| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:46267951-46268041 | Common:1; Rare:39 | ||||
| chr22:46335616-46335760 | Common:2; Rare:61; Clinvar:5; Clinvar (benign):6 | ||||
| chr22:46762496-46762706 | Common:3; Rare:80 | ||||
| chr22:49853601-49853913 | Common:2; Rare:112 | ||||
| chr22:50244960-50245111 | Common:2; Rare:61 | ||||
| chr22:50628139-50628270 | Common:6; Rare:64; Clinvar:1 | ||||
| chr22:50783628-50783859 | Common:1; Rare:66 | ||||
| chr3:2098607-2098914 | Common:4; Rare:120 | ||||
| chr3:3126813-3126975 | Common:4; Rare:70; Clinvar (benign):1 | ||||
| chr3:4493109-4493348 | Common:2; Rare:86 | ||||
| chr3:8501616-8501854 | Rare:85 | ||||
| chr3:8652046-8652208 | Common:1; Rare:38 | ||||
| chr3:9362978-9363088 | Common:1; Rare:42 | ||||
| chr3:9397437-9397676 | Rare:77 | ||||
| chr3:9792414-9792570 | Rare:40 |