chr start stop reference nuc variant nuc depth genic status zygosity variant ID X 114928688 114928689 G A 18 GENIC possibly homozygous 595333678 X 114929263 114929264 T A 1 GENIC homozygous 595333679 X 114929559 114929560 G A 10 GENIC homozygous 595333680 X 114934944 114934945 A C 8 GENIC homozygous 595333681 X 114935007 114935008 T A 3 GENIC heterozygous 595333682 X 114935946 114935947 C T 26 GENIC possibly homozygous 595333683 X 114937245 114937246 G C 21 GENIC possibly homozygous 595333684 X 114937462 114937463 T C 14 GENIC homozygous 595333685 X 114938934 114938941 TGTCCAA ------- 7 GENIC possibly homozygous 727325047 X 114939476 114939477 G A 24 GENIC homozygous 595333686 X 114939824 114939825 A G 8 GENIC homozygous 595333687 X 114940124 114940125 G T 12 GENIC homozygous 595333688 X 114941790 114941791 G A 17 GENIC homozygous 595333689 X 114943654 114943655 C T 16 GENIC homozygous 595333690 X 114945819 114945820 G - 27 GENIC homozygous 727325048 X 114946263 114946264 C CTACA 12 GENIC possibly homozygous 727325049 X 114946536 114946537 C T 17 GENIC homozygous 595333691 X 114946573 114946574 T C 21 GENIC possibly homozygous 595333692 X 114946839 114946840 G T 16 GENIC possibly homozygous 595333693