| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:201642653-201642722 | Rare:37 | ||||
| chr2:202265656-202265947 | Common:1; Rare:111 | ||||
| chr2:202377058-202377310 | Common:2; Rare:56; Clinvar:1; Clinvar (benign):3 | ||||
| chr2:202634852-202634997 | Common:1; Rare:53 | ||||
| chr2:202912138-202912554 | Common:4; Rare:124 | ||||
| chr2:203014633-203014920 | Common:1; Rare:85 | ||||
| chr2:203238768-203239050 | Common:2; Rare:99 | ||||
| chr2:203239229-203239344 | Rare:40 | ||||
| chr2:206085772-206085960 | Common:1; Rare:54 | ||||
| chr2:206086281-206086303 | Rare:3 | ||||
| chr2:206159396-206159977 | Common:3; Rare:172 | ||||
| chr2:206765297-206765654 | Common:3; Rare:95; Clinvar:4; Clinvar (benign):5 | ||||
| chr2:207529607-207530108 | Common:3; Rare:136 | ||||
| chr2:207625204-207625498 | Common:1; Rare:84 | ||||
| chr2:208255019-208255228 | Common:2; Rare:55 |