chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
8
37307810
37307811
C
T
57
GENIC
homozygous
142063886
8
37308280
37308281
G
C
54
GENIC
homozygous
142063887
8
37308419
37308420
T
C
59
GENIC
homozygous
142063888
8
37308432
37308433
C
T
59
GENIC
homozygous
142063889
8
37308964
37308965
T
C
58
GENIC
homozygous
142063890
8
37309367
37309376
AGACCTTTC
53
GENIC
homozygous
142022411
8
37310705
37310706
C
T
52
GENIC
homozygous
142063891
8
37311465
37311561
AGTATAAACATTTTTTTTTTCTTTTCTTTTTTTCGGAGCTGGGGACTGAACCCAGGGCCTTGCGCTTCCTAGGTAAGCGCTCTACCACTGAGCTAA
34
GENIC
homozygous
142022412
8
37312982
37313009
ATATGGCCCTTAAATGAAATGACTGAA
38
GENIC
homozygous
142022413
8
37313543
37313563
TATGTATGTATGTATGTATA
44
GENIC
heterozygous
145213234
8
37314858
37314859
A
G
73
GENIC
homozygous
142063892
8
37315952
37315953
A
C
63
GENIC
homozygous
142063893
8
37316792
37316794
AC
39
GENIC
homozygous
142022414
8
37316830
37316831
G
A
43
GENIC
homozygous
142063894
8
37317038
37317039
T
41
GENIC
possibly homozygous
142022415
8
37317086
37317087
A
G
55
GENIC
possibly homozygous
142063895
8
37317190
37317193
TTT
37
GENIC
homozygous
142022416
8
37317297
37317298
C
T
32
GENIC
homozygous
142063896
8
37317301
37317302
C
T
36
GENIC
homozygous
142063897
8
37317975
37317976
C
T
58
GENIC
homozygous
142063898
8
37318176
37318177
T
A
57
GENIC
homozygous
142063899
