| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:107459490-107459738 | Common:2; Rare:64; Clinvar:1 | ||||
| chr6:107490470-107490628 | Common:2; Rare:58 | ||||
| chr6:107824207-107824748 | Common:3; Rare:94 | ||||
| chr6:107957225-107957433 | Rare:43 | ||||
| chr6:107957939-107958220 | Common:1; Rare:91; Clinvar (benign):1 | ||||
| chr6:107958265-107958383 | Common:1; Rare:40; Clinvar (benign):2 | ||||
| chr6:108074653-108074889 | Common:1; Rare:84; Clinvar:1 | ||||
| chr6:108260918-108261040 | Rare:69 | ||||
| chr6:108294765-108295158 | Common:2; Rare:129 | ||||
| chr6:108477132-108477239 | Rare:25 | ||||
| chr6:108560072-108560354 | Rare:87 | ||||
| chr6:108560729-108560844 | Rare:50 | ||||
| chr6:108848332-108848503 | Rare:62 | ||||
| chr6:109094471-109094541 | Rare:17 | ||||
| chr6:109095043-109095567 | Common:4; Rare:127 |