| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:161273961-161274181 | Rare:42 | ||||
| chr6:162727688-162728070 | Common:3; Rare:138; Clinvar:4 | ||||
| chr6:163415113-163415328 | Common:6; Rare:79 | ||||
| chr6:166342496-166342665 | Common:3; Rare:67 | ||||
| chr6:166999081-166999409 | Common:1; Rare:112 | ||||
| chr6:167826759-167827142 | Common:2; Rare:220 | ||||
| chr6:167827554-167827761 | Common:1; Rare:74 | ||||
| chr6:169702031-169702176 | Common:2; Rare:68 | ||||
| chr6:169725529-169725644 | Common:1; Rare:28 | ||||
| chr6:169751471-169751645 | Common:1; Rare:73; Clinvar (benign):1 | ||||
| chr6:170306597-170306824 | Common:3; Rare:67 | ||||
| chr6:170554221-170554409 | Common:1; Rare:63 | ||||
| chr7:727238-727297 | Rare:18; Clinvar:1 | ||||
| chr7:945790-945826 | Rare:6 | ||||
| chr7:975513-975674 | Common:1; Rare:64 |