| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:79545093-79545112 | Common:1; Rare:5 | ||||
| chr6:81938435-81938697 | Rare:61 | ||||
| chr6:82959414-82959705 | Rare:48 | ||||
| chr6:83028910-83029190 | Common:2; Rare:56 | ||||
| chr6:83160536-83160649 | Common:1; Rare:16 | ||||
| chr6:83174300-83174419 | Rare:31 | ||||
| chr6:85451626-85452024 | Common:1; Rare:76 | ||||
| chr6:85452103-85452195 | Rare:15 | ||||
| chr6:85510702-85510890 | Common:1; Rare:32 | ||||
| chr6:85512647-85512951 | Common:2; Rare:58 | ||||
| chr6:85513049-85513166 | Rare:16 | ||||
| chr6:85565366-85565719 | Rare:70 | ||||
| chr6:85572138-85572315 | Rare:47; Clinvar (pathogenic):1 | ||||
| chr6:85637075-85637282 | Rare:46 | ||||
| chr6:85640218-85640499 | Rare:68 |