| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:49918406-49918684 | Common:1; Rare:100 | ||||
| chr22:50244949-50245080 | Common:2; Rare:49 | ||||
| chr22:50261002-50261167 | Common:2; Rare:51 | ||||
| chr22:50506629-50506828 | Common:3; Rare:103 | ||||
| chr22:50525509-50525712 | Common:4; Rare:102; Clinvar:3; Clinvar (benign):2 | ||||
| chr22:50562887-50563039 | Common:3; Rare:44 | ||||
| chr22:50582786-50583132 | Common:7; Rare:110; Clinvar:2; Clinvar (benign):3 | ||||
| chr22:50628087-50628252 | Common:8; Rare:81; Clinvar:3; Clinvar (benign):1 | ||||
| chr22:50783581-50783904 | Common:2; Rare:106 | ||||
| chr3:196707-196902 | Common:1; Rare:62 | ||||
| chr3:197186-197347 | Rare:52 | ||||
| chr3:3126768-3127059 | Common:4; Rare:124; Clinvar (benign):4 | ||||
| chr3:4303253-4303412 | Common:1; Rare:62 | ||||
| chr3:4467220-4467282 | Rare:32; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:4493165-4493524 | Rare:123; Clinvar:1; Clinvar (benign):1 |