Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:4767114-4767330 | Common:2; Rare:72 | ||||
chr16:5033928-5033962 | Rare:10 | ||||
chr16:5071739-5071861 | Rare:55; Clinvar (benign):1 | ||||
chr16:5097735-5097977 | Common:4; Rare:93 | ||||
chr16:8797621-8797866 | Rare:93; Clinvar:2; Clinvar (benign):1 | ||||
chr16:8868966-8869226 | Common:4; Rare:119 | ||||
chr16:10743580-10743882 | Rare:107 | ||||
chr16:10944300-10944658 | Common:1; Rare:113 | ||||
chr16:11586889-11587036 | Common:1; Rare:44 | ||||
chr16:11851513-11851653 | Rare:69 | ||||
chr16:11915889-11916202 | Common:2; Rare:128 | ||||
chr16:11976615-11976794 | Common:2; Rare:72 | ||||
chr16:14071017-14071370 | Common:4; Rare:121 | ||||
chr16:14630188-14630405 | Rare:95 | ||||
chr16:14632687-14632990 | Common:1; Rare:106 |