chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
18
69209001
69209002
T
TGCATGAGCCTCCCAACTCACAGACCGAGAGCATGATGGGATAAGTTGGTCCTAGC
47
GENIC
homozygous
46799836
18
69209165
69209166
A
G
27
GENIC
homozygous
46744837
18
69209191
69209192
G
A
27
GENIC
homozygous
46975805
18
69209553
69209554
G
-
33
GENIC
homozygous
46744838
18
69209557
69209558
C
-
34
GENIC
homozygous
46744839
18
69210934
69210936
GG
--
15
GENIC
homozygous
46744842
18
69211443
69211444
G
A
50
GENIC
homozygous
46744843
18
69211452
69211453
G
A
49
GENIC
homozygous
46744844
18
69211894
69211895
T
C
13
GENIC
homozygous
46799848
18
69212168
69212169
G
C
41
GENIC
homozygous
46918013
18
69212475
69212476
G
GTTTTGAGGCCCTGTAATGTGGAGGCCTGGAGTGCCAGGCACAGCATTGTTCTTTACCAATGGCCATTCT
46
GENIC
homozygous
46799850
18
69212663
69212664
T
C
53
GENIC
homozygous
46744845
18
69212701
69212702
G
T
62
GENIC
homozygous
46744846
18
69212735
69212736
T
C
78
GENIC
homozygous
46744847
18
69212849
69212850
T
C
58
GENIC
homozygous
46744848
18
69212905
69212906
A
C
64
GENIC
homozygous
46744849
18
69212966
69212967
G
A
66
GENIC
homozygous
46744850
18
69213963
69213964
G
T
36
GENIC
homozygous
46744851