| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:50267405-50267652 | Common:2; Rare:83 | ||||
| chr3:50299329-50299671 | Common:1; Rare:86 | ||||
| chr3:50328155-50328352 | Rare:61 | ||||
| chr3:50350677-50350924 | Common:1; Rare:43 | ||||
| chr3:50351055-50351221 | Common:2; Rare:30 | ||||
| chr3:50359301-50359411 | Common:1; Rare:24 | ||||
| chr3:50359435-50359597 | Common:2; Rare:46 | ||||
| chr3:50365190-50365382 | Common:1; Rare:75; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:50569421-50569569 | Common:1; Rare:35 | ||||
| chr3:50611737-50611883 | Rare:34 | ||||
| chr3:50617412-50617586 | Common:1; Rare:31 | ||||
| chr3:51385012-51385423 | Common:2; Rare:124 | ||||
| chr3:51500008-51500366 | Common:1; Rare:74 | ||||
| chr3:51670964-51671288 | Common:2; Rare:95 | ||||
| chr3:51941837-51942405 | Common:4; Rare:169 |