| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:57317539-57317660 | Rare:36 | ||||
| chr6:62286019-62286352 | Common:1; Rare:103 | ||||
| chr6:63572250-63572616 | Rare:138 | ||||
| chr6:63636043-63636139 | Rare:31 | ||||
| chr6:68634867-68635382 | Common:2; Rare:138 | ||||
| chr6:68635817-68635947 | Rare:26 | ||||
| chr6:69232631-69232780 | Rare:26 | ||||
| chr6:69232971-69233014 | Common:1; Rare:18 | ||||
| chr6:69796546-69796651 | Common:1; Rare:18 | ||||
| chr6:69796825-69797126 | Common:1; Rare:100; Clinvar:4; Clinvar (benign):2 | ||||
| chr6:70413182-70413577 | Common:2; Rare:116 | ||||
| chr6:70566837-70566967 | Common:1; Rare:46 | ||||
| chr6:70667696-70667970 | Common:2; Rare:96 | ||||
| chr6:70955921-70956163 | Common:1; Rare:86 | ||||
| chr6:71886416-71887003 | Common:3; Rare:167; Clinvar:3; Clinvar (benign):3 |