| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:47841218-47841390 | Rare:35 | ||||
| chr17:47896282-47896565 | Common:3; Rare:68 | ||||
| chr17:47941335-47941652 | Rare:72; Clinvar:1; Clinvar (benign):1 | ||||
| chr17:47970783-47971171 | Common:4; Rare:87 | ||||
| chr17:48048039-48048416 | Common:1; Rare:104 | ||||
| chr17:48048602-48048813 | Common:4; Rare:30 | ||||
| chr17:48101266-48101634 | Common:3; Rare:102 | ||||
| chr17:48107427-48107817 | Common:5; Rare:94 | ||||
| chr17:48604010-48604029 | Rare:6 | ||||
| chr17:48604037-48604091 | Rare:17 | ||||
| chr17:48604955-48605066 | Common:1; Rare:21 | ||||
| chr17:48610537-48610705 | Common:1; Rare:57 | ||||
| chr17:48610707-48611081 | Common:4; Rare:113 | ||||
| chr17:48625854-48626087 | Rare:82 | ||||
| chr17:48892341-48892628 | Common:10; Rare:86 |