chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	9234790	9234790		T	20	GENIC	homozygous	130949913
5	9237938	9237938		AC	9	GENIC	homozygous	130949914
5	9238377	9238378	T	G	37	GENIC	heterozygous	119051035
5	9238378	9238379	A	T	37	GENIC	heterozygous	113640771
5	9241298	9241299	G	T	31	GENIC	homozygous	114170569
5	9243120	9243120		T	18	GENIC	homozygous	128149043
5	9243692	9243693	G	A	21	GENIC	homozygous	114170570
5	9244154	9244155	A		19	GENIC	possibly homozygous	128149044
5	9244301	9244301		CAATCTTTATCA	20	GENIC	homozygous	130949915
5	9244808	9244809	G		8	GENIC	homozygous	130949916
5	9244821	9244825	TTTA		8	GENIC	heterozygous	130949917
5	9245009	9245010	T		18	GENIC	homozygous	128149045
5	9245013	9245014	T	A	18	GENIC	homozygous	118941821
5	9245787	9245787		T	9	GENIC	heterozygous	130949918
5	9245813	9245814	C	T	15	GENIC	homozygous	114170571
5	9245931	9245932	C	T	23	GENIC	homozygous	114170572
5	9246653	9246655	TG		22	GENIC	heterozygous	131377557
5	9250246	9250247	A		20	GENIC	homozygous	130949919
5	9251220	9251221	T		17	GENIC	homozygous	128149046
5	9253133	9253133		TT	22	GENIC	homozygous	130949920
5	9253788	9253789	G	A	20	GENIC	homozygous	113640779
5	9255998	9255999	C	G	4	GENIC	homozygous	114170573
5	9256009	9256010	G	T	5	GENIC	homozygous	113640781
5	9256012	9256013	T	C	5	GENIC	homozygous	113640783
5	9256512	9256512		T	19	GENIC	homozygous	128149047