| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:166999017-166999424 | Common:1; Rare:137 | ||||
| chr6:167826755-167827123 | Common:2; Rare:220 | ||||
| chr6:169701977-169702390 | Common:5; Rare:171 | ||||
| chr6:169751507-169751651 | Rare:56; Clinvar (benign):2 | ||||
| chr6:170306568-170306830 | Common:3; Rare:82 | ||||
| chr6:170553035-170553376 | Common:3; Rare:126 | ||||
| chr6:170554211-170554457 | Common:2; Rare:76 | ||||
| chr6:170584586-170584793 | Common:1; Rare:69 | ||||
| chr7:727224-727339 | Rare:39; Clinvar:1; Clinvar (benign):1 | ||||
| chr7:975486-975660 | Common:1; Rare:82 | ||||
| chr7:1028301-1028476 | Rare:65 | ||||
| chr7:1044306-1044639 | Common:6; Rare:122 | ||||
| chr7:1055304-1055399 | Rare:44 | ||||
| chr7:1448381-1448622 | Rare:68 | ||||
| chr7:1504338-1504526 | Common:3; Rare:87 |