| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:61251376-61251593 | Common:4; Rare:55 | ||||
| chr3:62318932-62319088 | Rare:63 | ||||
| chr3:63863749-63864126 | Common:7; Rare:124 | ||||
| chr3:67654582-67654776 | Common:2; Rare:71 | ||||
| chr3:69084762-69085063 | Common:3; Rare:76 | ||||
| chr3:71130556-71130655 | Rare:38; Clinvar:1 | ||||
| chr3:79018999-79019061 | Rare:21 | ||||
| chr3:81761515-81761735 | Common:8; Rare:80; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:81761738-81761839 | Rare:26 | ||||
| chr3:87227137-87227382 | Common:1; Rare:88; Clinvar:1; Clinvar (benign):2 | ||||
| chr3:88058923-88059294 | Common:3; Rare:137 | ||||
| chr3:88149627-88150043 | Common:5; Rare:124 | ||||
| chr3:93979907-93980207 | Common:4; Rare:109; Clinvar:1; Clinvar (benign):2 | ||||
| chr3:94062897-94063101 | Rare:49 | ||||
| chr3:97764706-97764811 | Common:1; Rare:24; Clinvar:1; Clinvar (benign):1 |