| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:126211644-126211812 | Rare:78 | ||||
| chr11:126268814-126269198 | Common:1; Rare:148; Clinvar:2; Clinvar (benign):3 | ||||
| chr11:126303966-126304083 | Rare:67 | ||||
| chr11:126355552-126355755 | Rare:52 | ||||
| chr11:134223925-134224125 | Common:2; Rare:59 | ||||
| chr11:134253298-134253586 | Common:2; Rare:94; Clinvar (benign):1 | ||||
| chr12:389249-389358 | Rare:39 | ||||
| chr12:401436-401682 | Rare:68 | ||||
| chr12:2004430-2004715 | Common:2; Rare:86 | ||||
| chr12:2812589-2812705 | Common:1; Rare:35 | ||||
| chr12:2877005-2877260 | Rare:76 | ||||
| chr12:4538436-4538934 | Common:3; Rare:113 | ||||
| chr12:4648966-4649143 | Common:2; Rare:55; Clinvar (benign):1 | ||||
| chr12:6493224-6493502 | Common:7; Rare:82 | ||||
| chr12:6493767-6494140 | Common:2; Rare:110 |