chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
8
50487088
50487089
T
TTGA
5
GENIC
homozygous
52625841
8
50487119
50487120
C
-
8
GENIC
homozygous
52625843
8
50487322
50487323
T
G
18
GENIC
homozygous
52625845
8
50503687
50503688
A
C
4
GENIC
homozygous
52625853
8
50504387
50504388
C
CA
6
GENIC
homozygous
52625867
8
50504394
50504395
C
A
4
GENIC
homozygous
52625869
8
50504397
50504398
G
T
3
GENIC
homozygous
52625871
8
50504405
50504406
G
T
1
GENIC
homozygous
52625873
8
50504411
50504412
C
-
1
GENIC
homozygous
52625875
8
50504521
50504522
G
T
1
GENIC
homozygous
52625919
8
50504532
50504533
C
G
2
GENIC
heterozygous
53385994
8
50504533
50504534
G
T
2
GENIC
heterozygous
53385995
8
50504538
50504539
A
-
3
GENIC
heterozygous
52625921
8
50512470
50512471
C
-
2
GENIC
homozygous
52625923
8
50523584
50523585
T
TG
2
GENIC
heterozygous
52625943
8
50526172
50526173
C
CAT
3
GENIC
homozygous
52625945
8
50526178
50526179
T
C
4
GENIC
homozygous
52625947
8
50526553
50526554
T
TTG
12
GENIC
homozygous
52625949
8
50536741
50536742
T
TTA
1
GENIC
homozygous
53115820
8
50550301
50550302
T
C
24
GENIC
possibly homozygous
52625955
8
50550465
50550467
GC
--
8
GENIC
homozygous
52625957
8
50557350
50557354
TGTA
----
3
GENIC
heterozygous
52625966
8
50558643
50558644
T
TTCCCCCCTCCCTCCCTCCCTCCCTCCCTCCCTCCTTTTC
2
GENIC
heterozygous
53386013
8
50580851
50580852
G
GT
4
GENIC
heterozygous
52625980
8
50589592
50589593
T
-
8
GENIC
heterozygous
53206012
8
50595693
50595694
A
-
6
GENIC
heterozygous
52972462
8
50672944
50672945
C
-
3
GENIC
homozygous
52626014
8
50689684
50689685
C
T
13
GENIC
possibly homozygous
52626022
8
50691118
50691119
C
CG
9
GENIC
possibly homozygous
52626024
8
50773085
50773086
A
-
4
GENIC
heterozygous
53116198
8
50789156
50789157
G
GT
17
GENIC
homozygous
52626044
8
50789593
50789594
C
CA
10
GENIC
heterozygous
52626050
8
50789612
50789613
G
GT
13
GENIC
heterozygous
52626052
8
50795625
50795626
A
-
12
GENIC
homozygous
52626054
