chr start stop reference nuc variant nuc depth genic status zygosity variant ID 2 195650907 195650908 A G 28 GENIC homozygous 978335441 2 195651436 195651437 G T 42 GENIC homozygous 978335442 2 195655866 195655867 A G 25 GENIC homozygous 978335443 2 195658260 195658261 T A 26 GENIC homozygous 978335444 2 195660620 195660621 A G 28 GENIC homozygous 978335445 2 195661310 195661311 A G 19 GENIC homozygous 978335446 2 195661434 195661435 G C 20 GENIC homozygous 978335447 2 195661700 195661701 C G 18 GENIC homozygous 978335448 2 195661907 195661908 C T 17 GENIC homozygous 978335449 2 195661951 195661952 G T 13 GENIC homozygous 978335450 2 195665990 195665991 T C 13 GENIC homozygous 978335451 2 195667404 195667405 T C 17 GENIC homozygous 978335452 2 195667847 195667848 A T 35 GENIC homozygous 978335453 2 195668649 195668650 G A 29 GENIC homozygous 978335454 2 195671090 195671091 A G 34 GENIC homozygous 978335455 2 195672704 195672705 G A 29 GENIC homozygous 978335456 2 195672908 195672909 C T 38 GENIC possibly homozygous 978335457 2 195673468 195673469 C T 35 GENIC homozygous 978335458