chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104531894245318943G-6GENIChomozygous51442209
104531905145319052A-26GENIChomozygous51442210
104531928645319287GA45GENICheterozygous51442212
104531929845319299AG42GENICheterozygous51636197
104532053945320540AG40GENIChomozygous52052375
104532263545322640TTTTT-----2GENIChomozygous51873378
104532417045324171TTACTC21GENIChomozygous51442213
104532507245325075GGT---30GENIChomozygous51442216
104532852545328526TG49GENIChomozygous52052377
104532913945329140CT48GENIChomozygous51442220
104533059745330606TCTCACACT---------20GENIChomozygous51442222
104533059945330606TCACACT-------19GENICheterozygous51442223
104533060545330606T-23GENIChomozygous51442224
104533061845330619CCGT24GENIChomozygous51442225
104533251845332519A-16GENICpossibly homozygous51442226
104533267245332675AAA---9GENICpossibly homozygous51636205
104533327045333271CT27GENIChomozygous52052379
104533362745333628GGTAGCTAGC27GENIChomozygous51442227
104533398645333987AG35GENIChomozygous52052381