Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:20186280-20186814 | Common:6; Rare:315 | ||||
chr1:20485368-20486000 | Common:2; Rare:243 | ||||
chr1:20485970-20486684 | Rare:495 | ||||
chr1:20486610-20487000 | Common:4; Rare:179 | ||||
chr1:20507900-20508350 | Common:17; Rare:440 | ||||
chr1:20552099-20552630 | Common:3; Rare:185 | ||||
chr1:20633226-20633626 | Common:1; Rare:269; Clinvar:1 | ||||
chr1:20633816-20634216 | Common:2; Rare:245; Clinvar (benign):1 | ||||
chr1:20661294-20661770 | Common:18; Rare:959; Clinvar:26; Clinvar (benign):36 | ||||
chr1:20717334-20718230 | Common:9; Rare:352 | ||||
chr1:20732900-20733460 | Common:19; Rare:278 | ||||
chr1:20785936-20786336 | Common:6; Rare:202 | ||||
chr1:20786360-20786480 | Common:10; Rare:67 | ||||
chr1:20786558-20786958 | Rare:770 | ||||
chr1:20787030-20787180 | Rare:59 |