chr start stop reference nuc variant nuc depth genic status zygosity variant ID 10 94137026 94137027 A C 16 GENIC homozygous 116826030 10 94140872 94140873 A G 28 GENIC homozygous 116826042 10 94141606 94141607 A G 33 GENIC homozygous 116826044 10 94142247 94142247 CGGCA 30 GENIC homozygous 131903207 10 94146118 94146118 TGAGCT 21 GENIC homozygous 128847257 10 94140751 94140752 C 23 GENIC homozygous 128847254 10 94140757 94140757 C 22 GENIC homozygous 128847255 10 94143398 94143400 CC 25 GENIC homozygous 128847256 10 94142873 94142874 T C 31 GENIC homozygous 116684629 10 94143627 94143628 A C 21 GENIC homozygous 116684631 10 94147379 94147379 C 14 GENIC homozygous 128847258 10 94147399 94147399 C 16 GENIC homozygous 128847259 10 94147409 94147409 G 15 GENIC homozygous 128847260 10 94147418 94147418 G 14 GENIC homozygous 128847261 10 94147426 94147426 C 13 GENIC homozygous 128847262 10 94147443 94147443 G 12 GENIC homozygous 128847263 10 94147448 94147449 C 11 GENIC homozygous 128847264 10 94147469 94147469 C 9 GENIC homozygous 128847265 10 94147485 94147486 C G 7 GENIC homozygous 118076117 10 94147495 94147495 C 7 GENIC homozygous 128847266 10 94147561 94147562 T G 8 GENIC homozygous 123407997 10 94147562 94147563 G C 8 GENIC homozygous 123407998 10 94146411 94146412 G T 30 GENIC homozygous 116954639