chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
19
37082960
37082961
T
C
17
GENIC
homozygous
46110013
19
37083038
37083039
G
C
24
GENIC
homozygous
46551042
19
37084196
37084197
G
A
23
GENIC
homozygous
46551044
19
37084359
37084363
TCTG
----
14
GENIC
homozygous
46249589
19
37084397
37084398
T
A
19
GENIC
homozygous
46110016
19
37084449
37084450
A
T
32
GENIC
possibly homozygous
46551046
19
37085894
37085895
A
G
22
GENIC
homozygous
46551048
19
37085927
37085928
T
C
26
GENIC
homozygous
46110018
19
37086339
37086340
C
CT
11
GENIC
heterozygous
46249591
19
37086340
37086341
T
-
11
GENIC
heterozygous
46445105
19
37086366
37086367
T
C
8
GENIC
homozygous
46110019
19
37089102
37089103
T
-
3
GENIC
homozygous
46429732
19
37092622
37092623
G
GTGGACAGATGGATGGGTGGGTTGGTGGATGGACTGGCGGACAGATGGATGGATGGGTGGGTTGATGGATGGAGATGGATGGGTGGGTGGATGAGTGGGTGGATGGATGGAGACGGA
12
GENIC
homozygous
46380075
19
37094433
37094434
C
A
19
GENIC
homozygous
46110032
