| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:32844328-32844447 | Rare:30 | ||||
| chr6:32844598-32844848 | Common:1; Rare:53 | ||||
| chr6:32853250-32853577 | Rare:92; Clinvar:3; Clinvar (benign):2 | ||||
| chr6:32853660-32853777 | Common:1; Rare:51; Clinvar:2; Clinvar (benign):2 | ||||
| chr6:32854023-32854250 | Common:2; Rare:57 | ||||
| chr6:32953032-32953346 | Common:1; Rare:59 | ||||
| chr6:32968451-32968621 | Common:3; Rare:45 | ||||
| chr6:32968780-32968933 | Common:4; Rare:52 | ||||
| chr6:32969774-32970063 | Rare:74 | ||||
| chr6:32970802-32971066 | Common:4; Rare:79 | ||||
| chr6:33075795-33076032 | Common:3; Rare:30 | ||||
| chr6:33200356-33200432 | Rare:18 | ||||
| chr6:33200637-33200938 | Common:2; Rare:89 | ||||
| chr6:33202101-33202327 | Common:2; Rare:72 | ||||
| chr6:33208436-33208524 | Rare:22 |