Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:47745325-47745572 | Rare:106 | ||||
chr19:48170270-48170714 | Common:2; Rare:119 | ||||
chr19:48325261-48325609 | Common:2; Rare:77 | ||||
chr19:48391435-48391580 | Rare:46 | ||||
chr19:48445886-48446011 | Rare:45 | ||||
chr19:48619139-48619428 | Rare:92 | ||||
chr19:48646367-48646688 | Common:2; Rare:82 | ||||
chr19:48872221-48872427 | Common:2; Rare:63 | ||||
chr19:48993253-48993909 | Common:8; Rare:228; Clinvar:3; Clinvar (benign):2 | ||||
chr19:49085143-49085492 | Common:3; Rare:141 | ||||
chr19:49155353-49155551 | Rare:36 | ||||
chr19:49157644-49157835 | Rare:56; Clinvar:1 | ||||
chr19:49513331-49513403 | Rare:14 | ||||
chr19:49527864-49528031 | Common:3; Rare:51 | ||||
chr19:49580534-49580648 | Rare:38 |