chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
20
44092228
44092229
G
A
19
GENIC
homozygous
142738656
20
44092247
44092248
T
C
18
GENIC
homozygous
130114527
20
44092266
44092267
T
C
18
GENIC
homozygous
130114530
20
44096380
44096381
A
G
20
GENIC
homozygous
142738657
20
44096547
44096548
C
A
13
GENIC
homozygous
142738658
20
44096894
44096895
C
A
13
GENIC
homozygous
142738659
20
44097121
44097122
T
C
12
GENIC
homozygous
142738660
20
44097546
44097547
C
T
12
GENIC
homozygous
142738661
20
44097551
44097552
C
A
13
GENIC
homozygous
142738662
20
44098316
44098317
C
T
5
GENIC
homozygous
142738663
20
44101240
44101241
A
G
28
GENIC
homozygous
130114583
20
44101587
44101588
C
G
18
GENIC
possibly homozygous
142738664
20
44102758
44102759
T
C
16
GENIC
homozygous
142738665
20
44102955
44102956
A
G
19
GENIC
homozygous
142738666
20
44103184
44103185
C
T
14
GENIC
homozygous
142738667
20
44103225
44103226
T
C
14
GENIC
homozygous
130114593
20
44098291
44098291
TC
5
GENIC
homozygous
142715528
20
44099660
44099660
CAAGTTTAGTTACTGAACCATACTGAAG
13
GENIC
homozygous
130000657
20
44098297
44098297
TCTCTT
5
GENIC
homozygous
142715529
20
44103298
44103299
A
15
GENIC
homozygous
142715530
20
44099598
44099599
T
6
GENIC
homozygous
145086400
20
44099600
44099613
TCTCTCTCTCTCT
6
GENIC
homozygous
145086401
20
44103368
44103369
T
G
20
GENIC
homozygous
142738668
20
44103509
44103510
C
T
22
GENIC
homozygous
142738669
20
44103755
44103756
A
G
18
GENIC
homozygous
130114599
20
44106018
44106019
T
C
32
GENIC
homozygous
130114606
20
44106636
44106637
A
G
15
GENIC
homozygous
142738670
20
44107058
44107059
A
T
22
GENIC
homozygous
142738671
20
44107068
44107069
C
T
18
GENIC
homozygous
142738672
20
44107352
44107353
C
A
23
GENIC
homozygous
142738673
20
44107478
44107479
T
A
20
GENIC
homozygous
142738674
20
44108235
44108236
A
G
11
GENIC
homozygous
142738675
20
44109084
44109085
T
G
9
GENIC
homozygous
142738676
20
44109081
44109081
A
11
GENIC
homozygous
142715531