ID: 130066580 | ATAC-STARR-seq lymphoblastoid active region 18393 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (34047171..34047220) | | |
ID: 130066579 | ATAC-STARR-seq lymphoblastoid active region 18392 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (34032209..34032308) | | |
ID: 130066578 | ATAC-STARR-seq lymphoblastoid active region 18391 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (34020481..34020660) | | |
ID: 130066577 | ATAC-STARR-seq lymphoblastoid active region 18390 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (34018848..34019007) | | |
ID: 130066576 | ATAC-STARR-seq lymphoblastoid active region 18389 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (34018261..34018450) | | |
ID: 130066575 | ATAC-STARR-seq lymphoblastoid active region 18388 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (33984057..33984226) | | |
ID: 130066574 | ATAC-STARR-seq lymphoblastoid active region 18386 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (33948731..33948790) | | |
ID: 129664719 | ReSE screen-validated silencer GRCh37_chr21:35440377-35440478 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (34068077..34068178) | | |
ID: 127894578 | H3K27ac hESC enhancer GRCh37_chr21:35445789-35446739 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (34073026..34074439) | | |
ID: 127894577 | H3K4me1 hESC enhancer GRCh37_chr21:35439104-35439620 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (34066804..34067320) | | |
ID: 127894576 | OCT4-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr21:35303079-35303720 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (33930775..33931416) | | |
ID: 126653353 | MED14-independent group 3 enhancer GRCh37_chr21:35409658-35410857 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (34037358..34038557) | | |
ID: 126653352 | P300/CBP strongly-dependent group 1 enhancer GRCh37_chr21:35348180-35349379 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (33975879..33977078) | | |
ID: 125418064 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr21:35343981-35344670 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (33971680..33972369) | | |
ID: 125418063 | P300/CBP strongly-dependent group 1 enhancer GRCh37_chr21:35319651-35320850 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (33947347..33948546) | | |
ID: 124905013 | uncharacterized LOC124905013 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (33967101..33968464, complement) | | |
ID: 106479491 | RNA, 7SL, cytoplasmic 740, pseudogene [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (33918995..33919338, complement) | | |
ID: 105372790 | uncharacterized LOC105372790 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (33982836..34051948) | | |
ID: 105372789 | uncharacterized LOC105372789 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (34015945..34019036, complement) | | |
ID: 101928126 | uncharacterized LOC101928126 [Homo sapiens (human)] | Chromosome 21, NC_000021.9 (33976382..33977691) | | |