chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
14106382075106382076CT31GENIChomozygous113765135
14106383139106383140CT60GENIChomozygous113536213
14106384747106384748CT33GENIChomozygous113536217
14106385058106385059GA8GENICpossibly homozygous113536219
14106385278106385279TA50GENIChomozygous113536221
14106385389106385390CT51GENIChomozygous113536223
14106385713106385714AG30GENICpossibly homozygous113789655
14106385720106385721TC29GENIChomozygous113536225
14106385768106385769AC32GENIChomozygous113536227
14106385816106385817CT36GENIChomozygous113536229
14106385951106385952CT55GENIChomozygous113765137
14106387051106387052TC57GENIChomozygous113536231
14106387124106387125TC59GENIChomozygous113536233
14106390744106390745GA40GENICpossibly homozygous113536235
14106390931106390932CT42GENIChomozygous113536237
14106391110106391111GA43GENIChomozygous113765139
14106391980106391981TC49GENIChomozygous113536239
14106392345106392346CA57GENIChomozygous113765141
14106393043106393044GA37GENICpossibly homozygous113765143
14106393116106393117CT43GENICpossibly homozygous113536243
14106385056106385057TC8GENICpossibly homozygous114093323
14106385045106385046AT6GENICheterozygous118724766
14106385053106385054AC8GENICpossibly homozygous118724767