| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:46762450-46762706 | Common:3; Rare:98 | ||||
| chr22:50244949-50245067 | Common:2; Rare:44 | ||||
| chr22:50270321-50270430 | Common:1; Rare:38 | ||||
| chr22:50454923-50455067 | Rare:58; Clinvar:1 | ||||
| chr22:50525507-50525708 | Common:4; Rare:102; Clinvar:4; Clinvar (benign):2 | ||||
| chr22:50562887-50563044 | Common:3; Rare:45 | ||||
| chr22:50582790-50583142 | Common:7; Rare:117; Clinvar:2; Clinvar (benign):3 | ||||
| chr22:50628038-50628274 | Common:9; Rare:107; Clinvar:3; Clinvar (benign):1 | ||||
| chr22:50783585-50783859 | Common:2; Rare:91 | ||||
| chr3:196734-197051 | Common:2; Rare:99 | ||||
| chr3:197230-197341 | Rare:37 | ||||
| chr3:197358-197637 | Common:4; Rare:89 | ||||
| chr3:3126764-3127021 | Common:4; Rare:115; Clinvar (benign):4 | ||||
| chr3:3179644-3179799 | Common:1; Rare:73; Clinvar:4 | ||||
| chr3:4303247-4303405 | Common:2; Rare:62 |