chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	211028460	211028463	TTT	---	8	GENIC	possibly homozygous	57072888
4	211028536	211028537	G	GCA	20	GENIC	heterozygous	58303054
4	211028783	211028784	C	T	28	GENIC	homozygous	57072889
4	211029158	211029159	A	G	19	GENIC	homozygous	57072890
4	211029667	211029668	T	C	1	GENIC	homozygous	57072891
4	211030102	211030105	CCT	---	7	GENIC	heterozygous	57072892
4	211030133	211030134	A	G	13	GENIC	homozygous	57072895
4	211030470	211030471	C	T	24	GENIC	homozygous	57072896
4	211030592	211030593	A	C	16	GENIC	possibly homozygous	57072897
4	211030713	211030714	T	C	15	GENIC	homozygous	57072898
4	211030828	211030829	G	A	27	GENIC	homozygous	57072899
4	211031021	211031022	C	T	22	GENIC	possibly homozygous	57072900
4	211031835	211031836	T	C	24	GENIC	possibly homozygous	57072901
4	211032008	211032009	T	C	20	GENIC	possibly homozygous	57072902
4	211032962	211032963	G	-	22	GENIC	possibly homozygous	57072904
4	211033219	211033220	T	C	17	GENIC	heterozygous	57072905
4	211033354	211033355	A	G	22	GENIC	possibly homozygous	57072906
4	211033533	211033534	A	-	17	GENIC	homozygous	57072907
4	211033567	211033568	A	G	18	GENIC	homozygous	57072908
4	211034446	211034447	C	G	15	GENIC	homozygous	57072909
4	211034932	211034936	AAGA	----	10	GENIC	possibly homozygous	57072910
4	211035531	211035532	C	T	15	GENIC	possibly homozygous	57072911
4	211036619	211036620	A	G	11	GENIC	homozygous	57072913
4	211037591	211037592	T	C	7	GENIC	homozygous	57072915
4	211037751	211037752	C	A	20	GENIC	homozygous	57072916
4	211038677	211038678	G	A	7	GENIC	homozygous	57072917
4	211039802	211039803	T	C	20	GENIC	homozygous	57072918