| ID: 132090715 | Neanderthal introgressed variant-containing enhancer experimental_75023 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (156485019..156485188) | | |
| ID: 132089057 | Neanderthal introgressed variant-containing enhancer experimental_75074 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (156794892..156795061) | | |
| ID: 132089056 | Neanderthal introgressed variant-containing enhancer experimental_75051 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (156513072..156513241) | | |
| ID: 132089055 | Neanderthal introgressed variant-containing enhancer experimental_74995 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (156391776..156391945) | | |
| ID: 127401801 | H3K27ac hESC enhancer GRCh37_chr4:157920440-157921219 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (156999288..157000067) | | |
| ID: 127401800 | H3K27ac hESC enhancer GRCh37_chr4:157919659-157920439 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (156998507..156999287) | | |
| ID: 127401799 | H3K4me1 hESC enhancer GRCh37_chr4:157892738-157893238 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (156971586..156972086) | | |
| ID: 127401798 | H3K4me1 hESC enhancer GRCh37_chr4:157718592-157719092 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (156797440..156797940) | | |
| ID: 127401797 | NANOG hESC enhancer GRCh37_chr4:157555350-157555851 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (156634198..156634699) | | |
| ID: 127401796 | OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr4:157526591-157527116 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (156605439..156605964) | | |
| ID: 127401795 | NANOG-H3K27ac hESC enhancer GRCh37_chr4:157521211-157521946 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (156600059..156600794) | | |
| ID: 127401794 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr4:157426362-157427068 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (156505210..156505916) | | |
| ID: 126807199 | BRD4-independent group 4 enhancer GRCh37_chr4:157519367-157520566 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (156598215..156599414) | | |
| ID: 123493222 | Sharpr-MPRA regulatory region 1911 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (157073257..157073551) | | |
| ID: 112939921 | NANOG hESC enhancer GRCh37_chr4:157692390-157692891 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (156771238..156771739) | | |
| ID: 107986322 | long intergenic non-protein coding RNA 2272 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (156623025..156642503, complement) | | |
| ID: 106479602 | ribonuclease P RNA component H1, 3 pseudogene [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (156986372..156986693, complement) | | |
| ID: 105377508 | uncharacterized LOC105377508 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (156308598..156330601, complement) | | |
| ID: 56034 | platelet derived growth factor C [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (156760454..156971799, complement) | FALLOTEIN, SCDGF | 608452 |
| ID: 2743 | glycine receptor beta [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (157076150..157172090) | HKPX2 | 138492 |