| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:47477696-47478255 | Common:5; Rare:160; Clinvar:7; Clinvar (benign):7 | ||||
| chr6:49463146-49463430 | Common:1; Rare:80; Clinvar:1; Clinvar (benign):1 | ||||
| chr6:52284709-52285094 | Common:2; Rare:125 | ||||
| chr6:52361969-52362157 | Common:2; Rare:66 | ||||
| chr6:52420122-52420376 | Common:3; Rare:105; Clinvar:1; Clinvar (benign):2 | ||||
| chr6:52576987-52577292 | Common:5; Rare:114 | ||||
| chr6:52577319-52577466 | Common:1; Rare:51 | ||||
| chr6:52671013-52671167 | Rare:46 | ||||
| chr6:52995267-52995814 | Common:4; Rare:227 | ||||
| chr6:53061690-53061916 | Rare:53 | ||||
| chr6:53348847-53349167 | Common:2; Rare:142 | ||||
| chr6:53545098-53545224 | Rare:38 | ||||
| chr6:53665582-53665968 | Common:5; Rare:79 | ||||
| chr6:56060739-56060891 | Rare:54 | ||||
| chr6:56091474-56091793 | Common:1; Rare:58 |