Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:3982894-3983294 | Common:4; Rare:144; Clinvar (benign):5 | ||||
chr19:4007502-4007771 | Common:3; Rare:105 | ||||
chr19:4124090-4124261 | Common:4; Rare:73; Clinvar (benign):3 | ||||
chr19:4182494-4182735 | Common:1; Rare:92; Clinvar:1 | ||||
chr19:4229178-4229547 | Common:3; Rare:114 | ||||
chr19:4246911-4247157 | Common:2; Rare:81 | ||||
chr19:4343420-4343613 | Rare:58 | ||||
chr19:4471927-4472337 | Common:7; Rare:154 | ||||
chr19:4474650-4474898 | Common:3; Rare:61 | ||||
chr19:4639219-4639573 | Common:1; Rare:120 | ||||
chr19:4670161-4670573 | Common:7; Rare:165 | ||||
chr19:4723709-4723863 | Common:1; Rare:50 | ||||
chr19:4791412-4791797 | Common:1; Rare:117 | ||||
chr19:4867621-4867864 | Common:3; Rare:74 | ||||
chr19:4909400-4909509 | Rare:30 |