| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:44361420-44362068 | Common:20; Rare:1033 | ||||
| chr2:44362120-44362520 | Common:2; Rare:101 | ||||
| chr2:45567915-45568315 | Common:5; Rare:170 | ||||
| chr2:45610633-45611701 | Common:14; Rare:951 | ||||
| chr2:45650840-45651430 | Common:16; Rare:626 | ||||
| chr2:46297059-46297459 | Common:28; Rare:598; Clinvar (benign):1 | ||||
| chr2:46297515-46298759 | Common:12; Rare:802; Clinvar:24; Clinvar (benign):16 | ||||
| chr2:46428703-46429530 | Common:14; Rare:951 | ||||
| chr2:46429479-46430096 | Common:7; Rare:171 | ||||
| chr2:46541809-46543218 | Common:27; Rare:1395 | ||||
| chr2:46544000-46544409 | Rare:352 | ||||
| chr2:46616082-46616483 | Common:4; Rare:109 | ||||
| chr2:46616836-46617390 | Common:59; Rare:1000; Clinvar (pathogenic):2 | ||||
| chr2:46698370-46698630 | Common:5; Rare:105 | ||||
| chr2:46698620-46699340 | Common:17; Rare:919 |