chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
2
30180066
30180066
T
38
GENIC
homozygous
127607275
2
30180073
30180074
C
35
GENIC
homozygous
127607276
2
30180076
30180077
G
A
34
GENIC
homozygous
120122962
2
30180084
30180084
C
37
GENIC
homozygous
127607277
2
30180081
30180082
C
T
37
GENIC
homozygous
109672753
2
30180100
30180101
C
T
40
GENIC
homozygous
109672755
2
30182001
30182001
G
51
GENIC
homozygous
127607278
2
30183293
30183294
T
30
GENIC
homozygous
127607279
2
30188370
30188371
A
G
10
GENIC
homozygous
109672775
2
30188399
30188400
C
T
11
GENIC
homozygous
109672777
2
30198550
30198551
G
A
39
GENIC
heterozygous
127785860
2
30198555
30198556
A
G
39
GENIC
heterozygous
127785861
2
30201551
30201552
C
T
32
GENIC
homozygous
109672829
2
30201658
30201662
CCCC
41
GENIC
homozygous
127607283
2
30201663
30201663
AAT
42
GENIC
homozygous
127607284
2
30207831
30207832
T
6
GENIC
homozygous
129863666
2
30207847
30207848
C
11
GENIC
homozygous
129863667
2
30207855
30207855
C
13
GENIC
homozygous
129863668
2
30207857
30207864
CCATAGA
13
GENIC
homozygous
129863669
2
30195449
30195452
CCT
19
GENIC
heterozygous
135148299
2
30198515
30198516
G
A
37
GENIC
heterozygous
132388183
2
30201576
30201577
A
29
GENIC
heterozygous
130630643
2
30207843
30207844
A
C
11
GENIC
homozygous
120165314
2
30213630
30213631
G
A
43
GENIC
heterozygous
110500779
2
30213631
30213632
G
T
41
GENIC
heterozygous
110500781
2
30213633
30213634
T
A
41
GENIC
heterozygous
110500783
2
30213656
30213657
A
G
43
GENIC
heterozygous
109672865
2
30213661
30213662
C
T
42
GENIC
heterozygous
109672867
2
30213669
30213670
G
A
42
GENIC
heterozygous
109672869
2
30233786
30233854
ATGTAGCCTGGCTGTCTTGCCCAACCAGAACCTCACGCGGTTCTTGAAACTTTGGATACAGACCCTTA
19
GENIC
homozygous
130244041
2
30234516
30234516
GTG
26
GENIC
possibly homozygous
130860654