chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	42266504	42266505	G	T	16	GENIC	homozygous	114330535
13	42303685	42303686	G	T	21	GENIC	homozygous	114330603
13	42340503	42340504	G	T	26	GENIC	homozygous	114665178
13	42341532	42341533	C	A	23	GENIC	homozygous	114719453
13	42397424	42397425	A	C	16	GENIC	homozygous	114330627
13	42397430	42397431	G	T	14	GENIC	homozygous	114330629
13	42397431	42397432	T	C	14	GENIC	homozygous	114330631
13	42512278	42512279	T	G	2	GENIC	homozygous	114871639
13	42589731	42589732	G	C	31	GENIC	homozygous	114857356
13	42771944	42771945	C	T	25	GENIC	homozygous	114331706
13	42779074	42779075	A	C	25	GENIC	homozygous	114331748
13	42955092	42955093	A	T	33	GENIC	homozygous	114543411
13	42967834	42967835	G	A	23	GENIC	homozygous	114332225
13	42968237	42968238	T	A	21	GENIC	homozygous	114332227
13	42968243	42968244	T	C	22	GENIC	homozygous	114332229
13	42969445	42969446	T	A	23	GENIC	homozygous	114332233
13	42969446	42969447	A	G	24	GENIC	homozygous	114332235
13	43003990	43003991	T	G	1	GENIC	homozygous	114871641
13	43003991	43003992	G	T	2	GENIC	homozygous	114871644
13	43004330	43004331	A	T	32	GENIC	homozygous	114332345
13	43004333	43004334	C	T	31	GENIC	homozygous	114332347
13	43010844	43010845	C	A	33	GENIC	homozygous	114543450
13	43010845	43010846	G	C	32	GENIC	homozygous	114332380
13	43010850	43010851	G	C	33	GENIC	homozygous	114543452