chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	107835795	107835796	C	T	25	GENIC	homozygous	114236320
5	107839142	107839143	G	A	24	GENIC	homozygous	114236321
5	107839671	107839672	C	T	21	GENIC	homozygous	114236322
5	107841173	107841174	C	T	36	GENIC	homozygous	114236324
5	107842620	107842621	C	T	15	GENIC	homozygous	113956446
5	107842983	107842984	A	G	17	GENIC	homozygous	114236325
5	107843791	107843792	T	C	23	GENIC	homozygous	114236326
5	107844357	107844358	A	T	26	GENIC	homozygous	114236327
5	107844789	107844790	C	T	11	GENIC	homozygous	114236328
5	107845017	107845018	G	A	17	GENIC	homozygous	114236329
5	107845237	107845238	T	C	23	GENIC	homozygous	113956447
5	107845265	107845266	C	G	18	GENIC	homozygous	114236330
5	107845283	107845284	G	A	18	GENIC	homozygous	113956448
5	107845643	107845644	G	C	13	GENIC	homozygous	114236331
5	107846855	107846856	C	T	20	GENIC	homozygous	114236332
5	107847349	107847350	C	T	26	GENIC	homozygous	114236333
5	107848422	107848423	A	G	38	GENIC	homozygous	114236334
5	107848543	107848544	T	C	23	GENIC	homozygous	113956449
5	107848588	107848589	G	A	17	GENIC	homozygous	114236335
5	107849329	107849330	A	G	25	GENIC	homozygous	113956450
5	107849729	107849730	G	T	33	GENIC	homozygous	114236336
5	107850238	107850239	T	A	22	GENIC	homozygous	114236337
5	107851848	107851849	C	T	19	GENIC	homozygous	114236338
5	107852132	107852133	A	G	13	GENIC	homozygous	113956452
5	107853769	107853770	A	G	22	GENIC	homozygous	114236339
5	107854025	107854026	C	T	9	GENIC	homozygous	114236340
5	107855256	107855257	A	G	3	GENIC	homozygous	114236341
5	107857364	107857365	T	C	33	GENIC	homozygous	113956458