chr start stop reference nuc variant nuc depth genic status zygosity variant ID 15 99762123 99762124 G T 9 GENIC homozygous 112616604 15 99762197 99762198 C G 17 GENIC homozygous 112616605 15 99762208 99762209 A G 16 GENIC homozygous 112616606 15 99762838 99762839 T A 14 GENIC homozygous 112616607 15 99762994 99762995 C T 25 GENIC homozygous 112616608 15 99763005 99763006 G A 22 GENIC homozygous 112616609 15 99763450 99763451 A G 17 GENIC homozygous 112616610 15 99763640 99763641 A G 18 GENIC homozygous 112616611 15 99763923 99763924 G A 28 GENIC homozygous 112616612 15 99764001 99764002 A G 28 GENIC homozygous 112616614 15 99764197 99764198 C G 20 GENIC homozygous 112616616 15 99764261 99764262 G A 14 GENIC homozygous 112616618 15 99764535 99764536 T C 16 GENIC homozygous 112616620 15 99764584 99764585 C G 13 GENIC homozygous 112616622 15 99764585 99764586 T A 13 GENIC homozygous 112616624 15 99764870 99764871 T C 18 GENIC homozygous 112616633 15 99765048 99765049 G A 23 GENIC homozygous 112616635 15 99765365 99765366 T C 14 GENIC homozygous 112616637 15 99765442 99765443 T A 15 GENIC homozygous 112616639 15 99765787 99765788 G A 19 GENIC homozygous 112616641 15 99765905 99765906 G T 10 GENIC homozygous 112616643 15 99766733 99766734 G C 19 GENIC homozygous 112616645 15 99767101 99767102 T C 16 GENIC homozygous 112616647 15 99767199 99767200 C T 17 GENIC homozygous 112616649 15 99768019 99768020 T A 27 GENIC homozygous 112760505 15 99769819 99769820 A G 21 GENIC homozygous 113067411 15 99769840 99769841 G A 25 GENIC homozygous 113067413 15 99770785 99770786 T C 17 GENIC homozygous 112616655 15 99770875 99770876 G T 15 GENIC homozygous 112616657 15 99770948 99770949 A G 13 GENIC homozygous 112616659 15 99771323 99771324 A G 21 GENIC homozygous 112616661 15 99771352 99771353 C A 20 GENIC homozygous 112616663 15 99767963 99767964 C A 29 GENIC homozygous 112826739