geneid | 57479 |
---|---|
ensemblid | ENSG00000126464.15 |
hgncid | 29217 |
symbol | PRR12 |
name | proline rich 12 |
refseq_nuc | NM_020719.3 |
refseq_prot | NP_065770.1 |
ensembl_nuc | ENST00000418929.7 |
ensembl_prot | ENSP00000394510.1 |
mane_status | MANE Select |
chr | chr19 |
start | 49591182 |
end | 49626439 |
strand | + |
ver | v1.2 |
region | chr19:49591182-49626439 |
region5000 | chr19:49586182-49631439 |
regionname0 | PRR12_chr19_49591182_49626439 |
regionname5000 | PRR12_chr19_49586182_49631439 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 2036 | 279 | 76 | 54 | 98 | 12 | 37 | 65 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0002 | 0/0 | 2036 | 12 | 3 | 4 | 0 | 0 | 5 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0003 | 0/0 | 935 | 7 | 1 | 3 | 3 | 0 | 0 | 3 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0004 | 0/0 | 935 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0005 | 0/0 | 2036 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0006 | 0/0 | 2036 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0007 | 0/0 | 2036 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0008 | 0/0 | 2036 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0009 | 0/0 | 2036 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0010 | 0/0 | 2036 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0011 | 0/0 | 2036 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0012 | 0/0 | 2036 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0013 | 0/0 | 2036 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0014 | 0/0 | 2036 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0015 | 0/0 | 2036 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0016 | 0/0 | 2036 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0017 | 0/0 | 2036 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0018 | 0/0 | 2036 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0019 | 0/0 | 2036 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0020 | 0/0 | 2036 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0021 | 0/0 | 2036 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0022 | 0/0 | 2036 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0023 | 0/0 | 2036 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0024 | 0/0 | 2036 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/0 | 6111 | 147 | 27 | 32 | 58 | 8 | 21 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
c0002 | 0/0 | 6111 | 57 | 23 | 10 | 24 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
c0003 | 0/1 | 6111 | 32 | 8 | 4 | 8 | 3 | 8 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
c0004 | 0/0 | 6111 | 8 | 1 | 3 | 0 | 0 | 4 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
c0005 | 0/0 | 6112 | 7 | 1 | 3 | 3 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
c0006 | 0/0 | 6111 | 4 | 3 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
c0007 | 0/0 | 6111 | 4 | 0 | 1 | 0 | 0 | 3 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
c0008 | 0/0 | 6111 | 4 | 0 | 0 | 4 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
c0009 | 0/0 | 6111 | 3 | 3 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
c0010 | 0/0 | 6111 | 2 | 0 | 2 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
c0011 | 0/0 | 6112 | 2 | 1 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
c0012 | 0/0 | 6111 | 2 | 2 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
c0013 | 0/0 | 6111 | 2 | 2 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
c0014 | 0/0 | 6111 | 2 | 0 | 1 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
c0015 | 0/0 | 6111 | 2 | 2 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
c0016 | 0/0 | 6111 | 2 | 2 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
c0017 | 0/0 | 6111 | 2 | 1 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
c0018 | 0/0 | 6111 | 2 | 0 | 1 | 0 | 1 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
c0019 | 0/0 | 6111 | 2 | 2 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
c0020 | 0/0 | 6111 | 2 | 2 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
c0021 | 0/0 | 6111 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
c0022 | 0/0 | 6111 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
c0023 | 0/0 | 6111 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
c0024 | 0/0 | 6111 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
c0025 | 0/0 | 6111 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
c0026 | 0/0 | 6111 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
c0027 | 0/0 | 6111 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
c0028 | 0/0 | 6111 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
c0029 | 0/0 | 6111 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
c0030 | 0/0 | 6111 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
c0031 | 0/0 | 6111 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
c0032 | 0/0 | 6111 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
c0033 | 0/0 | 6111 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
c0034 | 0/0 | 6111 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
c0035 | 0/0 | 6111 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
c0036 | 0/0 | 6111 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
c0037 | 0/0 | 6111 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
c0038 | 0/0 | 6111 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
c0039 | 0/0 | 6111 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
c0040 | 0/0 | 6111 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
c0041 | 0/0 | 6111 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
c0042 | 0/0 | 6111 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
c0043 | 0/0 | 6111 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
c0044 | 0/0 | 6111 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
c0045 | 0/0 | 6111 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
c0046 | 0/0 | 6111 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
c0047 | 0/0 | 6111 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
c0048 | 0/0 | 6111 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
c0049 | 0/0 | 6111 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
c0050 | 0/0 | 6111 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
c0051 | 0/0 | 6111 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
c0052 | 0/0 | 6111 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
c0053 | 0/0 | 6111 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
c0054 | 0/0 | 6111 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 1306 | 258 | 72 | 48 | 91 | 12 | 33 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
t0002 | 0/0 | 1302 | 28 | 6 | 9 | 13 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
t0003 | 0/0 | 1307 | 10 | 1 | 3 | 3 | 0 | 3 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
t0004 | 0/0 | 1303 | 7 | 0 | 1 | 0 | 0 | 6 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
t0005 | 0/0 | 1302 | 4 | 4 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
t0006 | 0/0 | 1306 | 3 | 3 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
t0007 | 0/0 | 1306 | 3 | 1 | 2 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
t0008 | 0/0 | 1306 | 3 | 3 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
t0009 | 0/0 | 1306 | 2 | 0 | 0 | 0 | 0 | 2 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
t0010 | 0/0 | 1306 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
t0011 | 0/0 | 1306 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
t0012 | 0/0 | 1280 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
t0013 | 0/0 | 1306 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0002 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0006 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0007 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0008 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0010 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0026 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0205 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0275 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0287 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0293 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0295 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 6111 | 147 | 27 | 32 | 58 | 8 | 21 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0001c0002 | 0/0 | 6111 | 57 | 23 | 10 | 24 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0001c0003 | 0/1 | 6111 | 32 | 8 | 4 | 8 | 3 | 8 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0001c0006 | 0/0 | 6111 | 4 | 3 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0001c0007 | 0/0 | 6111 | 4 | 0 | 1 | 0 | 0 | 3 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0001c0008 | 0/0 | 6111 | 4 | 0 | 0 | 4 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0001c0009 | 0/0 | 6111 | 3 | 3 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0001c0012 | 0/0 | 6111 | 2 | 2 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0001c0014 | 0/0 | 6111 | 2 | 0 | 1 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0001c0016 | 0/0 | 6111 | 2 | 2 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0001c0017 | 0/0 | 6111 | 2 | 1 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0001c0018 | 0/0 | 6111 | 2 | 0 | 1 | 0 | 1 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0001c0019 | 0/0 | 6111 | 2 | 2 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0001c0020 | 0/0 | 6111 | 2 | 2 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0001c0021 | 0/0 | 6111 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0001c0024 | 0/0 | 6111 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0001c0029 | 0/0 | 6111 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0001c0031 | 0/0 | 6111 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0001c0037 | 0/0 | 6111 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0001c0043 | 0/0 | 6111 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0001c0044 | 0/0 | 6111 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0001c0045 | 0/0 | 6111 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0001c0047 | 0/0 | 6111 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0001c0048 | 0/0 | 6111 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0001c0049 | 0/0 | 6111 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0001c0051 | 0/0 | 6111 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0001c0052 | 0/0 | 6111 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0001c0054 | 0/0 | 6111 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0002c0004 | 0/0 | 6111 | 8 | 1 | 3 | 0 | 0 | 4 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0002c0015 | 0/0 | 6111 | 2 | 2 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0002c0034 | 0/0 | 6111 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0002c0035 | 0/0 | 6111 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0003c0005 | 0/0 | 6112 | 7 | 1 | 3 | 3 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0004c0011 | 0/0 | 6112 | 2 | 1 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0005c0013 | 0/0 | 6111 | 2 | 2 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0006c0010 | 0/0 | 6111 | 2 | 0 | 2 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0007c0041 | 0/0 | 6111 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0008c0042 | 0/0 | 6111 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0009c0050 | 0/0 | 6111 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0010c0032 | 0/0 | 6111 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0011c0026 | 0/0 | 6111 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0012c0028 | 0/0 | 6111 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0013c0033 | 0/0 | 6111 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0014c0023 | 0/0 | 6111 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0015c0025 | 0/0 | 6111 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0016c0039 | 0/0 | 6111 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0017c0027 | 0/0 | 6111 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0018c0046 | 0/0 | 6111 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0019c0022 | 0/0 | 6111 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0020c0040 | 0/0 | 6111 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0021c0038 | 0/0 | 6111 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0022c0030 | 0/0 | 6111 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0023c0053 | 0/0 | 6111 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0024c0036 | 0/0 | 6111 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 7416 | 139 | 27 | 30 | 56 | 8 | 17 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0001c0001t0003 | 0/0 | 7417 | 6 | 0 | 2 | 2 | 0 | 2 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0001c0001t0009 | 0/0 | 7416 | 2 | 0 | 0 | 0 | 0 | 2 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0001c0002t0001 | 0/0 | 7416 | 26 | 15 | 2 | 9 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0001c0002t0002 | 0/0 | 7412 | 21 | 0 | 8 | 13 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0001c0002t0003 | 0/0 | 7417 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0001c0002t0005 | 0/0 | 7412 | 2 | 2 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0001c0002t0006 | 0/0 | 7416 | 3 | 3 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0001c0002t0008 | 0/0 | 7416 | 3 | 3 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0001c0002t0013 | 0/0 | 7416 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0001c0003t0001 | 0/1 | 7416 | 30 | 7 | 4 | 8 | 3 | 7 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0001c0003t0002 | 0/0 | 7412 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0001c0003t0011 | 0/0 | 7416 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0001c0006t0001 | 0/0 | 7416 | 3 | 2 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0001c0006t0003 | 0/0 | 7417 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0001c0007t0001 | 0/0 | 7416 | 4 | 0 | 1 | 0 | 0 | 3 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0001c0008t0001 | 0/0 | 7416 | 4 | 0 | 0 | 4 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0001c0009t0002 | 0/0 | 7412 | 3 | 3 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0001c0012t0001 | 0/0 | 7416 | 2 | 2 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0001c0014t0001 | 0/0 | 7416 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0001c0014t0003 | 0/0 | 7417 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0001c0016t0001 | 0/0 | 7416 | 2 | 2 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0001c0017t0001 | 0/0 | 7416 | 2 | 1 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0001c0018t0001 | 0/0 | 7416 | 2 | 0 | 1 | 0 | 1 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0001c0019t0001 | 0/0 | 7416 | 2 | 2 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0001c0020t0002 | 0/0 | 7412 | 2 | 2 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0001c0021t0001 | 0/0 | 7416 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0001c0024t0003 | 0/0 | 7417 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0001c0029t0001 | 0/0 | 7416 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0001c0031t0001 | 0/0 | 7416 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0001c0037t0001 | 0/0 | 7416 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0001c0043t0012 | 0/0 | 7390 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0001c0044t0001 | 0/0 | 7416 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0001c0045t0001 | 0/0 | 7416 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0001c0047t0010 | 0/0 | 7416 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0001c0048t0001 | 0/0 | 7416 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0001c0049t0001 | 0/0 | 7416 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0001c0051t0001 | 0/0 | 7416 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0001c0052t0001 | 0/0 | 7416 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0001c0054t0001 | 0/0 | 7416 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0002c0004t0004 | 0/0 | 7413 | 5 | 0 | 1 | 0 | 0 | 4 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0002c0004t0007 | 0/0 | 7416 | 3 | 1 | 2 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0002c0015t0001 | 0/0 | 7416 | 2 | 2 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0002c0034t0001 | 0/0 | 7416 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0002c0035t0004 | 0/0 | 7413 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0003c0005t0001 | 0/0 | 7417 | 7 | 1 | 3 | 3 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0004c0011t0001 | 0/0 | 7417 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0004c0011t0002 | 0/0 | 7413 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0005c0013t0005 | 0/0 | 7412 | 2 | 2 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0006c0010t0001 | 0/0 | 7416 | 2 | 0 | 2 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0007c0041t0001 | 0/0 | 7416 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0008c0042t0001 | 0/0 | 7416 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0009c0050t0001 | 0/0 | 7416 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0010c0032t0004 | 0/0 | 7413 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0011c0026t0001 | 0/0 | 7416 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0012c0028t0001 | 0/0 | 7416 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0013c0033t0001 | 0/0 | 7416 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0014c0023t0001 | 0/0 | 7416 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0015c0025t0001 | 0/0 | 7416 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0016c0039t0001 | 0/0 | 7416 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0017c0027t0001 | 0/0 | 7416 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0018c0046t0001 | 0/0 | 7416 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0019c0022t0001 | 0/0 | 7416 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0020c0040t0001 | 0/0 | 7416 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0021c0038t0001 | 0/0 | 7416 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0022c0030t0001 | 0/0 | 7416 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0023c0053t0001 | 0/0 | 7416 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
a0024c0036t0001 | 0/0 | 7416 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | copy fasta | chr19 | 49586182 | 49631439 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0205 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0003g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0003g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0003g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0003g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0003g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0003g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0001t0009g0010 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0002t0001g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0002t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0002t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0002t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0002t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0002t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0002t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0002t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0002t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0002t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0002t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0002t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0002t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0002t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0002t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0002t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0002t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0002t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0002t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0002t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0002t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0002t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0002t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0002t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0002t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0002t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0002t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0002t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0002t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0002t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0002t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0002t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0002t0002g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0002t0002g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0002t0002g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0002t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0002t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0002t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0002t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0002t0005g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0002t0005g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0002t0006g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0002t0006g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0002t0006g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0002t0008g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0002t0008g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0002t0008g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0002t0013g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0003t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0003t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0003t0001g0026 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0003t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0003t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0003t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0003t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0003t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0003t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0003t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0003t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0003t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0003t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0003t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0003t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0003t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0003t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0003t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0003t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0003t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0003t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0003t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0003t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0003t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0003t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0003t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0003t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0003t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0003t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0003t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0003t0002g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0003t0011g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0006t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0006t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0006t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0006t0003g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0007t0001g0008 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0007t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0007t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0008t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0008t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0008t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0008t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0009t0002g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0009t0002g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0009t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0012t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0012t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0014t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0014t0003g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0016t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0016t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0017t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0017t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0018t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0018t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0019t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0019t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0020t0002g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0020t0002g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0021t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0024t0003g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0029t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0031t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0037t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0043t0012g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0044t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0045t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0047t0010g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0048t0001g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0049t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0051t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0052t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0001c0054t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0002c0004t0004g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0002c0004t0004g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0002c0004t0004g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0002c0004t0004g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0002c0004t0004g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0002c0004t0007g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0002c0004t0007g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0002c0004t0007g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0002c0015t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0002c0015t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0002c0034t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0002c0035t0004g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0003c0005t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0003c0005t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0003c0005t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0003c0005t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0003c0005t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0003c0005t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0003c0005t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0004c0011t0001g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0004c0011t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0005c0013t0005g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0005c0013t0005g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0006c0010t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0006c0010t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0007c0041t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0008c0042t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0009c0050t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0010c0032t0004g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0011c0026t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0012c0028t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0013c0033t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0014c0023t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0015c0025t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0016c0039t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0017c0027t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0018c0046t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0019c0022t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0020c0040t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0021c0038t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0022c0030t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0023c0053t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
a0024c0036t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0231 | EUR | GBR | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0214 | EUR | GBR | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0183 | EUR | GBR | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG00140 | hp2 | a0001 | c0003 | t0001 | g0110 | EUR | GBR | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0295 | EUR | FIN | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG00280 | hp2 | a0001 | c0003 | t0001 | g0025 | EUR | FIN | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG00408 | hp1 | a0001 | c0002 | t0002 | g0070 | EAS | CHS | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG00408 | hp2 | a0001 | c0044 | t0001 | g0218 | EAS | CHS | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | CHS | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG00423 | hp2 | a0001 | c0002 | t0002 | g0076 | EAS | CHS | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG00438 | hp1 | a0001 | c0003 | t0001 | g0133 | EAS | CHS | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG00438 | hp2 | a0020 | c0040 | t0001 | g0193 | EAS | CHS | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG00544 | hp1 | a0001 | c0003 | t0001 | g0122 | EAS | CHS | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | CHS | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | CHS | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG00597 | hp2 | a0001 | c0054 | t0001 | g0227 | EAS | CHS | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | CHS | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | CHS | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0241 | AMR | PUR | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | PUR | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG00642 | hp1 | a0001 | c0003 | t0001 | g0101 | AMR | PUR | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG00642 | hp2 | a0001 | c0002 | t0002 | g0075 | AMR | PUR | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG00673 | hp1 | a0001 | c0002 | t0002 | g0082 | EAS | CHS | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | CHS | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0234 | AMR | PUR | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG00733 | hp2 | a0001 | c0002 | t0001 | g0084 | AMR | PUR | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG00735 | hp1 | a0001 | c0017 | t0001 | g0018 | AMR | PUR | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG00735 | hp2 | a0003 | c0005 | t0001 | g0271 | AMR | PUR | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0299 | AMR | PUR | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG00738 | hp2 | a0001 | c0002 | t0002 | g0071 | AMR | PUR | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG01069 | hp1 | a0001 | c0002 | t0002 | g0066 | AMR | PUR | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0277 | AMR | PUR | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG01070 | hp1 | a0002 | c0004 | t0007 | g0036 | AMR | PUR | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG01071 | hp1 | a0002 | c0004 | t0007 | g0035 | AMR | PUR | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0274 | AMR | PUR | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG01081 | hp1 | a0001 | c0018 | t0001 | g0192 | AMR | PUR | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0243 | AMR | PUR | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG01099 | hp1 | a0001 | c0014 | t0001 | g0136 | AMR | PUR | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG01099 | hp2 | a0003 | c0005 | t0001 | g0288 | AMR | PUR | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0289 | AMR | PUR | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG01106 | hp2 | a0001 | c0007 | t0001 | g0008 | AMR | PUR | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0157 | AMR | PUR | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0258 | AMR | PUR | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0250 | AMR | PUR | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG01167 | hp2 | a0001 | c0003 | t0001 | g0103 | AMR | PUR | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0223 | AMR | PUR | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG01168 | hp2 | a0006 | c0010 | t0001 | g0131 | AMR | PUR | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG01169 | hp1 | a0001 | c0003 | t0001 | g0109 | AMR | PUR | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG01169 | hp2 | a0006 | c0010 | t0001 | g0132 | AMR | PUR | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG01175 | hp1 | a0003 | c0005 | t0001 | g0232 | AMR | PUR | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG01175 | hp2 | a0002 | c0004 | t0004 | g0045 | AMR | PUR | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG01192 | hp1 | a0001 | c0001 | t0003 | g0269 | AMR | PUR | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG01192 | hp2 | a0002 | c0034 | t0001 | g0037 | AMR | PUR | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0252 | AMR | PUR | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0260 | AMR | CLM | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0170 | AMR | CLM | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0292 | AMR | CLM | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0300 | AMR | CLM | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG01261 | hp1 | a0001 | c0024 | t0003 | g0085 | AMR | CLM | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0286 | AMR | CLM | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0224 | AMR | CLM | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG01346 | hp2 | a0001 | c0006 | t0001 | g0033 | AMR | CLM | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0180 | AMR | CLM | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG01358 | hp2 | a0001 | c0047 | t0010 | g0298 | AMR | CLM | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG01433 | hp1 | a0001 | c0002 | t0001 | g0054 | AMR | CLM | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG01433 | hp2 | a0001 | c0002 | t0002 | g0080 | AMR | CLM | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0265 | AMR | CLM | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0302 | AMR | CLM | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0287 | EUR | IBS | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG01515 | hp2 | a0001 | c0018 | t0001 | g0190 | EUR | IBS | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0256 | EUR | IBS | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0275 | EUR | IBS | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG01884 | hp1 | a0001 | c0002 | t0008 | g0126 | AFR | ACB | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | ACB | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG01928 | hp1 | a0001 | c0002 | t0002 | g0079 | AMR | PEL | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0303 | AMR | PEL | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG01934 | hp1 | a0001 | c0002 | t0002 | g0049 | AMR | PEL | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG01934 | hp2 | a0001 | c0001 | t0003 | g0011 | AMR | PEL | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0247 | AMR | PEL | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG01943 | hp2 | a0001 | c0003 | t0001 | g0120 | AMR | PEL | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG01981 | hp1 | a0001 | c0002 | t0002 | g0068 | AMR | PEL | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0311 | AMR | PEL | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG01993 | hp1 | a0004 | c0011 | t0002 | g0072 | AMR | PEL | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0312 | AMR | PEL | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02004 | hp1 | a0001 | c0049 | t0001 | g0278 | AMR | PEL | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0242 | AMR | PEL | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02040 | hp1 | a0001 | c0008 | t0001 | g0235 | EAS | KHV | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02040 | hp2 | a0001 | c0002 | t0002 | g0151 | EAS | KHV | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02055 | hp1 | a0001 | c0002 | t0001 | g0052 | AFR | ACB | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | ACB | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | KHV | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | KHV | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | KHV | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | KHV | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | KHV | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | KHV | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02083 | hp1 | a0001 | c0003 | t0001 | g0135 | EAS | KHV | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | KHV | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02129 | hp2 | a0001 | c0002 | t0001 | g0028 | EAS | KHV | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02132 | hp1 | a0001 | c0003 | t0001 | g0134 | EAS | KHV | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02132 | hp2 | a0001 | c0008 | t0001 | g0007 | EAS | KHV | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02135 | hp1 | a0001 | c0002 | t0003 | g0064 | EAS | KHV | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02135 | hp2 | a0001 | c0001 | t0003 | g0014 | EAS | KHV | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02145 | hp1 | a0002 | c0015 | t0001 | g0039 | AFR | ACB | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02145 | hp2 | a0001 | c0003 | t0001 | g0099 | AFR | ACB | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | CDX | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02155 | hp2 | a0001 | c0002 | t0002 | g0051 | EAS | CDX | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | CDX | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | CDX | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | ACB | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02257 | hp2 | a0001 | c0002 | t0006 | g0094 | AFR | ACB | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | ACB | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02258 | hp2 | a0001 | c0020 | t0002 | g0147 | AFR | ACB | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02273 | hp1 | a0001 | c0002 | t0002 | g0078 | AMR | PEL | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0219 | AMR | PEL | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0204 | AFR | ACB | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | ACB | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02451 | hp1 | a0001 | c0016 | t0001 | g0156 | AFR | ACB | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02451 | hp2 | a0001 | c0002 | t0001 | g0091 | AFR | ACB | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02572 | hp1 | a0001 | c0012 | t0001 | g0128 | AFR | GWD | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | GWD | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0273 | SAS | PJL | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02602 | hp2 | a0007 | c0041 | t0001 | g0182 | SAS | PJL | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02615 | hp1 | a0001 | c0002 | t0006 | g0138 | AFR | GWD | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02615 | hp2 | a0001 | c0002 | t0001 | g0093 | AFR | GWD | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02622 | hp1 | a0001 | c0002 | t0001 | g0143 | AFR | GWD | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | GWD | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02630 | hp1 | a0001 | c0002 | t0001 | g0001 | AFR | GWD | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02630 | hp2 | a0022 | c0030 | t0001 | g0124 | AFR | GWD | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0272 | SAS | PJL | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0188 | SAS | PJL | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02698 | hp1 | a0001 | c0007 | t0001 | g0233 | SAS | PJL | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0276 | SAS | PJL | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02717 | hp1 | a0001 | c0002 | t0001 | g0142 | AFR | GWD | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02717 | hp2 | a0001 | c0002 | t0001 | g0056 | AFR | GWD | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | GWD | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02723 | hp2 | a0002 | c0015 | t0001 | g0038 | AFR | GWD | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02735 | hp1 | a0001 | c0048 | t0001 | g0007 | SAS | PJL | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02735 | hp2 | a0001 | c0001 | t0009 | g0010 | SAS | PJL | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02738 | hp1 | a0001 | c0001 | t0003 | g0270 | SAS | PJL | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02738 | hp2 | a0001 | c0007 | t0001 | g0196 | SAS | PJL | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02809 | hp1 | a0005 | c0013 | t0005 | g0089 | AFR | GWD | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02809 | hp2 | a0001 | c0002 | t0008 | g0125 | AFR | GWD | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02818 | hp1 | a0001 | c0002 | t0005 | g0087 | AFR | GWD | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02818 | hp2 | a0001 | c0006 | t0001 | g0032 | AFR | GWD | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02886 | hp2 | a0001 | c0002 | t0001 | g0092 | AFR | GWD | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02895 | hp1 | a0001 | c0019 | t0001 | g0016 | AFR | GWD | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02895 | hp2 | a0011 | c0026 | t0001 | g0083 | AFR | GWD | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02896 | hp1 | a0001 | c0003 | t0001 | g0098 | AFR | GWD | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02896 | hp2 | a0001 | c0009 | t0002 | g0144 | AFR | GWD | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02897 | hp1 | a0001 | c0009 | t0002 | g0146 | AFR | GWD | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02897 | hp2 | a0001 | c0019 | t0001 | g0017 | AFR | GWD | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02922 | hp1 | a0001 | c0002 | t0001 | g0141 | AFR | ESN | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02922 | hp2 | a0005 | c0013 | t0005 | g0090 | AFR | ESN | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02965 | hp1 | a0001 | c0002 | t0001 | g0061 | AFR | ESN | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0255 | AFR | ESN | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02970 | hp1 | a0001 | c0003 | t0001 | g0107 | AFR | ESN | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02970 | hp2 | a0001 | c0002 | t0005 | g0088 | AFR | ESN | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | ESN | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0168 | AFR | ESN | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG03017 | hp1 | a0017 | c0027 | t0001 | g0130 | SAS | PJL | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0262 | SAS | PJL | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | GWD | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG03041 | hp2 | a0001 | c0012 | t0001 | g0095 | AFR | GWD | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0261 | AFR | MSL | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG03098 | hp2 | a0001 | c0002 | t0001 | g0150 | AFR | MSL | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG03130 | hp1 | a0001 | c0002 | t0001 | g0059 | AFR | ESN | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG03130 | hp2 | a0001 | c0003 | t0002 | g0149 | AFR | ESN | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | ESN | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG03139 | hp2 | a0001 | c0003 | t0001 | g0108 | AFR | ESN | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG03195 | hp1 | a0001 | c0003 | t0001 | g0119 | AFR | ESN | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | ESN | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | MSL | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG03209 | hp2 | a0001 | c0002 | t0001 | g0060 | AFR | MSL | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG03225 | hp1 | a0001 | c0020 | t0002 | g0148 | AFR | MSL | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG03225 | hp2 | a0023 | c0053 | t0001 | g0254 | AFR | MSL | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG03239 | hp1 | a0001 | c0003 | t0001 | g0024 | SAS | PJL | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0264 | SAS | PJL | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG03453 | hp1 | a0001 | c0017 | t0001 | g0020 | AFR | MSL | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG03453 | hp2 | a0013 | c0033 | t0001 | g0029 | AFR | MSL | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG03486 | hp1 | a0001 | c0006 | t0001 | g0031 | AFR | MSL | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | MSL | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG03490 | hp1 | a0009 | c0050 | t0001 | g0294 | SAS | PJL | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0217 | SAS | PJL | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0237 | SAS | PJL | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0301 | SAS | PJL | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG03516 | hp1 | a0003 | c0005 | t0001 | g0009 | AFR | ESN | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG03516 | hp2 | a0001 | c0031 | t0001 | g0096 | AFR | ESN | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG03540 | hp1 | a0001 | c0002 | t0006 | g0139 | AFR | GWD | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | GWD | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG03654 | hp1 | a0002 | c0004 | t0004 | g0043 | SAS | PJL | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG03654 | hp2 | a0001 | c0003 | t0001 | g0118 | SAS | PJL | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG03688 | hp1 | a0001 | c0043 | t0012 | g0153 | SAS | STU | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0282 | SAS | STU | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG03704 | hp1 | a0001 | c0001 | t0009 | g0010 | SAS | PJL | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG03704 | hp2 | a0002 | c0035 | t0004 | g0042 | SAS | PJL | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG03710 | hp1 | a0002 | c0004 | t0004 | g0040 | SAS | PJL | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0206 | SAS | BEB | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG03831 | hp2 | a0010 | c0032 | t0004 | g0046 | SAS | BEB | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG03834 | hp1 | a0001 | c0052 | t0001 | g0245 | SAS | BEB | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0251 | SAS | BEB | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG03927 | hp1 | a0001 | c0037 | t0001 | g0194 | SAS | BEB | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG03927 | hp2 | a0002 | c0004 | t0004 | g0044 | SAS | BEB | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0176 | SAS | BEB | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG03942 | hp2 | a0001 | c0003 | t0001 | g0102 | SAS | BEB | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG04115 | hp1 | a0001 | c0003 | t0001 | g0116 | SAS | STU | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG04115 | hp2 | a0001 | c0007 | t0001 | g0008 | SAS | STU | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG04184 | hp1 | a0001 | c0001 | t0003 | g0207 | SAS | BEB | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG04184 | hp2 | a0001 | c0014 | t0003 | g0137 | SAS | BEB | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG04199 | hp1 | a0001 | c0003 | t0001 | g0115 | SAS | STU | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG04199 | hp2 | a0002 | c0004 | t0004 | g0041 | SAS | STU | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0297 | SAS | STU | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG04204 | hp2 | a0001 | c0003 | t0001 | g0111 | SAS | STU | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG04228 | hp1 | a0001 | c0003 | t0001 | g0113 | SAS | STU | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0281 | SAS | STU | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA18906 | hp1 | a0004 | c0011 | t0001 | g0001 | AFR | YRI | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA18906 | hp2 | a0001 | c0003 | t0001 | g0106 | AFR | YRI | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA18942 | hp1 | a0001 | c0002 | t0001 | g0057 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA18948 | hp1 | a0001 | c0003 | t0001 | g0100 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA18948 | hp2 | a0008 | c0042 | t0001 | g0238 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA18951 | hp2 | a0021 | c0038 | t0001 | g0285 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA18954 | hp1 | a0001 | c0002 | t0002 | g0067 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA18957 | hp1 | a0001 | c0003 | t0001 | g0123 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA18959 | hp2 | a0001 | c0051 | t0001 | g0015 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA18967 | hp1 | a0001 | c0003 | t0001 | g0117 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA18967 | hp2 | a0001 | c0008 | t0001 | g0210 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA18970 | hp2 | a0001 | c0002 | t0002 | g0074 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA18971 | hp1 | a0001 | c0002 | t0001 | g0055 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA18977 | hp1 | a0016 | c0039 | t0001 | g0179 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA18979 | hp1 | a0003 | c0005 | t0001 | g0279 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA18980 | hp2 | a0001 | c0002 | t0002 | g0077 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA18981 | hp1 | a0001 | c0002 | t0001 | g0062 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA18982 | hp2 | a0003 | c0005 | t0001 | g0284 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA18986 | hp1 | a0001 | c0002 | t0001 | g0154 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA18986 | hp2 | a0001 | c0008 | t0001 | g0177 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA18990 | hp2 | a0001 | c0002 | t0002 | g0069 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA18992 | hp1 | a0001 | c0029 | t0001 | g0097 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA18992 | hp2 | a0001 | c0002 | t0002 | g0065 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA18995 | hp1 | a0001 | c0002 | t0002 | g0081 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA18998 | hp1 | a0001 | c0001 | t0003 | g0307 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA18998 | hp2 | a0001 | c0002 | t0013 | g0063 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA19004 | hp2 | a0001 | c0003 | t0001 | g0105 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA19006 | hp2 | a0001 | c0002 | t0001 | g0058 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA19010 | hp1 | a0001 | c0002 | t0001 | g0053 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA19010 | hp2 | a0001 | c0002 | t0002 | g0073 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | LWK | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA19030 | hp2 | a0001 | c0021 | t0001 | g0050 | AFR | LWK | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA19043 | hp1 | a0002 | c0004 | t0007 | g0034 | AFR | LWK | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA19043 | hp2 | a0001 | c0002 | t0001 | g0140 | AFR | LWK | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA19065 | hp1 | a0003 | c0005 | t0001 | g0216 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA19065 | hp2 | a0012 | c0028 | t0001 | g0112 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA19077 | hp1 | a0001 | c0002 | t0001 | g0152 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA19080 | hp1 | a0001 | c0002 | t0001 | g0047 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA19088 | hp2 | a0018 | c0046 | t0001 | g0259 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA19089 | hp1 | a0024 | c0036 | t0001 | g0197 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA19089 | hp2 | a0001 | c0002 | t0002 | g0048 | EAS | JPT | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA19240 | hp1 | a0001 | c0016 | t0001 | g0155 | AFR | YRI | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0253 | AFR | YRI | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA20129 | hp1 | a0001 | c0009 | t0002 | g0145 | AFR | ASW | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA20129 | hp2 | a0001 | c0003 | t0001 | g0104 | AFR | ASW | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0293 | EUR | TSI | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA20752 | hp2 | a0001 | c0003 | t0001 | g0114 | EUR | TSI | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA20905 | hp1 | a0001 | c0003 | t0011 | g0121 | SAS | GIH | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0246 | SAS | GIH | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02109 | hp1 | a0001 | c0002 | t0008 | g0127 | AFR | ACB | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02109 | hp2 | a0015 | c0025 | t0001 | g0027 | AFR | ACB | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02486 | hp1 | a0001 | c0006 | t0003 | g0030 | AFR | ACB | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02486 | hp2 | a0014 | c0023 | t0001 | g0086 | AFR | ACB | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | ACB | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG02559 | hp2 | a0001 | c0045 | t0001 | g0211 | AFR | ACB | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG03471 | hp1 | a0001 | c0002 | t0001 | g0129 | AFR | MSL | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | MSL | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | USA | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0291 | AFR | USA | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA20300 | hp1 | a0019 | c0022 | t0001 | g0023 | AFR | USA | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0290 | AFR | USA | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
homoSapiens_chm13v2 | hp1 | a0001 | c0003 | t0001 | g0026 | REF | REF | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0205 | REF | REF | PRR12_chr19_49586182_49631439 | PRR12 | chr19 | 49586182 | 49631439 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:49594570
|
G | A | 1 | a0024 | 1 | NA19089.hp1 | missense_variant | MODERATE | c.316G>A | p.Ala106Thr | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 3/14 | 789/7416 | 316/6111 | 106/2036 | chr19 | 49594570 | ||
chr19:49595011
|
C | A | 1 | a0006 | 2 | HG01168.hp2 HG01169.hp2 |
missense_variant | MODERATE | c.676C>A | p.Pro226Thr | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 4/14 | 1149/7416 | 676/6111 | 226/2036 | chr19 | 49595011 | ||
chr19:49595011
|
C | T | 1 | a0023 | 1 | HG03225.hp2 | missense_variant | MODERATE | c.676C>T | p.Pro226Ser | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 4/14 | 1149/7416 | 676/6111 | 226/2036 | chr19 | 49595011 | ||
chr19:49596308
|
C | T | 1 | a0022 | 1 | HG02630.hp2 | missense_variant | MODERATE | c.1973C>T | p.Ala658Val | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 4/14 | 2446/7416 | 1973/6111 | 658/2036 | chr19 | 49596308 | ||
chr19:49596376
|
G | A | 1 | a0021 | 1 | NA18951.hp2 | missense_variant | MODERATE | c.2041G>A | p.Gly681Arg | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 4/14 | 2514/7416 | 2041/6111 | 681/2036 | chr19 | 49596376 | ||
chr19:49596781
|
G | A | 1 | a0020 | 1 | HG00438.hp2 | missense_variant | MODERATE | c.2446G>A | p.Ala816Thr | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 4/14 | 2919/7416 | 2446/6111 | 816/2036 | chr19 | 49596781 | ||
chr19:49596852
|
A | AC | 2 | a0003a0004 | 9 | HG00735.hp2 HG01099.hp2 HG01175.hp1 others(6): Show |
frameshift_variant | HIGH | c.2522dupC | p.Pro842fs | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 4/14 | 2996/7416 | 2523/6111 | 841/2036 | INFO_REALIGN_3_PRIME | chr19 | 49596852 | |
chr19:49596935
|
G | A | 1 | a0007 | 1 | HG02602.hp2 | missense_variant | MODERATE | c.2600G>A | p.Arg867His | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 4/14 | 3073/7416 | 2600/6111 | 867/2036 | chr19 | 49596935 | ||
chr19:49597016
|
C | A | 1 | a0008 | 1 | NA18948.hp2 | missense_variant | MODERATE | c.2681C>A | p.Pro894His | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 4/14 | 3154/7416 | 2681/6111 | 894/2036 | chr19 | 49597016 | ||
chr19:49597168
|
A | G | 1 | a0009 | 1 | HG03490.hp1 | missense_variant | MODERATE | c.2833A>G | p.Ser945Gly | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 4/14 | 3306/7416 | 2833/6111 | 945/2036 | chr19 | 49597168 | ||
chr19:49597261
|
G | C | 1 | a0019 | 1 | NA20300.hp1 | missense_variant | MODERATE | c.2926G>C | p.Ala976Pro | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 4/14 | 3399/7416 | 2926/6111 | 976/2036 | chr19 | 49597261 | ||
chr19:49597283
|
G | C | 1 | a0010 | 1 | HG03831.hp2 | missense_variant | MODERATE | c.2948G>C | p.Gly983Ala | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 4/14 | 3421/7416 | 2948/6111 | 983/2036 | chr19 | 49597283 | ||
chr19:49597327
|
G | T | 1 | a0005 | 2 | HG02809.hp1 HG02922.hp2 |
missense_variant | MODERATE | c.2992G>T | p.Ala998Ser | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 4/14 | 3465/7416 | 2992/6111 | 998/2036 | chr19 | 49597327 | ||
chr19:49597510
|
C | T | 1 | a0011 | 1 | HG02895.hp2 | missense_variant | MODERATE | c.3175C>T | p.Leu1059Phe | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 4/14 | 3648/7416 | 3175/6111 | 1059/2036 | chr19 | 49597510 | ||
chr19:49597880
|
C | T | 1 | a0012 | 1 | NA19065.hp2 | missense_variant | MODERATE | c.3545C>T | p.Pro1182Leu | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 4/14 | 4018/7416 | 3545/6111 | 1182/2036 | chr19 | 49597880 | ||
chr19:49599351
|
G | T | 1 | a0019 | 1 | NA20300.hp1 | missense_variant | MODERATE | c.3758G>T | p.Ser1253Ile | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 5/14 | 4231/7416 | 3758/6111 | 1253/2036 | chr19 | 49599351 | ||
chr19:49599594
|
A | G | 1 | a0018 | 1 | NA19088.hp2 | missense_variant | MODERATE | c.4001A>G | p.His1334Arg | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 5/14 | 4474/7416 | 4001/6111 | 1334/2036 | chr19 | 49599594 | ||
chr19:49599927
|
A | G | 1 | a0017 | 1 | HG03017.hp1 | missense_variant | MODERATE | c.4334A>G | p.Asn1445Ser | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 5/14 | 4807/7416 | 4334/6111 | 1445/2036 | chr19 | 49599927 | ||
chr19:49601554
|
A | C | 1 | a0013 | 1 | HG03453.hp2 | missense_variant | MODERATE | c.4409A>C | p.Gln1470Pro | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/14 | 4882/7416 | 4409/6111 | 1470/2036 | chr19 | 49601554 | ||
chr19:49601568
|
C | A | 1 | a0006 | 2 | HG01168.hp2 HG01169.hp2 |
missense_variant | MODERATE | c.4423C>A | p.Pro1475Thr | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/14 | 4896/7416 | 4423/6111 | 1475/2036 | chr19 | 49601568 | ||
chr19:49601590
|
T | C | 1 | a0016 | 1 | NA18977.hp1 | missense_variant | MODERATE | c.4445T>C | p.Leu1482Pro | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/14 | 4918/7416 | 4445/6111 | 1482/2036 | chr19 | 49601590 | ||
chr19:49601611
|
T | C | 1 | a0014 | 1 | HG02486.hp2 | missense_variant | MODERATE | c.4466T>C | p.Val1489Ala | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/14 | 4939/7416 | 4466/6111 | 1489/2036 | chr19 | 49601611 | ||
chr19:49601620
|
C | T | 1 | a0015 | 1 | HG02109.hp2 | missense_variant | MODERATE | c.4475C>T | p.Thr1492Met | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/14 | 4948/7416 | 4475/6111 | 1492/2036 | chr19 | 49601620 | ||
chr19:49601683
|
C | A | 1 | a0016 | 1 | NA18977.hp1 | missense_variant | MODERATE | c.4538C>A | p.Pro1513Gln | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/14 | 5011/7416 | 4538/6111 | 1513/2036 | chr19 | 49601683 | ||
chr19:49601691
|
C | A | 2 | a0002a0010 | 13 | HG01070.hp1 HG01071.hp1 HG01175.hp2 others(10): Show |
missense_variant | MODERATE | c.4546C>A | p.Pro1516Thr | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/14 | 5019/7416 | 4546/6111 | 1516/2036 | chr19 | 49601691 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:49594527
|
T | C | 25 | a0001c0002a0001c0003a0001c0006others(22): Show | 128 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(125): Show |
synonymous_variant | LOW | c.273T>C | p.Leu91Leu | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 3/14 | 746/7416 | 273/6111 | 91/2036 | chr19 | 49594527 | ||
chr19:49594554
|
C | T | 1 | a0001c0054 | 1 | HG00597.hp2 | synonymous_variant | LOW | c.300C>T | p.Pro100Pro | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 3/14 | 773/7416 | 300/6111 | 100/2036 | chr19 | 49594554 | ||
chr19:49594569
|
C | T | 1 | a0002c0035 | 1 | HG03704.hp2 | synonymous_variant | LOW | c.315C>T | p.Ser105Ser | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 3/14 | 788/7416 | 315/6111 | 105/2036 | chr19 | 49594569 | ||
chr19:49594815
|
C | T | 1 | a0001c0008 | 4 | HG02040.hp1 HG02132.hp2 NA18967.hp2 others(1): Show |
synonymous_variant | LOW | c.480C>T | p.Arg160Arg | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 4/14 | 953/7416 | 480/6111 | 160/2036 | chr19 | 49594815 | ||
chr19:49595091
|
C | T | 1 | a0001c0052 | 1 | HG03834.hp1 | synonymous_variant | LOW | c.756C>T | p.Ser252Ser | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 4/14 | 1229/7416 | 756/6111 | 252/2036 | chr19 | 49595091 | ||
chr19:49595112
|
G | A | 1 | a0001c0037 | 1 | HG03927.hp1 | synonymous_variant | LOW | c.777G>A | p.Glu259Glu | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 4/14 | 1250/7416 | 777/6111 | 259/2036 | chr19 | 49595112 | ||
chr19:49595166
|
G | A | 17 | a0001c0002a0001c0003a0001c0012others(14): Show | 108 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(105): Show |
synonymous_variant | LOW | c.831G>A | p.Pro277Pro | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 4/14 | 1304/7416 | 831/6111 | 277/2036 | chr19 | 49595166 | ||
chr19:49595335
|
C | T | 2 | a0001c0009a0001c0020 | 5 | HG02258.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
synonymous_variant | LOW | c.1000C>T | p.Leu334Leu | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 4/14 | 1473/7416 | 1000/6111 | 334/2036 | chr19 | 49595335 | ||
chr19:49596000
|
C | T | 1 | a0001c0031 | 1 | HG03516.hp2 | synonymous_variant | LOW | c.1665C>T | p.Gly555Gly | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 4/14 | 2138/7416 | 1665/6111 | 555/2036 | chr19 | 49596000 | ||
chr19:49596075
|
C | T | 1 | a0001c0051 | 1 | NA18959.hp2 | synonymous_variant | LOW | c.1740C>T | p.Val580Val | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 4/14 | 2213/7416 | 1740/6111 | 580/2036 | chr19 | 49596075 | ||
chr19:49596102
|
C | T | 1 | a0002c0034 | 1 | HG01192.hp2 | synonymous_variant | LOW | c.1767C>T | p.Tyr589Tyr | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 4/14 | 2240/7416 | 1767/6111 | 589/2036 | chr19 | 49596102 | ||
chr19:49596144
|
G | A | 1 | a0001c0016 | 2 | HG02451.hp1 NA19240.hp1 |
synonymous_variant | LOW | c.1809G>A | p.Pro603Pro | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 4/14 | 2282/7416 | 1809/6111 | 603/2036 | chr19 | 49596144 | ||
chr19:49596165
|
C | T | 8 | a0001c0003a0001c0019a0001c0029others(5): Show | 41 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(38): Show |
synonymous_variant | LOW | c.1830C>T | p.Ala610Ala | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 4/14 | 2303/7416 | 1830/6111 | 610/2036 | chr19 | 49596165 | ||
chr19:49596234
|
G | A | 1 | a0001c0021 | 1 | NA19030.hp2 | synonymous_variant | LOW | c.1899G>A | p.Ala633Ala | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 4/14 | 2372/7416 | 1899/6111 | 633/2036 | chr19 | 49596234 | ||
chr19:49596312
|
C | T | 1 | a0001c0018 | 2 | HG01081.hp1 HG01515.hp2 |
synonymous_variant | LOW | c.1977C>T | p.Asp659Asp | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 4/14 | 2450/7416 | 1977/6111 | 659/2036 | chr19 | 49596312 | ||
chr19:49596399
|
C | T | 1 | a0001c0029 | 1 | NA18992.hp1 | synonymous_variant | LOW | c.2064C>T | p.Tyr688Tyr | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 4/14 | 2537/7416 | 2064/6111 | 688/2036 | chr19 | 49596399 | ||
chr19:49596447
|
C | T | 1 | a0011c0026 | 1 | HG02895.hp2 | synonymous_variant | LOW | c.2112C>T | p.Ile704Ile | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 4/14 | 2585/7416 | 2112/6111 | 704/2036 | chr19 | 49596447 | ||
chr19:49596540
|
T | G | 1 | a0016c0039 | 1 | NA18977.hp1 | synonymous_variant | LOW | c.2205T>G | p.Gly735Gly | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 4/14 | 2678/7416 | 2205/6111 | 735/2036 | chr19 | 49596540 | ||
chr19:49597038
|
A | G | 27 | a0001c0002a0001c0003a0001c0006others(24): Show | 133 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(130): Show |
synonymous_variant | LOW | c.2703A>G | p.Pro901Pro | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 4/14 | 3176/7416 | 2703/6111 | 901/2036 | chr19 | 49597038 | ||
chr19:49597147
|
T | C | 2 | a0001c0009a0001c0020 | 5 | HG02258.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
synonymous_variant | LOW | c.2812T>C | p.Leu938Leu | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 4/14 | 3285/7416 | 2812/6111 | 938/2036 | chr19 | 49597147 | ||
chr19:49597215
|
C | T | 1 | a0001c0049 | 1 | HG02004.hp1 | synonymous_variant | LOW | c.2880C>T | p.Asp960Asp | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 4/14 | 3353/7416 | 2880/6111 | 960/2036 | chr19 | 49597215 | ||
chr19:49597227
|
G | A | 7 | a0001c0006a0002c0004a0002c0015others(4): Show | 18 | HG01070.hp1 HG01071.hp1 HG01175.hp2 others(15): Show |
synonymous_variant | LOW | c.2892G>A | p.Lys964Lys | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 4/14 | 3365/7416 | 2892/6111 | 964/2036 | chr19 | 49597227 | ||
chr19:49597407
|
C | T | 1 | a0001c0009 | 3 | HG02896.hp2 HG02897.hp1 NA20129.hp1 |
synonymous_variant | LOW | c.3072C>T | p.Ala1024Ala | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 4/14 | 3545/7416 | 3072/6111 | 1024/2036 | chr19 | 49597407 | ||
chr19:49597419
|
C | T | 1 | a0001c0048 | 1 | HG02735.hp1 | synonymous_variant | LOW | c.3084C>T | p.Gly1028Gly | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 4/14 | 3557/7416 | 3084/6111 | 1028/2036 | chr19 | 49597419 | ||
chr19:49597563
|
C | T | 1 | a0001c0047 | 1 | HG01358.hp2 | synonymous_variant | LOW | c.3228C>T | p.Ser1076Ser | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 4/14 | 3701/7416 | 3228/6111 | 1076/2036 | chr19 | 49597563 | ||
chr19:49597617
|
G | A | 2 | a0001c0007a0007c0041 | 5 | HG01106.hp2 HG02602.hp2 HG02698.hp1 others(2): Show |
synonymous_variant | LOW | c.3282G>A | p.Leu1094Leu | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 4/14 | 3755/7416 | 3282/6111 | 1094/2036 | chr19 | 49597617 | ||
chr19:49597635
|
G | A | 1 | a0001c0017 | 2 | HG00735.hp1 HG03453.hp1 |
synonymous_variant | LOW | c.3300G>A | p.Glu1100Glu | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 4/14 | 3773/7416 | 3300/6111 | 1100/2036 | chr19 | 49597635 | ||
chr19:49599394
|
T | C | 3 | a0001c0009a0001c0016a0001c0020 | 7 | HG02258.hp2 HG02451.hp1 HG02896.hp2 others(4): Show |
synonymous_variant | LOW | c.3801T>C | p.Ile1267Ile | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 5/14 | 4274/7416 | 3801/6111 | 1267/2036 | chr19 | 49599394 | ||
chr19:49599418
|
G | A | 1 | a0001c0016 | 2 | HG02451.hp1 NA19240.hp1 |
synonymous_variant | LOW | c.3825G>A | p.Pro1275Pro | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 5/14 | 4298/7416 | 3825/6111 | 1275/2036 | chr19 | 49599418 | ||
chr19:49599847
|
C | A | 1 | a0001c0016 | 2 | HG02451.hp1 NA19240.hp1 |
synonymous_variant | LOW | c.4254C>A | p.Thr1418Thr | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 5/14 | 4727/7416 | 4254/6111 | 1418/2036 | chr19 | 49599847 | ||
chr19:49601678
|
G | A | 3 | a0001c0009a0001c0016a0001c0020 | 7 | HG02258.hp2 HG02451.hp1 HG02896.hp2 others(4): Show |
synonymous_variant | LOW | c.4533G>A | p.Ser1511Ser | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/14 | 5006/7416 | 4533/6111 | 1511/2036 | chr19 | 49601678 | ||
chr19:49601684
|
A | C | 1 | a0016c0039 | 1 | NA18977.hp1 | synonymous_variant | LOW | c.4539A>C | p.Pro1513Pro | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/14 | 5012/7416 | 4539/6111 | 1513/2036 | chr19 | 49601684 | ||
chr19:49601747
|
T | C | 3 | a0001c0009a0001c0016a0001c0020 | 7 | HG02258.hp2 HG02451.hp1 HG02896.hp2 others(4): Show |
synonymous_variant | LOW | c.4602T>C | p.Ser1534Ser | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/14 | 5075/7416 | 4602/6111 | 1534/2036 | chr19 | 49601747 | ||
chr19:49601807
|
G | A | 1 | a0001c0043 | 1 | HG03688.hp1 | synonymous_variant | LOW | c.4662G>A | p.Thr1554Thr | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/14 | 5135/7416 | 4662/6111 | 1554/2036 | chr19 | 49601807 | ||
chr19:49615870
|
G | A | 1 | a0001c0020 | 2 | HG02258.hp2 HG03225.hp1 |
synonymous_variant | LOW | c.5148G>A | p.Glu1716Glu | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/14 | 5621/7416 | 5148/6111 | 1716/2036 | chr19 | 49615870 | ||
chr19:49615966
|
A | G | 2 | a0001c0009a0001c0020 | 5 | HG02258.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
synonymous_variant | LOW | c.5244A>G | p.Thr1748Thr | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/14 | 5717/7416 | 5244/6111 | 1748/2036 | chr19 | 49615966 | ||
chr19:49616047
|
A | G | 2 | a0001c0009a0001c0020 | 5 | HG02258.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
synonymous_variant | LOW | c.5325A>G | p.Gln1775Gln | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/14 | 5798/7416 | 5325/6111 | 1775/2036 | chr19 | 49616047 | ||
chr19:49616104
|
C | T | 1 | a0001c0045 | 1 | HG02559.hp2 | synonymous_variant | LOW | c.5382C>T | p.Pro1794Pro | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/14 | 5855/7416 | 5382/6111 | 1794/2036 | chr19 | 49616104 | ||
chr19:49616212
|
C | T | 1 | a0001c0024 | 1 | HG01261.hp1 | synonymous_variant | LOW | c.5490C>T | p.Ser1830Ser | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/14 | 5963/7416 | 5490/6111 | 1830/2036 | chr19 | 49616212 | ||
chr19:49621541
|
C | T | 5 | a0001c0009a0001c0020a0002c0004others(2): Show | 15 | HG01070.hp1 HG01071.hp1 HG01175.hp2 others(12): Show |
synonymous_variant | LOW | c.5640C>T | p.Pro1880Pro | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/14 | 6113/7416 | 5640/6111 | 1880/2036 | chr19 | 49621541 | ||
chr19:49621599
|
C | T | 1 | a0001c0044 | 1 | HG00408.hp2 | synonymous_variant | LOW | c.5698C>T | p.Leu1900Leu | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/14 | 6171/7416 | 5698/6111 | 1900/2036 | chr19 | 49621599 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:49591240
|
AGGC | A | 3 | a0002c0004t0004a0002c0035t0004a0010c0032t0004 | 7 | HG01175.hp2 HG03654.hp1 HG03704.hp2 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-398_-396delGCG | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 1/14 | 396 | INFO_REALIGN_3_PRIME | chr19 | 49591240 | ||||
chr19:49591326
|
G | GC | 5 | a0001c0001t0003a0001c0002t0003a0001c0006t0003others(2): Show | 10 | HG01192.hp1 HG01261.hp1 HG01934.hp2 others(7): Show |
5_prime_UTR_variant | MODIFIER | c.-322dupC | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 1/14 | 321 | INFO_REALIGN_3_PRIME | chr19 | 49591326 | ||||
chr19:49591328
|
C | T | 1 | a0001c0002t0013 | 1 | NA18998.hp2 | 5_prime_UTR_variant | MODIFIER | c.-327C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 1/14 | 327 | chr19 | 49591328 | |||||
chr19:49591527
|
AAAAG | A | 2 | a0001c0002t0005a0005c0013t0005 | 4 | HG02809.hp1 HG02818.hp1 HG02922.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-126_-123delAAGA | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 1/14 | 123 | INFO_REALIGN_3_PRIME | chr19 | 49591527 | ||||
chr19:49591540
|
A | C | 1 | a0001c0002t0008 | 3 | HG01884.hp1 HG02109.hp1 HG02809.hp2 |
5_prime_UTR_variant | MODIFIER | c.-115A>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 1/14 | 115 | chr19 | 49591540 | |||||
chr19:49591601
|
CCCCT | C | 5 | a0001c0002t0002a0001c0003t0002a0001c0009t0002others(2): Show | 28 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(25): Show |
5_prime_UTR_variant | MODIFIER | c.-34_-31delTCCC | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 1/14 | 31 | INFO_REALIGN_3_PRIME | chr19 | 49591601 | ||||
chr19:49625648
|
C | T | 4 | a0002c0004t0004a0002c0004t0007a0002c0035t0004others(1): Show | 10 | HG01070.hp1 HG01071.hp1 HG01175.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*41C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 14/14 | 41 | chr19 | 49625648 | |||||
chr19:49625766
|
C | T | 1 | a0001c0002t0006 | 3 | HG02257.hp2 HG02615.hp1 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*159C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 14/14 | 159 | chr19 | 49625766 | |||||
chr19:49625895
|
ACCCCCCC others(19): Show |
A | 1 | a0001c0043t0012 | 1 | HG03688.hp1 | 3_prime_UTR_variant | MODIFIER | c.*294_*319delCCTCCA others(20): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 14/14 | 294 | INFO_REALIGN_3_PRIME | chr19 | 49625895 | ||||
chr19:49626013
|
C | G | 1 | a0001c0003t0011 | 1 | NA20905.hp1 | 3_prime_UTR_variant | MODIFIER | c.*406C>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 14/14 | 406 | chr19 | 49626013 | |||||
chr19:49626317
|
C | T | 1 | a0001c0001t0009 | 2 | HG02735.hp2 HG03704.hp1 |
3_prime_UTR_variant | MODIFIER | c.*710C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 14/14 | 710 | chr19 | 49626317 | |||||
chr19:49626426
|
C | T | 1 | a0001c0047t0010 | 1 | HG01358.hp2 | 3_prime_UTR_variant | MODIFIER | c.*819C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 14/14 | 819 | chr19 | 49626426 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:49591754
|
G | A | 1 | a0001c0001t0003g0011 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.86+14G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 1/13 | chr19 | 49591754 | ||||||
chr19:49591790
|
AGCCGG | A | 132 | a0001c0002t0001g0001a0001c0002t0001g0028a0001c0002t0001g0047others(129): Show | 132 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.86+74_86+78delGGGC others(1): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 49591790 | |||||
chr19:49591790
|
AGCCGGGC others(3): Show |
A | 7 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0022others(4): Show | 7 | HG00735.hp1 HG02258.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.86+69_86+78delGGGC others(6): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 49591790 | |||||
chr19:49591794
|
G | A | 4 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0003g0014others(1): Show | 4 | HG02135.hp2 NA18959.hp2 NA18995.hp2 others(1): Show |
intron_variant | MODIFIER | c.86+54G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 1/13 | chr19 | 49591794 | ||||||
chr19:49592062
|
C | T | 1 | a0001c0001t0001g0312 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.86+322C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 1/13 | chr19 | 49592062 | ||||||
chr19:49592113
|
G | T | 9 | a0001c0001t0001g0303a0001c0001t0001g0304a0001c0001t0001g0305others(6): Show | 9 | HG01928.hp2 HG01981.hp2 NA18969.hp1 others(6): Show |
intron_variant | MODIFIER | c.86+373G>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 1/13 | chr19 | 49592113 | ||||||
chr19:49592270
|
T | TTG | 17 | a0001c0001t0001g0287a0001c0001t0001g0289a0001c0001t0001g0290others(14): Show | 18 | HG00280.hp1 HG00738.hp1 HG01099.hp2 others(15): Show |
intron_variant | MODIFIER | c.86+540_86+541dupGT | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr19 | 49592270 | |||||
chr19:49592319
|
A | G | 1 | a0001c0001t0001g0302 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.86+579A>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 1/13 | chr19 | 49592319 | ||||||
chr19:49592406
|
C | T | 1 | a0001c0002t0001g0152 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.86+666C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 1/13 | chr19 | 49592406 | ||||||
chr19:49592454
|
T | C | 1 | a0019c0022t0001g0023 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.86+714T>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 1/13 | chr19 | 49592454 | ||||||
chr19:49592569
|
C | A | 1 | a0001c0043t0012g0153 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.87-758C>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 1/13 | chr19 | 49592569 | ||||||
chr19:49592704
|
T | C | 154 | a0001c0001t0001g0002a0001c0001t0001g0157a0001c0001t0001g0158others(151): Show | 155 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(152): Show |
intron_variant | MODIFIER | c.87-623T>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 1/13 | chr19 | 49592704 | ||||||
chr19:49592727
|
A | G | 1 | a0001c0002t0001g0150 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.87-600A>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 1/13 | chr19 | 49592727 | ||||||
chr19:49592858
|
C | A | 1 | a0001c0001t0001g0176 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.87-469C>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 1/13 | chr19 | 49592858 | ||||||
chr19:49592887
|
T | C | 126 | a0001c0002t0001g0001a0001c0002t0001g0028a0001c0002t0001g0047others(123): Show | 126 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(123): Show |
intron_variant | MODIFIER | c.87-440T>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 1/13 | chr19 | 49592887 | ||||||
chr19:49592970
|
G | C | 1 | a0001c0008t0001g0177 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.87-357G>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 1/13 | chr19 | 49592970 | ||||||
chr19:49592971
|
C | T | 1 | a0001c0008t0001g0177 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.87-356C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 1/13 | chr19 | 49592971 | ||||||
chr19:49592972
|
T | G | 1 | a0001c0008t0001g0177 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.87-355T>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 1/13 | chr19 | 49592972 | ||||||
chr19:49593036
|
C | T | 3 | a0001c0002t0001g0141a0001c0002t0001g0142a0001c0002t0001g0143 | 3 | HG02622.hp1 HG02717.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.87-291C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 1/13 | chr19 | 49593036 | ||||||
chr19:49593164
|
C | G | 126 | a0001c0002t0001g0001a0001c0002t0001g0028a0001c0002t0001g0047others(123): Show | 126 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(123): Show |
intron_variant | MODIFIER | c.87-163C>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 1/13 | chr19 | 49593164 | ||||||
chr19:49593602
|
G | C | 135 | a0001c0002t0001g0001a0001c0002t0001g0028a0001c0002t0001g0047others(132): Show | 135 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.199+163G>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 2/13 | chr19 | 49593602 | ||||||
chr19:49593840
|
C | T | 1 | a0001c0001t0001g0286 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.199+401C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 2/13 | chr19 | 49593840 | ||||||
chr19:49594170
|
G | A | 3 | a0001c0003t0001g0024a0001c0003t0001g0025a0001c0003t0001g0026 | 3 | HG00280.hp2 HG03239.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.200-284G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 2/13 | chr19 | 49594170 | ||||||
chr19:49594268
|
T | C | 1 | a0015c0025t0001g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.200-186T>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 2/13 | chr19 | 49594268 | ||||||
chr19:49594290
|
A | G | 129 | a0001c0001t0001g0311a0001c0002t0001g0001a0001c0002t0001g0028others(126): Show | 129 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(126): Show |
intron_variant | MODIFIER | c.200-164A>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 2/13 | chr19 | 49594290 | ||||||
chr19:49594340
|
C | T | 1 | a0001c0002t0001g0140 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.200-114C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 2/13 | chr19 | 49594340 | ||||||
chr19:49594350
|
C | T | 63 | a0001c0002t0001g0001a0001c0002t0001g0084a0001c0002t0001g0091others(60): Show | 63 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(60): Show |
intron_variant | MODIFIER | c.200-104C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 2/13 | chr19 | 49594350 | ||||||
chr19:49594648
|
T | G | 1 | a0001c0002t0001g0028 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.361+33T>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 3/13 | chr19 | 49594648 | ||||||
chr19:49594675
|
G | C | 134 | a0001c0002t0001g0001a0001c0002t0001g0028a0001c0002t0001g0047others(131): Show | 134 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(131): Show |
intron_variant | MODIFIER | c.362-22G>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 3/13 | chr19 | 49594675 | ||||||
chr19:49598031
|
C | T | 7 | a0001c0009t0002g0144a0001c0009t0002g0145a0001c0009t0002g0146others(4): Show | 7 | HG02258.hp2 HG02451.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.3678+18C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 4/13 | chr19 | 49598031 | ||||||
chr19:49598075
|
CT | C | 25 | a0001c0001t0001g0178a0001c0006t0001g0031a0001c0006t0001g0032others(22): Show | 25 | HG01070.hp1 HG01071.hp1 HG01175.hp2 others(22): Show |
intron_variant | MODIFIER | c.3678+78delT | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr19 | 49598075 | |||||
chr19:49598096
|
C | CA | 18 | a0001c0006t0001g0031a0001c0006t0001g0032a0001c0006t0001g0033others(15): Show | 18 | HG01070.hp1 HG01071.hp1 HG01175.hp2 others(15): Show |
intron_variant | MODIFIER | c.3678+84dupA | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr19 | 49598096 | |||||
chr19:49598113
|
G | T | 7 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(4): Show | 7 | HG01070.hp2 HG01255.hp2 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.3678+100G>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 4/13 | chr19 | 49598113 | ||||||
chr19:49598114
|
T | C | 1 | a0013c0033t0001g0029 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3678+101T>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 4/13 | chr19 | 49598114 | ||||||
chr19:49598117
|
A | C | 3 | a0001c0001t0001g0283a0003c0005t0001g0284a0021c0038t0001g0285 | 3 | NA18951.hp2 NA18982.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.3678+104A>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 4/13 | chr19 | 49598117 | ||||||
chr19:49598145
|
T | C | 7 | a0001c0009t0002g0144a0001c0009t0002g0145a0001c0009t0002g0146others(4): Show | 7 | HG02258.hp2 HG02451.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.3678+132T>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 4/13 | chr19 | 49598145 | ||||||
chr19:49598164
|
C | T | 13 | a0002c0004t0004g0040a0002c0004t0004g0041a0002c0004t0004g0043others(10): Show | 13 | HG01070.hp1 HG01071.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.3678+151C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 4/13 | chr19 | 49598164 | ||||||
chr19:49598174
|
C | T | 13 | a0002c0004t0004g0040a0002c0004t0004g0041a0002c0004t0004g0043others(10): Show | 13 | HG01070.hp1 HG01071.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.3678+161C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 4/13 | chr19 | 49598174 | ||||||
chr19:49598240
|
GT | G | 8 | a0001c0009t0002g0144a0001c0009t0002g0145a0001c0009t0002g0146others(5): Show | 8 | HG02258.hp2 HG02451.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.3678+234delT | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr19 | 49598240 | |||||
chr19:49598242
|
T | G | 13 | a0001c0002t0001g0001a0001c0002t0001g0084a0001c0002t0001g0091others(10): Show | 13 | HG00733.hp2 HG01261.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.3678+229T>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 4/13 | chr19 | 49598242 | ||||||
chr19:49598285
|
A | G | 18 | a0001c0006t0001g0031a0001c0006t0001g0032a0001c0006t0001g0033others(15): Show | 18 | HG01070.hp1 HG01071.hp1 HG01175.hp2 others(15): Show |
intron_variant | MODIFIER | c.3678+272A>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 4/13 | chr19 | 49598285 | ||||||
chr19:49598365
|
C | T | 2 | a0001c0002t0006g0138a0001c0002t0006g0139 | 2 | HG02615.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.3678+352C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 4/13 | chr19 | 49598365 | ||||||
chr19:49598456
|
T | C | 136 | a0001c0001t0001g0157a0001c0002t0001g0001a0001c0002t0001g0028others(133): Show | 136 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.3678+443T>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 4/13 | chr19 | 49598456 | ||||||
chr19:49598459
|
A | G | 1 | a0001c0001t0001g0282 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.3678+446A>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 4/13 | chr19 | 49598459 | ||||||
chr19:49598480
|
G | A | 1 | a0001c0001t0001g0180 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.3678+467G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 4/13 | chr19 | 49598480 | ||||||
chr19:49598545
|
C | G | 3 | a0001c0003t0001g0133a0001c0003t0001g0134a0001c0003t0001g0135 | 3 | HG00438.hp1 HG02083.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.3678+532C>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 4/13 | chr19 | 49598545 | ||||||
chr19:49598618
|
G | C | 1 | a0001c0002t0001g0047 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.3678+605G>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 4/13 | chr19 | 49598618 | ||||||
chr19:49598801
|
A | G | 3 | a0006c0010t0001g0131a0006c0010t0001g0132a0017c0027t0001g0130 | 3 | HG01168.hp2 HG01169.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.3679-471A>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 4/13 | chr19 | 49598801 | ||||||
chr19:49598941
|
C | G | 1 | a0001c0051t0001g0015 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.3679-331C>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 4/13 | chr19 | 49598941 | ||||||
chr19:49599032
|
C | T | 17 | a0001c0002t0001g0001a0001c0002t0001g0084a0001c0002t0001g0091others(14): Show | 17 | HG00733.hp2 HG01261.hp1 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.3679-240C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 4/13 | chr19 | 49599032 | ||||||
chr19:49599067
|
AG | A | 136 | a0001c0001t0001g0157a0001c0002t0001g0001a0001c0002t0001g0028others(133): Show | 136 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.3679-203delG | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr19 | 49599067 | |||||
chr19:49599088
|
C | T | 7 | a0001c0009t0002g0144a0001c0009t0002g0145a0001c0009t0002g0146others(4): Show | 7 | HG02258.hp2 HG02451.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.3679-184C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 4/13 | chr19 | 49599088 | ||||||
chr19:49599140
|
G | T | 1 | a0001c0001t0001g0281 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.3679-132G>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 4/13 | chr19 | 49599140 | ||||||
chr19:49599185
|
G | A | 1 | a0001c0002t0001g0129 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3679-87G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 4/13 | chr19 | 49599185 | ||||||
chr19:49599195
|
A | G | 1 | a0001c0002t0001g0140 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3679-77A>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 4/13 | chr19 | 49599195 | ||||||
chr19:49599995
|
G | A | 136 | a0001c0001t0001g0157a0001c0002t0001g0001a0001c0002t0001g0028others(133): Show | 136 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.4345+57G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 5/13 | chr19 | 49599995 | ||||||
chr19:49600048
|
T | G | 2 | a0001c0016t0001g0155a0001c0016t0001g0156 | 2 | HG02451.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.4345+110T>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 5/13 | chr19 | 49600048 | ||||||
chr19:49600104
|
G | C | 1 | a0001c0001t0001g0012 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.4345+166G>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 5/13 | chr19 | 49600104 | ||||||
chr19:49600109
|
A | G | 1 | a0001c0001t0001g0301 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.4345+171A>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 5/13 | chr19 | 49600109 | ||||||
chr19:49600121
|
T | C | 1 | a0001c0001t0001g0181 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.4345+183T>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 5/13 | chr19 | 49600121 | ||||||
chr19:49600480
|
C | CA | 13 | a0001c0001t0001g0183a0001c0001t0001g0283a0001c0001t0001g0303others(10): Show | 13 | HG00140.hp1 HG01928.hp2 HG01981.hp2 others(10): Show |
intron_variant | MODIFIER | c.4345+557dupA | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr19 | 49600480 | |||||
chr19:49600480
|
C | CAA | 11 | a0002c0004t0004g0040a0002c0004t0004g0041a0002c0004t0004g0043others(8): Show | 11 | HG01070.hp1 HG01071.hp1 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.4345+556_4345+557d others(4): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr19 | 49600480 | |||||
chr19:49600694
|
G | A | 1 | a0001c0002t0002g0049 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.4345+756G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 5/13 | chr19 | 49600694 | ||||||
chr19:49600729
|
A | G | 2 | a0001c0001t0001g0280a0003c0005t0001g0279 | 2 | NA18971.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.4346-762A>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 5/13 | chr19 | 49600729 | ||||||
chr19:49600795
|
G | A | 1 | a0001c0001t0001g0184 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.4346-696G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 5/13 | chr19 | 49600795 | ||||||
chr19:49600947
|
A | T | 1 | a0001c0001t0001g0157 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.4346-544A>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 5/13 | chr19 | 49600947 | ||||||
chr19:49601087
|
T | A | 1 | a0016c0039t0001g0179 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.4346-404T>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 5/13 | chr19 | 49601087 | ||||||
chr19:49601144
|
G | A | 1 | a0001c0002t0001g0084 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.4346-347G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 5/13 | chr19 | 49601144 | ||||||
chr19:49601221
|
A | T | 1 | a0016c0039t0001g0179 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.4346-270A>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 5/13 | chr19 | 49601221 | ||||||
chr19:49601305
|
TCTC | T | 7 | a0001c0009t0002g0144a0001c0009t0002g0145a0001c0009t0002g0146others(4): Show | 7 | HG02258.hp2 HG02451.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.4346-183_4346-181d others(5): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr19 | 49601305 | |||||
chr19:49601431
|
A | G | 1 | a0001c0049t0001g0278 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.4346-60A>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 5/13 | chr19 | 49601431 | ||||||
chr19:49601449
|
ATGATGAA others(13): Show |
A | 1 | a0001c0012t0001g0128 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.4346-36_4346-17del others(20): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr19 | 49601449 | |||||
chr19:49601982
|
C | T | 145 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0022others(142): Show | 145 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.4773+64C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49601982 | ||||||
chr19:49602120
|
A | G | 1 | a0001c0001t0001g0168 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.4773+202A>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49602120 | ||||||
chr19:49602150
|
T | C | 1 | a0001c0001t0001g0185 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.4773+232T>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49602150 | ||||||
chr19:49602158
|
C | T | 1 | a0001c0001t0001g0022 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.4773+240C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49602158 | ||||||
chr19:49602164
|
T | C | 1 | a0001c0001t0001g0186 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.4773+246T>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49602164 | ||||||
chr19:49602198
|
C | G | 7 | a0001c0009t0002g0144a0001c0009t0002g0145a0001c0009t0002g0146others(4): Show | 7 | HG02258.hp2 HG02451.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.4773+280C>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49602198 | ||||||
chr19:49602236
|
G | A | 1 | a0001c0031t0001g0096 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.4773+318G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49602236 | ||||||
chr19:49602241
|
A | T | 1 | a0016c0039t0001g0179 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.4773+323A>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49602241 | ||||||
chr19:49602484
|
T | C | 1 | a0001c0049t0001g0278 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.4773+566T>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49602484 | ||||||
chr19:49602508
|
A | G | 1 | a0001c0002t0006g0094 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.4773+590A>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49602508 | ||||||
chr19:49602554
|
A | G | 1 | a0015c0025t0001g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.4773+636A>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49602554 | ||||||
chr19:49602584
|
C | T | 6 | a0001c0006t0001g0031a0001c0006t0001g0032a0001c0006t0001g0033others(3): Show | 6 | HG01346.hp2 HG02486.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.4773+666C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49602584 | ||||||
chr19:49602647
|
G | A | 1 | a0001c0002t0001g0129 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.4773+729G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49602647 | ||||||
chr19:49602713
|
G | A | 1 | a0001c0001t0001g0187 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.4773+795G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49602713 | ||||||
chr19:49602772
|
G | A | 13 | a0002c0004t0004g0040a0002c0004t0004g0041a0002c0004t0004g0043others(10): Show | 13 | HG01070.hp1 HG01071.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.4773+854G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49602772 | ||||||
chr19:49602951
|
C | G | 130 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0022others(127): Show | 130 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.4773+1033C>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49602951 | ||||||
chr19:49602965
|
C | A | 5 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0022others(2): Show | 5 | HG00735.hp1 HG02258.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.4773+1047C>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49602965 | ||||||
chr19:49603051
|
T | C | 5 | a0001c0009t0002g0144a0001c0009t0002g0145a0001c0009t0002g0146others(2): Show | 5 | HG02258.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.4773+1133T>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49603051 | ||||||
chr19:49603159
|
T | A | 1 | a0001c0001t0001g0158 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.4773+1241T>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49603159 | ||||||
chr19:49603276
|
GTCAGCCC others(8): Show |
G | 1 | a0001c0002t0006g0094 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.4773+1359_4773+137 others(19): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49603276 | ||||||
chr19:49603282
|
C | T | 2 | a0001c0001t0001g0267a0001c0001t0001g0268 | 2 | NA18950.hp1 NA18954.hp2 |
intron_variant | MODIFIER | c.4773+1364C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49603282 | ||||||
chr19:49603363
|
C | T | 5 | a0001c0006t0001g0031a0001c0006t0001g0032a0001c0006t0001g0033others(2): Show | 5 | HG01346.hp2 HG02486.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.4773+1445C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49603363 | ||||||
chr19:49603384
|
C | T | 1 | a0001c0002t0006g0094 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.4773+1466C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49603384 | ||||||
chr19:49603410
|
G | A | 1 | a0001c0001t0001g0159 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.4773+1492G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49603410 | ||||||
chr19:49603467
|
G | C | 1 | a0001c0021t0001g0050 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.4773+1549G>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49603467 | ||||||
chr19:49603504
|
A | G | 1 | a0001c0002t0001g0129 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.4773+1586A>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49603504 | ||||||
chr19:49603562
|
C | T | 1 | a0011c0026t0001g0083 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.4773+1644C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49603562 | ||||||
chr19:49603627
|
G | C | 1 | a0001c0002t0002g0051 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.4773+1709G>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49603627 | ||||||
chr19:49603649
|
G | T | 130 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0022others(127): Show | 130 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.4773+1731G>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49603649 | ||||||
chr19:49603734
|
T | C | 1 | a0001c0024t0003g0085 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.4773+1816T>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49603734 | ||||||
chr19:49603753
|
G | A | 1 | a0001c0001t0001g0168 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.4773+1835G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49603753 | ||||||
chr19:49603782
|
T | A | 1 | a0001c0001t0001g0188 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.4773+1864T>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49603782 | ||||||
chr19:49603801
|
A | T | 7 | a0001c0009t0002g0144a0001c0009t0002g0145a0001c0009t0002g0146others(4): Show | 7 | HG02258.hp2 HG02451.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.4773+1883A>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49603801 | ||||||
chr19:49603810
|
A | G | 28 | a0001c0002t0001g0047a0001c0002t0001g0141a0001c0002t0001g0142others(25): Show | 28 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.4773+1892A>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49603810 | ||||||
chr19:49603824
|
T | G | 28 | a0001c0002t0001g0047a0001c0002t0001g0141a0001c0002t0001g0142others(25): Show | 28 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.4773+1906T>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49603824 | ||||||
chr19:49603881
|
C | T | 5 | a0001c0009t0002g0144a0001c0009t0002g0145a0001c0009t0002g0146others(2): Show | 5 | HG02258.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.4773+1963C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49603881 | ||||||
chr19:49603913
|
C | T | 1 | a0001c0001t0001g0266 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.4773+1995C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49603913 | ||||||
chr19:49603916
|
G | A | 13 | a0002c0004t0004g0040a0002c0004t0004g0041a0002c0004t0004g0043others(10): Show | 13 | HG01070.hp1 HG01071.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.4773+1998G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49603916 | ||||||
chr19:49604003
|
T | C | 40 | a0001c0001t0001g0300a0001c0003t0001g0024a0001c0003t0001g0025others(37): Show | 40 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(37): Show |
intron_variant | MODIFIER | c.4773+2085T>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49604003 | ||||||
chr19:49604189
|
A | G | 2 | a0001c0002t0003g0064a0001c0002t0013g0063 | 2 | HG02135.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.4773+2271A>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49604189 | ||||||
chr19:49604296
|
A | G | 1 | a0001c0001t0001g0187 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.4773+2378A>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49604296 | ||||||
chr19:49604345
|
A | C | 1 | a0019c0022t0001g0023 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.4773+2427A>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49604345 | ||||||
chr19:49604353
|
G | A | 13 | a0002c0004t0004g0040a0002c0004t0004g0041a0002c0004t0004g0043others(10): Show | 13 | HG01070.hp1 HG01071.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.4773+2435G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49604353 | ||||||
chr19:49604363
|
CA | C | 9 | a0001c0001t0001g0159a0001c0001t0001g0178a0001c0001t0001g0263others(6): Show | 9 | HG01496.hp1 HG01993.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.4773+2461delA | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr19 | 49604363 | |||||
chr19:49604384
|
A | C | 1 | a0001c0001t0001g0175 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.4773+2466A>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49604384 | ||||||
chr19:49604503
|
G | C | 149 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0022others(146): Show | 149 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(146): Show |
intron_variant | MODIFIER | c.4773+2585G>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49604503 | ||||||
chr19:49604585
|
G | A | 13 | a0002c0004t0004g0040a0002c0004t0004g0041a0002c0004t0004g0043others(10): Show | 13 | HG01070.hp1 HG01071.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.4773+2667G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49604585 | ||||||
chr19:49604977
|
G | A | 2 | a0002c0004t0007g0035a0002c0004t0007g0036 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.4773+3059G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49604977 | ||||||
chr19:49605462
|
A | G | 1 | a0001c0001t0001g0300 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.4773+3544A>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49605462 | ||||||
chr19:49605482
|
G | A | 2 | a0001c0001t0001g0304a0001c0001t0001g0305 | 2 | NA18969.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.4773+3564G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49605482 | ||||||
chr19:49605558
|
A | G | 7 | a0001c0009t0002g0144a0001c0009t0002g0145a0001c0009t0002g0146others(4): Show | 7 | HG02258.hp2 HG02451.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.4773+3640A>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49605558 | ||||||
chr19:49605618
|
C | T | 28 | a0001c0002t0001g0047a0001c0002t0001g0141a0001c0002t0001g0142others(25): Show | 28 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.4773+3700C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49605618 | ||||||
chr19:49605726
|
G | A | 13 | a0002c0004t0004g0040a0002c0004t0004g0041a0002c0004t0004g0043others(10): Show | 13 | HG01070.hp1 HG01071.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.4773+3808G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49605726 | ||||||
chr19:49605733
|
C | T | 2 | a0001c0016t0001g0155a0001c0016t0001g0156 | 2 | HG02451.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.4773+3815C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49605733 | ||||||
chr19:49605777
|
C | T | 5 | a0001c0009t0002g0144a0001c0009t0002g0145a0001c0009t0002g0146others(2): Show | 5 | HG02258.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.4773+3859C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49605777 | ||||||
chr19:49605841
|
G | T | 6 | a0001c0006t0001g0031a0001c0006t0001g0032a0001c0006t0001g0033others(3): Show | 6 | HG01346.hp2 HG02486.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.4773+3923G>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49605841 | ||||||
chr19:49605973
|
C | T | 13 | a0002c0004t0004g0040a0002c0004t0004g0041a0002c0004t0004g0043others(10): Show | 13 | HG01070.hp1 HG01071.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.4773+4055C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49605973 | ||||||
chr19:49606004
|
T | G | 5 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0162others(2): Show | 5 | HG02451.hp1 HG02723.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.4773+4086T>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49606004 | ||||||
chr19:49606034
|
CT | C | 5 | a0001c0009t0002g0144a0001c0009t0002g0145a0001c0009t0002g0146others(2): Show | 5 | HG02258.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.4773+4118delT | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr19 | 49606034 | |||||
chr19:49606155
|
C | T | 17 | a0001c0002t0001g0001a0001c0002t0001g0084a0001c0002t0001g0091others(14): Show | 17 | HG00733.hp2 HG01261.hp1 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.4773+4237C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49606155 | ||||||
chr19:49606198
|
C | G | 1 | a0001c0002t0001g0129 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.4773+4280C>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49606198 | ||||||
chr19:49606315
|
C | CT | 9 | a0001c0001t0001g0261a0001c0001t0001g0262a0001c0002t0006g0094others(6): Show | 9 | HG02257.hp2 HG02258.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.4773+4411dupT | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr19 | 49606315 | |||||
chr19:49606315
|
CT | C | 84 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0022others(81): Show | 84 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.4773+4411delT | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr19 | 49606315 | |||||
chr19:49606323
|
T | G | 1 | a0001c0002t0002g0065 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.4773+4405T>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49606323 | ||||||
chr19:49606508
|
TGGTCAGG others(3): Show |
T | 1 | a0001c0001t0001g0283 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.4773+4592_4773+460 others(14): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr19 | 49606508 | |||||
chr19:49606645
|
C | CT | 13 | a0001c0001t0001g0176a0001c0001t0001g0260a0001c0001t0001g0283others(10): Show | 13 | HG01255.hp1 HG01261.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.4773+4746dupT | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr19 | 49606645 | |||||
chr19:49606645
|
CT | C | 10 | a0001c0001t0001g0191a0001c0001t0001g0287a0001c0002t0001g0141others(7): Show | 10 | HG01069.hp1 HG01081.hp1 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.4773+4746delT | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr19 | 49606645 | |||||
chr19:49606855
|
C | T | 1 | a0015c0025t0001g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.4773+4937C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49606855 | ||||||
chr19:49606872
|
C | T | 1 | a0001c0001t0001g0167 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.4773+4954C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49606872 | ||||||
chr19:49606895
|
A | T | 2 | a0001c0020t0002g0147a0001c0020t0002g0148 | 2 | HG02258.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.4773+4977A>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49606895 | ||||||
chr19:49606920
|
A | G | 5 | a0001c0009t0002g0144a0001c0009t0002g0145a0001c0009t0002g0146others(2): Show | 5 | HG02258.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.4773+5002A>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49606920 | ||||||
chr19:49606953
|
C | A | 13 | a0002c0004t0004g0040a0002c0004t0004g0041a0002c0004t0004g0043others(10): Show | 13 | HG01070.hp1 HG01071.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.4773+5035C>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49606953 | ||||||
chr19:49607060
|
G | A | 1 | a0002c0034t0001g0037 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.4773+5142G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49607060 | ||||||
chr19:49607121
|
C | G | 1 | a0001c0001t0001g0310 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.4773+5203C>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49607121 | ||||||
chr19:49607255
|
G | T | 1 | a0002c0004t0004g0045 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.4773+5337G>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49607255 | ||||||
chr19:49607333
|
G | A | 5 | a0001c0009t0002g0144a0001c0009t0002g0145a0001c0009t0002g0146others(2): Show | 5 | HG02258.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.4773+5415G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49607333 | ||||||
chr19:49607356
|
C | CAT | 12 | a0001c0002t0001g0001a0001c0002t0001g0084a0001c0002t0001g0091others(9): Show | 12 | HG00733.hp2 HG01261.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.4773+5438_4773+543 others(6): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49607356 | ||||||
chr19:49607360
|
T | C | 12 | a0001c0002t0001g0001a0001c0002t0001g0084a0001c0002t0001g0091others(9): Show | 12 | HG00733.hp2 HG01261.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.4773+5442T>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49607360 | ||||||
chr19:49607361
|
G | GCA | 29 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0022others(26): Show | 29 | HG00735.hp1 HG00735.hp2 HG01069.hp2 others(26): Show |
intron_variant | MODIFIER | c.4773+5462_4773+546 others(6): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr19 | 49607361 | |||||
chr19:49607361
|
G | GCACACA | 4 | a0001c0009t0002g0144a0001c0009t0002g0145a0001c0009t0002g0146others(1): Show | 4 | HG02896.hp2 HG02897.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.4773+5458_4773+546 others(10): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr19 | 49607361 | |||||
chr19:49607361
|
G | GCGCACAC others(9): Show |
3 | a0002c0004t0007g0034a0002c0015t0001g0038a0002c0015t0001g0039 | 3 | HG02145.hp1 HG02723.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.4773+5444_4773+544 others(20): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr19 | 49607361 | |||||
chr19:49607361
|
G | GCGCACAC others(13): Show |
2 | a0002c0004t0007g0035a0002c0004t0007g0036 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.4773+5444_4773+544 others(24): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr19 | 49607361 | |||||
chr19:49607361
|
G | GCGCACAC others(15): Show |
1 | a0002c0034t0001g0037 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.4773+5444_4773+544 others(26): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr19 | 49607361 | |||||
chr19:49607361
|
G | GCGCGCAC others(7): Show |
1 | a0002c0035t0004g0042 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.4773+5444_4773+544 others(18): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr19 | 49607361 | |||||
chr19:49607361
|
G | GCGCGCAC others(9): Show |
2 | a0002c0004t0004g0041a0002c0004t0004g0044 | 2 | HG03927.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.4773+5444_4773+544 others(20): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr19 | 49607361 | |||||
chr19:49607361
|
G | GCGCGCAC others(11): Show |
2 | a0002c0004t0004g0040a0010c0032t0004g0046 | 2 | HG03710.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.4773+5444_4773+544 others(22): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr19 | 49607361 | |||||
chr19:49607361
|
G | GCGCGCAC others(13): Show |
1 | a0002c0004t0004g0045 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.4773+5444_4773+544 others(24): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr19 | 49607361 | |||||
chr19:49607361
|
G | GCGCGCGC others(13): Show |
1 | a0002c0004t0004g0043 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.4773+5444_4773+544 others(24): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr19 | 49607361 | |||||
chr19:49607363
|
A | G | 1 | a0001c0001t0001g0174 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.4773+5445A>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49607363 | ||||||
chr19:49607372
|
C | T | 1 | a0001c0002t0002g0082 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.4773+5454C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49607372 | ||||||
chr19:49607382
|
G | C | 6 | a0001c0002t0001g0001a0001c0002t0001g0091a0001c0002t0001g0092others(3): Show | 6 | HG01261.hp1 HG02451.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.4773+5464G>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49607382 | ||||||
chr19:49607531
|
C | T | 2 | a0002c0004t0004g0043a0010c0032t0004g0046 | 2 | HG03654.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.4773+5613C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49607531 | ||||||
chr19:49607532
|
G | A | 1 | a0001c0002t0002g0068 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.4773+5614G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49607532 | ||||||
chr19:49607532
|
G | GC | 21 | a0001c0001t0001g0012a0001c0001t0001g0159a0001c0001t0001g0195others(18): Show | 21 | HG00438.hp1 HG00438.hp2 HG00642.hp1 others(18): Show |
intron_variant | MODIFIER | c.4773+5621dupC | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr19 | 49607532 | |||||
chr19:49607657
|
G | A | 1 | a0001c0001t0001g0159 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.4773+5739G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49607657 | ||||||
chr19:49607658
|
A | T | 1 | a0001c0001t0001g0310 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.4773+5740A>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49607658 | ||||||
chr19:49607666
|
G | C | 150 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0022others(147): Show | 150 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(147): Show |
intron_variant | MODIFIER | c.4773+5748G>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49607666 | ||||||
chr19:49607699
|
C | A | 2 | a0001c0002t0006g0138a0001c0002t0006g0139 | 2 | HG02615.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.4773+5781C>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49607699 | ||||||
chr19:49607796
|
G | A | 1 | a0001c0001t0001g0163 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.4773+5878G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49607796 | ||||||
chr19:49607880
|
G | A | 10 | a0001c0001t0001g0003a0001c0001t0001g0191a0001c0001t0001g0198others(7): Show | 11 | HG01934.hp2 HG02056.hp2 HG02071.hp2 others(8): Show |
intron_variant | MODIFIER | c.4773+5962G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49607880 | ||||||
chr19:49607880
|
G | C | 130 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0022others(127): Show | 130 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.4773+5962G>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49607880 | ||||||
chr19:49608005
|
G | C | 5 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0022others(2): Show | 5 | HG00735.hp1 HG02258.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.4773+6087G>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49608005 | ||||||
chr19:49608051
|
T | A | 2 | a0001c0002t0006g0138a0001c0002t0006g0139 | 2 | HG02615.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.4773+6133T>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49608051 | ||||||
chr19:49608198
|
C | T | 1 | a0018c0046t0001g0259 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.4773+6280C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49608198 | ||||||
chr19:49608334
|
T | G | 130 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0022others(127): Show | 130 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.4774-6199T>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49608334 | ||||||
chr19:49608344
|
T | A | 1 | a0002c0004t0004g0044 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.4774-6189T>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49608344 | ||||||
chr19:49608345
|
A | T | 23 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(20): Show | 23 | HG01070.hp2 HG01109.hp2 HG01255.hp2 others(20): Show |
intron_variant | MODIFIER | c.4774-6188A>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49608345 | ||||||
chr19:49608346
|
A | T | 5 | a0001c0009t0002g0144a0001c0009t0002g0145a0001c0009t0002g0146others(2): Show | 5 | HG02258.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.4774-6187A>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49608346 | ||||||
chr19:49608405
|
C | T | 5 | a0001c0001t0001g0300a0001c0003t0001g0101a0001c0003t0001g0122others(2): Show | 5 | HG00544.hp1 HG00642.hp1 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.4774-6128C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49608405 | ||||||
chr19:49608444
|
C | T | 1 | a0002c0004t0004g0041 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.4774-6089C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49608444 | ||||||
chr19:49608503
|
G | A | 2 | a0001c0002t0005g0087a0001c0002t0005g0088 | 2 | HG02818.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.4774-6030G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49608503 | ||||||
chr19:49608510
|
A | G | 13 | a0002c0004t0004g0040a0002c0004t0004g0041a0002c0004t0004g0043others(10): Show | 13 | HG01070.hp1 HG01071.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.4774-6023A>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49608510 | ||||||
chr19:49608590
|
C | T | 1 | a0019c0022t0001g0023 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.4774-5943C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49608590 | ||||||
chr19:49608659
|
G | A | 1 | a0002c0004t0007g0034 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.4774-5874G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49608659 | ||||||
chr19:49608751
|
A | C | 1 | a0001c0001t0001g0256 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.4774-5782A>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49608751 | ||||||
chr19:49608841
|
C | CA | 17 | a0001c0002t0001g0028a0001c0002t0001g0052a0001c0002t0001g0053others(14): Show | 17 | HG01433.hp1 HG02055.hp1 HG02129.hp2 others(14): Show |
intron_variant | MODIFIER | c.4774-5681dupA | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr19 | 49608841 | |||||
chr19:49608853
|
C | A | 1 | a0001c0001t0001g0310 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.4774-5680C>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49608853 | ||||||
chr19:49608854
|
A | C | 1 | a0001c0001t0001g0310 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.4774-5679A>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49608854 | ||||||
chr19:49608883
|
A | G | 5 | a0001c0001t0001g0009a0001c0001t0001g0253a0001c0001t0001g0255others(2): Show | 5 | HG02886.hp1 HG02965.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.4774-5650A>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49608883 | ||||||
chr19:49608900
|
C | T | 5 | a0001c0009t0002g0144a0001c0009t0002g0145a0001c0009t0002g0146others(2): Show | 5 | HG02258.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.4774-5633C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49608900 | ||||||
chr19:49609114
|
C | A | 2 | a0001c0016t0001g0155a0001c0016t0001g0156 | 2 | HG02451.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.4774-5419C>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49609114 | ||||||
chr19:49609133
|
G | A | 13 | a0002c0004t0004g0040a0002c0004t0004g0041a0002c0004t0004g0043others(10): Show | 13 | HG01070.hp1 HG01071.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.4774-5400G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49609133 | ||||||
chr19:49609134
|
C | T | 4 | a0001c0001t0001g0183a0001c0001t0001g0252a0001c0018t0001g0190others(1): Show | 4 | HG00140.hp1 HG01081.hp1 HG01243.hp1 others(1): Show |
intron_variant | MODIFIER | c.4774-5399C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49609134 | ||||||
chr19:49609329
|
G | T | 1 | a0001c0001t0001g0310 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.4774-5204G>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49609329 | ||||||
chr19:49609346
|
A | G | 1 | a0001c0001t0001g0310 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.4774-5187A>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49609346 | ||||||
chr19:49609408
|
C | T | 1 | a0001c0001t0001g0258 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.4774-5125C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49609408 | ||||||
chr19:49609469
|
C | T | 1 | a0002c0004t0004g0041 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.4774-5064C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49609469 | ||||||
chr19:49609472
|
G | T | 5 | a0001c0009t0002g0144a0001c0009t0002g0145a0001c0009t0002g0146others(2): Show | 5 | HG02258.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.4774-5061G>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49609472 | ||||||
chr19:49609556
|
A | G | 5 | a0001c0009t0002g0144a0001c0009t0002g0145a0001c0009t0002g0146others(2): Show | 5 | HG02258.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.4774-4977A>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49609556 | ||||||
chr19:49609592
|
C | A | 17 | a0001c0002t0001g0001a0001c0002t0001g0084a0001c0002t0001g0091others(14): Show | 17 | HG00733.hp2 HG01261.hp1 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.4774-4941C>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49609592 | ||||||
chr19:49609598
|
C | T | 2 | a0001c0002t0001g0059a0001c0002t0001g0060 | 2 | HG03130.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.4774-4935C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49609598 | ||||||
chr19:49609598
|
CA | C | 142 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0022others(139): Show | 142 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(139): Show |
intron_variant | MODIFIER | c.4774-4915delA | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr19 | 49609598 | |||||
chr19:49609598
|
CAA | C | 9 | a0001c0001t0001g0277a0001c0002t0001g0061a0001c0002t0001g0154others(6): Show | 9 | HG01069.hp2 HG01070.hp1 HG01943.hp2 others(6): Show |
intron_variant | MODIFIER | c.4774-4916_4774-491 others(6): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr19 | 49609598 | |||||
chr19:49609599
|
A | C | 2 | a0001c0002t0001g0059a0001c0002t0001g0060 | 2 | HG03130.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.4774-4934A>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49609599 | ||||||
chr19:49609633
|
A | G | 1 | a0001c0003t0001g0119 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.4774-4900A>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49609633 | ||||||
chr19:49609718
|
G | A | 1 | a0001c0001t0001g0159 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.4774-4815G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49609718 | ||||||
chr19:49609766
|
G | T | 1 | a0001c0001t0001g0310 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.4774-4767G>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49609766 | ||||||
chr19:49609852
|
G | A | 2 | a0001c0020t0002g0147a0001c0020t0002g0148 | 2 | HG02258.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.4774-4681G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49609852 | ||||||
chr19:49609942
|
C | T | 1 | a0001c0003t0001g0118 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.4774-4591C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49609942 | ||||||
chr19:49609979
|
CT | C | 31 | a0001c0001t0001g0310a0001c0002t0001g0047a0001c0002t0001g0084others(28): Show | 31 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(28): Show |
intron_variant | MODIFIER | c.4774-4542delT | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr19 | 49609979 | |||||
chr19:49610119
|
C | T | 46 | a0001c0001t0001g0157a0001c0001t0001g0300a0001c0002t0008g0125others(43): Show | 46 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(43): Show |
intron_variant | MODIFIER | c.4774-4414C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49610119 | ||||||
chr19:49610131
|
C | T | 9 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(6): Show | 9 | HG01070.hp2 HG01255.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.4774-4402C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49610131 | ||||||
chr19:49610186
|
G | A | 1 | a0001c0003t0001g0102 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.4774-4347G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49610186 | ||||||
chr19:49610203
|
G | A | 13 | a0001c0002t0001g0001a0001c0002t0001g0084a0001c0002t0001g0091others(10): Show | 13 | HG00733.hp2 HG01261.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.4774-4330G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49610203 | ||||||
chr19:49610298
|
T | C | 1 | a0001c0001t0001g0289 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.4774-4235T>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49610298 | ||||||
chr19:49610341
|
G | A | 13 | a0002c0004t0004g0040a0002c0004t0004g0041a0002c0004t0004g0043others(10): Show | 13 | HG01070.hp1 HG01071.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.4774-4192G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49610341 | ||||||
chr19:49610546
|
A | ATTTTTTT others(2): Show |
14 | a0001c0001t0001g0159a0001c0001t0001g0163a0001c0001t0001g0169others(11): Show | 14 | HG01070.hp2 HG01167.hp2 HG01255.hp2 others(11): Show |
intron_variant | MODIFIER | c.4774-3981_4774-397 others(13): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr19 | 49610546 | |||||
chr19:49610546
|
A | ATTTTTTT others(3): Show |
75 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0022others(72): Show | 75 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.4774-3982_4774-397 others(14): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr19 | 49610546 | |||||
chr19:49610546
|
A | ATTTTTTT others(4): Show |
42 | a0001c0001t0003g0270a0001c0002t0001g0047a0001c0002t0001g0062others(39): Show | 42 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.4774-3983_4774-397 others(15): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr19 | 49610546 | |||||
chr19:49610546
|
A | ATTTTTTT others(5): Show |
25 | a0001c0002t0001g0001a0001c0002t0001g0084a0001c0002t0001g0092others(22): Show | 25 | HG00733.hp2 HG01070.hp1 HG01071.hp1 others(22): Show |
intron_variant | MODIFIER | c.4774-3984_4774-397 others(16): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr19 | 49610546 | |||||
chr19:49610546
|
A | ATTTTTTT others(6): Show |
6 | a0001c0002t0001g0093a0001c0002t0001g0129a0001c0002t0001g0140others(3): Show | 6 | HG01175.hp2 HG01261.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.4774-3985_4774-397 others(17): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr19 | 49610546 | |||||
chr19:49610629
|
G | A | 6 | a0001c0009t0002g0144a0001c0009t0002g0145a0001c0009t0002g0146others(3): Show | 6 | HG02258.hp2 HG02896.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.4774-3904G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49610629 | ||||||
chr19:49610658
|
C | T | 1 | a0001c0003t0001g0115 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.4774-3875C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49610658 | ||||||
chr19:49610661
|
C | T | 1 | a0001c0001t0001g0249 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.4774-3872C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49610661 | ||||||
chr19:49610702
|
C | T | 1 | a0001c0001t0001g0248 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.4774-3831C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49610702 | ||||||
chr19:49610725
|
A | T | 1 | a0001c0003t0001g0115 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.4774-3808A>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49610725 | ||||||
chr19:49610789
|
C | T | 1 | a0001c0001t0001g0251 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.4774-3744C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49610789 | ||||||
chr19:49610790
|
G | A | 14 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(11): Show | 14 | HG01070.hp2 HG01255.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.4774-3743G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49610790 | ||||||
chr19:49610949
|
A | G | 5 | a0001c0009t0002g0144a0001c0009t0002g0145a0001c0009t0002g0146others(2): Show | 5 | HG02258.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.4774-3584A>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49610949 | ||||||
chr19:49611015
|
G | A | 1 | a0001c0001t0001g0204 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.4774-3518G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49611015 | ||||||
chr19:49611083
|
C | T | 1 | a0017c0027t0001g0130 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.4774-3450C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49611083 | ||||||
chr19:49611093
|
C | T | 110 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0022others(107): Show | 110 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.4774-3440C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49611093 | ||||||
chr19:49611163
|
A | G | 5 | a0001c0009t0002g0144a0001c0009t0002g0145a0001c0009t0002g0146others(2): Show | 5 | HG02258.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.4774-3370A>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49611163 | ||||||
chr19:49611384
|
C | T | 19 | a0001c0001t0001g0157a0001c0001t0001g0163a0001c0002t0001g0028others(16): Show | 19 | HG01109.hp1 HG01192.hp2 HG01433.hp1 others(16): Show |
intron_variant | MODIFIER | c.4774-3149C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49611384 | ||||||
chr19:49611632
|
AAAAAAAA others(283): Show |
A | 5 | a0001c0009t0002g0144a0001c0009t0002g0145a0001c0009t0002g0146others(2): Show | 5 | HG02258.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.4774-2891_4774-260 others(4): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr19 | 49611632 | |||||
chr19:49611748
|
C | T | 2 | a0001c0016t0001g0155a0001c0016t0001g0156 | 2 | HG02451.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.4774-2785C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49611748 | ||||||
chr19:49611765
|
T | A | 1 | a0001c0001t0001g0283 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.4774-2768T>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49611765 | ||||||
chr19:49611767
|
C | A | 1 | a0001c0001t0001g0283 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.4774-2766C>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49611767 | ||||||
chr19:49611774
|
A | T | 149 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0022others(146): Show | 149 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(146): Show |
intron_variant | MODIFIER | c.4774-2759A>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49611774 | ||||||
chr19:49611779
|
C | T | 2 | a0001c0001t0001g0246a0001c0001t0001g0281 | 2 | HG04228.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.4774-2754C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49611779 | ||||||
chr19:49611796
|
G | A | 1 | a0001c0001t0001g0250 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.4774-2737G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49611796 | ||||||
chr19:49611800
|
G | A | 82 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0022others(79): Show | 82 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.4774-2733G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49611800 | ||||||
chr19:49611884
|
C | T | 1 | a0001c0052t0001g0245 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.4774-2649C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49611884 | ||||||
chr19:49611889
|
C | T | 12 | a0002c0004t0004g0040a0002c0004t0004g0041a0002c0004t0004g0043others(9): Show | 12 | HG01070.hp1 HG01071.hp1 HG01175.hp2 others(9): Show |
intron_variant | MODIFIER | c.4774-2644C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49611889 | ||||||
chr19:49611902
|
G | A | 1 | a0001c0001t0001g0302 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.4774-2631G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49611902 | ||||||
chr19:49611922
|
CAAAAA | C | 40 | a0001c0001t0001g0159a0001c0001t0001g0176a0001c0001t0001g0183others(37): Show | 40 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(37): Show |
intron_variant | MODIFIER | c.4774-2589_4774-258 others(9): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr19 | 49611922 | |||||
chr19:49611922
|
CAAAAAA | C | 259 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(256): Show | 265 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(262): Show |
intron_variant | MODIFIER | c.4774-2590_4774-258 others(10): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr19 | 49611922 | |||||
chr19:49611922
|
CAAAAAAA | C | 8 | a0001c0001t0001g0002a0001c0001t0001g0021a0001c0001t0001g0164others(5): Show | 9 | HG01243.hp2 HG01943.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.4774-2591_4774-258 others(11): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr19 | 49611922 | |||||
chr19:49611934
|
A | C | 5 | a0001c0009t0002g0144a0001c0009t0002g0145a0001c0009t0002g0146others(2): Show | 5 | HG02258.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.4774-2599A>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49611934 | ||||||
chr19:49611942
|
A | C | 5 | a0001c0009t0002g0144a0001c0009t0002g0145a0001c0009t0002g0146others(2): Show | 5 | HG02258.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.4774-2591A>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49611942 | ||||||
chr19:49611955
|
G | A | 2 | a0001c0001t0001g0246a0001c0001t0001g0281 | 2 | HG04228.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.4774-2578G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49611955 | ||||||
chr19:49611999
|
C | G | 5 | a0001c0009t0002g0144a0001c0009t0002g0145a0001c0009t0002g0146others(2): Show | 5 | HG02258.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.4774-2534C>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49611999 | ||||||
chr19:49612041
|
G | A | 4 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0200others(1): Show | 4 | HG02056.hp2 HG02071.hp2 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.4774-2492G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49612041 | ||||||
chr19:49612056
|
C | A | 2 | a0001c0016t0001g0155a0001c0016t0001g0156 | 2 | HG02451.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.4774-2477C>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49612056 | ||||||
chr19:49612208
|
G | A | 1 | a0001c0003t0001g0106 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.4774-2325G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49612208 | ||||||
chr19:49612211
|
AGAGCAAG others(5): Show |
A | 7 | a0001c0002t0001g0154a0001c0002t0002g0048a0001c0002t0002g0067others(4): Show | 7 | HG01433.hp2 HG01928.hp1 HG02273.hp1 others(4): Show |
intron_variant | MODIFIER | c.4774-2320_4774-230 others(16): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr19 | 49612211 | |||||
chr19:49612225
|
T | G | 7 | a0001c0002t0001g0154a0001c0002t0002g0048a0001c0002t0002g0067others(4): Show | 7 | HG01433.hp2 HG01928.hp1 HG02273.hp1 others(4): Show |
intron_variant | MODIFIER | c.4774-2308T>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49612225 | ||||||
chr19:49612228
|
C | CA | 19 | a0001c0001t0001g0203a0001c0001t0001g0206a0001c0001t0001g0257others(16): Show | 19 | HG00438.hp2 HG00735.hp1 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.4774-2286dupA | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr19 | 49612228 | |||||
chr19:49612228
|
CA | C | 7 | a0001c0001t0001g0189a0001c0001t0001g0244a0001c0001t0001g0283others(4): Show | 7 | HG01943.hp2 HG02895.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.4774-2286delA | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr19 | 49612228 | |||||
chr19:49612344
|
G | A | 5 | a0001c0001t0001g0009a0001c0001t0001g0253a0001c0001t0001g0255others(2): Show | 5 | HG02886.hp1 HG02965.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.4774-2189G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49612344 | ||||||
chr19:49612355
|
T | C | 5 | a0001c0009t0002g0144a0001c0009t0002g0145a0001c0009t0002g0146others(2): Show | 5 | HG02258.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.4774-2178T>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49612355 | ||||||
chr19:49612427
|
G | A | 1 | a0001c0003t0001g0135 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.4774-2106G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49612427 | ||||||
chr19:49612480
|
G | A | 5 | a0001c0009t0002g0144a0001c0009t0002g0145a0001c0009t0002g0146others(2): Show | 5 | HG02258.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.4774-2053G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49612480 | ||||||
chr19:49612488
|
G | C | 1 | a0001c0001t0001g0159 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.4774-2045G>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49612488 | ||||||
chr19:49612505
|
T | G | 5 | a0001c0009t0002g0144a0001c0009t0002g0145a0001c0009t0002g0146others(2): Show | 5 | HG02258.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.4774-2028T>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49612505 | ||||||
chr19:49612746
|
C | G | 1 | a0001c0001t0001g0188 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.4774-1787C>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49612746 | ||||||
chr19:49612812
|
G | A | 9 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(6): Show | 9 | HG01070.hp2 HG01255.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.4774-1721G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49612812 | ||||||
chr19:49612876
|
C | T | 2 | a0001c0016t0001g0155a0001c0016t0001g0156 | 2 | HG02451.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.4774-1657C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49612876 | ||||||
chr19:49612924
|
A | G | 2 | a0006c0010t0001g0131a0006c0010t0001g0132 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.4774-1609A>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49612924 | ||||||
chr19:49612984
|
T | G | 118 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0022others(115): Show | 118 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.4774-1549T>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49612984 | ||||||
chr19:49613057
|
A | C | 5 | a0001c0009t0002g0144a0001c0009t0002g0145a0001c0009t0002g0146others(2): Show | 5 | HG02258.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.4774-1476A>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49613057 | ||||||
chr19:49613145
|
C | T | 1 | a0001c0043t0012g0153 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.4774-1388C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49613145 | ||||||
chr19:49613284
|
G | A | 12 | a0002c0004t0004g0040a0002c0004t0004g0041a0002c0004t0004g0043others(9): Show | 12 | HG01070.hp1 HG01071.hp1 HG01175.hp2 others(9): Show |
intron_variant | MODIFIER | c.4774-1249G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49613284 | ||||||
chr19:49613330
|
C | CA | 13 | a0001c0001t0001g0019a0001c0001t0001g0258a0001c0001t0001g0264others(10): Show | 13 | HG00735.hp1 HG01099.hp1 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.4774-1181dupA | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr19 | 49613330 | |||||
chr19:49613330
|
CA | C | 79 | a0001c0001t0001g0159a0001c0001t0001g0162a0001c0001t0001g0163others(76): Show | 79 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(76): Show |
intron_variant | MODIFIER | c.4774-1181delA | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr19 | 49613330 | |||||
chr19:49613661
|
C | T | 1 | a0001c0001t0001g0242 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.4774-872C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49613661 | ||||||
chr19:49614033
|
C | T | 1 | a0001c0001t0001g0263 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.4774-500C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49614033 | ||||||
chr19:49614299
|
C | T | 1 | a0001c0052t0001g0245 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.4774-234C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49614299 | ||||||
chr19:49614347
|
C | T | 1 | a0001c0003t0001g0120 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.4774-186C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 6/13 | chr19 | 49614347 | ||||||
chr19:49614773
|
G | A | 1 | a0001c0001t0001g0291 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.4891-103G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 7/13 | chr19 | 49614773 | ||||||
chr19:49614804
|
A | G | 5 | a0001c0009t0002g0144a0001c0009t0002g0145a0001c0009t0002g0146others(2): Show | 5 | HG02258.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.4891-72A>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 7/13 | chr19 | 49614804 | ||||||
chr19:49615060
|
A | T | 5 | a0001c0009t0002g0144a0001c0009t0002g0145a0001c0009t0002g0146others(2): Show | 5 | HG02258.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.5024+51A>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 8/13 | chr19 | 49615060 | ||||||
chr19:49615133
|
G | C | 5 | a0001c0009t0002g0144a0001c0009t0002g0145a0001c0009t0002g0146others(2): Show | 5 | HG02258.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.5024+124G>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 8/13 | chr19 | 49615133 | ||||||
chr19:49615154
|
G | A | 5 | a0001c0009t0002g0144a0001c0009t0002g0145a0001c0009t0002g0146others(2): Show | 5 | HG02258.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.5024+145G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 8/13 | chr19 | 49615154 | ||||||
chr19:49615357
|
C | A | 279 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(276): Show | 285 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(282): Show |
intron_variant | MODIFIER | c.5024+348C>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 8/13 | chr19 | 49615357 | ||||||
chr19:49615379
|
CG | C | 12 | a0002c0004t0004g0040a0002c0004t0004g0041a0002c0004t0004g0043others(9): Show | 12 | HG01070.hp1 HG01071.hp1 HG01175.hp2 others(9): Show |
intron_variant | MODIFIER | c.5025-365delG | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 49615379 | |||||
chr19:49615434
|
C | G | 135 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0022others(132): Show | 135 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.5025-313C>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 8/13 | chr19 | 49615434 | ||||||
chr19:49615479
|
C | T | 2 | a0001c0001t0001g0003a0001c0001t0001g0202 | 3 | NA18982.hp1 NA18983.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.5025-268C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 8/13 | chr19 | 49615479 | ||||||
chr19:49615525
|
A | T | 6 | a0001c0002t0001g0129a0001c0009t0002g0144a0001c0009t0002g0145others(3): Show | 6 | HG02258.hp2 HG02896.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.5025-222A>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 8/13 | chr19 | 49615525 | ||||||
chr19:49615525
|
ACCCAGAG others(17): Show |
A | 12 | a0002c0004t0004g0040a0002c0004t0004g0041a0002c0004t0004g0043others(9): Show | 12 | HG01070.hp1 HG01071.hp1 HG01175.hp2 others(9): Show |
intron_variant | MODIFIER | c.5025-157_5025-134d others(26): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 49615525 | |||||
chr19:49615590
|
G | A | 17 | a0001c0002t0001g0141a0001c0002t0001g0142a0001c0002t0001g0143others(14): Show | 17 | HG01070.hp1 HG01071.hp1 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.5025-157G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 8/13 | chr19 | 49615590 | ||||||
chr19:49615590
|
G | GGTCAGAG others(67): Show |
5 | a0001c0009t0002g0144a0001c0009t0002g0145a0001c0009t0002g0146others(2): Show | 5 | HG02258.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.5025-157_5025-156i others(76): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 8/13 | chr19 | 49615590 | ||||||
chr19:49615590
|
G | GTCAGAGT others(17): Show |
142 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0022others(139): Show | 142 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(139): Show |
intron_variant | MODIFIER | c.5025-156_5025-133d others(26): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr19 | 49615590 | |||||
chr19:49615683
|
A | G | 5 | a0001c0009t0002g0144a0001c0009t0002g0145a0001c0009t0002g0146others(2): Show | 5 | HG02258.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.5025-64A>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 8/13 | chr19 | 49615683 | ||||||
chr19:49616369
|
CA | C | 135 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0022others(132): Show | 135 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.5497+151delA | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | chr19 | 49616369 | ||||||
chr19:49616372
|
TACAC | T | 135 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0022others(132): Show | 135 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.5497+154_5497+157d others(6): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | chr19 | 49616372 | ||||||
chr19:49616447
|
C | T | 4 | a0001c0003t0001g0024a0001c0003t0001g0025a0001c0003t0001g0026others(1): Show | 4 | HG00280.hp2 HG03239.hp1 NA20752.hp2 others(1): Show |
intron_variant | MODIFIER | c.5497+228C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | chr19 | 49616447 | ||||||
chr19:49616507
|
G | A | 1 | a0001c0001t0001g0187 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.5497+288G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | chr19 | 49616507 | ||||||
chr19:49616864
|
C | T | 4 | a0001c0002t0001g0129a0001c0002t0001g0140a0001c0002t0006g0138others(1): Show | 4 | HG02615.hp1 HG03471.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.5497+645C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | chr19 | 49616864 | ||||||
chr19:49616903
|
C | T | 1 | a0001c0001t0001g0187 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.5497+684C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | chr19 | 49616903 | ||||||
chr19:49616994
|
G | A | 1 | a0001c0001t0003g0207 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.5497+775G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | chr19 | 49616994 | ||||||
chr19:49617000
|
T | C | 5 | a0001c0009t0002g0144a0001c0009t0002g0145a0001c0009t0002g0146others(2): Show | 5 | HG02258.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.5497+781T>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | chr19 | 49617000 | ||||||
chr19:49617006
|
T | C | 2 | a0001c0002t0006g0138a0001c0002t0006g0139 | 2 | HG02615.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.5497+787T>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | chr19 | 49617006 | ||||||
chr19:49617025
|
C | T | 2 | a0001c0012t0001g0095a0001c0012t0001g0128 | 2 | HG02572.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.5497+806C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | chr19 | 49617025 | ||||||
chr19:49617130
|
CA | C | 7 | a0001c0001t0001g0167a0001c0001t0001g0237a0001c0001t0001g0277others(4): Show | 7 | HG01069.hp2 HG01099.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.5497+927delA | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr19 | 49617130 | |||||
chr19:49617155
|
A | G | 1 | a0001c0003t0001g0104 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.5497+936A>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | chr19 | 49617155 | ||||||
chr19:49617231
|
A | C | 16 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0022others(13): Show | 16 | HG00735.hp1 HG00735.hp2 HG01069.hp2 others(13): Show |
intron_variant | MODIFIER | c.5497+1012A>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | chr19 | 49617231 | ||||||
chr19:49617346
|
G | A | 29 | a0001c0001t0001g0247a0001c0002t0001g0047a0001c0002t0001g0141others(26): Show | 29 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.5497+1127G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | chr19 | 49617346 | ||||||
chr19:49617369
|
G | A | 7 | a0001c0009t0002g0144a0001c0009t0002g0145a0001c0009t0002g0146others(4): Show | 7 | HG02258.hp2 HG02451.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.5497+1150G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | chr19 | 49617369 | ||||||
chr19:49617492
|
T | C | 5 | a0001c0009t0002g0144a0001c0009t0002g0145a0001c0009t0002g0146others(2): Show | 5 | HG02258.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.5497+1273T>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | chr19 | 49617492 | ||||||
chr19:49617714
|
AG | A | 4 | a0001c0002t0001g0129a0001c0002t0001g0140a0001c0002t0006g0138others(1): Show | 4 | HG02615.hp1 HG03471.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.5497+1499delG | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr19 | 49617714 | |||||
chr19:49617727
|
T | C | 1 | a0001c0001t0001g0246 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.5497+1508T>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | chr19 | 49617727 | ||||||
chr19:49617762
|
A | C | 30 | a0001c0001t0001g0163a0001c0001t0001g0247a0001c0002t0001g0047others(27): Show | 30 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(27): Show |
intron_variant | MODIFIER | c.5497+1543A>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | chr19 | 49617762 | ||||||
chr19:49617765
|
C | T | 135 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0022others(132): Show | 135 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.5497+1546C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | chr19 | 49617765 | ||||||
chr19:49617772
|
G | C | 15 | a0001c0009t0002g0144a0001c0009t0002g0145a0001c0009t0002g0146others(12): Show | 15 | HG01070.hp1 HG01071.hp1 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.5497+1553G>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | chr19 | 49617772 | ||||||
chr19:49617824
|
G | A | 1 | a0001c0002t0001g0059 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.5497+1605G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | chr19 | 49617824 | ||||||
chr19:49617864
|
G | A | 1 | a0001c0002t0008g0127 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.5497+1645G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | chr19 | 49617864 | ||||||
chr19:49617954
|
C | T | 16 | a0001c0001t0001g0176a0001c0009t0002g0144a0001c0009t0002g0145others(13): Show | 16 | HG01070.hp1 HG01071.hp1 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.5497+1735C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | chr19 | 49617954 | ||||||
chr19:49618017
|
G | A | 52 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0188others(49): Show | 54 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(51): Show |
intron_variant | MODIFIER | c.5497+1798G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | chr19 | 49618017 | ||||||
chr19:49618058
|
A | G | 15 | a0001c0009t0002g0144a0001c0009t0002g0145a0001c0009t0002g0146others(12): Show | 15 | HG01070.hp1 HG01071.hp1 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.5497+1839A>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | chr19 | 49618058 | ||||||
chr19:49618092
|
G | T | 15 | a0001c0009t0002g0144a0001c0009t0002g0145a0001c0009t0002g0146others(12): Show | 15 | HG01070.hp1 HG01071.hp1 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.5497+1873G>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | chr19 | 49618092 | ||||||
chr19:49618155
|
C | T | 1 | a0001c0001t0001g0241 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.5497+1936C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | chr19 | 49618155 | ||||||
chr19:49618194
|
G | T | 25 | a0001c0001t0001g0247a0001c0002t0001g0047a0001c0002t0001g0154others(22): Show | 25 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.5497+1975G>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | chr19 | 49618194 | ||||||
chr19:49618294
|
T | C | 15 | a0001c0009t0002g0144a0001c0009t0002g0145a0001c0009t0002g0146others(12): Show | 15 | HG01070.hp1 HG01071.hp1 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.5498-2058T>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | chr19 | 49618294 | ||||||
chr19:49618387
|
T | C | 2 | a0001c0001t0001g0292a0001c0001t0001g0302 | 2 | HG01258.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.5498-1965T>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | chr19 | 49618387 | ||||||
chr19:49618410
|
G | A | 1 | a0001c0016t0001g0155 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.5498-1942G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | chr19 | 49618410 | ||||||
chr19:49618491
|
G | A | 16 | a0001c0001t0001g0157a0001c0002t0001g0028a0001c0002t0001g0052others(13): Show | 16 | HG01109.hp1 HG01433.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.5498-1861G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | chr19 | 49618491 | ||||||
chr19:49618713
|
C | T | 1 | a0001c0001t0001g0204 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.5498-1639C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | chr19 | 49618713 | ||||||
chr19:49618773
|
G | T | 1 | a0001c0003t0001g0115 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.5498-1579G>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | chr19 | 49618773 | ||||||
chr19:49618821
|
T | C | 152 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0022others(149): Show | 152 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.5498-1531T>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | chr19 | 49618821 | ||||||
chr19:49618965
|
A | T | 3 | a0001c0002t0001g0084a0001c0002t0006g0094a0014c0023t0001g0086 | 3 | HG00733.hp2 HG02257.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.5498-1387A>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | chr19 | 49618965 | ||||||
chr19:49619027
|
C | T | 1 | a0001c0001t0001g0230 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.5498-1325C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | chr19 | 49619027 | ||||||
chr19:49619047
|
A | G | 5 | a0001c0009t0002g0144a0001c0009t0002g0145a0001c0009t0002g0146others(2): Show | 5 | HG02258.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.5498-1305A>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | chr19 | 49619047 | ||||||
chr19:49619141
|
C | A | 1 | a0001c0001t0001g0173 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.5498-1211C>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | chr19 | 49619141 | ||||||
chr19:49619174
|
C | A | 3 | a0002c0004t0007g0034a0002c0004t0007g0035a0002c0004t0007g0036 | 3 | HG01070.hp1 HG01071.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.5498-1178C>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | chr19 | 49619174 | ||||||
chr19:49619224
|
G | GT | 127 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0021others(124): Show | 129 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.5498-1103dupT | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr19 | 49619224 | |||||
chr19:49619224
|
G | GTT | 43 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0163others(40): Show | 43 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(40): Show |
intron_variant | MODIFIER | c.5498-1104_5498-110 others(6): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr19 | 49619224 | |||||
chr19:49619224
|
G | GTTT | 14 | a0001c0001t0001g0157a0001c0002t0001g0028a0001c0002t0001g0054others(11): Show | 14 | HG01109.hp1 HG01433.hp1 HG02129.hp2 others(11): Show |
intron_variant | MODIFIER | c.5498-1105_5498-110 others(7): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr19 | 49619224 | |||||
chr19:49619224
|
G | GTTTT | 9 | a0001c0002t0001g0052a0001c0002t0001g0053a0001c0002t0001g0060others(6): Show | 9 | HG01346.hp2 HG02055.hp1 HG02135.hp1 others(6): Show |
intron_variant | MODIFIER | c.5498-1106_5498-110 others(8): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr19 | 49619224 | |||||
chr19:49619224
|
GTT | G | 12 | a0001c0009t0002g0144a0001c0009t0002g0146a0001c0020t0002g0147others(9): Show | 12 | HG01070.hp1 HG01071.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.5498-1104_5498-110 others(6): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr19 | 49619224 | |||||
chr19:49619224
|
GTTTTTTT others(5): Show |
G | 1 | a0019c0022t0001g0023 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.5498-1114_5498-110 others(16): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr19 | 49619224 | |||||
chr19:49619280
|
A | G | 15 | a0001c0009t0002g0144a0001c0009t0002g0145a0001c0009t0002g0146others(12): Show | 15 | HG01070.hp1 HG01071.hp1 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.5498-1072A>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | chr19 | 49619280 | ||||||
chr19:49619312
|
C | T | 1 | a0001c0001t0001g0260 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.5498-1040C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | chr19 | 49619312 | ||||||
chr19:49619501
|
G | C | 152 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0022others(149): Show | 152 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.5498-851G>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | chr19 | 49619501 | ||||||
chr19:49619535
|
C | CT | 81 | a0001c0001t0001g0012a0001c0001t0001g0159a0001c0001t0001g0161others(78): Show | 81 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.5498-794dupT | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr19 | 49619535 | |||||
chr19:49619535
|
C | CTT | 74 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0022others(71): Show | 74 | HG00423.hp2 HG00642.hp2 HG00735.hp1 others(71): Show |
intron_variant | MODIFIER | c.5498-795_5498-794d others(4): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr19 | 49619535 | |||||
chr19:49619535
|
C | CTTT | 25 | a0001c0001t0001g0274a0001c0002t0001g0058a0001c0002t0001g0061others(22): Show | 25 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(22): Show |
intron_variant | MODIFIER | c.5498-796_5498-794d others(5): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr19 | 49619535 | |||||
chr19:49619535
|
CTT | C | 9 | a0001c0016t0001g0155a0001c0016t0001g0156a0002c0004t0004g0040others(6): Show | 9 | HG02451.hp1 HG03654.hp1 HG03704.hp2 others(6): Show |
intron_variant | MODIFIER | c.5498-795_5498-794d others(4): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr19 | 49619535 | |||||
chr19:49619563
|
C | T | 15 | a0001c0009t0002g0144a0001c0009t0002g0145a0001c0009t0002g0146others(12): Show | 15 | HG01070.hp1 HG01071.hp1 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.5498-789C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | chr19 | 49619563 | ||||||
chr19:49619659
|
A | C | 1 | a0010c0032t0004g0046 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.5498-693A>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | chr19 | 49619659 | ||||||
chr19:49619703
|
G | A | 1 | a0001c0001t0001g0181 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.5498-649G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | chr19 | 49619703 | ||||||
chr19:49619715
|
A | G | 2 | a0001c0001t0001g0296a0003c0005t0001g0288 | 2 | HG01099.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.5498-637A>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | chr19 | 49619715 | ||||||
chr19:49619769
|
C | G | 1 | a0001c0003t0001g0098 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.5498-583C>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | chr19 | 49619769 | ||||||
chr19:49619770
|
G | A | 1 | a0001c0003t0001g0098 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.5498-582G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | chr19 | 49619770 | ||||||
chr19:49619771
|
A | G | 1 | a0001c0003t0001g0098 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.5498-581A>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | chr19 | 49619771 | ||||||
chr19:49619781
|
A | T | 1 | a0001c0003t0001g0098 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.5498-571A>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | chr19 | 49619781 | ||||||
chr19:49619792
|
T | C | 15 | a0001c0009t0002g0144a0001c0009t0002g0145a0001c0009t0002g0146others(12): Show | 15 | HG01070.hp1 HG01071.hp1 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.5498-560T>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | chr19 | 49619792 | ||||||
chr19:49619793
|
C | T | 1 | a0001c0002t0001g0093 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.5498-559C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | chr19 | 49619793 | ||||||
chr19:49619851
|
C | CT | 84 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0009others(81): Show | 87 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.5498-476dupT | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr19 | 49619851 | |||||
chr19:49619851
|
C | CTT | 45 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0168others(42): Show | 45 | HG00280.hp2 HG00544.hp1 HG00733.hp2 others(42): Show |
intron_variant | MODIFIER | c.5498-477_5498-476d others(4): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr19 | 49619851 | |||||
chr19:49619851
|
C | CTTT | 61 | a0001c0001t0001g0019a0001c0001t0001g0157a0001c0001t0001g0272others(58): Show | 61 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(58): Show |
intron_variant | MODIFIER | c.5498-478_5498-476d others(5): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr19 | 49619851 | |||||
chr19:49619851
|
C | CTTTT | 24 | a0001c0001t0001g0163a0001c0001t0001g0247a0001c0001t0003g0269others(21): Show | 24 | HG00423.hp2 HG00642.hp2 HG00738.hp2 others(21): Show |
intron_variant | MODIFIER | c.5498-479_5498-476d others(6): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr19 | 49619851 | |||||
chr19:49619851
|
CTTTT | C | 9 | a0002c0004t0004g0040a0002c0004t0004g0043a0002c0004t0004g0044others(6): Show | 9 | HG01070.hp1 HG01071.hp1 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.5498-479_5498-476d others(6): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr19 | 49619851 | |||||
chr19:49619851
|
CTTTTTTT others(6): Show |
C | 1 | a0001c0003t0001g0104 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.5498-488_5498-476d others(15): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr19 | 49619851 | |||||
chr19:49619997
|
C | T | 1 | a0002c0004t0004g0043 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.5498-355C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | chr19 | 49619997 | ||||||
chr19:49620009
|
C | T | 10 | a0002c0004t0004g0040a0002c0004t0004g0041a0002c0004t0004g0043others(7): Show | 10 | HG01070.hp1 HG01071.hp1 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.5498-343C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | chr19 | 49620009 | ||||||
chr19:49620055
|
G | A | 15 | a0001c0009t0002g0144a0001c0009t0002g0145a0001c0009t0002g0146others(12): Show | 15 | HG01070.hp1 HG01071.hp1 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.5498-297G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | chr19 | 49620055 | ||||||
chr19:49620055
|
G | T | 1 | a0001c0001t0001g0301 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.5498-297G>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | chr19 | 49620055 | ||||||
chr19:49620302
|
G | A | 15 | a0001c0009t0002g0144a0001c0009t0002g0145a0001c0009t0002g0146others(12): Show | 15 | HG01070.hp1 HG01071.hp1 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.5498-50G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | chr19 | 49620302 | ||||||
chr19:49620333
|
C | T | 10 | a0002c0004t0004g0040a0002c0004t0004g0041a0002c0004t0004g0043others(7): Show | 10 | HG01070.hp1 HG01071.hp1 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.5498-19C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 9/13 | chr19 | 49620333 | ||||||
chr19:49620499
|
A | AG | 36 | a0001c0001t0001g0012a0001c0001t0001g0157a0001c0001t0001g0159others(33): Show | 36 | HG00597.hp1 HG00597.hp2 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.5623+32dupG | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 49620499 | |||||
chr19:49620499
|
A | G | 1 | a0001c0001t0003g0270 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.5623+22A>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 10/13 | chr19 | 49620499 | ||||||
chr19:49620502
|
G | C | 7 | a0001c0001t0001g0189a0001c0001t0001g0212a0001c0001t0001g0239others(4): Show | 7 | HG00544.hp2 NA18957.hp2 NA18981.hp2 others(4): Show |
intron_variant | MODIFIER | c.5623+25G>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 10/13 | chr19 | 49620502 | ||||||
chr19:49620504
|
G | T | 15 | a0001c0009t0002g0144a0001c0009t0002g0145a0001c0009t0002g0146others(12): Show | 15 | HG01070.hp1 HG01071.hp1 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.5623+27G>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 10/13 | chr19 | 49620504 | ||||||
chr19:49620768
|
A | AGGGCTGG others(30): Show |
25 | a0001c0001t0001g0247a0001c0002t0001g0047a0001c0002t0001g0154others(22): Show | 25 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.5623+317_5623+353d others(39): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 49620768 | |||||
chr19:49620882
|
G | T | 1 | a0001c0001t0001g0230 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.5623+405G>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 10/13 | chr19 | 49620882 | ||||||
chr19:49620965
|
G | A | 1 | a0001c0001t0001g0241 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.5623+488G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 10/13 | chr19 | 49620965 | ||||||
chr19:49620982
|
A | G | 1 | a0001c0001t0001g0260 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.5623+505A>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 10/13 | chr19 | 49620982 | ||||||
chr19:49621012
|
G | A | 2 | a0001c0002t0006g0138a0001c0002t0006g0139 | 2 | HG02615.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.5624-513G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 10/13 | chr19 | 49621012 | ||||||
chr19:49621020
|
T | TGGGGGTC others(9): Show |
5 | a0001c0009t0002g0144a0001c0009t0002g0145a0001c0009t0002g0146others(2): Show | 5 | HG02258.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.5624-501_5624-500i others(18): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 49621020 | |||||
chr19:49621022
|
GGGTCTGG others(6): Show |
G | 10 | a0002c0004t0004g0040a0002c0004t0004g0041a0002c0004t0004g0043others(7): Show | 10 | HG01070.hp1 HG01071.hp1 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.5624-500_5624-488d others(15): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 49621022 | |||||
chr19:49621040
|
CTGAGGGA others(1): Show |
C | 10 | a0002c0004t0004g0040a0002c0004t0004g0041a0002c0004t0004g0043others(7): Show | 10 | HG01070.hp1 HG01071.hp1 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.5624-484_5624-477d others(10): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 10/13 | chr19 | 49621040 | ||||||
chr19:49621054
|
G | C | 10 | a0002c0004t0004g0040a0002c0004t0004g0041a0002c0004t0004g0043others(7): Show | 10 | HG01070.hp1 HG01071.hp1 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.5624-471G>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 10/13 | chr19 | 49621054 | ||||||
chr19:49621056
|
T | TG | 10 | a0002c0004t0004g0040a0002c0004t0004g0041a0002c0004t0004g0043others(7): Show | 10 | HG01070.hp1 HG01071.hp1 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.5624-465dupG | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 49621056 | |||||
chr19:49621061
|
C | T | 10 | a0002c0004t0004g0040a0002c0004t0004g0041a0002c0004t0004g0043others(7): Show | 10 | HG01070.hp1 HG01071.hp1 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.5624-464C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 10/13 | chr19 | 49621061 | ||||||
chr19:49621090
|
A | G | 15 | a0001c0009t0002g0144a0001c0009t0002g0145a0001c0009t0002g0146others(12): Show | 15 | HG01070.hp1 HG01071.hp1 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.5624-435A>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 10/13 | chr19 | 49621090 | ||||||
chr19:49621092
|
T | TG | 15 | a0001c0009t0002g0144a0001c0009t0002g0145a0001c0009t0002g0146others(12): Show | 15 | HG01070.hp1 HG01071.hp1 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.5624-429dupG | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 49621092 | |||||
chr19:49621097
|
C | T | 15 | a0001c0009t0002g0144a0001c0009t0002g0145a0001c0009t0002g0146others(12): Show | 15 | HG01070.hp1 HG01071.hp1 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.5624-428C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 10/13 | chr19 | 49621097 | ||||||
chr19:49621128
|
TGGGGGTC others(9): Show |
T | 15 | a0001c0009t0002g0144a0001c0009t0002g0145a0001c0009t0002g0146others(12): Show | 15 | HG01070.hp1 HG01071.hp1 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.5624-392_5624-377d others(18): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 49621128 | |||||
chr19:49621149
|
T | C | 15 | a0001c0009t0002g0144a0001c0009t0002g0145a0001c0009t0002g0146others(12): Show | 15 | HG01070.hp1 HG01071.hp1 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.5624-376T>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 10/13 | chr19 | 49621149 | ||||||
chr19:49621180
|
T | TG | 15 | a0001c0009t0002g0144a0001c0009t0002g0145a0001c0009t0002g0146others(12): Show | 15 | HG01070.hp1 HG01071.hp1 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.5624-341dupG | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 49621180 | |||||
chr19:49621185
|
C | T | 15 | a0001c0009t0002g0144a0001c0009t0002g0145a0001c0009t0002g0146others(12): Show | 15 | HG01070.hp1 HG01071.hp1 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.5624-340C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 10/13 | chr19 | 49621185 | ||||||
chr19:49621194
|
C | T | 15 | a0001c0009t0002g0144a0001c0009t0002g0145a0001c0009t0002g0146others(12): Show | 15 | HG01070.hp1 HG01071.hp1 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.5624-331C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 10/13 | chr19 | 49621194 | ||||||
chr19:49621201
|
T | A | 15 | a0001c0009t0002g0144a0001c0009t0002g0145a0001c0009t0002g0146others(12): Show | 15 | HG01070.hp1 HG01071.hp1 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.5624-324T>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 10/13 | chr19 | 49621201 | ||||||
chr19:49621205
|
G | A | 15 | a0001c0009t0002g0144a0001c0009t0002g0145a0001c0009t0002g0146others(12): Show | 15 | HG01070.hp1 HG01071.hp1 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.5624-320G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 10/13 | chr19 | 49621205 | ||||||
chr19:49621231
|
T | C | 15 | a0001c0009t0002g0144a0001c0009t0002g0145a0001c0009t0002g0146others(12): Show | 15 | HG01070.hp1 HG01071.hp1 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.5624-294T>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 10/13 | chr19 | 49621231 | ||||||
chr19:49621238
|
A | T | 15 | a0001c0009t0002g0144a0001c0009t0002g0145a0001c0009t0002g0146others(12): Show | 15 | HG01070.hp1 HG01071.hp1 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.5624-287A>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 10/13 | chr19 | 49621238 | ||||||
chr19:49621241
|
G | A | 1 | a0015c0025t0001g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.5624-284G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 10/13 | chr19 | 49621241 | ||||||
chr19:49621242
|
A | G | 15 | a0001c0009t0002g0144a0001c0009t0002g0145a0001c0009t0002g0146others(12): Show | 15 | HG01070.hp1 HG01071.hp1 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.5624-283A>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 10/13 | chr19 | 49621242 | ||||||
chr19:49621249
|
G | C | 15 | a0001c0009t0002g0144a0001c0009t0002g0145a0001c0009t0002g0146others(12): Show | 15 | HG01070.hp1 HG01071.hp1 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.5624-276G>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 10/13 | chr19 | 49621249 | ||||||
chr19:49621249
|
GGGCTGGG others(30): Show |
G | 1 | a0001c0002t0001g0061 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.5624-202_5624-166d others(39): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr19 | 49621249 | |||||
chr19:49621406
|
G | A | 118 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0022others(115): Show | 118 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.5624-119G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 10/13 | chr19 | 49621406 | ||||||
chr19:49621625
|
G | A | 1 | a0001c0001t0001g0248 | 1 | HG00544.hp2 | splice_region_variant&intron_variant | LOW | c.5721+3G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49621625 | ||||||
chr19:49621670
|
G | A | 15 | a0001c0009t0002g0144a0001c0009t0002g0145a0001c0009t0002g0146others(12): Show | 15 | HG01070.hp1 HG01071.hp1 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.5721+48G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49621670 | ||||||
chr19:49621689
|
C | T | 8 | a0001c0001t0001g0002a0001c0001t0001g0158a0001c0001t0001g0160others(5): Show | 9 | HG01243.hp2 HG02572.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.5721+67C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49621689 | ||||||
chr19:49621690
|
G | C | 1 | a0001c0002t0005g0088 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.5721+68G>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49621690 | ||||||
chr19:49621872
|
T | G | 15 | a0001c0009t0002g0144a0001c0009t0002g0145a0001c0009t0002g0146others(12): Show | 15 | HG01070.hp1 HG01071.hp1 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.5721+250T>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49621872 | ||||||
chr19:49621907
|
C | T | 2 | a0001c0002t0001g0142a0001c0002t0001g0143 | 2 | HG02622.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.5721+285C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49621907 | ||||||
chr19:49621935
|
T | C | 1 | a0001c0001t0001g0204 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.5721+313T>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49621935 | ||||||
chr19:49621960
|
G | C | 1 | a0001c0001t0001g0241 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.5721+338G>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49621960 | ||||||
chr19:49622033
|
TCAGGGCT others(8): Show |
T | 2 | a0001c0002t0001g0061a0002c0034t0001g0037 | 2 | HG01192.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.5721+415_5721+429d others(17): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 49622033 | |||||
chr19:49622319
|
G | A | 2 | a0001c0016t0001g0155a0001c0016t0001g0156 | 2 | HG02451.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.5721+697G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49622319 | ||||||
chr19:49622472
|
G | C | 1 | a0001c0052t0001g0245 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.5721+850G>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49622472 | ||||||
chr19:49622527
|
G | A | 2 | a0001c0001t0001g0304a0001c0001t0001g0305 | 2 | NA18969.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.5721+905G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49622527 | ||||||
chr19:49622555
|
G | A | 1 | a0001c0024t0003g0085 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.5721+933G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49622555 | ||||||
chr19:49622597
|
G | GA | 152 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0022others(149): Show | 152 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.5721+985dupA | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 49622597 | |||||
chr19:49622687
|
C | T | 10 | a0002c0004t0004g0040a0002c0004t0004g0041a0002c0004t0004g0043others(7): Show | 10 | HG01070.hp1 HG01071.hp1 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.5721+1065C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49622687 | ||||||
chr19:49622760
|
C | T | 2 | a0001c0016t0001g0155a0001c0016t0001g0156 | 2 | HG02451.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.5721+1138C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49622760 | ||||||
chr19:49622824
|
G | A | 130 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0022others(127): Show | 130 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.5721+1202G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49622824 | ||||||
chr19:49622840
|
C | T | 8 | a0001c0001t0001g0002a0001c0001t0001g0158a0001c0001t0001g0160others(5): Show | 9 | HG01243.hp2 HG02572.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.5721+1218C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49622840 | ||||||
chr19:49622846
|
C | T | 1 | a0001c0001t0001g0241 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.5721+1224C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49622846 | ||||||
chr19:49622869
|
G | A | 2 | a0001c0016t0001g0155a0001c0016t0001g0156 | 2 | HG02451.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.5721+1247G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49622869 | ||||||
chr19:49622891
|
C | CA | 94 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0022others(91): Show | 94 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.5721+1279dupA | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 49622891 | |||||
chr19:49622900
|
A | C | 1 | a0001c0001t0001g0229 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.5721+1278A>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49622900 | ||||||
chr19:49622901
|
AC | A | 5 | a0001c0002t0001g0093a0001c0003t0001g0024a0001c0003t0001g0107others(2): Show | 5 | HG01261.hp1 HG02615.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.5721+1280delC | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49622901 | ||||||
chr19:49622902
|
C | A | 147 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0022others(144): Show | 147 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(144): Show |
intron_variant | MODIFIER | c.5721+1280C>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49622902 | ||||||
chr19:49622906
|
A | AAAC | 14 | a0001c0002t0001g0047a0001c0002t0002g0048a0001c0002t0002g0051others(11): Show | 14 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(11): Show |
intron_variant | MODIFIER | c.5721+1285_5721+128 others(7): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 49622906 | |||||
chr19:49622906
|
A | AAACATAT | 4 | a0001c0002t0002g0077a0001c0002t0002g0078a0001c0002t0013g0063others(1): Show | 4 | HG02132.hp1 HG02273.hp1 NA18980.hp2 others(1): Show |
intron_variant | MODIFIER | c.5721+1285_5721+128 others(11): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 49622906 | |||||
chr19:49622906
|
A | AAACATAT others(2): Show |
4 | a0001c0001t0001g0157a0001c0002t0001g0028a0001c0002t0001g0056others(1): Show | 4 | HG01109.hp1 HG02129.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.5721+1285_5721+128 others(13): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 49622906 | |||||
chr19:49622906
|
A | AAACATAT others(4): Show |
2 | a0001c0002t0001g0052a0001c0002t0001g0054 | 2 | HG01433.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.5721+1285_5721+128 others(15): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 49622906 | |||||
chr19:49622906
|
A | AAACATAT others(6): Show |
2 | a0001c0002t0001g0057a0001c0002t0003g0064 | 2 | HG02135.hp1 NA18942.hp1 |
intron_variant | MODIFIER | c.5721+1285_5721+128 others(17): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 49622906 | |||||
chr19:49622906
|
A | AAACATAT others(10): Show |
1 | a0001c0002t0001g0150 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.5721+1285_5721+128 others(21): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 49622906 | |||||
chr19:49622907
|
ACATAT | A | 3 | a0001c0002t0008g0125a0001c0002t0008g0126a0001c0002t0008g0127 | 3 | HG01884.hp1 HG02109.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.5721+1286_5721+129 others(9): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49622907 | ||||||
chr19:49622908
|
C | A | 8 | a0001c0002t0001g0093a0001c0002t0002g0080a0001c0003t0001g0024others(5): Show | 8 | HG01261.hp1 HG01433.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.5721+1286C>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49622908 | ||||||
chr19:49622908
|
C | CAT | 5 | a0001c0001t0001g0187a0001c0001t0001g0198a0001c0001t0001g0263others(2): Show | 5 | HG00639.hp2 HG02071.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.5721+1306_5721+130 others(6): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 49622908 | |||||
chr19:49622908
|
C | CATAT | 3 | a0001c0001t0001g0003a0001c0001t0001g0202a0001c0001t0001g0257 | 4 | HG02056.hp1 NA18982.hp1 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.5721+1304_5721+130 others(8): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 49622908 | |||||
chr19:49622908
|
C | CATATATA others(3): Show |
1 | a0001c0002t0001g0058 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.5721+1298_5721+130 others(14): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 49622908 | |||||
chr19:49622908
|
C | T | 29 | a0001c0001t0001g0157a0001c0002t0001g0028a0001c0002t0001g0047others(26): Show | 29 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.5721+1286C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49622908 | ||||||
chr19:49622908
|
CAT | C | 7 | a0001c0001t0001g0002a0001c0001t0001g0160a0001c0001t0001g0161others(4): Show | 8 | HG01243.hp2 HG02572.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.5721+1306_5721+130 others(6): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 49622908 | |||||
chr19:49622908
|
CATAT | C | 11 | a0001c0001t0001g0159a0001c0001t0001g0169a0001c0001t0001g0171others(8): Show | 11 | HG01070.hp2 HG01255.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.5721+1304_5721+130 others(8): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 49622908 | |||||
chr19:49622910
|
T | C | 8 | a0001c0002t0001g0093a0001c0002t0002g0080a0001c0003t0001g0024others(5): Show | 8 | HG01261.hp1 HG01433.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.5721+1288T>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49622910 | ||||||
chr19:49622914
|
T | C | 3 | a0001c0002t0008g0125a0001c0002t0008g0126a0001c0002t0008g0127 | 3 | HG01884.hp1 HG02109.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.5721+1292T>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49622914 | ||||||
chr19:49622922
|
T | C | 2 | a0001c0001t0001g0275a0001c0001t0003g0270 | 2 | HG01516.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.5721+1300T>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49622922 | ||||||
chr19:49622924
|
T | G | 7 | a0001c0001t0001g0213a0001c0001t0001g0222a0001c0001t0001g0249others(4): Show | 7 | HG00673.hp2 HG01175.hp1 NA18950.hp1 others(4): Show |
intron_variant | MODIFIER | c.5721+1302T>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49622924 | ||||||
chr19:49622924
|
T | TAGAG | 3 | a0001c0001t0001g0244a0001c0001t0001g0283a0003c0005t0001g0284 | 3 | NA18982.hp2 NA19006.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.5721+1303_5721+130 others(8): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 49622924 | |||||
chr19:49622926
|
T | G | 24 | a0001c0001t0001g0006a0001c0001t0001g0013a0001c0001t0001g0213others(21): Show | 26 | HG00673.hp2 HG01106.hp2 HG01168.hp1 others(23): Show |
intron_variant | MODIFIER | c.5721+1304T>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49622926 | ||||||
chr19:49622926
|
T | TAG | 3 | a0001c0001t0001g0191a0001c0001t0001g0201a0001c0001t0001g0303 | 3 | HG01928.hp2 HG02155.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.5721+1305_5721+130 others(6): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 49622926 | |||||
chr19:49622926
|
TATAG | T | 9 | a0001c0001t0001g0170a0001c0001t0001g0173a0001c0001t0001g0178others(6): Show | 9 | HG00597.hp1 HG01255.hp2 HG02080.hp2 others(6): Show |
intron_variant | MODIFIER | c.5721+1306_5721+130 others(8): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 49622926 | |||||
chr19:49622926
|
TATAGAG | T | 3 | a0001c0001t0001g0292a0001c0001t0001g0297a0001c0001t0001g0302 | 3 | HG01258.hp1 HG01496.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.5721+1306_5721+131 others(10): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 49622926 | |||||
chr19:49622928
|
T | G | 57 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0013others(54): Show | 59 | HG00099.hp2 HG00408.hp2 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.5721+1306T>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49622928 | ||||||
chr19:49622928
|
T | TAGAG | 4 | a0001c0001t0001g0209a0001c0001t0001g0221a0001c0001t0003g0011others(1): Show | 4 | HG01934.hp2 HG02080.hp1 NA19065.hp1 others(1): Show |
intron_variant | MODIFIER | c.5721+1332_5721+133 others(8): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 49622928 | |||||
chr19:49622928
|
T | TATATATA others(9): Show |
1 | a0001c0002t0001g0152 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.5721+1307_5721+130 others(20): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 49622928 | |||||
chr19:49622928
|
T | TATATATA others(5): Show |
2 | a0001c0002t0001g0053a0001c0002t0001g0055 | 2 | NA18971.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.5721+1307_5721+130 others(16): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 49622928 | |||||
chr19:49622928
|
TAG | T | 4 | a0001c0001t0001g0158a0001c0001t0001g0165a0001c0001t0001g0167others(1): Show | 4 | HG00609.hp2 HG02622.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.5721+1334_5721+133 others(6): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 49622928 | |||||
chr19:49622928
|
TAGAG | T | 4 | a0001c0001t0001g0199a0001c0001t0001g0220a0001c0001t0001g0231others(1): Show | 4 | HG00099.hp1 HG01358.hp2 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.5721+1332_5721+133 others(8): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 49622928 | |||||
chr19:49622928
|
TAGAGAG | T | 12 | a0001c0001t0001g0287a0001c0001t0001g0289a0001c0001t0001g0290others(9): Show | 13 | HG00280.hp1 HG00738.hp1 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.5721+1330_5721+133 others(10): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 49622928 | |||||
chr19:49622930
|
G | T | 150 | a0001c0001t0001g0009a0001c0001t0001g0019a0001c0001t0001g0021others(147): Show | 150 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(147): Show |
intron_variant | MODIFIER | c.5721+1308G>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49622930 | ||||||
chr19:49622932
|
G | T | 112 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0022others(109): Show | 112 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.5721+1310G>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49622932 | ||||||
chr19:49622934
|
G | T | 84 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0157others(81): Show | 84 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.5721+1312G>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49622934 | ||||||
chr19:49622936
|
G | T | 51 | a0001c0001t0001g0163a0001c0001t0001g0199a0001c0001t0001g0262others(48): Show | 51 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(48): Show |
intron_variant | MODIFIER | c.5721+1314G>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49622936 | ||||||
chr19:49622938
|
G | T | 24 | a0001c0001t0001g0199a0001c0001t0001g0262a0001c0001t0001g0274others(21): Show | 24 | HG00438.hp1 HG00735.hp2 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.5721+1316G>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49622938 | ||||||
chr19:49622940
|
G | T | 13 | a0001c0001t0001g0262a0001c0002t0001g0154a0001c0003t0001g0113others(10): Show | 13 | HG00438.hp1 HG01943.hp2 HG02083.hp1 others(10): Show |
intron_variant | MODIFIER | c.5721+1318G>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49622940 | ||||||
chr19:49622940
|
GAGAGAGA others(11): Show |
G | 2 | a0001c0003t0001g0025a0001c0003t0001g0026 | 2 | HG00280.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.5721+1336_5721+135 others(22): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 49622940 | |||||
chr19:49622942
|
G | T | 3 | a0001c0001t0001g0262a0001c0003t0001g0133a0001c0003t0001g0134 | 3 | HG00438.hp1 HG02132.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.5721+1320G>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49622942 | ||||||
chr19:49622944
|
G | A | 1 | a0001c0002t0002g0051 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.5721+1322G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49622944 | ||||||
chr19:49622944
|
GAGAGAGA others(7): Show |
G | 3 | a0001c0003t0001g0119a0005c0013t0005g0089a0005c0013t0005g0090 | 3 | HG02809.hp1 HG02922.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.5721+1336_5721+134 others(18): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 49622944 | |||||
chr19:49622946
|
GAGAGAGA others(5): Show |
G | 11 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0022others(8): Show | 11 | HG00733.hp2 HG00735.hp1 HG01167.hp2 others(8): Show |
intron_variant | MODIFIER | c.5721+1336_5721+134 others(16): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 49622946 | |||||
chr19:49622948
|
GAGAGAGA others(3): Show |
G | 7 | a0001c0002t0006g0138a0001c0002t0006g0139a0001c0003t0001g0107others(4): Show | 7 | HG02615.hp1 HG02970.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.5721+1336_5721+134 others(14): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 49622948 | |||||
chr19:49622950
|
GAGAGAGA others(1): Show |
G | 25 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(22): Show | 25 | HG00735.hp2 HG01069.hp2 HG01071.hp2 others(22): Show |
intron_variant | MODIFIER | c.5721+1336_5721+134 others(12): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 49622950 | |||||
chr19:49622952
|
GAGAGAA | G | 16 | a0001c0001t0001g0300a0001c0002t0001g0093a0001c0002t0001g0129others(13): Show | 16 | HG00544.hp1 HG01070.hp1 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.5721+1336_5721+134 others(10): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 49622952 | |||||
chr19:49622954
|
GAGAA | G | 22 | a0001c0001t0001g0168a0001c0001t0001g0262a0001c0002t0001g0061others(19): Show | 22 | HG00140.hp2 HG01168.hp2 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.5721+1336_5721+133 others(8): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 49622954 | |||||
chr19:49622956
|
G | A | 1 | a0002c0015t0001g0039 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.5721+1334G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49622956 | ||||||
chr19:49622956
|
GAA | G | 12 | a0001c0001t0001g0163a0001c0002t0001g0141a0001c0002t0002g0151others(9): Show | 12 | HG00642.hp1 HG01943.hp2 HG02040.hp2 others(9): Show |
intron_variant | MODIFIER | c.5721+1336_5721+133 others(6): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 49622956 | |||||
chr19:49622958
|
A | G | 55 | a0001c0001t0001g0157a0001c0001t0001g0247a0001c0002t0001g0028others(52): Show | 55 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(52): Show |
intron_variant | MODIFIER | c.5721+1336A>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49622958 | ||||||
chr19:49622974
|
G | T | 3 | a0001c0001t0001g0167a0001c0001t0001g0273a0001c0001t0001g0289 | 3 | HG01106.hp1 HG02602.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.5721+1352G>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49622974 | ||||||
chr19:49623201
|
A | G | 1 | a0002c0004t0004g0043 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.5721+1579A>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49623201 | ||||||
chr19:49623265
|
A | G | 3 | a0001c0016t0001g0155a0001c0016t0001g0156a0015c0025t0001g0027 | 3 | HG02109.hp2 HG02451.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.5722-1579A>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49623265 | ||||||
chr19:49623278
|
G | T | 1 | a0001c0003t0001g0098 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.5722-1566G>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49623278 | ||||||
chr19:49623314
|
T | C | 19 | a0001c0001t0001g0262a0001c0003t0001g0100a0001c0003t0001g0101others(16): Show | 19 | HG00140.hp2 HG00438.hp1 HG00642.hp1 others(16): Show |
intron_variant | MODIFIER | c.5722-1530T>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49623314 | ||||||
chr19:49623319
|
C | T | 1 | a0001c0031t0001g0096 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.5722-1525C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49623319 | ||||||
chr19:49623328
|
G | A | 1 | a0001c0044t0001g0218 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.5722-1516G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49623328 | ||||||
chr19:49623423
|
A | G | 1 | a0001c0001t0001g0301 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.5722-1421A>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49623423 | ||||||
chr19:49623488
|
C | T | 1 | a0003c0005t0001g0232 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.5722-1356C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49623488 | ||||||
chr19:49623494
|
T | C | 1 | a0001c0003t0001g0119 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.5722-1350T>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49623494 | ||||||
chr19:49623573
|
A | G | 125 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0022others(122): Show | 125 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.5722-1271A>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49623573 | ||||||
chr19:49623619
|
G | A | 2 | a0001c0016t0001g0155a0001c0016t0001g0156 | 2 | HG02451.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.5722-1225G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49623619 | ||||||
chr19:49623631
|
T | TA | 6 | a0001c0001t0001g0215a0001c0001t0001g0261a0001c0002t0002g0051others(3): Show | 6 | HG01884.hp1 HG02155.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.5722-1197dupA | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 49623631 | |||||
chr19:49623631
|
TA | T | 9 | a0001c0001t0001g0164a0001c0001t0001g0243a0001c0001t0001g0268others(6): Show | 9 | HG00738.hp1 HG01081.hp2 HG01167.hp2 others(6): Show |
intron_variant | MODIFIER | c.5722-1197delA | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 49623631 | |||||
chr19:49623729
|
ATAGATGG others(59): Show |
A | 4 | a0001c0001t0001g0157a0001c0002t0001g0052a0001c0002t0001g0054others(1): Show | 4 | HG01109.hp1 HG01433.hp1 HG02055.hp1 others(1): Show |
intron_variant | MODIFIER | c.5722-1095_5722-103 others(70): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 49623729 | |||||
chr19:49623799
|
A | ATGGTTAG others(125): Show |
12 | a0001c0002t0001g0001a0001c0002t0001g0084a0001c0002t0001g0091others(9): Show | 12 | HG00733.hp2 HG01261.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.5722-1016_5722-885 others(135): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 49623799 | |||||
chr19:49623799
|
ATGGTTAG others(59): Show |
A | 17 | a0001c0009t0002g0144a0001c0009t0002g0145a0001c0009t0002g0146others(14): Show | 17 | HG01070.hp1 HG01071.hp1 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.5722-950_5722-885d others(68): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 49623799 | |||||
chr19:49623815
|
T | C | 2 | a0001c0002t0001g0061a0002c0034t0001g0037 | 2 | HG01192.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.5722-1029T>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49623815 | ||||||
chr19:49623832
|
C | CTGGTTAG others(493): Show |
1 | a0015c0025t0001g0027 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.5722-951_5722-950i others(502): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 49623832 | |||||
chr19:49623898
|
C | CTGGTTAG others(26): Show |
1 | a0001c0021t0001g0050 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.5722-915_5722-883d others(35): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 49623898 | |||||
chr19:49623934
|
G | T | 5 | a0001c0006t0001g0031a0001c0006t0001g0032a0001c0006t0001g0033others(2): Show | 5 | HG01346.hp2 HG02486.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.5722-910G>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49623934 | ||||||
chr19:49623947
|
T | C | 1 | a0001c0001t0001g0250 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.5722-897T>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49623947 | ||||||
chr19:49623957
|
G | A | 1 | a0003c0005t0001g0216 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.5722-887G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49623957 | ||||||
chr19:49623981
|
A | G | 1 | a0001c0001t0001g0244 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.5722-863A>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49623981 | ||||||
chr19:49623995
|
G | A | 142 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0022others(139): Show | 142 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(139): Show |
intron_variant | MODIFIER | c.5722-849G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49623995 | ||||||
chr19:49624080
|
A | G | 26 | a0001c0001t0001g0247a0001c0002t0001g0047a0001c0002t0001g0154others(23): Show | 26 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(23): Show |
intron_variant | MODIFIER | c.5722-764A>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49624080 | ||||||
chr19:49624136
|
G | C | 1 | a0021c0038t0001g0285 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.5722-708G>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49624136 | ||||||
chr19:49624229
|
GTAGGTGG others(26): Show |
G | 2 | a0001c0001t0001g0272a0001c0001t0001g0276 | 2 | HG02683.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.5722-595_5722-563d others(35): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 49624229 | |||||
chr19:49624262
|
A | ATAGGTGG others(26): Show |
1 | a0001c0001t0001g0260 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.5722-565_5722-533d others(35): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 49624262 | |||||
chr19:49624279
|
GGCTGAGA others(26): Show |
G | 3 | a0001c0002t0001g0141a0001c0002t0001g0142a0001c0002t0001g0143 | 3 | HG02622.hp1 HG02717.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.5722-516_5722-484d others(35): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 49624279 | |||||
chr19:49624312
|
T | G | 311 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(308): Show | 318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.5722-532T>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49624312 | ||||||
chr19:49624317
|
A | G | 3 | a0001c0002t0008g0125a0001c0002t0008g0126a0001c0002t0008g0127 | 3 | HG01884.hp1 HG02109.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.5722-527A>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49624317 | ||||||
chr19:49624328
|
G | GTGGGTGG others(295): Show |
3 | a0001c0002t0008g0125a0001c0002t0008g0126a0001c0002t0008g0127 | 3 | HG01884.hp1 HG02109.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.5722-515_5722-514i others(304): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 49624328 | |||||
chr19:49624328
|
GTAGGTGG others(26): Show |
G | 1 | a0001c0001t0001g0239 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.5722-499_5722-467d others(35): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 49624328 | |||||
chr19:49624345
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T | G | 3 | a0001c0002t0001g0141a0001c0002t0001g0142a0001c0002t0001g0143 | 3 | HG02622.hp1 HG02717.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.5722-499T>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49624345 | ||||||
chr19:49624413
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C | T | 125 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0022others(122): Show | 125 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.5722-431C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49624413 | ||||||
chr19:49624416
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A | AGAATTCT others(26): Show |
1 | a0001c0001t0001g0299 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.5722-401_5722-400i others(35): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 49624416 | |||||
chr19:49624416
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A | AGAATTCT others(59): Show |
2 | a0001c0001t0001g0304a0001c0001t0001g0305 | 2 | NA18969.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.5722-400_5722-335d others(68): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 49624416 | |||||
chr19:49624450
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A | G | 1 | a0001c0001t0001g0176 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.5722-394A>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49624450 | ||||||
chr19:49624455
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T | C | 1 | a0001c0001t0001g0176 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.5722-389T>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49624455 | ||||||
chr19:49624460
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G | A | 1 | a0001c0001t0001g0176 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.5722-384G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49624460 | ||||||
chr19:49624466
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G | GGTTAGGA others(26): Show |
1 | a0001c0001t0001g0176 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.5722-363_5722-362i others(35): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 49624466 | |||||
chr19:49624493
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G | A | 1 | a0001c0003t0001g0119 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.5722-351G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49624493 | ||||||
chr19:49624497
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GTGGTTAG others(26): Show |
G | 3 | a0001c0003t0001g0098a0001c0003t0001g0099a0001c0003t0002g0149 | 3 | HG02145.hp2 HG02896.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.5722-329_5722-297d others(35): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 49624497 | |||||
chr19:49624508
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G | A | 1 | a0001c0001t0001g0187 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.5722-336G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49624508 | ||||||
chr19:49624531
|
T | C | 1 | a0019c0022t0001g0023 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.5722-313T>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49624531 | ||||||
chr19:49624559
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ATAGATGG others(26): Show |
A | 1 | a0001c0049t0001g0278 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.5722-247_5722-215d others(35): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr19 | 49624559 | |||||
chr19:49624710
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C | G | 1 | a0001c0002t0008g0125 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.5722-134C>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49624710 | ||||||
chr19:49624795
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G | A | 1 | a0001c0001t0001g0213 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.5722-49G>A | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49624795 | ||||||
chr19:49624814
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G | T | 17 | a0001c0009t0002g0144a0001c0009t0002g0145a0001c0009t0002g0146others(14): Show | 17 | HG01070.hp1 HG01071.hp1 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.5722-30G>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49624814 | ||||||
chr19:49624815
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C | T | 17 | a0001c0009t0002g0144a0001c0009t0002g0145a0001c0009t0002g0146others(14): Show | 17 | HG01070.hp1 HG01071.hp1 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.5722-29C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49624815 | ||||||
chr19:49624820
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A | G | 15 | a0001c0001t0001g0157a0001c0001t0001g0163a0001c0002t0001g0028others(12): Show | 15 | HG01109.hp1 HG01433.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.5722-24A>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 11/13 | chr19 | 49624820 | ||||||
chr19:49625086
|
C | T | 1 | a0001c0001t0001g0229 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.5869-19C>T | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 12/13 | chr19 | 49625086 | ||||||
chr19:49625265
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T | C | 17 | a0001c0009t0002g0144a0001c0009t0002g0145a0001c0009t0002g0146others(14): Show | 17 | HG01070.hp1 HG01071.hp1 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.5964+65T>C | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 13/13 | chr19 | 49625265 | ||||||
chr19:49625286
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A | G | 142 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0022others(139): Show | 142 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(139): Show |
intron_variant | MODIFIER | c.5964+86A>G | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 13/13 | chr19 | 49625286 | ||||||
chr19:49625393
|
GCCCCAGC others(33): Show |
G | 5 | a0001c0009t0002g0144a0001c0009t0002g0145a0001c0009t0002g0146others(2): Show | 5 | HG02258.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.5965-61_5965-22del others(40): Show |
PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr19 | 49625393 | |||||
chr19:49625441
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G | GC | 5 | a0001c0009t0002g0144a0001c0009t0002g0145a0001c0009t0002g0146others(2): Show | 5 | HG02258.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.5965-18dupC | PRR12 | ENSG00000126464.15 | transcript | ENST00000418929.7 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr19 | 49625441 |