| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:7035773-7036108 | Rare:79 | ||||
| chr17:7042988-7043154 | Common:3; Rare:63 | ||||
| chr17:7114959-7115162 | Common:2; Rare:36 | ||||
| chr17:7219793-7219956 | Common:3; Rare:74; Clinvar:5; Clinvar (benign):2 | ||||
| chr17:7221737-7222011 | Common:3; Rare:67; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
| chr17:7241772-7241886 | Common:1; Rare:26 | ||||
| chr17:7242244-7242486 | Common:1; Rare:74 | ||||
| chr17:7242937-7243107 | Common:1; Rare:82 | ||||
| chr17:7251927-7252321 | Common:2; Rare:154 | ||||
| chr17:7313369-7313605 | Common:1; Rare:97 | ||||
| chr17:7315036-7315429 | Common:4; Rare:139 | ||||
| chr17:7343433-7343728 | Common:4; Rare:83 | ||||
| chr17:7352051-7352212 | Rare:52 | ||||
| chr17:7438183-7438316 | Rare:31 | ||||
| chr17:7479490-7479713 | Common:1; Rare:38 |