chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
10
55572039
55572039
A
16
GENIC
homozygous
131094347
10
55572271
55572272
A
G
17
GENIC
homozygous
116934859
10
55572718
55572719
A
G
27
GENIC
homozygous
116782666
10
55572908
55572909
T
25
GENIC
homozygous
131094348
10
55573072
55573073
A
G
20
GENIC
possibly homozygous
116934861
10
55573990
55573991
G
A
20
GENIC
homozygous
116934863
10
55574976
55574977
T
A
21
GENIC
homozygous
116978011
10
55575797
55575798
A
G
22
GENIC
homozygous
116934865
10
55576556
55576557
G
A
21
GENIC
homozygous
116934867
10
55577586
55577587
G
A
34
GENIC
homozygous
116934869
10
55578017
55578018
A
G
23
GENIC
homozygous
116934871
10
55585184
55585184
GGGCGGGTAGTGAGTGT
19
GENIC
homozygous
128818965
10
55573312
55573313
A
24
GENIC
homozygous
131094349
10
55576561
55576561
GA
20
GENIC
homozygous
131094350
10
55575798
55575799
C
T
22
GENIC
homozygous
116602605
10
55576276
55576277
A
T
22
GENIC
homozygous
116602607
10
55581417
55581418
A
C
8
GENIC
homozygous
116602611
10
55583055
55583056
T
C
14
GENIC
homozygous
116602613
10
55583484
55583485
A
G
26
GENIC
homozygous
116602615
10
55580020
55580020
AAGCAAAGCAACAT
18
GENIC
homozygous
128818963
10
55584861
55585033
TAAGCTGCTGTCTCTTTTTTTTTTTTTTTGGTTCTTTTTTTTTTTTTTTTTTTACTTTTTTTTTTTTTTTTTTTTGGTTCTTTTTTTTTTTTTTTTTCGGAGCTGGGGACCGAACCCAGGGCCTTGCGCTTCTTAGGCAAGCGCTCTACCACTGAGCTAAATCCCCAACCCC
11
GENIC
homozygous
128818964
10
55585200
55585201
A
G
19
GENIC
homozygous
116602619
10
55586612
55586613
A
G
21
GENIC
homozygous
116602623
10
55587635
55587636
T
C
29
GENIC
homozygous
116602625
10
55589499
55589499
GAG
23
GENIC
homozygous
128818966
10
55590430
55590431
C
T
16
GENIC
homozygous
116602627
10
55591979
55591986
TGTTTTT
25
GENIC
homozygous
131094351
10
55593013
55593014
C
T
25
GENIC
possibly homozygous
116890218
