| ID: 130066689 | ATAC-STARR-seq lymphoblastoid silent region 13328 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (39445689..39445948) | | |
| ID: 130066688 | ATAC-STARR-seq lymphoblastoid active region 18469 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (39388116..39388285) | | |
| ID: 130066687 | ATAC-STARR-seq lymphoblastoid active region 18468 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (39386091..39386140) | | |
| ID: 127894680 | NANOG hESC enhancer GRCh37_chr21:40931347-40931936 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (39559420..39560009) | | |
| ID: 127894679 | NANOG hESC enhancer GRCh37_chr21:40923594-40924095 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (39551667..39552168) | | |
| ID: 127894678 | OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr21:40909281-40910174 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (39537354..39538247) | | |
| ID: 127894677 | H3K27ac hESC enhancer GRCh37_chr21:40907492-40908386 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (39535565..39536459) | | |
| ID: 127894676 | H3K4me1 hESC enhancer GRCh37_chr21:40899605-40900600 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (39527678..39528673) | | |
| ID: 127894675 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr21:40823338-40823876 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (39451412..39451950) | | |
| ID: 121627923 | Sharpr-MPRA regulatory region 12540 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (39430483..39430777) | | |
| ID: 106865373 | GET1-SH3BGR readthrough [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (39380326..39515504) | WRB-SH3BGR | |
| ID: 102466972 | microRNA 6508 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (39447010..39447069) | hsa-mir-6508 | |
| ID: 100431168 | MYL6 pseudogene 2 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (39488309..39488955) | | |
| ID: 100420924 | ring finger protein 6 pseudogene 1 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (39373763..39374421, complement) | | |
| ID: 729056 | JCAD pseudogene 1 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (39526359..39529810) | | |
| ID: 692146 | ribosomal protein S26 pseudogene 4 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (39491476..39491918, complement) | RPS26_32_1733 | |
| ID: 150082 | lebercilin LCA5 like [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (39405728..39445778, complement) | C21orf13 | |
| ID: 114041 | B3GALT5 antisense RNA 1 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (39597147..39612822, complement) | C21orf88 | |
| ID: 7485 | guided entry of tail-anchored proteins factor 1 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (39380326..39428528) | CHD5, WRB | 602915 |
| ID: 6450 | SH3 domain binding glutamate rich protein [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (39445865..39515506) | 21-GARP | 602230 |