| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:109382372-109382838 | Common:6; Rare:153; Clinvar (benign):1 | ||||
| chr6:109440592-109440833 | Common:1; Rare:83 | ||||
| chr6:109455690-109455865 | Common:3; Rare:51 | ||||
| chr6:109691163-109691329 | Common:3; Rare:38; Clinvar:4; Clinvar (benign):3 | ||||
| chr6:110981975-110982098 | Common:2; Rare:62 | ||||
| chr6:111483214-111483537 | Common:1; Rare:115 | ||||
| chr6:112087424-112087684 | Rare:85 | ||||
| chr6:113971090-113971495 | Common:3; Rare:131 | ||||
| chr6:116100695-116100895 | Common:1; Rare:72 | ||||
| chr6:116126133-116126235 | Common:1; Rare:18 | ||||
| chr6:116254068-116254265 | Common:4; Rare:49 | ||||
| chr6:116279834-116280108 | Common:2; Rare:94 | ||||
| chr6:116370708-116370976 | Common:1; Rare:61 | ||||
| chr6:116571190-116571588 | Common:3; Rare:112 | ||||
| chr6:117265460-117265632 | Rare:45 |