| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:43226554-43226869 | Common:3; Rare:131 | ||||
| chr2:43595947-43596203 | Common:1; Rare:92 | ||||
| chr2:44303892-44304334 | Common:1; Rare:169; Clinvar:4 | ||||
| chr2:44361479-44362010 | Common:4; Rare:166 | ||||
| chr2:46297097-46297437 | Common:6; Rare:131 | ||||
| chr2:46617005-46617261 | Common:6; Rare:113 | ||||
| chr2:46915724-46915953 | Common:2; Rare:76; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:46941333-46941587 | Common:3; Rare:77; Clinvar (benign):1 | ||||
| chr2:46941640-46941667 | Rare:7 | ||||
| chr2:46941694-46941819 | Common:3; Rare:43; Clinvar (benign):1 | ||||
| chr2:47176374-47176813 | Common:4; Rare:217; Clinvar (benign):5 | ||||
| chr2:47345053-47345338 | Common:1; Rare:78 | ||||
| chr2:47369151-47369601 | Common:4; Rare:190; Clinvar:19; Clinvar (benign):7 | ||||
| chr2:47782971-47783195 | Common:2; Rare:95; Clinvar:4; Clinvar (benign):5 | ||||
| chr2:48314624-48314787 | Rare:64 |