Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:24745228-24745625 | Common:2; Rare:138 | ||||
chr1:25232442-25232657 | Rare:87 | ||||
chr1:25247419-25247661 | Common:3; Rare:96 | ||||
chr1:25338214-25338453 | Common:1; Rare:82 | ||||
chr1:25819878-25820219 | Common:4; Rare:101 | ||||
chr1:25859370-25859580 | Common:2; Rare:85 | ||||
chr1:25906392-25906580 | Rare:74 | ||||
chr1:26021623-26021779 | Common:1; Rare:23 | ||||
chr1:26067587-26067817 | Common:2; Rare:33 | ||||
chr1:26257299-26257538 | Common:4; Rare:42 | ||||
chr1:26279934-26280162 | Rare:127 | ||||
chr1:26432100-26432443 | Common:5; Rare:93; Clinvar:2; Clinvar (benign):1 | ||||
chr1:26472143-26472550 | Common:5; Rare:133 | ||||
chr1:26695847-26696047 | Rare:66 | ||||
chr1:26787865-26788207 | Common:3; Rare:94; Clinvar:2; Clinvar (benign):2 |