| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:132687285-132687669 | Common:5; Rare:268; Clinvar:16; Clinvar (benign):20; Clinvar (pathogenic):2 | ||||
| chr12:132710534-132710882 | Common:10; Rare:238 | ||||
| chr12:132761388-132761594 | Common:2; Rare:61 | ||||
| chr12:132761634-132762233 | Common:6; Rare:357 | ||||
| chr12:132828670-132828925 | Common:6; Rare:104 | ||||
| chr12:132829030-132829310 | Rare:112 | ||||
| chr12:132956280-132956435 | Common:2; Rare:54 | ||||
| chr12:132986160-132986490 | Rare:146 | ||||
| chr12:133079950-133080500 | Common:18; Rare:306 | ||||
| chr12:133080520-133081098 | Common:7; Rare:308 | ||||
| chr12:133130228-133130652 | Common:10; Rare:210 | ||||
| chr12:133181391-133181546 | Common:1; Rare:42 | ||||
| chr13:19633411-19633752 | Common:2; Rare:246 | ||||
| chr13:19782876-19783090 | Common:4; Rare:148 | ||||
| chr13:19863445-19863937 | Common:11; Rare:302 |