| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:5260690-5261025 | Common:3; Rare:111; Clinvar (benign):4 | ||||
| chr6:5261268-5261563 | Common:9; Rare:76 | ||||
| chr6:7108566-7108665 | Rare:34 | ||||
| chr6:7313127-7313380 | Common:4; Rare:93 | ||||
| chr6:7389734-7389999 | Common:1; Rare:70 | ||||
| chr6:7541349-7541827 | Common:1; Rare:138; Clinvar:2; Clinvar (benign):1 | ||||
| chr6:7541841-7542040 | Common:2; Rare:82; Clinvar:11; Clinvar (benign):8; Clinvar (pathogenic):1 | ||||
| chr6:7590075-7590247 | Common:5; Rare:50 | ||||
| chr6:7910633-7910893 | Common:3; Rare:103 | ||||
| chr6:8064332-8064472 | Common:4; Rare:55 | ||||
| chr6:8102490-8102784 | Common:2; Rare:95 | ||||
| chr6:8435491-8435659 | Common:3; Rare:66 | ||||
| chr6:10415030-10415202 | Common:1; Rare:56 | ||||
| chr6:10419542-10419660 | Rare:22 | ||||
| chr6:10521182-10521526 | Common:1; Rare:84 |