| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:109382239-109382852 | Common:6; Rare:216; Clinvar (benign):2 | ||||
| chr6:109440529-109440849 | Common:1; Rare:118 | ||||
| chr6:109455692-109455985 | Common:3; Rare:83 | ||||
| chr6:109483140-109483266 | Rare:54 | ||||
| chr6:109691151-109691329 | Common:3; Rare:43; Clinvar:4; Clinvar (benign):3 | ||||
| chr6:110179941-110180160 | Common:2; Rare:63 | ||||
| chr6:110814299-110814638 | Common:1; Rare:105 | ||||
| chr6:110874687-110874791 | Common:3; Rare:36 | ||||
| chr6:110958549-110958772 | Common:4; Rare:77 | ||||
| chr6:110981959-110982109 | Common:2; Rare:76 | ||||
| chr6:111483192-111483544 | Common:1; Rare:126 | ||||
| chr6:111483707-111483775 | Common:1; Rare:31 | ||||
| chr6:112087253-112087684 | Common:1; Rare:148 | ||||
| chr6:113857260-113857430 | Common:1; Rare:37 | ||||
| chr6:116100709-116100928 | Common:1; Rare:90 |