Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:41860825-41861212 | Common:2; Rare:117; Clinvar:2; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
chr19:42075817-42076186 | Rare:101 | ||||
chr19:42220120-42220333 | Common:2; Rare:59 | ||||
chr19:43670129-43670292 | Common:2; Rare:39 | ||||
chr19:43754901-43755088 | Common:3; Rare:65 | ||||
chr19:43901764-43901882 | Common:1; Rare:24 | ||||
chr19:44002779-44003006 | Common:4; Rare:61 | ||||
chr19:44071991-44072181 | Common:1; Rare:43 | ||||
chr19:44113145-44113440 | Common:4; Rare:68 | ||||
chr19:44141472-44141703 | Common:2; Rare:33 | ||||
chr19:44212429-44212575 | Rare:37 | ||||
chr19:44305001-44305164 | Rare:43 | ||||
chr19:44356645-44356851 | Common:1; Rare:43 | ||||
chr19:44643801-44643918 | Rare:35 | ||||
chr19:45406341-45406676 | Common:1; Rare:81 |