chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	62778575	62778575		ATCA	16	GENIC	homozygous	136887504
4	62779140	62779141	A	G	20	GENIC	homozygous	137064969
4	62782463	62782464	G	T	15	GENIC	homozygous	137064970
4	62782464	62782465	A	C	15	GENIC	homozygous	137064971
4	62783405	62783406	T	A	15	GENIC	homozygous	137064972
4	62783480	62783481	T	C	14	GENIC	homozygous	137064973
4	62785098	62785099	G	A	21	GENIC	homozygous	137064974
4	62785466	62785467	A	G	15	GENIC	homozygous	137064975
4	62786069	62786070	C	G	10	GENIC	homozygous	137064976
4	62787488	62787489	G	A	23	GENIC	homozygous	137064977
4	62790178	62790288	TCAAAAATATTTTTTTTTTTTTTGGTTCTTTTTTTCGGAGCTGGGAACCGAACCCAGGGCCTTGCGCTTCCTAGGCAAGCGCTCTACCACTGAGCTAAATCCCCAACCCC		9	GENIC	homozygous	136887505
4	62791497	62791498	T	C	23	GENIC	homozygous	137064978
4	62791768	62791769	T	C	28	GENIC	homozygous	137064979
4	62793665	62793666	A	G	18	GENIC	homozygous	137064980
4	62793740	62793741	T	C	22	GENIC	homozygous	137064981
4	62794116	62794117	C	T	13	GENIC	homozygous	137064982
4	62794353	62794354	T	C	19	GENIC	homozygous	137064983
4	62794910	62794911	G	A	10	GENIC	homozygous	137064984
4	62795487	62795488	G	A	15	GENIC	homozygous	137064985
4	62795608	62795608		AC	5	GENIC	homozygous	136887506
4	62797405	62797406	T	C	15	GENIC	homozygous	137064991
4	62797587	62797588	T	C	12	GENIC	homozygous	137064992
4	62797603	62797603		CATTTTCATATTCTTATC	11	GENIC	homozygous	136887507
4	62798286	62798287	A	C	14	GENIC	homozygous	137064993
4	62798507	62798508	T	C	14	GENIC	homozygous	137064994