chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	100849916	100849917	C	T	5	GENIC	heterozygous	126522613
9	100849923	100849924	A	C	8	GENIC	heterozygous	117400470
9	100850066	100850067	G	A	23	GENIC	homozygous	120283414
9	100850507	100850508	A	G	18	GENIC	homozygous	117620189
9	100851661	100851662	C	T	13	GENIC	homozygous	120283416
9	100851797	100851798	G	A	8	GENIC	homozygous	126556287
9	100853680	100853681	G	A	21	GENIC	homozygous	120283417
9	100854250	100854251	A	T	9	GENIC	heterozygous	120364144
9	100854684	100854685	G	A	11	GENIC	homozygous	117764437
9	100857003	100857004	G	A	14	GENIC	homozygous	117620200
9	100858535	100858536	T	A	17	GENIC	homozygous	120283418
9	100860210	100860211	G	C	19	GENIC	homozygous	120283419
9	100861713	100861714	G	A	21	GENIC	homozygous	120283420
9	100875115	100875116	C	T	21	GENIC	homozygous	117620224
9	100875529	100875530	A	C	11	GENIC	homozygous	117620226
9	100876814	100876815	A	C	8	GENIC	homozygous	120283422
9	100876818	100876819	A	C	8	GENIC	homozygous	117620228
9	100878674	100878675	C	T	16	GENIC	homozygous	117620230
9	100879200	100879201	T	A	27	GENIC	homozygous	117620232
9	100880142	100880143	A	C	10	GENIC	homozygous	126556288
9	100884477	100884478	G	A	8	GENIC	homozygous	117620236
9	100885091	100885092	T	C	11	GENIC	homozygous	117620238
9	100885551	100885552	G	T	22	GENIC	heterozygous	117400502
9	100885856	100885857	C	T	12	GENIC	homozygous	120283423
9	100886289	100886290	A	G	16	GENIC	homozygous	117620240
9	100886740	100886741	A	G	9	GENIC	heterozygous	126556289
9	100886741	100886742	A	G	8	GENIC	heterozygous	117794998
9	100887509	100887510	A	G	4	GENIC	homozygous	117620242