chr start stop reference nuc variant nuc depth genic status zygosity variant ID 7 140326408 140326409 T G 21 GENIC homozygous 115938484 7 140327563 140327564 T G 16 GENIC homozygous 115938485 7 140327957 140327958 A G 27 GENIC homozygous 115938486 7 140328432 140328433 T C 31 GENIC possibly homozygous 115938487 7 140328770 140328771 A G 21 GENIC homozygous 115938488 7 140329694 140329695 T C 17 GENIC homozygous 115938493 7 140332112 140332113 A G 21 GENIC homozygous 115938494 7 140332864 140332865 C T 31 GENIC homozygous 115938495 7 140333359 140333360 A C 32 GENIC homozygous 115938496 7 140333762 140333763 G A 33 GENIC homozygous 115938497 7 140334643 140334644 T C 29 GENIC homozygous 115938498 7 140336378 140336379 C T 12 GENIC homozygous 115938499 7 140336420 140336421 T C 18 GENIC homozygous 115938500 7 140336592 140336593 A G 9 GENIC homozygous 115938501 7 140337405 140337406 T C 18 GENIC homozygous 115938502 7 140338881 140338882 A G 33 GENIC homozygous 115938503 7 140339564 140339565 T C 30 GENIC homozygous 115938505 7 140340988 140340989 T C 21 GENIC homozygous 115938514 7 140341199 140341200 A G 19 GENIC homozygous 115938515 7 140341814 140341815 C T 25 GENIC homozygous 115938516 7 140342282 140342283 T A 20 GENIC homozygous 115938517