Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:18317525-18317532 | Rare:2 | ||||
chr17:30804055-30804276 | Rare:39 | ||||
chr17:35567878-35568139 | Common:2; Rare:78 | ||||
chr17:38738765-38738933 | Rare:57 | ||||
chr17:38739085-38739172 | Rare:26 | ||||
chr17:38739220-38739418 | Common:2; Rare:41 | ||||
chr17:40444782-40444826 | Common:1; Rare:7 | ||||
chr17:41983573-41983691 | Rare:26 | ||||
chr17:42337546-42337861 | Common:3; Rare:73; Clinvar:1; Clinvar (benign):2 | ||||
chr17:42422614-42422888 | Rare:112; Clinvar:2; Clinvar (pathogenic):2 | ||||
chr17:42851695-42851902 | Common:1; Rare:92 | ||||
chr17:45149055-45149373 | Common:3; Rare:105 | ||||
chr17:45149882-45150116 | Rare:45 | ||||
chr17:45150259-45150273 | Rare:4 | ||||
chr17:47100248-47100384 | Rare:38 |