chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	148434636	148434637	C	T	17	GENIC	homozygous	114153735
5	148435112	148435113	C	A	16	GENIC	homozygous	114153736
5	148439173	148439174	C	T	10	GENIC	homozygous	114049269
5	148439189	148439190	C	T	7	GENIC	homozygous	114153737
5	148439641	148439642	C	G	17	GENIC	homozygous	114049283
5	148439654	148439655	G	A	15	GENIC	homozygous	114049284
5	148440589	148440590	T	C	13	GENIC	homozygous	114049288
5	148440663	148440664	G	A	17	GENIC	possibly homozygous	114153738
5	148441218	148441219	T	C	17	GENIC	homozygous	114049290
5	148441249	148441250	A	G	22	GENIC	homozygous	114153739
5	148441714	148441715	G	A	11	GENIC	homozygous	114153740
5	148441847	148441848	C	T	24	GENIC	homozygous	114153741
5	148442183	148442184	T	C	22	GENIC	homozygous	114153742
5	148442812	148442813	A	G	16	GENIC	homozygous	114049292
5	148442951	148442952	A	G	9	GENIC	homozygous	114049294
5	148443134	148443135	C	T	13	GENIC	homozygous	114049296
5	148443683	148443684	G	A	9	GENIC	homozygous	114153743
5	148443720	148443721	A	C	10	GENIC	homozygous	114153744
5	148443899	148443900	C	T	16	GENIC	homozygous	114153745
5	148443983	148443984	T	C	15	GENIC	homozygous	114153746
5	148444051	148444052	C	T	18	GENIC	homozygous	114153747
5	148440914	148440914		CC	11	GENIC	homozygous	128255082
5	148442407	148442408	T		15	GENIC	homozygous	132079859
5	148443452	148443454	TC		14	GENIC	homozygous	132079860