Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:36916027-36916392 | Common:3; Rare:66 | ||||
chr19:37594736-37594886 | Rare:43 | ||||
chr19:38618912-38619259 | Common:3; Rare:102 | ||||
chr19:38831777-38832056 | Common:3; Rare:76 | ||||
chr19:38842211-38842441 | Rare:44 | ||||
chr19:38849885-38850079 | Common:1; Rare:85 | ||||
chr19:38852324-38852414 | Rare:22 | ||||
chr19:38899528-38900001 | Rare:141 | ||||
chr19:38930726-38930996 | Common:3; Rare:78; Clinvar:2; Clinvar (benign):3 | ||||
chr19:39084136-39084369 | Rare:57 | ||||
chr19:39391045-39391418 | Common:1; Rare:152 | ||||
chr19:39435848-39436167 | Common:7; Rare:117 | ||||
chr19:39445480-39445849 | Common:2; Rare:98 | ||||
chr19:39480591-39480927 | Common:3; Rare:162; Clinvar (pathogenic):1 | ||||
chr19:39834078-39834481 | Common:3; Rare:107 |