Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:48445899-48446035 | Common:1; Rare:54 | ||||
chr19:48469082-48469396 | Common:3; Rare:93 | ||||
chr19:48619139-48619459 | Common:1; Rare:104 | ||||
chr19:48624074-48624417 | Common:1; Rare:86 | ||||
chr19:48810988-48811065 | Rare:31 | ||||
chr19:48835815-48835996 | Common:1; Rare:54 | ||||
chr19:48872208-48872517 | Common:2; Rare:108 | ||||
chr19:48900101-48900431 | Common:2; Rare:98 | ||||
chr19:48918773-48919127 | Common:3; Rare:119 | ||||
chr19:48964929-48965355 | Common:1; Rare:105; Clinvar (pathogenic):4 | ||||
chr19:48965357-48965609 | Rare:80; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):3 | ||||
chr19:48993266-48993503 | Common:2; Rare:110; Clinvar:3; Clinvar (benign):2 | ||||
chr19:48993553-48993914 | Common:5; Rare:94 | ||||
chr19:49085109-49085492 | Common:3; Rare:153 | ||||
chr19:49157689-49157827 | Rare:37; Clinvar:1 |