chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
8
50979719
50979720
A
G
21
GENIC
homozygous
138329685
8
50980135
50980136
C
T
29
GENIC
homozygous
138329686
8
50980562
50980563
T
C
30
GENIC
homozygous
142070051
8
50981010
50981010
A
26
GENIC
homozygous
138244863
8
50981539
50981540
G
C
28
GENIC
homozygous
138329687
8
50981663
50981664
T
A
22
GENIC
homozygous
138329688
8
50981860
50981861
T
C
32
GENIC
homozygous
138329689
8
50983266
50983267
A
G
14
GENIC
homozygous
138329690
8
50983869
50983870
C
T
7
GENIC
homozygous
138329691
8
50984413
50984414
T
C
19
GENIC
homozygous
138329692
8
50989252
50989253
A
C
18
GENIC
possibly homozygous
138329693
8
50981987
50981987
CACACACG
16
GENIC
homozygous
142023735
8
50988317
50988317
AGGAGTAGCTGGTTCCACAGGAGTAGCTGGTTCCAC
17
GENIC
homozygous
142023736
8
50991473
50991474
G
A
17
GENIC
homozygous
138329694
8
50992439
50992440
C
G
28
GENIC
homozygous
138329696
8
50993580
50993581
T
A
15
GENIC
homozygous
138329697
8
50996221
50996222
C
T
11
GENIC
homozygous
138329698
8
50998931
50998931
TCC
16
GENIC
homozygous
138244865
8
51001033
51001033
TG
13
GENIC
homozygous
138244866
8
51001077
51001077
TG
12
GENIC
homozygous
138244867
8
51002590
51002591
C
A
18
GENIC
heterozygous
403237545
8
50996251
50996252
C
T
18
GENIC
homozygous
154518244
8
50997824
50997825
A
T
26
GENIC
homozygous
138329699
8
50998519
50998520
G
A
24
GENIC
homozygous
138329700
8
50999666
50999667
G
A
21
GENIC
homozygous
138329701
8
50996251
50996252
C
18
GENIC
heterozygous
403237543
8
51002590
51002591
C
18
GENIC
possibly homozygous
403237544
