chr start stop reference nuc variant nuc depth genic status zygosity variant ID 10 74862924 74862925 C T 25 GENIC homozygous 116637931 10 74866176 74866177 C T 9 GENIC homozygous 126385884 10 74866491 74866492 G A 4 GENIC homozygous 126442409 10 74866601 74866602 A T 13 GENIC homozygous 126385885 10 74866715 74866716 C A 26 GENIC homozygous 117065294 10 74866867 74866868 A G 18 GENIC homozygous 117065296 10 74868947 74868948 C T 30 GENIC homozygous 116637939 10 74869657 74869658 A G 24 GENIC homozygous 118001544 10 74870411 74870412 A G 20 GENIC homozygous 126385886 10 74870770 74870771 A G 36 GENIC homozygous 126385887 10 74873401 74873402 G T 9 GENIC homozygous 126385890 10 74873675 74873676 G A 17 GENIC homozygous 116637941 10 74874273 74874274 C T 28 GENIC homozygous 126462182 10 74876643 74876644 G T 18 GENIC homozygous 116637943 10 74877526 74877527 G A 19 GENIC homozygous 126462183 10 74878845 74878846 G A 22 GENIC homozygous 126462184 10 74879095 74879096 G A 19 GENIC homozygous 126462185 10 74879637 74879638 A G 10 GENIC heterozygous 126462186 10 74879959 74879960 C T 22 GENIC homozygous 126462187 10 74881334 74881335 T C 7 GENIC homozygous 118001546 10 74882077 74882078 G A 16 GENIC homozygous 116637953