chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	155093955	155093956	A	C	12	GENIC	homozygous	113246602
4	155094026	155094027	C	G	18	GENIC	homozygous	113246603
4	155095139	155095140	C	T	14	GENIC	homozygous	113246604
4	155095214	155095215	T	C	19	GENIC	homozygous	113246605
4	155096621	155096622	C	T	24	GENIC	homozygous	113246606
4	155097042	155097043	T	G	28	GENIC	homozygous	113246607
4	155099029	155099030	C	T	7	GENIC	homozygous	112894461
4	155100131	155100132	G	A	18	GENIC	homozygous	113246610
4	155100416	155100417	C	T	12	GENIC	homozygous	113246611
4	155100488	155100489	T	G	7	GENIC	homozygous	113246612
4	155100742	155100743	G	A	14	GENIC	homozygous	112894465
4	155101275	155101276	A	G	32	GENIC	homozygous	113246614
4	155101319	155101320	G	C	31	GENIC	homozygous	113246615
4	155102745	155102746	A	G	27	GENIC	homozygous	112894467
4	155103801	155103802	A	G	4	GENIC	homozygous	119370374
4	155103803	155103804	A	G	4	GENIC	homozygous	119370375
4	155103805	155103806	A	G	3	GENIC	homozygous	119370376
4	155103898	155103899	C	A	6	GENIC	homozygous	113246617
4	155104812	155104813	G	A	33	GENIC	homozygous	113246618
4	155105445	155105446	T	C	34	GENIC	homozygous	113246619
4	155106010	155106011	G	A	23	GENIC	homozygous	113246620
4	155106301	155106302	T	C	17	GENIC	homozygous	113246621
4	155106499	155106500	A	G	23	GENIC	homozygous	113246622
4	155108707	155108708	T	C	22	GENIC	homozygous	113246627
4	155110445	155110446	T	C	23	GENIC	homozygous	113246628
4	155110563	155110564	T	G	30	GENIC	homozygous	112894483
4	155111469	155111470	T	A	16	GENIC	homozygous	113246632
4	155110767	155110768	A	G	19	GENIC	homozygous	113246629
4	155110893	155110894	T	C	36	GENIC	homozygous	113246630
4	155110940	155110941	G	A	34	GENIC	homozygous	113246631