chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
19
10340593
10340594
C
T
22
GENIC
homozygous
109633596
19
10341178
10341179
A
C
25
GENIC
homozygous
109633598
19
10342191
10342192
G
A
27
GENIC
homozygous
109633600
19
10342841
10342842
A
G
20
GENIC
homozygous
109633602
19
10342891
10342892
A
G
17
GENIC
homozygous
109633604
19
10345773
10345774
C
T
17
GENIC
homozygous
109633606
19
10345778
10345779
A
G
18
GENIC
homozygous
109633608
19
10348263
10348264
T
C
22
GENIC
homozygous
109633610
19
10349567
10349568
C
T
14
GENIC
homozygous
109633612
19
10350452
10350453
G
A
19
GENIC
homozygous
109633614
19
10353725
10353725
G
19
GENIC
homozygous
129583443
19
10341308
10341309
A
G
28
GENIC
homozygous
109764542
19
10346630
10346667
TTCCTCCGTAGGCCTGCCTTCACCTCCTCCAGTCCAG
13
GENIC
homozygous
129583439
19
10349055
10349062
GGGGAGT
19
GENIC
homozygous
129583440
19
10352595
10352596
C
17
GENIC
homozygous
129583441
19
10353717
10353723
TCTCTC
19
GENIC
homozygous
129583442
19
10353726
10353726
ACATGAGC
19
GENIC
homozygous
129583444
19
10354967
10354968
T
C
20
GENIC
homozygous
109633616
19
10355021
10355022
T
C
18
GENIC
homozygous
109633618
19
10355526
10355527
G
A
19
GENIC
homozygous
109633620
19
10357629
10357630
A
G
11
GENIC
homozygous
109633622
19
10358482
10358483
C
T
13
GENIC
homozygous
109633624
19
10359004
10359005
G
T
27
GENIC
homozygous
109633626
19
10359212
10359213
A
G
21
GENIC
homozygous
109633628
