| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:43637122-43637324 | Common:2; Rare:69 | ||||
| chr2:46617012-46617263 | Common:7; Rare:110 | ||||
| chr2:46915733-46915869 | Common:1; Rare:34; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:46916032-46916154 | Common:2; Rare:41 | ||||
| chr2:46941694-46941758 | Common:2; Rare:26; Clinvar (benign):1 | ||||
| chr2:47782946-47783210 | Common:2; Rare:118; Clinvar:5; Clinvar (benign):10 | ||||
| chr2:48440631-48440837 | Common:5; Rare:97 | ||||
| chr2:53767740-53767865 | Common:1; Rare:45 | ||||
| chr2:53786848-53787169 | Common:1; Rare:118 | ||||
| chr2:53970788-53971133 | Common:10; Rare:118 | ||||
| chr2:55050321-55050375 | Rare:22 | ||||
| chr2:55050441-55050818 | Common:4; Rare:115 | ||||
| chr2:55519406-55519786 | Common:1; Rare:113 | ||||
| chr2:60756140-60756277 | Rare:44 | ||||
| chr2:60881322-60881562 | Common:1; Rare:97 |