| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:1294968-1295224 | Rare:122; Clinvar:2 | ||||
| chr5:1344961-1345233 | Common:3; Rare:200 | ||||
| chr5:1523853-1524087 | Rare:136 | ||||
| chr5:1524140-1524470 | Common:4; Rare:157 | ||||
| chr5:1799776-1799996 | Common:16; Rare:202 | ||||
| chr5:1801283-1801532 | Common:8; Rare:202; Clinvar:6; Clinvar (benign):4 | ||||
| chr5:5422250-5422752 | Common:5; Rare:303 | ||||
| chr5:6378492-6378688 | Rare:162 | ||||
| chr5:6632955-6633460 | Common:18; Rare:317; Clinvar:20; Clinvar (benign):10 | ||||
| chr5:6713140-6713500 | Common:6; Rare:231 | ||||
| chr5:7868984-7869235 | Common:2; Rare:133; Clinvar:2; Clinvar (benign):3 | ||||
| chr5:10249853-10250363 | Common:38; Rare:479; Clinvar:8; Clinvar (benign):4 | ||||
| chr5:10307420-10307733 | Common:1; Rare:99 | ||||
| chr5:10353548-10353968 | Common:8; Rare:294 | ||||
| chr5:10761067-10761477 | Common:27; Rare:261 |