geneid | 339855 |
---|---|
ensemblid | ENSG00000174611.12 |
hgncid | 26576 |
symbol | KY |
name | kyphoscoliosis peptidase |
refseq_nuc | NM_178554.6 |
refseq_prot | NP_848649.3 |
ensembl_nuc | ENST00000423778.7 |
ensembl_prot | ENSP00000397598.2 |
mane_status | MANE Select |
chr | chr3 |
start | 134599923 |
end | 134651022 |
strand | - |
ver | v1.2 |
region | chr3:134599923-134651022 |
region5000 | chr3:134594923-134656022 |
regionname0 | KY_chr3_134599923_134651022 |
regionname5000 | KY_chr3_134594923_134656022 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aa |
---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 661 | 288 | 84 | 60 | 84 | 14 | 44 | KY_chr3_134594923_134656022 | KY | copy fasta |
a0002 | 0/0 | 661 | 2 | 0 | 0 | 2 | 0 | 0 | KY_chr3_134594923_134656022 | KY | copy fasta |
a0003 | 0/0 | 661 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | copy fasta |
a0004 | 0/0 | 661 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY | copy fasta |
a0005 | 0/0 | 661 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY | copy fasta |
a0006 | 0/0 | 661 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | copy fasta |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq |
---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/1 | 1986 | 145 | 27 | 36 | 49 | 10 | 22 | KY_chr3_134594923_134656022 | KY | copy fasta |
c0002 | 0/0 | 1986 | 61 | 21 | 8 | 18 | 1 | 13 | KY_chr3_134594923_134656022 | KY | copy fasta |
c0003 | 0/0 | 1986 | 29 | 7 | 7 | 7 | 2 | 6 | KY_chr3_134594923_134656022 | KY | copy fasta |
c0004 | 0/0 | 1986 | 18 | 16 | 2 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | copy fasta |
c0005 | 0/0 | 1986 | 14 | 6 | 1 | 7 | 0 | 0 | KY_chr3_134594923_134656022 | KY | copy fasta |
c0006 | 0/0 | 1986 | 12 | 3 | 5 | 0 | 1 | 3 | KY_chr3_134594923_134656022 | KY | copy fasta |
c0007 | 0/0 | 1986 | 3 | 2 | 1 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | copy fasta |
c0008 | 0/0 | 1986 | 3 | 0 | 0 | 3 | 0 | 0 | KY_chr3_134594923_134656022 | KY | copy fasta |
c0009 | 1/0 | 1986 | 2 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | copy fasta |
c0010 | 0/0 | 1986 | 2 | 0 | 0 | 2 | 0 | 0 | KY_chr3_134594923_134656022 | KY | copy fasta |
c0011 | 0/0 | 1986 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | copy fasta |
c0012 | 0/0 | 1986 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | copy fasta |
c0013 | 0/0 | 1986 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY | copy fasta |
c0014 | 0/0 | 1986 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | copy fasta |
c0015 | 0/0 | 1986 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY | copy fasta |
thapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq |
---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 3729 | 134 | 38 | 30 | 45 | 8 | 12 | KY_chr3_134594923_134656022 | KY | copy fasta |
t0002 | 0/0 | 3730 | 75 | 24 | 14 | 16 | 3 | 18 | KY_chr3_134594923_134656022 | KY | copy fasta |
t0003 | 0/0 | 3729 | 15 | 0 | 5 | 0 | 3 | 7 | KY_chr3_134594923_134656022 | KY | copy fasta |
t0004 | 0/0 | 3730 | 13 | 2 | 0 | 11 | 0 | 0 | KY_chr3_134594923_134656022 | KY | copy fasta |
t0005 | 0/0 | 3729 | 10 | 0 | 5 | 5 | 0 | 0 | KY_chr3_134594923_134656022 | KY | copy fasta |
t0006 | 0/0 | 3730 | 8 | 1 | 0 | 7 | 0 | 0 | KY_chr3_134594923_134656022 | KY | copy fasta |
t0007 | 0/0 | 3730 | 5 | 4 | 1 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | copy fasta |
t0008 | 0/0 | 3729 | 4 | 4 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | copy fasta |
t0009 | 1/0 | 3719 | 3 | 2 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | copy fasta |
t0010 | 0/0 | 3730 | 3 | 2 | 1 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | copy fasta |
t0011 | 0/0 | 3729 | 3 | 3 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | copy fasta |
t0012 | 0/0 | 3729 | 2 | 0 | 2 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | copy fasta |
t0013 | 0/0 | 3729 | 2 | 0 | 0 | 0 | 0 | 2 | KY_chr3_134594923_134656022 | KY | copy fasta |
t0014 | 0/0 | 3729 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | copy fasta |
t0015 | 0/0 | 3730 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY | copy fasta |
t0016 | 0/0 | 3730 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | copy fasta |
t0017 | 0/0 | 3719 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | copy fasta |
t0018 | 0/0 | 3729 | 1 | 0 | 0 | 0 | 0 | 1 | KY_chr3_134594923_134656022 | KY | copy fasta |
t0019 | 0/0 | 3730 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | copy fasta |
t0020 | 0/0 | 3719 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY | copy fasta |
t0021 | 0/0 | 3730 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | copy fasta |
t0022 | 0/0 | 3729 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY | copy fasta |
t0023 | 0/0 | 3729 | 1 | 0 | 1 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | copy fasta |
t0024 | 0/0 | 3729 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY | copy fasta |
t0025 | 0/0 | 3729 | 1 | 0 | 0 | 0 | 0 | 1 | KY_chr3_134594923_134656022 | KY | copy fasta |
t0026 | 0/0 | 3729 | 1 | 0 | 0 | 0 | 0 | 1 | KY_chr3_134594923_134656022 | KY | copy fasta |
t0027 | 0/0 | 3729 | 1 | 0 | 0 | 0 | 0 | 1 | KY_chr3_134594923_134656022 | KY | copy fasta |
t0028 | 0/0 | 3729 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | copy fasta |
t0029 | 0/0 | 3729 | 1 | 0 | 0 | 0 | 0 | 1 | KY_chr3_134594923_134656022 | KY | copy fasta |
t0030 | 0/0 | 3730 | 1 | 0 | 1 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | copy fasta |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename |
---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 8 | 1 | 4 | 3 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0002 | 0/0 | 7 | 0 | 2 | 2 | 1 | 2 | KY_chr3_134594923_134656022 | KY |
g0003 | 0/0 | 6 | 1 | 0 | 5 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0005 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0006 | 0/0 | 4 | 0 | 0 | 1 | 0 | 3 | KY_chr3_134594923_134656022 | KY |
g0007 | 0/0 | 4 | 1 | 1 | 0 | 2 | 0 | KY_chr3_134594923_134656022 | KY |
g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0009 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0010 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0011 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0013 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | KY_chr3_134594923_134656022 | KY |
g0014 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0015 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0017 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | KY_chr3_134594923_134656022 | KY |
g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0021 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0022 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0023 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | KY_chr3_134594923_134656022 | KY |
g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KY_chr3_134594923_134656022 | KY |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KY_chr3_134594923_134656022 | KY |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KY_chr3_134594923_134656022 | KY |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KY_chr3_134594923_134656022 | KY |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KY_chr3_134594923_134656022 | KY |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KY_chr3_134594923_134656022 | KY |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KY_chr3_134594923_134656022 | KY |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KY_chr3_134594923_134656022 | KY |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KY_chr3_134594923_134656022 | KY |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KY_chr3_134594923_134656022 | KY |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KY_chr3_134594923_134656022 | KY |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KY_chr3_134594923_134656022 | KY |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KY_chr3_134594923_134656022 | KY |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KY_chr3_134594923_134656022 | KY |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KY_chr3_134594923_134656022 | KY |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KY_chr3_134594923_134656022 | KY |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KY_chr3_134594923_134656022 | KY |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0142 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KY_chr3_134594923_134656022 | KY |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KY_chr3_134594923_134656022 | KY |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KY_chr3_134594923_134656022 | KY |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KY_chr3_134594923_134656022 | KY |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KY_chr3_134594923_134656022 | KY |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KY_chr3_134594923_134656022 | KY |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KY_chr3_134594923_134656022 | KY |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KY_chr3_134594923_134656022 | KY |
g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KY_chr3_134594923_134656022 | KY |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KY_chr3_134594923_134656022 | KY |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KY_chr3_134594923_134656022 | KY |
g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KY_chr3_134594923_134656022 | KY |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KY_chr3_134594923_134656022 | KY |
g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KY_chr3_134594923_134656022 | KY |
g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KY_chr3_134594923_134656022 | KY |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KY_chr3_134594923_134656022 | KY |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KY_chr3_134594923_134656022 | KY |
g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KY_chr3_134594923_134656022 | KY |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KY_chr3_134594923_134656022 | KY |
g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KY_chr3_134594923_134656022 | KY |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KY_chr3_134594923_134656022 | KY |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KY_chr3_134594923_134656022 | KY |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KY_chr3_134594923_134656022 | KY |
g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KY_chr3_134594923_134656022 | KY |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KY_chr3_134594923_134656022 | KY |
g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KY_chr3_134594923_134656022 | KY |
g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KY_chr3_134594923_134656022 | KY |
g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KY_chr3_134594923_134656022 | KY |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
achapid | ahapid | chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2 |
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | acseq |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | a0001 | c0001 | 0/1 | 145 | 27 | 36 | 49 | 10 | 22 | KY_chr3_134594923_134656022 | KY | copy fasta |
a0001c0002 | a0001 | c0002 | 0/0 | 61 | 21 | 8 | 18 | 1 | 13 | KY_chr3_134594923_134656022 | KY | copy fasta |
a0001c0003 | a0001 | c0003 | 0/0 | 29 | 7 | 7 | 7 | 2 | 6 | KY_chr3_134594923_134656022 | KY | copy fasta |
a0001c0004 | a0001 | c0004 | 0/0 | 18 | 16 | 2 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | copy fasta |
a0001c0005 | a0001 | c0005 | 0/0 | 14 | 6 | 1 | 7 | 0 | 0 | KY_chr3_134594923_134656022 | KY | copy fasta |
a0001c0006 | a0001 | c0006 | 0/0 | 12 | 3 | 5 | 0 | 1 | 3 | KY_chr3_134594923_134656022 | KY | copy fasta |
a0001c0007 | a0001 | c0007 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | copy fasta |
a0001c0008 | a0001 | c0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | KY_chr3_134594923_134656022 | KY | copy fasta |
a0001c0009 | a0001 | c0009 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | copy fasta |
a0001c0012 | a0001 | c0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | copy fasta |
a0002c0010 | a0002 | c0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KY_chr3_134594923_134656022 | KY | copy fasta |
a0003c0014 | a0003 | c0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | copy fasta |
a0004c0015 | a0004 | c0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY | copy fasta |
a0005c0013 | a0005 | c0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY | copy fasta |
a0006c0011 | a0006 | c0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | copy fasta |
acthapid | ahapid | chapid | thapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2 |
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | actseq |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | a0001 | c0001 | t0001 | 0/1 | 111 | 22 | 27 | 42 | 7 | 12 | KY_chr3_134594923_134656022 | KY | copy fasta |
a0001c0001t0003 | a0001 | c0001 | t0003 | 0/0 | 9 | 0 | 1 | 0 | 3 | 5 | KY_chr3_134594923_134656022 | KY | copy fasta |
a0001c0001t0005 | a0001 | c0001 | t0005 | 0/0 | 10 | 0 | 5 | 5 | 0 | 0 | KY_chr3_134594923_134656022 | KY | copy fasta |
a0001c0001t0008 | a0001 | c0001 | t0008 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | copy fasta |
a0001c0001t0012 | a0001 | c0001 | t0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | copy fasta |
a0001c0001t0013 | a0001 | c0001 | t0013 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | KY_chr3_134594923_134656022 | KY | copy fasta |
a0001c0001t0014 | a0001 | c0001 | t0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | copy fasta |
a0001c0001t0022 | a0001 | c0001 | t0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY | copy fasta |
a0001c0001t0023 | a0001 | c0001 | t0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | copy fasta |
a0001c0001t0024 | a0001 | c0001 | t0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY | copy fasta |
a0001c0001t0025 | a0001 | c0001 | t0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KY_chr3_134594923_134656022 | KY | copy fasta |
a0001c0001t0027 | a0001 | c0001 | t0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KY_chr3_134594923_134656022 | KY | copy fasta |
a0001c0001t0029 | a0001 | c0001 | t0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KY_chr3_134594923_134656022 | KY | copy fasta |
a0001c0002t0002 | a0001 | c0002 | t0002 | 0/0 | 42 | 17 | 7 | 5 | 1 | 12 | KY_chr3_134594923_134656022 | KY | copy fasta |
a0001c0002t0004 | a0001 | c0002 | t0004 | 0/0 | 13 | 2 | 0 | 11 | 0 | 0 | KY_chr3_134594923_134656022 | KY | copy fasta |
a0001c0002t0015 | a0001 | c0002 | t0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY | copy fasta |
a0001c0002t0018 | a0001 | c0002 | t0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KY_chr3_134594923_134656022 | KY | copy fasta |
a0001c0002t0019 | a0001 | c0002 | t0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | copy fasta |
a0001c0002t0020 | a0001 | c0002 | t0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY | copy fasta |
a0001c0002t0021 | a0001 | c0002 | t0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | copy fasta |
a0001c0002t0030 | a0001 | c0002 | t0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | copy fasta |
a0001c0003t0002 | a0001 | c0003 | t0002 | 0/0 | 29 | 7 | 7 | 7 | 2 | 6 | KY_chr3_134594923_134656022 | KY | copy fasta |
a0001c0004t0001 | a0001 | c0004 | t0001 | 0/0 | 15 | 13 | 2 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | copy fasta |
a0001c0004t0011 | a0001 | c0004 | t0011 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | copy fasta |
a0001c0005t0006 | a0001 | c0005 | t0006 | 0/0 | 8 | 1 | 0 | 7 | 0 | 0 | KY_chr3_134594923_134656022 | KY | copy fasta |
a0001c0005t0007 | a0001 | c0005 | t0007 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | copy fasta |
a0001c0005t0016 | a0001 | c0005 | t0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | copy fasta |
a0001c0006t0001 | a0001 | c0006 | t0001 | 0/0 | 5 | 3 | 1 | 0 | 1 | 0 | KY_chr3_134594923_134656022 | KY | copy fasta |
a0001c0006t0003 | a0001 | c0006 | t0003 | 0/0 | 6 | 0 | 4 | 0 | 0 | 2 | KY_chr3_134594923_134656022 | KY | copy fasta |
a0001c0006t0026 | a0001 | c0006 | t0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KY_chr3_134594923_134656022 | KY | copy fasta |
a0001c0007t0010 | a0001 | c0007 | t0010 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | copy fasta |
a0001c0008t0001 | a0001 | c0008 | t0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | KY_chr3_134594923_134656022 | KY | copy fasta |
a0001c0009t0009 | a0001 | c0009 | t0009 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | copy fasta |
a0001c0012t0028 | a0001 | c0012 | t0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | copy fasta |
a0002c0010t0002 | a0002 | c0010 | t0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KY_chr3_134594923_134656022 | KY | copy fasta |
a0003c0014t0017 | a0003 | c0014 | t0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | copy fasta |
a0004c0015t0002 | a0004 | c0015 | t0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY | copy fasta |
a0005c0013t0002 | a0005 | c0013 | t0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY | copy fasta |
a0006c0011t0009 | a0006 | c0011 | t0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY | copy fasta |
actghapid | ahapid | chapid | thapid | ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2 |
total | AFR | AMR | EAS | EUR | SAS | regionname | genename |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | a0001 | c0001 | t0001 | g0001 | 0/0 | 8 | 1 | 4 | 3 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0001t0001g0002 | a0001 | c0001 | t0001 | g0002 | 0/0 | 7 | 0 | 2 | 2 | 1 | 2 | KY_chr3_134594923_134656022 | KY |
a0001c0001t0001g0003 | a0001 | c0001 | t0001 | g0003 | 0/0 | 6 | 1 | 0 | 5 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0001t0001g0005 | a0001 | c0001 | t0001 | g0005 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0001t0001g0016 | a0001 | c0001 | t0001 | g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0001t0001g0017 | a0001 | c0001 | t0001 | g0017 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0001t0001g0018 | a0001 | c0001 | t0001 | g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0001t0001g0021 | a0001 | c0001 | t0001 | g0021 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0001t0001g0022 | a0001 | c0001 | t0001 | g0022 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0001t0001g0023 | a0001 | c0001 | t0001 | g0023 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | KY_chr3_134594923_134656022 | KY |
a0001c0001t0001g0024 | a0001 | c0001 | t0001 | g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0001t0001g0030 | a0001 | c0001 | t0001 | g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0001t0001g0032 | a0001 | c0001 | t0001 | g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0001t0001g0036 | a0001 | c0001 | t0001 | g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0001t0001g0040 | a0001 | c0001 | t0001 | g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0001t0001g0056 | a0001 | c0001 | t0001 | g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0001t0001g0061 | a0001 | c0001 | t0001 | g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0001t0001g0064 | a0001 | c0001 | t0001 | g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0001t0001g0068 | a0001 | c0001 | t0001 | g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0001t0001g0070 | a0001 | c0001 | t0001 | g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0001t0001g0071 | a0001 | c0001 | t0001 | g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0001t0001g0072 | a0001 | c0001 | t0001 | g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0001t0001g0073 | a0001 | c0001 | t0001 | g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0001t0001g0074 | a0001 | c0001 | t0001 | g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0001t0001g0075 | a0001 | c0001 | t0001 | g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0001t0001g0076 | a0001 | c0001 | t0001 | g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0001t0001g0077 | a0001 | c0001 | t0001 | g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0001t0001g0078 | a0001 | c0001 | t0001 | g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0001t0001g0079 | a0001 | c0001 | t0001 | g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0001t0001g0080 | a0001 | c0001 | t0001 | g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0001t0001g0084 | a0001 | c0001 | t0001 | g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0001t0001g0085 | a0001 | c0001 | t0001 | g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0001t0001g0086 | a0001 | c0001 | t0001 | g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0001t0001g0089 | a0001 | c0001 | t0001 | g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KY_chr3_134594923_134656022 | KY |
a0001c0001t0001g0091 | a0001 | c0001 | t0001 | g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0001t0001g0092 | a0001 | c0001 | t0001 | g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0001t0001g0093 | a0001 | c0001 | t0001 | g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0001t0001g0097 | a0001 | c0001 | t0001 | g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KY_chr3_134594923_134656022 | KY |
a0001c0001t0001g0099 | a0001 | c0001 | t0001 | g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0001t0001g0100 | a0001 | c0001 | t0001 | g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0001t0001g0101 | a0001 | c0001 | t0001 | g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0001t0001g0108 | a0001 | c0001 | t0001 | g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0001t0001g0109 | a0001 | c0001 | t0001 | g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0001t0001g0116 | a0001 | c0001 | t0001 | g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0001t0001g0128 | a0001 | c0001 | t0001 | g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0001t0001g0129 | a0001 | c0001 | t0001 | g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0001t0001g0130 | a0001 | c0001 | t0001 | g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0001t0001g0131 | a0001 | c0001 | t0001 | g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0001t0001g0132 | a0001 | c0001 | t0001 | g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0001t0001g0133 | a0001 | c0001 | t0001 | g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0001t0001g0134 | a0001 | c0001 | t0001 | g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0001t0001g0135 | a0001 | c0001 | t0001 | g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0001t0001g0137 | a0001 | c0001 | t0001 | g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0001t0001g0138 | a0001 | c0001 | t0001 | g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0001t0001g0142 | a0001 | c0001 | t0001 | g0142 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0001t0001g0143 | a0001 | c0001 | t0001 | g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KY_chr3_134594923_134656022 | KY |
a0001c0001t0001g0144 | a0001 | c0001 | t0001 | g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0001t0001g0150 | a0001 | c0001 | t0001 | g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0001t0001g0151 | a0001 | c0001 | t0001 | g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0001t0001g0155 | a0001 | c0001 | t0001 | g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KY_chr3_134594923_134656022 | KY |
a0001c0001t0001g0156 | a0001 | c0001 | t0001 | g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0001t0001g0157 | a0001 | c0001 | t0001 | g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0001t0001g0161 | a0001 | c0001 | t0001 | g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0001t0001g0162 | a0001 | c0001 | t0001 | g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0001t0001g0165 | a0001 | c0001 | t0001 | g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0001t0001g0167 | a0001 | c0001 | t0001 | g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0001t0001g0168 | a0001 | c0001 | t0001 | g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0001t0001g0177 | a0001 | c0001 | t0001 | g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0001t0001g0178 | a0001 | c0001 | t0001 | g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0001t0001g0179 | a0001 | c0001 | t0001 | g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0001t0001g0180 | a0001 | c0001 | t0001 | g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0001t0001g0181 | a0001 | c0001 | t0001 | g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0001t0001g0182 | a0001 | c0001 | t0001 | g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0001t0001g0186 | a0001 | c0001 | t0001 | g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0001t0001g0187 | a0001 | c0001 | t0001 | g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0001t0001g0188 | a0001 | c0001 | t0001 | g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0001t0001g0192 | a0001 | c0001 | t0001 | g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0001t0001g0193 | a0001 | c0001 | t0001 | g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KY_chr3_134594923_134656022 | KY |
a0001c0001t0001g0194 | a0001 | c0001 | t0001 | g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KY_chr3_134594923_134656022 | KY |
a0001c0001t0001g0197 | a0001 | c0001 | t0001 | g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0001t0001g0198 | a0001 | c0001 | t0001 | g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0001t0001g0204 | a0001 | c0001 | t0001 | g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KY_chr3_134594923_134656022 | KY |
a0001c0001t0001g0205 | a0001 | c0001 | t0001 | g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KY_chr3_134594923_134656022 | KY |
a0001c0001t0003g0013 | a0001 | c0001 | t0003 | g0013 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0001t0003g0063 | a0001 | c0001 | t0003 | g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KY_chr3_134594923_134656022 | KY |
a0001c0001t0003g0065 | a0001 | c0001 | t0003 | g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0001t0003g0066 | a0001 | c0001 | t0003 | g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0001t0003g0069 | a0001 | c0001 | t0003 | g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KY_chr3_134594923_134656022 | KY |
a0001c0001t0003g0096 | a0001 | c0001 | t0003 | g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KY_chr3_134594923_134656022 | KY |
a0001c0001t0003g0183 | a0001 | c0001 | t0003 | g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KY_chr3_134594923_134656022 | KY |
a0001c0001t0003g0184 | a0001 | c0001 | t0003 | g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KY_chr3_134594923_134656022 | KY |
a0001c0001t0005g0019 | a0001 | c0001 | t0005 | g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0001t0005g0020 | a0001 | c0001 | t0005 | g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0001t0005g0110 | a0001 | c0001 | t0005 | g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0001t0005g0139 | a0001 | c0001 | t0005 | g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0001t0005g0140 | a0001 | c0001 | t0005 | g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0001t0005g0141 | a0001 | c0001 | t0005 | g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0001t0005g0154 | a0001 | c0001 | t0005 | g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0001t0005g0176 | a0001 | c0001 | t0005 | g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0001t0008g0053 | a0001 | c0001 | t0008 | g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0001t0008g0054 | a0001 | c0001 | t0008 | g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0001t0008g0055 | a0001 | c0001 | t0008 | g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0001t0008g0175 | a0001 | c0001 | t0008 | g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0001t0012g0169 | a0001 | c0001 | t0012 | g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0001t0012g0171 | a0001 | c0001 | t0012 | g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0001t0013g0189 | a0001 | c0001 | t0013 | g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KY_chr3_134594923_134656022 | KY |
a0001c0001t0013g0190 | a0001 | c0001 | t0013 | g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KY_chr3_134594923_134656022 | KY |
a0001c0001t0014g0052 | a0001 | c0001 | t0014 | g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0001t0022g0136 | a0001 | c0001 | t0022 | g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0001t0023g0191 | a0001 | c0001 | t0023 | g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0001t0024g0196 | a0001 | c0001 | t0024 | g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0001t0025g0170 | a0001 | c0001 | t0025 | g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KY_chr3_134594923_134656022 | KY |
a0001c0001t0027g0148 | a0001 | c0001 | t0027 | g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KY_chr3_134594923_134656022 | KY |
a0001c0001t0029g0195 | a0001 | c0001 | t0029 | g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KY_chr3_134594923_134656022 | KY |
a0001c0002t0002g0006 | a0001 | c0002 | t0002 | g0006 | 0/0 | 4 | 0 | 0 | 1 | 0 | 3 | KY_chr3_134594923_134656022 | KY |
a0001c0002t0002g0012 | a0001 | c0002 | t0002 | g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0002t0002g0029 | a0001 | c0002 | t0002 | g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0002t0002g0037 | a0001 | c0002 | t0002 | g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0002t0002g0049 | a0001 | c0002 | t0002 | g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0002t0002g0050 | a0001 | c0002 | t0002 | g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0002t0002g0051 | a0001 | c0002 | t0002 | g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0002t0002g0057 | a0001 | c0002 | t0002 | g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0002t0002g0058 | a0001 | c0002 | t0002 | g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0002t0002g0059 | a0001 | c0002 | t0002 | g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0002t0002g0062 | a0001 | c0002 | t0002 | g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0002t0002g0067 | a0001 | c0002 | t0002 | g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0002t0002g0090 | a0001 | c0002 | t0002 | g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0002t0002g0094 | a0001 | c0002 | t0002 | g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0002t0002g0095 | a0001 | c0002 | t0002 | g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0002t0002g0102 | a0001 | c0002 | t0002 | g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0002t0002g0103 | a0001 | c0002 | t0002 | g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0002t0002g0107 | a0001 | c0002 | t0002 | g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0002t0002g0111 | a0001 | c0002 | t0002 | g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KY_chr3_134594923_134656022 | KY |
a0001c0002t0002g0112 | a0001 | c0002 | t0002 | g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0002t0002g0113 | a0001 | c0002 | t0002 | g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KY_chr3_134594923_134656022 | KY |
a0001c0002t0002g0114 | a0001 | c0002 | t0002 | g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KY_chr3_134594923_134656022 | KY |
a0001c0002t0002g0117 | a0001 | c0002 | t0002 | g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KY_chr3_134594923_134656022 | KY |
a0001c0002t0002g0118 | a0001 | c0002 | t0002 | g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KY_chr3_134594923_134656022 | KY |
a0001c0002t0002g0119 | a0001 | c0002 | t0002 | g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KY_chr3_134594923_134656022 | KY |
a0001c0002t0002g0120 | a0001 | c0002 | t0002 | g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0002t0002g0121 | a0001 | c0002 | t0002 | g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0002t0002g0122 | a0001 | c0002 | t0002 | g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0002t0002g0123 | a0001 | c0002 | t0002 | g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0002t0002g0124 | a0001 | c0002 | t0002 | g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0002t0002g0125 | a0001 | c0002 | t0002 | g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KY_chr3_134594923_134656022 | KY |
a0001c0002t0002g0126 | a0001 | c0002 | t0002 | g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0002t0002g0127 | a0001 | c0002 | t0002 | g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0002t0002g0152 | a0001 | c0002 | t0002 | g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KY_chr3_134594923_134656022 | KY |
a0001c0002t0002g0163 | a0001 | c0002 | t0002 | g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KY_chr3_134594923_134656022 | KY |
a0001c0002t0002g0164 | a0001 | c0002 | t0002 | g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0002t0002g0172 | a0001 | c0002 | t0002 | g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0002t0002g0201 | a0001 | c0002 | t0002 | g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0002t0004g0004 | a0001 | c0002 | t0004 | g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0002t0004g0034 | a0001 | c0002 | t0004 | g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0002t0004g0035 | a0001 | c0002 | t0004 | g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0002t0004g0038 | a0001 | c0002 | t0004 | g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0002t0004g0041 | a0001 | c0002 | t0004 | g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0002t0004g0042 | a0001 | c0002 | t0004 | g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0002t0004g0043 | a0001 | c0002 | t0004 | g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0002t0004g0044 | a0001 | c0002 | t0004 | g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0002t0004g0045 | a0001 | c0002 | t0004 | g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0002t0004g0087 | a0001 | c0002 | t0004 | g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0002t0015g0088 | a0001 | c0002 | t0015 | g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0002t0018g0106 | a0001 | c0002 | t0018 | g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KY_chr3_134594923_134656022 | KY |
a0001c0002t0019g0098 | a0001 | c0002 | t0019 | g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0002t0020g0039 | a0001 | c0002 | t0020 | g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0002t0021g0060 | a0001 | c0002 | t0021 | g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0002t0030g0239 | a0001 | c0002 | t0030 | g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0003t0002g0007 | a0001 | c0003 | t0002 | g0007 | 0/0 | 4 | 1 | 1 | 0 | 2 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0003t0002g0027 | a0001 | c0003 | t0002 | g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0003t0002g0206 | a0001 | c0003 | t0002 | g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0003t0002g0209 | a0001 | c0003 | t0002 | g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KY_chr3_134594923_134656022 | KY |
a0001c0003t0002g0210 | a0001 | c0003 | t0002 | g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0003t0002g0211 | a0001 | c0003 | t0002 | g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0003t0002g0214 | a0001 | c0003 | t0002 | g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0003t0002g0215 | a0001 | c0003 | t0002 | g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0003t0002g0216 | a0001 | c0003 | t0002 | g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KY_chr3_134594923_134656022 | KY |
a0001c0003t0002g0217 | a0001 | c0003 | t0002 | g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0003t0002g0219 | a0001 | c0003 | t0002 | g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0003t0002g0220 | a0001 | c0003 | t0002 | g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0003t0002g0221 | a0001 | c0003 | t0002 | g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0003t0002g0222 | a0001 | c0003 | t0002 | g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0003t0002g0223 | a0001 | c0003 | t0002 | g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0003t0002g0224 | a0001 | c0003 | t0002 | g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KY_chr3_134594923_134656022 | KY |
a0001c0003t0002g0225 | a0001 | c0003 | t0002 | g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KY_chr3_134594923_134656022 | KY |
a0001c0003t0002g0226 | a0001 | c0003 | t0002 | g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0003t0002g0227 | a0001 | c0003 | t0002 | g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KY_chr3_134594923_134656022 | KY |
a0001c0003t0002g0228 | a0001 | c0003 | t0002 | g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KY_chr3_134594923_134656022 | KY |
a0001c0003t0002g0229 | a0001 | c0003 | t0002 | g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0003t0002g0230 | a0001 | c0003 | t0002 | g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0003t0002g0231 | a0001 | c0003 | t0002 | g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0003t0002g0232 | a0001 | c0003 | t0002 | g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0003t0002g0233 | a0001 | c0003 | t0002 | g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0004t0001g0009 | a0001 | c0004 | t0001 | g0009 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0004t0001g0010 | a0001 | c0004 | t0001 | g0010 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0004t0001g0026 | a0001 | c0004 | t0001 | g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0004t0001g0145 | a0001 | c0004 | t0001 | g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0004t0001g0146 | a0001 | c0004 | t0001 | g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0004t0001g0147 | a0001 | c0004 | t0001 | g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0004t0001g0149 | a0001 | c0004 | t0001 | g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0004t0001g0173 | a0001 | c0004 | t0001 | g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0004t0001g0174 | a0001 | c0004 | t0001 | g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0004t0001g0202 | a0001 | c0004 | t0001 | g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0004t0011g0008 | a0001 | c0004 | t0011 | g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0005t0006g0104 | a0001 | c0005 | t0006 | g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0005t0006g0105 | a0001 | c0005 | t0006 | g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0005t0006g0158 | a0001 | c0005 | t0006 | g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0005t0006g0159 | a0001 | c0005 | t0006 | g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0005t0006g0160 | a0001 | c0005 | t0006 | g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0005t0006g0166 | a0001 | c0005 | t0006 | g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0005t0006g0199 | a0001 | c0005 | t0006 | g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0005t0006g0200 | a0001 | c0005 | t0006 | g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0005t0007g0033 | a0001 | c0005 | t0007 | g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0005t0007g0046 | a0001 | c0005 | t0007 | g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0005t0007g0047 | a0001 | c0005 | t0007 | g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0005t0007g0048 | a0001 | c0005 | t0007 | g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0005t0007g0082 | a0001 | c0005 | t0007 | g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0005t0016g0153 | a0001 | c0005 | t0016 | g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0006t0001g0011 | a0001 | c0006 | t0001 | g0011 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0006t0001g0208 | a0001 | c0006 | t0001 | g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0006t0001g0218 | a0001 | c0006 | t0001 | g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0006t0003g0028 | a0001 | c0006 | t0003 | g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0006t0003g0234 | a0001 | c0006 | t0003 | g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0006t0003g0235 | a0001 | c0006 | t0003 | g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KY_chr3_134594923_134656022 | KY |
a0001c0006t0003g0236 | a0001 | c0006 | t0003 | g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0006t0003g0237 | a0001 | c0006 | t0003 | g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KY_chr3_134594923_134656022 | KY |
a0001c0006t0026g0207 | a0001 | c0006 | t0026 | g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KY_chr3_134594923_134656022 | KY |
a0001c0007t0010g0015 | a0001 | c0007 | t0010 | g0015 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0007t0010g0083 | a0001 | c0007 | t0010 | g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0008t0001g0025 | a0001 | c0008 | t0001 | g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0008t0001g0185 | a0001 | c0008 | t0001 | g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0009t0009g0014 | a0001 | c0009 | t0009 | g0014 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0001c0012t0028g0203 | a0001 | c0012 | t0028 | g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0002c0010t0002g0212 | a0002 | c0010 | t0002 | g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0002c0010t0002g0213 | a0002 | c0010 | t0002 | g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0003c0014t0017g0081 | a0003 | c0014 | t0017 | g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0004c0015t0002g0238 | a0004 | c0015 | t0002 | g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0005c0013t0002g0115 | a0005 | c0013 | t0002 | g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
a0006c0011t0009g0031 | a0006 | c0011 | t0009 | g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KY_chr3_134594923_134656022 | KY |
sampleid | haplotypeid | ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename |
---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0002 | t0002 | g0120 | EUR | GBR | KY_chr3_134594923_134656022 | KY |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0017 | EUR | GBR | KY_chr3_134594923_134656022 | KY |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0116 | EUR | GBR | KY_chr3_134594923_134656022 | KY |
HG00140 | hp2 | a0001 | c0001 | t0003 | g0066 | EUR | GBR | KY_chr3_134594923_134656022 | KY |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0187 | EUR | FIN | KY_chr3_134594923_134656022 | KY |
HG00280 | hp2 | a0001 | c0001 | t0003 | g0065 | EUR | FIN | KY_chr3_134594923_134656022 | KY |
HG00323 | hp1 | a0001 | c0001 | t0003 | g0013 | EUR | FIN | KY_chr3_134594923_134656022 | KY |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0017 | EUR | FIN | KY_chr3_134594923_134656022 | KY |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | CHS | KY_chr3_134594923_134656022 | KY |
HG00544 | hp2 | a0001 | c0002 | t0002 | g0121 | EAS | CHS | KY_chr3_134594923_134656022 | KY |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | KY_chr3_134594923_134656022 | KY |
HG00558 | hp2 | a0001 | c0001 | t0005 | g0176 | EAS | CHS | KY_chr3_134594923_134656022 | KY |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | CHS | KY_chr3_134594923_134656022 | KY |
HG00609 | hp2 | a0001 | c0002 | t0002 | g0006 | EAS | CHS | KY_chr3_134594923_134656022 | KY |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | KY_chr3_134594923_134656022 | KY |
HG00621 | hp2 | a0005 | c0013 | t0002 | g0115 | EAS | CHS | KY_chr3_134594923_134656022 | KY |
HG00642 | hp1 | a0001 | c0006 | t0003 | g0236 | AMR | PUR | KY_chr3_134594923_134656022 | KY |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0182 | AMR | PUR | KY_chr3_134594923_134656022 | KY |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | KY_chr3_134594923_134656022 | KY |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | PUR | KY_chr3_134594923_134656022 | KY |
HG00738 | hp1 | a0001 | c0002 | t0002 | g0057 | AMR | PUR | KY_chr3_134594923_134656022 | KY |
HG00738 | hp2 | a0001 | c0006 | t0001 | g0208 | AMR | PUR | KY_chr3_134594923_134656022 | KY |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | KY_chr3_134594923_134656022 | KY |
HG00741 | hp2 | a0001 | c0006 | t0003 | g0234 | AMR | PUR | KY_chr3_134594923_134656022 | KY |
HG01069 | hp1 | a0001 | c0003 | t0002 | g0217 | AMR | PUR | KY_chr3_134594923_134656022 | KY |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | PUR | KY_chr3_134594923_134656022 | KY |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | KY_chr3_134594923_134656022 | KY |
HG01071 | hp2 | a0001 | c0002 | t0002 | g0067 | AMR | PUR | KY_chr3_134594923_134656022 | KY |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | KY_chr3_134594923_134656022 | KY |
HG01081 | hp2 | a0001 | c0001 | t0023 | g0191 | AMR | PUR | KY_chr3_134594923_134656022 | KY |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0157 | AMR | PUR | KY_chr3_134594923_134656022 | KY |
HG01099 | hp2 | a0001 | c0003 | t0002 | g0230 | AMR | PUR | KY_chr3_134594923_134656022 | KY |
HG01106 | hp1 | a0001 | c0002 | t0002 | g0102 | AMR | PUR | KY_chr3_134594923_134656022 | KY |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0180 | AMR | PUR | KY_chr3_134594923_134656022 | KY |
HG01109 | hp1 | a0001 | c0005 | t0007 | g0033 | AMR | PUR | KY_chr3_134594923_134656022 | KY |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | KY_chr3_134594923_134656022 | KY |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | KY_chr3_134594923_134656022 | KY |
HG01167 | hp2 | a0001 | c0004 | t0001 | g0010 | AMR | PUR | KY_chr3_134594923_134656022 | KY |
HG01168 | hp1 | a0001 | c0003 | t0002 | g0027 | AMR | PUR | KY_chr3_134594923_134656022 | KY |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | KY_chr3_134594923_134656022 | KY |
HG01169 | hp1 | a0001 | c0004 | t0001 | g0010 | AMR | PUR | KY_chr3_134594923_134656022 | KY |
HG01169 | hp2 | a0001 | c0003 | t0002 | g0027 | AMR | PUR | KY_chr3_134594923_134656022 | KY |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | PUR | KY_chr3_134594923_134656022 | KY |
HG01175 | hp2 | a0001 | c0002 | t0002 | g0107 | AMR | PUR | KY_chr3_134594923_134656022 | KY |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | KY_chr3_134594923_134656022 | KY |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0181 | AMR | PUR | KY_chr3_134594923_134656022 | KY |
HG01243 | hp1 | a0001 | c0002 | t0002 | g0123 | AMR | PUR | KY_chr3_134594923_134656022 | KY |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | KY_chr3_134594923_134656022 | KY |
HG01255 | hp1 | a0001 | c0001 | t0005 | g0020 | AMR | CLM | KY_chr3_134594923_134656022 | KY |
HG01255 | hp2 | a0001 | c0002 | t0030 | g0239 | AMR | CLM | KY_chr3_134594923_134656022 | KY |
HG01256 | hp1 | a0001 | c0003 | t0002 | g0229 | AMR | CLM | KY_chr3_134594923_134656022 | KY |
HG01256 | hp2 | a0001 | c0006 | t0003 | g0028 | AMR | CLM | KY_chr3_134594923_134656022 | KY |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | KY_chr3_134594923_134656022 | KY |
HG01257 | hp2 | a0001 | c0001 | t0005 | g0020 | AMR | CLM | KY_chr3_134594923_134656022 | KY |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | KY_chr3_134594923_134656022 | KY |
HG01258 | hp2 | a0001 | c0006 | t0003 | g0028 | AMR | CLM | KY_chr3_134594923_134656022 | KY |
HG01261 | hp1 | a0001 | c0002 | t0002 | g0062 | AMR | CLM | KY_chr3_134594923_134656022 | KY |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0092 | AMR | CLM | KY_chr3_134594923_134656022 | KY |
HG01346 | hp1 | a0001 | c0003 | t0002 | g0007 | AMR | CLM | KY_chr3_134594923_134656022 | KY |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | KY_chr3_134594923_134656022 | KY |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | CLM | KY_chr3_134594923_134656022 | KY |
HG01496 | hp2 | a0001 | c0002 | t0002 | g0095 | AMR | CLM | KY_chr3_134594923_134656022 | KY |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0167 | EUR | IBS | KY_chr3_134594923_134656022 | KY |
HG01516 | hp2 | a0001 | c0006 | t0001 | g0218 | EUR | IBS | KY_chr3_134594923_134656022 | KY |
HG01884 | hp1 | a0003 | c0014 | t0017 | g0081 | AFR | ACB | KY_chr3_134594923_134656022 | KY |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | KY_chr3_134594923_134656022 | KY |
HG01891 | hp1 | a0001 | c0004 | t0011 | g0008 | AFR | ACB | KY_chr3_134594923_134656022 | KY |
HG01891 | hp2 | a0001 | c0001 | t0008 | g0055 | AFR | ACB | KY_chr3_134594923_134656022 | KY |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | PEL | KY_chr3_134594923_134656022 | KY |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | KY_chr3_134594923_134656022 | KY |
HG01952 | hp1 | a0001 | c0001 | t0005 | g0110 | AMR | PEL | KY_chr3_134594923_134656022 | KY |
HG01952 | hp2 | a0001 | c0001 | t0012 | g0171 | AMR | PEL | KY_chr3_134594923_134656022 | KY |
HG01981 | hp1 | a0001 | c0003 | t0002 | g0206 | AMR | PEL | KY_chr3_134594923_134656022 | KY |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0056 | AMR | PEL | KY_chr3_134594923_134656022 | KY |
HG02004 | hp1 | a0001 | c0001 | t0012 | g0169 | AMR | PEL | KY_chr3_134594923_134656022 | KY |
HG02004 | hp2 | a0001 | c0001 | t0005 | g0141 | AMR | PEL | KY_chr3_134594923_134656022 | KY |
HG02055 | hp1 | a0001 | c0007 | t0010 | g0083 | AFR | ACB | KY_chr3_134594923_134656022 | KY |
HG02055 | hp2 | a0001 | c0002 | t0002 | g0112 | AFR | ACB | KY_chr3_134594923_134656022 | KY |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | KY_chr3_134594923_134656022 | KY |
HG02056 | hp2 | a0001 | c0008 | t0001 | g0185 | EAS | KHV | KY_chr3_134594923_134656022 | KY |
HG02074 | hp1 | a0004 | c0015 | t0002 | g0238 | EAS | KHV | KY_chr3_134594923_134656022 | KY |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | KHV | KY_chr3_134594923_134656022 | KY |
HG02145 | hp1 | a0001 | c0003 | t0002 | g0210 | AFR | ACB | KY_chr3_134594923_134656022 | KY |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | ACB | KY_chr3_134594923_134656022 | KY |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | ACB | KY_chr3_134594923_134656022 | KY |
HG02258 | hp2 | a0001 | c0001 | t0008 | g0175 | AFR | ACB | KY_chr3_134594923_134656022 | KY |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PEL | KY_chr3_134594923_134656022 | KY |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | KY_chr3_134594923_134656022 | KY |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | ACB | KY_chr3_134594923_134656022 | KY |
HG02280 | hp2 | a0001 | c0003 | t0002 | g0215 | AFR | ACB | KY_chr3_134594923_134656022 | KY |
HG02300 | hp1 | a0001 | c0001 | t0003 | g0013 | AMR | PEL | KY_chr3_134594923_134656022 | KY |
HG02300 | hp2 | a0001 | c0001 | t0005 | g0140 | AMR | PEL | KY_chr3_134594923_134656022 | KY |
HG02451 | hp1 | a0001 | c0002 | t0019 | g0098 | AFR | ACB | KY_chr3_134594923_134656022 | KY |
HG02451 | hp2 | a0001 | c0001 | t0008 | g0054 | AFR | ACB | KY_chr3_134594923_134656022 | KY |
HG02523 | hp1 | a0001 | c0001 | t0005 | g0139 | EAS | KHV | KY_chr3_134594923_134656022 | KY |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | KHV | KY_chr3_134594923_134656022 | KY |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | GWD | KY_chr3_134594923_134656022 | KY |
HG02572 | hp2 | a0001 | c0005 | t0007 | g0048 | AFR | GWD | KY_chr3_134594923_134656022 | KY |
HG02602 | hp1 | a0001 | c0003 | t0002 | g0209 | SAS | PJL | KY_chr3_134594923_134656022 | KY |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0194 | SAS | PJL | KY_chr3_134594923_134656022 | KY |
HG02615 | hp1 | a0001 | c0003 | t0002 | g0007 | AFR | GWD | KY_chr3_134594923_134656022 | KY |
HG02615 | hp2 | a0001 | c0002 | t0002 | g0058 | AFR | GWD | KY_chr3_134594923_134656022 | KY |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | GWD | KY_chr3_134594923_134656022 | KY |
HG02622 | hp2 | a0001 | c0002 | t0021 | g0060 | AFR | GWD | KY_chr3_134594923_134656022 | KY |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | GWD | KY_chr3_134594923_134656022 | KY |
HG02647 | hp2 | a0001 | c0003 | t0002 | g0214 | AFR | GWD | KY_chr3_134594923_134656022 | KY |
HG02683 | hp1 | a0001 | c0006 | t0026 | g0207 | SAS | PJL | KY_chr3_134594923_134656022 | KY |
HG02683 | hp2 | a0001 | c0002 | t0002 | g0114 | SAS | PJL | KY_chr3_134594923_134656022 | KY |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0089 | SAS | PJL | KY_chr3_134594923_134656022 | KY |
HG02698 | hp2 | a0001 | c0001 | t0029 | g0195 | SAS | PJL | KY_chr3_134594923_134656022 | KY |
HG02717 | hp1 | a0001 | c0003 | t0002 | g0211 | AFR | GWD | KY_chr3_134594923_134656022 | KY |
HG02717 | hp2 | a0001 | c0001 | t0008 | g0053 | AFR | GWD | KY_chr3_134594923_134656022 | KY |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | GWD | KY_chr3_134594923_134656022 | KY |
HG02723 | hp2 | a0001 | c0005 | t0006 | g0166 | AFR | GWD | KY_chr3_134594923_134656022 | KY |
HG02735 | hp1 | a0001 | c0001 | t0013 | g0189 | SAS | PJL | KY_chr3_134594923_134656022 | KY |
HG02735 | hp2 | a0001 | c0003 | t0002 | g0216 | SAS | PJL | KY_chr3_134594923_134656022 | KY |
HG02738 | hp1 | a0001 | c0006 | t0003 | g0235 | SAS | PJL | KY_chr3_134594923_134656022 | KY |
HG02738 | hp2 | a0001 | c0003 | t0002 | g0225 | SAS | PJL | KY_chr3_134594923_134656022 | KY |
HG02809 | hp1 | a0001 | c0002 | t0002 | g0094 | AFR | GWD | KY_chr3_134594923_134656022 | KY |
HG02809 | hp2 | a0001 | c0004 | t0001 | g0146 | AFR | GWD | KY_chr3_134594923_134656022 | KY |
HG02818 | hp1 | a0001 | c0005 | t0016 | g0153 | AFR | GWD | KY_chr3_134594923_134656022 | KY |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | GWD | KY_chr3_134594923_134656022 | KY |
HG02896 | hp1 | a0001 | c0012 | t0028 | g0203 | AFR | GWD | KY_chr3_134594923_134656022 | KY |
HG02896 | hp2 | a0001 | c0003 | t0002 | g0220 | AFR | GWD | KY_chr3_134594923_134656022 | KY |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | GWD | KY_chr3_134594923_134656022 | KY |
HG02897 | hp2 | a0001 | c0003 | t0002 | g0221 | AFR | GWD | KY_chr3_134594923_134656022 | KY |
HG02922 | hp1 | a0001 | c0004 | t0001 | g0202 | AFR | ESN | KY_chr3_134594923_134656022 | KY |
HG02922 | hp2 | a0001 | c0002 | t0004 | g0042 | AFR | ESN | KY_chr3_134594923_134656022 | KY |
HG02970 | hp1 | a0001 | c0002 | t0002 | g0103 | AFR | ESN | KY_chr3_134594923_134656022 | KY |
HG02970 | hp2 | a0001 | c0004 | t0011 | g0008 | AFR | ESN | KY_chr3_134594923_134656022 | KY |
HG02976 | hp1 | a0001 | c0002 | t0002 | g0201 | AFR | ESN | KY_chr3_134594923_134656022 | KY |
HG02976 | hp2 | a0001 | c0002 | t0002 | g0049 | AFR | ESN | KY_chr3_134594923_134656022 | KY |
HG03041 | hp1 | a0001 | c0002 | t0004 | g0045 | AFR | GWD | KY_chr3_134594923_134656022 | KY |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | GWD | KY_chr3_134594923_134656022 | KY |
HG03098 | hp1 | a0001 | c0002 | t0002 | g0172 | AFR | MSL | KY_chr3_134594923_134656022 | KY |
HG03098 | hp2 | a0001 | c0002 | t0002 | g0127 | AFR | MSL | KY_chr3_134594923_134656022 | KY |
HG03139 | hp1 | a0001 | c0005 | t0007 | g0082 | AFR | ESN | KY_chr3_134594923_134656022 | KY |
HG03139 | hp2 | a0001 | c0004 | t0001 | g0026 | AFR | ESN | KY_chr3_134594923_134656022 | KY |
HG03195 | hp1 | a0001 | c0002 | t0002 | g0059 | AFR | ESN | KY_chr3_134594923_134656022 | KY |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | ESN | KY_chr3_134594923_134656022 | KY |
HG03209 | hp1 | a0001 | c0007 | t0010 | g0015 | AFR | MSL | KY_chr3_134594923_134656022 | KY |
HG03209 | hp2 | a0001 | c0004 | t0001 | g0173 | AFR | MSL | KY_chr3_134594923_134656022 | KY |
HG03225 | hp1 | a0001 | c0004 | t0001 | g0009 | AFR | MSL | KY_chr3_134594923_134656022 | KY |
HG03225 | hp2 | a0001 | c0006 | t0001 | g0011 | AFR | MSL | KY_chr3_134594923_134656022 | KY |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0204 | SAS | PJL | KY_chr3_134594923_134656022 | KY |
HG03239 | hp2 | a0001 | c0001 | t0003 | g0069 | SAS | PJL | KY_chr3_134594923_134656022 | KY |
HG03453 | hp1 | a0001 | c0009 | t0009 | g0014 | AFR | MSL | KY_chr3_134594923_134656022 | KY |
HG03453 | hp2 | a0001 | c0004 | t0011 | g0008 | AFR | MSL | KY_chr3_134594923_134656022 | KY |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | MSL | KY_chr3_134594923_134656022 | KY |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | MSL | KY_chr3_134594923_134656022 | KY |
HG03490 | hp1 | a0001 | c0002 | t0002 | g0113 | SAS | PJL | KY_chr3_134594923_134656022 | KY |
HG03490 | hp2 | a0001 | c0002 | t0002 | g0006 | SAS | PJL | KY_chr3_134594923_134656022 | KY |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0097 | SAS | PJL | KY_chr3_134594923_134656022 | KY |
HG03491 | hp2 | a0001 | c0001 | t0003 | g0184 | SAS | PJL | KY_chr3_134594923_134656022 | KY |
HG03492 | hp1 | a0001 | c0002 | t0002 | g0006 | SAS | PJL | KY_chr3_134594923_134656022 | KY |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | KY_chr3_134594923_134656022 | KY |
HG03516 | hp1 | a0001 | c0004 | t0001 | g0174 | AFR | ESN | KY_chr3_134594923_134656022 | KY |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | ESN | KY_chr3_134594923_134656022 | KY |
HG03540 | hp1 | a0001 | c0002 | t0002 | g0012 | AFR | GWD | KY_chr3_134594923_134656022 | KY |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | GWD | KY_chr3_134594923_134656022 | KY |
HG03579 | hp1 | a0001 | c0004 | t0001 | g0009 | AFR | MSL | KY_chr3_134594923_134656022 | KY |
HG03579 | hp2 | a0001 | c0005 | t0007 | g0046 | AFR | MSL | KY_chr3_134594923_134656022 | KY |
HG03654 | hp1 | a0001 | c0002 | t0002 | g0152 | SAS | PJL | KY_chr3_134594923_134656022 | KY |
HG03654 | hp2 | a0001 | c0003 | t0002 | g0224 | SAS | PJL | KY_chr3_134594923_134656022 | KY |
HG03669 | hp1 | a0001 | c0006 | t0003 | g0237 | SAS | PJL | KY_chr3_134594923_134656022 | KY |
HG03669 | hp2 | a0001 | c0002 | t0002 | g0163 | SAS | PJL | KY_chr3_134594923_134656022 | KY |
HG03688 | hp1 | a0001 | c0003 | t0002 | g0228 | SAS | STU | KY_chr3_134594923_134656022 | KY |
HG03688 | hp2 | a0001 | c0002 | t0002 | g0118 | SAS | STU | KY_chr3_134594923_134656022 | KY |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0205 | SAS | PJL | KY_chr3_134594923_134656022 | KY |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | KY_chr3_134594923_134656022 | KY |
HG03710 | hp1 | a0001 | c0003 | t0002 | g0227 | SAS | PJL | KY_chr3_134594923_134656022 | KY |
HG03710 | hp2 | a0001 | c0002 | t0002 | g0117 | SAS | PJL | KY_chr3_134594923_134656022 | KY |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0023 | SAS | BEB | KY_chr3_134594923_134656022 | KY |
HG03831 | hp2 | a0001 | c0001 | t0027 | g0148 | SAS | BEB | KY_chr3_134594923_134656022 | KY |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0155 | SAS | BEB | KY_chr3_134594923_134656022 | KY |
HG03834 | hp2 | a0001 | c0002 | t0018 | g0106 | SAS | BEB | KY_chr3_134594923_134656022 | KY |
HG03942 | hp1 | a0001 | c0002 | t0002 | g0111 | SAS | BEB | KY_chr3_134594923_134656022 | KY |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0193 | SAS | BEB | KY_chr3_134594923_134656022 | KY |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0143 | SAS | STU | KY_chr3_134594923_134656022 | KY |
HG04115 | hp2 | a0001 | c0002 | t0002 | g0006 | SAS | STU | KY_chr3_134594923_134656022 | KY |
HG04184 | hp1 | a0001 | c0002 | t0002 | g0125 | SAS | BEB | KY_chr3_134594923_134656022 | KY |
HG04184 | hp2 | a0001 | c0001 | t0025 | g0170 | SAS | BEB | KY_chr3_134594923_134656022 | KY |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0023 | SAS | STU | KY_chr3_134594923_134656022 | KY |
HG04199 | hp2 | a0001 | c0001 | t0003 | g0183 | SAS | STU | KY_chr3_134594923_134656022 | KY |
HG04204 | hp1 | a0001 | c0001 | t0013 | g0190 | SAS | STU | KY_chr3_134594923_134656022 | KY |
HG04204 | hp2 | a0001 | c0002 | t0002 | g0119 | SAS | STU | KY_chr3_134594923_134656022 | KY |
NA18522 | hp1 | a0001 | c0004 | t0001 | g0009 | AFR | YRI | KY_chr3_134594923_134656022 | KY |
NA18522 | hp2 | a0001 | c0002 | t0002 | g0012 | AFR | YRI | KY_chr3_134594923_134656022 | KY |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | CHB | KY_chr3_134594923_134656022 | KY |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | CHB | KY_chr3_134594923_134656022 | KY |
NA18906 | hp1 | a0001 | c0004 | t0001 | g0149 | AFR | YRI | KY_chr3_134594923_134656022 | KY |
NA18906 | hp2 | a0001 | c0005 | t0007 | g0047 | AFR | YRI | KY_chr3_134594923_134656022 | KY |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | KY_chr3_134594923_134656022 | KY |
NA18939 | hp2 | a0002 | c0010 | t0002 | g0212 | EAS | JPT | KY_chr3_134594923_134656022 | KY |
NA18941 | hp1 | a0001 | c0002 | t0020 | g0039 | EAS | JPT | KY_chr3_134594923_134656022 | KY |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | KY_chr3_134594923_134656022 | KY |
NA18951 | hp1 | a0001 | c0005 | t0006 | g0105 | EAS | JPT | KY_chr3_134594923_134656022 | KY |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | KY_chr3_134594923_134656022 | KY |
NA18956 | hp1 | a0001 | c0003 | t0002 | g0232 | EAS | JPT | KY_chr3_134594923_134656022 | KY |
NA18956 | hp2 | a0001 | c0008 | t0001 | g0025 | EAS | JPT | KY_chr3_134594923_134656022 | KY |
NA18959 | hp1 | a0001 | c0001 | t0005 | g0154 | EAS | JPT | KY_chr3_134594923_134656022 | KY |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | KY_chr3_134594923_134656022 | KY |
NA18960 | hp1 | a0001 | c0002 | t0004 | g0087 | EAS | JPT | KY_chr3_134594923_134656022 | KY |
NA18960 | hp2 | a0001 | c0005 | t0006 | g0160 | EAS | JPT | KY_chr3_134594923_134656022 | KY |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | KY_chr3_134594923_134656022 | KY |
NA18965 | hp2 | a0001 | c0002 | t0004 | g0044 | EAS | JPT | KY_chr3_134594923_134656022 | KY |
NA18967 | hp1 | a0001 | c0002 | t0004 | g0035 | EAS | JPT | KY_chr3_134594923_134656022 | KY |
NA18967 | hp2 | a0001 | c0005 | t0006 | g0199 | EAS | JPT | KY_chr3_134594923_134656022 | KY |
NA18968 | hp1 | a0001 | c0002 | t0015 | g0088 | EAS | JPT | KY_chr3_134594923_134656022 | KY |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | KY_chr3_134594923_134656022 | KY |
NA18969 | hp1 | a0001 | c0005 | t0006 | g0158 | EAS | JPT | KY_chr3_134594923_134656022 | KY |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | KY_chr3_134594923_134656022 | KY |
NA18981 | hp1 | a0001 | c0002 | t0004 | g0004 | EAS | JPT | KY_chr3_134594923_134656022 | KY |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | KY_chr3_134594923_134656022 | KY |
NA18982 | hp1 | a0001 | c0002 | t0004 | g0004 | EAS | JPT | KY_chr3_134594923_134656022 | KY |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | KY_chr3_134594923_134656022 | KY |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | KY_chr3_134594923_134656022 | KY |
NA18984 | hp2 | a0001 | c0005 | t0006 | g0104 | EAS | JPT | KY_chr3_134594923_134656022 | KY |
NA18989 | hp1 | a0001 | c0003 | t0002 | g0233 | EAS | JPT | KY_chr3_134594923_134656022 | KY |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | KY_chr3_134594923_134656022 | KY |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | KY_chr3_134594923_134656022 | KY |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | KY_chr3_134594923_134656022 | KY |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | KY_chr3_134594923_134656022 | KY |
NA18999 | hp2 | a0001 | c0003 | t0002 | g0226 | EAS | JPT | KY_chr3_134594923_134656022 | KY |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | KY_chr3_134594923_134656022 | KY |
NA19003 | hp2 | a0001 | c0002 | t0004 | g0038 | EAS | JPT | KY_chr3_134594923_134656022 | KY |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | KY_chr3_134594923_134656022 | KY |
NA19007 | hp2 | a0001 | c0002 | t0002 | g0126 | EAS | JPT | KY_chr3_134594923_134656022 | KY |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | KY_chr3_134594923_134656022 | KY |
NA19010 | hp2 | a0001 | c0008 | t0001 | g0025 | EAS | JPT | KY_chr3_134594923_134656022 | KY |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | KY_chr3_134594923_134656022 | KY |
NA19012 | hp2 | a0001 | c0002 | t0004 | g0041 | EAS | JPT | KY_chr3_134594923_134656022 | KY |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | LWK | KY_chr3_134594923_134656022 | KY |
NA19030 | hp2 | a0006 | c0011 | t0009 | g0031 | AFR | LWK | KY_chr3_134594923_134656022 | KY |
NA19043 | hp1 | a0001 | c0001 | t0014 | g0052 | AFR | LWK | KY_chr3_134594923_134656022 | KY |
NA19043 | hp2 | a0001 | c0004 | t0001 | g0147 | AFR | LWK | KY_chr3_134594923_134656022 | KY |
NA19054 | hp1 | a0001 | c0002 | t0004 | g0004 | EAS | JPT | KY_chr3_134594923_134656022 | KY |
NA19054 | hp2 | a0001 | c0001 | t0005 | g0019 | EAS | JPT | KY_chr3_134594923_134656022 | KY |
NA19056 | hp1 | a0001 | c0002 | t0002 | g0164 | EAS | JPT | KY_chr3_134594923_134656022 | KY |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | KY_chr3_134594923_134656022 | KY |
NA19057 | hp1 | a0001 | c0005 | t0006 | g0200 | EAS | JPT | KY_chr3_134594923_134656022 | KY |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | KY_chr3_134594923_134656022 | KY |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | KY_chr3_134594923_134656022 | KY |
NA19064 | hp2 | a0001 | c0003 | t0002 | g0219 | EAS | JPT | KY_chr3_134594923_134656022 | KY |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | KY_chr3_134594923_134656022 | KY |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | KY_chr3_134594923_134656022 | KY |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | KY_chr3_134594923_134656022 | KY |
NA19066 | hp2 | a0001 | c0003 | t0002 | g0223 | EAS | JPT | KY_chr3_134594923_134656022 | KY |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | KY_chr3_134594923_134656022 | KY |
NA19067 | hp2 | a0001 | c0002 | t0002 | g0090 | EAS | JPT | KY_chr3_134594923_134656022 | KY |
NA19068 | hp1 | a0002 | c0010 | t0002 | g0213 | EAS | JPT | KY_chr3_134594923_134656022 | KY |
NA19068 | hp2 | a0001 | c0001 | t0005 | g0019 | EAS | JPT | KY_chr3_134594923_134656022 | KY |
NA19074 | hp1 | a0001 | c0003 | t0002 | g0222 | EAS | JPT | KY_chr3_134594923_134656022 | KY |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | KY_chr3_134594923_134656022 | KY |
NA19076 | hp1 | a0001 | c0003 | t0002 | g0231 | EAS | JPT | KY_chr3_134594923_134656022 | KY |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | KY_chr3_134594923_134656022 | KY |
NA19077 | hp1 | a0001 | c0001 | t0024 | g0196 | EAS | JPT | KY_chr3_134594923_134656022 | KY |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | KY_chr3_134594923_134656022 | KY |
NA19082 | hp1 | a0001 | c0001 | t0022 | g0136 | EAS | JPT | KY_chr3_134594923_134656022 | KY |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | KY_chr3_134594923_134656022 | KY |
NA19084 | hp1 | a0001 | c0002 | t0004 | g0004 | EAS | JPT | KY_chr3_134594923_134656022 | KY |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | KY_chr3_134594923_134656022 | KY |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | KY_chr3_134594923_134656022 | KY |
NA19090 | hp2 | a0001 | c0002 | t0004 | g0043 | EAS | JPT | KY_chr3_134594923_134656022 | KY |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | KY_chr3_134594923_134656022 | KY |
NA19091 | hp2 | a0001 | c0005 | t0006 | g0159 | EAS | JPT | KY_chr3_134594923_134656022 | KY |
NA19240 | hp1 | a0001 | c0002 | t0002 | g0037 | AFR | YRI | KY_chr3_134594923_134656022 | KY |
NA19240 | hp2 | a0001 | c0006 | t0001 | g0011 | AFR | YRI | KY_chr3_134594923_134656022 | KY |
NA20129 | hp1 | a0001 | c0006 | t0001 | g0011 | AFR | ASW | KY_chr3_134594923_134656022 | KY |
NA20129 | hp2 | a0001 | c0004 | t0001 | g0145 | AFR | ASW | KY_chr3_134594923_134656022 | KY |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0198 | EUR | TSI | KY_chr3_134594923_134656022 | KY |
NA20752 | hp2 | a0001 | c0003 | t0002 | g0007 | EUR | TSI | KY_chr3_134594923_134656022 | KY |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | KY_chr3_134594923_134656022 | KY |
NA20805 | hp2 | a0001 | c0003 | t0002 | g0007 | EUR | TSI | KY_chr3_134594923_134656022 | KY |
NA20905 | hp1 | a0001 | c0001 | t0003 | g0063 | SAS | GIH | KY_chr3_134594923_134656022 | KY |
NA20905 | hp2 | a0001 | c0001 | t0003 | g0096 | SAS | GIH | KY_chr3_134594923_134656022 | KY |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | KY_chr3_134594923_134656022 | KY |
HG01123 | hp2 | a0001 | c0007 | t0010 | g0015 | AMR | CLM | KY_chr3_134594923_134656022 | KY |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | ACB | KY_chr3_134594923_134656022 | KY |
HG02109 | hp2 | a0001 | c0002 | t0002 | g0124 | AFR | ACB | KY_chr3_134594923_134656022 | KY |
HG02559 | hp1 | a0001 | c0002 | t0002 | g0051 | AFR | ACB | KY_chr3_134594923_134656022 | KY |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | ACB | KY_chr3_134594923_134656022 | KY |
HG03471 | hp1 | a0001 | c0004 | t0001 | g0026 | AFR | MSL | KY_chr3_134594923_134656022 | KY |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | MSL | KY_chr3_134594923_134656022 | KY |
HG06807 | hp1 | a0001 | c0004 | t0001 | g0010 | AFR | USA | KY_chr3_134594923_134656022 | KY |
HG06807 | hp2 | a0001 | c0002 | t0002 | g0050 | AFR | USA | KY_chr3_134594923_134656022 | KY |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | KY_chr3_134594923_134656022 | KY |
NA18955 | hp2 | a0001 | c0002 | t0004 | g0034 | EAS | JPT | KY_chr3_134594923_134656022 | KY |
NA20300 | hp1 | a0001 | c0002 | t0002 | g0122 | AFR | USA | KY_chr3_134594923_134656022 | KY |
NA20300 | hp2 | a0001 | c0002 | t0002 | g0029 | AFR | USA | KY_chr3_134594923_134656022 | KY |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | LWK | KY_chr3_134594923_134656022 | KY |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | LWK | KY_chr3_134594923_134656022 | KY |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0142 | REF | REF | KY_chr3_134594923_134656022 | KY |
homoSapiens_grch38 | hp1 | a0001 | c0009 | t0009 | g0014 | REF | REF | KY_chr3_134594923_134656022 | KY |
chr:pos | ref | alt | # # of ahapid:amio-acid(protein) level
|
ahapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:134603788
|
G | A | 1 | a0005 | 1 | HG00621.hp2 | missense_variant | MODERATE | c.1777C>T | p.Arg593Trp | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 11/11 | 1839/5704 | 1777/1986 | 593/661 | chr3 | 134603788 | ||
chr3:134603805
|
C | G | 1 | a0004 | 1 | HG02074.hp1 | missense_variant | MODERATE | c.1760G>C | p.Gly587Ala | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 11/11 | 1822/5704 | 1760/1986 | 587/661 | chr3 | 134603805 | ||
chr3:134610219
|
G | C | 1 | a0003 | 1 | HG01884.hp1 | missense_variant | MODERATE | c.875C>G | p.Thr292Ser | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 9/11 | 937/5704 | 875/1986 | 292/661 | chr3 | 134610219 | ||
chr3:134610363
|
A | G | 1 | a0002 | 2 | NA18939.hp2 NA19068.hp1 |
missense_variant | MODERATE | c.731T>C | p.Met244Thr | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 9/11 | 793/5704 | 731/1986 | 244/661 | chr3 | 134610363 | ||
chr3:134620833
|
C | T | 1 | a0006 | 1 | NA19030.hp2 | missense_variant | MODERATE | c.508G>A | p.Glu170Lys | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 7/11 | 570/5704 | 508/1986 | 170/661 | chr3 | 134620833 |
chr:pos | ref | alt | # # of chapid
|
chapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:134603672
|
T | C | 2 | a0001c0004a0001c0012 | 19 | HG01167.hp2 HG01169.hp1 HG01891.hp1 others(16): Show |
synonymous_variant | LOW | c.1893A>G | p.Thr631Thr | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 11/11 | 1955/5704 | 1893/1986 | 631/661 | chr3 | 134603672 | ||
chr3:134603831
|
G | A | 1 | a0001c0012 | 1 | HG02896.hp1 | synonymous_variant | LOW | c.1734C>T | p.Asp578Asp | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 11/11 | 1796/5704 | 1734/1986 | 578/661 | chr3 | 134603831 | ||
chr3:134603900
|
A | G | 5 | a0001c0001a0001c0004a0001c0006others(2): Show | 179 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(176): Show |
synonymous_variant | LOW | c.1665T>C | p.Leu555Leu | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 11/11 | 1727/5704 | 1665/1986 | 555/661 | chr3 | 134603900 | ||
chr3:134603972
|
G | C | 6 | a0001c0002a0001c0003a0001c0007others(3): Show | 97 | HG00099.hp1 HG00544.hp2 HG00609.hp2 others(94): Show |
synonymous_variant | LOW | c.1593C>G | p.Gly531Gly | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 11/11 | 1655/5704 | 1593/1986 | 531/661 | chr3 | 134603972 | ||
chr3:134604002
|
G | A | 1 | a0001c0007 | 3 | HG01123.hp2 HG02055.hp1 HG03209.hp1 |
synonymous_variant | LOW | c.1563C>T | p.Thr521Thr | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 11/11 | 1625/5704 | 1563/1986 | 521/661 | chr3 | 134604002 | ||
chr3:134604074
|
G | A | 1 | a0001c0008 | 3 | HG02056.hp2 NA18956.hp2 NA19010.hp2 |
synonymous_variant | LOW | c.1491C>T | p.His497His | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 11/11 | 1553/5704 | 1491/1986 | 497/661 | chr3 | 134604074 | ||
chr3:134604314
|
A | G | 13 | a0001c0001a0001c0002a0001c0003others(10): Show | 291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
synonymous_variant | LOW | c.1251T>C | p.Phe417Phe | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 11/11 | 1313/5704 | 1251/1986 | 417/661 | chr3 | 134604314 | ||
chr3:134650874
|
C | A | 4 | a0001c0003a0001c0006a0002c0010others(1): Show | 44 | HG00642.hp1 HG00738.hp2 HG00741.hp2 others(41): Show |
synonymous_variant | LOW | c.87G>T | p.Thr29Thr | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 1/11 | 149/5704 | 87/1986 | 29/661 | chr3 | 134650874 |
chr:pos | ref | alt | # # of thapid:transcript level
|
thapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:134600000
|
G | A | 1 | a0003c0014t0017 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3579C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 11/11 | 3579 | chr3 | 134600000 | |||||
chr3:134600007
|
A | G | 3 | a0001c0002t0004a0001c0002t0015a0001c0002t0020 | 15 | HG02922.hp2 HG03041.hp1 NA18941.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*3572T>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 11/11 | 3572 | chr3 | 134600007 | |||||
chr3:134600130
|
G | A | 1 | a0001c0001t0025 | 1 | HG04184.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3449C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 11/11 | 3449 | chr3 | 134600130 | |||||
chr3:134600606
|
C | G | 21 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(18): Show | 180 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(177): Show |
3_prime_UTR_variant | MODIFIER | c.*2973G>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 11/11 | 2973 | chr3 | 134600606 | |||||
chr3:134600613
|
C | T | 20 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(17): Show | 176 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(173): Show |
3_prime_UTR_variant | MODIFIER | c.*2966G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 11/11 | 2966 | chr3 | 134600613 | |||||
chr3:134600715
|
T | C | 1 | a0001c0001t0008 | 4 | HG01891.hp2 HG02258.hp2 HG02451.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2864A>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 11/11 | 2864 | chr3 | 134600715 | |||||
chr3:134600881
|
T | A | 21 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(18): Show | 180 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(177): Show |
3_prime_UTR_variant | MODIFIER | c.*2698A>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 11/11 | 2698 | chr3 | 134600881 | |||||
chr3:134600908
|
C | G | 1 | a0001c0001t0005 | 10 | HG00558.hp2 HG01255.hp1 HG01257.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2671G>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 11/11 | 2671 | chr3 | 134600908 | |||||
chr3:134601018
|
C | T | 1 | a0001c0001t0022 | 1 | NA19082.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2561G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 11/11 | 2561 | chr3 | 134601018 | |||||
chr3:134601262
|
GA | G | 21 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(18): Show | 180 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(177): Show |
3_prime_UTR_variant | MODIFIER | c.*2316delT | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 11/11 | 2316 | chr3 | 134601262 | |||||
chr3:134601451
|
T | C | 1 | a0001c0001t0023 | 1 | HG01081.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2128A>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 11/11 | 2128 | chr3 | 134601451 | |||||
chr3:134601462
|
C | T | 1 | a0001c0001t0014 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2117G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 11/11 | 2117 | chr3 | 134601462 | |||||
chr3:134601540
|
C | T | 1 | a0001c0001t0012 | 2 | HG01952.hp2 HG02004.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2039G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 11/11 | 2039 | chr3 | 134601540 | |||||
chr3:134601657
|
G | A | 1 | a0001c0001t0013 | 2 | HG02735.hp1 HG04204.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1922C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 11/11 | 1922 | chr3 | 134601657 | |||||
chr3:134601737
|
C | T | 1 | a0001c0002t0019 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1842G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 11/11 | 1842 | chr3 | 134601737 | |||||
chr3:134601923
|
A | G | 21 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(18): Show | 180 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(177): Show |
3_prime_UTR_variant | MODIFIER | c.*1656T>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 11/11 | 1656 | chr3 | 134601923 | |||||
chr3:134601983
|
T | TTACCAAG others(4): Show |
36 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(33): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
3_prime_UTR_variant | MODIFIER | c.*1595_*1596insGTGC others(7): Show |
KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 11/11 | 1595 | chr3 | 134601983 | |||||
chr3:134602161
|
C | T | 3 | a0001c0001t0003a0001c0001t0027a0001c0006t0003 | 16 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1418G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 11/11 | 1418 | chr3 | 134602161 | |||||
chr3:134602220
|
CAGTGGCC others(4): Show |
C | 1 | a0001c0002t0020 | 1 | NA18941.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1348_*1358delACAT others(7): Show |
KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 11/11 | 1348 | chr3 | 134602220 | |||||
chr3:134602229
|
T | C | 1 | a0001c0005t0016 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1350A>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 11/11 | 1350 | chr3 | 134602229 | |||||
chr3:134602240
|
T | A | 1 | a0001c0002t0020 | 1 | NA18941.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1339A>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 11/11 | 1339 | chr3 | 134602240 | |||||
chr3:134602244
|
G | A | 1 | a0001c0002t0020 | 1 | NA18941.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1335C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 11/11 | 1335 | chr3 | 134602244 | |||||
chr3:134602245
|
C | T | 1 | a0001c0002t0020 | 1 | NA18941.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1334G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 11/11 | 1334 | chr3 | 134602245 | |||||
chr3:134602247
|
T | C | 1 | a0001c0002t0020 | 1 | NA18941.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1332A>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 11/11 | 1332 | chr3 | 134602247 | |||||
chr3:134602249
|
T | G | 1 | a0001c0002t0020 | 1 | NA18941.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1330A>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 11/11 | 1330 | chr3 | 134602249 | |||||
chr3:134602253
|
T | A | 1 | a0001c0002t0020 | 1 | NA18941.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1326A>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 11/11 | 1326 | chr3 | 134602253 | |||||
chr3:134602255
|
T | A | 1 | a0001c0002t0020 | 1 | NA18941.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1324A>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 11/11 | 1324 | chr3 | 134602255 | |||||
chr3:134602256
|
T | G | 1 | a0001c0002t0020 | 1 | NA18941.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1323A>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 11/11 | 1323 | chr3 | 134602256 | |||||
chr3:134602280
|
T | G | 1 | a0001c0005t0007 | 5 | HG01109.hp1 HG02572.hp2 HG03139.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1299A>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 11/11 | 1299 | chr3 | 134602280 | |||||
chr3:134602288
|
G | A | 1 | a0001c0004t0011 | 3 | HG01891.hp1 HG02970.hp2 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1291C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 11/11 | 1291 | chr3 | 134602288 | |||||
chr3:134602310
|
G | C | 1 | a0001c0002t0020 | 1 | NA18941.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1269C>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 11/11 | 1269 | chr3 | 134602310 | |||||
chr3:134602313
|
G | T | 1 | a0001c0002t0020 | 1 | NA18941.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1266C>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 11/11 | 1266 | chr3 | 134602313 | |||||
chr3:134602314
|
C | G | 1 | a0001c0002t0020 | 1 | NA18941.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1265G>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 11/11 | 1265 | chr3 | 134602314 | |||||
chr3:134602315
|
G | C | 1 | a0001c0002t0020 | 1 | NA18941.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1264C>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 11/11 | 1264 | chr3 | 134602315 | |||||
chr3:134602317
|
T | C | 1 | a0001c0002t0020 | 1 | NA18941.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1262A>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 11/11 | 1262 | chr3 | 134602317 | |||||
chr3:134602318
|
G | C | 1 | a0001c0002t0020 | 1 | NA18941.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1261C>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 11/11 | 1261 | chr3 | 134602318 | |||||
chr3:134602572
|
G | A | 2 | a0001c0002t0021a0001c0007t0010 | 4 | HG01123.hp2 HG02055.hp1 HG02622.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1007C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 11/11 | 1007 | chr3 | 134602572 | |||||
chr3:134602681
|
T | C | 20 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(17): Show | 179 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(176): Show |
3_prime_UTR_variant | MODIFIER | c.*898A>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 11/11 | 898 | chr3 | 134602681 | |||||
chr3:134602738
|
A | C | 2 | a0001c0005t0006a0001c0005t0016 | 9 | HG02723.hp2 HG02818.hp1 NA18951.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*841T>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 11/11 | 841 | chr3 | 134602738 | |||||
chr3:134602757
|
G | A | 1 | a0001c0002t0021 | 1 | HG02622.hp2 | 3_prime_UTR_variant | MODIFIER | c.*822C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 11/11 | 822 | chr3 | 134602757 | |||||
chr3:134602824
|
G | C | 1 | a0001c0001t0024 | 1 | NA19077.hp1 | 3_prime_UTR_variant | MODIFIER | c.*755C>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 11/11 | 755 | chr3 | 134602824 | |||||
chr3:134602827
|
T | A | 19 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(16): Show | 175 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(172): Show |
3_prime_UTR_variant | MODIFIER | c.*752A>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 11/11 | 752 | chr3 | 134602827 | |||||
chr3:134602909
|
C | T | 1 | a0001c0002t0015 | 1 | NA18968.hp1 | 3_prime_UTR_variant | MODIFIER | c.*670G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 11/11 | 670 | chr3 | 134602909 | |||||
chr3:134602936
|
G | C | 1 | a0001c0001t0025 | 1 | HG04184.hp2 | 3_prime_UTR_variant | MODIFIER | c.*643C>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 11/11 | 643 | chr3 | 134602936 | |||||
chr3:134602966
|
G | A | 20 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(17): Show | 179 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(176): Show |
3_prime_UTR_variant | MODIFIER | c.*613C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 11/11 | 613 | chr3 | 134602966 | |||||
chr3:134602986
|
T | C | 1 | a0001c0006t0026 | 1 | HG02683.hp1 | 3_prime_UTR_variant | MODIFIER | c.*593A>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 11/11 | 593 | chr3 | 134602986 | |||||
chr3:134603166
|
A | T | 1 | a0001c0001t0029 | 1 | HG02698.hp2 | 3_prime_UTR_variant | MODIFIER | c.*413T>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 11/11 | 413 | chr3 | 134603166 | |||||
chr3:134603207
|
T | C | 1 | a0001c0001t0027 | 1 | HG03831.hp2 | 3_prime_UTR_variant | MODIFIER | c.*372A>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 11/11 | 372 | chr3 | 134603207 | |||||
chr3:134603271
|
G | A | 20 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(17): Show | 179 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(176): Show |
3_prime_UTR_variant | MODIFIER | c.*308C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 11/11 | 308 | chr3 | 134603271 | |||||
chr3:134603321
|
C | A | 20 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(17): Show | 179 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(176): Show |
3_prime_UTR_variant | MODIFIER | c.*258G>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 11/11 | 258 | chr3 | 134603321 | |||||
chr3:134603375
|
C | G | 1 | a0001c0005t0007 | 5 | HG01109.hp1 HG02572.hp2 HG03139.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*204G>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 11/11 | 204 | chr3 | 134603375 | |||||
chr3:134603377
|
C | A | 1 | a0001c0012t0028 | 1 | HG02896.hp1 | 3_prime_UTR_variant | MODIFIER | c.*202G>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 11/11 | 202 | chr3 | 134603377 | |||||
chr3:134603404
|
G | C | 1 | a0001c0002t0015 | 1 | NA18968.hp1 | 3_prime_UTR_variant | MODIFIER | c.*175C>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 11/11 | 175 | chr3 | 134603404 | |||||
chr3:134603405
|
C | G | 1 | a0001c0002t0015 | 1 | NA18968.hp1 | 3_prime_UTR_variant | MODIFIER | c.*174G>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 11/11 | 174 | chr3 | 134603405 | |||||
chr3:134603442
|
G | A | 1 | a0001c0001t0029 | 1 | HG02698.hp2 | 3_prime_UTR_variant | MODIFIER | c.*137C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 11/11 | 137 | chr3 | 134603442 | |||||
chr3:134603578
|
C | T | 1 | a0001c0001t0014 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 11/11 | 1 | chr3 | 134603578 | |||||
chr3:134651016
|
T | C | 1 | a0001c0002t0030 | 1 | HG01255.hp2 | 5_prime_UTR_variant | MODIFIER | c.-56A>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 1/11 | 56 | chr3 | 134651016 |
chr:pos | ref | alt | # # of ghapid:genebody level
|
ghapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:134604597
|
C | T | 1 | a0001c0001t0014g0052 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1091-123G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 10/10 | chr3 | 134604597 | ||||||
chr3:134604680
|
G | A | 137 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(134): Show | 179 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.1091-206C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 10/10 | chr3 | 134604680 | ||||||
chr3:134604733
|
C | T | 1 | a0001c0001t0001g0061 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1091-259G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 10/10 | chr3 | 134604733 | ||||||
chr3:134604779
|
C | G | 4 | a0001c0001t0008g0053a0001c0001t0008g0054a0001c0001t0008g0055others(1): Show | 4 | HG01891.hp2 HG02258.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.1091-305G>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 10/10 | chr3 | 134604779 | ||||||
chr3:134604868
|
T | C | 1 | a0001c0005t0006g0159 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1091-394A>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 10/10 | chr3 | 134604868 | ||||||
chr3:134604977
|
T | C | 137 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(134): Show | 179 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.1091-503A>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 10/10 | chr3 | 134604977 | ||||||
chr3:134605042
|
G | A | 1 | a0001c0001t0008g0053 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1091-568C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 10/10 | chr3 | 134605042 | ||||||
chr3:134605182
|
G | C | 137 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(134): Show | 179 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.1091-708C>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 10/10 | chr3 | 134605182 | ||||||
chr3:134605212
|
G | A | 2 | a0001c0005t0007g0046a0001c0005t0007g0048 | 2 | HG02572.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1091-738C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 10/10 | chr3 | 134605212 | ||||||
chr3:134605267
|
G | A | 2 | a0001c0002t0002g0006a0001c0002t0002g0152 | 5 | HG00609.hp2 HG03490.hp2 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.1091-793C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 10/10 | chr3 | 134605267 | ||||||
chr3:134605378
|
G | A | 9 | a0001c0003t0002g0219a0001c0003t0002g0222a0001c0003t0002g0223others(6): Show | 9 | NA18939.hp2 NA18956.hp1 NA18989.hp1 others(6): Show |
intron_variant | MODIFIER | c.1091-904C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 10/10 | chr3 | 134605378 | ||||||
chr3:134605435
|
G | A | 1 | a0001c0001t0001g0143 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1091-961C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 10/10 | chr3 | 134605435 | ||||||
chr3:134605761
|
C | T | 1 | a0004c0015t0002g0238 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1091-1287G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 10/10 | chr3 | 134605761 | ||||||
chr3:134605762
|
G | A | 1 | a0001c0002t0002g0090 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1091-1288C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 10/10 | chr3 | 134605762 | ||||||
chr3:134606414
|
T | G | 137 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(134): Show | 179 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.1091-1940A>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 10/10 | chr3 | 134606414 | ||||||
chr3:134606484
|
G | A | 3 | a0001c0002t0021g0060a0001c0007t0010g0015a0001c0007t0010g0083 | 4 | HG01123.hp2 HG02055.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.1091-2010C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 10/10 | chr3 | 134606484 | ||||||
chr3:134606527
|
C | A | 1 | a0004c0015t0002g0238 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1091-2053G>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 10/10 | chr3 | 134606527 | ||||||
chr3:134606665
|
C | T | 3 | a0001c0002t0002g0113a0001c0002t0002g0114a0001c0002t0002g0120 | 3 | HG00099.hp1 HG02683.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.1090+1984G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 10/10 | chr3 | 134606665 | ||||||
chr3:134606686
|
G | A | 1 | a0003c0014t0017g0081 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1090+1963C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 10/10 | chr3 | 134606686 | ||||||
chr3:134606694
|
G | A | 85 | a0001c0002t0002g0006a0001c0002t0002g0012a0001c0002t0002g0029others(82): Show | 97 | HG00099.hp1 HG00544.hp2 HG00609.hp2 others(94): Show |
intron_variant | MODIFIER | c.1090+1955C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 10/10 | chr3 | 134606694 | ||||||
chr3:134606784
|
A | G | 79 | a0001c0002t0002g0006a0001c0002t0002g0012a0001c0002t0002g0029others(76): Show | 90 | HG00099.hp1 HG00544.hp2 HG00609.hp2 others(87): Show |
intron_variant | MODIFIER | c.1090+1865T>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 10/10 | chr3 | 134606784 | ||||||
chr3:134606815
|
T | G | 137 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(134): Show | 179 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.1090+1834A>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 10/10 | chr3 | 134606815 | ||||||
chr3:134606895
|
T | C | 1 | a0001c0003t0002g0209 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1090+1754A>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 10/10 | chr3 | 134606895 | ||||||
chr3:134607139
|
C | T | 2 | a0001c0001t0005g0019a0001c0001t0005g0139 | 3 | HG02523.hp1 NA19054.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.1090+1510G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 10/10 | chr3 | 134607139 | ||||||
chr3:134607151
|
G | A | 1 | a0001c0001t0001g0178 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1090+1498C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 10/10 | chr3 | 134607151 | ||||||
chr3:134607225
|
C | T | 4 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0078others(1): Show | 4 | HG01243.hp2 HG02559.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.1090+1424G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 10/10 | chr3 | 134607225 | ||||||
chr3:134607306
|
T | C | 222 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(219): Show | 276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.1090+1343A>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 10/10 | chr3 | 134607306 | ||||||
chr3:134607420
|
C | A | 3 | a0001c0001t0003g0013a0001c0001t0003g0069a0001c0001t0003g0096 | 4 | HG00323.hp1 HG02300.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.1090+1229G>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 10/10 | chr3 | 134607420 | ||||||
chr3:134607483
|
G | A | 10 | a0001c0002t0004g0004a0001c0002t0004g0034a0001c0002t0004g0035others(7): Show | 13 | NA18941.hp1 NA18955.hp2 NA18960.hp1 others(10): Show |
intron_variant | MODIFIER | c.1090+1166C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 10/10 | chr3 | 134607483 | ||||||
chr3:134607693
|
A | G | 1 | a0001c0001t0001g0071 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1090+956T>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 10/10 | chr3 | 134607693 | ||||||
chr3:134607768
|
G | A | 54 | a0001c0001t0001g0002a0001c0001t0001g0024a0001c0001t0001g0030others(51): Show | 72 | HG00280.hp1 HG00642.hp1 HG00642.hp2 others(69): Show |
intron_variant | MODIFIER | c.1090+881C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 10/10 | chr3 | 134607768 | ||||||
chr3:134607784
|
G | A | 4 | a0001c0001t0008g0053a0001c0001t0008g0054a0001c0001t0008g0055others(1): Show | 4 | HG01891.hp2 HG02258.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.1090+865C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 10/10 | chr3 | 134607784 | ||||||
chr3:134607842
|
G | A | 137 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(134): Show | 179 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.1090+807C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 10/10 | chr3 | 134607842 | ||||||
chr3:134608640
|
C | T | 2 | a0001c0001t0001g0064a0001c0001t0001g0181 | 2 | HG01069.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.1090+9G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 10/10 | chr3 | 134608640 | ||||||
chr3:134608913
|
G | T | 8 | a0001c0005t0006g0104a0001c0005t0006g0105a0001c0005t0006g0158others(5): Show | 8 | HG02818.hp1 NA18951.hp1 NA18960.hp2 others(5): Show |
intron_variant | MODIFIER | c.900-74C>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 9/10 | chr3 | 134608913 | ||||||
chr3:134608953
|
G | T | 4 | a0001c0001t0008g0053a0001c0001t0008g0054a0001c0001t0008g0055others(1): Show | 4 | HG01891.hp2 HG02258.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.900-114C>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 9/10 | chr3 | 134608953 | ||||||
chr3:134609088
|
G | A | 3 | a0001c0002t0002g0049a0001c0002t0002g0050a0001c0002t0002g0051 | 3 | HG02559.hp1 HG02976.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.900-249C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 9/10 | chr3 | 134609088 | ||||||
chr3:134609137
|
G | C | 1 | a0001c0001t0001g0116 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.900-298C>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 9/10 | chr3 | 134609137 | ||||||
chr3:134609196
|
G | A | 9 | a0001c0005t0006g0104a0001c0005t0006g0105a0001c0005t0006g0158others(6): Show | 9 | HG02723.hp2 HG02818.hp1 NA18951.hp1 others(6): Show |
intron_variant | MODIFIER | c.900-357C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 9/10 | chr3 | 134609196 | ||||||
chr3:134609368
|
G | C | 1 | a0001c0002t0002g0117 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.900-529C>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 9/10 | chr3 | 134609368 | ||||||
chr3:134609464
|
T | C | 1 | a0001c0001t0001g0130 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.900-625A>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 9/10 | chr3 | 134609464 | ||||||
chr3:134609491
|
A | G | 136 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(133): Show | 178 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.900-652T>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 9/10 | chr3 | 134609491 | ||||||
chr3:134609496
|
T | G | 1 | a0001c0005t0006g0166 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.900-657A>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 9/10 | chr3 | 134609496 | ||||||
chr3:134609519
|
C | T | 136 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(133): Show | 178 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.899+676G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 9/10 | chr3 | 134609519 | ||||||
chr3:134609654
|
C | T | 4 | a0001c0001t0008g0053a0001c0001t0008g0054a0001c0001t0008g0055others(1): Show | 4 | HG01891.hp2 HG02258.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.899+541G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 9/10 | chr3 | 134609654 | ||||||
chr3:134609832
|
G | C | 1 | a0001c0001t0001g0133 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.899+363C>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 9/10 | chr3 | 134609832 | ||||||
chr3:134609898
|
A | G | 136 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(133): Show | 178 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.899+297T>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 9/10 | chr3 | 134609898 | ||||||
chr3:134610022
|
C | T | 136 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(133): Show | 178 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.899+173G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 9/10 | chr3 | 134610022 | ||||||
chr3:134610129
|
A | G | 2 | a0001c0002t0002g0006a0001c0002t0002g0152 | 5 | HG00609.hp2 HG03490.hp2 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.899+66T>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 9/10 | chr3 | 134610129 | ||||||
chr3:134610166
|
C | T | 1 | a0001c0005t0016g0153 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.899+29G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 9/10 | chr3 | 134610166 | ||||||
chr3:134610176
|
A | T | 1 | a0001c0001t0001g0155 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.899+19T>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 9/10 | chr3 | 134610176 | ||||||
chr3:134610414
|
G | A | 1 | a0001c0001t0008g0053 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.711-31C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134610414 | ||||||
chr3:134610495
|
A | G | 1 | a0001c0001t0001g0130 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.711-112T>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134610495 | ||||||
chr3:134610551
|
G | A | 1 | a0001c0001t0001g0205 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.711-168C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134610551 | ||||||
chr3:134610693
|
G | A | 84 | a0001c0001t0001g0116a0001c0002t0002g0006a0001c0002t0002g0012others(81): Show | 95 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.711-310C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134610693 | ||||||
chr3:134610734
|
C | T | 1 | a0001c0005t0006g0166 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.711-351G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134610734 | ||||||
chr3:134610758
|
G | A | 84 | a0001c0001t0001g0116a0001c0002t0002g0006a0001c0002t0002g0012others(81): Show | 95 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.711-375C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134610758 | ||||||
chr3:134610799
|
T | A | 1 | a0001c0001t0001g0108 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.711-416A>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134610799 | ||||||
chr3:134610979
|
G | A | 136 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(133): Show | 178 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.711-596C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134610979 | ||||||
chr3:134610994
|
C | G | 27 | a0001c0002t0002g0062a0001c0002t0002g0067a0001c0002t0002g0107others(24): Show | 31 | HG01069.hp1 HG01071.hp2 HG01099.hp2 others(28): Show |
intron_variant | MODIFIER | c.711-611G>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134610994 | ||||||
chr3:134611185
|
C | T | 136 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(133): Show | 178 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.711-802G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134611185 | ||||||
chr3:134611200
|
G | A | 3 | a0001c0004t0001g0009a0001c0004t0001g0026a0001c0004t0001g0202 | 6 | HG02922.hp1 HG03139.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.711-817C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134611200 | ||||||
chr3:134611241
|
C | T | 136 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(133): Show | 178 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.711-858G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134611241 | ||||||
chr3:134611249
|
G | T | 1 | a0001c0001t0027g0148 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.711-866C>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134611249 | ||||||
chr3:134611371
|
C | G | 136 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(133): Show | 178 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.711-988G>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134611371 | ||||||
chr3:134611477
|
C | T | 1 | a0001c0001t0024g0196 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.711-1094G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134611477 | ||||||
chr3:134611532
|
T | G | 136 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(133): Show | 178 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.711-1149A>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134611532 | ||||||
chr3:134611602
|
G | A | 1 | a0001c0001t0001g0162 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.711-1219C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134611602 | ||||||
chr3:134611770
|
C | T | 136 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(133): Show | 178 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.711-1387G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134611770 | ||||||
chr3:134611867
|
T | C | 136 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(133): Show | 178 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.711-1484A>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134611867 | ||||||
chr3:134611912
|
C | A | 1 | a0001c0002t0004g0045 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.711-1529G>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134611912 | ||||||
chr3:134612134
|
T | C | 136 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(133): Show | 178 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.711-1751A>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134612134 | ||||||
chr3:134612137
|
C | T | 4 | a0001c0005t0007g0046a0001c0005t0007g0047a0001c0005t0007g0048others(1): Show | 4 | HG02572.hp2 HG03139.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.711-1754G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134612137 | ||||||
chr3:134612196
|
G | A | 7 | a0001c0004t0001g0009a0001c0004t0001g0010a0001c0004t0001g0026others(4): Show | 12 | HG01167.hp2 HG01169.hp1 HG02896.hp1 others(9): Show |
intron_variant | MODIFIER | c.711-1813C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134612196 | ||||||
chr3:134612200
|
T | A | 42 | a0001c0001t0001g0002a0001c0001t0001g0024a0001c0001t0001g0030others(39): Show | 53 | HG00280.hp1 HG00642.hp1 HG00642.hp2 others(50): Show |
intron_variant | MODIFIER | c.711-1817A>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134612200 | ||||||
chr3:134612206
|
A | G | 136 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(133): Show | 178 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.711-1823T>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134612206 | ||||||
chr3:134612246
|
G | A | 1 | a0001c0001t0001g0193 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.711-1863C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134612246 | ||||||
chr3:134612325
|
C | T | 84 | a0001c0001t0001g0116a0001c0002t0002g0006a0001c0002t0002g0012others(81): Show | 95 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.711-1942G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134612325 | ||||||
chr3:134612362
|
G | A | 1 | a0001c0001t0001g0132 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.711-1979C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134612362 | ||||||
chr3:134612624
|
A | T | 136 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(133): Show | 178 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.711-2241T>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134612624 | ||||||
chr3:134612684
|
C | A | 1 | a0001c0002t0002g0058 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.711-2301G>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134612684 | ||||||
chr3:134612751
|
C | CTG | 43 | a0001c0001t0001g0091a0001c0001t0001g0116a0001c0001t0001g0198others(40): Show | 50 | HG00099.hp1 HG00140.hp1 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.711-2370_711-2369d others(4): Show |
KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134612751 | ||||||
chr3:134612751
|
C | CTGTG | 27 | a0001c0001t0001g0056a0001c0001t0001g0134a0001c0001t0001g0138others(24): Show | 34 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(31): Show |
intron_variant | MODIFIER | c.711-2372_711-2369d others(6): Show |
KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134612751 | ||||||
chr3:134612751
|
C | CTGTGTG | 43 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0017others(40): Show | 57 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(54): Show |
intron_variant | MODIFIER | c.711-2374_711-2369d others(8): Show |
KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134612751 | ||||||
chr3:134612751
|
C | CTGTGTGT others(1): Show |
29 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0021others(26): Show | 41 | HG00609.hp1 HG00642.hp2 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.711-2376_711-2369d others(10): Show |
KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134612751 | ||||||
chr3:134612751
|
C | CTGTGTGT others(3): Show |
19 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0077others(16): Show | 26 | HG00280.hp1 HG00544.hp1 HG01106.hp2 others(23): Show |
intron_variant | MODIFIER | c.711-2378_711-2369d others(12): Show |
KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134612751 | ||||||
chr3:134612751
|
C | CTGTGTGT others(5): Show |
8 | a0001c0001t0001g0068a0001c0001t0001g0075a0001c0001t0001g0076others(5): Show | 8 | HG01109.hp2 HG01261.hp2 HG02698.hp1 others(5): Show |
intron_variant | MODIFIER | c.711-2380_711-2369d others(14): Show |
KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134612751 | ||||||
chr3:134612751
|
C | CTGTGTGT others(7): Show |
3 | a0001c0001t0001g0024a0001c0001t0001g0093a0001c0005t0007g0033 | 4 | HG01109.hp1 NA18982.hp2 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.711-2382_711-2369d others(16): Show |
KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134612751 | ||||||
chr3:134612751
|
CTG | C | 7 | a0001c0001t0001g0070a0001c0001t0001g0074a0001c0001t0001g0084others(4): Show | 7 | HG01099.hp2 HG01256.hp1 HG01496.hp1 others(4): Show |
intron_variant | MODIFIER | c.711-2370_711-2369d others(4): Show |
KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134612751 | ||||||
chr3:134612751
|
CTGTGTGT others(13): Show |
C | 5 | a0001c0002t0004g0004a0001c0002t0004g0041a0001c0002t0004g0044others(2): Show | 8 | NA18960.hp1 NA18965.hp2 NA18968.hp1 others(5): Show |
intron_variant | MODIFIER | c.711-2388_711-2369d others(22): Show |
KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134612751 | ||||||
chr3:134612756
|
T | TGTGTGTG others(4): Show |
1 | a0001c0001t0001g0194 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.711-2384_711-2374d others(13): Show |
KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134612756 | ||||||
chr3:134612795
|
G | GTGTGTGT others(8): Show |
1 | a0001c0001t0001g0188 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.711-2413_711-2412i others(17): Show |
KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134612795 | ||||||
chr3:134613032
|
T | C | 234 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(231): Show | 287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.711-2649A>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134613032 | ||||||
chr3:134613138
|
C | T | 136 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(133): Show | 178 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.711-2755G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134613138 | ||||||
chr3:134613308
|
G | T | 1 | a0001c0001t0001g0180 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.711-2925C>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134613308 | ||||||
chr3:134613309
|
T | C | 4 | a0001c0005t0007g0046a0001c0005t0007g0047a0001c0005t0007g0048others(1): Show | 4 | HG02572.hp2 HG03139.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.711-2926A>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134613309 | ||||||
chr3:134613380
|
C | A | 136 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(133): Show | 178 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.711-2997G>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134613380 | ||||||
chr3:134613407
|
G | A | 1 | a0001c0005t0006g0160 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.711-3024C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134613407 | ||||||
chr3:134613417
|
C | T | 3 | a0001c0001t0008g0054a0001c0001t0008g0055a0001c0001t0008g0175 | 3 | HG01891.hp2 HG02258.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.711-3034G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134613417 | ||||||
chr3:134613455
|
C | T | 1 | a0001c0001t0005g0154 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.711-3072G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134613455 | ||||||
chr3:134613469
|
G | T | 136 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(133): Show | 178 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.711-3086C>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134613469 | ||||||
chr3:134613477
|
C | T | 136 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(133): Show | 178 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.711-3094G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134613477 | ||||||
chr3:134613921
|
C | T | 3 | a0001c0001t0003g0013a0001c0001t0003g0069a0001c0001t0003g0096 | 4 | HG00323.hp1 HG02300.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.711-3538G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134613921 | ||||||
chr3:134613934
|
T | A | 136 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(133): Show | 178 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.711-3551A>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134613934 | ||||||
chr3:134614062
|
T | C | 1 | a0001c0002t0002g0057 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.711-3679A>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134614062 | ||||||
chr3:134614084
|
A | G | 136 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(133): Show | 178 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.711-3701T>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134614084 | ||||||
chr3:134614319
|
C | T | 88 | a0001c0001t0001g0116a0001c0002t0002g0006a0001c0002t0002g0012others(85): Show | 99 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(96): Show |
intron_variant | MODIFIER | c.711-3936G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134614319 | ||||||
chr3:134614612
|
G | A | 1 | a0001c0001t0001g0144 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.711-4229C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134614612 | ||||||
chr3:134614869
|
C | T | 1 | a0001c0006t0003g0237 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.710+4279G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134614869 | ||||||
chr3:134614870
|
G | A | 8 | a0001c0005t0006g0104a0001c0005t0006g0105a0001c0005t0006g0158others(5): Show | 8 | HG02818.hp1 NA18951.hp1 NA18960.hp2 others(5): Show |
intron_variant | MODIFIER | c.710+4278C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134614870 | ||||||
chr3:134614932
|
G | C | 1 | a0001c0002t0002g0124 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.710+4216C>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134614932 | ||||||
chr3:134615283
|
G | A | 231 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(228): Show | 284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.710+3865C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134615283 | ||||||
chr3:134615306
|
G | A | 11 | a0001c0001t0008g0054a0001c0001t0008g0055a0001c0001t0008g0175others(8): Show | 11 | HG01891.hp2 HG02258.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.710+3842C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134615306 | ||||||
chr3:134615349
|
C | CT | 131 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(128): Show | 171 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.710+3798dupA | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134615349 | ||||||
chr3:134615349
|
C | CTT | 6 | a0001c0001t0001g0073a0001c0001t0001g0078a0001c0001t0022g0136others(3): Show | 8 | HG01167.hp2 HG01169.hp1 HG01243.hp2 others(5): Show |
intron_variant | MODIFIER | c.710+3797_710+3798d others(4): Show |
KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134615349 | ||||||
chr3:134615349
|
CT | C | 16 | a0001c0002t0002g0012a0001c0002t0002g0058a0001c0002t0002g0118others(13): Show | 17 | HG02615.hp2 HG02622.hp2 HG02818.hp1 others(14): Show |
intron_variant | MODIFIER | c.710+3798delA | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134615349 | ||||||
chr3:134615394
|
A | G | 234 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(231): Show | 287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.710+3754T>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134615394 | ||||||
chr3:134615469
|
A | C | 1 | a0001c0001t0001g0179 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.710+3679T>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134615469 | ||||||
chr3:134615485
|
G | A | 97 | a0001c0001t0001g0032a0001c0001t0001g0116a0001c0002t0002g0006others(94): Show | 108 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(105): Show |
intron_variant | MODIFIER | c.710+3663C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134615485 | ||||||
chr3:134615530
|
C | T | 2 | a0001c0002t0002g0094a0001c0002t0002g0095 | 2 | HG01496.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.710+3618G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134615530 | ||||||
chr3:134615531
|
ACCAGCTC others(164): Show |
A | 2 | a0001c0002t0002g0094a0001c0002t0002g0095 | 2 | HG01496.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.710+3446_710+3616d others(2): Show |
KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134615531 | ||||||
chr3:134615605
|
G | A | 7 | a0001c0005t0006g0104a0001c0005t0006g0105a0001c0005t0006g0158others(4): Show | 7 | NA18951.hp1 NA18960.hp2 NA18967.hp2 others(4): Show |
intron_variant | MODIFIER | c.710+3543C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134615605 | ||||||
chr3:134615622
|
C | A | 1 | a0001c0001t0001g0186 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.710+3526G>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134615622 | ||||||
chr3:134615671
|
G | A | 88 | a0001c0001t0001g0032a0001c0001t0001g0116a0001c0002t0002g0006others(85): Show | 99 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(96): Show |
intron_variant | MODIFIER | c.710+3477C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134615671 | ||||||
chr3:134615678
|
A | T | 1 | a0001c0001t0001g0167 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.710+3470T>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134615678 | ||||||
chr3:134615680
|
G | T | 1 | a0001c0001t0001g0167 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.710+3468C>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134615680 | ||||||
chr3:134615682
|
T | A | 1 | a0001c0001t0001g0167 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.710+3466A>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134615682 | ||||||
chr3:134615704
|
C | A | 2 | a0001c0002t0002g0094a0001c0002t0002g0095 | 2 | HG01496.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.710+3444G>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134615704 | ||||||
chr3:134615705
|
A | T | 2 | a0001c0002t0002g0094a0001c0002t0002g0095 | 2 | HG01496.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.710+3443T>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134615705 | ||||||
chr3:134615707
|
C | A | 2 | a0001c0002t0002g0094a0001c0002t0002g0095 | 2 | HG01496.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.710+3441G>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134615707 | ||||||
chr3:134615787
|
T | G | 1 | a0006c0011t0009g0031 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.710+3361A>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134615787 | ||||||
chr3:134615896
|
G | A | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(135): Show | 178 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.710+3252C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134615896 | ||||||
chr3:134616015
|
G | A | 1 | a0001c0001t0023g0191 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.710+3133C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134616015 | ||||||
chr3:134616082
|
G | A | 3 | a0001c0004t0001g0145a0001c0004t0001g0146a0001c0004t0001g0149 | 3 | HG02809.hp2 NA18906.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.710+3066C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134616082 | ||||||
chr3:134616132
|
C | T | 2 | a0001c0001t0014g0052a0001c0006t0026g0207 | 2 | HG02683.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.710+3016G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134616132 | ||||||
chr3:134616133
|
A | G | 141 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(138): Show | 181 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.710+3015T>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134616133 | ||||||
chr3:134616192
|
T | C | 133 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(130): Show | 173 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.710+2956A>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134616192 | ||||||
chr3:134616412
|
C | T | 1 | a0001c0005t0006g0158 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.710+2736G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134616412 | ||||||
chr3:134616629
|
T | C | 141 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(138): Show | 181 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.710+2519A>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134616629 | ||||||
chr3:134616684
|
T | G | 3 | a0001c0002t0021g0060a0001c0004t0001g0173a0001c0004t0001g0174 | 3 | HG02622.hp2 HG03209.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.710+2464A>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134616684 | ||||||
chr3:134616763
|
T | C | 4 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0078others(1): Show | 4 | HG01243.hp2 HG02559.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.710+2385A>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134616763 | ||||||
chr3:134616806
|
G | A | 1 | a0001c0001t0014g0052 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.710+2342C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134616806 | ||||||
chr3:134617132
|
C | T | 3 | a0001c0002t0021g0060a0001c0004t0001g0173a0001c0004t0001g0174 | 3 | HG02622.hp2 HG03209.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.710+2016G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134617132 | ||||||
chr3:134617151
|
T | C | 86 | a0001c0001t0001g0032a0001c0001t0001g0116a0001c0001t0001g0150others(83): Show | 101 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.710+1997A>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134617151 | ||||||
chr3:134617167
|
A | T | 1 | a0001c0003t0002g0223 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.710+1981T>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134617167 | ||||||
chr3:134617253
|
A | T | 84 | a0001c0001t0001g0032a0001c0001t0001g0116a0001c0002t0002g0006others(81): Show | 97 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(94): Show |
intron_variant | MODIFIER | c.710+1895T>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134617253 | ||||||
chr3:134617262
|
C | A | 3 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0080 | 3 | HG03041.hp2 HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.710+1886G>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134617262 | ||||||
chr3:134617524
|
C | A | 1 | a0001c0001t0001g0100 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.710+1624G>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134617524 | ||||||
chr3:134617720
|
G | A | 1 | a0006c0011t0009g0031 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.710+1428C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134617720 | ||||||
chr3:134617813
|
G | A | 1 | a0001c0006t0003g0028 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.710+1335C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134617813 | ||||||
chr3:134617962
|
C | T | 1 | a0001c0003t0002g0214 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.710+1186G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134617962 | ||||||
chr3:134618010
|
G | C | 1 | a0001c0002t0002g0120 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.710+1138C>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134618010 | ||||||
chr3:134618054
|
C | T | 3 | a0001c0002t0002g0049a0001c0002t0002g0050a0001c0002t0002g0051 | 3 | HG02559.hp1 HG02976.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.710+1094G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134618054 | ||||||
chr3:134618055
|
C | T | 132 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(129): Show | 172 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.710+1093G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134618055 | ||||||
chr3:134618092
|
C | A | 1 | a0001c0004t0001g0010 | 3 | HG01167.hp2 HG01169.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.710+1056G>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134618092 | ||||||
chr3:134618114
|
T | A | 238 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(235): Show | 292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.710+1034A>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134618114 | ||||||
chr3:134618199
|
G | A | 1 | a0001c0001t0001g0187 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.710+949C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134618199 | ||||||
chr3:134618298
|
G | A | 1 | a0001c0003t0002g0227 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.710+850C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134618298 | ||||||
chr3:134618434
|
T | A | 10 | a0001c0002t0002g0006a0001c0002t0002g0152a0001c0005t0006g0104others(7): Show | 13 | HG00609.hp2 HG02818.hp1 HG03490.hp2 others(10): Show |
intron_variant | MODIFIER | c.710+714A>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134618434 | ||||||
chr3:134618762
|
C | A | 11 | a0001c0001t0014g0052a0001c0002t0002g0006a0001c0002t0002g0152others(8): Show | 14 | HG00609.hp2 HG02818.hp1 HG03490.hp2 others(11): Show |
intron_variant | MODIFIER | c.710+386G>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134618762 | ||||||
chr3:134618881
|
C | T | 1 | a0001c0001t0008g0053 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.710+267G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134618881 | ||||||
chr3:134619023
|
G | A | 4 | a0001c0002t0002g0059a0001c0002t0002g0123a0001c0002t0002g0124others(1): Show | 4 | HG01243.hp1 HG02109.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.710+125C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 8/10 | chr3 | 134619023 | ||||||
chr3:134619324
|
C | T | 6 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0108others(3): Show | 8 | HG00741.hp1 HG02109.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.593-59G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 7/10 | chr3 | 134619324 | ||||||
chr3:134619346
|
G | A | 1 | a0001c0006t0001g0208 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.593-81C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 7/10 | chr3 | 134619346 | ||||||
chr3:134619543
|
G | A | 1 | a0001c0002t0002g0029 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.593-278C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 7/10 | chr3 | 134619543 | ||||||
chr3:134619640
|
T | C | 9 | a0001c0001t0001g0005a0001c0001t0001g0022a0001c0001t0001g0099others(6): Show | 13 | HG01934.hp2 HG02074.hp2 HG02273.hp1 others(10): Show |
intron_variant | MODIFIER | c.593-375A>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 7/10 | chr3 | 134619640 | ||||||
chr3:134619696
|
C | T | 1 | a0001c0001t0005g0141 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.593-431G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 7/10 | chr3 | 134619696 | ||||||
chr3:134619746
|
T | C | 11 | a0001c0001t0014g0052a0001c0002t0002g0006a0001c0002t0002g0152others(8): Show | 14 | HG00609.hp2 HG02818.hp1 HG03490.hp2 others(11): Show |
intron_variant | MODIFIER | c.593-481A>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 7/10 | chr3 | 134619746 | ||||||
chr3:134619788
|
T | C | 4 | a0001c0004t0001g0145a0001c0004t0001g0146a0001c0004t0001g0147others(1): Show | 4 | HG02809.hp2 NA18906.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.593-523A>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 7/10 | chr3 | 134619788 | ||||||
chr3:134619927
|
A | C | 1 | a0001c0001t0001g0188 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.593-662T>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 7/10 | chr3 | 134619927 | ||||||
chr3:134620260
|
C | T | 1 | a0001c0005t0006g0166 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.592+489G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 7/10 | chr3 | 134620260 | ||||||
chr3:134620312
|
C | T | 1 | a0001c0003t0002g0210 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.592+437G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 7/10 | chr3 | 134620312 | ||||||
chr3:134620527
|
G | A | 3 | a0001c0002t0002g0049a0001c0002t0002g0050a0001c0002t0002g0051 | 3 | HG02559.hp1 HG02976.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.592+222C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 7/10 | chr3 | 134620527 | ||||||
chr3:134620896
|
G | A | 2 | a0001c0001t0001g0023a0001c0001t0025g0170 | 3 | HG03831.hp1 HG04184.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.484-39C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 6/10 | chr3 | 134620896 | ||||||
chr3:134620948
|
C | G | 3 | a0001c0002t0002g0049a0001c0002t0002g0050a0001c0002t0002g0051 | 3 | HG02559.hp1 HG02976.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.484-91G>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 6/10 | chr3 | 134620948 | ||||||
chr3:134621037
|
C | T | 3 | a0001c0001t0001g0017a0001c0001t0001g0100a0001c0001t0001g0101 | 4 | HG00099.hp2 HG00323.hp2 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.484-180G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 6/10 | chr3 | 134621037 | ||||||
chr3:134621125
|
A | C | 11 | a0001c0001t0014g0052a0001c0002t0002g0006a0001c0002t0002g0152others(8): Show | 14 | HG00609.hp2 HG02818.hp1 HG03490.hp2 others(11): Show |
intron_variant | MODIFIER | c.484-268T>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 6/10 | chr3 | 134621125 | ||||||
chr3:134621219
|
C | T | 1 | a0001c0001t0003g0063 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.484-362G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 6/10 | chr3 | 134621219 | ||||||
chr3:134621421
|
C | T | 1 | a0001c0006t0001g0208 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.484-564G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 6/10 | chr3 | 134621421 | ||||||
chr3:134621437
|
G | A | 1 | a0006c0011t0009g0031 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.484-580C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 6/10 | chr3 | 134621437 | ||||||
chr3:134621511
|
C | T | 132 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(129): Show | 172 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.484-654G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 6/10 | chr3 | 134621511 | ||||||
chr3:134621592
|
A | G | 1 | a0001c0005t0006g0166 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.484-735T>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 6/10 | chr3 | 134621592 | ||||||
chr3:134621637
|
C | A | 1 | a0001c0006t0003g0237 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.484-780G>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 6/10 | chr3 | 134621637 | ||||||
chr3:134621700
|
G | GA | 4 | a0001c0001t0001g0161a0001c0002t0002g0049a0001c0002t0002g0050others(1): Show | 4 | HG02559.hp1 HG02976.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.484-844dupT | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 6/10 | chr3 | 134621700 | ||||||
chr3:134621724
|
G | A | 1 | a0001c0001t0005g0140 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.484-867C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 6/10 | chr3 | 134621724 | ||||||
chr3:134622008
|
A | G | 128 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(125): Show | 168 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.484-1151T>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 6/10 | chr3 | 134622008 | ||||||
chr3:134622218
|
A | C | 144 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(141): Show | 187 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.484-1361T>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 6/10 | chr3 | 134622218 | ||||||
chr3:134622265
|
A | G | 2 | a0001c0001t0001g0064a0001c0006t0001g0218 | 2 | HG01069.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.484-1408T>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 6/10 | chr3 | 134622265 | ||||||
chr3:134622381
|
C | T | 225 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(222): Show | 278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.484-1524G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 6/10 | chr3 | 134622381 | ||||||
chr3:134622455
|
G | A | 5 | a0001c0002t0002g0062a0001c0002t0002g0107a0001c0003t0002g0007others(2): Show | 8 | HG01175.hp2 HG01261.hp1 HG01346.hp1 others(5): Show |
intron_variant | MODIFIER | c.484-1598C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 6/10 | chr3 | 134622455 | ||||||
chr3:134622543
|
C | T | 3 | a0001c0001t0001g0070a0001c0001t0001g0074a0001c0001t0001g0084 | 3 | HG01496.hp1 HG02280.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.484-1686G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 6/10 | chr3 | 134622543 | ||||||
chr3:134622723
|
G | A | 2 | a0001c0005t0006g0166a0001c0006t0003g0235 | 2 | HG02723.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.484-1866C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 6/10 | chr3 | 134622723 | ||||||
chr3:134622793
|
A | G | 2 | a0001c0002t0002g0094a0001c0002t0002g0095 | 2 | HG01496.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.484-1936T>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 6/10 | chr3 | 134622793 | ||||||
chr3:134622866
|
C | A | 1 | a0001c0005t0006g0166 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.484-2009G>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 6/10 | chr3 | 134622866 | ||||||
chr3:134623285
|
C | T | 135 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(132): Show | 175 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.483+1768G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 6/10 | chr3 | 134623285 | ||||||
chr3:134623345
|
T | C | 231 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(228): Show | 284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.483+1708A>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 6/10 | chr3 | 134623345 | ||||||
chr3:134623551
|
C | T | 1 | a0001c0001t0001g0132 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.483+1502G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 6/10 | chr3 | 134623551 | ||||||
chr3:134623756
|
T | A | 3 | a0001c0002t0002g0111a0001c0002t0002g0112a0001c0002t0002g0172 | 3 | HG02055.hp2 HG03098.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.483+1297A>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 6/10 | chr3 | 134623756 | ||||||
chr3:134623760
|
G | A | 1 | a0001c0001t0005g0139 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.483+1293C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 6/10 | chr3 | 134623760 | ||||||
chr3:134623836
|
G | A | 4 | a0001c0002t0002g0059a0001c0002t0002g0123a0001c0002t0002g0124others(1): Show | 4 | HG01243.hp1 HG02109.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.483+1217C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 6/10 | chr3 | 134623836 | ||||||
chr3:134623916
|
T | C | 133 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(130): Show | 173 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.483+1137A>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 6/10 | chr3 | 134623916 | ||||||
chr3:134623916
|
T | G | 1 | a0001c0006t0003g0235 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.483+1137A>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 6/10 | chr3 | 134623916 | ||||||
chr3:134624226
|
G | T | 3 | a0001c0002t0002g0049a0001c0002t0002g0050a0001c0002t0002g0051 | 3 | HG02559.hp1 HG02976.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.483+827C>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 6/10 | chr3 | 134624226 | ||||||
chr3:134624246
|
C | T | 1 | a0001c0002t0002g0107 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.483+807G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 6/10 | chr3 | 134624246 | ||||||
chr3:134624372
|
T | A | 1 | a0001c0003t0002g0227 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.483+681A>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 6/10 | chr3 | 134624372 | ||||||
chr3:134624710
|
G | A | 1 | a0001c0005t0006g0166 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.483+343C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 6/10 | chr3 | 134624710 | ||||||
chr3:134624798
|
G | A | 1 | a0001c0005t0006g0166 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.483+255C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 6/10 | chr3 | 134624798 | ||||||
chr3:134624846
|
C | G | 237 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(234): Show | 291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.483+207G>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 6/10 | chr3 | 134624846 | ||||||
chr3:134625032
|
C | G | 2 | a0001c0001t0013g0189a0001c0001t0013g0190 | 2 | HG02735.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.483+21G>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 6/10 | chr3 | 134625032 | ||||||
chr3:134625215
|
A | G | 1 | a0001c0005t0006g0166 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.401-80T>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 5/10 | chr3 | 134625215 | ||||||
chr3:134625340
|
C | T | 80 | a0001c0001t0001g0032a0001c0001t0001g0116a0001c0002t0002g0012others(77): Show | 90 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(87): Show |
intron_variant | MODIFIER | c.401-205G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 5/10 | chr3 | 134625340 | ||||||
chr3:134625488
|
G | A | 1 | a0001c0001t0001g0157 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.401-353C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 5/10 | chr3 | 134625488 | ||||||
chr3:134625593
|
C | T | 134 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(131): Show | 174 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.401-458G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 5/10 | chr3 | 134625593 | ||||||
chr3:134625663
|
G | A | 145 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(142): Show | 188 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.401-528C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 5/10 | chr3 | 134625663 | ||||||
chr3:134625683
|
G | A | 1 | a0001c0001t0008g0053 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.401-548C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 5/10 | chr3 | 134625683 | ||||||
chr3:134625852
|
A | G | 231 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(228): Show | 284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.401-717T>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 5/10 | chr3 | 134625852 | ||||||
chr3:134625876
|
G | C | 1 | a0001c0001t0001g0086 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.401-741C>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 5/10 | chr3 | 134625876 | ||||||
chr3:134625882
|
C | T | 2 | a0001c0002t0002g0029a0001c0005t0007g0033 | 2 | HG01109.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.401-747G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 5/10 | chr3 | 134625882 | ||||||
chr3:134625938
|
C | A | 1 | a0001c0002t0002g0029 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.401-803G>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 5/10 | chr3 | 134625938 | ||||||
chr3:134625957
|
G | C | 231 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(228): Show | 284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.401-822C>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 5/10 | chr3 | 134625957 | ||||||
chr3:134625966
|
T | C | 1 | a0001c0001t0008g0055 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.401-831A>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 5/10 | chr3 | 134625966 | ||||||
chr3:134625997
|
G | A | 1 | a0001c0002t0002g0121 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.401-862C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 5/10 | chr3 | 134625997 | ||||||
chr3:134626053
|
A | G | 1 | a0001c0003t0002g0209 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.401-918T>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 5/10 | chr3 | 134626053 | ||||||
chr3:134626086
|
T | G | 83 | a0001c0001t0001g0032a0001c0001t0001g0116a0001c0002t0002g0012others(80): Show | 93 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(90): Show |
intron_variant | MODIFIER | c.401-951A>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 5/10 | chr3 | 134626086 | ||||||
chr3:134626090
|
C | G | 5 | a0001c0001t0001g0068a0001c0001t0001g0075a0001c0001t0001g0076others(2): Show | 5 | HG01109.hp2 HG02818.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.401-955G>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 5/10 | chr3 | 134626090 | ||||||
chr3:134626114
|
C | T | 4 | a0001c0001t0008g0053a0001c0001t0008g0054a0001c0001t0008g0055others(1): Show | 4 | HG01891.hp2 HG02258.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.401-979G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 5/10 | chr3 | 134626114 | ||||||
chr3:134626306
|
T | C | 229 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(226): Show | 282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.401-1171A>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 5/10 | chr3 | 134626306 | ||||||
chr3:134626472
|
G | A | 1 | a0001c0004t0001g0147 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.400+1284C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 5/10 | chr3 | 134626472 | ||||||
chr3:134626485
|
C | G | 145 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(142): Show | 188 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.400+1271G>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 5/10 | chr3 | 134626485 | ||||||
chr3:134626555
|
G | A | 1 | a0001c0001t0014g0052 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.400+1201C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 5/10 | chr3 | 134626555 | ||||||
chr3:134626746
|
C | A | 11 | a0001c0001t0014g0052a0001c0002t0002g0006a0001c0002t0002g0152others(8): Show | 14 | HG00609.hp2 HG02818.hp1 HG03490.hp2 others(11): Show |
intron_variant | MODIFIER | c.400+1010G>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 5/10 | chr3 | 134626746 | ||||||
chr3:134626842
|
T | G | 1 | a0001c0005t0006g0166 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.400+914A>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 5/10 | chr3 | 134626842 | ||||||
chr3:134626877
|
C | T | 134 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(131): Show | 174 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.400+879G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 5/10 | chr3 | 134626877 | ||||||
chr3:134626882
|
T | C | 145 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(142): Show | 188 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.400+874A>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 5/10 | chr3 | 134626882 | ||||||
chr3:134626939
|
A | C | 11 | a0001c0001t0014g0052a0001c0002t0002g0006a0001c0002t0002g0152others(8): Show | 14 | HG00609.hp2 HG02818.hp1 HG03490.hp2 others(11): Show |
intron_variant | MODIFIER | c.400+817T>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 5/10 | chr3 | 134626939 | ||||||
chr3:134626946
|
T | C | 145 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(142): Show | 188 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.400+810A>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 5/10 | chr3 | 134626946 | ||||||
chr3:134627183
|
G | A | 145 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(142): Show | 188 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.400+573C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 5/10 | chr3 | 134627183 | ||||||
chr3:134627265
|
G | C | 1 | a0001c0001t0005g0141 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.400+491C>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 5/10 | chr3 | 134627265 | ||||||
chr3:134627296
|
C | G | 1 | a0001c0005t0006g0166 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.400+460G>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 5/10 | chr3 | 134627296 | ||||||
chr3:134627375
|
C | T | 1 | a0001c0001t0014g0052 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.400+381G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 5/10 | chr3 | 134627375 | ||||||
chr3:134627473
|
G | A | 5 | a0001c0001t0005g0020a0001c0001t0005g0110a0001c0001t0005g0140others(2): Show | 6 | HG00558.hp2 HG01255.hp1 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.400+283C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 5/10 | chr3 | 134627473 | ||||||
chr3:134627480
|
G | A | 11 | a0001c0001t0014g0052a0001c0002t0002g0006a0001c0002t0002g0152others(8): Show | 14 | HG00609.hp2 HG02818.hp1 HG03490.hp2 others(11): Show |
intron_variant | MODIFIER | c.400+276C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 5/10 | chr3 | 134627480 | ||||||
chr3:134627518
|
T | C | 1 | a0001c0001t0001g0193 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.400+238A>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 5/10 | chr3 | 134627518 | ||||||
chr3:134627525
|
G | C | 3 | a0001c0002t0002g0111a0001c0002t0002g0112a0001c0002t0002g0172 | 3 | HG02055.hp2 HG03098.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.400+231C>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 5/10 | chr3 | 134627525 | ||||||
chr3:134627839
|
G | A | 1 | a0001c0001t0001g0188 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.338-21C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 4/10 | chr3 | 134627839 | ||||||
chr3:134627920
|
C | A | 1 | a0001c0005t0006g0166 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.338-102G>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 4/10 | chr3 | 134627920 | ||||||
chr3:134628123
|
C | A | 2 | a0001c0001t0013g0189a0001c0001t0013g0190 | 2 | HG02735.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.338-305G>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 4/10 | chr3 | 134628123 | ||||||
chr3:134628148
|
G | T | 231 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(228): Show | 284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.338-330C>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 4/10 | chr3 | 134628148 | ||||||
chr3:134628211
|
A | G | 1 | a0001c0002t0002g0126 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.338-393T>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 4/10 | chr3 | 134628211 | ||||||
chr3:134628619
|
C | A | 231 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(228): Show | 284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.338-801G>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 4/10 | chr3 | 134628619 | ||||||
chr3:134628644
|
G | A | 2 | a0001c0006t0003g0028a0001c0006t0003g0236 | 3 | HG00642.hp1 HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.338-826C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 4/10 | chr3 | 134628644 | ||||||
chr3:134628651
|
T | C | 1 | a0001c0001t0023g0191 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.338-833A>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 4/10 | chr3 | 134628651 | ||||||
chr3:134628742
|
C | T | 12 | a0001c0001t0014g0052a0001c0002t0002g0006a0001c0002t0002g0152others(9): Show | 15 | HG00609.hp2 HG02818.hp1 HG03490.hp2 others(12): Show |
intron_variant | MODIFIER | c.337+879G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 4/10 | chr3 | 134628742 | ||||||
chr3:134628809
|
G | C | 1 | a0001c0001t0027g0148 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.337+812C>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 4/10 | chr3 | 134628809 | ||||||
chr3:134628816
|
C | G | 1 | a0001c0001t0003g0063 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.337+805G>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 4/10 | chr3 | 134628816 | ||||||
chr3:134629034
|
C | G | 145 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(142): Show | 188 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.337+587G>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 4/10 | chr3 | 134629034 | ||||||
chr3:134629434
|
C | T | 1 | a0001c0001t0001g0074 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.337+187G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 4/10 | chr3 | 134629434 | ||||||
chr3:134629796
|
C | A | 19 | a0001c0001t0001g0032a0001c0001t0001g0116a0001c0002t0002g0090others(16): Show | 19 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(16): Show |
intron_variant | MODIFIER | c.263-101G>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134629796 | ||||||
chr3:134629895
|
G | T | 1 | a0001c0002t0021g0060 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.263-200C>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134629895 | ||||||
chr3:134629952
|
A | C | 2 | a0001c0001t0001g0150a0001c0006t0001g0011 | 4 | HG02109.hp1 HG03225.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.263-257T>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134629952 | ||||||
chr3:134629954
|
G | A | 27 | a0001c0002t0002g0062a0001c0002t0002g0107a0001c0002t0002g0122others(24): Show | 31 | HG01099.hp2 HG01168.hp1 HG01169.hp2 others(28): Show |
intron_variant | MODIFIER | c.263-259C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134629954 | ||||||
chr3:134630088
|
T | G | 80 | a0001c0001t0001g0032a0001c0001t0001g0116a0001c0002t0002g0012others(77): Show | 90 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(87): Show |
intron_variant | MODIFIER | c.263-393A>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134630088 | ||||||
chr3:134630363
|
A | T | 132 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(129): Show | 172 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.263-668T>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134630363 | ||||||
chr3:134630403
|
G | GT | 82 | a0001c0001t0001g0032a0001c0001t0001g0036a0001c0001t0001g0040others(79): Show | 92 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.263-709dupA | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134630403 | ||||||
chr3:134630505
|
G | A | 5 | a0001c0002t0002g0029a0001c0002t0002g0049a0001c0002t0002g0050others(2): Show | 5 | HG01109.hp1 HG02559.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.263-810C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134630505 | ||||||
chr3:134630868
|
G | C | 80 | a0001c0001t0001g0032a0001c0001t0001g0036a0001c0001t0001g0040others(77): Show | 90 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(87): Show |
intron_variant | MODIFIER | c.263-1173C>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134630868 | ||||||
chr3:134631041
|
G | A | 1 | a0001c0001t0001g0130 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.263-1346C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134631041 | ||||||
chr3:134631153
|
G | A | 80 | a0001c0001t0001g0032a0001c0001t0001g0036a0001c0001t0001g0040others(77): Show | 90 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(87): Show |
intron_variant | MODIFIER | c.263-1458C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134631153 | ||||||
chr3:134631387
|
C | T | 2 | a0001c0002t0002g0029a0001c0005t0007g0033 | 2 | HG01109.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.263-1692G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134631387 | ||||||
chr3:134631404
|
G | A | 2 | a0001c0003t0002g0211a0001c0003t0002g0215 | 2 | HG02280.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.263-1709C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134631404 | ||||||
chr3:134631545
|
TTTTGATA | T | 130 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(127): Show | 170 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(167): Show |
intron_variant | MODIFIER | c.263-1857_263-1851d others(9): Show |
KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134631545 | ||||||
chr3:134631877
|
G | A | 1 | a0001c0001t0008g0053 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.263-2182C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134631877 | ||||||
chr3:134631914
|
A | G | 1 | a0001c0005t0006g0166 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.263-2219T>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134631914 | ||||||
chr3:134631929
|
C | G | 231 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(228): Show | 284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.263-2234G>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134631929 | ||||||
chr3:134632072
|
C | G | 1 | a0001c0002t0002g0094 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.263-2377G>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134632072 | ||||||
chr3:134632170
|
C | G | 232 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(229): Show | 285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.263-2475G>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134632170 | ||||||
chr3:134632181
|
C | T | 8 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0072others(5): Show | 8 | HG01243.hp2 HG01496.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.263-2486G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134632181 | ||||||
chr3:134632302
|
C | A | 2 | a0001c0003t0002g0220a0001c0003t0002g0221 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.263-2607G>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134632302 | ||||||
chr3:134632308
|
G | A | 2 | a0001c0003t0002g0216a0001c0003t0002g0228 | 2 | HG02735.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.263-2613C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134632308 | ||||||
chr3:134632456
|
G | A | 1 | a0001c0001t0001g0074 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.263-2761C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134632456 | ||||||
chr3:134632489
|
C | T | 1 | a0001c0003t0002g0230 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.263-2794G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134632489 | ||||||
chr3:134632882
|
A | G | 134 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(131): Show | 174 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.263-3187T>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134632882 | ||||||
chr3:134632923
|
G | T | 231 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(228): Show | 284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.263-3228C>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134632923 | ||||||
chr3:134632941
|
C | T | 1 | a0001c0001t0014g0052 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.263-3246G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134632941 | ||||||
chr3:134633124
|
T | C | 231 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(228): Show | 284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.263-3429A>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134633124 | ||||||
chr3:134633363
|
C | T | 1 | a0001c0004t0001g0145 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.263-3668G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134633363 | ||||||
chr3:134633379
|
A | T | 1 | a0001c0001t0014g0052 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.263-3684T>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134633379 | ||||||
chr3:134633502
|
A | G | 134 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(131): Show | 174 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.263-3807T>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134633502 | ||||||
chr3:134633556
|
G | A | 3 | a0001c0001t0008g0054a0001c0001t0008g0055a0001c0001t0008g0175 | 3 | HG01891.hp2 HG02258.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.263-3861C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134633556 | ||||||
chr3:134633592
|
A | G | 1 | a0001c0003t0002g0222 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.263-3897T>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134633592 | ||||||
chr3:134633817
|
T | C | 231 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(228): Show | 284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.263-4122A>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134633817 | ||||||
chr3:134633912
|
G | A | 11 | a0001c0002t0002g0012a0001c0002t0002g0037a0001c0002t0002g0057others(8): Show | 12 | HG00738.hp1 HG01243.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.263-4217C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134633912 | ||||||
chr3:134633924
|
T | C | 3 | a0001c0002t0002g0049a0001c0002t0002g0050a0001c0002t0002g0051 | 3 | HG02559.hp1 HG02976.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.263-4229A>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134633924 | ||||||
chr3:134633933
|
A | C | 1 | a0001c0001t0003g0096 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.263-4238T>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134633933 | ||||||
chr3:134634070
|
C | T | 1 | a0001c0005t0006g0166 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.263-4375G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134634070 | ||||||
chr3:134634200
|
A | T | 1 | a0001c0001t0001g0161 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.263-4505T>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134634200 | ||||||
chr3:134634443
|
A | G | 1 | a0001c0001t0001g0131 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.263-4748T>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134634443 | ||||||
chr3:134634532
|
T | A | 231 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(228): Show | 284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.263-4837A>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134634532 | ||||||
chr3:134635040
|
C | T | 1 | a0001c0001t0001g0130 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.263-5345G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134635040 | ||||||
chr3:134635143
|
A | T | 1 | a0001c0001t0001g0129 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.263-5448T>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134635143 | ||||||
chr3:134635246
|
C | T | 1 | a0001c0001t0008g0053 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.263-5551G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134635246 | ||||||
chr3:134635412
|
G | A | 1 | a0001c0001t0029g0195 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.263-5717C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134635412 | ||||||
chr3:134635429
|
G | A | 1 | a0001c0003t0002g0229 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.263-5734C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134635429 | ||||||
chr3:134635445
|
C | T | 1 | a0001c0001t0001g0128 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.263-5750G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134635445 | ||||||
chr3:134635493
|
T | TA | 5 | a0001c0003t0002g0220a0001c0003t0002g0231a0001c0005t0006g0166others(2): Show | 6 | HG01123.hp2 HG02723.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.263-5799dupT | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134635493 | ||||||
chr3:134635493
|
T | TAA | 73 | a0001c0001t0001g0036a0001c0001t0001g0040a0001c0001t0001g0116others(70): Show | 83 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(80): Show |
intron_variant | MODIFIER | c.263-5800_263-5799d others(4): Show |
KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134635493 | ||||||
chr3:134635493
|
T | TAAA | 81 | a0001c0001t0001g0002a0001c0001t0001g0024a0001c0001t0001g0030others(78): Show | 98 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(95): Show |
intron_variant | MODIFIER | c.263-5801_263-5799d others(5): Show |
KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134635493 | ||||||
chr3:134635493
|
T | TAAAA | 55 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(52): Show | 77 | HG00099.hp2 HG00323.hp2 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.263-5802_263-5799d others(6): Show |
KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134635493 | ||||||
chr3:134635493
|
T | TAAAAA | 6 | a0001c0001t0001g0021a0001c0001t0001g0101a0001c0001t0001g0142others(3): Show | 7 | HG00735.hp1 HG01175.hp1 HG04115.hp1 others(4): Show |
intron_variant | MODIFIER | c.263-5803_263-5799d others(7): Show |
KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134635493 | ||||||
chr3:134635493
|
T | TTAAA | 3 | a0001c0001t0008g0054a0001c0001t0008g0055a0001c0001t0008g0175 | 3 | HG01891.hp2 HG02258.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.263-5799_263-5798i others(6): Show |
KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134635493 | ||||||
chr3:134635532
|
A | G | 1 | a0001c0005t0006g0166 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.263-5837T>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134635532 | ||||||
chr3:134636216
|
T | A | 2 | a0001c0007t0010g0015a0001c0007t0010g0083 | 3 | HG01123.hp2 HG02055.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.263-6521A>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134636216 | ||||||
chr3:134636236
|
C | T | 55 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(52): Show | 78 | HG00099.hp2 HG00323.hp2 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.263-6541G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134636236 | ||||||
chr3:134636272
|
C | T | 1 | a0001c0006t0003g0237 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.263-6577G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134636272 | ||||||
chr3:134636347
|
G | T | 80 | a0001c0001t0001g0032a0001c0001t0001g0036a0001c0001t0001g0040others(77): Show | 90 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(87): Show |
intron_variant | MODIFIER | c.263-6652C>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134636347 | ||||||
chr3:134636589
|
C | T | 11 | a0001c0001t0014g0052a0001c0002t0002g0006a0001c0002t0002g0152others(8): Show | 14 | HG00609.hp2 HG02818.hp1 HG03490.hp2 others(11): Show |
intron_variant | MODIFIER | c.262+6727G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134636589 | ||||||
chr3:134636655
|
A | G | 1 | a0001c0001t0001g0205 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.262+6661T>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134636655 | ||||||
chr3:134636691
|
C | T | 1 | a0001c0005t0006g0166 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.262+6625G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134636691 | ||||||
chr3:134636828
|
T | G | 1 | a0001c0001t0001g0074 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.262+6488A>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134636828 | ||||||
chr3:134637900
|
A | C | 12 | a0001c0001t0001g0036a0001c0001t0001g0040a0001c0002t0004g0004others(9): Show | 15 | HG02922.hp2 HG03041.hp1 NA18747.hp1 others(12): Show |
intron_variant | MODIFIER | c.262+5416T>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134637900 | ||||||
chr3:134637928
|
C | T | 2 | a0001c0002t0030g0239a0001c0004t0011g0008 | 4 | HG01255.hp2 HG01891.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.262+5388G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134637928 | ||||||
chr3:134638895
|
C | T | 1 | a0001c0002t0002g0029 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.262+4421G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134638895 | ||||||
chr3:134638907
|
GGT | G | 134 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(131): Show | 174 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.262+4407_262+4408d others(4): Show |
KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134638907 | ||||||
chr3:134638939
|
C | T | 1 | a0001c0006t0003g0237 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.262+4377G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134638939 | ||||||
chr3:134638990
|
A | G | 8 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0072others(5): Show | 8 | HG01243.hp2 HG01496.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.262+4326T>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134638990 | ||||||
chr3:134639047
|
C | CT | 232 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(229): Show | 286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.262+4268dupA | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134639047 | ||||||
chr3:134639061
|
T | G | 1 | a0001c0005t0007g0033 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.262+4255A>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134639061 | ||||||
chr3:134639070
|
G | GT | 15 | a0001c0001t0001g0150a0001c0001t0014g0052a0001c0002t0002g0006others(12): Show | 18 | HG00609.hp2 HG02109.hp1 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.262+4245dupA | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134639070 | ||||||
chr3:134639070
|
G | GTT | 78 | a0001c0001t0001g0032a0001c0001t0001g0036a0001c0001t0001g0040others(75): Show | 88 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(85): Show |
intron_variant | MODIFIER | c.262+4244_262+4245d others(4): Show |
KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134639070 | ||||||
chr3:134639202
|
T | C | 1 | a0001c0005t0006g0166 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.262+4114A>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134639202 | ||||||
chr3:134639227
|
G | A | 2 | a0001c0003t0002g0211a0001c0003t0002g0215 | 2 | HG02280.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.262+4089C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134639227 | ||||||
chr3:134639267
|
C | A | 1 | a0001c0001t0014g0052 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.262+4049G>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134639267 | ||||||
chr3:134639267
|
C | G | 90 | a0001c0001t0001g0032a0001c0001t0001g0036a0001c0001t0001g0040others(87): Show | 103 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(100): Show |
intron_variant | MODIFIER | c.262+4049G>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134639267 | ||||||
chr3:134639321
|
C | T | 1 | a0001c0003t0002g0231 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.262+3995G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134639321 | ||||||
chr3:134639789
|
C | T | 3 | a0001c0001t0008g0054a0001c0001t0008g0055a0001c0001t0008g0175 | 3 | HG01891.hp2 HG02258.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.262+3527G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134639789 | ||||||
chr3:134639949
|
C | CA | 16 | a0001c0001t0014g0052a0001c0002t0002g0051a0001c0002t0002g0090others(13): Show | 16 | HG01175.hp2 HG02280.hp2 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.262+3366dupT | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134639949 | ||||||
chr3:134639949
|
CA | C | 14 | a0001c0001t0001g0061a0001c0001t0001g0068a0001c0001t0001g0193others(11): Show | 15 | HG01123.hp2 HG02258.hp1 HG02622.hp2 others(12): Show |
intron_variant | MODIFIER | c.262+3366delT | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134639949 | ||||||
chr3:134639949
|
CAA | C | 48 | a0001c0001t0001g0002a0001c0001t0001g0024a0001c0001t0001g0030others(45): Show | 59 | HG00280.hp1 HG00642.hp1 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.262+3365_262+3366d others(4): Show |
KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134639949 | ||||||
chr3:134639949
|
CAAA | C | 80 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(77): Show | 109 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.262+3364_262+3366d others(5): Show |
KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134639949 | ||||||
chr3:134640105
|
C | T | 80 | a0001c0001t0001g0032a0001c0001t0001g0036a0001c0001t0001g0040others(77): Show | 90 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(87): Show |
intron_variant | MODIFIER | c.262+3211G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134640105 | ||||||
chr3:134640306
|
C | T | 1 | a0001c0003t0002g0219 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.262+3010G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134640306 | ||||||
chr3:134640523
|
A | G | 1 | a0001c0001t0005g0110 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.262+2793T>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134640523 | ||||||
chr3:134640553
|
C | A | 1 | a0001c0001t0014g0052 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.262+2763G>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134640553 | ||||||
chr3:134640622
|
G | A | 1 | a0001c0002t0002g0029 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.262+2694C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134640622 | ||||||
chr3:134641029
|
C | T | 7 | a0001c0002t0002g0012a0001c0002t0002g0037a0001c0002t0002g0057others(4): Show | 8 | HG00738.hp1 HG02280.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.262+2287G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134641029 | ||||||
chr3:134641083
|
C | T | 5 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0001g0086others(2): Show | 5 | HG00741.hp1 HG02647.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.262+2233G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134641083 | ||||||
chr3:134641318
|
T | C | 4 | a0001c0001t0008g0053a0001c0001t0008g0054a0001c0001t0008g0055others(1): Show | 4 | HG01891.hp2 HG02258.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.262+1998A>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134641318 | ||||||
chr3:134641570
|
G | A | 1 | a0001c0006t0026g0207 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.262+1746C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134641570 | ||||||
chr3:134641683
|
T | C | 1 | a0001c0005t0007g0033 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.262+1633A>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134641683 | ||||||
chr3:134641712
|
C | T | 1 | a0001c0002t0002g0090 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.262+1604G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134641712 | ||||||
chr3:134641736
|
C | T | 1 | a0001c0001t0001g0036 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.262+1580G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134641736 | ||||||
chr3:134641737
|
G | A | 26 | a0001c0002t0002g0107a0001c0003t0002g0007a0001c0003t0002g0027others(23): Show | 30 | HG01099.hp2 HG01168.hp1 HG01169.hp2 others(27): Show |
intron_variant | MODIFIER | c.262+1579C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134641737 | ||||||
chr3:134641791
|
C | T | 5 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0001g0086others(2): Show | 5 | HG00741.hp1 HG02647.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.262+1525G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134641791 | ||||||
chr3:134641866
|
G | T | 1 | a0001c0002t0002g0029 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.262+1450C>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134641866 | ||||||
chr3:134641994
|
A | G | 237 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(234): Show | 291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.262+1322T>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134641994 | ||||||
chr3:134642187
|
G | T | 3 | a0001c0002t0002g0029a0001c0007t0010g0015a0001c0007t0010g0083 | 4 | HG01123.hp2 HG02055.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.262+1129C>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134642187 | ||||||
chr3:134642228
|
C | A | 29 | a0001c0002t0002g0107a0001c0003t0002g0007a0001c0003t0002g0027others(26): Show | 35 | HG01069.hp1 HG01099.hp2 HG01168.hp1 others(32): Show |
intron_variant | MODIFIER | c.262+1088G>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134642228 | ||||||
chr3:134642536
|
T | TAG | 141 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(138): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.262+778_262+779dup others(2): Show |
KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134642536 | ||||||
chr3:134642886
|
A | G | 1 | a0001c0002t0004g0004 | 4 | NA18981.hp1 NA18982.hp1 NA19054.hp1 others(1): Show |
intron_variant | MODIFIER | c.262+430T>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134642886 | ||||||
chr3:134643003
|
ATAGT | A | 3 | a0001c0003t0002g0231a0001c0003t0002g0232a0001c0003t0002g0233 | 3 | NA18956.hp1 NA18989.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.262+309_262+312del others(4): Show |
KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 3/10 | chr3 | 134643003 | ||||||
chr3:134643485
|
G | C | 4 | a0001c0001t0001g0022a0001c0001t0001g0099a0001c0001t0001g0161others(1): Show | 5 | HG02074.hp2 HG02273.hp1 NA18959.hp2 others(2): Show |
intron_variant | MODIFIER | c.200-107C>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 2/10 | chr3 | 134643485 | ||||||
chr3:134643491
|
C | T | 1 | a0001c0006t0026g0207 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.200-113G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 2/10 | chr3 | 134643491 | ||||||
chr3:134643559
|
G | A | 1 | a0001c0002t0002g0163 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.200-181C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 2/10 | chr3 | 134643559 | ||||||
chr3:134643805
|
G | C | 1 | a0001c0002t0002g0164 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.200-427C>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 2/10 | chr3 | 134643805 | ||||||
chr3:134643829
|
C | CT | 39 | a0001c0001t0001g0002a0001c0001t0001g0024a0001c0001t0001g0030others(36): Show | 48 | HG00280.hp1 HG00642.hp1 HG00642.hp2 others(45): Show |
intron_variant | MODIFIER | c.200-452dupA | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 2/10 | chr3 | 134643829 | ||||||
chr3:134643829
|
C | CTT | 104 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(101): Show | 135 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(132): Show |
intron_variant | MODIFIER | c.200-453_200-452dup others(2): Show |
KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 2/10 | chr3 | 134643829 | ||||||
chr3:134643829
|
C | CTTT | 5 | a0001c0001t0008g0175a0001c0002t0002g0172a0001c0004t0001g0173others(2): Show | 7 | HG01891.hp1 HG02258.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.200-454_200-452dup others(3): Show |
KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 2/10 | chr3 | 134643829 | ||||||
chr3:134643870
|
A | C | 1 | a0001c0002t0018g0106 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.200-492T>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 2/10 | chr3 | 134643870 | ||||||
chr3:134643888
|
G | A | 1 | a0006c0011t0009g0031 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.200-510C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 2/10 | chr3 | 134643888 | ||||||
chr3:134643946
|
C | T | 2 | a0001c0005t0006g0104a0001c0005t0006g0105 | 2 | NA18951.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.200-568G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 2/10 | chr3 | 134643946 | ||||||
chr3:134643957
|
G | A | 13 | a0001c0001t0001g0068a0001c0001t0001g0070a0001c0001t0001g0071others(10): Show | 13 | HG01109.hp2 HG01243.hp2 HG01255.hp2 others(10): Show |
intron_variant | MODIFIER | c.200-579C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 2/10 | chr3 | 134643957 | ||||||
chr3:134644016
|
G | A | 139 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(136): Show | 181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.200-638C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 2/10 | chr3 | 134644016 | ||||||
chr3:134644019
|
G | T | 1 | a0001c0005t0006g0199 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.200-641C>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 2/10 | chr3 | 134644019 | ||||||
chr3:134644072
|
G | A | 1 | a0001c0001t0001g0091 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.200-694C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 2/10 | chr3 | 134644072 | ||||||
chr3:134644125
|
G | A | 1 | a0001c0001t0001g0030 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.200-747C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 2/10 | chr3 | 134644125 | ||||||
chr3:134644152
|
C | CAGG | 3 | a0001c0001t0001g0017a0001c0001t0001g0100a0001c0001t0001g0101 | 4 | HG00099.hp2 HG00323.hp2 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.200-777_200-775dup others(3): Show |
KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 2/10 | chr3 | 134644152 | ||||||
chr3:134644364
|
G | A | 33 | a0001c0001t0001g0032a0001c0003t0002g0007a0001c0003t0002g0027others(30): Show | 39 | HG00738.hp2 HG01069.hp1 HG01099.hp2 others(36): Show |
intron_variant | MODIFIER | c.200-986C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 2/10 | chr3 | 134644364 | ||||||
chr3:134644498
|
C | A | 25 | a0001c0001t0001g0064a0001c0001t0001g0068a0001c0001t0001g0070others(22): Show | 26 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(23): Show |
intron_variant | MODIFIER | c.200-1120G>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 2/10 | chr3 | 134644498 | ||||||
chr3:134644529
|
C | T | 1 | a0001c0004t0001g0010 | 3 | HG01167.hp2 HG01169.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.200-1151G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 2/10 | chr3 | 134644529 | ||||||
chr3:134644584
|
C | A | 1 | a0001c0001t0001g0030 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.200-1206G>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 2/10 | chr3 | 134644584 | ||||||
chr3:134644750
|
G | T | 3 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0001g0086 | 3 | HG02647.hp1 HG02897.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.200-1372C>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 2/10 | chr3 | 134644750 | ||||||
chr3:134645102
|
T | C | 9 | a0001c0001t0001g0023a0001c0001t0001g0056a0001c0001t0001g0089others(6): Show | 10 | HG01952.hp2 HG01981.hp2 HG02004.hp1 others(7): Show |
intron_variant | MODIFIER | c.200-1724A>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 2/10 | chr3 | 134645102 | ||||||
chr3:134645267
|
C | T | 1 | a0001c0001t0001g0099 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.200-1889G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 2/10 | chr3 | 134645267 | ||||||
chr3:134645268
|
G | A | 6 | a0001c0001t0008g0175a0001c0001t0029g0195a0001c0002t0002g0172others(3): Show | 8 | HG01891.hp1 HG02258.hp2 HG02698.hp2 others(5): Show |
intron_variant | MODIFIER | c.200-1890C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 2/10 | chr3 | 134645268 | ||||||
chr3:134645287
|
A | G | 33 | a0001c0001t0001g0032a0001c0003t0002g0007a0001c0003t0002g0027others(30): Show | 39 | HG00738.hp2 HG01069.hp1 HG01099.hp2 others(36): Show |
intron_variant | MODIFIER | c.200-1909T>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 2/10 | chr3 | 134645287 | ||||||
chr3:134645306
|
T | C | 1 | a0001c0006t0003g0237 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.200-1928A>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 2/10 | chr3 | 134645306 | ||||||
chr3:134645320
|
C | G | 1 | a0001c0004t0001g0009 | 3 | HG03225.hp1 HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.200-1942G>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 2/10 | chr3 | 134645320 | ||||||
chr3:134645549
|
C | T | 4 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0001g0086others(1): Show | 4 | HG02451.hp1 HG02647.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.199+1886G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 2/10 | chr3 | 134645549 | ||||||
chr3:134645789
|
G | A | 1 | a0001c0001t0024g0196 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.199+1646C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 2/10 | chr3 | 134645789 | ||||||
chr3:134645988
|
G | A | 5 | a0001c0001t0008g0175a0001c0002t0002g0172a0001c0004t0001g0173others(2): Show | 7 | HG01891.hp1 HG02258.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.199+1447C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 2/10 | chr3 | 134645988 | ||||||
chr3:134646047
|
T | C | 26 | a0001c0001t0001g0002a0001c0001t0001g0024a0001c0001t0001g0177others(23): Show | 34 | HG00280.hp1 HG00558.hp2 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.199+1388A>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 2/10 | chr3 | 134646047 | ||||||
chr3:134646114
|
T | C | 1 | a0001c0001t0001g0030 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.199+1321A>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 2/10 | chr3 | 134646114 | ||||||
chr3:134646211
|
G | A | 1 | a0001c0001t0001g0197 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.199+1224C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 2/10 | chr3 | 134646211 | ||||||
chr3:134646222
|
T | C | 148 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(145): Show | 190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.199+1213A>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 2/10 | chr3 | 134646222 | ||||||
chr3:134646289
|
C | T | 2 | a0001c0002t0002g0094a0001c0002t0002g0095 | 2 | HG01496.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.199+1146G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 2/10 | chr3 | 134646289 | ||||||
chr3:134646437
|
A | G | 1 | a0001c0002t0002g0201 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.199+998T>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 2/10 | chr3 | 134646437 | ||||||
chr3:134646654
|
C | T | 2 | a0001c0007t0010g0015a0001c0007t0010g0083 | 3 | HG01123.hp2 HG02055.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.199+781G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 2/10 | chr3 | 134646654 | ||||||
chr3:134646730
|
T | C | 1 | a0001c0001t0001g0198 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.199+705A>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 2/10 | chr3 | 134646730 | ||||||
chr3:134646786
|
G | A | 1 | a0001c0001t0003g0069 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.199+649C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 2/10 | chr3 | 134646786 | ||||||
chr3:134646911
|
C | G | 237 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(234): Show | 291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.199+524G>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 2/10 | chr3 | 134646911 | ||||||
chr3:134647032
|
T | C | 2 | a0001c0002t0004g0087a0001c0002t0015g0088 | 2 | NA18960.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.199+403A>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 2/10 | chr3 | 134647032 | ||||||
chr3:134647043
|
T | G | 2 | a0001c0005t0006g0199a0001c0005t0006g0200 | 2 | NA18967.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.199+392A>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 2/10 | chr3 | 134647043 | ||||||
chr3:134647069
|
C | T | 1 | a0001c0001t0001g0093 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.199+366G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 2/10 | chr3 | 134647069 | ||||||
chr3:134647173
|
C | T | 1 | a0001c0003t0002g0211 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.199+262G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 2/10 | chr3 | 134647173 | ||||||
chr3:134647248
|
G | A | 1 | a0001c0002t0002g0201 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.199+187C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 2/10 | chr3 | 134647248 | ||||||
chr3:134647273
|
A | C | 2 | a0001c0001t0001g0016a0001c0001t0001g0092 | 3 | HG01257.hp1 HG01258.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.199+162T>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 2/10 | chr3 | 134647273 | ||||||
chr3:134647578
|
G | A | 11 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0072others(8): Show | 11 | HG01109.hp2 HG01243.hp2 HG01496.hp1 others(8): Show |
intron_variant | MODIFIER | c.137-81C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 1/10 | chr3 | 134647578 | ||||||
chr3:134647594
|
C | T | 1 | a0001c0003t0002g0210 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.137-97G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 1/10 | chr3 | 134647594 | ||||||
chr3:134647611
|
CTG | C | 5 | a0001c0004t0001g0009a0001c0004t0001g0010a0001c0004t0001g0026others(2): Show | 10 | HG01167.hp2 HG01169.hp1 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.137-116_137-115del others(2): Show |
KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 1/10 | chr3 | 134647611 | ||||||
chr3:134647715
|
G | T | 1 | a0001c0001t0001g0030 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.137-218C>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 1/10 | chr3 | 134647715 | ||||||
chr3:134647765
|
TTTCCAC | T | 3 | a0001c0002t0002g0029a0001c0007t0010g0015a0001c0007t0010g0083 | 4 | HG01123.hp2 HG02055.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.137-274_137-269del others(6): Show |
KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 1/10 | chr3 | 134647765 | ||||||
chr3:134647920
|
A | G | 1 | a0001c0001t0001g0091 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.137-423T>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 1/10 | chr3 | 134647920 | ||||||
chr3:134647959
|
C | T | 1 | a0001c0002t0002g0090 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.137-462G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 1/10 | chr3 | 134647959 | ||||||
chr3:134648083
|
C | T | 2 | a0001c0003t0002g0027a0001c0003t0002g0209 | 3 | HG01168.hp1 HG01169.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.137-586G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 1/10 | chr3 | 134648083 | ||||||
chr3:134648084
|
G | A | 1 | a0003c0014t0017g0081 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.137-587C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 1/10 | chr3 | 134648084 | ||||||
chr3:134648114
|
C | T | 1 | a0001c0001t0001g0089 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.137-617G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 1/10 | chr3 | 134648114 | ||||||
chr3:134648209
|
C | T | 13 | a0001c0001t0001g0036a0001c0001t0001g0040a0001c0002t0002g0037others(10): Show | 16 | HG02922.hp2 HG03041.hp1 NA18747.hp1 others(13): Show |
intron_variant | MODIFIER | c.137-712G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 1/10 | chr3 | 134648209 | ||||||
chr3:134648352
|
C | T | 207 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(204): Show | 258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.137-855G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 1/10 | chr3 | 134648352 | ||||||
chr3:134648543
|
G | A | 1 | a0004c0015t0002g0238 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.137-1046C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 1/10 | chr3 | 134648543 | ||||||
chr3:134648768
|
G | A | 1 | a0001c0001t0001g0204 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.137-1271C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 1/10 | chr3 | 134648768 | ||||||
chr3:134648997
|
C | T | 2 | a0001c0002t0004g0087a0001c0002t0015g0088 | 2 | NA18960.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.137-1500G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 1/10 | chr3 | 134648997 | ||||||
chr3:134649130
|
A | T | 3 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0001g0086 | 3 | HG02647.hp1 HG02897.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.137-1633T>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 1/10 | chr3 | 134649130 | ||||||
chr3:134649131
|
G | T | 3 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0001g0086 | 3 | HG02647.hp1 HG02897.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.137-1634C>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 1/10 | chr3 | 134649131 | ||||||
chr3:134649132
|
A | ATTCTG | 3 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0001g0086 | 3 | HG02647.hp1 HG02897.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.137-1636_137-1635i others(7): Show |
KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 1/10 | chr3 | 134649132 | ||||||
chr3:134649792
|
A | T | 181 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(178): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.136+1033T>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 1/10 | chr3 | 134649792 | ||||||
chr3:134649972
|
C | T | 1 | a0001c0002t0002g0029 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.136+853G>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 1/10 | chr3 | 134649972 | ||||||
chr3:134650123
|
GGATCCTG others(17): Show |
G | 1 | a0001c0005t0007g0082 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.136+678_136+701del others(24): Show |
KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 1/10 | chr3 | 134650123 | ||||||
chr3:134650140
|
A | G | 1 | a0006c0011t0009g0031 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.136+685T>C | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 1/10 | chr3 | 134650140 | ||||||
chr3:134650219
|
T | A | 1 | a0001c0001t0001g0205 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.136+606A>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 1/10 | chr3 | 134650219 | ||||||
chr3:134650366
|
G | T | 2 | a0001c0006t0001g0208a0001c0006t0026g0207 | 2 | HG00738.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.136+459C>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 1/10 | chr3 | 134650366 | ||||||
chr3:134650436
|
G | A | 1 | a0001c0002t0004g0004 | 4 | NA18981.hp1 NA18982.hp1 NA19054.hp1 others(1): Show |
intron_variant | MODIFIER | c.136+389C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 1/10 | chr3 | 134650436 | ||||||
chr3:134650488
|
G | A | 3 | a0001c0002t0002g0029a0001c0007t0010g0015a0001c0007t0010g0083 | 4 | HG01123.hp2 HG02055.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.136+337C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 1/10 | chr3 | 134650488 | ||||||
chr3:134650578
|
G | A | 141 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(138): Show | 182 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(179): Show |
intron_variant | MODIFIER | c.136+247C>T | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 1/10 | chr3 | 134650578 | ||||||
chr3:134650627
|
GCTGCGCG others(11): Show |
G | 1 | a0001c0003t0002g0206 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.136+180_136+197del others(18): Show |
KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 1/10 | chr3 | 134650627 | ||||||
chr3:134650722
|
A | C | 1 | a0001c0001t0001g0030 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.136+103T>G | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 1/10 | chr3 | 134650722 | ||||||
chr3:134650779
|
G | T | 1 | a0001c0002t0002g0029 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.136+46C>A | KY | ENSG00000174611.12 | transcript | ENST00000423778.7 | protein_coding | 1/10 | chr3 | 134650779 |