| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:203238847-203239092 | Common:2; Rare:98 | ||||
| chr2:203239226-203239320 | Rare:31 | ||||
| chr2:203535139-203535557 | Common:3; Rare:157 | ||||
| chr2:206085763-206085983 | Common:1; Rare:64 | ||||
| chr2:206086081-206086303 | Rare:28 | ||||
| chr2:206159362-206160057 | Common:4; Rare:210; Clinvar (benign):1 | ||||
| chr2:206765278-206765627 | Common:2; Rare:89; Clinvar:4; Clinvar (benign):1 | ||||
| chr2:207529553-207530119 | Common:3; Rare:145 | ||||
| chr2:207625183-207625378 | Common:1; Rare:59 | ||||
| chr2:207769865-207770186 | Common:1; Rare:102 | ||||
| chr2:208025466-208025618 | Common:1; Rare:41 | ||||
| chr2:208254418-208254507 | Rare:23 | ||||
| chr2:208254965-208255238 | Common:2; Rare:69 | ||||
| chr2:208266074-208266302 | Common:7; Rare:76; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:210002532-210002664 | Common:4; Rare:55 |