chr start stop reference nuc variant nuc depth genic status zygosity variant ID 7 131967494 131967495 G C 23 GENIC homozygous 69139889 7 131968785 131968786 T C 27 GENIC homozygous 69139893 7 131969781 131969782 A G 32 GENIC homozygous 69139898 7 131970287 131970288 G A 38 GENIC homozygous 69139900 7 131970691 131970692 G A 23 GENIC homozygous 69139909 7 131971092 131971093 G A 26 GENIC homozygous 69139913 7 131972405 131972406 T C 16 GENIC homozygous 69139916 7 131973621 131973622 T A 26 GENIC homozygous 69139920 7 131976210 131976211 G A 29 GENIC homozygous 69139924 7 131976230 131976231 G A 29 GENIC homozygous 69139928 7 131976351 131976352 A G 23 GENIC homozygous 69139932 7 131977104 131977105 G A 23 GENIC homozygous 69139936 7 131977129 131977130 A G 19 GENIC homozygous 69139940 7 131977573 131977574 A G 18 GENIC homozygous 69139943 7 131977797 131977798 C T 22 GENIC homozygous 69139947 7 131979444 131979445 A C 45 GENIC possibly homozygous 69139951 7 131979670 131979671 T C 15 GENIC homozygous 69139955 7 131979822 131979823 G C 23 GENIC homozygous 69139957 7 131980524 131980525 G A 28 GENIC homozygous 69139962 7 131980768 131980769 A C 4 GENIC heterozygous 69139965 7 131980993 131980994 T C 9 GENIC homozygous 69139968 7 131981061 131981062 T C 15 GENIC possibly homozygous 69139972 7 131981077 131981078 C T 16 GENIC possibly homozygous 69139976 7 131981399 131981400 T C 28 GENIC homozygous 69139980 7 131981980 131981981 C T 36 GENIC possibly homozygous 69139983 7 131982332 131982333 A G 29 GENIC homozygous 69139987 7 131983111 131983112 T C 27 GENIC homozygous 69139991 7 131983962 131983963 T C 40 GENIC homozygous 69139995 7 131984731 131984732 C T 29 GENIC homozygous 69139999 7 131985013 131985014 T C 24 GENIC homozygous 69140003 7 131985162 131985163 T G 40 GENIC homozygous 69140007