| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:39037120-39037520 | Common:1; Rare:103 | ||||
| chr13:39037689-39038493 | Common:7; Rare:752 | ||||
| chr13:39038559-39038971 | Common:7; Rare:219 | ||||
| chr13:39655400-39655920 | Common:21; Rare:559; Clinvar:15; Clinvar (benign):22; Clinvar (pathogenic):4 | ||||
| chr13:40666505-40667150 | Common:12; Rare:584 | ||||
| chr13:40770568-40771133 | Common:2; Rare:213 | ||||
| chr13:40771054-40771476 | Common:12; Rare:387 | ||||
| chr13:40789180-40789896 | Common:15; Rare:717; Clinvar:29; Clinvar (benign):10 | ||||
| chr13:40789993-40790393 | Common:5; Rare:80 | ||||
| chr13:40981334-40981820 | Common:8; Rare:119 | ||||
| chr13:40981986-40983170 | Common:27; Rare:636 | ||||
| chr13:41018902-41019580 | Common:2; Rare:240 | ||||
| chr13:41060089-41060656 | Common:9; Rare:616 | ||||
| chr13:41060579-41061300 | Common:91; Rare:1310 | ||||
| chr13:41061320-41061625 | Common:15; Rare:474 |