chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
10104227701104227702GA16GENICheterozygous51947783
10104227759104227760GC17GENICheterozygous51947786
10104228266104228267TA10GENICheterozygous51947789
10104228510104228511GC16GENICheterozygous51947792
10104228997104228998TC11GENIChomozygous51589276
10104229004104229005TTC10GENIChomozygous51589278
10104229013104229014CT11GENIChomozygous51589280
10104229026104229027TTC9GENIChomozygous51589282
10104229046104229047G-11GENICheterozygous52329193
10104229051104229052GGCT10GENICheterozygous52329195
10104229150104229151AG11GENICheterozygous51947798
10104229710104229711GA7GENICheterozygous52329197
10104231881104231882CT6GENICheterozygous52329199
10104233109104233110AG13GENICheterozygous51947836
10104233698104233699TC15GENICheterozygous52079888
10104234897104234898TTA16GENICheterozygous51947845
10104235383104235384AG13GENICheterozygous51947850
10104235523104235524TC11GENICheterozygous51947856
10104235680104235681CT18GENICheterozygous52079898
10104235746104235747TC18GENICheterozygous52329202
10104235966104235967AG18GENICheterozygous52079900
10104236493104236494CT15GENICheterozygous52329204
10104236501104236502AAG15GENIChomozygous51589290
10104236507104236508T-14GENIChomozygous51589292
10104236541104236542G-13GENIChomozygous51589294
10104236721104236722CT13GENICheterozygous52329208
10104236904104236905TC11GENICheterozygous51947866
10104237280104237281GT19GENICheterozygous52329210
10104238201104238202CT7GENICheterozygous52329212
10104240296104240297AG9GENICheterozygous51947887
10104240348104240349CT12GENICheterozygous51947890
10104240636104240637TC10GENICheterozygous52329216
10104241083104241084GA10GENICheterozygous53561692
10104242057104242058AAT8GENICheterozygous51947917
10104243344104243345TC7GENICheterozygous52329224