chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
191064511110645112TC20GENIChomozygous46059628
191064519710645198AG20GENIChomozygous46059630
191064526210645263TG28GENIChomozygous46486199
191064577110645772GA25GENIChomozygous46486204
191064579210645793AG28GENIChomozygous46486206
191064610310646104CT23GENIChomozygous46788841
191064621610646217TC19GENIChomozygous46059633
191064673710646738TC27GENIChomozygous46059639
191064674510646746TA24GENIChomozygous46059640
191064719410647202GGGTGGGA--------2GENIChomozygous46059642
191064740510647406TTC19GENIChomozygous46059643
191064782310647824CT16GENIChomozygous46279901
191064820510648206TG8INTERGENIChomozygous46059646
191064837910648380GC9INTERGENIChomozygous46059648
191064912910649130CT20INTERGENIChomozygous46788843
191064959710649598GA12INTERGENIChomozygous46788845
191064977910649780CT4INTERGENIChomozygous46556264
191065046210650463TTCTC25INTERGENIChomozygous46279903
191065065710650658AG30INTERGENIChomozygous46788847
191065067310650675TT--28INTERGENICpossibly homozygous46788849
191065092210650923GA21INTERGENIChomozygous46788851
191065129610651297AC27INTERGENIChomozygous46059650
191065154710651548GA24INTERGENIChomozygous46788853
191065183410651835CT22INTERGENIChomozygous46059653
191065193110651933GC--3INTERGENIChomozygous46817194
191065193410651940TGCTTG------3INTERGENIChomozygous46817197
191065220910652210CT23INTERGENIChomozygous46788855
191065357610653577CT26INTERGENIChomozygous46788857
191065447610654477GA20INTERGENIChomozygous46788859