| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:166342513-166342665 | Common:3; Rare:59 | ||||
| chr6:166382889-166383196 | Common:4; Rare:110 | ||||
| chr6:166956501-166956687 | Common:4; Rare:60; Clinvar:3; Clinvar (benign):2 | ||||
| chr6:166999081-166999412 | Common:1; Rare:113 | ||||
| chr6:166999889-166999927 | Rare:12 | ||||
| chr6:167826367-167826599 | Common:5; Rare:68 | ||||
| chr6:167826810-167827235 | Common:2; Rare:201 | ||||
| chr6:169701958-169702207 | Common:3; Rare:123 | ||||
| chr6:169751497-169751660 | Rare:67; Clinvar (benign):2 | ||||
| chr6:170290527-170290648 | Rare:23 | ||||
| chr6:170290925-170290961 | Rare:7 | ||||
| chr6:170306554-170306809 | Common:1; Rare:86 | ||||
| chr6:170584577-170584773 | Common:1; Rare:64 | ||||
| chr7:519119-519294 | Rare:47 | ||||
| chr7:727242-727303 | Rare:19; Clinvar:1 |