| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:190408650-190408870 | Common:6; Rare:83 | ||||
| chr2:190534310-190534610 | Common:7; Rare:93 | ||||
| chr2:190534530-190534885 | Common:5; Rare:185 | ||||
| chr2:190648655-190649326 | Common:6; Rare:341 | ||||
| chr2:190649420-190649850 | Common:6; Rare:115 | ||||
| chr2:190880631-190880859 | Common:4; Rare:77 | ||||
| chr2:191014132-191014357 | Common:3; Rare:135; Clinvar:4; Clinvar (benign):4 | ||||
| chr2:191020240-191020541 | Common:3; Rare:161 | ||||
| chr2:191245285-191245524 | Common:2; Rare:75 | ||||
| chr2:191677852-191678171 | Common:8; Rare:179 | ||||
| chr2:191678566-191679030 | Common:2; Rare:229 | ||||
| chr2:195575370-195576189 | Common:8; Rare:256 | ||||
| chr2:195656623-195657340 | Common:4; Rare:321 | ||||
| chr2:196171517-196171845 | Common:1; Rare:99 | ||||
| chr2:196639340-196639770 | Rare:181 |