| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:32896761-32896847 | Rare:33; Clinvar:4; Clinvar (benign):2 | ||||
| chr12:38905497-38905736 | Common:3; Rare:66 | ||||
| chr12:42237417-42237673 | Rare:68 | ||||
| chr12:42326004-42326225 | Common:1; Rare:72 | ||||
| chr12:43758749-43758997 | Common:2; Rare:68; Clinvar:2 | ||||
| chr12:43806309-43806407 | Common:1; Rare:23 | ||||
| chr12:45215982-45216134 | Common:1; Rare:54 | ||||
| chr12:45990373-45990479 | Rare:32 | ||||
| chr12:45990513-45990920 | Common:2; Rare:131 | ||||
| chr12:46269097-46269160 | Common:1; Rare:12 | ||||
| chr12:46372651-46372965 | Rare:131 | ||||
| chr12:47705962-47706124 | Rare:69 | ||||
| chr12:47758445-47758563 | Rare:27 | ||||
| chr12:48106041-48106124 | Common:1; Rare:27 | ||||
| chr12:48350795-48351046 | Common:4; Rare:95 |