| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:42217826-42217967 | Common:3; Rare:44 | ||||
| chr6:42879585-42879935 | Rare:101 | ||||
| chr6:42929238-42929556 | Common:3; Rare:86 | ||||
| chr6:42984333-42984619 | Rare:68 | ||||
| chr6:43013793-43014268 | Common:2; Rare:123 | ||||
| chr6:43059812-43059854 | Rare:16 | ||||
| chr6:43516861-43517106 | Common:3; Rare:93; Clinvar:2 | ||||
| chr6:43575918-43576199 | Common:1; Rare:106; Clinvar:4 | ||||
| chr6:43770081-43770213 | Common:2; Rare:42 | ||||
| chr6:44127358-44127623 | Common:4; Rare:73 | ||||
| chr6:44223441-44223613 | Common:1; Rare:51 | ||||
| chr6:44387620-44387747 | Common:2; Rare:41 | ||||
| chr6:46129816-46130113 | Common:5; Rare:99 | ||||
| chr6:49463186-49463430 | Common:1; Rare:73; Clinvar:1; Clinvar (benign):1 | ||||
| chr6:52284682-52285091 | Common:2; Rare:139 |