| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:75602327-75602534 | Common:1; Rare:58 | ||||
| chr6:78867470-78867621 | Rare:73 | ||||
| chr6:79078156-79078652 | Common:1; Rare:204 | ||||
| chr6:79537351-79537650 | Common:2; Rare:90; Clinvar:4 | ||||
| chr6:80004505-80004675 | Common:3; Rare:39 | ||||
| chr6:80106383-80106708 | Common:2; Rare:109; Clinvar (pathogenic):1 | ||||
| chr6:82247715-82247860 | Common:1; Rare:46 | ||||
| chr6:82363493-82363857 | Common:2; Rare:108 | ||||
| chr6:83193197-83193397 | Common:3; Rare:68 | ||||
| chr6:85593812-85593955 | Rare:49 | ||||
| chr6:85643808-85643902 | Rare:31 | ||||
| chr6:87155268-87155594 | Rare:87 | ||||
| chr6:87472900-87472997 | Common:1; Rare:38; Clinvar (benign):4 | ||||
| chr6:87589959-87590165 | Common:2; Rare:89; Clinvar (benign):4 | ||||
| chr6:87702203-87702497 | Common:1; Rare:93 |