| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:70413222-70413580 | Common:2; Rare:101 | ||||
| chr6:73462037-73462069 | Rare:11; Clinvar (benign):1 | ||||
| chr6:73521202-73521406 | Rare:37 | ||||
| chr6:73521537-73521634 | Rare:24 | ||||
| chr6:73523793-73523884 | Rare:27 | ||||
| chr6:73653873-73654123 | Common:2; Rare:66; Clinvar:3 | ||||
| chr6:73696019-73696207 | Common:1; Rare:37 | ||||
| chr6:75243718-75243978 | Common:1; Rare:115 | ||||
| chr6:75284553-75284654 | Rare:43 | ||||
| chr6:75284668-75285070 | Common:1; Rare:127 | ||||
| chr6:75493489-75493659 | Common:1; Rare:30 | ||||
| chr6:75493778-75493857 | Rare:20 | ||||
| chr6:75601789-75601916 | Rare:51 | ||||
| chr6:78867465-78867564 | Rare:33 | ||||
| chr6:79078241-79078584 | Common:1; Rare:149 |