| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:178790375-178790849 | Common:1; Rare:97; Clinvar:3; Clinvar (benign):7; Clinvar (pathogenic):2 | ||||
| chr2:178791338-178791634 | Rare:49 | ||||
| chr2:178791919-178792201 | Common:2; Rare:63; Clinvar:7; Clinvar (benign):3 | ||||
| chr2:178804459-178804659 | Common:3; Rare:63; Clinvar:6; Clinvar (benign):8 | ||||
| chr2:178805074-178805097 | Rare:4 | ||||
| chr2:182056101-182056179 | Rare:12 | ||||
| chr2:188994043-188994327 | Common:1; Rare:79; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):7 | ||||
| chr2:188996175-188996456 | Common:12; Rare:64; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr2:189004034-189004300 | Rare:79; Clinvar:7; Clinvar (benign):3; Clinvar (pathogenic):12 | ||||
| chr2:191846498-191846737 | Common:4; Rare:79 | ||||
| chr2:201644163-201644285 | Common:1; Rare:18 | ||||
| chr2:202376111-202376209 | Rare:55 | ||||
| chr2:206452775-206453083 | Common:2; Rare:62 | ||||
| chr2:206846957-206847147 | Rare:23 | ||||
| chr2:215378177-215378511 | Common:1; Rare:72; Clinvar:1 |