| ID: 129389754 | MPRA-validated peak6401 silencer [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (14051911..14052111) | | |
| ID: 127408538 | NANOG hESC enhancer GRCh37_chr7:14104855-14105356 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (14065230..14065731) | | |
| ID: 127408537 | NANOG-H3K27ac hESC enhancer GRCh37_chr7:14030811-14031312 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (13991186..13991687) | | |
| ID: 127408536 | OCT4-NANOG hESC enhancer GRCh37_chr7:14024671-14025465 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (13985046..13985840) | | |
| ID: 127408535 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr7:13846329-13847091 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (13806704..13807466) | | |
| ID: 127408534 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr7:13845564-13846328 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (13805939..13806703) | | |
| ID: 127408533 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr7:13805522-13806099 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (13765897..13766474) | | |
| ID: 127408532 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr7:13804943-13805521 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (13765318..13765896) | | |
| ID: 126859947 | P300/CBP strongly-dependent group 1 enhancer GRCh37_chr7:13818290-13819489 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (13778665..13779864) | | |
| ID: 105375162 | uncharacterized LOC105375162 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (14051127..14061685) | | |
| ID: 105375161 | uncharacterized LOC105375161 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (13712690..13750538) | | |
| ID: 100423044 | solute carrier family 34 member 2 pseudogene [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (14053009..14054039) | | |
| ID: 100270846 | ribosomal protein L6 pseudogene 21 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (14070501..14071399, complement) | RPL6_5_786 | |
| ID: 646161 | ribosomal protein L26 pseudogene 21 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (13871823..13872556) | RPL26_11_785 | |
| ID: 2115 | ETS variant transcription factor 1 [Homo sapiens (human)] | Chromosome 7, NC_000007.14 (13891229..13991425, complement) | ER81 | 600541 |