chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
14	43963540	43963541	G	A	41	GENIC	possibly homozygous	113443892
14	43964268	43964269	A	G	48	GENIC	homozygous	113443894
14	43964433	43964434	A	T	41	GENIC	homozygous	113443896
14	43964893	43964894	A	C	19	GENIC	heterozygous	113443898
14	43965365	43965366	A	C	20	GENIC	homozygous	113592935
14	43968724	43968725	T	C	20	GENIC	homozygous	113592937
14	43968879	43968880	C	G	37	GENIC	homozygous	113443900
14	43969190	43969191	T	C	37	GENIC	homozygous	113443902
14	43971684	43971685	C	T	33	GENIC	homozygous	113443904
14	43972359	43972360	T	G	41	GENIC	homozygous	113443906
14	43973211	43973212	C	G	28	GENIC	homozygous	113443908
14	43974423	43974424	T	C	42	GENIC	homozygous	113443910
14	43975293	43975294	G	A	40	GENIC	homozygous	113443912
14	43975308	43975309	G	T	37	GENIC	possibly homozygous	113443914
14	43975618	43975619	C	T	42	GENIC	homozygous	113443916
14	43967131	43967132	A	T	31	GENIC	homozygous	118691485
14	43968185	43968186	A	G	20	GENIC	homozygous	118691487
14	43980375	43980376	A	G	40	GENIC	possibly homozygous	113443918
14	43980614	43980615	G	C	34	GENIC	homozygous	113443920
14	43981829	43981830	T	A	39	GENIC	homozygous	113443922
14	43983433	43983434	C	T	29	GENIC	homozygous	113443924
14	43984374	43984375	C	T	40	GENIC	homozygous	113443926
14	43984867	43984868	C	T	41	GENIC	homozygous	113443928
14	43987575	43987576	C	T	52	GENIC	possibly homozygous	113443930
14	43987653	43987654	A	G	49	GENIC	homozygous	113443932
14	43987744	43987745	C	T	65	GENIC	heterozygous	118691491
14	43991951	43991952	A	G	42	GENIC	homozygous	113443934
14	43992171	43992172	T	C	43	GENIC	homozygous	113443936