Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:37507023-37507168 | Common:2; Rare:43 | ||||
chr19:37594719-37594917 | Rare:57 | ||||
chr19:37692172-37692421 | Common:2; Rare:51 | ||||
chr19:37779579-37779662 | Rare:18 | ||||
chr19:38264256-38264676 | Common:6; Rare:103 | ||||
chr19:38315926-38316114 | Rare:48 | ||||
chr19:38618947-38619252 | Common:3; Rare:90 | ||||
chr19:38831748-38832030 | Common:4; Rare:93; Clinvar (benign):1 | ||||
chr19:38899572-38900039 | Rare:138 | ||||
chr19:38930723-38930988 | Common:2; Rare:75; Clinvar:2; Clinvar (benign):3 | ||||
chr19:39390640-39390800 | Rare:38 | ||||
chr19:39390840-39391487 | Common:1; Rare:246 | ||||
chr19:39406699-39406928 | Rare:92 | ||||
chr19:39407588-39407724 | Rare:31 | ||||
chr19:39435838-39436163 | Common:6; Rare:118 |