| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:42169222-42169880 | Common:6; Rare:546 | ||||
| chr2:42493952-42494368 | Common:3; Rare:278 | ||||
| chr2:42568373-42568768 | Common:11; Rare:159 | ||||
| chr2:42792510-42792820 | Common:5; Rare:166 | ||||
| chr2:43225899-43226070 | Common:2; Rare:107 | ||||
| chr2:43226060-43226260 | Common:1; Rare:79 | ||||
| chr2:43226335-43226895 | Common:7; Rare:405 | ||||
| chr2:43595917-43596217 | Common:2; Rare:203 | ||||
| chr2:43676370-43676630 | Common:2; Rare:144 | ||||
| chr2:43838414-43838760 | Common:1; Rare:167; Clinvar:20; Clinvar (benign):2 | ||||
| chr2:43838833-43839016 | Rare:60; Clinvar:1 | ||||
| chr2:43839102-43839296 | Common:1; Rare:50; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr2:43995882-43996335 | Common:11; Rare:361; Clinvar:5; Clinvar (benign):6; Clinvar (pathogenic):2 | ||||
| chr2:44361476-44362129 | Common:8; Rare:418 | ||||
| chr2:45611084-45611701 | Common:4; Rare:324 |