| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:41781680-41781914 | Rare:51 | ||||
| chr17:41782137-41782389 | Common:1; Rare:45 | ||||
| chr17:41784233-41784525 | Common:4; Rare:61 | ||||
| chr17:41793242-41793499 | Common:3; Rare:55 | ||||
| chr17:42422720-42422855 | Rare:54; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr17:43315632-43315917 | Common:6; Rare:121 | ||||
| chr17:44797748-44797906 | Rare:25 | ||||
| chr17:47618912-47618952 | Rare:4 | ||||
| chr17:51119491-51119693 | Common:3; Rare:30 | ||||
| chr17:58332513-58332662 | Common:2; Rare:39 | ||||
| chr17:59681384-59681695 | Common:1; Rare:56 | ||||
| chr17:60085136-60085159 | Rare:4 | ||||
| chr17:64145764-64145975 | Common:2; Rare:55 | ||||
| chr17:64385178-64385511 | Common:2; Rare:52 | ||||
| chr17:64781279-64781437 | Rare:27 |