| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:191014133-191014333 | Common:1; Rare:64; Clinvar:2; Clinvar (benign):2 | ||||
| chr2:191245231-191245525 | Common:3; Rare:92 | ||||
| chr2:191246162-191246305 | Common:1; Rare:41 | ||||
| chr2:191677856-191678161 | Common:4; Rare:86 | ||||
| chr2:191846722-191846843 | Rare:34 | ||||
| chr2:191847187-191847478 | Rare:43 | ||||
| chr2:196799605-196799827 | Common:2; Rare:73 | ||||
| chr2:197434973-197435198 | Rare:76 | ||||
| chr2:197453239-197453554 | Rare:106 | ||||
| chr2:197499807-197500430 | Common:1; Rare:239; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:197500658-197500725 | Rare:18 | ||||
| chr2:197515884-197516087 | Common:1; Rare:80 | ||||
| chr2:197705212-197705392 | Common:2; Rare:67 | ||||
| chr2:200510040-200510141 | Rare:32 | ||||
| chr2:200811432-200811589 | Common:1; Rare:57 |