chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
121409896214098963TA32GENIChomozygous115262269
121409946514099466GA20GENIChomozygous115262271
121410192014101921AG20GENIChomozygous115262273
121410228514102286CT19GENIChomozygous115262275
121410687914106880AG20GENIChomozygous115262277
121413470214134703TG19GENIChomozygous115262283
121413794614137947GT22GENIChomozygous115262285
121413799614137997TC20GENIChomozygous115262287
121414100414141005GA21GENIChomozygous115262289
121414101714141018AG21GENIChomozygous115262291
121414172314141724AT22GENIChomozygous115262293
121414393814143939AG13GENIChomozygous115262295
121414457614144577AC20GENIChomozygous115262297
121414560614145607CT19GENIChomozygous115262299
121414645914146460TC19GENIChomozygous115262303
121414705214147053TC21GENIChomozygous115262305
121414729114147292TC14GENIChomozygous115262307
121414791614147917CT29GENIChomozygous115262309
121414834914148350GT15GENIChomozygous115262311
121414858714148588GT18GENIChomozygous115262313
121414860614148607TC21GENIChomozygous115262315
121414865914148660CT19GENIChomozygous115262317
121414954614149547TA30GENIChomozygous115262319
121415301814153019GA11GENIChomozygous115262321
121414424314144244AG11GENIChomozygous115437978
121414467614144677CT20GENIChomozygous115437979
121414659814146599AG15GENIChomozygous115437980