chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
10
66341936
66341937
C
A
23
GENIC
homozygous
51479540
10
66342188
66342189
A
AGAGGCCTGGGTTCTTTTTTTTTTTTTTGAGCTGGGGACCGAACCCAGGGCTTTGTGCTTCCTAGGTAAGCGCTCTACCACTGAGCTAAATCCCCAGCCCC
2
GENIC
homozygous
52382616
10
66343029
66343030
C
T
19
GENIC
homozygous
51479541
10
66350666
66350667
A
G
26
GENIC
homozygous
51479543
10
66350764
66350765
A
ATTTTTT
8
GENIC
homozygous
51907945
10
66351483
66351484
C
T
24
GENIC
homozygous
51479547
10
66351527
66351528
G
A
27
GENIC
homozygous
51907947
10
66352061
66352062
T
A
22
GENIC
homozygous
51479548
10
66352225
66352226
G
A
23
GENIC
homozygous
51479549
10
66352692
66352693
T
-
5
GENIC
heterozygous
51907949
10
66353719
66353720
C
T
14
GENIC
homozygous
51479554
10
66354076
66354077
G
-
9
GENIC
homozygous
51907951
10
66354336
66354337
G
A
28
GENIC
homozygous
51479561
10
66354736
66354737
A
G
21
GENIC
homozygous
51479562
10
66354841
66354856
TGCCCTCTTCTGGTG
---------------
20
GENIC
homozygous
51479563
10
66354898
66354899
T
TAA
22
GENIC
homozygous
52382620
10
66354911
66354915
AACC
----
22
GENIC
homozygous
52382622
10
66354929
66354930
C
A
24
GENIC
homozygous
52382624
10
66354930
66354931
C
A
26
GENIC
homozygous
51907953
10
66355017
66355018
A
-
20
GENIC
possibly homozygous
51479566
10
66355169
66355170
C
CAAAA
4
GENIC
heterozygous
51479567
10
66355169
66355170
C
CAA
4
GENIC
heterozygous
52503853
10
66355372
66355373
T
TA
17
GENIC
homozygous
51479568
10
66355389
66355390
A
-
12
GENIC
homozygous
51907955
10
66355414
66355415
G
T
14
GENIC
homozygous
51479569
10
66355169
66355170
C
CAAA
4
GENIC
heterozygous
52320381
10
66355454
66355455
C
A
12
GENIC
homozygous
51678708