| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:99425219-99425442 | Common:2; Rare:66 | ||||
| chr6:100881293-100881482 | Common:5; Rare:84 | ||||
| chr6:105137132-105137276 | Common:1; Rare:58 | ||||
| chr6:105179841-105180111 | Common:5; Rare:77 | ||||
| chr6:106629432-106629624 | Common:2; Rare:44 | ||||
| chr6:107958012-107958450 | Common:2; Rare:145; Clinvar:2; Clinvar (benign):3 | ||||
| chr6:108074250-108074326 | Rare:24 | ||||
| chr6:108260790-108260805 | Rare:5 | ||||
| chr6:108294838-108295071 | Common:1; Rare:63 | ||||
| chr6:109382374-109382803 | Common:5; Rare:142; Clinvar (benign):1 | ||||
| chr6:109440608-109440784 | Rare:59 | ||||
| chr6:109455690-109455852 | Common:3; Rare:46 | ||||
| chr6:109691151-109691315 | Common:1; Rare:41; Clinvar:4; Clinvar (benign):1 | ||||
| chr6:110874633-110874801 | Common:4; Rare:54 | ||||
| chr6:110981975-110982097 | Common:2; Rare:61 |