chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
105357145253571458ACACAC------10GENIChomozygous52460367
105357408753574088CCTT10GENIChomozygous51648515
105357562353575624TTA12GENIChomozygous52057760
105357250353572504GA22GENIChomozygous52057756
105357489553574896CA23GENIChomozygous52057758
105357403653574046TTTTTTTGTT----------6GENICheterozygous51455633
105357407553574076CCT14GENIChomozygous51455635
105357579453575795CA24GENIChomozygous52057762
105357644053576441CG17GENIChomozygous52057764
105358054253580543AATTGTTG19GENIChomozygous51648518
105358067153580672CT26GENIChomozygous51648519
105358072753580728AC19GENIChomozygous51648520
105358392153583922TG32GENIChomozygous51648528
105358392653583927AG34GENIChomozygous51648529
105358450553584506AC38GENIChomozygous52057766
105358564053585641GA19GENIChomozygous52057768
105358566753585681ACCCCACACCTTGT--------------14GENIChomozygous52057770
105358602853586029AG21GENIChomozygous51648534
105358621753586218GT17GENIChomozygous52057772
105358651853586519GA28GENIChomozygous52057774
105358665153586652CT45GENIChomozygous51648536
105358673953586740GA40GENIChomozygous52057776
105358878653588787CG16GENIChomozygous51648542
105358888653588887CT24GENIChomozygous51648544
105358909053589091GT22GENIChomozygous52057778
105358993753589939CT--2GENIChomozygous52376561
105359171153591712G-29GENIChomozygous51455640
105359178853591789TTGGCCCACGCCCTGCAGTCCTCCCGCCACGACTGTGACCTGCTTCGGGAACAGTACGAG9GENIChomozygous52376563
105359742553597426AAC12GENICheterozygous51648552
105357650153576505ACAC----7GENICpossibly homozygous52439587