chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
106715390067153901GA55GENICpossibly homozygous51680483
106715419067154191CG56GENIChomozygous51680485
106715474567154749TGTT----24GENICheterozygous51680487
106715492367154924GGTCGCTCCAGCCC27GENIChomozygous51480516
106715492967154930GC20GENICpossibly homozygous51680489
106715512867155129GC64GENICpossibly homozygous51480517
106715551867155519GA49GENIChomozygous51680491
106715668767156688TC32GENIChomozygous51680493
106715856467158565CA30GENIChomozygous51680503
106715674567156746TC37GENICpossibly homozygous51680495
106715771167157712CA44GENICheterozygous51680497
106715771167157712CCCGGTGGGCGAAGGCA35GENIChomozygous51680499
106715820267158203CT40GENIChomozygous51680501
106715881167158812CA72GENIChomozygous51680504
106715960767159611TGTA----28GENICpossibly homozygous51680506
106716050467160505CCT36GENICpossibly homozygous51680508
106716057767160578GA48GENICpossibly homozygous51680510
106716071567160716CCTTTCTTTTTTTTTTT24GENICpossibly homozygous51680512
106716089167160892AC64GENIChomozygous51680514
106716122367161224TG42GENIChomozygous51680516
106716159867161599TC57GENIChomozygous51680519
106716185667161857CT49GENIChomozygous51680521
106716195267161957TTTTG-----36GENIChomozygous51680523
106716195467161957TTG---40GENIChomozygous51680525
106716195667161957G-41GENIChomozygous51680527
106716197067161971C-41GENICheterozygous51680529
106716230067162308AAACAAAC--------20GENIChomozygous51680531
106716237967162380TC52GENIChomozygous51680533
106716314667163147A-72GENIChomozygous51680535
106716336567163366GGAA53GENIChomozygous51680537
106716357967163580GC1GENIChomozygous51680539
106716411267164113GC33GENICheterozygous51680541
106716486167164862CT76GENICheterozygous51680543
106716508967165090TC47GENICheterozygous51680545
106716537767165378GGT50GENIChomozygous51680547
106716555867165559TTG32GENIChomozygous51680549
106716594167165942GC60GENIChomozygous51680550