chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	2828703	2828704	C	T	8	GENIC	homozygous	116311533
7	2830391	2830392	G	A	13	GENIC	homozygous	116311535
7	2830424	2830424		ATA	11	GENIC	homozygous	128432357
7	2831465	2831466	G	A	20	GENIC	homozygous	116311537
7	2831504	2831505	A	G	21	GENIC	homozygous	115545942
7	2831998	2832004	GCTACG		22	GENIC	homozygous	131007020
7	2832655	2832656	T	G	21	GENIC	homozygous	115545944
7	2835191	2835191		TTTATGTATTTTTTTTTTCTTTCTCTTTTTTTCGGGGCTGGGGATCGAACCCATGACCTTGCGCTTCCTAGGCAAGCGCTCTACCACTGAGCCAAATCCCCAATCCC	9	GENIC	heterozygous	131007021
7	2836371	2836372	C	T	15	GENIC	homozygous	116311541
7	2837580	2837580		A	5	GENIC	heterozygous	131007022
7	2837727	2837728	C	T	13	GENIC	homozygous	116311543
7	2839134	2839135	G	A	12	GENIC	homozygous	115977181
7	2839440	2839441	A	G	19	GENIC	homozygous	116311547
7	2839666	2839667	T	A	17	GENIC	homozygous	116311549
7	2840852	2840853	T	C	16	GENIC	homozygous	115545952
7	2841489	2841490	T	G	16	GENIC	homozygous	115977185
7	2843605	2843606	A	G	17	GENIC	homozygous	115545956
7	2845315	2845316	A	T	13	GENIC	homozygous	116311551
7	2846879	2846880	A	T	10	GENIC	homozygous	116311553
7	2849307	2849308	A	G	17	GENIC	homozygous	115545968
7	2849772	2849773	G	A	14	GENIC	homozygous	116311559
7	2849937	2849938	G	T	13	GENIC	homozygous	115977201
7	2850319	2850322	CCT		16	GENIC	homozygous	131007023
7	2851008	2851009	T	C	16	GENIC	homozygous	115977205
7	2851964	2851965	A	G	16	GENIC	homozygous	116311561
7	2852025	2852026	C	T	17	GENIC	homozygous	115977207
7	2852051	2852100	GAGTGAGGCATTTCTACACTTGATCTTAGCCAAAAGGCCGAGAAGCGAT		8	GENIC	homozygous	131007024
7	2852462	2852463	T		18	GENIC	homozygous	131007025
7	2852654	2852654		A	8	GENIC	heterozygous	131007026
7	2853409	2853410	A	G	12	GENIC	homozygous	115545974