| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:163120020-163120309 | Common:1; Rare:73 | ||||
| chr2:163121504-163121535 | Rare:2 | ||||
| chr2:163121543-163121908 | Common:5; Rare:60 | ||||
| chr2:163122410-163122502 | Common:1; Rare:17 | ||||
| chr2:168456756-168456845 | Rare:21 | ||||
| chr2:168644105-168644253 | Common:2; Rare:18 | ||||
| chr2:169510239-169510329 | Rare:24; Clinvar (benign):1 | ||||
| chr2:170770785-170771137 | Common:3; Rare:65 | ||||
| chr2:171878550-171878632 | Common:2; Rare:16 | ||||
| chr2:172558346-172558615 | Rare:52 | ||||
| chr2:177727706-177727849 | Common:1; Rare:39 | ||||
| chr2:178523205-178523221 | Rare:6 | ||||
| chr2:178527470-178527967 | Rare:107; Clinvar:10; Clinvar (benign):6; Clinvar (pathogenic):3 | ||||
| chr2:178597732-178598066 | Common:1; Rare:85; Clinvar:9; Clinvar (benign):9 | ||||
| chr2:178611197-178611330 | Rare:33; Clinvar:5; Clinvar (benign):2 |