chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
108910778589107786A-3INTERGENICheterozygous51731629
108911357689113579AAA---6INTERGENIChomozygous51536550
108911393689113937GGTT1INTERGENIChomozygous52445295
108911485789114858CCAA1INTERGENIChomozygous51536553
108911886689118867GGA3GENICheterozygous51731740
108912833489128335TC18GENICpossibly homozygous51536557
108913127989131280GA11GENIChomozygous51536558
108913136989131370TC14GENIChomozygous51536559
108913142289131423AG6GENIChomozygous51536560
108913150089131501GT6GENICheterozygous51536561
108913173189131732AT3GENIChomozygous51536562
108913173989131740AG4GENIChomozygous51536563
108913253789132538CT5GENIChomozygous51536566
108913283889132839AG11GENIChomozygous51536567
108913292989132930GGGTTTTGTTTT2GENIChomozygous51536568
108913357989133580AG11GENICheterozygous51536572
108913391389133914TC4GENIChomozygous51536574
108913410589134106AT9GENIChomozygous51536575
108913445489134455GA6GENIChomozygous51536579
108913460189134605TTTT----7GENICheterozygous52508070
108913460689134619TTTTCTTTTCTTT-------------7GENICheterozygous52394338
108913460989134610T-7GENICheterozygous52508072
108913493889134939AC16GENIChomozygous51536585
108913538189135382CT4GENICheterozygous51536591
108913549489135495CA13GENICheterozygous51536592
108913573289135733TC11GENIChomozygous51536593
108913607889136079TG7GENIChomozygous51536594
108913669589136696TC3INTERGENIChomozygous51536595
108913670389136704AATCTGC2INTERGENIChomozygous51536596
108913681989136820TC8INTERGENIChomozygous51536597
108913682489136825TC9INTERGENIChomozygous51536598
108913817989138180AT5GENIChomozygous51536599
108913818389138184AT6GENIChomozygous51536600
108913859789138598GA11GENICpossibly homozygous51536601
108913873389138734CT8GENIChomozygous51536602
108913884489138845TC14GENICpossibly homozygous51536604
108913916489139165AC14GENIChomozygous51536605
108913925989139260T-2GENIChomozygous51536606
108913994689139947AG12GENIChomozygous51536607