chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2250076799250076800CT11GENIChomozygous110849771
2250077470250077471TC12GENIChomozygous110377250
2250077712250077713TC4GENICheterozygous125751448
2250079265250079266GA11GENIChomozygous110377254
2250080072250080073AG12GENIChomozygous110377256
2250082699250082700CT14GENIChomozygous110377262
2250082875250082876TC23GENIChomozygous110377264
2250086206250086207TC11GENIChomozygous110377270
2250084659250084660GA19GENIChomozygous110377266
2250084933250084934AG23GENIChomozygous110377268
2250086226250086227CT13GENIChomozygous110849775
2250086745250086746GA20GENIChomozygous110377272
2250086801250086802TC19GENIChomozygous110377274
2250087303250087304CT16GENIChomozygous110377276
2250087673250087674TC13GENIChomozygous110377278
2250087697250087698CT13GENIChomozygous110377280
2250087922250087923CT10GENIChomozygous110377282
2250088110250088111GA12GENIChomozygous110377284
2250088335250088336TA10GENICheterozygous110377292
2250089220250089221AG16GENIChomozygous110377294
2250090804250090805GA8GENIChomozygous110849777
2250090900250090901CT13GENIChomozygous110849779
2250091415250091416CT22GENIChomozygous110377298
2250091431250091432TC23GENIChomozygous110377300
2250091463250091464GA21GENIChomozygous110377302
2250092082250092083GA22GENIChomozygous110849780
2250092272250092273CT27GENIChomozygous110849782
2250092652250092653AG14GENIChomozygous110377306
2250092765250092766AC18GENIChomozygous110377308
2250092821250092822TC19GENIChomozygous110377310
2250092968250092969GA8GENIChomozygous120176928
2250093324250093325GA10GENIChomozygous110849784
2250093529250093530TC31GENIChomozygous110377312
2250093852250093853CA17GENIChomozygous110849786
2250096544250096545CA25GENIChomozygous110377332
2250097127250097128CT24GENIChomozygous110849793
2250097547250097548TC27GENIChomozygous110377334
2250097979250097980GT16GENIChomozygous110377338
2250098613250098614GC18GENIChomozygous110377340
2250098673250098674GA13GENIChomozygous110377342