chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	44150891	44150892	C	T	23	GENIC	homozygous	112118384
3	44150904	44150905	A	T	22	GENIC	homozygous	111552170
3	44151166	44151167	A	T	27	GENIC	homozygous	111552171
3	44151715	44151716	A	T	16	GENIC	homozygous	111552172
3	44152119	44152120	T	C	25	GENIC	homozygous	111552173
3	44152254	44152255	T	A	28	GENIC	homozygous	111552174
3	44152439	44152440	T	C	39	GENIC	homozygous	112118385
3	44152632	44152633	T	C	31	GENIC	homozygous	111552175
3	44154269	44154270	A	G	22	GENIC	homozygous	111552179
3	44154306	44154307	A	G	17	GENIC	homozygous	111552180
3	44154376	44154377	C	T	23	GENIC	homozygous	111552181
3	44154618	44154619	C	T	20	GENIC	homozygous	111552182
3	44154926	44154927	G	A	47	GENIC	homozygous	111552184
3	44155344	44155345	T	C	9	GENIC	homozygous	111552186
3	44156101	44156102	T	G	22	GENIC	homozygous	111552190
3	44157145	44157146	A	G	46	GENIC	homozygous	112118386
3	44157881	44157882	T	C	18	GENIC	homozygous	112118387
3	44157994	44157995	A	G	27	GENIC	homozygous	111552193
3	44158462	44158463	T	C	23	GENIC	homozygous	112118388
3	44158503	44158504	T	C	21	GENIC	homozygous	111552194
3	44158666	44158667	C	T	26	GENIC	homozygous	111552195
3	44159058	44159059	A	G	46	GENIC	homozygous	111552196
3	44159109	44159110	A	G	41	GENIC	homozygous	112118389
3	44159182	44159183	G	A	32	GENIC	homozygous	112118390
3	44160575	44160576	T	C	28	GENIC	homozygous	111552200
3	44161165	44161166	T	C	18	GENIC	homozygous	111552201
3	44162618	44162619	G	T	34	GENIC	homozygous	112118391
3	44182329	44182330	A	G	33	GENIC	homozygous	112379993