Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:110308510-110308610 | Common:1; Rare:22 | ||||
chr13:110424784-110424986 | Common:4; Rare:64; Clinvar:3; Clinvar (benign):2 | ||||
chr13:110449511-110449786 | Common:4; Rare:74; Clinvar:1; Clinvar (benign):2 | ||||
chr13:110482266-110482628 | Common:4; Rare:87; Clinvar:1; Clinvar (benign):1 | ||||
chr13:110503929-110504255 | Common:3; Rare:111; Clinvar:1; Clinvar (benign):2 | ||||
chr13:111169567-111169767 | Common:1; Rare:26 | ||||
chr13:112694035-112694458 | Common:1; Rare:76 | ||||
chr13:112819905-112820009 | Rare:34 | ||||
chr13:113820961-113821244 | Common:3; Rare:95 | ||||
chr13:113852765-113852809 | Rare:9 | ||||
chr13:113854265-113854361 | Common:1; Rare:18 | ||||
chr13:113859309-113859660 | Common:7; Rare:124 | ||||
chr13:114065810-114065917 | Rare:24 | ||||
chr14:21500665-21500830 | Common:1; Rare:40 | ||||
chr14:22770640-22770907 | Common:2; Rare:59 |