chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
124092606740926068GGTGT19GENIChomozygous50205024
124092780140927810CATACACAC---------35GENIChomozygous50205026
124094148440941485A-1GENIChomozygous50205046
124095012940950131AG--4GENICheterozygous50543804
124095024740950248GGT19GENIChomozygous50205054
124095170040951701C-6GENICheterozygous50571830
124098175440981755G-4GENIChomozygous50205096
124098176040981761T-3GENIChomozygous50205097
124098360940983610GA12GENIChomozygous50205108
124098363540983636GGA5GENIChomozygous50205109
124098364440983645AAC6GENIChomozygous50205110
124098364740983648GGA5GENIChomozygous50205111
124098368640983688AA--1GENIChomozygous50615574
124098682940986833TGTT----13GENICheterozygous50323568
124099075240990753T-10GENICheterozygous50205133
124099292740992928AG25GENIChomozygous50205143
124099292940992930AG26GENIChomozygous50205144
124099301640993017AAG16GENIChomozygous50205147
124099730440997305A-19GENICheterozygous50205161
124099826240998263CCG22GENIChomozygous50205162
124099912440999125CCA1GENIChomozygous50543810
124100479741004798TC31GENICpossibly homozygous50205174
124100836141008362TTACACACACACACACAC2GENIChomozygous50543813
124101143941011440C-8GENICheterozygous50610488
124101525641015257CCTT7GENICheterozygous50205226
124101525741015258T-7GENICheterozygous50205227
124102241141022412C-6GENICheterozygous50323669
124103326741033268CCTT1GENIChomozygous50543820
124103588341035884AT14GENIChomozygous50205263
124103588541035886TG13GENIChomozygous50205264
124103590041035901TA12GENIChomozygous50205265
124103590641035907GA13GENIChomozygous50205266
124104920541049206TTGTAGGCATCC40GENIChomozygous50205288
124104920741049208AG40GENIChomozygous50205290
124105118041051181CCTTTT8GENICheterozygous50205294