| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:80101315-80101745 | Common:5; Rare:168; Clinvar:1; Clinvar (benign):5 | ||||
| chr17:80112621-80112910 | Common:2; Rare:116; Clinvar:11; Clinvar (benign):9; Clinvar (pathogenic):7 | ||||
| chr17:80146942-80147260 | Common:8; Rare:157 | ||||
| chr17:80220309-80220468 | Common:1; Rare:61; Clinvar:1; Clinvar (pathogenic):2 | ||||
| chr17:80415076-80415509 | Common:5; Rare:221 | ||||
| chr17:80991777-80991928 | Common:1; Rare:57 | ||||
| chr17:81034924-81035158 | Common:2; Rare:98 | ||||
| chr17:81239009-81239203 | Common:2; Rare:69 | ||||
| chr17:81295278-81295442 | Common:2; Rare:41 | ||||
| chr17:81395263-81395475 | Common:1; Rare:55 | ||||
| chr17:81512225-81512618 | Common:4; Rare:192; Clinvar:2; Clinvar (benign):12 | ||||
| chr17:81512708-81513047 | Common:7; Rare:190; Clinvar (benign):14 | ||||
| chr17:81552314-81552494 | Common:1; Rare:70 | ||||
| chr17:81666554-81666779 | Common:1; Rare:101 | ||||
| chr17:81683621-81684076 | Common:5; Rare:244 |