Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:106844744-106844906 | Rare:36 | ||||
chr14:106845857-106846045 | Common:1; Rare:46 | ||||
chr15:25375683-25375884 | Common:1; Rare:35; Clinvar:1; Clinvar (benign):1 | ||||
chr15:34334055-34334208 | Common:1; Rare:41 | ||||
chr15:40325478-40325712 | Common:1; Rare:29 | ||||
chr15:44717267-44717483 | Common:2; Rare:35 | ||||
chr15:44726773-44727072 | Common:1; Rare:41 | ||||
chr15:59688026-59688113 | Rare:16 | ||||
chr15:65132913-65133104 | Rare:82 | ||||
chr15:67091264-67091443 | Rare:41 | ||||
chr15:71165480-71165709 | Common:1; Rare:35 | ||||
chr15:72759988-72760087 | Rare:18 | ||||
chr15:73927695-73927846 | Common:1; Rare:45 | ||||
chr15:74490260-74490398 | Common:1; Rare:21 | ||||
chr15:75738604-75738823 | Common:3; Rare:67 |