chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	72751260	72751261	T	G	45	GENIC	possibly homozygous	115899864
11	72755007	72755008	G	A	55	GENIC	possibly homozygous	115899870
11	72798825	72798826	A	G	39	GENIC	homozygous	118226124
11	72805035	72805036	T	C	39	GENIC	heterozygous	118226125
11	72805184	72805185	G	A	18	GENIC	homozygous	118226126
11	72824307	72824308	C	T	3	GENIC	homozygous	118226127
11	72824550	72824551	A	G	12	GENIC	heterozygous	118163992
11	72824553	72824554	T	G	12	GENIC	homozygous	118195683
11	72824587	72824588	G	A	5	GENIC	homozygous	118226128
11	72824640	72824641	A	T	8	GENIC	homozygous	118163993
11	72824776	72824777	G	A	42	GENIC	possibly homozygous	115987549
11	72824952	72824953	A	G	43	GENIC	homozygous	116161721
11	72849817	72849818	A	G	22	GENIC	homozygous	118226129
11	72849850	72849851	T	C	24	GENIC	heterozygous	118226130
11	72849875	72849876	C	T	17	GENIC	heterozygous	118226131
11	73000436	73000437	G	T	14	GENIC	homozygous	118163994
11	73019302	73019303	T	G	36	GENIC	heterozygous	116052802
11	73027343	73027344	G	T	45	GENIC	heterozygous	116052806
11	73029581	73029582	C	T	5	GENIC	homozygous	118226132
11	73029606	73029607	C	A	17	GENIC	homozygous	116161725
11	73029880	73029881	A	T	28	GENIC	homozygous	116161727
11	73030018	73030019	C	A	48	GENIC	homozygous	115899880