| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:45490680-45490950 | Common:7; Rare:84 | ||||
| chr17:45620164-45620264 | Rare:21 | ||||
| chr17:46192771-46193029 | Common:3; Rare:63; Clinvar (benign):2 | ||||
| chr17:46193318-46193614 | Common:5; Rare:85 | ||||
| chr17:46193935-46194303 | Common:5; Rare:57 | ||||
| chr17:46225456-46225548 | Common:3; Rare:24 | ||||
| chr17:46922768-46923274 | Common:5; Rare:163; Clinvar:5; Clinvar (benign):12; Clinvar (pathogenic):1 | ||||
| chr17:47188283-47188447 | Rare:29 | ||||
| chr17:47188845-47189068 | Common:2; Rare:44 | ||||
| chr17:47189072-47189130 | Rare:19 | ||||
| chr17:47189135-47189665 | Common:1; Rare:136 | ||||
| chr17:47200132-47200349 | Common:1; Rare:26 | ||||
| chr17:47200398-47200496 | Common:3; Rare:20 | ||||
| chr17:47253857-47253953 | Common:1; Rare:32; Clinvar:1; Clinvar (benign):3 | ||||
| chr17:47323671-47324080 | Common:5; Rare:136 |