| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:167880513-167880816 | Rare:52 | ||||
| chr6:169702011-169702149 | Common:1; Rare:60 | ||||
| chr6:169725509-169725570 | Rare:21 | ||||
| chr6:169751479-169751660 | Common:1; Rare:79; Clinvar (benign):2 | ||||
| chr6:170306579-170306824 | Common:3; Rare:76 | ||||
| chr6:170553164-170553423 | Common:3; Rare:101 | ||||
| chr6:170554184-170554454 | Common:2; Rare:80 | ||||
| chr7:519095-519271 | Rare:44 | ||||
| chr7:727212-727308 | Rare:32; Clinvar:2 | ||||
| chr7:975480-975650 | Common:1; Rare:83 | ||||
| chr7:1028296-1028522 | Common:1; Rare:83 | ||||
| chr7:1087829-1088122 | Common:1; Rare:61 | ||||
| chr7:1138198-1138461 | Common:2; Rare:82 | ||||
| chr7:1530601-1530887 | Common:1; Rare:103 | ||||
| chr7:1538074-1538289 | Common:1; Rare:70 |