chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
99431048494310484C4GENIChomozygous128733225
99431049494310495G6GENIChomozygous128733226
99431050194310501CG6GENIChomozygous128733227
99431050594310506A7GENIChomozygous128733228
99431051194310512A10GENIChomozygous128733229
99431051894310520GG12GENIChomozygous128733230
99431052194310522GT12GENIChomozygous120385829
99431052494310525G13GENIChomozygous128733231
99431053294310533A15GENIChomozygous128733232
99431055794310558A24GENIChomozygous128733233
99431056294310562AC24GENIChomozygous128733234
99431056794310568T24GENIChomozygous128733235
99431057894310578TGA24GENIChomozygous128733236
99431058194310583AT24GENIChomozygous128733237
99431059194310592C26GENIChomozygous128733238
99431060094310600GG27GENIChomozygous128733239
99431060894310609TC27GENIChomozygous117602015
99431061994310620C25GENIChomozygous128733240
99431082794310828GT19GENIChomozygous130775808
99431083094310831A20GENIChomozygous128733241
99431083394310834G20GENIChomozygous128733242
99431084294310842CCTGGTGGGT20GENIChomozygous128733243
99431084694310850ATTT19GENIChomozygous128733244
99431085294310852TGCCG19GENIChomozygous128733245
99431085694310862CATGAA22GENIChomozygous128733246
99431087394310874G24GENIChomozygous128733247
99431088794310887T27GENIChomozygous128733248
99431090394310903C28GENIChomozygous128733249
99431091194310911CT28GENIChomozygous128733250
99431091394310913T28GENIChomozygous128733251
99431206994312070T37GENICheterozygous128733252
99431215694312157AC60GENIChomozygous117605057
99431240494312405AG42GENIChomozygous117605061
99432102694321027GT6GENIChomozygous117605083
99432102994321030CT6GENIChomozygous117390314
99432398794323988TC21GENICheterozygous117390323
99432398794323987C20GENICheterozygous128733254