chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
6	93423699	93423700	T	C	15	GENIC	homozygous	115139376
6	93423896	93423897	G	A	13	GENIC	heterozygous	115139377
6	93423898	93423899	G	A	13	GENIC	heterozygous	114903420
6	93424711	93424712	A	G	7	GENIC	homozygous	115139378
6	93425161	93425162	A	G	34	GENIC	homozygous	115139379
6	93425226	93425227	C	T	36	GENIC	heterozygous	115139380
6	93425287	93425288	G	C	25	GENIC	possibly homozygous	115139381
6	93430412	93430413	A	G	17	GENIC	homozygous	115139382
6	93432037	93432038	G	A	12	GENIC	homozygous	114903430
6	93433235	93433236	A	T	22	GENIC	homozygous	115139384
6	93433865	93433866	T	A	13	GENIC	homozygous	114903434
6	93436504	93436505	G	A	13	GENIC	heterozygous	114903442
6	93436520	93436521	C	T	9	GENIC	possibly homozygous	114903444
6	93436543	93436544	G	T	10	GENIC	homozygous	114903446
6	93436549	93436550	C	T	12	GENIC	homozygous	114903448
6	93436589	93436590	C	G	14	GENIC	homozygous	114903450
6	93436779	93436780	C	T	10	GENIC	homozygous	115139388
6	93437242	93437243	G	T	12	GENIC	homozygous	114903454
6	93437539	93437540	G	A	20	GENIC	homozygous	115139389
6	93441743	93441744	T	C	8	GENIC	homozygous	115139390
6	93442979	93442980	T	C	15	GENIC	homozygous	115139391