| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:6686911-6687168 | Common:3; Rare:52 | ||||
| chr6:6695011-6695263 | Common:2; Rare:50 | ||||
| chr6:6700103-6700289 | Common:1; Rare:28 | ||||
| chr6:7542404-7542711 | Common:3; Rare:79 | ||||
| chr6:7542899-7543332 | Common:3; Rare:124 | ||||
| chr6:7545968-7546127 | Common:1; Rare:23 | ||||
| chr6:7561415-7561681 | Common:2; Rare:46 | ||||
| chr6:7567747-7568012 | Rare:59; Clinvar:4; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr6:7571363-7571764 | Common:3; Rare:93; Clinvar:5; Clinvar (benign):11; Clinvar (pathogenic):1 | ||||
| chr6:7577920-7578137 | Common:2; Rare:41 | ||||
| chr6:7891624-7891916 | Common:2; Rare:63 | ||||
| chr6:9482039-9482435 | Common:3; Rare:76 | ||||
| chr6:10414036-10414097 | Common:1; Rare:19 | ||||
| chr6:13643226-13643339 | Rare:19 | ||||
| chr6:13710800-13710915 | Rare:44 |