| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:48119181-48119414 | Common:2; Rare:47; Clinvar:4; Clinvar (benign):2 | ||||
| chr12:48350790-48350959 | Rare:63 | ||||
| chr12:48716621-48717013 | Common:4; Rare:117 | ||||
| chr12:48814747-48814880 | Rare:25 | ||||
| chr12:48815480-48815617 | Common:1; Rare:30 | ||||
| chr12:48852086-48852387 | Common:2; Rare:86 | ||||
| chr12:48957367-48957565 | Common:2; Rare:54 | ||||
| chr12:49018733-49018935 | Common:1; Rare:83 | ||||
| chr12:49069882-49070144 | Common:2; Rare:64 | ||||
| chr12:49131280-49131671 | Common:2; Rare:155 | ||||
| chr12:49188492-49188607 | Common:2; Rare:17 | ||||
| chr12:49188981-49189274 | Rare:81; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:49264749-49265092 | Common:5; Rare:120 | ||||
| chr12:49297554-49297659 | Common:3; Rare:38; Clinvar:3 | ||||
| chr12:49322986-49323336 | Common:3; Rare:78 |