| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:75493761-75493805 | Rare:10 | ||||
| chr6:75493812-75493926 | Common:1; Rare:21 | ||||
| chr6:75601767-75601899 | Rare:50 | ||||
| chr6:75602114-75602534 | Common:1; Rare:106 | ||||
| chr6:75748986-75749420 | Common:6; Rare:139; Clinvar:3 | ||||
| chr6:78867465-78867594 | Rare:54 | ||||
| chr6:79077701-79077841 | Common:1; Rare:39 | ||||
| chr6:79078126-79078588 | Common:1; Rare:186 | ||||
| chr6:79234564-79235037 | Common:4; Rare:101 | ||||
| chr6:79537309-79537658 | Common:2; Rare:108; Clinvar:5 | ||||
| chr6:79630857-79630956 | Common:2; Rare:17 | ||||
| chr6:79631154-79631503 | Common:2; Rare:93 | ||||
| chr6:79947526-79947807 | Common:1; Rare:103; Clinvar:7; Clinvar (benign):1 | ||||
| chr6:80004382-80004687 | Common:6; Rare:75 | ||||
| chr6:82247693-82247839 | Rare:46 |