Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:36605268-36605350 | Rare:19 | ||||
chr19:36687423-36687633 | Common:3; Rare:64 | ||||
chr19:36772803-36773120 | Common:4; Rare:77 | ||||
chr19:37078172-37078473 | Common:3; Rare:71 | ||||
chr19:37467425-37467519 | Common:1; Rare:23 | ||||
chr19:37907016-37907293 | Common:1; Rare:64 | ||||
chr19:38315877-38316130 | Rare:77 | ||||
chr19:38618896-38619252 | Common:4; Rare:107 | ||||
chr19:38647372-38647737 | Common:3; Rare:129 | ||||
chr19:38831777-38832052 | Common:3; Rare:75 | ||||
chr19:38899592-38900018 | Rare:125 | ||||
chr19:38930723-38931013 | Common:3; Rare:82; Clinvar:2; Clinvar (benign):3 | ||||
chr19:39342396-39342512 | Common:2; Rare:41 | ||||
chr19:39391025-39391418 | Common:1; Rare:158 | ||||
chr19:39406706-39406857 | Rare:57 |