chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	115466775	115466776	T	C	24	GENIC	homozygous	112815658
4	115467688	115467689	T	C	23	GENIC	homozygous	112815660
4	115468457	115468458	C	T	30	GENIC	homozygous	112815662
4	115469206	115469207	A	G	28	GENIC	homozygous	119527312
4	115469911	115469912	T	G	20	GENIC	homozygous	119406518
4	115470182	115470183	C	T	26	GENIC	homozygous	112815668
4	115470313	115470314	A	G	31	GENIC	homozygous	112815670
4	115470420	115470421	T	C	33	GENIC	homozygous	112815672
4	115470489	115470490	A	G	30	GENIC	homozygous	112815674
4	115470523	115470524	C	T	38	GENIC	homozygous	112815676
4	115470542	115470543	T	A	37	GENIC	homozygous	112815678
4	115470849	115470850	T	G	24	GENIC	homozygous	112815680
4	115471144	115471145	A	G	40	GENIC	homozygous	112815682
4	115471502	115471503	T	C	27	GENIC	homozygous	112815684
4	115471507	115471508	C	T	29	GENIC	homozygous	119527314
4	115471569	115471570	A	G	27	GENIC	homozygous	112815686
4	115471628	115471629	C	T	24	GENIC	homozygous	112815690
4	115471693	115471694	A	G	20	GENIC	homozygous	112815692
4	115471791	115471792	T	A	24	GENIC	homozygous	112815694
4	115471964	115471965	A	T	29	GENIC	homozygous	112815696
4	115472156	115472157	C	T	29	GENIC	possibly homozygous	112815698
4	115472532	115472533	A	C	45	GENIC	homozygous	112815702