| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:2593437-2593767 | Common:4; Rare:122; Clinvar:3; Clinvar (benign):2 | ||||
| chr17:2593924-2594231 | Rare:85; Clinvar:1 | ||||
| chr17:2711228-2711350 | Common:1; Rare:34 | ||||
| chr17:2711684-2712078 | Common:2; Rare:106 | ||||
| chr17:2796333-2796416 | Rare:15 | ||||
| chr17:3557786-3557969 | Common:4; Rare:37; Clinvar:4; Clinvar (benign):5 | ||||
| chr17:3636178-3636560 | Common:5; Rare:119; Clinvar (benign):2 | ||||
| chr17:3636630-3636824 | Common:1; Rare:49; Clinvar:5; Clinvar (benign):1 | ||||
| chr17:3668422-3668929 | Common:3; Rare:198 | ||||
| chr17:3696036-3696347 | Common:1; Rare:72 | ||||
| chr17:3723731-3724155 | Common:1; Rare:213 | ||||
| chr17:3724302-3724360 | Common:1; Rare:17 | ||||
| chr17:3846158-3846469 | Common:1; Rare:107 | ||||
| chr17:3893072-3893318 | Rare:76 | ||||
| chr17:3893446-3893603 | Common:3; Rare:28 |