chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	101797067	101797068	G	A	15	GENIC	homozygous	114654884
13	101797172	101797173	A	G	13	GENIC	homozygous	114654885
13	101797224	101797225	G	T	8	GENIC	homozygous	126072908
13	101800013	101800014	A	G	9	GENIC	homozygous	126111917
13	101800861	101800862	T	A	15	GENIC	homozygous	114654891
13	101801091	101801092	T	C	6	GENIC	heterozygous	126111918
13	101801200	101801201	T	C	11	GENIC	homozygous	114654892
13	101801293	101801294	G	A	27	GENIC	homozygous	114654893
13	101801327	101801328	C	T	21	GENIC	homozygous	114654894
13	101801558	101801559	G	A	28	GENIC	homozygous	114654895
13	101801644	101801645	G	A	20	GENIC	homozygous	114654896
13	101801662	101801663	G	A	25	GENIC	homozygous	114654897
13	101802335	101802336	G	A	22	GENIC	homozygous	114654898
13	101803515	101803516	A	G	15	GENIC	homozygous	114654899
13	101803579	101803580	G	A	22	GENIC	homozygous	114654900
13	101803611	101803612	A	G	19	GENIC	homozygous	114654901
13	101803911	101803912	T	C	15	GENIC	homozygous	114654902
13	101803923	101803924	C	T	17	GENIC	homozygous	114654903
13	101804463	101804464	T	G	8	GENIC	heterozygous	118550336
13	101804467	101804468	T	G	9	GENIC	heterozygous	118550337
13	101804588	101804589	A	C	9	GENIC	homozygous	114654904
13	101804602	101804603	T	C	11	GENIC	homozygous	114654905
13	101804723	101804724	A	G	22	GENIC	homozygous	114654906
13	101806523	101806524	C	A	19	GENIC	heterozygous	114654907
13	101806531	101806532	T	C	20	GENIC	heterozygous	114654908
13	101807054	101807055	C	G	13	GENIC	homozygous	114654909
13	101807437	101807438	G	A	12	GENIC	homozygous	114654910