| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:107958032-107958399 | Common:2; Rare:112; Clinvar:2; Clinvar (benign):3 | ||||
| chr6:108260781-108261262 | Common:2; Rare:184 | ||||
| chr6:109009541-109009685 | Common:2; Rare:38 | ||||
| chr6:109094811-109095153 | Common:3; Rare:96 | ||||
| chr6:109382221-109382250 | Rare:15 | ||||
| chr6:109382383-109382573 | Common:4; Rare:78; Clinvar (benign):1 | ||||
| chr6:109440529-109440919 | Common:2; Rare:138 | ||||
| chr6:109483115-109483294 | Rare:78 | ||||
| chr6:109691104-109691326 | Common:3; Rare:56; Clinvar:4; Clinvar (benign):3 | ||||
| chr6:110179917-110180162 | Common:2; Rare:69 | ||||
| chr6:110815833-110815910 | Common:1; Rare:24 | ||||
| chr6:110874604-110874925 | Common:4; Rare:97 | ||||
| chr6:110958621-110958817 | Common:3; Rare:86 | ||||
| chr6:110981808-110982113 | Common:3; Rare:125 | ||||
| chr6:111483085-111483597 | Common:1; Rare:180 |