geneid | 1071 |
---|---|
ensemblid | ENSG00000087237.12 |
hgncid | 1869 |
symbol | CETP |
name | cholesteryl ester transfer protein |
refseq_nuc | NM_000078.3 |
refseq_prot | NP_000069.2 |
ensembl_nuc | ENST00000200676.8 |
ensembl_prot | ENSP00000200676.3 |
mane_status | MANE Select |
chr | chr16 |
start | 56961950 |
end | 56983845 |
strand | + |
ver | v1.2 |
region | chr16:56961950-56983845 |
region5000 | chr16:56956950-56988845 |
regionname0 | CETP_chr16_56961950_56983845 |
regionname5000 | CETP_chr16_56956950_56988845 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 493 | 211 | 29 | 42 | 97 | 13 | 29 | 65 | CETP_chr16_56956950_56988845 | CETP | copy fasta | chr16 | 56956950 | 56988845 |
a0002 | 1/0 | 493 | 209 | 56 | 26 | 108 | 3 | 15 | 91 | CETP_chr16_56956950_56988845 | CETP | copy fasta | chr16 | 56956950 | 56988845 |
a0003 | 0/0 | 493 | 12 | 0 | 11 | 0 | 0 | 1 | 0 | CETP_chr16_56956950_56988845 | CETP | copy fasta | chr16 | 56956950 | 56988845 |
a0004 | 0/0 | 493 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | copy fasta | chr16 | 56956950 | 56988845 |
a0005 | 0/0 | 493 | 5 | 0 | 0 | 5 | 0 | 0 | 5 | CETP_chr16_56956950_56988845 | CETP | copy fasta | chr16 | 56956950 | 56988845 |
a0006 | 0/0 | 493 | 3 | 0 | 1 | 0 | 0 | 2 | 0 | CETP_chr16_56956950_56988845 | CETP | copy fasta | chr16 | 56956950 | 56988845 |
a0007 | 0/0 | 493 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | copy fasta | chr16 | 56956950 | 56988845 |
a0008 | 0/0 | 493 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | copy fasta | chr16 | 56956950 | 56988845 |
a0009 | 0/0 | 493 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | CETP_chr16_56956950_56988845 | CETP | copy fasta | chr16 | 56956950 | 56988845 |
a0010 | 0/0 | 493 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | copy fasta | chr16 | 56956950 | 56988845 |
a0011 | 0/0 | 493 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CETP_chr16_56956950_56988845 | CETP | copy fasta | chr16 | 56956950 | 56988845 |
a0012 | 0/0 | 493 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | copy fasta | chr16 | 56956950 | 56988845 |
a0013 | 0/0 | 493 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CETP_chr16_56956950_56988845 | CETP | copy fasta | chr16 | 56956950 | 56988845 |
a0014 | 0/0 | 493 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CETP_chr16_56956950_56988845 | CETP | copy fasta | chr16 | 56956950 | 56988845 |
a0015 | 0/0 | 493 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | copy fasta | chr16 | 56956950 | 56988845 |
a0016 | 0/0 | 493 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CETP_chr16_56956950_56988845 | CETP | copy fasta | chr16 | 56956950 | 56988845 |
a0017 | 0/0 | 493 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | copy fasta | chr16 | 56956950 | 56988845 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/1 | 1482 | 207 | 29 | 42 | 93 | 13 | 29 | CETP_chr16_56956950_56988845 | CETP | copy fasta | chr16 | 56956950 | 56988845 |
c0002 | 1/0 | 1482 | 168 | 29 | 25 | 101 | 2 | 10 | CETP_chr16_56956950_56988845 | CETP | copy fasta | chr16 | 56956950 | 56988845 |
c0003 | 0/0 | 1482 | 17 | 12 | 1 | 0 | 1 | 3 | CETP_chr16_56956950_56988845 | CETP | copy fasta | chr16 | 56956950 | 56988845 |
c0004 | 0/0 | 1482 | 12 | 0 | 11 | 0 | 0 | 1 | CETP_chr16_56956950_56988845 | CETP | copy fasta | chr16 | 56956950 | 56988845 |
c0005 | 0/0 | 1482 | 9 | 0 | 0 | 7 | 0 | 2 | CETP_chr16_56956950_56988845 | CETP | copy fasta | chr16 | 56956950 | 56988845 |
c0006 | 0/0 | 1482 | 6 | 6 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | copy fasta | chr16 | 56956950 | 56988845 |
c0007 | 0/0 | 1482 | 6 | 6 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | copy fasta | chr16 | 56956950 | 56988845 |
c0008 | 0/0 | 1482 | 5 | 0 | 0 | 5 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | copy fasta | chr16 | 56956950 | 56988845 |
c0009 | 0/0 | 1482 | 5 | 5 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | copy fasta | chr16 | 56956950 | 56988845 |
c0010 | 0/0 | 1482 | 3 | 0 | 0 | 3 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | copy fasta | chr16 | 56956950 | 56988845 |
c0011 | 0/0 | 1482 | 3 | 0 | 1 | 0 | 0 | 2 | CETP_chr16_56956950_56988845 | CETP | copy fasta | chr16 | 56956950 | 56988845 |
c0012 | 0/0 | 1482 | 3 | 3 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | copy fasta | chr16 | 56956950 | 56988845 |
c0013 | 0/0 | 1482 | 3 | 2 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | copy fasta | chr16 | 56956950 | 56988845 |
c0014 | 0/0 | 1482 | 2 | 2 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | copy fasta | chr16 | 56956950 | 56988845 |
c0015 | 0/0 | 1482 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | copy fasta | chr16 | 56956950 | 56988845 |
c0016 | 0/0 | 1482 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | copy fasta | chr16 | 56956950 | 56988845 |
c0017 | 0/0 | 1482 | 1 | 0 | 0 | 0 | 0 | 1 | CETP_chr16_56956950_56988845 | CETP | copy fasta | chr16 | 56956950 | 56988845 |
c0018 | 0/0 | 1482 | 1 | 0 | 0 | 0 | 0 | 1 | CETP_chr16_56956950_56988845 | CETP | copy fasta | chr16 | 56956950 | 56988845 |
c0019 | 0/0 | 1482 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | copy fasta | chr16 | 56956950 | 56988845 |
c0020 | 0/0 | 1482 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | copy fasta | chr16 | 56956950 | 56988845 |
c0021 | 0/0 | 1482 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | copy fasta | chr16 | 56956950 | 56988845 |
c0022 | 0/0 | 1482 | 1 | 0 | 0 | 0 | 0 | 1 | CETP_chr16_56956950_56988845 | CETP | copy fasta | chr16 | 56956950 | 56988845 |
c0023 | 0/0 | 1482 | 1 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | copy fasta | chr16 | 56956950 | 56988845 |
c0024 | 0/0 | 1482 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | copy fasta | chr16 | 56956950 | 56988845 |
c0025 | 0/0 | 1482 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | copy fasta | chr16 | 56956950 | 56988845 |
c0026 | 0/0 | 1482 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | copy fasta | chr16 | 56956950 | 56988845 |
c0027 | 0/0 | 1482 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | copy fasta | chr16 | 56956950 | 56988845 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 210 | 404 | 82 | 75 | 190 | 14 | 41 | CETP_chr16_56956950_56988845 | CETP | copy fasta | chr16 | 56956950 | 56988845 |
t0002 | 0/0 | 210 | 57 | 15 | 7 | 24 | 2 | 9 | CETP_chr16_56956950_56988845 | CETP | copy fasta | chr16 | 56956950 | 56988845 |
t0003 | 0/0 | 210 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | copy fasta | chr16 | 56956950 | 56988845 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 15 | 2 | 2 | 8 | 1 | 2 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0002 | 0/0 | 15 | 4 | 3 | 4 | 3 | 1 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0003 | 0/0 | 8 | 0 | 2 | 6 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0004 | 0/0 | 8 | 0 | 1 | 7 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0005 | 0/0 | 7 | 1 | 0 | 5 | 1 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0006 | 0/0 | 6 | 0 | 2 | 4 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0007 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0008 | 0/0 | 5 | 0 | 4 | 0 | 0 | 1 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0009 | 0/0 | 5 | 0 | 0 | 3 | 1 | 1 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0010 | 0/0 | 5 | 0 | 4 | 0 | 0 | 1 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0011 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0013 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0014 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0015 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0016 | 0/0 | 4 | 0 | 2 | 0 | 1 | 1 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0017 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0018 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0019 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0021 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0024 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0025 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0026 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0027 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0028 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0029 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0030 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0031 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0032 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0034 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0035 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0037 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0042 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0044 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0045 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0047 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0049 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0050 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0051 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0052 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0053 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0054 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0055 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0056 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0057 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0058 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0059 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0060 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0061 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0062 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0063 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0064 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0065 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0265 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0269 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0272 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0285 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0288 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 1482 | 207 | 29 | 42 | 93 | 13 | 29 | CETP_chr16_56956950_56988845 | CETP | copy fasta | chr16 | 56956950 | 56988845 |
a0001c0010 | 0/0 | 1482 | 3 | 0 | 0 | 3 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | copy fasta | chr16 | 56956950 | 56988845 |
a0001c0016 | 0/0 | 1482 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | copy fasta | chr16 | 56956950 | 56988845 |
a0002c0002 | 1/0 | 1482 | 168 | 29 | 25 | 101 | 2 | 10 | CETP_chr16_56956950_56988845 | CETP | copy fasta | chr16 | 56956950 | 56988845 |
a0002c0003 | 0/0 | 1482 | 17 | 12 | 1 | 0 | 1 | 3 | CETP_chr16_56956950_56988845 | CETP | copy fasta | chr16 | 56956950 | 56988845 |
a0002c0005 | 0/0 | 1482 | 9 | 0 | 0 | 7 | 0 | 2 | CETP_chr16_56956950_56988845 | CETP | copy fasta | chr16 | 56956950 | 56988845 |
a0002c0006 | 0/0 | 1482 | 6 | 6 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | copy fasta | chr16 | 56956950 | 56988845 |
a0002c0009 | 0/0 | 1482 | 5 | 5 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | copy fasta | chr16 | 56956950 | 56988845 |
a0002c0014 | 0/0 | 1482 | 2 | 2 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | copy fasta | chr16 | 56956950 | 56988845 |
a0002c0019 | 0/0 | 1482 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | copy fasta | chr16 | 56956950 | 56988845 |
a0002c0025 | 0/0 | 1482 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | copy fasta | chr16 | 56956950 | 56988845 |
a0003c0004 | 0/0 | 1482 | 12 | 0 | 11 | 0 | 0 | 1 | CETP_chr16_56956950_56988845 | CETP | copy fasta | chr16 | 56956950 | 56988845 |
a0004c0007 | 0/0 | 1482 | 6 | 6 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | copy fasta | chr16 | 56956950 | 56988845 |
a0005c0008 | 0/0 | 1482 | 5 | 0 | 0 | 5 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | copy fasta | chr16 | 56956950 | 56988845 |
a0006c0011 | 0/0 | 1482 | 3 | 0 | 1 | 0 | 0 | 2 | CETP_chr16_56956950_56988845 | CETP | copy fasta | chr16 | 56956950 | 56988845 |
a0007c0012 | 0/0 | 1482 | 3 | 3 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | copy fasta | chr16 | 56956950 | 56988845 |
a0008c0013 | 0/0 | 1482 | 3 | 2 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | copy fasta | chr16 | 56956950 | 56988845 |
a0009c0017 | 0/0 | 1482 | 1 | 0 | 0 | 0 | 0 | 1 | CETP_chr16_56956950_56988845 | CETP | copy fasta | chr16 | 56956950 | 56988845 |
a0009c0018 | 0/0 | 1482 | 1 | 0 | 0 | 0 | 0 | 1 | CETP_chr16_56956950_56988845 | CETP | copy fasta | chr16 | 56956950 | 56988845 |
a0010c0027 | 0/0 | 1482 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | copy fasta | chr16 | 56956950 | 56988845 |
a0011c0020 | 0/0 | 1482 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | copy fasta | chr16 | 56956950 | 56988845 |
a0012c0021 | 0/0 | 1482 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | copy fasta | chr16 | 56956950 | 56988845 |
a0013c0022 | 0/0 | 1482 | 1 | 0 | 0 | 0 | 0 | 1 | CETP_chr16_56956950_56988845 | CETP | copy fasta | chr16 | 56956950 | 56988845 |
a0014c0024 | 0/0 | 1482 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | copy fasta | chr16 | 56956950 | 56988845 |
a0015c0023 | 0/0 | 1482 | 1 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | copy fasta | chr16 | 56956950 | 56988845 |
a0016c0015 | 0/0 | 1482 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | copy fasta | chr16 | 56956950 | 56988845 |
a0017c0026 | 0/0 | 1482 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | copy fasta | chr16 | 56956950 | 56988845 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 1691 | 207 | 29 | 42 | 93 | 13 | 29 | CETP_chr16_56956950_56988845 | CETP | copy fasta | chr16 | 56956950 | 56988845 |
a0001c0010t0001 | 0/0 | 1691 | 3 | 0 | 0 | 3 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | copy fasta | chr16 | 56956950 | 56988845 |
a0001c0016t0001 | 0/0 | 1691 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | copy fasta | chr16 | 56956950 | 56988845 |
a0002c0002t0001 | 1/0 | 1691 | 130 | 25 | 19 | 77 | 1 | 7 | CETP_chr16_56956950_56988845 | CETP | copy fasta | chr16 | 56956950 | 56988845 |
a0002c0002t0002 | 0/0 | 1691 | 37 | 3 | 6 | 24 | 1 | 3 | CETP_chr16_56956950_56988845 | CETP | copy fasta | chr16 | 56956950 | 56988845 |
a0002c0002t0003 | 0/0 | 1691 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | copy fasta | chr16 | 56956950 | 56988845 |
a0002c0003t0002 | 0/0 | 1691 | 17 | 12 | 1 | 0 | 1 | 3 | CETP_chr16_56956950_56988845 | CETP | copy fasta | chr16 | 56956950 | 56988845 |
a0002c0005t0001 | 0/0 | 1691 | 9 | 0 | 0 | 7 | 0 | 2 | CETP_chr16_56956950_56988845 | CETP | copy fasta | chr16 | 56956950 | 56988845 |
a0002c0006t0001 | 0/0 | 1691 | 6 | 6 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | copy fasta | chr16 | 56956950 | 56988845 |
a0002c0009t0001 | 0/0 | 1691 | 5 | 5 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | copy fasta | chr16 | 56956950 | 56988845 |
a0002c0014t0001 | 0/0 | 1691 | 2 | 2 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | copy fasta | chr16 | 56956950 | 56988845 |
a0002c0019t0001 | 0/0 | 1691 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | copy fasta | chr16 | 56956950 | 56988845 |
a0002c0025t0001 | 0/0 | 1691 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | copy fasta | chr16 | 56956950 | 56988845 |
a0003c0004t0001 | 0/0 | 1691 | 12 | 0 | 11 | 0 | 0 | 1 | CETP_chr16_56956950_56988845 | CETP | copy fasta | chr16 | 56956950 | 56988845 |
a0004c0007t0001 | 0/0 | 1691 | 6 | 6 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | copy fasta | chr16 | 56956950 | 56988845 |
a0005c0008t0001 | 0/0 | 1691 | 5 | 0 | 0 | 5 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | copy fasta | chr16 | 56956950 | 56988845 |
a0006c0011t0001 | 0/0 | 1691 | 3 | 0 | 1 | 0 | 0 | 2 | CETP_chr16_56956950_56988845 | CETP | copy fasta | chr16 | 56956950 | 56988845 |
a0007c0012t0001 | 0/0 | 1691 | 3 | 3 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | copy fasta | chr16 | 56956950 | 56988845 |
a0008c0013t0001 | 0/0 | 1691 | 3 | 2 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | copy fasta | chr16 | 56956950 | 56988845 |
a0009c0017t0002 | 0/0 | 1691 | 1 | 0 | 0 | 0 | 0 | 1 | CETP_chr16_56956950_56988845 | CETP | copy fasta | chr16 | 56956950 | 56988845 |
a0009c0018t0002 | 0/0 | 1691 | 1 | 0 | 0 | 0 | 0 | 1 | CETP_chr16_56956950_56988845 | CETP | copy fasta | chr16 | 56956950 | 56988845 |
a0010c0027t0001 | 0/0 | 1691 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | copy fasta | chr16 | 56956950 | 56988845 |
a0011c0020t0001 | 0/0 | 1691 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | copy fasta | chr16 | 56956950 | 56988845 |
a0012c0021t0001 | 0/0 | 1691 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | copy fasta | chr16 | 56956950 | 56988845 |
a0013c0022t0002 | 0/0 | 1691 | 1 | 0 | 0 | 0 | 0 | 1 | CETP_chr16_56956950_56988845 | CETP | copy fasta | chr16 | 56956950 | 56988845 |
a0014c0024t0001 | 0/0 | 1691 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | copy fasta | chr16 | 56956950 | 56988845 |
a0015c0023t0001 | 0/0 | 1691 | 1 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | copy fasta | chr16 | 56956950 | 56988845 |
a0016c0015t0001 | 0/0 | 1691 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | copy fasta | chr16 | 56956950 | 56988845 |
a0017c0026t0001 | 0/0 | 1691 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | copy fasta | chr16 | 56956950 | 56988845 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 15 | 2 | 2 | 8 | 1 | 2 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0001c0001t0001g0002 | 0/0 | 15 | 4 | 3 | 4 | 3 | 1 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0001c0001t0001g0004 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0001c0001t0001g0005 | 0/0 | 7 | 1 | 0 | 5 | 1 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0001c0001t0001g0008 | 0/0 | 5 | 0 | 4 | 0 | 0 | 1 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0001c0001t0001g0011 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0001c0001t0001g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0001c0001t0001g0016 | 0/0 | 4 | 0 | 2 | 0 | 1 | 1 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0001c0001t0001g0019 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0001c0001t0001g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0001c0001t0001g0021 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0001c0001t0001g0024 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0001c0001t0001g0027 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0001c0001t0001g0031 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0001c0001t0001g0032 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0001c0001t0001g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0001c0001t0001g0047 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0001c0001t0001g0049 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0001c0001t0001g0050 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0001c0001t0001g0051 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0001c0001t0001g0052 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0001c0001t0001g0055 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0001c0001t0001g0056 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0001c0001t0001g0057 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0001c0001t0001g0059 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0001c0001t0001g0061 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0001c0001t0001g0062 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0001c0001t0001g0063 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0001c0001t0001g0064 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0001c0001t0001g0269 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0001c0001t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0001c0010t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0001c0010t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0001c0010t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0001c0016t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0002t0001g0003 | 0/0 | 8 | 0 | 2 | 6 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0002t0001g0006 | 0/0 | 6 | 0 | 2 | 4 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0002t0001g0009 | 0/0 | 5 | 0 | 0 | 3 | 1 | 1 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0002t0001g0014 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0002t0001g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0002t0001g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0002t0001g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0002t0001g0025 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0002t0001g0028 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0002t0001g0030 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0002t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0002t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0002t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0002t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0002t0001g0042 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0002t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0002t0001g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0002t0001g0053 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0002t0001g0065 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0002t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0002t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0002t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0002t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0002t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0002t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0002t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0002t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0002t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0002t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0002t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0002t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0002t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0002t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0002t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0002t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0002t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0002t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0002t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0002t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0002t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0002t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0002t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0002t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0002t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0002t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0002t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0002t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0002t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0002t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0002t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0002t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0002t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0002t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0002t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0002t0001g0285 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0002t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0002t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0002t0002g0007 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0002t0002g0015 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0002t0002g0029 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0002t0002g0060 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0002t0002g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0002t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0002t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0002t0002g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0002t0002g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0002t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0002t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0002t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0002t0002g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0002t0002g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0002t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0002t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0002t0002g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0002t0002g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0002t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0002t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0002t0002g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0002t0002g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0002t0002g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0002t0002g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0002t0002g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0002t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0002t0003g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0003t0002g0013 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0003t0002g0034 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0003t0002g0037 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0003t0002g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0003t0002g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0003t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0003t0002g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0003t0002g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0003t0002g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0003t0002g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0003t0002g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0005t0001g0018 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0005t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0005t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0005t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0005t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0005t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0006t0001g0054 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0006t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0006t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0006t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0006t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0009t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0009t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0009t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0009t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0009t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0014t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0014t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0019t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0002c0025t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0003c0004t0001g0010 | 0/0 | 5 | 0 | 4 | 0 | 0 | 1 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0003c0004t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0003c0004t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0003c0004t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0003c0004t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0003c0004t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0003c0004t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0003c0004t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0004c0007t0001g0026 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0004c0007t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0004c0007t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0004c0007t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0005c0008t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0005c0008t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0005c0008t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0005c0008t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0006c0011t0001g0058 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0006c0011t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0007c0012t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0007c0012t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0007c0012t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0008c0013t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0008c0013t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0008c0013t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0009c0017t0002g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0009c0018t0002g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0010c0027t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0011c0020t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0012c0021t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0013c0022t0002g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0014c0024t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0015c0023t0001g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0016c0015t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
a0017c0026t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0288 | EUR | GBR | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG00099 | hp2 | a0002 | c0003 | t0002 | g0037 | EUR | GBR | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0016 | EUR | GBR | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0061 | EUR | GBR | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | FIN | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0272 | EUR | FIN | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG00323 | hp1 | a0002 | c0002 | t0001 | g0009 | EUR | FIN | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0265 | EUR | FIN | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | CHS | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | CHS | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG00438 | hp1 | a0002 | c0005 | t0001 | g0210 | EAS | CHS | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG00438 | hp2 | a0001 | c0010 | t0001 | g0212 | EAS | CHS | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | CHS | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG00544 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | CHS | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG00558 | hp1 | a0002 | c0002 | t0001 | g0033 | EAS | CHS | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | CHS | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | CHS | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | CHS | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | CHS | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | CHS | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG00621 | hp2 | a0002 | c0002 | t0001 | g0023 | EAS | CHS | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0254 | AMR | PUR | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG00642 | hp1 | a0002 | c0002 | t0001 | g0114 | AMR | PUR | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0225 | AMR | PUR | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | CHS | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG00673 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | CHS | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG00733 | hp1 | a0003 | c0004 | t0001 | g0228 | AMR | PUR | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0238 | AMR | PUR | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | PUR | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0206 | AMR | PUR | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG00738 | hp1 | a0002 | c0002 | t0002 | g0129 | AMR | PUR | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0284 | AMR | PUR | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG00741 | hp1 | a0002 | c0003 | t0002 | g0297 | AMR | PUR | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG00741 | hp2 | a0002 | c0002 | t0001 | g0003 | AMR | PUR | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG01069 | hp2 | a0002 | c0002 | t0001 | g0065 | AMR | PUR | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | PUR | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG01071 | hp1 | a0002 | c0002 | t0001 | g0065 | AMR | PUR | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | PUR | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0304 | AMR | PUR | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG01081 | hp2 | a0002 | c0002 | t0002 | g0007 | AMR | PUR | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG01099 | hp1 | a0002 | c0002 | t0001 | g0107 | AMR | PUR | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG01106 | hp2 | a0002 | c0002 | t0002 | g0296 | AMR | PUR | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0218 | AMR | PUR | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG01109 | hp2 | a0002 | c0002 | t0001 | g0255 | AMR | PUR | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG01167 | hp1 | a0003 | c0004 | t0001 | g0045 | AMR | PUR | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0159 | AMR | PUR | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0219 | AMR | PUR | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG01168 | hp2 | a0002 | c0002 | t0001 | g0157 | AMR | PUR | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG01169 | hp1 | a0003 | c0004 | t0001 | g0164 | AMR | PUR | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG01169 | hp2 | a0002 | c0002 | t0001 | g0160 | AMR | PUR | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG01175 | hp1 | a0002 | c0002 | t0001 | g0106 | AMR | PUR | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG01175 | hp2 | a0002 | c0002 | t0002 | g0276 | AMR | PUR | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0207 | AMR | PUR | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0205 | AMR | PUR | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG01255 | hp2 | a0003 | c0004 | t0001 | g0010 | AMR | CLM | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | CLM | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | CLM | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0049 | AMR | CLM | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | CLM | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0049 | AMR | CLM | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | CLM | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG01261 | hp1 | a0002 | c0002 | t0002 | g0150 | AMR | CLM | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | CLM | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG01346 | hp1 | a0002 | c0002 | t0001 | g0155 | AMR | CLM | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG01346 | hp2 | a0002 | c0002 | t0002 | g0264 | AMR | CLM | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG01433 | hp1 | a0015 | c0023 | t0001 | g0004 | AMR | CLM | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0222 | AMR | CLM | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG01496 | hp2 | a0002 | c0002 | t0001 | g0278 | AMR | CLM | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0035 | EUR | IBS | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0035 | EUR | IBS | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG01884 | hp1 | a0002 | c0002 | t0001 | g0193 | AFR | ACB | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | ACB | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG01891 | hp1 | a0002 | c0006 | t0001 | g0196 | AFR | ACB | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG01928 | hp1 | a0002 | c0002 | t0001 | g0006 | AMR | PEL | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG01928 | hp2 | a0003 | c0004 | t0001 | g0010 | AMR | PEL | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG01952 | hp1 | a0003 | c0004 | t0001 | g0010 | AMR | PEL | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG01952 | hp2 | a0002 | c0002 | t0001 | g0003 | AMR | PEL | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG01975 | hp1 | a0003 | c0004 | t0001 | g0010 | AMR | PEL | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG01975 | hp2 | a0002 | c0002 | t0001 | g0006 | AMR | PEL | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG01978 | hp2 | a0006 | c0011 | t0001 | g0223 | AMR | PEL | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG01981 | hp1 | a0002 | c0002 | t0001 | g0025 | AMR | PEL | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | PEL | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG01993 | hp2 | a0002 | c0002 | t0001 | g0108 | AMR | PEL | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG02004 | hp1 | a0002 | c0002 | t0001 | g0025 | AMR | PEL | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | KHV | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG02015 | hp2 | a0002 | c0002 | t0002 | g0260 | EAS | KHV | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | KHV | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | KHV | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | KHV | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG02055 | hp1 | a0007 | c0012 | t0001 | g0197 | AFR | ACB | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | ACB | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG02056 | hp1 | a0002 | c0002 | t0002 | g0149 | EAS | KHV | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG02056 | hp2 | a0010 | c0027 | t0001 | g0142 | EAS | KHV | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG02071 | hp1 | a0002 | c0002 | t0001 | g0033 | EAS | KHV | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG02071 | hp2 | a0002 | c0002 | t0001 | g0161 | EAS | KHV | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | KHV | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG02080 | hp1 | a0002 | c0002 | t0001 | g0256 | EAS | KHV | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | KHV | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG02083 | hp1 | a0002 | c0002 | t0001 | g0135 | EAS | KHV | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | KHV | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG02129 | hp2 | a0002 | c0002 | t0001 | g0014 | EAS | KHV | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG02132 | hp1 | a0002 | c0002 | t0001 | g0113 | EAS | KHV | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG02132 | hp2 | a0002 | c0002 | t0002 | g0007 | EAS | KHV | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG02135 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | KHV | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | KHV | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG02145 | hp1 | a0002 | c0002 | t0001 | g0204 | AFR | ACB | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | ACB | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | PEL | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG02148 | hp2 | a0003 | c0004 | t0001 | g0220 | AMR | PEL | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | CDX | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | CDX | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0301 | EAS | CDX | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG02165 | hp2 | a0002 | c0002 | t0002 | g0130 | EAS | CDX | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG02257 | hp1 | a0002 | c0002 | t0001 | g0028 | AFR | ACB | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | ACB | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG02258 | hp2 | a0012 | c0021 | t0001 | g0095 | AFR | ACB | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG02273 | hp1 | a0003 | c0004 | t0001 | g0109 | AMR | PEL | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG02273 | hp2 | a0002 | c0002 | t0001 | g0025 | AMR | PEL | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG02280 | hp1 | a0002 | c0003 | t0002 | g0013 | AFR | ACB | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG02280 | hp2 | a0002 | c0002 | t0001 | g0243 | AFR | ACB | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG02293 | hp1 | a0002 | c0002 | t0001 | g0145 | AMR | PEL | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG02300 | hp1 | a0003 | c0004 | t0001 | g0217 | AMR | PEL | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | PEL | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG02451 | hp1 | a0002 | c0003 | t0002 | g0083 | AFR | ACB | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG02451 | hp2 | a0002 | c0009 | t0001 | g0178 | AFR | ACB | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG02523 | hp1 | a0002 | c0002 | t0002 | g0015 | EAS | KHV | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG02572 | hp1 | a0002 | c0002 | t0001 | g0203 | AFR | GWD | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | GWD | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0056 | SAS | PJL | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG02615 | hp1 | a0002 | c0002 | t0001 | g0235 | AFR | GWD | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG02622 | hp1 | a0002 | c0002 | t0001 | g0188 | AFR | GWD | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG02622 | hp2 | a0002 | c0009 | t0001 | g0154 | AFR | GWD | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG02630 | hp1 | a0007 | c0012 | t0001 | g0200 | AFR | GWD | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | GWD | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG02647 | hp1 | a0004 | c0007 | t0001 | g0026 | AFR | GWD | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG02647 | hp2 | a0002 | c0002 | t0001 | g0166 | AFR | GWD | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0226 | SAS | PJL | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0121 | SAS | PJL | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG02717 | hp1 | a0002 | c0002 | t0001 | g0022 | AFR | GWD | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG02717 | hp2 | a0002 | c0014 | t0001 | g0098 | AFR | GWD | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG02723 | hp1 | a0002 | c0025 | t0001 | g0082 | AFR | GWD | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0239 | AFR | GWD | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0165 | SAS | PJL | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG02735 | hp2 | a0003 | c0004 | t0001 | g0010 | SAS | PJL | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0208 | SAS | PJL | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG02738 | hp2 | a0002 | c0002 | t0001 | g0042 | SAS | PJL | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG02809 | hp2 | a0002 | c0002 | t0001 | g0022 | AFR | GWD | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG02818 | hp1 | a0002 | c0009 | t0001 | g0177 | AFR | GWD | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | GWD | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG02886 | hp1 | a0002 | c0006 | t0001 | g0054 | AFR | GWD | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | GWD | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG02895 | hp1 | a0002 | c0003 | t0002 | g0048 | AFR | GWD | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG02896 | hp1 | a0002 | c0003 | t0002 | g0013 | AFR | GWD | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG02897 | hp2 | a0002 | c0003 | t0002 | g0048 | AFR | GWD | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG02922 | hp1 | a0002 | c0002 | t0001 | g0092 | AFR | ESN | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG02922 | hp2 | a0002 | c0002 | t0001 | g0176 | AFR | ESN | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG02965 | hp1 | a0008 | c0013 | t0001 | g0167 | AFR | ESN | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG02965 | hp2 | a0002 | c0002 | t0001 | g0237 | AFR | ESN | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG02970 | hp1 | a0002 | c0006 | t0001 | g0054 | AFR | ESN | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG02970 | hp2 | a0002 | c0002 | t0001 | g0174 | AFR | ESN | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | ESN | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG02976 | hp2 | a0002 | c0002 | t0001 | g0191 | AFR | ESN | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG03017 | hp1 | a0013 | c0022 | t0002 | g0120 | SAS | PJL | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG03017 | hp2 | a0002 | c0002 | t0002 | g0163 | SAS | PJL | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | GWD | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG03041 | hp2 | a0002 | c0002 | t0001 | g0236 | AFR | GWD | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG03098 | hp1 | a0002 | c0002 | t0001 | g0067 | AFR | MSL | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | MSL | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG03130 | hp1 | a0002 | c0003 | t0002 | g0013 | AFR | ESN | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG03130 | hp2 | a0002 | c0009 | t0001 | g0090 | AFR | ESN | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG03139 | hp1 | a0007 | c0012 | t0001 | g0199 | AFR | ESN | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0293 | AFR | ESN | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG03195 | hp1 | a0002 | c0019 | t0001 | g0242 | AFR | ESN | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | ESN | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG03209 | hp1 | a0002 | c0002 | t0002 | g0282 | AFR | MSL | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG03209 | hp2 | a0002 | c0002 | t0001 | g0181 | AFR | MSL | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG03225 | hp1 | a0002 | c0002 | t0001 | g0066 | AFR | MSL | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | MSL | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0221 | SAS | PJL | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG03239 | hp2 | a0002 | c0002 | t0001 | g0014 | SAS | PJL | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG03453 | hp1 | a0002 | c0006 | t0001 | g0194 | AFR | MSL | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG03453 | hp2 | a0002 | c0002 | t0001 | g0028 | AFR | MSL | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG03486 | hp1 | a0002 | c0002 | t0001 | g0216 | AFR | MSL | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG03486 | hp2 | a0002 | c0003 | t0002 | g0084 | AFR | MSL | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG03490 | hp1 | a0002 | c0003 | t0002 | g0034 | SAS | PJL | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0062 | SAS | PJL | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG03491 | hp1 | a0006 | c0011 | t0001 | g0058 | SAS | PJL | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0290 | SAS | PJL | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0062 | SAS | PJL | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG03492 | hp2 | a0006 | c0011 | t0001 | g0058 | SAS | PJL | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG03516 | hp1 | a0002 | c0003 | t0002 | g0013 | AFR | ESN | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG03516 | hp2 | a0002 | c0014 | t0001 | g0099 | AFR | ESN | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG03540 | hp1 | a0004 | c0007 | t0001 | g0026 | AFR | GWD | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG03540 | hp2 | a0002 | c0003 | t0002 | g0085 | AFR | GWD | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | MSL | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG03579 | hp2 | a0008 | c0013 | t0001 | g0172 | AFR | MSL | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG03654 | hp1 | a0002 | c0003 | t0002 | g0071 | SAS | PJL | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0056 | SAS | PJL | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG03669 | hp1 | a0002 | c0002 | t0001 | g0268 | SAS | PJL | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0044 | SAS | PJL | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0097 | SAS | STU | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0224 | SAS | STU | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0156 | SAS | PJL | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG03704 | hp2 | a0002 | c0005 | t0001 | g0018 | SAS | PJL | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0057 | SAS | PJL | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG03710 | hp2 | a0009 | c0017 | t0002 | g0234 | SAS | PJL | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG03831 | hp1 | a0002 | c0003 | t0002 | g0034 | SAS | BEB | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG03831 | hp2 | a0002 | c0002 | t0002 | g0151 | SAS | BEB | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0305 | SAS | BEB | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0016 | SAS | BEB | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG03927 | hp1 | a0009 | c0018 | t0002 | g0231 | SAS | BEB | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0057 | SAS | BEB | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0187 | SAS | BEB | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0032 | SAS | BEB | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG04115 | hp1 | a0002 | c0002 | t0001 | g0141 | SAS | STU | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0189 | SAS | STU | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG04184 | hp2 | a0002 | c0005 | t0001 | g0072 | SAS | BEB | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0279 | SAS | STU | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0287 | SAS | STU | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG04204 | hp1 | a0002 | c0002 | t0001 | g0081 | SAS | STU | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG04204 | hp2 | a0002 | c0002 | t0001 | g0009 | SAS | STU | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0044 | SAS | STU | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG04228 | hp2 | a0002 | c0002 | t0001 | g0139 | SAS | STU | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA18522 | hp1 | a0002 | c0002 | t0002 | g0281 | AFR | YRI | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA18522 | hp2 | a0002 | c0002 | t0002 | g0175 | AFR | YRI | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | CHB | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA18612 | hp2 | a0001 | c0010 | t0001 | g0215 | EAS | CHB | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | CHB | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHB | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | YRI | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA18906 | hp2 | a0002 | c0002 | t0001 | g0180 | AFR | YRI | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA18939 | hp2 | a0002 | c0002 | t0001 | g0080 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA18940 | hp1 | a0005 | c0008 | t0001 | g0247 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA18940 | hp2 | a0002 | c0002 | t0001 | g0123 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA18941 | hp1 | a0002 | c0005 | t0001 | g0214 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA18942 | hp1 | a0002 | c0005 | t0001 | g0213 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA18943 | hp1 | a0002 | c0002 | t0002 | g0007 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA18943 | hp2 | a0002 | c0002 | t0001 | g0117 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA18944 | hp1 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA18945 | hp1 | a0002 | c0002 | t0001 | g0277 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA18945 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA18948 | hp1 | a0002 | c0002 | t0001 | g0248 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA18950 | hp1 | a0002 | c0002 | t0001 | g0023 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA18951 | hp1 | a0002 | c0002 | t0002 | g0182 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA18951 | hp2 | a0002 | c0002 | t0001 | g0039 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA18952 | hp1 | a0002 | c0002 | t0001 | g0043 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA18952 | hp2 | a0005 | c0008 | t0001 | g0040 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA18953 | hp2 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA18954 | hp2 | a0002 | c0002 | t0001 | g0103 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA18957 | hp1 | a0002 | c0002 | t0001 | g0014 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA18957 | hp2 | a0002 | c0002 | t0001 | g0162 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA18959 | hp1 | a0002 | c0002 | t0002 | g0060 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA18959 | hp2 | a0002 | c0002 | t0002 | g0122 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA18960 | hp2 | a0002 | c0002 | t0001 | g0075 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA18961 | hp1 | a0002 | c0002 | t0001 | g0292 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA18961 | hp2 | a0002 | c0002 | t0001 | g0192 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA18962 | hp1 | a0002 | c0002 | t0002 | g0127 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA18963 | hp1 | a0014 | c0024 | t0001 | g0186 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA18964 | hp1 | a0002 | c0002 | t0002 | g0007 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA18968 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA18970 | hp1 | a0002 | c0002 | t0001 | g0069 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA18970 | hp2 | a0002 | c0002 | t0002 | g0007 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA18971 | hp1 | a0002 | c0002 | t0002 | g0015 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA18971 | hp2 | a0002 | c0005 | t0001 | g0018 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA18972 | hp1 | a0002 | c0002 | t0001 | g0185 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA18973 | hp2 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA18975 | hp1 | a0002 | c0002 | t0001 | g0046 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA18977 | hp1 | a0002 | c0002 | t0001 | g0042 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA18977 | hp2 | a0001 | c0010 | t0001 | g0211 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA18978 | hp1 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA18978 | hp2 | a0005 | c0008 | t0001 | g0004 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA18979 | hp1 | a0002 | c0002 | t0001 | g0017 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA18979 | hp2 | a0002 | c0002 | t0001 | g0124 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA18980 | hp1 | a0002 | c0002 | t0001 | g0043 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA18980 | hp2 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA18983 | hp2 | a0002 | c0002 | t0001 | g0132 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA18984 | hp1 | a0002 | c0002 | t0001 | g0271 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA18984 | hp2 | a0002 | c0002 | t0001 | g0140 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA18986 | hp2 | a0002 | c0002 | t0001 | g0036 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA18988 | hp1 | a0002 | c0002 | t0001 | g0014 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA18988 | hp2 | a0002 | c0002 | t0001 | g0046 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA18989 | hp1 | a0002 | c0002 | t0002 | g0148 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA18990 | hp1 | a0002 | c0002 | t0001 | g0053 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA18990 | hp2 | a0011 | c0020 | t0001 | g0289 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA18991 | hp1 | a0005 | c0008 | t0001 | g0253 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA18992 | hp1 | a0002 | c0002 | t0001 | g0112 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA18992 | hp2 | a0002 | c0002 | t0002 | g0029 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA18993 | hp1 | a0002 | c0002 | t0001 | g0030 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA18994 | hp2 | a0002 | c0002 | t0001 | g0184 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA18995 | hp1 | a0002 | c0002 | t0001 | g0262 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA18995 | hp2 | a0002 | c0002 | t0001 | g0053 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA18998 | hp1 | a0002 | c0002 | t0002 | g0015 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA18998 | hp2 | a0002 | c0002 | t0001 | g0302 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA18999 | hp1 | a0002 | c0002 | t0001 | g0131 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA18999 | hp2 | a0002 | c0002 | t0001 | g0030 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA19001 | hp1 | a0002 | c0002 | t0002 | g0152 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA19002 | hp1 | a0002 | c0002 | t0001 | g0017 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA19003 | hp1 | a0002 | c0002 | t0001 | g0190 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA19003 | hp2 | a0002 | c0002 | t0002 | g0007 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA19005 | hp1 | a0002 | c0002 | t0002 | g0029 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA19009 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA19012 | hp2 | a0002 | c0002 | t0001 | g0039 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA19030 | hp1 | a0004 | c0007 | t0001 | g0171 | AFR | LWK | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | LWK | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | LWK | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA19043 | hp2 | a0002 | c0006 | t0001 | g0179 | AFR | LWK | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA19054 | hp2 | a0002 | c0002 | t0001 | g0041 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA19055 | hp1 | a0002 | c0002 | t0001 | g0086 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA19055 | hp2 | a0002 | c0002 | t0001 | g0068 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA19056 | hp1 | a0002 | c0005 | t0001 | g0018 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA19057 | hp1 | a0002 | c0002 | t0001 | g0036 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA19060 | hp1 | a0002 | c0002 | t0001 | g0227 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA19060 | hp2 | a0001 | c0016 | t0001 | g0283 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA19062 | hp1 | a0002 | c0002 | t0002 | g0153 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA19062 | hp2 | a0002 | c0002 | t0001 | g0183 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA19063 | hp1 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA19064 | hp1 | a0002 | c0002 | t0002 | g0029 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA19066 | hp1 | a0002 | c0002 | t0001 | g0030 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA19066 | hp2 | a0002 | c0005 | t0001 | g0018 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA19070 | hp2 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA19075 | hp1 | a0002 | c0005 | t0001 | g0209 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA19075 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA19077 | hp1 | a0016 | c0015 | t0001 | g0017 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA19077 | hp2 | a0002 | c0002 | t0001 | g0105 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA19080 | hp1 | a0005 | c0008 | t0001 | g0040 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA19081 | hp1 | a0002 | c0002 | t0002 | g0303 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA19082 | hp1 | a0002 | c0002 | t0002 | g0060 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA19083 | hp1 | a0002 | c0002 | t0002 | g0015 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA19083 | hp2 | a0002 | c0002 | t0001 | g0134 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA19085 | hp1 | a0002 | c0002 | t0001 | g0017 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA19085 | hp2 | a0002 | c0002 | t0001 | g0041 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA19086 | hp1 | a0002 | c0002 | t0001 | g0094 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA19086 | hp2 | a0002 | c0002 | t0001 | g0023 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA19087 | hp1 | a0002 | c0002 | t0001 | g0070 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA19089 | hp1 | a0002 | c0002 | t0001 | g0104 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA19091 | hp1 | a0002 | c0002 | t0001 | g0146 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA19091 | hp2 | a0002 | c0002 | t0001 | g0143 | EAS | JPT | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA19240 | hp1 | a0004 | c0007 | t0001 | g0169 | AFR | YRI | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | YRI | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA20129 | hp1 | a0002 | c0002 | t0001 | g0028 | AFR | ASW | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA20129 | hp2 | a0002 | c0002 | t0003 | g0088 | AFR | ASW | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA20805 | hp1 | a0002 | c0002 | t0002 | g0128 | EUR | TSI | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0047 | EUR | TSI | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0087 | SAS | GIH | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA20905 | hp2 | a0002 | c0002 | t0002 | g0119 | SAS | GIH | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG01123 | hp1 | a0003 | c0004 | t0001 | g0110 | AMR | CLM | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG01123 | hp2 | a0008 | c0013 | t0001 | g0168 | AMR | CLM | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG02109 | hp1 | a0002 | c0009 | t0001 | g0091 | AFR | ACB | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG02109 | hp2 | a0002 | c0003 | t0002 | g0299 | AFR | ACB | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG02486 | hp2 | a0002 | c0003 | t0002 | g0037 | AFR | ACB | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | ACB | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG02559 | hp2 | a0017 | c0026 | t0001 | g0201 | AFR | ACB | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG03471 | hp1 | a0002 | c0002 | t0001 | g0022 | AFR | MSL | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG03471 | hp2 | a0002 | c0006 | t0001 | g0195 | AFR | MSL | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG06807 | hp1 | a0002 | c0003 | t0002 | g0298 | AFR | USA | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
HG06807 | hp2 | a0004 | c0007 | t0001 | g0026 | AFR | USA | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA20300 | hp1 | a0004 | c0007 | t0001 | g0170 | AFR | USA | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
NA20300 | hp2 | a0002 | c0002 | t0001 | g0093 | AFR | USA | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0269 | REF | REF | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
homoSapiens_grch38 | hp1 | a0002 | c0002 | t0001 | g0285 | REF | REF | CETP_chr16_56956950_56988845 | CETP | chr16 | 56956950 | 56988845 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:56962023
|
C | G | 2 | a0004a0008 | 9 | HG01123.hp2 HG02647.hp1 HG02965.hp1 others(6): Show |
missense_variant | MODERATE | c.44C>G | p.Ala15Gly | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 1/16 | 74/1691 | 44/1482 | 15/493 | chr16 | 56962023 | ||
chr16:56962047
|
C | T | 1 | a0010 | 1 | HG02056.hp2 | missense_variant | MODERATE | c.68C>T | p.Ser23Leu | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 1/16 | 98/1691 | 68/1482 | 23/493 | chr16 | 56962047 | ||
chr16:56969934
|
C | T | 2 | a0007a0017 | 4 | HG02055.hp1 HG02559.hp2 HG02630.hp1 others(1): Show |
missense_variant | MODERATE | c.460C>T | p.Arg154Trp | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 5/16 | 490/1691 | 460/1482 | 154/493 | chr16 | 56969934 | ||
chr16:56971324
|
T | G | 1 | a0016 | 1 | NA19077.hp1 | missense_variant | MODERATE | c.601T>G | p.Cys201Gly | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 7/16 | 631/1691 | 601/1482 | 201/493 | chr16 | 56971324 | ||
chr16:56971996
|
C | A | 1 | a0009 | 2 | HG03710.hp2 HG03927.hp1 |
missense_variant | MODERATE | c.663C>A | p.Ser221Arg | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 8/16 | 693/1691 | 663/1482 | 221/493 | chr16 | 56971996 | ||
chr16:56973364
|
C | A | 1 | a0011 | 1 | NA18990.hp2 | missense_variant | MODERATE | c.784C>A | p.Leu262Ile | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 9/16 | 814/1691 | 784/1482 | 262/493 | chr16 | 56973364 | ||
chr16:56981164
|
G | A | 1 | a0012 | 1 | HG02258.hp2 | missense_variant | MODERATE | c.1153G>A | p.Val385Met | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 12/16 | 1183/1691 | 1153/1482 | 385/493 | chr16 | 56981164 | ||
chr16:56981179
|
G | C | 2 | a0003a0006 | 15 | HG00733.hp1 HG01123.hp1 HG01167.hp1 others(12): Show |
missense_variant | MODERATE | c.1168G>C | p.Ala390Pro | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 12/16 | 1198/1691 | 1168/1482 | 390/493 | chr16 | 56981179 | ||
chr16:56981201
|
T | A | 1 | a0013 | 1 | HG03017.hp1 | missense_variant | MODERATE | c.1190T>A | p.Leu397His | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 12/16 | 1220/1691 | 1190/1482 | 397/493 | chr16 | 56981201 | ||
chr16:56982180
|
G | A | 9 | a0001a0003a0005others(6): Show | 240 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(237): Show |
missense_variant | MODERATE | c.1264G>A | p.Val422Ile | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 14/16 | 1294/1691 | 1264/1482 | 422/493 | chr16 | 56982180 | ||
chr16:56983331
|
G | A | 1 | a0015 | 1 | HG01433.hp1 | missense_variant | MODERATE | c.1327G>A | p.Glu443Lys | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 15/16 | 1357/1691 | 1327/1482 | 443/493 | chr16 | 56983331 | ||
chr16:56983370
|
A | C | 1 | a0014 | 1 | NA18963.hp1 | missense_variant | MODERATE | c.1366A>C | p.Ser456Arg | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 15/16 | 1396/1691 | 1366/1482 | 456/493 | chr16 | 56983370 | ||
chr16:56983380
|
A | G | 1 | a0005 | 5 | NA18940.hp1 NA18952.hp2 NA18978.hp2 others(2): Show |
missense_variant | MODERATE | c.1376A>G | p.Asp459Gly | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 15/16 | 1406/1691 | 1376/1482 | 459/493 | chr16 | 56983380 | ||
chr16:56983407
|
G | A | 1 | a0003 | 12 | HG00733.hp1 HG01123.hp1 HG01167.hp1 others(9): Show |
missense_variant | MODERATE | c.1403G>A | p.Arg468Gln | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 15/16 | 1433/1691 | 1403/1482 | 468/493 | chr16 | 56983407 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:56962045
|
C | A | 1 | a0002c0006 | 6 | HG01891.hp1 HG02886.hp1 HG02970.hp1 others(3): Show |
synonymous_variant | LOW | c.66C>A | p.Thr22Thr | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 1/16 | 96/1691 | 66/1482 | 22/493 | chr16 | 56962045 | ||
chr16:56971039
|
G | A | 2 | a0001c0010a0002c0005 | 12 | HG00438.hp1 HG00438.hp2 HG03704.hp2 others(9): Show |
synonymous_variant | LOW | c.534G>A | p.Gly178Gly | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 6/16 | 564/1691 | 534/1482 | 178/493 | chr16 | 56971039 | ||
chr16:56971359
|
C | T | 1 | a0002c0014 | 2 | HG02717.hp2 HG03516.hp2 |
synonymous_variant | LOW | c.636C>T | p.Ala212Ala | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 7/16 | 666/1691 | 636/1482 | 212/493 | chr16 | 56971359 | ||
chr16:56971362
|
T | C | 1 | a0001c0016 | 1 | NA19060.hp2 | synonymous_variant | LOW | c.639T>C | p.Asp213Asp | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 7/16 | 669/1691 | 639/1482 | 213/493 | chr16 | 56971362 | ||
chr16:56973336
|
T | C | 1 | a0002c0019 | 1 | HG03195.hp1 | synonymous_variant | LOW | c.756T>C | p.His252His | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 9/16 | 786/1691 | 756/1482 | 252/493 | chr16 | 56973336 | ||
chr16:56973441
|
C | T | 2 | a0002c0003a0009c0018 | 18 | HG00099.hp2 HG00741.hp1 HG02109.hp2 others(15): Show |
synonymous_variant | LOW | c.861C>T | p.Phe287Phe | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 9/16 | 891/1691 | 861/1482 | 287/493 | chr16 | 56973441 | ||
chr16:56981172
|
C | G | 1 | a0002c0009 | 5 | HG02109.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
synonymous_variant | LOW | c.1161C>G | p.Thr387Thr | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 12/16 | 1191/1691 | 1161/1482 | 387/493 | chr16 | 56981172 | ||
chr16:56981172
|
C | T | 2 | a0002c0025a0017c0026 | 2 | HG02559.hp2 HG02723.hp1 |
synonymous_variant | LOW | c.1161C>T | p.Thr387Thr | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 12/16 | 1191/1691 | 1161/1482 | 387/493 | chr16 | 56981172 | ||
chr16:56982215
|
G | A | 1 | a0002c0009 | 5 | HG02109.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
synonymous_variant | LOW | c.1299G>A | p.Val433Val | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 14/16 | 1329/1691 | 1299/1482 | 433/493 | chr16 | 56982215 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:56983711
|
C | G | 1 | a0002c0002t0003 | 1 | NA20129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*45C>G | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 16/16 | 45 | chr16 | 56983711 | |||||
chr16:56983750
|
G | A | 5 | a0002c0002t0002a0002c0003t0002a0009c0017t0002others(2): Show | 57 | HG00099.hp2 HG00738.hp1 HG00741.hp1 others(54): Show |
3_prime_UTR_variant | MODIFIER | c.*84G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 16/16 | 84 | chr16 | 56983750 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:56962130
|
G | A | 1 | a0002c0002t0001g0066 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.118+33G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 1/15 | chr16 | 56962130 | ||||||
chr16:56962148
|
C | A | 1 | a0002c0002t0001g0067 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.118+51C>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 1/15 | chr16 | 56962148 | ||||||
chr16:56962155
|
G | A | 4 | a0001c0001t0001g0020a0002c0002t0001g0068a0002c0002t0001g0069others(1): Show | 6 | HG00544.hp1 HG02155.hp2 NA18969.hp2 others(3): Show |
intron_variant | MODIFIER | c.118+58G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 1/15 | chr16 | 56962155 | ||||||
chr16:56962192
|
C | A | 23 | a0001c0001t0001g0012a0001c0001t0001g0021a0001c0001t0001g0035others(20): Show | 36 | HG00099.hp2 HG00423.hp1 HG00558.hp1 others(33): Show |
intron_variant | MODIFIER | c.118+95C>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 1/15 | chr16 | 56962192 | ||||||
chr16:56962246
|
T | C | 174 | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0016others(171): Show | 253 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(250): Show |
intron_variant | MODIFIER | c.118+149T>C | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 1/15 | chr16 | 56962246 | ||||||
chr16:56962299
|
G | A | 114 | a0001c0001t0001g0008a0001c0001t0001g0016a0001c0001t0001g0024others(111): Show | 170 | HG00140.hp1 HG00323.hp1 HG00544.hp2 others(167): Show |
intron_variant | MODIFIER | c.118+202G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 1/15 | chr16 | 56962299 | ||||||
chr16:56962367
|
C | T | 2 | a0001c0001t0001g0304a0001c0001t0001g0305 | 2 | HG01081.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.118+270C>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 1/15 | chr16 | 56962367 | ||||||
chr16:56962376
|
G | A | 114 | a0001c0001t0001g0008a0001c0001t0001g0016a0001c0001t0001g0024others(111): Show | 170 | HG00140.hp1 HG00323.hp1 HG00544.hp2 others(167): Show |
intron_variant | MODIFIER | c.118+279G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 1/15 | chr16 | 56962376 | ||||||
chr16:56962391
|
T | A | 1 | a0001c0001t0001g0202 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.118+294T>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 1/15 | chr16 | 56962391 | ||||||
chr16:56962677
|
G | A | 1 | a0002c0002t0001g0203 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.119-333G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 1/15 | chr16 | 56962677 | ||||||
chr16:56962733
|
GCC | G | 107 | a0001c0001t0001g0008a0001c0001t0001g0016a0001c0001t0001g0024others(104): Show | 161 | HG00140.hp1 HG00323.hp1 HG00544.hp2 others(158): Show |
intron_variant | MODIFIER | c.119-274_119-273del others(2): Show |
CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 56962733 | |||||
chr16:56962737
|
C | A | 107 | a0001c0001t0001g0008a0001c0001t0001g0016a0001c0001t0001g0024others(104): Show | 161 | HG00140.hp1 HG00323.hp1 HG00544.hp2 others(158): Show |
intron_variant | MODIFIER | c.119-273C>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 1/15 | chr16 | 56962737 | ||||||
chr16:56962751
|
G | A | 3 | a0002c0002t0001g0204a0002c0003t0002g0071a0008c0013t0001g0167 | 3 | HG02145.hp1 HG02965.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.119-259G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 1/15 | chr16 | 56962751 | ||||||
chr16:56962795
|
G | T | 2 | a0001c0001t0001g0050a0002c0002t0001g0166 | 3 | HG02647.hp2 HG03041.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.119-215G>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 1/15 | chr16 | 56962795 | ||||||
chr16:56962860
|
C | A | 1 | a0002c0002t0001g0086 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.119-150C>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 1/15 | chr16 | 56962860 | ||||||
chr16:56963160
|
A | G | 9 | a0001c0001t0001g0198a0002c0006t0001g0054a0002c0006t0001g0194others(6): Show | 10 | HG01891.hp1 HG02055.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.233+36A>G | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56963160 | ||||||
chr16:56963168
|
G | A | 1 | a0001c0001t0001g0087 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.233+44G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56963168 | ||||||
chr16:56963277
|
C | A | 1 | a0002c0002t0003g0088 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.233+153C>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56963277 | ||||||
chr16:56963321
|
G | A | 57 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0038others(54): Show | 92 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.233+197G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56963321 | ||||||
chr16:56963406
|
G | A | 5 | a0001c0001t0001g0027a0001c0001t0001g0173a0002c0002t0001g0174others(2): Show | 7 | HG02615.hp2 HG02896.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.233+282G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56963406 | ||||||
chr16:56963437
|
C | CA | 79 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0027others(76): Show | 119 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(116): Show |
intron_variant | MODIFIER | c.233+315dupA | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 56963437 | |||||
chr16:56963456
|
T | A | 1 | a0002c0002t0001g0180 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.233+332T>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56963456 | ||||||
chr16:56963457
|
A | T | 210 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0012others(207): Show | 313 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(310): Show |
intron_variant | MODIFIER | c.233+333A>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56963457 | ||||||
chr16:56963458
|
A | T | 1 | a0001c0001t0001g0049 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.233+334A>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56963458 | ||||||
chr16:56963639
|
C | T | 198 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0012others(195): Show | 299 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(296): Show |
intron_variant | MODIFIER | c.233+515C>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56963639 | ||||||
chr16:56963744
|
G | C | 35 | a0001c0001t0001g0012a0001c0001t0001g0021a0001c0001t0001g0035others(32): Show | 52 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.233+620G>C | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56963744 | ||||||
chr16:56963990
|
T | TTTTA | 8 | a0001c0001t0001g0087a0001c0001t0001g0165a0001c0001t0001g0295others(5): Show | 8 | HG01169.hp1 HG02109.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.233+917_233+920dup others(4): Show |
CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 56963990 | |||||
chr16:56963990
|
TTTTA | T | 115 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0012others(112): Show | 169 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(166): Show |
intron_variant | MODIFIER | c.233+917_233+920del others(4): Show |
CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 56963990 | |||||
chr16:56963990
|
TTTTATTT others(1): Show |
T | 52 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0024others(49): Show | 83 | HG00408.hp2 HG00544.hp2 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.233+913_233+920del others(8): Show |
CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 56963990 | |||||
chr16:56963990
|
TTTTATTT others(5): Show |
T | 10 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0244others(7): Show | 10 | HG01884.hp1 HG02165.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.233+909_233+920del others(12): Show |
CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 56963990 | |||||
chr16:56963990
|
TTTTATTT others(13): Show |
T | 11 | a0001c0010t0001g0211a0001c0010t0001g0212a0001c0010t0001g0215others(8): Show | 14 | HG00438.hp1 HG00438.hp2 HG02717.hp2 others(11): Show |
intron_variant | MODIFIER | c.233+901_233+920del others(20): Show |
CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 56963990 | |||||
chr16:56963990
|
TTTTATTT others(17): Show |
T | 41 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0027others(38): Show | 74 | HG00408.hp1 HG00597.hp1 HG00609.hp1 others(71): Show |
intron_variant | MODIFIER | c.233+897_233+920del others(24): Show |
CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 56963990 | |||||
chr16:56963994
|
A | T | 4 | a0002c0003t0002g0048a0002c0003t0002g0083a0002c0003t0002g0084others(1): Show | 5 | HG02451.hp1 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.233+870A>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56963994 | ||||||
chr16:56964002
|
ATTTATTT others(18): Show |
A | 1 | a0002c0002t0001g0216 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.233+881_233+905del others(25): Show |
CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 56964002 | |||||
chr16:56964034
|
ATTTATTT others(2): Show |
A | 6 | a0001c0001t0001g0096a0001c0001t0001g0102a0002c0002t0001g0023others(3): Show | 9 | HG00621.hp2 NA18942.hp2 NA18950.hp1 others(6): Show |
intron_variant | MODIFIER | c.233+912_233+920del others(9): Show |
CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 56964034 | |||||
chr16:56964108
|
C | G | 1 | a0002c0002t0001g0243 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.233+984C>G | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56964108 | ||||||
chr16:56964425
|
T | A | 1 | a0001c0001t0001g0245 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.233+1301T>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56964425 | ||||||
chr16:56964656
|
ACCCGCGC others(4): Show |
A | 4 | a0001c0001t0001g0011a0001c0001t0001g0258a0001c0001t0001g0259others(1): Show | 8 | NA18944.hp2 NA18953.hp1 NA18960.hp1 others(5): Show |
intron_variant | MODIFIER | c.233+1533_233+1543d others(13): Show |
CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56964656 | ||||||
chr16:56964660
|
G | C | 77 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0019others(74): Show | 125 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(122): Show |
intron_variant | MODIFIER | c.233+1536G>C | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56964660 | ||||||
chr16:56964797
|
C | T | 2 | a0007c0012t0001g0200a0017c0026t0001g0201 | 2 | HG02559.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.233+1673C>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56964797 | ||||||
chr16:56964849
|
T | G | 23 | a0001c0001t0001g0024a0002c0002t0001g0003a0002c0002t0001g0014others(20): Show | 39 | HG00544.hp2 HG00558.hp1 HG00673.hp2 others(36): Show |
intron_variant | MODIFIER | c.233+1725T>G | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56964849 | ||||||
chr16:56964982
|
G | A | 1 | a0002c0002t0002g0260 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.233+1858G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56964982 | ||||||
chr16:56965006
|
A | G | 79 | a0001c0001t0001g0008a0001c0001t0001g0016a0001c0001t0001g0044others(76): Show | 114 | HG00140.hp1 HG00323.hp1 HG00621.hp2 others(111): Show |
intron_variant | MODIFIER | c.233+1882A>G | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56965006 | ||||||
chr16:56965015
|
G | A | 2 | a0002c0009t0001g0177a0002c0009t0001g0178 | 2 | HG02451.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.233+1891G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56965015 | ||||||
chr16:56965040
|
A | T | 2 | a0002c0014t0001g0098a0002c0014t0001g0099 | 2 | HG02717.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.233+1916A>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56965040 | ||||||
chr16:56965133
|
G | C | 1 | a0001c0001t0001g0073 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.233+2009G>C | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56965133 | ||||||
chr16:56965146
|
C | T | 1 | a0002c0002t0001g0203 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.233+2022C>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56965146 | ||||||
chr16:56965188
|
T | A | 4 | a0007c0012t0001g0197a0007c0012t0001g0199a0007c0012t0001g0200others(1): Show | 4 | HG02055.hp1 HG02559.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.233+2064T>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56965188 | ||||||
chr16:56965267
|
C | T | 1 | a0002c0006t0001g0179 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.233+2143C>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56965267 | ||||||
chr16:56965272
|
AT | A | 21 | a0001c0001t0001g0012a0001c0001t0001g0021a0001c0001t0001g0035others(18): Show | 33 | HG00099.hp2 HG00423.hp1 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.233+2149delT | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56965272 | ||||||
chr16:56965346
|
A | C | 97 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0024others(94): Show | 151 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(148): Show |
intron_variant | MODIFIER | c.233+2222A>C | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56965346 | ||||||
chr16:56965416
|
C | T | 78 | a0001c0001t0001g0008a0001c0001t0001g0016a0001c0001t0001g0044others(75): Show | 113 | HG00140.hp1 HG00323.hp1 HG00621.hp2 others(110): Show |
intron_variant | MODIFIER | c.233+2292C>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56965416 | ||||||
chr16:56965440
|
TC | T | 44 | a0001c0001t0001g0012a0001c0001t0001g0021a0001c0001t0001g0035others(41): Show | 65 | HG00099.hp2 HG00423.hp1 HG00741.hp1 others(62): Show |
intron_variant | MODIFIER | c.233+2317delC | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56965440 | ||||||
chr16:56965470
|
G | A | 2 | a0002c0014t0001g0098a0002c0014t0001g0099 | 2 | HG02717.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.233+2346G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56965470 | ||||||
chr16:56965651
|
C | A | 3 | a0002c0002t0001g0174a0002c0002t0001g0193a0002c0025t0001g0082 | 3 | HG01884.hp1 HG02723.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.233+2527C>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56965651 | ||||||
chr16:56965866
|
C | T | 7 | a0002c0002t0001g0022a0002c0002t0001g0028a0002c0002t0001g0092others(4): Show | 11 | HG02257.hp1 HG02622.hp1 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.233+2742C>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56965866 | ||||||
chr16:56965866
|
CG | C | 57 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0027others(54): Show | 95 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.233+2744delG | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 56965866 | |||||
chr16:56965925
|
C | T | 1 | a0001c0001t0001g0239 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.233+2801C>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56965925 | ||||||
chr16:56966036
|
C | T | 1 | a0001c0010t0001g0215 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.233+2912C>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56966036 | ||||||
chr16:56966037
|
A | G | 229 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0012others(226): Show | 340 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(337): Show |
intron_variant | MODIFIER | c.233+2913A>G | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56966037 | ||||||
chr16:56966048
|
G | C | 2 | a0002c0002t0001g0176a0002c0002t0002g0175 | 2 | HG02922.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.233+2924G>C | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56966048 | ||||||
chr16:56966072
|
T | TA | 7 | a0002c0002t0001g0104a0002c0002t0002g0281a0002c0002t0002g0282others(4): Show | 9 | HG01123.hp2 HG02647.hp1 HG03209.hp1 others(6): Show |
intron_variant | MODIFIER | c.233+2956dupA | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 56966072 | |||||
chr16:56966090
|
G | A | 1 | a0001c0001t0001g0118 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.233+2966G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56966090 | ||||||
chr16:56966232
|
G | A | 2 | a0002c0002t0002g0119a0013c0022t0002g0120 | 2 | HG03017.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.233+3108G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56966232 | ||||||
chr16:56966233
|
C | T | 19 | a0001c0001t0001g0024a0002c0002t0001g0003a0002c0002t0001g0014others(16): Show | 35 | HG00544.hp2 HG00558.hp1 HG00673.hp2 others(32): Show |
intron_variant | MODIFIER | c.233+3109C>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56966233 | ||||||
chr16:56966234
|
T | C | 1 | a0002c0003t0002g0071 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.233+3110T>C | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56966234 | ||||||
chr16:56966279
|
A | G | 2 | a0002c0009t0001g0177a0002c0009t0001g0178 | 2 | HG02451.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.234-3107A>G | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56966279 | ||||||
chr16:56966297
|
C | A | 8 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0111others(5): Show | 8 | HG02055.hp1 HG02145.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.234-3089C>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56966297 | ||||||
chr16:56966300
|
G | A | 1 | a0001c0001t0001g0246 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.234-3086G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56966300 | ||||||
chr16:56966309
|
C | T | 3 | a0002c0002t0001g0174a0002c0002t0001g0193a0002c0025t0001g0082 | 3 | HG01884.hp1 HG02723.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.234-3077C>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56966309 | ||||||
chr16:56966330
|
A | G | 14 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0001g0187others(11): Show | 19 | HG03942.hp1 HG04115.hp2 NA18612.hp1 others(16): Show |
intron_variant | MODIFIER | c.234-3056A>G | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56966330 | ||||||
chr16:56966364
|
T | A | 5 | a0002c0002t0001g0033a0002c0002t0001g0036a0002c0002t0001g0039others(2): Show | 8 | HG00558.hp1 HG02071.hp1 NA18939.hp2 others(5): Show |
intron_variant | MODIFIER | c.234-3022T>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56966364 | ||||||
chr16:56966372
|
G | A | 166 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0016others(163): Show | 255 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(252): Show |
intron_variant | MODIFIER | c.234-3014G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56966372 | ||||||
chr16:56966463
|
G | T | 1 | a0002c0002t0002g0282 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.234-2923G>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56966463 | ||||||
chr16:56966484
|
C | T | 1 | a0002c0002t0001g0145 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.234-2902C>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56966484 | ||||||
chr16:56966485
|
G | A | 2 | a0002c0009t0001g0177a0002c0009t0001g0178 | 2 | HG02451.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.234-2901G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56966485 | ||||||
chr16:56966524
|
T | C | 1 | a0012c0021t0001g0095 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.234-2862T>C | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56966524 | ||||||
chr16:56966593
|
T | G | 1 | a0001c0001t0001g0115 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.234-2793T>G | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56966593 | ||||||
chr16:56966598
|
T | G | 1 | a0002c0002t0001g0104 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.234-2788T>G | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56966598 | ||||||
chr16:56966599
|
G | T | 1 | a0002c0002t0001g0104 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.234-2787G>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56966599 | ||||||
chr16:56966761
|
G | A | 1 | a0002c0005t0001g0209 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.234-2625G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56966761 | ||||||
chr16:56966764
|
TA | T | 18 | a0001c0001t0001g0024a0002c0002t0001g0003a0002c0002t0001g0014others(15): Show | 34 | HG00544.hp2 HG00558.hp1 HG00673.hp2 others(31): Show |
intron_variant | MODIFIER | c.234-2620delA | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 56966764 | |||||
chr16:56966768
|
CT | C | 99 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0024others(96): Show | 154 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(151): Show |
intron_variant | MODIFIER | c.234-2602delT | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 56966768 | |||||
chr16:56966770
|
T | C | 1 | a0002c0002t0001g0105 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.234-2616T>C | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56966770 | ||||||
chr16:56966784
|
T | A | 84 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0024others(81): Show | 138 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(135): Show |
intron_variant | MODIFIER | c.234-2602T>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56966784 | ||||||
chr16:56966973
|
G | A | 56 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0027others(53): Show | 93 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.234-2413G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56966973 | ||||||
chr16:56967026
|
G | A | 16 | a0001c0001t0001g0057a0001c0001t0001g0218a0001c0001t0001g0219others(13): Show | 22 | HG00642.hp2 HG00733.hp1 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.234-2360G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56967026 | ||||||
chr16:56967119
|
G | A | 1 | a0001c0001t0001g0205 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.234-2267G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56967119 | ||||||
chr16:56967173
|
C | G | 6 | a0002c0002t0002g0281a0002c0002t0002g0282a0004c0007t0001g0026others(3): Show | 8 | HG01123.hp2 HG02647.hp1 HG03209.hp1 others(5): Show |
intron_variant | MODIFIER | c.234-2213C>G | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56967173 | ||||||
chr16:56967191
|
T | C | 2 | a0002c0009t0001g0177a0002c0009t0001g0178 | 2 | HG02451.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.234-2195T>C | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56967191 | ||||||
chr16:56967202
|
C | A | 1 | a0001c0001t0001g0229 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.234-2184C>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56967202 | ||||||
chr16:56967304
|
C | T | 82 | a0001c0001t0001g0008a0001c0001t0001g0016a0001c0001t0001g0044others(79): Show | 117 | HG00140.hp1 HG00323.hp1 HG00621.hp2 others(114): Show |
intron_variant | MODIFIER | c.234-2082C>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56967304 | ||||||
chr16:56967338
|
T | C | 9 | a0002c0002t0001g0066a0002c0002t0001g0174a0002c0002t0001g0176others(6): Show | 9 | HG01884.hp1 HG02717.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.234-2048T>C | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56967338 | ||||||
chr16:56967342
|
T | TCACA | 55 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0027others(52): Show | 93 | HG00408.hp1 HG00438.hp2 HG00597.hp1 others(90): Show |
intron_variant | MODIFIER | c.234-2041_234-2038d others(6): Show |
CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 56967342 | |||||
chr16:56967349
|
A | C | 2 | a0002c0005t0001g0210a0003c0004t0001g0217 | 2 | HG00438.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.234-2037A>C | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56967349 | ||||||
chr16:56967362
|
AC | A | 49 | a0001c0001t0001g0008a0001c0001t0001g0016a0001c0001t0001g0044others(46): Show | 74 | HG00140.hp1 HG00323.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.234-2023delC | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56967362 | ||||||
chr16:56967363
|
C | A | 32 | a0001c0001t0001g0049a0001c0001t0001g0121a0001c0001t0001g0125others(29): Show | 42 | HG00673.hp1 HG00738.hp1 HG01081.hp2 others(39): Show |
intron_variant | MODIFIER | c.234-2023C>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56967363 | ||||||
chr16:56967425
|
G | A | 1 | a0001c0001t0001g0206 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.234-1961G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56967425 | ||||||
chr16:56967475
|
T | G | 20 | a0001c0001t0001g0024a0002c0002t0001g0003a0002c0002t0001g0014others(17): Show | 36 | HG00544.hp2 HG00558.hp1 HG00673.hp2 others(33): Show |
intron_variant | MODIFIER | c.234-1911T>G | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56967475 | ||||||
chr16:56967526
|
G | A | 82 | a0001c0001t0001g0008a0001c0001t0001g0016a0001c0001t0001g0044others(79): Show | 117 | HG00140.hp1 HG00323.hp1 HG00621.hp2 others(114): Show |
intron_variant | MODIFIER | c.234-1860G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56967526 | ||||||
chr16:56967604
|
G | A | 21 | a0001c0001t0001g0012a0001c0001t0001g0021a0001c0001t0001g0035others(18): Show | 33 | HG00099.hp2 HG00423.hp1 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.234-1782G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56967604 | ||||||
chr16:56967654
|
C | CA | 19 | a0001c0001t0001g0077a0001c0001t0001g0115a0001c0001t0001g0218others(16): Show | 20 | HG00438.hp1 HG01109.hp1 HG01175.hp1 others(17): Show |
intron_variant | MODIFIER | c.234-1715dupA | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 56967654 | |||||
chr16:56967654
|
CA | C | 9 | a0002c0002t0001g0066a0002c0002t0001g0176a0002c0002t0001g0216others(6): Show | 9 | HG02451.hp2 HG02717.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.234-1715delA | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 56967654 | |||||
chr16:56967661
|
A | G | 3 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0111 | 3 | HG02630.hp2 HG02886.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.234-1725A>G | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56967661 | ||||||
chr16:56967668
|
AAAAC | A | 8 | a0002c0002t0001g0112a0002c0002t0001g0114a0002c0002t0001g0162others(5): Show | 8 | HG00642.hp1 HG02055.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.234-1715_234-1712d others(6): Show |
CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 56967668 | |||||
chr16:56967669
|
AAAC | A | 76 | a0001c0001t0001g0008a0001c0001t0001g0016a0001c0001t0001g0044others(73): Show | 111 | HG00140.hp1 HG00323.hp1 HG00621.hp2 others(108): Show |
intron_variant | MODIFIER | c.234-1714_234-1712d others(5): Show |
CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 56967669 | |||||
chr16:56967672
|
C | A | 1 | a0001c0001t0001g0173 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.234-1714C>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56967672 | ||||||
chr16:56967680
|
T | C | 2 | a0001c0001t0001g0012a0001c0001t0001g0076 | 5 | NA18947.hp1 NA18973.hp1 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.234-1706T>C | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56967680 | ||||||
chr16:56967792
|
C | T | 2 | a0002c0006t0001g0179a0004c0007t0001g0170 | 2 | NA19043.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.234-1594C>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56967792 | ||||||
chr16:56967795
|
A | G | 1 | a0012c0021t0001g0095 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.234-1591A>G | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56967795 | ||||||
chr16:56967882
|
G | A | 7 | a0002c0002t0001g0025a0002c0002t0001g0043a0002c0002t0001g0117others(4): Show | 10 | HG01346.hp1 HG01981.hp1 HG02004.hp1 others(7): Show |
intron_variant | MODIFIER | c.234-1504G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56967882 | ||||||
chr16:56967900
|
AGTGAACT | A | 4 | a0002c0009t0001g0090a0002c0009t0001g0091a0002c0009t0001g0177others(1): Show | 4 | HG02109.hp1 HG02451.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.234-1481_234-1475d others(9): Show |
CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 56967900 | |||||
chr16:56967977
|
TA | T | 279 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(276): Show | 414 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(411): Show |
intron_variant | MODIFIER | c.234-1396delA | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 56967977 | |||||
chr16:56968053
|
T | A | 8 | a0001c0001t0001g0032a0001c0001t0001g0097a0001c0001t0001g0263others(5): Show | 10 | HG00423.hp2 HG02015.hp1 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.234-1333T>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56968053 | ||||||
chr16:56968073
|
A | C | 84 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(81): Show | 131 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.234-1313A>C | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56968073 | ||||||
chr16:56968180
|
C | A | 1 | a0008c0013t0001g0168 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.234-1206C>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56968180 | ||||||
chr16:56968189
|
A | G | 1 | a0001c0001t0001g0280 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.234-1197A>G | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56968189 | ||||||
chr16:56968206
|
G | T | 2 | a0001c0001t0001g0044a0001c0001t0001g0133 | 3 | HG01981.hp2 HG03669.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.234-1180G>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56968206 | ||||||
chr16:56968209
|
A | T | 2 | a0001c0001t0001g0044a0001c0001t0001g0133 | 3 | HG01981.hp2 HG03669.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.234-1177A>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56968209 | ||||||
chr16:56968240
|
T | C | 37 | a0001c0001t0001g0035a0001c0001t0001g0051a0001c0001t0001g0052others(34): Show | 53 | HG00099.hp2 HG00741.hp1 HG01515.hp2 others(50): Show |
intron_variant | MODIFIER | c.234-1146T>C | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56968240 | ||||||
chr16:56968330
|
C | T | 41 | a0001c0001t0001g0035a0001c0001t0001g0051a0001c0001t0001g0052others(38): Show | 58 | HG00099.hp2 HG00741.hp1 HG01515.hp2 others(55): Show |
intron_variant | MODIFIER | c.234-1056C>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56968330 | ||||||
chr16:56968336
|
C | G | 4 | a0002c0002t0001g0243a0002c0006t0001g0054a0002c0006t0001g0179others(1): Show | 5 | HG02280.hp2 HG02886.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.234-1050C>G | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56968336 | ||||||
chr16:56968346
|
C | T | 4 | a0001c0001t0001g0012a0001c0001t0001g0076a0001c0001t0001g0078others(1): Show | 7 | HG00423.hp1 NA18947.hp1 NA18973.hp1 others(4): Show |
intron_variant | MODIFIER | c.234-1040C>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56968346 | ||||||
chr16:56968359
|
T | C | 1 | a0001c0001t0001g0156 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.234-1027T>C | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56968359 | ||||||
chr16:56968376
|
G | A | 1 | a0002c0003t0002g0083 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.234-1010G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56968376 | ||||||
chr16:56968387
|
A | G | 3 | a0002c0002t0001g0174a0002c0002t0001g0193a0002c0025t0001g0082 | 3 | HG01884.hp1 HG02723.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.234-999A>G | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56968387 | ||||||
chr16:56968463
|
A | G | 4 | a0002c0009t0001g0090a0002c0009t0001g0091a0002c0009t0001g0177others(1): Show | 4 | HG02109.hp1 HG02451.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.234-923A>G | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56968463 | ||||||
chr16:56968478
|
C | T | 1 | a0002c0003t0002g0085 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.234-908C>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56968478 | ||||||
chr16:56968492
|
C | A | 85 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(82): Show | 132 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.234-894C>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56968492 | ||||||
chr16:56968729
|
C | CT | 35 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0001g0077others(32): Show | 51 | HG00099.hp2 HG00733.hp2 HG02109.hp2 others(48): Show |
intron_variant | MODIFIER | c.234-642dupT | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 56968729 | |||||
chr16:56968729
|
CT | C | 24 | a0001c0001t0001g0024a0002c0002t0001g0003a0002c0002t0001g0014others(21): Show | 40 | HG00544.hp2 HG00558.hp1 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.234-642delT | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 56968729 | |||||
chr16:56968751
|
C | G | 177 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(174): Show | 258 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(255): Show |
intron_variant | MODIFIER | c.234-635C>G | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56968751 | ||||||
chr16:56968798
|
A | G | 4 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0111others(1): Show | 4 | HG02145.hp2 HG02630.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.234-588A>G | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56968798 | ||||||
chr16:56968820
|
T | G | 248 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(245): Show | 362 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(359): Show |
intron_variant | MODIFIER | c.234-566T>G | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56968820 | ||||||
chr16:56969113
|
G | T | 20 | a0001c0001t0001g0024a0002c0002t0001g0003a0002c0002t0001g0014others(17): Show | 36 | HG00544.hp2 HG00558.hp1 HG00673.hp2 others(33): Show |
intron_variant | MODIFIER | c.234-273G>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56969113 | ||||||
chr16:56969131
|
C | T | 6 | a0002c0009t0001g0090a0002c0009t0001g0091a0002c0009t0001g0177others(3): Show | 6 | HG02109.hp1 HG02451.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.234-255C>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56969131 | ||||||
chr16:56969234
|
T | C | 23 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0027others(20): Show | 50 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(47): Show |
intron_variant | MODIFIER | c.234-152T>C | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56969234 | ||||||
chr16:56969278
|
G | A | 1 | a0002c0002t0001g0107 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.234-108G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56969278 | ||||||
chr16:56969322
|
A | T | 1 | a0002c0009t0001g0154 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.234-64A>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56969322 | ||||||
chr16:56969338
|
C | A | 9 | a0001c0010t0001g0211a0001c0010t0001g0212a0001c0010t0001g0215others(6): Show | 12 | HG00438.hp1 HG00438.hp2 HG03704.hp2 others(9): Show |
intron_variant | MODIFIER | c.234-48C>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 2/15 | chr16 | 56969338 | ||||||
chr16:56969549
|
T | C | 2 | a0002c0002t0001g0176a0002c0002t0002g0175 | 2 | HG02922.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.368+29T>C | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 3/15 | chr16 | 56969549 | ||||||
chr16:56969811
|
G | T | 289 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(286): Show | 437 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(434): Show |
intron_variant | MODIFIER | c.440-103G>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 4/15 | chr16 | 56969811 | ||||||
chr16:56969877
|
G | A | 1 | a0002c0002t0002g0119 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.440-37G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 4/15 | chr16 | 56969877 | ||||||
chr16:56970065
|
T | C | 293 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(290): Show | 441 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(438): Show |
intron_variant | MODIFIER | c.527+64T>C | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 5/15 | chr16 | 56970065 | ||||||
chr16:56970068
|
T | C | 302 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(299): Show | 453 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(450): Show |
intron_variant | MODIFIER | c.527+67T>C | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 5/15 | chr16 | 56970068 | ||||||
chr16:56970402
|
G | A | 1 | a0002c0014t0001g0098 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.527+401G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 5/15 | chr16 | 56970402 | ||||||
chr16:56970547
|
G | A | 6 | a0002c0009t0001g0090a0002c0009t0001g0091a0002c0009t0001g0177others(3): Show | 6 | HG02109.hp1 HG02451.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.528-486G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 5/15 | chr16 | 56970547 | ||||||
chr16:56970551
|
C | T | 1 | a0002c0002t0002g0163 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.528-482C>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 5/15 | chr16 | 56970551 | ||||||
chr16:56970576
|
C | T | 1 | a0002c0002t0001g0094 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.528-457C>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 5/15 | chr16 | 56970576 | ||||||
chr16:56970750
|
C | T | 6 | a0002c0009t0001g0090a0002c0009t0001g0091a0002c0009t0001g0177others(3): Show | 6 | HG02109.hp1 HG02451.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.528-283C>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 5/15 | chr16 | 56970750 | ||||||
chr16:56970756
|
C | T | 1 | a0001c0001t0001g0121 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.528-277C>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 5/15 | chr16 | 56970756 | ||||||
chr16:56970757
|
A | G | 1 | a0003c0004t0001g0228 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.528-276A>G | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 5/15 | chr16 | 56970757 | ||||||
chr16:56970835
|
A | G | 6 | a0002c0009t0001g0090a0002c0009t0001g0091a0002c0009t0001g0177others(3): Show | 6 | HG02109.hp1 HG02451.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.528-198A>G | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 5/15 | chr16 | 56970835 | ||||||
chr16:56970859
|
A | G | 2 | a0002c0002t0002g0152a0002c0002t0002g0153 | 2 | NA19001.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.528-174A>G | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 5/15 | chr16 | 56970859 | ||||||
chr16:56970898
|
G | A | 1 | a0004c0007t0001g0171 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.528-135G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 5/15 | chr16 | 56970898 | ||||||
chr16:56970956
|
G | C | 1 | a0001c0001t0001g0249 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.528-77G>C | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 5/15 | chr16 | 56970956 | ||||||
chr16:56970977
|
G | A | 95 | a0001c0001t0001g0008a0001c0001t0001g0016a0001c0001t0001g0044others(92): Show | 133 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(130): Show |
intron_variant | MODIFIER | c.528-56G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 5/15 | chr16 | 56970977 | ||||||
chr16:56970999
|
G | A | 1 | a0002c0002t0001g0216 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.528-34G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 5/15 | chr16 | 56970999 | ||||||
chr16:56971389
|
C | T | 86 | a0001c0001t0001g0008a0001c0001t0001g0016a0001c0001t0001g0044others(83): Show | 121 | HG00140.hp1 HG00323.hp1 HG00621.hp2 others(118): Show |
splice_region_variant&intron_variant | LOW | c.658+8C>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 7/15 | chr16 | 56971389 | ||||||
chr16:56971468
|
A | G | 1 | a0002c0002t0003g0088 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.658+87A>G | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 7/15 | chr16 | 56971468 | ||||||
chr16:56971513
|
T | C | 8 | a0002c0002t0001g0022a0002c0002t0001g0028a0002c0002t0001g0092others(5): Show | 12 | HG02257.hp1 HG02622.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.658+132T>C | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 7/15 | chr16 | 56971513 | ||||||
chr16:56971567
|
C | A | 86 | a0001c0001t0001g0008a0001c0001t0001g0016a0001c0001t0001g0044others(83): Show | 121 | HG00140.hp1 HG00323.hp1 HG00621.hp2 others(118): Show |
intron_variant | MODIFIER | c.658+186C>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 7/15 | chr16 | 56971567 | ||||||
chr16:56971638
|
C | T | 26 | a0001c0001t0001g0049a0001c0001t0001g0121a0001c0001t0001g0125others(23): Show | 35 | HG00673.hp1 HG00738.hp1 HG01081.hp2 others(32): Show |
intron_variant | MODIFIER | c.658+257C>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 7/15 | chr16 | 56971638 | ||||||
chr16:56971690
|
T | C | 1 | a0001c0001t0001g0097 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.659-302T>C | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 7/15 | chr16 | 56971690 | ||||||
chr16:56971708
|
T | C | 39 | a0001c0001t0001g0024a0001c0001t0001g0100a0001c0001t0001g0101others(36): Show | 58 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.659-284T>C | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 7/15 | chr16 | 56971708 | ||||||
chr16:56971852
|
C | G | 10 | a0002c0002t0001g0066a0002c0002t0001g0176a0002c0002t0002g0175others(7): Show | 10 | HG02055.hp1 HG02559.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.659-140C>G | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 7/15 | chr16 | 56971852 | ||||||
chr16:56971970
|
C | T | 10 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0111others(7): Show | 10 | HG02109.hp1 HG02451.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.659-22C>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 7/15 | chr16 | 56971970 | ||||||
chr16:56972160
|
G | A | 2 | a0002c0003t0002g0297a0002c0003t0002g0298 | 2 | HG00741.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.750+77G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 8/15 | chr16 | 56972160 | ||||||
chr16:56972387
|
GC | G | 208 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0016others(205): Show | 312 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(309): Show |
intron_variant | MODIFIER | c.750+313delC | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr16 | 56972387 | |||||
chr16:56972393
|
C | T | 84 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(81): Show | 131 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.750+310C>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 8/15 | chr16 | 56972393 | ||||||
chr16:56972394
|
C | A | 2 | a0001c0001t0001g0218a0001c0001t0001g0239 | 2 | HG01109.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.750+311C>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 8/15 | chr16 | 56972394 | ||||||
chr16:56972402
|
G | A | 1 | a0002c0002t0002g0152 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.750+319G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 8/15 | chr16 | 56972402 | ||||||
chr16:56972440
|
A | G | 1 | a0001c0001t0001g0257 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.750+357A>G | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 8/15 | chr16 | 56972440 | ||||||
chr16:56972466
|
A | G | 42 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0027others(39): Show | 75 | HG00408.hp1 HG00597.hp1 HG00609.hp1 others(72): Show |
intron_variant | MODIFIER | c.750+383A>G | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 8/15 | chr16 | 56972466 | ||||||
chr16:56972493
|
C | G | 1 | a0004c0007t0001g0170 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.750+410C>G | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 8/15 | chr16 | 56972493 | ||||||
chr16:56972533
|
C | T | 1 | a0002c0003t0002g0299 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.750+450C>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 8/15 | chr16 | 56972533 | ||||||
chr16:56972535
|
C | T | 1 | a0001c0001t0001g0073 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.750+452C>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 8/15 | chr16 | 56972535 | ||||||
chr16:56972678
|
C | T | 77 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0027others(74): Show | 119 | HG00408.hp1 HG00597.hp1 HG00609.hp1 others(116): Show |
intron_variant | MODIFIER | c.750+595C>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 8/15 | chr16 | 56972678 | ||||||
chr16:56972684
|
G | C | 2 | a0002c0002t0002g0148a0002c0002t0002g0260 | 2 | HG02015.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.750+601G>C | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 8/15 | chr16 | 56972684 | ||||||
chr16:56972806
|
C | T | 1 | a0001c0001t0001g0294 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.751-525C>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 8/15 | chr16 | 56972806 | ||||||
chr16:56972917
|
T | A | 212 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(209): Show | 310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.751-414T>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 8/15 | chr16 | 56972917 | ||||||
chr16:56972970
|
C | T | 1 | a0002c0002t0001g0067 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.751-361C>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 8/15 | chr16 | 56972970 | ||||||
chr16:56973023
|
G | A | 1 | a0002c0002t0001g0248 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.751-308G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 8/15 | chr16 | 56973023 | ||||||
chr16:56973027
|
T | A | 2 | a0002c0002t0001g0174a0002c0002t0001g0193 | 2 | HG01884.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.751-304T>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 8/15 | chr16 | 56973027 | ||||||
chr16:56973038
|
G | A | 2 | a0002c0002t0001g0174a0002c0002t0001g0193 | 2 | HG01884.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.751-293G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 8/15 | chr16 | 56973038 | ||||||
chr16:56973128
|
C | T | 2 | a0001c0001t0001g0055a0002c0002t0001g0256 | 3 | HG01070.hp1 HG01071.hp2 HG02080.hp1 |
intron_variant | MODIFIER | c.751-203C>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 8/15 | chr16 | 56973128 | ||||||
chr16:56973280
|
T | C | 15 | a0001c0001t0001g0057a0001c0001t0001g0118a0001c0001t0001g0288others(12): Show | 22 | HG00099.hp1 HG00099.hp2 HG00741.hp1 others(19): Show |
intron_variant | MODIFIER | c.751-51T>C | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 8/15 | chr16 | 56973280 | ||||||
chr16:56973534
|
T | G | 92 | a0001c0001t0001g0001a0001c0001t0001g0019a0001c0001t0001g0027others(89): Show | 147 | HG00099.hp1 HG00408.hp1 HG00544.hp2 others(144): Show |
intron_variant | MODIFIER | c.930+24T>G | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 9/15 | chr16 | 56973534 | ||||||
chr16:56973539
|
G | A | 208 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(205): Show | 304 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(301): Show |
intron_variant | MODIFIER | c.930+29G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 9/15 | chr16 | 56973539 | ||||||
chr16:56973600
|
G | A | 22 | a0001c0010t0001g0211a0002c0002t0001g0003a0002c0002t0001g0014others(19): Show | 37 | HG00544.hp2 HG00558.hp1 HG00673.hp2 others(34): Show |
intron_variant | MODIFIER | c.930+90G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 9/15 | chr16 | 56973600 | ||||||
chr16:56973698
|
G | A | 135 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(132): Show | 199 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.930+188G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 9/15 | chr16 | 56973698 | ||||||
chr16:56973716
|
C | T | 1 | a0001c0001t0001g0125 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.930+206C>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 9/15 | chr16 | 56973716 | ||||||
chr16:56973740
|
A | G | 2 | a0002c0003t0002g0297a0002c0003t0002g0298 | 2 | HG00741.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.930+230A>G | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 9/15 | chr16 | 56973740 | ||||||
chr16:56973774
|
C | T | 1 | a0002c0002t0001g0203 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.930+264C>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 9/15 | chr16 | 56973774 | ||||||
chr16:56973806
|
C | T | 1 | a0004c0007t0001g0169 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.930+296C>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 9/15 | chr16 | 56973806 | ||||||
chr16:56973822
|
A | C | 133 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(130): Show | 199 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.930+312A>C | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 9/15 | chr16 | 56973822 | ||||||
chr16:56973906
|
C | T | 1 | a0002c0002t0001g0216 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.930+396C>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 9/15 | chr16 | 56973906 | ||||||
chr16:56973921
|
C | T | 1 | a0006c0011t0001g0223 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.930+411C>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 9/15 | chr16 | 56973921 | ||||||
chr16:56973928
|
C | T | 1 | a0001c0001t0001g0035 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.930+418C>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 9/15 | chr16 | 56973928 | ||||||
chr16:56973980
|
T | C | 1 | a0002c0002t0001g0248 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.930+470T>C | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 9/15 | chr16 | 56973980 | ||||||
chr16:56974017
|
G | A | 1 | a0001c0001t0001g0286 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.930+507G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 9/15 | chr16 | 56974017 | ||||||
chr16:56974075
|
G | C | 1 | a0005c0008t0001g0040 | 2 | NA18952.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.930+565G>C | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 9/15 | chr16 | 56974075 | ||||||
chr16:56974136
|
G | A | 129 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(126): Show | 195 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.930+626G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 9/15 | chr16 | 56974136 | ||||||
chr16:56974212
|
G | A | 1 | a0001c0001t0001g0059 | 2 | HG01884.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.930+702G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 9/15 | chr16 | 56974212 | ||||||
chr16:56974249
|
G | A | 9 | a0002c0002t0001g0022a0002c0002t0001g0028a0002c0002t0001g0092others(6): Show | 13 | HG02257.hp1 HG02622.hp1 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.930+739G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 9/15 | chr16 | 56974249 | ||||||
chr16:56974275
|
A | G | 1 | a0003c0004t0001g0109 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.930+765A>G | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 9/15 | chr16 | 56974275 | ||||||
chr16:56974288
|
TAA | T | 2 | a0001c0001t0001g0047a0001c0001t0001g0144 | 3 | HG01074.hp2 HG01256.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.930+779_930+780del others(2): Show |
CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 9/15 | chr16 | 56974288 | ||||||
chr16:56974315
|
G | A | 187 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(184): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.931-786G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 9/15 | chr16 | 56974315 | ||||||
chr16:56974316
|
G | A | 1 | a0001c0001t0001g0224 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.931-785G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 9/15 | chr16 | 56974316 | ||||||
chr16:56974375
|
A | G | 200 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(197): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.931-726A>G | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 9/15 | chr16 | 56974375 | ||||||
chr16:56974465
|
C | A | 1 | a0001c0001t0001g0125 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.931-636C>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 9/15 | chr16 | 56974465 | ||||||
chr16:56974493
|
T | A | 1 | a0001c0001t0001g0205 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.931-608T>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 9/15 | chr16 | 56974493 | ||||||
chr16:56974586
|
T | G | 20 | a0002c0002t0001g0003a0002c0002t0001g0014a0002c0002t0001g0033others(17): Show | 35 | HG00544.hp2 HG00558.hp1 HG00673.hp2 others(32): Show |
intron_variant | MODIFIER | c.931-515T>G | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 9/15 | chr16 | 56974586 | ||||||
chr16:56974596
|
A | T | 233 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(230): Show | 359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.931-505A>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 9/15 | chr16 | 56974596 | ||||||
chr16:56974857
|
G | A | 1 | a0011c0020t0001g0289 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.931-244G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 9/15 | chr16 | 56974857 | ||||||
chr16:56974993
|
G | A | 4 | a0001c0001t0001g0126a0001c0001t0001g0258a0001c0001t0001g0263others(1): Show | 4 | NA18960.hp1 NA18993.hp2 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.931-108G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 9/15 | chr16 | 56974993 | ||||||
chr16:56975189
|
G | A | 1 | a0002c0002t0001g0131 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.981+38G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 10/15 | chr16 | 56975189 | ||||||
chr16:56975253
|
A | G | 2 | a0002c0002t0002g0281a0002c0002t0002g0282 | 2 | HG03209.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.981+102A>G | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 10/15 | chr16 | 56975253 | ||||||
chr16:56975283
|
T | G | 33 | a0002c0002t0001g0003a0002c0002t0001g0014a0002c0002t0001g0022others(30): Show | 52 | HG00544.hp2 HG00558.hp1 HG00673.hp2 others(49): Show |
intron_variant | MODIFIER | c.981+132T>G | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 10/15 | chr16 | 56975283 | ||||||
chr16:56975288
|
C | T | 5 | a0002c0009t0001g0090a0002c0009t0001g0091a0002c0009t0001g0154others(2): Show | 5 | HG02109.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.981+137C>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 10/15 | chr16 | 56975288 | ||||||
chr16:56975289
|
G | A | 2 | a0002c0002t0001g0046a0002c0002t0001g0162 | 3 | NA18957.hp2 NA18975.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.981+138G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 10/15 | chr16 | 56975289 | ||||||
chr16:56975329
|
T | G | 1 | a0001c0001t0001g0246 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.981+178T>G | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 10/15 | chr16 | 56975329 | ||||||
chr16:56975464
|
T | A | 162 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(159): Show | 256 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(253): Show |
intron_variant | MODIFIER | c.981+313T>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 10/15 | chr16 | 56975464 | ||||||
chr16:56975476
|
G | A | 88 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(85): Show | 137 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.981+325G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 10/15 | chr16 | 56975476 | ||||||
chr16:56975599
|
C | T | 9 | a0002c0002t0001g0022a0002c0002t0001g0092a0002c0002t0001g0093others(6): Show | 11 | HG02572.hp1 HG02717.hp1 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.981+448C>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 10/15 | chr16 | 56975599 | ||||||
chr16:56975632
|
T | C | 20 | a0002c0002t0001g0003a0002c0002t0001g0014a0002c0002t0001g0033others(17): Show | 35 | HG00544.hp2 HG00558.hp1 HG00673.hp2 others(32): Show |
intron_variant | MODIFIER | c.981+481T>C | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 10/15 | chr16 | 56975632 | ||||||
chr16:56975696
|
A | G | 13 | a0002c0002t0001g0022a0002c0002t0001g0028a0002c0002t0001g0092others(10): Show | 17 | HG02257.hp1 HG02572.hp1 HG02622.hp1 others(14): Show |
intron_variant | MODIFIER | c.981+545A>G | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 10/15 | chr16 | 56975696 | ||||||
chr16:56975739
|
TC | T | 163 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(160): Show | 257 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(254): Show |
intron_variant | MODIFIER | c.981+594delC | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr16 | 56975739 | |||||
chr16:56975857
|
T | A | 29 | a0002c0002t0001g0006a0002c0002t0001g0009a0002c0002t0001g0023others(26): Show | 42 | HG00323.hp1 HG00621.hp2 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.981+706T>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 10/15 | chr16 | 56975857 | ||||||
chr16:56975887
|
C | A | 15 | a0001c0001t0001g0250a0001c0001t0001g0251a0002c0002t0001g0022others(12): Show | 19 | HG02257.hp1 HG02572.hp1 HG02622.hp1 others(16): Show |
intron_variant | MODIFIER | c.981+736C>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 10/15 | chr16 | 56975887 | ||||||
chr16:56975916
|
C | A | 1 | a0002c0002t0003g0088 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.981+765C>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 10/15 | chr16 | 56975916 | ||||||
chr16:56975939
|
G | A | 1 | a0013c0022t0002g0120 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.981+788G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 10/15 | chr16 | 56975939 | ||||||
chr16:56975966
|
G | A | 4 | a0002c0002t0001g0143a0002c0005t0001g0018a0002c0005t0001g0209others(1): Show | 7 | HG03704.hp2 NA18942.hp1 NA18971.hp2 others(4): Show |
intron_variant | MODIFIER | c.981+815G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 10/15 | chr16 | 56975966 | ||||||
chr16:56975970
|
C | G | 13 | a0002c0002t0001g0022a0002c0002t0001g0028a0002c0002t0001g0092others(10): Show | 17 | HG02257.hp1 HG02572.hp1 HG02622.hp1 others(14): Show |
intron_variant | MODIFIER | c.981+819C>G | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 10/15 | chr16 | 56975970 | ||||||
chr16:56976005
|
C | T | 2 | a0002c0002t0001g0107a0002c0002t0001g0108 | 2 | HG01099.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.981+854C>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 10/15 | chr16 | 56976005 | ||||||
chr16:56976020
|
C | T | 182 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(179): Show | 291 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(288): Show |
intron_variant | MODIFIER | c.981+869C>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 10/15 | chr16 | 56976020 | ||||||
chr16:56976029
|
T | C | 187 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(184): Show | 296 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(293): Show |
intron_variant | MODIFIER | c.981+878T>C | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 10/15 | chr16 | 56976029 | ||||||
chr16:56976073
|
T | C | 74 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0016others(71): Show | 119 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.981+922T>C | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 10/15 | chr16 | 56976073 | ||||||
chr16:56976075
|
T | G | 20 | a0002c0002t0001g0003a0002c0002t0001g0014a0002c0002t0001g0033others(17): Show | 35 | HG00544.hp2 HG00558.hp1 HG00673.hp2 others(32): Show |
intron_variant | MODIFIER | c.981+924T>G | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 10/15 | chr16 | 56976075 | ||||||
chr16:56976119
|
A | G | 1 | a0001c0001t0001g0121 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.981+968A>G | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 10/15 | chr16 | 56976119 | ||||||
chr16:56976197
|
C | T | 1 | a0001c0001t0001g0275 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.981+1046C>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 10/15 | chr16 | 56976197 | ||||||
chr16:56976203
|
G | A | 13 | a0002c0002t0001g0022a0002c0002t0001g0028a0002c0002t0001g0092others(10): Show | 17 | HG02257.hp1 HG02572.hp1 HG02622.hp1 others(14): Show |
intron_variant | MODIFIER | c.981+1052G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 10/15 | chr16 | 56976203 | ||||||
chr16:56976205
|
G | A | 3 | a0001c0001t0001g0062a0001c0001t0001g0279a0001c0001t0001g0293 | 4 | HG03139.hp2 HG03490.hp2 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.981+1054G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 10/15 | chr16 | 56976205 | ||||||
chr16:56976320
|
C | T | 3 | a0001c0001t0001g0016a0001c0001t0001g0044a0001c0001t0001g0133 | 7 | HG00140.hp1 HG01361.hp2 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.981+1169C>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 10/15 | chr16 | 56976320 | ||||||
chr16:56976420
|
A | G | 13 | a0002c0002t0001g0022a0002c0002t0001g0028a0002c0002t0001g0092others(10): Show | 17 | HG02257.hp1 HG02572.hp1 HG02622.hp1 others(14): Show |
intron_variant | MODIFIER | c.981+1269A>G | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 10/15 | chr16 | 56976420 | ||||||
chr16:56976470
|
T | G | 9 | a0001c0001t0001g0055a0001c0001t0001g0077a0001c0001t0001g0205others(6): Show | 10 | HG00280.hp2 HG00735.hp2 HG01070.hp1 others(7): Show |
intron_variant | MODIFIER | c.981+1319T>G | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 10/15 | chr16 | 56976470 | ||||||
chr16:56976475
|
CT | C | 8 | a0001c0001t0001g0064a0001c0001t0001g0158a0001c0001t0001g0189others(5): Show | 9 | HG01069.hp1 HG02148.hp2 HG03209.hp2 others(6): Show |
intron_variant | MODIFIER | c.981+1338delT | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr16 | 56976475 | |||||
chr16:56976574
|
C | T | 7 | a0003c0004t0001g0010a0003c0004t0001g0109a0003c0004t0001g0110others(4): Show | 11 | HG00733.hp1 HG01123.hp1 HG01255.hp2 others(8): Show |
intron_variant | MODIFIER | c.981+1423C>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 10/15 | chr16 | 56976574 | ||||||
chr16:56976769
|
G | A | 1 | a0002c0002t0001g0081 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.982-1322G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 10/15 | chr16 | 56976769 | ||||||
chr16:56976915
|
T | A | 2 | a0001c0001t0001g0252a0002c0002t0001g0204 | 2 | HG02145.hp1 NA18946.hp2 |
intron_variant | MODIFIER | c.982-1176T>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 10/15 | chr16 | 56976915 | ||||||
chr16:56976916
|
A | G | 72 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0016others(69): Show | 117 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.982-1175A>G | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 10/15 | chr16 | 56976916 | ||||||
chr16:56976929
|
A | T | 1 | a0001c0001t0001g0246 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.982-1162A>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 10/15 | chr16 | 56976929 | ||||||
chr16:56976940
|
C | T | 1 | a0002c0002t0002g0130 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.982-1151C>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 10/15 | chr16 | 56976940 | ||||||
chr16:56976992
|
T | A | 1 | a0002c0019t0001g0242 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.982-1099T>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 10/15 | chr16 | 56976992 | ||||||
chr16:56977036
|
T | G | 227 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(224): Show | 349 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(346): Show |
intron_variant | MODIFIER | c.982-1055T>G | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 10/15 | chr16 | 56977036 | ||||||
chr16:56977043
|
G | C | 14 | a0001c0001t0001g0187a0001c0001t0001g0189a0002c0002t0001g0017others(11): Show | 19 | HG00438.hp1 HG03942.hp1 HG04115.hp2 others(16): Show |
intron_variant | MODIFIER | c.982-1048G>C | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 10/15 | chr16 | 56977043 | ||||||
chr16:56977082
|
T | G | 21 | a0002c0002t0002g0007a0002c0002t0002g0015a0002c0002t0002g0029others(18): Show | 32 | HG01081.hp2 HG01175.hp2 HG01346.hp2 others(29): Show |
intron_variant | MODIFIER | c.982-1009T>G | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 10/15 | chr16 | 56977082 | ||||||
chr16:56977201
|
G | A | 1 | a0001c0016t0001g0283 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.982-890G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 10/15 | chr16 | 56977201 | ||||||
chr16:56977208
|
G | A | 1 | a0002c0002t0001g0237 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.982-883G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 10/15 | chr16 | 56977208 | ||||||
chr16:56977211
|
G | A | 5 | a0002c0009t0001g0090a0002c0009t0001g0091a0002c0009t0001g0154others(2): Show | 5 | HG02109.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.982-880G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 10/15 | chr16 | 56977211 | ||||||
chr16:56977273
|
G | A | 108 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(105): Show | 172 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(169): Show |
intron_variant | MODIFIER | c.982-818G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 10/15 | chr16 | 56977273 | ||||||
chr16:56977331
|
C | T | 21 | a0002c0002t0002g0007a0002c0002t0002g0015a0002c0002t0002g0029others(18): Show | 32 | HG01081.hp2 HG01175.hp2 HG01346.hp2 others(29): Show |
intron_variant | MODIFIER | c.982-760C>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 10/15 | chr16 | 56977331 | ||||||
chr16:56977342
|
A | G | 1 | a0002c0002t0001g0161 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.982-749A>G | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 10/15 | chr16 | 56977342 | ||||||
chr16:56977540
|
G | A | 88 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(85): Show | 137 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.982-551G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 10/15 | chr16 | 56977540 | ||||||
chr16:56977632
|
G | A | 1 | a0002c0002t0001g0176 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.982-459G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 10/15 | chr16 | 56977632 | ||||||
chr16:56977665
|
CT | C | 1 | a0001c0001t0001g0027 | 3 | HG02615.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.982-425delT | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 10/15 | chr16 | 56977665 | ||||||
chr16:56977794
|
C | T | 1 | a0001c0001t0001g0173 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.982-297C>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 10/15 | chr16 | 56977794 | ||||||
chr16:56977847
|
G | A | 1 | a0001c0001t0001g0290 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.982-244G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 10/15 | chr16 | 56977847 | ||||||
chr16:56977884
|
T | A | 2 | a0005c0008t0001g0247a0005c0008t0001g0253 | 2 | NA18940.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.982-207T>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 10/15 | chr16 | 56977884 | ||||||
chr16:56977905
|
A | G | 1 | a0002c0002t0001g0161 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.982-186A>G | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 10/15 | chr16 | 56977905 | ||||||
chr16:56977914
|
C | T | 20 | a0002c0002t0001g0003a0002c0002t0001g0014a0002c0002t0001g0033others(17): Show | 35 | HG00544.hp2 HG00558.hp1 HG00673.hp2 others(32): Show |
intron_variant | MODIFIER | c.982-177C>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 10/15 | chr16 | 56977914 | ||||||
chr16:56977944
|
C | G | 1 | a0001c0001t0001g0035 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.982-147C>G | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 10/15 | chr16 | 56977944 | ||||||
chr16:56977972
|
C | T | 2 | a0002c0002t0001g0174a0002c0002t0001g0193 | 2 | HG01884.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.982-119C>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 10/15 | chr16 | 56977972 | ||||||
chr16:56978024
|
C | T | 40 | a0002c0002t0001g0003a0002c0002t0001g0014a0002c0002t0001g0022others(37): Show | 58 | HG00544.hp2 HG00558.hp1 HG00673.hp2 others(55): Show |
intron_variant | MODIFIER | c.982-67C>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 10/15 | chr16 | 56978024 | ||||||
chr16:56978262
|
C | T | 1 | a0001c0001t0001g0222 | 1 | HG01496.hp1 | splice_region_variant&intron_variant | LOW | c.1146+7C>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 11/15 | chr16 | 56978262 | ||||||
chr16:56978442
|
C | T | 2 | a0002c0002t0001g0067a0002c0002t0001g0243 | 2 | HG02280.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1146+187C>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 11/15 | chr16 | 56978442 | ||||||
chr16:56978467
|
T | G | 69 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0016others(66): Show | 110 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.1146+212T>G | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 11/15 | chr16 | 56978467 | ||||||
chr16:56978548
|
A | G | 1 | a0002c0003t0002g0298 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1146+293A>G | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 11/15 | chr16 | 56978548 | ||||||
chr16:56978650
|
T | A | 1 | a0001c0001t0001g0089 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1146+395T>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 11/15 | chr16 | 56978650 | ||||||
chr16:56978650
|
TA | T | 21 | a0002c0002t0001g0003a0002c0002t0001g0014a0002c0002t0001g0033others(18): Show | 36 | HG00544.hp2 HG00558.hp1 HG00673.hp2 others(33): Show |
intron_variant | MODIFIER | c.1146+406delA | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr16 | 56978650 | |||||
chr16:56978651
|
A | T | 71 | a0002c0002t0001g0006a0002c0002t0001g0009a0002c0002t0001g0023others(68): Show | 101 | HG00099.hp2 HG00323.hp1 HG00621.hp2 others(98): Show |
intron_variant | MODIFIER | c.1146+396A>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 11/15 | chr16 | 56978651 | ||||||
chr16:56978787
|
A | G | 90 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(87): Show | 141 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.1146+532A>G | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 11/15 | chr16 | 56978787 | ||||||
chr16:56978880
|
C | T | 1 | a0010c0027t0001g0142 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1146+625C>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 11/15 | chr16 | 56978880 | ||||||
chr16:56978975
|
G | A | 21 | a0002c0002t0002g0007a0002c0002t0002g0015a0002c0002t0002g0029others(18): Show | 32 | HG01081.hp2 HG01175.hp2 HG01346.hp2 others(29): Show |
intron_variant | MODIFIER | c.1146+720G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 11/15 | chr16 | 56978975 | ||||||
chr16:56979019
|
G | A | 1 | a0001c0001t0001g0138 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1146+764G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 11/15 | chr16 | 56979019 | ||||||
chr16:56979024
|
G | A | 1 | a0001c0001t0001g0019 | 4 | HG02055.hp2 HG02559.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.1146+769G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 11/15 | chr16 | 56979024 | ||||||
chr16:56979104
|
G | A | 20 | a0002c0002t0001g0003a0002c0002t0001g0014a0002c0002t0001g0033others(17): Show | 35 | HG00544.hp2 HG00558.hp1 HG00673.hp2 others(32): Show |
intron_variant | MODIFIER | c.1146+849G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 11/15 | chr16 | 56979104 | ||||||
chr16:56979484
|
G | C | 1 | a0002c0002t0002g0128 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1146+1229G>C | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 11/15 | chr16 | 56979484 | ||||||
chr16:56979517
|
A | AT | 28 | a0001c0001t0001g0076a0002c0002t0001g0003a0002c0002t0001g0014others(25): Show | 43 | HG00544.hp2 HG00558.hp1 HG00673.hp2 others(40): Show |
intron_variant | MODIFIER | c.1146+1273dupT | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr16 | 56979517 | |||||
chr16:56979517
|
A | ATT | 200 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(197): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.1146+1272_1146+127 others(6): Show |
CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr16 | 56979517 | |||||
chr16:56979572
|
G | A | 1 | a0002c0002t0001g0243 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1146+1317G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 11/15 | chr16 | 56979572 | ||||||
chr16:56979614
|
G | A | 5 | a0002c0009t0001g0090a0002c0009t0001g0091a0002c0009t0001g0154others(2): Show | 5 | HG02109.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1146+1359G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 11/15 | chr16 | 56979614 | ||||||
chr16:56979619
|
G | A | 2 | a0002c0002t0001g0069a0002c0002t0001g0292 | 2 | NA18961.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.1146+1364G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 11/15 | chr16 | 56979619 | ||||||
chr16:56979659
|
C | T | 8 | a0002c0002t0001g0067a0002c0002t0001g0174a0002c0002t0001g0193others(5): Show | 8 | HG01884.hp1 HG02280.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1146+1404C>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 11/15 | chr16 | 56979659 | ||||||
chr16:56979660
|
G | A | 5 | a0002c0009t0001g0090a0002c0009t0001g0091a0002c0009t0001g0154others(2): Show | 5 | HG02109.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1146+1405G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 11/15 | chr16 | 56979660 | ||||||
chr16:56979661
|
C | T | 2 | a0002c0002t0001g0014a0002c0002t0001g0262 | 5 | HG02129.hp2 HG03239.hp2 NA18957.hp1 others(2): Show |
intron_variant | MODIFIER | c.1146+1406C>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 11/15 | chr16 | 56979661 | ||||||
chr16:56979671
|
C | T | 1 | a0001c0001t0001g0274 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1146+1416C>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 11/15 | chr16 | 56979671 | ||||||
chr16:56979672
|
G | A | 1 | a0002c0002t0001g0123 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1146+1417G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 11/15 | chr16 | 56979672 | ||||||
chr16:56979753
|
T | C | 5 | a0002c0009t0001g0090a0002c0009t0001g0091a0002c0009t0001g0154others(2): Show | 5 | HG02109.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1147-1405T>C | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 11/15 | chr16 | 56979753 | ||||||
chr16:56979787
|
A | G | 11 | a0002c0002t0001g0022a0002c0002t0001g0028a0002c0002t0001g0092others(8): Show | 15 | HG02257.hp1 HG02622.hp1 HG02717.hp1 others(12): Show |
intron_variant | MODIFIER | c.1147-1371A>G | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 11/15 | chr16 | 56979787 | ||||||
chr16:56979822
|
A | G | 2 | a0001c0001t0001g0187a0001c0001t0001g0189 | 2 | HG03942.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.1147-1336A>G | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 11/15 | chr16 | 56979822 | ||||||
chr16:56979831
|
TA | T | 21 | a0002c0002t0002g0007a0002c0002t0002g0015a0002c0002t0002g0029others(18): Show | 32 | HG01081.hp2 HG01175.hp2 HG01346.hp2 others(29): Show |
intron_variant | MODIFIER | c.1147-1324delA | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr16 | 56979831 | |||||
chr16:56979842
|
G | A | 5 | a0002c0009t0001g0090a0002c0009t0001g0091a0002c0009t0001g0154others(2): Show | 5 | HG02109.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1147-1316G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 11/15 | chr16 | 56979842 | ||||||
chr16:56979934
|
G | T | 5 | a0002c0009t0001g0090a0002c0009t0001g0091a0002c0009t0001g0154others(2): Show | 5 | HG02109.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1147-1224G>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 11/15 | chr16 | 56979934 | ||||||
chr16:56980123
|
G | A | 1 | a0001c0001t0001g0206 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1147-1035G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 11/15 | chr16 | 56980123 | ||||||
chr16:56980125
|
C | T | 5 | a0002c0009t0001g0090a0002c0009t0001g0091a0002c0009t0001g0154others(2): Show | 5 | HG02109.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1147-1033C>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 11/15 | chr16 | 56980125 | ||||||
chr16:56980137
|
C | T | 1 | a0006c0011t0001g0058 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1147-1021C>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 11/15 | chr16 | 56980137 | ||||||
chr16:56980144
|
C | T | 1 | a0002c0002t0001g0183 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1147-1014C>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 11/15 | chr16 | 56980144 | ||||||
chr16:56980296
|
G | A | 4 | a0001c0001t0001g0031a0001c0001t0001g0245a0001c0001t0001g0267others(1): Show | 6 | HG00609.hp2 HG00621.hp1 NA18939.hp1 others(3): Show |
intron_variant | MODIFIER | c.1147-862G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 11/15 | chr16 | 56980296 | ||||||
chr16:56980337
|
T | C | 5 | a0002c0009t0001g0090a0002c0009t0001g0091a0002c0009t0001g0154others(2): Show | 5 | HG02109.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1147-821T>C | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 11/15 | chr16 | 56980337 | ||||||
chr16:56980407
|
A | G | 204 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(201): Show | 315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.1147-751A>G | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 11/15 | chr16 | 56980407 | ||||||
chr16:56980427
|
C | T | 5 | a0002c0009t0001g0090a0002c0009t0001g0091a0002c0009t0001g0154others(2): Show | 5 | HG02109.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1147-731C>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 11/15 | chr16 | 56980427 | ||||||
chr16:56980483
|
T | C | 3 | a0002c0002t0002g0015a0002c0002t0002g0130a0002c0002t0002g0149 | 6 | HG02056.hp1 HG02165.hp2 HG02523.hp1 others(3): Show |
intron_variant | MODIFIER | c.1147-675T>C | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 11/15 | chr16 | 56980483 | ||||||
chr16:56980510
|
C | T | 5 | a0002c0009t0001g0090a0002c0009t0001g0091a0002c0009t0001g0154others(2): Show | 5 | HG02109.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1147-648C>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 11/15 | chr16 | 56980510 | ||||||
chr16:56980625
|
A | T | 1 | a0002c0002t0001g0103 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1147-533A>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 11/15 | chr16 | 56980625 | ||||||
chr16:56980646
|
G | A | 1 | a0002c0002t0001g0066 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1147-512G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 11/15 | chr16 | 56980646 | ||||||
chr16:56980694
|
T | C | 5 | a0002c0009t0001g0090a0002c0009t0001g0091a0002c0009t0001g0154others(2): Show | 5 | HG02109.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1147-464T>C | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 11/15 | chr16 | 56980694 | ||||||
chr16:56980698
|
T | C | 238 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(235): Show | 364 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(361): Show |
intron_variant | MODIFIER | c.1147-460T>C | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 11/15 | chr16 | 56980698 | ||||||
chr16:56980778
|
C | T | 1 | a0002c0002t0001g0176 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1147-380C>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 11/15 | chr16 | 56980778 | ||||||
chr16:56980852
|
G | A | 1 | a0002c0002t0001g0139 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1147-306G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 11/15 | chr16 | 56980852 | ||||||
chr16:56980897
|
G | A | 3 | a0002c0006t0001g0194a0002c0006t0001g0195a0002c0006t0001g0196 | 3 | HG01891.hp1 HG03453.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1147-261G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 11/15 | chr16 | 56980897 | ||||||
chr16:56980908
|
T | C | 5 | a0002c0009t0001g0090a0002c0009t0001g0091a0002c0009t0001g0154others(2): Show | 5 | HG02109.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1147-250T>C | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 11/15 | chr16 | 56980908 | ||||||
chr16:56980932
|
A | G | 1 | a0017c0026t0001g0201 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1147-226A>G | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 11/15 | chr16 | 56980932 | ||||||
chr16:56980963
|
A | G | 88 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(85): Show | 138 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.1147-195A>G | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 11/15 | chr16 | 56980963 | ||||||
chr16:56981333
|
T | C | 5 | a0002c0009t0001g0090a0002c0009t0001g0091a0002c0009t0001g0154others(2): Show | 5 | HG02109.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1214+108T>C | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 12/15 | chr16 | 56981333 | ||||||
chr16:56981377
|
A | C | 3 | a0002c0002t0001g0081a0002c0002t0002g0281a0002c0002t0002g0282 | 3 | HG03209.hp1 HG04204.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1214+152A>C | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 12/15 | chr16 | 56981377 | ||||||
chr16:56981390
|
G | C | 2 | a0002c0014t0001g0098a0002c0014t0001g0099 | 2 | HG02717.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1214+165G>C | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 12/15 | chr16 | 56981390 | ||||||
chr16:56981423
|
GCTGCCAG others(5): Show |
G | 230 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(227): Show | 356 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(353): Show |
intron_variant | MODIFIER | c.1214+199_1214+210d others(14): Show |
CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 12/15 | chr16 | 56981423 | ||||||
chr16:56981464
|
G | A | 1 | a0002c0014t0001g0099 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1215-183G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 12/15 | chr16 | 56981464 | ||||||
chr16:56981468
|
A | G | 5 | a0002c0009t0001g0090a0002c0009t0001g0091a0002c0009t0001g0154others(2): Show | 5 | HG02109.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1215-179A>G | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 12/15 | chr16 | 56981468 | ||||||
chr16:56981507
|
G | A | 3 | a0002c0002t0001g0081a0002c0002t0002g0281a0002c0002t0002g0282 | 3 | HG03209.hp1 HG04204.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1215-140G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 12/15 | chr16 | 56981507 | ||||||
chr16:56981535
|
C | G | 5 | a0002c0009t0001g0090a0002c0009t0001g0091a0002c0009t0001g0154others(2): Show | 5 | HG02109.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1215-112C>G | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 12/15 | chr16 | 56981535 | ||||||
chr16:56981551
|
G | A | 297 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(294): Show | 448 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(445): Show |
intron_variant | MODIFIER | c.1215-96G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 12/15 | chr16 | 56981551 | ||||||
chr16:56981632
|
G | T | 5 | a0002c0009t0001g0090a0002c0009t0001g0091a0002c0009t0001g0154others(2): Show | 5 | HG02109.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1215-15G>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 12/15 | chr16 | 56981632 | ||||||
chr16:56981633
|
C | T | 61 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0016others(58): Show | 102 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.1215-14C>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 12/15 | chr16 | 56981633 | ||||||
chr16:56981796
|
A | T | 1 | a0002c0002t0001g0141 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1248+116A>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 13/15 | chr16 | 56981796 | ||||||
chr16:56981813
|
T | C | 5 | a0002c0009t0001g0090a0002c0009t0001g0091a0002c0009t0001g0154others(2): Show | 5 | HG02109.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1248+133T>C | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 13/15 | chr16 | 56981813 | ||||||
chr16:56981869
|
A | G | 1 | a0013c0022t0002g0120 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1248+189A>G | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 13/15 | chr16 | 56981869 | ||||||
chr16:56982238
|
G | A | 1 | a0001c0001t0001g0051 | 2 | NA18948.hp2 NA19081.hp2 |
splice_donor_variant&intron_variant | HIGH | c.1321+1G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 14/15 | chr16 | 56982238 | ||||||
chr16:56982366
|
C | T | 1 | a0001c0001t0001g0241 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1321+129C>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 14/15 | chr16 | 56982366 | ||||||
chr16:56982390
|
T | C | 25 | a0002c0002t0001g0003a0002c0002t0001g0014a0002c0002t0001g0033others(22): Show | 40 | HG00544.hp2 HG00558.hp1 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.1321+153T>C | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 14/15 | chr16 | 56982390 | ||||||
chr16:56982397
|
C | A | 2 | a0002c0014t0001g0098a0002c0014t0001g0099 | 2 | HG02717.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1321+160C>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 14/15 | chr16 | 56982397 | ||||||
chr16:56982479
|
C | A | 1 | a0002c0002t0001g0271 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1321+242C>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 14/15 | chr16 | 56982479 | ||||||
chr16:56982503
|
T | TTTGGTGT others(17): Show |
1 | a0001c0001t0001g0159 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1321+266_1321+267i others(26): Show |
CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 14/15 | chr16 | 56982503 | ||||||
chr16:56982533
|
C | G | 25 | a0002c0002t0001g0003a0002c0002t0001g0014a0002c0002t0001g0033others(22): Show | 40 | HG00544.hp2 HG00558.hp1 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.1321+296C>G | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 14/15 | chr16 | 56982533 | ||||||
chr16:56982573
|
C | A | 5 | a0001c0001t0001g0011a0001c0001t0001g0102a0001c0001t0001g0259others(2): Show | 9 | NA18944.hp2 NA18953.hp1 NA18966.hp2 others(6): Show |
intron_variant | MODIFIER | c.1321+336C>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 14/15 | chr16 | 56982573 | ||||||
chr16:56982607
|
T | C | 25 | a0002c0002t0001g0003a0002c0002t0001g0014a0002c0002t0001g0033others(22): Show | 40 | HG00544.hp2 HG00558.hp1 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.1321+370T>C | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 14/15 | chr16 | 56982607 | ||||||
chr16:56982610
|
T | C | 1 | a0002c0005t0001g0213 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1321+373T>C | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 14/15 | chr16 | 56982610 | ||||||
chr16:56982615
|
T | G | 5 | a0002c0009t0001g0090a0002c0009t0001g0091a0002c0009t0001g0154others(2): Show | 5 | HG02109.hp1 HG02451.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1321+378T>G | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 14/15 | chr16 | 56982615 | ||||||
chr16:56982672
|
G | T | 2 | a0001c0010t0001g0211a0001c0010t0001g0215 | 2 | NA18612.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.1321+435G>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 14/15 | chr16 | 56982672 | ||||||
chr16:56982693
|
T | C | 1 | a0001c0001t0001g0254 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1321+456T>C | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 14/15 | chr16 | 56982693 | ||||||
chr16:56982736
|
G | A | 26 | a0002c0002t0001g0003a0002c0002t0001g0014a0002c0002t0001g0033others(23): Show | 41 | HG00544.hp2 HG00558.hp1 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.1321+499G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 14/15 | chr16 | 56982736 | ||||||
chr16:56982888
|
G | A | 1 | a0002c0002t0001g0140 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1322-438G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 14/15 | chr16 | 56982888 | ||||||
chr16:56982911
|
A | T | 1 | a0001c0001t0001g0078 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1322-415A>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 14/15 | chr16 | 56982911 | ||||||
chr16:56983038
|
C | T | 302 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(299): Show | 453 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(450): Show |
intron_variant | MODIFIER | c.1322-288C>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 14/15 | chr16 | 56983038 | ||||||
chr16:56983090
|
T | G | 17 | a0002c0002t0002g0128a0002c0002t0002g0129a0002c0002t0002g0150others(14): Show | 23 | HG00099.hp2 HG00738.hp1 HG00741.hp1 others(20): Show |
intron_variant | MODIFIER | c.1322-236T>G | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 14/15 | chr16 | 56983090 | ||||||
chr16:56983178
|
G | T | 1 | a0001c0001t0001g0258 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1322-148G>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 14/15 | chr16 | 56983178 | ||||||
chr16:56983254
|
C | T | 2 | a0002c0002t0001g0067a0002c0002t0001g0243 | 2 | HG02280.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1322-72C>T | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 14/15 | chr16 | 56983254 | ||||||
chr16:56983487
|
G | A | 1 | a0002c0002t0002g0029 | 3 | NA18992.hp2 NA19005.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.1407+76G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 15/15 | chr16 | 56983487 | ||||||
chr16:56983562
|
G | A | 171 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(168): Show | 276 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(273): Show |
intron_variant | MODIFIER | c.1408-30G>A | CETP | ENSG00000087237.12 | transcript | ENST00000200676.8 | protein_coding | 15/15 | chr16 | 56983562 |