chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	71721738	71721739	A		34	GENIC	possibly homozygous	128921769
11	71721784	71721785	C	A	48	GENIC	homozygous	115985141
11	71722808	71722809	A	G	37	GENIC	homozygous	115985143
11	71724135	71724136	T	C	27	GENIC	homozygous	118226028
11	71724180	71724181	T	C	46	GENIC	homozygous	116267078
11	71724932	71724933	T	A	57	GENIC	homozygous	115985147
11	71725114	71725115	C	G	61	GENIC	homozygous	115985149
11	71725250	71725251	A	T	50	GENIC	homozygous	115985151
11	71726314	71726315	C	T	41	GENIC	homozygous	115985153
11	71723438	71723439	C	T	43	GENIC	homozygous	116051206
11	71724536	71724537	T	C	51	GENIC	homozygous	116051208
11	71726801	71726802	T	A	31	GENIC	homozygous	116051210
11	71725021	71725022	A		60	GENIC	homozygous	131108317
11	71726822	71726822		G	26	GENIC	possibly homozygous	131480230
11	71727971	71727971		C	25	GENIC	homozygous	131480231
11	71727990	71727991	C	G	28	GENIC	homozygous	116051212
11	71728055	71728056	T	C	38	GENIC	homozygous	115985161
11	71728327	71728328	A	G	59	GENIC	homozygous	115985163
11	71729734	71729735	C		45	GENIC	homozygous	131108325
11	71730379	71730379		GCCTTGGCTGTGATAT	37	GENIC	homozygous	131108327
11	71730383	71730383		TGGGGTGG	38	GENIC	homozygous	131108328
11	71734439	71734440	C	T	33	GENIC	homozygous	116267079
11	71739206	71739207	T		48	GENIC	homozygous	128921770
11	71739510	71739511	G	A	28	GENIC	possibly homozygous	115985177
11	71741452	71741453	C	T	8	GENIC	homozygous	118226032
11	71741531	71741532	T	C	20	GENIC	homozygous	116051214
11	71743320	71743321	A	T	49	GENIC	homozygous	115985181
11	71731371	71731372	C	A	5	GENIC	homozygous	118185475
11	71729768	71729769	C	A	40	GENIC	homozygous	116247718