| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:166382889-166383158 | Common:2; Rare:97 | ||||
| chr6:166627970-166628062 | Rare:19 | ||||
| chr6:166956550-166956715 | Common:3; Rare:60; Clinvar:3 | ||||
| chr6:166999081-166999415 | Common:1; Rare:114 | ||||
| chr6:167271103-167271376 | Common:4; Rare:42 | ||||
| chr6:167826759-167827235 | Common:2; Rare:237 | ||||
| chr6:169237213-169237458 | Common:3; Rare:51 | ||||
| chr6:169701993-169702266 | Common:5; Rare:128 | ||||
| chr6:169751521-169751660 | Rare:54; Clinvar (benign):2 | ||||
| chr6:170306571-170306805 | Common:1; Rare:76 | ||||
| chr6:170554211-170554404 | Common:1; Rare:63 | ||||
| chr6:170584433-170584539 | Rare:34 | ||||
| chr7:519070-519294 | Rare:53 | ||||
| chr7:727243-727308 | Rare:21; Clinvar:1 | ||||
| chr7:832276-832594 | Common:2; Rare:89; Clinvar:4 |