chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
3
21706323
21706323
G
29
GENIC
homozygous
127859506
3
21710174
21710175
T
39
GENIC
heterozygous
127859507
3
21723599
21723600
T
G
35
GENIC
heterozygous
111504302
3
21746148
21746149
G
34
GENIC
homozygous
127859515
3
21746154
21746154
T
34
GENIC
homozygous
127859516
3
21746193
21746194
C
T
32
GENIC
homozygous
111504330
3
21746196
21746197
G
31
GENIC
homozygous
127859517
3
21746214
21746214
C
29
GENIC
homozygous
127859518
3
21747498
21747499
C
A
35
GENIC
homozygous
111504331
3
21747504
21747505
A
34
GENIC
homozygous
127859519
3
21747510
21747511
G
C
34
GENIC
homozygous
111504333
3
21747532
21747533
C
A
36
GENIC
homozygous
111504335
3
21747551
21747553
TG
35
GENIC
homozygous
127859520
3
21747716
21747716
T
1
GENIC
homozygous
127859521
3
21747928
21747929
A
6
GENIC
homozygous
127859522
3
21748047
21748047
G
18
GENIC
possibly homozygous
127859523
3
21748123
21748124
G
20
GENIC
homozygous
127859524
3
21748166
21748167
G
31
GENIC
homozygous
127859525
3
21768419
21768419
TGGGG
20
GENIC
homozygous
127859528
3
21768420
21768420
TTTAGCTCAGTGGTAGAGCGCTTGCCTAGC
20
GENIC
homozygous
127859529
3
21768423
21768424
G
A
27
GENIC
homozygous
121755751
3
21800987
21800988
C
G
37
GENIC
heterozygous
130644811
3
21747609
21747610
G
17
GENIC
homozygous
129888256
3
21800967
21800968
C
G
37
GENIC
heterozygous
130644810