chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
7
92161599
92161600
G
GA
27
GENIC
possibly homozygous
54208607
7
92161600
92161601
A
-
27
GENIC
heterozygous
54798497
7
92162777
92162778
T
C
24
GENIC
homozygous
54022516
7
92162815
92162816
G
A
19
GENIC
homozygous
54208608
7
92163749
92163750
G
-
13
GENIC
homozygous
54208610
7
92164525
92164526
A
G
15
GENIC
homozygous
54208611
7
92167625
92167626
C
T
20
GENIC
homozygous
54208612
7
92168246
92168247
A
G
26
GENIC
homozygous
54022520
7
92170426
92170427
A
G
12
GENIC
homozygous
54022522
7
92171520
92171521
T
C
23
GENIC
homozygous
54208613
7
92171839
92171840
G
GA
23
GENIC
homozygous
54022525
7
92172529
92172530
A
-
19
GENIC
homozygous
54022526
7
92176534
92176535
T
TA
5
GENIC
heterozygous
54988457
7
92176536
92176537
A
-
5
GENIC
heterozygous
55028483
7
92177811
92177812
T
C
10
GENIC
homozygous
54022535
7
92177977
92177978
T
C
26
GENIC
homozygous
54022536
7
92178113
92178115
AC
--
18
GENIC
possibly homozygous
54988461
7
92178630
92178631
C
CTAGTGTATAAGCAAACCTAGCGAAT
23
GENIC
homozygous
54022538
7
92179089
92179090
G
GA
23
GENIC
possibly homozygous
54208615
7
92179642
92179643
A
G
19
GENIC
homozygous
54022542
7
92180119
92180120
T
TA
22
GENIC
homozygous
54208616
7
92180443
92180444
C
G
27
GENIC
homozygous
54208617
7
92180793
92180794
C
T
22
GENIC
homozygous
54208618
7
92180878
92180879
A
ACTC
16
GENIC
homozygous
54208619
7
92181884
92181885
T
TA
18
GENIC
homozygous
54208620
7
92181960
92181961
C
A
11
GENIC
homozygous
54208621
7
92182055
92182056
A
G
4
GENIC
homozygous
54208622
7
92182068
92182069
C
T
3
GENIC
homozygous
54208623
7
92182255
92182256
T
C
3
GENIC
homozygous
54208624