| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:47810280-47810880 | Common:3; Rare:136 | ||||
| chr17:47895346-47895460 | Rare:21 | ||||
| chr17:47936117-47936299 | Common:2; Rare:20 | ||||
| chr17:47947115-47947285 | Common:2; Rare:15; Clinvar (benign):1 | ||||
| chr17:47948787-47948922 | Common:1; Rare:19; Clinvar (benign):1 | ||||
| chr17:47949173-47949524 | Common:1; Rare:73; Clinvar:1; Clinvar (benign):1 | ||||
| chr17:48012329-48012570 | Common:2; Rare:45 | ||||
| chr17:48023435-48023614 | Common:2; Rare:36 | ||||
| chr17:48023920-48024052 | Rare:26 | ||||
| chr17:48024165-48024305 | Rare:33 | ||||
| chr17:48025062-48025480 | Common:2; Rare:89 | ||||
| chr17:48026567-48026708 | Rare:23 | ||||
| chr17:48194128-48194538 | Common:1; Rare:71 | ||||
| chr17:48199197-48199701 | Common:5; Rare:141 | ||||
| chr17:48240645-48240767 | Common:1; Rare:21 |