| ID: 132089057 | Neanderthal introgressed variant-containing enhancer experimental_75074 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (156794892..156795061) | | |
| 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: 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: 106481365 | RNA, U6 small nuclear 582, pseudogene [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (157201563..157201667, complement) | | |
| ID: 106479602 | ribonuclease P RNA component H1, 3 pseudogene [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (156986372..156986693, complement) | | |
| ID: 391707 | chromatin accessibility complex subunit 1 pseudogene [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (157204267..157204864, 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 |