chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
18249176782491768CT4GENICheterozygous61449832
18249179682491797CG5GENICheterozygous61449833
18249190382491904TA26GENIChomozygous61449834
18249236682492367TC13GENICpossibly homozygous61449837
18249253482492535TG18GENIChomozygous61449838
18249283782492838GA24GENIChomozygous61449840
18249310882493109CT17GENICpossibly homozygous61449842
18249337182493372CCAT4GENICheterozygous61449843
18249448182494482GC11GENICpossibly homozygous61449844
18249490382494904TG8GENIChomozygous61669473
18249519982495200AG5GENIChomozygous61669474
18249547482495475TA19GENIChomozygous61449846
18249600282496003CT4GENICheterozygous61669476
18249676282496764CA--3GENIChomozygous61669477
18249751982497520AG3GENIChomozygous61449857
18249756482497565TG13GENICpossibly homozygous61449858
18249774982497750TC2GENIChomozygous61449859
18249846482498465AG6GENIChomozygous61449860
18249876882498769CT20GENICpossibly homozygous61669483
18249882282498823CCACAG1GENIChomozygous61449861
18249901482499015CG3GENIChomozygous61669484
18249963382499634CT13GENICheterozygous61449866
18249969082499691GA3GENIChomozygous61669485
18249986182499862TC6GENICheterozygous61669486
18250022882500229TC15GENICpossibly homozygous61449873
18250050582500506CT5GENIChomozygous61669487
18250191582501916AAC5GENICheterozygous61449886
18250192482501925AC9GENIChomozygous61449887
18250255582502556GA14GENIChomozygous61669488
18250303482503035AG15GENIChomozygous61449896
18250327782503278CA2GENIChomozygous61669491
18250331982503320AC13GENIChomozygous61449899
18250576082505761GA5GENICheterozygous61669495
18250595582505956AC9GENICpossibly homozygous61449915
18250687082506871A-8GENIChomozygous61669496
18250690282506903AC5GENIChomozygous61449919
18250731482507315TTGCA2GENIChomozygous61449922
18250792082507921CT20GENICpossibly homozygous61669497