chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3112042902112042926ATATATATATATATATATATATAT------------------------14GENIChomozygous59630648
3112043449112043450GC26GENIChomozygous59630649
3112043943112043944TTA17GENICpossibly homozygous57990888
3112044915112044916GA21GENIChomozygous57990891
3112045592112045593TTAAAA24GENIChomozygous57990893
3112046063112046064TC24INTERGENIChomozygous57990902
3112046687112046688AG20INTERGENIChomozygous57990908
3112048396112048397T-15GENIChomozygous59630650
3112048641112048642TA28GENIChomozygous59630651
3112051176112051177CT31GENIChomozygous57990937
3112051260112051261A-16GENIChomozygous59630652
3112051535112051536TTA33GENIChomozygous57990943
3112051539112051540TA34GENIChomozygous57990945
3112051630112051631GT27GENIChomozygous58690241
3112051631112051632TA28GENIChomozygous58424387
3112051703112051704TTA23GENICpossibly homozygous59630653
3112052221112052222AG30GENIChomozygous59630654
3112052686112052687CT37GENIChomozygous57990954
3112052805112052806AG33GENIChomozygous57990957
3112053590112053594GATT----18GENIChomozygous58424389
3112053941112053942AAT20GENIChomozygous59630655
3112054364112054365GA26GENIChomozygous59630656
3112054979112054981CT--35GENIChomozygous59630657
3112055400112055401TTCAGGTGGTGA24GENIChomozygous57990966
3112056912112056913AG29GENIChomozygous57990969
3112056939112056940TC26GENIChomozygous57990971
3112057096112057097CT38GENIChomozygous59630658
3112058740112058741AG33GENIChomozygous57990988
3112059776112059777GC22GENIChomozygous59630659
3112060787112060788AT36GENIChomozygous59630660
3112054603112054604TTACAC5GENIChomozygous57603003