| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:27620465-27620812 | Common:2; Rare:117 | ||||
| chr13:28138147-28138206 | Rare:13 | ||||
| chr13:28659076-28659184 | Rare:48; Clinvar (pathogenic):1 | ||||
| chr13:28718823-28718916 | Rare:25 | ||||
| chr13:29850069-29850225 | Rare:50 | ||||
| chr13:30306959-30307231 | Common:5; Rare:73 | ||||
| chr13:30307377-30307605 | Common:3; Rare:77 | ||||
| chr13:30464208-30464372 | Common:1; Rare:49 | ||||
| chr13:30465756-30466113 | Common:1; Rare:112 | ||||
| chr13:30616931-30617146 | Rare:44 | ||||
| chr13:30617233-30618019 | Common:1; Rare:238 | ||||
| chr13:30932560-30932710 | Rare:33 | ||||
| chr13:31162302-31162473 | Common:1; Rare:57 | ||||
| chr13:32031035-32031451 | Common:2; Rare:98 | ||||
| chr13:32031571-32031816 | Common:1; Rare:66 |