| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:7389740-7389966 | Common:1; Rare:60 | ||||
| chr6:7541409-7541741 | Rare:103; Clinvar:1; Clinvar (benign):1 | ||||
| chr6:7541845-7542051 | Common:3; Rare:84; Clinvar:11; Clinvar (benign):9; Clinvar (pathogenic):1 | ||||
| chr6:7590116-7590281 | Common:3; Rare:62 | ||||
| chr6:7910633-7910888 | Common:3; Rare:100 | ||||
| chr6:8064332-8064485 | Common:4; Rare:60 | ||||
| chr6:8102520-8102712 | Common:1; Rare:64 | ||||
| chr6:8435491-8435714 | Common:6; Rare:85 | ||||
| chr6:10412156-10412325 | Rare:57 | ||||
| chr6:10415072-10415196 | Common:1; Rare:43 | ||||
| chr6:10694570-10695019 | Common:7; Rare:135 | ||||
| chr6:10747582-10747858 | Common:3; Rare:106 | ||||
| chr6:11044244-11044598 | Common:3; Rare:119 | ||||
| chr6:11232590-11232825 | Rare:51 | ||||
| chr6:13328523-13328630 | Common:1; Rare:35 |