| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:109373133-109373413 | Common:1; Rare:70 | ||||
| chr6:109382369-109382806 | Common:5; Rare:148; Clinvar (benign):1 | ||||
| chr6:109440575-109440872 | Common:2; Rare:104 | ||||
| chr6:109455702-109456074 | Common:2; Rare:96 | ||||
| chr6:109483129-109483258 | Rare:58 | ||||
| chr6:109691135-109691319 | Common:3; Rare:47; Clinvar:4; Clinvar (benign):3 | ||||
| chr6:110815124-110815341 | Common:1; Rare:75 | ||||
| chr6:110815850-110816106 | Common:2; Rare:61 | ||||
| chr6:110874602-110874861 | Common:4; Rare:86 | ||||
| chr6:110958595-110958784 | Common:4; Rare:69 | ||||
| chr6:110981910-110982097 | Common:3; Rare:86 | ||||
| chr6:111259071-111259339 | Common:1; Rare:76 | ||||
| chr6:111483108-111483619 | Common:1; Rare:181 | ||||
| chr6:112087461-112087685 | Rare:65 | ||||
| chr6:113970966-113971472 | Common:4; Rare:186 |