chr
start
stop
reference nuc
variant nuc
depth
genic status
zygosity
variant ID
13
47663864
47663865
A
T
16
GENIC
homozygous
114615086
13
47664327
47664328
A
C
10
GENIC
homozygous
114615087
13
47664651
47664652
C
T
8
GENIC
homozygous
114615088
13
47665421
47665422
A
C
17
GENIC
homozygous
114615089
13
47665613
47665614
G
A
10
GENIC
homozygous
114615090
13
47666831
47666832
C
T
15
GENIC
possibly homozygous
114615091
13
47667513
47667514
T
C
8
GENIC
homozygous
114615092
13
47668092
47668093
T
A
15
GENIC
homozygous
114615093
13
47670285
47670286
A
G
13
GENIC
homozygous
114615094
13
47670944
47670945
T
C
19
GENIC
homozygous
114615095
13
47673926
47673927
G
A
13
GENIC
homozygous
114615096
13
47675818
47675819
C
T
11
GENIC
homozygous
114615097
13
47676823
47676824
A
T
6
GENIC
homozygous
114615098
13
47677353
47677354
T
G
16
GENIC
homozygous
114615099
13
47667938
47667939
A
G
17
GENIC
possibly homozygous
114548339
13
47670861
47670862
G
A
12
GENIC
homozygous
118497551
13
47670701
47670702
A
G
9
GENIC
homozygous
115182096
13
47671136
47671137
T
A
12
GENIC
homozygous
114923041
13
47676534
47676534
CATACATCAG
11
GENIC
homozygous
132171404
13
47670744
47670744
TTGGGGATTTAGCTCAGTGGTAGAGCGCTTGCCTAGCAAGC
6
GENIC
homozygous
129051004
13
47672327
47672327
A
9
GENIC
homozygous
131501504
13
47671915
47671915
T
13
GENIC
homozygous
132171403
13
47676634
47676634
GAGT
12
GENIC
homozygous
132171405
13
47676671
47676731
AGAGGGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGACAGAGACAGAGACAGAGGAGGAG
8
GENIC
homozygous
132171406
13
47676645
47676646
C
T
11
GENIC
homozygous
115118379
