| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:46479407-46479561 | Common:2; Rare:41 | ||||
| chr2:46519950-46520048 | Rare:21 | ||||
| chr2:46580168-46580355 | Rare:32 | ||||
| chr2:46617019-46617270 | Common:7; Rare:112 | ||||
| chr2:46698766-46698952 | Common:1; Rare:52 | ||||
| chr2:46699024-46699372 | Common:1; Rare:103 | ||||
| chr2:46699422-46699556 | Common:1; Rare:42 | ||||
| chr2:46915709-46915944 | Common:2; Rare:80; Clinvar:3; Clinvar (benign):1 | ||||
| chr2:46916007-46916174 | Common:2; Rare:56 | ||||
| chr2:46940780-46940942 | Common:3; Rare:34 | ||||
| chr2:46941701-46941731 | Rare:14; Clinvar (benign):1 | ||||
| chr2:47176204-47176920 | Common:6; Rare:322; Clinvar (benign):5 | ||||
| chr2:47369095-47369591 | Common:4; Rare:210; Clinvar:19; Clinvar (benign):7 | ||||
| chr2:47402943-47403202 | Common:1; Rare:121; Clinvar:39; Clinvar (benign):29; Clinvar (pathogenic):1 | ||||
| chr2:47782946-47783214 | Common:2; Rare:119; Clinvar:6; Clinvar (benign):10 |