chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
12
39952289
39952290
C
T
13
GENIC
homozygous
50422071
12
39952444
39952445
T
C
22
GENIC
homozygous
50422072
12
39952655
39952656
T
A
29
GENIC
homozygous
50202253
12
39953171
39953222
CTGCTGCACTTACACTGCTGTTGGTCATTACACAGCATGCCTCGGCAACAG
---------------------------------------------------
18
GENIC
homozygous
50543424
12
39953357
39953358
T
C
4
GENIC
homozygous
50202261
12
39953362
39953363
A
AAT
5
GENIC
heterozygous
50543425
12
39953548
39953549
G
GGA
16
GENIC
homozygous
50422073
12
39953549
39953550
C
G
15
GENIC
homozygous
50543426
12
39953835
39953836
G
A
5
GENIC
homozygous
50422074
12
39954012
39954013
A
-
12
GENIC
homozygous
50202265
12
39954275
39954276
A
G
27
GENIC
homozygous
50202267
12
39954283
39954284
G
A
27
GENIC
homozygous
50202269
12
39954650
39954651
T
C
14
GENIC
homozygous
50202273
12
39955001
39955002
G
A
35
GENIC
homozygous
50202279
12
39955889
39955890
A
G
25
GENIC
homozygous
50202281
12
39956067
39956068
T
TA
11
GENIC
homozygous
50422075
12
39956087
39956088
C
CAGGG
7
GENIC
homozygous
50512180
12
39956167
39956168
G
A
26
GENIC
homozygous
50422076
12
39956202
39956206
GAAG
----
14
GENIC
homozygous
50202285
12
39957320
39957321
T
TACACACACACACAC
8
GENIC
homozygous
50543428
12
39957365
39957366
G
GT
7
GENIC
homozygous
50381035
12
39957377
39957378
G
GT
7
GENIC
possibly homozygous
50202295
12
39958244
39958245
C
T
23
GENIC
homozygous
50202299
12
39958725
39958726
A
G
13
GENIC
homozygous
50422077
12
39958936
39958937
C
A
17
GENIC
homozygous
50422078
