chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	83098210	83098211	T	C	49	GENIC	homozygous	116660492
10	83101581	83101582	C	T	55	GENIC	possibly homozygous	116660494
10	83101627	83101628	T	G	49	GENIC	homozygous	116660496
10	83114989	83114990	T	C	47	GENIC	homozygous	116660498
10	83115192	83115193	C	T	50	GENIC	possibly homozygous	116660500
10	83115364	83115365	A	G	39	GENIC	homozygous	116660502
10	83115365	83115366	A	C	40	GENIC	homozygous	116660504
10	83115580	83115581	C	T	67	GENIC	homozygous	116660506
10	83116363	83116364	A	G	44	GENIC	homozygous	116660508
10	83116598	83116599	C	A	55	GENIC	homozygous	116660510
10	83118061	83118062	T	A	23	GENIC	homozygous	116660512
10	83121369	83121370	G	A	18	GENIC	homozygous	116660514
10	83121396	83121397	A	G	16	GENIC	homozygous	116660516
10	83121892	83121893	T	C	30	GENIC	homozygous	116660517
10	83125782	83125783	G	A	44	GENIC	homozygous	116660519
10	83125869	83125870	A	C	40	GENIC	homozygous	116660521
10	83126340	83126341	C	T	36	GENIC	homozygous	116660523
10	83126635	83126636	T	A	48	GENIC	heterozygous	118003976