| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:43013901-43014268 | Common:1; Rare:76 | ||||
| chr6:43516891-43517106 | Common:3; Rare:84; Clinvar:2 | ||||
| chr6:43576013-43576190 | Rare:61; Clinvar:4 | ||||
| chr6:43770087-43770231 | Common:2; Rare:44 | ||||
| chr6:44127369-44127657 | Common:4; Rare:84 | ||||
| chr6:44387445-44387729 | Common:4; Rare:71 | ||||
| chr6:49463191-49463407 | Common:1; Rare:62; Clinvar:1; Clinvar (benign):1 | ||||
| chr6:52995303-52995770 | Common:4; Rare:189 | ||||
| chr6:54846432-54846786 | Common:2; Rare:87 | ||||
| chr6:73521193-73521406 | Rare:38 | ||||
| chr6:75284728-75285033 | Common:1; Rare:88 | ||||
| chr6:78867471-78867585 | Rare:47 | ||||
| chr6:83193222-83193364 | Common:3; Rare:52 | ||||
| chr6:85449905-85450245 | Common:1; Rare:99 | ||||
| chr6:85593821-85594038 | Rare:71 |