Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:21140259-21140615 | Rare:150 | ||||
chr13:21176557-21176704 | Rare:76 | ||||
chr13:23579252-23579383 | Common:2; Rare:37 | ||||
chr13:24512739-24512843 | Common:3; Rare:31 | ||||
chr13:24922810-24923145 | Common:2; Rare:116; Clinvar:1 | ||||
chr13:25301312-25301696 | Common:2; Rare:119 | ||||
chr13:26221791-26221972 | Rare:51 | ||||
chr13:26222259-26222391 | Common:2; Rare:38 | ||||
chr13:27251235-27251626 | Common:8; Rare:121 | ||||
chr13:27450062-27450215 | Common:3; Rare:47 | ||||
chr13:27450529-27450648 | Common:2; Rare:48 | ||||
chr13:28659071-28659184 | Rare:48; Clinvar (pathogenic):1 | ||||
chr13:30306968-30307234 | Common:5; Rare:73 | ||||
chr13:30465824-30466059 | Common:1; Rare:79 | ||||
chr13:30617255-30617392 | Rare:29 |