| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:162838548-162839163 | Common:1; Rare:130 | ||||
| chr2:163735853-163736423 | Common:5; Rare:160 | ||||
| chr2:164840534-164840778 | Common:1; Rare:44 | ||||
| chr2:164841821-164841906 | Common:1; Rare:24 | ||||
| chr2:164842052-164842139 | Rare:29 | ||||
| chr2:165469539-165469717 | Rare:34 | ||||
| chr2:165953723-165954089 | Common:3; Rare:127; Clinvar:6; Clinvar (benign):2 | ||||
| chr2:166375899-166376110 | Common:4; Rare:63; Clinvar:1; Clinvar (benign):5 | ||||
| chr2:169362524-169362623 | Common:1; Rare:19; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:169510123-169510202 | Rare:18; Clinvar (benign):1 | ||||
| chr2:169584307-169584674 | Common:1; Rare:137 | ||||
| chr2:169584760-169584811 | Rare:15 | ||||
| chr2:169694376-169694529 | Common:4; Rare:45 | ||||
| chr2:169733779-169734080 | Common:2; Rare:85 | ||||
| chr2:169798739-169798965 | Rare:62 |