Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:134632737-134632937 | Rare:40 | ||||
chr5:134648425-134648681 | Common:1; Rare:46 | ||||
chr5:134648682-134648859 | Rare:57 | ||||
chr5:134874254-134874454 | Common:1; Rare:100 | ||||
chr5:135399100-135399494 | Common:1; Rare:93 | ||||
chr5:136028823-136029091 | Rare:77; Clinvar:2 | ||||
chr5:137880335-137880731 | Common:2; Rare:67 | ||||
chr5:138032964-138033180 | Common:1; Rare:73 | ||||
chr5:138178604-138178739 | Rare:32 | ||||
chr5:138465829-138465884 | Rare:23 | ||||
chr5:138543070-138543506 | Common:3; Rare:128 | ||||
chr5:138753261-138753507 | Common:2; Rare:85 | ||||
chr5:138930302-138930649 | Common:1; Rare:70; Clinvar (benign):1 | ||||
chr5:138930735-138930930 | Common:2; Rare:34; Clinvar:1; Clinvar (benign):1 | ||||
chr5:139198274-139198526 | Rare:82; Clinvar (benign):1 |