Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:49635600-49635896 | Common:1; Rare:106; Clinvar:3; Clinvar (benign):5 | ||||
chr19:50491024-50491350 | Common:6; Rare:61 | ||||
chr19:50494623-50494746 | Common:1; Rare:19 | ||||
chr19:50495990-50496085 | Common:1; Rare:14 | ||||
chr19:50496180-50496359 | Common:3; Rare:43 | ||||
chr19:50496362-50496726 | Common:3; Rare:78 | ||||
chr19:50496913-50497474 | Common:3; Rare:112 | ||||
chr19:50498246-50498340 | Common:1; Rare:10 | ||||
chr19:50500276-50500527 | Common:2; Rare:60 | ||||
chr19:50500709-50500948 | Common:1; Rare:49 | ||||
chr19:50501876-50502016 | Common:2; Rare:25 | ||||
chr19:50724813-50725155 | Common:1; Rare:117 | ||||
chr19:51354282-51354475 | Common:3; Rare:71; Clinvar (benign):4 | ||||
chr19:51354769-51354974 | Common:1; Rare:32 | ||||
chr19:51594356-51594602 | Common:2; Rare:65 |