chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4110800534110800535CG8GENICheterozygous187184021
4111080875111080876GC14GENIChomozygous187184022
4111089179111089180GT11GENICheterozygous187184023
4111153709111153710GA24GENIChomozygous187184024
4111218840111218841GA14GENIChomozygous187184025
4111273875111273876GT18GENIChomozygous187184026
4111325010111325011GA8GENIChomozygous185311526
4111325011111325012AT8GENIChomozygous185311527
4111380289111380290AG27GENIChomozygous187184027
4111382095111382096AG7GENIChomozygous187184028
4111382804111382805TA19GENIChomozygous187184029
4111382921111382922GA15GENIChomozygous185311528
4111386104111386105TA24GENIChomozygous187184030
4111386117111386118GT6GENIChomozygous187184031
4111386206111386207GC17GENIChomozygous187184032
4111386262111386263GT19GENIChomozygous187184033
4111420589111420590TG19GENIChomozygous185311529
4111425684111425685GT6GENIChomozygous185311530
4111425686111425687GT7GENIChomozygous185311531
4111429268111429269TC9GENIChomozygous185311532
4111430537111430538CA21GENIChomozygous187184034
4111430602111430603CG14GENIChomozygous187184035
4111430653111430654TC8GENIChomozygous187184036
4111444566111444567CT12GENIChomozygous187184037
4111504899111504900GA9GENIChomozygous185311533
4111525105111525106TA30GENICheterozygous187184038
4111525230111525231GT34GENICheterozygous187184039
4111554282111554283CA8GENICheterozygous187184040
4111557607111557608CT13GENIChomozygous185311534
4111612895111612896GC6GENICheterozygous187184041
4111616321111616322CT3GENIChomozygous187184042
4111616821111616822GT13GENIChomozygous187184043
4111697739111697740GC10GENIChomozygous187184044
4111697798111697799CA13GENIChomozygous187184045
4111711584111711585GT10GENICheterozygous187184046
4111733580111733581CT12GENIChomozygous187184047
4111771531111771532GA10GENICheterozygous187184048
4111860970111860971TC17GENIChomozygous187184049