| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:34961404-34961575 | Common:1; Rare:82 | ||||
| chr17:34980455-34980597 | Common:4; Rare:42 | ||||
| chr17:35242901-35243130 | Rare:79 | ||||
| chr17:35373609-35373778 | Common:3; Rare:34 | ||||
| chr17:35578545-35578707 | Common:1; Rare:43; Clinvar (benign):1 | ||||
| chr17:35795604-35795731 | Rare:29 | ||||
| chr17:36486496-36486716 | Common:2; Rare:83 | ||||
| chr17:36534852-36535020 | Common:2; Rare:77 | ||||
| chr17:36544789-36544968 | Common:3; Rare:58 | ||||
| chr17:36601491-36601616 | Rare:38 | ||||
| chr17:37406762-37406929 | Rare:71 | ||||
| chr17:37491418-37491554 | Common:2; Rare:35 | ||||
| chr17:38428294-38428488 | Common:8; Rare:75 | ||||
| chr17:38705021-38705306 | Common:2; Rare:70 | ||||
| chr17:38706078-38706141 | Rare:26 |