chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
10
40258441
40258442
G
19
GENIC
homozygous
128809837
10
40258595
40258596
G
A
19
GENIC
homozygous
116927514
10
40261770
40261770
G
4
GENIC
homozygous
128809838
10
40261913
40261916
AGA
11
GENIC
homozygous
128809840
10
40264857
40264858
T
C
27
GENIC
homozygous
116568903
10
40259135
40259136
G
A
16
GENIC
homozygous
117057569
10
40271009
40271010
G
C
25
GENIC
homozygous
116568911
10
40278647
40278648
C
T
16
GENIC
homozygous
116927516
10
40278649
40278650
C
16
GENIC
homozygous
128809842
10
40278651
40278652
C
16
GENIC
homozygous
128809843
10
40280808
40280809
A
G
21
GENIC
homozygous
116568921
10
40281377
40281378
C
T
30
GENIC
homozygous
116927518
10
40281934
40281935
C
A
29
GENIC
homozygous
116568925
10
40281971
40281971
CTGC
27
GENIC
homozygous
128809847
10
40283538
40283539
C
T
18
GENIC
homozygous
116927520
10
40284775
40284776
A
G
33
GENIC
homozygous
116568927
10
40286273
40286274
A
C
23
GENIC
homozygous
116927522
10
40288651
40288652
T
C
24
GENIC
homozygous
116764200
10
40289598
40289599
G
A
28
GENIC
possibly homozygous
116927526
10
40289974
40289975
G
A
30
GENIC
homozygous
116927528
10
40290288
40290289
T
A
23
GENIC
homozygous
116764206
10
40291912
40291913
C
T
30
GENIC
homozygous
116764210
10
40292690
40292718
CCCATGCCTGGGATCTTTGGGGGGCTTA
13
GENIC
homozygous
132691058
10
40293042
40293043
G
A
27
GENIC
homozygous
116927530
10
40295113
40295113
G
13
GENIC
homozygous
132691059
10
40296115
40296116
A
G
25
GENIC
homozygous
116568933
10
40296474
40296475
C
G
35
GENIC
homozygous
116927532
10
40296928
40296929
A
G
21
GENIC
homozygous
116568943
10
40298427
40298428
G
A
26
GENIC
homozygous
116568949
10
40299353
40299354
C
T
16
GENIC
homozygous
116927534
10
40300024
40300025
T
C
19
GENIC
homozygous
116764212
10
40300027
40300028
A
T
19
GENIC
homozygous
116764214
10
40301683
40301684
C
A
20
GENIC
homozygous
116927536
10
40295080
40295081
C
A
9
GENIC
homozygous
116977344
