| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:78130459-78130828 | Common:3; Rare:71 | ||||
| chr17:78168508-78168691 | Common:2; Rare:51 | ||||
| chr17:78187018-78187431 | Common:3; Rare:150 | ||||
| chr17:78359944-78360255 | Common:2; Rare:85 | ||||
| chr17:78379134-78379217 | Rare:19 | ||||
| chr17:78736683-78736911 | Common:1; Rare:49 | ||||
| chr17:78782213-78782572 | Common:9; Rare:120 | ||||
| chr17:78840745-78841114 | Common:2; Rare:139 | ||||
| chr17:78873793-78873978 | Common:1; Rare:38 | ||||
| chr17:78979827-78980201 | Common:2; Rare:76 | ||||
| chr17:79009663-79009902 | Common:9; Rare:71; Clinvar:3; Clinvar (benign):1 | ||||
| chr17:80035824-80036012 | Common:1; Rare:64 | ||||
| chr17:80036576-80036665 | Common:2; Rare:24; Clinvar (benign):2 | ||||
| chr17:80146999-80147315 | Common:8; Rare:139 | ||||
| chr17:80220304-80220478 | Common:1; Rare:67; Clinvar:1; Clinvar (pathogenic):2 |