Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:7943649-7943988 | Rare:87 | ||||
chr19:8321328-8321557 | Common:2; Rare:109 | ||||
chr19:8390064-8390411 | Common:1; Rare:98 | ||||
chr19:8444697-8445040 | Common:4; Rare:144 | ||||
chr19:9584482-9584596 | Common:1; Rare:36 | ||||
chr19:9621186-9621529 | Common:3; Rare:96 | ||||
chr19:9827815-9827974 | Common:1; Rare:59 | ||||
chr19:10333517-10333701 | Rare:62 | ||||
chr19:10380499-10380811 | Common:12; Rare:88; Clinvar:5 | ||||
chr19:10403478-10403733 | Rare:117 | ||||
chr19:10653839-10653987 | Common:1; Rare:54 | ||||
chr19:10960712-10961059 | Common:3; Rare:136 | ||||
chr19:11089312-11089516 | Rare:35; Clinvar:9; Clinvar (pathogenic):1 | ||||
chr19:11155768-11156086 | Common:3; Rare:80 | ||||
chr19:11197517-11197652 | Common:1; Rare:42 |