| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:46915722-46915910 | Common:1; Rare:57; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:46916012-46916135 | Common:2; Rare:38 | ||||
| chr2:47176429-47176759 | Common:4; Rare:164; Clinvar (benign):5 | ||||
| chr2:47345053-47345149 | Rare:26 | ||||
| chr2:47402951-47403189 | Common:1; Rare:107; Clinvar:32; Clinvar (benign):26 | ||||
| chr2:48314413-48314744 | Rare:118 | ||||
| chr2:48440609-48440837 | Common:6; Rare:104 | ||||
| chr2:53767559-53767867 | Common:5; Rare:106 | ||||
| chr2:53786842-53787209 | Common:1; Rare:141 | ||||
| chr2:53970788-53971157 | Common:11; Rare:134 | ||||
| chr2:55050287-55050369 | Rare:37 | ||||
| chr2:55050389-55050763 | Common:5; Rare:111 | ||||
| chr2:55232249-55232881 | Common:5; Rare:202 | ||||
| chr2:55419851-55420140 | Common:4; Rare:111 | ||||
| chr2:55519404-55519825 | Common:2; Rare:132 |