| ID: 132090606 | Neanderthal introgressed variant-containing enhancer experimental_61302 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (63881641..63881810) | | |
| ID: 132090605 | Neanderthal introgressed variant-containing enhancer experimental_61295 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (63880930..63881099) | | |
| ID: 132090604 | Neanderthal introgressed variant-containing enhancer experimental_61287 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (63878169..63878338) | | |
| ID: 130066405 | ATAC-STARR-seq lymphoblastoid silent region 13191 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (63894968..63895207) | | |
| ID: 130066404 | ATAC-STARR-seq lymphoblastoid active region 18254 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (63863998..63864227) | | |
| ID: 129664683 | ReSE screen-validated silencer GRCh37_chr20:62517585-62517755 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (63886232..63886402) | | |
| ID: 127894297 | H3K4me1 hESC enhancer GRCh37_chr20:62573671-62574384 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (63942318..63943031) | | |
| ID: 127894296 | H3K4me1 hESC enhancer GRCh37_chr20:62563589-62564090 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (63932236..63932737) | | |
| ID: 127894295 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr20:62551107-62551809 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (63919754..63920456) | | |
| ID: 127894294 | H3K4me1 hESC enhancer GRCh37_chr20:62543630-62544130 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (63912277..63912777) | | |
| ID: 127894293 | H3K4me1 hESC enhancer GRCh37_chr20:62541709-62542208 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (63910356..63910855) | | |
| ID: 127894292 | H3K4me1 hESC enhancer GRCh37_chr20:62525794-62526321 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (63894339..63894968) | | |
| ID: 127894291 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr20:62497355-62498074 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (63866002..63866721) | | |
| ID: 126863088 | BRD4-independent group 4 enhancer GRCh37_chr20:62495674-62496873 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (63864321..63865520) | | |
| ID: 124904951 | uncharacterized LOC124904951 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (63917759..63920435) | | |
| ID: 112268269 | uncharacterized LOC112268269 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (63861215..63865073, complement) | | |
| ID: 106480194 | RNA, U1 small nuclear 134, pseudogene [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (63908955..63909119) | | |
| ID: 103504732 | microRNA 941-5 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (63919868..63919939) | | |
| ID: 100302137 | microRNA 1914 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (63941465..63941544, complement) | MIRN1914, hsa-mir-1914 | |
| ID: 100126352 | microRNA 941-3 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (63919561..63919632) | MIRN941-3 | |