Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:81891418-81891775 | Common:3; Rare:144 | ||||
chr19:2328567-2328696 | Rare:66 | ||||
chr19:7636983-7637145 | Common:2; Rare:51; Clinvar (benign):1 | ||||
chr19:8321358-8321649 | Common:2; Rare:121 | ||||
chr19:8390054-8390416 | Common:1; Rare:102 | ||||
chr19:10928536-10928841 | Common:2; Rare:98 | ||||
chr19:14529272-14529653 | Common:1; Rare:161 | ||||
chr19:18919352-18919722 | Common:2; Rare:120 | ||||
chr19:39391086-39391398 | Common:1; Rare:123 | ||||
chr2:27370297-27370636 | Common:1; Rare:138 | ||||
chr2:43226604-43226862 | Common:2; Rare:102 | ||||
chr2:61888586-61888693 | Common:1; Rare:47 | ||||
chr2:74529676-74530036 | Rare:107; Clinvar:3; Clinvar (benign):1 | ||||
chr2:98608483-98608601 | Common:1; Rare:50 | ||||
chr2:206159394-206159673 | Common:2; Rare:95 |