| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:50783621-50783859 | Common:2; Rare:71 | ||||
| chr3:2098605-2098923 | Common:4; Rare:123 | ||||
| chr3:3126795-3127016 | Common:4; Rare:96; Clinvar (benign):4 | ||||
| chr3:3179679-3179772 | Common:1; Rare:35; Clinvar:1 | ||||
| chr3:4303247-4303399 | Common:2; Rare:58 | ||||
| chr3:4467246-4467325 | Rare:34; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:4493176-4493348 | Rare:61 | ||||
| chr3:8501641-8501963 | Common:2; Rare:116 | ||||
| chr3:8733574-8733831 | Common:5; Rare:53; Clinvar:2; Clinvar (benign):2 | ||||
| chr3:9362970-9363117 | Common:1; Rare:54 | ||||
| chr3:9397433-9397679 | Rare:81 | ||||
| chr3:9792376-9792570 | Rare:55 | ||||
| chr3:9792726-9793125 | Common:3; Rare:140 | ||||
| chr3:9843986-9844115 | Common:2; Rare:49 | ||||
| chr3:9890473-9890667 | Common:2; Rare:72 |