chr start stop reference nuc variant nuc depth genic status zygosity variant ID 2 143893156 143893157 G C 38 GENIC homozygous 110038643 2 143897498 143897499 G A 39 GENIC homozygous 110761082 2 143900941 143900942 C T 45 GENIC homozygous 110761083 2 143902757 143902758 T C 24 GENIC homozygous 110761084 2 143904679 143904680 G A 38 GENIC homozygous 110761085 2 143904961 143904962 C T 52 GENIC homozygous 110761086 2 143905700 143905701 A G 58 GENIC homozygous 110038655 2 143908649 143908650 C T 49 GENIC homozygous 110761087 2 143909624 143909625 A G 49 GENIC homozygous 110038662 2 143910190 143910191 A C 62 GENIC homozygous 110038664 2 143910525 143910526 T A 31 GENIC homozygous 110761088 2 143910940 143910941 A G 52 GENIC homozygous 110761089 2 143912117 143912118 A G 57 GENIC possibly homozygous 110038666 2 143914519 143914520 A G 32 GENIC homozygous 110761090 2 143914528 143914529 T C 35 GENIC homozygous 110038668 2 143915327 143915328 A T 43 GENIC possibly homozygous 110761091 2 143916086 143916087 C A 43 GENIC homozygous 110038669 2 143917310 143917311 G A 48 GENIC homozygous 110761092 2 143917420 143917421 T G 33 GENIC heterozygous 110761093 2 143917456 143917457 T A 45 GENIC heterozygous 111330354 2 143918369 143918370 C T 61 GENIC homozygous 110761094 2 143921988 143921989 G A 49 GENIC homozygous 110761095 2 143923832 143923833 C T 49 GENIC homozygous 110038678 2 143923868 143923869 T A 51 GENIC homozygous 110038679 2 143925217 143925218 T C 60 GENIC homozygous 110761096