chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
8
50979719
50979720
A
G
49
GENIC
homozygous
138329685
8
50980135
50980136
C
T
51
GENIC
homozygous
138329686
8
50980562
50980563
T
C
54
GENIC
homozygous
142070051
8
50981010
50981010
A
62
GENIC
homozygous
138244863
8
50981539
50981540
G
C
61
GENIC
homozygous
138329687
8
50981663
50981664
T
A
60
GENIC
possibly homozygous
138329688
8
50981860
50981861
T
C
48
GENIC
homozygous
138329689
8
50983266
50983267
A
G
46
GENIC
homozygous
138329690
8
50983869
50983870
C
T
26
GENIC
homozygous
138329691
8
50984413
50984414
T
C
53
GENIC
homozygous
138329692
8
50989252
50989253
A
C
54
GENIC
homozygous
138329693
8
50991473
50991474
G
A
52
GENIC
homozygous
138329694
8
50992439
50992440
C
G
56
GENIC
homozygous
138329696
8
50993580
50993581
T
A
40
GENIC
homozygous
138329697
8
50996221
50996222
C
T
21
GENIC
homozygous
138329698
8
50997824
50997825
A
T
56
GENIC
homozygous
138329699
8
50998519
50998520
G
A
36
GENIC
homozygous
138329700
8
51002445
51002445
A
10
GENIC
heterozygous
145145493
8
50996251
50996252
C
T
27
GENIC
homozygous
154518244
8
50998931
50998931
TCC
37
GENIC
possibly homozygous
138244865
8
51001033
51001033
TG
30
GENIC
possibly homozygous
138244866
8
51001077
51001077
TG
21
GENIC
homozygous
138244867
8
50999666
50999667
G
A
49
GENIC
homozygous
138329701
8
50981987
50981987
CACACACG
29
GENIC
heterozygous
142023735
8
50988317
50988317
AGGAGTAGCTGGTTCCACAGGAGTAGCTGGTTCCAC
37
GENIC
possibly homozygous
142023736
8
50996251
50996252
C
27
GENIC
heterozygous
403237543
8
51002590
51002591
C
36
GENIC
homozygous
403237544
8
51002590
51002591
C
A
36
GENIC
heterozygous
403237545
8
51000271
51000272
G
A
29
GENIC
homozygous
145146252
