| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:139293896-139294018 | Rare:34 | ||||
| chr5:139341689-139341911 | Common:1; Rare:53 | ||||
| chr5:139404072-139404260 | Rare:54 | ||||
| chr5:139439453-139439597 | Common:1; Rare:40 | ||||
| chr5:139561732-139561794 | Rare:28 | ||||
| chr5:140303063-140303171 | Common:1; Rare:32 | ||||
| chr5:140557427-140557510 | Rare:45 | ||||
| chr5:140564567-140564837 | Rare:74 | ||||
| chr5:140647585-140647889 | Common:5; Rare:124; Clinvar:4; Clinvar (benign):3 | ||||
| chr5:140664747-140664904 | Common:2; Rare:38 | ||||
| chr5:140691313-140691633 | Common:1; Rare:111; Clinvar:8; Clinvar (benign):1 | ||||
| chr5:140800761-140801104 | Common:4; Rare:45 | ||||
| chr5:141172525-141172689 | Common:1; Rare:29 | ||||
| chr5:141245218-141245417 | Common:1; Rare:43 | ||||
| chr5:141320742-141320928 | Common:2; Rare:64 |