chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
121409896214098963TA27GENIChomozygous115262269
121409946514099466GA11GENIChomozygous115262271
121410192014101921AG18GENIChomozygous115262273
121410228514102286CT13GENIChomozygous115262275
121410687914106880AG24GENIChomozygous115262277
121411738614117387CA12GENIChomozygous126167794
121412846914128470CA4GENIChomozygous126167796
121412862514128626CA16GENIChomozygous126167797
121413278614132787AC13GENIChomozygous126167798
121413371214133713GT7GENIChomozygous115262281
121413794614137947GT16GENIChomozygous115262285
121413799614137997TC20GENIChomozygous115262287
121414100414141005GA4GENIChomozygous115262289
121414172314141724AT5GENIChomozygous115262293
121414416014144161TC24GENIChomozygous118245609
121414424314144244AG23GENIChomozygous115437978
121414457614144577AC17GENIChomozygous115262297
121414467614144677CT29GENIChomozygous115437979
121414560614145607CT21GENIChomozygous115262299
121414608314146084AC26GENIChomozygous115262301
121414645914146460TC22GENIChomozygous115262303
121414659814146599AG20GENIChomozygous115437980
121414705214147053TC28GENIChomozygous115262305
121414729114147292TC20GENIChomozygous115262307
121414743514147436CT20GENIChomozygous115417741
121414791614147917CT17GENIChomozygous115262309
121414834914148350GT11GENIChomozygous115262311
121414858714148588GT5GENIChomozygous115262313
121414860614148607TC10GENIChomozygous115262315
121414865914148660CT13GENIChomozygous115262317
121414923014149231GT6GENICheterozygous126240279
121414923114149232GT6GENICheterozygous126240281
121414954614149547TA20GENIChomozygous115262319
121415301814153019GA10GENIChomozygous115262321
121415646714156468AG10GENIChomozygous115363028
121415647814156479CA9GENIChomozygous115262323