chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
141714613117146132GA8GENIChomozygous113908521
141714694517146946TC12GENIChomozygous113361106
141714752017147521TC19GENIChomozygous113361108
141714758017147581TC20GENIChomozygous113361110
141714930917149310AG26GENIChomozygous113361118
141715124617151247TC4GENIChomozygous113361120
141715414617154147TC20GENIChomozygous113361138
141715641617156417AG28GENIChomozygous113577785
141715669917156700GA10GENIChomozygous113361142
141715674817156749TC12GENIChomozygous113361144
141715710217157103GA27GENIChomozygous113577786
141715789717157898CT10GENIChomozygous113577787
141715872317158724GA23GENIChomozygous113577788
141715874817158749CG10GENICheterozygous113361169
141715908417159085AG17GENIChomozygous113577789
141715928317159284TC20GENIChomozygous113361197
141715996617159967TC10GENIChomozygous113361227
141715996817159969TC11GENIChomozygous113361229
141716873017168731TC16GENIChomozygous113361367
141717103317171034TC11GENIChomozygous113577791
141717359517173596TG10GENIChomozygous118747275
141717551317175514GA20GENIChomozygous113361473
141718164517181646GA11GENIChomozygous113577792
141719145117191452AT13GENIChomozygous113361609
141719214217192143AG17GENIChomozygous113361611
141720356317203564GA14GENICheterozygous113577794
141721912417219125TC18GENIChomozygous113577795
141721929217219293AC14GENICheterozygous113577796
141721972817219729CT28GENIChomozygous113577797
141721976917219770AG13GENIChomozygous113809545
141722331717223318CT13GENIChomozygous113577799
141722365217223653TA7GENICheterozygous113361697
141722411417224115CT20GENIChomozygous113577800
141722430317224304GA13GENIChomozygous113361699
141722451917224520TG3GENICheterozygous113852839
141722452217224523TG4GENIChomozygous113944095
141719915017199151AC3GENICheterozygous125945114
141721991417219915GA10GENIChomozygous125978924
141722327317223274CA4GENICheterozygous125978926