| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:203328138-203328516 | Common:2; Rare:137 | ||||
| chr2:206085923-206085965 | Rare:11 | ||||
| chr2:206086185-206086229 | Rare:5 | ||||
| chr2:206086278-206086303 | Rare:3 | ||||
| chr2:206159347-206159681 | Common:3; Rare:104; Clinvar (benign):1 | ||||
| chr2:206274551-206274741 | Common:1; Rare:56 | ||||
| chr2:206274917-206275041 | Rare:46 | ||||
| chr2:206765284-206765653 | Common:3; Rare:102; Clinvar:4; Clinvar (benign):5 | ||||
| chr2:207529701-207529993 | Common:3; Rare:95 | ||||
| chr2:207625185-207625364 | Common:1; Rare:49 | ||||
| chr2:208254979-208255232 | Common:2; Rare:65 | ||||
| chr2:208266121-208266355 | Common:6; Rare:84; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:209423970-209424252 | Common:3; Rare:79 | ||||
| chr2:209579391-209579739 | Common:1; Rare:61 | ||||
| chr2:210002473-210002659 | Common:5; Rare:60 |