| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:190880467-190881028 | Common:5; Rare:198 | ||||
| chr2:190881503-190881678 | Common:1; Rare:81 | ||||
| chr2:191013872-191014583 | Common:6; Rare:185; Clinvar:2; Clinvar (benign):3 | ||||
| chr2:191020218-191020936 | Common:3; Rare:208 | ||||
| chr2:191020967-191021204 | Common:2; Rare:37 | ||||
| chr2:191150979-191151086 | Rare:14 | ||||
| chr2:191677634-191678227 | Common:5; Rare:152 | ||||
| chr2:195656811-195656868 | Rare:19 | ||||
| chr2:195656972-195657370 | Common:2; Rare:114 | ||||
| chr2:196068835-196068962 | Rare:39 | ||||
| chr2:196171471-196171936 | Common:1; Rare:139 | ||||
| chr2:196176184-196176454 | Rare:41 | ||||
| chr2:196639465-196639805 | Rare:111 | ||||
| chr2:196639830-196639932 | Rare:21 | ||||
| chr2:196799394-196799857 | Common:2; Rare:150 |