| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:47705960-47706088 | Rare:58 | ||||
| chr12:47758819-47759011 | Common:1; Rare:38 | ||||
| chr12:48105828-48105938 | Rare:25 | ||||
| chr12:48105985-48106196 | Common:2; Rare:69 | ||||
| chr12:48106276-48106385 | Rare:34 | ||||
| chr12:48119190-48119382 | Common:2; Rare:37; Clinvar:4; Clinvar (benign):2 | ||||
| chr12:48350814-48351105 | Common:5; Rare:107 | ||||
| chr12:48716678-48717008 | Common:4; Rare:99 | ||||
| chr12:48814709-48814863 | Rare:29 | ||||
| chr12:48815432-48815624 | Common:1; Rare:43 | ||||
| chr12:48852102-48852397 | Common:2; Rare:80 | ||||
| chr12:48957325-48957509 | Common:1; Rare:52 | ||||
| chr12:48957512-48957566 | Common:1; Rare:13 | ||||
| chr12:49018739-49018947 | Common:1; Rare:86 | ||||
| chr12:49110647-49111058 | Rare:94 |