| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:75881432-75881802 | Rare:64 | ||||
| chr6:75906813-75907108 | Common:1; Rare:42 | ||||
| chr6:76593770-76593966 | Common:1; Rare:42 | ||||
| chr6:77087346-77087640 | Common:1; Rare:59 | ||||
| chr6:77369063-77369219 | Common:3; Rare:51 | ||||
| chr6:77403394-77403657 | Common:1; Rare:46 | ||||
| chr6:77650550-77650668 | Common:1; Rare:32 | ||||
| chr6:78030567-78030879 | Rare:57 | ||||
| chr6:78597966-78598098 | Rare:35 | ||||
| chr6:79025557-79025863 | Rare:54; Clinvar (pathogenic):1 | ||||
| chr6:79041510-79041714 | Rare:39 | ||||
| chr6:79233442-79233716 | Common:3; Rare:50 | ||||
| chr6:79233896-79234018 | Rare:33 | ||||
| chr6:79539178-79539439 | Common:2; Rare:35 | ||||
| chr6:79545198-79545542 | Common:1; Rare:61 |