chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5145361099145361100AG2GENIChomozygous567718388
5145361900145361901GC13GENIChomozygous567718389
5145363123145363126CCA---12GENIChomozygous710113821
5145363320145363321AC24GENIChomozygous567718390
5145364001145364002CT22GENIChomozygous565658677
5145364976145364977AG18GENIChomozygous567718391
5145365273145365274CCAGTT14GENIChomozygous710113822
5145365654145365655AT15GENIChomozygous567718392
5145365891145365892CT25GENIChomozygous565658678
5145366834145366835GA20GENIChomozygous565658679
5145367301145367302TG27GENIChomozygous565658680
5145368243145368244GGA11GENIChomozygous710113823
5145369071145369072AG17GENIChomozygous567718393
5145369147145369148TC15GENIChomozygous567718394
5145370295145370296A-8GENICpossibly homozygous710113824
5145370312145370313CCA8GENICheterozygous710113826
5145370313145370314A-8GENICheterozygous710113825
5145371450145371458GTGTGTGT--------14GENICheterozygous710113827
5145371452145371458GTGTGT------14GENICpossibly homozygous710113828
5145373072145373073CT21GENIChomozygous565658681
5145373159145373160TC15GENIChomozygous565658682
5145373253145373254TG23GENIChomozygous565658683
5145373669145373670CT25GENIChomozygous565658684
5145373689145373695TGTGTG------19GENICheterozygous710113831
5145373691145373695TGTG----19GENICpossibly homozygous710113832
5145374274145374275CG2GENIChomozygous567718395
5145375208145375209CCT18GENIChomozygous710113834
5145376435145376436GA20GENIChomozygous565658685
5145376586145376587GA23GENIChomozygous565658686
5145377734145377735TG23GENIChomozygous567718396
5145377759145377760AG23GENIChomozygous567718397
5145377938145377939TC20GENIChomozygous567718398
5145378460145378461AG27GENIChomozygous565658687
5145378986145378987GA21GENIChomozygous565658688