| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:55231931-55232051 | Common:2; Rare:30 | ||||
| chr2:55232191-55232730 | Common:4; Rare:147 | ||||
| chr2:55269157-55269342 | Common:2; Rare:56 | ||||
| chr2:55419287-55419406 | Rare:25 | ||||
| chr2:55419755-55420179 | Common:5; Rare:165 | ||||
| chr2:55519406-55519753 | Common:1; Rare:97 | ||||
| chr2:55616438-55617106 | Common:8; Rare:267 | ||||
| chr2:55617575-55617968 | Common:4; Rare:157 | ||||
| chr2:55618815-55618983 | Rare:48 | ||||
| chr2:55693813-55693997 | Common:1; Rare:55; Clinvar (benign):2 | ||||
| chr2:55923660-55924000 | Common:5; Rare:120; Clinvar:2; Clinvar (benign):9 | ||||
| chr2:58046470-58046910 | Common:2; Rare:125 | ||||
| chr2:58046930-58047300 | Common:1; Rare:120 | ||||
| chr2:58240786-58241186 | Rare:174 | ||||
| chr2:58241302-58241477 | Common:1; Rare:91; Clinvar:5; Clinvar (benign):1 |