chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
108213131982131320G-3GENIChomozygous51516668
108213134682131347C-1GENIChomozygous51516669
108213362782133628A-11GENIChomozygous52068528
108213449582134496GT6GENIChomozygous51516690
108213897882138979GT14GENIChomozygous51516720
108213898382138984CT14GENIChomozygous51516721
108213899882138999GT13GENIChomozygous51516722
108213900082139001AT13GENIChomozygous51516723
108213900782139008AT13GENIChomozygous51516724
108213901982139020AT14GENIChomozygous51516725
108213925882139259CG8GENIChomozygous51516729
108213926282139263AAG8GENIChomozygous51516730
108213926882139269A-7GENIChomozygous51516731
108214005982140061TT--3GENICheterozygous51717142
108214458682144588CA--2GENIChomozygous51516752
108213896182138962GT11GENIChomozygous52390726
108214005882140059CCT3GENICheterozygous52461988
108215116782151168A-11INTERGENICheterozygous52506282
108215976882159772ATTT----1GENIChomozygous51717191
108216039082160391TG2INTERGENIChomozygous51516792
108216039182160392TA2INTERGENIChomozygous51516793
108216039682160397C-3INTERGENIChomozygous51516794
108216039782160398CG3INTERGENIChomozygous52390728
108216161582161616G-11INTERGENICheterozygous51516802
108217776782177768CCT3GENICheterozygous52390732
108218064082180641T-2GENICheterozygous51717237
108218548182185482CCA8GENIChomozygous51516834