Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:660824-661065 | Common:22; Rare:111 | ||||
chr16:679783-680140 | Common:8; Rare:92 | ||||
chr16:684291-684505 | Common:3; Rare:121 | ||||
chr16:721076-721184 | Common:3; Rare:27 | ||||
chr16:721366-721539 | Common:2; Rare:57 | ||||
chr16:726877-727143 | Common:5; Rare:68 | ||||
chr16:740942-741131 | Rare:66 | ||||
chr16:1308887-1309187 | Common:2; Rare:80 | ||||
chr16:1333524-1333649 | Common:1; Rare:56 | ||||
chr16:1351831-1351983 | Common:2; Rare:77; Clinvar:6; Clinvar (benign):1 | ||||
chr16:1474987-1475141 | Common:3; Rare:56; Clinvar:1; Clinvar (benign):1 | ||||
chr16:1493241-1493599 | Common:4; Rare:110 | ||||
chr16:1706042-1706300 | Common:2; Rare:83 | ||||
chr16:1771502-1771868 | Common:3; Rare:144 | ||||
chr16:1773126-1773213 | Rare:21 |