chr start stop reference nuc variant nuc depth genic status zygosity variant ID 12 30161084 30161085 A G 3 GENIC homozygous 1001341556 12 30161822 30161823 G A 4 GENIC homozygous 1001341557 12 30163459 30163460 G T 5 GENIC homozygous 1001341558 12 30164304 30164305 C T 7 GENIC homozygous 1001341559 12 30164486 30164487 A C 4 GENIC homozygous 1001341560 12 30165458 30165459 G T 9 GENIC homozygous 1001341561 12 30165523 30165524 C A 7 GENIC homozygous 1001341562 12 30166404 30166405 C T 9 GENIC homozygous 1001341563 12 30166449 30166450 C T 7 GENIC homozygous 1001341564 12 30166464 30166465 C A 8 GENIC homozygous 1001341565 12 30166659 30166660 A T 6 GENIC homozygous 1001341566 12 30166830 30166831 G T 10 GENIC homozygous 1001341567 12 30166831 30166832 G A 10 GENIC homozygous 1001341568 12 30170287 30170288 A G 6 GENIC homozygous 1001341569 12 30171217 30171218 T C 8 GENIC homozygous 1001341570 12 30172654 30172655 G A 2 GENIC homozygous 1001341571 12 30172688 30172689 T G 6 GENIC homozygous 1001341572 12 30172829 30172830 A C 6 GENIC homozygous 1001341573 12 30173785 30173786 C T 3 GENIC homozygous 1001341574 12 30174333 30174334 G A 3 GENIC homozygous 1001341575 12 30175060 30175061 A G 3 GENIC homozygous 1001341576 12 30175440 30175441 G A 6 GENIC homozygous 1001341577 12 30175611 30175612 G A 7 GENIC homozygous 1001341578 12 30176130 30176131 G A 12 GENIC homozygous 1001341579 12 30176322 30176323 T G 5 GENIC homozygous 1001341580 12 30177010 30177011 T C 5 GENIC homozygous 1001341581 12 30177099 30177100 T C 4 GENIC homozygous 1001341582 12 30177201 30177202 T C 9 GENIC homozygous 1001341583 12 30177264 30177265 A G 4 GENIC homozygous 1001341584 12 30177318 30177319 G A 7 GENIC homozygous 1001341585 12 30177583 30177584 T C 4 GENIC homozygous 1001341586