| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:56682787-56682809 | Rare:3 | ||||
| chr3:56682822-56683027 | Common:2; Rare:80 | ||||
| chr3:56683035-56683370 | Common:4; Rare:114 | ||||
| chr3:57227637-57227913 | Common:3; Rare:88 | ||||
| chr3:57555992-57556329 | Rare:84 | ||||
| chr3:57597294-57597785 | Common:5; Rare:145 | ||||
| chr3:57889883-57890084 | Rare:44; Clinvar (benign):2 | ||||
| chr3:58008325-58008853 | Common:1; Rare:157; Clinvar:8; Clinvar (benign):5 | ||||
| chr3:58149882-58150227 | Rare:117; Clinvar:2; Clinvar (benign):3 | ||||
| chr3:58332636-58332977 | Common:10; Rare:79 | ||||
| chr3:58433787-58433968 | Common:1; Rare:76; Clinvar:2; Clinvar (benign):3 | ||||
| chr3:58666555-58666629 | Common:1; Rare:14 | ||||
| chr3:58666632-58666979 | Common:1; Rare:58 | ||||
| chr3:61251308-61251594 | Common:4; Rare:71 | ||||
| chr3:61561410-61561656 | Common:2; Rare:88 |