| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:130314709-130315114 | Common:8; Rare:261 | ||||
| chr11:130448251-130448786 | Common:1; Rare:236 | ||||
| chr11:130916371-130916687 | Common:7; Rare:98 | ||||
| chr11:133956883-133957448 | Common:6; Rare:311 | ||||
| chr11:134223872-134224192 | Common:6; Rare:277 | ||||
| chr11:134224464-134224837 | Common:2; Rare:350 | ||||
| chr11:134253298-134253645 | Common:8; Rare:347; Clinvar:3; Clinvar (benign):5; Clinvar (pathogenic):2 | ||||
| chr11:134331520-134332170 | Common:21; Rare:270 | ||||
| chr12:389205-389432 | Common:2; Rare:207 | ||||
| chr12:389450-389738 | Common:19; Rare:299 | ||||
| chr12:401426-401717 | Common:1; Rare:152 | ||||
| chr12:401740-402100 | Common:3; Rare:61 | ||||
| chr12:459514-460170 | Common:4; Rare:278 | ||||
| chr12:643150-643631 | Common:11; Rare:168 | ||||
| chr12:752279-752653 | Common:3; Rare:327 |