| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:159761665-159762097 | Common:8; Rare:176 | ||||
| chr6:159762305-159762564 | Common:2; Rare:69 | ||||
| chr6:159762766-159763010 | Rare:66 | ||||
| chr6:159789538-159790000 | Common:4; Rare:154 | ||||
| chr6:160121693-160121907 | Common:1; Rare:44 | ||||
| chr6:160122269-160122383 | Rare:39 | ||||
| chr6:160664210-160664423 | Common:2; Rare:48 | ||||
| chr6:160702096-160702362 | Common:3; Rare:66 | ||||
| chr6:161273974-161274183 | Rare:39 | ||||
| chr6:162726897-162727176 | Common:4; Rare:54 | ||||
| chr6:162727695-162727944 | Rare:95; Clinvar:4 | ||||
| chr6:163415243-163415321 | Rare:17 | ||||
| chr6:166342505-166342686 | Common:3; Rare:73 | ||||
| chr6:166382860-166383175 | Common:2; Rare:110 | ||||
| chr6:166956501-166956698 | Common:4; Rare:65; Clinvar:3; Clinvar (benign):2 |