| ID: 127457012 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr7:95570872-95571471 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (95941560..95942159) | | |
| ID: 127457011 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr7:95570271-95570871 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (95940959..95941559) | | |
| ID: 127457010 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr7:95466378-95466994 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (95837066..95837682) | | |
| ID: 126860115 | CDK7 strongly-dependent group 2 enhancer GRCh37_chr7:95405912-95407111 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (95776600..95777799) | | |
| ID: 124901701 | uncharacterized LOC124901701 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (96049982..96058256) | | |
| ID: 124901700 | uncharacterized LOC124901700 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (96014948..96033159, complement) | | |
| ID: 121740691 | Sharpr-MPRA regulatory region 1852 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (95793697..95793991) | | |
| ID: 114827816 | eDlx#27 enhancer in SHFM1 region [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (95902183..95902774) | | |
| ID: 114827815 | eDlx#26 enhancer in SHFM1 region [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (95953351..95954041) | | |
| ID: 114827814 | eDlx#24 enhancer in SHFM1 region [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (96067218..96067717) | | |
| ID: 110121296 | eDlx#23 enhancer in SHFM1 region [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (96136568..96137161) | | |
| ID: 110121293 | eExon 17 DLX5/6 limb enhancer [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (96096967..96098368) | | |
| ID: 110121292 | eExon 15 DLX5/6 limb enhancer [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (96075777..96076384) | | |
| ID: 107986746 | uncharacterized LOC107986746 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (95645859..95654617) | | |
| ID: 105375409 | uncharacterized LOC105375409 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (95660317..95719901) | | |
| ID: 360173 | CYCS pseudogene 18 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (96127827..96128062, complement) | HCP18 | |
| ID: 10165 | solute carrier family 25 member 13 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (96120220..96322098, complement) | ARALAR2, CITRIN, CTLN2, NICCD | 603859 |
| ID: 1780 | dynein cytoplasmic 1 intermediate chain 1 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (95772554..96110322) | DNCI1, DNCIC1 | 603772 |