Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:24502743-24502856 | Rare:35 | ||||
chr1:24642890-24643355 | Common:2; Rare:151 | ||||
chr1:24745293-24745620 | Common:2; Rare:115 | ||||
chr1:25232428-25232654 | Rare:91 | ||||
chr1:25247392-25247611 | Common:2; Rare:84 | ||||
chr1:25337773-25337999 | Rare:28 | ||||
chr1:25338038-25338484 | Common:2; Rare:128 | ||||
chr1:25819855-25820032 | Common:4; Rare:55 | ||||
chr1:25859447-25859555 | Rare:31 | ||||
chr1:26279791-26280204 | Common:1; Rare:212 | ||||
chr1:26432091-26432445 | Common:5; Rare:93; Clinvar:2; Clinvar (benign):1 | ||||
chr1:26695576-26695752 | Rare:61 | ||||
chr1:26695914-26696047 | Rare:40 | ||||
chr1:26787706-26788004 | Common:3; Rare:96; Clinvar:2; Clinvar (benign):2 | ||||
chr1:26788069-26788227 | Rare:41 |