| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:80654514-80654760 | Common:5; Rare:143 | ||||
| chr5:80960447-80960672 | Common:5; Rare:54 | ||||
| chr5:81233176-81233359 | Rare:51 | ||||
| chr5:81301464-81301829 | Common:5; Rare:115 | ||||
| chr5:81751024-81751461 | Common:1; Rare:128 | ||||
| chr5:81971845-81972075 | Common:2; Rare:95 | ||||
| chr5:81972245-81972295 | Common:1; Rare:12 | ||||
| chr5:82278319-82278702 | Common:4; Rare:126 | ||||
| chr5:83077330-83077619 | Common:1; Rare:87 | ||||
| chr5:83077861-83078086 | Common:1; Rare:41 | ||||
| chr5:83471592-83471824 | Rare:49; Clinvar:2 | ||||
| chr5:86617772-86618125 | Common:2; Rare:118 | ||||
| chr5:87267673-87267986 | Common:4; Rare:119 | ||||
| chr5:87268174-87268291 | Common:1; Rare:30; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:87268833-87269000 | Rare:61; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):1 |