chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7137148586137148587CT17GENIChomozygous554738365
7137148798137148799AG23GENIChomozygous554738366
7137148956137148957TA23GENIChomozygous554295533
7137149002137149003TG12GENIChomozygous554295534
7137149347137149349AA--15GENIChomozygous703190398
7137149410137149411AT19GENIChomozygous554738367
7137149534137149535GA10GENIChomozygous554738368
7137149644137149645GA11GENIChomozygous554738369
7137149935137149936AT9GENIChomozygous554295535
7137149997137149998CCTTGTTTGT14GENIChomozygous703190400
7137150134137150135T-12GENIChomozygous703190402
7137150222137150223TG12GENIChomozygous554295536
7137150351137150352AG17GENIChomozygous554295537
7137151268137151269GA25GENICpossibly homozygous554738370
7137151311137151312GGTGTC32GENIChomozygous703190403
7137151529137151530GA36GENIChomozygous554295538
7137151732137151733GA17GENIChomozygous554295539
7137152106137152110TTTT----1GENIChomozygous703190406
7137152162137152163TC4GENIChomozygous554738371
7137152231137152232TTTTTC4GENIChomozygous703190407
7137152239137152240CCTT3GENIChomozygous703190410
7137152728137152729AG21GENIChomozygous554295540
7137152829137152830AATGTATATGTATG2GENIChomozygous703190411
7137152946137152947AG29GENIChomozygous554295541
7137153127137153128GA20GENIChomozygous554295542
7137153207137153208GGA13GENIChomozygous703190413
7137153658137153659CA31GENIChomozygous554295543
7137153697137153698TA37GENIChomozygous554295544
7137153848137153849GA24GENIChomozygous554295545
7137154398137154399CT23GENIChomozygous554295546
7137154438137154439TG26GENIChomozygous554295547
7137154578137154579AG24GENIChomozygous554295548
7137154902137154903CA36GENIChomozygous554295549
7137154909137154910TA36GENIChomozygous554738372