| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:78378440-78378677 | Rare:73 | ||||
| chr17:78840745-78841037 | Common:2; Rare:105 | ||||
| chr17:78979827-78980202 | Common:2; Rare:77 | ||||
| chr17:79074709-79074947 | Common:4; Rare:65 | ||||
| chr17:80035849-80036037 | Common:1; Rare:65 | ||||
| chr17:80036540-80036665 | Common:2; Rare:34; Clinvar (benign):2 | ||||
| chr17:80147095-80147260 | Common:4; Rare:81 | ||||
| chr17:80220309-80220468 | Common:1; Rare:61; Clinvar:1; Clinvar (pathogenic):2 | ||||
| chr17:80415095-80415189 | Common:1; Rare:61 | ||||
| chr17:80415377-80415492 | Common:4; Rare:45 | ||||
| chr17:80991804-80991960 | Common:1; Rare:62 | ||||
| chr17:81057542-81057772 | Common:2; Rare:47 | ||||
| chr17:81239020-81239317 | Common:2; Rare:100 | ||||
| chr17:81295216-81295380 | Common:1; Rare:37 | ||||
| chr17:81512733-81513117 | Common:7; Rare:201; Clinvar (benign):14 |