| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:1112006-1112112 | Rare:44 | ||||
| chr5:1326448-1326588 | Common:1; Rare:21 | ||||
| chr5:1326736-1326759 | Common:1; Rare:3 | ||||
| chr5:1345019-1345127 | Common:1; Rare:41 | ||||
| chr5:1799775-1799993 | Common:8; Rare:102 | ||||
| chr5:1801256-1801531 | Common:4; Rare:144; Clinvar:3; Clinvar (benign):3 | ||||
| chr5:5422342-5422722 | Common:2; Rare:127 | ||||
| chr5:5422836-5422983 | Rare:33 | ||||
| chr5:6378362-6378594 | Rare:81 | ||||
| chr5:6632952-6633498 | Common:10; Rare:167; Clinvar:10; Clinvar (benign):6 | ||||
| chr5:7868991-7869243 | Common:2; Rare:133; Clinvar:2; Clinvar (benign):3 | ||||
| chr5:10249861-10250440 | Common:19; Rare:271; Clinvar:5; Clinvar (benign):2 | ||||
| chr5:10307732-10308052 | Common:1; Rare:63 | ||||
| chr5:10353576-10353920 | Common:3; Rare:131 | ||||
| chr5:10354036-10354282 | Rare:88 |