chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
155203782352037824GT20GENIChomozygous112508562
155204073952040740GA20GENIChomozygous112508564
155204132752041328TC22GENIChomozygous112508566
155204472252044723AG41GENIChomozygous112508568
155204516152045162TC28GENIChomozygous112508570
155204609352046094GA31GENIChomozygous112508572
155204748652047487GA45GENIChomozygous112508574
155205053352050534GA49GENIChomozygous112508576
155205197452051975TA41GENIChomozygous112508578
155205342652053427AG32GENIChomozygous112508580
155205553652055537TC41GENIChomozygous112508582
155205884352058844TC32GENIChomozygous112508584
155205993552059936GT36GENIChomozygous112508586
155206154752061548AG37GENIChomozygous112508588
155206300352063004GT48GENIChomozygous112508590
155206435952064360AG28GENIChomozygous112508592
155206514052065141TG45GENIChomozygous112508594
155206562652065627GA37GENIChomozygous112508596
155206619152066192GA34GENIChomozygous112508598
155206766052067661TG36GENIChomozygous112508600
155206780552067806AG42GENIChomozygous112508602
155207046252070463GT37GENIChomozygous112508604
155208459152084592GT38GENIChomozygous112508606
155208626552086266AG47GENIChomozygous112508608
155208680652086807GT21GENIChomozygous112508610
155208791152087912CA31GENIChomozygous112508612
155208848452088485CT30GENIChomozygous112508614
155208909552089096CT31GENIChomozygous112508616
155209599852095999AG27GENIChomozygous112508618
155210570252105703GA44GENIChomozygous112508620
155211094352110944GA27GENIChomozygous112508622
155211150952111510TC26GENIChomozygous112508624
155211225852112259CT28GENIChomozygous112508626
155211391552113916AC47GENIChomozygous112508628
155211414852114149GA10GENIChomozygous112508630
155211564052115641TC47GENIChomozygous112508632
155211617652116177AG36GENIChomozygous112508634