Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr18:63367143-63367394 | Common:1; Rare:86 | ||||
chr18:63422360-63422710 | Common:2; Rare:100 | ||||
chr18:68714979-68715296 | Common:7; Rare:134 | ||||
chr18:70205650-70205750 | Common:2; Rare:48; Clinvar (benign):2 | ||||
chr18:74148346-74148570 | Common:1; Rare:73 | ||||
chr18:74499788-74499958 | Common:2; Rare:38 | ||||
chr18:74597801-74597907 | Common:1; Rare:26 | ||||
chr19:572322-572610 | Rare:144 | ||||
chr19:633525-633838 | Common:8; Rare:123 | ||||
chr19:893165-893484 | Common:3; Rare:133 | ||||
chr19:1026469-1026706 | Common:1; Rare:90 | ||||
chr19:1103749-1104115 | Common:7; Rare:153 | ||||
chr19:1354702-1354996 | Common:3; Rare:122 | ||||
chr19:2256389-2256580 | Common:1; Rare:33 | ||||
chr19:2269251-2269560 | Common:1; Rare:133 |