chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	2666740	2666741	C	T	21	GENIC	homozygous	116312405
11	2666957	2666958	T	C	24	GENIC	homozygous	116013787
11	2667518	2667519	C	T	25	GENIC	homozygous	116013789
11	2667554	2667555	T	C	23	GENIC	homozygous	116013791
11	2667689	2667690	C	T	13	GENIC	homozygous	116312407
11	2668179	2668180	A	C	16	GENIC	homozygous	116013793
11	2669061	2669062	C	T	31	GENIC	homozygous	116013795
11	2669450	2669451	C	T	21	GENIC	possibly homozygous	118217728
11	2669474	2669475	T	C	17	GENIC	homozygous	118217729
11	2669586	2669587	C	T	21	GENIC	possibly homozygous	116013797
11	2670018	2670019	G	T	18	GENIC	homozygous	116013799
11	2670497	2670498	G	A	7	GENIC	homozygous	118217730
11	2671389	2671390	G	C	24	GENIC	homozygous	116013801
11	2672951	2672952	C	T	18	GENIC	homozygous	116312409
11	2675000	2675001	C	T	14	GENIC	possibly homozygous	116013805
11	2677364	2677365	T	A	20	GENIC	homozygous	115733217
11	2678031	2678032	G	T	11	GENIC	homozygous	115733219
11	2680528	2680529	G	A	16	GENIC	homozygous	116312411
11	2681066	2681067	T	C	29	GENIC	homozygous	116013811
11	2681444	2681445	C	A	15	GENIC	homozygous	118173501
11	2681504	2681505	C	A	10	GENIC	homozygous	118133200
11	2681598	2681599	C	A	9	GENIC	homozygous	118133201
11	2685612	2685613	G	T	30	GENIC	homozygous	116013813
11	2690015	2690016	T	C	14	GENIC	homozygous	116312413
11	2691619	2691620	G	C	37	GENIC	possibly homozygous	116013817