chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
6	122249598	122249599	G	A	37	GENIC	homozygous	115162712
6	122250051	122250051		C	39	GENIC	homozygous	128390550
6	122250495	122250496	A	G	31	GENIC	homozygous	114973359
6	122250552	122250553	T	C	39	GENIC	homozygous	114973360
6	122250910	122250911	T	C	38	GENIC	homozygous	114973361
6	122251926	122251927	C	T	21	GENIC	homozygous	115162713
6	122253332	122253333	C	A	36	GENIC	homozygous	115162714
6	122253381	122253382	C	T	35	GENIC	homozygous	115162715
6	122253460	122253461	T	C	52	GENIC	homozygous	115162716
6	122253872	122253873	G	A	47	GENIC	homozygous	115162717
6	122254124	122254125	T	C	36	GENIC	possibly homozygous	115162718
6	122254346	122254346		T	45	GENIC	homozygous	132645387
6	122252818	122252821	GAC		36	GENIC	homozygous	132645383
6	122253567	122253567		TCTTTTC	47	GENIC	possibly homozygous	132645384
6	122253784	122253786	TC		46	GENIC	possibly homozygous	132645385
6	122254172	122254172		AA	33	GENIC	homozygous	132645386
6	122254538	122254538		T	38	GENIC	homozygous	132645388
6	122254587	122254588	T	C	44	GENIC	homozygous	115162719
6	122254675	122254676	G	A	40	GENIC	homozygous	115162720
6	122254850	122254851	G	A	45	GENIC	homozygous	115162721
6	122255108	122255109	C	T	39	GENIC	homozygous	115162722
6	122255126	122255127	C	A	40	GENIC	homozygous	115162723
6	122255690	122255691	T	C	53	GENIC	homozygous	115162724