chr start stop reference nuc variant nuc depth genic status zygosity variant ID 11 77287683 77287684 G A 32 GENIC possibly homozygous 597649940 11 77287715 77287716 G A 24 GENIC possibly homozygous 597649941 11 77287731 77287732 G A 26 GENIC possibly homozygous 597649942 11 77287775 77287776 T C 29 GENIC homozygous 596349128 11 77288251 77288252 A C 12 GENIC homozygous 596349129 11 77288260 77288261 C G 12 GENIC homozygous 596349130 11 77288542 77288543 G A 24 GENIC possibly homozygous 597649943 11 77288767 77288768 G A 27 GENIC heterozygous 597649944 11 77289213 77289214 G A 2 GENIC homozygous 597649945 11 77289219 77289220 A G 2 GENIC homozygous 596349131 11 77289374 77289375 T C 27 GENIC possibly homozygous 596349132 11 77289694 77289695 G GTCTGTC 1 GENIC homozygous 726479716 11 77289755 77289756 C T 15 GENIC heterozygous 596349133 11 77290309 77290310 A G 18 GENIC possibly homozygous 596349134 11 77291908 77291909 T TTCCC 4 GENIC homozygous 726479717 11 77292515 77292516 A G 19 GENIC homozygous 597649946 11 77292654 77292655 T C 24 GENIC possibly homozygous 597649947 11 77293286 77293287 G A 16 GENIC possibly homozygous 597649948 11 77293754 77293755 C T 28 GENIC possibly homozygous 597649949 11 77293936 77293937 T A 28 GENIC possibly homozygous 597649950 11 77297096 77297097 A G 19 GENIC homozygous 596349135 11 77298674 77298675 G T 3 GENIC homozygous 597649951 11 77300459 77300460 A G 17 GENIC possibly homozygous 596349136 11 77304169 77304170 C T 21 GENIC possibly homozygous 597649952 11 77305215 77305216 G GT 4 GENIC homozygous 726479718 11 77305245 77305246 C T 3 GENIC heterozygous 596349137 11 77305591 77305592 A G 11 GENIC possibly homozygous 596349138