| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:69796546-69796643 | Common:1; Rare:16 | ||||
| chr6:69796867-69797151 | Common:1; Rare:85; Clinvar:4; Clinvar (benign):2 | ||||
| chr6:69866550-69866608 | Rare:10 | ||||
| chr6:70413222-70413603 | Common:2; Rare:107 | ||||
| chr6:70566850-70566967 | Common:1; Rare:43 | ||||
| chr6:70667707-70667960 | Common:2; Rare:84 | ||||
| chr6:70955919-70956165 | Common:1; Rare:86 | ||||
| chr6:73263127-73263296 | Common:4; Rare:48 | ||||
| chr6:73521180-73521406 | Rare:40 | ||||
| chr6:73521555-73521640 | Rare:21 | ||||
| chr6:75284722-75285033 | Common:1; Rare:89 | ||||
| chr6:75493489-75493814 | Common:1; Rare:61 | ||||
| chr6:75601795-75601902 | Rare:44 | ||||
| chr6:75602290-75602527 | Common:1; Rare:68 | ||||
| chr6:75749106-75749303 | Common:3; Rare:58; Clinvar:3 |