Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:3900180-3900539 | Common:13; Rare:153 | ||||
chr1:5992411-5992765 | Common:4; Rare:112; Clinvar:4 | ||||
chr1:7961457-7961787 | Common:4; Rare:110; Clinvar:2; Clinvar (benign):3 | ||||
chr1:8878582-8878874 | Rare:155 | ||||
chr1:9943348-9943494 | Common:2; Rare:35 | ||||
chr1:11654745-11654918 | Common:3; Rare:49 | ||||
chr1:11691511-11691710 | Common:3; Rare:42 | ||||
chr1:11805918-11806248 | Common:2; Rare:88; Clinvar:1 | ||||
chr1:15526649-15526908 | Common:2; Rare:84 | ||||
chr1:16352424-16352567 | Common:2; Rare:79 | ||||
chr1:17044760-17045014 | Common:1; Rare:74; Clinvar:11; Clinvar (benign):6; Clinvar (pathogenic):6 | ||||
chr1:19210241-19210368 | Rare:47 | ||||
chr1:19251516-19251849 | Common:6; Rare:107 | ||||
chr1:19312091-19312356 | Common:5; Rare:121 | ||||
chr1:19485437-19485731 | Common:1; Rare:96 |