chr start stop reference nuc variant nuc depth genic status zygosity variant ID 13 100666740 100666741 T C 26 GENIC possibly homozygous 114653472 13 100666936 100666937 T C 24 GENIC homozygous 114653473 13 100666959 100666960 T A 27 GENIC homozygous 114653474 13 100667074 100667075 C T 29 GENIC homozygous 114653475 13 100667694 100667695 T C 16 GENIC homozygous 114653476 13 100667872 100667873 G A 19 GENIC homozygous 114653477 13 100668106 100668107 C T 29 GENIC homozygous 114653478 13 100668122 100668123 T C 24 GENIC homozygous 114653479 13 100668483 100668484 C T 25 GENIC homozygous 114653480 13 100668890 100668891 T C 22 GENIC homozygous 114653481 13 100669242 100669243 A G 28 GENIC homozygous 114653482 13 100670808 100670809 G T 16 GENIC homozygous 114653483 13 100671422 100671423 C T 27 GENIC homozygous 114653484 13 100671838 100671839 T C 23 GENIC homozygous 114653485 13 100672433 100672434 A G 4 GENIC homozygous 114653486 13 100672437 100672438 C A 3 GENIC homozygous 114653487