Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr20:2652452-2652636 | Common:6; Rare:59 | ||||
chr20:3209438-3209534 | Rare:31 | ||||
chr20:3820502-3820579 | Rare:31 | ||||
chr20:3889072-3889396 | Common:2; Rare:179; Clinvar:8; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr20:4148562-4148921 | Rare:97 | ||||
chr20:5119903-5120209 | Common:1; Rare:108 | ||||
chr20:5126569-5126852 | Common:3; Rare:81 | ||||
chr20:11890642-11890916 | Common:2; Rare:105 | ||||
chr20:13784894-13785074 | Common:2; Rare:77; Clinvar (benign):3 | ||||
chr20:17569747-17570191 | Common:5; Rare:151 | ||||
chr20:17968409-17968610 | Common:4; Rare:86 | ||||
chr20:17968700-17969119 | Common:5; Rare:155 | ||||
chr20:18467065-18467399 | Rare:67 | ||||
chr20:20017193-20017388 | Rare:65 | ||||
chr20:23361874-23362196 | Common:3; Rare:103 |