chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	124006400	124006401	C	T	11	GENIC	homozygous	134539644
4	124006473	124006474	T	C	12	GENIC	homozygous	113380660
4	124006486	124006486		T	13	GENIC	homozygous	131361932
4	124010841	124010842	C	T	29	GENIC	homozygous	134539645
4	124010907	124010908	T		29	GENIC	possibly homozygous	133730386
4	124012891	124012892	T	G	23	GENIC	homozygous	113380668
4	124013217	124013218	C	T	22	GENIC	homozygous	113380670
4	124014205	124014206	A	C	24	GENIC	homozygous	113380672
4	124016845	124016846	A	G	27	GENIC	homozygous	119407869
4	124016680	124016681	G	C	20	GENIC	homozygous	119407868
4	124007262	124007262		A	25	GENIC	homozygous	134530996
4	124016086	124016087	C		18	GENIC	homozygous	134530997
4	124017064	124017069	TTTCG		19	GENIC	homozygous	131361933
4	124017969	124017970	G	A	32	GENIC	homozygous	113380674
4	124018839	124018840	T	C	29	GENIC	homozygous	119407872
4	124020155	124020155		A	17	GENIC	homozygous	131361934
4	124020473	124020474	T	A	30	GENIC	homozygous	119407873
4	124020815	124020816	A	T	21	GENIC	homozygous	113380678
4	124020886	124020886		GCTAGCTGATGGCTAGCACTAGCTGATTCCAGGTGGCATTG	22	GENIC	homozygous	131361935
4	124021917	124021918	T	C	29	GENIC	homozygous	119407874
4	124022611	124022612	C	T	35	GENIC	homozygous	119407875
4	124023106	124023107	C	T	24	GENIC	homozygous	119407876
4	124023420	124023421	T	C	14	GENIC	homozygous	113380680
4	124023601	124023602	A	G	21	GENIC	homozygous	113380682
4	124028109	124028110	A		20	GENIC	homozygous	131361937
4	124028126	124028126		AA	22	GENIC	homozygous	134530998
4	124028740	124028741	T	A	33	GENIC	homozygous	134539646
4	124029281	124029282	C	T	23	GENIC	homozygous	119407878
4	124029491	124029491		G	19	GENIC	homozygous	134530999