| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:50582779-50583161 | Common:8; Rare:136; Clinvar:2; Clinvar (benign):3 | ||||
| chr22:50628082-50628274 | Common:9; Rare:93; Clinvar:3; Clinvar (benign):1 | ||||
| chr22:50783592-50783822 | Common:2; Rare:78 | ||||
| chr3:3126808-3127101 | Common:5; Rare:116; Clinvar (benign):4 | ||||
| chr3:4303029-4303587 | Common:3; Rare:172 | ||||
| chr3:4979401-4979820 | Common:2; Rare:102 | ||||
| chr3:4979829-4980035 | Common:1; Rare:63 | ||||
| chr3:4980290-4980615 | Common:1; Rare:77 | ||||
| chr3:5122486-5122559 | Rare:11 | ||||
| chr3:8501532-8501968 | Common:3; Rare:158 | ||||
| chr3:8768356-8768874 | Common:8; Rare:91 | ||||
| chr3:8769205-8769653 | Common:4; Rare:98 | ||||
| chr3:9249631-9249757 | Common:1; Rare:35 | ||||
| chr3:9362964-9363123 | Common:2; Rare:58 | ||||
| chr3:9397417-9397942 | Common:1; Rare:162 |