chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
19
52826470
52826470
G
58
GENIC
homozygous
140394444
19
52827447
52827448
G
C
55
GENIC
possibly homozygous
140475774
19
52828051
52828052
T
C
55
GENIC
homozygous
140475775
19
52828157
52828158
G
A
50
GENIC
homozygous
140475776
19
52828228
52828229
C
T
45
GENIC
homozygous
140475777
19
52831063
52831064
T
C
39
GENIC
homozygous
140475778
19
52831672
52831673
A
G
49
GENIC
homozygous
140475779
19
52833217
52833218
G
A
62
GENIC
homozygous
140475780
19
52834361
52834362
T
C
67
GENIC
homozygous
140475781
19
52834404
52834405
A
G
55
GENIC
homozygous
140475782
19
52839635
52839635
C
27
GENIC
possibly homozygous
140394445
19
52839691
52839692
C
T
30
GENIC
homozygous
140475783
19
52840362
52840370
CACATGTA
41
GENIC
homozygous
140394446
19
52840377
52840429
AAGTGTGTGTGTGCATGCACATGTATGTGTTGTGGAGTGAGTGTGTGTGCAC
34
GENIC
homozygous
140394447
19
52840479
52840480
G
A
43
GENIC
homozygous
140475784
19
52847025
52847026
A
G
42
GENIC
homozygous
140475785
19
52847225
52847226
G
A
57
GENIC
homozygous
140475786
19
52847467
52847468
C
T
50
GENIC
homozygous
140475787
19
52848431
52848432
G
T
56
GENIC
homozygous
140475788
19
52848781
52848785
TTTG
39
GENIC
homozygous
140394448