chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
13103523263103523264CA16GENIChomozygous51203306
13103525420103525421TC3GENIChomozygous49872698
13103525975103525976GA7GENIChomozygous49872699
13103526655103526656TC9GENIChomozygous49872700
13103528280103528281AG2GENIChomozygous49872706
13103529761103529762AG23GENIChomozygous49872708
13103531404103531405TC1GENIChomozygous49872712
13103531595103531596AG6GENIChomozygous49872714
13103532107103532108AG13GENIChomozygous51203311
13103532369103532370CCG8GENIChomozygous49872715
13103532980103532981AG11GENIChomozygous49872716
13103534836103534837GA14GENICpossibly homozygous51203314
13103535663103535664TC4GENICheterozygous49872717
13103536058103536080TCTCTCTCTCTCTCTCTCTCTC----------------------3GENICheterozygous51203317
13103537529103537530TC20GENIChomozygous49872721
13103538671103538672CT13GENIChomozygous51203322
13103538930103538931CT14GENIChomozygous51203325
13103539887103539888A-1GENIChomozygous50746490
13103540451103540452GGT5GENICheterozygous49872725
13103540783103540784AG3GENIChomozygous49872726
13103541164103541165TG15GENIChomozygous51203330
13103541194103541195TC14GENIChomozygous49872727
13103541519103541520CT19GENICpossibly homozygous51203333
13103541924103541929TTTGT-----5GENIChomozygous51203336
13103543361103543362CT9GENIChomozygous51203339
13103543882103543883CT8GENICpossibly homozygous51203341
13103545051103545052TTAA1GENIChomozygous51203347
13103545417103545418CT11GENICheterozygous51203350
13103545507103545509GA--5GENIChomozygous51203352
13103545622103545624TT--7GENICpossibly homozygous51203355
13103542702103542810GAGAATGTTCTCATGTTGGGCTGGGGATTTAGCTCAGTGGTAGAGCGCTTACCTAGGAAGCGCAAGGCCCTGGGTTCGGTCCCCAGCTCCGAAAAAAAAAAAAAAAAA------------------------------------------------------------------------------------------------------------14GENIChomozygous50498712