| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:1111997-1112112 | Rare:48 | ||||
| chr5:1326160-1327141 | Common:40; Rare:269 | ||||
| chr5:1344937-1345299 | Common:4; Rare:250 | ||||
| chr5:1494743-1495201 | Common:8; Rare:271 | ||||
| chr5:1523733-1524115 | Common:1; Rare:184 | ||||
| chr5:1524160-1524430 | Common:2; Rare:88 | ||||
| chr5:1799778-1800027 | Common:19; Rare:217 | ||||
| chr5:1801254-1801539 | Common:8; Rare:285; Clinvar:6; Clinvar (benign):6 | ||||
| chr5:5422102-5422823 | Common:5; Rare:365 | ||||
| chr5:6378462-6378733 | Rare:203 | ||||
| chr5:6632890-6633695 | Common:20; Rare:427; Clinvar:20; Clinvar (benign):11 | ||||
| chr5:6713160-6713654 | Common:5; Rare:145 | ||||
| chr5:6714410-6714950 | Common:3; Rare:157 | ||||
| chr5:7868959-7869253 | Common:4; Rare:289; Clinvar:2; Clinvar (benign):5 | ||||
| chr5:10249846-10250371 | Common:38; Rare:493; Clinvar:8; Clinvar (benign):4 |