| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:138773655-138773787 | Common:1; Rare:61 | ||||
| chr6:143060711-143060922 | Common:7; Rare:71 | ||||
| chr6:143450671-143450831 | Rare:68; Clinvar:2 | ||||
| chr6:158168237-158168388 | Common:2; Rare:55 | ||||
| chr6:158644713-158644936 | Common:2; Rare:81 | ||||
| chr6:159726948-159727139 | Rare:71 | ||||
| chr6:159727327-159727604 | Common:5; Rare:119 | ||||
| chr6:159762278-159762569 | Common:3; Rare:83 | ||||
| chr6:159789617-159789952 | Common:3; Rare:111 | ||||
| chr6:166342529-166342628 | Common:2; Rare:37 | ||||
| chr6:166999050-166999404 | Common:1; Rare:120 | ||||
| chr6:169701986-169702366 | Common:5; Rare:160 | ||||
| chr6:169751528-169751679 | Common:1; Rare:62; Clinvar (benign):4 | ||||
| chr7:727238-727285 | Rare:14; Clinvar:1 | ||||
| chr7:2242176-2242241 | Common:2; Rare:40 |