chr start stop reference nuc variant nuc depth genic status zygosity variant ID X 65371014 65371015 T A 5 GENIC homozygous 805578667 X 65373166 65373167 G A 20 GENIC homozygous 805578668 X 65374185 65374186 G A 12 GENIC homozygous 805578669 X 65375904 65375905 A G 10 GENIC homozygous 805578670 X 65376727 65376728 G A 6 GENIC homozygous 805578671 X 65382251 65382252 T A 13 GENIC homozygous 805578672 X 65383157 65383158 T C 5 GENIC homozygous 805578673 X 65384653 65384654 T C 2 GENIC homozygous 805578674 X 65385056 65385057 C T 5 GENIC homozygous 805578675 X 65389102 65389103 G A 17 GENIC heterozygous 805578676 X 65390170 65390171 A G 10 GENIC homozygous 805578677 X 65390772 65390773 T A 12 GENIC heterozygous 805578678 X 65390779 65390780 G T 18 GENIC heterozygous 805578679 X 65390869 65390870 A G 55 GENIC heterozygous 805578680 X 65390870 65390871 C G 58 GENIC heterozygous 805578681 X 65390929 65390930 C T 44 GENIC heterozygous 805578682 X 65391025 65391026 T C 11 GENIC heterozygous 805578683 X 65391598 65391599 G A 12 GENIC heterozygous 805578684 X 65391656 65391657 C T 10 GENIC heterozygous 805578685 X 65392053 65392054 A C 13 GENIC homozygous 805578686 X 65392210 65392211 G A 8 GENIC homozygous 805578687 X 65393956 65393957 G A 13 GENIC homozygous 805578688 X 65394247 65394248 A T 12 GENIC possibly homozygous 805578689 X 65394268 65394269 T A 12 GENIC possibly homozygous 805578690 X 65394962 65394963 G A 18 GENIC heterozygous 805578691 X 65395038 65395039 A G 15 GENIC heterozygous 805578692 X 65395559 65395560 T A 31 GENIC heterozygous 805578693 X 65398257 65398258 A G 3 GENIC homozygous 805578694 X 65398941 65398942 T C 5 GENIC homozygous 805578695