chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104775511647755117CG22GENIChomozygous51446410
104775522147755222GT24GENICpossibly homozygous51446411
104775562347755624GA33GENIChomozygous51446412
104775647147756472TC31GENIChomozygous51446413
104775772347757724AG32GENIChomozygous51446414
104775971447759715GC42GENIChomozygous51446415
104775980047759808TTTTTTTT--------11GENIChomozygous51446416
104776035847760359AG23GENIChomozygous51446417
104776161547761616TG34GENIChomozygous51446418
104776234647762347TTC36GENICpossibly homozygous51446419
104776545447765455TC43GENIChomozygous51446420
104776850347768504AAC38GENIChomozygous51446421
104776861747768618AG38GENIChomozygous51446422
104777025447770255TC14GENIChomozygous51446423
104777447747774492CCCTGACCCTCCTAA---------------23GENICheterozygous52799985