| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:46297091-46297444 | Common:7; Rare:134; Clinvar (benign):1 | ||||
| chr2:46297495-46297948 | Common:2; Rare:148; Clinvar:7; Clinvar (benign):5 | ||||
| chr2:46616974-46617301 | Common:7; Rare:138; Clinvar (pathogenic):1 | ||||
| chr2:46698769-46698947 | Common:1; Rare:52 | ||||
| chr2:46698998-46699446 | Common:2; Rare:133 | ||||
| chr2:46915723-46915949 | Common:2; Rare:75; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:46915987-46916081 | Common:1; Rare:25 | ||||
| chr2:46916085-46916114 | Common:1; Rare:9 | ||||
| chr2:46941113-46941592 | Common:4; Rare:170; Clinvar (benign):1 | ||||
| chr2:46941680-46941808 | Common:3; Rare:48; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:47176394-47176406 | Rare:10 | ||||
| chr2:47176424-47176577 | Rare:109; Clinvar (benign):5 | ||||
| chr2:47345075-47345351 | Common:1; Rare:76 | ||||
| chr2:47402871-47403197 | Common:1; Rare:152; Clinvar:51; Clinvar (benign):28 | ||||
| chr2:47782918-47783214 | Common:2; Rare:133; Clinvar:6; Clinvar (benign):10 |