chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
13
101019184
101019185
G
A
31
GENIC
possibly homozygous
50266963
13
101019189
101019190
G
T
31
GENIC
possibly homozygous
50266964
13
101019474
101019475
T
TACATGCACATGCACACACATGCACATGCACAC
15
GENIC
homozygous
50586629
13
101019516
101019517
C
T
34
GENIC
homozygous
50266965
13
101023763
101023764
A
G
23
GENIC
homozygous
50266970
13
101024704
101024706
AC
--
30
GENIC
homozygous
50586630
13
101025844
101025845
T
TACATACAG
19
GENIC
homozygous
50586631
13
101026227
101026228
C
A
25
GENIC
homozygous
50586632
13
101026608
101026609
C
A
20
GENIC
possibly homozygous
50586633
13
101027840
101027841
A
AACACTC
26
GENIC
homozygous
50586634
13
101028261
101028262
G
A
37
GENIC
possibly homozygous
50586635
13
101028459
101028460
C
T
33
GENIC
possibly homozygous
50586636
13
101029439
101029440
C
CA
26
GENIC
homozygous
50586637
13
101030019
101030020
G
A
23
GENIC
possibly homozygous
50586638
13
101030033
101030034
C
T
22
GENIC
homozygous
50266983
13
101030210
101030211
T
A
29
GENIC
possibly homozygous
50586639
13
101030337
101030338
T
C
36
GENIC
possibly homozygous
50266984
13
101030635
101030636
C
CAG
11
GENIC
heterozygous
50586640
13
101031400
101031401
A
G
16
GENIC
possibly homozygous
50266985
13
101031586
101031587
C
T
21
GENIC
possibly homozygous
50586641
13
101032080
101032081
A
C
30
GENIC
possibly homozygous
50586642
13
101032812
101032813
G
A
38
GENIC
possibly homozygous
50586643
13
101033176
101033177
T
TC
2
GENIC
heterozygous
50586644
13
101033230
101033231
C
G
2
GENIC
heterozygous
50586645
13
101034200
101034201
T
C
10
GENIC
homozygous
50586651
13
101034755
101034756
T
C
23
GENIC
homozygous
50266986
13
101034892
101034893
A
G
25
GENIC
homozygous
50586652
13
101035105
101035106
G
GT
25
GENIC
homozygous
49867472
13
101035062
101035063
G
GA
22
GENIC
homozygous
49867470
13
101035091
101035092
A
G
28
GENIC
homozygous
49867471
13
101035095
101035096
C
A
28
GENIC
homozygous
50498664
13
101035096
101035097
A
G
28
GENIC
homozygous
50498665
13
101035108
101035109
A
G
24
GENIC
homozygous
49867473
13
101035111
101035112
C
A
21
GENIC
homozygous
49867474
13
101035474
101035475
C
A
21
GENIC
possibly homozygous
50586653
13
101036360
101036372
CACCATCACCAC
------------
13
GENIC
possibly homozygous
50586654
13
101036452
101036453
C
T
26
GENIC
homozygous
50586655
13
101037323
101037324
T
-
27
GENIC
possibly homozygous
50266991
13
101037729
101037730
T
TC
25
GENIC
possibly homozygous
50266992
13
101037741
101037758
GCATGCATGCATCCATC
-----------------
19
GENIC
possibly homozygous
50586656
13
101038462
101038463
T
G
26
GENIC
homozygous
50586657
13
101038503
101038504
G
A
28
GENIC
homozygous
50266997
13
101038986
101038987
C
T
28
GENIC
homozygous
50586661
13
101038678
101038679
C
T
28
GENIC
possibly homozygous
50586658
13
101038718
101038719
A
ACTG
7
GENIC
homozygous
50267000
13
101038764
101038765
C
G
18
GENIC
possibly homozygous
50586659
13
101038949
101038950
C
A
30
GENIC
homozygous
50586660
13
101036714
101036715
T
TA
18
GENIC
possibly homozygous
49974001
13
101039167
101039168
G
A
18
GENIC
possibly homozygous
50586662
13
101039174
101039175
A
AT
20
GENIC
possibly homozygous
50586663
