chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	12117918	12117919	G	A	15	GENIC	homozygous	109095690
20	12118109	12118110	G	A	23	GENIC	homozygous	109095692
20	12118625	12118626	G	A	38	GENIC	homozygous	109095694
20	12119311	12119312	T	C	20	GENIC	homozygous	109095696
20	12119329	12119330	C	T	21	GENIC	homozygous	109095698
20	12120088	12120089	G	T	24	GENIC	homozygous	109095700
20	12120316	12120317	A	G	32	GENIC	homozygous	109095702
20	12120319	12120320	G	T	34	GENIC	homozygous	109095704
20	12121920	12121921	A	G	29	GENIC	homozygous	109095706
20	12122318	12122319	A	G	23	GENIC	homozygous	109095708
20	12123008	12123009	A	G	22	GENIC	homozygous	109095710
20	12123427	12123428	G	A	29	GENIC	homozygous	109095712
20	12123944	12123945	T	A	25	GENIC	homozygous	109095714
20	12123996	12123997	A	G	27	GENIC	homozygous	109095716
20	12124267	12124268	A	G	25	GENIC	homozygous	109095718
20	12124470	12124471	A	C	17	GENIC	homozygous	109095720
20	12124487	12124488	T	C	18	GENIC	homozygous	109095722
20	12125147	12125148	A	G	23	GENIC	homozygous	109095724
20	12125194	12125195	G	C	36	GENIC	homozygous	109095726
20	12125317	12125318	C	A	23	GENIC	homozygous	109095728
20	12125525	12125526	A	T	35	GENIC	homozygous	109095730
20	12125590	12125591	A	G	35	GENIC	homozygous	109095732
20	12126132	12126133	T	C	35	GENIC	homozygous	109095734
20	12126189	12126190	A	G	24	GENIC	homozygous	109095736
20	12126259	12126260	A	G	40	GENIC	homozygous	109095738
20	12128208	12128209	T	C	32	GENIC	homozygous	109095746