| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:132807205-132807547 | Common:2; Rare:86 | ||||
| chr5:132830585-132831170 | Common:2; Rare:223 | ||||
| chr5:132866307-132866734 | Common:6; Rare:250; Clinvar:2; Clinvar (benign):2 | ||||
| chr5:132873380-132873680 | Common:4; Rare:116 | ||||
| chr5:132963264-132963424 | Common:1; Rare:64 | ||||
| chr5:132963499-132964036 | Common:2; Rare:259 | ||||
| chr5:133026512-133026803 | Common:5; Rare:70 | ||||
| chr5:133051605-133052108 | Common:4; Rare:353 | ||||
| chr5:133968538-133968741 | Rare:154 | ||||
| chr5:134004625-134004922 | Common:2; Rare:200 | ||||
| chr5:134004970-134005220 | Rare:102 | ||||
| chr5:134005230-134005530 | Common:1; Rare:76 | ||||
| chr5:134114529-134114829 | Common:1; Rare:162 | ||||
| chr5:134225310-134225700 | Common:5; Rare:229 | ||||
| chr5:134225988-134226421 | Common:2; Rare:270 |