| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:109691158-109691353 | Common:3; Rare:44; Clinvar:5; Clinvar (benign):3 | ||||
| chr6:109766270-109766468 | Common:2; Rare:32 | ||||
| chr6:110415508-110415726 | Rare:49 | ||||
| chr6:112087452-112087663 | Rare:65 | ||||
| chr6:116100690-116100909 | Common:1; Rare:83 | ||||
| chr6:116254068-116254164 | Common:1; Rare:20 | ||||
| chr6:116278730-116279004 | Rare:84 | ||||
| chr6:116279432-116279526 | Common:1; Rare:38 | ||||
| chr6:116279540-116279795 | Common:2; Rare:88 | ||||
| chr6:116279826-116280086 | Common:1; Rare:91 | ||||
| chr6:116571170-116571665 | Common:3; Rare:140 | ||||
| chr6:116681041-116681303 | Common:4; Rare:76 | ||||
| chr6:117265383-117265718 | Common:1; Rare:95 | ||||
| chr6:117602197-117602363 | Rare:65 | ||||
| chr6:118894109-118894292 | Common:1; Rare:44 |