chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
11
3339171
3339172
T
C
16
GENIC
homozygous
144886913
11
3339732
3339733
C
T
25
GENIC
homozygous
144886914
11
3339768
3339769
T
C
23
GENIC
homozygous
144886915
11
3340393
3340394
A
C
20
GENIC
homozygous
144886916
11
3340620
3340660
AGAGCAAGAATGTGATGCAGTGCTCTAGAAGTAAGCTTCT
12
GENIC
homozygous
144877413
11
3341275
3341276
C
T
13
GENIC
homozygous
144886917
11
3341688
3341689
T
C
11
GENIC
homozygous
144886918
11
3341800
3341801
C
T
13
GENIC
homozygous
144886919
11
3341897
3341897
TA
12
GENIC
homozygous
144877414
11
3342232
3342233
G
T
21
GENIC
homozygous
144886920
11
3343603
3343604
G
C
16
GENIC
homozygous
144886921
11
3343888
3343889
A
15
GENIC
homozygous
144877415
11
3345584
3345585
G
A
19
GENIC
homozygous
144886922
11
3346863
3346864
C
T
18
GENIC
homozygous
144886923
11
3347231
3347232
G
A
20
GENIC
homozygous
144886924
11
3347986
3347987
A
16
GENIC
homozygous
144877416
11
3348514
3348515
C
G
20
GENIC
homozygous
144886925
11
3348547
3348548
C
T
20
GENIC
homozygous
144886926
11
3348638
3348639
A
G
14
GENIC
homozygous
144886927
11
3349629
3349630
T
G
20
GENIC
possibly homozygous
144886928
11
3352903
3352904
T
C
20
GENIC
homozygous
144886929
11
3353710
3353711
G
C
17
GENIC
homozygous
144886930
11
3353821
3353822
G
A
7
GENIC
possibly homozygous
138901870
11
3356232
3356232
ACT
11
GENIC
homozygous
144877418
11
3357443
3357444
G
T
16
GENIC
homozygous
144886931
11
3358425
3358426
G
A
19
GENIC
homozygous
144886932
11
3359137
3359158
AGAAGAAGAAGAAGAAGAAGC
17
GENIC
possibly homozygous
144877420
11
3363458
3363459
G
C
17
GENIC
homozygous
144886934
11
3348714
3348715
C
A
17
GENIC
homozygous
403297894
