Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr4:184474512-184474812 | Rare:65 | ||||
chr4:184649429-184649796 | Common:4; Rare:117 | ||||
chr4:184734066-184734419 | Common:6; Rare:122 | ||||
chr4:185396569-185396843 | Rare:88 | ||||
chr4:185425872-185426265 | Common:4; Rare:120 | ||||
chr4:186191482-186191814 | Common:5; Rare:110; Clinvar:2; Clinvar (benign):5 | ||||
chr4:189940655-189941012 | Common:14; Rare:131 | ||||
chr5:218114-218403 | Common:3; Rare:118; Clinvar:11; Clinvar (benign):9; Clinvar (pathogenic):2 | ||||
chr5:443080-443280 | Common:10; Rare:93 | ||||
chr5:693289-693630 | Common:6; Rare:100 | ||||
chr5:892710-892923 | Common:5; Rare:81 | ||||
chr5:1799785-1799986 | Common:7; Rare:95 | ||||
chr5:1801300-1801494 | Common:4; Rare:105; Clinvar:3; Clinvar (benign):2 | ||||
chr5:7869000-7869204 | Common:2; Rare:103; Clinvar (benign):1 | ||||
chr5:9545988-9546333 | Common:8; Rare:84 |