| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:3751396-3751551 | Common:1; Rare:70 | ||||
| chr6:3849114-3849439 | Common:3; Rare:92 | ||||
| chr6:4021149-4021464 | Common:1; Rare:128 | ||||
| chr6:5003662-5003843 | Common:5; Rare:56 | ||||
| chr6:5260677-5261017 | Common:3; Rare:116; Clinvar (benign):4 | ||||
| chr6:5261238-5261557 | Common:9; Rare:80 | ||||
| chr6:7107512-7107843 | Rare:110 | ||||
| chr6:7108073-7108447 | Rare:106 | ||||
| chr6:7108497-7108684 | Common:1; Rare:59 | ||||
| chr6:7313042-7313343 | Common:5; Rare:115 | ||||
| chr6:7389676-7390059 | Common:2; Rare:121 | ||||
| chr6:7541314-7541528 | Common:2; Rare:69 | ||||
| chr6:7541536-7542207 | Common:4; Rare:219; Clinvar:18; Clinvar (benign):12; Clinvar (pathogenic):1 | ||||
| chr6:8102524-8102761 | Common:1; Rare:77 | ||||
| chr6:8435343-8435659 | Common:4; Rare:109 |