| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:15424392-15424767 | Common:3; Rare:90 | ||||
| chr2:15560798-15561134 | Common:2; Rare:78 | ||||
| chr2:15561186-15561507 | Rare:110 | ||||
| chr2:15561702-15562068 | Common:3; Rare:69 | ||||
| chr2:15590460-15590961 | Common:6; Rare:98 | ||||
| chr2:15591069-15591178 | Rare:18 | ||||
| chr2:15591493-15592109 | Common:3; Rare:161 | ||||
| chr2:15592145-15592257 | Common:2; Rare:28 | ||||
| chr2:15592285-15592382 | Common:1; Rare:24 | ||||
| chr2:15940062-15940796 | Common:2; Rare:170 | ||||
| chr2:15940963-15940987 | Rare:7 | ||||
| chr2:17518464-17518660 | Common:1; Rare:50 | ||||
| chr2:17753689-17754202 | Common:6; Rare:156; Clinvar (benign):1 | ||||
| chr2:18560649-18560801 | Rare:43 | ||||
| chr2:19901628-19901759 | Common:1; Rare:70 |