| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:7687436-7687631 | Rare:69; Clinvar:2 | ||||
| chr17:7688179-7688532 | Common:5; Rare:89; Clinvar:3; Clinvar (benign):2 | ||||
| chr17:7803760-7804370 | Common:1; Rare:196 | ||||
| chr17:7843953-7844230 | Common:6; Rare:113 | ||||
| chr17:7844760-7845060 | Common:2; Rare:162 | ||||
| chr17:7857088-7857338 | Common:2; Rare:192 | ||||
| chr17:7857465-7858355 | Common:8; Rare:453 | ||||
| chr17:7884411-7885361 | Common:10; Rare:327 | ||||
| chr17:7931845-7932280 | Common:10; Rare:233 | ||||
| chr17:8087690-8088180 | Common:2; Rare:183 | ||||
| chr17:8103623-8103984 | Common:2; Rare:97 | ||||
| chr17:8118360-8119261 | Common:15; Rare:526 | ||||
| chr17:8123604-8123729 | Rare:25 | ||||
| chr17:8124060-8124450 | Common:5; Rare:180 | ||||
| chr17:8156307-8156444 | Common:1; Rare:44 |