| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:58499142-58499672 | Common:4; Rare:185; Clinvar:10; Clinvar (benign):2 | ||||
| chr19:58519765-58520059 | Rare:79 | ||||
| chr19:58554903-58555184 | Common:1; Rare:92 | ||||
| chr19:58558880-58559151 | Common:1; Rare:85 | ||||
| chr19:58573274-58573764 | Common:4; Rare:123 | ||||
| chr2:264012-264121 | Common:2; Rare:40 | ||||
| chr2:264558-264998 | Common:4; Rare:169 | ||||
| chr2:676957-677199 | Common:1; Rare:72 | ||||
| chr2:677301-677535 | Common:1; Rare:98 | ||||
| chr2:1979178-1979292 | Rare:30 | ||||
| chr2:2324325-2324758 | Common:1; Rare:85 | ||||
| chr2:2324935-2325159 | Common:1; Rare:45 | ||||
| chr2:2326272-2326405 | Common:1; Rare:28 | ||||
| chr2:2326489-2326624 | Common:4; Rare:32 | ||||
| chr2:2331005-2331134 | Common:1; Rare:24 |