| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:39461809-39462088 | Common:3; Rare:73 | ||||
| chr17:39636973-39637388 | Common:5; Rare:144 | ||||
| chr17:39668489-39668616 | Rare:56 | ||||
| chr17:39687763-39687950 | Rare:78; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr17:39687981-39688224 | Rare:74 | ||||
| chr17:39695200-39695371 | Rare:23 | ||||
| chr17:39699811-39700083 | Rare:55 | ||||
| chr17:39700669-39700790 | Rare:26 | ||||
| chr17:39730209-39730362 | Rare:52 | ||||
| chr17:39730387-39730669 | Common:1; Rare:90 | ||||
| chr17:39730763-39730856 | Rare:11 | ||||
| chr17:39737341-39737526 | Common:1; Rare:31 | ||||
| chr17:39737816-39738000 | Rare:31 | ||||
| chr17:39738117-39738441 | Common:1; Rare:69 | ||||
| chr17:39738601-39738819 | Rare:36 |