| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:75493412-75494052 | Common:3; Rare:111 | ||||
| chr6:75601747-75601910 | Common:1; Rare:55 | ||||
| chr6:75602373-75602570 | Common:1; Rare:60 | ||||
| chr6:75749022-75749303 | Common:5; Rare:95; Clinvar:3 | ||||
| chr6:78867470-78867621 | Rare:73 | ||||
| chr6:79078117-79078627 | Common:1; Rare:205 | ||||
| chr6:79234551-79234725 | Common:1; Rare:51 | ||||
| chr6:79234731-79234779 | Common:1; Rare:7 | ||||
| chr6:79234863-79235139 | Common:1; Rare:42 | ||||
| chr6:79537132-79537228 | Rare:24; Clinvar:1 | ||||
| chr6:79537286-79537690 | Common:3; Rare:130; Clinvar:5 | ||||
| chr6:79631173-79631397 | Common:2; Rare:51 | ||||
| chr6:79947534-79947706 | Rare:74; Clinvar:6; Clinvar (benign):1 | ||||
| chr6:80004491-80004728 | Common:4; Rare:52 | ||||
| chr6:80106422-80106711 | Common:2; Rare:100; Clinvar (pathogenic):1 |