| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:79993102-79993342 | Common:2; Rare:59 | ||||
| chr17:79993363-79993844 | Common:3; Rare:165 | ||||
| chr17:79993960-79994330 | Common:3; Rare:176 | ||||
| chr17:80034927-80035760 | Common:2; Rare:199 | ||||
| chr17:80035782-80036121 | Common:4; Rare:260 | ||||
| chr17:80036447-80036718 | Common:7; Rare:162; Clinvar:1; Clinvar (benign):6 | ||||
| chr17:80101343-80101697 | Common:14; Rare:366; Clinvar:1; Clinvar (benign):15 | ||||
| chr17:80146921-80147476 | Common:25; Rare:499 | ||||
| chr17:80169854-80170112 | Common:3; Rare:87 | ||||
| chr17:80220236-80220497 | Common:3; Rare:241; Clinvar:3; Clinvar (pathogenic):6 | ||||
| chr17:80220530-80220860 | Common:5; Rare:73 | ||||
| chr17:80260436-80261031 | Common:21; Rare:175 | ||||
| chr17:80261264-80261673 | Common:6; Rare:96 | ||||
| chr17:80414787-80415565 | Common:18; Rare:718 | ||||
| chr17:80544750-80545001 | Common:2; Rare:59 |