| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:32853680-32853819 | Rare:67; Clinvar:2; Clinvar (benign):2 | ||||
| chr6:32853985-32854209 | Common:2; Rare:52 | ||||
| chr6:32953038-32953261 | Rare:44 | ||||
| chr6:32968446-32968616 | Common:3; Rare:44 | ||||
| chr6:32968619-32968933 | Common:7; Rare:91 | ||||
| chr6:32970643-32970952 | Common:2; Rare:83 | ||||
| chr6:32977529-32977945 | Common:4; Rare:150; Clinvar:1; Clinvar (benign):1 | ||||
| chr6:33075812-33076008 | Common:2; Rare:21 | ||||
| chr6:33200356-33200449 | Rare:24 | ||||
| chr6:33200654-33201002 | Common:3; Rare:94 | ||||
| chr6:33201024-33201255 | Rare:42 | ||||
| chr6:33201801-33202099 | Common:4; Rare:79 | ||||
| chr6:33208425-33208882 | Common:3; Rare:120 | ||||
| chr6:33271631-33272131 | Common:4; Rare:182 | ||||
| chr6:33277077-33277326 | Common:1; Rare:82 |