chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
108213131982131320G-20GENIChomozygous51516668
108213134682131347C-20GENIChomozygous51516669
108213447482134476TT--14GENICheterozygous52390722
108213449582134496GT20GENIChomozygous51516690
108213769082137691C-9GENIChomozygous51516710
108213896182138962GT17GENIChomozygous52390726
108213897882138979GT19GENIChomozygous51516720
108213898382138984CT19GENIChomozygous51516721
108213899882138999GT20GENIChomozygous51516722
108213900082139001AT20GENIChomozygous51516723
108213900782139008AT20GENIChomozygous51516724
108213901982139020AT21GENIChomozygous51516725
108213925882139259CG23GENIChomozygous51516729
108213926282139263AAG23GENIChomozygous51516730
108213926882139269A-24GENIChomozygous51516731
108214005882140059CCT6GENICheterozygous52461988
108214005982140061TT--6GENICheterozygous51717142
108214006082140061T-6GENICheterozygous51516732
108214458682144588CA--13GENICheterozygous51516752
108214536782145368GGAGGA13GENIChomozygous51516756
108215116782151168A-11INTERGENICheterozygous52506282
108215976882159772ATTT----4GENIChomozygous51717191
108216039082160391TG31INTERGENIChomozygous51516792
108216039182160392TA31INTERGENIChomozygous51516793
108216039682160397C-29INTERGENIChomozygous51516794
108216039782160398CG30INTERGENIChomozygous52390728
108216161582161616G-28INTERGENICheterozygous51516802
108216395382163957AACC----24INTERGENICheterozygous52444014
108216397582163976CT30INTERGENICheterozygous51516809
108216441582164416A-1INTERGENIChomozygous52068562
108217032182170325TATG----10INTERGENIChomozygous51717210
108218548182185482CCA23GENIChomozygous51516834