| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:162727688-162728063 | Common:3; Rare:136; Clinvar:4 | ||||
| chr6:163415107-163415328 | Common:6; Rare:82 | ||||
| chr6:166342519-166342659 | Common:3; Rare:54 | ||||
| chr6:166627901-166628142 | Rare:56 | ||||
| chr6:166999074-166999410 | Common:1; Rare:114 | ||||
| chr6:169702027-169702149 | Common:1; Rare:51 | ||||
| chr6:169751591-169751645 | Rare:23; Clinvar (benign):1 | ||||
| chr6:170554211-170554420 | Common:1; Rare:65 | ||||
| chr7:519143-519265 | Rare:33 | ||||
| chr7:727249-727282 | Rare:10; Clinvar:1 | ||||
| chr7:727283-727308 | Rare:6 | ||||
| chr7:1055304-1055393 | Rare:44 | ||||
| chr7:1537274-1537483 | Rare:71 | ||||
| chr7:1537946-1538312 | Common:1; Rare:124 | ||||
| chr7:1570012-1570146 | Common:1; Rare:43 |