chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7125742672125742673CG21GENIChomozygous554733018
7125743637125743638TC22GENIChomozygous554733019
7125743757125743758G-8GENICheterozygous703177434
7125745057125745058AT17GENIChomozygous554274061
7125747420125747421GA33GENIChomozygous554274062
7125747571125747572GA33GENIChomozygous554274063
7125748235125748236TC24GENIChomozygous554274064
7125748640125748641CG16GENIChomozygous554274065
7125748927125748928GA28GENIChomozygous554274066
7125749347125749348TG25GENIChomozygous554274067
7125749414125749415AG24GENIChomozygous554274068
7125749577125749578GGGCAGTCAGTGCCC28GENIChomozygous703177435
7125751462125751463CT27GENICpossibly homozygous554274069
7125751521125751522AAT13GENICheterozygous703177436
7125751521125751522AATT13GENICheterozygous703177437
7125752000125752001TC26GENIChomozygous554274070
7125752841125752842AG32GENIChomozygous554733020
7125753821125753822CT25GENIChomozygous554733021
7125753949125753950GA25GENIChomozygous554274071
7125754274125754275AG15GENIChomozygous554274072
7125754320125754321CT18GENIChomozygous554274073
7125754542125754543GA20GENIChomozygous554733022
7125754626125754627GA21GENIChomozygous554733023
7125755403125755404AAT36GENIChomozygous703177438
7125755666125755667CT26GENIChomozygous554274074
7125756500125756501TC34GENIChomozygous554274075
7125756582125756583GA31GENIChomozygous554733024
7125756849125756850AG12GENIChomozygous554274076
7125756965125756966GGA7GENICheterozygous703177439
7125756965125756966GGAAAAAAAAAAA7GENICheterozygous703177441
7125757153125757154TTA9GENICheterozygous703177442
7125757153125757154TTAA9GENICpossibly homozygous703177443
7125757211125757212CT18GENIChomozygous554274077