| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:159726918-159727221 | Common:1; Rare:107 | ||||
| chr6:159727328-159727703 | Common:5; Rare:152 | ||||
| chr6:159761690-159762066 | Common:8; Rare:154 | ||||
| chr6:159789515-159789990 | Common:4; Rare:162 | ||||
| chr6:159790259-159790529 | Common:8; Rare:87 | ||||
| chr6:159968941-159969121 | Common:1; Rare:78 | ||||
| chr6:161274040-161274228 | Rare:30 | ||||
| chr6:162727757-162728088 | Common:3; Rare:90; Clinvar:1 | ||||
| chr6:166342544-166342648 | Common:3; Rare:39 | ||||
| chr6:166956260-166956327 | Rare:11; Clinvar:2 | ||||
| chr6:166956457-166956687 | Common:4; Rare:68; Clinvar:3; Clinvar (benign):2 | ||||
| chr6:167122618-167122760 | Common:1; Rare:23 | ||||
| chr6:169701997-169702322 | Common:5; Rare:141 | ||||
| chr6:169751545-169751650 | Rare:44; Clinvar (benign):2 | ||||
| chr6:170553250-170553364 | Rare:47 |