| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:46335634-46335797 | Common:5; Rare:74; Clinvar:6; Clinvar (benign):9; Clinvar (pathogenic):1 | ||||
| chr22:46762519-46762669 | Common:3; Rare:50 | ||||
| chr22:50582370-50582435 | Rare:31 | ||||
| chr22:50582818-50583120 | Common:5; Rare:83; Clinvar:2; Clinvar (benign):1 | ||||
| chr22:50628052-50628270 | Common:8; Rare:99; Clinvar:3; Clinvar (benign):1 | ||||
| chr22:50783606-50783836 | Common:2; Rare:70 | ||||
| chr3:197178-197334 | Rare:51 | ||||
| chr3:3126813-3126975 | Common:4; Rare:70; Clinvar (benign):1 | ||||
| chr3:4493167-4493349 | Rare:64 | ||||
| chr3:5187321-5187658 | Common:5; Rare:129 | ||||
| chr3:8501536-8501947 | Common:3; Rare:151 | ||||
| chr3:9249627-9249771 | Common:2; Rare:37 | ||||
| chr3:9362966-9363098 | Common:1; Rare:48 | ||||
| chr3:9397437-9397688 | Common:1; Rare:92 | ||||
| chr3:9749814-9749963 | Rare:41 |