chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
10
90521372
90521373
G
GC
5
GENIC
homozygous
51538631
10
90521433
90521434
G
GT
4
GENIC
homozygous
51538633
10
90521475
90521476
G
GC
2
GENIC
homozygous
51538634
10
90521495
90521496
T
TC
5
GENIC
homozygous
51538635
10
90522496
90522497
C
T
24
GENIC
homozygous
51736877
10
90522619
90522620
C
A
26
GENIC
homozygous
51736881
10
90523477
90523478
A
T
22
GENIC
homozygous
51736886
10
90523662
90523663
G
A
30
GENIC
homozygous
51736888
10
90523679
90523680
C
A
27
GENIC
homozygous
52165642
10
90523889
90523890
C
A
19
GENIC
homozygous
51736890
10
90524611
90524612
T
C
22
GENIC
homozygous
51736892
10
90524927
90524928
C
A
19
GENIC
homozygous
52165643
10
90525183
90525184
G
A
28
GENIC
possibly homozygous
52165644
10
90525549
90525550
C
T
42
GENIC
homozygous
52165645
10
90526087
90526088
G
GA
20
GENIC
homozygous
52396549
10
90526089
90526090
A
ACTCAGTTTGAGATCTGTGAGTGAGCTGAGCCTTCTGGGGACTGGCAGGGATTGGCTCTGCAGATGAGGCC
20
GENIC
homozygous
52396550
10
90526093
90526094
G
T
19
GENIC
homozygous
52396552
10
90529817
90529818
T
C
19
GENIC
homozygous
52165646
10
90530156
90530157
T
TG
20
GENIC
homozygous
52165647
10
90530165
90530166
C
G
24
GENIC
homozygous
52508471
10
90531806
90531807
T
C
20
GENIC
homozygous
51736905
10
90532766
90532767
T
C
19
GENIC
homozygous
51736909
10
90532827
90532828
T
G
26
GENIC
homozygous
51736911
10
90533671
90533672
A
G
14
GENIC
homozygous
52165648
10
90533861
90533862
C
T
22
GENIC
homozygous
52165649
10
90534748
90534749
G
A
33
GENIC
homozygous
52165650
10
90534757
90534758
G
T
32
GENIC
homozygous
52165651
10
90534813
90534825
TCTCTCTCTCTG
------------
12
GENIC
heterozygous
52508473
10
90534856
90534857
C
T
26
GENIC
homozygous
51736915
10
90535440
90535441
C
T
25
GENIC
homozygous
51736917
10
90536309
90536310
T
C
30
GENIC
homozygous
51736919
10
90538001
90538002
A
AAAATCCTC
3
GENIC
homozygous
52165652
10
90538034
90538035
A
ACCCC
2
GENIC
homozygous
52508475
10
90538183
90538184
A
C
24
GENIC
homozygous
51736923
