| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:109455705-109455835 | Common:1; Rare:36 | ||||
| chr6:109483122-109483236 | Rare:55 | ||||
| chr6:109691151-109691348 | Common:3; Rare:46; Clinvar:4; Clinvar (benign):3 | ||||
| chr6:110415525-110415670 | Rare:31 | ||||
| chr6:110815168-110815264 | Common:1; Rare:33 | ||||
| chr6:110874633-110874798 | Common:4; Rare:54 | ||||
| chr6:110958423-110958542 | Common:2; Rare:31 | ||||
| chr6:110958589-110958941 | Common:8; Rare:132 | ||||
| chr6:110981959-110982125 | Common:2; Rare:87 | ||||
| chr6:111259210-111259407 | Common:3; Rare:68 | ||||
| chr6:111483211-111483572 | Common:1; Rare:128 | ||||
| chr6:111483574-111483662 | Rare:34 | ||||
| chr6:111483730-111483900 | Common:1; Rare:78 | ||||
| chr6:111484118-111484275 | Rare:58 | ||||
| chr6:111567067-111567264 | Rare:48 |