geneid | 83986 |
---|---|
ensemblid | ENSG00000167930.17 |
hgncid | 14163 |
symbol | FAM234A |
name | family with sequence similarity 234 member A |
refseq_nuc | NM_032039.4 |
refseq_prot | NP_114428.1 |
ensembl_nuc | ENST00000399932.8 |
ensembl_prot | ENSP00000382814.3 |
mane_status | MANE Select |
chr | chr16 |
start | 234821 |
end | 266096 |
strand | + |
ver | v1.2 |
region | chr16:234821-266096 |
region5000 | chr16:229821-271096 |
regionname0 | FAM234A_chr16_234821_266096 |
regionname5000 | FAM234A_chr16_229821_271096 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 552 | 368 | 87 | 70 | 152 | 14 | 43 | 115 | FAM234A_chr16_229821_271096 | FAM234A | copy fasta | chr16 | 229821 | 271096 |
a0002 | 0/0 | 552 | 14 | 0 | 1 | 13 | 0 | 0 | 9 | FAM234A_chr16_229821_271096 | FAM234A | copy fasta | chr16 | 229821 | 271096 |
a0003 | 0/0 | 552 | 8 | 0 | 3 | 5 | 0 | 0 | 4 | FAM234A_chr16_229821_271096 | FAM234A | copy fasta | chr16 | 229821 | 271096 |
a0004 | 0/0 | 552 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | copy fasta | chr16 | 229821 | 271096 |
a0005 | 0/0 | 552 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | copy fasta | chr16 | 229821 | 271096 |
a0006 | 0/0 | 552 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | copy fasta | chr16 | 229821 | 271096 |
a0007 | 0/0 | 552 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | copy fasta | chr16 | 229821 | 271096 |
a0008 | 0/0 | 552 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | copy fasta | chr16 | 229821 | 271096 |
a0009 | 0/0 | 552 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | copy fasta | chr16 | 229821 | 271096 |
a0010 | 0/0 | 552 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | copy fasta | chr16 | 229821 | 271096 |
a0011 | 0/0 | 552 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | copy fasta | chr16 | 229821 | 271096 |
a0012 | 0/0 | 552 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | copy fasta | chr16 | 229821 | 271096 |
a0013 | 0/0 | 552 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | copy fasta | chr16 | 229821 | 271096 |
a0014 | 0/0 | 552 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FAM234A_chr16_229821_271096 | FAM234A | copy fasta | chr16 | 229821 | 271096 |
a0015 | 0/0 | 552 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | copy fasta | chr16 | 229821 | 271096 |
a0016 | 0/0 | 552 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | copy fasta | chr16 | 229821 | 271096 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1659 | 262 | 67 | 52 | 100 | 11 | 30 | FAM234A_chr16_229821_271096 | FAM234A | copy fasta | chr16 | 229821 | 271096 |
c0002 | 0/0 | 1659 | 84 | 10 | 14 | 45 | 3 | 12 | FAM234A_chr16_229821_271096 | FAM234A | copy fasta | chr16 | 229821 | 271096 |
c0003 | 0/0 | 1659 | 14 | 0 | 1 | 13 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | copy fasta | chr16 | 229821 | 271096 |
c0004 | 0/0 | 1659 | 8 | 0 | 3 | 5 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | copy fasta | chr16 | 229821 | 271096 |
c0005 | 0/0 | 1659 | 6 | 6 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | copy fasta | chr16 | 229821 | 271096 |
c0006 | 0/0 | 1659 | 5 | 3 | 2 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | copy fasta | chr16 | 229821 | 271096 |
c0007 | 0/0 | 1659 | 3 | 3 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | copy fasta | chr16 | 229821 | 271096 |
c0008 | 0/0 | 1659 | 2 | 2 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | copy fasta | chr16 | 229821 | 271096 |
c0009 | 0/0 | 1659 | 2 | 0 | 0 | 2 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | copy fasta | chr16 | 229821 | 271096 |
c0010 | 0/0 | 1659 | 2 | 0 | 0 | 2 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | copy fasta | chr16 | 229821 | 271096 |
c0011 | 0/0 | 1659 | 2 | 0 | 2 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | copy fasta | chr16 | 229821 | 271096 |
c0012 | 0/0 | 1659 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | copy fasta | chr16 | 229821 | 271096 |
c0013 | 0/0 | 1659 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | copy fasta | chr16 | 229821 | 271096 |
c0014 | 0/0 | 1659 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | copy fasta | chr16 | 229821 | 271096 |
c0015 | 0/0 | 1659 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | copy fasta | chr16 | 229821 | 271096 |
c0016 | 0/0 | 1659 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | copy fasta | chr16 | 229821 | 271096 |
c0017 | 0/0 | 1659 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | copy fasta | chr16 | 229821 | 271096 |
c0018 | 0/0 | 1659 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | copy fasta | chr16 | 229821 | 271096 |
c0019 | 0/0 | 1659 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | copy fasta | chr16 | 229821 | 271096 |
c0020 | 0/0 | 1659 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | copy fasta | chr16 | 229821 | 271096 |
c0021 | 0/0 | 1659 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | copy fasta | chr16 | 229821 | 271096 |
c0022 | 0/0 | 1659 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | copy fasta | chr16 | 229821 | 271096 |
c0023 | 0/0 | 1659 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | copy fasta | chr16 | 229821 | 271096 |
c0024 | 0/0 | 1659 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | copy fasta | chr16 | 229821 | 271096 |
c0025 | 0/0 | 1659 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | copy fasta | chr16 | 229821 | 271096 |
c0026 | 0/0 | 1659 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | copy fasta | chr16 | 229821 | 271096 |
c0027 | 0/0 | 1659 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | copy fasta | chr16 | 229821 | 271096 |
c0028 | 0/0 | 1659 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | copy fasta | chr16 | 229821 | 271096 |
c0029 | 0/0 | 1659 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | copy fasta | chr16 | 229821 | 271096 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 1251 | 249 | 44 | 51 | 113 | 10 | 30 | FAM234A_chr16_229821_271096 | FAM234A | copy fasta | chr16 | 229821 | 271096 |
t0002 | 0/0 | 1251 | 107 | 22 | 18 | 52 | 3 | 12 | FAM234A_chr16_229821_271096 | FAM234A | copy fasta | chr16 | 229821 | 271096 |
t0003 | 0/0 | 1251 | 22 | 8 | 3 | 9 | 1 | 1 | FAM234A_chr16_229821_271096 | FAM234A | copy fasta | chr16 | 229821 | 271096 |
t0004 | 0/0 | 1251 | 6 | 6 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | copy fasta | chr16 | 229821 | 271096 |
t0005 | 0/0 | 1251 | 6 | 6 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | copy fasta | chr16 | 229821 | 271096 |
t0006 | 0/0 | 1251 | 2 | 1 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | copy fasta | chr16 | 229821 | 271096 |
t0007 | 0/0 | 1251 | 2 | 2 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | copy fasta | chr16 | 229821 | 271096 |
t0008 | 0/0 | 1251 | 2 | 1 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | copy fasta | chr16 | 229821 | 271096 |
t0009 | 0/0 | 1251 | 2 | 0 | 2 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | copy fasta | chr16 | 229821 | 271096 |
t0010 | 0/0 | 1251 | 2 | 2 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | copy fasta | chr16 | 229821 | 271096 |
t0011 | 0/0 | 1251 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | copy fasta | chr16 | 229821 | 271096 |
t0012 | 0/0 | 1251 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | copy fasta | chr16 | 229821 | 271096 |
t0013 | 0/0 | 1251 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | copy fasta | chr16 | 229821 | 271096 |
t0014 | 0/0 | 1251 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | copy fasta | chr16 | 229821 | 271096 |
t0015 | 0/0 | 1251 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | copy fasta | chr16 | 229821 | 271096 |
t0016 | 0/0 | 1251 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | copy fasta | chr16 | 229821 | 271096 |
t0017 | 0/0 | 1251 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | copy fasta | chr16 | 229821 | 271096 |
t0018 | 1/0 | 1251 | 1 | 0 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | copy fasta | chr16 | 229821 | 271096 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 6 | 0 | 4 | 2 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0002 | 0/0 | 4 | 1 | 0 | 0 | 1 | 2 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0005 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0008 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0014 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0019 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0033 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0145 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0252 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0275 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0345 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0351 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0362 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0366 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0374 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0375 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0376 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0377 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0378 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0379 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
g0380 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1659 | 262 | 67 | 52 | 100 | 11 | 30 | FAM234A_chr16_229821_271096 | FAM234A | copy fasta | chr16 | 229821 | 271096 |
a0001c0002 | 0/0 | 1659 | 84 | 10 | 14 | 45 | 3 | 12 | FAM234A_chr16_229821_271096 | FAM234A | copy fasta | chr16 | 229821 | 271096 |
a0001c0005 | 0/0 | 1659 | 6 | 6 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | copy fasta | chr16 | 229821 | 271096 |
a0001c0006 | 0/0 | 1659 | 5 | 3 | 2 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | copy fasta | chr16 | 229821 | 271096 |
a0001c0009 | 0/0 | 1659 | 2 | 0 | 0 | 2 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | copy fasta | chr16 | 229821 | 271096 |
a0001c0012 | 0/0 | 1659 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | copy fasta | chr16 | 229821 | 271096 |
a0001c0017 | 0/0 | 1659 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | copy fasta | chr16 | 229821 | 271096 |
a0001c0018 | 0/0 | 1659 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | copy fasta | chr16 | 229821 | 271096 |
a0001c0019 | 0/0 | 1659 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | copy fasta | chr16 | 229821 | 271096 |
a0001c0020 | 0/0 | 1659 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | copy fasta | chr16 | 229821 | 271096 |
a0001c0021 | 0/0 | 1659 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | copy fasta | chr16 | 229821 | 271096 |
a0001c0024 | 0/0 | 1659 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | copy fasta | chr16 | 229821 | 271096 |
a0001c0027 | 0/0 | 1659 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | copy fasta | chr16 | 229821 | 271096 |
a0001c0029 | 0/0 | 1659 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | copy fasta | chr16 | 229821 | 271096 |
a0002c0003 | 0/0 | 1659 | 14 | 0 | 1 | 13 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | copy fasta | chr16 | 229821 | 271096 |
a0003c0004 | 0/0 | 1659 | 8 | 0 | 3 | 5 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | copy fasta | chr16 | 229821 | 271096 |
a0004c0007 | 0/0 | 1659 | 3 | 3 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | copy fasta | chr16 | 229821 | 271096 |
a0005c0011 | 0/0 | 1659 | 2 | 0 | 2 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | copy fasta | chr16 | 229821 | 271096 |
a0006c0010 | 0/0 | 1659 | 2 | 0 | 0 | 2 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | copy fasta | chr16 | 229821 | 271096 |
a0007c0008 | 0/0 | 1659 | 2 | 2 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | copy fasta | chr16 | 229821 | 271096 |
a0008c0015 | 0/0 | 1659 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | copy fasta | chr16 | 229821 | 271096 |
a0009c0025 | 0/0 | 1659 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | copy fasta | chr16 | 229821 | 271096 |
a0010c0016 | 0/0 | 1659 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | copy fasta | chr16 | 229821 | 271096 |
a0011c0028 | 0/0 | 1659 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | copy fasta | chr16 | 229821 | 271096 |
a0012c0026 | 0/0 | 1659 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | copy fasta | chr16 | 229821 | 271096 |
a0013c0022 | 0/0 | 1659 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | copy fasta | chr16 | 229821 | 271096 |
a0014c0014 | 0/0 | 1659 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | copy fasta | chr16 | 229821 | 271096 |
a0015c0013 | 0/0 | 1659 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | copy fasta | chr16 | 229821 | 271096 |
a0016c0023 | 0/0 | 1659 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | copy fasta | chr16 | 229821 | 271096 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 2909 | 218 | 38 | 47 | 94 | 10 | 28 | FAM234A_chr16_229821_271096 | FAM234A | copy fasta | chr16 | 229821 | 271096 |
a0001c0001t0002 | 0/0 | 2909 | 3 | 3 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | copy fasta | chr16 | 229821 | 271096 |
a0001c0001t0003 | 0/0 | 2909 | 18 | 8 | 3 | 5 | 1 | 1 | FAM234A_chr16_229821_271096 | FAM234A | copy fasta | chr16 | 229821 | 271096 |
a0001c0001t0004 | 0/0 | 2909 | 5 | 5 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | copy fasta | chr16 | 229821 | 271096 |
a0001c0001t0005 | 0/0 | 2909 | 6 | 6 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | copy fasta | chr16 | 229821 | 271096 |
a0001c0001t0007 | 0/0 | 2909 | 2 | 2 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | copy fasta | chr16 | 229821 | 271096 |
a0001c0001t0008 | 0/0 | 2909 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | copy fasta | chr16 | 229821 | 271096 |
a0001c0001t0009 | 0/0 | 2909 | 2 | 0 | 2 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | copy fasta | chr16 | 229821 | 271096 |
a0001c0001t0010 | 0/0 | 2909 | 2 | 2 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | copy fasta | chr16 | 229821 | 271096 |
a0001c0001t0011 | 0/0 | 2909 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | copy fasta | chr16 | 229821 | 271096 |
a0001c0001t0013 | 0/0 | 2909 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | copy fasta | chr16 | 229821 | 271096 |
a0001c0001t0015 | 0/0 | 2909 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | copy fasta | chr16 | 229821 | 271096 |
a0001c0001t0016 | 0/0 | 2909 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | copy fasta | chr16 | 229821 | 271096 |
a0001c0001t0018 | 1/0 | 2909 | 1 | 0 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | copy fasta | chr16 | 229821 | 271096 |
a0001c0002t0001 | 0/0 | 2909 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | copy fasta | chr16 | 229821 | 271096 |
a0001c0002t0002 | 0/0 | 2909 | 80 | 10 | 13 | 43 | 3 | 11 | FAM234A_chr16_229821_271096 | FAM234A | copy fasta | chr16 | 229821 | 271096 |
a0001c0002t0012 | 0/0 | 2909 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | copy fasta | chr16 | 229821 | 271096 |
a0001c0002t0014 | 0/0 | 2909 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | copy fasta | chr16 | 229821 | 271096 |
a0001c0002t0017 | 0/0 | 2909 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | copy fasta | chr16 | 229821 | 271096 |
a0001c0005t0002 | 0/0 | 2909 | 6 | 6 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | copy fasta | chr16 | 229821 | 271096 |
a0001c0006t0001 | 0/0 | 2909 | 3 | 2 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | copy fasta | chr16 | 229821 | 271096 |
a0001c0006t0006 | 0/0 | 2909 | 2 | 1 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | copy fasta | chr16 | 229821 | 271096 |
a0001c0009t0003 | 0/0 | 2909 | 2 | 0 | 0 | 2 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | copy fasta | chr16 | 229821 | 271096 |
a0001c0012t0004 | 0/0 | 2909 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | copy fasta | chr16 | 229821 | 271096 |
a0001c0017t0001 | 0/0 | 2909 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | copy fasta | chr16 | 229821 | 271096 |
a0001c0018t0001 | 0/0 | 2909 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | copy fasta | chr16 | 229821 | 271096 |
a0001c0019t0001 | 0/0 | 2909 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | copy fasta | chr16 | 229821 | 271096 |
a0001c0020t0001 | 0/0 | 2909 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | copy fasta | chr16 | 229821 | 271096 |
a0001c0021t0003 | 0/0 | 2909 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | copy fasta | chr16 | 229821 | 271096 |
a0001c0024t0002 | 0/0 | 2909 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | copy fasta | chr16 | 229821 | 271096 |
a0001c0027t0002 | 0/0 | 2909 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | copy fasta | chr16 | 229821 | 271096 |
a0001c0029t0002 | 0/0 | 2909 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | copy fasta | chr16 | 229821 | 271096 |
a0002c0003t0001 | 0/0 | 2909 | 14 | 0 | 1 | 13 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | copy fasta | chr16 | 229821 | 271096 |
a0003c0004t0002 | 0/0 | 2909 | 8 | 0 | 3 | 5 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | copy fasta | chr16 | 229821 | 271096 |
a0004c0007t0001 | 0/0 | 2909 | 3 | 3 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | copy fasta | chr16 | 229821 | 271096 |
a0005c0011t0002 | 0/0 | 2909 | 2 | 0 | 2 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | copy fasta | chr16 | 229821 | 271096 |
a0006c0010t0001 | 0/0 | 2909 | 2 | 0 | 0 | 2 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | copy fasta | chr16 | 229821 | 271096 |
a0007c0008t0002 | 0/0 | 2909 | 2 | 2 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | copy fasta | chr16 | 229821 | 271096 |
a0008c0015t0001 | 0/0 | 2909 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | copy fasta | chr16 | 229821 | 271096 |
a0009c0025t0002 | 0/0 | 2909 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | copy fasta | chr16 | 229821 | 271096 |
a0010c0016t0001 | 0/0 | 2909 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | copy fasta | chr16 | 229821 | 271096 |
a0011c0028t0002 | 0/0 | 2909 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | copy fasta | chr16 | 229821 | 271096 |
a0012c0026t0002 | 0/0 | 2909 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | copy fasta | chr16 | 229821 | 271096 |
a0013c0022t0001 | 0/0 | 2909 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | copy fasta | chr16 | 229821 | 271096 |
a0014c0014t0001 | 0/0 | 2909 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | copy fasta | chr16 | 229821 | 271096 |
a0015c0013t0008 | 0/0 | 2909 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | copy fasta | chr16 | 229821 | 271096 |
a0016c0023t0003 | 0/0 | 2909 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | copy fasta | chr16 | 229821 | 271096 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 4 | 1 | 0 | 0 | 1 | 2 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0005 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0252 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0351 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0379 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0001g0380 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0002g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0002g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0003g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0003g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0003g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0003g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0003g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0003g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0003g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0003g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0003g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0003g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0003g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0003g0275 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0003g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0003g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0003g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0003g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0003g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0003g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0004g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0004g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0004g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0004g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0004g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0005g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0005g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0005g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0005g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0005g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0005g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0007g0377 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0007g0378 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0008g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0009g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0009g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0010g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0010g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0011g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0013g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0015g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0016g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0001t0018g0145 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0001g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0001 | 0/0 | 5 | 0 | 4 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0033 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0345 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0002g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0012g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0014g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0002t0017g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0005t0002g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0005t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0005t0002g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0005t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0005t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0006t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0006t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0006t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0006t0006g0362 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0006t0006g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0009t0003g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0009t0003g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0012t0004g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0017t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0018t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0019t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0020t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0021t0003g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0024t0002g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0027t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0001c0029t0002g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0002c0003t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0002c0003t0001g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0002c0003t0001g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0002c0003t0001g0366 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0002c0003t0001g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0002c0003t0001g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0002c0003t0001g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0002c0003t0001g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0002c0003t0001g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0002c0003t0001g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0002c0003t0001g0374 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0002c0003t0001g0375 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0002c0003t0001g0376 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0003c0004t0002g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0003c0004t0002g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0003c0004t0002g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0003c0004t0002g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0003c0004t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0003c0004t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0003c0004t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0003c0004t0002g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0004c0007t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0004c0007t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0004c0007t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0005c0011t0002g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0005c0011t0002g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0006c0010t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0006c0010t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0007c0008t0002g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0007c0008t0002g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0008c0015t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0009c0025t0002g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0010c0016t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0011c0028t0002g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0012c0026t0002g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0013c0022t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0014c0014t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0015c0013t0008g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
a0016c0023t0003g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0003 | g0275 | EUR | GBR | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0264 | EUR | GBR | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0269 | EUR | GBR | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0097 | EUR | GBR | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0166 | EUR | FIN | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | CHS | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG00423 | hp2 | a0006 | c0010 | t0001 | g0074 | EAS | CHS | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | CHS | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG00438 | hp2 | a0003 | c0004 | t0002 | g0174 | EAS | CHS | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG00544 | hp1 | a0001 | c0002 | t0002 | g0346 | EAS | CHS | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG00597 | hp1 | a0001 | c0027 | t0002 | g0307 | EAS | CHS | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | CHS | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | CHS | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | CHS | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG00621 | hp1 | a0002 | c0003 | t0001 | g0371 | EAS | CHS | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG00621 | hp2 | a0001 | c0021 | t0003 | g0216 | EAS | CHS | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | PUR | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG00642 | hp1 | a0003 | c0004 | t0002 | g0165 | AMR | PUR | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG00642 | hp2 | a0001 | c0002 | t0002 | g0302 | AMR | PUR | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | CHS | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG00673 | hp2 | a0001 | c0001 | t0003 | g0213 | EAS | CHS | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG00733 | hp1 | a0001 | c0002 | t0002 | g0310 | AMR | PUR | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG00733 | hp2 | a0001 | c0001 | t0003 | g0290 | AMR | PUR | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | PUR | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG00738 | hp1 | a0001 | c0006 | t0006 | g0362 | AMR | PUR | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | PUR | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG01069 | hp1 | a0001 | c0001 | t0009 | g0124 | AMR | PUR | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0281 | AMR | PUR | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG01070 | hp2 | a0001 | c0002 | t0002 | g0001 | AMR | PUR | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG01071 | hp1 | a0001 | c0001 | t0009 | g0125 | AMR | PUR | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG01071 | hp2 | a0001 | c0002 | t0002 | g0001 | AMR | PUR | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG01074 | hp1 | a0001 | c0002 | t0002 | g0251 | AMR | PUR | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0280 | AMR | PUR | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG01099 | hp2 | a0001 | c0020 | t0001 | g0192 | AMR | PUR | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0231 | AMR | PUR | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG01106 | hp2 | a0001 | c0001 | t0003 | g0078 | AMR | PUR | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG01109 | hp2 | a0001 | c0001 | t0003 | g0355 | AMR | PUR | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | PUR | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0279 | AMR | PUR | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0183 | AMR | PUR | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG01168 | hp2 | a0005 | c0011 | t0002 | g0308 | AMR | PUR | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG01169 | hp1 | a0005 | c0011 | t0002 | g0014 | AMR | PUR | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0266 | AMR | PUR | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0260 | AMR | PUR | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG01175 | hp2 | a0001 | c0002 | t0002 | g0305 | AMR | PUR | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG01192 | hp1 | a0001 | c0002 | t0017 | g0028 | AMR | PUR | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG01243 | hp2 | a0001 | c0006 | t0001 | g0055 | AMR | PUR | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | CLM | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG01255 | hp2 | a0001 | c0002 | t0002 | g0309 | AMR | CLM | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | CLM | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0211 | AMR | CLM | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0273 | AMR | CLM | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0267 | AMR | CLM | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0210 | AMR | CLM | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0278 | AMR | CLM | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0208 | AMR | CLM | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0207 | AMR | CLM | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG01361 | hp1 | a0001 | c0002 | t0002 | g0030 | AMR | CLM | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG01361 | hp2 | a0002 | c0003 | t0001 | g0366 | AMR | CLM | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0271 | AMR | CLM | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0185 | AMR | CLM | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0190 | AMR | CLM | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0072 | AMR | CLM | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG01515 | hp1 | a0001 | c0002 | t0002 | g0032 | EUR | IBS | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0153 | EUR | IBS | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG01517 | hp1 | a0001 | c0002 | t0002 | g0033 | EUR | IBS | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0019 | EUR | IBS | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0352 | AFR | ACB | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG01884 | hp2 | a0001 | c0002 | t0002 | g0068 | AFR | ACB | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG01891 | hp1 | a0001 | c0002 | t0002 | g0237 | AFR | ACB | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0341 | AFR | ACB | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG01928 | hp1 | a0001 | c0002 | t0002 | g0322 | AMR | PEL | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PEL | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG01943 | hp1 | a0001 | c0002 | t0002 | g0001 | AMR | PEL | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0268 | AMR | PEL | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG01975 | hp1 | a0003 | c0004 | t0002 | g0138 | AMR | PEL | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG01975 | hp2 | a0001 | c0002 | t0002 | g0317 | AMR | PEL | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PEL | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG01978 | hp2 | a0003 | c0004 | t0002 | g0136 | AMR | PEL | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG01981 | hp1 | a0001 | c0019 | t0001 | g0081 | AMR | PEL | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG01981 | hp2 | a0001 | c0002 | t0002 | g0315 | AMR | PEL | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | PEL | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | PEL | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | KHV | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02015 | hp2 | a0002 | c0003 | t0001 | g0372 | EAS | KHV | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02027 | hp1 | a0002 | c0003 | t0001 | g0373 | EAS | KHV | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | KHV | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02040 | hp2 | a0001 | c0002 | t0002 | g0335 | EAS | KHV | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | ACB | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02055 | hp2 | a0001 | c0001 | t0002 | g0126 | AFR | ACB | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | KHV | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02056 | hp2 | a0001 | c0009 | t0003 | g0292 | EAS | KHV | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02074 | hp1 | a0001 | c0002 | t0002 | g0329 | EAS | KHV | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02074 | hp2 | a0002 | c0003 | t0001 | g0376 | EAS | KHV | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | KHV | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02080 | hp2 | a0001 | c0009 | t0003 | g0257 | EAS | KHV | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02083 | hp2 | a0015 | c0013 | t0008 | g0368 | EAS | KHV | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02129 | hp2 | a0001 | c0002 | t0002 | g0286 | EAS | KHV | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02132 | hp1 | a0001 | c0002 | t0014 | g0319 | EAS | KHV | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02132 | hp2 | a0012 | c0026 | t0002 | g0014 | EAS | KHV | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | KHV | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | KHV | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | ACB | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0176 | AMR | PEL | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0332 | AMR | PEL | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02155 | hp1 | a0001 | c0002 | t0002 | g0311 | EAS | CDX | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CDX | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02165 | hp1 | a0001 | c0002 | t0002 | g0285 | EAS | CDX | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02165 | hp2 | a0001 | c0002 | t0002 | g0293 | EAS | CDX | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | ACB | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02257 | hp2 | a0001 | c0002 | t0002 | g0301 | AFR | ACB | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02258 | hp1 | a0001 | c0002 | t0002 | g0229 | AFR | ACB | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02258 | hp2 | a0001 | c0006 | t0001 | g0037 | AFR | ACB | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02273 | hp2 | a0001 | c0002 | t0002 | g0001 | AMR | PEL | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02280 | hp1 | a0001 | c0001 | t0003 | g0347 | AFR | ACB | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0282 | AMR | PEL | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | PEL | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | PEL | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PEL | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | ACB | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | ACB | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02523 | hp1 | a0016 | c0023 | t0003 | g0291 | EAS | KHV | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | KHV | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02572 | hp1 | a0001 | c0002 | t0002 | g0358 | AFR | GWD | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02572 | hp2 | a0007 | c0008 | t0002 | g0360 | AFR | GWD | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0241 | SAS | PJL | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0087 | SAS | PJL | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | GWD | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0353 | AFR | GWD | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0236 | AFR | GWD | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | GWD | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02630 | hp1 | a0008 | c0015 | t0001 | g0059 | AFR | GWD | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | GWD | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | GWD | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02647 | hp2 | a0001 | c0002 | t0002 | g0255 | AFR | GWD | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0272 | SAS | PJL | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0094 | SAS | PJL | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02698 | hp1 | a0001 | c0002 | t0002 | g0123 | SAS | PJL | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02698 | hp2 | a0001 | c0002 | t0002 | g0327 | SAS | PJL | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0287 | AFR | GWD | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02717 | hp2 | a0001 | c0001 | t0004 | g0245 | AFR | GWD | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0224 | AFR | GWD | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02723 | hp2 | a0001 | c0001 | t0005 | g0009 | AFR | GWD | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02735 | hp1 | a0001 | c0002 | t0002 | g0303 | SAS | PJL | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0198 | SAS | PJL | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0351 | SAS | PJL | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0150 | SAS | PJL | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02809 | hp1 | a0001 | c0002 | t0002 | g0357 | AFR | GWD | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02809 | hp2 | a0001 | c0005 | t0002 | g0010 | AFR | GWD | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | GWD | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02818 | hp2 | a0001 | c0005 | t0002 | g0129 | AFR | GWD | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02886 | hp1 | a0001 | c0001 | t0003 | g0253 | AFR | GWD | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02886 | hp2 | a0001 | c0001 | t0004 | g0244 | AFR | GWD | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | GWD | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02895 | hp2 | a0001 | c0002 | t0002 | g0330 | AFR | GWD | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02896 | hp1 | a0001 | c0001 | t0003 | g0233 | AFR | GWD | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02896 | hp2 | a0007 | c0008 | t0002 | g0359 | AFR | GWD | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | GWD | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02897 | hp2 | a0001 | c0001 | t0003 | g0234 | AFR | GWD | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02970 | hp1 | a0001 | c0001 | t0005 | g0240 | AFR | ESN | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02970 | hp2 | a0001 | c0001 | t0002 | g0128 | AFR | ESN | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02976 | hp2 | a0011 | c0028 | t0002 | g0256 | AFR | ESN | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0225 | AFR | GWD | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0361 | AFR | GWD | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG03098 | hp1 | a0001 | c0001 | t0010 | g0248 | AFR | MSL | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0356 | AFR | MSL | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG03130 | hp1 | a0001 | c0001 | t0007 | g0377 | AFR | ESN | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG03130 | hp2 | a0001 | c0005 | t0002 | g0130 | AFR | ESN | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0209 | AFR | ESN | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG03139 | hp2 | a0001 | c0001 | t0004 | g0226 | AFR | ESN | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0232 | AFR | ESN | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG03195 | hp2 | a0001 | c0002 | t0002 | g0062 | AFR | ESN | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0246 | AFR | MSL | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG03209 | hp2 | a0001 | c0006 | t0006 | g0363 | AFR | MSL | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG03225 | hp1 | a0001 | c0001 | t0005 | g0027 | AFR | MSL | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG03225 | hp2 | a0001 | c0012 | t0004 | g0238 | AFR | MSL | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG03239 | hp2 | a0001 | c0001 | t0003 | g0096 | SAS | PJL | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | MSL | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG03453 | hp2 | a0001 | c0001 | t0005 | g0026 | AFR | MSL | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG03486 | hp1 | a0001 | c0001 | t0010 | g0250 | AFR | MSL | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG03486 | hp2 | a0001 | c0001 | t0003 | g0036 | AFR | MSL | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG03491 | hp1 | a0014 | c0014 | t0001 | g0270 | SAS | PJL | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG03491 | hp2 | a0001 | c0002 | t0002 | g0040 | SAS | PJL | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG03492 | hp2 | a0001 | c0002 | t0002 | g0041 | SAS | PJL | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG03516 | hp1 | a0001 | c0001 | t0003 | g0288 | AFR | ESN | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG03516 | hp2 | a0001 | c0005 | t0002 | g0131 | AFR | ESN | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG03540 | hp1 | a0001 | c0005 | t0002 | g0043 | AFR | GWD | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG03540 | hp2 | a0001 | c0001 | t0005 | g0127 | AFR | GWD | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG03579 | hp1 | a0001 | c0001 | t0016 | g0009 | AFR | MSL | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0261 | SAS | PJL | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0173 | SAS | PJL | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0164 | SAS | STU | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0102 | SAS | STU | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0265 | SAS | PJL | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0218 | SAS | PJL | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG03710 | hp1 | a0001 | c0002 | t0002 | g0046 | SAS | PJL | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0259 | SAS | PJL | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0101 | SAS | BEB | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0137 | SAS | BEB | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0086 | SAS | BEB | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0277 | SAS | BEB | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG03927 | hp1 | a0001 | c0001 | t0015 | g0093 | SAS | BEB | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | BEB | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG03942 | hp1 | a0001 | c0002 | t0002 | g0029 | SAS | BEB | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0262 | SAS | BEB | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0025 | SAS | STU | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0276 | SAS | STU | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0263 | SAS | BEB | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG04184 | hp2 | a0001 | c0002 | t0002 | g0034 | SAS | BEB | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG04199 | hp1 | a0001 | c0002 | t0002 | g0296 | SAS | STU | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG04199 | hp2 | a0001 | c0002 | t0002 | g0254 | SAS | STU | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0092 | SAS | STU | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG04228 | hp1 | a0001 | c0024 | t0002 | g0312 | SAS | STU | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0221 | SAS | STU | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | CHB | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | CHB | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | CHB | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18747 | hp2 | a0001 | c0002 | t0002 | g0206 | EAS | CHB | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0230 | AFR | YRI | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18906 | hp2 | a0001 | c0002 | t0002 | g0239 | AFR | YRI | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18939 | hp1 | a0001 | c0001 | t0003 | g0214 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18939 | hp2 | a0001 | c0002 | t0002 | g0333 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0350 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18943 | hp1 | a0002 | c0003 | t0001 | g0017 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18945 | hp2 | a0001 | c0002 | t0002 | g0015 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18946 | hp2 | a0001 | c0002 | t0002 | g0299 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18947 | hp2 | a0001 | c0002 | t0002 | g0314 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18949 | hp1 | a0001 | c0002 | t0002 | g0326 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18950 | hp1 | a0003 | c0004 | t0002 | g0294 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18952 | hp1 | a0001 | c0002 | t0002 | g0219 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18952 | hp2 | a0001 | c0001 | t0003 | g0217 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18953 | hp1 | a0001 | c0002 | t0002 | g0338 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18954 | hp2 | a0001 | c0029 | t0002 | g0001 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18959 | hp2 | a0002 | c0003 | t0001 | g0365 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18963 | hp1 | a0001 | c0002 | t0002 | g0340 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18964 | hp1 | a0001 | c0002 | t0002 | g0295 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18965 | hp2 | a0001 | c0002 | t0002 | g0318 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18966 | hp1 | a0001 | c0001 | t0003 | g0220 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18966 | hp2 | a0001 | c0002 | t0002 | g0316 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18969 | hp1 | a0002 | c0003 | t0001 | g0369 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18972 | hp1 | a0001 | c0001 | t0003 | g0215 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18975 | hp1 | a0001 | c0002 | t0002 | g0013 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18978 | hp1 | a0001 | c0002 | t0002 | g0304 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18978 | hp2 | a0001 | c0001 | t0011 | g0106 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18979 | hp1 | a0001 | c0002 | t0002 | g0306 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18982 | hp2 | a0002 | c0003 | t0001 | g0370 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18983 | hp1 | a0001 | c0002 | t0002 | g0337 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18984 | hp1 | a0001 | c0002 | t0002 | g0313 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18987 | hp1 | a0001 | c0002 | t0002 | g0325 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18997 | hp1 | a0001 | c0002 | t0002 | g0348 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18997 | hp2 | a0001 | c0018 | t0001 | g0151 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18998 | hp2 | a0003 | c0004 | t0002 | g0015 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA18999 | hp2 | a0001 | c0017 | t0001 | g0187 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA19001 | hp1 | a0002 | c0003 | t0001 | g0375 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA19002 | hp1 | a0001 | c0002 | t0002 | g0334 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA19003 | hp2 | a0002 | c0003 | t0001 | g0364 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA19004 | hp1 | a0002 | c0003 | t0001 | g0017 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA19005 | hp1 | a0003 | c0004 | t0002 | g0188 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA19007 | hp1 | a0002 | c0003 | t0001 | g0367 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA19009 | hp1 | a0001 | c0002 | t0002 | g0323 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA19010 | hp1 | a0001 | c0002 | t0002 | g0047 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA19012 | hp1 | a0010 | c0016 | t0001 | g0116 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA19030 | hp1 | a0001 | c0001 | t0003 | g0283 | AFR | LWK | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | LWK | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0243 | AFR | LWK | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA19043 | hp2 | a0004 | c0007 | t0001 | g0049 | AFR | LWK | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA19054 | hp2 | a0001 | c0002 | t0002 | g0321 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA19057 | hp2 | a0001 | c0002 | t0002 | g0328 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA19060 | hp1 | a0013 | c0022 | t0001 | g0114 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA19063 | hp2 | a0001 | c0002 | t0002 | g0048 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA19064 | hp2 | a0002 | c0003 | t0001 | g0374 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA19066 | hp2 | a0001 | c0002 | t0002 | g0284 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA19067 | hp1 | a0001 | c0002 | t0002 | g0339 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA19068 | hp1 | a0001 | c0002 | t0002 | g0343 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA19070 | hp2 | a0001 | c0002 | t0002 | g0300 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA19074 | hp2 | a0001 | c0002 | t0002 | g0298 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA19079 | hp1 | a0001 | c0002 | t0012 | g0320 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA19079 | hp2 | a0003 | c0004 | t0002 | g0324 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA19082 | hp1 | a0006 | c0010 | t0001 | g0076 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA19084 | hp1 | a0001 | c0002 | t0002 | g0342 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA19084 | hp2 | a0001 | c0002 | t0002 | g0344 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA19085 | hp1 | a0001 | c0002 | t0002 | g0336 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA19087 | hp2 | a0001 | c0002 | t0002 | g0349 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA19090 | hp1 | a0009 | c0025 | t0002 | g0013 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA19090 | hp2 | a0001 | c0002 | t0002 | g0297 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA19091 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA19240 | hp1 | a0004 | c0007 | t0001 | g0051 | AFR | YRI | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | YRI | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA20129 | hp1 | a0001 | c0001 | t0007 | g0378 | AFR | ASW | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA20129 | hp2 | a0001 | c0001 | t0004 | g0228 | AFR | ASW | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0172 | EUR | TSI | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0379 | EUR | TSI | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0274 | EUR | TSI | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA20805 | hp2 | a0001 | c0002 | t0002 | g0345 | EUR | TSI | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA20905 | hp1 | a0001 | c0002 | t0001 | g0331 | SAS | GIH | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA20905 | hp2 | a0001 | c0002 | t0002 | g0031 | SAS | GIH | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | CLM | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02109 | hp1 | a0001 | c0006 | t0001 | g0038 | AFR | ACB | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0354 | AFR | ACB | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02486 | hp1 | a0001 | c0001 | t0008 | g0247 | AFR | ACB | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02486 | hp2 | a0001 | c0001 | t0004 | g0227 | AFR | ACB | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02559 | hp1 | a0001 | c0005 | t0002 | g0010 | AFR | ACB | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG02559 | hp2 | a0001 | c0001 | t0005 | g0242 | AFR | ACB | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0235 | AFR | MSL | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG03471 | hp2 | a0001 | c0001 | t0002 | g0249 | AFR | MSL | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | USA | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0258 | AFR | USA | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0380 | AFR | USA | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA20300 | hp2 | a0004 | c0007 | t0001 | g0050 | AFR | USA | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA21309 | hp1 | a0001 | c0001 | t0013 | g0035 | AFR | LWK | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
NA21309 | hp2 | a0001 | c0001 | t0003 | g0289 | AFR | LWK | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0252 | REF | REF | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0018 | g0145 | REF | REF | FAM234A_chr16_229821_271096 | FAM234A | chr16 | 229821 | 271096 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:254562
|
C | T | 1 | a0016 | 1 | HG02523.hp1 | missense_variant | MODERATE | c.149C>T | p.Ala50Val | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/13 | 325/2909 | 149/1659 | 50/552 | chr16 | 254562 | ||
chr16:259525
|
G | A | 1 | a0005 | 2 | HG01168.hp2 HG01169.hp1 |
missense_variant | MODERATE | c.311G>A | p.Arg104Lys | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 4/13 | 487/2909 | 311/1659 | 104/552 | chr16 | 259525 | ||
chr16:259593
|
G | A | 1 | a0015 | 1 | HG02083.hp2 | missense_variant | MODERATE | c.379G>A | p.Asp127Asn | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 4/13 | 555/2909 | 379/1659 | 127/552 | chr16 | 259593 | ||
chr16:259999
|
C | T | 2 | a0002a0015 | 15 | HG00621.hp1 HG01361.hp2 HG02015.hp2 others(12): Show |
missense_variant | MODERATE | c.416C>T | p.Ala139Val | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 5/13 | 592/2909 | 416/1659 | 139/552 | chr16 | 259999 | ||
chr16:260031
|
G | A | 1 | a0014 | 1 | HG03491.hp1 | missense_variant | MODERATE | c.448G>A | p.Glu150Lys | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 5/13 | 624/2909 | 448/1659 | 150/552 | chr16 | 260031 | ||
chr16:260139
|
A | G | 1 | a0013 | 1 | NA19060.hp1 | missense_variant | MODERATE | c.556A>G | p.Ile186Val | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 5/13 | 732/2909 | 556/1659 | 186/552 | chr16 | 260139 | ||
chr16:261417
|
G | A | 1 | a0008 | 1 | HG02630.hp1 | missense_variant | MODERATE | c.611G>A | p.Ser204Asn | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 6/13 | 787/2909 | 611/1659 | 204/552 | chr16 | 261417 | ||
chr16:261462
|
T | G | 1 | a0009 | 1 | NA19090.hp1 | missense_variant | MODERATE | c.656T>G | p.Val219Gly | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 6/13 | 832/2909 | 656/1659 | 219/552 | chr16 | 261462 | ||
chr16:261507
|
G | A | 1 | a0004 | 3 | NA19043.hp2 NA19240.hp1 NA20300.hp2 |
missense_variant | MODERATE | c.701G>A | p.Arg234Gln | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 6/13 | 877/2909 | 701/1659 | 234/552 | chr16 | 261507 | ||
chr16:264166
|
G | A | 1 | a0012 | 1 | HG02132.hp2 | missense_variant | MODERATE | c.1339G>A | p.Glu447Lys | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 11/13 | 1515/2909 | 1339/1659 | 447/552 | chr16 | 264166 | ||
chr16:264659
|
C | G | 1 | a0011 | 1 | HG02976.hp2 | missense_variant | MODERATE | c.1390C>G | p.Leu464Val | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 12/13 | 1566/2909 | 1390/1659 | 464/552 | chr16 | 264659 | ||
chr16:264665
|
C | T | 1 | a0006 | 2 | HG00423.hp2 NA19082.hp1 |
missense_variant | MODERATE | c.1396C>T | p.Arg466Cys | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 12/13 | 1572/2909 | 1396/1659 | 466/552 | chr16 | 264665 | ||
chr16:264963
|
G | A | 1 | a0007 | 2 | HG02572.hp2 HG02896.hp2 |
missense_variant | MODERATE | c.1600G>A | p.Asp534Asn | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 13/13 | 1776/2909 | 1600/1659 | 534/552 | chr16 | 264963 | ||
chr16:264997
|
G | A | 1 | a0010 | 1 | NA19012.hp1 | missense_variant | MODERATE | c.1634G>A | p.Arg545Gln | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 13/13 | 1810/2909 | 1634/1659 | 545/552 | chr16 | 264997 | ||
chr16:265009
|
A | G | 1 | a0003 | 8 | HG00438.hp2 HG00642.hp1 HG01975.hp1 others(5): Show |
missense_variant | MODERATE | c.1646A>G | p.Gln549Arg | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 13/13 | 1822/2909 | 1646/1659 | 549/552 | chr16 | 265009 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:254515
|
C | T | 10 | a0001c0002a0001c0005a0001c0024others(7): Show | 106 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(103): Show |
synonymous_variant | LOW | c.102C>T | p.Asn34Asn | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/13 | 278/2909 | 102/1659 | 34/552 | chr16 | 254515 | ||
chr16:254579
|
T | C | 1 | a0001c0024 | 1 | HG04228.hp1 | synonymous_variant | LOW | c.166T>C | p.Leu56Leu | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/13 | 342/2909 | 166/1659 | 56/552 | chr16 | 254579 | ||
chr16:254662
|
G | A | 1 | a0001c0012 | 1 | HG03225.hp2 | synonymous_variant | LOW | c.249G>A | p.Arg83Arg | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/13 | 425/2909 | 249/1659 | 83/552 | chr16 | 254662 | ||
chr16:259517
|
C | T | 1 | a0001c0005 | 6 | HG02559.hp1 HG02809.hp2 HG02818.hp2 others(3): Show |
synonymous_variant | LOW | c.303C>T | p.Asn101Asn | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 4/13 | 479/2909 | 303/1659 | 101/552 | chr16 | 259517 | ||
chr16:260006
|
G | A | 1 | a0001c0006 | 5 | HG00738.hp1 HG01243.hp2 HG02109.hp1 others(2): Show |
synonymous_variant | LOW | c.423G>A | p.Ser141Ser | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 5/13 | 599/2909 | 423/1659 | 141/552 | chr16 | 260006 | ||
chr16:261496
|
C | T | 1 | a0001c0021 | 1 | HG00621.hp2 | synonymous_variant | LOW | c.690C>T | p.Leu230Leu | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 6/13 | 866/2909 | 690/1659 | 230/552 | chr16 | 261496 | ||
chr16:263262
|
C | T | 1 | a0001c0020 | 1 | HG01099.hp2 | splice_region_variant&synonymous_variant | LOW | c.972C>T | p.Ser324Ser | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 9/13 | 1148/2909 | 972/1659 | 324/552 | chr16 | 263262 | ||
chr16:263766
|
C | T | 1 | a0001c0029 | 1 | NA18954.hp2 | synonymous_variant | LOW | c.1179C>T | p.Thr393Thr | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 10/13 | 1355/2909 | 1179/1659 | 393/552 | chr16 | 263766 | ||
chr16:264144
|
C | G | 1 | a0001c0019 | 1 | HG01981.hp1 | synonymous_variant | LOW | c.1317C>G | p.Leu439Leu | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 11/13 | 1493/2909 | 1317/1659 | 439/552 | chr16 | 264144 | ||
chr16:264812
|
C | T | 1 | a0001c0018 | 1 | NA18997.hp2 | splice_region_variant&synonymous_variant | LOW | c.1449C>T | p.Ala483Ala | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 13/13 | 1625/2909 | 1449/1659 | 483/552 | chr16 | 264812 | ||
chr16:264830
|
C | T | 1 | a0001c0009 | 2 | HG02056.hp2 HG02080.hp2 |
synonymous_variant | LOW | c.1467C>T | p.Ser489Ser | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 13/13 | 1643/2909 | 1467/1659 | 489/552 | chr16 | 264830 | ||
chr16:264863
|
G | T | 1 | a0001c0027 | 1 | HG00597.hp1 | synonymous_variant | LOW | c.1500G>T | p.Pro500Pro | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 13/13 | 1676/2909 | 1500/1659 | 500/552 | chr16 | 264863 | ||
chr16:264971
|
C | T | 1 | a0001c0017 | 1 | NA18999.hp2 | synonymous_variant | LOW | c.1608C>T | p.Asp536Asp | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 13/13 | 1784/2909 | 1608/1659 | 536/552 | chr16 | 264971 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:234834
|
T | G | 46 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(43): Show | 407 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(404): Show |
5_prime_UTR_variant | MODIFIER | c.-163T>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/13 | 19580 | chr16 | 234834 | |||||
chr16:234850
|
G | C | 1 | a0001c0006t0006 | 2 | HG00738.hp1 HG03209.hp2 |
5_prime_UTR_variant | MODIFIER | c.-147G>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/13 | 19564 | chr16 | 234850 | |||||
chr16:249611
|
A | G | 1 | a0001c0001t0010 | 2 | HG03098.hp1 HG03486.hp1 |
5_prime_UTR_variant | MODIFIER | c.-77A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/13 | 4803 | chr16 | 249611 | |||||
chr16:254410
|
C | T | 1 | a0001c0002t0017 | 1 | HG01192.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-4C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/13 | chr16 | 254410 | ||||||
chr16:265028
|
C | A | 1 | a0001c0001t0011 | 1 | NA18978.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6C>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 13/13 | 6 | chr16 | 265028 | |||||
chr16:265205
|
G | A | 1 | a0001c0001t0011 | 1 | NA18978.hp2 | 3_prime_UTR_variant | MODIFIER | c.*183G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 13/13 | 183 | chr16 | 265205 | |||||
chr16:265286
|
C | T | 1 | a0001c0001t0009 | 2 | HG01069.hp1 HG01071.hp1 |
3_prime_UTR_variant | MODIFIER | c.*264C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 13/13 | 264 | chr16 | 265286 | |||||
chr16:265308
|
T | G | 3 | a0001c0001t0004a0001c0001t0007a0001c0012t0004 | 8 | HG02486.hp2 HG02717.hp2 HG02886.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*286T>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 13/13 | 286 | chr16 | 265308 | |||||
chr16:265355
|
C | T | 2 | a0001c0001t0009a0001c0001t0016 | 3 | HG01069.hp1 HG01071.hp1 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*333C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 13/13 | 333 | chr16 | 265355 | |||||
chr16:265382
|
C | T | 1 | a0001c0001t0015 | 1 | HG03927.hp1 | 3_prime_UTR_variant | MODIFIER | c.*360C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 13/13 | 360 | chr16 | 265382 | |||||
chr16:265413
|
C | T | 1 | a0001c0001t0007 | 2 | HG03130.hp1 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*391C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 13/13 | 391 | chr16 | 265413 | |||||
chr16:265437
|
G | A | 18 | a0001c0001t0002a0001c0001t0004a0001c0001t0013others(15): Show | 117 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(114): Show |
3_prime_UTR_variant | MODIFIER | c.*415G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 13/13 | 415 | chr16 | 265437 | |||||
chr16:265446
|
C | T | 1 | a0001c0001t0005 | 6 | HG02559.hp2 HG02723.hp2 HG02970.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*424C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 13/13 | 424 | chr16 | 265446 | |||||
chr16:265558
|
C | G | 27 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(24): Show | 150 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(147): Show |
3_prime_UTR_variant | MODIFIER | c.*536C>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 13/13 | 536 | chr16 | 265558 | |||||
chr16:265587
|
G | A | 2 | a0001c0001t0009a0001c0001t0016 | 3 | HG01069.hp1 HG01071.hp1 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*565G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 13/13 | 565 | chr16 | 265587 | |||||
chr16:265703
|
C | T | 2 | a0001c0001t0009a0001c0001t0016 | 3 | HG01069.hp1 HG01071.hp1 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*681C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 13/13 | 681 | chr16 | 265703 | |||||
chr16:265840
|
G | A | 4 | a0001c0001t0003a0001c0009t0003a0001c0021t0003others(1): Show | 22 | HG00099.hp1 HG00621.hp2 HG00673.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*818G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 13/13 | 818 | chr16 | 265840 | |||||
chr16:265876
|
C | A | 1 | a0001c0002t0012 | 1 | NA19079.hp1 | 3_prime_UTR_variant | MODIFIER | c.*854C>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 13/13 | 854 | chr16 | 265876 | |||||
chr16:265915
|
G | A | 1 | a0001c0001t0013 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*893G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 13/13 | 893 | chr16 | 265915 | |||||
chr16:265986
|
T | C | 3 | a0001c0001t0009a0001c0001t0010a0001c0001t0016 | 5 | HG01069.hp1 HG01071.hp1 HG03098.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*964T>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 13/13 | 964 | chr16 | 265986 | |||||
chr16:265988
|
C | T | 1 | a0001c0002t0014 | 1 | HG02132.hp1 | 3_prime_UTR_variant | MODIFIER | c.*966C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 13/13 | 966 | chr16 | 265988 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:234909
|
G | A | 1 | a0001c0001t0001g0018 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.-140+52G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 234909 | ||||||
chr16:234914
|
C | T | 1 | a0001c0001t0001g0380 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-140+57C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 234914 | ||||||
chr16:234920
|
C | G | 1 | a0001c0001t0001g0379 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-140+63C>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 234920 | ||||||
chr16:234931
|
C | T | 2 | a0001c0001t0007g0377a0001c0001t0007g0378 | 2 | HG03130.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-140+74C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 234931 | ||||||
chr16:234939
|
C | T | 14 | a0002c0003t0001g0017a0002c0003t0001g0364a0002c0003t0001g0365others(11): Show | 15 | HG00621.hp1 HG01361.hp2 HG02015.hp2 others(12): Show |
intron_variant | MODIFIER | c.-140+82C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 234939 | ||||||
chr16:234987
|
C | T | 10 | a0001c0001t0001g0354a0001c0001t0001g0356a0001c0001t0001g0361others(7): Show | 10 | HG00738.hp1 HG01109.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.-140+130C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 234987 | ||||||
chr16:235044
|
A | C | 2 | a0001c0001t0001g0352a0001c0001t0001g0353 | 2 | HG01884.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.-140+187A>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 235044 | ||||||
chr16:235064
|
A | G | 1 | a0001c0001t0001g0351 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-140+207A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 235064 | ||||||
chr16:235118
|
G | A | 7 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(4): Show | 7 | HG01256.hp1 HG01517.hp2 HG01928.hp2 others(4): Show |
intron_variant | MODIFIER | c.-140+261G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 235118 | ||||||
chr16:235120
|
T | G | 2 | a0001c0001t0005g0026a0001c0001t0005g0027 | 2 | HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-140+263T>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 235120 | ||||||
chr16:235300
|
G | A | 13 | a0001c0001t0003g0036a0001c0001t0007g0377a0001c0001t0007g0378others(10): Show | 13 | HG01192.hp1 HG01361.hp1 HG01515.hp1 others(10): Show |
intron_variant | MODIFIER | c.-140+443G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 235300 | ||||||
chr16:235314
|
C | T | 136 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0019others(133): Show | 145 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(142): Show |
intron_variant | MODIFIER | c.-140+457C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 235314 | ||||||
chr16:235340
|
C | G | 1 | a0001c0001t0008g0247 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-140+483C>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 235340 | ||||||
chr16:235362
|
C | G | 1 | a0001c0001t0001g0246 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-140+505C>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 235362 | ||||||
chr16:235382
|
A | C | 2 | a0001c0001t0004g0244a0001c0001t0004g0245 | 2 | HG02717.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.-140+525A>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 235382 | ||||||
chr16:235440
|
A | G | 1 | a0001c0001t0001g0350 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.-140+583A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 235440 | ||||||
chr16:235511
|
A | T | 1 | a0001c0001t0001g0243 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-140+654A>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 235511 | ||||||
chr16:235513
|
A | C | 2 | a0001c0006t0006g0362a0001c0006t0006g0363 | 2 | HG00738.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-140+656A>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 235513 | ||||||
chr16:235590
|
C | T | 1 | a0001c0001t0005g0242 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-140+733C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 235590 | ||||||
chr16:235683
|
A | G | 1 | a0001c0001t0001g0241 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-140+826A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 235683 | ||||||
chr16:235789
|
A | C | 1 | a0001c0001t0005g0240 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-140+932A>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 235789 | ||||||
chr16:235811
|
G | A | 1 | a0001c0001t0001g0039 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-140+954G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 235811 | ||||||
chr16:235927
|
C | T | 20 | a0001c0001t0001g0224a0001c0001t0001g0225a0001c0001t0001g0230others(17): Show | 20 | HG01106.hp1 HG01891.hp1 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.-140+1070C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 235927 | ||||||
chr16:235946
|
A | G | 2 | a0001c0001t0001g0222a0001c0001t0001g0223 | 2 | NA19005.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.-140+1089A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 235946 | ||||||
chr16:235969
|
A | G | 2 | a0001c0006t0001g0037a0001c0006t0001g0038 | 2 | HG02109.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.-140+1112A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 235969 | ||||||
chr16:235983
|
T | G | 1 | a0001c0001t0001g0224 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-140+1126T>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 235983 | ||||||
chr16:235998
|
A | C | 1 | a0001c0001t0003g0036 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-140+1141A>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 235998 | ||||||
chr16:236009
|
T | C | 122 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0018others(119): Show | 126 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(123): Show |
intron_variant | MODIFIER | c.-140+1152T>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 236009 | ||||||
chr16:236088
|
G | C | 5 | a0001c0001t0002g0249a0001c0001t0010g0248a0001c0001t0010g0250others(2): Show | 5 | HG00738.hp1 HG03098.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.-140+1231G>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 236088 | ||||||
chr16:236243
|
A | G | 9 | a0001c0001t0001g0218a0001c0001t0001g0221a0001c0001t0003g0213others(6): Show | 9 | HG00621.hp2 HG00673.hp2 HG03704.hp2 others(6): Show |
intron_variant | MODIFIER | c.-140+1386A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 236243 | ||||||
chr16:236249
|
A | C | 2 | a0001c0006t0006g0362a0001c0006t0006g0363 | 2 | HG00738.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-140+1392A>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 236249 | ||||||
chr16:236334
|
A | T | 3 | a0001c0001t0001g0212a0001c0006t0006g0362a0001c0006t0006g0363 | 3 | HG00738.hp1 HG03209.hp2 NA18945.hp1 |
intron_variant | MODIFIER | c.-140+1477A>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 236334 | ||||||
chr16:236353
|
A | G | 2 | a0001c0001t0001g0210a0001c0001t0001g0211 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.-140+1496A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 236353 | ||||||
chr16:236358
|
C | G | 1 | a0001c0002t0002g0123 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-140+1501C>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 236358 | ||||||
chr16:236388
|
T | G | 2 | a0001c0006t0006g0362a0001c0006t0006g0363 | 2 | HG00738.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-140+1531T>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 236388 | ||||||
chr16:236389
|
T | C | 2 | a0001c0006t0006g0362a0001c0006t0006g0363 | 2 | HG00738.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-140+1532T>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 236389 | ||||||
chr16:236502
|
A | G | 2 | a0001c0006t0006g0362a0001c0006t0006g0363 | 2 | HG00738.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-140+1645A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 236502 | ||||||
chr16:236568
|
A | C | 2 | a0001c0006t0006g0362a0001c0006t0006g0363 | 2 | HG00738.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-140+1711A>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 236568 | ||||||
chr16:236580
|
A | G | 2 | a0001c0006t0006g0362a0001c0006t0006g0363 | 2 | HG00738.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-140+1723A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 236580 | ||||||
chr16:236588
|
G | A | 2 | a0001c0006t0006g0362a0001c0006t0006g0363 | 2 | HG00738.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-140+1731G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 236588 | ||||||
chr16:236595
|
A | C | 2 | a0001c0006t0006g0362a0001c0006t0006g0363 | 2 | HG00738.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-140+1738A>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 236595 | ||||||
chr16:236629
|
G | A | 2 | a0001c0006t0006g0362a0001c0006t0006g0363 | 2 | HG00738.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-140+1772G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 236629 | ||||||
chr16:236644
|
C | A | 2 | a0001c0002t0002g0013a0009c0025t0002g0013 | 2 | NA18975.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.-140+1787C>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 236644 | ||||||
chr16:236681
|
C | T | 14 | a0002c0003t0001g0017a0002c0003t0001g0364a0002c0003t0001g0365others(11): Show | 15 | HG00621.hp1 HG01361.hp2 HG02015.hp2 others(12): Show |
intron_variant | MODIFIER | c.-140+1824C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 236681 | ||||||
chr16:236712
|
G | C | 2 | a0001c0006t0006g0362a0001c0006t0006g0363 | 2 | HG00738.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-140+1855G>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 236712 | ||||||
chr16:236797
|
G | T | 133 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0019others(130): Show | 141 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(138): Show |
intron_variant | MODIFIER | c.-140+1940G>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 236797 | ||||||
chr16:236798
|
C | T | 133 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0019others(130): Show | 141 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(138): Show |
intron_variant | MODIFIER | c.-140+1941C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 236798 | ||||||
chr16:236803
|
G | A | 4 | a0001c0001t0001g0225a0001c0001t0004g0226a0001c0001t0004g0227others(1): Show | 4 | HG02486.hp2 HG03041.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.-140+1946G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 236803 | ||||||
chr16:236824
|
G | T | 132 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0019others(129): Show | 140 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(137): Show |
intron_variant | MODIFIER | c.-140+1967G>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 236824 | ||||||
chr16:236825
|
A | G | 134 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0019others(131): Show | 142 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(139): Show |
intron_variant | MODIFIER | c.-140+1968A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 236825 | ||||||
chr16:236827
|
AC | A | 132 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0019others(129): Show | 140 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(137): Show |
intron_variant | MODIFIER | c.-140+1974delC | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 236827 | |||||
chr16:236835
|
G | A | 131 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0019others(128): Show | 139 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(136): Show |
intron_variant | MODIFIER | c.-140+1978G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 236835 | ||||||
chr16:236844
|
C | T | 131 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0019others(128): Show | 139 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(136): Show |
intron_variant | MODIFIER | c.-140+1987C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 236844 | ||||||
chr16:236862
|
G | C | 132 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0019others(129): Show | 140 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(137): Show |
intron_variant | MODIFIER | c.-140+2005G>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 236862 | ||||||
chr16:236885
|
C | CGA | 132 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0019others(129): Show | 140 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(137): Show |
intron_variant | MODIFIER | c.-140+2028_-140+202 others(6): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 236885 | ||||||
chr16:236888
|
C | G | 132 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0019others(129): Show | 140 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(137): Show |
intron_variant | MODIFIER | c.-140+2031C>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 236888 | ||||||
chr16:236897
|
T | TCC | 132 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0019others(129): Show | 140 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(137): Show |
intron_variant | MODIFIER | c.-140+2040_-140+204 others(6): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 236897 | ||||||
chr16:236903
|
A | AAAAAAAA others(8): Show |
2 | a0001c0006t0001g0037a0001c0006t0001g0038 | 2 | HG02109.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.-140+2052_-140+205 others(19): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 236903 | |||||
chr16:236903
|
A | AAAAAAAT others(8): Show |
1 | a0001c0001t0013g0035 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-140+2056_-140+205 others(19): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 236903 | |||||
chr16:236905
|
A | AAAAAAAA others(13): Show |
10 | a0001c0001t0007g0377a0001c0001t0007g0378a0001c0002t0002g0029others(7): Show | 10 | HG01074.hp1 HG01192.hp1 HG01361.hp1 others(7): Show |
intron_variant | MODIFIER | c.-140+2052_-140+205 others(24): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 236905 | |||||
chr16:236905
|
A | AAAAAAAA others(14): Show |
1 | a0001c0001t0003g0253 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-140+2052_-140+205 others(25): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 236905 | |||||
chr16:236905
|
A | AAAAAAAA others(13): Show |
117 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0019others(114): Show | 125 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(122): Show |
intron_variant | MODIFIER | c.-140+2052_-140+205 others(24): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 236905 | |||||
chr16:236905
|
A | AAAAAAAA others(13): Show |
1 | a0001c0002t0002g0349 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.-140+2052_-140+205 others(24): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 236905 | |||||
chr16:236929
|
A | T | 1 | a0001c0001t0001g0205 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-140+2072A>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 236929 | ||||||
chr16:236983
|
T | C | 286 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(283): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.-140+2126T>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 236983 | ||||||
chr16:237058
|
T | C | 1 | a0001c0002t0002g0254 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-140+2201T>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 237058 | ||||||
chr16:237071
|
A | AT | 87 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0018others(84): Show | 90 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.-140+2221dupT | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 237071 | |||||
chr16:237078
|
T | A | 2 | a0001c0006t0006g0362a0001c0006t0006g0363 | 2 | HG00738.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-140+2221T>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 237078 | ||||||
chr16:237079
|
A | T | 268 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(265): Show | 281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.-140+2222A>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 237079 | ||||||
chr16:237080
|
A | T | 2 | a0001c0001t0001g0122a0001c0001t0005g0242 | 2 | HG02451.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.-140+2223A>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 237080 | ||||||
chr16:237092
|
G | A | 1 | a0001c0001t0001g0052 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.-140+2235G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 237092 | ||||||
chr16:237211
|
T | C | 2 | a0001c0006t0006g0362a0001c0006t0006g0363 | 2 | HG00738.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-140+2354T>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 237211 | ||||||
chr16:237235
|
C | T | 4 | a0001c0001t0001g0012a0001c0001t0001g0202a0001c0001t0001g0203others(1): Show | 5 | NA18612.hp1 NA18949.hp2 NA18981.hp1 others(2): Show |
intron_variant | MODIFIER | c.-140+2378C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 237235 | ||||||
chr16:237324
|
T | A | 1 | a0001c0001t0001g0039 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-140+2467T>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 237324 | ||||||
chr16:237383
|
G | A | 18 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0056others(15): Show | 18 | HG00639.hp1 HG01243.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.-140+2526G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 237383 | ||||||
chr16:237389
|
C | T | 14 | a0002c0003t0001g0017a0002c0003t0001g0364a0002c0003t0001g0365others(11): Show | 15 | HG00621.hp1 HG01361.hp2 HG02015.hp2 others(12): Show |
intron_variant | MODIFIER | c.-140+2532C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 237389 | ||||||
chr16:237485
|
A | G | 1 | a0001c0002t0002g0348 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-140+2628A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 237485 | ||||||
chr16:237557
|
C | T | 1 | a0001c0002t0002g0251 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-140+2700C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 237557 | ||||||
chr16:237713
|
C | CT | 84 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0016others(81): Show | 88 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.-140+2872dupT | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 237713 | |||||
chr16:237742
|
T | C | 2 | a0001c0006t0006g0362a0001c0006t0006g0363 | 2 | HG00738.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-140+2885T>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 237742 | ||||||
chr16:237791
|
G | A | 2 | a0001c0006t0006g0362a0001c0006t0006g0363 | 2 | HG00738.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-140+2934G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 237791 | ||||||
chr16:237844
|
C | A | 2 | a0001c0002t0002g0040a0001c0002t0002g0041 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.-140+2987C>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 237844 | ||||||
chr16:237892
|
C | T | 12 | a0001c0001t0001g0354a0001c0001t0001g0356a0001c0001t0001g0361others(9): Show | 13 | HG01109.hp2 HG02109.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.-140+3035C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 237892 | ||||||
chr16:237918
|
C | G | 113 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0016others(110): Show | 118 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.-140+3061C>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 237918 | ||||||
chr16:237951
|
G | T | 2 | a0001c0006t0006g0362a0001c0006t0006g0363 | 2 | HG00738.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-140+3094G>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 237951 | ||||||
chr16:238007
|
GTTATTTA others(3): Show |
G | 2 | a0001c0006t0006g0362a0001c0006t0006g0363 | 2 | HG00738.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-140+3161_-140+317 others(14): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 238007 | |||||
chr16:238010
|
ATTTATT | A | 269 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(266): Show | 282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.-140+3161_-140+316 others(10): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 238010 | |||||
chr16:238045
|
T | G | 1 | a0001c0001t0001g0019 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.-140+3188T>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 238045 | ||||||
chr16:238185
|
A | G | 13 | a0002c0003t0001g0017a0002c0003t0001g0365a0002c0003t0001g0366others(10): Show | 14 | HG00621.hp1 HG01361.hp2 HG02015.hp2 others(11): Show |
intron_variant | MODIFIER | c.-140+3328A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 238185 | ||||||
chr16:238216
|
G | C | 3 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135 | 3 | HG02135.hp2 NA18965.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.-140+3359G>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 238216 | ||||||
chr16:238303
|
A | G | 2 | a0001c0006t0006g0362a0001c0006t0006g0363 | 2 | HG00738.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-140+3446A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 238303 | ||||||
chr16:238325
|
G | A | 1 | a0001c0001t0003g0036 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-140+3468G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 238325 | ||||||
chr16:238519
|
C | A | 1 | a0001c0001t0001g0042 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-140+3662C>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 238519 | ||||||
chr16:238542
|
A | G | 4 | a0001c0001t0004g0244a0001c0001t0004g0245a0001c0006t0006g0362others(1): Show | 4 | HG00738.hp1 HG02717.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.-140+3685A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 238542 | ||||||
chr16:238543
|
G | A | 1 | a0001c0009t0003g0257 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-140+3686G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 238543 | ||||||
chr16:238562
|
C | G | 111 | a0001c0001t0001g0016a0001c0001t0001g0052a0001c0001t0001g0073others(108): Show | 116 | HG00544.hp1 HG00597.hp1 HG00642.hp2 others(113): Show |
intron_variant | MODIFIER | c.-140+3705C>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 238562 | ||||||
chr16:238562
|
C | T | 2 | a0001c0006t0006g0362a0001c0006t0006g0363 | 2 | HG00738.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-140+3705C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 238562 | ||||||
chr16:238583
|
A | G | 18 | a0001c0001t0001g0196a0001c0001t0001g0197a0001c0001t0003g0253others(15): Show | 19 | HG00733.hp2 HG02056.hp2 HG02080.hp2 others(16): Show |
intron_variant | MODIFIER | c.-140+3726A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 238583 | ||||||
chr16:238619
|
A | T | 1 | a0001c0001t0001g0102 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-140+3762A>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 238619 | ||||||
chr16:238691
|
G | A | 1 | a0001c0001t0001g0258 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-140+3834G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 238691 | ||||||
chr16:238720
|
C | A | 1 | a0001c0002t0002g0293 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-140+3863C>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 238720 | ||||||
chr16:238727
|
C | T | 2 | a0001c0006t0006g0362a0001c0006t0006g0363 | 2 | HG00738.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-140+3870C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 238727 | ||||||
chr16:238763
|
C | G | 2 | a0001c0006t0006g0362a0001c0006t0006g0363 | 2 | HG00738.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-140+3906C>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 238763 | ||||||
chr16:238765
|
C | CA | 130 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(127): Show | 136 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(133): Show |
intron_variant | MODIFIER | c.-140+3929dupA | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 238765 | |||||
chr16:238765
|
C | CAA | 32 | a0001c0001t0001g0016a0001c0001t0001g0020a0001c0001t0001g0042others(29): Show | 34 | HG00423.hp2 HG00621.hp1 HG00673.hp1 others(31): Show |
intron_variant | MODIFIER | c.-140+3928_-140+392 others(6): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 238765 | |||||
chr16:238765
|
CAAAAAAA others(4): Show |
C | 2 | a0001c0001t0001g0100a0001c0001t0001g0101 | 2 | HG03831.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.-140+3919_-140+392 others(15): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 238765 | |||||
chr16:238775
|
A | G | 2 | a0001c0006t0006g0362a0001c0006t0006g0363 | 2 | HG00738.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-140+3918A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 238775 | ||||||
chr16:238776
|
AAAAAAAA others(4): Show |
A | 2 | a0001c0006t0006g0362a0001c0006t0006g0363 | 2 | HG00738.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-140+3930_-140+394 others(15): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 238776 | |||||
chr16:238780
|
A | G | 82 | a0001c0001t0001g0209a0001c0001t0001g0287a0001c0001t0001g0332others(79): Show | 86 | HG00544.hp1 HG00597.hp1 HG00642.hp2 others(83): Show |
intron_variant | MODIFIER | c.-140+3923A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 238780 | ||||||
chr16:238781
|
A | G | 3 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195 | 3 | NA18999.hp1 NA19009.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.-140+3924A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 238781 | ||||||
chr16:238782
|
A | G | 1 | a0001c0001t0001g0221 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-140+3925A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 238782 | ||||||
chr16:238850
|
T | C | 88 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0016others(85): Show | 92 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.-140+3993T>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 238850 | ||||||
chr16:238896
|
A | G | 2 | a0001c0001t0002g0126a0001c0001t0002g0128 | 2 | HG02055.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.-140+4039A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 238896 | ||||||
chr16:238919
|
C | CAAAAAA | 8 | a0002c0003t0001g0017a0002c0003t0001g0369a0002c0003t0001g0370others(5): Show | 9 | HG00621.hp1 HG02015.hp2 HG02027.hp1 others(6): Show |
intron_variant | MODIFIER | c.-140+4070_-140+407 others(10): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 238919 | |||||
chr16:238919
|
C | CAAAAAAA | 6 | a0001c0001t0003g0036a0002c0003t0001g0365a0002c0003t0001g0366others(3): Show | 6 | HG01361.hp2 HG03486.hp2 NA18959.hp2 others(3): Show |
intron_variant | MODIFIER | c.-140+4069_-140+407 others(11): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 238919 | |||||
chr16:239021
|
G | A | 3 | a0001c0001t0002g0249a0001c0001t0010g0248a0001c0001t0010g0250 | 3 | HG03098.hp1 HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-140+4164G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 239021 | ||||||
chr16:239022
|
C | T | 1 | a0001c0001t0001g0099 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-140+4165C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 239022 | ||||||
chr16:239076
|
C | T | 4 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0002t0002g0046others(1): Show | 4 | HG00140.hp2 HG02698.hp1 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.-140+4219C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 239076 | ||||||
chr16:239168
|
C | T | 1 | a0002c0003t0001g0373 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-140+4311C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 239168 | ||||||
chr16:239175
|
C | CTGTAGTC others(1020): Show |
1 | a0001c0001t0007g0377 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-140+4341_-140+434 others(1031): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 239175 | |||||
chr16:239175
|
C | CTGTAGTC others(1013): Show |
1 | a0001c0001t0001g0146 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-140+4341_-140+434 others(1024): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 239175 | |||||
chr16:239175
|
C | CTGTAGTC others(1013): Show |
1 | a0001c0001t0001g0198 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-140+4341_-140+434 others(1024): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 239175 | |||||
chr16:239175
|
C | CTGTAGTC others(1021): Show |
1 | a0001c0002t0017g0028 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-140+4341_-140+434 others(1032): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 239175 | |||||
chr16:239175
|
C | CTGTAGTC others(1030): Show |
1 | a0004c0007t0001g0049 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-140+4341_-140+434 others(1041): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 239175 | |||||
chr16:239175
|
C | CTGTAGTC others(1029): Show |
1 | a0004c0007t0001g0050 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-140+4341_-140+434 others(1040): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 239175 | |||||
chr16:239175
|
C | CTGTAGTC others(1027): Show |
3 | a0001c0001t0001g0231a0001c0001t0010g0248a0001c0002t0002g0229 | 3 | HG01106.hp1 HG02258.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-140+4341_-140+434 others(1038): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 239175 | |||||
chr16:239175
|
C | CTGTAGTC others(1026): Show |
4 | a0001c0001t0001g0232a0001c0001t0002g0249a0001c0001t0003g0355others(1): Show | 4 | HG01109.hp2 HG03195.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.-140+4341_-140+434 others(1037): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 239175 | |||||
chr16:239175
|
C | CTGTAGTC others(1025): Show |
1 | a0004c0007t0001g0051 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-140+4341_-140+434 others(1036): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 239175 | |||||
chr16:239175
|
C | CTGTAGTC others(1025): Show |
10 | a0001c0001t0001g0224a0001c0001t0001g0230a0001c0001t0001g0235others(7): Show | 10 | HG02109.hp2 HG02622.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.-140+4341_-140+434 others(1036): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 239175 | |||||
chr16:239175
|
C | CTGTAGTC others(1024): Show |
1 | a0001c0001t0001g0356 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-140+4341_-140+434 others(1035): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 239175 | |||||
chr16:239175
|
C | CTGTAGTC others(1024): Show |
1 | a0001c0001t0003g0036 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-140+4341_-140+434 others(1035): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 239175 | |||||
chr16:239175
|
C | CTGTAGTC others(1023): Show |
1 | a0001c0001t0003g0253 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-140+4341_-140+434 others(1034): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 239175 | |||||
chr16:239175
|
C | CTGTAGTC others(1023): Show |
3 | a0001c0006t0001g0037a0001c0006t0001g0038a0001c0006t0001g0055 | 3 | HG01243.hp2 HG02109.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.-140+4341_-140+434 others(1034): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 239175 | |||||
chr16:239175
|
C | CTGTAGTC others(1023): Show |
5 | a0001c0001t0001g0361a0001c0002t0002g0357a0001c0002t0002g0358others(2): Show | 5 | HG02572.hp1 HG02572.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.-140+4341_-140+434 others(1034): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 239175 | |||||
chr16:239175
|
C | CTGTAGTC others(1021): Show |
1 | a0001c0002t0002g0295 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-140+4341_-140+434 others(1032): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 239175 | |||||
chr16:239175
|
C | CTGTAGTC others(1022): Show |
1 | a0001c0005t0002g0129 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-140+4341_-140+434 others(1033): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 239175 | |||||
chr16:239175
|
C | CTGTAGTC others(1020): Show |
5 | a0001c0002t0002g0296a0001c0002t0002g0297a0001c0002t0002g0298others(2): Show | 5 | HG04199.hp1 NA18946.hp2 NA19070.hp2 others(2): Show |
intron_variant | MODIFIER | c.-140+4341_-140+434 others(1031): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 239175 | |||||
chr16:239175
|
C | CTGTAGTC others(1021): Show |
2 | a0001c0001t0013g0035a0001c0005t0002g0130 | 2 | HG03130.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-140+4341_-140+434 others(1032): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 239175 | |||||
chr16:239175
|
C | CTGTAGTC others(1021): Show |
9 | a0001c0002t0002g0029a0001c0002t0002g0030a0001c0002t0002g0254others(6): Show | 9 | HG00642.hp2 HG01361.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.-140+4341_-140+434 others(1032): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 239175 | |||||
chr16:239175
|
C | CTGTAGTC others(1020): Show |
1 | a0001c0002t0002g0237 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-140+4341_-140+434 others(1031): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 239175 | |||||
chr16:239175
|
C | CTGTAGTC others(1019): Show |
28 | a0001c0002t0002g0001a0001c0002t0002g0206a0001c0002t0002g0285others(25): Show | 32 | HG00597.hp1 HG00733.hp1 HG01070.hp2 others(29): Show |
intron_variant | MODIFIER | c.-140+4341_-140+434 others(1030): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 239175 | |||||
chr16:239175
|
C | CTGTAGTC others(1020): Show |
3 | a0001c0005t0002g0010a0001c0005t0002g0131a0001c0012t0004g0238 | 4 | HG02559.hp1 HG02809.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-140+4341_-140+434 others(1031): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 239175 | |||||
chr16:239175
|
C | CTGTAGTC others(1020): Show |
33 | a0001c0001t0001g0209a0001c0001t0001g0287a0001c0001t0001g0332others(30): Show | 33 | HG01074.hp1 HG01515.hp1 HG01517.hp1 others(30): Show |
intron_variant | MODIFIER | c.-140+4341_-140+434 others(1031): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 239175 | |||||
chr16:239175
|
C | CTGTAGTC others(1019): Show |
1 | a0011c0028t0002g0256 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-140+4341_-140+434 others(1030): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 239175 | |||||
chr16:239175
|
C | CTGTAGTC others(1019): Show |
1 | a0001c0002t0002g0239 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-140+4341_-140+434 others(1030): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 239175 | |||||
chr16:239175
|
C | CTGTAGTC others(1018): Show |
2 | a0001c0002t0002g0343a0001c0002t0002g0344 | 2 | NA19068.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.-140+4341_-140+434 others(1029): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 239175 | |||||
chr16:239175
|
C | CTGTAGTC others(1019): Show |
1 | a0001c0002t0002g0345 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-140+4341_-140+434 others(1030): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 239175 | |||||
chr16:239175
|
C | CTGTAGTC others(1013): Show |
5 | a0001c0001t0001g0147a0001c0001t0001g0148a0001c0001t0002g0126others(2): Show | 5 | HG00609.hp2 HG01978.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.-140+4341_-140+434 others(1024): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 239175 | |||||
chr16:239175
|
C | CTGTAGTC others(1011): Show |
13 | a0002c0003t0001g0017a0002c0003t0001g0365a0002c0003t0001g0366others(10): Show | 14 | HG00621.hp1 HG01361.hp2 HG02015.hp2 others(11): Show |
intron_variant | MODIFIER | c.-140+4341_-140+434 others(1022): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 239175 | |||||
chr16:239175
|
C | CTGTAGTC others(1012): Show |
124 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(121): Show | 137 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(134): Show |
intron_variant | MODIFIER | c.-140+4341_-140+434 others(1023): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 239175 | |||||
chr16:239175
|
C | CTGTAGTC others(1011): Show |
1 | a0001c0001t0001g0189 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-140+4341_-140+434 others(1022): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 239175 | |||||
chr16:239175
|
C | CTGTAGTC others(1011): Show |
13 | a0001c0001t0001g0024a0001c0001t0001g0190a0001c0001t0001g0191others(10): Show | 13 | HG00738.hp1 HG01070.hp1 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.-140+4341_-140+434 others(1022): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 239175 | |||||
chr16:239175
|
C | CTGTAGTC others(1008): Show |
7 | a0001c0001t0001g0258a0001c0001t0003g0288a0001c0001t0003g0289others(4): Show | 7 | HG00733.hp2 HG02080.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-140+4341_-140+434 others(1019): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 239175 | |||||
chr16:239175
|
C | CTGTAGTC others(1009): Show |
1 | a0001c0009t0003g0292 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-140+4341_-140+434 others(1020): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 239175 | |||||
chr16:239175
|
C | CTGTAGTC others(1005): Show |
4 | a0001c0001t0001g0225a0001c0001t0004g0226a0001c0001t0004g0227others(1): Show | 4 | HG02486.hp2 HG03041.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.-140+4341_-140+434 others(1016): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 239175 | |||||
chr16:239175
|
C | CTGTAGTC others(1005): Show |
1 | a0001c0001t0003g0214 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.-140+4341_-140+434 others(1016): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 239175 | |||||
chr16:239175
|
C | CTGTAGTC others(1012): Show |
1 | a0001c0001t0001g0282 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-140+4341_-140+434 others(1023): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 239175 | |||||
chr16:239175
|
C | CTGTAGTC others(1011): Show |
2 | a0001c0001t0005g0026a0001c0001t0005g0027 | 2 | HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-140+4341_-140+434 others(1022): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 239175 | |||||
chr16:239175
|
C | CTGTAGTC others(1007): Show |
1 | a0001c0001t0003g0283 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-140+4341_-140+434 others(1018): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 239175 | |||||
chr16:239175
|
C | CTGTAGTC others(1022): Show |
5 | a0001c0001t0001g0054a0001c0001t0001g0079a0001c0001t0001g0080others(2): Show | 5 | HG02027.hp2 HG02145.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.-140+4332_-140+433 others(1033): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 239175 | |||||
chr16:239175
|
C | CTGTAGTC others(1022): Show |
5 | a0001c0001t0001g0073a0001c0001t0001g0105a0001c0001t0001g0107others(2): Show | 5 | HG01123.hp1 NA18967.hp2 NA18978.hp2 others(2): Show |
intron_variant | MODIFIER | c.-140+4332_-140+433 others(1033): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 239175 | |||||
chr16:239175
|
C | CTGTAGTC others(1021): Show |
18 | a0001c0001t0001g0018a0001c0001t0001g0042a0001c0001t0001g0044others(15): Show | 18 | HG00423.hp2 HG00673.hp1 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.-140+4332_-140+433 others(1032): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 239175 | |||||
chr16:239175
|
C | CTGTAGTC others(1021): Show |
15 | a0001c0001t0001g0052a0001c0001t0001g0108a0001c0001t0001g0109others(12): Show | 15 | HG01255.hp1 HG01993.hp2 HG02293.hp2 others(12): Show |
intron_variant | MODIFIER | c.-140+4332_-140+433 others(1032): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 239175 | |||||
chr16:239175
|
C | CTGTAGTC others(1020): Show |
15 | a0001c0001t0001g0008a0001c0001t0001g0056a0001c0001t0001g0071others(12): Show | 16 | HG00408.hp2 HG00609.hp1 HG00639.hp1 others(13): Show |
intron_variant | MODIFIER | c.-140+4332_-140+433 others(1031): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 239175 | |||||
chr16:239175
|
C | CTGTAGTC others(1022): Show |
1 | a0001c0001t0001g0121 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-140+4332_-140+433 others(1033): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 239175 | |||||
chr16:239175
|
C | CTGTAGTC others(1021): Show |
1 | a0001c0001t0001g0072 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-140+4332_-140+433 others(1032): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 239175 | |||||
chr16:239175
|
C | CTGTAGTC others(1019): Show |
1 | a0001c0001t0015g0093 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-140+4332_-140+433 others(1030): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 239175 | |||||
chr16:239175
|
C | CTGTAGTC others(1019): Show |
5 | a0001c0001t0001g0003a0001c0001t0001g0077a0001c0001t0001g0094others(2): Show | 7 | HG00738.hp2 HG01167.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.-140+4332_-140+433 others(1030): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 239175 | |||||
chr16:239175
|
C | CTGTAGTC others(1021): Show |
1 | a0001c0001t0001g0057 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-140+4332_-140+433 others(1032): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 239175 | |||||
chr16:239175
|
C | CTGTAGTC others(1020): Show |
11 | a0001c0001t0001g0053a0001c0001t0001g0058a0001c0001t0001g0060others(8): Show | 11 | HG01884.hp1 HG02055.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.-140+4332_-140+433 others(1031): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 239175 | |||||
chr16:239175
|
C | CTGTAGTC others(1019): Show |
1 | a0001c0001t0001g0066 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-140+4332_-140+433 others(1030): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 239175 | |||||
chr16:239175
|
C | CTGTAGTC others(1021): Show |
1 | a0001c0001t0001g0067 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-140+4332_-140+433 others(1032): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 239175 | |||||
chr16:239175
|
C | CTGTAGTC others(1020): Show |
1 | a0001c0002t0002g0068 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-140+4332_-140+433 others(1031): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 239175 | |||||
chr16:239175
|
C | CTGTAGTC others(1020): Show |
3 | a0001c0001t0001g0016a0001c0001t0003g0078a0001c0001t0003g0096 | 4 | HG01074.hp2 HG01106.hp2 HG01123.hp2 others(1): Show |
intron_variant | MODIFIER | c.-140+4332_-140+433 others(1031): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 239175 | |||||
chr16:239175
|
C | CTGTAGTC others(1022): Show |
2 | a0001c0001t0001g0097a0001c0002t0002g0123 | 2 | HG00140.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.-140+4332_-140+433 others(1033): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 239175 | |||||
chr16:239175
|
C | CTGTAGTC others(1021): Show |
2 | a0001c0001t0001g0098a0001c0002t0002g0046 | 2 | HG03239.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.-140+4332_-140+433 others(1032): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 239175 | |||||
chr16:239199
|
A | G | 1 | a0001c0001t0005g0027 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-140+4342A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 239199 | ||||||
chr16:239278
|
C | T | 1 | a0001c0002t0002g0342 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-140+4421C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 239278 | ||||||
chr16:239294
|
T | C | 5 | a0001c0001t0002g0249a0001c0001t0004g0244a0001c0001t0004g0245others(2): Show | 5 | HG02717.hp2 HG02886.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.-140+4437T>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 239294 | ||||||
chr16:239336
|
G | A | 22 | a0001c0001t0001g0224a0001c0001t0001g0230a0001c0001t0001g0231others(19): Show | 22 | HG01106.hp1 HG01109.hp2 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.-140+4479G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 239336 | ||||||
chr16:239342
|
G | A | 1 | a0001c0001t0013g0035 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-140+4485G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 239342 | ||||||
chr16:239410
|
G | A | 1 | a0001c0001t0001g0042 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-140+4553G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 239410 | ||||||
chr16:239614
|
C | CA | 35 | a0001c0001t0001g0025a0001c0001t0001g0053a0001c0001t0001g0072others(32): Show | 36 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(33): Show |
intron_variant | MODIFIER | c.-140+4775dupA | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 239614 | |||||
chr16:239614
|
C | CAA | 88 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0016others(85): Show | 92 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.-140+4774_-140+477 others(6): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 239614 | |||||
chr16:239614
|
CA | C | 19 | a0001c0001t0001g0186a0001c0001t0001g0279a0001c0001t0003g0253others(16): Show | 20 | HG00621.hp1 HG01167.hp2 HG01361.hp2 others(17): Show |
intron_variant | MODIFIER | c.-140+4775delA | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 239614 | |||||
chr16:239688
|
G | A | 1 | a0001c0001t0003g0036 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-140+4831G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 239688 | ||||||
chr16:239695
|
T | C | 237 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0016others(234): Show | 247 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(244): Show |
intron_variant | MODIFIER | c.-140+4838T>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 239695 | ||||||
chr16:239699
|
T | C | 3 | a0001c0001t0001g0231a0001c0001t0003g0233a0001c0001t0003g0234 | 3 | HG01106.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-140+4842T>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 239699 | ||||||
chr16:239840
|
T | C | 3 | a0004c0007t0001g0049a0004c0007t0001g0050a0004c0007t0001g0051 | 3 | NA19043.hp2 NA19240.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-140+4983T>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 239840 | ||||||
chr16:239938
|
G | C | 1 | a0001c0001t0001g0205 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-140+5081G>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 239938 | ||||||
chr16:239977
|
A | G | 1 | a0001c0001t0001g0122 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-140+5120A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 239977 | ||||||
chr16:240166
|
C | A | 2 | a0001c0001t0001g0264a0001c0001t0001g0265 | 2 | HG00099.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.-140+5309C>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 240166 | ||||||
chr16:240193
|
G | A | 1 | a0001c0001t0005g0240 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-140+5336G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 240193 | ||||||
chr16:240305
|
C | T | 35 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0020others(32): Show | 38 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(35): Show |
intron_variant | MODIFIER | c.-140+5448C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 240305 | ||||||
chr16:240500
|
GTA | G | 9 | a0001c0001t0001g0224a0001c0001t0001g0230a0001c0001t0001g0231others(6): Show | 9 | HG01106.hp1 HG02622.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.-140+5645_-140+564 others(6): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 240500 | |||||
chr16:240502
|
A | AT | 18 | a0001c0001t0001g0023a0001c0001t0001g0091a0001c0001t0001g0092others(15): Show | 18 | HG00423.hp2 HG00609.hp1 HG00733.hp2 others(15): Show |
intron_variant | MODIFIER | c.-140+5662dupT | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 240502 | |||||
chr16:240502
|
AT | A | 108 | a0001c0001t0001g0085a0001c0001t0001g0120a0001c0001t0001g0209others(105): Show | 113 | HG00544.hp1 HG00597.hp1 HG00621.hp1 others(110): Show |
intron_variant | MODIFIER | c.-140+5662delT | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 240502 | |||||
chr16:240543
|
C | T | 1 | a0001c0002t0002g0123 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-140+5686C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 240543 | ||||||
chr16:240593
|
C | T | 1 | a0001c0001t0001g0277 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-140+5736C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 240593 | ||||||
chr16:240602
|
A | T | 1 | a0001c0002t0017g0028 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-140+5745A>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 240602 | ||||||
chr16:240626
|
C | T | 7 | a0001c0001t0001g0224a0001c0001t0001g0230a0001c0001t0001g0232others(4): Show | 7 | HG02258.hp1 HG02622.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.-140+5769C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 240626 | ||||||
chr16:240925
|
C | T | 1 | a0001c0001t0001g0380 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-140+6068C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 240925 | ||||||
chr16:240927
|
TTTAAAAC others(4): Show |
T | 1 | a0001c0001t0001g0090 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.-140+6073_-140+608 others(15): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 240927 | |||||
chr16:241048
|
C | T | 1 | a0001c0001t0001g0103 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-140+6191C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 241048 | ||||||
chr16:241275
|
G | GAA | 234 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0016others(231): Show | 244 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(241): Show |
intron_variant | MODIFIER | c.-140+6428_-140+642 others(6): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 241275 | |||||
chr16:241350
|
G | C | 1 | a0001c0001t0003g0036 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-140+6493G>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 241350 | ||||||
chr16:241406
|
G | T | 14 | a0002c0003t0001g0017a0002c0003t0001g0364a0002c0003t0001g0365others(11): Show | 15 | HG00621.hp1 HG01361.hp2 HG02015.hp2 others(12): Show |
intron_variant | MODIFIER | c.-140+6549G>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 241406 | ||||||
chr16:241476
|
C | A | 14 | a0002c0003t0001g0017a0002c0003t0001g0364a0002c0003t0001g0365others(11): Show | 15 | HG00621.hp1 HG01361.hp2 HG02015.hp2 others(12): Show |
intron_variant | MODIFIER | c.-140+6619C>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 241476 | ||||||
chr16:241535
|
G | A | 1 | a0004c0007t0001g0050 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-140+6678G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 241535 | ||||||
chr16:241588
|
C | CA | 16 | a0001c0001t0001g0150a0001c0002t0002g0326a0002c0003t0001g0017others(13): Show | 17 | HG00621.hp1 HG01361.hp2 HG02015.hp2 others(14): Show |
intron_variant | MODIFIER | c.-140+6743dupA | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 241588 | |||||
chr16:241645
|
C | T | 12 | a0001c0001t0001g0258a0001c0001t0003g0283a0001c0001t0003g0288others(9): Show | 12 | HG00733.hp2 HG02056.hp2 HG02080.hp2 others(9): Show |
intron_variant | MODIFIER | c.-140+6788C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 241645 | ||||||
chr16:241655
|
G | C | 12 | a0001c0001t0001g0258a0001c0001t0003g0283a0001c0001t0003g0288others(9): Show | 12 | HG00733.hp2 HG02056.hp2 HG02080.hp2 others(9): Show |
intron_variant | MODIFIER | c.-140+6798G>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 241655 | ||||||
chr16:241671
|
A | C | 21 | a0001c0002t0002g0001a0001c0002t0002g0206a0001c0002t0002g0293others(18): Show | 25 | HG01070.hp2 HG01071.hp2 HG01928.hp1 others(22): Show |
intron_variant | MODIFIER | c.-140+6814A>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 241671 | ||||||
chr16:241683
|
C | T | 1 | a0001c0001t0001g0276 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-140+6826C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 241683 | ||||||
chr16:241708
|
C | G | 19 | a0001c0001t0001g0225a0001c0001t0003g0253a0001c0001t0004g0226others(16): Show | 20 | HG00621.hp1 HG01361.hp2 HG02015.hp2 others(17): Show |
intron_variant | MODIFIER | c.-140+6851C>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 241708 | ||||||
chr16:241734
|
A | G | 2 | a0001c0002t0002g0032a0001c0002t0002g0033 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.-140+6877A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 241734 | ||||||
chr16:241745
|
A | G | 1 | a0001c0001t0013g0035 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-140+6888A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 241745 | ||||||
chr16:241905
|
C | CA | 18 | a0001c0001t0001g0069a0001c0001t0001g0108a0001c0001t0001g0109others(15): Show | 18 | HG00438.hp1 HG00735.hp2 HG01169.hp2 others(15): Show |
intron_variant | MODIFIER | c.-140+7066dupA | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 241905 | |||||
chr16:241905
|
CA | C | 104 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0001g0209others(101): Show | 108 | HG00544.hp1 HG00597.hp1 HG00642.hp2 others(105): Show |
intron_variant | MODIFIER | c.-140+7066delA | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 241905 | |||||
chr16:241905
|
CAA | C | 25 | a0001c0001t0001g0224a0001c0001t0001g0230a0001c0001t0001g0231others(22): Show | 26 | HG00621.hp1 HG01106.hp1 HG01361.hp2 others(23): Show |
intron_variant | MODIFIER | c.-140+7065_-140+706 others(6): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 241905 | |||||
chr16:242066
|
G | A | 3 | a0001c0002t0002g0306a0001c0002t0002g0343a0001c0002t0002g0344 | 3 | NA18979.hp1 NA19068.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.-140+7209G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 242066 | ||||||
chr16:242079
|
G | A | 3 | a0001c0001t0001g0153a0001c0001t0001g0154a0001c0001t0001g0190 | 3 | HG01109.hp1 HG01496.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.-140+7222G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 242079 | ||||||
chr16:242251
|
A | G | 2 | a0001c0001t0005g0026a0001c0001t0005g0027 | 2 | HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-139-7298A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 242251 | ||||||
chr16:242325
|
G | A | 1 | a0001c0002t0002g0328 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.-139-7224G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 242325 | ||||||
chr16:242389
|
T | A | 1 | a0001c0001t0001g0205 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-139-7160T>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 242389 | ||||||
chr16:242394
|
A | G | 1 | a0001c0001t0001g0205 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-139-7155A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 242394 | ||||||
chr16:242406
|
G | C | 1 | a0001c0002t0002g0343 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.-139-7143G>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 242406 | ||||||
chr16:242495
|
C | T | 3 | a0001c0001t0001g0107a0001c0001t0001g0118a0001c0001t0001g0119 | 3 | HG01123.hp1 HG01255.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.-139-7054C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 242495 | ||||||
chr16:242578
|
C | T | 1 | a0001c0001t0003g0283 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-139-6971C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 242578 | ||||||
chr16:242612
|
C | CT | 6 | a0001c0001t0001g0119a0001c0001t0001g0144a0001c0001t0001g0182others(3): Show | 6 | HG01993.hp2 NA18967.hp1 NA18979.hp2 others(3): Show |
intron_variant | MODIFIER | c.-139-6921dupT | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 242612 | |||||
chr16:242612
|
CT | C | 19 | a0001c0001t0001g0110a0001c0001t0001g0135a0001c0001t0001g0191others(16): Show | 19 | HG00733.hp2 HG00738.hp1 HG01257.hp2 others(16): Show |
intron_variant | MODIFIER | c.-139-6921delT | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 242612 | |||||
chr16:242669
|
A | G | 10 | a0001c0001t0002g0126a0001c0001t0002g0128a0001c0001t0005g0009others(7): Show | 10 | HG01069.hp1 HG01071.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.-139-6880A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 242669 | ||||||
chr16:242706
|
G | C | 1 | a0001c0001t0001g0102 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-139-6843G>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 242706 | ||||||
chr16:242770
|
G | A | 6 | a0001c0001t0001g0053a0001c0001t0001g0057a0001c0001t0001g0058others(3): Show | 6 | HG01884.hp1 HG02615.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.-139-6779G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 242770 | ||||||
chr16:242773
|
T | C | 249 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0016others(246): Show | 259 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(256): Show |
intron_variant | MODIFIER | c.-139-6776T>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 242773 | ||||||
chr16:242913
|
G | A | 1 | a0001c0002t0002g0206 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-139-6636G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 242913 | ||||||
chr16:242981
|
C | CT | 6 | a0001c0001t0001g0007a0001c0001t0001g0090a0001c0001t0001g0144others(3): Show | 8 | HG00609.hp2 HG02083.hp1 HG02155.hp2 others(5): Show |
intron_variant | MODIFIER | c.-139-6552dupT | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 242981 | |||||
chr16:242981
|
CT | C | 9 | a0001c0001t0001g0072a0001c0001t0001g0153a0001c0001t0001g0186others(6): Show | 9 | HG01081.hp1 HG01257.hp2 HG01496.hp2 others(6): Show |
intron_variant | MODIFIER | c.-139-6552delT | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 242981 | |||||
chr16:243022
|
C | G | 1 | a0001c0001t0003g0036 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-139-6527C>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 243022 | ||||||
chr16:243156
|
T | G | 1 | a0001c0001t0007g0378 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-139-6393T>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 243156 | ||||||
chr16:243168
|
G | T | 10 | a0001c0001t0001g0224a0001c0001t0001g0230a0001c0001t0001g0231others(7): Show | 10 | HG01106.hp1 HG02258.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.-139-6381G>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 243168 | ||||||
chr16:243198
|
C | T | 1 | a0001c0002t0002g0322 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-139-6351C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 243198 | ||||||
chr16:243258
|
C | T | 13 | a0002c0003t0001g0017a0002c0003t0001g0365a0002c0003t0001g0366others(10): Show | 14 | HG00621.hp1 HG01361.hp2 HG02015.hp2 others(11): Show |
intron_variant | MODIFIER | c.-139-6291C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 243258 | ||||||
chr16:243275
|
G | A | 1 | a0001c0017t0001g0187 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.-139-6274G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 243275 | ||||||
chr16:243315
|
C | A | 4 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0066others(1): Show | 4 | HG02257.hp1 HG03195.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.-139-6234C>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 243315 | ||||||
chr16:243496
|
A | C | 1 | a0001c0001t0001g0039 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-139-6053A>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 243496 | ||||||
chr16:243530
|
A | G | 3 | a0004c0007t0001g0049a0004c0007t0001g0050a0004c0007t0001g0051 | 3 | NA19043.hp2 NA19240.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-139-6019A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 243530 | ||||||
chr16:243563
|
T | C | 191 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0016others(188): Show | 200 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(197): Show |
intron_variant | MODIFIER | c.-139-5986T>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 243563 | ||||||
chr16:243588
|
G | C | 3 | a0001c0001t0002g0249a0001c0001t0010g0248a0001c0001t0010g0250 | 3 | HG03098.hp1 HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-139-5961G>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 243588 | ||||||
chr16:243594
|
C | T | 2 | a0001c0006t0006g0362a0001c0006t0006g0363 | 2 | HG00738.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-139-5955C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 243594 | ||||||
chr16:243779
|
G | T | 5 | a0001c0001t0001g0356a0001c0001t0001g0361a0001c0001t0003g0355others(2): Show | 5 | HG01109.hp2 HG02572.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.-139-5770G>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 243779 | ||||||
chr16:243916
|
G | A | 30 | a0001c0001t0001g0008a0001c0001t0001g0018a0001c0001t0001g0069others(27): Show | 31 | HG00408.hp2 HG00423.hp2 HG00609.hp1 others(28): Show |
intron_variant | MODIFIER | c.-139-5633G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 243916 | ||||||
chr16:243942
|
C | T | 1 | a0001c0002t0002g0327 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-139-5607C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 243942 | ||||||
chr16:243972
|
A | AT | 85 | a0001c0001t0001g0020a0001c0001t0001g0090a0001c0001t0001g0179others(82): Show | 89 | HG00544.hp1 HG00597.hp1 HG00642.hp2 others(86): Show |
intron_variant | MODIFIER | c.-139-5563dupT | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 243972 | |||||
chr16:244008
|
A | G | 1 | a0001c0001t0001g0354 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-139-5541A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 244008 | ||||||
chr16:244024
|
A | G | 3 | a0001c0001t0001g0354a0001c0002t0002g0357a0001c0002t0002g0358 | 3 | HG02109.hp2 HG02572.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.-139-5525A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 244024 | ||||||
chr16:244028
|
G | C | 5 | a0001c0001t0001g0003a0001c0001t0001g0042a0001c0001t0001g0077others(2): Show | 7 | HG00738.hp2 HG01099.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.-139-5521G>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 244028 | ||||||
chr16:244029
|
T | C | 1 | a0002c0003t0001g0373 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-139-5520T>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 244029 | ||||||
chr16:244030
|
G | A | 1 | a0002c0003t0001g0373 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-139-5519G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 244030 | ||||||
chr16:244031
|
C | T | 1 | a0002c0003t0001g0373 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-139-5518C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 244031 | ||||||
chr16:244032
|
C | G | 2 | a0001c0001t0001g0354a0002c0003t0001g0373 | 2 | HG02027.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.-139-5517C>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 244032 | ||||||
chr16:244037
|
C | A | 1 | a0002c0003t0001g0373 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-139-5512C>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 244037 | ||||||
chr16:244050
|
C | G | 1 | a0001c0001t0001g0354 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-139-5499C>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 244050 | ||||||
chr16:244070
|
A | G | 2 | a0001c0001t0007g0377a0001c0001t0007g0378 | 2 | HG03130.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-139-5479A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 244070 | ||||||
chr16:244080
|
T | C | 3 | a0004c0007t0001g0049a0004c0007t0001g0050a0004c0007t0001g0051 | 3 | NA19043.hp2 NA19240.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-139-5469T>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 244080 | ||||||
chr16:244086
|
A | C | 1 | a0001c0009t0003g0257 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-139-5463A>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 244086 | ||||||
chr16:244093
|
T | C | 2 | a0001c0001t0005g0026a0001c0001t0005g0027 | 2 | HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-139-5456T>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 244093 | ||||||
chr16:244094
|
G | C | 2 | a0001c0001t0005g0026a0001c0001t0005g0027 | 2 | HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-139-5455G>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 244094 | ||||||
chr16:244103
|
G | A | 2 | a0001c0001t0005g0026a0001c0001t0005g0027 | 2 | HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-139-5446G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 244103 | ||||||
chr16:244104
|
G | C | 1 | a0001c0001t0001g0198 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-139-5445G>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 244104 | ||||||
chr16:244114
|
A | G | 17 | a0001c0001t0001g0209a0001c0001t0001g0224a0001c0001t0001g0230others(14): Show | 17 | HG01106.hp1 HG01891.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.-139-5435A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 244114 | ||||||
chr16:244130
|
G | A | 1 | a0001c0001t0004g0244 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-139-5419G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 244130 | ||||||
chr16:244158
|
T | C | 103 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(100): Show | 110 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.-139-5391T>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 244158 | ||||||
chr16:244162
|
G | T | 1 | a0001c0001t0001g0052 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.-139-5387G>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 244162 | ||||||
chr16:244170
|
G | A | 2 | a0002c0003t0001g0369a0015c0013t0008g0368 | 2 | HG02083.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.-139-5379G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 244170 | ||||||
chr16:244178
|
T | C | 210 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(207): Show | 221 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.-139-5371T>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 244178 | ||||||
chr16:244182
|
A | G | 1 | a0001c0001t0001g0089 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.-139-5367A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 244182 | ||||||
chr16:244183
|
T | C | 1 | a0001c0002t0002g0315 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-139-5366T>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 244183 | ||||||
chr16:244190
|
G | A | 7 | a0001c0001t0001g0224a0001c0001t0001g0230a0001c0001t0001g0235others(4): Show | 7 | HG01891.hp2 HG02622.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.-139-5359G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 244190 | ||||||
chr16:244190
|
G | C | 55 | a0001c0001t0001g0070a0001c0001t0001g0094a0001c0001t0001g0095others(52): Show | 59 | HG00597.hp1 HG00642.hp2 HG00733.hp1 others(56): Show |
intron_variant | MODIFIER | c.-139-5359G>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 244190 | ||||||
chr16:244203
|
T | C | 11 | a0001c0001t0001g0091a0001c0001t0001g0231a0001c0001t0003g0233others(8): Show | 11 | HG00423.hp2 HG00609.hp1 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.-139-5346T>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 244203 | ||||||
chr16:244211
|
A | G | 207 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0016others(204): Show | 216 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(213): Show |
intron_variant | MODIFIER | c.-139-5338A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 244211 | ||||||
chr16:244215
|
G | A | 2 | a0001c0001t0001g0063a0001c0001t0001g0098 | 2 | HG02055.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.-139-5334G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 244215 | ||||||
chr16:244219
|
T | C | 9 | a0001c0001t0001g0003a0001c0001t0001g0077a0001c0001t0001g0098others(6): Show | 12 | HG00738.hp2 HG02280.hp2 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.-139-5330T>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 244219 | ||||||
chr16:244219
|
TG | T | 3 | a0001c0001t0002g0249a0001c0001t0010g0248a0001c0001t0010g0250 | 3 | HG03098.hp1 HG03471.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-139-5328delG | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 244219 | |||||
chr16:244244
|
A | G | 65 | a0001c0001t0001g0016a0001c0001t0001g0225a0001c0001t0001g0332others(62): Show | 70 | HG00597.hp1 HG00642.hp2 HG00733.hp1 others(67): Show |
intron_variant | MODIFIER | c.-139-5305A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 244244 | ||||||
chr16:244248
|
G | A | 2 | a0001c0002t0002g0047a0001c0002t0002g0048 | 2 | NA19010.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.-139-5301G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 244248 | ||||||
chr16:244255
|
A | C | 5 | a0001c0001t0001g0356a0001c0001t0001g0361a0001c0001t0003g0283others(2): Show | 5 | HG02280.hp1 HG03041.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.-139-5294A>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 244255 | ||||||
chr16:244260
|
G | A | 2 | a0001c0001t0004g0244a0001c0001t0004g0245 | 2 | HG02717.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.-139-5289G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 244260 | ||||||
chr16:244263
|
C | T | 2 | a0001c0001t0001g0063a0001c0001t0003g0253 | 2 | HG02055.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.-139-5286C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 244263 | ||||||
chr16:244264
|
G | A | 1 | a0001c0001t0001g0113 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-139-5285G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 244264 | ||||||
chr16:244386
|
C | T | 2 | a0001c0001t0005g0240a0001c0001t0008g0247 | 2 | HG02486.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.-139-5163C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 244386 | ||||||
chr16:244387
|
A | G | 21 | a0001c0001t0001g0224a0001c0001t0001g0230a0001c0001t0001g0232others(18): Show | 21 | HG00738.hp1 HG01069.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.-139-5162A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 244387 | ||||||
chr16:244401
|
T | C | 1 | a0001c0002t0002g0346 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-139-5148T>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 244401 | ||||||
chr16:244533
|
C | G | 1 | a0001c0001t0003g0288 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-139-5016C>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 244533 | ||||||
chr16:244672
|
A | G | 2 | a0001c0001t0010g0248a0001c0001t0010g0250 | 2 | HG03098.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-139-4877A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 244672 | ||||||
chr16:244682
|
C | CT | 21 | a0001c0001t0001g0150a0001c0001t0001g0201a0001c0001t0001g0210others(18): Show | 21 | HG01071.hp1 HG01256.hp2 HG01258.hp1 others(18): Show |
intron_variant | MODIFIER | c.-139-4844dupT | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 244682 | |||||
chr16:244682
|
CT | C | 122 | a0001c0001t0001g0058a0001c0001t0001g0085a0001c0001t0001g0090others(119): Show | 126 | HG00544.hp1 HG00597.hp1 HG00642.hp2 others(123): Show |
intron_variant | MODIFIER | c.-139-4844delT | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 244682 | |||||
chr16:244682
|
CTT | C | 19 | a0001c0001t0001g0225a0001c0002t0002g0032a0001c0002t0002g0251others(16): Show | 20 | HG00621.hp1 HG01074.hp1 HG01361.hp2 others(17): Show |
intron_variant | MODIFIER | c.-139-4845_-139-484 others(6): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 244682 | |||||
chr16:244683
|
T | C | 1 | a0001c0009t0003g0292 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-139-4866T>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 244683 | ||||||
chr16:244710
|
C | T | 14 | a0001c0001t0008g0247a0002c0003t0001g0017a0002c0003t0001g0365others(11): Show | 15 | HG00621.hp1 HG01361.hp2 HG02015.hp2 others(12): Show |
intron_variant | MODIFIER | c.-139-4839C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 244710 | ||||||
chr16:244750
|
A | G | 162 | a0001c0001t0001g0067a0001c0001t0001g0224a0001c0001t0001g0225others(159): Show | 168 | HG00099.hp1 HG00544.hp1 HG00597.hp1 others(165): Show |
intron_variant | MODIFIER | c.-139-4799A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 244750 | ||||||
chr16:244751
|
C | T | 1 | a0001c0001t0001g0143 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-139-4798C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 244751 | ||||||
chr16:244798
|
C | T | 4 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0118others(1): Show | 4 | HG01123.hp1 HG01255.hp1 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.-139-4751C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 244798 | ||||||
chr16:244854
|
A | G | 2 | a0001c0002t0002g0034a0001c0002t0002g0251 | 2 | HG01074.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.-139-4695A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 244854 | ||||||
chr16:244872
|
A | G | 13 | a0002c0003t0001g0017a0002c0003t0001g0365a0002c0003t0001g0366others(10): Show | 14 | HG00621.hp1 HG01361.hp2 HG02015.hp2 others(11): Show |
intron_variant | MODIFIER | c.-139-4677A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 244872 | ||||||
chr16:244879
|
ATGGGGTT others(2076): Show |
A | 1 | a0001c0001t0007g0378 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-139-4660_-139-257 others(4): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 244879 | |||||
chr16:244892
|
A | G | 4 | a0001c0001t0001g0003a0001c0001t0001g0077a0001c0001t0001g0099others(1): Show | 6 | HG00738.hp2 HG02280.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-139-4657A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 244892 | ||||||
chr16:244912
|
A | T | 1 | a0001c0001t0001g0350 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.-139-4637A>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 244912 | ||||||
chr16:244919
|
C | T | 1 | a0001c0001t0001g0101 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-139-4630C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 244919 | ||||||
chr16:244982
|
G | A | 1 | a0001c0001t0007g0377 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-139-4567G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 244982 | ||||||
chr16:245054
|
C | G | 1 | a0001c0002t0002g0310 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-139-4495C>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 245054 | ||||||
chr16:245085
|
C | T | 1 | a0001c0001t0001g0180 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.-139-4464C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 245085 | ||||||
chr16:245118
|
A | G | 90 | a0001c0001t0004g0244a0001c0001t0004g0245a0001c0002t0001g0331others(87): Show | 94 | HG00544.hp1 HG00597.hp1 HG00642.hp2 others(91): Show |
intron_variant | MODIFIER | c.-139-4431A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 245118 | ||||||
chr16:245353
|
A | G | 8 | a0001c0006t0001g0037a0001c0006t0001g0038a0001c0006t0001g0055others(5): Show | 8 | HG00738.hp1 HG01243.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.-139-4196A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 245353 | ||||||
chr16:245365
|
G | C | 1 | a0001c0001t0001g0281 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.-139-4184G>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 245365 | ||||||
chr16:245446
|
C | T | 1 | a0001c0001t0001g0016 | 2 | HG01074.hp2 HG01123.hp2 |
intron_variant | MODIFIER | c.-139-4103C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 245446 | ||||||
chr16:245602
|
G | A | 15 | a0001c0001t0004g0244a0001c0001t0004g0245a0002c0003t0001g0017others(12): Show | 16 | HG00621.hp1 HG01361.hp2 HG02015.hp2 others(13): Show |
intron_variant | MODIFIER | c.-139-3947G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 245602 | ||||||
chr16:245626
|
A | G | 1 | a0001c0001t0003g0253 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-139-3923A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 245626 | ||||||
chr16:245664
|
GA | G | 120 | a0001c0001t0001g0361a0001c0001t0002g0249a0001c0001t0003g0078others(117): Show | 125 | HG00099.hp1 HG00544.hp1 HG00597.hp1 others(122): Show |
intron_variant | MODIFIER | c.-139-3874delA | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 245664 | |||||
chr16:245715
|
A | C | 26 | a0001c0001t0003g0078a0001c0001t0003g0096a0001c0001t0003g0213others(23): Show | 27 | HG00099.hp1 HG00621.hp2 HG00673.hp2 others(24): Show |
intron_variant | MODIFIER | c.-139-3834A>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 245715 | ||||||
chr16:245719
|
A | G | 175 | a0001c0001t0001g0224a0001c0001t0001g0225a0001c0001t0001g0230others(172): Show | 181 | HG00099.hp1 HG00544.hp1 HG00597.hp1 others(178): Show |
intron_variant | MODIFIER | c.-139-3830A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 245719 | ||||||
chr16:245793
|
A | G | 13 | a0002c0003t0001g0017a0002c0003t0001g0365a0002c0003t0001g0366others(10): Show | 14 | HG00621.hp1 HG01361.hp2 HG02015.hp2 others(11): Show |
intron_variant | MODIFIER | c.-139-3756A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 245793 | ||||||
chr16:245796
|
T | C | 136 | a0001c0001t0002g0249a0001c0001t0003g0036a0001c0001t0003g0078others(133): Show | 142 | HG00099.hp1 HG00544.hp1 HG00597.hp1 others(139): Show |
intron_variant | MODIFIER | c.-139-3753T>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 245796 | ||||||
chr16:245825
|
C | T | 1 | a0001c0001t0003g0253 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-139-3724C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 245825 | ||||||
chr16:245839
|
G | A | 1 | a0001c0001t0001g0155 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.-139-3710G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 245839 | ||||||
chr16:245958
|
G | A | 16 | a0001c0001t0003g0036a0001c0001t0004g0244a0001c0001t0004g0245others(13): Show | 17 | HG00621.hp1 HG01361.hp2 HG02015.hp2 others(14): Show |
intron_variant | MODIFIER | c.-139-3591G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 245958 | ||||||
chr16:245964
|
T | A | 2 | a0001c0001t0004g0244a0001c0001t0004g0245 | 2 | HG02717.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.-139-3585T>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 245964 | ||||||
chr16:246055
|
T | C | 2 | a0001c0001t0010g0248a0001c0001t0010g0250 | 2 | HG03098.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-139-3494T>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 246055 | ||||||
chr16:246185
|
C | A | 175 | a0001c0001t0001g0224a0001c0001t0001g0225a0001c0001t0001g0230others(172): Show | 181 | HG00099.hp1 HG00544.hp1 HG00597.hp1 others(178): Show |
intron_variant | MODIFIER | c.-139-3364C>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 246185 | ||||||
chr16:246219
|
A | AAAT | 17 | a0001c0001t0001g0011a0001c0001t0003g0036a0001c0001t0004g0244others(14): Show | 19 | HG00621.hp1 HG01361.hp2 HG02015.hp2 others(16): Show |
intron_variant | MODIFIER | c.-139-3311_-139-330 others(7): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 246219 | |||||
chr16:246219
|
A | T | 18 | a0001c0001t0001g0224a0001c0001t0001g0225a0001c0001t0001g0230others(15): Show | 18 | HG01106.hp1 HG01891.hp2 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.-139-3330A>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 246219 | ||||||
chr16:246222
|
T | A | 4 | a0001c0001t0001g0157a0001c0001t0010g0248a0001c0001t0010g0250others(1): Show | 4 | HG02165.hp1 HG03098.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-139-3327T>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 246222 | ||||||
chr16:246283
|
A | AT | 18 | a0001c0001t0001g0061a0001c0001t0001g0108a0001c0001t0001g0144others(15): Show | 18 | HG02257.hp1 HG02293.hp2 HG02698.hp2 others(15): Show |
intron_variant | MODIFIER | c.-139-3251dupT | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 246283 | |||||
chr16:246293
|
T | G | 3 | a0001c0002t0002g0062a0001c0002t0002g0255a0011c0028t0002g0256 | 3 | HG02647.hp2 HG02976.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-139-3256T>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 246293 | ||||||
chr16:246295
|
T | G | 3 | a0001c0002t0002g0062a0001c0002t0002g0255a0011c0028t0002g0256 | 3 | HG02647.hp2 HG02976.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-139-3254T>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 246295 | ||||||
chr16:246297
|
T | G | 3 | a0001c0002t0002g0062a0001c0002t0002g0255a0011c0028t0002g0256 | 3 | HG02647.hp2 HG02976.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-139-3252T>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 246297 | ||||||
chr16:246355
|
C | T | 2 | a0001c0001t0001g0022a0001c0002t0002g0031 | 2 | HG01978.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.-139-3194C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 246355 | ||||||
chr16:246382
|
A | G | 1 | a0001c0001t0001g0039 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-139-3167A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 246382 | ||||||
chr16:246383
|
G | A | 1 | a0001c0001t0001g0039 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-139-3166G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 246383 | ||||||
chr16:246417
|
C | CT | 33 | a0001c0001t0001g0069a0001c0001t0001g0087a0001c0001t0001g0088others(30): Show | 33 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(30): Show |
intron_variant | MODIFIER | c.-139-3110dupT | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 246417 | |||||
chr16:246417
|
C | CTT | 102 | a0001c0001t0001g0176a0001c0001t0002g0249a0001c0001t0003g0096others(99): Show | 107 | HG00099.hp1 HG00544.hp1 HG00597.hp1 others(104): Show |
intron_variant | MODIFIER | c.-139-3111_-139-311 others(6): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 246417 | |||||
chr16:246417
|
C | CTTT | 16 | a0001c0001t0003g0078a0001c0001t0003g0290a0001c0001t0003g0347others(13): Show | 16 | HG00733.hp2 HG01106.hp2 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.-139-3112_-139-311 others(7): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 246417 | |||||
chr16:246417
|
CT | C | 14 | a0001c0001t0001g0085a0001c0001t0001g0139a0001c0001t0001g0158others(11): Show | 14 | HG01069.hp2 HG01106.hp1 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.-139-3110delT | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 246417 | |||||
chr16:246417
|
CTTT | C | 12 | a0002c0003t0001g0017a0002c0003t0001g0365a0002c0003t0001g0366others(9): Show | 13 | HG00621.hp1 HG01361.hp2 HG02015.hp2 others(10): Show |
intron_variant | MODIFIER | c.-139-3112_-139-311 others(7): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 246417 | |||||
chr16:246458
|
C | T | 1 | a0001c0001t0001g0147 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-139-3091C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 246458 | ||||||
chr16:246459
|
G | A | 8 | a0001c0006t0001g0037a0001c0006t0001g0038a0001c0006t0001g0055others(5): Show | 8 | HG00738.hp1 HG01243.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.-139-3090G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 246459 | ||||||
chr16:246503
|
T | G | 1 | a0001c0001t0001g0085 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.-139-3046T>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 246503 | ||||||
chr16:246512
|
C | T | 1 | a0001c0001t0001g0067 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-139-3037C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 246512 | ||||||
chr16:246513
|
G | A | 1 | a0001c0002t0002g0301 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-139-3036G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 246513 | ||||||
chr16:246524
|
A | G | 1 | a0001c0001t0001g0225 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-139-3025A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 246524 | ||||||
chr16:246568
|
C | T | 2 | a0001c0001t0001g0172a0001c0001t0001g0208 | 2 | HG01261.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.-139-2981C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 246568 | ||||||
chr16:246666
|
G | A | 1 | a0001c0001t0001g0258 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-139-2883G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 246666 | ||||||
chr16:246691
|
T | C | 2 | a0001c0001t0004g0244a0001c0001t0004g0245 | 2 | HG02717.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.-139-2858T>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 246691 | ||||||
chr16:246726
|
GT | G | 10 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0045others(7): Show | 10 | HG00735.hp1 HG01099.hp1 HG01167.hp1 others(7): Show |
intron_variant | MODIFIER | c.-139-2811delT | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 246726 | |||||
chr16:246739
|
C | T | 1 | a0001c0001t0003g0036 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-139-2810C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 246739 | ||||||
chr16:246749
|
GTGTTT | G | 9 | a0001c0002t0001g0331a0001c0002t0002g0046a0001c0002t0002g0123others(6): Show | 9 | HG00738.hp1 HG01243.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.-139-2778_-139-277 others(9): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 246749 | |||||
chr16:246801
|
G | A | 1 | a0001c0001t0001g0086 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-139-2748G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 246801 | ||||||
chr16:246997
|
A | G | 15 | a0001c0001t0002g0126a0001c0001t0002g0128a0001c0001t0004g0226others(12): Show | 15 | HG01069.hp1 HG01071.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.-139-2552A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 246997 | ||||||
chr16:247025
|
G | A | 2 | a0001c0002t0002g0357a0001c0002t0002g0358 | 2 | HG02572.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.-139-2524G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 247025 | ||||||
chr16:247027
|
C | A | 1 | a0001c0001t0001g0258 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-139-2522C>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 247027 | ||||||
chr16:247077
|
G | T | 2 | a0001c0001t0010g0248a0001c0001t0010g0250 | 2 | HG03098.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-139-2472G>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 247077 | ||||||
chr16:247202
|
C | G | 1 | a0001c0001t0003g0253 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-139-2347C>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 247202 | ||||||
chr16:247232
|
G | A | 1 | a0001c0001t0001g0089 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.-139-2317G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 247232 | ||||||
chr16:247265
|
G | A | 31 | a0001c0001t0001g0224a0001c0001t0001g0225a0001c0001t0001g0230others(28): Show | 31 | HG01069.hp1 HG01071.hp1 HG01106.hp1 others(28): Show |
intron_variant | MODIFIER | c.-139-2284G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 247265 | ||||||
chr16:247289
|
C | T | 1 | a0001c0001t0001g0183 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.-139-2260C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 247289 | ||||||
chr16:247322
|
C | T | 13 | a0001c0001t0002g0126a0001c0001t0002g0128a0001c0001t0004g0226others(10): Show | 13 | HG01069.hp1 HG01071.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.-139-2227C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 247322 | ||||||
chr16:247426
|
G | T | 2 | a0001c0001t0007g0377a0001c0001t0007g0378 | 2 | HG03130.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-139-2123G>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 247426 | ||||||
chr16:247511
|
C | A | 158 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0094others(155): Show | 166 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(163): Show |
intron_variant | MODIFIER | c.-139-2038C>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 247511 | ||||||
chr16:247525
|
C | G | 8 | a0001c0006t0001g0037a0001c0006t0001g0038a0001c0006t0001g0055others(5): Show | 8 | HG00738.hp1 HG01243.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.-139-2024C>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 247525 | ||||||
chr16:247604
|
G | A | 1 | a0001c0001t0003g0253 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-139-1945G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 247604 | ||||||
chr16:247672
|
C | A | 219 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0094others(216): Show | 228 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(225): Show |
intron_variant | MODIFIER | c.-139-1877C>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 247672 | ||||||
chr16:247751
|
T | C | 221 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0094others(218): Show | 230 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(227): Show |
intron_variant | MODIFIER | c.-139-1798T>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 247751 | ||||||
chr16:247782
|
T | C | 4 | a0001c0001t0003g0253a0001c0001t0003g0355a0007c0008t0002g0359others(1): Show | 4 | HG01109.hp2 HG02572.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-139-1767T>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 247782 | ||||||
chr16:247836
|
T | G | 1 | a0001c0001t0001g0272 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-139-1713T>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 247836 | ||||||
chr16:247939
|
C | T | 1 | a0001c0001t0001g0137 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-139-1610C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 247939 | ||||||
chr16:248098
|
T | C | 1 | a0001c0001t0003g0253 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-139-1451T>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 248098 | ||||||
chr16:248132
|
C | T | 1 | a0001c0001t0001g0102 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-139-1417C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 248132 | ||||||
chr16:248138
|
A | C | 378 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(375): Show | 401 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(398): Show |
intron_variant | MODIFIER | c.-139-1411A>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 248138 | ||||||
chr16:248241
|
C | G | 2 | a0001c0002t0002g0357a0001c0002t0002g0358 | 2 | HG02572.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.-139-1308C>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 248241 | ||||||
chr16:248251
|
C | T | 5 | a0001c0001t0001g0224a0001c0001t0001g0230a0001c0001t0001g0235others(2): Show | 5 | HG02622.hp1 HG02723.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.-139-1298C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 248251 | ||||||
chr16:248588
|
G | A | 11 | a0001c0001t0004g0226a0001c0001t0004g0227a0001c0001t0004g0228others(8): Show | 11 | HG01069.hp1 HG01071.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.-139-961G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 248588 | ||||||
chr16:248589
|
A | G | 8 | a0001c0006t0001g0037a0001c0006t0001g0038a0001c0006t0001g0055others(5): Show | 8 | HG00738.hp1 HG01243.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.-139-960A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 248589 | ||||||
chr16:248690
|
C | G | 26 | a0001c0001t0003g0036a0001c0001t0003g0253a0001c0001t0004g0244others(23): Show | 27 | HG00621.hp1 HG00738.hp1 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.-139-859C>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 248690 | ||||||
chr16:248755
|
G | A | 1 | a0001c0002t0001g0331 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-139-794G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 248755 | ||||||
chr16:248861
|
C | A | 1 | a0001c0001t0003g0253 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-139-688C>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 248861 | ||||||
chr16:249003
|
C | T | 1 | a0001c0001t0003g0036 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-139-546C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 249003 | ||||||
chr16:249466
|
T | C | 1 | a0001c0002t0002g0314 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.-139-83T>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 249466 | ||||||
chr16:249503
|
G | A | 8 | a0001c0006t0001g0037a0001c0006t0001g0038a0001c0006t0001g0055others(5): Show | 8 | HG00738.hp1 HG01243.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.-139-46G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 1/12 | chr16 | 249503 | ||||||
chr16:249716
|
C | T | 9 | a0001c0002t0002g0284a0001c0002t0002g0329a0001c0002t0002g0334others(6): Show | 9 | HG02040.hp2 HG02074.hp1 NA18953.hp1 others(6): Show |
intron_variant | MODIFIER | c.-34+62C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 249716 | ||||||
chr16:249808
|
G | A | 1 | a0001c0001t0001g0282 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-34+154G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 249808 | ||||||
chr16:249924
|
A | G | 5 | a0001c0006t0001g0037a0001c0006t0001g0038a0001c0006t0001g0055others(2): Show | 5 | HG00738.hp1 HG01243.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.-34+270A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 249924 | ||||||
chr16:249946
|
A | T | 10 | a0001c0001t0005g0009a0001c0001t0005g0026a0001c0001t0005g0027others(7): Show | 10 | HG01069.hp1 HG01071.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.-34+292A>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 249946 | ||||||
chr16:249959
|
C | T | 3 | a0001c0001t0003g0253a0001c0001t0010g0248a0001c0001t0010g0250 | 3 | HG02886.hp1 HG03098.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-34+305C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 249959 | ||||||
chr16:249981
|
T | C | 94 | a0001c0001t0002g0126a0001c0001t0002g0128a0001c0001t0002g0249others(91): Show | 98 | HG00099.hp1 HG00544.hp1 HG00597.hp1 others(95): Show |
intron_variant | MODIFIER | c.-34+327T>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 249981 | ||||||
chr16:250007
|
G | A | 3 | a0001c0001t0001g0137a0001c0001t0001g0210a0001c0001t0001g0211 | 3 | HG01256.hp2 HG01258.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.-34+353G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 250007 | ||||||
chr16:250008
|
C | T | 1 | a0001c0001t0001g0178 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.-34+354C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 250008 | ||||||
chr16:250077
|
G | C | 17 | a0001c0001t0001g0224a0001c0001t0001g0225a0001c0001t0001g0230others(14): Show | 17 | HG01106.hp1 HG01891.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.-34+423G>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 250077 | ||||||
chr16:250097
|
A | G | 14 | a0002c0003t0001g0017a0002c0003t0001g0364a0002c0003t0001g0365others(11): Show | 15 | HG00621.hp1 HG01361.hp2 HG02015.hp2 others(12): Show |
intron_variant | MODIFIER | c.-34+443A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 250097 | ||||||
chr16:250174
|
T | G | 15 | a0001c0001t0003g0036a0002c0003t0001g0017a0002c0003t0001g0364others(12): Show | 16 | HG00621.hp1 HG01361.hp2 HG02015.hp2 others(13): Show |
intron_variant | MODIFIER | c.-34+520T>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 250174 | ||||||
chr16:250178
|
A | G | 147 | a0001c0001t0002g0126a0001c0001t0002g0128a0001c0001t0002g0249others(144): Show | 153 | HG00099.hp1 HG00544.hp1 HG00597.hp1 others(150): Show |
intron_variant | MODIFIER | c.-34+524A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 250178 | ||||||
chr16:250240
|
T | C | 14 | a0002c0003t0001g0017a0002c0003t0001g0364a0002c0003t0001g0365others(11): Show | 15 | HG00621.hp1 HG01361.hp2 HG02015.hp2 others(12): Show |
intron_variant | MODIFIER | c.-34+586T>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 250240 | ||||||
chr16:250264
|
T | G | 2 | a0001c0001t0001g0352a0001c0001t0001g0353 | 2 | HG01884.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.-34+610T>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 250264 | ||||||
chr16:250277
|
T | C | 14 | a0002c0003t0001g0017a0002c0003t0001g0364a0002c0003t0001g0365others(11): Show | 15 | HG00621.hp1 HG01361.hp2 HG02015.hp2 others(12): Show |
intron_variant | MODIFIER | c.-34+623T>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 250277 | ||||||
chr16:250389
|
T | C | 140 | a0001c0001t0001g0003a0001c0001t0001g0077a0001c0001t0001g0099others(137): Show | 148 | HG00099.hp1 HG00544.hp1 HG00597.hp1 others(145): Show |
intron_variant | MODIFIER | c.-34+735T>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 250389 | ||||||
chr16:250394
|
AC | A | 23 | a0001c0001t0003g0036a0001c0001t0003g0253a0001c0001t0004g0226others(20): Show | 23 | HG00738.hp1 HG01069.hp1 HG01071.hp1 others(20): Show |
intron_variant | MODIFIER | c.-34+742delC | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr16 | 250394 | |||||
chr16:250396
|
C | T | 16 | a0001c0001t0001g0224a0001c0001t0001g0225a0001c0001t0001g0230others(13): Show | 16 | HG01106.hp1 HG01891.hp2 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.-34+742C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 250396 | ||||||
chr16:250396
|
CT | C | 10 | a0001c0001t0002g0126a0001c0001t0002g0128a0001c0001t0002g0249others(7): Show | 10 | HG02055.hp2 HG02572.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.-34+746delT | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr16 | 250396 | |||||
chr16:250400
|
T | C | 129 | a0001c0001t0001g0003a0001c0001t0001g0077a0001c0001t0003g0078others(126): Show | 137 | HG00099.hp1 HG00544.hp1 HG00597.hp1 others(134): Show |
intron_variant | MODIFIER | c.-34+746T>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 250400 | ||||||
chr16:250491
|
G | C | 1 | a0001c0001t0001g0077 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-34+837G>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 250491 | ||||||
chr16:250642
|
G | A | 178 | a0001c0001t0001g0087a0001c0001t0001g0154a0001c0001t0001g0224others(175): Show | 184 | HG00099.hp1 HG00544.hp1 HG00597.hp1 others(181): Show |
intron_variant | MODIFIER | c.-34+988G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 250642 | ||||||
chr16:250682
|
C | T | 1 | a0001c0001t0003g0036 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-34+1028C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 250682 | ||||||
chr16:250697
|
T | A | 175 | a0001c0001t0001g0087a0001c0001t0001g0224a0001c0001t0001g0225others(172): Show | 181 | HG00099.hp1 HG00544.hp1 HG00597.hp1 others(178): Show |
intron_variant | MODIFIER | c.-34+1043T>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 250697 | ||||||
chr16:250773
|
T | C | 1 | a0001c0001t0001g0225 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-34+1119T>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 250773 | ||||||
chr16:250993
|
A | G | 1 | a0001c0001t0003g0096 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-34+1339A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 250993 | ||||||
chr16:251012
|
A | AAT | 6 | a0001c0001t0001g0079a0001c0001t0001g0082a0001c0001t0001g0085others(3): Show | 6 | HG02027.hp2 NA18949.hp2 NA18969.hp2 others(3): Show |
intron_variant | MODIFIER | c.-34+1359_-34+1360d others(4): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr16 | 251012 | |||||
chr16:251013
|
A | G | 1 | a0001c0001t0001g0099 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-34+1359A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 251013 | ||||||
chr16:251025
|
T | C | 1 | a0001c0002t0002g0335 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-34+1371T>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 251025 | ||||||
chr16:251042
|
C | T | 2 | a0001c0001t0005g0026a0001c0001t0005g0027 | 2 | HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-34+1388C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 251042 | ||||||
chr16:251113
|
T | C | 1 | a0002c0003t0001g0373 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-34+1459T>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 251113 | ||||||
chr16:251147
|
T | C | 1 | a0001c0001t0001g0332 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.-34+1493T>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 251147 | ||||||
chr16:251182
|
G | A | 2 | a0001c0001t0001g0134a0001c0001t0001g0135 | 2 | NA18965.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.-34+1528G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 251182 | ||||||
chr16:251325
|
A | G | 3 | a0004c0007t0001g0049a0004c0007t0001g0050a0004c0007t0001g0051 | 3 | NA19043.hp2 NA19240.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-34+1671A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 251325 | ||||||
chr16:251396
|
A | G | 1 | a0001c0002t0002g0318 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-34+1742A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 251396 | ||||||
chr16:251397
|
T | A | 1 | a0001c0002t0002g0318 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-34+1743T>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 251397 | ||||||
chr16:251398
|
G | T | 1 | a0001c0002t0002g0318 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-34+1744G>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 251398 | ||||||
chr16:251499
|
C | T | 1 | a0001c0001t0001g0079 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-34+1845C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 251499 | ||||||
chr16:251515
|
C | T | 1 | a0001c0002t0002g0327 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-34+1861C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 251515 | ||||||
chr16:251524
|
G | A | 2 | a0001c0001t0001g0146a0001c0001t0001g0156 | 2 | NA19063.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.-34+1870G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 251524 | ||||||
chr16:251526
|
C | T | 1 | a0001c0002t0017g0028 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-34+1872C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 251526 | ||||||
chr16:251528
|
C | T | 1 | a0001c0001t0001g0177 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-34+1874C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 251528 | ||||||
chr16:251679
|
G | GT | 43 | a0001c0001t0001g0022a0001c0001t0001g0025a0001c0001t0001g0045others(40): Show | 43 | HG00738.hp1 HG01069.hp1 HG01071.hp1 others(40): Show |
intron_variant | MODIFIER | c.-34+2052dupT | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr16 | 251679 | |||||
chr16:251679
|
G | GTT | 24 | a0001c0001t0001g0271a0001c0001t0005g0026a0001c0001t0005g0127others(21): Show | 25 | HG00621.hp1 HG01361.hp2 HG01433.hp1 others(22): Show |
intron_variant | MODIFIER | c.-34+2051_-34+2052d others(4): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr16 | 251679 | |||||
chr16:251679
|
G | GTTT | 92 | a0001c0001t0001g0171a0001c0001t0002g0126a0001c0001t0002g0128others(89): Show | 96 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.-34+2050_-34+2052d others(5): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr16 | 251679 | |||||
chr16:251679
|
G | GTTTT | 29 | a0001c0001t0003g0283a0001c0001t0003g0288a0001c0001t0003g0289others(26): Show | 30 | HG00642.hp2 HG01109.hp2 HG01255.hp2 others(27): Show |
intron_variant | MODIFIER | c.-34+2049_-34+2052d others(6): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr16 | 251679 | |||||
chr16:251679
|
GT | G | 11 | a0001c0001t0001g0018a0001c0001t0001g0024a0001c0001t0001g0058others(8): Show | 11 | HG01256.hp1 HG01256.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.-34+2052delT | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr16 | 251679 | |||||
chr16:251679
|
GTTTTTTT others(5): Show |
G | 1 | a0001c0001t0003g0253 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-34+2041_-34+2052d others(14): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr16 | 251679 | |||||
chr16:251687
|
T | TTTG | 14 | a0001c0001t0001g0224a0001c0001t0001g0230a0001c0001t0001g0231others(11): Show | 14 | HG01106.hp1 HG01891.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.-34+2035_-34+2036i others(5): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr16 | 251687 | |||||
chr16:251741
|
T | C | 185 | a0001c0001t0001g0171a0001c0001t0001g0224a0001c0001t0001g0225others(182): Show | 191 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(188): Show |
intron_variant | MODIFIER | c.-34+2087T>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 251741 | ||||||
chr16:251895
|
C | T | 4 | a0001c0001t0004g0226a0001c0001t0004g0227a0001c0001t0004g0228others(1): Show | 4 | HG02486.hp2 HG03130.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.-34+2241C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 251895 | ||||||
chr16:251896
|
G | A | 1 | a0001c0001t0003g0253 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-34+2242G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 251896 | ||||||
chr16:251942
|
A | G | 187 | a0001c0001t0001g0054a0001c0001t0001g0056a0001c0001t0001g0171others(184): Show | 193 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(190): Show |
intron_variant | MODIFIER | c.-34+2288A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 251942 | ||||||
chr16:251952
|
A | G | 1 | a0001c0001t0003g0036 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-34+2298A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 251952 | ||||||
chr16:251972
|
T | C | 1 | a0001c0002t0002g0062 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-34+2318T>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 251972 | ||||||
chr16:252002
|
C | CA | 24 | a0001c0001t0001g0063a0001c0001t0001g0088a0001c0001t0001g0144others(21): Show | 24 | HG00597.hp1 HG01261.hp2 HG01433.hp2 others(21): Show |
intron_variant | MODIFIER | c.-33-2360dupA | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr16 | 252002 | |||||
chr16:252002
|
CA | C | 3 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0143 | 6 | HG02040.hp1 HG02080.hp1 NA18612.hp2 others(3): Show |
intron_variant | MODIFIER | c.-33-2360delA | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr16 | 252002 | |||||
chr16:252003
|
A | C | 1 | a0001c0001t0001g0231 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-34+2349A>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 252003 | ||||||
chr16:252029
|
G | A | 1 | a0001c0001t0005g0240 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-33-2352G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 252029 | ||||||
chr16:252033
|
C | CT | 113 | a0001c0001t0002g0126a0001c0001t0002g0128a0001c0001t0002g0249others(110): Show | 118 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(115): Show |
intron_variant | MODIFIER | c.-33-2347dupT | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr16 | 252033 | |||||
chr16:252086
|
G | A | 3 | a0001c0001t0001g0262a0001c0001t0001g0269a0001c0001t0001g0276 | 3 | HG00140.hp1 HG03942.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.-33-2295G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 252086 | ||||||
chr16:252162
|
A | G | 2 | a0001c0006t0006g0362a0001c0006t0006g0363 | 2 | HG00738.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-33-2219A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 252162 | ||||||
chr16:252185
|
G | GT | 55 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0025others(52): Show | 58 | HG00408.hp1 HG00438.hp2 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.-33-2180dupT | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr16 | 252185 | |||||
chr16:252185
|
G | T | 9 | a0001c0001t0001g0185a0001c0001t0001g0264a0001c0001t0001g0265others(6): Show | 9 | HG00099.hp2 HG01167.hp2 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.-33-2196G>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 252185 | ||||||
chr16:252185
|
GT | G | 131 | a0001c0001t0001g0224a0001c0001t0001g0225a0001c0001t0001g0230others(128): Show | 137 | HG00099.hp1 HG00597.hp1 HG00621.hp1 others(134): Show |
intron_variant | MODIFIER | c.-33-2180delT | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr16 | 252185 | |||||
chr16:252190
|
T | G | 1 | a0001c0001t0001g0271 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-33-2191T>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 252190 | ||||||
chr16:252326
|
C | A | 1 | a0001c0002t0002g0339 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-33-2055C>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 252326 | ||||||
chr16:252405
|
T | C | 3 | a0001c0002t0002g0062a0001c0002t0002g0255a0011c0028t0002g0256 | 3 | HG02647.hp2 HG02976.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-33-1976T>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 252405 | ||||||
chr16:252433
|
G | A | 13 | a0001c0001t0003g0078a0001c0001t0003g0096a0001c0001t0003g0213others(10): Show | 13 | HG00099.hp1 HG00621.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.-33-1948G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 252433 | ||||||
chr16:252507
|
G | T | 1 | a0001c0001t0007g0378 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-33-1874G>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 252507 | ||||||
chr16:252627
|
C | G | 1 | a0001c0002t0002g0254 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-33-1754C>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 252627 | ||||||
chr16:253021
|
G | T | 14 | a0002c0003t0001g0017a0002c0003t0001g0364a0002c0003t0001g0365others(11): Show | 15 | HG00621.hp1 HG01361.hp2 HG02015.hp2 others(12): Show |
intron_variant | MODIFIER | c.-33-1360G>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 253021 | ||||||
chr16:253024
|
C | A | 29 | a0001c0002t0002g0013a0001c0002t0002g0015a0001c0002t0002g0219others(26): Show | 29 | HG00438.hp2 HG00544.hp1 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.-33-1357C>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 253024 | ||||||
chr16:253028
|
A | T | 14 | a0002c0003t0001g0017a0002c0003t0001g0364a0002c0003t0001g0365others(11): Show | 15 | HG00621.hp1 HG01361.hp2 HG02015.hp2 others(12): Show |
intron_variant | MODIFIER | c.-33-1353A>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 253028 | ||||||
chr16:253400
|
A | T | 115 | a0001c0001t0002g0126a0001c0001t0002g0128a0001c0001t0002g0249others(112): Show | 120 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(117): Show |
intron_variant | MODIFIER | c.-33-981A>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 253400 | ||||||
chr16:253422
|
G | A | 4 | a0001c0002t0002g0040a0001c0002t0002g0041a0001c0002t0002g0305others(1): Show | 4 | HG01175.hp2 HG01255.hp2 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.-33-959G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 253422 | ||||||
chr16:253567
|
C | T | 1 | a0001c0027t0002g0307 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.-33-814C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 253567 | ||||||
chr16:253663
|
A | G | 1 | a0001c0001t0001g0350 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.-33-718A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 253663 | ||||||
chr16:253664
|
T | C | 184 | a0001c0001t0001g0224a0001c0001t0001g0225a0001c0001t0001g0230others(181): Show | 190 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(187): Show |
intron_variant | MODIFIER | c.-33-717T>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 253664 | ||||||
chr16:253699
|
C | T | 2 | a0001c0001t0007g0377a0001c0001t0007g0378 | 2 | HG03130.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-33-682C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 253699 | ||||||
chr16:253725
|
C | A | 2 | a0001c0001t0001g0210a0001c0001t0001g0211 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.-33-656C>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 253725 | ||||||
chr16:253725
|
C | T | 1 | a0001c0001t0001g0189 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-33-656C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 253725 | ||||||
chr16:253859
|
C | T | 1 | a0001c0002t0002g0334 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.-33-522C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 253859 | ||||||
chr16:253964
|
A | T | 1 | a0001c0001t0001g0218 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-33-417A>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 253964 | ||||||
chr16:254023
|
G | A | 1 | a0001c0001t0001g0172 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-33-358G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 254023 | ||||||
chr16:254041
|
G | T | 8 | a0001c0006t0001g0037a0001c0006t0001g0038a0001c0006t0001g0055others(5): Show | 8 | HG00738.hp1 HG01243.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.-33-340G>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 254041 | ||||||
chr16:254119
|
A | G | 1 | a0001c0002t0002g0029 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-33-262A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 254119 | ||||||
chr16:254270
|
A | G | 1 | a0001c0001t0001g0354 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-33-111A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 254270 | ||||||
chr16:254316
|
C | T | 3 | a0001c0006t0001g0037a0001c0006t0001g0038a0001c0006t0001g0055 | 3 | HG01243.hp2 HG02109.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.-33-65C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 2/12 | chr16 | 254316 | ||||||
chr16:254737
|
G | A | 3 | a0004c0007t0001g0049a0004c0007t0001g0050a0004c0007t0001g0051 | 3 | NA19043.hp2 NA19240.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.268+56G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 254737 | ||||||
chr16:254787
|
A | C | 4 | a0001c0001t0007g0377a0001c0001t0007g0378a0001c0001t0010g0248others(1): Show | 4 | HG03098.hp1 HG03130.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.268+106A>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 254787 | ||||||
chr16:254796
|
A | G | 1 | a0001c0001t0001g0252 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.268+115A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 254796 | ||||||
chr16:254804
|
A | T | 265 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0016others(262): Show | 275 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(272): Show |
intron_variant | MODIFIER | c.268+123A>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 254804 | ||||||
chr16:254850
|
G | A | 4 | a0001c0001t0002g0126a0001c0001t0002g0128a0001c0001t0002g0249others(1): Show | 4 | HG02055.hp2 HG02970.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.268+169G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 254850 | ||||||
chr16:255089
|
C | T | 5 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0001g0163others(2): Show | 5 | HG01261.hp2 HG01993.hp1 NA18948.hp1 others(2): Show |
intron_variant | MODIFIER | c.268+408C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 255089 | ||||||
chr16:255139
|
C | T | 17 | a0001c0001t0003g0078a0001c0001t0003g0096a0001c0001t0003g0213others(14): Show | 17 | HG00099.hp1 HG00621.hp2 HG00673.hp2 others(14): Show |
intron_variant | MODIFIER | c.268+458C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 255139 | ||||||
chr16:255146
|
G | A | 10 | a0001c0001t0005g0009a0001c0001t0005g0026a0001c0001t0005g0027others(7): Show | 10 | HG01069.hp1 HG01071.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.268+465G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 255146 | ||||||
chr16:255146
|
G | T | 2 | a0001c0001t0001g0163a0001c0001t0001g0207 | 2 | HG01261.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.268+465G>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 255146 | ||||||
chr16:255269
|
T | C | 185 | a0001c0001t0001g0054a0001c0001t0001g0224a0001c0001t0001g0225others(182): Show | 191 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(188): Show |
intron_variant | MODIFIER | c.268+588T>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 255269 | ||||||
chr16:255270
|
G | A | 1 | a0002c0003t0001g0371 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.268+589G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 255270 | ||||||
chr16:255274
|
G | A | 1 | a0001c0002t0002g0029 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.268+593G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 255274 | ||||||
chr16:255302
|
T | C | 3 | a0001c0002t0002g0337a0001c0002t0002g0338a0001c0002t0002g0340 | 3 | NA18953.hp1 NA18963.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.268+621T>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 255302 | ||||||
chr16:255378
|
G | C | 168 | a0001c0001t0002g0126a0001c0001t0002g0128a0001c0001t0002g0249others(165): Show | 174 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(171): Show |
intron_variant | MODIFIER | c.268+697G>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 255378 | ||||||
chr16:255400
|
C | T | 2 | a0001c0001t0001g0134a0001c0001t0001g0354 | 2 | HG02109.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.268+719C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 255400 | ||||||
chr16:255426
|
C | T | 1 | a0001c0001t0001g0260 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.268+745C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 255426 | ||||||
chr16:255457
|
C | G | 1 | a0001c0002t0002g0335 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.268+776C>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 255457 | ||||||
chr16:255541
|
T | A | 2 | a0001c0001t0007g0377a0001c0001t0007g0378 | 2 | HG03130.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.268+860T>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 255541 | ||||||
chr16:255647
|
C | A | 1 | a0001c0002t0002g0293 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.268+966C>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 255647 | ||||||
chr16:255732
|
C | A | 8 | a0001c0006t0001g0037a0001c0006t0001g0038a0001c0006t0001g0055others(5): Show | 8 | HG00738.hp1 HG01243.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.268+1051C>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 255732 | ||||||
chr16:255829
|
A | G | 113 | a0001c0001t0002g0126a0001c0001t0002g0128a0001c0001t0002g0249others(110): Show | 118 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(115): Show |
intron_variant | MODIFIER | c.268+1148A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 255829 | ||||||
chr16:255863
|
G | A | 8 | a0001c0006t0001g0037a0001c0006t0001g0038a0001c0006t0001g0055others(5): Show | 8 | HG00738.hp1 HG01243.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.268+1182G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 255863 | ||||||
chr16:255873
|
G | A | 1 | a0001c0002t0002g0310 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.268+1192G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 255873 | ||||||
chr16:255888
|
C | T | 1 | a0001c0001t0001g0201 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.268+1207C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 255888 | ||||||
chr16:256045
|
G | A | 8 | a0001c0006t0001g0037a0001c0006t0001g0038a0001c0006t0001g0055others(5): Show | 8 | HG00738.hp1 HG01243.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.268+1364G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 256045 | ||||||
chr16:256063
|
C | G | 3 | a0001c0001t0001g0082a0001c0001t0001g0085a0001c0001t0001g0088 | 3 | NA18969.hp2 NA18981.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.268+1382C>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 256063 | ||||||
chr16:256161
|
G | A | 2 | a0001c0001t0001g0069a0001c0001t0001g0072 | 2 | HG00735.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.268+1480G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 256161 | ||||||
chr16:256173
|
G | A | 1 | a0010c0016t0001g0116 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.268+1492G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 256173 | ||||||
chr16:256239
|
A | T | 1 | a0001c0001t0001g0350 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.268+1558A>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 256239 | ||||||
chr16:256244
|
A | G | 141 | a0001c0001t0002g0126a0001c0001t0002g0128a0001c0001t0002g0249others(138): Show | 146 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(143): Show |
intron_variant | MODIFIER | c.268+1563A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 256244 | ||||||
chr16:256317
|
T | TA | 14 | a0002c0003t0001g0017a0002c0003t0001g0364a0002c0003t0001g0365others(11): Show | 15 | HG00621.hp1 HG01361.hp2 HG02015.hp2 others(12): Show |
intron_variant | MODIFIER | c.268+1636_268+1637i others(3): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 256317 | ||||||
chr16:256403
|
T | C | 2 | a0001c0001t0003g0078a0001c0001t0003g0096 | 2 | HG01106.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.268+1722T>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 256403 | ||||||
chr16:256609
|
A | C | 1 | a0001c0001t0001g0191 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.268+1928A>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 256609 | ||||||
chr16:256673
|
C | T | 14 | a0002c0003t0001g0017a0002c0003t0001g0364a0002c0003t0001g0365others(11): Show | 15 | HG00621.hp1 HG01361.hp2 HG02015.hp2 others(12): Show |
intron_variant | MODIFIER | c.268+1992C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 256673 | ||||||
chr16:256740
|
A | AT | 107 | a0001c0001t0001g0169a0001c0001t0001g0189a0001c0001t0001g0209others(104): Show | 112 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(109): Show |
intron_variant | MODIFIER | c.268+2078dupT | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr16 | 256740 | |||||
chr16:256740
|
AT | A | 24 | a0001c0001t0001g0085a0001c0001t0001g0090a0001c0001t0001g0095others(21): Show | 24 | HG00099.hp1 HG00621.hp2 HG00673.hp2 others(21): Show |
intron_variant | MODIFIER | c.268+2078delT | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr16 | 256740 | |||||
chr16:256743
|
T | A | 1 | a0001c0001t0001g0112 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.268+2062T>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 256743 | ||||||
chr16:256989
|
G | A | 14 | a0002c0003t0001g0017a0002c0003t0001g0364a0002c0003t0001g0365others(11): Show | 15 | HG00621.hp1 HG01361.hp2 HG02015.hp2 others(12): Show |
intron_variant | MODIFIER | c.268+2308G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 256989 | ||||||
chr16:257068
|
G | A | 14 | a0002c0003t0001g0017a0002c0003t0001g0364a0002c0003t0001g0365others(11): Show | 15 | HG00621.hp1 HG01361.hp2 HG02015.hp2 others(12): Show |
intron_variant | MODIFIER | c.268+2387G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 257068 | ||||||
chr16:257075
|
C | T | 1 | a0001c0001t0003g0220 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.268+2394C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 257075 | ||||||
chr16:257083
|
T | C | 15 | a0001c0001t0001g0224a0001c0001t0001g0225a0001c0001t0001g0230others(12): Show | 15 | HG01106.hp1 HG01891.hp2 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.269-2400T>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 257083 | ||||||
chr16:257170
|
C | T | 2 | a0001c0001t0005g0026a0001c0001t0005g0027 | 2 | HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.269-2313C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 257170 | ||||||
chr16:257189
|
C | G | 1 | a0001c0002t0002g0255 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.269-2294C>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 257189 | ||||||
chr16:257236
|
C | CT | 54 | a0001c0001t0001g0025a0001c0001t0001g0042a0001c0001t0001g0044others(51): Show | 54 | HG00423.hp2 HG00544.hp1 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.269-2221dupT | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr16 | 257236 | |||||
chr16:257236
|
CT | C | 55 | a0001c0001t0001g0024a0001c0001t0001g0090a0001c0001t0001g0135others(52): Show | 56 | HG00738.hp1 HG01069.hp1 HG01071.hp1 others(53): Show |
intron_variant | MODIFIER | c.269-2221delT | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr16 | 257236 | |||||
chr16:257236
|
CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0003g0253 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.269-2230_269-2221d others(12): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr16 | 257236 | |||||
chr16:257236
|
CTTTTTTT others(6): Show |
C | 1 | a0001c0002t0002g0293 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.269-2233_269-2221d others(15): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr16 | 257236 | |||||
chr16:257257
|
T | G | 10 | a0001c0001t0005g0009a0001c0001t0005g0026a0001c0001t0005g0027others(7): Show | 10 | HG01069.hp1 HG01071.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.269-2226T>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 257257 | ||||||
chr16:257435
|
G | A | 1 | a0001c0001t0008g0247 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.269-2048G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 257435 | ||||||
chr16:257539
|
C | T | 2 | a0001c0001t0007g0377a0001c0001t0007g0378 | 2 | HG03130.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.269-1944C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 257539 | ||||||
chr16:257560
|
A | G | 2 | a0001c0001t0001g0193a0001c0001t0001g0194 | 2 | NA18999.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.269-1923A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 257560 | ||||||
chr16:257615
|
T | C | 106 | a0001c0001t0002g0126a0001c0001t0002g0128a0001c0001t0002g0249others(103): Show | 111 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(108): Show |
intron_variant | MODIFIER | c.269-1868T>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 257615 | ||||||
chr16:257618
|
A | G | 10 | a0001c0001t0005g0009a0001c0001t0005g0026a0001c0001t0005g0027others(7): Show | 10 | HG01069.hp1 HG01071.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.269-1865A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 257618 | ||||||
chr16:257780
|
G | C | 2 | a0001c0001t0010g0248a0001c0001t0010g0250 | 2 | HG03098.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.269-1703G>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 257780 | ||||||
chr16:257858
|
T | G | 32 | a0001c0001t0003g0078a0001c0001t0003g0096a0001c0001t0003g0213others(29): Show | 32 | HG00099.hp1 HG00621.hp2 HG00673.hp2 others(29): Show |
intron_variant | MODIFIER | c.269-1625T>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 257858 | ||||||
chr16:257983
|
G | A | 2 | a0007c0008t0002g0359a0007c0008t0002g0360 | 2 | HG02572.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.269-1500G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 257983 | ||||||
chr16:258003
|
G | A | 9 | a0001c0001t0003g0253a0001c0006t0001g0037a0001c0006t0001g0038others(6): Show | 9 | HG00738.hp1 HG01243.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.269-1480G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 258003 | ||||||
chr16:258004
|
C | G | 1 | a0001c0001t0001g0271 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.269-1479C>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 258004 | ||||||
chr16:258023
|
A | G | 1 | a0001c0001t0003g0289 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.269-1460A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 258023 | ||||||
chr16:258056
|
G | A | 9 | a0001c0001t0001g0100a0001c0001t0001g0104a0001c0001t0001g0120others(6): Show | 9 | HG02015.hp1 HG02486.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.269-1427G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 258056 | ||||||
chr16:258109
|
C | G | 8 | a0001c0006t0001g0037a0001c0006t0001g0038a0001c0006t0001g0055others(5): Show | 8 | HG00738.hp1 HG01243.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.269-1374C>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 258109 | ||||||
chr16:258150
|
G | A | 3 | a0001c0001t0004g0226a0001c0001t0004g0227a0001c0001t0004g0228 | 3 | HG02486.hp2 HG03139.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.269-1333G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 258150 | ||||||
chr16:258155
|
A | AT | 35 | a0001c0001t0001g0054a0001c0001t0001g0140a0001c0001t0001g0225others(32): Show | 36 | HG00621.hp1 HG00738.hp1 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.269-1310dupT | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr16 | 258155 | |||||
chr16:258155
|
AT | A | 37 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0064others(34): Show | 37 | HG00099.hp1 HG00621.hp2 HG00673.hp2 others(34): Show |
intron_variant | MODIFIER | c.269-1310delT | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr16 | 258155 | |||||
chr16:258173
|
T | A | 19 | a0001c0001t0003g0036a0001c0001t0003g0078a0001c0001t0003g0096others(16): Show | 19 | HG00099.hp1 HG00621.hp2 HG00673.hp2 others(16): Show |
intron_variant | MODIFIER | c.269-1310T>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 258173 | ||||||
chr16:258192
|
T | G | 1 | a0001c0001t0001g0200 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.269-1291T>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 258192 | ||||||
chr16:258319
|
G | A | 1 | a0001c0001t0001g0272 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.269-1164G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 258319 | ||||||
chr16:258361
|
C | A | 1 | a0001c0001t0003g0355 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.269-1122C>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 258361 | ||||||
chr16:258501
|
CAGA | C | 154 | a0001c0001t0002g0126a0001c0001t0002g0128a0001c0001t0002g0249others(151): Show | 159 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(156): Show |
intron_variant | MODIFIER | c.269-976_269-974del others(3): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr16 | 258501 | |||||
chr16:258563
|
C | T | 1 | a0001c0001t0001g0354 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.269-920C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 258563 | ||||||
chr16:258609
|
C | A | 1 | a0006c0010t0001g0076 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.269-874C>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 258609 | ||||||
chr16:258650
|
G | T | 1 | a0001c0002t0002g0255 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.269-833G>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 258650 | ||||||
chr16:258683
|
C | T | 1 | a0001c0001t0003g0289 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.269-800C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 258683 | ||||||
chr16:258733
|
G | A | 2 | a0007c0008t0002g0359a0007c0008t0002g0360 | 2 | HG02572.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.269-750G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 258733 | ||||||
chr16:258761
|
G | C | 14 | a0002c0003t0001g0017a0002c0003t0001g0364a0002c0003t0001g0365others(11): Show | 15 | HG00621.hp1 HG01361.hp2 HG02015.hp2 others(12): Show |
intron_variant | MODIFIER | c.269-722G>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 258761 | ||||||
chr16:258929
|
C | T | 1 | a0001c0001t0001g0200 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.269-554C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 258929 | ||||||
chr16:258940
|
A | G | 5 | a0001c0005t0002g0010a0001c0005t0002g0043a0001c0005t0002g0129others(2): Show | 6 | HG02559.hp1 HG02809.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.269-543A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 258940 | ||||||
chr16:259032
|
C | T | 1 | a0001c0002t0002g0255 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.269-451C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 259032 | ||||||
chr16:259061
|
G | A | 1 | a0014c0014t0001g0270 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.269-422G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 259061 | ||||||
chr16:259092
|
T | G | 2 | a0001c0001t0005g0026a0001c0001t0005g0027 | 2 | HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.269-391T>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 259092 | ||||||
chr16:259156
|
C | A | 76 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0016others(73): Show | 80 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.269-327C>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 259156 | ||||||
chr16:259358
|
C | T | 1 | a0001c0001t0001g0147 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.269-125C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 259358 | ||||||
chr16:259378
|
A | C | 1 | a0001c0001t0001g0354 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.269-105A>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 259378 | ||||||
chr16:259413
|
G | A | 1 | a0001c0002t0002g0029 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.269-70G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 259413 | ||||||
chr16:259427
|
C | T | 10 | a0001c0001t0005g0009a0001c0001t0005g0026a0001c0001t0005g0027others(7): Show | 10 | HG01069.hp1 HG01071.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.269-56C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 259427 | ||||||
chr16:259446
|
TG | T | 14 | a0001c0001t0001g0224a0001c0001t0001g0230a0001c0001t0001g0231others(11): Show | 14 | HG01106.hp1 HG01891.hp2 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.269-35delG | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr16 | 259446 | |||||
chr16:259448
|
G | C | 14 | a0001c0001t0001g0224a0001c0001t0001g0230a0001c0001t0001g0231others(11): Show | 14 | HG01106.hp1 HG01891.hp2 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.269-35G>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 3/12 | chr16 | 259448 | ||||||
chr16:259706
|
T | C | 1 | a0001c0001t0005g0240 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.385+107T>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 4/12 | chr16 | 259706 | ||||||
chr16:259721
|
C | T | 109 | a0001c0001t0002g0126a0001c0001t0002g0128a0001c0001t0002g0249others(106): Show | 114 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(111): Show |
intron_variant | MODIFIER | c.385+122C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 4/12 | chr16 | 259721 | ||||||
chr16:259837
|
A | C | 1 | a0001c0001t0003g0253 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.386-132A>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 4/12 | chr16 | 259837 | ||||||
chr16:259895
|
C | T | 6 | a0001c0001t0004g0226a0001c0001t0004g0227a0001c0001t0004g0228others(3): Show | 6 | HG02486.hp2 HG02717.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.386-74C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 4/12 | chr16 | 259895 | ||||||
chr16:259937
|
C | T | 1 | a0001c0001t0001g0090 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.386-32C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 4/12 | chr16 | 259937 | ||||||
chr16:259951
|
C | T | 38 | a0001c0002t0001g0331a0001c0002t0002g0013a0001c0002t0002g0015others(35): Show | 38 | HG00438.hp2 HG00544.hp1 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.386-18C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 4/12 | chr16 | 259951 | ||||||
chr16:260244
|
G | A | 112 | a0001c0001t0002g0126a0001c0001t0002g0128a0001c0001t0002g0249others(109): Show | 117 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(114): Show |
intron_variant | MODIFIER | c.577+84G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 5/12 | chr16 | 260244 | ||||||
chr16:260246
|
C | T | 1 | a0001c0012t0004g0238 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.577+86C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 5/12 | chr16 | 260246 | ||||||
chr16:260294
|
T | C | 3 | a0001c0001t0001g0167a0001c0001t0001g0171a0001c0001t0001g0177 | 3 | HG02615.hp1 HG02630.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.577+134T>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 5/12 | chr16 | 260294 | ||||||
chr16:260355
|
C | T | 8 | a0001c0006t0001g0037a0001c0006t0001g0038a0001c0006t0001g0055others(5): Show | 8 | HG00738.hp1 HG01243.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.577+195C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 5/12 | chr16 | 260355 | ||||||
chr16:260381
|
G | A | 8 | a0001c0006t0001g0037a0001c0006t0001g0038a0001c0006t0001g0055others(5): Show | 8 | HG00738.hp1 HG01243.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.577+221G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 5/12 | chr16 | 260381 | ||||||
chr16:260469
|
C | T | 1 | a0001c0001t0001g0282 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.577+309C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 5/12 | chr16 | 260469 | ||||||
chr16:260503
|
C | A | 4 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195others(1): Show | 4 | NA18989.hp2 NA18999.hp1 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.577+343C>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 5/12 | chr16 | 260503 | ||||||
chr16:260508
|
C | T | 1 | a0001c0001t0001g0258 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.577+348C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 5/12 | chr16 | 260508 | ||||||
chr16:260598
|
C | T | 1 | a0001c0001t0005g0127 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.577+438C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 5/12 | chr16 | 260598 | ||||||
chr16:260845
|
G | C | 3 | a0001c0001t0004g0226a0001c0001t0004g0227a0001c0001t0004g0228 | 3 | HG02486.hp2 HG03139.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.578-539G>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 5/12 | chr16 | 260845 | ||||||
chr16:260871
|
T | G | 2 | a0001c0001t0007g0377a0001c0001t0007g0378 | 2 | HG03130.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.578-513T>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 5/12 | chr16 | 260871 | ||||||
chr16:260887
|
C | T | 2 | a0001c0001t0001g0356a0001c0001t0001g0361 | 2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.578-497C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 5/12 | chr16 | 260887 | ||||||
chr16:260968
|
G | T | 2 | a0001c0001t0001g0193a0001c0001t0001g0194 | 2 | NA18999.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.578-416G>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 5/12 | chr16 | 260968 | ||||||
chr16:261108
|
G | A | 5 | a0001c0006t0001g0037a0001c0006t0001g0038a0001c0006t0001g0055others(2): Show | 5 | HG00738.hp1 HG01243.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.578-276G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 5/12 | chr16 | 261108 | ||||||
chr16:261133
|
G | A | 8 | a0001c0006t0001g0037a0001c0006t0001g0038a0001c0006t0001g0055others(5): Show | 8 | HG00738.hp1 HG01243.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.578-251G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 5/12 | chr16 | 261133 | ||||||
chr16:261181
|
C | T | 1 | a0001c0001t0001g0122 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.578-203C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 5/12 | chr16 | 261181 | ||||||
chr16:261235
|
T | G | 4 | a0001c0001t0002g0126a0001c0001t0002g0128a0001c0001t0002g0249others(1): Show | 4 | HG02055.hp2 HG02970.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.578-149T>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 5/12 | chr16 | 261235 | ||||||
chr16:261362
|
G | A | 3 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0001g0196 | 3 | NA18948.hp1 NA18975.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.578-22G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 5/12 | chr16 | 261362 | ||||||
chr16:261368
|
G | A | 8 | a0001c0001t0004g0226a0001c0001t0004g0227a0001c0001t0004g0228others(5): Show | 8 | HG01891.hp1 HG02486.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.578-16G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 5/12 | chr16 | 261368 | ||||||
chr16:261651
|
G | A | 1 | a0002c0003t0001g0375 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.708+137G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 6/12 | chr16 | 261651 | ||||||
chr16:261671
|
C | T | 2 | a0001c0001t0010g0248a0001c0001t0010g0250 | 2 | HG03098.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.708+157C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 6/12 | chr16 | 261671 | ||||||
chr16:261823
|
C | T | 14 | a0002c0003t0001g0017a0002c0003t0001g0364a0002c0003t0001g0365others(11): Show | 15 | HG00621.hp1 HG01361.hp2 HG02015.hp2 others(12): Show |
intron_variant | MODIFIER | c.709-270C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 6/12 | chr16 | 261823 | ||||||
chr16:261854
|
A | G | 172 | a0001c0001t0001g0354a0001c0001t0002g0126a0001c0001t0002g0128others(169): Show | 178 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(175): Show |
intron_variant | MODIFIER | c.709-239A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 6/12 | chr16 | 261854 | ||||||
chr16:261860
|
C | T | 1 | a0001c0001t0001g0379 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.709-233C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 6/12 | chr16 | 261860 | ||||||
chr16:261971
|
CTCTCTTC others(38): Show |
C | 158 | a0001c0001t0001g0354a0001c0001t0002g0126a0001c0001t0002g0128others(155): Show | 163 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(160): Show |
intron_variant | MODIFIER | c.709-100_709-56delA others(44): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr16 | 261971 | |||||
chr16:262250
|
G | C | 8 | a0001c0001t0001g0007a0001c0001t0001g0144a0001c0001t0001g0147others(5): Show | 10 | HG00423.hp1 HG00609.hp2 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.841+25G>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 7/12 | chr16 | 262250 | ||||||
chr16:262254
|
A | G | 180 | a0001c0001t0001g0007a0001c0001t0001g0144a0001c0001t0001g0147others(177): Show | 188 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(185): Show |
intron_variant | MODIFIER | c.841+29A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 7/12 | chr16 | 262254 | ||||||
chr16:262288
|
C | T | 1 | a0002c0003t0001g0369 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.841+63C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 7/12 | chr16 | 262288 | ||||||
chr16:262369
|
G | A | 1 | a0001c0001t0001g0077 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.842-55G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 7/12 | chr16 | 262369 | ||||||
chr16:262621
|
C | T | 1 | a0001c0001t0001g0243 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.971+68C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 8/12 | chr16 | 262621 | ||||||
chr16:262636
|
T | C | 115 | a0001c0001t0001g0067a0001c0001t0001g0354a0001c0001t0002g0126others(112): Show | 120 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(117): Show |
intron_variant | MODIFIER | c.971+83T>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 8/12 | chr16 | 262636 | ||||||
chr16:262806
|
G | GT | 33 | a0001c0001t0001g0069a0001c0001t0001g0141a0001c0001t0001g0156others(30): Show | 34 | HG00621.hp1 HG00735.hp2 HG01069.hp1 others(31): Show |
intron_variant | MODIFIER | c.971+267dupT | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr16 | 262806 | |||||
chr16:262814
|
T | A | 6 | a0001c0001t0004g0226a0001c0001t0004g0227a0001c0001t0004g0228others(3): Show | 6 | HG02486.hp2 HG02717.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.971+261T>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 8/12 | chr16 | 262814 | ||||||
chr16:262824
|
T | G | 14 | a0001c0001t0001g0054a0001c0001t0001g0224a0001c0001t0001g0225others(11): Show | 14 | HG01106.hp1 HG01891.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.971+271T>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 8/12 | chr16 | 262824 | ||||||
chr16:262888
|
C | T | 2 | a0001c0001t0010g0248a0001c0001t0010g0250 | 2 | HG03098.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.971+335C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 8/12 | chr16 | 262888 | ||||||
chr16:263203
|
C | A | 133 | a0001c0001t0001g0354a0001c0001t0002g0126a0001c0001t0002g0128others(130): Show | 138 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(135): Show |
intron_variant | MODIFIER | c.972-59C>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 8/12 | chr16 | 263203 | ||||||
chr16:263206
|
G | A | 1 | a0001c0021t0003g0216 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.972-56G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 8/12 | chr16 | 263206 | ||||||
chr16:263407
|
A | G | 174 | a0001c0001t0001g0077a0001c0001t0001g0354a0001c0001t0002g0126others(171): Show | 180 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(177): Show |
splice_region_variant&intron_variant | LOW | c.1112+5A>G | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 9/12 | chr16 | 263407 | ||||||
chr16:263466
|
C | T | 6 | a0001c0001t0004g0226a0001c0001t0004g0227a0001c0001t0004g0228others(3): Show | 6 | HG02486.hp2 HG02717.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1112+64C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 9/12 | chr16 | 263466 | ||||||
chr16:263510
|
G | A | 1 | a0001c0001t0001g0153 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1112+108G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 9/12 | chr16 | 263510 | ||||||
chr16:263520
|
G | T | 1 | a0001c0001t0001g0198 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1112+118G>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 9/12 | chr16 | 263520 | ||||||
chr16:263574
|
C | T | 2 | a0001c0001t0001g0102a0001c0012t0004g0238 | 2 | HG03225.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.1113-126C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 9/12 | chr16 | 263574 | ||||||
chr16:263645
|
C | T | 3 | a0004c0007t0001g0049a0004c0007t0001g0050a0004c0007t0001g0051 | 3 | NA19043.hp2 NA19240.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1113-55C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 9/12 | chr16 | 263645 | ||||||
chr16:263647
|
T | C | 1 | a0001c0001t0003g0036 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1113-53T>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 9/12 | chr16 | 263647 | ||||||
chr16:263849
|
C | T | 101 | a0001c0001t0001g0354a0001c0001t0002g0126a0001c0001t0002g0128others(98): Show | 106 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(103): Show |
intron_variant | MODIFIER | c.1188+74C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 10/12 | chr16 | 263849 | ||||||
chr16:263983
|
C | T | 1 | a0001c0001t0001g0260 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1189-33C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 10/12 | chr16 | 263983 | ||||||
chr16:264256
|
C | T | 8 | a0001c0001t0005g0009a0001c0001t0005g0127a0001c0001t0005g0240others(5): Show | 8 | HG01069.hp1 HG01071.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.1344+85C>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 11/12 | chr16 | 264256 | ||||||
chr16:264262
|
G | C | 1 | a0001c0001t0001g0086 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1344+91G>C | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 11/12 | chr16 | 264262 | ||||||
chr16:264452
|
G | A | 1 | a0001c0001t0001g0205 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1345-162G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 11/12 | chr16 | 264452 | ||||||
chr16:264520
|
AGACATAG others(35): Show |
A | 5 | a0001c0002t0002g0040a0001c0002t0002g0041a0001c0002t0002g0305others(2): Show | 5 | HG00733.hp1 HG01175.hp2 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.1345-92_1345-51del others(42): Show |
FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr16 | 264520 | |||||
chr16:264535
|
G | T | 9 | a0001c0001t0005g0009a0001c0001t0005g0026a0001c0001t0005g0027others(6): Show | 9 | HG01069.hp1 HG01071.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.1345-79G>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 11/12 | chr16 | 264535 | ||||||
chr16:264754
|
G | A | 1 | a0001c0001t0001g0089 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1447+38G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 12/12 | chr16 | 264754 | ||||||
chr16:264757
|
G | A | 1 | a0001c0001t0001g0183 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1447+41G>A | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 12/12 | chr16 | 264757 | ||||||
chr16:264781
|
G | T | 5 | a0001c0006t0001g0037a0001c0006t0001g0038a0001c0006t0001g0055others(2): Show | 5 | HG00738.hp1 HG01243.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.1448-30G>T | FAM234A | ENSG00000167930.17 | transcript | ENST00000399932.8 | protein_coding | 12/12 | chr16 | 264781 |