chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4149261124149261125AG10GENICheterozygous57516786
4149261125149261126GA10GENICheterozygous58285641
4149261548149261549TC11GENIChomozygous56977807
4149261573149261575TG--10GENIChomozygous56977808
4149262006149262007CT14GENICpossibly homozygous56977809
4149262868149262869GC8GENIChomozygous56977811
4149263336149263337TC21GENIChomozygous56977813
4149263730149263731TG23GENICpossibly homozygous56977814
4149263841149263842CA17GENIChomozygous56977815
4149264090149264091GA14GENICpossibly homozygous56977816
4149264309149264310AAG1GENIChomozygous56977818
4149264343149264344AT12GENIChomozygous56977819
4149264640149264641AG5GENIChomozygous56977820
4149264823149264824GA26GENICpossibly homozygous56977821
4149264856149264857TC26GENICpossibly homozygous56977822
4149265319149265320GT20GENICpossibly homozygous56977823
4149265836149265837T-4GENIChomozygous56977825
4149266081149266082TC13GENIChomozygous56977828
4149266377149266378AT3GENICheterozygous56977829
4149267285149267286GGC7GENIChomozygous56977830
4149269529149269530CG10GENICpossibly homozygous56977835