| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:7541836-7542085 | Common:3; Rare:102; Clinvar:15; Clinvar (benign):11; Clinvar (pathogenic):1 | ||||
| chr6:8435405-8435654 | Common:4; Rare:88 | ||||
| chr6:10694620-10694984 | Common:4; Rare:90 | ||||
| chr6:10723005-10723230 | Common:3; Rare:90 | ||||
| chr6:10747493-10747865 | Common:4; Rare:132 | ||||
| chr6:11232633-11232736 | Rare:25 | ||||
| chr6:13328515-13328615 | Common:2; Rare:34 | ||||
| chr6:13615180-13615426 | Common:2; Rare:106 | ||||
| chr6:13615428-13615559 | Rare:40 | ||||
| chr6:13814041-13814289 | Common:3; Rare:78 | ||||
| chr6:16761430-16761960 | Common:4; Rare:148 | ||||
| chr6:17706388-17706516 | Rare:59 | ||||
| chr6:17706752-17707042 | Common:1; Rare:78 | ||||
| chr6:18122624-18122763 | Common:1; Rare:32; Clinvar (benign):2 | ||||
| chr6:18155209-18155534 | Common:1; Rare:97 |