| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:127294088-127294212 | Common:2; Rare:49; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:128091004-128091335 | Common:8; Rare:119 | ||||
| chr2:130181543-130181710 | Common:1; Rare:66 | ||||
| chr2:130342127-130342217 | Rare:37 | ||||
| chr2:130342642-130342932 | Common:5; Rare:91 | ||||
| chr2:131105214-131105381 | Common:1; Rare:76 | ||||
| chr2:131493052-131493113 | Common:1; Rare:18 | ||||
| chr2:134918718-134918857 | Rare:55 | ||||
| chr2:135531167-135531508 | Common:1; Rare:72 | ||||
| chr2:148020686-148021068 | Common:2; Rare:81; Clinvar (benign):2 | ||||
| chr2:152717829-152717880 | Rare:23 | ||||
| chr2:152717991-152718078 | Rare:26 | ||||
| chr2:152718491-152718654 | Rare:65 | ||||
| chr2:153478775-153479052 | Common:1; Rare:66 | ||||
| chr2:156436118-156436410 | Common:3; Rare:86 |