Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:46601016-46601367 | Common:4; Rare:111 | ||||
chr19:46745872-46746066 | Common:3; Rare:39 | ||||
chr19:46787275-46787362 | Rare:17 | ||||
chr19:46788582-46788726 | Rare:36 | ||||
chr19:47484162-47484289 | Common:2; Rare:42 | ||||
chr19:48170245-48170705 | Common:2; Rare:127 | ||||
chr19:48619141-48619683 | Common:1; Rare:166 | ||||
chr19:48868129-48868691 | Common:2; Rare:104 | ||||
chr19:48993234-48993556 | Common:4; Rare:142; Clinvar:3; Clinvar (benign):3 | ||||
chr19:49453086-49453311 | Common:1; Rare:72 | ||||
chr19:49580525-49580650 | Rare:44 | ||||
chr19:49640192-49640503 | Rare:88 | ||||
chr19:49665600-49666041 | Common:6; Rare:204; Clinvar (pathogenic):1 | ||||
chr19:49801485-49801806 | Common:1; Rare:91 | ||||
chr19:49877268-49877724 | Common:2; Rare:116 |