chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
3
177015193
177015194
G
C
16
GENIC
homozygous
111843010
3
177015478
177015479
G
T
14
GENIC
homozygous
111843012
3
177016773
177016774
A
G
19
GENIC
homozygous
111843014
3
177017850
177017851
A
G
22
GENIC
homozygous
111843016
3
177019326
177019327
A
C
10
GENIC
homozygous
111843018
3
177019372
177019375
CAC
8
GENIC
homozygous
127965528
3
177020639
177020640
T
11
GENIC
homozygous
127965529
3
177023243
177023244
T
28
GENIC
possibly homozygous
127965530
3
177024104
177024105
A
C
14
GENIC
homozygous
119653220
3
177025987
177025988
A
G
21
GENIC
homozygous
111843020
3
177027334
177027335
A
G
13
GENIC
homozygous
111843022
3
177033894
177033895
C
G
31
GENIC
homozygous
111843024
3
177039682
177039683
G
C
26
GENIC
homozygous
111843028
3
177042791
177042791
G
16
GENIC
homozygous
127965537
3
177024103
177024103
C
13
GENIC
homozygous
127965531
3
177033054
177033066
CCACCATCACCA
7
GENIC
homozygous
127965532
3
177033351
177033401
TTTAAAGACAATATTTACTGTAAGTAGAATGATCAAAAGATGTGCCTATA
10
GENIC
homozygous
127965533
3
177035790
177035794
TTTC
14
GENIC
homozygous
127965534
3
177038352
177038352
T
22
GENIC
possibly homozygous
127965535
3
177038745
177038748
CAA
13
GENIC
homozygous
127965536
3
177043355
177043356
T
C
18
GENIC
homozygous
111843030
3
177045519
177045520
T
C
13
GENIC
homozygous
111843032