chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
41415370914153710AG39GENICheterozygous112512558
41415371214153713TC37GENICheterozygous112512560
41415372214153723TA37GENICheterozygous112512562
41415374714153748TA34GENICheterozygous119273568
41415384714153848CT66GENICheterozygous112512575
41415385614153857AG65GENICheterozygous112512577
41415386314153864CA65GENICheterozygous112512579
41415403414154035AG48GENICheterozygous112512603
41415409614154097TC49GENICheterozygous112512605
41415413014154131TC43GENICheterozygous112512607
41415415114154152GT42GENICheterozygous112512609
41415417314154174CT44GENICheterozygous112512611
41415426114154262GT37GENICheterozygous119302980
41415426814154269AT38GENICheterozygous112512613
41415439914154400CT33GENICheterozygous112512621
41415440314154404GC31GENICheterozygous112512623
41415441714154418GA32GENICheterozygous112512625
41415471514154716GC53GENICheterozygous112512649
41415474914154750TG44GENICheterozygous112512651
41415476114154762GA43GENICheterozygous112512653
41415476414154765AC42GENICheterozygous112512655
41415479514154796TA33GENICheterozygous112512657
41416032014160321TG19GENIChomozygous112512713
41417190714171908CT10GENIChomozygous112512767
41417888614178887AT10GENIChomozygous112512795
41417944714179448CA17GENIChomozygous112512797
41418003214180033GT27GENIChomozygous112512805
41418045014180451AG31GENIChomozygous112512809
41418105714181058GT20GENIChomozygous112512813
41418207814182079AG17GENICpossibly homozygous119452571
41418208014182081AG20GENIChomozygous119452574
41418209614182097AC23GENICpossibly homozygous112998192