| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:38905567-38905710 | Common:3; Rare:38 | ||||
| chr12:39619785-39619919 | Common:1; Rare:25 | ||||
| chr12:42326065-42326215 | Common:1; Rare:47 | ||||
| chr12:43758749-43759000 | Common:2; Rare:69; Clinvar:2 | ||||
| chr12:44876052-44876474 | Common:3; Rare:131 | ||||
| chr12:45216011-45216188 | Rare:53 | ||||
| chr12:45990533-45990900 | Common:2; Rare:115 | ||||
| chr12:46267353-46267409 | Rare:12 | ||||
| chr12:46269137-46269191 | Rare:12 | ||||
| chr12:46372724-46373004 | Rare:112 | ||||
| chr12:47705962-47706088 | Rare:57 | ||||
| chr12:48105843-48105923 | Rare:19 | ||||
| chr12:48105985-48106196 | Common:2; Rare:69 | ||||
| chr12:48119181-48119379 | Common:2; Rare:36; Clinvar:4; Clinvar (benign):2 | ||||
| chr12:48818583-48818854 | Common:1; Rare:95 |