| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:72615206-72615556 | Common:1; Rare:64 | ||||
| chr17:72618073-72618338 | Rare:50 | ||||
| chr17:72622815-72622992 | Common:1; Rare:26 | ||||
| chr17:72632326-72632452 | Rare:32 | ||||
| chr17:72661490-72661793 | Common:2; Rare:58 | ||||
| chr17:72661816-72661992 | Rare:35 | ||||
| chr17:72681936-72682101 | Common:4; Rare:37 | ||||
| chr17:72683580-72684200 | Common:3; Rare:108 | ||||
| chr17:72716220-72716546 | Common:7; Rare:67 | ||||
| chr17:72896229-72896629 | Common:8; Rare:94 | ||||
| chr17:72977867-72978007 | Rare:23 | ||||
| chr17:72978083-72978314 | Common:2; Rare:42 | ||||
| chr17:72985017-72985125 | Common:5; Rare:25 | ||||
| chr17:73191462-73191709 | Common:5; Rare:55 | ||||
| chr17:73196536-73197001 | Common:6; Rare:282; Clinvar:8; Clinvar (benign):6 |