chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
12
40270951
40270952
G
T
19
GENIC
homozygous
115328003
12
40275731
40275732
G
A
12
GENIC
homozygous
115328005
12
40275735
40275736
G
A
13
GENIC
homozygous
115328007
12
40275743
40275743
A
14
GENIC
homozygous
128989139
12
40275744
40275745
T
G
14
GENIC
homozygous
115328009
12
40276358
40276359
T
C
11
GENIC
homozygous
115328011
12
40276526
40276526
AAAACA
16
GENIC
homozygous
128989140
12
40278185
40278185
CCCG
16
GENIC
homozygous
128989141
12
40284220
40284220
GATGGTTACAGAT
15
GENIC
homozygous
128989144
12
40278188
40278192
ATAG
16
GENIC
homozygous
128989142
12
40279676
40279678
CT
16
GENIC
homozygous
128989143
12
40297155
40297167
TTTTTTTTCTTT
16
GENIC
homozygous
128989145
12
40313861
40313862
C
G
11
GENIC
homozygous
115328013
12
40313871
40313872
C
A
12
GENIC
homozygous
115328015
12
40313887
40313888
C
A
12
GENIC
homozygous
115328017
12
40313893
40313894
C
A
12
GENIC
homozygous
115328019
12
40313908
40313909
G
A
10
GENIC
homozygous
115328021
12
40313912
40313913
C
A
10
GENIC
homozygous
115328023
12
40313920
40313921
C
A
9
GENIC
homozygous
115328025
12
40314365
40314365
TCTGTAATGGGATCTGATGCCTTCTTCTAGTGTGTCTGAAGACAGCTACAGTGTAC
4
GENIC
homozygous
128989146
12
40321633
40321633
AC
6
GENIC
homozygous
132167230
12
40322048
40322048
C
16
GENIC
homozygous
128989147
12
40322611
40322612
G
A
20
GENIC
homozygous
115328027
12
40326937
40326938
C
T
11
GENIC
homozygous
115328029
12
40326939
40326941
CT
11
GENIC
homozygous
128989148
12
40326942
40326943
C
11
GENIC
homozygous
128989149
12
40326962
40326962
T
14
GENIC
homozygous
128989150
12
40329811
40329812
A
G
11
GENIC
homozygous
115328031
12
40303616
40303617
A
C
12
GENIC
homozygous
115426758
12
40334432
40334433
G
A
19
GENIC
homozygous
115328033
