| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:19004149-19004312 | Rare:39 | ||||
| chr17:19377905-19378037 | Common:1; Rare:30 | ||||
| chr17:19378044-19378542 | Common:3; Rare:112 | ||||
| chr17:19533766-19533966 | Common:3; Rare:64 | ||||
| chr17:19647889-19648187 | Common:2; Rare:62 | ||||
| chr17:19648692-19649110 | Common:3; Rare:153; Clinvar (benign):1 | ||||
| chr17:19741003-19741209 | Common:2; Rare:64 | ||||
| chr17:19748212-19748694 | Common:3; Rare:118 | ||||
| chr17:19749134-19749158 | Rare:5 | ||||
| chr17:19749320-19749541 | Common:2; Rare:32 | ||||
| chr17:19977793-19977945 | Common:1; Rare:51 | ||||
| chr17:20008589-20008875 | Common:1; Rare:65 | ||||
| chr17:20009173-20009428 | Common:5; Rare:77 | ||||
| chr17:21011026-21011234 | Rare:63 | ||||
| chr17:21042230-21042407 | Common:1; Rare:70 |