Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:153608903-153608963 | Common:1; Rare:7 | ||||
chr1:153612956-153613177 | Common:1; Rare:41 | ||||
chr1:153627633-153627903 | Common:2; Rare:59 | ||||
chr1:153633984-153634166 | Common:1; Rare:56 | ||||
chr1:153634238-153634435 | Common:1; Rare:54 | ||||
chr1:153658561-153658791 | Common:2; Rare:72 | ||||
chr1:153664049-153664476 | Common:2; Rare:88 | ||||
chr1:153923088-153923385 | Common:1; Rare:83 | ||||
chr1:153963310-153963385 | Rare:18 | ||||
chr1:153963490-153963738 | Common:2; Rare:68 | ||||
chr1:153967301-153967528 | Common:1; Rare:47 | ||||
chr1:153967723-153967945 | Rare:39 | ||||
chr1:153977946-153978103 | Rare:38 | ||||
chr1:153990658-153990829 | Common:2; Rare:85 | ||||
chr1:154170401-154170706 | Rare:64; Clinvar (benign):1 |