chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	23537876	23537877	C	T	17	GENIC	homozygous	143562247
13	23538377	23538378	G	T	25	GENIC	homozygous	143562248
13	23543998	23543999	C	T	9	GENIC	homozygous	143562249
13	23544058	23544059	G		10	GENIC	homozygous	403332432
13	23544058	23544059	G	A	10	GENIC	heterozygous	403332433
13	23544341	23544342	G	A	19	GENIC	homozygous	143562250
13	23545266	23545267	G	C	14	GENIC	homozygous	139250257
13	23547462	23547463	T	C	26	GENIC	homozygous	139250263
13	23547577	23547578	C	T	19	GENIC	homozygous	139250264
13	23547615	23547616	T	A	19	GENIC	homozygous	143562251
13	23549181	23549182	G	A	20	GENIC	homozygous	143562254
13	23540978	23540978		A	24	GENIC	possibly homozygous	139164094
13	23548646	23548647	G	C	22	GENIC	homozygous	143562252
13	23548682	23548683	C	G	21	GENIC	homozygous	139250267
13	23548717	23548718	C	T	26	GENIC	homozygous	143562253
13	23546660	23546666	CTTCTG		7	GENIC	homozygous	143546263
13	23546672	23546675	CTC		7	GENIC	homozygous	143546264
13	23546696	23546705	CTCCTCCTG		7	GENIC	homozygous	143546265
13	23550150	23550151	C		25	GENIC	homozygous	143546266
13	23550225	23550226	C	T	24	GENIC	homozygous	143562255
13	23550941	23550942	G	A	21	GENIC	homozygous	143562256
13	23550150	23550151	C	T	25	GENIC	heterozygous	154768837