| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:176002221-176002407 | Common:3; Rare:81 | ||||
| chr2:177212441-177212802 | Common:4; Rare:146 | ||||
| chr2:177264651-177264854 | Common:2; Rare:65 | ||||
| chr2:177392672-177392813 | Rare:39; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:178451090-178451297 | Common:5; Rare:65; Clinvar:4; Clinvar (benign):3 | ||||
| chr2:178478538-178478677 | Common:1; Rare:44 | ||||
| chr2:186486075-186486354 | Common:3; Rare:89 | ||||
| chr2:186590082-186590355 | Rare:83 | ||||
| chr2:188974437-188974564 | Rare:42; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr2:189783965-189784096 | Common:3; Rare:45; Clinvar (benign):1 | ||||
| chr2:189784305-189784506 | Common:3; Rare:65; Clinvar:6; Clinvar (benign):1 | ||||
| chr2:197434999-197435238 | Rare:78 | ||||
| chr2:197499813-197500167 | Rare:126; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:197500234-197500430 | Common:1; Rare:80 | ||||
| chr2:197515941-197516107 | Rare:66 |