| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:163416006-163416210 | Common:2; Rare:56 | ||||
| chr6:166342508-166342686 | Common:3; Rare:72 | ||||
| chr6:166956535-166956678 | Common:2; Rare:50; Clinvar:3 | ||||
| chr6:166999074-166999424 | Common:1; Rare:118 | ||||
| chr6:167826771-167827123 | Common:2; Rare:211 | ||||
| chr6:167827210-167827227 | Rare:1 | ||||
| chr6:169701993-169702377 | Common:5; Rare:157 | ||||
| chr6:169724494-169724832 | Rare:95 | ||||
| chr6:169751440-169751829 | Common:3; Rare:150; Clinvar (benign):5 | ||||
| chr6:170306548-170306805 | Common:1; Rare:87 | ||||
| chr6:170553196-170553423 | Common:3; Rare:89 | ||||
| chr6:170554211-170554445 | Common:2; Rare:74 | ||||
| chr6:170584466-170584784 | Common:2; Rare:104 | ||||
| chr7:519105-519228 | Rare:33 | ||||
| chr7:519242-519307 | Rare:16 |