| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:63572448-63572587 | Rare:49 | ||||
| chr6:63636053-63636149 | Rare:31 | ||||
| chr6:69796847-69797169 | Common:1; Rare:101; Clinvar:6; Clinvar (benign):3 | ||||
| chr6:70413213-70413595 | Common:2; Rare:106 | ||||
| chr6:70667707-70668009 | Common:4; Rare:113 | ||||
| chr6:73262923-73263273 | Common:4; Rare:91 | ||||
| chr6:73310144-73310232 | Common:1; Rare:22 | ||||
| chr6:73394603-73394862 | Common:4; Rare:74 | ||||
| chr6:73523793-73523837 | Rare:15 | ||||
| chr6:73653912-73654174 | Common:3; Rare:71; Clinvar:3 | ||||
| chr6:75284695-75285033 | Common:1; Rare:101 | ||||
| chr6:75493761-75493851 | Rare:20 | ||||
| chr6:75601771-75601904 | Rare:50 | ||||
| chr6:75602333-75602520 | Common:1; Rare:54 | ||||
| chr6:75749080-75749327 | Common:3; Rare:80; Clinvar:3 |