chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
56078079060780795GCTCG52GENIChomozygous141682657
56078082460780825AG62GENIChomozygous141727800
56078367760783678CT61GENIChomozygous141727806
56078121660781217GC49GENIChomozygous146131338
56078158660781587AT35GENIChomozygous141727801
56078215060782151TA52GENIChomozygous141727802
56078234060782341TG59GENIChomozygous141727803
56078331860783319AG47GENIChomozygous141727805
56078146460781465C14GENICpossibly homozygous146120573
56078383460783835CT50GENIChomozygous141727807
56078478460784785AG43GENIChomozygous141727809
56078487860784879GA43GENIChomozygous146131339
56078544560785446TC58GENIChomozygous141727810
56078635860786359CT50GENIChomozygous146131340
56078645960786459T42GENIChomozygous146120574
56078663860786639TG46GENIChomozygous146131341
56078663960786640CA47GENIChomozygous146131342
56078753960787540CT56GENIChomozygous146131343
56078791660787916GGGT28GENIChomozygous141682658
56078856860788569AT45GENIChomozygous146131344
56079212360792124TC68GENIChomozygous137482132
56078313560783135T53GENIChomozygous137311563
56078498960784999GTGTGTGTGC32GENICheterozygous147865970
56078801460788015CT57GENIChomozygous137482127
56079015960790160AC40GENIChomozygous137482129
56078906460789076TCCTCCTCTTCC30GENIChomozygous147664270
56078919960789241TCCTCCTCCTCTTCCTCCTCCTCTTCTTCCTCCTCCTCCTTT35GENIChomozygous147664271
56079255160792552TG63GENIChomozygous137482133
56079322960793230TC56GENIChomozygous137482134
56079421360794214GT53GENIChomozygous146131345
56079474260794743CT68GENIChomozygous146131346
56079523060795231CT52GENIChomozygous146131347
56079586460795865CT53GENIChomozygous146131348
56079688960796890AG44GENIChomozygous137482136
56079721460797215AG55GENIChomozygous137482137