| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:190648502-190649119 | Common:10; Rare:323 | ||||
| chr2:190880590-190880925 | Common:9; Rare:229 | ||||
| chr2:191014127-191014379 | Common:3; Rare:161; Clinvar:4; Clinvar (benign):4 | ||||
| chr2:191245342-191245527 | Common:1; Rare:60 | ||||
| chr2:191245990-191246450 | Common:2; Rare:193 | ||||
| chr2:191677856-191678171 | Common:8; Rare:179 | ||||
| chr2:195656833-195657327 | Common:3; Rare:181 | ||||
| chr2:196639340-196639810 | Rare:228 | ||||
| chr2:196719050-196719330 | Common:2; Rare:72 | ||||
| chr2:196926960-196927290 | Common:1; Rare:106 | ||||
| chr2:197434991-197435288 | Rare:174 | ||||
| chr2:197453125-197453580 | Rare:278 | ||||
| chr2:197453871-197454006 | Rare:75 | ||||
| chr2:197499779-197500440 | Common:4; Rare:501; Clinvar:2; Clinvar (benign):4 | ||||
| chr2:197515752-197516121 | Common:2; Rare:195 |