| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:166999044-166999424 | Common:1; Rare:131 | ||||
| chr6:167826724-167827093 | Common:2; Rare:215 | ||||
| chr6:169702000-169702138 | Common:1; Rare:56 | ||||
| chr6:169751471-169751663 | Common:1; Rare:83; Clinvar (benign):3 | ||||
| chr6:170306629-170306783 | Rare:41 | ||||
| chr6:170554211-170554409 | Common:1; Rare:64 | ||||
| chr7:975513-975674 | Common:1; Rare:64 | ||||
| chr7:1028329-1028526 | Common:1; Rare:67 | ||||
| chr7:1138213-1138461 | Common:2; Rare:74 | ||||
| chr7:1570007-1570087 | Common:1; Rare:26 | ||||
| chr7:2242168-2242283 | Common:2; Rare:62 | ||||
| chr7:5513746-5513876 | Common:1; Rare:55 | ||||
| chr7:5530522-5530866 | Common:1; Rare:127; Clinvar (benign):4 | ||||
| chr7:6009029-6009355 | Common:4; Rare:137; Clinvar:3; Clinvar (benign):15 | ||||
| chr7:6059033-6059338 | Common:5; Rare:116 |