geneid | 339778 |
---|---|
ensemblid | ENSG00000173557.15 |
hgncid | 27938 |
symbol | FAM166C |
name | ciliary microtubule inner protein 2C |
refseq_nuc | NM_001105519.3 |
refseq_prot | NP_001098989.1 |
ensembl_nuc | ENST00000329615.4 |
ensembl_prot | ENSP00000332875.3 |
mane_status | MANE Select |
chr | chr2 |
start | 26562587 |
end | 26579524 |
strand | + |
ver | v1.2 |
region | chr2:26562587-26579524 |
region5000 | chr2:26557587-26584524 |
regionname0 | FAM166C_chr2_26562587_26579524 |
regionname5000 | FAM166C_chr2_26557587_26584524 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 201 | 272 | 82 | 59 | 107 | 7 | 15 | 86 | FAM166C_chr2_26557587_26584524 | FAM166C | copy fasta | chr2 | 26557587 | 26584524 |
a0002 | 0/0 | 201 | 134 | 10 | 14 | 79 | 5 | 26 | 60 | FAM166C_chr2_26557587_26584524 | FAM166C | copy fasta | chr2 | 26557587 | 26584524 |
a0003 | 0/0 | 201 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | copy fasta | chr2 | 26557587 | 26584524 |
a0004 | 0/0 | 157 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FAM166C_chr2_26557587_26584524 | FAM166C | copy fasta | chr2 | 26557587 | 26584524 |
a0005 | 0/0 | 162 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FAM166C_chr2_26557587_26584524 | FAM166C | copy fasta | chr2 | 26557587 | 26584524 |
a0006 | 0/0 | 201 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | copy fasta | chr2 | 26557587 | 26584524 |
a0007 | 0/0 | 201 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | copy fasta | chr2 | 26557587 | 26584524 |
a0008 | 0/0 | 201 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | copy fasta | chr2 | 26557587 | 26584524 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/0 | 606 | 146 | 18 | 42 | 70 | 6 | 10 | FAM166C_chr2_26557587_26584524 | FAM166C | copy fasta | chr2 | 26557587 | 26584524 |
c0002 | 0/0 | 606 | 131 | 10 | 13 | 78 | 5 | 25 | FAM166C_chr2_26557587_26584524 | FAM166C | copy fasta | chr2 | 26557587 | 26584524 |
c0003 | 1/1 | 606 | 118 | 58 | 15 | 37 | 1 | 5 | FAM166C_chr2_26557587_26584524 | FAM166C | copy fasta | chr2 | 26557587 | 26584524 |
c0004 | 0/0 | 606 | 4 | 2 | 2 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | copy fasta | chr2 | 26557587 | 26584524 |
c0005 | 0/0 | 606 | 4 | 4 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | copy fasta | chr2 | 26557587 | 26584524 |
c0006 | 0/0 | 606 | 2 | 0 | 1 | 1 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | copy fasta | chr2 | 26557587 | 26584524 |
c0007 | 0/0 | 606 | 1 | 1 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | copy fasta | chr2 | 26557587 | 26584524 |
c0008 | 0/0 | 606 | 1 | 1 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | copy fasta | chr2 | 26557587 | 26584524 |
c0009 | 0/0 | 606 | 1 | 0 | 1 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | copy fasta | chr2 | 26557587 | 26584524 |
c0010 | 0/0 | 606 | 1 | 0 | 0 | 0 | 0 | 1 | FAM166C_chr2_26557587_26584524 | FAM166C | copy fasta | chr2 | 26557587 | 26584524 |
c0011 | 0/0 | 606 | 1 | 0 | 0 | 1 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | copy fasta | chr2 | 26557587 | 26584524 |
c0012 | 0/0 | 606 | 1 | 0 | 0 | 1 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | copy fasta | chr2 | 26557587 | 26584524 |
c0013 | 0/0 | 606 | 1 | 0 | 0 | 0 | 0 | 1 | FAM166C_chr2_26557587_26584524 | FAM166C | copy fasta | chr2 | 26557587 | 26584524 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 113 | 270 | 80 | 58 | 107 | 7 | 16 | FAM166C_chr2_26557587_26584524 | FAM166C | copy fasta | chr2 | 26557587 | 26584524 |
t0002 | 0/0 | 113 | 140 | 14 | 15 | 80 | 5 | 26 | FAM166C_chr2_26557587_26584524 | FAM166C | copy fasta | chr2 | 26557587 | 26584524 |
t0003 | 0/0 | 113 | 1 | 0 | 0 | 1 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | copy fasta | chr2 | 26557587 | 26584524 |
t0004 | 0/0 | 113 | 1 | 0 | 1 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | copy fasta | chr2 | 26557587 | 26584524 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 45 | 1 | 15 | 25 | 2 | 2 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0002 | 0/0 | 41 | 3 | 5 | 26 | 1 | 6 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0003 | 0/0 | 35 | 0 | 0 | 28 | 0 | 7 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0004 | 0/0 | 18 | 0 | 0 | 18 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0005 | 0/0 | 13 | 0 | 1 | 9 | 0 | 3 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0006 | 0/0 | 13 | 0 | 13 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0007 | 0/0 | 12 | 4 | 3 | 0 | 0 | 5 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0008 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0009 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0010 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0011 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0012 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0013 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0014 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0015 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0016 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0017 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0018 | 0/0 | 4 | 2 | 2 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0019 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0020 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0021 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0023 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0024 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0025 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0026 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0027 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0028 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0029 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0034 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0035 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0036 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0037 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0038 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0140 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 606 | 146 | 18 | 42 | 70 | 6 | 10 | FAM166C_chr2_26557587_26584524 | FAM166C | copy fasta | chr2 | 26557587 | 26584524 |
a0001c0003 | 1/1 | 606 | 118 | 58 | 15 | 37 | 1 | 5 | FAM166C_chr2_26557587_26584524 | FAM166C | copy fasta | chr2 | 26557587 | 26584524 |
a0001c0004 | 0/0 | 606 | 4 | 2 | 2 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | copy fasta | chr2 | 26557587 | 26584524 |
a0001c0005 | 0/0 | 606 | 4 | 4 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | copy fasta | chr2 | 26557587 | 26584524 |
a0002c0002 | 0/0 | 606 | 131 | 10 | 13 | 78 | 5 | 25 | FAM166C_chr2_26557587_26584524 | FAM166C | copy fasta | chr2 | 26557587 | 26584524 |
a0002c0006 | 0/0 | 606 | 2 | 0 | 1 | 1 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | copy fasta | chr2 | 26557587 | 26584524 |
a0002c0013 | 0/0 | 606 | 1 | 0 | 0 | 0 | 0 | 1 | FAM166C_chr2_26557587_26584524 | FAM166C | copy fasta | chr2 | 26557587 | 26584524 |
a0003c0007 | 0/0 | 606 | 1 | 1 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | copy fasta | chr2 | 26557587 | 26584524 |
a0004c0011 | 0/0 | 606 | 1 | 0 | 0 | 1 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | copy fasta | chr2 | 26557587 | 26584524 |
a0005c0012 | 0/0 | 606 | 1 | 0 | 0 | 1 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | copy fasta | chr2 | 26557587 | 26584524 |
a0006c0008 | 0/0 | 606 | 1 | 1 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | copy fasta | chr2 | 26557587 | 26584524 |
a0007c0009 | 0/0 | 606 | 1 | 0 | 1 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | copy fasta | chr2 | 26557587 | 26584524 |
a0008c0010 | 0/0 | 606 | 1 | 0 | 0 | 0 | 0 | 1 | FAM166C_chr2_26557587_26584524 | FAM166C | copy fasta | chr2 | 26557587 | 26584524 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 718 | 143 | 17 | 41 | 69 | 6 | 10 | FAM166C_chr2_26557587_26584524 | FAM166C | copy fasta | chr2 | 26557587 | 26584524 |
a0001c0001t0002 | 0/0 | 718 | 1 | 1 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | copy fasta | chr2 | 26557587 | 26584524 |
a0001c0001t0003 | 0/0 | 718 | 1 | 0 | 0 | 1 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | copy fasta | chr2 | 26557587 | 26584524 |
a0001c0001t0004 | 0/0 | 718 | 1 | 0 | 1 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | copy fasta | chr2 | 26557587 | 26584524 |
a0001c0003t0001 | 1/1 | 718 | 118 | 58 | 15 | 37 | 1 | 5 | FAM166C_chr2_26557587_26584524 | FAM166C | copy fasta | chr2 | 26557587 | 26584524 |
a0001c0004t0002 | 0/0 | 718 | 4 | 2 | 2 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | copy fasta | chr2 | 26557587 | 26584524 |
a0001c0005t0001 | 0/0 | 718 | 4 | 4 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | copy fasta | chr2 | 26557587 | 26584524 |
a0002c0002t0002 | 0/0 | 718 | 131 | 10 | 13 | 78 | 5 | 25 | FAM166C_chr2_26557587_26584524 | FAM166C | copy fasta | chr2 | 26557587 | 26584524 |
a0002c0006t0001 | 0/0 | 718 | 2 | 0 | 1 | 1 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | copy fasta | chr2 | 26557587 | 26584524 |
a0002c0013t0002 | 0/0 | 718 | 1 | 0 | 0 | 0 | 0 | 1 | FAM166C_chr2_26557587_26584524 | FAM166C | copy fasta | chr2 | 26557587 | 26584524 |
a0003c0007t0002 | 0/0 | 718 | 1 | 1 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | copy fasta | chr2 | 26557587 | 26584524 |
a0004c0011t0002 | 0/0 | 718 | 1 | 0 | 0 | 1 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | copy fasta | chr2 | 26557587 | 26584524 |
a0005c0012t0002 | 0/0 | 718 | 1 | 0 | 0 | 1 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | copy fasta | chr2 | 26557587 | 26584524 |
a0006c0008t0001 | 0/0 | 718 | 1 | 1 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | copy fasta | chr2 | 26557587 | 26584524 |
a0007c0009t0001 | 0/0 | 718 | 1 | 0 | 1 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | copy fasta | chr2 | 26557587 | 26584524 |
a0008c0010t0001 | 0/0 | 718 | 1 | 0 | 0 | 0 | 0 | 1 | FAM166C_chr2_26557587_26584524 | FAM166C | copy fasta | chr2 | 26557587 | 26584524 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 43 | 1 | 13 | 25 | 2 | 2 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0001c0001t0001g0005 | 0/0 | 12 | 0 | 1 | 8 | 0 | 3 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0001c0001t0001g0006 | 0/0 | 13 | 0 | 13 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0001c0001t0001g0008 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0001c0001t0001g0011 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0001c0001t0001g0012 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0001c0001t0001g0020 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0001c0001t0001g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0001c0001t0001g0026 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0001c0001t0001g0034 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0001c0001t0001g0038 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0001c0001t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0001c0001t0003g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0001c0001t0004g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0001c0003t0001g0004 | 0/0 | 18 | 0 | 0 | 18 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0001c0003t0001g0007 | 0/0 | 12 | 4 | 3 | 0 | 0 | 5 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0001c0003t0001g0009 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0001c0003t0001g0013 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0001c0003t0001g0014 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0001c0003t0001g0015 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0001c0003t0001g0016 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0001c0003t0001g0019 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0001c0003t0001g0021 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0001c0003t0001g0024 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0001c0003t0001g0027 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0001c0003t0001g0029 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0001c0003t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0001c0003t0001g0035 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0001c0003t0001g0037 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0001c0003t0001g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0001c0003t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0001c0003t0001g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0001c0003t0001g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0001c0003t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0001c0003t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0001c0003t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0001c0003t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0001c0003t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0001c0003t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0001c0003t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0001c0003t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0001c0003t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0001c0003t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0001c0003t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0001c0003t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0001c0003t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0001c0003t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0001c0003t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0001c0003t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0001c0003t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0001c0003t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0001c0003t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0001c0003t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0001c0003t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0001c0003t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0001c0003t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0001c0003t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0001c0003t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0001c0003t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0001c0003t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0001c0003t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0001c0003t0001g0140 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0001c0003t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0001c0003t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0001c0003t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0001c0003t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0001c0003t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0001c0004t0002g0018 | 0/0 | 4 | 2 | 2 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0001c0005t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0001c0005t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0001c0005t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0001c0005t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0002c0002t0002g0002 | 0/0 | 39 | 2 | 5 | 26 | 1 | 5 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0002c0002t0002g0003 | 0/0 | 34 | 0 | 0 | 27 | 0 | 7 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0002c0002t0002g0010 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0002c0002t0002g0017 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0002c0002t0002g0023 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0002c0002t0002g0025 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0002c0002t0002g0028 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0002c0002t0002g0036 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0002c0002t0002g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0002c0002t0002g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0002c0002t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0002c0002t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0002c0002t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0002c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0002c0002t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0002c0002t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0002c0002t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0002c0002t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0002c0002t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0002c0002t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0002c0002t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0002c0002t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0002c0002t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0002c0002t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0002c0002t0002g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0002c0002t0002g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0002c0002t0002g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0002c0002t0002g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0002c0002t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0002c0002t0002g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0002c0002t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0002c0002t0002g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0002c0002t0002g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0002c0002t0002g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0002c0002t0002g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0002c0002t0002g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0002c0002t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0002c0002t0002g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0002c0002t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0002c0002t0002g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0002c0002t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0002c0002t0002g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0002c0002t0002g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0002c0002t0002g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0002c0006t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0002c0006t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0002c0013t0002g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0003c0007t0002g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0004c0011t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0005c0012t0002g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0006c0008t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0007c0009t0001g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
a0008c0010t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0038 | EUR | GBR | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG00140 | hp1 | a0001 | c0003 | t0001 | g0037 | EUR | GBR | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG00140 | hp2 | a0002 | c0002 | t0002 | g0002 | EUR | GBR | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG00280 | hp1 | a0002 | c0002 | t0002 | g0110 | EUR | FIN | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0099 | EUR | FIN | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG00323 | hp1 | a0002 | c0002 | t0002 | g0135 | EUR | FIN | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG00323 | hp2 | a0002 | c0002 | t0002 | g0137 | EUR | FIN | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG00408 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | CHS | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG00408 | hp2 | a0002 | c0002 | t0002 | g0084 | EAS | CHS | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG00423 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | CHS | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG00438 | hp1 | a0001 | c0003 | t0001 | g0127 | EAS | CHS | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG00544 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | CHS | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG00544 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | CHS | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG00558 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | CHS | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG00558 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | CHS | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG00621 | hp1 | a0001 | c0003 | t0001 | g0004 | EAS | CHS | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG00621 | hp2 | a0002 | c0002 | t0002 | g0081 | EAS | CHS | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG00639 | hp1 | a0001 | c0003 | t0001 | g0122 | AMR | PUR | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG00639 | hp2 | a0001 | c0003 | t0001 | g0075 | AMR | PUR | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG00642 | hp2 | a0001 | c0001 | t0004 | g0001 | AMR | PUR | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG00733 | hp1 | a0002 | c0002 | t0002 | g0002 | AMR | PUR | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG00733 | hp2 | a0001 | c0003 | t0001 | g0021 | AMR | PUR | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG00735 | hp1 | a0002 | c0002 | t0002 | g0090 | AMR | PUR | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG00735 | hp2 | a0001 | c0003 | t0001 | g0007 | AMR | PUR | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG00738 | hp1 | a0001 | c0004 | t0002 | g0018 | AMR | PUR | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | PUR | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG01071 | hp1 | a0002 | c0002 | t0002 | g0111 | AMR | PUR | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG01074 | hp1 | a0001 | c0003 | t0001 | g0053 | AMR | PUR | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG01081 | hp2 | a0002 | c0002 | t0002 | g0002 | AMR | PUR | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG01099 | hp1 | a0001 | c0003 | t0001 | g0037 | AMR | PUR | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG01106 | hp1 | a0001 | c0003 | t0001 | g0060 | AMR | PUR | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG01106 | hp2 | a0001 | c0003 | t0001 | g0120 | AMR | PUR | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0101 | AMR | PUR | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG01167 | hp1 | a0001 | c0003 | t0001 | g0021 | AMR | PUR | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0071 | AMR | PUR | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | PUR | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG01255 | hp1 | a0002 | c0002 | t0002 | g0002 | AMR | CLM | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG01257 | hp1 | a0002 | c0006 | t0001 | g0086 | AMR | CLM | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG01257 | hp2 | a0001 | c0003 | t0001 | g0042 | AMR | CLM | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG01258 | hp2 | a0001 | c0003 | t0001 | g0042 | AMR | CLM | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG01346 | hp2 | a0001 | c0004 | t0002 | g0018 | AMR | CLM | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG01361 | hp1 | a0002 | c0002 | t0002 | g0082 | AMR | CLM | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | CLM | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG01433 | hp1 | a0001 | c0003 | t0001 | g0007 | AMR | CLM | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG01433 | hp2 | a0007 | c0009 | t0001 | g0001 | AMR | CLM | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG01496 | hp1 | a0001 | c0003 | t0001 | g0014 | AMR | CLM | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG01496 | hp2 | a0001 | c0003 | t0001 | g0079 | AMR | CLM | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG01515 | hp1 | a0002 | c0002 | t0002 | g0139 | EUR | IBS | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG01884 | hp2 | a0002 | c0002 | t0002 | g0023 | AFR | ACB | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG01891 | hp1 | a0001 | c0001 | t0002 | g0068 | AFR | ACB | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG01891 | hp2 | a0002 | c0002 | t0002 | g0097 | AFR | ACB | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG01928 | hp2 | a0001 | c0003 | t0001 | g0007 | AMR | PEL | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | PEL | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG01952 | hp2 | a0002 | c0002 | t0002 | g0002 | AMR | PEL | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG01981 | hp1 | a0002 | c0002 | t0002 | g0028 | AMR | PEL | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | PEL | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | PEL | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG02004 | hp1 | a0002 | c0002 | t0002 | g0028 | AMR | PEL | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG02004 | hp2 | a0002 | c0002 | t0002 | g0098 | AMR | PEL | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG02015 | hp1 | a0001 | c0003 | t0001 | g0019 | EAS | KHV | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG02015 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | KHV | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG02055 | hp2 | a0001 | c0003 | t0001 | g0045 | AFR | ACB | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | KHV | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG02056 | hp2 | a0002 | c0002 | t0002 | g0017 | EAS | KHV | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG02071 | hp1 | a0001 | c0003 | t0001 | g0004 | EAS | KHV | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG02074 | hp1 | a0001 | c0003 | t0001 | g0019 | EAS | KHV | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG02074 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | KHV | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG02080 | hp2 | a0001 | c0003 | t0001 | g0004 | EAS | KHV | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG02083 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | KHV | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG02129 | hp1 | a0002 | c0002 | t0002 | g0085 | EAS | KHV | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG02129 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | KHV | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG02132 | hp1 | a0001 | c0003 | t0001 | g0004 | EAS | KHV | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG02132 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | KHV | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG02145 | hp1 | a0001 | c0004 | t0002 | g0018 | AFR | ACB | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG02145 | hp2 | a0001 | c0003 | t0001 | g0007 | AFR | ACB | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG02155 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | CDX | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | CDX | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG02165 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | CDX | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG02165 | hp2 | a0001 | c0003 | t0001 | g0131 | EAS | CDX | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG02257 | hp1 | a0001 | c0003 | t0001 | g0029 | AFR | ACB | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG02257 | hp2 | a0001 | c0003 | t0001 | g0013 | AFR | ACB | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG02258 | hp1 | a0002 | c0002 | t0002 | g0002 | AFR | ACB | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG02280 | hp1 | a0002 | c0002 | t0002 | g0039 | AFR | ACB | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG02280 | hp2 | a0001 | c0003 | t0001 | g0024 | AFR | ACB | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | PEL | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | PEL | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG02300 | hp2 | a0002 | c0002 | t0002 | g0028 | AMR | PEL | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG02451 | hp1 | a0001 | c0005 | t0001 | g0153 | AFR | ACB | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG02451 | hp2 | a0001 | c0003 | t0001 | g0024 | AFR | ACB | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG02523 | hp1 | a0001 | c0003 | t0001 | g0004 | EAS | KHV | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG02523 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | KHV | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG02572 | hp1 | a0001 | c0003 | t0001 | g0007 | AFR | GWD | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG02572 | hp2 | a0001 | c0003 | t0001 | g0009 | AFR | GWD | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG02602 | hp1 | a0002 | c0002 | t0002 | g0002 | SAS | PJL | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG02615 | hp1 | a0001 | c0003 | t0001 | g0013 | AFR | GWD | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG02615 | hp2 | a0001 | c0003 | t0001 | g0009 | AFR | GWD | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG02622 | hp1 | a0001 | c0003 | t0001 | g0029 | AFR | GWD | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG02622 | hp2 | a0001 | c0003 | t0001 | g0016 | AFR | GWD | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG02630 | hp1 | a0001 | c0003 | t0001 | g0016 | AFR | GWD | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG02630 | hp2 | a0001 | c0003 | t0001 | g0070 | AFR | GWD | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | GWD | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG02647 | hp2 | a0001 | c0003 | t0001 | g0009 | AFR | GWD | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG02698 | hp1 | a0002 | c0002 | t0002 | g0141 | SAS | PJL | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG02698 | hp2 | a0002 | c0013 | t0002 | g0002 | SAS | PJL | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG02717 | hp1 | a0002 | c0002 | t0002 | g0123 | AFR | GWD | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG02717 | hp2 | a0001 | c0005 | t0001 | g0055 | AFR | GWD | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG02723 | hp1 | a0001 | c0005 | t0001 | g0152 | AFR | GWD | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG02723 | hp2 | a0001 | c0003 | t0001 | g0013 | AFR | GWD | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG02735 | hp2 | a0002 | c0002 | t0002 | g0002 | SAS | PJL | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG02738 | hp1 | a0001 | c0003 | t0001 | g0007 | SAS | PJL | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG02809 | hp1 | a0001 | c0003 | t0001 | g0047 | AFR | GWD | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG02809 | hp2 | a0001 | c0003 | t0001 | g0015 | AFR | GWD | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG02818 | hp1 | a0001 | c0003 | t0001 | g0030 | AFR | GWD | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG02818 | hp2 | a0001 | c0003 | t0001 | g0016 | AFR | GWD | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | GWD | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | GWD | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG02895 | hp1 | a0001 | c0003 | t0001 | g0014 | AFR | GWD | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG02895 | hp2 | a0001 | c0003 | t0001 | g0007 | AFR | GWD | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG02897 | hp1 | a0001 | c0003 | t0001 | g0007 | AFR | GWD | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG02897 | hp2 | a0001 | c0003 | t0001 | g0014 | AFR | GWD | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG02922 | hp1 | a0001 | c0003 | t0001 | g0061 | AFR | ESN | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG02922 | hp2 | a0001 | c0003 | t0001 | g0016 | AFR | ESN | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG02965 | hp2 | a0002 | c0002 | t0002 | g0087 | AFR | ESN | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG02970 | hp1 | a0001 | c0003 | t0001 | g0021 | AFR | ESN | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG02970 | hp2 | a0001 | c0003 | t0001 | g0065 | AFR | ESN | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG02976 | hp1 | a0001 | c0003 | t0001 | g0015 | AFR | ESN | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0115 | SAS | PJL | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG03017 | hp2 | a0002 | c0002 | t0002 | g0106 | SAS | PJL | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG03041 | hp1 | a0001 | c0004 | t0002 | g0018 | AFR | GWD | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG03041 | hp2 | a0001 | c0003 | t0001 | g0143 | AFR | GWD | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG03098 | hp1 | a0001 | c0003 | t0001 | g0051 | AFR | MSL | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG03098 | hp2 | a0001 | c0003 | t0001 | g0013 | AFR | MSL | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG03130 | hp1 | a0001 | c0003 | t0001 | g0074 | AFR | ESN | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG03139 | hp1 | a0001 | c0003 | t0001 | g0009 | AFR | ESN | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG03209 | hp1 | a0001 | c0003 | t0001 | g0013 | AFR | MSL | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | MSL | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG03225 | hp1 | a0001 | c0003 | t0001 | g0130 | AFR | MSL | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG03225 | hp2 | a0001 | c0003 | t0001 | g0035 | AFR | MSL | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG03239 | hp1 | a0002 | c0002 | t0002 | g0002 | SAS | PJL | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG03239 | hp2 | a0002 | c0002 | t0002 | g0025 | SAS | PJL | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG03453 | hp1 | a0001 | c0003 | t0001 | g0073 | AFR | MSL | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG03453 | hp2 | a0001 | c0003 | t0001 | g0015 | AFR | MSL | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | MSL | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG03486 | hp2 | a0003 | c0007 | t0002 | g0002 | AFR | MSL | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG03490 | hp1 | a0002 | c0002 | t0002 | g0003 | SAS | PJL | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG03490 | hp2 | a0001 | c0003 | t0001 | g0007 | SAS | PJL | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG03492 | hp1 | a0002 | c0002 | t0002 | g0003 | SAS | PJL | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0113 | SAS | PJL | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | ESN | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG03516 | hp2 | a0001 | c0003 | t0001 | g0072 | AFR | ESN | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG03540 | hp1 | a0001 | c0003 | t0001 | g0030 | AFR | GWD | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG03540 | hp2 | a0001 | c0003 | t0001 | g0151 | AFR | GWD | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG03579 | hp1 | a0001 | c0003 | t0001 | g0029 | AFR | MSL | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG03579 | hp2 | a0001 | c0003 | t0001 | g0009 | AFR | MSL | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG03654 | hp1 | a0002 | c0002 | t0002 | g0093 | SAS | PJL | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG03654 | hp2 | a0001 | c0003 | t0001 | g0007 | SAS | PJL | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG03669 | hp1 | a0008 | c0010 | t0001 | g0103 | SAS | PJL | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG03669 | hp2 | a0002 | c0002 | t0002 | g0036 | SAS | PJL | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG03688 | hp1 | a0002 | c0002 | t0002 | g0089 | SAS | STU | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG03688 | hp2 | a0002 | c0002 | t0002 | g0003 | SAS | STU | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG03704 | hp2 | a0002 | c0002 | t0002 | g0003 | SAS | PJL | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG03710 | hp1 | a0001 | c0003 | t0001 | g0007 | SAS | PJL | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG03710 | hp2 | a0002 | c0002 | t0002 | g0025 | SAS | PJL | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG03831 | hp1 | a0002 | c0002 | t0002 | g0003 | SAS | BEB | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG03831 | hp2 | a0002 | c0002 | t0002 | g0002 | SAS | BEB | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG03927 | hp2 | a0002 | c0002 | t0002 | g0003 | SAS | BEB | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG03942 | hp1 | a0002 | c0002 | t0002 | g0092 | SAS | BEB | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG03942 | hp2 | a0001 | c0003 | t0001 | g0007 | SAS | BEB | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0064 | SAS | BEB | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG04184 | hp2 | a0002 | c0002 | t0002 | g0002 | SAS | BEB | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0114 | SAS | STU | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0144 | SAS | STU | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG04204 | hp1 | a0002 | c0002 | t0002 | g0108 | SAS | STU | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG04204 | hp2 | a0002 | c0002 | t0002 | g0095 | SAS | STU | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG04228 | hp1 | a0002 | c0002 | t0002 | g0054 | SAS | STU | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG04228 | hp2 | a0002 | c0002 | t0002 | g0036 | SAS | STU | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA18522 | hp1 | a0001 | c0003 | t0001 | g0014 | AFR | YRI | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA18522 | hp2 | a0006 | c0008 | t0001 | g0049 | AFR | YRI | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHB | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA18612 | hp2 | a0001 | c0003 | t0001 | g0126 | EAS | CHB | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA18747 | hp1 | a0001 | c0003 | t0001 | g0004 | EAS | CHB | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA18747 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | CHB | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | YRI | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA18906 | hp2 | a0001 | c0003 | t0001 | g0142 | AFR | YRI | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA18939 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA18939 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA18940 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA18940 | hp2 | a0001 | c0003 | t0001 | g0027 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA18941 | hp1 | a0002 | c0002 | t0002 | g0138 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA18941 | hp2 | a0001 | c0003 | t0001 | g0019 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA18942 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA18942 | hp2 | a0002 | c0002 | t0002 | g0088 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA18945 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA18945 | hp2 | a0002 | c0002 | t0002 | g0017 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA18946 | hp1 | a0002 | c0002 | t0002 | g0010 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA18946 | hp2 | a0002 | c0002 | t0002 | g0010 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA18949 | hp1 | a0004 | c0011 | t0002 | g0096 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA18953 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA18954 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA18956 | hp2 | a0002 | c0002 | t0002 | g0010 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA18957 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA18959 | hp1 | a0002 | c0002 | t0002 | g0069 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA18960 | hp1 | a0001 | c0003 | t0001 | g0004 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA18960 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA18963 | hp1 | a0001 | c0003 | t0001 | g0004 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA18963 | hp2 | a0002 | c0002 | t0002 | g0010 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA18964 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA18965 | hp1 | a0001 | c0003 | t0001 | g0150 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA18965 | hp2 | a0002 | c0002 | t0002 | g0077 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA18966 | hp2 | a0005 | c0012 | t0002 | g0003 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA18968 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA18969 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA18970 | hp2 | a0002 | c0002 | t0002 | g0017 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA18971 | hp1 | a0001 | c0003 | t0001 | g0004 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA18977 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA18979 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA18980 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA18980 | hp2 | a0001 | c0003 | t0001 | g0004 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA18981 | hp1 | a0001 | c0003 | t0001 | g0044 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA18982 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA18982 | hp2 | a0001 | c0003 | t0001 | g0004 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA18984 | hp1 | a0002 | c0002 | t0002 | g0058 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA18985 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA18989 | hp2 | a0001 | c0003 | t0001 | g0043 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA18991 | hp2 | a0002 | c0002 | t0002 | g0136 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA18993 | hp1 | a0001 | c0003 | t0001 | g0004 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA18994 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA18995 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA18995 | hp2 | a0001 | c0003 | t0001 | g0019 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA18997 | hp1 | a0001 | c0003 | t0001 | g0004 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA18998 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA18999 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA19001 | hp1 | a0002 | c0002 | t0002 | g0083 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA19001 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA19002 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA19003 | hp1 | a0001 | c0003 | t0001 | g0125 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA19003 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA19004 | hp2 | a0002 | c0002 | t0002 | g0094 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA19005 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA19009 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA19009 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA19010 | hp1 | a0002 | c0002 | t0002 | g0010 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA19011 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA19030 | hp1 | a0001 | c0003 | t0001 | g0121 | AFR | LWK | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA19030 | hp2 | a0001 | c0003 | t0001 | g0015 | AFR | LWK | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA19043 | hp1 | a0002 | c0002 | t0002 | g0023 | AFR | LWK | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA19043 | hp2 | a0001 | c0003 | t0001 | g0105 | AFR | LWK | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA19054 | hp1 | a0002 | c0002 | t0002 | g0078 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA19055 | hp1 | a0002 | c0002 | t0002 | g0076 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA19055 | hp2 | a0001 | c0003 | t0001 | g0124 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA19056 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA19057 | hp1 | a0001 | c0003 | t0001 | g0004 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA19060 | hp1 | a0001 | c0003 | t0001 | g0004 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA19060 | hp2 | a0001 | c0003 | t0001 | g0128 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA19062 | hp2 | a0001 | c0003 | t0001 | g0004 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA19064 | hp2 | a0001 | c0003 | t0001 | g0004 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA19065 | hp1 | a0002 | c0006 | t0001 | g0091 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA19067 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA19068 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA19070 | hp1 | a0001 | c0003 | t0001 | g0044 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA19070 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA19074 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA19076 | hp2 | a0001 | c0003 | t0001 | g0027 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA19077 | hp2 | a0001 | c0003 | t0001 | g0129 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA19078 | hp2 | a0002 | c0002 | t0002 | g0010 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA19079 | hp1 | a0001 | c0003 | t0001 | g0027 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA19079 | hp2 | a0001 | c0003 | t0001 | g0004 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA19080 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA19080 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA19081 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA19082 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA19084 | hp1 | a0002 | c0002 | t0002 | g0080 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA19085 | hp1 | a0001 | c0003 | t0001 | g0043 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA19085 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA19088 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA19090 | hp1 | a0002 | c0002 | t0002 | g0017 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA19090 | hp2 | a0002 | c0002 | t0002 | g0057 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | YRI | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA19240 | hp2 | a0001 | c0003 | t0001 | g0148 | AFR | YRI | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0109 | EUR | TSI | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0118 | EUR | TSI | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA20905 | hp1 | a0002 | c0002 | t0002 | g0025 | SAS | GIH | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA20905 | hp2 | a0002 | c0002 | t0002 | g0003 | SAS | GIH | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG01123 | hp1 | a0002 | c0002 | t0002 | g0145 | AMR | CLM | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG01123 | hp2 | a0002 | c0002 | t0002 | g0002 | AMR | CLM | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG02109 | hp1 | a0001 | c0003 | t0001 | g0009 | AFR | ACB | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG02109 | hp2 | a0001 | c0003 | t0001 | g0024 | AFR | ACB | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG02486 | hp1 | a0001 | c0003 | t0001 | g0104 | AFR | ACB | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG02486 | hp2 | a0001 | c0003 | t0001 | g0045 | AFR | ACB | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG02559 | hp1 | a0001 | c0003 | t0001 | g0056 | AFR | ACB | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG02559 | hp2 | a0001 | c0005 | t0001 | g0100 | AFR | ACB | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG03471 | hp1 | a0002 | c0002 | t0002 | g0039 | AFR | MSL | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG03471 | hp2 | a0001 | c0003 | t0001 | g0009 | AFR | MSL | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | USA | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
HG06807 | hp2 | a0001 | c0003 | t0001 | g0052 | AFR | USA | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA20300 | hp1 | a0002 | c0002 | t0002 | g0002 | AFR | USA | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA20300 | hp2 | a0001 | c0003 | t0001 | g0059 | AFR | USA | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | LWK | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
NA21309 | hp2 | a0002 | c0002 | t0002 | g0023 | AFR | LWK | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
homoSapiens_chm13v2 | hp1 | a0001 | c0003 | t0001 | g0140 | REF | REF | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
homoSapiens_grch38 | hp1 | a0001 | c0003 | t0001 | g0035 | REF | REF | FAM166C_chr2_26557587_26584524 | FAM166C | chr2 | 26557587 | 26584524 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:26576006
|
G | A | 1 | a0003 | 1 | HG03486.hp2 | missense_variant | MODERATE | c.179G>A | p.Ser60Asn | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 2/4 | 205/718 | 179/606 | 60/201 | chr2 | 26576006 | ||
chr2:26576025
|
A | T | 4 | a0002a0003a0004others(1): Show | 137 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(134): Show |
missense_variant | MODERATE | c.198A>T | p.Gln66His | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 2/4 | 224/718 | 198/606 | 66/201 | chr2 | 26576025 | ||
chr2:26576093
|
G | A | 1 | a0006 | 1 | NA18522.hp2 | missense_variant | MODERATE | c.266G>A | p.Arg89Gln | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 2/4 | 292/718 | 266/606 | 89/201 | chr2 | 26576093 | ||
chr2:26576165
|
A | G | 1 | a0008 | 1 | HG03669.hp1 | missense_variant | MODERATE | c.338A>G | p.Asn113Ser | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 2/4 | 364/718 | 338/606 | 113/201 | chr2 | 26576165 | ||
chr2:26579306
|
C | A | 1 | a0004 | 1 | NA18949.hp1 | stop_gained | HIGH | c.474C>A | p.Cys158* | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 4/4 | 500/718 | 474/606 | 158/201 | chr2 | 26579306 | ||
chr2:26579320
|
G | A | 1 | a0005 | 1 | NA18966.hp2 | stop_gained | HIGH | c.488G>A | p.Trp163* | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 4/4 | 514/718 | 488/606 | 163/201 | chr2 | 26579320 | ||
chr2:26579343
|
G | A | 1 | a0007 | 1 | HG01433.hp2 | missense_variant | MODERATE | c.511G>A | p.Glu171Lys | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 4/4 | 537/718 | 511/606 | 171/201 | chr2 | 26579343 | ||
chr2:26579362
|
A | T | 1 | a0005 | 1 | NA18966.hp2 | missense_variant | MODERATE | c.530A>T | p.Gln177Leu | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 4/4 | 556/718 | 530/606 | 177/201 | chr2 | 26579362 | ||
chr2:26579524
|
A | T | 5 | a0001a0002a0003others(2): Show | 140 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(137): Show |
splice_region_variant | LOW | c.*86A>T | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 4/4 | chr2 | 26579524 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:26576163
|
G | A | 7 | a0001c0004a0002c0002a0002c0006others(4): Show | 141 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(138): Show |
synonymous_variant | LOW | c.336G>A | p.Thr112Thr | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 2/4 | 362/718 | 336/606 | 112/201 | chr2 | 26576163 | ||
chr2:26577554
|
G | A | 3 | a0001c0001a0002c0006a0007c0009 | 149 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(146): Show |
synonymous_variant | LOW | c.387G>A | p.Thr129Thr | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 3/4 | 413/718 | 387/606 | 129/201 | chr2 | 26577554 | ||
chr2:26577569
|
A | G | 1 | a0001c0005 | 4 | HG02451.hp1 HG02559.hp2 HG02717.hp2 others(1): Show |
synonymous_variant | LOW | c.402A>G | p.Arg134Arg | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 3/4 | 428/718 | 402/606 | 134/201 | chr2 | 26577569 | ||
chr2:26579354
|
G | A | 1 | a0002c0013 | 1 | HG02698.hp2 | synonymous_variant | LOW | c.522G>A | p.Lys174Lys | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 4/4 | 548/718 | 522/606 | 174/201 | chr2 | 26579354 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:26562590
|
C | A | 1 | a0001c0001t0003 | 1 | NA19080.hp1 | 5_prime_UTR_variant | MODIFIER | c.-23C>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/4 | 23 | chr2 | 26562590 | |||||
chr2:26579480
|
G | A | 1 | a0001c0001t0004 | 1 | HG00642.hp2 | 3_prime_UTR_variant | MODIFIER | c.*42G>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 4/4 | 42 | chr2 | 26579480 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:26562694
|
C | T | 3 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0003t0001g0045 | 4 | HG02055.hp2 HG02486.hp2 HG02886.hp1 others(1): Show |
splice_region_variant&intron_variant | LOW | c.74+8C>T | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26562694 | ||||||
chr2:26562695
|
G | A | 1 | a0001c0003t0001g0014 | 4 | HG01496.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.74+9G>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26562695 | ||||||
chr2:26562738
|
C | T | 2 | a0001c0005t0001g0152a0001c0005t0001g0153 | 2 | HG02451.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.74+52C>T | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26562738 | ||||||
chr2:26562766
|
C | A | 3 | a0001c0001t0001g0046a0001c0001t0001g0048a0001c0003t0001g0047 | 3 | HG02809.hp1 HG02886.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.74+80C>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26562766 | ||||||
chr2:26562842
|
G | T | 1 | a0001c0003t0001g0151 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.74+156G>T | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26562842 | ||||||
chr2:26562901
|
G | A | 1 | a0006c0008t0001g0049 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.74+215G>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26562901 | ||||||
chr2:26562968
|
G | A | 5 | a0001c0001t0001g0050a0001c0003t0001g0021a0001c0003t0001g0051others(2): Show | 7 | HG00733.hp2 HG01074.hp1 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.74+282G>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26562968 | ||||||
chr2:26562969
|
G | A | 5 | a0001c0001t0001g0050a0001c0003t0001g0021a0001c0003t0001g0051others(2): Show | 7 | HG00733.hp2 HG01074.hp1 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.74+283G>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26562969 | ||||||
chr2:26562998
|
G | T | 1 | a0001c0003t0001g0150 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.74+312G>T | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26562998 | ||||||
chr2:26563113
|
A | G | 1 | a0001c0001t0001g0149 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.74+427A>G | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26563113 | ||||||
chr2:26563160
|
C | T | 1 | a0001c0003t0001g0148 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.74+474C>T | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26563160 | ||||||
chr2:26563206
|
G | T | 2 | a0001c0001t0001g0146a0001c0001t0001g0147 | 2 | HG02647.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.74+520G>T | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26563206 | ||||||
chr2:26563239
|
T | C | 1 | a0002c0002t0002g0054 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.74+553T>C | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26563239 | ||||||
chr2:26563392
|
T | C | 1 | a0001c0005t0001g0055 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.74+706T>C | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26563392 | ||||||
chr2:26563420
|
T | C | 23 | a0001c0001t0001g0005a0001c0001t0001g0031a0001c0001t0001g0032others(20): Show | 38 | HG00609.hp2 HG01106.hp1 HG01175.hp1 others(35): Show |
intron_variant | MODIFIER | c.74+734T>C | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26563420 | ||||||
chr2:26563458
|
G | A | 1 | a0001c0003t0001g0070 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.74+772G>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26563458 | ||||||
chr2:26563460
|
A | G | 2 | a0001c0003t0001g0009a0001c0003t0001g0029 | 10 | HG02109.hp1 HG02257.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.74+774A>G | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26563460 | ||||||
chr2:26563462
|
C | G | 1 | a0002c0002t0002g0145 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.74+776C>G | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26563462 | ||||||
chr2:26563511
|
T | C | 2 | a0001c0001t0001g0034a0001c0001t0001g0071 | 3 | HG01167.hp2 HG01169.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.74+825T>C | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26563511 | ||||||
chr2:26563967
|
C | T | 2 | a0001c0003t0001g0009a0001c0003t0001g0029 | 10 | HG02109.hp1 HG02257.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.74+1281C>T | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26563967 | ||||||
chr2:26563981
|
G | A | 22 | a0001c0001t0001g0005a0001c0001t0001g0031a0001c0001t0001g0032others(19): Show | 37 | HG00609.hp2 HG01106.hp1 HG01175.hp1 others(34): Show |
intron_variant | MODIFIER | c.74+1295G>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26563981 | ||||||
chr2:26564259
|
A | G | 1 | a0001c0001t0001g0144 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.74+1573A>G | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26564259 | ||||||
chr2:26564284
|
A | G | 1 | a0001c0001t0001g0155 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.74+1598A>G | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26564284 | ||||||
chr2:26564325
|
A | G | 158 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(155): Show | 405 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(402): Show |
intron_variant | MODIFIER | c.74+1639A>G | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26564325 | ||||||
chr2:26564419
|
C | T | 3 | a0001c0001t0001g0046a0001c0001t0001g0048a0001c0003t0001g0047 | 3 | HG02809.hp1 HG02886.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.74+1733C>T | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26564419 | ||||||
chr2:26564518
|
C | G | 1 | a0001c0003t0001g0143 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.74+1832C>G | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26564518 | ||||||
chr2:26564623
|
A | G | 1 | a0001c0003t0001g0142 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.74+1937A>G | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26564623 | ||||||
chr2:26564669
|
C | T | 1 | a0002c0002t0002g0141 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.74+1983C>T | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26564669 | ||||||
chr2:26564815
|
G | A | 2 | a0001c0003t0001g0073a0001c0003t0001g0074 | 2 | HG03130.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.74+2129G>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26564815 | ||||||
chr2:26565015
|
T | TTTC | 1 | a0001c0001t0001g0020 | 4 | NA18953.hp2 NA18954.hp2 NA18991.hp1 others(1): Show |
intron_variant | MODIFIER | c.74+2346_74+2348dup others(3): Show |
FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 26565015 | |||||
chr2:26565029
|
T | TCTTCTC | 4 | a0001c0001t0001g0012a0001c0001t0001g0022a0001c0001t0002g0068others(1): Show | 10 | HG00639.hp2 HG01884.hp1 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.74+2367_74+2372dup others(6): Show |
FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 26565029 | |||||
chr2:26565029
|
TCTTCTC | T | 5 | a0001c0003t0001g0140a0002c0002t0002g0137a0002c0002t0002g0138others(2): Show | 5 | HG00323.hp2 HG01515.hp1 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.74+2367_74+2372del others(6): Show |
FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 26565029 | |||||
chr2:26565053
|
CCTTCTT | C | 2 | a0001c0003t0001g0030a0001c0003t0001g0056 | 3 | HG02559.hp1 HG02818.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.74+2372_74+2377del others(6): Show |
FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 26565053 | |||||
chr2:26565059
|
T | C | 21 | a0001c0001t0001g0005a0001c0001t0001g0031a0001c0001t0001g0032others(18): Show | 35 | HG00609.hp2 HG01106.hp1 HG01175.hp1 others(32): Show |
intron_variant | MODIFIER | c.74+2373T>C | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26565059 | ||||||
chr2:26565059
|
T | TCTTCCC | 3 | a0002c0002t0002g0028a0002c0002t0002g0135a0002c0002t0002g0136 | 5 | HG00323.hp1 HG01981.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.74+2400_74+2405dup others(6): Show |
FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 26565059 | |||||
chr2:26565059
|
TCTTCCC | T | 3 | a0001c0003t0001g0009a0001c0003t0001g0016a0001c0003t0001g0151 | 12 | HG02109.hp1 HG02572.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.74+2400_74+2405del others(6): Show |
FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 26565059 | |||||
chr2:26565223
|
T | C | 47 | a0001c0001t0001g0038a0001c0003t0001g0037a0001c0003t0001g0079others(44): Show | 134 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(131): Show |
intron_variant | MODIFIER | c.74+2537T>C | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26565223 | ||||||
chr2:26565239
|
C | T | 6 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0003t0001g0045others(3): Show | 7 | HG01074.hp1 HG02055.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.74+2553C>T | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26565239 | ||||||
chr2:26565337
|
C | T | 1 | a0001c0001t0001g0067 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.74+2651C>T | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26565337 | ||||||
chr2:26565377
|
C | T | 1 | a0002c0002t0002g0039 | 2 | HG02280.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.74+2691C>T | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26565377 | ||||||
chr2:26565382
|
C | T | 1 | a0006c0008t0001g0049 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.74+2696C>T | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26565382 | ||||||
chr2:26565468
|
G | A | 1 | a0001c0001t0001g0099 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.74+2782G>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26565468 | ||||||
chr2:26565503
|
C | T | 3 | a0001c0001t0001g0012a0001c0001t0001g0022a0001c0003t0001g0075 | 9 | HG00639.hp2 HG01884.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.74+2817C>T | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26565503 | ||||||
chr2:26565664
|
CT | C | 3 | a0001c0005t0001g0100a0001c0005t0001g0152a0001c0005t0001g0153 | 3 | HG02451.hp1 HG02559.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.74+2979delT | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26565664 | ||||||
chr2:26565665
|
T | C | 1 | a0001c0005t0001g0055 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.74+2979T>C | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26565665 | ||||||
chr2:26565808
|
G | A | 1 | a0001c0003t0001g0051 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.74+3122G>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26565808 | ||||||
chr2:26565822
|
C | T | 1 | a0001c0001t0001g0033 | 2 | NA18943.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.74+3136C>T | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26565822 | ||||||
chr2:26565862
|
G | A | 1 | a0002c0002t0002g0076 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.74+3176G>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26565862 | ||||||
chr2:26565865
|
G | A | 1 | a0002c0002t0002g0135 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.74+3179G>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26565865 | ||||||
chr2:26566118
|
C | A | 1 | a0001c0003t0001g0142 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.74+3432C>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26566118 | ||||||
chr2:26566346
|
G | A | 2 | a0001c0001t0001g0067a0001c0001t0002g0068 | 2 | HG01891.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.74+3660G>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26566346 | ||||||
chr2:26566381
|
G | T | 4 | a0001c0001t0001g0006a0001c0001t0001g0132a0001c0001t0001g0133others(1): Show | 16 | HG01081.hp1 HG01192.hp2 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.74+3695G>T | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26566381 | ||||||
chr2:26566384
|
G | T | 1 | a0001c0001t0001g0048 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.74+3698G>T | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26566384 | ||||||
chr2:26566436
|
G | A | 7 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0146others(4): Show | 8 | HG01109.hp2 HG02055.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.74+3750G>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26566436 | ||||||
chr2:26566463
|
C | G | 1 | a0002c0002t0002g0098 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.74+3777C>G | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26566463 | ||||||
chr2:26566500
|
C | T | 1 | a0001c0003t0001g0142 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.74+3814C>T | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26566500 | ||||||
chr2:26566583
|
G | A | 1 | a0008c0010t0001g0103 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.74+3897G>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26566583 | ||||||
chr2:26566954
|
C | A | 7 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0146others(4): Show | 8 | HG01109.hp2 HG02055.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.74+4268C>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26566954 | ||||||
chr2:26566991
|
C | T | 1 | a0001c0001t0001g0067 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.74+4305C>T | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26566991 | ||||||
chr2:26566992
|
C | G | 1 | a0001c0001t0001g0144 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.74+4306C>G | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26566992 | ||||||
chr2:26567118
|
G | A | 1 | a0002c0002t0002g0077 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.74+4432G>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26567118 | ||||||
chr2:26567129
|
C | G | 16 | a0001c0001t0001g0011a0001c0003t0001g0004a0001c0003t0001g0019others(13): Show | 45 | HG00438.hp1 HG00438.hp2 HG00621.hp1 others(42): Show |
intron_variant | MODIFIER | c.74+4443C>G | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26567129 | ||||||
chr2:26567170
|
G | A | 1 | a0008c0010t0001g0103 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.74+4484G>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26567170 | ||||||
chr2:26567390
|
A | G | 154 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(151): Show | 397 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(394): Show |
intron_variant | MODIFIER | c.74+4704A>G | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26567390 | ||||||
chr2:26567505
|
G | A | 3 | a0001c0003t0001g0051a0001c0003t0001g0052a0001c0003t0001g0053 | 3 | HG01074.hp1 HG03098.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.74+4819G>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26567505 | ||||||
chr2:26567592
|
G | A | 1 | a0002c0002t0002g0078 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.74+4906G>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26567592 | ||||||
chr2:26567624
|
C | G | 1 | a0001c0003t0001g0075 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.74+4938C>G | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26567624 | ||||||
chr2:26567653
|
C | T | 8 | a0001c0001t0001g0119a0001c0003t0001g0007a0001c0003t0001g0042others(5): Show | 20 | HG00639.hp1 HG00735.hp2 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.74+4967C>T | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26567653 | ||||||
chr2:26567853
|
T | C | 122 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0008others(119): Show | 332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.74+5167T>C | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26567853 | ||||||
chr2:26567947
|
A | G | 1 | a0001c0003t0001g0131 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.74+5261A>G | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26567947 | ||||||
chr2:26567966
|
T | C | 1 | a0001c0005t0001g0055 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.74+5280T>C | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26567966 | ||||||
chr2:26568040
|
G | A | 1 | a0001c0003t0001g0124 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.74+5354G>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26568040 | ||||||
chr2:26568096
|
G | T | 1 | a0002c0002t0002g0139 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.74+5410G>T | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26568096 | ||||||
chr2:26568186
|
C | A | 2 | a0001c0001t0001g0031a0001c0001t0001g0032 | 4 | NA18956.hp1 NA18984.hp2 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.74+5500C>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26568186 | ||||||
chr2:26568235
|
C | G | 1 | a0001c0001t0001g0118 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.74+5549C>G | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26568235 | ||||||
chr2:26568468
|
C | A | 1 | a0001c0003t0001g0105 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.74+5782C>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26568468 | ||||||
chr2:26568572
|
G | A | 3 | a0001c0003t0001g0043a0001c0003t0001g0125a0001c0003t0001g0150 | 4 | NA18965.hp1 NA18989.hp2 NA19003.hp1 others(1): Show |
intron_variant | MODIFIER | c.74+5886G>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26568572 | ||||||
chr2:26568586
|
A | C | 105 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0008others(102): Show | 297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.74+5900A>C | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26568586 | ||||||
chr2:26568791
|
C | T | 1 | a0001c0003t0001g0143 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.74+6105C>T | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26568791 | ||||||
chr2:26568793
|
G | C | 1 | a0001c0003t0001g0072 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.74+6107G>C | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26568793 | ||||||
chr2:26568842
|
A | G | 8 | a0001c0001t0001g0012a0001c0001t0001g0022a0001c0003t0001g0009others(5): Show | 25 | HG00639.hp2 HG01496.hp1 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.74+6156A>G | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26568842 | ||||||
chr2:26568861
|
A | G | 1 | a0001c0001t0002g0068 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.74+6175A>G | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26568861 | ||||||
chr2:26569016
|
CA | C | 37 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0012others(34): Show | 79 | HG00438.hp2 HG00609.hp2 HG00621.hp2 others(76): Show |
intron_variant | MODIFIER | c.74+6345delA | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 26569016 | |||||
chr2:26569016
|
CAA | C | 111 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0008others(108): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.74+6344_74+6345del others(2): Show |
FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 26569016 | |||||
chr2:26569020
|
A | C | 1 | a0002c0002t0002g0097 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.74+6334A>C | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26569020 | ||||||
chr2:26569167
|
G | A | 120 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0008others(117): Show | 341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.74+6481G>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26569167 | ||||||
chr2:26569187
|
T | C | 1 | a0002c0002t0002g0082 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.74+6501T>C | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26569187 | ||||||
chr2:26569205
|
G | A | 4 | a0001c0003t0001g0021a0001c0003t0001g0051a0001c0003t0001g0052others(1): Show | 6 | HG00733.hp2 HG01074.hp1 HG01167.hp1 others(3): Show |
intron_variant | MODIFIER | c.74+6519G>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26569205 | ||||||
chr2:26569220
|
C | T | 1 | a0001c0001t0001g0117 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.74+6534C>T | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26569220 | ||||||
chr2:26569228
|
A | C | 4 | a0001c0003t0001g0105a0001c0005t0001g0100a0001c0005t0001g0152others(1): Show | 4 | HG02451.hp1 HG02559.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.74+6542A>C | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26569228 | ||||||
chr2:26569266
|
C | T | 109 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0008others(106): Show | 305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.74+6580C>T | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26569266 | ||||||
chr2:26569493
|
G | A | 1 | a0002c0002t0002g0083 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.75-6409G>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26569493 | ||||||
chr2:26569554
|
A | C | 1 | a0004c0011t0002g0096 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.75-6348A>C | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26569554 | ||||||
chr2:26569647
|
G | T | 1 | a0002c0002t0002g0095 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.75-6255G>T | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26569647 | ||||||
chr2:26569903
|
T | C | 1 | a0001c0003t0001g0142 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.75-5999T>C | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26569903 | ||||||
chr2:26569946
|
G | A | 1 | a0001c0003t0001g0021 | 3 | HG00733.hp2 HG01167.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.75-5956G>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26569946 | ||||||
chr2:26570035
|
A | G | 1 | a0006c0008t0001g0049 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.75-5867A>G | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26570035 | ||||||
chr2:26570043
|
C | T | 14 | a0001c0001t0001g0012a0001c0001t0001g0022a0001c0001t0001g0119others(11): Show | 40 | HG00639.hp1 HG00639.hp2 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.75-5859C>T | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26570043 | ||||||
chr2:26570247
|
A | C | 89 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0008others(86): Show | 258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.75-5655A>C | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26570247 | ||||||
chr2:26570278
|
G | A | 1 | a0001c0003t0001g0027 | 3 | NA18940.hp2 NA19076.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.75-5624G>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26570278 | ||||||
chr2:26570302
|
C | A | 1 | a0001c0003t0001g0044 | 2 | NA18981.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.75-5600C>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26570302 | ||||||
chr2:26570344
|
C | T | 1 | a0001c0001t0001g0066 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.75-5558C>T | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26570344 | ||||||
chr2:26570363
|
C | T | 1 | a0001c0001t0001g0066 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.75-5539C>T | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26570363 | ||||||
chr2:26570429
|
T | C | 1 | a0002c0002t0002g0106 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.75-5473T>C | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26570429 | ||||||
chr2:26570491
|
C | T | 1 | a0001c0001t0001g0041 | 2 | NA18949.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.75-5411C>T | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26570491 | ||||||
chr2:26570496
|
G | A | 1 | a0001c0003t0001g0126 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.75-5406G>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26570496 | ||||||
chr2:26570740
|
T | G | 154 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(151): Show | 397 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(394): Show |
intron_variant | MODIFIER | c.75-5162T>G | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26570740 | ||||||
chr2:26570776
|
T | C | 8 | a0001c0001t0001g0119a0001c0003t0001g0007a0001c0003t0001g0042others(5): Show | 20 | HG00639.hp1 HG00735.hp2 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.75-5126T>C | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26570776 | ||||||
chr2:26570779
|
A | G | 154 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(151): Show | 397 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(394): Show |
intron_variant | MODIFIER | c.75-5123A>G | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26570779 | ||||||
chr2:26570787
|
C | A | 1 | a0001c0003t0001g0052 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.75-5115C>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26570787 | ||||||
chr2:26570797
|
G | C | 21 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0031others(18): Show | 41 | HG00438.hp2 HG00609.hp2 HG01106.hp1 others(38): Show |
intron_variant | MODIFIER | c.75-5105G>C | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26570797 | ||||||
chr2:26570940
|
GTGGAGGG others(3): Show |
G | 1 | a0001c0003t0001g0056 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.75-4946_75-4937del others(10): Show |
FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 26570940 | |||||
chr2:26571008
|
G | A | 1 | a0001c0003t0001g0150 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.75-4894G>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26571008 | ||||||
chr2:26571023
|
T | C | 3 | a0001c0001t0001g0012a0001c0001t0001g0022a0001c0003t0001g0075 | 9 | HG00639.hp2 HG01884.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.75-4879T>C | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26571023 | ||||||
chr2:26571050
|
G | A | 1 | a0001c0001t0001g0101 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.75-4852G>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26571050 | ||||||
chr2:26571121
|
G | A | 160 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(157): Show | 410 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(407): Show |
intron_variant | MODIFIER | c.75-4781G>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26571121 | ||||||
chr2:26571141
|
TAG | T | 153 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(150): Show | 396 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(393): Show |
intron_variant | MODIFIER | c.75-4756_75-4755del others(2): Show |
FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 26571141 | |||||
chr2:26571258
|
G | A | 1 | a0002c0002t0002g0084 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.75-4644G>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26571258 | ||||||
chr2:26571653
|
T | C | 1 | a0001c0001t0001g0132 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.75-4249T>C | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26571653 | ||||||
chr2:26571658
|
C | T | 1 | a0002c0002t0002g0094 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.75-4244C>T | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26571658 | ||||||
chr2:26571659
|
G | A | 1 | a0001c0001t0001g0107 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.75-4243G>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26571659 | ||||||
chr2:26571739
|
C | T | 27 | a0001c0001t0001g0012a0001c0001t0001g0022a0001c0001t0001g0119others(24): Show | 70 | HG00438.hp1 HG00621.hp1 HG00639.hp1 others(67): Show |
intron_variant | MODIFIER | c.75-4163C>T | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26571739 | ||||||
chr2:26571882
|
A | C | 3 | a0001c0001t0001g0012a0001c0001t0001g0022a0001c0003t0001g0075 | 9 | HG00639.hp2 HG01884.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.75-4020A>C | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26571882 | ||||||
chr2:26571927
|
GAACTT | G | 57 | a0001c0003t0001g0014a0001c0003t0001g0016a0001c0003t0001g0024others(54): Show | 153 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(150): Show |
intron_variant | MODIFIER | c.75-3970_75-3966del others(5): Show |
FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 26571927 | |||||
chr2:26571976
|
AT | A | 57 | a0001c0003t0001g0014a0001c0003t0001g0016a0001c0003t0001g0024others(54): Show | 153 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(150): Show |
intron_variant | MODIFIER | c.75-3923delT | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 26571976 | |||||
chr2:26572122
|
T | G | 2 | a0001c0003t0001g0019a0002c0002t0002g0083 | 5 | HG02015.hp1 HG02074.hp1 NA18941.hp2 others(2): Show |
intron_variant | MODIFIER | c.75-3780T>G | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26572122 | ||||||
chr2:26572125
|
G | T | 3 | a0001c0001t0001g0046a0001c0001t0001g0048a0001c0003t0001g0047 | 3 | HG02809.hp1 HG02886.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.75-3777G>T | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26572125 | ||||||
chr2:26572223
|
G | A | 1 | a0002c0002t0002g0085 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.75-3679G>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26572223 | ||||||
chr2:26572278
|
T | C | 1 | a0001c0003t0001g0151 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.75-3624T>C | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26572278 | ||||||
chr2:26572347
|
TG | T | 5 | a0001c0003t0001g0016a0001c0003t0001g0024a0001c0003t0001g0073others(2): Show | 10 | HG02109.hp2 HG02280.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.75-3553delG | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 26572347 | |||||
chr2:26572349
|
GT | G | 119 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0008others(116): Show | 329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.75-3538delT | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 26572349 | |||||
chr2:26572349
|
GTT | G | 5 | a0001c0001t0001g0071a0001c0003t0001g0021a0001c0003t0001g0105others(2): Show | 7 | HG00733.hp2 HG01167.hp1 HG01167.hp2 others(4): Show |
intron_variant | MODIFIER | c.75-3539_75-3538del others(2): Show |
FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 26572349 | |||||
chr2:26572367
|
C | T | 57 | a0001c0003t0001g0009a0001c0003t0001g0014a0001c0003t0001g0016others(54): Show | 161 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(158): Show |
intron_variant | MODIFIER | c.75-3535C>T | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26572367 | ||||||
chr2:26572655
|
G | T | 1 | a0002c0002t0002g0023 | 3 | HG01884.hp2 NA19043.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.75-3247G>T | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26572655 | ||||||
chr2:26572780
|
G | A | 1 | a0001c0003t0001g0014 | 4 | HG01496.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.75-3122G>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26572780 | ||||||
chr2:26573093
|
T | C | 11 | a0001c0001t0001g0119a0001c0003t0001g0007a0001c0003t0001g0009others(8): Show | 31 | HG00639.hp1 HG00735.hp2 HG01106.hp2 others(28): Show |
intron_variant | MODIFIER | c.75-2809T>C | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26573093 | ||||||
chr2:26573189
|
G | C | 1 | a0001c0003t0001g0142 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.75-2713G>C | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26573189 | ||||||
chr2:26573211
|
C | T | 1 | a0001c0001t0001g0022 | 3 | HG01884.hp1 HG02055.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.75-2691C>T | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26573211 | ||||||
chr2:26573223
|
C | T | 1 | a0001c0003t0001g0019 | 4 | HG02015.hp1 HG02074.hp1 NA18941.hp2 others(1): Show |
intron_variant | MODIFIER | c.75-2679C>T | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26573223 | ||||||
chr2:26573294
|
G | C | 1 | a0001c0001t0001g0062 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.75-2608G>C | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26573294 | ||||||
chr2:26573398
|
G | GGGGAAGA others(38): Show |
3 | a0001c0001t0001g0012a0001c0001t0001g0022a0001c0003t0001g0015 | 12 | HG01884.hp1 HG02055.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.75-2500_75-2456dup others(45): Show |
FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr2 | 26573398 | |||||
chr2:26573400
|
G | A | 2 | a0001c0001t0001g0034a0001c0001t0001g0071 | 3 | HG01167.hp2 HG01169.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.75-2502G>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26573400 | ||||||
chr2:26573442
|
A | G | 22 | a0001c0003t0001g0004a0001c0003t0001g0007a0001c0003t0001g0009others(19): Show | 66 | HG00438.hp1 HG00621.hp1 HG00639.hp1 others(63): Show |
intron_variant | MODIFIER | c.75-2460A>G | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26573442 | ||||||
chr2:26573592
|
A | C | 1 | a0001c0001t0002g0068 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.75-2310A>C | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26573592 | ||||||
chr2:26573609
|
G | A | 14 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0012others(11): Show | 39 | HG00438.hp2 HG00609.hp2 HG01175.hp1 others(36): Show |
intron_variant | MODIFIER | c.75-2293G>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26573609 | ||||||
chr2:26573659
|
G | A | 1 | a0001c0003t0001g0120 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.75-2243G>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26573659 | ||||||
chr2:26573660
|
C | T | 2 | a0002c0002t0002g0039a0002c0002t0002g0123 | 3 | HG02280.hp1 HG02717.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.75-2242C>T | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26573660 | ||||||
chr2:26573666
|
A | G | 2 | a0002c0002t0002g0092a0002c0002t0002g0093 | 2 | HG03654.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.75-2236A>G | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26573666 | ||||||
chr2:26573706
|
A | G | 1 | a0001c0003t0001g0042 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.75-2196A>G | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26573706 | ||||||
chr2:26573710
|
G | C | 14 | a0001c0003t0001g0004a0001c0003t0001g0019a0001c0003t0001g0027others(11): Show | 41 | HG00438.hp1 HG00621.hp1 HG00639.hp2 others(38): Show |
intron_variant | MODIFIER | c.75-2192G>C | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26573710 | ||||||
chr2:26573917
|
C | T | 2 | a0002c0002t0002g0025a0002c0002t0002g0106 | 4 | HG03017.hp2 HG03239.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.75-1985C>T | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26573917 | ||||||
chr2:26573988
|
C | A | 1 | a0001c0001t0001g0109 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.75-1914C>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26573988 | ||||||
chr2:26574051
|
G | A | 137 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(134): Show | 361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
intron_variant | MODIFIER | c.75-1851G>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26574051 | ||||||
chr2:26574119
|
C | T | 2 | a0002c0002t0002g0017a0002c0006t0001g0091 | 5 | HG02056.hp2 NA18945.hp2 NA18970.hp2 others(2): Show |
intron_variant | MODIFIER | c.75-1783C>T | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26574119 | ||||||
chr2:26574208
|
A | T | 1 | a0002c0002t0002g0090 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.75-1694A>T | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26574208 | ||||||
chr2:26574232
|
G | A | 1 | a0002c0002t0002g0110 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.75-1670G>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26574232 | ||||||
chr2:26574246
|
G | A | 1 | a0001c0003t0001g0143 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.75-1656G>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26574246 | ||||||
chr2:26574423
|
G | A | 51 | a0001c0004t0002g0018a0002c0002t0002g0002a0002c0002t0002g0003others(48): Show | 141 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.75-1479G>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26574423 | ||||||
chr2:26574490
|
G | A | 1 | a0001c0003t0001g0140 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.75-1412G>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26574490 | ||||||
chr2:26574599
|
C | T | 1 | a0001c0003t0001g0142 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.75-1303C>T | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26574599 | ||||||
chr2:26574660
|
G | A | 1 | a0001c0003t0001g0014 | 4 | HG01496.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.75-1242G>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26574660 | ||||||
chr2:26574662
|
A | G | 1 | a0001c0003t0001g0105 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.75-1240A>G | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26574662 | ||||||
chr2:26574754
|
G | A | 1 | a0001c0001t0001g0063 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.75-1148G>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26574754 | ||||||
chr2:26574768
|
C | T | 7 | a0001c0003t0001g0007a0001c0003t0001g0009a0001c0003t0001g0029others(4): Show | 27 | HG00639.hp1 HG00735.hp2 HG01106.hp2 others(24): Show |
intron_variant | MODIFIER | c.75-1134C>T | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26574768 | ||||||
chr2:26574775
|
G | A | 2 | a0001c0004t0002g0018a0002c0002t0002g0092 | 5 | HG00738.hp1 HG01346.hp2 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.75-1127G>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26574775 | ||||||
chr2:26574820
|
C | T | 1 | a0001c0003t0001g0061 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.75-1082C>T | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26574820 | ||||||
chr2:26574850
|
G | A | 1 | a0001c0003t0001g0142 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.75-1052G>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26574850 | ||||||
chr2:26574938
|
T | G | 154 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(151): Show | 401 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(398): Show |
intron_variant | MODIFIER | c.75-964T>G | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26574938 | ||||||
chr2:26574939
|
G | C | 1 | a0001c0001t0001g0008 | 9 | NA18950.hp2 NA18977.hp1 NA18994.hp1 others(6): Show |
intron_variant | MODIFIER | c.75-963G>C | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26574939 | ||||||
chr2:26574939
|
G | T | 2 | a0001c0001t0001g0064a0001c0003t0001g0122 | 2 | HG00639.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.75-963G>T | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26574939 | ||||||
chr2:26574953
|
G | A | 1 | a0001c0001t0001g0133 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.75-949G>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26574953 | ||||||
chr2:26575033
|
T | G | 1 | a0001c0003t0001g0125 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.75-869T>G | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26575033 | ||||||
chr2:26575114
|
C | T | 51 | a0001c0004t0002g0018a0002c0002t0002g0002a0002c0002t0002g0003others(48): Show | 141 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.75-788C>T | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26575114 | ||||||
chr2:26575188
|
T | A | 13 | a0002c0002t0002g0003a0002c0002t0002g0028a0002c0002t0002g0076others(10): Show | 48 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(45): Show |
intron_variant | MODIFIER | c.75-714T>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26575188 | ||||||
chr2:26575227
|
G | A | 2 | a0001c0003t0001g0021a0001c0003t0001g0073 | 4 | HG00733.hp2 HG01167.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.75-675G>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26575227 | ||||||
chr2:26575262
|
G | A | 17 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0012others(14): Show | 42 | HG00438.hp2 HG00609.hp2 HG01175.hp1 others(39): Show |
intron_variant | MODIFIER | c.75-640G>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26575262 | ||||||
chr2:26575277
|
C | G | 89 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(86): Show | 236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.75-625C>G | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26575277 | ||||||
chr2:26575306
|
C | T | 1 | a0001c0003t0001g0056 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.75-596C>T | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26575306 | ||||||
chr2:26575381
|
G | C | 1 | a0001c0003t0001g0142 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.75-521G>C | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26575381 | ||||||
chr2:26575470
|
G | C | 1 | a0001c0001t0001g0101 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.75-432G>C | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26575470 | ||||||
chr2:26575470
|
G | T | 1 | a0001c0003t0001g0125 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.75-432G>T | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26575470 | ||||||
chr2:26575475
|
G | T | 1 | a0001c0001t0001g0116 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.75-427G>T | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26575475 | ||||||
chr2:26575610
|
A | T | 1 | a0001c0003t0001g0142 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.75-292A>T | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26575610 | ||||||
chr2:26575692
|
T | A | 1 | a0001c0003t0001g0009 | 7 | HG02109.hp1 HG02572.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.75-210T>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26575692 | ||||||
chr2:26575723
|
G | A | 85 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(82): Show | 232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.75-179G>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 1/3 | chr2 | 26575723 | ||||||
chr2:26576223
|
C | A | 17 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0012others(14): Show | 42 | HG00438.hp2 HG00609.hp2 HG01175.hp1 others(39): Show |
intron_variant | MODIFIER | c.348+48C>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 2/3 | chr2 | 26576223 | ||||||
chr2:26576256
|
C | A | 1 | a0001c0001t0001g0112 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.348+81C>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 2/3 | chr2 | 26576256 | ||||||
chr2:26576355
|
G | A | 2 | a0002c0002t0002g0137a0002c0002t0002g0139 | 2 | HG00323.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.348+180G>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 2/3 | chr2 | 26576355 | ||||||
chr2:26576523
|
A | G | 6 | a0001c0003t0001g0013a0001c0003t0001g0047a0001c0003t0001g0059others(3): Show | 10 | HG00639.hp2 HG01106.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.348+348A>G | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 2/3 | chr2 | 26576523 | ||||||
chr2:26576588
|
C | T | 1 | a0001c0001t0001g0022 | 3 | HG01884.hp1 HG02055.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.348+413C>T | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 2/3 | chr2 | 26576588 | ||||||
chr2:26576600
|
C | T | 3 | a0001c0003t0001g0051a0001c0003t0001g0052a0001c0003t0001g0053 | 3 | HG01074.hp1 HG03098.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.348+425C>T | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 2/3 | chr2 | 26576600 | ||||||
chr2:26576623
|
G | T | 3 | a0001c0001t0001g0050a0001c0001t0001g0067a0001c0001t0002g0068 | 3 | HG01243.hp2 HG01891.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.348+448G>T | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 2/3 | chr2 | 26576623 | ||||||
chr2:26576671
|
G | A | 1 | a0001c0003t0001g0021 | 3 | HG00733.hp2 HG01167.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.348+496G>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 2/3 | chr2 | 26576671 | ||||||
chr2:26576742
|
G | A | 1 | a0001c0003t0001g0127 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.348+567G>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 2/3 | chr2 | 26576742 | ||||||
chr2:26576851
|
T | C | 92 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(89): Show | 239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.349-665T>C | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 2/3 | chr2 | 26576851 | ||||||
chr2:26576865
|
C | A | 2 | a0002c0002t0002g0087a0002c0002t0002g0097 | 2 | HG01891.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.349-651C>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 2/3 | chr2 | 26576865 | ||||||
chr2:26576870
|
A | G | 1 | a0001c0001t0001g0134 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.349-646A>G | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 2/3 | chr2 | 26576870 | ||||||
chr2:26576955
|
C | G | 1 | a0002c0002t0002g0036 | 2 | HG03669.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.349-561C>G | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 2/3 | chr2 | 26576955 | ||||||
chr2:26576955
|
C | T | 1 | a0001c0001t0001g0115 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.349-561C>T | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 2/3 | chr2 | 26576955 | ||||||
chr2:26577002
|
G | A | 1 | a0001c0001t0001g0113 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.349-514G>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 2/3 | chr2 | 26577002 | ||||||
chr2:26577042
|
G | A | 1 | a0001c0003t0001g0121 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.349-474G>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 2/3 | chr2 | 26577042 | ||||||
chr2:26577213
|
C | T | 1 | a0001c0001t0001g0032 | 2 | NA18984.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.349-303C>T | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 2/3 | chr2 | 26577213 | ||||||
chr2:26577219
|
C | T | 1 | a0001c0001t0001g0102 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.349-297C>T | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 2/3 | chr2 | 26577219 | ||||||
chr2:26577312
|
A | C | 1 | a0002c0002t0002g0058 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.349-204A>C | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 2/3 | chr2 | 26577312 | ||||||
chr2:26577325
|
G | A | 1 | a0001c0003t0001g0142 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.349-191G>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 2/3 | chr2 | 26577325 | ||||||
chr2:26577327
|
C | T | 1 | a0001c0003t0001g0142 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.349-189C>T | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 2/3 | chr2 | 26577327 | ||||||
chr2:26577365
|
G | A | 1 | a0006c0008t0001g0049 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.349-151G>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 2/3 | chr2 | 26577365 | ||||||
chr2:26577384
|
C | T | 1 | a0002c0002t0002g0089 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.349-132C>T | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 2/3 | chr2 | 26577384 | ||||||
chr2:26577395
|
C | T | 1 | a0001c0001t0001g0147 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.349-121C>T | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 2/3 | chr2 | 26577395 | ||||||
chr2:26577838
|
A | G | 2 | a0001c0001t0001g0034a0001c0001t0001g0071 | 3 | HG01167.hp2 HG01169.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.461+210A>G | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 3/3 | chr2 | 26577838 | ||||||
chr2:26577915
|
A | G | 2 | a0001c0001t0001g0046a0001c0001t0001g0048 | 2 | HG02886.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.461+287A>G | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 3/3 | chr2 | 26577915 | ||||||
chr2:26577975
|
T | A | 5 | a0001c0003t0001g0016a0001c0003t0001g0024a0001c0003t0001g0073others(2): Show | 10 | HG02109.hp2 HG02280.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.461+347T>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 3/3 | chr2 | 26577975 | ||||||
chr2:26578040
|
C | CT | 4 | a0001c0003t0001g0014a0001c0003t0001g0051a0001c0003t0001g0052others(1): Show | 7 | HG01074.hp1 HG01496.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.461+413dupT | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr2 | 26578040 | |||||
chr2:26578046
|
C | T | 1 | a0001c0003t0001g0060 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.461+418C>T | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 3/3 | chr2 | 26578046 | ||||||
chr2:26578051
|
C | T | 1 | a0001c0003t0001g0142 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.461+423C>T | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 3/3 | chr2 | 26578051 | ||||||
chr2:26578123
|
C | G | 1 | a0001c0005t0001g0055 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.461+495C>G | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 3/3 | chr2 | 26578123 | ||||||
chr2:26578273
|
G | A | 1 | a0001c0003t0001g0009 | 7 | HG02109.hp1 HG02572.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.461+645G>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 3/3 | chr2 | 26578273 | ||||||
chr2:26578275
|
G | T | 1 | a0002c0002t0002g0136 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.461+647G>T | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 3/3 | chr2 | 26578275 | ||||||
chr2:26578295
|
G | A | 13 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0012others(10): Show | 38 | HG00438.hp2 HG00609.hp2 HG01175.hp1 others(35): Show |
intron_variant | MODIFIER | c.461+667G>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 3/3 | chr2 | 26578295 | ||||||
chr2:26578443
|
G | C | 51 | a0001c0003t0001g0037a0001c0003t0001g0079a0001c0004t0002g0018others(48): Show | 142 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.461+815G>C | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 3/3 | chr2 | 26578443 | ||||||
chr2:26578523
|
G | A | 4 | a0001c0003t0001g0047a0001c0003t0001g0059a0001c0003t0001g0060others(1): Show | 4 | HG01106.hp1 HG02809.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.462-771G>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 3/3 | chr2 | 26578523 | ||||||
chr2:26578523
|
G | C | 1 | a0001c0003t0001g0105 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.462-771G>C | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 3/3 | chr2 | 26578523 | ||||||
chr2:26578524
|
C | A | 1 | a0001c0003t0001g0065 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.462-770C>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 3/3 | chr2 | 26578524 | ||||||
chr2:26578532
|
A | G | 1 | a0002c0002t0002g0088 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.462-762A>G | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 3/3 | chr2 | 26578532 | ||||||
chr2:26578546
|
G | T | 1 | a0001c0003t0001g0013 | 5 | HG02257.hp2 HG02615.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.462-748G>T | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 3/3 | chr2 | 26578546 | ||||||
chr2:26578661
|
T | C | 1 | a0001c0001t0001g0115 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.462-633T>C | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 3/3 | chr2 | 26578661 | ||||||
chr2:26578718
|
G | A | 35 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0008others(32): Show | 106 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.462-576G>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 3/3 | chr2 | 26578718 | ||||||
chr2:26578878
|
C | G | 1 | a0001c0003t0001g0014 | 4 | HG01496.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.462-416C>G | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 3/3 | chr2 | 26578878 | ||||||
chr2:26578927
|
C | T | 7 | a0001c0003t0001g0007a0001c0003t0001g0009a0001c0003t0001g0029others(4): Show | 27 | HG00639.hp1 HG00735.hp2 HG01106.hp2 others(24): Show |
intron_variant | MODIFIER | c.462-367C>T | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 3/3 | chr2 | 26578927 | ||||||
chr2:26578944
|
C | G | 1 | a0001c0003t0001g0143 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.462-350C>G | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 3/3 | chr2 | 26578944 | ||||||
chr2:26578973
|
T | C | 3 | a0001c0005t0001g0100a0001c0005t0001g0152a0001c0005t0001g0153 | 3 | HG02451.hp1 HG02559.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.462-321T>C | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 3/3 | chr2 | 26578973 | ||||||
chr2:26579067
|
C | T | 1 | a0008c0010t0001g0103 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.462-227C>T | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 3/3 | chr2 | 26579067 | ||||||
chr2:26579153
|
G | A | 1 | a0001c0001t0001g0114 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.462-141G>A | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 3/3 | chr2 | 26579153 | ||||||
chr2:26579276
|
TC | T | 1 | a0001c0003t0001g0024 | 3 | HG02109.hp2 HG02280.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.462-15delC | FAM166C | ENSG00000173557.15 | transcript | ENST00000329615.4 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr2 | 26579276 |