| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:7583719-7583911 | Common:1; Rare:86; Clinvar:3; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr17:7584053-7584299 | Common:1; Rare:60 | ||||
| chr17:7586392-7586724 | Common:1; Rare:77 | ||||
| chr17:7586963-7587492 | Common:2; Rare:158; Clinvar:3; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr17:7627791-7627994 | Common:2; Rare:64 | ||||
| chr17:7685450-7685630 | Common:1; Rare:31 | ||||
| chr17:7687378-7687431 | Rare:8; Clinvar:1 | ||||
| chr17:7687460-7687606 | Rare:32 | ||||
| chr17:7705036-7705246 | Common:1; Rare:42 | ||||
| chr17:7843644-7843733 | Rare:32 | ||||
| chr17:7857155-7857368 | Common:1; Rare:116 | ||||
| chr17:7857382-7858113 | Common:5; Rare:242 | ||||
| chr17:7931817-7932295 | Common:5; Rare:134 | ||||
| chr17:7947944-7948325 | Common:1; Rare:99 | ||||
| chr17:8210536-8210744 | Common:2; Rare:39 |