chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
121409896214098963TA36GENIChomozygous115262269
121409946514099466GA44GENIChomozygous115262271
121410192014101921AG32GENIChomozygous115262273
121410228514102286CT38GENIChomozygous115262275
121410414814104149CG38GENICheterozygous115522399
121410687914106880AG31GENIChomozygous115262277
121410899914109000CT13GENICheterozygous118292393
121410900314109004CT11GENICheterozygous118292394
121412846314128464GT15GENIChomozygous115362955
121413794614137947GT37GENIChomozygous115262285
121413799614137997TC26GENIChomozygous115262287
121414100414141005GA20GENIChomozygous115262289
121414101714141018AG23GENIChomozygous115262291
121414172314141724AT23GENIChomozygous115262293
121414393814143939AG31GENIChomozygous115262295
121414416014144161TC34GENIChomozygous118245609
121414424314144244AG23GENIChomozygous115437978
121414457614144577AC29GENIChomozygous115262297
121414467614144677CT27GENIChomozygous115437979
121414560614145607CT34GENIChomozygous115262299
121414608314146084AC29GENIChomozygous115262301
121414645914146460TC32GENIChomozygous115262303
121414659814146599AG42GENIChomozygous115437980
121414705214147053TC40GENIChomozygous115262305
121414729114147292TC24GENIChomozygous115262307
121414743514147436CT17GENIChomozygous115417741
121414791614147917CT35GENIChomozygous115262309
121414834914148350GT29GENIChomozygous115262311
121414858714148588GT17GENIChomozygous115262313
121414860614148607TC24GENIChomozygous115262315
121414865914148660CT32GENIChomozygous115262317
121414916314149164AC37GENICheterozygous118330229
121414919814149199AC60GENICheterozygous118292395
121414924914149250TC60GENICheterozygous118245610
121414925014149251AC61GENICheterozygous118292397
121414934914149350TG45GENICheterozygous118245611
121414935414149355TC43GENICheterozygous118245612
121414954614149547TA32GENIChomozygous115262319
121415301814153019GA23GENICpossibly homozygous115262321
121415646714156468AG23GENIChomozygous115363028
121415647814156479CA25GENICpossibly homozygous115262323