ID: 130066438 | ATAC-STARR-seq lymphoblastoid silent region 13214 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (14572332..14572391) | | |
ID: 130066437 | ATAC-STARR-seq lymphoblastoid active region 18275 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (14544125..14544174) | | |
ID: 130066436 | ATAC-STARR-seq lymphoblastoid active region 18274 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (14542360..14542409) | | |
ID: 130066435 | ATAC-STARR-seq lymphoblastoid active region 18272 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (14415249..14415388) | | |
ID: 130066434 | ATAC-STARR-seq lymphoblastoid active region 18271 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (14383553..14383682) | | |
ID: 130066433 | ATAC-STARR-seq lymphoblastoid active region 18270 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (14382853..14383162) | | |
ID: 130066432 | ATAC-STARR-seq lymphoblastoid silent region 13213 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (14215974..14216203) | | |
ID: 129664697 | ReSE screen-validated silencer GRCh37_chr21:15821444-15821607 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (14449123..14449286) | | |
ID: 127894404 | OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr21:15653463-15654235 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (14281142..14281914) | | |
ID: 126653312 | P300/CBP strongly-dependent group 1 enhancer GRCh37_chr21:15905912-15907111 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (14533591..14534790) | | |
ID: 124905053 | uncharacterized LOC124905053 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (14477329..14538528) | | |
ID: 121853023 | Sharpr-MPRA regulatory region 5316 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (14578188..14578482) | | |
ID: 116309121 | CRISPRi-validated cis-regulatory element chr21.64 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (14454237..14454893) | | |
ID: 116309120 | CRISPRi-validated cis-regulatory element chr21.63 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (14452120..14452281) | | |
ID: 105369304 | uncharacterized LOC105369304 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (14382766..14393537) | | |
ID: 100874190 | SAMSN1 antisense RNA 1 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (14582202..14598303) | | |
ID: 150000 | ATP binding cassette subfamily C member 13 (pseudogene) [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (14273799..14301386) | ABCC13P, C21orf73, PRED6 | 608835 |
ID: 64092 | SAM domain, SH3 domain and nuclear localization signals 1 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (14485228..14659417, complement) | HACS1, NASH1, SASH2, SH3D6B, SLy2 | 607978 |
ID: 54033 | RNA binding motif protein 11 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (14216157..14228372) | | 617937 |
ID: 6782 | heat shock protein family A (Hsp70) member 13 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (14371115..14383146, complement) | STCH | 601100 |