| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:42938541-42938671 | Common:2; Rare:30 | ||||
| chr22:42995164-42995459 | Rare:49 | ||||
| chr22:46069854-46070067 | Rare:46 | ||||
| chr22:49657421-49657735 | Common:2; Rare:110 | ||||
| chr22:50267686-50267852 | Common:1; Rare:63 | ||||
| chr22:50293537-50293677 | Common:1; Rare:46 | ||||
| chr22:50314508-50314643 | Common:1; Rare:59 | ||||
| chr22:50466186-50466417 | Rare:83 | ||||
| chr3:4683402-4683795 | Common:2; Rare:94; Clinvar:3; Clinvar (benign):5 | ||||
| chr3:4831322-4831391 | Rare:12 | ||||
| chr3:4977115-4977391 | Rare:53 | ||||
| chr3:9396636-9396705 | Rare:30 | ||||
| chr3:9780426-9780693 | Common:2; Rare:70 | ||||
| chr3:9977387-9977606 | Common:1; Rare:40 | ||||
| chr3:12994102-12994398 | Common:2; Rare:65 |