chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
156072235060722351AG21GENIChomozygous894278297
156072251560722516CT19GENIChomozygous894278298
156072300660723007TG8GENIChomozygous894278299
156072320060723201AC20GENIChomozygous894278300
156072339460723395TA17GENIChomozygous894278301
156072348160723482CG25GENIChomozygous894278302
156072358960723590CT22GENIChomozygous894278303
156072390560723906AT4GENIChomozygous894278304
156072404160724042TG12GENIChomozygous894278305
156072406660724067AG10GENIChomozygous894278306
156072410360724104TC9GENIChomozygous894278307
156072411160724112AC10GENIChomozygous894278308
156072418360724184TC16GENIChomozygous894278309
156072436260724363TA17GENICpossibly homozygous894278310
156073627660736277GA3GENICheterozygous894278311
156073820660738207AG10GENIChomozygous894278312
156073851760738518CT12GENIChomozygous894278313
156073854060738541GA8GENIChomozygous894278314
156073867560738676AG6GENIChomozygous894278315
156073906260739063GA18GENIChomozygous894278316
156074476160744762TC11GENIChomozygous894278317
156074745360747454AG27GENIChomozygous894278318
156075076960750770AC20GENIChomozygous894278319
156075079060750791TC20GENIChomozygous894278320
156075372560753726GA21GENIChomozygous894278321
156075599360755994AG6GENIChomozygous894278322
156075849060758491GC19GENIChomozygous894278323
156075857460758575AC12GENIChomozygous894278324