chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
175398448153984482TC20GENIChomozygous791653322
175398519453985195AC16GENIChomozygous791653323
175398725053987251AG8GENIChomozygous791653324
175399013353990134TC22GENIChomozygous791653325
175399017853990179AG24GENIChomozygous791653326
175399094453990945GA24GENIChomozygous791653327
175399096053990961GA23GENICheterozygous791653328
175399432053994321GA26GENIChomozygous791653329
175399545853995459CT23GENIChomozygous791653330
175399565353995654CT19GENIChomozygous791653331
175399769653997697AT5GENIChomozygous791653332
175399836253998363AT29GENIChomozygous791653333
175400060254000603AT25GENIChomozygous791653334
175400081854000819CT18GENIChomozygous791653335
175400221054002211TA12GENIChomozygous791653336
175400437254004373AG27GENIChomozygous791653337
175400446654004467CT39GENIChomozygous791653338
175400870554008706AC21GENIChomozygous791653339
175401080154010802AG29GENIChomozygous791653340
175401434654014347AG32GENIChomozygous791653341
175401471654014717AG9GENICpossibly homozygous791653342
175401594854015949CT31GENICheterozygous791653343
175401603854016039CT36GENICheterozygous791653344
175401771154017712CT19GENIChomozygous791653345
175401795154017952TC22GENIChomozygous791653346
175402084754020848CT23GENIChomozygous791653347
175402283554022836GA27GENIChomozygous791653348
175402461054024611CG32GENIChomozygous791653349
175402475754024758AG35GENIChomozygous791653350
175402624054026241CT24GENIChomozygous791653351
175402688154026882CT20GENIChomozygous791653352
175402690454026905GA21GENIChomozygous791653353
175402787554027876TC10GENIChomozygous791653354