| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:106973973-106974150 | Common:1; Rare:39 | ||||
| chr6:106975241-106975421 | Rare:55 | ||||
| chr6:107028161-107028253 | Common:1; Rare:25 | ||||
| chr6:107459551-107459703 | Common:1; Rare:32 | ||||
| chr6:107490466-107490605 | Common:2; Rare:54 | ||||
| chr6:107958131-107958428 | Common:1; Rare:91; Clinvar:2; Clinvar (benign):2 | ||||
| chr6:108074647-108074871 | Common:1; Rare:80; Clinvar:1 | ||||
| chr6:108165857-108166120 | Rare:53 | ||||
| chr6:108260881-108261023 | Rare:77 | ||||
| chr6:108294756-108295147 | Common:2; Rare:125 | ||||
| chr6:108848356-108848496 | Rare:53 | ||||
| chr6:109382348-109382566 | Common:4; Rare:94; Clinvar (benign):1 | ||||
| chr6:109440551-109440872 | Common:2; Rare:122 | ||||
| chr6:109455630-109455865 | Common:4; Rare:67 | ||||
| chr6:109483140-109483283 | Rare:61 |