| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:7313043-7313385 | Common:5; Rare:126 | ||||
| chr6:7389250-7389600 | Common:1; Rare:77 | ||||
| chr6:7389672-7389878 | Common:2; Rare:69 | ||||
| chr6:7541120-7541630 | Common:5; Rare:146 | ||||
| chr6:7590060-7590262 | Common:5; Rare:68 | ||||
| chr6:7909940-7910562 | Common:16; Rare:297 | ||||
| chr6:7910712-7910954 | Common:1; Rare:97 | ||||
| chr6:8064297-8064632 | Common:4; Rare:107 | ||||
| chr6:8102493-8102829 | Common:3; Rare:102 | ||||
| chr6:8435518-8435654 | Common:3; Rare:49 | ||||
| chr6:10404090-10404660 | Common:5; Rare:217; Clinvar (pathogenic):2 | ||||
| chr6:10412056-10412456 | Common:1; Rare:182 | ||||
| chr6:10555651-10555764 | Common:2; Rare:24; Clinvar (benign):1 | ||||
| chr6:10556189-10556321 | Rare:28; Clinvar:1 | ||||
| chr6:10694409-10694993 | Common:12; Rare:172 |