Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:33080985-33081157 | Common:2; Rare:39 | ||||
chr1:33472384-33472668 | Rare:65 | ||||
chr1:34985292-34985393 | Common:1; Rare:37 | ||||
chr1:35079337-35079396 | Common:1; Rare:21 | ||||
chr1:35268631-35269033 | Rare:142 | ||||
chr1:35557360-35557442 | Rare:20 | ||||
chr1:35557597-35557845 | Common:2; Rare:94 | ||||
chr1:35641486-35641629 | Rare:30 | ||||
chr1:35930629-35930774 | Rare:44 | ||||
chr1:36450422-36450595 | Common:1; Rare:54 | ||||
chr1:36464189-36464468 | Common:2; Rare:81 | ||||
chr1:36475573-36475840 | Common:1; Rare:70; Clinvar:4; Clinvar (benign):2 | ||||
chr1:37474373-37474585 | Common:1; Rare:83 | ||||
chr1:37692177-37692496 | Common:3; Rare:68 | ||||
chr1:37859569-37859836 | Common:4; Rare:96 |