chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	10280298	10280299	C	T	35	GENIC	homozygous	141598934
4	10282830	10282831	T	A	32	GENIC	possibly homozygous	141598935
4	10285480	10285481	C	T	24	GENIC	homozygous	141598936
4	10285684	10285685	A	G	26	GENIC	homozygous	141598937
4	10286187	10286188	T	C	22	GENIC	homozygous	141598938
4	10286781	10286782	A	C	18	GENIC	homozygous	141598939
4	10287672	10287673	C	T	34	GENIC	homozygous	141598940
4	10290498	10290499	C	T	23	GENIC	homozygous	141598941
4	10291909	10291910	C	T	21	GENIC	homozygous	141598942
4	10298767	10298768	A	G	17	GENIC	homozygous	141598943
4	10299397	10299398	C	T	22	GENIC	homozygous	141598944
4	10299528	10299529	A	C	36	GENIC	homozygous	141598945
4	10299529	10299530	C	T	36	GENIC	homozygous	141598946
4	10306564	10306565	G	A	25	GENIC	homozygous	141598947
4	10308187	10308188	G	A	16	GENIC	homozygous	141598948
4	10309175	10309175		G	21	GENIC	homozygous	141574765
4	10283570	10283571	T	C	23	GENIC	homozygous	136969701
4	10295400	10295401	T	C	22	GENIC	homozygous	136969702
4	10296060	10296061	T		14	GENIC	possibly homozygous	136866363
4	10297877	10297878	T		14	GENIC	homozygous	143045100
4	10297986	10297991	TTTTC		8	GENIC	homozygous	143045101
4	10298391	10298391		T	14	GENIC	possibly homozygous	141574761
4	10301489	10301489		T	14	GENIC	homozygous	141574762
4	10301505	10301506	T		12	GENIC	homozygous	141574763
4	10302183	10302185	TA		15	GENIC	homozygous	141574764
4	10309724	10309724		GTCTTACGT	19	GENIC	homozygous	141574766
4	10312387	10312387		TC	17	GENIC	homozygous	141574767
4	10313781	10313782	T	G	18	GENIC	homozygous	141598949
4	10314161	10314162	G	A	24	GENIC	homozygous	141598950
4	10317169	10317170	C	G	19	GENIC	homozygous	141598951
4	10318976	10318977	C	T	13	GENIC	homozygous	141598952
4	10319332	10319332		AGTC	18	GENIC	homozygous	141574768
4	10319397	10319398	G	T	21	GENIC	homozygous	141598953
4	10319524	10319525	C	T	16	GENIC	homozygous	141598954