| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:48939655-48940128 | Common:3; Rare:101 | ||||
| chr12:49018733-49019157 | Common:2; Rare:137; Clinvar (benign):3 | ||||
| chr12:49131300-49131606 | Common:2; Rare:124 | ||||
| chr12:49188447-49188611 | Common:2; Rare:22 | ||||
| chr12:49188975-49189165 | Rare:56; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:49264752-49265209 | Common:6; Rare:167 | ||||
| chr12:49322949-49323293 | Common:3; Rare:86 | ||||
| chr12:49367159-49367586 | Common:1; Rare:116 | ||||
| chr12:49489777-49490099 | Common:2; Rare:50 | ||||
| chr12:49514243-49514348 | Common:1; Rare:22 | ||||
| chr12:49567819-49568177 | Common:1; Rare:94 | ||||
| chr12:49623286-49623591 | Common:1; Rare:82 | ||||
| chr12:49741391-49741626 | Rare:73 | ||||
| chr12:49750604-49750685 | Rare:14 | ||||
| chr12:49758192-49758478 | Common:5; Rare:85 |