chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
191064446910644470GA29GENIChomozygous46279896
191064520210645203TA37GENIChomozygous46279897
191064528010645281GA43GENIChomozygous46279898
191064604110646042CG39GENIChomozygous46279899
191064621610646217TC24GENIChomozygous46059633
191064631310646314CCTTTT24GENICheterozygous46059636
191064631410646315T-24GENICpossibly homozygous46279900
191064673710646738TC31GENIChomozygous46059639
191064674510646746TA30GENIChomozygous46059640
191064718910647190T-15GENIChomozygous46059641
191064719410647202GGGTGGGA--------25GENIChomozygous46059642
191064740510647406TTC38GENIChomozygous46059643
191064782310647824CT26GENICpossibly homozygous46279901
191064820510648206TG38INTERGENIChomozygous46059646
191064837910648380GC18INTERGENIChomozygous46059648
191065019110650192AT35INTERGENIChomozygous46279902
191065046210650463TTCTC36INTERGENIChomozygous46279903
191065067210650673CCT28INTERGENIChomozygous46279904
191065129610651297AC40INTERGENIChomozygous46059650
191065173710651738A-11INTERGENICheterozygous46059652
191065194710651948TG31INTERGENICheterozygous46279905
191065199110651992TC26INTERGENICheterozygous46279906
191065216110652162AG35INTERGENIChomozygous46279907
191065453910654540GA33INTERGENIChomozygous46279908
191064717710647183GGGGGG------18GENIChomozygous46208041
191064832110648322AAC8INTERGENICheterozygous46232784