Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:14953994-14954195 | Rare:71 | ||||
chr10:15097301-15097381 | Common:1; Rare:39 | ||||
chr10:15860323-15860562 | Common:1; Rare:66 | ||||
chr10:16817328-16817744 | Common:5; Rare:149 | ||||
chr10:17228607-17228675 | Common:1; Rare:22 | ||||
chr10:17228882-17229399 | Common:6; Rare:117 | ||||
chr10:17643875-17644300 | Common:2; Rare:130 | ||||
chr10:17951791-17951971 | Rare:25 | ||||
chr10:18340572-18340685 | Common:3; Rare:28; Clinvar (benign):2 | ||||
chr10:18651564-18651773 | Common:1; Rare:89 | ||||
chr10:18659230-18659625 | Common:2; Rare:136 | ||||
chr10:19816106-19816472 | Common:5; Rare:78 | ||||
chr10:21173832-21173955 | Common:3; Rare:39; Clinvar (benign):1 | ||||
chr10:22316231-22316456 | Common:1; Rare:103 | ||||
chr10:22325513-22325671 | Rare:69 |