chr start stop reference nuc variant nuc depth genic status zygosity variant ID 9 121808496 121808497 T G 39 GENIC possibly homozygous 117788580 9 121823429 121823430 T C 39 GENIC homozygous 117641641 9 121824767 121824768 G A 47 GENIC homozygous 117655249 9 121825659 121825660 T A 58 GENIC heterozygous 117451710 9 121825663 121825664 T C 59 GENIC heterozygous 117451712 9 121828958 121828959 A G 46 GENIC homozygous 117655250 9 121831456 121831457 A T 42 GENIC homozygous 117641667 9 121833764 121833765 A G 44 GENIC homozygous 117655251 9 121843468 121843469 A G 30 GENIC homozygous 117641669 9 121848250 121848251 C G 39 GENIC heterozygous 117641671 9 121848283 121848284 G A 48 GENIC heterozygous 117641675 9 121849318 121849319 G A 28 GENIC heterozygous 117451732 9 121849325 121849326 A G 13 GENIC heterozygous 117451734 9 121849645 121849646 C T 83 GENIC heterozygous 117641678 9 121852847 121852848 T G 19 GENIC heterozygous 117641686 9 121853567 121853568 G A 29 GENIC possibly homozygous 117641688 9 121856840 121856841 C T 60 GENIC possibly homozygous 117655255 9 121867193 121867194 A G 41 GENIC homozygous 117655256 9 121872320 121872321 A G 50 GENIC heterozygous 117781070 9 121880259 121880260 C G 29 GENIC homozygous 117641690 9 121880485 121880486 C T 39 GENIC possibly homozygous 117641692 9 121881126 121881127 T A 58 GENIC heterozygous 120285560 9 121882751 121882752 A T 75 GENIC heterozygous 120285561 9 121882796 121882797 C T 66 GENIC heterozygous 117836370 9 121896003 121896004 C T 55 GENIC homozygous 117641734 9 121896536 121896537 A G 33 GENIC possibly homozygous 117641736 9 121896543 121896544 A G 39 GENIC possibly homozygous 117641738 9 121902634 121902635 C A 53 GENIC homozygous 117655257 9 121903692 121903693 C A 48 GENIC homozygous 117655258 9 121909387 121909388 C T 58 GENIC homozygous 117655259 9 121913143 121913144 A G 46 GENIC homozygous 117655261