| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:80386062-80386258 | Common:3; Rare:41 | ||||
| chr17:80415105-80415189 | Common:1; Rare:56 | ||||
| chr17:80991807-80991948 | Common:1; Rare:57 | ||||
| chr17:81057549-81057846 | Common:3; Rare:66 | ||||
| chr17:81084572-81084783 | Common:2; Rare:53 | ||||
| chr17:81087242-81087549 | Common:2; Rare:87 | ||||
| chr17:81239029-81239308 | Common:2; Rare:93 | ||||
| chr17:81511677-81512161 | Common:7; Rare:268; Clinvar:6; Clinvar (benign):24; Clinvar (pathogenic):2 | ||||
| chr17:81512696-81513155 | Common:8; Rare:236; Clinvar (benign):14 | ||||
| chr17:81636983-81637232 | Common:2; Rare:101 | ||||
| chr17:81666552-81666833 | Common:1; Rare:121 | ||||
| chr17:81683685-81684102 | Common:4; Rare:207 | ||||
| chr17:81703286-81703517 | Common:2; Rare:64; Clinvar (benign):2 | ||||
| chr17:81833251-81833390 | Rare:63 | ||||
| chr17:81855453-81855699 | Rare:69 |