chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	50197272	50197273	G	A	16	GENIC	homozygous	114339615
13	50197525	50197526	G	A	16	GENIC	homozygous	114339617
13	50197573	50197574	T	C	20	GENIC	homozygous	114339619
13	50198814	50198815	C	T	27	GENIC	homozygous	114339621
13	50200872	50200873	A	T	16	GENIC	homozygous	114339623
13	50198496	50198497	T	A	21	GENIC	homozygous	114671061
13	50212242	50212243	C	T	17	GENIC	homozygous	114339627
13	50213396	50213397	G	C	28	GENIC	homozygous	114339629
13	50214944	50214945	A	G	23	GENIC	homozygous	114339639
13	50215369	50215370	G	A	19	GENIC	homozygous	114339641
13	50215876	50215877	G	A	24	GENIC	homozygous	114339643
13	50219198	50219199	A	T	31	GENIC	homozygous	114339645
13	50221511	50221512	T	C	18	GENIC	homozygous	114339649
13	50222240	50222241	A	G	30	GENIC	homozygous	114339653
13	50224340	50224341	T	C	13	GENIC	homozygous	114339657
13	50227626	50227627	A	T	21	GENIC	homozygous	114339661
13	50227817	50227818	T	C	24	GENIC	homozygous	114339663
13	50227846	50227847	C	T	25	GENIC	homozygous	114339665
13	50229486	50229487	G	T	22	GENIC	homozygous	114671063
13	50229757	50229758	T	A	32	GENIC	homozygous	114339667
13	50230161	50230162	A	G	23	GENIC	homozygous	114339669
13	50232057	50232058	T	C	34	GENIC	homozygous	114339673