| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:75749005-75749308 | Common:6; Rare:105; Clinvar:3 | ||||
| chr6:78867465-78867670 | Rare:91 | ||||
| chr6:78867811-78868034 | Common:1; Rare:64 | ||||
| chr6:79078116-79078768 | Common:1; Rare:249 | ||||
| chr6:79234556-79234897 | Common:4; Rare:86 | ||||
| chr6:79537132-79537253 | Rare:30; Clinvar:2 | ||||
| chr6:79537309-79537697 | Common:2; Rare:123; Clinvar:5 | ||||
| chr6:79631156-79631358 | Common:2; Rare:51 | ||||
| chr6:79947549-79947716 | Common:1; Rare:64; Clinvar:4 | ||||
| chr6:80004473-80004702 | Common:5; Rare:57 | ||||
| chr6:80106401-80106715 | Common:2; Rare:111; Clinvar (pathogenic):1 | ||||
| chr6:82247704-82247846 | Common:1; Rare:44 | ||||
| chr6:82363515-82363838 | Common:2; Rare:95 | ||||
| chr6:83065733-83065928 | Common:1; Rare:70 | ||||
| chr6:83067541-83067767 | Common:1; Rare:64 |