chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
155546486855464869CG50GENIChomozygous113001007
155546672055466721TC66GENIChomozygous112515533
155547140355471404CT48GENIChomozygous112515556
155547152455471525GA52GENIChomozygous113001009
155547156455471565CG54GENIChomozygous112686922
155547182455471825AG48GENIChomozygous113001011
155547652655476527TC52GENIChomozygous112515566
155547656655476567AG51GENIChomozygous112515568
155547853355478534AG30GENIChomozygous113001013
155548231855482319TC39GENIChomozygous112515598
155548310555483106TC55GENIChomozygous112515602
155548623155486231T34GENIChomozygous129258015
155547151955471519A51GENIChomozygous133500890
155547930955479315TCTCTC10GENICheterozygous133500891
155547932055479321CT6GENICheterozygous133779209
155547932555479327TT6GENICheterozygous133776150
155548405055484051TA43GENIChomozygous133504187
155549230255492302T26GENICheterozygous133776151
155549258255492583C42GENIChomozygous133500892
155549330855493309AC35GENIChomozygous133504188
155549483455494835GA35GENIChomozygous118919567
155549553355495534T3GENIChomozygous133776152
155549644955496450GA37GENIChomozygous133504189
155549376155493762T15GENICpossibly homozygous130789304
155549405755494073GTCCCTGGAAGCTCTG7GENIChomozygous130592708
155549692855496929GT42GENIChomozygous133504190
155549750755497508CG10GENIChomozygous133504191
155549976355499764CA55GENICpossibly homozygous125875650
155550426055504261GA33GENICheterozygous130449209
155550148755501488GT22GENIChomozygous118919589
155550173755501738TA38GENIChomozygous112515648
155550464555504646GC46GENICheterozygous118919593
155550470555504706GA54GENICheterozygous118919595
155551426755514268T49GENIChomozygous129258040
155550474455504745TA47GENICheterozygous118919596
155550771055507711TC44GENIChomozygous112515663
155551211955512120AT56GENIChomozygous113001015
155551251255512513GT47GENIChomozygous113001018
155551626355516264AG46GENIChomozygous112515691