chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
84450310144503102CT32GENICpossibly homozygous503393235
84450321244503213TTA31GENIChomozygous684218382
84450324744503248TC30GENIChomozygous503393236
84450432844504329GGA24GENIChomozygous684218383
84450467444504675TC54GENIChomozygous503393237
84450530544505306AG44GENIChomozygous503393238
84450660744506608CT50GENIChomozygous506079548
84450710644507107TC50GENIChomozygous503393239
84450792544507926TC28GENIChomozygous503393240
84450956044509561GA39GENIChomozygous503393241
84450957244509573GT45GENIChomozygous506079549
84450992644509927GC41GENIChomozygous503393242
84451006244510063GA50GENIChomozygous503393243
84451020744510208TC46GENIChomozygous506079550
84451076344510764GA22GENIChomozygous506079551
84451173744511738AG34GENIChomozygous503393244
84451292044512921AT31GENIChomozygous506079552
84451312444513128TTTA----28GENIChomozygous684218385
84451328644513287AC22GENIChomozygous503393245
84451363044513631TA48GENIChomozygous503393246
84451376644513767CCA17GENICheterozygous684218387
84451504244515043TC51GENIChomozygous503393247
84451512844515129GA38GENIChomozygous503393248
84451533944515340TTTTTA3GENIChomozygous684218388
84451572844515729CCTAGG2GENIChomozygous684218389
84451573944515740CCA2GENIChomozygous684218390
84451653744516538AT51GENIChomozygous503393249