chr start stop reference nuc variant nuc depth genic status zygosity variant ID 13 93946740 93946741 T C 20 GENIC homozygous 144936896 13 93947226 93947266 AGCCGGAAATTACGTCAGCGAGCCGGAAATTACGTCAGCG 11 GENIC homozygous 144926859 13 93947629 93947630 T C 17 GENIC homozygous 144936897 13 93947825 93947826 T C 18 GENIC homozygous 144936898 13 93947847 93947847 T 18 GENIC homozygous 144926860 13 93947848 93947849 T A 18 GENIC homozygous 144936899 13 93947851 93947851 A 18 GENIC homozygous 144926861 13 93947852 93947852 TAACACAAGAA 18 GENIC homozygous 144926862 13 93947963 93947964 C T 22 GENIC homozygous 144936900 13 93948208 93948209 A 15 GENIC homozygous 144926863 13 93948583 93948584 T C 21 GENIC homozygous 144936901 13 93948761 93948762 G A 16 GENIC homozygous 144936902 13 93948995 93948996 C T 19 GENIC homozygous 144936903 13 93949011 93949012 T C 19 GENIC homozygous 144936904 13 93949372 93949373 C T 21 GENIC homozygous 144936905 13 93949779 93949780 T C 13 GENIC homozygous 144936906 13 93950131 93950132 A G 14 GENIC homozygous 144936907 13 93950478 93950478 TA 13 GENIC homozygous 144926864 13 93951697 93951698 G T 15 GENIC homozygous 144936908 13 93951794 93951795 T G 5 GENIC homozygous 144936909 13 93951812 93951813 A 3 GENIC homozygous 144926865 13 93951890 93951891 A T 8 GENIC homozygous 144936910 13 93952311 93952312 C T 18 GENIC homozygous 144936911 13 93952727 93952728 T C 22 GENIC homozygous 144936912 13 93953322 93953323 A G 21 GENIC homozygous 144936913 13 93953326 93953327 C A 21 GENIC homozygous 144936914