| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:56557086-56557238 | Common:2; Rare:60 | ||||
| chr3:57227600-57227922 | Common:4; Rare:107 | ||||
| chr3:57292673-57293025 | Common:2; Rare:54 | ||||
| chr3:57555996-57556307 | Rare:76 | ||||
| chr3:57597331-57597661 | Common:4; Rare:104 | ||||
| chr3:57756181-57756323 | Rare:34 | ||||
| chr3:58491828-58492161 | Common:3; Rare:90 | ||||
| chr3:61251376-61251594 | Common:4; Rare:55 | ||||
| chr3:61561434-61561656 | Common:2; Rare:71 | ||||
| chr3:63863777-63864150 | Common:7; Rare:123 | ||||
| chr3:67654582-67654799 | Common:2; Rare:77 | ||||
| chr3:69013202-69013417 | Rare:60 | ||||
| chr3:69013590-69013790 | Common:1; Rare:58 | ||||
| chr3:73624101-73624477 | Common:6; Rare:117 | ||||
| chr3:87227189-87227392 | Common:1; Rare:69; Clinvar:1; Clinvar (benign):2 |