Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:30968695-30968802 | Rare:17 | ||||
chr17:30970584-30970699 | Rare:24 | ||||
chr17:30970822-30970914 | Common:2; Rare:25 | ||||
chr17:32350012-32350200 | Rare:97 | ||||
chr17:34980315-34980589 | Common:4; Rare:78 | ||||
chr17:35242901-35243090 | Rare:62 | ||||
chr17:35373580-35373751 | Common:3; Rare:38 | ||||
chr17:35578545-35578769 | Common:2; Rare:57; Clinvar (benign):1 | ||||
chr17:35587184-35587541 | Rare:90 | ||||
chr17:36195845-36195967 | Common:2; Rare:6 | ||||
chr17:36196751-36197052 | Common:1; Rare:33 | ||||
chr17:36534816-36535039 | Common:3; Rare:102 | ||||
chr17:36544789-36544976 | Common:3; Rare:60 | ||||
chr17:37406831-37406893 | Rare:21 | ||||
chr17:38296965-38297181 | Common:4; Rare:62 |