| ID: 132089076 | Neanderthal introgressed variant-containing enhancer experimental_75752 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (164727635..164727804) | | |
| ID: 129389246 | MPRA-validated peak5144 silencer [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (164459724..164459924) | | |
| ID: 127401859 | H3K4me1 hESC enhancer GRCh37_chr4:165597429-165597929 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (164676277..164676777) | | |
| ID: 127401858 | H3K4me1 hESC enhancer GRCh37_chr4:165304399-165304900 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (164383247..164383748) | | |
| ID: 127401857 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr4:165272175-165272792 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (164351023..164351640) | | |
| ID: 127401856 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr4:165162965-165163475 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (164241813..164242323) | | |
| ID: 127401855 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr4:165162454-165162964 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (164241302..164241812) | | |
| ID: 127401854 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr4:165063227-165063816 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (164142075..164142664) | | |
| ID: 127401853 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr4:165062637-165063226 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (164141485..164142074) | | |
| ID: 127401852 | H3K4me1 hESC enhancer GRCh37_chr4:164871577-164872076 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (163950425..163950924) | | |
| ID: 106481268 | RNA, U6 small nuclear 284, pseudogene [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (164620732..164620837) | | |
| ID: 100288073 | heat shock protein family A (Hsp70) member 5 pseudogene [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (164188233..164190633) | | |
| ID: 100133261 | CHORDC1 pseudogene 3 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (164725576..164727661) | | |
| ID: 646954 | YWHAQ pseudogene 4 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (163932520..163933441) | | |
| ID: 55016 | membrane associated ring-CH-type finger 1 [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (163524298..164384019, complement) | MARCH-I, MARCH1, RNF171 | 613331 |
| ID: 23520 | acidic nuclear phosphoprotein 32 family member C, pseudogene [Homo sapiens (human)] | Chromosome 4, NC_000004.12 (164196840..164197821, complement) | ANP32C, PP32R1 | 606877 |