| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:162727736-162727985 | Rare:69; Clinvar:1 | ||||
| chr6:163416006-163416166 | Common:2; Rare:45 | ||||
| chr6:166342512-166342675 | Common:3; Rare:64 | ||||
| chr6:166999035-166999415 | Common:1; Rare:131 | ||||
| chr6:167826759-167827123 | Common:2; Rare:217 | ||||
| chr6:169253840-169254072 | Rare:35 | ||||
| chr6:169702018-169702138 | Common:1; Rare:47 | ||||
| chr6:169751534-169751645 | Rare:40; Clinvar (benign):1 | ||||
| chr6:170306603-170306809 | Common:1; Rare:61 | ||||
| chr6:170553196-170553397 | Common:3; Rare:85 | ||||
| chr6:170554150-170554404 | Common:1; Rare:78 | ||||
| chr7:519154-519312 | Rare:40 | ||||
| chr7:712428-712656 | Common:1; Rare:49 | ||||
| chr7:727246-727281 | Rare:13; Clinvar:1 | ||||
| chr7:975519-975722 | Common:1; Rare:74 |