| ID: 127893626 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr20:48505417-48506228 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (49888880..49889691) | | |
| ID: 127893625 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr20:48504605-48505416 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (49888068..49888879) | | |
| ID: 127893624 | H3K4me1 hESC enhancer GRCh37_chr20:48453109-48453609 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (49836572..49837072) | | |
| ID: 127893623 | H3K4me1 hESC enhancer GRCh37_chr20:48452608-48453108 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (49836071..49836571) | | |
| ID: 127893622 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr20:48400170-48400693 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (49783633..49784156) | | |
| ID: 125387286 | Sharpr-MPRA regulatory region 9917 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (49928692..49928986) | | |
| ID: 121853012 | Sharpr-MPRA regulatory region 10189 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (49909912..49910206) | | |
| ID: 113219455 | microRNA 12122 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (49863859..49863953) | | |
| ID: 106479972 | RNA, U6 small nuclear 919, pseudogene [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (49794811..49794914) | | |
| ID: 105372653 | uncharacterized LOC105372653 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (49915822..49928821) | | |
| ID: 100421569 | GLYR1 pseudogene 1 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (49829102..49831365) | | |
| ID: 100151669 | RNA, U7 small nuclear 72 pseudogene [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (49827996..49828052) | U7.72 | |
| ID: 23315 | solute carrier family 9 member A8 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (49812828..49892242) | NHE-8, NHE8 | 612730 |
| ID: 9825 | spermatogenesis associated 2 [Homo sapiens (human)] | Chromosome 20, NC_000020.11 (49903391..49915529, complement) | PD1, PPP1R145, tamo | 607662 |