| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:31901624-31901786 | Common:2; Rare:55 | ||||
| chr17:32142341-32142714 | Common:8; Rare:150 | ||||
| chr17:32350026-32350204 | Rare:98 | ||||
| chr17:32444202-32444523 | Common:2; Rare:107 | ||||
| chr17:34156725-34156886 | Rare:22 | ||||
| chr17:34961423-34961589 | Common:1; Rare:85 | ||||
| chr17:34980411-34980604 | Common:4; Rare:57 | ||||
| chr17:35119814-35119919 | Rare:39; Clinvar:2; Clinvar (benign):1 | ||||
| chr17:35242901-35243081 | Rare:59 | ||||
| chr17:35578478-35578721 | Common:1; Rare:62; Clinvar:1; Clinvar (benign):1 | ||||
| chr17:35587184-35587640 | Rare:111 | ||||
| chr17:36090137-36090422 | Common:1; Rare:56 | ||||
| chr17:36486476-36486735 | Common:3; Rare:95 | ||||
| chr17:36534830-36535016 | Common:3; Rare:82 | ||||
| chr17:36544787-36544968 | Common:3; Rare:60 |