chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	30663781	30663782	T	C	35	GENIC	heterozygous	51389292
10	30663985	30663986	C	T	37	GENIC	heterozygous	51389293
10	30678336	30678337	C	T	82	GENIC	heterozygous	51389336
10	30706622	30706623	C	G	34	GENIC	heterozygous	51389398
10	30706709	30706710	G	A	39	GENIC	heterozygous	51389399
10	30711002	30711003	C	T	36	GENIC	heterozygous	51389440
10	30716959	30716960	T	C	16	GENIC	heterozygous	51389481
10	30720371	30720372	A	T	18	GENIC	heterozygous	51389509
10	30778490	30778491	T	G	11	GENIC	heterozygous	51633728
10	30778491	30778492	C	T	11	GENIC	heterozygous	51389819
10	30800764	30800765	T	C	22	GENIC	heterozygous	51389868
10	30801001	30801002	C	T	36	GENIC	heterozygous	51389869
10	30803107	30803108	G	A	11	GENIC	heterozygous	51389871
10	30805995	30805996	T	TTAGTGTCCCCA	20	GENIC	heterozygous	51389878
10	30819704	30819705	G	C	27	GENIC	heterozygous	51389907
10	30825578	30825579	C	CA	24	GENIC	heterozygous	51389911
10	30825645	30825646	C	G	23	GENIC	heterozygous	51389912
10	30829455	30829456	T	-	71	GENIC	heterozygous	51389914