| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:108260927-108261065 | Rare:72 | ||||
| chr6:108294786-108295107 | Common:1; Rare:90 | ||||
| chr6:109382221-109382286 | Rare:28 | ||||
| chr6:109382297-109382316 | Rare:7 | ||||
| chr6:109691151-109691315 | Common:1; Rare:41; Clinvar:4; Clinvar (benign):1 | ||||
| chr6:110958582-110958781 | Common:4; Rare:69 | ||||
| chr6:110981977-110982104 | Common:2; Rare:67 | ||||
| chr6:111259061-111259385 | Common:3; Rare:99 | ||||
| chr6:112087443-112087684 | Rare:76 | ||||
| chr6:113971116-113971490 | Common:3; Rare:117 | ||||
| chr6:116254068-116254183 | Common:2; Rare:24 | ||||
| chr6:116279846-116280120 | Common:2; Rare:91 | ||||
| chr6:116571100-116571593 | Common:3; Rare:142 | ||||
| chr6:117602457-117602683 | Common:3; Rare:63 | ||||
| chr6:117675294-117675489 | Common:3; Rare:56 |