| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:31859119-31859397 | Common:3; Rare:78 | ||||
| chr17:31901632-31901809 | Common:2; Rare:64 | ||||
| chr17:31936782-31937067 | Rare:83 | ||||
| chr17:32020915-32021108 | Rare:49 | ||||
| chr17:32142387-32142709 | Common:8; Rare:131 | ||||
| chr17:32350002-32350228 | Rare:114 | ||||
| chr17:32444222-32444561 | Common:1; Rare:119 | ||||
| chr17:32445540-32445657 | Common:2; Rare:18 | ||||
| chr17:32876778-32876791 | Rare:2 | ||||
| chr17:32991716-32991935 | Common:2; Rare:42 | ||||
| chr17:34255133-34255317 | Rare:50 | ||||
| chr17:34961273-34961585 | Common:2; Rare:135 | ||||
| chr17:34980196-34980613 | Common:4; Rare:104 | ||||
| chr17:34981121-34981479 | Common:2; Rare:68 | ||||
| chr17:35119776-35119854 | Rare:40; Clinvar:1; Clinvar (benign):1 |