chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104531894245318943G-11GENIChomozygous51442209
104531905145319052A-27GENIChomozygous51442210
104531928645319287GA58GENICheterozygous51442212
104531929845319299AG53GENICheterozygous51636197
104531948745319488AG29GENICheterozygous51873360
104532417045324171TTACTC23GENIChomozygous51442213
104532431545324317GC--21GENIChomozygous51442214
104532433245324354AGAGCGCACACACACACACACA----------------------18GENIChomozygous51442215
104532507245325075GGT---29GENIChomozygous51442216
104532520745325208GA50GENICpossibly homozygous51442217
104532791145327912AAAC33GENIChomozygous51442218
104532842845328429CT45GENIChomozygous51442219
104532913945329140CT46GENIChomozygous51442220
104533059745330606TCTCACACT---------3GENIChomozygous51442222
104533059945330606TCACACT-------3GENIChomozygous51442223
104533060545330606T-4GENICheterozygous51442224
104533061845330619CCGT1GENIChomozygous51442225
104533251845332519A-8GENICheterozygous51442226
104533362745333628GGTAGCTAGC28GENIChomozygous51442227
104533412245334123AT36GENIChomozygous51442228