| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:159693242-159693611 | Common:5; Rare:107 | ||||
| chr6:159726911-159727175 | Common:1; Rare:103 | ||||
| chr6:159727337-159727624 | Common:5; Rare:124 | ||||
| chr6:159761828-159762073 | Common:4; Rare:120 | ||||
| chr6:159789553-159789984 | Common:4; Rare:148 | ||||
| chr6:159790257-159790539 | Common:8; Rare:94 | ||||
| chr6:162727766-162727963 | Rare:51; Clinvar:1 | ||||
| chr6:166342496-166342665 | Common:3; Rare:67 | ||||
| chr6:166999017-166999424 | Common:1; Rare:137 | ||||
| chr6:169702004-169702196 | Common:3; Rare:99 | ||||
| chr6:169751459-169751644 | Common:2; Rare:78; Clinvar (benign):1 | ||||
| chr6:170553226-170553371 | Common:2; Rare:61 | ||||
| chr6:170554162-170554416 | Common:1; Rare:77 | ||||
| chr7:727236-727315 | Rare:27; Clinvar:1 | ||||
| chr7:727598-727971 | Common:1; Rare:72 |