chr start stop reference nuc variant nuc depth genic status zygosity variant ID 12 1721786 1721787 G A 10 GENIC homozygous 139061479 12 1721791 1721792 C T 10 GENIC homozygous 139061480 12 1721792 1721793 A G 10 GENIC homozygous 139061481 12 1721847 1721849 CA 25 GENIC possibly homozygous 145216736 12 1722108 1722109 T C 18 GENIC homozygous 139061482 12 1722635 1722636 A G 21 GENIC homozygous 139061483 12 1722687 1722688 G C 18 GENIC homozygous 139061484 12 1722748 1722749 C A 25 GENIC homozygous 139061485 12 1722912 1722913 C T 16 GENIC homozygous 139061486 12 1723273 1723274 C T 15 GENIC homozygous 139061487 12 1723410 1723411 T A 11 GENIC homozygous 139061488 12 1723603 1723604 T G 18 GENIC homozygous 139061489 12 1723912 1723913 T C 27 GENIC homozygous 139061490 12 1725303 1725304 T C 17 GENIC homozygous 139061491 12 1725867 1725868 C T 20 GENIC homozygous 139061492 12 1727332 1727333 G T 25 GENIC possibly homozygous 139061493 12 1722834 1722834 T 17 GENIC homozygous 139035731