geneid | 2487 |
---|---|
ensemblid | ENSG00000162998.5 |
hgncid | 3959 |
symbol | FRZB |
name | frizzled related protein |
refseq_nuc | NM_001463.4 |
refseq_prot | NP_001454.2 |
ensembl_nuc | ENST00000295113.5 |
ensembl_prot | ENSP00000295113.4 |
mane_status | MANE Select |
chr | chr2 |
start | 182833275 |
end | 182866637 |
strand | - |
ver | v1.2 |
region | chr2:182833275-182866637 |
region5000 | chr2:182828275-182871637 |
regionname0 | FRZB_chr2_182833275_182866637 |
regionname5000 | FRZB_chr2_182828275_182871637 |
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 | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 325 | 321 | 65 | 53 | 160 | 8 | 34 | 123 | FRZB_chr2_182828275_182871637 | FRZB | copy fasta | chr2 | 182828275 | 182871637 |
a0002 | 0/1 | 325 | 32 | 26 | 1 | 1 | 3 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | copy fasta | chr2 | 182828275 | 182871637 |
a0003 | 0/0 | 325 | 9 | 1 | 6 | 0 | 1 | 1 | 0 | FRZB_chr2_182828275_182871637 | FRZB | copy fasta | chr2 | 182828275 | 182871637 |
a0004 | 0/0 | 325 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | copy fasta | chr2 | 182828275 | 182871637 |
a0005 | 0/0 | 325 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | copy fasta | chr2 | 182828275 | 182871637 |
a0006 | 0/0 | 325 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FRZB_chr2_182828275_182871637 | FRZB | copy fasta | chr2 | 182828275 | 182871637 |
a0007 | 0/0 | 325 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | copy fasta | chr2 | 182828275 | 182871637 |
a0008 | 0/0 | 325 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FRZB_chr2_182828275_182871637 | FRZB | copy fasta | chr2 | 182828275 | 182871637 |
a0009 | 0/0 | 325 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | copy fasta | chr2 | 182828275 | 182871637 |
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 | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/0 | 978 | 316 | 60 | 53 | 160 | 8 | 34 | FRZB_chr2_182828275_182871637 | FRZB | copy fasta | chr2 | 182828275 | 182871637 |
c0002 | 0/1 | 978 | 31 | 25 | 1 | 1 | 3 | 0 | FRZB_chr2_182828275_182871637 | FRZB | copy fasta | chr2 | 182828275 | 182871637 |
c0003 | 0/0 | 978 | 8 | 0 | 6 | 0 | 1 | 1 | FRZB_chr2_182828275_182871637 | FRZB | copy fasta | chr2 | 182828275 | 182871637 |
c0004 | 0/0 | 978 | 5 | 5 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | copy fasta | chr2 | 182828275 | 182871637 |
c0005 | 0/0 | 978 | 2 | 0 | 2 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | copy fasta | chr2 | 182828275 | 182871637 |
c0006 | 0/0 | 978 | 2 | 0 | 2 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | copy fasta | chr2 | 182828275 | 182871637 |
c0007 | 0/0 | 978 | 1 | 0 | 1 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | copy fasta | chr2 | 182828275 | 182871637 |
c0008 | 0/0 | 978 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | copy fasta | chr2 | 182828275 | 182871637 |
c0009 | 0/0 | 978 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | copy fasta | chr2 | 182828275 | 182871637 |
c0010 | 0/0 | 978 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | copy fasta | chr2 | 182828275 | 182871637 |
c0011 | 0/0 | 978 | 1 | 0 | 0 | 0 | 0 | 1 | FRZB_chr2_182828275_182871637 | FRZB | copy fasta | chr2 | 182828275 | 182871637 |
c0012 | 0/0 | 978 | 1 | 0 | 1 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | copy fasta | chr2 | 182828275 | 182871637 |
thapid | grch38chm13v2 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 | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 1660 | 229 | 43 | 21 | 137 | 4 | 22 | FRZB_chr2_182828275_182871637 | FRZB | copy fasta | chr2 | 182828275 | 182871637 |
t0002 | 0/0 | 1660 | 80 | 8 | 35 | 21 | 5 | 11 | FRZB_chr2_182828275_182871637 | FRZB | copy fasta | chr2 | 182828275 | 182871637 |
t0003 | 0/0 | 1659 | 35 | 26 | 5 | 1 | 3 | 0 | FRZB_chr2_182828275_182871637 | FRZB | copy fasta | chr2 | 182828275 | 182871637 |
t0004 | 0/0 | 1660 | 8 | 8 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | copy fasta | chr2 | 182828275 | 182871637 |
t0005 | 0/0 | 1659 | 4 | 1 | 0 | 3 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | copy fasta | chr2 | 182828275 | 182871637 |
t0006 | 0/0 | 1659 | 4 | 0 | 1 | 0 | 0 | 3 | FRZB_chr2_182828275_182871637 | FRZB | copy fasta | chr2 | 182828275 | 182871637 |
t0007 | 0/0 | 1660 | 3 | 2 | 1 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | copy fasta | chr2 | 182828275 | 182871637 |
t0008 | 0/0 | 1660 | 2 | 2 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | copy fasta | chr2 | 182828275 | 182871637 |
t0009 | 0/0 | 1660 | 2 | 2 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | copy fasta | chr2 | 182828275 | 182871637 |
t0010 | 0/0 | 1660 | 2 | 0 | 2 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | copy fasta | chr2 | 182828275 | 182871637 |
t0011 | 0/0 | 1660 | 1 | 0 | 1 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | copy fasta | chr2 | 182828275 | 182871637 |
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 | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 20 | 2 | 1 | 17 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0002 | 0/0 | 16 | 0 | 5 | 9 | 0 | 2 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0003 | 0/0 | 15 | 3 | 6 | 2 | 1 | 3 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0004 | 0/0 | 9 | 0 | 7 | 2 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0005 | 0/0 | 8 | 8 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0006 | 0/0 | 7 | 0 | 0 | 6 | 0 | 1 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0007 | 0/0 | 7 | 0 | 2 | 5 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0008 | 0/0 | 7 | 0 | 0 | 6 | 0 | 1 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0009 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0010 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0011 | 0/0 | 5 | 0 | 1 | 1 | 0 | 3 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0012 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0015 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0016 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0018 | 1/0 | 3 | 2 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0020 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0022 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0026 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0030 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0034 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0040 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0043 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0046 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0047 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0048 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0049 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0051 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0195 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
achapid | 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 | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 978 | 316 | 60 | 53 | 160 | 8 | 34 | FRZB_chr2_182828275_182871637 | FRZB | copy fasta | chr2 | 182828275 | 182871637 |
a0001c0004 | 0/0 | 978 | 5 | 5 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | copy fasta | chr2 | 182828275 | 182871637 |
a0002c0002 | 0/1 | 978 | 31 | 25 | 1 | 1 | 3 | 0 | FRZB_chr2_182828275_182871637 | FRZB | copy fasta | chr2 | 182828275 | 182871637 |
a0002c0010 | 0/0 | 978 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | copy fasta | chr2 | 182828275 | 182871637 |
a0003c0003 | 0/0 | 978 | 8 | 0 | 6 | 0 | 1 | 1 | FRZB_chr2_182828275_182871637 | FRZB | copy fasta | chr2 | 182828275 | 182871637 |
a0003c0009 | 0/0 | 978 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | copy fasta | chr2 | 182828275 | 182871637 |
a0004c0005 | 0/0 | 978 | 2 | 0 | 2 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | copy fasta | chr2 | 182828275 | 182871637 |
a0005c0006 | 0/0 | 978 | 2 | 0 | 2 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | copy fasta | chr2 | 182828275 | 182871637 |
a0006c0008 | 0/0 | 978 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | copy fasta | chr2 | 182828275 | 182871637 |
a0007c0007 | 0/0 | 978 | 1 | 0 | 1 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | copy fasta | chr2 | 182828275 | 182871637 |
a0008c0011 | 0/0 | 978 | 1 | 0 | 0 | 0 | 0 | 1 | FRZB_chr2_182828275_182871637 | FRZB | copy fasta | chr2 | 182828275 | 182871637 |
a0009c0012 | 0/0 | 978 | 1 | 0 | 1 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | copy fasta | chr2 | 182828275 | 182871637 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 2637 | 219 | 40 | 18 | 137 | 3 | 20 | FRZB_chr2_182828275_182871637 | FRZB | copy fasta | chr2 | 182828275 | 182871637 |
a0001c0001t0002 | 0/0 | 2637 | 74 | 8 | 30 | 20 | 5 | 11 | FRZB_chr2_182828275_182871637 | FRZB | copy fasta | chr2 | 182828275 | 182871637 |
a0001c0001t0004 | 0/0 | 2637 | 5 | 5 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | copy fasta | chr2 | 182828275 | 182871637 |
a0001c0001t0005 | 0/0 | 2636 | 4 | 1 | 0 | 3 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | copy fasta | chr2 | 182828275 | 182871637 |
a0001c0001t0006 | 0/0 | 2636 | 4 | 0 | 1 | 0 | 0 | 3 | FRZB_chr2_182828275_182871637 | FRZB | copy fasta | chr2 | 182828275 | 182871637 |
a0001c0001t0007 | 0/0 | 2637 | 3 | 2 | 1 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | copy fasta | chr2 | 182828275 | 182871637 |
a0001c0001t0008 | 0/0 | 2637 | 2 | 2 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | copy fasta | chr2 | 182828275 | 182871637 |
a0001c0001t0009 | 0/0 | 2637 | 2 | 2 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | copy fasta | chr2 | 182828275 | 182871637 |
a0001c0001t0010 | 0/0 | 2637 | 2 | 0 | 2 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | copy fasta | chr2 | 182828275 | 182871637 |
a0001c0001t0011 | 0/0 | 2637 | 1 | 0 | 1 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | copy fasta | chr2 | 182828275 | 182871637 |
a0001c0004t0001 | 0/0 | 2637 | 3 | 3 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | copy fasta | chr2 | 182828275 | 182871637 |
a0001c0004t0004 | 0/0 | 2637 | 2 | 2 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | copy fasta | chr2 | 182828275 | 182871637 |
a0002c0002t0001 | 0/1 | 2637 | 1 | 0 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | copy fasta | chr2 | 182828275 | 182871637 |
a0002c0002t0003 | 0/0 | 2636 | 30 | 25 | 1 | 1 | 3 | 0 | FRZB_chr2_182828275_182871637 | FRZB | copy fasta | chr2 | 182828275 | 182871637 |
a0002c0010t0003 | 0/0 | 2636 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | copy fasta | chr2 | 182828275 | 182871637 |
a0003c0003t0001 | 0/0 | 2637 | 4 | 0 | 2 | 0 | 1 | 1 | FRZB_chr2_182828275_182871637 | FRZB | copy fasta | chr2 | 182828275 | 182871637 |
a0003c0003t0002 | 0/0 | 2637 | 4 | 0 | 4 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | copy fasta | chr2 | 182828275 | 182871637 |
a0003c0009t0004 | 0/0 | 2637 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | copy fasta | chr2 | 182828275 | 182871637 |
a0004c0005t0003 | 0/0 | 2636 | 2 | 0 | 2 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | copy fasta | chr2 | 182828275 | 182871637 |
a0005c0006t0003 | 0/0 | 2636 | 2 | 0 | 2 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | copy fasta | chr2 | 182828275 | 182871637 |
a0006c0008t0002 | 0/0 | 2637 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | copy fasta | chr2 | 182828275 | 182871637 |
a0007c0007t0002 | 0/0 | 2637 | 1 | 0 | 1 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | copy fasta | chr2 | 182828275 | 182871637 |
a0008c0011t0001 | 0/0 | 2637 | 1 | 0 | 0 | 0 | 0 | 1 | FRZB_chr2_182828275_182871637 | FRZB | copy fasta | chr2 | 182828275 | 182871637 |
a0009c0012t0001 | 0/0 | 2637 | 1 | 0 | 1 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | copy fasta | chr2 | 182828275 | 182871637 |
actghapid | 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 | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 20 | 2 | 1 | 17 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0001g0002 | 0/0 | 16 | 0 | 5 | 9 | 0 | 2 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0001g0005 | 0/0 | 8 | 8 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0001g0006 | 0/0 | 7 | 0 | 0 | 6 | 0 | 1 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0001g0007 | 0/0 | 7 | 0 | 2 | 5 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0001g0008 | 0/0 | 7 | 0 | 0 | 6 | 0 | 1 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0001g0009 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0001g0010 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0001g0011 | 0/0 | 5 | 0 | 1 | 1 | 0 | 3 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0001g0012 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0001g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0001g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0001g0015 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0001g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0001g0018 | 1/0 | 3 | 2 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0001g0034 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0001g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0001g0046 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0001g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0002g0003 | 0/0 | 15 | 3 | 6 | 2 | 1 | 3 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0002g0004 | 0/0 | 9 | 0 | 7 | 2 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0002g0016 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0002g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0002g0030 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0002g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0002g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0002g0047 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0002g0049 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0002g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0002g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0002g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0002g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0002g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0002g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0002g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0002g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0002g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0002g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0002g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0002g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0002g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0002g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0004g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0004g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0004g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0004g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0004g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0005g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0005g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0005g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0005g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0006g0020 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0006g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0007g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0007g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0007g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0008g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0008g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0009g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0010g0040 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0001t0011g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0004t0001g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0004t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0001c0004t0004g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0002c0002t0001g0195 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0002c0002t0003g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0002c0002t0003g0048 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0002c0002t0003g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0002c0002t0003g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0002c0002t0003g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0002c0002t0003g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0002c0002t0003g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0002c0002t0003g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0002c0002t0003g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0002c0002t0003g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0002c0002t0003g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0002c0002t0003g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0002c0002t0003g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0002c0002t0003g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0002c0002t0003g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0002c0002t0003g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0002c0002t0003g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0002c0002t0003g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0002c0002t0003g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0002c0002t0003g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0002c0002t0003g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0002c0002t0003g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0002c0002t0003g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0002c0002t0003g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0002c0002t0003g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0002c0002t0003g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0002c0002t0003g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0002c0002t0003g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0002c0010t0003g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0003c0003t0001g0022 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0003c0003t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0003c0003t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0003c0003t0002g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0003c0003t0002g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0003c0003t0002g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0003c0003t0002g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0003c0009t0004g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0004c0005t0003g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0005c0006t0003g0051 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0006c0008t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0007c0007t0002g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0008c0011t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
a0009c0012t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0002 | g0003 | EUR | GBR | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG00099 | hp2 | a0003 | c0003 | t0001 | g0132 | EUR | GBR | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG00140 | hp1 | a0001 | c0001 | t0002 | g0135 | EUR | GBR | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG00140 | hp2 | a0001 | c0001 | t0002 | g0016 | EUR | GBR | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0046 | EUR | FIN | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0043 | EUR | FIN | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | CHS | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | CHS | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG00438 | hp1 | a0001 | c0001 | t0002 | g0100 | EAS | CHS | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | CHS | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | CHS | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG00558 | hp2 | a0001 | c0001 | t0002 | g0113 | EAS | CHS | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG00597 | hp1 | a0002 | c0002 | t0003 | g0145 | EAS | CHS | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | CHS | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | CHS | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | CHS | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG00639 | hp1 | a0001 | c0001 | t0006 | g0199 | AMR | PUR | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG00642 | hp1 | a0001 | c0001 | t0002 | g0151 | AMR | PUR | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG00642 | hp2 | a0003 | c0003 | t0002 | g0052 | AMR | PUR | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | CHS | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | CHS | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG00733 | hp2 | a0001 | c0001 | t0002 | g0031 | AMR | PUR | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG00735 | hp1 | a0003 | c0003 | t0002 | g0125 | AMR | PUR | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG01071 | hp1 | a0003 | c0003 | t0002 | g0131 | AMR | PUR | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG01071 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG01074 | hp1 | a0001 | c0001 | t0002 | g0160 | AMR | PUR | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG01081 | hp1 | a0001 | c0001 | t0007 | g0150 | AMR | PUR | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG01081 | hp2 | a0001 | c0001 | t0002 | g0120 | AMR | PUR | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG01099 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG01099 | hp2 | a0009 | c0012 | t0001 | g0221 | AMR | PUR | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG01109 | hp2 | a0003 | c0003 | t0001 | g0022 | AMR | PUR | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG01168 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG01169 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG01169 | hp2 | a0003 | c0003 | t0002 | g0053 | AMR | PUR | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG01175 | hp1 | a0001 | c0001 | t0002 | g0016 | AMR | PUR | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG01175 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG01192 | hp1 | a0004 | c0005 | t0003 | g0023 | AMR | PUR | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG01243 | hp1 | a0007 | c0007 | t0002 | g0062 | AMR | PUR | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG01255 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | CLM | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | CLM | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG01257 | hp1 | a0001 | c0001 | t0002 | g0049 | AMR | CLM | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0114 | AMR | CLM | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG01261 | hp2 | a0002 | c0002 | t0003 | g0074 | AMR | CLM | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG01346 | hp1 | a0004 | c0005 | t0003 | g0023 | AMR | CLM | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG01346 | hp2 | a0001 | c0001 | t0002 | g0033 | AMR | CLM | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG01358 | hp1 | a0005 | c0006 | t0003 | g0051 | AMR | CLM | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0181 | AMR | CLM | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG01361 | hp1 | a0005 | c0006 | t0003 | g0051 | AMR | CLM | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG01361 | hp2 | a0001 | c0001 | t0011 | g0122 | AMR | CLM | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG01496 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0033 | AMR | CLM | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG01515 | hp1 | a0001 | c0001 | t0002 | g0047 | EUR | IBS | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG01515 | hp2 | a0002 | c0002 | t0003 | g0048 | EUR | IBS | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG01517 | hp1 | a0002 | c0002 | t0003 | g0048 | EUR | IBS | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG01517 | hp2 | a0001 | c0001 | t0002 | g0030 | EUR | IBS | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | ACB | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG01884 | hp2 | a0001 | c0004 | t0004 | g0037 | AFR | ACB | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG01943 | hp1 | a0001 | c0001 | t0002 | g0031 | AMR | PEL | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG01952 | hp1 | a0001 | c0001 | t0002 | g0204 | AMR | PEL | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG01952 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG01978 | hp1 | a0003 | c0003 | t0001 | g0054 | AMR | PEL | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG01978 | hp2 | a0001 | c0001 | t0002 | g0091 | AMR | PEL | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG01981 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG01981 | hp2 | a0001 | c0001 | t0010 | g0040 | AMR | PEL | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG01993 | hp1 | a0001 | c0001 | t0002 | g0166 | AMR | PEL | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG01993 | hp2 | a0001 | c0001 | t0002 | g0157 | AMR | PEL | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG02004 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG02004 | hp2 | a0001 | c0001 | t0002 | g0202 | AMR | PEL | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | KHV | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG02040 | hp1 | a0001 | c0001 | t0002 | g0136 | EAS | KHV | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | KHV | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG02055 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | ACB | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | KHV | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | KHV | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | KHV | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | KHV | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG02083 | hp2 | a0001 | c0001 | t0002 | g0078 | EAS | KHV | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG02132 | hp1 | a0001 | c0001 | t0002 | g0162 | EAS | KHV | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | KHV | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG02145 | hp1 | a0002 | c0002 | t0003 | g0070 | AFR | ACB | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG02145 | hp2 | a0001 | c0001 | t0002 | g0056 | AFR | ACB | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG02148 | hp1 | a0001 | c0001 | t0010 | g0040 | AMR | PEL | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG02148 | hp2 | a0001 | c0001 | t0002 | g0124 | AMR | PEL | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG02257 | hp1 | a0002 | c0002 | t0003 | g0167 | AFR | ACB | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG02257 | hp2 | a0001 | c0004 | t0001 | g0137 | AFR | ACB | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG02258 | hp1 | a0001 | c0004 | t0001 | g0038 | AFR | ACB | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | ACB | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG02273 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG02273 | hp2 | a0001 | c0001 | t0002 | g0148 | AMR | PEL | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG02280 | hp1 | a0003 | c0009 | t0004 | g0178 | AFR | ACB | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG02293 | hp1 | a0001 | c0001 | t0002 | g0049 | AMR | PEL | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG02293 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG02300 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG02451 | hp1 | a0002 | c0002 | t0003 | g0075 | AFR | ACB | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | ACB | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG02572 | hp1 | a0001 | c0001 | t0004 | g0083 | AFR | GWD | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG02572 | hp2 | a0002 | c0002 | t0003 | g0127 | AFR | GWD | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG02602 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0081 | SAS | PJL | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | GWD | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | GWD | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG02622 | hp2 | a0002 | c0002 | t0003 | g0024 | AFR | GWD | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | GWD | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG02647 | hp1 | a0001 | c0001 | t0008 | g0096 | AFR | GWD | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG02647 | hp2 | a0001 | c0001 | t0002 | g0187 | AFR | GWD | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG02698 | hp1 | a0001 | c0001 | t0002 | g0156 | SAS | PJL | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG02698 | hp2 | a0001 | c0001 | t0002 | g0047 | SAS | PJL | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | GWD | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG02717 | hp2 | a0001 | c0001 | t0004 | g0141 | AFR | GWD | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG02723 | hp1 | a0001 | c0001 | t0002 | g0169 | AFR | GWD | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG02723 | hp2 | a0001 | c0001 | t0004 | g0153 | AFR | GWD | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG02809 | hp2 | a0001 | c0001 | t0002 | g0196 | AFR | GWD | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG02818 | hp1 | a0002 | c0002 | t0003 | g0176 | AFR | GWD | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | GWD | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG02886 | hp1 | a0002 | c0002 | t0003 | g0175 | AFR | GWD | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | GWD | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG02896 | hp1 | a0001 | c0001 | t0009 | g0045 | AFR | GWD | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG02896 | hp2 | a0001 | c0001 | t0007 | g0059 | AFR | GWD | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG02897 | hp1 | a0001 | c0001 | t0009 | g0045 | AFR | GWD | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG02897 | hp2 | a0002 | c0002 | t0003 | g0064 | AFR | GWD | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ESN | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG02922 | hp2 | a0001 | c0001 | t0002 | g0177 | AFR | ESN | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG02965 | hp1 | a0002 | c0002 | t0003 | g0139 | AFR | ESN | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG02965 | hp2 | a0002 | c0002 | t0003 | g0065 | AFR | ESN | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | ESN | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG02976 | hp1 | a0002 | c0002 | t0003 | g0179 | AFR | ESN | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG03017 | hp1 | a0003 | c0003 | t0001 | g0022 | SAS | PJL | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG03017 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG03041 | hp1 | a0002 | c0002 | t0003 | g0069 | AFR | GWD | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG03041 | hp2 | a0002 | c0002 | t0003 | g0060 | AFR | GWD | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG03098 | hp1 | a0001 | c0004 | t0004 | g0037 | AFR | MSL | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG03098 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | MSL | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG03130 | hp1 | a0002 | c0002 | t0003 | g0143 | AFR | ESN | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | ESN | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | ESN | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG03195 | hp2 | a0002 | c0002 | t0003 | g0140 | AFR | ESN | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | MSL | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | MSL | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG03225 | hp1 | a0001 | c0001 | t0004 | g0144 | AFR | MSL | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG03225 | hp2 | a0001 | c0004 | t0001 | g0038 | AFR | MSL | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | MSL | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG03453 | hp2 | a0002 | c0002 | t0003 | g0174 | AFR | MSL | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG03486 | hp2 | a0002 | c0002 | t0003 | g0072 | AFR | MSL | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG03490 | hp1 | a0001 | c0001 | t0006 | g0020 | SAS | PJL | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG03490 | hp2 | a0001 | c0001 | t0002 | g0016 | SAS | PJL | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG03492 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG03492 | hp2 | a0001 | c0001 | t0006 | g0020 | SAS | PJL | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG03540 | hp2 | a0002 | c0010 | t0003 | g0063 | AFR | GWD | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG03579 | hp1 | a0001 | c0001 | t0008 | g0099 | AFR | MSL | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG03579 | hp2 | a0002 | c0002 | t0003 | g0066 | AFR | MSL | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0121 | SAS | PJL | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG03654 | hp2 | a0001 | c0001 | t0002 | g0161 | SAS | PJL | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | STU | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | STU | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0206 | SAS | PJL | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0182 | SAS | PJL | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0116 | SAS | BEB | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | BEB | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG03942 | hp1 | a0001 | c0001 | t0002 | g0129 | SAS | BEB | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG03942 | hp2 | a0001 | c0001 | t0002 | g0133 | SAS | BEB | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0168 | SAS | STU | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0088 | SAS | STU | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | BEB | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0219 | SAS | BEB | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0026 | SAS | STU | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG04199 | hp2 | a0001 | c0001 | t0002 | g0030 | SAS | STU | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG04204 | hp1 | a0001 | c0001 | t0002 | g0193 | SAS | STU | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG04204 | hp2 | a0001 | c0001 | t0006 | g0020 | SAS | STU | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG04228 | hp1 | a0008 | c0011 | t0001 | g0220 | SAS | STU | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0212 | SAS | STU | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA18522 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | YRI | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | YRI | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | CHB | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | CHB | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | CHB | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | CHB | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA18906 | hp1 | a0002 | c0002 | t0003 | g0068 | AFR | YRI | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | YRI | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA18940 | hp2 | a0001 | c0001 | t0002 | g0192 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA18950 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA18952 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA18954 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA18969 | hp2 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA18972 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA18979 | hp2 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA18982 | hp2 | a0001 | c0001 | t0002 | g0190 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA18985 | hp2 | a0001 | c0001 | t0005 | g0200 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA18986 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA18991 | hp2 | a0001 | c0001 | t0002 | g0210 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA19006 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA19043 | hp1 | a0001 | c0001 | t0007 | g0097 | AFR | LWK | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | LWK | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA19056 | hp2 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA19057 | hp1 | a0001 | c0001 | t0002 | g0185 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA19067 | hp2 | a0001 | c0001 | t0005 | g0214 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA19072 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA19082 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA19084 | hp1 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA19084 | hp2 | a0001 | c0001 | t0005 | g0194 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA19085 | hp1 | a0006 | c0008 | t0002 | g0184 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | YRI | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | YRI | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | ASW | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | ASW | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0043 | EUR | TSI | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA20752 | hp2 | a0002 | c0002 | t0003 | g0119 | EUR | TSI | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0117 | SAS | GIH | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0208 | SAS | GIH | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG02109 | hp1 | a0002 | c0002 | t0003 | g0061 | AFR | ACB | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG02109 | hp2 | a0001 | c0001 | t0004 | g0172 | AFR | ACB | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG02486 | hp2 | a0002 | c0002 | t0003 | g0173 | AFR | ACB | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG02559 | hp1 | a0002 | c0002 | t0003 | g0154 | AFR | ACB | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG03471 | hp1 | a0002 | c0002 | t0003 | g0152 | AFR | MSL | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG06807 | hp1 | a0002 | c0002 | t0003 | g0067 | AFR | USA | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0084 | AFR | USA | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA20300 | hp1 | a0002 | c0002 | t0003 | g0024 | AFR | USA | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | USA | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA21309 | hp1 | a0001 | c0001 | t0005 | g0142 | AFR | LWK | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
homoSapiens_chm13v2 | hp1 | a0002 | c0002 | t0001 | g0195 | REF | REF | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0018 | REF | REF | FRZB_chr2_182828275_182871637 | FRZB | chr2 | 182828275 | 182871637 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:182834856
|
C | T | 1 | a0006 | 1 | NA19085.hp1 | missense_variant | MODERATE | c.971G>A | p.Arg324His | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 6/6 | 1056/2637 | 971/978 | 324/325 | chr2 | 182834856 | ||
chr2:182834857
|
G | C | 3 | a0002a0004a0005 | 36 | HG00597.hp1 HG01192.hp1 HG01261.hp2 others(33): Show |
missense_variant | MODERATE | c.970C>G | p.Arg324Gly | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 6/6 | 1055/2637 | 970/978 | 324/325 | chr2 | 182834857 | ||
chr2:182838419
|
C | T | 1 | a0007 | 1 | HG01243.hp1 | missense_variant | MODERATE | c.787G>A | p.Glu263Lys | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 4/6 | 872/2637 | 787/978 | 263/325 | chr2 | 182838419 | ||
chr2:182838608
|
G | A | 2 | a0003a0004 | 11 | HG00099.hp2 HG00642.hp2 HG00735.hp1 others(8): Show |
missense_variant | MODERATE | c.598C>T | p.Arg200Trp | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 4/6 | 683/2637 | 598/978 | 200/325 | chr2 | 182838608 | ||
chr2:182866405
|
T | C | 1 | a0008 | 1 | HG04228.hp1 | missense_variant | MODERATE | c.148A>G | p.Met50Val | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/6 | 233/2637 | 148/978 | 50/325 | chr2 | 182866405 | ||
chr2:182866465
|
C | A | 2 | a0005a0009 | 3 | HG01099.hp2 HG01358.hp1 HG01361.hp1 |
missense_variant | MODERATE | c.88G>T | p.Ala30Ser | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/6 | 173/2637 | 88/978 | 30/325 | chr2 | 182866465 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:182837963
|
G | A | 1 | a0003c0009 | 1 | HG02280.hp1 | synonymous_variant | LOW | c.846C>T | p.Leu282Leu | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 5/6 | 931/2637 | 846/978 | 282/325 | chr2 | 182837963 | ||
chr2:182842533
|
T | C | 1 | a0002c0010 | 1 | HG03540.hp2 | synonymous_variant | LOW | c.537A>G | p.Lys179Lys | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 3/6 | 622/2637 | 537/978 | 179/325 | chr2 | 182842533 | ||
chr2:182858811
|
G | A | 1 | a0001c0004 | 5 | HG01884.hp2 HG02257.hp2 HG02258.hp1 others(2): Show |
synonymous_variant | LOW | c.501C>T | p.Asn167Asn | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/6 | 586/2637 | 501/978 | 167/325 | chr2 | 182858811 |
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 cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:182833364
|
A | G | 5 | a0001c0001t0002a0001c0001t0005a0003c0003t0002others(2): Show | 84 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(81): Show |
3_prime_UTR_variant | MODIFIER | c.*1485T>C | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 6/6 | 1485 | chr2 | 182833364 | |||||
chr2:182833427
|
C | T | 3 | a0001c0001t0004a0001c0004t0004a0003c0009t0004 | 8 | HG01884.hp2 HG02109.hp2 HG02280.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1422G>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 6/6 | 1422 | chr2 | 182833427 | |||||
chr2:182833506
|
T | A | 4 | a0001c0001t0004a0001c0001t0008a0001c0004t0004others(1): Show | 10 | HG01884.hp2 HG02109.hp2 HG02280.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1343A>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 6/6 | 1343 | chr2 | 182833506 | |||||
chr2:182833520
|
T | C | 1 | a0001c0001t0011 | 1 | HG01361.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1329A>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 6/6 | 1329 | chr2 | 182833520 | |||||
chr2:182833834
|
C | T | 1 | a0001c0001t0009 | 2 | HG02896.hp1 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1015G>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 6/6 | 1015 | chr2 | 182833834 | |||||
chr2:182833858
|
CA | C | 2 | a0001c0001t0005a0001c0001t0006 | 8 | HG00639.hp1 HG03490.hp1 HG03492.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*990delT | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 6/6 | 990 | chr2 | 182833858 | |||||
chr2:182833872
|
T | C | 4 | a0002c0002t0003a0002c0010t0003a0004c0005t0003others(1): Show | 35 | HG00597.hp1 HG01192.hp1 HG01261.hp2 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*977A>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 6/6 | 977 | chr2 | 182833872 | |||||
chr2:182833964
|
G | A | 4 | a0002c0002t0003a0002c0010t0003a0004c0005t0003others(1): Show | 35 | HG00597.hp1 HG01192.hp1 HG01261.hp2 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*885C>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 6/6 | 885 | chr2 | 182833964 | |||||
chr2:182833970
|
A | G | 1 | a0001c0001t0007 | 3 | HG01081.hp1 HG02896.hp2 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*879T>C | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 6/6 | 879 | chr2 | 182833970 | |||||
chr2:182834000
|
GA | G | 4 | a0002c0002t0003a0002c0010t0003a0004c0005t0003others(1): Show | 35 | HG00597.hp1 HG01192.hp1 HG01261.hp2 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*848delT | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 6/6 | 848 | chr2 | 182834000 | |||||
chr2:182834453
|
A | G | 1 | a0001c0001t0008 | 2 | HG02647.hp1 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*396T>C | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 6/6 | 396 | chr2 | 182834453 | |||||
chr2:182834637
|
C | T | 4 | a0002c0002t0003a0002c0010t0003a0004c0005t0003others(1): Show | 35 | HG00597.hp1 HG01192.hp1 HG01261.hp2 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*212G>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 6/6 | 212 | chr2 | 182834637 | |||||
chr2:182834684
|
G | A | 1 | a0001c0001t0010 | 2 | HG01981.hp2 HG02148.hp1 |
3_prime_UTR_variant | MODIFIER | c.*165C>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 6/6 | 165 | chr2 | 182834684 |
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 cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:182834983
|
G | A | 2 | a0001c0001t0002g0092a0001c0001t0002g0136 | 2 | HG02040.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.862-18C>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 5/5 | chr2 | 182834983 | ||||||
chr2:182835041
|
G | A | 19 | a0001c0001t0001g0009a0001c0001t0001g0036a0001c0001t0001g0041others(16): Show | 29 | HG00408.hp1 HG00597.hp1 HG01192.hp1 others(26): Show |
intron_variant | MODIFIER | c.862-76C>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 5/5 | chr2 | 182835041 | ||||||
chr2:182835079
|
C | G | 4 | a0001c0001t0001g0058a0001c0001t0001g0128a0001c0004t0001g0038others(1): Show | 5 | HG02257.hp2 HG02258.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.862-114G>C | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 5/5 | chr2 | 182835079 | ||||||
chr2:182835225
|
T | C | 2 | a0001c0001t0008g0096a0001c0001t0008g0099 | 2 | HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.862-260A>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 5/5 | chr2 | 182835225 | ||||||
chr2:182835227
|
T | C | 26 | a0001c0001t0001g0005a0001c0001t0001g0039a0001c0001t0001g0055others(23): Show | 36 | HG00609.hp2 HG00621.hp1 HG01081.hp1 others(33): Show |
intron_variant | MODIFIER | c.862-262A>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 5/5 | chr2 | 182835227 | ||||||
chr2:182835328
|
C | T | 1 | a0001c0001t0001g0121 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.862-363G>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 5/5 | chr2 | 182835328 | ||||||
chr2:182835365
|
C | T | 14 | a0001c0001t0001g0089a0001c0001t0001g0118a0001c0001t0001g0126others(11): Show | 14 | HG00642.hp2 HG00673.hp1 HG00735.hp2 others(11): Show |
intron_variant | MODIFIER | c.862-400G>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 5/5 | chr2 | 182835365 | ||||||
chr2:182835447
|
T | TG | 19 | a0001c0001t0001g0009a0001c0001t0001g0036a0001c0001t0001g0041others(16): Show | 28 | HG00408.hp1 HG00597.hp1 HG01192.hp1 others(25): Show |
intron_variant | MODIFIER | c.862-483dupC | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 5/5 | chr2 | 182835447 | ||||||
chr2:182835538
|
A | T | 1 | a0001c0001t0002g0187 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.862-573T>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 5/5 | chr2 | 182835538 | ||||||
chr2:182835539
|
A | T | 1 | a0001c0001t0002g0187 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.862-574T>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 5/5 | chr2 | 182835539 | ||||||
chr2:182835568
|
AC | A | 49 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(46): Show | 99 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(96): Show |
intron_variant | MODIFIER | c.862-604delG | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 5/5 | chr2 | 182835568 | ||||||
chr2:182835703
|
G | A | 1 | a0001c0001t0001g0170 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.862-738C>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 5/5 | chr2 | 182835703 | ||||||
chr2:182835913
|
G | A | 2 | a0001c0001t0002g0187a0005c0006t0003g0051 | 3 | HG01358.hp1 HG01361.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.862-948C>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 5/5 | chr2 | 182835913 | ||||||
chr2:182835935
|
A | T | 2 | a0002c0002t0003g0175a0002c0002t0003g0176 | 2 | HG02818.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.862-970T>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 5/5 | chr2 | 182835935 | ||||||
chr2:182836059
|
T | C | 1 | a0001c0001t0001g0170 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.862-1094A>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 5/5 | chr2 | 182836059 | ||||||
chr2:182836076
|
C | T | 54 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0012others(51): Show | 97 | HG00323.hp1 HG00423.hp2 HG00544.hp2 others(94): Show |
intron_variant | MODIFIER | c.862-1111G>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 5/5 | chr2 | 182836076 | ||||||
chr2:182836139
|
T | A | 15 | a0001c0001t0001g0170a0001c0001t0002g0187a0001c0001t0004g0083others(12): Show | 18 | HG01261.hp2 HG01358.hp1 HG01361.hp1 others(15): Show |
intron_variant | MODIFIER | c.862-1174A>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 5/5 | chr2 | 182836139 | ||||||
chr2:182836155
|
C | T | 9 | a0001c0001t0001g0117a0003c0003t0001g0022a0003c0003t0001g0054others(6): Show | 11 | HG00099.hp2 HG00642.hp2 HG00735.hp1 others(8): Show |
intron_variant | MODIFIER | c.862-1190G>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 5/5 | chr2 | 182836155 | ||||||
chr2:182836173
|
T | C | 15 | a0001c0001t0001g0170a0001c0001t0002g0187a0001c0001t0004g0083others(12): Show | 18 | HG01261.hp2 HG01358.hp1 HG01361.hp1 others(15): Show |
intron_variant | MODIFIER | c.862-1208A>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 5/5 | chr2 | 182836173 | ||||||
chr2:182836232
|
T | A | 1 | a0001c0001t0001g0171 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.862-1267A>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 5/5 | chr2 | 182836232 | ||||||
chr2:182836286
|
T | A | 8 | a0001c0001t0001g0008a0001c0001t0001g0035a0001c0001t0001g0103others(5): Show | 15 | HG03688.hp2 NA18747.hp1 NA18747.hp2 others(12): Show |
intron_variant | MODIFIER | c.862-1321A>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 5/5 | chr2 | 182836286 | ||||||
chr2:182836459
|
C | T | 1 | a0001c0001t0001g0046 | 2 | HG00323.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.861+1489G>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 5/5 | chr2 | 182836459 | ||||||
chr2:182836510
|
G | A | 1 | a0001c0001t0001g0170 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.861+1438C>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 5/5 | chr2 | 182836510 | ||||||
chr2:182836580
|
C | A | 18 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0026others(15): Show | 33 | HG00597.hp1 HG00609.hp2 HG00621.hp1 others(30): Show |
intron_variant | MODIFIER | c.861+1368G>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 5/5 | chr2 | 182836580 | ||||||
chr2:182836860
|
A | G | 137 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(134): Show | 210 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(207): Show |
intron_variant | MODIFIER | c.861+1088T>C | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 5/5 | chr2 | 182836860 | ||||||
chr2:182836979
|
A | T | 4 | a0001c0001t0001g0170a0001c0004t0001g0038a0001c0004t0001g0137others(1): Show | 6 | HG01884.hp2 HG02257.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.861+969T>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 5/5 | chr2 | 182836979 | ||||||
chr2:182837054
|
T | C | 1 | a0001c0001t0006g0199 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.861+894A>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 5/5 | chr2 | 182837054 | ||||||
chr2:182837199
|
A | T | 1 | a0001c0001t0001g0206 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.861+749T>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 5/5 | chr2 | 182837199 | ||||||
chr2:182837344
|
T | C | 1 | a0001c0001t0002g0177 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.861+604A>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 5/5 | chr2 | 182837344 | ||||||
chr2:182837505
|
TG | T | 19 | a0001c0001t0001g0010a0001c0001t0001g0071a0001c0001t0001g0073others(16): Show | 26 | HG00099.hp2 HG00642.hp2 HG00735.hp1 others(23): Show |
intron_variant | MODIFIER | c.861+442delC | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 5/5 | chr2 | 182837505 | ||||||
chr2:182837541
|
C | T | 5 | a0001c0001t0001g0010a0001c0001t0005g0142a0002c0002t0003g0139others(2): Show | 9 | HG02257.hp1 HG02559.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.861+407G>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 5/5 | chr2 | 182837541 | ||||||
chr2:182837729
|
T | A | 1 | a0002c0002t0003g0140 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.861+219A>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 5/5 | chr2 | 182837729 | ||||||
chr2:182837780
|
A | C | 1 | a0001c0001t0004g0172 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.861+168T>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 5/5 | chr2 | 182837780 | ||||||
chr2:182837824
|
C | T | 1 | a0005c0006t0003g0051 | 2 | HG01358.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.861+124G>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 5/5 | chr2 | 182837824 | ||||||
chr2:182838102
|
T | C | 19 | a0001c0001t0001g0058a0001c0001t0001g0171a0001c0001t0002g0169others(16): Show | 20 | HG01243.hp1 HG01358.hp1 HG01361.hp1 others(17): Show |
intron_variant | MODIFIER | c.798-91A>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 4/5 | chr2 | 182838102 | ||||||
chr2:182838164
|
C | T | 1 | a0001c0001t0001g0215 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.798-153G>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 4/5 | chr2 | 182838164 | ||||||
chr2:182838236
|
G | A | 8 | a0003c0003t0001g0022a0003c0003t0001g0054a0003c0003t0001g0132others(5): Show | 10 | HG00099.hp2 HG00642.hp2 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.797+173C>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 4/5 | chr2 | 182838236 | ||||||
chr2:182838958
|
G | A | 1 | a0001c0001t0001g0168 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.593-345C>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 3/5 | chr2 | 182838958 | ||||||
chr2:182838966
|
A | C | 1 | a0001c0001t0002g0113 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.593-353T>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 3/5 | chr2 | 182838966 | ||||||
chr2:182839057
|
C | T | 1 | a0001c0001t0004g0172 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.593-444G>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 3/5 | chr2 | 182839057 | ||||||
chr2:182839136
|
G | A | 3 | a0002c0002t0003g0174a0002c0002t0003g0175a0002c0002t0003g0176 | 3 | HG02818.hp1 HG02886.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.593-523C>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 3/5 | chr2 | 182839136 | ||||||
chr2:182839321
|
A | G | 1 | a0001c0001t0001g0088 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.593-708T>C | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 3/5 | chr2 | 182839321 | ||||||
chr2:182839356
|
A | G | 72 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(69): Show | 146 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(143): Show |
intron_variant | MODIFIER | c.593-743T>C | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 3/5 | chr2 | 182839356 | ||||||
chr2:182839409
|
T | A | 67 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(64): Show | 115 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.593-796A>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 3/5 | chr2 | 182839409 | ||||||
chr2:182839433
|
C | G | 1 | a0001c0001t0007g0150 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.593-820G>C | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 3/5 | chr2 | 182839433 | ||||||
chr2:182839444
|
C | T | 1 | a0001c0001t0004g0172 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.593-831G>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 3/5 | chr2 | 182839444 | ||||||
chr2:182839517
|
T | C | 1 | a0003c0009t0004g0178 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.593-904A>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 3/5 | chr2 | 182839517 | ||||||
chr2:182839534
|
C | T | 1 | a0001c0001t0001g0134 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.593-921G>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 3/5 | chr2 | 182839534 | ||||||
chr2:182839761
|
C | A | 3 | a0001c0001t0001g0171a0001c0001t0002g0169a0002c0002t0003g0173 | 3 | HG02486.hp2 HG02622.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.593-1148G>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 3/5 | chr2 | 182839761 | ||||||
chr2:182839855
|
T | C | 59 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(56): Show | 106 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.593-1242A>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 3/5 | chr2 | 182839855 | ||||||
chr2:182839891
|
A | G | 4 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0002g0169others(1): Show | 4 | HG02486.hp2 HG02622.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.593-1278T>C | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 3/5 | chr2 | 182839891 | ||||||
chr2:182839911
|
T | C | 1 | a0001c0001t0001g0029 | 2 | NA18962.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.593-1298A>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 3/5 | chr2 | 182839911 | ||||||
chr2:182839913
|
T | C | 1 | a0001c0001t0004g0172 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.593-1300A>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 3/5 | chr2 | 182839913 | ||||||
chr2:182839931
|
T | C | 5 | a0003c0003t0001g0022a0003c0003t0001g0054a0003c0003t0002g0052others(2): Show | 7 | HG00642.hp2 HG01109.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.593-1318A>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 3/5 | chr2 | 182839931 | ||||||
chr2:182839953
|
C | G | 22 | a0001c0001t0001g0010a0001c0001t0001g0071a0001c0001t0001g0073others(19): Show | 31 | HG00642.hp2 HG01109.hp2 HG01169.hp2 others(28): Show |
intron_variant | MODIFIER | c.593-1340G>C | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 3/5 | chr2 | 182839953 | ||||||
chr2:182839991
|
C | T | 21 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0026others(18): Show | 36 | HG00597.hp1 HG00609.hp2 HG00621.hp1 others(33): Show |
intron_variant | MODIFIER | c.593-1378G>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 3/5 | chr2 | 182839991 | ||||||
chr2:182840469
|
A | G | 7 | a0001c0001t0001g0058a0001c0001t0007g0059a0002c0002t0003g0060others(4): Show | 7 | HG01243.hp1 HG02109.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.593-1856T>C | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 3/5 | chr2 | 182840469 | ||||||
chr2:182841047
|
G | C | 2 | a0003c0003t0001g0022a0003c0003t0001g0054 | 3 | HG01109.hp2 HG01978.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.592+1431C>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 3/5 | chr2 | 182841047 | ||||||
chr2:182841090
|
C | T | 1 | a0001c0001t0004g0172 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.592+1388G>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 3/5 | chr2 | 182841090 | ||||||
chr2:182841129
|
A | G | 1 | a0001c0001t0002g0177 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.592+1349T>C | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 3/5 | chr2 | 182841129 | ||||||
chr2:182841410
|
G | A | 1 | a0001c0001t0002g0185 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.592+1068C>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 3/5 | chr2 | 182841410 | ||||||
chr2:182841437
|
T | C | 190 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(187): Show | 331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.592+1041A>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 3/5 | chr2 | 182841437 | ||||||
chr2:182841540
|
C | T | 1 | a0007c0007t0002g0062 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.592+938G>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 3/5 | chr2 | 182841540 | ||||||
chr2:182841713
|
A | C | 4 | a0001c0001t0001g0041a0001c0001t0001g0155a0001c0001t0001g0158others(1): Show | 5 | NA18969.hp1 NA18972.hp1 NA18995.hp2 others(2): Show |
intron_variant | MODIFIER | c.592+765T>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 3/5 | chr2 | 182841713 | ||||||
chr2:182841726
|
T | A | 1 | a0001c0001t0002g0161 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.592+752A>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 3/5 | chr2 | 182841726 | ||||||
chr2:182841784
|
G | T | 79 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(76): Show | 141 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(138): Show |
intron_variant | MODIFIER | c.592+694C>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 3/5 | chr2 | 182841784 | ||||||
chr2:182841792
|
T | C | 12 | a0001c0001t0001g0010a0001c0001t0001g0071a0001c0001t0001g0073others(9): Show | 17 | HG01261.hp2 HG02145.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.592+686A>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 3/5 | chr2 | 182841792 | ||||||
chr2:182841827
|
A | G | 3 | a0001c0004t0001g0038a0001c0004t0001g0137a0001c0004t0004g0037 | 5 | HG01884.hp2 HG02257.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.592+651T>C | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 3/5 | chr2 | 182841827 | ||||||
chr2:182841948
|
C | T | 1 | a0001c0001t0002g0210 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.592+530G>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 3/5 | chr2 | 182841948 | ||||||
chr2:182842076
|
T | G | 5 | a0003c0003t0001g0022a0003c0003t0001g0054a0003c0003t0002g0052others(2): Show | 7 | HG00642.hp2 HG01109.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.592+402A>C | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 3/5 | chr2 | 182842076 | ||||||
chr2:182842098
|
T | C | 2 | a0001c0001t0001g0107a0001c0001t0002g0104 | 2 | NA18969.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.592+380A>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 3/5 | chr2 | 182842098 | ||||||
chr2:182842127
|
G | A | 82 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(79): Show | 146 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(143): Show |
intron_variant | MODIFIER | c.592+351C>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 3/5 | chr2 | 182842127 | ||||||
chr2:182842129
|
A | G | 1 | a0001c0001t0001g0116 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.592+349T>C | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 3/5 | chr2 | 182842129 | ||||||
chr2:182842200
|
T | A | 5 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0002g0169others(2): Show | 5 | HG02486.hp2 HG02622.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.592+278A>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 3/5 | chr2 | 182842200 | ||||||
chr2:182842302
|
T | C | 2 | a0002c0002t0003g0074a0002c0002t0003g0075 | 2 | HG01261.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.592+176A>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 3/5 | chr2 | 182842302 | ||||||
chr2:182842445
|
C | A | 1 | a0001c0001t0001g0205 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.592+33G>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 3/5 | chr2 | 182842445 | ||||||
chr2:182842972
|
T | C | 116 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(113): Show | 200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.527-429A>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182842972 | ||||||
chr2:182843077
|
G | C | 3 | a0001c0001t0002g0157a0001c0001t0002g0162a0001c0001t0002g0166 | 3 | HG01993.hp1 HG01993.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.527-534C>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182843077 | ||||||
chr2:182843080
|
G | A | 71 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(68): Show | 142 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(139): Show |
intron_variant | MODIFIER | c.527-537C>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182843080 | ||||||
chr2:182843468
|
T | C | 200 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(197): Show | 343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.527-925A>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182843468 | ||||||
chr2:182843511
|
C | A | 1 | a0001c0001t0001g0171 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.527-968G>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182843511 | ||||||
chr2:182843528
|
G | T | 33 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0026others(30): Show | 50 | HG00597.hp1 HG00609.hp2 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.527-985C>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182843528 | ||||||
chr2:182843656
|
C | T | 2 | a0001c0001t0001g0055a0001c0001t0002g0056 | 2 | HG02145.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.527-1113G>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182843656 | ||||||
chr2:182843676
|
A | G | 1 | a0001c0001t0004g0141 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.527-1133T>C | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182843676 | ||||||
chr2:182843761
|
G | A | 1 | a0002c0002t0003g0072 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.527-1218C>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182843761 | ||||||
chr2:182843797
|
G | A | 1 | a0001c0001t0001g0110 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.527-1254C>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182843797 | ||||||
chr2:182843799
|
C | T | 1 | a0001c0001t0002g0192 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.527-1256G>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182843799 | ||||||
chr2:182843800
|
G | A | 1 | a0003c0009t0004g0178 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.527-1257C>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182843800 | ||||||
chr2:182843880
|
A | C | 1 | a0002c0002t0003g0069 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.527-1337T>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182843880 | ||||||
chr2:182844507
|
T | C | 1 | a0001c0001t0002g0033 | 2 | HG01346.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.527-1964A>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182844507 | ||||||
chr2:182844803
|
C | G | 12 | a0001c0001t0001g0010a0001c0001t0001g0071a0001c0001t0001g0073others(9): Show | 17 | HG01261.hp2 HG02145.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.527-2260G>C | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182844803 | ||||||
chr2:182845005
|
C | T | 1 | a0001c0001t0004g0172 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.527-2462G>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182845005 | ||||||
chr2:182845258
|
T | C | 3 | a0001c0004t0001g0038a0001c0004t0001g0137a0001c0004t0004g0037 | 5 | HG01884.hp2 HG02257.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.527-2715A>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182845258 | ||||||
chr2:182845269
|
C | CT | 3 | a0001c0001t0004g0172a0005c0006t0003g0051a0009c0012t0001g0221 | 4 | HG01099.hp2 HG01358.hp1 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.527-2727dupA | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182845269 | ||||||
chr2:182845409
|
C | T | 112 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(109): Show | 191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.527-2866G>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182845409 | ||||||
chr2:182845562
|
GA | G | 13 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0134others(10): Show | 24 | HG00423.hp1 HG00558.hp2 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.527-3020delT | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182845562 | ||||||
chr2:182845711
|
C | G | 71 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(68): Show | 142 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(139): Show |
intron_variant | MODIFIER | c.527-3168G>C | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182845711 | ||||||
chr2:182845951
|
C | G | 1 | a0001c0001t0001g0043 | 2 | HG00323.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.527-3408G>C | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182845951 | ||||||
chr2:182846170
|
T | C | 5 | a0003c0003t0001g0022a0003c0003t0001g0054a0003c0003t0002g0052others(2): Show | 7 | HG00642.hp2 HG01109.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.527-3627A>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182846170 | ||||||
chr2:182846200
|
A | G | 1 | a0001c0001t0002g0190 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.527-3657T>C | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182846200 | ||||||
chr2:182846216
|
A | C | 1 | a0001c0001t0002g0177 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.527-3673T>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182846216 | ||||||
chr2:182846223
|
T | C | 197 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(194): Show | 340 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(337): Show |
intron_variant | MODIFIER | c.527-3680A>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182846223 | ||||||
chr2:182846262
|
A | C | 1 | a0003c0009t0004g0178 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.527-3719T>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182846262 | ||||||
chr2:182846325
|
T | A | 1 | a0002c0002t0003g0048 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.527-3782A>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182846325 | ||||||
chr2:182846414
|
T | C | 1 | a0002c0002t0003g0048 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.527-3871A>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182846414 | ||||||
chr2:182846499
|
A | G | 1 | a0001c0001t0008g0096 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.527-3956T>C | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182846499 | ||||||
chr2:182846689
|
G | A | 213 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(210): Show | 358 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(355): Show |
intron_variant | MODIFIER | c.527-4146C>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182846689 | ||||||
chr2:182846709
|
T | C | 1 | a0002c0002t0003g0179 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.527-4166A>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182846709 | ||||||
chr2:182846800
|
C | T | 1 | a0001c0001t0001g0080 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.527-4257G>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182846800 | ||||||
chr2:182846920
|
T | C | 1 | a0001c0001t0001g0077 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.527-4377A>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182846920 | ||||||
chr2:182847021
|
T | C | 20 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0026others(17): Show | 33 | HG00597.hp1 HG00609.hp2 HG00621.hp1 others(30): Show |
intron_variant | MODIFIER | c.527-4478A>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182847021 | ||||||
chr2:182847155
|
T | C | 17 | a0001c0001t0001g0055a0001c0001t0001g0057a0001c0001t0001g0058others(14): Show | 18 | HG01099.hp2 HG01243.hp1 HG01358.hp1 others(15): Show |
intron_variant | MODIFIER | c.527-4612A>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182847155 | ||||||
chr2:182847242
|
C | G | 5 | a0003c0003t0001g0022a0003c0003t0001g0054a0003c0003t0002g0052others(2): Show | 7 | HG00642.hp2 HG01109.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.527-4699G>C | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182847242 | ||||||
chr2:182847251
|
T | C | 107 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(104): Show | 184 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(181): Show |
intron_variant | MODIFIER | c.527-4708A>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182847251 | ||||||
chr2:182847412
|
G | A | 2 | a0001c0001t0001g0055a0001c0001t0002g0056 | 2 | HG02145.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.527-4869C>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182847412 | ||||||
chr2:182847432
|
G | A | 1 | a0001c0001t0001g0108 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.527-4889C>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182847432 | ||||||
chr2:182847444
|
T | G | 5 | a0003c0003t0001g0022a0003c0003t0001g0054a0003c0003t0002g0052others(2): Show | 7 | HG00642.hp2 HG01109.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.527-4901A>C | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182847444 | ||||||
chr2:182847620
|
G | A | 112 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(109): Show | 191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.527-5077C>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182847620 | ||||||
chr2:182847796
|
T | C | 1 | a0001c0001t0004g0172 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.527-5253A>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182847796 | ||||||
chr2:182847867
|
G | T | 1 | a0001c0001t0001g0164 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.527-5324C>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182847867 | ||||||
chr2:182848070
|
T | TA | 19 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0026others(16): Show | 31 | HG00621.hp2 HG01884.hp1 HG02056.hp2 others(28): Show |
intron_variant | MODIFIER | c.527-5528dupT | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182848070 | ||||||
chr2:182848070
|
TA | T | 115 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(112): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.527-5528delT | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182848070 | ||||||
chr2:182848083
|
A | C | 102 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(99): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.527-5540T>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182848083 | ||||||
chr2:182848360
|
C | T | 112 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(109): Show | 192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.527-5817G>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182848360 | ||||||
chr2:182848551
|
C | A | 3 | a0001c0004t0001g0038a0001c0004t0001g0137a0001c0004t0004g0037 | 5 | HG01884.hp2 HG02257.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.527-6008G>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182848551 | ||||||
chr2:182848584
|
A | G | 1 | a0001c0001t0002g0169 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.527-6041T>C | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182848584 | ||||||
chr2:182848598
|
T | C | 1 | a0002c0002t0003g0145 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.527-6055A>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182848598 | ||||||
chr2:182848616
|
C | T | 7 | a0001c0001t0001g0058a0001c0001t0007g0059a0002c0002t0003g0060others(4): Show | 7 | HG01243.hp1 HG02109.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.527-6073G>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182848616 | ||||||
chr2:182848709
|
C | T | 1 | a0001c0001t0002g0112 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.527-6166G>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182848709 | ||||||
chr2:182848963
|
C | T | 1 | a0002c0002t0003g0068 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.527-6420G>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182848963 | ||||||
chr2:182849009
|
C | T | 3 | a0002c0002t0003g0066a0002c0002t0003g0179a0003c0009t0004g0178 | 3 | HG02280.hp1 HG02976.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.527-6466G>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182849009 | ||||||
chr2:182849088
|
G | A | 1 | a0001c0001t0002g0177 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.527-6545C>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182849088 | ||||||
chr2:182849097
|
A | G | 107 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(104): Show | 184 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(181): Show |
intron_variant | MODIFIER | c.527-6554T>C | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182849097 | ||||||
chr2:182849155
|
G | C | 5 | a0003c0003t0001g0022a0003c0003t0001g0054a0003c0003t0002g0052others(2): Show | 7 | HG00642.hp2 HG01109.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.527-6612C>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182849155 | ||||||
chr2:182849227
|
A | AAAAT | 8 | a0001c0001t0001g0019a0001c0001t0001g0155a0001c0001t0001g0189others(5): Show | 10 | HG01261.hp2 HG02015.hp1 HG02056.hp1 others(7): Show |
intron_variant | MODIFIER | c.527-6688_527-6685d others(6): Show |
FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182849227 | ||||||
chr2:182849227
|
A | AAAATAAA others(5): Show |
1 | a0001c0001t0009g0045 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.527-6696_527-6685d others(14): Show |
FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182849227 | ||||||
chr2:182849227
|
AAAAT | A | 40 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0012others(37): Show | 65 | HG00408.hp1 HG00558.hp1 HG00597.hp1 others(62): Show |
intron_variant | MODIFIER | c.527-6688_527-6685d others(6): Show |
FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182849227 | ||||||
chr2:182849227
|
AAAATAAA others(1): Show |
A | 12 | a0001c0001t0001g0026a0001c0001t0001g0050a0001c0001t0001g0058others(9): Show | 15 | HG00642.hp2 HG01109.hp2 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.527-6692_527-6685d others(10): Show |
FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182849227 | ||||||
chr2:182849227
|
AAAATAAA others(5): Show |
A | 6 | a0001c0001t0001g0027a0001c0001t0001g0076a0002c0002t0003g0024others(3): Show | 9 | HG01192.hp1 HG01346.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.527-6696_527-6685d others(14): Show |
FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182849227 | ||||||
chr2:182849227
|
AAAATAAA others(9): Show |
A | 1 | a0002c0002t0003g0064 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.527-6700_527-6685d others(18): Show |
FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182849227 | ||||||
chr2:182849227
|
AAAATAAA others(13): Show |
A | 3 | a0001c0001t0001g0079a0001c0001t0002g0133a0003c0003t0001g0054 | 3 | HG01978.hp1 HG02074.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.527-6704_527-6685d others(22): Show |
FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182849227 | ||||||
chr2:182849227
|
AAAATAAA others(17): Show |
A | 81 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(78): Show | 153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): Show |
intron_variant | MODIFIER | c.527-6708_527-6685d others(26): Show |
FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182849227 | ||||||
chr2:182849748
|
A | G | 1 | a0001c0001t0001g0170 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.527-7205T>C | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182849748 | ||||||
chr2:182849797
|
A | G | 13 | a0001c0001t0001g0055a0001c0001t0001g0057a0001c0001t0001g0058others(10): Show | 13 | HG01243.hp1 HG02109.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.527-7254T>C | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182849797 | ||||||
chr2:182850185
|
TTA | T | 115 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(112): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.527-7644_527-7643d others(4): Show |
FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182850185 | ||||||
chr2:182850225
|
G | T | 4 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0002g0169others(1): Show | 4 | HG02486.hp2 HG02622.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.527-7682C>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182850225 | ||||||
chr2:182850266
|
G | A | 12 | a0001c0001t0001g0010a0001c0001t0001g0071a0001c0001t0001g0073others(9): Show | 17 | HG01261.hp2 HG02145.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.527-7723C>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182850266 | ||||||
chr2:182850400
|
T | A | 1 | a0001c0001t0004g0172 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.527-7857A>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182850400 | ||||||
chr2:182850544
|
A | G | 99 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(96): Show | 177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
intron_variant | MODIFIER | c.527-8001T>C | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182850544 | ||||||
chr2:182850560
|
C | CT | 16 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0002g0169others(13): Show | 19 | HG00642.hp2 HG01099.hp2 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.527-8018dupA | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182850560 | ||||||
chr2:182850690
|
G | C | 5 | a0001c0001t0001g0005a0001c0001t0001g0109a0001c0001t0001g0110others(2): Show | 12 | HG02055.hp2 HG02572.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.526+8096C>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182850690 | ||||||
chr2:182850876
|
C | T | 1 | a0001c0001t0001g0170 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.526+7910G>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182850876 | ||||||
chr2:182850883
|
G | A | 11 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0026others(8): Show | 22 | HG00621.hp2 HG02056.hp2 HG02074.hp2 others(19): Show |
intron_variant | MODIFIER | c.526+7903C>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182850883 | ||||||
chr2:182850982
|
T | G | 3 | a0002c0002t0003g0066a0002c0002t0003g0179a0003c0009t0004g0178 | 3 | HG02280.hp1 HG02976.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.526+7804A>C | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182850982 | ||||||
chr2:182850988
|
A | G | 220 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(217): Show | 367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): Show |
intron_variant | MODIFIER | c.526+7798T>C | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182850988 | ||||||
chr2:182850991
|
T | C | 1 | a0002c0002t0003g0173 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.526+7795A>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182850991 | ||||||
chr2:182851213
|
G | C | 1 | a0001c0001t0002g0129 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.526+7573C>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182851213 | ||||||
chr2:182851259
|
C | T | 2 | a0001c0001t0004g0083a0001c0001t0004g0141 | 2 | HG02572.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.526+7527G>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182851259 | ||||||
chr2:182851306
|
G | A | 1 | a0001c0001t0004g0172 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.526+7480C>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182851306 | ||||||
chr2:182851458
|
C | A | 1 | a0001c0001t0002g0187 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.526+7328G>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182851458 | ||||||
chr2:182851645
|
G | C | 5 | a0003c0003t0001g0022a0003c0003t0001g0054a0003c0003t0002g0052others(2): Show | 7 | HG00642.hp2 HG01109.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.526+7141C>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182851645 | ||||||
chr2:182851654
|
T | C | 1 | a0001c0001t0001g0094 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.526+7132A>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182851654 | ||||||
chr2:182851851
|
C | T | 12 | a0001c0001t0001g0010a0001c0001t0001g0071a0001c0001t0001g0073others(9): Show | 17 | HG01261.hp2 HG02145.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.526+6935G>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182851851 | ||||||
chr2:182852079
|
T | C | 70 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(67): Show | 141 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(138): Show |
intron_variant | MODIFIER | c.526+6707A>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182852079 | ||||||
chr2:182852172
|
C | A | 114 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(111): Show | 195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.526+6614G>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182852172 | ||||||
chr2:182852246
|
T | C | 2 | a0001c0001t0001g0182a0001c0001t0001g0219 | 2 | HG03704.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.526+6540A>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182852246 | ||||||
chr2:182852323
|
G | A | 1 | a0001c0001t0001g0103 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.526+6463C>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182852323 | ||||||
chr2:182852373
|
G | A | 112 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(109): Show | 193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.526+6413C>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182852373 | ||||||
chr2:182852377
|
G | A | 5 | a0003c0003t0001g0022a0003c0003t0001g0054a0003c0003t0002g0052others(2): Show | 7 | HG00642.hp2 HG01109.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.526+6409C>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182852377 | ||||||
chr2:182852689
|
T | C | 10 | a0001c0001t0001g0055a0001c0001t0001g0057a0001c0001t0001g0058others(7): Show | 10 | HG01243.hp1 HG02109.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.526+6097A>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182852689 | ||||||
chr2:182852883
|
T | C | 1 | a0002c0002t0003g0179 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.526+5903A>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182852883 | ||||||
chr2:182852944
|
C | T | 10 | a0001c0001t0001g0010a0001c0001t0001g0071a0001c0001t0001g0073others(7): Show | 15 | HG02145.hp1 HG02559.hp2 HG02622.hp2 others(12): Show |
intron_variant | MODIFIER | c.526+5842G>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182852944 | ||||||
chr2:182853043
|
AC | A | 13 | a0001c0001t0001g0055a0001c0001t0001g0057a0001c0001t0001g0058others(10): Show | 13 | HG01243.hp1 HG02109.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.526+5742delG | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182853043 | ||||||
chr2:182853150
|
G | T | 1 | a0001c0001t0001g0077 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.526+5636C>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182853150 | ||||||
chr2:182853332
|
C | T | 3 | a0001c0001t0004g0172a0005c0006t0003g0051a0009c0012t0001g0221 | 4 | HG01099.hp2 HG01358.hp1 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.526+5454G>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182853332 | ||||||
chr2:182853400
|
A | C | 4 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0002g0169others(1): Show | 4 | HG02486.hp2 HG02622.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.526+5386T>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182853400 | ||||||
chr2:182853421
|
A | G | 2 | a0001c0001t0001g0087a0001c0001t0001g0111 | 2 | NA18944.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.526+5365T>C | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182853421 | ||||||
chr2:182853430
|
C | A | 8 | a0001c0001t0001g0039a0001c0001t0001g0138a0001c0001t0001g0147others(5): Show | 10 | HG00597.hp1 HG00609.hp2 HG00621.hp1 others(7): Show |
intron_variant | MODIFIER | c.526+5356G>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182853430 | ||||||
chr2:182853441
|
G | A | 1 | a0001c0001t0001g0080 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.526+5345C>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182853441 | ||||||
chr2:182853577
|
T | A | 1 | a0001c0001t0001g0188 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.526+5209A>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182853577 | ||||||
chr2:182853579
|
A | T | 1 | a0001c0001t0001g0188 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.526+5207T>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182853579 | ||||||
chr2:182853588
|
T | C | 1 | a0001c0001t0001g0206 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.526+5198A>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182853588 | ||||||
chr2:182853620
|
C | A | 1 | a0001c0001t0001g0188 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.526+5166G>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182853620 | ||||||
chr2:182853622
|
T | C | 1 | a0001c0001t0001g0188 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.526+5164A>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182853622 | ||||||
chr2:182853625
|
G | T | 1 | a0001c0001t0001g0188 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.526+5161C>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182853625 | ||||||
chr2:182853772
|
C | A | 1 | a0001c0001t0002g0207 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.526+5014G>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182853772 | ||||||
chr2:182853817
|
G | C | 3 | a0002c0002t0003g0066a0002c0002t0003g0179a0003c0009t0004g0178 | 3 | HG02280.hp1 HG02976.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.526+4969C>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182853817 | ||||||
chr2:182853849
|
C | T | 13 | a0001c0001t0001g0055a0001c0001t0001g0057a0001c0001t0001g0058others(10): Show | 13 | HG01243.hp1 HG02109.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.526+4937G>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182853849 | ||||||
chr2:182853879
|
G | A | 1 | a0001c0001t0001g0208 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.526+4907C>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182853879 | ||||||
chr2:182854106
|
T | C | 1 | a0001c0001t0001g0130 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.526+4680A>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182854106 | ||||||
chr2:182854151
|
G | T | 1 | a0002c0002t0003g0174 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.526+4635C>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182854151 | ||||||
chr2:182854205
|
A | G | 1 | a0001c0001t0007g0059 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.526+4581T>C | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182854205 | ||||||
chr2:182854232
|
T | C | 12 | a0001c0001t0001g0010a0001c0001t0001g0071a0001c0001t0001g0073others(9): Show | 17 | HG01261.hp2 HG02145.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.526+4554A>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182854232 | ||||||
chr2:182854361
|
A | G | 2 | a0001c0001t0004g0083a0001c0001t0004g0141 | 2 | HG02572.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.526+4425T>C | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182854361 | ||||||
chr2:182854411
|
T | G | 1 | a0001c0001t0002g0177 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.526+4375A>C | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182854411 | ||||||
chr2:182854519
|
G | A | 2 | a0005c0006t0003g0051a0009c0012t0001g0221 | 3 | HG01099.hp2 HG01358.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.526+4267C>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182854519 | ||||||
chr2:182854720
|
G | A | 10 | a0001c0001t0001g0055a0001c0001t0001g0057a0001c0001t0001g0058others(7): Show | 10 | HG01243.hp1 HG02109.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.526+4066C>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182854720 | ||||||
chr2:182854744
|
T | C | 1 | a0002c0002t0003g0140 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.526+4042A>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182854744 | ||||||
chr2:182854992
|
A | G | 2 | a0005c0006t0003g0051a0009c0012t0001g0221 | 3 | HG01099.hp2 HG01358.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.526+3794T>C | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182854992 | ||||||
chr2:182855025
|
C | T | 3 | a0001c0004t0001g0038a0001c0004t0001g0137a0001c0004t0004g0037 | 5 | HG01884.hp2 HG02257.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.526+3761G>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182855025 | ||||||
chr2:182855070
|
T | C | 2 | a0003c0003t0001g0132a0003c0003t0002g0131 | 2 | HG00099.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.526+3716A>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182855070 | ||||||
chr2:182855304
|
G | GA | 3 | a0001c0004t0001g0038a0001c0004t0001g0137a0001c0004t0004g0037 | 5 | HG01884.hp2 HG02257.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.526+3481dupT | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182855304 | ||||||
chr2:182855947
|
A | G | 12 | a0001c0001t0001g0010a0001c0001t0001g0071a0001c0001t0001g0073others(9): Show | 17 | HG01261.hp2 HG02145.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.526+2839T>C | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182855947 | ||||||
chr2:182856138
|
C | T | 3 | a0001c0001t0004g0153a0002c0002t0003g0152a0002c0002t0003g0154 | 3 | HG02559.hp1 HG02723.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.526+2648G>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182856138 | ||||||
chr2:182856147
|
G | A | 1 | a0001c0001t0001g0057 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.526+2639C>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182856147 | ||||||
chr2:182856262
|
G | A | 1 | a0001c0001t0002g0177 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.526+2524C>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182856262 | ||||||
chr2:182856373
|
A | T | 70 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(67): Show | 141 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(138): Show |
intron_variant | MODIFIER | c.526+2413T>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182856373 | ||||||
chr2:182856375
|
A | T | 1 | a0001c0001t0001g0086 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.526+2411T>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182856375 | ||||||
chr2:182856385
|
A | G | 1 | a0001c0001t0002g0151 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.526+2401T>C | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182856385 | ||||||
chr2:182856396
|
C | T | 3 | a0001c0004t0001g0038a0001c0004t0001g0137a0001c0004t0004g0037 | 5 | HG01884.hp2 HG02257.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.526+2390G>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182856396 | ||||||
chr2:182856593
|
C | T | 2 | a0001c0001t0001g0182a0001c0001t0001g0219 | 2 | HG03704.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.526+2193G>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182856593 | ||||||
chr2:182856669
|
C | G | 139 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(136): Show | 233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.526+2117G>C | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182856669 | ||||||
chr2:182856731
|
A | G | 114 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(111): Show | 195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.526+2055T>C | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182856731 | ||||||
chr2:182856800
|
G | A | 70 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(67): Show | 141 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(138): Show |
intron_variant | MODIFIER | c.526+1986C>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182856800 | ||||||
chr2:182856980
|
G | A | 70 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(67): Show | 141 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(138): Show |
intron_variant | MODIFIER | c.526+1806C>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182856980 | ||||||
chr2:182857073
|
A | G | 1 | a0002c0002t0003g0145 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.526+1713T>C | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182857073 | ||||||
chr2:182857206
|
A | G | 3 | a0001c0001t0001g0055a0001c0001t0001g0057a0001c0001t0002g0056 | 3 | HG02145.hp2 HG02451.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.526+1580T>C | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182857206 | ||||||
chr2:182857419
|
G | C | 70 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(67): Show | 141 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(138): Show |
intron_variant | MODIFIER | c.526+1367C>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182857419 | ||||||
chr2:182857472
|
T | C | 98 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(95): Show | 176 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(173): Show |
intron_variant | MODIFIER | c.526+1314A>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182857472 | ||||||
chr2:182857541
|
C | T | 1 | a0001c0001t0007g0150 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.526+1245G>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182857541 | ||||||
chr2:182857616
|
C | CA | 9 | a0001c0001t0001g0209a0001c0001t0001g0211a0001c0001t0002g0210others(6): Show | 11 | HG01884.hp2 HG02109.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.526+1169dupT | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182857616 | ||||||
chr2:182857774
|
T | C | 1 | a0001c0001t0002g0166 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.526+1012A>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182857774 | ||||||
chr2:182858149
|
T | A | 98 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(95): Show | 176 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(173): Show |
intron_variant | MODIFIER | c.526+637A>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182858149 | ||||||
chr2:182858201
|
A | G | 13 | a0001c0001t0001g0055a0001c0001t0001g0057a0001c0001t0001g0058others(10): Show | 13 | HG01243.hp1 HG02109.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.526+585T>C | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182858201 | ||||||
chr2:182858223
|
G | A | 3 | a0002c0002t0003g0174a0002c0002t0003g0175a0002c0002t0003g0176 | 3 | HG02818.hp1 HG02886.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.526+563C>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182858223 | ||||||
chr2:182858224
|
C | T | 1 | a0002c0002t0003g0174 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.526+562G>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182858224 | ||||||
chr2:182858238
|
T | C | 16 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0002g0169others(13): Show | 19 | HG00642.hp2 HG01099.hp2 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.526+548A>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182858238 | ||||||
chr2:182858292
|
A | G | 10 | a0001c0001t0001g0055a0001c0001t0001g0057a0001c0001t0001g0058others(7): Show | 10 | HG01243.hp1 HG02109.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.526+494T>C | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182858292 | ||||||
chr2:182858378
|
G | A | 3 | a0002c0002t0003g0066a0002c0002t0003g0179a0003c0009t0004g0178 | 3 | HG02280.hp1 HG02976.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.526+408C>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182858378 | ||||||
chr2:182858401
|
C | T | 114 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(111): Show | 195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.526+385G>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182858401 | ||||||
chr2:182858410
|
G | T | 1 | a0001c0001t0002g0187 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.526+376C>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182858410 | ||||||
chr2:182858509
|
G | A | 5 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0002g0169others(2): Show | 5 | HG02486.hp2 HG02622.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.526+277C>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182858509 | ||||||
chr2:182858739
|
A | T | 1 | a0001c0001t0001g0110 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.526+47T>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 2/5 | chr2 | 182858739 | ||||||
chr2:182858952
|
T | C | 1 | a0001c0001t0001g0101 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.479-119A>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182858952 | ||||||
chr2:182858967
|
G | A | 1 | a0001c0001t0001g0095 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.479-134C>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182858967 | ||||||
chr2:182858994
|
A | G | 114 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(111): Show | 195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.479-161T>C | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182858994 | ||||||
chr2:182859211
|
T | G | 20 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0026others(17): Show | 33 | HG00597.hp1 HG00609.hp2 HG00621.hp1 others(30): Show |
intron_variant | MODIFIER | c.479-378A>C | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182859211 | ||||||
chr2:182859220
|
G | A | 139 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(136): Show | 233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.479-387C>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182859220 | ||||||
chr2:182859510
|
G | A | 13 | a0001c0001t0001g0055a0001c0001t0001g0057a0001c0001t0001g0058others(10): Show | 13 | HG01243.hp1 HG02109.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.479-677C>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182859510 | ||||||
chr2:182859523
|
C | T | 5 | a0001c0001t0001g0044a0001c0001t0001g0186a0001c0001t0001g0213others(2): Show | 6 | HG00423.hp2 HG00544.hp2 NA18939.hp1 others(3): Show |
intron_variant | MODIFIER | c.479-690G>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182859523 | ||||||
chr2:182859700
|
G | T | 5 | a0003c0003t0001g0022a0003c0003t0001g0054a0003c0003t0002g0052others(2): Show | 7 | HG00642.hp2 HG01109.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.479-867C>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182859700 | ||||||
chr2:182859723
|
A | G | 8 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0002g0169others(5): Show | 8 | HG02280.hp1 HG02486.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.479-890T>C | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182859723 | ||||||
chr2:182859810
|
C | T | 198 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(195): Show | 341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.479-977G>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182859810 | ||||||
chr2:182859824
|
C | A | 12 | a0001c0001t0001g0010a0001c0001t0001g0071a0001c0001t0001g0073others(9): Show | 17 | HG01261.hp2 HG02145.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.479-991G>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182859824 | ||||||
chr2:182859884
|
A | T | 5 | a0003c0003t0001g0022a0003c0003t0001g0054a0003c0003t0002g0052others(2): Show | 7 | HG00642.hp2 HG01109.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.479-1051T>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182859884 | ||||||
chr2:182859894
|
A | G | 3 | a0001c0001t0004g0172a0005c0006t0003g0051a0009c0012t0001g0221 | 4 | HG01099.hp2 HG01358.hp1 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.479-1061T>C | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182859894 | ||||||
chr2:182860017
|
C | T | 28 | a0001c0001t0001g0010a0001c0001t0001g0071a0001c0001t0001g0073others(25): Show | 36 | HG00642.hp2 HG01099.hp2 HG01109.hp2 others(33): Show |
intron_variant | MODIFIER | c.479-1184G>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182860017 | ||||||
chr2:182860179
|
A | T | 3 | a0001c0004t0001g0038a0001c0004t0001g0137a0001c0004t0004g0037 | 5 | HG01884.hp2 HG02257.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.479-1346T>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182860179 | ||||||
chr2:182860260
|
C | T | 12 | a0001c0001t0001g0010a0001c0001t0001g0071a0001c0001t0001g0073others(9): Show | 17 | HG01261.hp2 HG02145.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.479-1427G>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182860260 | ||||||
chr2:182860493
|
A | G | 86 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(83): Show | 159 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(156): Show |
intron_variant | MODIFIER | c.479-1660T>C | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182860493 | ||||||
chr2:182860784
|
T | A | 1 | a0002c0002t0003g0167 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.479-1951A>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182860784 | ||||||
chr2:182860823
|
C | T | 1 | a0002c0002t0003g0140 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.479-1990G>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182860823 | ||||||
chr2:182860864
|
C | CA | 13 | a0001c0001t0001g0081a0001c0001t0001g0098a0001c0001t0001g0108others(10): Show | 13 | HG00423.hp1 HG00544.hp2 HG01192.hp2 others(10): Show |
intron_variant | MODIFIER | c.479-2032dupT | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182860864 | ||||||
chr2:182860864
|
C | CAA | 13 | a0001c0001t0001g0055a0001c0001t0001g0057a0001c0001t0001g0058others(10): Show | 13 | HG01243.hp1 HG02109.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.479-2033_479-2032d others(4): Show |
FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182860864 | ||||||
chr2:182860864
|
CA | C | 17 | a0001c0001t0001g0032a0001c0001t0001g0109a0001c0001t0001g0170others(14): Show | 20 | HG00642.hp2 HG01109.hp2 HG01169.hp2 others(17): Show |
intron_variant | MODIFIER | c.479-2032delT | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182860864 | ||||||
chr2:182860959
|
G | C | 4 | a0001c0001t0001g0215a0001c0001t0001g0216a0001c0001t0001g0217others(1): Show | 4 | HG00609.hp1 HG02040.hp2 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.479-2126C>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182860959 | ||||||
chr2:182860990
|
G | A | 1 | a0001c0001t0001g0082 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.479-2157C>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182860990 | ||||||
chr2:182861261
|
A | G | 1 | a0003c0009t0004g0178 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.479-2428T>C | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182861261 | ||||||
chr2:182861303
|
T | G | 70 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(67): Show | 141 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(138): Show |
intron_variant | MODIFIER | c.479-2470A>C | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182861303 | ||||||
chr2:182861316
|
A | C | 86 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(83): Show | 159 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(156): Show |
intron_variant | MODIFIER | c.479-2483T>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182861316 | ||||||
chr2:182861352
|
C | T | 28 | a0001c0001t0001g0010a0001c0001t0001g0071a0001c0001t0001g0073others(25): Show | 36 | HG00642.hp2 HG01099.hp2 HG01109.hp2 others(33): Show |
intron_variant | MODIFIER | c.479-2519G>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182861352 | ||||||
chr2:182861407
|
A | G | 1 | a0001c0001t0001g0076 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.479-2574T>C | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182861407 | ||||||
chr2:182861480
|
G | T | 2 | a0005c0006t0003g0051a0009c0012t0001g0221 | 3 | HG01099.hp2 HG01358.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.479-2647C>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182861480 | ||||||
chr2:182861500
|
T | C | 1 | a0001c0001t0002g0100 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.479-2667A>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182861500 | ||||||
chr2:182861957
|
C | T | 1 | a0001c0001t0001g0043 | 2 | HG00323.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.479-3124G>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182861957 | ||||||
chr2:182861973
|
C | T | 4 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0002g0169others(1): Show | 4 | HG02486.hp2 HG02622.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.479-3140G>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182861973 | ||||||
chr2:182861985
|
C | T | 70 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(67): Show | 141 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(138): Show |
intron_variant | MODIFIER | c.479-3152G>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182861985 | ||||||
chr2:182862201
|
A | G | 114 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(111): Show | 195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.479-3368T>C | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182862201 | ||||||
chr2:182862773
|
CTT | C | 28 | a0001c0001t0001g0010a0001c0001t0001g0071a0001c0001t0001g0073others(25): Show | 36 | HG00642.hp2 HG01099.hp2 HG01109.hp2 others(33): Show |
intron_variant | MODIFIER | c.478+3300_478+3301d others(4): Show |
FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182862773 | ||||||
chr2:182862773
|
CTTT | C | 86 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(83): Show | 160 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(157): Show |
intron_variant | MODIFIER | c.478+3299_478+3301d others(5): Show |
FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182862773 | ||||||
chr2:182862808
|
G | A | 2 | a0001c0001t0001g0182a0001c0001t0001g0219 | 2 | HG03704.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.478+3267C>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182862808 | ||||||
chr2:182862951
|
G | A | 1 | a0001c0001t0002g0135 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.478+3124C>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182862951 | ||||||
chr2:182863202
|
C | T | 1 | a0001c0001t0004g0172 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.478+2873G>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182863202 | ||||||
chr2:182863212
|
C | CT | 5 | a0003c0003t0001g0022a0003c0003t0001g0054a0003c0003t0002g0052others(2): Show | 7 | HG00642.hp2 HG01109.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.478+2862_478+2863i others(3): Show |
FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182863212 | ||||||
chr2:182863213
|
C | T | 5 | a0003c0003t0001g0022a0003c0003t0001g0054a0003c0003t0002g0052others(2): Show | 7 | HG00642.hp2 HG01109.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.478+2862G>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182863213 | ||||||
chr2:182863271
|
A | G | 1 | a0001c0001t0001g0103 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.478+2804T>C | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182863271 | ||||||
chr2:182863328
|
T | C | 3 | a0002c0002t0003g0174a0002c0002t0003g0175a0002c0002t0003g0176 | 3 | HG02818.hp1 HG02886.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.478+2747A>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182863328 | ||||||
chr2:182863393
|
C | G | 7 | a0001c0001t0001g0103a0001c0001t0001g0105a0001c0001t0001g0106others(4): Show | 8 | HG00733.hp2 HG01192.hp2 HG01943.hp1 others(5): Show |
intron_variant | MODIFIER | c.478+2682G>C | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182863393 | ||||||
chr2:182863417
|
C | A | 1 | a0001c0001t0001g0101 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.478+2658G>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182863417 | ||||||
chr2:182863483
|
A | G | 1 | a0001c0001t0001g0102 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.478+2592T>C | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182863483 | ||||||
chr2:182863562
|
C | T | 28 | a0001c0001t0001g0010a0001c0001t0001g0071a0001c0001t0001g0073others(25): Show | 36 | HG00642.hp2 HG01099.hp2 HG01109.hp2 others(33): Show |
intron_variant | MODIFIER | c.478+2513G>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182863562 | ||||||
chr2:182863625
|
T | C | 2 | a0002c0002t0003g0179a0003c0009t0004g0178 | 2 | HG02280.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.478+2450A>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182863625 | ||||||
chr2:182863685
|
G | GA | 47 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0032others(44): Show | 88 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(85): Show |
intron_variant | MODIFIER | c.478+2389dupT | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182863685 | ||||||
chr2:182863686
|
A | T | 1 | a0002c0002t0003g0173 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.478+2389T>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182863686 | ||||||
chr2:182863690
|
A | C | 1 | a0001c0001t0001g0182 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.478+2385T>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182863690 | ||||||
chr2:182863858
|
G | A | 3 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0002g0136 | 5 | HG02040.hp1 NA18950.hp1 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.478+2217C>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182863858 | ||||||
chr2:182863906
|
C | T | 89 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(86): Show | 163 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(160): Show |
intron_variant | MODIFIER | c.478+2169G>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182863906 | ||||||
chr2:182863980
|
C | T | 1 | a0002c0002t0003g0065 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.478+2095G>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182863980 | ||||||
chr2:182864122
|
T | G | 2 | a0002c0002t0003g0179a0003c0009t0004g0178 | 2 | HG02280.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.478+1953A>C | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182864122 | ||||||
chr2:182864129
|
A | T | 3 | a0001c0004t0001g0038a0001c0004t0001g0137a0001c0004t0004g0037 | 5 | HG01884.hp2 HG02257.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.478+1946T>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182864129 | ||||||
chr2:182864194
|
C | T | 1 | a0001c0001t0001g0084 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.478+1881G>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182864194 | ||||||
chr2:182864236
|
C | T | 20 | a0001c0001t0001g0010a0001c0001t0001g0071a0001c0001t0001g0073others(17): Show | 26 | HG01099.hp2 HG01261.hp2 HG01358.hp1 others(23): Show |
intron_variant | MODIFIER | c.478+1839G>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182864236 | ||||||
chr2:182864347
|
A | T | 71 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(68): Show | 143 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(140): Show |
intron_variant | MODIFIER | c.478+1728T>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182864347 | ||||||
chr2:182864469
|
C | T | 71 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(68): Show | 143 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(140): Show |
intron_variant | MODIFIER | c.478+1606G>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182864469 | ||||||
chr2:182864697
|
C | T | 20 | a0001c0001t0001g0010a0001c0001t0001g0071a0001c0001t0001g0073others(17): Show | 26 | HG01099.hp2 HG01261.hp2 HG01358.hp1 others(23): Show |
intron_variant | MODIFIER | c.478+1378G>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182864697 | ||||||
chr2:182864785
|
C | T | 109 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(106): Show | 189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.478+1290G>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182864785 | ||||||
chr2:182864805
|
A | G | 4 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0002g0169others(1): Show | 4 | HG02486.hp2 HG02622.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.478+1270T>C | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182864805 | ||||||
chr2:182864854
|
T | G | 2 | a0002c0002t0003g0179a0003c0009t0004g0178 | 2 | HG02280.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.478+1221A>C | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182864854 | ||||||
chr2:182864873
|
G | C | 1 | a0002c0002t0003g0173 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.478+1202C>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182864873 | ||||||
chr2:182864893
|
G | C | 20 | a0001c0001t0001g0010a0001c0001t0001g0071a0001c0001t0001g0073others(17): Show | 26 | HG01099.hp2 HG01261.hp2 HG01358.hp1 others(23): Show |
intron_variant | MODIFIER | c.478+1182C>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182864893 | ||||||
chr2:182864896
|
A | G | 1 | a0001c0001t0004g0083 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.478+1179T>C | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182864896 | ||||||
chr2:182865042
|
A | G | 12 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0025others(9): Show | 24 | HG00621.hp2 HG02056.hp2 HG02074.hp2 others(21): Show |
intron_variant | MODIFIER | c.478+1033T>C | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182865042 | ||||||
chr2:182865229
|
G | A | 16 | a0001c0001t0001g0055a0001c0001t0001g0057a0001c0001t0001g0058others(13): Show | 16 | HG01243.hp1 HG02109.hp1 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.478+846C>T | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182865229 | ||||||
chr2:182865252
|
C | T | 13 | a0001c0001t0001g0010a0001c0001t0001g0071a0001c0001t0001g0073others(10): Show | 18 | HG01261.hp2 HG02145.hp1 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.478+823G>A | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182865252 | ||||||
chr2:182865359
|
T | C | 1 | a0001c0001t0001g0180 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.478+716A>G | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182865359 | ||||||
chr2:182865381
|
A | G | 10 | a0001c0001t0001g0055a0001c0001t0001g0057a0001c0001t0001g0058others(7): Show | 10 | HG01243.hp1 HG02109.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.478+694T>C | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182865381 | ||||||
chr2:182865701
|
A | G | 5 | a0003c0003t0001g0022a0003c0003t0001g0054a0003c0003t0002g0052others(2): Show | 7 | HG00642.hp2 HG01109.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.478+374T>C | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182865701 | ||||||
chr2:182865799
|
T | G | 56 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(53): Show | 103 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.478+276A>C | FRZB | ENSG00000162998.5 | transcript | ENST00000295113.5 | protein_coding | 1/5 | chr2 | 182865799 |