| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:69866543-69866599 | Rare:13 | ||||
| chr6:70413222-70413613 | Common:2; Rare:110 | ||||
| chr6:70566852-70566963 | Common:1; Rare:41 | ||||
| chr6:70667707-70667970 | Common:2; Rare:91 | ||||
| chr6:70955846-70956178 | Common:1; Rare:116 | ||||
| chr6:71886607-71887059 | Common:1; Rare:141; Clinvar:3; Clinvar (benign):4 | ||||
| chr6:73263153-73263279 | Common:3; Rare:34 | ||||
| chr6:73451871-73452020 | Common:2; Rare:53; Clinvar:1 | ||||
| chr6:73461900-73461996 | Rare:34; Clinvar:2; Clinvar (benign):1 | ||||
| chr6:73521001-73521406 | Common:2; Rare:100 | ||||
| chr6:73521547-73521634 | Rare:22 | ||||
| chr6:73653934-73654151 | Common:2; Rare:57; Clinvar:3 | ||||
| chr6:73695928-73696213 | Common:1; Rare:54 | ||||
| chr6:75205804-75206080 | Common:1; Rare:76 | ||||
| chr6:75284678-75285033 | Common:1; Rare:108 |