| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:79023308-79023418 | Common:1; Rare:23 | ||||
| chr17:79024003-79024322 | Common:3; Rare:70 | ||||
| chr17:79025327-79025645 | Common:5; Rare:53 | ||||
| chr17:80035837-80036035 | Common:1; Rare:68 | ||||
| chr17:80036522-80036665 | Common:2; Rare:37; Clinvar (benign):2 | ||||
| chr17:80146993-80147360 | Common:8; Rare:153 | ||||
| chr17:80219529-80219828 | Common:1; Rare:54 | ||||
| chr17:80220304-80220468 | Common:1; Rare:64; Clinvar:1; Clinvar (pathogenic):2 | ||||
| chr17:80372778-80373090 | Common:2; Rare:95; Clinvar:1 | ||||
| chr17:80385288-80385589 | Common:1; Rare:87 | ||||
| chr17:80415098-80415189 | Common:1; Rare:58 | ||||
| chr17:80415377-80415509 | Common:4; Rare:49 | ||||
| chr17:80991786-80991955 | Common:1; Rare:65 | ||||
| chr17:81097418-81097618 | Rare:75 | ||||
| chr17:81239036-81239332 | Common:2; Rare:95 |