chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
12
42479561
42479562
A
T
19
GENIC
homozygous
50209153
12
42479566
42479567
T
G
16
GENIC
homozygous
50209154
12
42479572
42479573
T
C
17
GENIC
homozygous
50209155
12
42480660
42480661
C
CCA
4
GENIC
heterozygous
50209156
12
42480660
42480661
C
CCACA
4
GENIC
heterozygous
50544348
12
42483114
42483157
AGATGGGTGCTCTTAACCGCTGAGCCATCTCTCCAGCCCCCCC
-------------------------------------------
16
GENIC
heterozygous
50544349
12
42483953
42483955
TT
--
17
GENIC
heterozygous
50572255
12
42483954
42483955
T
-
17
GENIC
heterozygous
50563860
12
42485028
42485029
G
GT
6
GENIC
heterozygous
50572257
12
42485029
42485030
G
GT
11
GENIC
heterozygous
50572259
12
42486270
42486271
A
AC
5
INTERGENIC
homozygous
50209165
12
42487706
42487707
C
T
16
GENIC
homozygous
50209168
12
42488113
42488114
A
ATTTTT
4
GENIC
homozygous
50544352
12
42487194
42487195
G
A
13
GENIC
homozygous
50327513
12
42488411
42488421
TTTTTTTTAA
----------
22
GENIC
possibly homozygous
50209172
12
42488455
42488456
C
-
20
GENIC
homozygous
50327515
12
42490593
42490594
A
G
17
GENIC
homozygous
50327517
12
42490595
42490596
A
-
17
GENIC
homozygous
50327519
12
42490603
42490609
CACACA
------
19
GENIC
homozygous
50327521
12
42490657
42490658
C
T
26
GENIC
homozygous
50209180
12
42491236
42491237
A
-
19
GENIC
homozygous
50327525
12
42492918
42492919
C
T
23
GENIC
homozygous
50327527
12
42494101
42494102
C
A
14
INTERGENIC
homozygous
50209183
