| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:80036522-80036665 | Common:2; Rare:37; Clinvar (benign):2 | ||||
| chr17:80101309-80101668 | Common:5; Rare:146; Clinvar (benign):5 | ||||
| chr17:80146993-80147309 | Common:8; Rare:141 | ||||
| chr17:80192063-80192534 | Common:1; Rare:93; Clinvar (benign):1 | ||||
| chr17:80220309-80220469 | Common:1; Rare:62; Clinvar:1; Clinvar (pathogenic):2 | ||||
| chr17:80415126-80415197 | Common:1; Rare:50 | ||||
| chr17:80415385-80415492 | Common:4; Rare:40 | ||||
| chr17:80544801-80544914 | Rare:24 | ||||
| chr17:80545623-80545668 | Rare:13 | ||||
| chr17:80991806-80991930 | Common:1; Rare:50 | ||||
| chr17:81057500-81057656 | Common:3; Rare:34 | ||||
| chr17:81097506-81097618 | Rare:40 | ||||
| chr17:81239029-81239343 | Common:3; Rare:101 | ||||
| chr17:81295293-81295439 | Common:2; Rare:35 | ||||
| chr17:81395179-81395536 | Common:1; Rare:98 |