| ID: 130066686 | ATAC-STARR-seq lymphoblastoid active region 18467 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (39349491..39349770) | | |
| ID: 130066685 | ATAC-STARR-seq lymphoblastoid silent region 13327 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (39348681..39349280) | | |
| ID: 130066684 | ATAC-STARR-seq lymphoblastoid silent region 13326 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (39313946..39314115) | | |
| ID: 129664730 | ReSE screen-validated silencer GRCh37_chr21:40731973-40732197 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (39360047..39360271) | | |
| ID: 129664729 | ReSE screen-validated silencer GRCh37_chr21:40723570-40723774 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (39351644..39351848) | | |
| ID: 127894674 | H3K4me1 hESC enhancer GRCh37_chr21:40704110-40704610 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (39332184..39332684) | | |
| ID: 127894673 | H3K4me1 hESC enhancer GRCh37_chr21:40687047-40687741 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (39315121..39315815) | | |
| ID: 127894672 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr21:40686351-40687046 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (39314425..39315120) | | |
| ID: 124905074 | small nucleolar RNA U13 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (39345351..39345457, complement) | | |
| ID: 105372804 | uncharacterized LOC105372804 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (39349974..39370894) | | |
| ID: 103091865 | BRWD1 antisense RNA 2 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (39313907..39314915) | BRWD1-IT2, C21orf87, NCRNA00257 | |
| ID: 100874093 | BRWD1 antisense RNA 1 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (39315707..39323218) | BRWD1-AS2, BRWD1-IT2, C21orf87, NCRNA00257 | |
| ID: 100420924 | ring finger protein 6 pseudogene 1 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (39373763..39374421, complement) | | |
| ID: 54014 | bromodomain and WD repeat domain containing 1 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (39184176..39321212, complement) | C21orf107, CILD51, DCAF19, N143, WDR9, WRD9 | 617824 |
| ID: 3150 | high mobility group nucleosome binding domain 1 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (39342315..39349088, complement) | HMG14 | 163920 |