| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:80415105-80415184 | Common:1; Rare:51 | ||||
| chr17:81239048-81239342 | Common:3; Rare:93 | ||||
| chr17:81295297-81295401 | Common:1; Rare:18 | ||||
| chr17:81511677-81512371 | Common:7; Rare:377; Clinvar:8; Clinvar (benign):34; Clinvar (pathogenic):2 | ||||
| chr17:81512725-81513155 | Common:7; Rare:213; Clinvar (benign):14 | ||||
| chr17:81636983-81637246 | Common:3; Rare:103 | ||||
| chr17:81666558-81666783 | Common:1; Rare:102 | ||||
| chr17:81683702-81684052 | Common:4; Rare:173 | ||||
| chr17:81703283-81703517 | Common:2; Rare:67; Clinvar (benign):2 | ||||
| chr17:81833251-81833371 | Rare:52 | ||||
| chr17:81859276-81859516 | Common:2; Rare:58 | ||||
| chr17:81871298-81871415 | Rare:39 | ||||
| chr17:81937261-81937415 | Rare:56 | ||||
| chr17:82022863-82023195 | Common:5; Rare:114 | ||||
| chr17:82037668-82037878 | Common:1; Rare:84 |