chr start stop reference nuc variant nuc depth genic status zygosity variant ID 10 40742723 40742724 T C 21 GENIC homozygous 116570313 10 40743859 40743860 C T 23 GENIC possibly homozygous 116570315 10 40744007 40744008 T C 34 GENIC homozygous 116570319 10 40744265 40744266 C T 29 GENIC homozygous 116764658 10 40744297 40744298 A G 26 GENIC homozygous 116764660 10 40745948 40745949 A C 23 GENIC homozygous 116870800 10 40746784 40746785 G A 46 GENIC homozygous 116870802 10 40747091 40747092 T C 39 GENIC homozygous 116764672 10 40748128 40748129 A G 28 GENIC homozygous 116570323 10 40748363 40748364 G C 28 GENIC homozygous 116870804 10 40748562 40748563 T C 26 GENIC homozygous 116764682 10 40751282 40751283 G A 28 GENIC homozygous 116570337 10 40751355 40751356 G A 33 GENIC homozygous 116870806 10 40752102 40752103 T C 32 GENIC homozygous 116870808 10 40752235 40752236 C T 28 GENIC homozygous 116870810 10 40755326 40755327 G A 24 GENIC homozygous 116870812 10 40755514 40755515 T C 24 GENIC homozygous 116870814 10 40755828 40755829 A G 18 GENIC homozygous 116870816 10 40756811 40756812 T C 32 GENIC homozygous 116570357 10 40756863 40756864 C T 36 GENIC homozygous 116870818 10 40758542 40758543 C T 29 GENIC homozygous 116870820 10 40758944 40758945 G A 43 GENIC homozygous 116870822 10 40762747 40762748 G A 33 GENIC homozygous 116870824