Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:42132424-42132658 | Rare:47 | ||||
chr19:42220117-42220339 | Common:2; Rare:61 | ||||
chr19:42268265-42268559 | Rare:58 | ||||
chr19:42423587-42423813 | Common:1; Rare:69 | ||||
chr19:42528460-42528728 | Common:2; Rare:50 | ||||
chr19:43527170-43527310 | Common:5; Rare:55; Clinvar:3; Clinvar (benign):7; Clinvar (pathogenic):2 | ||||
chr19:43575477-43575778 | Common:2; Rare:86 | ||||
chr19:43596045-43596368 | Common:3; Rare:99 | ||||
chr19:43670155-43670309 | Common:2; Rare:32 | ||||
chr19:43827204-43827438 | Common:3; Rare:50 | ||||
chr19:43901782-43901873 | Rare:18 | ||||
chr19:44002819-44003021 | Common:4; Rare:51 | ||||
chr19:44071930-44072181 | Common:1; Rare:57 | ||||
chr19:44113197-44113440 | Common:3; Rare:52 | ||||
chr19:44141500-44141643 | Common:1; Rare:19 |