| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:55618847-55619035 | Common:1; Rare:45 | ||||
| chr2:55693804-55693897 | Rare:38; Clinvar (benign):2 | ||||
| chr2:58046619-58046712 | Rare:26 | ||||
| chr2:58046724-58046861 | Common:1; Rare:44 | ||||
| chr2:58047009-58047222 | Rare:62 | ||||
| chr2:58047224-58047407 | Rare:55 | ||||
| chr2:58241311-58241444 | Common:1; Rare:73; Clinvar:3; Clinvar (benign):1 | ||||
| chr2:60550894-60551031 | Rare:36 | ||||
| chr2:60881424-60881727 | Common:3; Rare:92 | ||||
| chr2:61017164-61017770 | Common:5; Rare:184; Clinvar:3; Clinvar (benign):2 | ||||
| chr2:61144901-61145176 | Common:3; Rare:91 | ||||
| chr2:61177252-61177472 | Common:5; Rare:96 | ||||
| chr2:61221520-61221694 | Common:2; Rare:54 | ||||
| chr2:61470664-61470991 | Rare:109 | ||||
| chr2:61471238-61471396 | Common:4; Rare:58 |