| ID: 127898550 | H3K27ac hESC enhancer GRCh37_chrX:154255797-154256700 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (155027522..155028425) | | |
| ID: 126863349 | P300/CBP strongly-dependent group 1 enhancer GRCh37_chrX:154195537-154196736 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (154967262..154968461) | | |
| ID: 125467795 | Sharpr-MPRA regulatory region 4209 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (155007074..155007368) | | |
| ID: 121627986 | H3K4me1 hESC enhancer GRCh37_chrX:154285543-154286044 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (155057268..155057769) | | |
| ID: 106146150 | int22h-1 recombination region [Homo sapiens (human)] | Chromosome X, NC_000023.11 (154880819..154890330) | | |
| ID: 106146143 | int1h-1 recombination region [Homo sapiens (human)] | Chromosome X, NC_000023.11 (155006107..155007182) | | |
| ID: 100419792 | ZNF622 pseudogene 1 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (154919433..154920182, complement) | | |
| ID: 100302111 | microRNA 1184-1 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (154887360..154887458, complement) | MIR1184, MIRN1184, hsa-mir-1184, hsa-mir-1184-1 | |
| ID: 100132963 | small integral membrane protein 9 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (154823348..154834662, complement) | CXorf68 | |
| ID: 728776 | high mobility group nucleosome binding domain 1 pseudogene 37 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (154816305..154817521, complement) | | |
| ID: 553820 | eukaryotic translation elongation factor 1 alpha 1 pseudogene 31 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (154908824..154919212, complement) | | |
| ID: 474382 | H2A.B variant histone 1 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (154884972..154885558) | H2A.B, H2A.B.2, H2A.Bbd, H2AFB1 | 301037 |
| ID: 65991 | FUN14 domain containing 2 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (155026844..155060304) | DC44, HCBP6, HCC3, PD03104 | 301042 |
| ID: 8263 | coagulation factor VIII associated 1 [Homo sapiens (human)] | Chromosome X, NC_000023.11 (154886355..154888061) | DXS522E, F8A, HAP40 | 305423 |
| ID: 2157 | coagulation factor VIII [Homo sapiens (human)] | Chromosome X, NC_000023.11 (154835792..155022723, complement) | AHF, DXS1253EB, F8C, FVIII, HEMA, THPH13, F8 | 300841 |