Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:17487142-17487385 | Common:3; Rare:76 | ||||
chr17:17836186-17836418 | Common:3; Rare:63 | ||||
chr17:19446875-19446992 | Common:1; Rare:27 | ||||
chr17:20321079-20321182 | Rare:27 | ||||
chr17:21612602-21612897 | Rare:81 | ||||
chr17:28227815-28227930 | Rare:38 | ||||
chr17:30731412-30731672 | Common:2; Rare:67 | ||||
chr17:31008536-31008630 | Common:2; Rare:23 | ||||
chr17:36483086-36483213 | Common:2; Rare:33 | ||||
chr17:38702211-38702479 | Common:1; Rare:86 | ||||
chr17:39726637-39726939 | Rare:77 | ||||
chr17:40093985-40094262 | Rare:72 | ||||
chr17:41515883-41516211 | Rare:122 | ||||
chr17:41586317-41586408 | Rare:23; Clinvar:1 | ||||
chr17:41755889-41756197 | Common:2; Rare:66; Clinvar:2; Clinvar (benign):3 |