Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:41500631-41500809 | Common:2; Rare:33 | ||||
chr19:41977967-41978322 | Rare:75; Clinvar:7; Clinvar (benign):2 | ||||
chr19:41981720-41982107 | Rare:85; Clinvar:6; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
chr19:42152258-42152536 | Rare:65 | ||||
chr19:42177276-42177314 | Common:1; Rare:9 | ||||
chr19:42287164-42287447 | Common:1; Rare:95; Clinvar:2 | ||||
chr19:42362131-42362447 | Rare:90 | ||||
chr19:42396872-42397184 | Common:1; Rare:77 | ||||
chr19:44977455-44977507 | Rare:16 | ||||
chr19:45717264-45717520 | Common:1; Rare:84 | ||||
chr19:46428846-46429066 | Common:1; Rare:41 | ||||
chr19:46494151-46494235 | Rare:34 | ||||
chr19:46530284-46530352 | Common:1; Rare:8 | ||||
chr19:46860829-46861141 | Common:3; Rare:97 | ||||
chr19:47047907-47048014 | Rare:22 |