Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:55140884-55141313 | Common:3; Rare:136; Clinvar:1; Clinvar (benign):4 | ||||
chr19:55146661-55146738 | Common:1; Rare:22; Clinvar:1; Clinvar (benign):2 | ||||
chr19:55146943-55147376 | Common:7; Rare:142; Clinvar:1; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
chr19:55149076-55149387 | Common:3; Rare:104; Clinvar:1; Clinvar (benign):2 | ||||
chr19:55385875-55385976 | Common:3; Rare:46 | ||||
chr19:55599491-55599764 | Common:2; Rare:91 | ||||
chr19:55600141-55600390 | Common:2; Rare:98 | ||||
chr19:55643434-55643656 | Common:3; Rare:71 | ||||
chr19:55653981-55654189 | Common:4; Rare:82 | ||||
chr19:55654851-55655110 | Rare:98 | ||||
chr19:55675087-55675419 | Common:4; Rare:146 | ||||
chr19:56314786-56314930 | Common:1; Rare:46 | ||||
chr19:56368036-56368347 | Common:3; Rare:110 | ||||
chr19:56393492-56393675 | Common:2; Rare:63 | ||||
chr19:56404011-56404376 | Common:6; Rare:104 |