Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:1605363-1605665 | Common:3; Rare:115 | ||||
chr19:2269664-2269769 | Common:2; Rare:55 | ||||
chr19:2328532-2328712 | Common:2; Rare:88 | ||||
chr19:2721318-2721514 | Common:1; Rare:49 | ||||
chr19:2770201-2770345 | Common:1; Rare:14 | ||||
chr19:2785266-2785566 | Common:5; Rare:93 | ||||
chr19:2841205-2841533 | Common:2; Rare:102 | ||||
chr19:2900632-2900966 | Common:10; Rare:131 | ||||
chr19:2944917-2945181 | Common:5; Rare:91 | ||||
chr19:3061357-3061433 | Rare:15 | ||||
chr19:3933225-3933693 | Common:2; Rare:130 | ||||
chr19:3936472-3936672 | Common:1; Rare:52 | ||||
chr19:3971026-3971383 | Common:2; Rare:129 | ||||
chr19:3982805-3983292 | Common:5; Rare:175; Clinvar:1; Clinvar (benign):6 | ||||
chr19:3985377-3985617 | Common:1; Rare:139 |