Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:64568137-64568288 | Common:1; Rare:30 | ||||
chr3:64568518-64568709 | Common:2; Rare:45 | ||||
chr3:64573869-64574027 | Common:1; Rare:27 | ||||
chr3:64684621-64685154 | Common:1; Rare:96 | ||||
chr3:75434995-75435388 | Common:6; Rare:133 | ||||
chr3:75641108-75641386 | Common:1; Rare:46 | ||||
chr3:81761504-81761599 | Common:5; Rare:30; Clinvar (benign):1 | ||||
chr3:101576978-101577013 | Common:1; Rare:7 | ||||
chr3:101676284-101676507 | Rare:74 | ||||
chr3:107240610-107240805 | Rare:74 | ||||
chr3:112409112-112409257 | Rare:26 | ||||
chr3:112409258-112409322 | Common:1; Rare:15 | ||||
chr3:120095037-120095268 | Common:1; Rare:67 | ||||
chr3:123629587-123629738 | Common:1; Rare:41; Clinvar (benign):1 | ||||
chr3:125916318-125916618 | Common:4; Rare:90 |