chr start stop reference nuc variant nuc depth genic status zygosity variant ID X 37793662 37793663 T G 14 GENIC homozygous 933910358 X 37793695 37793696 T G 12 GENIC homozygous 933910359 X 37824978 37824979 T G 3 GENIC homozygous 933910360 X 37931796 37931797 G T 5 GENIC homozygous 933910361 X 37937467 37937468 C T 12 GENIC homozygous 933910362 X 37937725 37937726 C T 5 GENIC homozygous 933910363 X 37937726 37937727 T C 5 GENIC homozygous 933910364 X 37967463 37967464 T G 10 GENIC homozygous 933910365 X 37995918 37995919 G T 15 GENIC homozygous 933910366 X 37998333 37998334 G A 9 GENIC homozygous 933910367 X 37998337 37998338 G A 10 GENIC homozygous 933910368 X 37998339 37998340 G A 10 GENIC homozygous 933910369 X 37998344 37998345 G A 10 GENIC homozygous 933910370 X 38005081 38005082 G T 6 GENIC homozygous 933910371 X 38013955 38013956 A T 4 GENIC homozygous 933910372 X 38062539 38062540 A T 8 GENIC homozygous 933910373 X 38062630 38062631 A T 4 GENIC homozygous 933910374 X 38062658 38062659 C A 2 GENIC homozygous 933910375 X 38135890 38135891 A C 6 GENIC homozygous 933910376 X 38170422 38170423 T G 13 GENIC homozygous 933910377