chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
55795046557950466GA14GENIChomozygous114673319
55795192657951927AG22GENIChomozygous114205838
55795417457954175CT14GENIChomozygous113816588
55795523757955238GA17GENIChomozygous113816590
55795803457958035TC23GENIChomozygous113816592
55796052957960530TC17GENIChomozygous113816594
55796111757961118CT8GENIChomozygous113816596
55796128957961290TC15GENIChomozygous113816598
55796169057961691CT7GENIChomozygous113816600
55796463357964634GA21GENIChomozygous113816606
55796576957965770TC17GENIChomozygous113816608
55796607257966073CT19GENIChomozygous113816610
55796648757966488TC10GENIChomozygous113816612
55796975157969752TC19GENIChomozygous113816614
55797017757970178GA10GENIChomozygous113816616
55796569057965691CT3GENICheterozygous126230935
55797623757976238CT13GENIChomozygous113816620
55797649057976491TC19GENIChomozygous113816622
55798009157980092GA6GENIChomozygous113816624
55798715157987152CT26GENIChomozygous113816626
55799168057991681TA12GENIChomozygous113816632
55799174357991744GA16GENIChomozygous113816634
55799226457992265CT22GENIChomozygous113816636
55799259257992593GA9GENIChomozygous113816638
55799336557993366GC7GENIChomozygous113816640
55799440357994404GC18GENIChomozygous113816642
55799465057994651CT13GENICheterozygous113816644
55799619357996194GA12GENIChomozygous113816646
55799738757997388TA19GENIChomozygous113816648
55799794657997947GA24GENIChomozygous113816650
55799858257998583GA20GENIChomozygous113816652
55799912257999123TC20GENIChomozygous113816654
55799940457999405TC16GENIChomozygous113816656
55801033358010334TC16GENIChomozygous113816686
55799991657999917GC15GENIChomozygous113816658
55800034558000346AG18GENIChomozygous113816660
55800060858000609GA15GENIChomozygous113816662
55800304858003049CT5GENICheterozygous114117755
55799983657999837TA5GENIChomozygous126188049
55800894158008942AC21GENIChomozygous126188050