chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
6	41059642	41059643	C	T	26	GENIC	homozygous	115374703
6	41059676	41059677	G	T	27	GENIC	homozygous	114768880
6	41060008	41060009	C	T	20	GENIC	homozygous	114768882
6	41061525	41061526	A	G	26	GENIC	possibly homozygous	114768888
6	41061680	41061681	A	G	20	GENIC	homozygous	114768890
6	41062607	41062608	C	A	25	GENIC	homozygous	114768892
6	41063044	41063045	G	A	17	GENIC	homozygous	114768894
6	41063781	41063782	G	T	30	GENIC	homozygous	114768896
6	41064148	41064149	A	G	16	GENIC	homozygous	114768900
6	41064899	41064900	G	C	18	GENIC	homozygous	114768904
6	41065666	41065667	A	T	15	GENIC	homozygous	115205740
6	41066241	41066242	A	G	17	GENIC	homozygous	118585372
6	41066243	41066244	A	G	17	GENIC	homozygous	118627510
6	41066245	41066246	A	G	17	GENIC	homozygous	118627511
6	41066247	41066248	A	G	17	GENIC	homozygous	118690515
6	41066484	41066485	A	G	21	GENIC	homozygous	115205742
6	41066720	41066721	G	A	26	GENIC	homozygous	115205743
6	41066741	41066742	T	C	24	GENIC	homozygous	115205744
6	41066892	41066893	A	G	24	GENIC	homozygous	114768908
6	41068080	41068081	T	C	20	GENIC	homozygous	115205746
6	41068103	41068104	C	T	24	GENIC	homozygous	115205747
6	41068424	41068425	T	C	35	GENIC	homozygous	115205748
6	41068520	41068521	C	T	23	GENIC	homozygous	114768918