| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:73461686-73461966 | Common:1; Rare:103; Clinvar:2; Clinvar (benign):3 | ||||
| chr6:73521545-73521634 | Rare:24 | ||||
| chr6:73653901-73654176 | Common:3; Rare:73; Clinvar:3 | ||||
| chr6:73696020-73696210 | Common:1; Rare:38 | ||||
| chr6:75284679-75285061 | Common:1; Rare:118 | ||||
| chr6:75493507-75493605 | Rare:15 | ||||
| chr6:75493778-75493884 | Common:1; Rare:23 | ||||
| chr6:75601771-75602038 | Common:2; Rare:91 | ||||
| chr6:75602370-75602534 | Common:1; Rare:43 | ||||
| chr6:75749024-75749330 | Common:5; Rare:102; Clinvar:3 | ||||
| chr6:78867465-78867600 | Rare:60 | ||||
| chr6:79077879-79077957 | Common:1; Rare:27 | ||||
| chr6:79078048-79078614 | Common:1; Rare:227 | ||||
| chr6:79537288-79537672 | Common:3; Rare:122; Clinvar:5 | ||||
| chr6:79631010-79631391 | Common:2; Rare:81 |