| ID: 130065570 | ATAC-STARR-seq lymphoblastoid active region 17662 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (25196708..25196857) | | |
| ID: 130065569 | ATAC-STARR-seq lymphoblastoid active region 17661 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (25196258..25196327) | | |
| ID: 130065568 | ATAC-STARR-seq lymphoblastoid silent region 12741 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (25195548..25195967) | | |
| ID: 130065567 | ATAC-STARR-seq lymphoblastoid active region 17660 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (25195168..25195407) | | |
| ID: 127892842 | H3K4me1 hESC enhancer GRCh37_chr20:25085805-25086741 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (25105169..25106105) | | |
| ID: 127892841 | H3K4me1 hESC enhancer GRCh37_chr20:25064664-25065269 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (25084028..25084633) | | |
| ID: 127892840 | H3K4me1 hESC enhancer GRCh37_chr20:25064059-25064663 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (25083423..25084027) | | |
| ID: 127892839 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr20:25062766-25063295 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (25082130..25082659) | | |
| ID: 127892838 | OCT4-NANOG hESC enhancer GRCh37_chr20:25052223-25052743 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (25071587..25072107) | | |
| ID: 112694695 | Sharpr-MPRA regulatory region 10160 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (25173973..25174267) | | |
| ID: 101926889 | uncharacterized LOC101926889 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (25184672..25196892, complement) | | |
| ID: 100128078 | NIPAL1 pseudogene 1 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (25160905..25162185, complement) | | |
| ID: 391239 | VTCN1 pseudogene 1 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (25099043..25100125) | | |
| ID: 284798 | uncharacterized LOC284798 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (25140798..25148790, complement) | | |
| ID: 30813 | visual system homeobox 1 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (25070880..25082141, complement) | CAASDS, KTCN, KTCN1, PPCD, PPCD1, PPD, RINX | 605020 |
| ID: 955 | ectonucleoside triphosphate diphosphohydrolase 6 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (25195712..25228075) | CD39L2, IL-6SAG, IL6ST2, NTPDase-6, dJ738P15.3 | 603160 |