chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5126165286126165286G14GENICpossibly homozygous132843587
5126166284126166285AC23GENIChomozygous113996572
5126166353126166354CT26GENIChomozygous119016615
5126166507126166508AC26GENIChomozygous113996576
5126166941126166942TC11GENIChomozygous113996579
5126168508126168508A9GENIChomozygous132843588
5126168624126168625TA13GENIChomozygous113996587
5126169113126169114CT10GENIChomozygous119016616
5126169988126169989AG18GENIChomozygous119016617
5126170176126170177TG31GENIChomozygous119016618
5126167389126167390CA18GENIChomozygous114137107
5126168430126168431GA16GENIChomozygous114137108
5126173281126173282CT17GENIChomozygous119016619
5126173825126173825G15GENIChomozygous128235418
5126178247126178248AC20GENIChomozygous119016620
5126178445126178446AG12GENIChomozygous113996624
5126178650126178655AGAAG17GENICheterozygous132843589
5126178670126178671AC22GENIChomozygous119016621
5126179112126179113AG17GENIChomozygous113996626
5126179863126179864CG14GENIChomozygous113996628
5126180718126180719G20GENIChomozygous132843590
5126181144126181145CT23GENIChomozygous119016622
5126182014126182015GA18GENIChomozygous119016623
5126182103126182104AG19GENIChomozygous113996630
5126182616126182617C13GENIChomozygous128235421
5126183898126183899CT15GENIChomozygous119016624
5126184187126184188CT19GENIChomozygous119016625
5126186543126186544GA21GENIChomozygous119016626
5126186603126186603ATAAAG14GENIChomozygous128235422
5126187664126187665AG22GENIChomozygous113996634
5126172393126172394TG9GENICheterozygous132848924