| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:43996217-43996335 | Common:2; Rare:35 | ||||
| chr2:44361776-44362005 | Common:1; Rare:67 | ||||
| chr2:46616978-46617263 | Common:7; Rare:124 | ||||
| chr2:46698749-46699012 | Common:1; Rare:81 | ||||
| chr2:46915738-46915914 | Common:2; Rare:54; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:46941711-46941850 | Common:2; Rare:47; Clinvar (benign):1 | ||||
| chr2:47176446-47176937 | Common:7; Rare:224; Clinvar (benign):5 | ||||
| chr2:47402984-47403218 | Common:1; Rare:114; Clinvar:41; Clinvar (benign):31; Clinvar (pathogenic):1 | ||||
| chr2:47695288-47695831 | Common:5; Rare:103 | ||||
| chr2:47782959-47783189 | Common:2; Rare:101; Clinvar:3; Clinvar (benign):5 | ||||
| chr2:48314411-48314731 | Rare:114 | ||||
| chr2:48440631-48440815 | Common:5; Rare:79 | ||||
| chr2:53767492-53767891 | Common:5; Rare:133 | ||||
| chr2:53786851-53787080 | Rare:76 | ||||
| chr2:53970766-53971148 | Common:11; Rare:138 |