| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:141738228-141738613 | Common:1; Rare:124 | ||||
| chr7:143380905-143381047 | Rare:35 | ||||
| chr7:149028655-149028894 | Common:1; Rare:79 | ||||
| chr7:149126234-149126431 | Common:6; Rare:66 | ||||
| chr7:150379073-150379321 | Common:1; Rare:86 | ||||
| chr7:151057856-151058198 | Common:3; Rare:97 | ||||
| chr7:151061045-151061273 | Rare:41 | ||||
| chr7:151062371-151062621 | Common:1; Rare:50 | ||||
| chr7:151736458-151736615 | Rare:24 | ||||
| chr7:155644375-155644719 | Common:2; Rare:118 | ||||
| chr7:157336778-157337102 | Common:3; Rare:155; Clinvar:3; Clinvar (benign):1 | ||||
| chr7:158856423-158856677 | Common:6; Rare:92 | ||||
| chr8:232200-232403 | Common:2; Rare:74 | ||||
| chr8:1755586-1755897 | Common:5; Rare:96 | ||||
| chr8:6406527-6406668 | Common:3; Rare:77; Clinvar:2; Clinvar (benign):1 |