Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr18:56651133-56651379 | Common:3; Rare:62 | ||||
chr18:62186985-62187320 | Common:5; Rare:95 | ||||
chr18:63367122-63367357 | Common:1; Rare:88 | ||||
chr18:63422360-63422710 | Common:2; Rare:100 | ||||
chr18:63476636-63476988 | Common:5; Rare:86 | ||||
chr18:68714988-68715250 | Common:5; Rare:119 | ||||
chr18:70205659-70205837 | Common:3; Rare:75; Clinvar (benign):2 | ||||
chr18:74148321-74148552 | Common:2; Rare:83 | ||||
chr18:74291876-74292267 | Common:4; Rare:118 | ||||
chr18:74597601-74597889 | Common:2; Rare:77 | ||||
chr18:79988352-79988667 | Common:4; Rare:111; Clinvar:1; Clinvar (pathogenic):2 | ||||
chr19:572344-572603 | Rare:135 | ||||
chr19:893177-893484 | Common:3; Rare:131 | ||||
chr19:913149-913274 | Rare:40 | ||||
chr19:984257-984348 | Rare:32 |