chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	144071155	144071156	A	C	23	GENIC	possibly homozygous	112869431
4	144071414	144071415	A	G	41	GENIC	homozygous	112869432
4	144071572	144071573	G	A	28	GENIC	homozygous	112869433
4	144073152	144073153	A	G	27	GENIC	homozygous	112869434
4	144073910	144073911	T	C	31	GENIC	homozygous	112869435
4	144075266	144075267	G	A	23	GENIC	homozygous	112869436
4	144076645	144076646	T	C	25	GENIC	homozygous	112869437
4	144076963	144076964	T	C	43	GENIC	homozygous	112869438
4	144078424	144078425	C	A	42	GENIC	homozygous	112869440
4	144079445	144079446	T	C	54	GENIC	homozygous	112869441
4	144079646	144079647	A	G	25	GENIC	homozygous	112869442
4	144080363	144080364	T	C	44	GENIC	homozygous	112869443
4	144080487	144080488	C	T	39	GENIC	homozygous	112869444
4	144080663	144080664	G	C	12	GENIC	homozygous	112869445
4	144080861	144080862	G	A	39	GENIC	homozygous	112869446
4	144081715	144081716	G	A	36	GENIC	homozygous	112869447
4	144082121	144082122	G	A	32	GENIC	possibly homozygous	112869448
4	144082693	144082694	C	T	30	GENIC	homozygous	112869449
4	144082959	144082960	G	A	32	GENIC	possibly homozygous	112869450
4	144083081	144083082	A	C	14	GENIC	homozygous	113178937
4	144100555	144100556	C	G	23	GENIC	heterozygous	112869451
4	144114702	144114703	A	G	58	GENIC	homozygous	112869453