| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:43006963-43007084 | Rare:31 | ||||
| chr17:43021936-43022023 | Common:1; Rare:29 | ||||
| chr17:43022031-43022188 | Common:1; Rare:55 | ||||
| chr17:43022290-43022503 | Rare:62 | ||||
| chr17:43024617-43024671 | Common:1; Rare:8 | ||||
| chr17:43025055-43025268 | Rare:48 | ||||
| chr17:43125058-43125142 | Rare:19; Clinvar (benign):1 | ||||
| chr17:43125321-43125722 | Rare:102; Clinvar:3; Clinvar (benign):3 | ||||
| chr17:43169751-43169919 | Common:4; Rare:27 | ||||
| chr17:43170019-43170135 | Rare:21 | ||||
| chr17:43170151-43170570 | Common:3; Rare:90 | ||||
| chr17:43170703-43170719 | Rare:4 | ||||
| chr17:43170904-43171365 | Common:1; Rare:150 | ||||
| chr17:43171451-43171545 | Rare:16 | ||||
| chr17:43171547-43171636 | Rare:14 |