chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	67517397	67517398	C	CTTTT	11	GENIC	homozygous	46569417
19	67521177	67521179	AA	--	11	GENIC	heterozygous	46193998
19	67521178	67521179	A	-	11	GENIC	heterozygous	46447089
19	67522417	67522418	T	C	34	GENIC	homozygous	46193999
19	67524910	67524911	A	G	25	GENIC	homozygous	46194001
19	67526360	67526361	T	G	30	GENIC	possibly homozygous	46194002
19	67518884	67518885	T	-	25	GENIC	possibly homozygous	46216761
19	67520963	67520964	C	T	22	GENIC	homozygous	46496150
19	67525973	67525974	G	C	34	GENIC	homozygous	46801965
19	67527264	67527265	T	TGTG	3	GENIC	homozygous	46801967
19	67526575	67526576	A	AG	19	GENIC	possibly homozygous	46474997
19	67526578	67526583	CTACA	-----	22	GENIC	possibly homozygous	46474999
19	67526583	67526584	G	GCC	20	GENIC	possibly homozygous	46475001
19	67527276	67527277	G	GT	3	GENIC	homozygous	46447091
19	67527292	67527293	G	GTTT	11	GENIC	homozygous	46801969
19	67527347	67527348	T	G	24	GENIC	homozygous	46194011
19	67527820	67527821	T	C	26	GENIC	homozygous	46194012
19	67527872	67527873	T	TATCACTA	26	GENIC	homozygous	46801971
19	67527874	67527875	A	AGGTACGGAAAGGGCCTC	27	GENIC	homozygous	46801973
19	67528960	67528961	G	A	28	GENIC	possibly homozygous	46194015
19	67530551	67530552	C	T	22	GENIC	homozygous	46496152
19	67530562	67530563	C	T	20	GENIC	homozygous	46194016
19	67530642	67530643	T	C	27	GENIC	homozygous	46194017
19	67530994	67530995	T	C	28	GENIC	homozygous	46194018
19	67531370	67531371	A	G	27	GENIC	homozygous	46194019
19	67531493	67531494	G	A	24	GENIC	homozygous	46496154
19	67532167	67532168	T	C	32	GENIC	homozygous	46194020
19	67533697	67533698	C	T	31	GENIC	homozygous	46496156
19	67533828	67533829	T	G	36	GENIC	possibly homozygous	46496158
19	67534191	67534192	A	G	31	GENIC	homozygous	46194021
19	67536046	67536047	G	A	20	GENIC	homozygous	46801975
19	67537651	67537652	A	G	30	GENIC	homozygous	46496162
19	67541703	67541704	G	A	17	GENIC	homozygous	46801977