chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
13779733737797338AG42GENIChomozygous60674711
13779734137797342AT45GENIChomozygous60674713
13779737537797376TG40GENIChomozygous60674715
13779749337797494CT34GENIChomozygous60674717
13779905237799053AG32GENICpossibly homozygous60674719
13780134337801344GGAAAC15GENIChomozygous60674721
13780305337803054A-29GENIChomozygous60674725
13780447337804474CCT16GENIChomozygous60674727
13780468337804685TC--28GENIChomozygous60674729
13780704437807045AATCACCCAGAAGTCACCAGG27GENIChomozygous60674731
13780787537807889AAGCTCTGTCATGT--------------33GENIChomozygous60674733
13780872037808721AAG18GENICpossibly homozygous60674735
13780875137808752CT34GENIChomozygous60674737
13780877537808776CT37GENIChomozygous60674739
13780894237808943CG19GENIChomozygous60674741
13780951437809515AG41GENIChomozygous60674743
13781150237811503TTATA28GENIChomozygous60674749
13781213437812135AG36GENIChomozygous60674753
13781312337813124AC32GENIChomozygous60674755
13781429737814298TG16GENIChomozygous60674759
13781678737816793TTGTTG------22GENIChomozygous60674761
13781680537816807TG--15GENICpossibly homozygous61401248
13781823137818232CA24GENIChomozygous60674763
13781944837819449AC21GENIChomozygous61985403
13781083437810835GGTGTCTGTGTC22GENIChomozygous62123956
13781754137817542CCAGTGTCTCGCTGTGGTCCAGGGTCTTGCTCTGGTCT23GENIChomozygous62123957
13781278837812789CT47GENIChomozygous61985399
13781969837819699TC40GENIChomozygous60674767
13781978937819790GT23GENIChomozygous60674769
13781996737819968AAT9GENIChomozygous60674771
13782441837824419GT20GENIChomozygous61985404
13782485037824854TATA----20GENIChomozygous60674773
13782551737825523ACAGAC------19GENICheterozygous62123958
13782568437825685TG16GENIChomozygous60674779
13782738037827381TC24GENIChomozygous60674783
13782896337828964AAGTCATCCCGACG32GENIChomozygous60674785
13782993837829939CT26GENIChomozygous60674787