Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:44909379-44909423 | Rare:4 | ||||
chr19:45075515-45075701 | Common:1; Rare:45 | ||||
chr19:45364933-45365110 | Common:3; Rare:57; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr19:45716511-45716866 | Common:2; Rare:70 | ||||
chr19:45717175-45717492 | Common:1; Rare:96 | ||||
chr19:46021422-46021429 | |||||
chr19:46278505-46278544 | Common:1; Rare:7 | ||||
chr19:46389930-46390127 | Common:3; Rare:44 | ||||
chr19:46639151-46639355 | Common:2; Rare:34 | ||||
chr19:46860080-46860481 | Common:2; Rare:123 | ||||
chr19:46860769-46861150 | Common:3; Rare:120 | ||||
chr19:46862241-46862510 | Rare:62 | ||||
chr19:47047894-47048056 | Rare:44 | ||||
chr19:47228513-47228655 | Common:2; Rare:22 | ||||
chr19:47243093-47243415 | Common:4; Rare:76 |