Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:37779566-37779667 | Rare:23 | ||||
chr19:37907052-37907296 | Rare:53 | ||||
chr19:38224150-38224439 | Common:1; Rare:82 | ||||
chr19:38617720-38618229 | Common:1; Rare:123 | ||||
chr19:38618767-38619253 | Common:4; Rare:140 | ||||
chr19:38647372-38647713 | Common:3; Rare:120 | ||||
chr19:38831761-38831943 | Common:3; Rare:66; Clinvar (benign):1 | ||||
chr19:38878233-38878343 | Rare:16 | ||||
chr19:38899581-38899971 | Rare:106 | ||||
chr19:38930723-38930996 | Common:3; Rare:78; Clinvar:2; Clinvar (benign):3 | ||||
chr19:39391025-39391418 | Common:1; Rare:158 | ||||
chr19:39406727-39406851 | Rare:51 | ||||
chr19:39435905-39436160 | Common:4; Rare:92 | ||||
chr19:39480559-39480918 | Common:3; Rare:166; Clinvar (pathogenic):1 | ||||
chr19:39846341-39846473 | Common:1; Rare:58 |