| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:134225624-134225844 | Common:1; Rare:52 | ||||
| chr11:134253301-134253754 | Common:3; Rare:165; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr11:134331635-134332086 | Common:10; Rare:106 | ||||
| chr11:134332296-134332414 | Rare:36 | ||||
| chr12:307348-307511 | Rare:43 | ||||
| chr12:388485-388720 | Common:1; Rare:53 | ||||
| chr12:388894-388967 | Rare:28 | ||||
| chr12:389000-389420 | Common:6; Rare:205 | ||||
| chr12:389436-389738 | Common:7; Rare:117 | ||||
| chr12:401362-401889 | Common:2; Rare:126 | ||||
| chr12:459840-460171 | Common:3; Rare:106 | ||||
| chr12:610303-610465 | Rare:27 | ||||
| chr12:642633-643166 | Common:5; Rare:156 | ||||
| chr12:752287-752669 | Common:1; Rare:121 | ||||
| chr12:752911-753281 | Common:3; Rare:97; Clinvar:3; Clinvar (benign):3 |