| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:159780471-159780651 | Common:1; Rare:55 | ||||
| chr6:159789553-159789966 | Common:4; Rare:140 | ||||
| chr6:159790244-159790514 | Common:7; Rare:86 | ||||
| chr6:161273985-161274192 | Rare:38 | ||||
| chr6:166342508-166342653 | Common:3; Rare:57 | ||||
| chr6:166999061-166999408 | Common:1; Rare:118 | ||||
| chr6:169702013-169702196 | Common:3; Rare:94 | ||||
| chr6:169751538-169751651 | Rare:45; Clinvar (benign):2 | ||||
| chr6:170553196-170553364 | Common:2; Rare:76 | ||||
| chr6:170554211-170554416 | Common:1; Rare:65 | ||||
| chr7:727236-727298 | Rare:20; Clinvar:1 | ||||
| chr7:975502-975655 | Common:1; Rare:69 | ||||
| chr7:1570012-1570142 | Common:1; Rare:41 | ||||
| chr7:2242168-2242270 | Common:2; Rare:61 | ||||
| chr7:2403278-2403619 | Common:1; Rare:135 |