| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:79839813-79840014 | Common:1; Rare:51 | ||||
| chr17:79950825-79950994 | Common:2; Rare:23 | ||||
| chr17:79951672-79951759 | Rare:21 | ||||
| chr17:79951916-79951999 | Common:1; Rare:19 | ||||
| chr17:79952002-79952046 | Rare:4 | ||||
| chr17:79993696-79993961 | Rare:52 | ||||
| chr17:80035412-80035479 | Rare:14 | ||||
| chr17:80035779-80036286 | Common:3; Rare:142 | ||||
| chr17:80036435-80036731 | Common:3; Rare:84; Clinvar:1; Clinvar (benign):2 | ||||
| chr17:80101343-80101679 | Common:5; Rare:138; Clinvar (benign):5 | ||||
| chr17:80147048-80147489 | Common:8; Rare:178 | ||||
| chr17:80147564-80147647 | Rare:14 | ||||
| chr17:80212368-80212518 | Common:1; Rare:30 | ||||
| chr17:80220296-80220468 | Common:1; Rare:69; Clinvar:1; Clinvar (pathogenic):2 | ||||
| chr17:80220900-80221023 | Common:1; Rare:30 |