chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
17	42087212	42087213	T	C	14	GENIC	homozygous	111049468
17	42088585	42088586	C	T	29	GENIC	homozygous	111528188
17	42088616	42088617	T	C	32	GENIC	homozygous	111049470
17	42088652	42088653	A	G	33	GENIC	homozygous	111203463
17	42089974	42089975	A	G	11	GENIC	homozygous	111049476
17	42090995	42090996	C	T	29	GENIC	homozygous	111049480
17	42091409	42091410	A	G	24	GENIC	homozygous	111203464
17	42094841	42094842	G	A	22	GENIC	homozygous	111203465
17	42097672	42097673	C	T	14	GENIC	homozygous	111528190
17	42098221	42098222	T	C	28	GENIC	homozygous	111049486
17	42098855	42098856	A	G	21	GENIC	homozygous	111049490
17	42099216	42099217	A	G	11	GENIC	homozygous	111203466
17	42100060	42100061	T	C	33	GENIC	homozygous	111049494
17	42100574	42100575	C	T	25	GENIC	homozygous	111528192
17	42102407	42102408	G	A	24	GENIC	homozygous	111203467
17	42105786	42105787	A	C	19	GENIC	homozygous	111049498
17	42105935	42105936	T	A	22	GENIC	homozygous	111049500
17	42106058	42106059	G	A	24	GENIC	homozygous	111528194
17	42106755	42106756	A	G	20	GENIC	homozygous	111049502
17	42108836	42108837	G	T	22	GENIC	homozygous	111528196
17	42109474	42109475	C	T	39	GENIC	homozygous	111203469
17	42110212	42110213	T	A	17	GENIC	homozygous	111528198
17	42112738	42112739	A	G	21	GENIC	homozygous	111049530
17	42114055	42114056	G	A	13	GENIC	homozygous	111049536
17	42115215	42115216	T	C	21	GENIC	homozygous	111049542
17	42115437	42115438	G	A	20	GENIC	homozygous	111528200
17	42117128	42117129	G	A	14	GENIC	homozygous	111528202
17	42117134	42117135	G	A	14	GENIC	homozygous	111049546
17	42118330	42118331	C	T	28	GENIC	homozygous	111049552
17	42118494	42118495	A	G	32	GENIC	homozygous	111049554
17	42128867	42128868	G	A	11	GENIC	homozygous	111528204