chr start stop reference nuc variant nuc depth genic status zygosity variant ID 7 12610888 12610889 T C 10 GENIC possibly homozygous 53791320 7 12614495 12614496 A C 14 GENIC homozygous 53791323 7 12614537 12614538 C T 12 GENIC homozygous 53791324 7 12618900 12618901 C A 19 GENIC homozygous 53791325 7 12618999 12619000 G A 14 GENIC possibly homozygous 53791326 7 12619188 12619189 G A 17 GENIC possibly homozygous 53791327 7 12619684 12619685 G A 21 GENIC possibly homozygous 53791328 7 12622061 12622062 G A 5 GENIC homozygous 53791330 7 12622383 12622384 A G 25 GENIC homozygous 53791335 7 12622659 12622660 A G 25 GENIC possibly homozygous 53791336 7 12624229 12624230 T TA 5 GENIC homozygous 53791337 7 12624768 12624769 C T 11 GENIC possibly homozygous 53791341 7 12625247 12625248 C T 11 GENIC possibly homozygous 53791342 7 12625260 12625261 G C 11 GENIC homozygous 53791343 7 12625357 12625358 C G 19 GENIC homozygous 53791344 7 12625409 12625410 C T 3 GENIC heterozygous 53791345 7 12625920 12625921 C A 5 GENIC homozygous 53791355 7 12625928 12625929 G A 5 GENIC homozygous 53791356 7 12626271 12626272 C T 3 GENIC homozygous 53791358 7 12627468 12627469 T C 2 GENIC homozygous 53791361