| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:160991564-160991784 | Common:3; Rare:67 | ||||
| chr6:161273981-161274272 | Rare:52 | ||||
| chr6:163414646-163414815 | Rare:71 | ||||
| chr6:163415162-163415331 | Common:2; Rare:59 | ||||
| chr6:165662303-165662455 | Common:1; Rare:46 | ||||
| chr6:166342425-166342662 | Common:5; Rare:95 | ||||
| chr6:166956255-166956308 | Rare:10; Clinvar:3 | ||||
| chr6:166956469-166956678 | Common:4; Rare:63; Clinvar:3; Clinvar (benign):2 | ||||
| chr6:166999074-166999333 | Rare:85 | ||||
| chr6:166999440-166999496 | Rare:17 | ||||
| chr6:169701597-169701631 | Rare:11 | ||||
| chr6:169701955-169702393 | Common:5; Rare:178 | ||||
| chr6:169702617-169702901 | Common:1; Rare:119 | ||||
| chr6:169751432-169751675 | Common:3; Rare:106; Clinvar (benign):4 | ||||
| chr6:170306579-170306820 | Common:2; Rare:74 |