| ID: 130066887 | ATAC-STARR-seq lymphoblastoid active region 18607 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (46661506..46661555) | | |
| ID: 130066886 | ATAC-STARR-seq lymphoblastoid silent region 13425 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (46661296..46661405) | | |
| ID: 130066885 | ATAC-STARR-seq lymphoblastoid silent region 13424 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (46635543..46636092) | | |
| ID: 129391255 | MPRA-validated peak4433 silencer [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (46675984..46676184) | | |
| ID: 127895164 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr21:48087547-48088284 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (46667635..46668372) | | |
| ID: 127895163 | H3K4me1 hESC enhancer GRCh37_chr21:48061114-48061614 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (46641202..46641702) | | |
| ID: 127895162 | H3K27ac hESC enhancer GRCh37_chr21:48054684-48055354 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (46634772..46635442) | | |
| ID: 127895161 | H3K4me1 hESC enhancer GRCh37_chr21:48044299-48044799 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (46624387..46624887) | | |
| ID: 127895160 | H3K4me1 hESC enhancer GRCh37_chr21:48026033-48026534 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (46606120..46606621) | | |
| ID: 124905058 | uncharacterized LOC124905058 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (46667389..46673549) | | |
| ID: 106481303 | RNA, U6 small nuclear 396, pseudogene [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (46525618..46525722) | | |
| ID: 387492 | DSTN pseudogene 1 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (46653130..46654115, complement) | | |
| ID: 54029 | ribosomal protein L23a pseudogene 4 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (46690750..46691275) | RPL23A_42_1735 | |
| ID: 23181 | disco interacting protein 2 homolog A [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (46458891..46583871) | C21orf106, DIP2 | 607711 |
| ID: 6285 | S100 calcium binding protein B [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (46598604..46605082, complement) | NEF, S100, S100-B, S100beta | 176990 |
| ID: 3275 | protein arginine methyltransferase 2 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (46635674..46665124) | HRMT1L1 | 601961 |