| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:47904954-47905295 | Common:1; Rare:96; Clinvar:1 | ||||
| chr12:47905311-47905536 | Rare:53 | ||||
| chr12:47963396-47963703 | Common:3; Rare:72 | ||||
| chr12:48004437-48004717 | Common:3; Rare:53; Clinvar (benign):2 | ||||
| chr12:48004795-48005002 | Rare:39 | ||||
| chr12:48105810-48106012 | Rare:54 | ||||
| chr12:48106016-48106469 | Common:2; Rare:130 | ||||
| chr12:48118623-48118750 | Common:1; Rare:21 | ||||
| chr12:48119148-48119426 | Common:2; Rare:56; Clinvar:4; Clinvar (benign):2 | ||||
| chr12:48119965-48120044 | Rare:17 | ||||
| chr12:48157079-48157229 | Rare:28 | ||||
| chr12:48157432-48157790 | Common:5; Rare:92 | ||||
| chr12:48183267-48183369 | Rare:23 | ||||
| chr12:48183482-48183858 | Common:1; Rare:99 | ||||
| chr12:48350781-48351097 | Common:5; Rare:116 |