chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	31081563	31081564	C	G	11	GENIC	homozygous	114818878
13	31081937	31081938	C	A	18	GENIC	homozygous	114309695
13	31084417	31084418	A	G	19	GENIC	homozygous	114818880
13	31089507	31089508	T	C	7	GENIC	homozygous	114818882
13	31093057	31093058	C	T	14	GENIC	homozygous	114522202
13	31093072	31093073	A	T	14	GENIC	homozygous	114522205
13	31098721	31098722	A	G	21	GENIC	homozygous	114309700
13	31099014	31099015	T	C	14	GENIC	homozygous	114818884
13	31100805	31100806	A	G	12	GENIC	homozygous	114309701
13	31105271	31105272	A	C	13	GENIC	homozygous	114309702
13	31108689	31108690	G	T	13	GENIC	homozygous	114818886
13	31109079	31109080	C	A	16	GENIC	homozygous	114309703
13	31113143	31113144	C	A	26	GENIC	homozygous	114309704
13	31114175	31114176	C	G	31	GENIC	homozygous	114818888
13	31114552	31114553	C	T	27	GENIC	homozygous	114818890
13	31127659	31127660	C	A	23	GENIC	homozygous	114818892
13	31132206	31132207	T	A	15	GENIC	homozygous	114818894
13	31140136	31140137	A	T	19	GENIC	homozygous	114818896
13	31140986	31140987	G	A	10	GENIC	homozygous	114309736
13	31178142	31178143	G	T	11	GENIC	heterozygous	114818898