| ID: 127460370 | H3K4me1 hESC enhancer GRCh37_chr8:131081877-131082759 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (130069631..130070513) | | |
| ID: 127460369 | H3K4me1 hESC enhancer GRCh37_chr8:131054337-131055152 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (130042091..130042906) | | |
| ID: 127460368 | H3K4me1 hESC enhancer GRCh37_chr8:131005193-131005693 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (129992947..129993447) | | |
| ID: 127460367 | H3K4me1 hESC enhancer GRCh37_chr8:130971367-130971867 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (129959121..129959621) | | |
| ID: 127460366 | H3K4me1 hESC enhancer GRCh37_chr8:130957594-130958094 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (129945348..129945848) | | |
| ID: 127460365 | H3K4me1 hESC enhancer GRCh37_chr8:130899605-130900116 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (129887359..129887870) | | |
| ID: 127460364 | H3K4me1 hESC enhancer GRCh37_chr8:130899091-130899604 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (129886845..129887358) | | |
| ID: 127460363 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr8:130882553-130883105 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (129870307..129870859) | | |
| ID: 127460362 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr8:130881998-130882552 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (129869752..129870306) | | |
| ID: 127460361 | OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr8:130845691-130846502 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (129833445..129834256) | | |
| ID: 127460360 | OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr8:130844878-130845690 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (129832632..129833444) | | |
| ID: 124902025 | uncharacterized LOC124902025 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (129988046..130011320, complement) | | |
| ID: 124900265 | uncharacterized LOC124900265 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (129868590..129868716, complement) | | |
| ID: 124188235 | Sharpr-MPRA regulatory region 603 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (129934063..129934671) | | |
| ID: 106481946 | RNA, U6 small nuclear 1255, pseudogene [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (130069573..130069652, complement) | | |
| ID: 106479093 | RNA, U7 small nuclear 181 pseudogene [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (130004528..130004601, complement) | | |
| ID: 100847051 | microRNA 5194 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (130008334..130008453, complement) | mir-5194 | |
| ID: 100131958 | ribosomal protein L15 pseudogene 12 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (129864469..129865363) | RPL15_6_949 | |
| ID: 51571 | CYFIP related Rac1 interactor B [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (129839593..130017129, complement) | BM-009, CYRI, CYRI-B, FAM49B, L1 | 617978 |
| ID: 50807 | ArfGAP with SH3 domain, ankyrin repeat and PH domain 1 [Homo sapiens (human)] | Chromosome 8, NC_000008.11 (130052104..130443674, complement) | AMAP1, CENTB4, DDEF1, PAG2, PAP, ZG14P | 605953 |