chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
7
108392673
108392674
G
A
56
GENIC
homozygous
138177771
7
108393849
108393850
G
T
52
GENIC
possibly homozygous
138177772
7
108394343
108394344
T
22
GENIC
homozygous
137973323
7
108394478
108394479
G
A
41
GENIC
homozygous
138177773
7
108394606
108394607
C
A
39
GENIC
homozygous
138177774
7
108394698
108394698
AAGAAACCCTGTCTTGGGGTTGGGGATTTAGCTCAGTGGCAGAGCGCTTGCCTAGGAAGAGCAAGGCCCTGGGTTCGGTCCCCAGCTCCGAAAAAAAGAACCAAAAAAAAAGAGA
17
GENIC
homozygous
137973324
7
108394826
108394827
T
C
54
GENIC
homozygous
138177775
7
108396342
108396343
T
C
29
GENIC
possibly homozygous
138177776
7
108397061
108397062
G
T
42
GENIC
homozygous
138177777
7
108400973
108400974
G
T
42
GENIC
possibly homozygous
138177778
7
108402938
108402939
A
T
50
GENIC
homozygous
138177779
7
108403544
108403545
C
T
46
GENIC
homozygous
138177780
7
108405289
108405290
T
C
39
GENIC
homozygous
138177781
7
108405467
108405468
G
A
43
GENIC
homozygous
138177782
7
108406022
108406023
A
T
50
GENIC
homozygous
138177783
7
108408800
108408801
C
T
56
GENIC
homozygous
138177784
7
108408885
108408886
A
G
57
GENIC
homozygous
138177785
7
108410072
108410073
G
A
68
GENIC
possibly homozygous
138177786
7
108410142
108410143
C
T
58
GENIC
homozygous
138177787
7
108410412
108410413
C
T
69
GENIC
possibly homozygous
138177788
7
108411088
108411089
C
A
41
GENIC
homozygous
138177789
7
108412104
108412105
G
A
55
GENIC
homozygous
138177790
7
108412404
108412405
T
C
52
GENIC
homozygous
138177791
7
108413095
108413096
G
A
40
GENIC
homozygous
138177792
7
108413366
108413367
A
G
51
GENIC
homozygous
138177793
