| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:43995946-43996325 | Common:5; Rare:165; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:44361479-44362025 | Common:4; Rare:172 | ||||
| chr2:46297110-46297431 | Common:5; Rare:127 | ||||
| chr2:46297682-46297820 | Rare:54; Clinvar:3; Clinvar (benign):1 | ||||
| chr2:46542559-46542693 | Rare:45 | ||||
| chr2:46616978-46617270 | Common:7; Rare:129 | ||||
| chr2:46915722-46916181 | Common:4; Rare:151; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:46941687-46941795 | Common:3; Rare:41; Clinvar (benign):1 | ||||
| chr2:47176441-47176864 | Common:4; Rare:188; Clinvar (benign):5 | ||||
| chr2:47402925-47403203 | Common:1; Rare:131; Clinvar:44; Clinvar (benign):29; Clinvar (pathogenic):1 | ||||
| chr2:47782918-47783198 | Common:2; Rare:122; Clinvar:4; Clinvar (benign):7 | ||||
| chr2:47905489-47905639 | Common:3; Rare:84 | ||||
| chr2:48314385-48314794 | Rare:145 | ||||
| chr2:48440619-48440876 | Common:8; Rare:118 | ||||
| chr2:53767494-53767889 | Common:5; Rare:131 |