chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2228504627228504628CA24GENIChomozygous636900839
2228504628228504629CA24GENIChomozygous636900840
2228504636228504637A-29GENIChomozygous749031426
2228504640228504641TC30GENIChomozygous636900841
2228504686228504687TC32GENIChomozygous636900842
2228504691228504692T-29GENIChomozygous749031427
2228505272228505273TC14GENIChomozygous636900843
2228505292228505293AAT13GENIChomozygous749031428
2228506041228506042TC15GENIChomozygous636900844
2228506291228506299TTTGTTTG--------9GENIChomozygous749031431
2228506325228506326TC20GENIChomozygous636900845
2228506491228506492CT17GENIChomozygous636900846
2228506503228506504CT19GENIChomozygous636900847
2228506548228506549CT17GENIChomozygous636900848
2228506621228506622AG17GENIChomozygous636900849
2228507182228507183AG31GENIChomozygous636900850
2228507496228507497CG28GENIChomozygous636900851
2228507947228507948TC29GENIChomozygous636900852
2228508507228508508TA26GENIChomozygous636900853
2228508626228508627TC35GENIChomozygous636900854
2228508825228508826GA37GENIChomozygous636900855
2228508827228508828GA36GENIChomozygous636900856
2228508897228508904GGGTTTA-------34GENIChomozygous749031432
2228509048228509050CG--26GENIChomozygous749031433
2228509053228509073GCGTGTGCGTGTGCGTGTGC--------------------12GENICpossibly homozygous749031435
2228509078228509079CT26GENIChomozygous636900857
2228509084228509085CT19GENIChomozygous636900858
2228509255228509256AC28GENIChomozygous636900859
2228509321228509322TA41GENIChomozygous636900860
2228509339228509340TC34GENIChomozygous636900861
2228509594228509595GA21GENIChomozygous636900862
2228509664228509665CT22GENIChomozygous636900863