chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1154148096154148097CT3GENIChomozygous120523053
1154148178154148179TC13GENIChomozygous108316032
1154148417154148418TA20GENIChomozygous108316034
1154148863154148864GA34GENIChomozygous108947442
1154153070154153071GA24GENIChomozygous108316042
1154155137154155138CA11GENIChomozygous108316046
1154156909154156910AG20GENIChomozygous108947443
1154158221154158222CA11GENIChomozygous108947444
1154159100154159101CT14GENIChomozygous108316052
1154159305154159306TC12GENIChomozygous108316054
1154159607154159608AG24GENIChomozygous108316056
1154160358154160359GA13GENIChomozygous108947445
1154160555154160556AG14GENIChomozygous108947446
1154163729154163730TC10GENIChomozygous108316064
1154165762154165763GA11GENIChomozygous108947448
1154166546154166547CT17GENIChomozygous108947449
1154167027154167028AC5GENIChomozygous108947450
1154167196154167197GC15GENIChomozygous108947451
1154167941154167942AT14GENIChomozygous108947452
1154168510154168511GA24GENIChomozygous108947453
1154168673154168674CA19GENIChomozygous108947454
1154169531154169532TC20GENIChomozygous108947455