chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	71721784	71721785	C	A	12	GENIC	homozygous	115985141
11	71722808	71722809	A	G	24	GENIC	homozygous	115985143
11	71723438	71723439	C	T	37	GENIC	homozygous	116051206
11	71724135	71724136	T	C	13	GENIC	homozygous	118226028
11	71724180	71724181	T	C	23	GENIC	homozygous	116267078
11	71724536	71724537	T	C	12	GENIC	homozygous	116051208
11	71724932	71724933	T	A	29	GENIC	homozygous	115985147
11	71725114	71725115	C	G	24	GENIC	homozygous	115985149
11	71725250	71725251	A	T	16	GENIC	homozygous	115985151
11	71726314	71726315	C	T	29	GENIC	homozygous	115985153
11	71726801	71726802	T	A	16	GENIC	homozygous	116051210
11	71727990	71727991	C	G	21	GENIC	homozygous	116051212
11	71728055	71728056	T	C	21	GENIC	homozygous	115985161
11	71728327	71728328	A	G	16	GENIC	possibly homozygous	115985163
11	71729580	71729581	C	A	13	GENIC	heterozygous	118226029
11	71734278	71734279	C	T	50	GENIC	possibly homozygous	118226030
11	71734293	71734294	C	T	37	GENIC	heterozygous	118195506
11	71734439	71734440	C	T	40	GENIC	homozygous	116267079
11	71736836	71736837	G	A	10	GENIC	heterozygous	118226031
11	71739510	71739511	G	A	11	GENIC	homozygous	115985177
11	71741531	71741532	T	C	19	GENIC	homozygous	116051214
11	71743320	71743321	A	T	46	GENIC	homozygous	115985181
11	71729517	71729518	C	T	29	GENIC	heterozygous	118229183
11	71729523	71729524	C	T	29	GENIC	possibly homozygous	118229184
11	71729768	71729769	C	A	27	GENIC	homozygous	116247718