chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
14	104475118	104475119	T	C	45	GENIC	heterozygous	118724097
14	104475129	104475130	G	A	48	GENIC	heterozygous	118724098
14	104475133	104475134	T	A	40	GENIC	heterozygous	118724099
14	104475140	104475141	G	A	39	GENIC	heterozygous	118724100
14	104475142	104475143	C	T	39	GENIC	heterozygous	118724101
14	104475153	104475154	C	A	38	GENIC	heterozygous	118724102
14	104475155	104475156	G	T	38	GENIC	heterozygous	118724103
14	104475184	104475185	T	A	27	GENIC	homozygous	113530450
14	104485550	104485551	C	T	45	GENIC	homozygous	113530452
14	104485640	104485641	C	T	21	GENIC	homozygous	113927805
14	104485663	104485664	G	C	6	GENIC	homozygous	118811493
14	104487534	104487535	G	A	42	GENIC	homozygous	113530454
14	104493931	104493932	T	C	31	GENIC	homozygous	113530456
14	104495232	104495233	G	A	5	GENIC	homozygous	118724104
14	104495233	104495234	G	C	5	GENIC	heterozygous	118724105
14	104495243	104495244	G	A	4	GENIC	homozygous	118724106
14	104495481	104495482	G	A	29	GENIC	homozygous	113530458
14	104496470	104496471	A	T	56	GENIC	homozygous	113530460
14	104496514	104496515	G	A	59	GENIC	homozygous	113530462
14	104496834	104496835	G	A	51	GENIC	homozygous	113530464
14	104497876	104497877	A	G	60	GENIC	homozygous	113530466
14	104499300	104499301	A	T	36	GENIC	homozygous	113530468
14	104499674	104499675	C	T	141	GENIC	heterozygous	118724107
14	104499714	104499715	A	T	187	GENIC	heterozygous	118724108
14	104499782	104499783	T	C	99	GENIC	heterozygous	118724109
14	104485938	104485939	A	C	25	GENIC	homozygous	114166543
14	104499638	104499639	T	C	82	GENIC	heterozygous	118772813
14	104499651	104499652	A	G	100	GENIC	heterozygous	118772814
14	104491325	104491326	A	C	29	GENIC	possibly homozygous	113827390
14	104492292	104492293	T	A	40	GENIC	possibly homozygous	113615489
14	104495227	104495228	C	T	6	GENIC	homozygous	114093228