| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:160407873-160408889 | Common:8; Rare:400 | ||||
| chr2:160492945-160493154 | Common:1; Rare:55 | ||||
| chr2:160493401-160493599 | Common:1; Rare:64 | ||||
| chr2:160493805-160493963 | Common:1; Rare:40 | ||||
| chr2:161160208-161160507 | Common:2; Rare:81 | ||||
| chr2:161308286-161308525 | Common:2; Rare:69 | ||||
| chr2:161423950-161424100 | Rare:32 | ||||
| chr2:162318557-162318957 | Common:2; Rare:110 | ||||
| chr2:162343856-162344199 | Common:1; Rare:106 | ||||
| chr2:162344387-162344808 | Common:6; Rare:129 | ||||
| chr2:162838560-162839230 | Common:1; Rare:132 | ||||
| chr2:163735987-163736193 | Rare:42 | ||||
| chr2:164841403-164841582 | Rare:57 | ||||
| chr2:164841701-164842101 | Common:3; Rare:152 | ||||
| chr2:165293743-165294198 | Common:1; Rare:82; Clinvar:4; Clinvar (benign):4 |