| ID: 130066502 | ATAC-STARR-seq lymphoblastoid active region 18322 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (28745611..28745700) | | |
| ID: 129391240 | MPRA-validated peak4395 silencer [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (28789513..28789713) | | |
| ID: 127894494 | OCT4-H3K27ac hESC enhancer GRCh37_chr21:30257548-30258106 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (28885221..28885784) | | |
| ID: 127894493 | OCT4-H3K27ac hESC enhancer GRCh37_chr21:30256988-30257547 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (28884666..28885225) | | |
| ID: 127894492 | H3K4me1 hESC enhancer GRCh37_chr21:30229227-30229726 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (28856905..28857404) | | |
| ID: 127894491 | H3K4me1 hESC enhancer GRCh37_chr21:30228725-30229226 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (28856403..28856904) | | |
| ID: 127894490 | OCT4-NANOG hESC enhancer GRCh37_chr21:29697851-29698465 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (28325532..28326146) | | |
| ID: 126653335 | MED14-independent group 3 enhancer GRCh37_chr21:30206496-30207695 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (28834174..28835373) | | |
| ID: 125418055 | Sharpr-MPRA regulatory region 7516 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (28742607..28742901) | | |
| ID: 124905067 | uncharacterized LOC124905067 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (28743192..28743291) | | |
| ID: 101927973 | long intergenic non-protein coding RNA 1695 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (28116094..28228667, complement) | | |
| ID: 391276 | THUMP domain containing 1 pseudogene 1 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (28901566..28903768, complement) | | |
| ID: 284825 | long intergenic non-protein coding RNA 1697 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (28048414..28137609) | | |
| ID: 118421 | long intergenic non-protein coding RNA 161 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (28539318..28540355) | C21orf100, Linc-USP16, NCRNA00161 | |
| ID: 54047 | heat shock protein family D (Hsp60) member 1 pseudogene 7 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (28886986..28889334, complement) | HSPD1-22P, HSPDP7 | |
| ID: 29104 | N-6 adenine-specific DNA methyltransferase 1 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (28575598..28885367, complement) | C21orf127, HEMK2, KMT9, MTQ2, N6AMT, PRED28, PrmC, m.HsaHemK2P | 614553 |