| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:50783585-50783916 | Common:2; Rare:107 | ||||
| chr3:196966-197314 | Common:3; Rare:124 | ||||
| chr3:3126769-3126990 | Common:4; Rare:98; Clinvar (benign):2 | ||||
| chr3:3128762-3129068 | Common:2; Rare:80; Clinvar (benign):2 | ||||
| chr3:3799642-3799853 | Common:1; Rare:67 | ||||
| chr3:4303253-4303424 | Common:1; Rare:66 | ||||
| chr3:4467189-4467299 | Rare:59; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:4493155-4493538 | Common:1; Rare:127; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:4979134-4979606 | Common:2; Rare:110 | ||||
| chr3:4979878-4980010 | Common:1; Rare:44 | ||||
| chr3:5187321-5187732 | Common:5; Rare:164 | ||||
| chr3:8501638-8501963 | Common:2; Rare:117 | ||||
| chr3:9362945-9363098 | Common:2; Rare:56 | ||||
| chr3:9397423-9397891 | Common:1; Rare:150 | ||||
| chr3:9731449-9731790 | Common:3; Rare:108 |