| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:46674413-46674604 | Common:3; Rare:44 | ||||
| chr22:46762455-46762701 | Common:3; Rare:92 | ||||
| chr22:50185690-50185949 | Common:4; Rare:109 | ||||
| chr22:50190399-50190950 | Common:10; Rare:150 | ||||
| chr22:50244960-50245086 | Common:2; Rare:50 | ||||
| chr22:50525552-50525697 | Common:3; Rare:72; Clinvar:2; Clinvar (benign):1 | ||||
| chr22:50582818-50583120 | Common:5; Rare:83; Clinvar:2; Clinvar (benign):1 | ||||
| chr22:50628135-50628280 | Common:7; Rare:73; Clinvar:1 | ||||
| chr22:50783606-50783842 | Common:2; Rare:72 | ||||
| chr3:3126813-3127021 | Common:4; Rare:95; Clinvar (benign):4 | ||||
| chr3:3179674-3179801 | Common:1; Rare:48; Clinvar:1 | ||||
| chr3:4303303-4303385 | Common:1; Rare:36 | ||||
| chr3:4493165-4493503 | Rare:115; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:5122125-5122365 | Common:2; Rare:108 | ||||
| chr3:5187321-5187663 | Common:5; Rare:133 |