Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr15:40807415-40807718 | Common:3; Rare:98 | ||||
chr15:40894200-40894477 | Rare:84 | ||||
chr15:41115982-41116044 | Rare:23 | ||||
chr15:41231206-41231446 | Rare:76; Clinvar (pathogenic):1 | ||||
chr15:41416969-41417213 | Common:3; Rare:111 | ||||
chr15:41621585-41621816 | Rare:57 | ||||
chr15:42273037-42273276 | Common:1; Rare:98 | ||||
chr15:42273312-42273481 | Common:1; Rare:73 | ||||
chr15:42273485-42273687 | Rare:59 | ||||
chr15:42273942-42274476 | Rare:120 | ||||
chr15:42490992-42491231 | Common:1; Rare:70 | ||||
chr15:42548711-42548875 | Common:2; Rare:90 | ||||
chr15:43330097-43330358 | Common:1; Rare:144 | ||||
chr15:43330546-43330781 | Common:1; Rare:80 | ||||
chr15:43371030-43371218 | Common:1; Rare:41 |