| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:135531174-135531502 | Common:1; Rare:65 | ||||
| chr2:135741742-135741951 | Common:1; Rare:82 | ||||
| chr2:135984903-135985160 | Common:1; Rare:59 | ||||
| chr2:148020682-148021125 | Common:2; Rare:105; Clinvar (benign):2 | ||||
| chr2:148021472-148021632 | Rare:48 | ||||
| chr2:149587318-149587370 | Rare:10 | ||||
| chr2:149587681-149587816 | Common:1; Rare:37; Clinvar:1 | ||||
| chr2:152717845-152717978 | Rare:55 | ||||
| chr2:152717995-152718029 | Rare:9 | ||||
| chr2:159712416-159712571 | Common:2; Rare:64 | ||||
| chr2:162073555-162073700 | Rare:38 | ||||
| chr2:162318650-162318794 | Rare:29 | ||||
| chr2:169584761-169584851 | Rare:31 | ||||
| chr2:171433973-171434275 | Common:2; Rare:76 | ||||
| chr2:171434753-171434858 | Common:1; Rare:23 |