| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:43219736-43219855 | Common:1; Rare:23 | ||||
| chr2:43220018-43220156 | Common:1; Rare:29 | ||||
| chr2:45888405-45888521 | Common:2; Rare:19 | ||||
| chr2:46818231-46818395 | Rare:46 | ||||
| chr2:47175672-47175899 | Common:3; Rare:80 | ||||
| chr2:47300842-47300969 | Rare:25 | ||||
| chr2:47335236-47335319 | Rare:16 | ||||
| chr2:47795719-47795995 | Common:4; Rare:78; Clinvar:18; Clinvar (benign):11; Clinvar (pathogenic):2 | ||||
| chr2:47798438-47798690 | Common:2; Rare:92; Clinvar:21; Clinvar (benign):15; Clinvar (pathogenic):2 | ||||
| chr2:47906306-47906363 | Rare:28 | ||||
| chr2:47906467-47906861 | Common:2; Rare:140 | ||||
| chr2:48315695-48315767 | Rare:24 | ||||
| chr2:48443071-48443148 | Rare:13 | ||||
| chr2:54560448-54560607 | Common:2; Rare:50 | ||||
| chr2:54571190-54571329 | Common:2; Rare:24 |