| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:49918286-49918710 | Common:4; Rare:150; Clinvar (benign):3 | ||||
| chr22:50200889-50201033 | Common:3; Rare:58 | ||||
| chr22:50244969-50245052 | Common:1; Rare:33 | ||||
| chr22:50278117-50278522 | Rare:121 | ||||
| chr22:50326935-50327161 | Common:3; Rare:77 | ||||
| chr22:50522825-50523151 | Common:1; Rare:115 | ||||
| chr22:50525461-50525761 | Common:6; Rare:152; Clinvar:5; Clinvar (benign):4 | ||||
| chr22:50532491-50532656 | Common:2; Rare:41 | ||||
| chr22:50582354-50582591 | Common:1; Rare:115; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr22:50582770-50583127 | Common:7; Rare:117; Clinvar:2; Clinvar (benign):3 | ||||
| chr22:50628082-50628282 | Common:9; Rare:100; Clinvar:3; Clinvar (benign):1 | ||||
| chr22:50783598-50783822 | Common:2; Rare:73 | ||||
| chr3:3126775-3127101 | Common:5; Rare:131; Clinvar (benign):4 | ||||
| chr3:4303253-4303422 | Common:1; Rare:66 | ||||
| chr3:4978612-4978724 | Common:1; Rare:35 |