| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:47344919-47345592 | Common:7; Rare:365 | ||||
| chr2:47368941-47370089 | Common:37; Rare:1382; Clinvar:75; Clinvar (benign):32 | ||||
| chr2:47402391-47402791 | Common:3; Rare:97; Clinvar (benign):1 | ||||
| chr2:47402829-47403229 | Common:6; Rare:854; Clinvar:284; Clinvar (benign):187; Clinvar (pathogenic):5 | ||||
| chr2:47403250-47404305 | Common:15; Rare:626; Clinvar:86; Clinvar (benign):55; Clinvar (pathogenic):13 | ||||
| chr2:47782369-47782769 | Common:2; Rare:111; Clinvar (benign):1 | ||||
| chr2:47782837-47783272 | Common:15; Rare:878; Clinvar:45; Clinvar (benign):87; Clinvar (pathogenic):4 | ||||
| chr2:47783381-47784062 | Common:39; Rare:518; Clinvar:25; Clinvar (benign):34 | ||||
| chr2:47904713-47905680 | Common:20; Rare:753 | ||||
| chr2:47905590-47905930 | Rare:232 | ||||
| chr2:47905917-47906317 | Common:2; Rare:226 | ||||
| chr2:47906290-47906880 | Common:2; Rare:221 | ||||
| chr2:48314082-48315435 | Common:9; Rare:1833 | ||||
| chr2:48440553-48440953 | Common:43; Rare:715 | ||||
| chr2:48529893-48530484 | Common:14; Rare:341 |