| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:50783628-50783785 | Common:1; Rare:45 | ||||
| chr3:3126783-3126990 | Common:4; Rare:88; Clinvar (benign):2 | ||||
| chr3:8501676-8501854 | Rare:59 | ||||
| chr3:9362978-9363098 | Common:1; Rare:45 | ||||
| chr3:9397437-9397688 | Common:1; Rare:92 | ||||
| chr3:9792789-9793112 | Common:3; Rare:112 | ||||
| chr3:10026351-10026484 | Rare:35 | ||||
| chr3:10115541-10115712 | Common:3; Rare:65 | ||||
| chr3:10141655-10141813 | Common:2; Rare:57; Clinvar:4; Clinvar (benign):7 | ||||
| chr3:12664093-12664351 | Common:1; Rare:76; Clinvar:1; Clinvar (benign):2 | ||||
| chr3:13420241-13420435 | Common:1; Rare:53 | ||||
| chr3:14124746-14125145 | Common:4; Rare:115; Clinvar:4; Clinvar (benign):1 | ||||
| chr3:14178569-14178862 | Common:2; Rare:151; Clinvar:4; Clinvar (benign):1 | ||||
| chr3:14651432-14651779 | Common:1; Rare:88 | ||||
| chr3:14947406-14947554 | Common:2; Rare:76 |