| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:108260914-108261296 | Common:2; Rare:155 | ||||
| chr6:108294798-108295085 | Common:1; Rare:75 | ||||
| chr6:108560726-108560960 | Rare:98 | ||||
| chr6:109095437-109095557 | Rare:23 | ||||
| chr6:109382209-109382298 | Rare:40 | ||||
| chr6:109382308-109382350 | Rare:17; Clinvar (benign):1 | ||||
| chr6:109382375-109382757 | Common:5; Rare:128; Clinvar (benign):1 | ||||
| chr6:109440577-109440868 | Common:2; Rare:101 | ||||
| chr6:109455696-109456040 | Common:3; Rare:89 | ||||
| chr6:109691151-109691322 | Common:3; Rare:43; Clinvar:4; Clinvar (benign):3 | ||||
| chr6:110179941-110180154 | Common:2; Rare:62 | ||||
| chr6:110958600-110958788 | Common:5; Rare:69 | ||||
| chr6:110981910-110982100 | Common:3; Rare:89 | ||||
| chr6:111483202-111483537 | Common:1; Rare:120 | ||||
| chr6:111483727-111483900 | Common:1; Rare:78 |