geneid | 143684 |
---|---|
ensemblid | ENSG00000077458.13 |
hgncid | 28492 |
symbol | FAM76B |
name | family with sequence similarity 76 member B |
refseq_nuc | NM_144664.5 |
refseq_prot | NP_653265.3 |
ensembl_nuc | ENST00000358780.10 |
ensembl_prot | ENSP00000351631.5 |
mane_status | MANE Select |
chr | chr11 |
start | 95768953 |
end | 95789782 |
strand | - |
ver | v1.2 |
region | chr11:95768953-95789782 |
region5000 | chr11:95763953-95794782 |
regionname0 | FAM76B_chr11_95768953_95789782 |
regionname5000 | FAM76B_chr11_95763953_95794782 |
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 | 1/1 | 339 | 416 | 100 | 76 | 178 | 14 | 46 | 132 | FAM76B_chr11_95763953_95794782 | FAM76B | copy fasta | chr11 | 95763953 | 95794782 |
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 | 0/1 | 1020 | 243 | 91 | 36 | 79 | 9 | 27 | FAM76B_chr11_95763953_95794782 | FAM76B | copy fasta | chr11 | 95763953 | 95794782 |
c0002 | 1/0 | 1020 | 166 | 5 | 39 | 97 | 5 | 19 | FAM76B_chr11_95763953_95794782 | FAM76B | copy fasta | chr11 | 95763953 | 95794782 |
c0003 | 0/0 | 1020 | 3 | 3 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | copy fasta | chr11 | 95763953 | 95794782 |
c0004 | 0/0 | 1020 | 2 | 0 | 0 | 2 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | copy fasta | chr11 | 95763953 | 95794782 |
c0005 | 0/0 | 1020 | 2 | 1 | 1 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | copy fasta | chr11 | 95763953 | 95794782 |
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 | 1/0 | 2913 | 276 | 77 | 53 | 114 | 6 | 25 | FAM76B_chr11_95763953_95794782 | FAM76B | copy fasta | chr11 | 95763953 | 95794782 |
t0002 | 0/0 | 2913 | 88 | 6 | 15 | 52 | 8 | 7 | FAM76B_chr11_95763953_95794782 | FAM76B | copy fasta | chr11 | 95763953 | 95794782 |
t0003 | 0/0 | 2910 | 15 | 7 | 1 | 0 | 0 | 7 | FAM76B_chr11_95763953_95794782 | FAM76B | copy fasta | chr11 | 95763953 | 95794782 |
t0004 | 0/1 | 2913 | 7 | 0 | 0 | 0 | 0 | 6 | FAM76B_chr11_95763953_95794782 | FAM76B | copy fasta | chr11 | 95763953 | 95794782 |
t0005 | 0/0 | 2913 | 3 | 3 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | copy fasta | chr11 | 95763953 | 95794782 |
t0006 | 0/0 | 2913 | 3 | 0 | 3 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | copy fasta | chr11 | 95763953 | 95794782 |
t0007 | 0/0 | 2913 | 3 | 0 | 0 | 3 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | copy fasta | chr11 | 95763953 | 95794782 |
t0008 | 0/0 | 2913 | 3 | 2 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | copy fasta | chr11 | 95763953 | 95794782 |
t0009 | 0/0 | 2913 | 2 | 0 | 0 | 2 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | copy fasta | chr11 | 95763953 | 95794782 |
t0010 | 0/0 | 2913 | 2 | 0 | 2 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | copy fasta | chr11 | 95763953 | 95794782 |
t0011 | 0/0 | 2913 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | copy fasta | chr11 | 95763953 | 95794782 |
t0012 | 0/0 | 2913 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | copy fasta | chr11 | 95763953 | 95794782 |
t0013 | 0/0 | 2913 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | copy fasta | chr11 | 95763953 | 95794782 |
t0014 | 0/0 | 2913 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | copy fasta | chr11 | 95763953 | 95794782 |
t0015 | 0/0 | 2913 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | copy fasta | chr11 | 95763953 | 95794782 |
t0016 | 0/0 | 2913 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | copy fasta | chr11 | 95763953 | 95794782 |
t0017 | 0/0 | 2913 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | copy fasta | chr11 | 95763953 | 95794782 |
t0018 | 0/0 | 2913 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | copy fasta | chr11 | 95763953 | 95794782 |
t0019 | 0/0 | 2913 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | copy fasta | chr11 | 95763953 | 95794782 |
t0020 | 0/0 | 2934 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | copy fasta | chr11 | 95763953 | 95794782 |
t0021 | 0/0 | 2913 | 1 | 0 | 0 | 0 | 0 | 1 | FAM76B_chr11_95763953_95794782 | FAM76B | copy fasta | chr11 | 95763953 | 95794782 |
t0022 | 0/0 | 2913 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | copy fasta | chr11 | 95763953 | 95794782 |
t0023 | 0/0 | 2913 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | copy fasta | chr11 | 95763953 | 95794782 |
t0024 | 0/0 | 2913 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | copy fasta | chr11 | 95763953 | 95794782 |
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 | 56 | 3 | 10 | 36 | 5 | 2 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0002 | 0/0 | 30 | 1 | 1 | 22 | 1 | 5 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0003 | 0/0 | 28 | 0 | 6 | 21 | 0 | 1 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0004 | 0/0 | 19 | 0 | 3 | 14 | 0 | 2 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0005 | 0/0 | 14 | 1 | 8 | 2 | 0 | 3 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0006 | 0/0 | 13 | 0 | 4 | 9 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0007 | 0/0 | 12 | 10 | 2 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0008 | 0/0 | 8 | 4 | 0 | 0 | 0 | 4 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0009 | 0/0 | 8 | 7 | 1 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0010 | 0/0 | 8 | 1 | 0 | 6 | 0 | 1 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0011 | 0/0 | 7 | 6 | 1 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0012 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0013 | 0/0 | 6 | 0 | 0 | 4 | 0 | 2 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0014 | 0/0 | 6 | 0 | 5 | 0 | 1 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0015 | 0/1 | 5 | 0 | 0 | 0 | 0 | 4 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0016 | 0/0 | 5 | 3 | 2 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0017 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0018 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0019 | 0/0 | 4 | 1 | 3 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0022 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0023 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0024 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0025 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0026 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0027 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0028 | 0/0 | 3 | 1 | 1 | 0 | 0 | 1 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0029 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0035 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0037 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0038 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0043 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0046 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0112 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
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 | 0/1 | 1020 | 243 | 91 | 36 | 79 | 9 | 27 | FAM76B_chr11_95763953_95794782 | FAM76B | copy fasta | chr11 | 95763953 | 95794782 |
a0001c0002 | 1/0 | 1020 | 166 | 5 | 39 | 97 | 5 | 19 | FAM76B_chr11_95763953_95794782 | FAM76B | copy fasta | chr11 | 95763953 | 95794782 |
a0001c0003 | 0/0 | 1020 | 3 | 3 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | copy fasta | chr11 | 95763953 | 95794782 |
a0001c0004 | 0/0 | 1020 | 2 | 0 | 0 | 2 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | copy fasta | chr11 | 95763953 | 95794782 |
a0001c0005 | 0/0 | 1020 | 2 | 1 | 1 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | copy fasta | chr11 | 95763953 | 95794782 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 3932 | 111 | 69 | 17 | 18 | 1 | 6 | FAM76B_chr11_95763953_95794782 | FAM76B | copy fasta | chr11 | 95763953 | 95794782 |
a0001c0001t0002 | 0/0 | 3932 | 88 | 6 | 15 | 52 | 8 | 7 | FAM76B_chr11_95763953_95794782 | FAM76B | copy fasta | chr11 | 95763953 | 95794782 |
a0001c0001t0003 | 0/0 | 3929 | 15 | 7 | 1 | 0 | 0 | 7 | FAM76B_chr11_95763953_95794782 | FAM76B | copy fasta | chr11 | 95763953 | 95794782 |
a0001c0001t0004 | 0/1 | 3932 | 7 | 0 | 0 | 0 | 0 | 6 | FAM76B_chr11_95763953_95794782 | FAM76B | copy fasta | chr11 | 95763953 | 95794782 |
a0001c0001t0005 | 0/0 | 3932 | 3 | 3 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | copy fasta | chr11 | 95763953 | 95794782 |
a0001c0001t0007 | 0/0 | 3932 | 3 | 0 | 0 | 3 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | copy fasta | chr11 | 95763953 | 95794782 |
a0001c0001t0008 | 0/0 | 3932 | 3 | 2 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | copy fasta | chr11 | 95763953 | 95794782 |
a0001c0001t0010 | 0/0 | 3932 | 2 | 0 | 2 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | copy fasta | chr11 | 95763953 | 95794782 |
a0001c0001t0011 | 0/0 | 3932 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | copy fasta | chr11 | 95763953 | 95794782 |
a0001c0001t0013 | 0/0 | 3932 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | copy fasta | chr11 | 95763953 | 95794782 |
a0001c0001t0015 | 0/0 | 3932 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | copy fasta | chr11 | 95763953 | 95794782 |
a0001c0001t0016 | 0/0 | 3932 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | copy fasta | chr11 | 95763953 | 95794782 |
a0001c0001t0018 | 0/0 | 3932 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | copy fasta | chr11 | 95763953 | 95794782 |
a0001c0001t0019 | 0/0 | 3932 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | copy fasta | chr11 | 95763953 | 95794782 |
a0001c0001t0020 | 0/0 | 3953 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | copy fasta | chr11 | 95763953 | 95794782 |
a0001c0001t0021 | 0/0 | 3932 | 1 | 0 | 0 | 0 | 0 | 1 | FAM76B_chr11_95763953_95794782 | FAM76B | copy fasta | chr11 | 95763953 | 95794782 |
a0001c0001t0022 | 0/0 | 3932 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | copy fasta | chr11 | 95763953 | 95794782 |
a0001c0001t0023 | 0/0 | 3932 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | copy fasta | chr11 | 95763953 | 95794782 |
a0001c0001t0024 | 0/0 | 3932 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | copy fasta | chr11 | 95763953 | 95794782 |
a0001c0002t0001 | 1/0 | 3932 | 158 | 4 | 35 | 94 | 5 | 19 | FAM76B_chr11_95763953_95794782 | FAM76B | copy fasta | chr11 | 95763953 | 95794782 |
a0001c0002t0006 | 0/0 | 3932 | 3 | 0 | 3 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | copy fasta | chr11 | 95763953 | 95794782 |
a0001c0002t0009 | 0/0 | 3932 | 2 | 0 | 0 | 2 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | copy fasta | chr11 | 95763953 | 95794782 |
a0001c0002t0012 | 0/0 | 3932 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | copy fasta | chr11 | 95763953 | 95794782 |
a0001c0002t0014 | 0/0 | 3932 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | copy fasta | chr11 | 95763953 | 95794782 |
a0001c0002t0017 | 0/0 | 3932 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | copy fasta | chr11 | 95763953 | 95794782 |
a0001c0003t0001 | 0/0 | 3932 | 3 | 3 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | copy fasta | chr11 | 95763953 | 95794782 |
a0001c0004t0001 | 0/0 | 3932 | 2 | 0 | 0 | 2 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | copy fasta | chr11 | 95763953 | 95794782 |
a0001c0005t0001 | 0/0 | 3932 | 2 | 1 | 1 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | copy fasta | chr11 | 95763953 | 95794782 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0007 | 0/0 | 12 | 10 | 2 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0001t0001g0009 | 0/0 | 8 | 7 | 1 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0001t0001g0010 | 0/0 | 8 | 1 | 0 | 6 | 0 | 1 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0001t0001g0011 | 0/0 | 7 | 6 | 1 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0001t0001g0013 | 0/0 | 6 | 0 | 0 | 4 | 0 | 2 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0001t0001g0016 | 0/0 | 5 | 3 | 2 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0001t0001g0017 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0001t0001g0018 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0001t0001g0019 | 0/0 | 4 | 1 | 3 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0001t0001g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0001t0001g0022 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0001t0001g0023 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0001t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0001t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0001t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0001t0001g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0001t0001g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0001t0002g0001 | 0/0 | 56 | 3 | 10 | 36 | 5 | 2 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0001t0002g0012 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0001t0002g0027 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0001t0002g0028 | 0/0 | 3 | 1 | 1 | 0 | 0 | 1 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0001t0002g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0001t0002g0043 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0001t0002g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0001t0002g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0001t0003g0008 | 0/0 | 8 | 4 | 0 | 0 | 0 | 4 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0001t0003g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0001t0003g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0001t0003g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0001t0003g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0001t0003g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0001t0003g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0001t0004g0015 | 0/1 | 5 | 0 | 0 | 0 | 0 | 4 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0001t0004g0029 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0001t0005g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0001t0007g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0001t0007g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0001t0008g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0001t0008g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0001t0010g0046 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0001t0011g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0001t0013g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0001t0015g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0001t0016g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0001t0018g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0001t0019g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0001t0020g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0001t0021g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0001t0022g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0001t0023g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0001t0024g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0002t0001g0002 | 0/0 | 30 | 1 | 1 | 22 | 1 | 5 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0002t0001g0003 | 0/0 | 28 | 0 | 6 | 21 | 0 | 1 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0002t0001g0004 | 0/0 | 19 | 0 | 3 | 14 | 0 | 2 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0002t0001g0005 | 0/0 | 14 | 1 | 8 | 2 | 0 | 3 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0002t0001g0006 | 0/0 | 13 | 0 | 4 | 9 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0002t0001g0014 | 0/0 | 6 | 0 | 5 | 0 | 1 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0002t0001g0025 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0002t0001g0026 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0002t0001g0035 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0002t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0002t0001g0037 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0002t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0002t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0002t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0002t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0002t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0002t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0002t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0002t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0002t0001g0112 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0002t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0002t0006g0024 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0002t0009g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0002t0012g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0002t0014g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0002t0017g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0003t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0003t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0003t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0004t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
a0001c0005t0001g0038 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0002 | t0001 | g0111 | EUR | GBR | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG00099 | hp2 | a0001 | c0001 | t0002 | g0001 | EUR | GBR | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG00140 | hp1 | a0001 | c0001 | t0002 | g0027 | EUR | GBR | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG00140 | hp2 | a0001 | c0001 | t0002 | g0001 | EUR | GBR | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG00280 | hp1 | a0001 | c0002 | t0001 | g0002 | EUR | FIN | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG00280 | hp2 | a0001 | c0001 | t0002 | g0151 | EUR | FIN | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG00323 | hp1 | a0001 | c0001 | t0002 | g0001 | EUR | FIN | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0080 | EUR | FIN | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG00408 | hp1 | a0001 | c0002 | t0001 | g0115 | EAS | CHS | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG00408 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | CHS | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG00423 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | CHS | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG00438 | hp1 | a0001 | c0001 | t0002 | g0043 | EAS | CHS | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG00438 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | CHS | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG00544 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG00544 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | CHS | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | CHS | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG00558 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | CHS | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG00597 | hp1 | a0001 | c0002 | t0001 | g0006 | EAS | CHS | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG00597 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG00609 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | CHS | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG00609 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG00621 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | CHS | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG00621 | hp2 | a0001 | c0002 | t0001 | g0106 | EAS | CHS | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG00639 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG00639 | hp2 | a0001 | c0001 | t0010 | g0046 | AMR | PUR | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG00642 | hp1 | a0001 | c0002 | t0001 | g0003 | AMR | PUR | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG00642 | hp2 | a0001 | c0002 | t0001 | g0014 | AMR | PUR | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG00673 | hp1 | a0001 | c0002 | t0001 | g0102 | EAS | CHS | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG00673 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | CHS | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG00733 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG00733 | hp2 | a0001 | c0001 | t0002 | g0154 | AMR | PUR | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG00735 | hp1 | a0001 | c0002 | t0001 | g0003 | AMR | PUR | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG00735 | hp2 | a0001 | c0002 | t0001 | g0014 | AMR | PUR | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG00738 | hp1 | a0001 | c0002 | t0001 | g0089 | AMR | PUR | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG00741 | hp1 | a0001 | c0001 | t0002 | g0027 | AMR | PUR | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG01069 | hp1 | a0001 | c0001 | t0010 | g0046 | AMR | PUR | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG01069 | hp2 | a0001 | c0002 | t0006 | g0024 | AMR | PUR | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG01071 | hp1 | a0001 | c0002 | t0006 | g0024 | AMR | PUR | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG01071 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG01074 | hp2 | a0001 | c0002 | t0006 | g0024 | AMR | PUR | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG01081 | hp2 | a0001 | c0002 | t0001 | g0095 | AMR | PUR | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG01099 | hp2 | a0001 | c0002 | t0001 | g0005 | AMR | PUR | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG01109 | hp1 | a0001 | c0002 | t0001 | g0014 | AMR | PUR | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG01167 | hp2 | a0001 | c0002 | t0001 | g0003 | AMR | PUR | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG01168 | hp2 | a0001 | c0001 | t0002 | g0042 | AMR | PUR | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG01169 | hp1 | a0001 | c0001 | t0002 | g0042 | AMR | PUR | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG01175 | hp1 | a0001 | c0002 | t0001 | g0005 | AMR | PUR | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG01175 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG01192 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG01192 | hp2 | a0001 | c0002 | t0001 | g0003 | AMR | PUR | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG01255 | hp1 | a0001 | c0002 | t0001 | g0101 | AMR | CLM | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG01255 | hp2 | a0001 | c0002 | t0001 | g0124 | AMR | CLM | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG01256 | hp1 | a0001 | c0002 | t0001 | g0006 | AMR | CLM | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG01256 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG01257 | hp1 | a0001 | c0001 | t0002 | g0028 | AMR | CLM | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG01257 | hp2 | a0001 | c0002 | t0001 | g0005 | AMR | CLM | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG01258 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG01258 | hp2 | a0001 | c0002 | t0001 | g0005 | AMR | CLM | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG01261 | hp1 | a0001 | c0002 | t0001 | g0004 | AMR | CLM | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG01261 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG01346 | hp1 | a0001 | c0005 | t0001 | g0038 | AMR | CLM | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG01346 | hp2 | a0001 | c0002 | t0001 | g0107 | AMR | CLM | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG01358 | hp1 | a0001 | c0002 | t0001 | g0005 | AMR | CLM | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG01358 | hp2 | a0001 | c0002 | t0014 | g0092 | AMR | CLM | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG01361 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG01433 | hp1 | a0001 | c0002 | t0001 | g0003 | AMR | CLM | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG01433 | hp2 | a0001 | c0002 | t0001 | g0093 | AMR | CLM | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG01496 | hp1 | a0001 | c0002 | t0001 | g0004 | AMR | CLM | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG01496 | hp2 | a0001 | c0002 | t0001 | g0014 | AMR | CLM | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG01516 | hp1 | a0001 | c0001 | t0002 | g0153 | EUR | IBS | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG01516 | hp2 | a0001 | c0002 | t0001 | g0088 | EUR | IBS | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG01884 | hp2 | a0001 | c0001 | t0002 | g0001 | AFR | ACB | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG01891 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | ACB | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | ACB | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PEL | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG01928 | hp2 | a0001 | c0002 | t0001 | g0003 | AMR | PEL | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG01952 | hp1 | a0001 | c0002 | t0001 | g0004 | AMR | PEL | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG01952 | hp2 | a0001 | c0002 | t0001 | g0006 | AMR | PEL | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG01975 | hp1 | a0001 | c0002 | t0001 | g0006 | AMR | PEL | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PEL | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG01978 | hp1 | a0001 | c0001 | t0013 | g0070 | AMR | PEL | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG01978 | hp2 | a0001 | c0002 | t0001 | g0005 | AMR | PEL | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG01981 | hp1 | a0001 | c0002 | t0001 | g0094 | AMR | PEL | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG01981 | hp2 | a0001 | c0002 | t0001 | g0006 | AMR | PEL | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG01993 | hp1 | a0001 | c0002 | t0001 | g0005 | AMR | PEL | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG01993 | hp2 | a0001 | c0002 | t0001 | g0097 | AMR | PEL | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | PEL | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PEL | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG02015 | hp1 | a0001 | c0002 | t0009 | g0034 | EAS | KHV | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG02015 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | KHV | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG02027 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | KHV | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG02027 | hp2 | a0001 | c0002 | t0001 | g0104 | EAS | KHV | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG02040 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG02040 | hp2 | a0001 | c0002 | t0001 | g0006 | EAS | KHV | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | ACB | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG02055 | hp2 | a0001 | c0002 | t0001 | g0103 | AFR | ACB | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG02056 | hp1 | a0001 | c0001 | t0024 | g0155 | EAS | KHV | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG02056 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG02071 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG02071 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | KHV | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG02074 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | KHV | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG02074 | hp2 | a0001 | c0002 | t0009 | g0034 | EAS | KHV | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG02080 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | KHV | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG02080 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | KHV | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG02129 | hp1 | a0001 | c0002 | t0001 | g0026 | EAS | KHV | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG02129 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | KHV | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG02132 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | KHV | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG02132 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | KHV | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG02135 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG02135 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | KHV | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG02145 | hp1 | a0001 | c0001 | t0002 | g0028 | AFR | ACB | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | ACB | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG02148 | hp1 | a0001 | c0002 | t0001 | g0005 | AMR | PEL | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG02148 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG02155 | hp1 | a0001 | c0002 | t0001 | g0087 | EAS | CDX | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG02155 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | CDX | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG02165 | hp1 | a0001 | c0002 | t0001 | g0110 | EAS | CDX | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG02165 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | CDX | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG02257 | hp1 | a0001 | c0002 | t0001 | g0002 | AFR | ACB | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | ACB | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG02258 | hp2 | a0001 | c0002 | t0012 | g0048 | AFR | ACB | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | ACB | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG02300 | hp1 | a0001 | c0001 | t0003 | g0052 | AMR | PEL | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG02300 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | PEL | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | GWD | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG02602 | hp2 | a0001 | c0002 | t0001 | g0003 | SAS | PJL | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | GWD | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | GWD | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | GWD | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG02647 | hp1 | a0001 | c0001 | t0003 | g0008 | AFR | GWD | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | GWD | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG02683 | hp1 | a0001 | c0002 | t0001 | g0090 | SAS | PJL | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG02683 | hp2 | a0001 | c0002 | t0001 | g0025 | SAS | PJL | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG02698 | hp1 | a0001 | c0002 | t0001 | g0099 | SAS | PJL | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG02698 | hp2 | a0001 | c0001 | t0002 | g0138 | SAS | PJL | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG02717 | hp1 | a0001 | c0005 | t0001 | g0038 | AFR | GWD | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG02735 | hp1 | a0001 | c0001 | t0002 | g0027 | SAS | PJL | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG02735 | hp2 | a0001 | c0001 | t0003 | g0059 | SAS | PJL | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG02738 | hp1 | a0001 | c0002 | t0001 | g0002 | SAS | PJL | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG02738 | hp2 | a0001 | c0002 | t0001 | g0005 | SAS | PJL | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG02818 | hp1 | a0001 | c0001 | t0003 | g0058 | AFR | GWD | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | GWD | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG02895 | hp1 | a0001 | c0001 | t0003 | g0030 | AFR | GWD | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG02895 | hp2 | a0001 | c0001 | t0002 | g0001 | AFR | GWD | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG02897 | hp1 | a0001 | c0001 | t0003 | g0030 | AFR | GWD | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | ESN | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | ESN | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | ESN | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG02965 | hp2 | a0001 | c0001 | t0003 | g0008 | AFR | ESN | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | ESN | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG02976 | hp1 | a0001 | c0001 | t0008 | g0045 | AFR | ESN | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG03041 | hp1 | a0001 | c0003 | t0001 | g0056 | AFR | GWD | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | GWD | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG03098 | hp1 | a0001 | c0001 | t0002 | g0147 | AFR | MSL | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | ESN | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG03139 | hp1 | a0001 | c0001 | t0003 | g0008 | AFR | ESN | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG03209 | hp1 | a0001 | c0001 | t0008 | g0045 | AFR | MSL | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG03209 | hp2 | a0001 | c0001 | t0018 | g0050 | AFR | MSL | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | MSL | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | MSL | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG03239 | hp1 | a0001 | c0001 | t0003 | g0060 | SAS | PJL | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG03239 | hp2 | a0001 | c0001 | t0004 | g0029 | SAS | PJL | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG03453 | hp1 | a0001 | c0001 | t0016 | g0049 | AFR | MSL | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | MSL | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | MSL | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | MSL | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG03490 | hp1 | a0001 | c0002 | t0001 | g0002 | SAS | PJL | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG03490 | hp2 | a0001 | c0001 | t0003 | g0008 | SAS | PJL | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG03491 | hp1 | a0001 | c0001 | t0004 | g0029 | SAS | PJL | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG03491 | hp2 | a0001 | c0002 | t0001 | g0005 | SAS | PJL | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG03492 | hp1 | a0001 | c0002 | t0001 | g0002 | SAS | PJL | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG03492 | hp2 | a0001 | c0002 | t0001 | g0005 | SAS | PJL | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | ESN | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG03516 | hp2 | a0001 | c0001 | t0011 | g0047 | AFR | ESN | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG03540 | hp1 | a0001 | c0001 | t0005 | g0020 | AFR | GWD | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | MSL | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG03654 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG03654 | hp2 | a0001 | c0001 | t0002 | g0140 | SAS | PJL | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG03669 | hp1 | a0001 | c0001 | t0003 | g0008 | SAS | PJL | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG03669 | hp2 | a0001 | c0002 | t0001 | g0004 | SAS | PJL | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0071 | SAS | STU | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG03688 | hp2 | a0001 | c0001 | t0004 | g0015 | SAS | STU | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0082 | SAS | PJL | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG03831 | hp1 | a0001 | c0001 | t0003 | g0008 | SAS | BEB | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG03831 | hp2 | a0001 | c0001 | t0002 | g0148 | SAS | BEB | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG03834 | hp1 | a0001 | c0002 | t0001 | g0091 | SAS | BEB | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG03834 | hp2 | a0001 | c0002 | t0001 | g0035 | SAS | BEB | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG03927 | hp1 | a0001 | c0002 | t0001 | g0002 | SAS | BEB | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG03927 | hp2 | a0001 | c0001 | t0002 | g0028 | SAS | BEB | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG03942 | hp1 | a0001 | c0001 | t0021 | g0143 | SAS | BEB | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG03942 | hp2 | a0001 | c0001 | t0003 | g0008 | SAS | BEB | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0083 | SAS | STU | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | STU | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG04184 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | BEB | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG04184 | hp2 | a0001 | c0002 | t0001 | g0025 | SAS | BEB | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG04199 | hp1 | a0001 | c0002 | t0001 | g0035 | SAS | STU | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG04199 | hp2 | a0001 | c0001 | t0004 | g0015 | SAS | STU | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG04204 | hp1 | a0001 | c0002 | t0001 | g0002 | SAS | STU | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG04204 | hp2 | a0001 | c0002 | t0001 | g0025 | SAS | STU | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG04228 | hp1 | a0001 | c0001 | t0003 | g0057 | SAS | STU | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG04228 | hp2 | a0001 | c0001 | t0004 | g0015 | SAS | STU | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | YRI | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | YRI | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA18612 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | CHB | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA18612 | hp2 | a0001 | c0002 | t0001 | g0006 | EAS | CHB | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA18747 | hp1 | a0001 | c0002 | t0001 | g0113 | EAS | CHB | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA18747 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | CHB | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA18906 | hp1 | a0001 | c0001 | t0023 | g0139 | AFR | YRI | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | YRI | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA18939 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA18940 | hp1 | a0001 | c0002 | t0001 | g0116 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA18941 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA18941 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA18942 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA18942 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA18943 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA18945 | hp2 | a0001 | c0001 | t0020 | g0134 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA18946 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA18947 | hp2 | a0001 | c0002 | t0001 | g0109 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA18948 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA18948 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA18951 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA18951 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA18953 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA18953 | hp2 | a0001 | c0002 | t0001 | g0119 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA18954 | hp1 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA18954 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA18956 | hp1 | a0001 | c0002 | t0001 | g0118 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA18956 | hp2 | a0001 | c0001 | t0002 | g0144 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA18957 | hp1 | a0001 | c0002 | t0001 | g0096 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA18957 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA18961 | hp2 | a0001 | c0001 | t0002 | g0141 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA18962 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA18962 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA18963 | hp2 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA18966 | hp1 | a0001 | c0001 | t0002 | g0152 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA18966 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA18968 | hp1 | a0001 | c0001 | t0002 | g0142 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA18968 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA18969 | hp1 | a0001 | c0001 | t0008 | g0145 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA18969 | hp2 | a0001 | c0002 | t0017 | g0108 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA18970 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA18970 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA18972 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA18972 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA18973 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA18973 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA18974 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA18974 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA18975 | hp1 | a0001 | c0004 | t0001 | g0039 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA18975 | hp2 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA18977 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA18977 | hp2 | a0001 | c0002 | t0001 | g0105 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA18979 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA18980 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA18980 | hp2 | a0001 | c0001 | t0019 | g0051 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA18982 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA18984 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA18984 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA18986 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA18986 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA18987 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA18988 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA18988 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA18989 | hp1 | a0001 | c0001 | t0002 | g0150 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA18989 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA18991 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA18991 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA18993 | hp1 | a0001 | c0002 | t0001 | g0026 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA18995 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA18995 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA18998 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA19000 | hp1 | a0001 | c0004 | t0001 | g0039 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA19000 | hp2 | a0001 | c0001 | t0022 | g0137 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA19001 | hp1 | a0001 | c0001 | t0007 | g0044 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA19001 | hp2 | a0001 | c0002 | t0001 | g0086 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA19004 | hp1 | a0001 | c0002 | t0001 | g0120 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA19004 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA19005 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA19005 | hp2 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA19007 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA19007 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA19009 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA19009 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA19010 | hp1 | a0001 | c0001 | t0002 | g0146 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA19010 | hp2 | a0001 | c0001 | t0002 | g0149 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA19011 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA19011 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | LWK | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA19030 | hp2 | a0001 | c0001 | t0005 | g0020 | AFR | LWK | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | LWK | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA19043 | hp2 | a0001 | c0003 | t0001 | g0054 | AFR | LWK | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA19054 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA19057 | hp1 | a0001 | c0002 | t0001 | g0122 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA19057 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA19058 | hp1 | a0001 | c0001 | t0007 | g0136 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA19059 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA19059 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA19060 | hp1 | a0001 | c0002 | t0001 | g0098 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA19060 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA19063 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA19063 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA19066 | hp1 | a0001 | c0001 | t0007 | g0044 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA19068 | hp1 | a0001 | c0002 | t0001 | g0100 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA19068 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA19070 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA19070 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA19072 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA19072 | hp2 | a0001 | c0002 | t0001 | g0117 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA19074 | hp1 | a0001 | c0002 | t0001 | g0121 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA19074 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA19078 | hp1 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA19078 | hp2 | a0001 | c0002 | t0001 | g0036 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA19079 | hp1 | a0001 | c0001 | t0015 | g0126 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA19079 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA19081 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA19081 | hp2 | a0001 | c0002 | t0001 | g0114 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA19082 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA19082 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA19084 | hp1 | a0001 | c0002 | t0001 | g0036 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA19084 | hp2 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA19086 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA19086 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA19088 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA19088 | hp2 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA19090 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA19090 | hp2 | a0001 | c0002 | t0001 | g0026 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA19091 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA19091 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | YRI | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | YRI | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA20129 | hp1 | a0001 | c0002 | t0001 | g0005 | AFR | ASW | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ASW | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA20752 | hp1 | a0001 | c0002 | t0001 | g0014 | EUR | TSI | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA20752 | hp2 | a0001 | c0001 | t0002 | g0001 | EUR | TSI | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA20805 | hp1 | a0001 | c0002 | t0001 | g0037 | EUR | TSI | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA20805 | hp2 | a0001 | c0001 | t0002 | g0001 | EUR | TSI | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA20905 | hp1 | a0001 | c0002 | t0001 | g0004 | SAS | GIH | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA20905 | hp2 | a0001 | c0001 | t0004 | g0015 | SAS | GIH | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG01123 | hp2 | a0001 | c0002 | t0001 | g0014 | AMR | CLM | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG02109 | hp2 | a0001 | c0001 | t0005 | g0020 | AFR | ACB | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | ACB | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG02559 | hp1 | a0001 | c0002 | t0001 | g0037 | AFR | ACB | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | MSL | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | USA | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
HG06807 | hp2 | a0001 | c0001 | t0003 | g0008 | AFR | USA | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA20300 | hp1 | a0001 | c0003 | t0001 | g0055 | AFR | USA | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | USA | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | LWK | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
NA21309 | hp2 | a0001 | c0001 | t0002 | g0043 | AFR | LWK | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0004 | g0015 | REF | REF | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
homoSapiens_grch38 | hp1 | a0001 | c0002 | t0001 | g0112 | REF | REF | FAM76B_chr11_95763953_95794782 | FAM76B | chr11 | 95763953 | 95794782 |
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 |
---|
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:95778896
|
A | G | 4 | a0001c0001a0001c0003a0001c0004others(1): Show | 250 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(247): Show |
synonymous_variant | LOW | c.754T>C | p.Leu252Leu | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 8/10 | 1058/3932 | 754/1020 | 252/339 | chr11 | 95778896 | ||
chr11:95778921
|
T | C | 1 | a0001c0003 | 3 | HG03041.hp1 NA19043.hp2 NA20300.hp1 |
synonymous_variant | LOW | c.729A>G | p.Thr243Thr | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 8/10 | 1033/3932 | 729/1020 | 243/339 | chr11 | 95778921 | ||
chr11:95783249
|
A | G | 1 | a0001c0004 | 2 | NA18975.hp1 NA19000.hp1 |
synonymous_variant | LOW | c.379T>C | p.Leu127Leu | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 5/10 | 683/3932 | 379/1020 | 127/339 | chr11 | 95783249 | ||
chr11:95788507
|
T | C | 1 | a0001c0005 | 2 | HG01346.hp1 HG02717.hp1 |
synonymous_variant | LOW | c.144A>G | p.Gln48Gln | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 2/10 | 448/3932 | 144/1020 | 48/339 | chr11 | 95788507 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:95768964
|
G | A | 1 | a0001c0002t0006 | 3 | HG01069.hp2 HG01071.hp1 HG01074.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2597C>T | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 10/10 | 2597 | chr11 | 95768964 | |||||
chr11:95768964
|
G | C | 6 | a0001c0001t0002a0001c0001t0007a0001c0001t0010others(3): Show | 96 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(93): Show |
3_prime_UTR_variant | MODIFIER | c.*2597C>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 10/10 | 2597 | chr11 | 95768964 | |||||
chr11:95769194
|
G | A | 1 | a0001c0001t0010 | 2 | HG00639.hp2 HG01069.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2367C>T | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 10/10 | 2367 | chr11 | 95769194 | |||||
chr11:95769748
|
A | G | 2 | a0001c0001t0004a0001c0001t0019 | 8 | HG03239.hp2 HG03491.hp1 HG03688.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1813T>C | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 10/10 | 1813 | chr11 | 95769748 | |||||
chr11:95770005
|
C | T | 1 | a0001c0001t0015 | 1 | NA19079.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1556G>A | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 10/10 | 1556 | chr11 | 95770005 | |||||
chr11:95770179
|
T | G | 1 | a0001c0002t0009 | 2 | HG02015.hp1 HG02074.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1382A>C | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 10/10 | 1382 | chr11 | 95770179 | |||||
chr11:95770238
|
C | T | 1 | a0001c0001t0022 | 1 | NA19000.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1323G>A | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 10/10 | 1323 | chr11 | 95770238 | |||||
chr11:95770472
|
T | C | 9 | a0001c0001t0002a0001c0001t0007a0001c0001t0008others(6): Show | 101 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(98): Show |
3_prime_UTR_variant | MODIFIER | c.*1089A>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 10/10 | 1089 | chr11 | 95770472 | |||||
chr11:95770486
|
A | C | 1 | a0001c0002t0012 | 1 | HG02258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1075T>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 10/10 | 1075 | chr11 | 95770486 | |||||
chr11:95770500
|
T | A | 1 | a0001c0002t0017 | 1 | NA18969.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1061A>T | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 10/10 | 1061 | chr11 | 95770500 | |||||
chr11:95770614
|
C | T | 1 | a0001c0001t0007 | 3 | NA19001.hp1 NA19058.hp1 NA19066.hp1 |
3_prime_UTR_variant | MODIFIER | c.*947G>A | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 10/10 | 947 | chr11 | 95770614 | |||||
chr11:95770993
|
CTAA | C | 1 | a0001c0001t0003 | 15 | HG02300.hp1 HG02647.hp1 HG02735.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*565_*567delTTA | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 10/10 | 565 | chr11 | 95770993 | |||||
chr11:95771065
|
T | G | 1 | a0001c0001t0018 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*496A>C | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 10/10 | 496 | chr11 | 95771065 | |||||
chr11:95771315
|
A | G | 1 | a0001c0002t0014 | 1 | HG01358.hp2 | 3_prime_UTR_variant | MODIFIER | c.*246T>C | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 10/10 | 246 | chr11 | 95771315 | |||||
chr11:95771378
|
A | C | 1 | a0001c0001t0021 | 1 | HG03942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*183T>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 10/10 | 183 | chr11 | 95771378 | |||||
chr11:95771436
|
C | A | 1 | a0001c0001t0023 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*125G>T | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 10/10 | 125 | chr11 | 95771436 | |||||
chr11:95771483
|
C | T | 1 | a0001c0001t0013 | 1 | HG01978.hp1 | 3_prime_UTR_variant | MODIFIER | c.*78G>A | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 10/10 | 78 | chr11 | 95771483 | |||||
chr11:95771523
|
T | C | 1 | a0001c0001t0019 | 1 | NA18980.hp2 | 3_prime_UTR_variant | MODIFIER | c.*38A>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 10/10 | 38 | chr11 | 95771523 | |||||
chr11:95789485
|
C | T | 1 | a0001c0001t0005 | 3 | HG02109.hp2 HG03540.hp1 NA19030.hp2 |
5_prime_UTR_variant | MODIFIER | c.-7G>A | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 1/10 | 7 | chr11 | 95789485 | |||||
chr11:95789602
|
A | ACCAGGGC others(14): Show |
1 | a0001c0001t0020 | 1 | NA18945.hp2 | 5_prime_UTR_variant | MODIFIER | c.-145_-125dupGCTCTC others(15): Show |
FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 1/10 | 125 | chr11 | 95789602 | |||||
chr11:95789638
|
A | G | 1 | a0001c0002t0012 | 1 | HG02258.hp2 | 5_prime_UTR_variant | MODIFIER | c.-160T>C | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 1/10 | 160 | chr11 | 95789638 | |||||
chr11:95789694
|
G | C | 8 | a0001c0001t0002a0001c0001t0007a0001c0001t0008others(5): Show | 100 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(97): Show |
5_prime_UTR_variant | MODIFIER | c.-216C>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 1/10 | 216 | chr11 | 95789694 | |||||
chr11:95789743
|
C | T | 1 | a0001c0001t0011 | 1 | HG03516.hp2 | 5_prime_UTR_variant | MODIFIER | c.-265G>A | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 1/10 | 265 | chr11 | 95789743 | |||||
chr11:95789758
|
T | C | 1 | a0001c0001t0024 | 1 | HG02056.hp1 | 5_prime_UTR_variant | MODIFIER | c.-280A>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 1/10 | 280 | chr11 | 95789758 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:95771762
|
G | C | 10 | a0001c0001t0001g0013a0001c0001t0001g0022a0001c0001t0001g0071others(7): Show | 17 | HG00423.hp1 HG00558.hp1 HG01928.hp1 others(14): Show |
intron_variant | MODIFIER | c.931-112C>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 9/9 | chr11 | 95771762 | ||||||
chr11:95771910
|
A | T | 1 | a0001c0001t0019g0051 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.931-260T>A | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 9/9 | chr11 | 95771910 | ||||||
chr11:95772063
|
G | A | 44 | a0001c0001t0001g0010a0001c0001t0001g0040a0001c0001t0001g0041others(41): Show | 124 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(121): Show |
intron_variant | MODIFIER | c.931-413C>T | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 9/9 | chr11 | 95772063 | ||||||
chr11:95772093
|
T | C | 14 | a0001c0001t0001g0010a0001c0001t0001g0040a0001c0001t0001g0041others(11): Show | 24 | HG01081.hp1 HG01167.hp1 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.931-443A>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 9/9 | chr11 | 95772093 | ||||||
chr11:95772110
|
T | C | 3 | a0001c0001t0002g0012a0001c0001t0002g0135a0001c0001t0002g0142 | 9 | HG02080.hp1 NA18747.hp2 NA18968.hp1 others(6): Show |
intron_variant | MODIFIER | c.931-460A>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 9/9 | chr11 | 95772110 | ||||||
chr11:95772486
|
A | C | 1 | a0001c0001t0002g0142 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.931-836T>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 9/9 | chr11 | 95772486 | ||||||
chr11:95772667
|
T | C | 1 | a0001c0001t0002g0149 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.931-1017A>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 9/9 | chr11 | 95772667 | ||||||
chr11:95772724
|
G | A | 31 | a0001c0001t0001g0073a0001c0001t0002g0001a0001c0001t0002g0012others(28): Show | 101 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(98): Show |
intron_variant | MODIFIER | c.931-1074C>T | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 9/9 | chr11 | 95772724 | ||||||
chr11:95772931
|
T | C | 1 | a0001c0001t0001g0019 | 4 | HG00738.hp2 HG00741.hp2 HG01099.hp1 others(1): Show |
intron_variant | MODIFIER | c.931-1281A>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 9/9 | chr11 | 95772931 | ||||||
chr11:95773120
|
GTTC | G | 30 | a0001c0001t0002g0001a0001c0001t0002g0012a0001c0001t0002g0027others(27): Show | 100 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(97): Show |
intron_variant | MODIFIER | c.931-1473_931-1471d others(5): Show |
FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 9/9 | chr11 | 95773120 | ||||||
chr11:95773429
|
T | C | 1 | a0001c0001t0001g0067 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.931-1779A>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 9/9 | chr11 | 95773429 | ||||||
chr11:95773458
|
C | CA | 63 | a0001c0001t0001g0011a0001c0001t0001g0017a0001c0001t0001g0021others(60): Show | 195 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.931-1809dupT | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 9/9 | chr11 | 95773458 | ||||||
chr11:95773458
|
C | CAA | 42 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0013others(39): Show | 91 | HG00323.hp2 HG00558.hp1 HG00738.hp2 others(88): Show |
intron_variant | MODIFIER | c.931-1810_931-1809d others(4): Show |
FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 9/9 | chr11 | 95773458 | ||||||
chr11:95773458
|
C | CAAAAA | 28 | a0001c0001t0002g0001a0001c0001t0002g0012a0001c0001t0002g0027others(25): Show | 97 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(94): Show |
intron_variant | MODIFIER | c.931-1813_931-1809d others(7): Show |
FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 9/9 | chr11 | 95773458 | ||||||
chr11:95773505
|
A | C | 1 | a0001c0001t0002g0141 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.931-1855T>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 9/9 | chr11 | 95773505 | ||||||
chr11:95773624
|
T | A | 1 | a0001c0002t0001g0107 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.931-1974A>T | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 9/9 | chr11 | 95773624 | ||||||
chr11:95773743
|
G | C | 31 | a0001c0001t0002g0001a0001c0001t0002g0012a0001c0001t0002g0027others(28): Show | 101 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(98): Show |
intron_variant | MODIFIER | c.931-2093C>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 9/9 | chr11 | 95773743 | ||||||
chr11:95773864
|
T | C | 8 | a0001c0001t0001g0031a0001c0001t0003g0008a0001c0001t0003g0030others(5): Show | 17 | HG02300.hp1 HG02630.hp1 HG02647.hp1 others(14): Show |
intron_variant | MODIFIER | c.930+2058A>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 9/9 | chr11 | 95773864 | ||||||
chr11:95773894
|
T | C | 1 | a0001c0002t0001g0106 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.930+2028A>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 9/9 | chr11 | 95773894 | ||||||
chr11:95774053
|
G | C | 8 | a0001c0001t0001g0011a0001c0001t0001g0017a0001c0001t0001g0062others(5): Show | 19 | HG01123.hp1 HG02055.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.930+1869C>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 9/9 | chr11 | 95774053 | ||||||
chr11:95774095
|
A | T | 1 | a0001c0001t0002g0154 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.930+1827T>A | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 9/9 | chr11 | 95774095 | ||||||
chr11:95774205
|
CAG | C | 1 | a0001c0002t0001g0025 | 3 | HG02683.hp2 HG04184.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.930+1715_930+1716d others(4): Show |
FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 9/9 | chr11 | 95774205 | ||||||
chr11:95774243
|
T | A | 3 | a0001c0001t0004g0015a0001c0001t0004g0029a0001c0001t0019g0051 | 8 | HG03239.hp2 HG03491.hp1 HG03688.hp2 others(5): Show |
intron_variant | MODIFIER | c.930+1679A>T | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 9/9 | chr11 | 95774243 | ||||||
chr11:95774460
|
C | A | 144 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(141): Show | 376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.930+1462G>T | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 9/9 | chr11 | 95774460 | ||||||
chr11:95774491
|
C | A | 1 | a0001c0001t0001g0129 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.930+1431G>T | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 9/9 | chr11 | 95774491 | ||||||
chr11:95774530
|
T | C | 1 | a0001c0002t0001g0121 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.930+1392A>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 9/9 | chr11 | 95774530 | ||||||
chr11:95774708
|
TATAAGA | T | 30 | a0001c0001t0002g0001a0001c0001t0002g0012a0001c0001t0002g0027others(27): Show | 100 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(97): Show |
intron_variant | MODIFIER | c.930+1208_930+1213d others(8): Show |
FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 9/9 | chr11 | 95774708 | ||||||
chr11:95774709
|
A | G | 1 | a0001c0002t0001g0116 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.930+1213T>C | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 9/9 | chr11 | 95774709 | ||||||
chr11:95774791
|
A | G | 1 | a0001c0001t0002g0027 | 3 | HG00140.hp1 HG00741.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.930+1131T>C | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 9/9 | chr11 | 95774791 | ||||||
chr11:95774856
|
T | C | 54 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0011others(51): Show | 116 | HG00323.hp2 HG00423.hp1 HG00558.hp1 others(113): Show |
intron_variant | MODIFIER | c.930+1066A>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 9/9 | chr11 | 95774856 | ||||||
chr11:95774875
|
A | T | 1 | a0001c0001t0001g0125 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.930+1047T>A | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 9/9 | chr11 | 95774875 | ||||||
chr11:95774957
|
A | G | 99 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(96): Show | 241 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(238): Show |
intron_variant | MODIFIER | c.930+965T>C | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 9/9 | chr11 | 95774957 | ||||||
chr11:95775003
|
G | GA | 21 | a0001c0001t0001g0053a0001c0001t0001g0061a0001c0001t0016g0049others(18): Show | 53 | HG00597.hp1 HG00673.hp1 HG01081.hp2 others(50): Show |
intron_variant | MODIFIER | c.930+918dupT | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 9/9 | chr11 | 95775003 | ||||||
chr11:95775003
|
GA | G | 20 | a0001c0001t0001g0010a0001c0001t0001g0040a0001c0001t0001g0041others(17): Show | 37 | HG01081.hp1 HG01167.hp1 HG01169.hp2 others(34): Show |
intron_variant | MODIFIER | c.930+918delT | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 9/9 | chr11 | 95775003 | ||||||
chr11:95775005
|
A | G | 14 | a0001c0001t0001g0010a0001c0001t0001g0040a0001c0001t0001g0041others(11): Show | 24 | HG01081.hp1 HG01167.hp1 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.930+917T>C | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 9/9 | chr11 | 95775005 | ||||||
chr11:95775013
|
A | C | 1 | a0001c0002t0001g0036 | 2 | NA19078.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.930+909T>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 9/9 | chr11 | 95775013 | ||||||
chr11:95775036
|
T | G | 14 | a0001c0001t0001g0010a0001c0001t0001g0040a0001c0001t0001g0041others(11): Show | 24 | HG01081.hp1 HG01167.hp1 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.930+886A>C | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 9/9 | chr11 | 95775036 | ||||||
chr11:95775188
|
T | C | 1 | a0001c0001t0001g0074 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.930+734A>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 9/9 | chr11 | 95775188 | ||||||
chr11:95775219
|
G | T | 45 | a0001c0001t0001g0010a0001c0001t0001g0040a0001c0001t0001g0041others(42): Show | 125 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(122): Show |
intron_variant | MODIFIER | c.930+703C>A | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 9/9 | chr11 | 95775219 | ||||||
chr11:95775220
|
T | C | 9 | a0001c0001t0001g0007a0001c0001t0001g0018a0001c0001t0001g0023others(6): Show | 27 | HG01074.hp1 HG01109.hp2 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.930+702A>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 9/9 | chr11 | 95775220 | ||||||
chr11:95775233
|
A | T | 14 | a0001c0001t0001g0010a0001c0001t0001g0040a0001c0001t0001g0041others(11): Show | 24 | HG01081.hp1 HG01167.hp1 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.930+689T>A | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 9/9 | chr11 | 95775233 | ||||||
chr11:95775240
|
C | A | 45 | a0001c0001t0001g0010a0001c0001t0001g0040a0001c0001t0001g0041others(42): Show | 125 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(122): Show |
intron_variant | MODIFIER | c.930+682G>T | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 9/9 | chr11 | 95775240 | ||||||
chr11:95775262
|
G | C | 1 | a0001c0001t0001g0075 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.930+660C>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 9/9 | chr11 | 95775262 | ||||||
chr11:95775360
|
C | A | 45 | a0001c0001t0001g0010a0001c0001t0001g0040a0001c0001t0001g0041others(42): Show | 125 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(122): Show |
intron_variant | MODIFIER | c.930+562G>T | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 9/9 | chr11 | 95775360 | ||||||
chr11:95775398
|
T | C | 14 | a0001c0001t0001g0010a0001c0001t0001g0040a0001c0001t0001g0041others(11): Show | 24 | HG01081.hp1 HG01167.hp1 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.930+524A>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 9/9 | chr11 | 95775398 | ||||||
chr11:95775571
|
T | C | 3 | a0001c0001t0004g0015a0001c0001t0004g0029a0001c0001t0019g0051 | 8 | HG03239.hp2 HG03491.hp1 HG03688.hp2 others(5): Show |
intron_variant | MODIFIER | c.930+351A>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 9/9 | chr11 | 95775571 | ||||||
chr11:95775599
|
A | G | 1 | a0001c0002t0001g0035 | 2 | HG03834.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.930+323T>C | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 9/9 | chr11 | 95775599 | ||||||
chr11:95775638
|
CA | C | 14 | a0001c0001t0001g0010a0001c0001t0001g0040a0001c0001t0001g0041others(11): Show | 24 | HG01081.hp1 HG01167.hp1 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.930+283delT | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 9/9 | chr11 | 95775638 | ||||||
chr11:95775757
|
C | T | 1 | a0001c0003t0001g0054 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.930+165G>A | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 9/9 | chr11 | 95775757 | ||||||
chr11:95775873
|
C | G | 29 | a0001c0001t0002g0001a0001c0001t0002g0012a0001c0001t0002g0027others(26): Show | 99 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(96): Show |
intron_variant | MODIFIER | c.930+49G>C | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 9/9 | chr11 | 95775873 | ||||||
chr11:95776178
|
G | C | 1 | a0001c0002t0001g0109 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.829-155C>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 8/9 | chr11 | 95776178 | ||||||
chr11:95776240
|
C | T | 14 | a0001c0001t0001g0010a0001c0001t0001g0040a0001c0001t0001g0041others(11): Show | 24 | HG01081.hp1 HG01167.hp1 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.829-217G>A | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 8/9 | chr11 | 95776240 | ||||||
chr11:95776474
|
T | C | 28 | a0001c0001t0002g0001a0001c0001t0002g0012a0001c0001t0002g0027others(25): Show | 97 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(94): Show |
intron_variant | MODIFIER | c.829-451A>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 8/9 | chr11 | 95776474 | ||||||
chr11:95776475
|
G | C | 1 | a0001c0001t0001g0128 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.829-452C>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 8/9 | chr11 | 95776475 | ||||||
chr11:95776533
|
T | C | 1 | a0001c0002t0001g0110 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.829-510A>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 8/9 | chr11 | 95776533 | ||||||
chr11:95776554
|
T | A | 1 | a0001c0001t0001g0068 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.829-531A>T | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 8/9 | chr11 | 95776554 | ||||||
chr11:95776913
|
G | A | 1 | a0001c0001t0002g0144 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.829-890C>T | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 8/9 | chr11 | 95776913 | ||||||
chr11:95776925
|
C | T | 30 | a0001c0001t0002g0001a0001c0001t0002g0012a0001c0001t0002g0027others(27): Show | 100 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(97): Show |
intron_variant | MODIFIER | c.829-902G>A | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 8/9 | chr11 | 95776925 | ||||||
chr11:95776930
|
TA | T | 6 | a0001c0001t0001g0017a0001c0001t0001g0062a0001c0001t0001g0063others(3): Show | 9 | HG02055.hp1 HG02257.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.829-908delT | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 8/9 | chr11 | 95776930 | ||||||
chr11:95777067
|
C | T | 1 | a0001c0001t0016g0049 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.829-1044G>A | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 8/9 | chr11 | 95777067 | ||||||
chr11:95777273
|
T | A | 1 | a0001c0001t0002g0146 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.829-1250A>T | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 8/9 | chr11 | 95777273 | ||||||
chr11:95777344
|
A | G | 33 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0013others(30): Show | 75 | HG00323.hp2 HG00423.hp1 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.829-1321T>C | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 8/9 | chr11 | 95777344 | ||||||
chr11:95777463
|
C | A | 1 | a0001c0002t0001g0117 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.828+1359G>T | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 8/9 | chr11 | 95777463 | ||||||
chr11:95777697
|
T | C | 1 | a0001c0001t0002g0147 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.828+1125A>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 8/9 | chr11 | 95777697 | ||||||
chr11:95777814
|
A | G | 1 | a0001c0001t0001g0071 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.828+1008T>C | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 8/9 | chr11 | 95777814 | ||||||
chr11:95777856
|
T | C | 1 | a0001c0001t0002g0148 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.828+966A>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 8/9 | chr11 | 95777856 | ||||||
chr11:95777858
|
T | C | 1 | a0001c0002t0001g0115 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.828+964A>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 8/9 | chr11 | 95777858 | ||||||
chr11:95777999
|
C | T | 1 | a0001c0002t0001g0105 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.828+823G>A | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 8/9 | chr11 | 95777999 | ||||||
chr11:95778234
|
C | A | 1 | a0001c0005t0001g0038 | 2 | HG01346.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.828+588G>T | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 8/9 | chr11 | 95778234 | ||||||
chr11:95778281
|
C | A | 30 | a0001c0001t0002g0001a0001c0001t0002g0012a0001c0001t0002g0027others(27): Show | 100 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(97): Show |
intron_variant | MODIFIER | c.828+541G>T | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 8/9 | chr11 | 95778281 | ||||||
chr11:95778343
|
G | C | 1 | a0001c0001t0016g0049 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.828+479C>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 8/9 | chr11 | 95778343 | ||||||
chr11:95778405
|
G | A | 1 | a0001c0002t0001g0111 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.828+417C>T | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 8/9 | chr11 | 95778405 | ||||||
chr11:95778484
|
A | C | 1 | a0001c0001t0002g0140 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.828+338T>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 8/9 | chr11 | 95778484 | ||||||
chr11:95778761
|
C | T | 1 | a0001c0001t0001g0019 | 4 | HG00738.hp2 HG00741.hp2 HG01099.hp1 others(1): Show |
intron_variant | MODIFIER | c.828+61G>A | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 8/9 | chr11 | 95778761 | ||||||
chr11:95779581
|
A | G | 1 | a0001c0002t0001g0104 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.692+26T>C | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 7/9 | chr11 | 95779581 | ||||||
chr11:95779593
|
G | A | 1 | a0001c0001t0001g0079 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.692+14C>T | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 7/9 | chr11 | 95779593 | ||||||
chr11:95779976
|
C | T | 1 | a0001c0001t0018g0050 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.564-50G>A | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 5/9 | chr11 | 95779976 | ||||||
chr11:95779993
|
C | A | 1 | a0001c0001t0001g0076 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.564-67G>T | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 5/9 | chr11 | 95779993 | ||||||
chr11:95780023
|
T | C | 1 | a0001c0002t0001g0103 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.564-97A>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 5/9 | chr11 | 95780023 | ||||||
chr11:95780044
|
G | A | 3 | a0001c0001t0001g0032a0001c0001t0001g0065a0001c0001t0001g0077 | 4 | HG02818.hp2 HG02922.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.564-118C>T | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 5/9 | chr11 | 95780044 | ||||||
chr11:95780194
|
A | C | 1 | a0001c0002t0001g0102 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.564-268T>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 5/9 | chr11 | 95780194 | ||||||
chr11:95780197
|
G | A | 1 | a0001c0002t0001g0102 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.564-271C>T | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 5/9 | chr11 | 95780197 | ||||||
chr11:95780198
|
T | A | 1 | a0001c0002t0001g0102 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.564-272A>T | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 5/9 | chr11 | 95780198 | ||||||
chr11:95780200
|
G | C | 1 | a0001c0001t0001g0033 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.564-274C>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 5/9 | chr11 | 95780200 | ||||||
chr11:95780208
|
A | G | 1 | a0001c0002t0001g0102 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.564-282T>C | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 5/9 | chr11 | 95780208 | ||||||
chr11:95780209
|
A | G | 1 | a0001c0002t0001g0102 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.564-283T>C | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 5/9 | chr11 | 95780209 | ||||||
chr11:95780211
|
T | G | 1 | a0001c0002t0001g0102 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.564-285A>C | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 5/9 | chr11 | 95780211 | ||||||
chr11:95780214
|
T | G | 1 | a0001c0002t0001g0102 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.564-288A>C | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 5/9 | chr11 | 95780214 | ||||||
chr11:95780220
|
T | G | 1 | a0001c0002t0001g0102 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.564-294A>C | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 5/9 | chr11 | 95780220 | ||||||
chr11:95780221
|
G | C | 1 | a0001c0002t0001g0102 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.564-295C>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 5/9 | chr11 | 95780221 | ||||||
chr11:95780227
|
G | C | 1 | a0001c0002t0001g0102 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.564-301C>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 5/9 | chr11 | 95780227 | ||||||
chr11:95780228
|
T | C | 1 | a0001c0002t0001g0102 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.564-302A>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 5/9 | chr11 | 95780228 | ||||||
chr11:95780230
|
T | C | 1 | a0001c0002t0001g0102 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.564-304A>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 5/9 | chr11 | 95780230 | ||||||
chr11:95780231
|
A | C | 1 | a0001c0002t0001g0102 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.564-305T>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 5/9 | chr11 | 95780231 | ||||||
chr11:95780232
|
G | C | 1 | a0001c0002t0001g0102 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.564-306C>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 5/9 | chr11 | 95780232 | ||||||
chr11:95780233
|
G | A | 1 | a0001c0002t0001g0102 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.564-307C>T | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 5/9 | chr11 | 95780233 | ||||||
chr11:95780234
|
T | C | 1 | a0001c0002t0001g0102 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.564-308A>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 5/9 | chr11 | 95780234 | ||||||
chr11:95780240
|
T | A | 1 | a0001c0002t0001g0102 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.564-314A>T | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 5/9 | chr11 | 95780240 | ||||||
chr11:95780245
|
T | C | 1 | a0001c0002t0001g0102 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.564-319A>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 5/9 | chr11 | 95780245 | ||||||
chr11:95780246
|
T | C | 1 | a0001c0002t0001g0102 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.564-320A>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 5/9 | chr11 | 95780246 | ||||||
chr11:95780247
|
T | C | 1 | a0001c0002t0001g0102 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.564-321A>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 5/9 | chr11 | 95780247 | ||||||
chr11:95780248
|
G | C | 1 | a0001c0002t0001g0102 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.564-322C>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 5/9 | chr11 | 95780248 | ||||||
chr11:95780249
|
G | C | 1 | a0001c0002t0001g0102 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.564-323C>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 5/9 | chr11 | 95780249 | ||||||
chr11:95780333
|
G | C | 54 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0011others(51): Show | 116 | HG00323.hp2 HG00423.hp1 HG00558.hp1 others(113): Show |
intron_variant | MODIFIER | c.564-407C>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 5/9 | chr11 | 95780333 | ||||||
chr11:95780353
|
A | G | 2 | a0001c0001t0001g0022a0001c0001t0013g0070 | 4 | HG01928.hp1 HG01975.hp2 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.564-427T>C | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 5/9 | chr11 | 95780353 | ||||||
chr11:95780428
|
A | G | 1 | a0001c0002t0001g0116 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.564-502T>C | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 5/9 | chr11 | 95780428 | ||||||
chr11:95780487
|
A | C | 1 | a0001c0002t0001g0103 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.564-561T>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 5/9 | chr11 | 95780487 | ||||||
chr11:95780621
|
A | G | 1 | a0001c0002t0001g0095 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.564-695T>C | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 5/9 | chr11 | 95780621 | ||||||
chr11:95780651
|
T | A | 1 | a0001c0001t0007g0136 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.564-725A>T | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 5/9 | chr11 | 95780651 | ||||||
chr11:95780740
|
C | T | 3 | a0001c0003t0001g0054a0001c0003t0001g0055a0001c0003t0001g0056 | 3 | HG03041.hp1 NA19043.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.564-814G>A | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 5/9 | chr11 | 95780740 | ||||||
chr11:95780789
|
T | C | 1 | a0001c0001t0002g0149 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.564-863A>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 5/9 | chr11 | 95780789 | ||||||
chr11:95780852
|
C | T | 1 | a0001c0003t0001g0054 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.564-926G>A | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 5/9 | chr11 | 95780852 | ||||||
chr11:95780862
|
C | T | 1 | a0001c0002t0001g0102 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.564-936G>A | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 5/9 | chr11 | 95780862 | ||||||
chr11:95780902
|
A | G | 1 | a0001c0001t0024g0155 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.564-976T>C | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 5/9 | chr11 | 95780902 | ||||||
chr11:95780927
|
G | T | 2 | a0001c0001t0003g0030a0001c0001t0003g0058 | 3 | HG02818.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.564-1001C>A | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 5/9 | chr11 | 95780927 | ||||||
chr11:95781000
|
T | A | 1 | a0001c0001t0002g0151 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.564-1074A>T | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 5/9 | chr11 | 95781000 | ||||||
chr11:95781011
|
A | G | 1 | a0001c0001t0001g0066 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.564-1085T>C | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 5/9 | chr11 | 95781011 | ||||||
chr11:95781077
|
TC | T | 3 | a0001c0001t0001g0062a0001c0001t0001g0069a0001c0001t0002g0153 | 3 | HG01516.hp1 HG02055.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.564-1152delG | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 5/9 | chr11 | 95781077 | ||||||
chr11:95781080
|
C | T | 151 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(148): Show | 412 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(409): Show |
intron_variant | MODIFIER | c.564-1154G>A | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 5/9 | chr11 | 95781080 | ||||||
chr11:95781092
|
T | C | 25 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0016others(22): Show | 54 | HG00323.hp2 HG00423.hp1 HG00558.hp1 others(51): Show |
intron_variant | MODIFIER | c.564-1166A>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 5/9 | chr11 | 95781092 | ||||||
chr11:95781357
|
C | T | 5 | a0001c0001t0001g0125a0001c0001t0001g0127a0001c0001t0001g0132others(2): Show | 6 | NA18940.hp2 NA18945.hp1 NA18975.hp1 others(3): Show |
intron_variant | MODIFIER | c.564-1431G>A | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 5/9 | chr11 | 95781357 | ||||||
chr11:95781435
|
T | A | 31 | a0001c0001t0002g0001a0001c0001t0002g0012a0001c0001t0002g0027others(28): Show | 101 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(98): Show |
intron_variant | MODIFIER | c.564-1509A>T | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 5/9 | chr11 | 95781435 | ||||||
chr11:95781622
|
G | A | 1 | a0001c0002t0001g0114 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.563+1443C>T | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 5/9 | chr11 | 95781622 | ||||||
chr11:95781656
|
G | A | 1 | a0001c0002t0012g0048 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.563+1409C>T | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 5/9 | chr11 | 95781656 | ||||||
chr11:95781825
|
CACT | C | 9 | a0001c0001t0001g0010a0001c0001t0001g0041a0001c0001t0001g0125others(6): Show | 18 | HG01167.hp1 HG01169.hp2 HG02056.hp1 others(15): Show |
intron_variant | MODIFIER | c.563+1237_563+1239d others(5): Show |
FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 5/9 | chr11 | 95781825 | ||||||
chr11:95781870
|
T | G | 1 | a0001c0002t0001g0115 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.563+1195A>C | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 5/9 | chr11 | 95781870 | ||||||
chr11:95781969
|
G | A | 1 | a0001c0003t0001g0056 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.563+1096C>T | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 5/9 | chr11 | 95781969 | ||||||
chr11:95782280
|
A | G | 1 | a0001c0002t0001g0101 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.563+785T>C | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 5/9 | chr11 | 95782280 | ||||||
chr11:95782328
|
C | A | 3 | a0001c0002t0001g0026a0001c0002t0001g0116a0001c0002t0001g0117 | 5 | HG02129.hp1 NA18940.hp1 NA18993.hp1 others(2): Show |
intron_variant | MODIFIER | c.563+737G>T | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 5/9 | chr11 | 95782328 | ||||||
chr11:95782328
|
C | T | 37 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0013others(34): Show | 79 | HG00323.hp2 HG00423.hp1 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.563+737G>A | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 5/9 | chr11 | 95782328 | ||||||
chr11:95782375
|
T | G | 1 | a0001c0001t0002g0150 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.563+690A>C | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 5/9 | chr11 | 95782375 | ||||||
chr11:95782556
|
G | A | 14 | a0001c0001t0001g0010a0001c0001t0001g0040a0001c0001t0001g0041others(11): Show | 24 | HG01081.hp1 HG01167.hp1 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.563+509C>T | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 5/9 | chr11 | 95782556 | ||||||
chr11:95782729
|
A | C | 1 | a0001c0001t0003g0057 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.563+336T>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 5/9 | chr11 | 95782729 | ||||||
chr11:95782745
|
T | C | 1 | a0001c0001t0003g0060 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.563+320A>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 5/9 | chr11 | 95782745 | ||||||
chr11:95782876
|
C | A | 45 | a0001c0001t0001g0010a0001c0001t0001g0040a0001c0001t0001g0041others(42): Show | 125 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(122): Show |
intron_variant | MODIFIER | c.563+189G>T | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 5/9 | chr11 | 95782876 | ||||||
chr11:95783372
|
A | G | 108 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(105): Show | 260 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(257): Show |
intron_variant | MODIFIER | c.364-108T>C | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 4/9 | chr11 | 95783372 | ||||||
chr11:95783394
|
T | G | 8 | a0001c0001t0001g0011a0001c0001t0001g0017a0001c0001t0001g0062others(5): Show | 19 | HG01123.hp1 HG02055.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.364-130A>C | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 4/9 | chr11 | 95783394 | ||||||
chr11:95783415
|
G | A | 1 | a0001c0001t0001g0131 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.364-151C>T | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 4/9 | chr11 | 95783415 | ||||||
chr11:95783459
|
G | C | 1 | a0001c0001t0001g0023 | 3 | HG01891.hp2 HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.364-195C>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 4/9 | chr11 | 95783459 | ||||||
chr11:95783553
|
A | G | 8 | a0001c0001t0001g0031a0001c0001t0003g0008a0001c0001t0003g0030others(5): Show | 17 | HG02300.hp1 HG02630.hp1 HG02647.hp1 others(14): Show |
intron_variant | MODIFIER | c.364-289T>C | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 4/9 | chr11 | 95783553 | ||||||
chr11:95783567
|
A | C | 24 | a0001c0001t0002g0001a0001c0001t0002g0012a0001c0001t0002g0042others(21): Show | 88 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.364-303T>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 4/9 | chr11 | 95783567 | ||||||
chr11:95783671
|
C | T | 1 | a0001c0001t0001g0065 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.364-407G>A | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 4/9 | chr11 | 95783671 | ||||||
chr11:95783721
|
C | T | 3 | a0001c0001t0004g0015a0001c0001t0004g0029a0001c0001t0019g0051 | 8 | HG03239.hp2 HG03491.hp1 HG03688.hp2 others(5): Show |
intron_variant | MODIFIER | c.364-457G>A | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 4/9 | chr11 | 95783721 | ||||||
chr11:95783982
|
T | C | 1 | a0001c0001t0016g0049 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.364-718A>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 4/9 | chr11 | 95783982 | ||||||
chr11:95784009
|
G | A | 4 | a0001c0001t0001g0040a0001c0001t0001g0129a0001c0001t0001g0130others(1): Show | 5 | HG01081.hp1 HG02280.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.364-745C>T | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 4/9 | chr11 | 95784009 | ||||||
chr11:95784074
|
T | C | 1 | a0001c0001t0001g0053 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.364-810A>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 4/9 | chr11 | 95784074 | ||||||
chr11:95784265
|
C | A | 1 | a0001c0001t0001g0063 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.364-1001G>T | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 4/9 | chr11 | 95784265 | ||||||
chr11:95784382
|
T | C | 1 | a0001c0002t0001g0118 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.364-1118A>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 4/9 | chr11 | 95784382 | ||||||
chr11:95784412
|
C | T | 32 | a0001c0001t0001g0130a0001c0001t0002g0001a0001c0001t0002g0012others(29): Show | 102 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(99): Show |
intron_variant | MODIFIER | c.364-1148G>A | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 4/9 | chr11 | 95784412 | ||||||
chr11:95784493
|
A | G | 1 | a0001c0001t0023g0139 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.364-1229T>C | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 4/9 | chr11 | 95784493 | ||||||
chr11:95784522
|
G | T | 1 | a0001c0001t0002g0042 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.364-1258C>A | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 4/9 | chr11 | 95784522 | ||||||
chr11:95784531
|
G | T | 1 | a0001c0001t0001g0053 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.364-1267C>A | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 4/9 | chr11 | 95784531 | ||||||
chr11:95784553
|
A | AGT | 1 | a0001c0001t0001g0019 | 4 | HG00738.hp2 HG00741.hp2 HG01099.hp1 others(1): Show |
intron_variant | MODIFIER | c.364-1291_364-1290d others(4): Show |
FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 4/9 | chr11 | 95784553 | ||||||
chr11:95784571
|
T | TAC | 19 | a0001c0001t0001g0011a0001c0001t0001g0017a0001c0001t0001g0062others(16): Show | 39 | HG00642.hp2 HG00735.hp2 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.364-1309_364-1308d others(4): Show |
FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 4/9 | chr11 | 95784571 | ||||||
chr11:95784573
|
C | T | 45 | a0001c0001t0001g0010a0001c0001t0001g0018a0001c0001t0001g0040others(42): Show | 128 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(125): Show |
intron_variant | MODIFIER | c.364-1309G>A | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 4/9 | chr11 | 95784573 | ||||||
chr11:95784593
|
A | T | 1 | a0001c0002t0001g0089 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.364-1329T>A | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 4/9 | chr11 | 95784593 | ||||||
chr11:95784622
|
C | G | 1 | a0001c0002t0001g0100 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.364-1358G>C | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 4/9 | chr11 | 95784622 | ||||||
chr11:95784681
|
G | C | 1 | a0001c0001t0001g0080 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.364-1417C>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 4/9 | chr11 | 95784681 | ||||||
chr11:95784818
|
A | T | 37 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0013others(34): Show | 79 | HG00323.hp2 HG00423.hp1 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.363+1301T>A | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 4/9 | chr11 | 95784818 | ||||||
chr11:95784942
|
G | C | 1 | a0001c0001t0001g0041 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.363+1177C>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 4/9 | chr11 | 95784942 | ||||||
chr11:95785341
|
T | C | 14 | a0001c0001t0001g0010a0001c0001t0001g0040a0001c0001t0001g0041others(11): Show | 24 | HG01081.hp1 HG01167.hp1 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.363+778A>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 4/9 | chr11 | 95785341 | ||||||
chr11:95785368
|
A | G | 1 | a0001c0001t0002g0138 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.363+751T>C | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 4/9 | chr11 | 95785368 | ||||||
chr11:95785443
|
C | G | 3 | a0001c0001t0004g0015a0001c0001t0004g0029a0001c0001t0019g0051 | 8 | HG03239.hp2 HG03491.hp1 HG03688.hp2 others(5): Show |
intron_variant | MODIFIER | c.363+676G>C | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 4/9 | chr11 | 95785443 | ||||||
chr11:95785452
|
A | G | 1 | a0001c0002t0009g0034 | 2 | HG02015.hp1 HG02074.hp2 |
intron_variant | MODIFIER | c.363+667T>C | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 4/9 | chr11 | 95785452 | ||||||
chr11:95785526
|
T | C | 1 | a0001c0001t0011g0047 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.363+593A>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 4/9 | chr11 | 95785526 | ||||||
chr11:95785698
|
A | C | 1 | a0001c0001t0003g0052 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.363+421T>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 4/9 | chr11 | 95785698 | ||||||
chr11:95785907
|
G | A | 1 | a0001c0002t0001g0121 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.363+212C>T | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 4/9 | chr11 | 95785907 | ||||||
chr11:95785914
|
T | C | 1 | a0001c0002t0001g0098 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.363+205A>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 4/9 | chr11 | 95785914 | ||||||
chr11:95785951
|
A | C | 1 | a0001c0001t0022g0137 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.363+168T>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 4/9 | chr11 | 95785951 | ||||||
chr11:95785993
|
T | C | 14 | a0001c0001t0001g0010a0001c0001t0001g0040a0001c0001t0001g0041others(11): Show | 24 | HG01081.hp1 HG01167.hp1 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.363+126A>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 4/9 | chr11 | 95785993 | ||||||
chr11:95786031
|
A | T | 45 | a0001c0001t0001g0010a0001c0001t0001g0040a0001c0001t0001g0041others(42): Show | 125 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(122): Show |
intron_variant | MODIFIER | c.363+88T>A | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 4/9 | chr11 | 95786031 | ||||||
chr11:95786079
|
T | C | 54 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0011others(51): Show | 116 | HG00323.hp2 HG00423.hp1 HG00558.hp1 others(113): Show |
intron_variant | MODIFIER | c.363+40A>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 4/9 | chr11 | 95786079 | ||||||
chr11:95786093
|
G | A | 2 | a0001c0002t0001g0087a0001c0002t0001g0098 | 2 | HG02155.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.363+26C>T | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 4/9 | chr11 | 95786093 | ||||||
chr11:95786323
|
G | A | 2 | a0001c0001t0001g0040a0001c0001t0001g0130 | 3 | HG02280.hp1 HG02630.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.208-49C>T | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 3/9 | chr11 | 95786323 | ||||||
chr11:95786342
|
G | A | 45 | a0001c0001t0001g0010a0001c0001t0001g0040a0001c0001t0001g0041others(42): Show | 125 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(122): Show |
intron_variant | MODIFIER | c.208-68C>T | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 3/9 | chr11 | 95786342 | ||||||
chr11:95786368
|
A | G | 1 | a0001c0002t0001g0088 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.208-94T>C | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 3/9 | chr11 | 95786368 | ||||||
chr11:95786475
|
G | T | 1 | a0001c0002t0001g0099 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.208-201C>A | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 3/9 | chr11 | 95786475 | ||||||
chr11:95786494
|
C | T | 14 | a0001c0001t0001g0010a0001c0001t0001g0040a0001c0001t0001g0041others(11): Show | 24 | HG01081.hp1 HG01167.hp1 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.208-220G>A | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 3/9 | chr11 | 95786494 | ||||||
chr11:95786623
|
C | T | 45 | a0001c0001t0001g0010a0001c0001t0001g0040a0001c0001t0001g0041others(42): Show | 125 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(122): Show |
intron_variant | MODIFIER | c.208-349G>A | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 3/9 | chr11 | 95786623 | ||||||
chr11:95786714
|
A | G | 1 | a0001c0001t0002g0042 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.208-440T>C | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 3/9 | chr11 | 95786714 | ||||||
chr11:95786775
|
A | G | 6 | a0001c0002t0001g0006a0001c0002t0001g0087a0001c0002t0001g0095others(3): Show | 18 | HG00597.hp1 HG01081.hp2 HG01256.hp1 others(15): Show |
intron_variant | MODIFIER | c.208-501T>C | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 3/9 | chr11 | 95786775 | ||||||
chr11:95786874
|
T | C | 1 | a0001c0001t0001g0131 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.208-600A>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 3/9 | chr11 | 95786874 | ||||||
chr11:95786910
|
T | G | 1 | a0001c0001t0001g0081 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.208-636A>C | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 3/9 | chr11 | 95786910 | ||||||
chr11:95787110
|
G | C | 1 | a0001c0001t0016g0049 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.207+514C>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 3/9 | chr11 | 95787110 | ||||||
chr11:95787140
|
T | G | 2 | a0001c0001t0001g0082a0001c0001t0001g0083 | 2 | HG03704.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.207+484A>C | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 3/9 | chr11 | 95787140 | ||||||
chr11:95787144
|
C | A | 1 | a0001c0001t0001g0064 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.207+480G>T | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 3/9 | chr11 | 95787144 | ||||||
chr11:95787242
|
T | G | 14 | a0001c0001t0001g0010a0001c0001t0001g0040a0001c0001t0001g0041others(11): Show | 24 | HG01081.hp1 HG01167.hp1 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.207+382A>C | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 3/9 | chr11 | 95787242 | ||||||
chr11:95787319
|
C | T | 11 | a0001c0002t0001g0005a0001c0002t0001g0014a0001c0002t0001g0088others(8): Show | 32 | HG00642.hp2 HG00735.hp2 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.207+305G>A | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 3/9 | chr11 | 95787319 | ||||||
chr11:95787356
|
C | T | 1 | a0001c0001t0007g0136 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.207+268G>A | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 3/9 | chr11 | 95787356 | ||||||
chr11:95787408
|
T | G | 1 | a0001c0002t0001g0122 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.207+216A>C | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 3/9 | chr11 | 95787408 | ||||||
chr11:95787430
|
T | C | 1 | a0001c0001t0001g0084 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.207+194A>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 3/9 | chr11 | 95787430 | ||||||
chr11:95787431
|
G | T | 1 | a0001c0002t0001g0087 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.207+193C>A | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 3/9 | chr11 | 95787431 | ||||||
chr11:95787482
|
C | A | 1 | a0001c0001t0001g0085 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.207+142G>T | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 3/9 | chr11 | 95787482 | ||||||
chr11:95787531
|
T | C | 102 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(99): Show | 249 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(246): Show |
intron_variant | MODIFIER | c.207+93A>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 3/9 | chr11 | 95787531 | ||||||
chr11:95787545
|
T | C | 33 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0013others(30): Show | 75 | HG00323.hp2 HG00423.hp1 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.207+79A>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 3/9 | chr11 | 95787545 | ||||||
chr11:95787780
|
T | A | 1 | a0001c0001t0001g0132 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.153-102A>T | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 2/9 | chr11 | 95787780 | ||||||
chr11:95787788
|
G | A | 1 | a0001c0001t0001g0041 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.153-110C>T | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 2/9 | chr11 | 95787788 | ||||||
chr11:95787851
|
T | C | 14 | a0001c0001t0001g0010a0001c0001t0001g0040a0001c0001t0001g0041others(11): Show | 24 | HG01081.hp1 HG01167.hp1 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.153-173A>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 2/9 | chr11 | 95787851 | ||||||
chr11:95787880
|
A | G | 45 | a0001c0001t0001g0010a0001c0001t0001g0040a0001c0001t0001g0041others(42): Show | 125 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(122): Show |
intron_variant | MODIFIER | c.153-202T>C | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 2/9 | chr11 | 95787880 | ||||||
chr11:95788156
|
G | T | 1 | a0001c0002t0001g0086 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.152+343C>A | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 2/9 | chr11 | 95788156 | ||||||
chr11:95788211
|
T | G | 54 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0011others(51): Show | 116 | HG00323.hp2 HG00423.hp1 HG00558.hp1 others(113): Show |
intron_variant | MODIFIER | c.152+288A>C | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 2/9 | chr11 | 95788211 | ||||||
chr11:95788276
|
T | A | 1 | a0001c0001t0001g0133 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.152+223A>T | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 2/9 | chr11 | 95788276 | ||||||
chr11:95788332
|
T | C | 1 | a0001c0001t0002g0153 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.152+167A>G | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 2/9 | chr11 | 95788332 | ||||||
chr11:95788484
|
A | G | 103 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(100): Show | 250 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(247): Show |
intron_variant | MODIFIER | c.152+15T>C | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 2/9 | chr11 | 95788484 | ||||||
chr11:95788763
|
T | G | 1 | a0001c0001t0002g0154 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.88-200A>C | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 1/9 | chr11 | 95788763 | ||||||
chr11:95788789
|
A | G | 31 | a0001c0001t0002g0001a0001c0001t0002g0012a0001c0001t0002g0027others(28): Show | 101 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(98): Show |
intron_variant | MODIFIER | c.88-226T>C | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 1/9 | chr11 | 95788789 | ||||||
chr11:95789054
|
AGAAAACC others(5): Show |
A | 1 | a0001c0001t0001g0123 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.87+326_87+337delAT others(10): Show |
FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 1/9 | chr11 | 95789054 | ||||||
chr11:95789089
|
C | T | 1 | a0001c0001t0002g0135 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.87+303G>A | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 1/9 | chr11 | 95789089 | ||||||
chr11:95789175
|
G | A | 1 | a0001c0001t0001g0123 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.87+217C>T | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 1/9 | chr11 | 95789175 | ||||||
chr11:95789265
|
G | A | 1 | a0001c0002t0001g0124 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.87+127C>T | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 1/9 | chr11 | 95789265 | ||||||
chr11:95789304
|
G | A | 14 | a0001c0001t0001g0010a0001c0001t0001g0040a0001c0001t0001g0041others(11): Show | 24 | HG01081.hp1 HG01167.hp1 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.87+88C>T | FAM76B | ENSG00000077458.13 | transcript | ENST00000358780.10 | protein_coding | 1/9 | chr11 | 95789304 |