| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:166956220-166956323 | Rare:14; Clinvar:3 | ||||
| chr6:166999031-166999443 | Common:2; Rare:143 | ||||
| chr6:167826688-167827072 | Common:2; Rare:214 | ||||
| chr6:167827188-167827665 | Common:5; Rare:130 | ||||
| chr6:169701987-169702322 | Common:5; Rare:147 | ||||
| chr6:169724471-169724803 | Rare:86 | ||||
| chr6:169751468-169751751 | Common:2; Rare:127; Clinvar (benign):5 | ||||
| chr6:170306673-170306803 | Common:1; Rare:43 | ||||
| chr6:170553177-170553354 | Common:2; Rare:81 | ||||
| chr6:170554154-170554445 | Common:2; Rare:89 | ||||
| chr6:170584588-170584819 | Common:1; Rare:71 | ||||
| chr7:194638-194796 | Common:6; Rare:45 | ||||
| chr7:519126-519272 | Rare:38 | ||||
| chr7:519836-519909 | Common:1; Rare:12 | ||||
| chr7:726616-726795 | Common:2; Rare:68; Clinvar:1; Clinvar (benign):3 |