Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:12649913-12650221 | Common:1; Rare:93; Clinvar:5; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr19:12782121-12782399 | Common:1; Rare:60 | ||||
chr19:12793213-12793313 | Common:1; Rare:26 | ||||
chr19:13839687-13839966 | Rare:68 | ||||
chr19:13846530-13846907 | Common:1; Rare:77 | ||||
chr19:14091632-14091755 | Rare:29 | ||||
chr19:14369750-14369936 | Common:1; Rare:35 | ||||
chr19:14369938-14370062 | Rare:25 | ||||
chr19:14370539-14370844 | Common:1; Rare:53 | ||||
chr19:14375166-14375535 | Common:4; Rare:75 | ||||
chr19:14390608-14390688 | Rare:8 | ||||
chr19:14408024-14408126 | Rare:46 | ||||
chr19:14408682-14408910 | Common:1; Rare:57 | ||||
chr19:14417719-14418036 | Common:4; Rare:51 | ||||
chr19:14595525-14595700 | Common:1; Rare:27 |