chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	44008955	44008956	T	A	46	GENIC	homozygous	115479374
12	44010252	44010253	A	T	30	GENIC	homozygous	115479376
12	44010315	44010318	CGT		30	GENIC	homozygous	133254984
12	44010405	44010406	G	A	34	GENIC	homozygous	115479378
12	44011190	44011191	T	G	32	GENIC	possibly homozygous	115390198
12	44014265	44014266	G	A	24	GENIC	homozygous	126245805
12	44014659	44014663	GGAT		32	GENIC	homozygous	133254986
12	44015301	44015302	T	C	35	GENIC	homozygous	126245807
12	44015731	44015732	G	A	50	GENIC	homozygous	115479382
12	44016186	44016187	A	T	37	GENIC	homozygous	115390200
12	44016227	44016228	G	A	42	GENIC	homozygous	115479384
12	44016306	44016307	A	G	52	GENIC	homozygous	115479386
12	44016438	44016439	G	T	44	GENIC	homozygous	126245808
12	44016887	44016888	A	G	23	GENIC	homozygous	115390202
12	44017080	44017081	C	A	49	GENIC	homozygous	115390204
12	44017186	44017187	A	G	43	GENIC	homozygous	115479388
12	44017455	44017456	A	T	46	GENIC	homozygous	115479390
12	44018559	44018563	AATC		22	GENIC	homozygous	133254987
12	44019153	44019154	C	T	40	GENIC	homozygous	115479392
12	44019879	44019880	C	T	48	GENIC	homozygous	115479394
12	44019964	44019965	T	A	54	GENIC	homozygous	115479396
12	44020780	44020781	T	C	29	GENIC	homozygous	115479398
12	44020947	44020948	A	G	22	GENIC	homozygous	115390208
12	44021179	44021179		GTG	35	GENIC	possibly homozygous	133254988
12	44021630	44021631	G	A	28	GENIC	homozygous	115390210
12	44011676	44011677	T	C	48	GENIC	homozygous	115336608
12	44012288	44012289	A	G	31	GENIC	homozygous	115336610
12	44022382	44022383	A	T	41	GENIC	homozygous	115390212
12	44022390	44022391	A		41	GENIC	homozygous	131119315
12	44022645	44022661	ATACATACATATGTAC		29	GENIC	homozygous	133254989
12	44022700	44022701	G	A	36	GENIC	homozygous	115479400
12	44029184	44029185	T	C	13	GENIC	homozygous	115336614
12	44029184	44029184		GGGCA	12	GENIC	homozygous	128993923
12	44022487	44022490	GCG		34	GENIC	homozygous	128993922