chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	4542407	4542408	T	C	39	GENIC	homozygous	109074694
20	4542415	4542416	A	G	41	GENIC	homozygous	109074696
20	4542956	4542957	A	G	31	GENIC	homozygous	109074698
20	4544975	4544976	C	T	29	GENIC	homozygous	109074700
20	4545440	4545441	C	T	21	GENIC	homozygous	109074702
20	4545577	4545578	T	A	14	GENIC	homozygous	109465785
20	4546251	4546252	A	G	33	GENIC	homozygous	109074704
20	4548233	4548234	C	A	35	GENIC	homozygous	109074708
20	4549064	4549065	G	T	31	GENIC	homozygous	109074710
20	4550464	4550465	G	C	16	GENIC	homozygous	109463080
20	4550971	4550972	A	G	29	GENIC	homozygous	109074712
20	4552076	4552077	C	A	25	GENIC	homozygous	109074716
20	4553033	4553034	G	T	23	GENIC	homozygous	109074718
20	4553251	4553252	C	T	9	GENIC	homozygous	109074720
20	4547272	4547273	G	A	37	GENIC	homozygous	109418820
20	4551495	4551496	T	C	30	GENIC	homozygous	109418822
20	4554392	4554393	T	C	28	GENIC	homozygous	109074722
20	4554839	4554840	G	T	35	GENIC	homozygous	109074726
20	4555267	4555268	G	A	39	GENIC	homozygous	109074728
20	4555559	4555560	G	A	36	GENIC	homozygous	109418824
20	4555666	4555667	A	G	36	GENIC	homozygous	109390042
20	4555730	4555731	A	G	31	GENIC	homozygous	109233515
20	4556045	4556046	G	A	23	GENIC	homozygous	109418826