chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5139689867139689868AG22GENICheterozygous114342294
5139690012139690013CT45GENIChomozygous114342296
5139693004139693005GA9GENICheterozygous114342298
5139693034139693035CA4GENIChomozygous114029115
5139693038139693039CA4GENIChomozygous114029116
5139693042139693043CA4GENIChomozygous114342300
5139693046139693047CA4GENIChomozygous114342302
5139694090139694091GA16GENICpossibly homozygous114342304
5139694279139694280AC15GENIChomozygous114029118
5139694442139694443GA28GENIChomozygous114029119
5139694920139694921CT15GENIChomozygous114342306
5139696549139696550AG20GENIChomozygous114029122
5139697356139697357CT27GENIChomozygous114029123
5139697456139697457AT24GENIChomozygous114342308
5139697670139697671GA23GENIChomozygous114342310
5139700094139700095CT23GENIChomozygous114029126
5139701742139701743TC36GENIChomozygous114029129
5139706788139706789CT35GENIChomozygous114342312
5139709936139709937CT11GENIChomozygous114148179
5139711213139711214GA6GENIChomozygous114029137
5139717152139717153CT32GENIChomozygous114342314
5139724327139724328TA14GENIChomozygous114148182
5139724858139724859CG30GENIChomozygous114342316
5139727912139727913TA20GENIChomozygous114029153
5139733451139733452AG13GENIChomozygous114029156
5139733937139733938AC32GENIChomozygous114029157
5139734191139734192TC10GENIChomozygous114029158
5139735976139735977AT28GENIChomozygous114342318
5139736164139736165CT20GENIChomozygous114029162