| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:96869393-96869578 | Common:2; Rare:47 | ||||
| chr2:97094806-97094966 | Common:1; Rare:36 | ||||
| chr2:97113444-97113702 | Common:1; Rare:63 | ||||
| chr2:97589662-97590015 | Common:7; Rare:96 | ||||
| chr2:97645780-97646196 | Common:3; Rare:123 | ||||
| chr2:97663902-97664255 | Common:1; Rare:110 | ||||
| chr2:97759657-97759854 | Rare:49 | ||||
| chr2:97995526-97995702 | Common:1; Rare:63 | ||||
| chr2:98086985-98087175 | Rare:49 | ||||
| chr2:98346438-98346456 | Rare:8 | ||||
| chr2:98444760-98445061 | Common:1; Rare:115 | ||||
| chr2:98608289-98608712 | Common:2; Rare:166; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:98608849-98608993 | Rare:37 | ||||
| chr2:98731062-98731308 | Common:3; Rare:88 | ||||
| chr2:98869223-98869420 | Common:1; Rare:45 |