chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
9100921631100921632TC18GENIChomozygous117795000
9100921975100921976TC21GENIChomozygous117620373
9100924209100924210AG18GENIChomozygous117620377
9100924641100924642TC17GENIChomozygous117620381
9100924781100924782GT29GENIChomozygous117620383
9100924791100924792GT30GENIChomozygous117620385
9100925833100925833AAT15GENIChomozygous128737671
9100926157100926158AG20GENIChomozygous117764533
9100923492100923576CATGACCATGTTCTGAATGGGGATATCGCATGACCATGTTCTGAATGGGGATATCACATGACCATGTTCTGAATGGGGATATCA6GENIChomozygous131073547
9100924594100924595TC17GENIChomozygous117764527
9100925866100925867CA12GENIChomozygous117764529
9100925928100925929TA12GENIChomozygous117764531
9100926331100926332TC17GENIChomozygous117620391
9100926905100926906TC23GENIChomozygous117764534
9100926927100926928GC19GENIChomozygous117764536
9100927227100927227GAAG14GENIChomozygous128737672
9100927360100927361A18GENIChomozygous128737673
9100928102100928104TC16GENIChomozygous131073548
9100928261100928261A21GENICpossibly homozygous131073549
9100928442100928443TC19GENIChomozygous117620403
9100928064100928065CT20GENIChomozygous117764538
9100928107100928108AG15GENIChomozygous123286331
9100928114100928115TC18GENIChomozygous117764540
9100928131100928132AG16GENIChomozygous117764542
9100928619100928620TC16GENIChomozygous117620407
9100928845100928846CT12GENIChomozygous117764546
9100929306100929307CT8GENIChomozygous117764548
9100929378100929379AG8GENIChomozygous117764550
9100929382100929383CA7GENIChomozygous117764552
9100929456100929459ACT15GENIChomozygous131073550
9100929465100929465A15GENIChomozygous131073551
9100929639100929639TGA15GENIChomozygous131073552
9100929680100929681TC19GENIChomozygous117764554