| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:5003662-5003834 | Common:5; Rare:52 | ||||
| chr6:5004007-5004088 | Rare:42 | ||||
| chr6:5260677-5261017 | Common:3; Rare:116; Clinvar (benign):4 | ||||
| chr6:5261263-5261554 | Common:9; Rare:73 | ||||
| chr6:6006858-6007082 | Common:3; Rare:51 | ||||
| chr6:7108381-7108665 | Common:1; Rare:84 | ||||
| chr6:7313052-7313380 | Common:5; Rare:124 | ||||
| chr6:7389740-7390003 | Common:1; Rare:70 | ||||
| chr6:7541409-7541678 | Rare:82; Clinvar (benign):1 | ||||
| chr6:8435484-8435678 | Common:4; Rare:80 | ||||
| chr6:10521229-10521431 | Common:1; Rare:46 | ||||
| chr6:10555962-10556267 | Common:1; Rare:66; Clinvar:2; Clinvar (benign):1 | ||||
| chr6:10694815-10694988 | Common:3; Rare:60 | ||||
| chr6:10722860-10723224 | Common:6; Rare:124 | ||||
| chr6:10747582-10747876 | Common:3; Rare:111 |