chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	21600896	21600896		TCTTC	13	GENIC	homozygous	140984824
3	21644638	21644639	C		16	GENIC	heterozygous	403765299
3	21644638	21644639	C	T	16	GENIC	heterozygous	403765300
3	21644641	21644642	T		16	GENIC	heterozygous	403765301
3	21644641	21644642	T	C	16	GENIC	heterozygous	403765302
3	21822803	21822804	A		11	GENIC	homozygous	403059186
3	21822803	21822804	A	G	11	GENIC	heterozygous	403059187
3	21822805	21822806	A		11	GENIC	homozygous	403059188
3	21822805	21822806	A	G	11	GENIC	heterozygous	403059189
3	21842355	21842356	G		20	GENIC	homozygous	403059196
3	21842355	21842356	G	A	20	GENIC	heterozygous	403059197
3	21842357	21842358	G		20	GENIC	homozygous	404061673
3	21842357	21842358	G	A	20	GENIC	heterozygous	404061674
3	21842359	21842360	G		20	GENIC	homozygous	404795678
3	21842359	21842360	G	A	20	GENIC	heterozygous	404795679
3	21863942	21863943	A		18	GENIC	heterozygous	403059202
3	21863942	21863943	A	G	18	GENIC	heterozygous	403059203
3	21866845	21866846	G		12	GENIC	heterozygous	403059212
3	21866845	21866846	G	C	12	GENIC	heterozygous	403059213
3	21869459	21869460	T		23	GENIC	heterozygous	403059218
3	21869459	21869460	T	A	23	GENIC	homozygous	403059219
3	21887552	21887553	G		66	GENIC	heterozygous	140984825
3	21937568	21937569	G		16	GENIC	heterozygous	403059224
3	21937568	21937569	G	C	16	GENIC	heterozygous	403059225
3	21943578	21943579	C		11	GENIC	homozygous	140984826
3	22004856	22004857	T		38	GENIC	possibly homozygous	136551962
3	22014535	22014536	G		33	GENIC	heterozygous	136551965
3	22014565	22014565		C	31	GENIC	heterozygous	136551966
3	22014591	22014592	G	A	31	GENIC	heterozygous	403059243
3	21838083	21838084	A	G	61	GENIC	homozygous	136653928
3	21937570	21937571	G		16	GENIC	heterozygous	403059226
3	21937570	21937571	G	C	16	GENIC	heterozygous	403059227
3	22014576	22014577	C	A	32	GENIC	heterozygous	403059241
3	22014587	22014588	G	A	31	GENIC	heterozygous	403059242
3	22014610	22014611	G		25	GENIC	heterozygous	140867915