| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:75589956-75590157 | Common:4; Rare:43 | ||||
| chr17:75617854-75618150 | Common:1; Rare:78 | ||||
| chr17:75633845-75634099 | Common:1; Rare:55 | ||||
| chr17:75667131-75667447 | Common:5; Rare:105 | ||||
| chr17:75721159-75721591 | Common:3; Rare:134; Clinvar:2 | ||||
| chr17:75765134-75765304 | Common:1; Rare:53; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr17:75779289-75779538 | Common:1; Rare:126 | ||||
| chr17:75779690-75780140 | Common:2; Rare:181 | ||||
| chr17:75784558-75784911 | Common:2; Rare:160 | ||||
| chr17:75834618-75834806 | Rare:61; Clinvar:3; Clinvar (benign):1 | ||||
| chr17:75843707-75843833 | Rare:31; Clinvar (pathogenic):1 | ||||
| chr17:75855242-75855699 | Common:1; Rare:131 | ||||
| chr17:75896949-75897153 | Common:2; Rare:83 | ||||
| chr17:75904871-75905218 | Common:4; Rare:94 | ||||
| chr17:75941023-75941233 | Common:1; Rare:66 |