| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:42746060-42746348 | Rare:86 | ||||
| chr6:42929226-42929525 | Common:3; Rare:79 | ||||
| chr6:43013869-43014280 | Common:2; Rare:90 | ||||
| chr6:43427783-43427886 | Rare:20 | ||||
| chr6:43516853-43517102 | Common:4; Rare:94; Clinvar:2 | ||||
| chr6:43687757-43687860 | Common:1; Rare:42 | ||||
| chr6:43770081-43770278 | Common:3; Rare:56 | ||||
| chr6:44127351-44127652 | Common:4; Rare:88 | ||||
| chr6:44247090-44247179 | Common:1; Rare:54 | ||||
| chr6:44387445-44387738 | Common:4; Rare:75 | ||||
| chr6:49463205-49463407 | Common:1; Rare:59; Clinvar (benign):1 | ||||
| chr6:52995269-52995819 | Common:4; Rare:226 | ||||
| chr6:53348904-53349272 | Common:2; Rare:123 | ||||
| chr6:54846574-54846764 | Common:1; Rare:48 | ||||
| chr6:56247519-56247680 | Common:2; Rare:29 |