chr start stop reference nuc variant nuc depth genic status zygosity variant ID 4 34755792 34755793 C T 23 GENIC homozygous 952117099 4 34756971 34756972 A G 6 GENIC homozygous 952117100 4 34757331 34757332 T C 42 GENIC homozygous 952117101 4 34758068 34758069 T C 37 GENIC homozygous 952117102 4 34758287 34758288 T C 22 GENIC homozygous 952117103 4 34759388 34759389 G A 27 GENIC homozygous 952117104 4 34759725 34759726 G T 9 GENIC homozygous 952117105 4 34760550 34760551 A G 21 GENIC homozygous 952117106 4 34760570 34760571 C T 17 GENIC homozygous 952117107 4 34760730 34760731 C T 21 GENIC homozygous 952117108 4 34760800 34760801 T A 14 GENIC homozygous 952117109 4 34760953 34760954 G A 27 GENIC homozygous 952117110 4 34760958 34760959 C A 27 GENIC homozygous 952117111 4 34760986 34760987 C T 21 GENIC homozygous 952117112 4 34761396 34761397 A G 28 GENIC homozygous 952117113 4 34761563 34761564 G T 25 GENIC homozygous 952117114 4 34762145 34762146 T C 17 GENIC homozygous 952117115 4 34762687 34762688 C T 30 GENIC homozygous 952117116 4 34763017 34763018 G A 14 GENIC homozygous 952117117 4 34763164 34763165 T C 18 GENIC homozygous 952117118 4 34763339 34763340 G A 34 GENIC homozygous 952117119 4 34763814 34763815 A G 30 GENIC homozygous 952117120 4 34764284 34764285 G A 25 GENIC homozygous 952117121 4 34764481 34764482 T C 29 GENIC homozygous 952117122