Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:1026488-1026664 | Rare:71 | ||||
chr19:1103755-1104109 | Common:7; Rare:152 | ||||
chr19:1242354-1242560 | Rare:68; Clinvar (pathogenic):1 | ||||
chr19:1269083-1269347 | Common:2; Rare:98 | ||||
chr19:1354817-1354996 | Rare:77 | ||||
chr19:1479183-1479335 | Common:1; Rare:53 | ||||
chr19:2328556-2328703 | Common:2; Rare:71 | ||||
chr19:2944917-2945250 | Common:7; Rare:114 | ||||
chr19:3366507-3366645 | Common:3; Rare:44 | ||||
chr19:3982805-3983194 | Common:5; Rare:139; Clinvar:1; Clinvar (benign):3 | ||||
chr19:4182535-4182683 | Rare:51 | ||||
chr19:4867613-4867938 | Common:4; Rare:93 | ||||
chr19:5293222-5293418 | Common:1; Rare:88 | ||||
chr19:5622720-5623262 | Common:6; Rare:221 | ||||
chr19:5978078-5978383 | Common:3; Rare:113 |