| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:76030875-76030956 | Rare:27 | ||||
| chr12:96436526-96436747 | Rare:36 | ||||
| chr12:103946615-103946916 | Rare:76 | ||||
| chr12:105935364-105935660 | Common:1; Rare:49 | ||||
| chr12:108852684-108852924 | Rare:60 | ||||
| chr12:122855339-122855612 | Rare:98 | ||||
| chr12:123270269-123270554 | Common:3; Rare:83 | ||||
| chr13:21297988-21298179 | Common:3; Rare:49 | ||||
| chr13:28329674-28329926 | Common:1; Rare:56 | ||||
| chr13:52194392-52194542 | Rare:44 | ||||
| chr13:52617359-52617537 | Rare:42 | ||||
| chr13:76885268-76885361 | Rare:28 | ||||
| chr13:98976034-98976216 | Common:2; Rare:33 | ||||
| chr13:110205351-110205541 | Common:1; Rare:74; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr13:110212415-110212619 | Common:1; Rare:60; Clinvar (benign):1 |