Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:24922801-24923032 | Common:1; Rare:69; Clinvar:1 | ||||
chr13:25301514-25301694 | Common:1; Rare:76 | ||||
chr13:26221798-26221923 | Rare:33 | ||||
chr13:27251235-27251626 | Common:8; Rare:121 | ||||
chr13:27424507-27424732 | Common:3; Rare:74 | ||||
chr13:27450119-27450230 | Common:3; Rare:33 | ||||
chr13:28659082-28659180 | Rare:44; Clinvar (pathogenic):1 | ||||
chr13:30306813-30307181 | Common:7; Rare:96 | ||||
chr13:30465784-30466134 | Common:1; Rare:108 | ||||
chr13:30617474-30617993 | Common:1; Rare:168 | ||||
chr13:32315445-32315536 | Rare:29; Clinvar:1; Clinvar (benign):1 | ||||
chr13:32538737-32538977 | Common:1; Rare:58 | ||||
chr13:33285683-33285880 | Rare:41 | ||||
chr13:33818017-33818190 | Common:1; Rare:75 | ||||
chr13:36297787-36297922 | Rare:49 |