| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:11746393-11746674 | Common:2; Rare:81; Clinvar:4 | ||||
| chr2:12716750-12717082 | Common:1; Rare:92 | ||||
| chr2:12718142-12718248 | Common:1; Rare:24 | ||||
| chr2:15561256-15561376 | Rare:62 | ||||
| chr2:17753643-17754195 | Common:6; Rare:171; Clinvar (benign):1 | ||||
| chr2:18560640-18560805 | Rare:47 | ||||
| chr2:19358406-19358434 | Common:1; Rare:4 | ||||
| chr2:19901628-19901803 | Common:1; Rare:97 | ||||
| chr2:19901938-19902049 | Common:1; Rare:37 | ||||
| chr2:20051258-20051874 | Common:2; Rare:189 | ||||
| chr2:20446831-20447106 | Common:3; Rare:120 | ||||
| chr2:20651040-20651253 | Rare:66 | ||||
| chr2:20823056-20823187 | Common:1; Rare:47 | ||||
| chr2:23927071-23927325 | Common:3; Rare:89 | ||||
| chr2:23940363-23940644 | Common:4; Rare:89 |