| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:188291822-188292083 | Common:4; Rare:87 | ||||
| chr2:188292692-188292869 | Common:1; Rare:44 | ||||
| chr2:188974234-188974568 | Rare:85; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr2:189007497-189007832 | Common:1; Rare:75; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):8 | ||||
| chr2:189179597-189179795 | Common:1; Rare:37; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr2:189441057-189441511 | Common:3; Rare:145 | ||||
| chr2:189783973-189784093 | Common:3; Rare:42; Clinvar (benign):1 | ||||
| chr2:189784281-189784543 | Common:4; Rare:96; Clinvar:8; Clinvar (benign):2 | ||||
| chr2:190319745-190319922 | Common:4; Rare:60; Clinvar (benign):5 | ||||
| chr2:190343873-190343955 | Rare:15 | ||||
| chr2:190534656-190534913 | Common:1; Rare:81 | ||||
| chr2:190648695-190648912 | Common:1; Rare:80 | ||||
| chr2:190880644-190880871 | Common:4; Rare:83 | ||||
| chr2:191014139-191014280 | Common:1; Rare:46; Clinvar:2; Clinvar (benign):2 | ||||
| chr2:191677856-191678161 | Common:4; Rare:86 |