geneid | 25797 |
---|---|
ensemblid | ENSG00000115828.17 |
hgncid | 9753 |
symbol | QPCT |
name | glutaminyl-peptide cyclotransferase |
refseq_nuc | NM_012413.4 |
refseq_prot | NP_036545.1 |
ensembl_nuc | ENST00000338415.8 |
ensembl_prot | ENSP00000344829.3 |
mane_status | MANE Select |
chr | chr2 |
start | 37344630 |
end | 37373322 |
strand | + |
ver | v1.2 |
region | chr2:37344630-37373322 |
region5000 | chr2:37339630-37378322 |
regionname0 | QPCT_chr2_37344630_37373322 |
regionname5000 | QPCT_chr2_37339630_37378322 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 361 | 318 | 89 | 64 | 111 | 12 | 40 | 86 | QPCT_chr2_37339630_37378322 | QPCT | copy fasta | chr2 | 37339630 | 37378322 |
a0002 | 0/0 | 361 | 71 | 0 | 9 | 62 | 0 | 0 | 48 | QPCT_chr2_37339630_37378322 | QPCT | copy fasta | chr2 | 37339630 | 37378322 |
a0003 | 0/0 | 361 | 32 | 0 | 4 | 25 | 2 | 1 | 22 | QPCT_chr2_37339630_37378322 | QPCT | copy fasta | chr2 | 37339630 | 37378322 |
a0004 | 0/0 | 361 | 19 | 5 | 3 | 10 | 0 | 1 | 8 | QPCT_chr2_37339630_37378322 | QPCT | copy fasta | chr2 | 37339630 | 37378322 |
a0005 | 0/0 | 361 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | QPCT_chr2_37339630_37378322 | QPCT | copy fasta | chr2 | 37339630 | 37378322 |
a0006 | 0/0 | 361 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | QPCT_chr2_37339630_37378322 | QPCT | copy fasta | chr2 | 37339630 | 37378322 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1086 | 262 | 42 | 60 | 110 | 10 | 38 | QPCT_chr2_37339630_37378322 | QPCT | copy fasta | chr2 | 37339630 | 37378322 |
c0002 | 0/0 | 1086 | 71 | 0 | 9 | 62 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | copy fasta | chr2 | 37339630 | 37378322 |
c0003 | 0/0 | 1086 | 55 | 47 | 4 | 0 | 2 | 2 | QPCT_chr2_37339630_37378322 | QPCT | copy fasta | chr2 | 37339630 | 37378322 |
c0004 | 0/0 | 1086 | 32 | 0 | 4 | 25 | 2 | 1 | QPCT_chr2_37339630_37378322 | QPCT | copy fasta | chr2 | 37339630 | 37378322 |
c0005 | 0/0 | 1086 | 19 | 5 | 3 | 10 | 0 | 1 | QPCT_chr2_37339630_37378322 | QPCT | copy fasta | chr2 | 37339630 | 37378322 |
c0006 | 0/0 | 1086 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | copy fasta | chr2 | 37339630 | 37378322 |
c0007 | 0/0 | 1086 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | copy fasta | chr2 | 37339630 | 37378322 |
c0008 | 0/0 | 1086 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | copy fasta | chr2 | 37339630 | 37378322 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 598 | 300 | 75 | 63 | 116 | 10 | 35 | QPCT_chr2_37339630_37378322 | QPCT | copy fasta | chr2 | 37339630 | 37378322 |
t0002 | 0/0 | 598 | 119 | 9 | 15 | 92 | 2 | 1 | QPCT_chr2_37339630_37378322 | QPCT | copy fasta | chr2 | 37339630 | 37378322 |
t0003 | 0/0 | 596 | 9 | 9 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | copy fasta | chr2 | 37339630 | 37378322 |
t0004 | 1/0 | 598 | 6 | 0 | 1 | 0 | 0 | 4 | QPCT_chr2_37339630_37378322 | QPCT | copy fasta | chr2 | 37339630 | 37378322 |
t0005 | 0/0 | 598 | 5 | 1 | 1 | 0 | 2 | 1 | QPCT_chr2_37339630_37378322 | QPCT | copy fasta | chr2 | 37339630 | 37378322 |
t0006 | 0/0 | 598 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | copy fasta | chr2 | 37339630 | 37378322 |
t0007 | 0/0 | 598 | 1 | 0 | 0 | 0 | 0 | 1 | QPCT_chr2_37339630_37378322 | QPCT | copy fasta | chr2 | 37339630 | 37378322 |
t0008 | 0/0 | 598 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | copy fasta | chr2 | 37339630 | 37378322 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 6 | 0 | 5 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0002 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0003 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0004 | 0/0 | 5 | 0 | 2 | 0 | 0 | 3 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0005 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0006 | 0/1 | 4 | 0 | 2 | 0 | 0 | 1 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0007 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0011 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0012 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0016 | 0/0 | 3 | 0 | 1 | 1 | 1 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0026 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0033 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0034 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0039 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0042 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0329 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0340 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0350 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0356 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0357 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0358 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1086 | 262 | 42 | 60 | 110 | 10 | 38 | QPCT_chr2_37339630_37378322 | QPCT | copy fasta | chr2 | 37339630 | 37378322 |
a0001c0003 | 0/0 | 1086 | 55 | 47 | 4 | 0 | 2 | 2 | QPCT_chr2_37339630_37378322 | QPCT | copy fasta | chr2 | 37339630 | 37378322 |
a0001c0006 | 0/0 | 1086 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | copy fasta | chr2 | 37339630 | 37378322 |
a0002c0002 | 0/0 | 1086 | 71 | 0 | 9 | 62 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | copy fasta | chr2 | 37339630 | 37378322 |
a0003c0004 | 0/0 | 1086 | 32 | 0 | 4 | 25 | 2 | 1 | QPCT_chr2_37339630_37378322 | QPCT | copy fasta | chr2 | 37339630 | 37378322 |
a0004c0005 | 0/0 | 1086 | 19 | 5 | 3 | 10 | 0 | 1 | QPCT_chr2_37339630_37378322 | QPCT | copy fasta | chr2 | 37339630 | 37378322 |
a0005c0007 | 0/0 | 1086 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | copy fasta | chr2 | 37339630 | 37378322 |
a0006c0008 | 0/0 | 1086 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | copy fasta | chr2 | 37339630 | 37378322 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 1683 | 240 | 35 | 57 | 105 | 10 | 32 | QPCT_chr2_37339630_37378322 | QPCT | copy fasta | chr2 | 37339630 | 37378322 |
a0001c0001t0002 | 0/0 | 1683 | 12 | 5 | 1 | 5 | 0 | 1 | QPCT_chr2_37339630_37378322 | QPCT | copy fasta | chr2 | 37339630 | 37378322 |
a0001c0001t0003 | 0/0 | 1681 | 2 | 2 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | copy fasta | chr2 | 37339630 | 37378322 |
a0001c0001t0004 | 1/0 | 1683 | 6 | 0 | 1 | 0 | 0 | 4 | QPCT_chr2_37339630_37378322 | QPCT | copy fasta | chr2 | 37339630 | 37378322 |
a0001c0001t0005 | 0/0 | 1683 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | copy fasta | chr2 | 37339630 | 37378322 |
a0001c0001t0007 | 0/0 | 1683 | 1 | 0 | 0 | 0 | 0 | 1 | QPCT_chr2_37339630_37378322 | QPCT | copy fasta | chr2 | 37339630 | 37378322 |
a0001c0003t0001 | 0/0 | 1683 | 41 | 36 | 3 | 0 | 0 | 2 | QPCT_chr2_37339630_37378322 | QPCT | copy fasta | chr2 | 37339630 | 37378322 |
a0001c0003t0002 | 0/0 | 1683 | 5 | 4 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | copy fasta | chr2 | 37339630 | 37378322 |
a0001c0003t0003 | 0/0 | 1681 | 6 | 6 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | copy fasta | chr2 | 37339630 | 37378322 |
a0001c0003t0005 | 0/0 | 1683 | 3 | 1 | 0 | 0 | 2 | 0 | QPCT_chr2_37339630_37378322 | QPCT | copy fasta | chr2 | 37339630 | 37378322 |
a0001c0006t0001 | 0/0 | 1683 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | copy fasta | chr2 | 37339630 | 37378322 |
a0002c0002t0002 | 0/0 | 1683 | 70 | 0 | 9 | 61 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | copy fasta | chr2 | 37339630 | 37378322 |
a0002c0002t0008 | 0/0 | 1683 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | copy fasta | chr2 | 37339630 | 37378322 |
a0003c0004t0002 | 0/0 | 1683 | 31 | 0 | 4 | 25 | 2 | 0 | QPCT_chr2_37339630_37378322 | QPCT | copy fasta | chr2 | 37339630 | 37378322 |
a0003c0004t0005 | 0/0 | 1683 | 1 | 0 | 0 | 0 | 0 | 1 | QPCT_chr2_37339630_37378322 | QPCT | copy fasta | chr2 | 37339630 | 37378322 |
a0004c0005t0001 | 0/0 | 1683 | 17 | 4 | 3 | 9 | 0 | 1 | QPCT_chr2_37339630_37378322 | QPCT | copy fasta | chr2 | 37339630 | 37378322 |
a0004c0005t0002 | 0/0 | 1683 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | copy fasta | chr2 | 37339630 | 37378322 |
a0004c0005t0003 | 0/0 | 1681 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | copy fasta | chr2 | 37339630 | 37378322 |
a0005c0007t0001 | 0/0 | 1683 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | copy fasta | chr2 | 37339630 | 37378322 |
a0006c0008t0006 | 0/0 | 1683 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | copy fasta | chr2 | 37339630 | 37378322 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0005 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0006 | 0/1 | 4 | 0 | 2 | 0 | 0 | 1 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0007 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0012 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0016 | 0/0 | 3 | 0 | 1 | 1 | 1 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0350 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0001g0358 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0002g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0002g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0002g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0002g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0002g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0002g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0002g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0002g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0003g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0003g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0004g0004 | 0/0 | 4 | 0 | 1 | 0 | 0 | 3 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0004g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0004g0357 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0005g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0001t0007g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0003t0001g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0003t0001g0026 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0003t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0003t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0003t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0003t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0003t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0003t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0003t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0003t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0003t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0003t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0003t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0003t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0003t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0003t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0003t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0003t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0003t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0003t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0003t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0003t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0003t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0003t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0003t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0003t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0003t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0003t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0003t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0003t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0003t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0003t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0003t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0003t0001g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0003t0001g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0003t0001g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0003t0001g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0003t0002g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0003t0002g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0003t0002g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0003t0002g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0003t0002g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0003t0003g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0003t0003g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0003t0003g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0003t0003g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0003t0003g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0003t0003g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0003t0005g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0003t0005g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0003t0005g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0001c0006t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0002c0002t0002g0001 | 0/0 | 6 | 0 | 5 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0002c0002t0002g0003 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0002c0002t0002g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0002c0002t0002g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0002c0002t0002g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0002c0002t0002g0033 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0002c0002t0002g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0002c0002t0002g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0002c0002t0002g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0002c0002t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0002c0002t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0002c0002t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0002c0002t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0002c0002t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0002c0002t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0002c0002t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0002c0002t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0002c0002t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0002c0002t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0002c0002t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0002c0002t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0002c0002t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0002c0002t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0002c0002t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0002c0002t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0002c0002t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0002c0002t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0002c0002t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0002c0002t0002g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0002c0002t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0002c0002t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0002c0002t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0002c0002t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0002c0002t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0002c0002t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0002c0002t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0002c0002t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0002c0002t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0002c0002t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0002c0002t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0002c0002t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0002c0002t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0002c0002t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0002c0002t0002g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0002c0002t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0002c0002t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0002c0002t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0002c0002t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0002c0002t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0002c0002t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0002c0002t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0002c0002t0002g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0002c0002t0008g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0003c0004t0002g0002 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0003c0004t0002g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0003c0004t0002g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0003c0004t0002g0042 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0003c0004t0002g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0003c0004t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0003c0004t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0003c0004t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0003c0004t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0003c0004t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0003c0004t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0003c0004t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0003c0004t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0003c0004t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0003c0004t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0003c0004t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0003c0004t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0003c0004t0002g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0003c0004t0002g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0003c0004t0002g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0003c0004t0002g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0003c0004t0002g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0003c0004t0002g0356 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0003c0004t0005g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0004c0005t0001g0034 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0004c0005t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0004c0005t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0004c0005t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0004c0005t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0004c0005t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0004c0005t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0004c0005t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0004c0005t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0004c0005t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0004c0005t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0004c0005t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0004c0005t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0004c0005t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0004c0005t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0004c0005t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0004c0005t0003g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0005c0007t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
a0006c0008t0006g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0039 | EUR | GBR | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0076 | EUR | GBR | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0329 | EUR | GBR | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0012 | EUR | GBR | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG00280 | hp1 | a0001 | c0003 | t0005 | g0127 | EUR | FIN | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0012 | EUR | FIN | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | CHS | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG00438 | hp2 | a0004 | c0005 | t0001 | g0285 | EAS | CHS | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | CHS | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG00544 | hp2 | a0002 | c0002 | t0002 | g0257 | EAS | CHS | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG00558 | hp1 | a0003 | c0004 | t0002 | g0020 | EAS | CHS | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | CHS | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG00597 | hp1 | a0003 | c0004 | t0002 | g0097 | EAS | CHS | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | CHS | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG00621 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | CHS | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG00639 | hp1 | a0001 | c0001 | t0002 | g0317 | AMR | PUR | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG00639 | hp2 | a0004 | c0005 | t0001 | g0289 | AMR | PUR | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG00673 | hp1 | a0002 | c0002 | t0002 | g0280 | EAS | CHS | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | CHS | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0215 | AMR | PUR | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG00738 | hp1 | a0003 | c0004 | t0002 | g0355 | AMR | PUR | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG00738 | hp2 | a0001 | c0003 | t0001 | g0149 | AMR | PUR | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0197 | AMR | PUR | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG00741 | hp2 | a0001 | c0001 | t0005 | g0336 | AMR | PUR | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG01069 | hp2 | a0003 | c0004 | t0002 | g0356 | AMR | PUR | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0226 | AMR | PUR | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | PUR | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0358 | AMR | PUR | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0323 | AMR | PUR | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0213 | AMR | PUR | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG01106 | hp1 | a0004 | c0005 | t0001 | g0138 | AMR | PUR | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0343 | AMR | PUR | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0333 | AMR | PUR | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0339 | AMR | PUR | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0325 | AMR | PUR | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | PUR | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | PUR | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0211 | AMR | PUR | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | PUR | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG01192 | hp2 | a0004 | c0005 | t0001 | g0034 | AMR | PUR | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG01243 | hp1 | a0001 | c0003 | t0001 | g0152 | AMR | PUR | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0204 | AMR | PUR | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0334 | AMR | CLM | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG01255 | hp2 | a0003 | c0004 | t0002 | g0045 | AMR | CLM | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | CLM | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | CLM | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG01257 | hp2 | a0002 | c0002 | t0002 | g0001 | AMR | CLM | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0351 | AMR | CLM | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0314 | AMR | CLM | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | CLM | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | CLM | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0312 | AMR | CLM | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG01361 | hp1 | a0001 | c0001 | t0004 | g0004 | AMR | CLM | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG01361 | hp2 | a0001 | c0003 | t0002 | g0232 | AMR | CLM | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG01433 | hp1 | a0002 | c0002 | t0002 | g0290 | AMR | CLM | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0321 | AMR | CLM | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0216 | AMR | CLM | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | CLM | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG01515 | hp1 | a0003 | c0004 | t0002 | g0042 | EUR | IBS | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0230 | EUR | IBS | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG01517 | hp1 | a0003 | c0004 | t0002 | g0042 | EUR | IBS | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0074 | EUR | IBS | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0309 | AFR | ACB | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG01884 | hp2 | a0001 | c0003 | t0001 | g0160 | AFR | ACB | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG01891 | hp1 | a0001 | c0003 | t0001 | g0147 | AFR | ACB | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG01891 | hp2 | a0001 | c0003 | t0001 | g0140 | AFR | ACB | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG01928 | hp2 | a0002 | c0002 | t0002 | g0001 | AMR | PEL | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG01934 | hp1 | a0003 | c0004 | t0002 | g0326 | AMR | PEL | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG01934 | hp2 | a0002 | c0002 | t0002 | g0033 | AMR | PEL | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | PEL | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0170 | AMR | PEL | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0354 | AMR | PEL | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG01975 | hp2 | a0002 | c0002 | t0002 | g0269 | AMR | PEL | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | PEL | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG01981 | hp2 | a0001 | c0003 | t0001 | g0026 | AMR | PEL | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG01993 | hp1 | a0002 | c0002 | t0002 | g0001 | AMR | PEL | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | PEL | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG02004 | hp1 | a0002 | c0002 | t0002 | g0300 | AMR | PEL | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0072 | AMR | PEL | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | KHV | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG02015 | hp2 | a0002 | c0002 | t0002 | g0277 | EAS | KHV | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG02027 | hp1 | a0001 | c0001 | t0002 | g0201 | EAS | KHV | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG02040 | hp2 | a0001 | c0001 | t0002 | g0306 | EAS | KHV | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0346 | AFR | ACB | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0303 | AFR | ACB | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | KHV | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG02056 | hp2 | a0002 | c0002 | t0002 | g0265 | EAS | KHV | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0332 | EAS | KHV | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG02071 | hp2 | a0003 | c0004 | t0002 | g0010 | EAS | KHV | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | KHV | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG02074 | hp2 | a0004 | c0005 | t0002 | g0283 | EAS | KHV | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG02080 | hp2 | a0002 | c0002 | t0008 | g0259 | EAS | KHV | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG02083 | hp1 | a0001 | c0001 | t0002 | g0353 | EAS | KHV | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG02083 | hp2 | a0002 | c0002 | t0002 | g0009 | EAS | KHV | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG02129 | hp1 | a0002 | c0002 | t0002 | g0274 | EAS | KHV | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG02129 | hp2 | a0001 | c0001 | t0002 | g0305 | EAS | KHV | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG02132 | hp1 | a0002 | c0002 | t0002 | g0254 | EAS | KHV | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG02132 | hp2 | a0002 | c0002 | t0002 | g0037 | EAS | KHV | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | KHV | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG02135 | hp2 | a0001 | c0001 | t0002 | g0320 | EAS | KHV | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG02145 | hp1 | a0001 | c0003 | t0001 | g0128 | AFR | ACB | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG02145 | hp2 | a0001 | c0003 | t0001 | g0150 | AFR | ACB | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG02155 | hp1 | a0002 | c0002 | t0002 | g0260 | EAS | CDX | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG02155 | hp2 | a0002 | c0002 | t0002 | g0256 | EAS | CDX | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | CDX | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | CDX | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | ACB | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0313 | AFR | ACB | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | ACB | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | ACB | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0198 | AMR | PEL | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0327 | AMR | PEL | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG02280 | hp1 | a0001 | c0003 | t0003 | g0231 | AFR | ACB | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0341 | AFR | ACB | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG02293 | hp1 | a0002 | c0002 | t0002 | g0001 | AMR | PEL | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG02300 | hp1 | a0002 | c0002 | t0002 | g0001 | AMR | PEL | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG02451 | hp1 | a0001 | c0003 | t0001 | g0027 | AFR | ACB | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG02451 | hp2 | a0001 | c0003 | t0003 | g0362 | AFR | ACB | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | KHV | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | KHV | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0345 | AFR | GWD | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | GWD | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG02602 | hp1 | a0001 | c0003 | t0001 | g0026 | SAS | PJL | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0100 | SAS | PJL | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG02615 | hp1 | a0001 | c0001 | t0002 | g0041 | AFR | GWD | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG02615 | hp2 | a0001 | c0003 | t0001 | g0156 | AFR | GWD | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | GWD | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | GWD | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG02630 | hp1 | a0001 | c0003 | t0001 | g0161 | AFR | GWD | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG02630 | hp2 | a0001 | c0003 | t0001 | g0363 | AFR | GWD | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG02647 | hp1 | a0001 | c0003 | t0001 | g0167 | AFR | GWD | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0214 | AFR | GWD | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0229 | SAS | PJL | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0194 | SAS | PJL | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG02698 | hp1 | a0001 | c0001 | t0004 | g0004 | SAS | PJL | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG02698 | hp2 | a0003 | c0004 | t0005 | g0291 | SAS | PJL | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG02717 | hp1 | a0004 | c0005 | t0003 | g0139 | AFR | GWD | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG02717 | hp2 | a0001 | c0001 | t0002 | g0199 | AFR | GWD | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG02723 | hp1 | a0001 | c0003 | t0001 | g0143 | AFR | GWD | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | GWD | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG02735 | hp1 | a0001 | c0001 | t0004 | g0004 | SAS | PJL | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0210 | SAS | PJL | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0350 | SAS | PJL | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0071 | SAS | PJL | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG02809 | hp1 | a0001 | c0003 | t0001 | g0146 | AFR | GWD | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG02809 | hp2 | a0001 | c0003 | t0001 | g0163 | AFR | GWD | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | GWD | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG02818 | hp2 | a0001 | c0003 | t0001 | g0132 | AFR | GWD | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | GWD | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG02895 | hp2 | a0001 | c0003 | t0001 | g0153 | AFR | GWD | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG02896 | hp1 | a0001 | c0001 | t0002 | g0347 | AFR | GWD | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0344 | AFR | GWD | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG02897 | hp1 | a0001 | c0001 | t0002 | g0349 | AFR | GWD | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0307 | AFR | GWD | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG02922 | hp1 | a0001 | c0003 | t0001 | g0015 | AFR | ESN | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0310 | AFR | ESN | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ESN | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0348 | AFR | ESN | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG02976 | hp1 | a0001 | c0003 | t0001 | g0245 | AFR | ESN | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG02976 | hp2 | a0001 | c0003 | t0003 | g0361 | AFR | ESN | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG03017 | hp1 | a0001 | c0001 | t0004 | g0322 | SAS | PJL | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | MSL | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG03098 | hp2 | a0001 | c0003 | t0003 | g0129 | AFR | MSL | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG03130 | hp1 | a0001 | c0003 | t0001 | g0155 | AFR | ESN | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG03130 | hp2 | a0001 | c0003 | t0001 | g0366 | AFR | ESN | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG03139 | hp1 | a0001 | c0001 | t0003 | g0244 | AFR | ESN | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG03139 | hp2 | a0001 | c0003 | t0001 | g0162 | AFR | ESN | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG03195 | hp1 | a0001 | c0003 | t0001 | g0027 | AFR | ESN | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG03195 | hp2 | a0001 | c0003 | t0003 | g0364 | AFR | ESN | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG03209 | hp1 | a0001 | c0003 | t0002 | g0233 | AFR | MSL | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG03209 | hp2 | a0001 | c0003 | t0001 | g0015 | AFR | MSL | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG03225 | hp1 | a0001 | c0003 | t0001 | g0158 | AFR | MSL | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0217 | AFR | MSL | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG03239 | hp1 | a0001 | c0001 | t0007 | g0011 | SAS | PJL | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0335 | SAS | PJL | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG03453 | hp1 | a0004 | c0005 | t0001 | g0131 | AFR | MSL | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG03453 | hp2 | a0001 | c0003 | t0001 | g0145 | AFR | MSL | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG03486 | hp1 | a0001 | c0001 | t0002 | g0041 | AFR | MSL | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG03486 | hp2 | a0001 | c0003 | t0001 | g0164 | AFR | MSL | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0208 | SAS | PJL | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0183 | SAS | PJL | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0182 | SAS | PJL | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG03492 | hp2 | a0001 | c0001 | t0004 | g0004 | SAS | PJL | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ESN | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | ESN | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG03540 | hp1 | a0001 | c0003 | t0001 | g0144 | AFR | GWD | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG03540 | hp2 | a0004 | c0005 | t0001 | g0141 | AFR | GWD | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG03579 | hp1 | a0001 | c0003 | t0002 | g0235 | AFR | MSL | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG03579 | hp2 | a0001 | c0003 | t0001 | g0015 | AFR | MSL | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0190 | SAS | PJL | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0205 | SAS | PJL | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0175 | SAS | PJL | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0311 | SAS | PJL | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0192 | SAS | STU | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0172 | SAS | STU | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0043 | SAS | PJL | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0316 | SAS | PJL | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0189 | SAS | BEB | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0179 | SAS | BEB | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0101 | SAS | BEB | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0039 | SAS | BEB | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG03942 | hp1 | a0001 | c0003 | t0001 | g0142 | SAS | BEB | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0103 | SAS | BEB | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0059 | SAS | BEB | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0206 | SAS | BEB | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG04199 | hp1 | a0004 | c0005 | t0001 | g0270 | SAS | STU | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0301 | SAS | STU | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0171 | SAS | STU | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0184 | SAS | STU | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0200 | SAS | STU | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0191 | SAS | STU | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA18522 | hp1 | a0001 | c0003 | t0001 | g0236 | AFR | YRI | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA18522 | hp2 | a0001 | c0003 | t0001 | g0165 | AFR | YRI | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | CHB | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA18612 | hp2 | a0002 | c0002 | t0002 | g0250 | EAS | CHB | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA18747 | hp1 | a0002 | c0002 | t0002 | g0266 | EAS | CHB | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | CHB | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0318 | AFR | YRI | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0328 | AFR | YRI | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA18940 | hp1 | a0002 | c0002 | t0002 | g0278 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA18941 | hp1 | a0003 | c0004 | t0002 | g0002 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA18941 | hp2 | a0002 | c0002 | t0002 | g0036 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA18942 | hp1 | a0005 | c0007 | t0001 | g0008 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA18944 | hp1 | a0002 | c0002 | t0002 | g0253 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA18944 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA18945 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA18946 | hp1 | a0002 | c0002 | t0002 | g0009 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA18946 | hp2 | a0003 | c0004 | t0002 | g0054 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA18947 | hp1 | a0002 | c0002 | t0002 | g0267 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA18948 | hp1 | a0002 | c0002 | t0002 | g0288 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA18949 | hp2 | a0002 | c0002 | t0002 | g0031 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0324 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA18951 | hp1 | a0003 | c0004 | t0002 | g0010 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA18952 | hp1 | a0002 | c0002 | t0002 | g0032 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA18956 | hp1 | a0002 | c0002 | t0002 | g0281 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0338 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA18959 | hp1 | a0003 | c0004 | t0002 | g0315 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA18960 | hp2 | a0003 | c0004 | t0002 | g0061 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA18961 | hp2 | a0002 | c0002 | t0002 | g0299 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA18962 | hp1 | a0002 | c0002 | t0002 | g0268 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA18962 | hp2 | a0002 | c0002 | t0002 | g0031 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA18963 | hp2 | a0002 | c0002 | t0002 | g0276 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA18964 | hp2 | a0002 | c0002 | t0002 | g0036 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA18965 | hp2 | a0002 | c0002 | t0002 | g0262 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0331 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA18968 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA18969 | hp1 | a0003 | c0004 | t0002 | g0053 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA18972 | hp1 | a0002 | c0002 | t0002 | g0038 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA18972 | hp2 | a0003 | c0004 | t0002 | g0091 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA18973 | hp2 | a0002 | c0002 | t0002 | g0249 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA18975 | hp2 | a0002 | c0002 | t0002 | g0294 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA18977 | hp2 | a0003 | c0004 | t0002 | g0298 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA18979 | hp1 | a0004 | c0005 | t0001 | g0275 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA18980 | hp1 | a0003 | c0004 | t0002 | g0002 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA18980 | hp2 | a0002 | c0002 | t0002 | g0296 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA18981 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA18984 | hp1 | a0004 | c0005 | t0001 | g0258 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA18986 | hp1 | a0004 | c0005 | t0001 | g0035 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA18986 | hp2 | a0003 | c0004 | t0002 | g0060 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA18987 | hp2 | a0003 | c0004 | t0002 | g0092 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA18988 | hp2 | a0004 | c0005 | t0001 | g0264 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA18989 | hp2 | a0002 | c0002 | t0002 | g0273 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA18991 | hp1 | a0002 | c0002 | t0002 | g0248 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA18994 | hp1 | a0002 | c0002 | t0002 | g0295 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA18995 | hp1 | a0003 | c0004 | t0002 | g0002 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA18995 | hp2 | a0002 | c0002 | t0002 | g0255 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA19000 | hp1 | a0002 | c0002 | t0002 | g0246 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA19002 | hp1 | a0002 | c0002 | t0002 | g0279 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA19002 | hp2 | a0003 | c0004 | t0002 | g0020 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA19003 | hp1 | a0003 | c0004 | t0002 | g0330 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA19004 | hp2 | a0002 | c0002 | t0002 | g0251 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA19005 | hp2 | a0004 | c0005 | t0001 | g0034 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA19007 | hp1 | a0001 | c0006 | t0001 | g0219 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA19011 | hp2 | a0002 | c0002 | t0002 | g0272 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA19030 | hp1 | a0001 | c0003 | t0001 | g0154 | AFR | LWK | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA19030 | hp2 | a0001 | c0003 | t0001 | g0157 | AFR | LWK | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | LWK | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0304 | AFR | LWK | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA19055 | hp1 | a0002 | c0002 | t0002 | g0282 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA19056 | hp2 | a0002 | c0002 | t0002 | g0009 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA19058 | hp1 | a0002 | c0002 | t0002 | g0286 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA19060 | hp2 | a0003 | c0004 | t0002 | g0010 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA19062 | hp1 | a0003 | c0004 | t0002 | g0056 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA19062 | hp2 | a0002 | c0002 | t0002 | g0284 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA19063 | hp1 | a0002 | c0002 | t0002 | g0037 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA19063 | hp2 | a0006 | c0008 | t0006 | g0337 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA19064 | hp2 | a0002 | c0002 | t0002 | g0297 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA19065 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA19066 | hp2 | a0002 | c0002 | t0002 | g0292 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA19067 | hp1 | a0003 | c0004 | t0002 | g0093 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA19067 | hp2 | a0002 | c0002 | t0002 | g0247 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA19070 | hp2 | a0002 | c0002 | t0002 | g0009 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA19074 | hp1 | a0003 | c0004 | t0002 | g0308 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA19074 | hp2 | a0004 | c0005 | t0001 | g0271 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA19077 | hp1 | a0003 | c0004 | t0002 | g0088 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA19078 | hp1 | a0002 | c0002 | t0002 | g0287 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA19079 | hp2 | a0004 | c0005 | t0001 | g0035 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA19082 | hp2 | a0002 | c0002 | t0002 | g0032 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA19083 | hp2 | a0002 | c0002 | t0002 | g0033 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA19085 | hp1 | a0004 | c0005 | t0001 | g0263 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA19086 | hp2 | a0002 | c0002 | t0002 | g0038 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA19087 | hp1 | a0002 | c0002 | t0002 | g0252 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA19087 | hp2 | a0003 | c0004 | t0002 | g0002 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA19088 | hp1 | a0003 | c0004 | t0002 | g0239 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA19088 | hp2 | a0003 | c0004 | t0002 | g0002 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA19090 | hp2 | a0002 | c0002 | t0002 | g0261 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA19091 | hp2 | a0002 | c0002 | t0002 | g0293 | EAS | JPT | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA19240 | hp1 | a0001 | c0003 | t0002 | g0166 | AFR | YRI | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA19240 | hp2 | a0001 | c0003 | t0003 | g0365 | AFR | YRI | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA20129 | hp1 | a0001 | c0003 | t0001 | g0151 | AFR | ASW | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA20129 | hp2 | a0001 | c0001 | t0003 | g0110 | AFR | ASW | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0016 | EUR | TSI | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0340 | EUR | TSI | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0228 | EUR | TSI | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA20805 | hp2 | a0001 | c0003 | t0005 | g0125 | EUR | TSI | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0193 | SAS | GIH | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA20905 | hp2 | a0001 | c0001 | t0002 | g0186 | SAS | GIH | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0352 | AMR | CLM | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | CLM | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG02109 | hp1 | a0001 | c0003 | t0001 | g0360 | AFR | ACB | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0243 | AFR | ACB | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0207 | AFR | ACB | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG02486 | hp2 | a0001 | c0003 | t0001 | g0148 | AFR | ACB | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG02559 | hp1 | a0001 | c0003 | t0001 | g0359 | AFR | ACB | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG02559 | hp2 | a0004 | c0005 | t0001 | g0137 | AFR | ACB | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG03471 | hp1 | a0001 | c0003 | t0001 | g0159 | AFR | MSL | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG03471 | hp2 | a0001 | c0003 | t0002 | g0234 | AFR | MSL | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG06807 | hp1 | a0004 | c0005 | t0001 | g0130 | AFR | USA | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | USA | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | USA | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | USA | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA21309 | hp1 | a0001 | c0003 | t0005 | g0126 | AFR | LWK | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0342 | AFR | LWK | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0006 | REF | REF | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0004 | g0357 | REF | REF | QPCT_chr2_37339630_37378322 | QPCT | chr2 | 37339630 | 37378322 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:37352828
|
C | T | 2 | a0002a0004 | 90 | HG00438.hp2 HG00544.hp2 HG00621.hp2 others(87): Show |
missense_variant | MODERATE | c.160C>T | p.Arg54Trp | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/7 | 262/1683 | 160/1086 | 54/361 | chr2 | 37352828 | ||
chr2:37372702
|
A | T | 1 | a0006 | 1 | NA19063.hp2 | missense_variant | MODERATE | c.961A>T | p.Ile321Leu | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 7/7 | 1063/1683 | 961/1086 | 321/361 | chr2 | 37372702 | ||
chr2:37372720
|
G | A | 1 | a0005 | 1 | NA18942.hp1 | missense_variant | MODERATE | c.979G>A | p.Glu327Lys | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 7/7 | 1081/1683 | 979/1086 | 327/361 | chr2 | 37372720 | ||
chr2:37372820
|
A | C | 2 | a0002a0003 | 103 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(100): Show |
missense_variant | MODERATE | c.1079A>C | p.His360Pro | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 7/7 | 1181/1683 | 1079/1086 | 360/361 | chr2 | 37372820 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:37344740
|
C | A | 1 | a0001c0006 | 1 | NA19007.hp1 | synonymous_variant | LOW | c.9C>A | p.Gly3Gly | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/7 | 111/1683 | 9/1086 | 3/361 | chr2 | 37344740 | ||
chr2:37352794
|
C | T | 3 | a0001c0003a0002c0002a0004c0005 | 145 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(142): Show |
synonymous_variant | LOW | c.126C>T | p.Tyr42Tyr | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/7 | 228/1683 | 126/1086 | 42/361 | chr2 | 37352794 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:37372836
|
T | A | 1 | a0006c0008t0006 | 1 | NA19063.hp2 | 3_prime_UTR_variant | MODIFIER | c.*9T>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 7/7 | 9 | chr2 | 37372836 | |||||
chr2:37372845
|
G | T | 9 | a0001c0001t0002a0001c0001t0003a0001c0003t0002others(6): Show | 129 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(126): Show |
3_prime_UTR_variant | MODIFIER | c.*18G>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 7/7 | 18 | chr2 | 37372845 | |||||
chr2:37372955
|
T | C | 1 | a0002c0002t0008 | 1 | HG02080.hp2 | 3_prime_UTR_variant | MODIFIER | c.*128T>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 7/7 | 128 | chr2 | 37372955 | |||||
chr2:37372989
|
T | C | 1 | a0001c0001t0007 | 1 | HG03239.hp1 | 3_prime_UTR_variant | MODIFIER | c.*162T>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 7/7 | 162 | chr2 | 37372989 | |||||
chr2:37373149
|
C | A | 19 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(16): Show | 436 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(433): Show |
3_prime_UTR_variant | MODIFIER | c.*322C>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 7/7 | 322 | chr2 | 37373149 | |||||
chr2:37373239
|
CAT | C | 3 | a0001c0001t0003a0001c0003t0003a0004c0005t0003 | 9 | HG02280.hp1 HG02451.hp2 HG02717.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*413_*414delAT | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 7/7 | 413 | chr2 | 37373239 | |||||
chr2:37373284
|
A | G | 12 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(9): Show | 134 | HG00280.hp1 HG00544.hp2 HG00558.hp1 others(131): Show |
3_prime_UTR_variant | MODIFIER | c.*457A>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 7/7 | 457 | chr2 | 37373284 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:37344900
|
G | T | 8 | a0001c0003t0001g0359a0001c0003t0001g0360a0001c0003t0001g0363others(5): Show | 8 | HG02109.hp1 HG02451.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.120+49G>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37344900 | ||||||
chr2:37345194
|
C | A | 1 | a0001c0001t0001g0043 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.120+343C>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37345194 | ||||||
chr2:37345207
|
G | C | 228 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(225): Show | 270 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.120+356G>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37345207 | ||||||
chr2:37345216
|
C | A | 2 | a0001c0001t0001g0243a0001c0001t0003g0244 | 2 | HG02109.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.120+365C>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37345216 | ||||||
chr2:37345231
|
GGGGCCGC others(2): Show |
G | 8 | a0001c0001t0001g0019a0001c0001t0001g0030a0001c0001t0001g0237others(5): Show | 11 | HG00544.hp1 HG00558.hp2 NA18947.hp2 others(8): Show |
intron_variant | MODIFIER | c.120+384_120+392del others(9): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37345231 | |||||
chr2:37345301
|
TGCTGGGG others(1): Show |
T | 103 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0012others(100): Show | 128 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.120+455_120+462del others(8): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37345301 | |||||
chr2:37345322
|
C | G | 7 | a0001c0003t0001g0360a0001c0003t0001g0363a0001c0003t0001g0366others(4): Show | 7 | HG02109.hp1 HG02451.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.120+471C>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37345322 | ||||||
chr2:37345420
|
C | A | 7 | a0001c0003t0001g0360a0001c0003t0001g0363a0001c0003t0001g0366others(4): Show | 7 | HG02109.hp1 HG02451.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.120+569C>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37345420 | ||||||
chr2:37345427
|
C | T | 1 | a0001c0003t0001g0236 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.120+576C>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37345427 | ||||||
chr2:37345458
|
C | T | 2 | a0001c0003t0002g0234a0001c0003t0002g0235 | 2 | HG03471.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.120+607C>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37345458 | ||||||
chr2:37345530
|
C | G | 7 | a0001c0003t0001g0360a0001c0003t0001g0363a0001c0003t0001g0366others(4): Show | 7 | HG02109.hp1 HG02451.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.120+679C>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37345530 | ||||||
chr2:37345544
|
G | A | 302 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(299): Show | 364 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(361): Show |
intron_variant | MODIFIER | c.120+693G>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37345544 | ||||||
chr2:37345573
|
C | T | 1 | a0001c0001t0001g0358 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.120+722C>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37345573 | ||||||
chr2:37345580
|
A | T | 1 | a0001c0003t0002g0233 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.120+729A>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37345580 | ||||||
chr2:37345663
|
G | T | 287 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(284): Show | 348 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(345): Show |
intron_variant | MODIFIER | c.120+812G>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37345663 | ||||||
chr2:37345764
|
G | A | 368 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(365): Show | 441 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(438): Show |
intron_variant | MODIFIER | c.120+913G>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37345764 | ||||||
chr2:37345826
|
A | C | 1 | a0001c0003t0001g0245 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.120+975A>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37345826 | ||||||
chr2:37345835
|
C | CA | 65 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0012others(62): Show | 80 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(77): Show |
intron_variant | MODIFIER | c.120+1004dupA | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37345835 | |||||
chr2:37345835
|
CA | C | 20 | a0001c0001t0001g0243a0001c0001t0001g0354a0001c0001t0002g0353others(17): Show | 21 | HG00738.hp1 HG01069.hp2 HG01361.hp2 others(18): Show |
intron_variant | MODIFIER | c.120+1004delA | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37345835 | |||||
chr2:37345908
|
G | T | 2 | a0001c0001t0001g0243a0001c0001t0003g0244 | 2 | HG02109.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.120+1057G>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37345908 | ||||||
chr2:37345976
|
T | C | 73 | a0001c0003t0001g0140a0002c0002t0002g0001a0002c0002t0002g0003others(70): Show | 93 | HG00438.hp2 HG00544.hp2 HG00621.hp2 others(90): Show |
intron_variant | MODIFIER | c.120+1125T>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37345976 | ||||||
chr2:37346051
|
T | C | 2 | a0001c0001t0001g0044a0003c0004t0002g0045 | 2 | HG01255.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.120+1200T>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37346051 | ||||||
chr2:37346068
|
C | T | 3 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0124 | 3 | HG02622.hp2 HG02818.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.120+1217C>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37346068 | ||||||
chr2:37346103
|
G | A | 294 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(291): Show | 356 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(353): Show |
intron_variant | MODIFIER | c.120+1252G>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37346103 | ||||||
chr2:37346116
|
C | T | 14 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0044others(11): Show | 19 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(16): Show |
intron_variant | MODIFIER | c.120+1265C>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37346116 | ||||||
chr2:37346136
|
C | CAT | 7 | a0001c0003t0001g0360a0001c0003t0001g0363a0001c0003t0001g0366others(4): Show | 7 | HG02109.hp1 HG02451.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.120+1294_120+1295d others(4): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37346136 | |||||
chr2:37346199
|
C | A | 1 | a0004c0005t0001g0137 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.120+1348C>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37346199 | ||||||
chr2:37346205
|
G | A | 3 | a0001c0003t0001g0128a0001c0003t0001g0359a0001c0003t0003g0129 | 3 | HG02145.hp1 HG02559.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.120+1354G>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37346205 | ||||||
chr2:37346299
|
A | G | 3 | a0001c0001t0001g0350a0001c0001t0001g0351a0001c0001t0001g0352 | 3 | HG01123.hp1 HG01261.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.120+1448A>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37346299 | ||||||
chr2:37346379
|
C | G | 1 | a0001c0001t0001g0120 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.120+1528C>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37346379 | ||||||
chr2:37346380
|
T | C | 1 | a0001c0003t0001g0142 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.120+1529T>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37346380 | ||||||
chr2:37346413
|
G | A | 302 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(299): Show | 364 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(361): Show |
intron_variant | MODIFIER | c.120+1562G>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37346413 | ||||||
chr2:37346444
|
T | C | 301 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(298): Show | 363 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(360): Show |
intron_variant | MODIFIER | c.120+1593T>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37346444 | ||||||
chr2:37346754
|
T | C | 301 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(298): Show | 363 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(360): Show |
intron_variant | MODIFIER | c.120+1903T>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37346754 | ||||||
chr2:37346847
|
C | G | 4 | a0001c0001t0001g0346a0001c0001t0001g0348a0001c0001t0002g0347others(1): Show | 4 | HG02055.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.120+1996C>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37346847 | ||||||
chr2:37346876
|
C | G | 3 | a0003c0004t0002g0042a0003c0004t0002g0355a0003c0004t0002g0356 | 4 | HG00738.hp1 HG01069.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.120+2025C>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37346876 | ||||||
chr2:37346983
|
G | A | 4 | a0001c0001t0001g0303a0003c0004t0002g0042a0003c0004t0002g0355others(1): Show | 5 | HG00738.hp1 HG01069.hp2 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.120+2132G>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37346983 | ||||||
chr2:37346991
|
G | C | 294 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(291): Show | 356 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(353): Show |
intron_variant | MODIFIER | c.120+2140G>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37346991 | ||||||
chr2:37347084
|
A | C | 181 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(178): Show | 219 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.120+2233A>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37347084 | ||||||
chr2:37347141
|
G | GT | 35 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0176others(32): Show | 48 | HG00438.hp2 HG00621.hp2 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.120+2294dupT | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347141 | |||||
chr2:37347141
|
G | GTT | 10 | a0001c0001t0001g0008a0001c0001t0001g0017a0001c0001t0001g0075others(7): Show | 14 | HG00597.hp2 HG02040.hp1 HG02165.hp1 others(11): Show |
intron_variant | MODIFIER | c.120+2293_120+2294d others(4): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347141 | |||||
chr2:37347144
|
T | TA | 4 | a0001c0003t0001g0359a0002c0002t0002g0246a0002c0002t0002g0250others(1): Show | 4 | HG02559.hp1 NA18612.hp2 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.120+2293_120+2294i others(3): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37347144 | ||||||
chr2:37347144
|
T | TTTA | 16 | a0002c0002t0002g0003a0002c0002t0002g0033a0002c0002t0002g0248others(13): Show | 21 | HG01934.hp2 HG01975.hp2 HG02015.hp2 others(18): Show |
intron_variant | MODIFIER | c.120+2294_120+2295i others(5): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347144 | |||||
chr2:37347144
|
T | TTTATA | 9 | a0002c0002t0002g0032a0002c0002t0002g0255a0002c0002t0002g0260others(6): Show | 10 | HG02004.hp1 HG02056.hp2 HG02155.hp1 others(7): Show |
intron_variant | MODIFIER | c.120+2294_120+2295i others(7): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347144 | |||||
chr2:37347144
|
T | TTTATATA | 4 | a0002c0002t0002g0031a0002c0002t0002g0257a0002c0002t0008g0259others(1): Show | 5 | HG00544.hp2 HG02080.hp2 NA18949.hp2 others(2): Show |
intron_variant | MODIFIER | c.120+2294_120+2295i others(9): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347144 | |||||
chr2:37347144
|
T | TTTTTTAT others(32): Show |
1 | a0001c0001t0001g0018 | 3 | HG02965.hp1 HG03098.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.120+2294_120+2295i others(41): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347144 | |||||
chr2:37347144
|
T | TTTTTTTT others(32): Show |
1 | a0001c0001t0001g0230 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.120+2294_120+2295i others(41): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347144 | |||||
chr2:37347144
|
TTA | T | 54 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0039others(51): Show | 64 | HG00099.hp1 HG00140.hp1 HG00621.hp1 others(61): Show |
intron_variant | MODIFIER | c.120+2312_120+2313d others(4): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347144 | |||||
chr2:37347146
|
A | T | 164 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0011others(161): Show | 198 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(195): Show |
intron_variant | MODIFIER | c.120+2295A>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37347146 | ||||||
chr2:37347148
|
A | T | 9 | a0001c0001t0001g0029a0001c0001t0001g0226a0001c0001t0001g0227others(6): Show | 10 | HG01070.hp1 HG01070.hp2 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.120+2297A>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37347148 | ||||||
chr2:37347151
|
T | TAAC | 2 | a0001c0001t0001g0018a0001c0001t0001g0230 | 4 | HG01515.hp2 HG02965.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.120+2301_120+2302i others(5): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347151 | |||||
chr2:37347151
|
T | TATATATA others(40): Show |
1 | a0001c0001t0001g0177 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.120+2309_120+2310i others(49): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347151 | |||||
chr2:37347151
|
T | TATATATA others(38): Show |
1 | a0001c0001t0001g0178 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.120+2309_120+2310i others(47): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347151 | |||||
chr2:37347151
|
T | TATATATA others(38): Show |
1 | a0001c0001t0001g0225 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.120+2308_120+2309i others(47): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347151 | |||||
chr2:37347153
|
T | TATATATA others(19): Show |
6 | a0001c0001t0001g0303a0001c0001t0001g0341a0001c0001t0001g0358others(3): Show | 7 | HG00738.hp1 HG01069.hp2 HG01074.hp2 others(4): Show |
intron_variant | MODIFIER | c.120+2311_120+2312i others(28): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347153 | |||||
chr2:37347153
|
T | TATATATA others(119): Show |
1 | a0001c0003t0003g0361 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.120+2313_120+2314i others(128): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347153 | |||||
chr2:37347153
|
T | TATATATA others(143): Show |
1 | a0001c0003t0001g0147 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.120+2313_120+2314i others(152): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347153 | |||||
chr2:37347153
|
T | TATATATA others(141): Show |
1 | a0001c0003t0001g0150 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.120+2313_120+2314i others(150): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347153 | |||||
chr2:37347153
|
T | TATATATA others(113): Show |
1 | a0001c0003t0003g0364 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.120+2313_120+2314i others(122): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347153 | |||||
chr2:37347153
|
T | TATATATA others(139): Show |
1 | a0001c0003t0001g0157 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.120+2313_120+2314i others(148): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347153 | |||||
chr2:37347155
|
T | TATATATA others(38): Show |
1 | a0001c0003t0001g0142 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.120+2313_120+2314i others(47): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347155 | |||||
chr2:37347155
|
T | TATATCAT others(65): Show |
2 | a0001c0003t0001g0015a0001c0003t0001g0165 | 4 | HG02922.hp1 HG03209.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.120+2308_120+2309i others(74): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347155 | |||||
chr2:37347155
|
T | TATATCAT others(67): Show |
1 | a0001c0003t0002g0234 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.120+2308_120+2309i others(76): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347155 | |||||
chr2:37347155
|
T | TATATCAT others(67): Show |
3 | a0001c0003t0001g0167a0001c0003t0002g0166a0001c0003t0002g0235 | 3 | HG02647.hp1 HG03579.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.120+2308_120+2309i others(76): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347155 | |||||
chr2:37347163
|
T | A | 5 | a0001c0001t0001g0243a0001c0001t0001g0342a0001c0001t0001g0343others(2): Show | 5 | HG01106.hp2 HG02109.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.120+2312T>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37347163 | ||||||
chr2:37347163
|
TA | T | 24 | a0001c0001t0001g0007a0001c0001t0001g0028a0001c0001t0001g0046others(21): Show | 29 | HG00642.hp2 HG00735.hp1 HG01069.hp1 others(26): Show |
intron_variant | MODIFIER | c.120+2314delA | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347163 | |||||
chr2:37347163
|
TAAC | T | 14 | a0001c0001t0001g0014a0001c0001t0001g0019a0001c0001t0001g0030others(11): Show | 19 | HG00544.hp1 HG02258.hp1 HG02572.hp2 others(16): Show |
intron_variant | MODIFIER | c.120+2314_120+2316d others(5): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347163 | |||||
chr2:37347164
|
A | AT | 200 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0012others(197): Show | 242 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(239): Show |
intron_variant | MODIFIER | c.120+2313_120+2314i others(3): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37347164 | ||||||
chr2:37347164
|
A | ATAT | 16 | a0001c0001t0001g0052a0001c0001t0001g0133a0001c0001t0001g0134others(13): Show | 16 | HG00438.hp1 HG01070.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.120+2313_120+2314i others(5): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37347164 | ||||||
chr2:37347164
|
A | ATATAT | 8 | a0001c0001t0001g0024a0001c0001t0001g0111a0001c0001t0001g0112others(5): Show | 10 | HG01981.hp2 HG02074.hp1 HG02602.hp1 others(7): Show |
intron_variant | MODIFIER | c.120+2313_120+2314i others(7): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37347164 | ||||||
chr2:37347164
|
A | ATATATAT | 3 | a0001c0001t0001g0113a0001c0003t0001g0162a0001c0003t0001g0236 | 3 | HG03139.hp2 NA18522.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.120+2313_120+2314i others(9): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37347164 | ||||||
chr2:37347164
|
A | ATATATAT others(4): Show |
1 | a0001c0003t0001g0143 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.120+2313_120+2314i others(13): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37347164 | ||||||
chr2:37347164
|
A | ATATATAT others(6): Show |
1 | a0001c0003t0005g0126 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.120+2313_120+2314i others(15): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37347164 | ||||||
chr2:37347164
|
A | ATATATAT others(8): Show |
1 | a0001c0003t0005g0127 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.120+2313_120+2314i others(17): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37347164 | ||||||
chr2:37347164
|
A | C | 4 | a0001c0001t0001g0243a0001c0001t0001g0342a0001c0001t0001g0343others(1): Show | 4 | HG01106.hp2 HG02109.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.120+2313A>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37347164 | ||||||
chr2:37347164
|
A | T | 1 | a0001c0001t0001g0344 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.120+2313A>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37347164 | ||||||
chr2:37347165
|
A | T | 13 | a0001c0001t0001g0008a0001c0001t0001g0017a0001c0001t0001g0075others(10): Show | 17 | HG00099.hp2 HG00597.hp2 HG02040.hp1 others(14): Show |
intron_variant | MODIFIER | c.120+2314A>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37347165 | ||||||
chr2:37347166
|
C | A | 1 | a0001c0006t0001g0219 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.120+2315C>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37347166 | ||||||
chr2:37347166
|
C | T | 262 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0011others(259): Show | 311 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(308): Show |
intron_variant | MODIFIER | c.120+2315C>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37347166 | ||||||
chr2:37347166
|
CAT | C | 5 | a0001c0003t0001g0015a0001c0003t0001g0167a0001c0003t0002g0166others(2): Show | 7 | HG02647.hp1 HG02922.hp1 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.120+2327_120+2328d others(4): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347166 | |||||
chr2:37347167
|
A | T | 1 | a0001c0006t0001g0219 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.120+2316A>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37347167 | ||||||
chr2:37347168
|
T | C | 1 | a0001c0006t0001g0219 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.120+2317T>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37347168 | ||||||
chr2:37347168
|
T | TATATATA others(91): Show |
1 | a0001c0003t0001g0128 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.120+2328_120+2329i others(100): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347168 | |||||
chr2:37347168
|
T | TATATATA others(67): Show |
1 | a0001c0003t0003g0129 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.120+2328_120+2329i others(76): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347168 | |||||
chr2:37347168
|
T | TATATATA others(63): Show |
1 | a0001c0003t0001g0359 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.120+2325_120+2326i others(72): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347168 | |||||
chr2:37347168
|
T | TATATATC others(72): Show |
1 | a0001c0001t0001g0117 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.120+2323_120+2324i others(81): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347168 | |||||
chr2:37347168
|
T | TATATCTC others(61): Show |
1 | a0001c0003t0002g0233 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.120+2321_120+2322i others(70): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347168 | |||||
chr2:37347168
|
T | TC | 4 | a0001c0001t0001g0113a0001c0001t0001g0118a0001c0001t0001g0119others(1): Show | 4 | NA18966.hp1 NA18966.hp2 NA18969.hp2 others(1): Show |
intron_variant | MODIFIER | c.120+2317_120+2318i others(3): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37347168 | ||||||
chr2:37347168
|
TATATATA others(6): Show |
T | 1 | a0001c0001t0001g0039 | 2 | HG00099.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.120+2353_120+2365d others(15): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347168 | |||||
chr2:37347170
|
T | C | 1 | a0001c0001t0001g0345 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.120+2319T>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37347170 | ||||||
chr2:37347170
|
T | TATATAAC | 5 | a0001c0001t0001g0018a0001c0001t0001g0177a0001c0001t0001g0178others(2): Show | 7 | HG01515.hp2 HG02965.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.120+2324_120+2325i others(9): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347170 | |||||
chr2:37347170
|
T | TATATATA others(37): Show |
1 | a0001c0001t0001g0076 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.120+2326_120+2327i others(46): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347170 | |||||
chr2:37347170
|
T | TATATATA others(28): Show |
10 | a0001c0001t0001g0008a0001c0001t0001g0017a0001c0001t0001g0075others(7): Show | 14 | HG00597.hp2 HG02040.hp1 HG02165.hp1 others(11): Show |
intron_variant | MODIFIER | c.120+2326_120+2327i others(37): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347170 | |||||
chr2:37347170
|
T | TATATATA others(30): Show |
1 | a0001c0001t0001g0224 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.120+2326_120+2327i others(39): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347170 | |||||
chr2:37347170
|
T | TATATATA others(30): Show |
1 | a0001c0003t0001g0245 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.120+2355_120+2391d others(39): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347170 | |||||
chr2:37347170
|
T | TATATATA others(46): Show |
1 | a0001c0003t0001g0144 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.120+2328_120+2329i others(55): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347170 | |||||
chr2:37347170
|
T | TATATATA others(57): Show |
1 | a0001c0003t0001g0360 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.120+2328_120+2329i others(66): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347170 | |||||
chr2:37347170
|
T | TATATATA others(53): Show |
2 | a0001c0003t0001g0145a0001c0003t0001g0146 | 2 | HG02809.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.120+2328_120+2329i others(62): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347170 | |||||
chr2:37347170
|
T | TATATATA others(49): Show |
1 | a0001c0003t0001g0149 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.120+2328_120+2329i others(58): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347170 | |||||
chr2:37347170
|
T | TATATATA others(51): Show |
6 | a0001c0003t0001g0152a0001c0003t0001g0153a0001c0003t0001g0154others(3): Show | 6 | HG01243.hp1 HG02451.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.120+2328_120+2329i others(60): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347170 | |||||
chr2:37347170
|
T | TATATATA others(55): Show |
1 | a0001c0001t0001g0180 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.120+2328_120+2329i others(64): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347170 | |||||
chr2:37347170
|
T | TATATATA others(47): Show |
1 | a0001c0003t0001g0156 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.120+2328_120+2329i others(56): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347170 | |||||
chr2:37347170
|
T | TATATATA others(101): Show |
1 | a0001c0003t0003g0231 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.120+2328_120+2329i others(110): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347170 | |||||
chr2:37347170
|
T | TATATATA others(49): Show |
3 | a0001c0003t0001g0158a0001c0003t0001g0159a0001c0003t0003g0365 | 3 | HG03225.hp1 HG03471.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.120+2328_120+2329i others(58): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347170 | |||||
chr2:37347170
|
T | TATATATA others(103): Show |
1 | a0001c0003t0002g0232 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.120+2328_120+2329i others(112): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347170 | |||||
chr2:37347170
|
T | TATATATA others(36): Show |
1 | a0001c0003t0001g0161 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.120+2328_120+2329i others(45): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347170 | |||||
chr2:37347170
|
T | TATATATA others(51): Show |
3 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0183 | 3 | HG03490.hp2 HG03492.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.120+2328_120+2329i others(60): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347170 | |||||
chr2:37347170
|
T | TATATATA others(45): Show |
1 | a0001c0003t0001g0366 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.120+2328_120+2329i others(54): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347170 | |||||
chr2:37347170
|
T | TATATATA others(56): Show |
1 | a0001c0001t0001g0086 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.120+2328_120+2329i others(65): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347170 | |||||
chr2:37347170
|
T | TATATATA others(47): Show |
1 | a0001c0001t0002g0186 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.120+2328_120+2329i others(56): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347170 | |||||
chr2:37347170
|
T | TATATATA others(91): Show |
3 | a0001c0001t0001g0187a0001c0001t0001g0188a0003c0004t0002g0020 | 4 | HG00558.hp1 HG02257.hp1 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.120+2328_120+2329i others(100): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347170 | |||||
chr2:37347170
|
T | TATATATA others(45): Show |
1 | a0001c0001t0001g0189 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.120+2328_120+2329i others(54): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347170 | |||||
chr2:37347170
|
T | TATATATA others(52): Show |
3 | a0001c0001t0001g0077a0001c0001t0001g0087a0003c0004t0002g0054 | 3 | HG01346.hp2 NA18946.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.120+2328_120+2329i others(61): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347170 | |||||
chr2:37347170
|
T | TATATATA others(48): Show |
1 | a0001c0001t0001g0120 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.120+2327_120+2328i others(57): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347170 | |||||
chr2:37347170
|
T | TATATATA others(50): Show |
13 | a0001c0001t0001g0013a0001c0001t0001g0023a0001c0001t0001g0047others(10): Show | 16 | HG01175.hp2 HG01256.hp1 HG01256.hp2 others(13): Show |
intron_variant | MODIFIER | c.120+2327_120+2328i others(59): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347170 | |||||
chr2:37347170
|
T | TATATATA others(87): Show |
1 | a0003c0004t0002g0056 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.120+2327_120+2328i others(96): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347170 | |||||
chr2:37347170
|
T | TATATATA others(41): Show |
3 | a0001c0001t0001g0212a0001c0001t0001g0213a0001c0001t0001g0214 | 3 | HG01099.hp2 HG02647.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.120+2327_120+2328i others(50): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347170 | |||||
chr2:37347170
|
T | TATATATC others(46): Show |
2 | a0003c0004t0002g0010a0003c0004t0002g0060 | 4 | HG02071.hp2 NA18951.hp1 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.120+2325_120+2326i others(55): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347170 | |||||
chr2:37347170
|
T | TATATATC others(48): Show |
43 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0012others(40): Show | 55 | HG00140.hp2 HG00280.hp2 HG00558.hp2 others(52): Show |
intron_variant | MODIFIER | c.120+2325_120+2326i others(57): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347170 | |||||
chr2:37347170
|
T | TATATATC others(85): Show |
1 | a0001c0001t0001g0049 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.120+2325_120+2326i others(94): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347170 | |||||
chr2:37347170
|
T | TATATATC others(39): Show |
2 | a0001c0001t0001g0043a0001c0001t0001g0216 | 2 | HG01496.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.120+2325_120+2326i others(48): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347170 | |||||
chr2:37347170
|
T | TATATCAT others(46): Show |
8 | a0001c0001t0001g0025a0001c0001t0001g0044a0001c0001t0001g0074others(5): Show | 9 | HG01255.hp2 HG01517.hp2 HG01981.hp1 others(6): Show |
intron_variant | MODIFIER | c.120+2323_120+2324i others(55): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347170 | |||||
chr2:37347170
|
T | TATATCAT others(83): Show |
2 | a0001c0001t0001g0122a0001c0001t0001g0123 | 2 | HG02818.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.120+2323_120+2324i others(92): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347170 | |||||
chr2:37347170
|
T | TATATCAT others(37): Show |
1 | a0001c0001t0001g0217 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.120+2323_120+2324i others(46): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347170 | |||||
chr2:37347170
|
T | TATCATAT others(20): Show |
1 | a0001c0003t0001g0027 | 2 | HG02451.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.120+2321_120+2322i others(29): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347170 | |||||
chr2:37347170
|
T | TC | 3 | a0001c0001t0001g0024a0001c0001t0001g0111a0001c0001t0001g0112 | 4 | HG02074.hp1 NA18948.hp2 NA18949.hp1 others(1): Show |
intron_variant | MODIFIER | c.120+2319_120+2320i others(3): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37347170 | ||||||
chr2:37347178
|
T | A | 1 | a0001c0003t0001g0142 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.120+2327T>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37347178 | ||||||
chr2:37347178
|
TA | T | 5 | a0001c0003t0001g0151a0002c0002t0002g0254a0002c0002t0002g0256others(2): Show | 5 | HG02132.hp1 HG02155.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.120+2329delA | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347178 | |||||
chr2:37347179
|
A | AT | 7 | a0001c0003t0001g0132a0001c0003t0001g0140a0001c0003t0001g0148others(4): Show | 7 | HG01884.hp2 HG01891.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.120+2328_120+2329i others(3): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37347179 | ||||||
chr2:37347179
|
A | C | 1 | a0001c0003t0001g0142 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.120+2328A>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37347179 | ||||||
chr2:37347179
|
A | T | 61 | a0002c0002t0002g0001a0002c0002t0002g0003a0002c0002t0002g0009others(58): Show | 81 | HG00438.hp2 HG00544.hp2 HG00621.hp2 others(78): Show |
intron_variant | MODIFIER | c.120+2328A>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37347179 | ||||||
chr2:37347180
|
A | T | 68 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0016others(65): Show | 80 | HG00438.hp1 HG00544.hp1 HG00642.hp2 others(77): Show |
intron_variant | MODIFIER | c.120+2329A>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37347180 | ||||||
chr2:37347181
|
C | T | 77 | a0001c0003t0001g0132a0001c0003t0001g0140a0001c0003t0001g0142others(74): Show | 97 | HG00438.hp2 HG00544.hp2 HG00621.hp2 others(94): Show |
intron_variant | MODIFIER | c.120+2330C>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37347181 | ||||||
chr2:37347183
|
T | C | 1 | a0001c0003t0001g0165 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.120+2332T>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37347183 | ||||||
chr2:37347183
|
T | TATATATA others(79): Show |
1 | a0002c0002t0002g0252 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.120+2339_120+2340i others(88): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347183 | |||||
chr2:37347183
|
T | TATATATA others(61): Show |
1 | a0001c0003t0001g0143 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.120+2339_120+2340i others(70): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347183 | |||||
chr2:37347183
|
T | TATATATA others(85): Show |
1 | a0001c0003t0001g0162 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.120+2339_120+2340i others(94): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347183 | |||||
chr2:37347183
|
T | TATATATA others(61): Show |
1 | a0001c0001t0001g0113 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.120+2339_120+2340i others(70): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347183 | |||||
chr2:37347183
|
T | TATATATA others(63): Show |
3 | a0001c0001t0001g0024a0001c0001t0001g0111a0001c0001t0001g0112 | 4 | HG02074.hp1 NA18948.hp2 NA18949.hp1 others(1): Show |
intron_variant | MODIFIER | c.120+2339_120+2340i others(72): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347183 | |||||
chr2:37347183
|
T | TATATATA others(4): Show |
1 | a0001c0001t0001g0052 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.120+2342_120+2352d others(13): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347183 | |||||
chr2:37347183
|
T | TATATATA others(76): Show |
8 | a0001c0001t0001g0014a0001c0001t0001g0019a0001c0001t0001g0030others(5): Show | 13 | HG00544.hp1 NA18947.hp2 NA18965.hp1 others(10): Show |
intron_variant | MODIFIER | c.120+2352_120+2353i others(85): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347183 | |||||
chr2:37347183
|
T | TATATATA others(67): Show |
1 | a0001c0001t0001g0195 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.120+2354_120+2355i others(76): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347183 | |||||
chr2:37347183
|
T | TATATATA others(91): Show |
1 | a0001c0001t0001g0133 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.120+2354_120+2355i others(100): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347183 | |||||
chr2:37347183
|
T | TATATATA others(54): Show |
2 | a0001c0001t0001g0118a0001c0001t0001g0119 | 2 | NA18966.hp2 NA18969.hp2 |
intron_variant | MODIFIER | c.120+2341_120+2342i others(63): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347183 | |||||
chr2:37347183
|
T | TATATATA others(96): Show |
1 | a0002c0002t0002g0297 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.120+2341_120+2342i others(105): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347183 | |||||
chr2:37347183
|
T | TATATCAT others(94): Show |
1 | a0001c0003t0001g0160 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.120+2336_120+2337i others(103): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347183 | |||||
chr2:37347183
|
T | TATTATAT others(72): Show |
1 | a0004c0005t0001g0137 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.120+2334_120+2335i others(81): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347183 | |||||
chr2:37347191
|
T | A | 1 | a0001c0001t0001g0117 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.120+2340T>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37347191 | ||||||
chr2:37347192
|
A | AT | 4 | a0001c0003t0001g0026a0001c0003t0005g0125a0001c0003t0005g0126others(1): Show | 5 | HG00280.hp1 HG01981.hp2 HG02602.hp1 others(2): Show |
intron_variant | MODIFIER | c.120+2341_120+2342i others(3): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37347192 | ||||||
chr2:37347192
|
A | C | 1 | a0001c0001t0001g0117 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.120+2341A>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37347192 | ||||||
chr2:37347192
|
A | T | 1 | a0002c0002t0002g0256 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.120+2341A>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37347192 | ||||||
chr2:37347193
|
A | T | 11 | a0001c0001t0001g0168a0001c0001t0001g0218a0001c0003t0001g0132others(8): Show | 11 | HG01891.hp2 HG02486.hp2 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.120+2342A>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37347193 | ||||||
chr2:37347194
|
C | A | 7 | a0001c0001t0001g0168a0001c0001t0001g0218a0001c0003t0001g0026others(4): Show | 8 | HG00280.hp1 HG01981.hp2 HG02602.hp1 others(5): Show |
intron_variant | MODIFIER | c.120+2343C>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37347194 | ||||||
chr2:37347194
|
C | T | 7 | a0001c0001t0001g0117a0001c0003t0001g0140a0002c0002t0002g0255others(4): Show | 7 | HG01891.hp2 HG02155.hp2 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.120+2343C>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37347194 | ||||||
chr2:37347194
|
CAT | C | 3 | a0001c0003t0001g0164a0001c0003t0001g0236a0004c0005t0001g0137 | 3 | HG02559.hp2 HG03486.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.120+2353_120+2354d others(4): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347194 | |||||
chr2:37347196
|
T | C | 3 | a0001c0001t0001g0168a0001c0001t0001g0218a0001c0006t0001g0219 | 3 | NA18966.hp1 NA19007.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.120+2345T>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37347196 | ||||||
chr2:37347196
|
T | TATATAAC others(99): Show |
3 | a0002c0002t0002g0246a0002c0002t0002g0250a0002c0002t0002g0251 | 3 | NA18612.hp2 NA19000.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.120+2350_120+2351i others(108): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347196 | |||||
chr2:37347196
|
T | TATATATA others(88): Show |
1 | a0002c0002t0002g0278 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.120+2352_120+2353i others(97): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347196 | |||||
chr2:37347196
|
T | TATATATA others(99): Show |
1 | a0002c0002t0002g0279 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.120+2352_120+2353i others(108): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347196 | |||||
chr2:37347196
|
T | TATATATA others(134): Show |
1 | a0002c0002t0002g0266 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.120+2352_120+2353i others(143): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347196 | |||||
chr2:37347196
|
T | TATATATA others(101): Show |
1 | a0002c0002t0002g0248 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.120+2352_120+2353i others(110): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347196 | |||||
chr2:37347196
|
T | TATATATA others(90): Show |
1 | a0002c0002t0002g0272 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.120+2352_120+2353i others(99): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347196 | |||||
chr2:37347196
|
T | TATATATA others(101): Show |
16 | a0002c0002t0002g0038a0002c0002t0002g0249a0002c0002t0002g0253others(13): Show | 19 | HG00438.hp2 HG01192.hp2 HG01975.hp2 others(16): Show |
intron_variant | MODIFIER | c.120+2352_120+2353i others(110): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347196 | |||||
chr2:37347196
|
T | TATATATA others(112): Show |
2 | a0002c0002t0002g0281a0002c0002t0002g0282 | 2 | NA18956.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.120+2352_120+2353i others(121): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347196 | |||||
chr2:37347196
|
T | TATATATA others(90): Show |
1 | a0002c0002t0002g0293 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.120+2352_120+2353i others(99): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347196 | |||||
chr2:37347196
|
T | TATATATA others(101): Show |
1 | a0002c0002t0002g0299 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.120+2352_120+2353i others(110): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347196 | |||||
chr2:37347196
|
T | TATATATA others(37): Show |
1 | a0004c0005t0001g0138 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.120+2352_120+2353i others(46): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347196 | |||||
chr2:37347196
|
T | TATATATA others(87): Show |
1 | a0003c0004t0002g0061 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.120+2352_120+2353i others(96): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347196 | |||||
chr2:37347196
|
T | TATATATA others(87): Show |
3 | a0001c0001t0001g0046a0001c0001t0001g0090a0003c0004t0002g0053 | 3 | NA18960.hp1 NA18969.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.120+2352_120+2353i others(96): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347196 | |||||
chr2:37347196
|
T | TATATATA others(85): Show |
1 | a0004c0005t0003g0139 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.120+2352_120+2353i others(94): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347196 | |||||
chr2:37347196
|
T | TATATATA others(6): Show |
1 | a0001c0001t0001g0204 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.120+2354_120+2355i others(15): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347196 | |||||
chr2:37347202
|
T | TAACATAT others(117): Show |
1 | a0002c0002t0002g0280 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.120+2352_120+2353i others(126): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347202 | |||||
chr2:37347202
|
T | TAACATAT others(108): Show |
1 | a0002c0002t0002g0260 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.120+2352_120+2353i others(117): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347202 | |||||
chr2:37347202
|
T | TAACATAT others(106): Show |
10 | a0002c0002t0002g0001a0002c0002t0002g0031a0002c0002t0002g0247others(7): Show | 16 | HG00621.hp2 HG00639.hp2 HG01257.hp2 others(13): Show |
intron_variant | MODIFIER | c.120+2352_120+2353i others(115): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347202 | |||||
chr2:37347202
|
T | TAACATAT others(84): Show |
1 | a0002c0002t0002g0292 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.120+2352_120+2353i others(93): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347202 | |||||
chr2:37347202
|
T | TAACATAT others(95): Show |
16 | a0002c0002t0002g0009a0002c0002t0002g0032a0002c0002t0002g0033others(13): Show | 22 | HG00544.hp2 HG01934.hp2 HG02083.hp2 others(19): Show |
intron_variant | MODIFIER | c.120+2352_120+2353i others(104): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347202 | |||||
chr2:37347202
|
T | TAACATAT others(106): Show |
1 | a0002c0002t0002g0003 | 5 | NA18944.hp2 NA18945.hp1 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.120+2352_120+2353i others(115): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347202 | |||||
chr2:37347202
|
T | TAACATAT others(106): Show |
2 | a0002c0002t0002g0265a0002c0002t0008g0259 | 2 | HG02056.hp2 HG02080.hp2 |
intron_variant | MODIFIER | c.120+2352_120+2353i others(115): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347202 | |||||
chr2:37347202
|
T | TAACATAT others(95): Show |
1 | a0002c0002t0002g0037 | 2 | HG02132.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.120+2352_120+2353i others(104): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347202 | |||||
chr2:37347202
|
T | TAACATAT others(106): Show |
1 | a0002c0002t0002g0277 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.120+2352_120+2353i others(115): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347202 | |||||
chr2:37347204
|
T | A | 7 | a0001c0001t0001g0049a0001c0001t0001g0122a0001c0001t0001g0123others(4): Show | 8 | HG00558.hp1 HG00673.hp2 HG01361.hp2 others(5): Show |
intron_variant | MODIFIER | c.120+2353T>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37347204 | ||||||
chr2:37347205
|
A | AT | 36 | a0002c0002t0002g0001a0002c0002t0002g0003a0002c0002t0002g0009others(33): Show | 53 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.120+2354_120+2355i others(3): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37347205 | ||||||
chr2:37347205
|
A | ATAACATA others(78): Show |
2 | a0001c0001t0001g0226a0001c0001t0001g0228 | 2 | HG01070.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.120+2354_120+2355i others(87): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37347205 | ||||||
chr2:37347205
|
A | ATAACATA others(78): Show |
1 | a0001c0001t0001g0179 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.120+2354_120+2355i others(87): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37347205 | ||||||
chr2:37347205
|
A | ATAACATA others(80): Show |
33 | a0001c0001t0001g0007a0001c0001t0001g0016a0001c0001t0001g0028others(30): Show | 40 | HG00642.hp2 HG00741.hp1 HG01069.hp1 others(37): Show |
intron_variant | MODIFIER | c.120+2354_120+2355i others(89): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37347205 | ||||||
chr2:37347205
|
A | ATAACATA others(79): Show |
1 | a0001c0001t0001g0215 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.120+2354_120+2355i others(88): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37347205 | ||||||
chr2:37347205
|
A | ATAACATA others(82): Show |
1 | a0001c0001t0002g0201 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.120+2354_120+2355i others(91): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37347205 | ||||||
chr2:37347205
|
A | ATAACATA others(82): Show |
1 | a0001c0001t0001g0202 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.120+2354_120+2355i others(91): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37347205 | ||||||
chr2:37347205
|
A | ATATAACA others(80): Show |
1 | a0001c0001t0001g0196 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.120+2354_120+2355i others(89): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37347205 | ||||||
chr2:37347205
|
A | ATATATAA others(3): Show |
3 | a0001c0003t0001g0147a0001c0003t0001g0150a0001c0003t0001g0157 | 3 | HG01891.hp1 HG02145.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.120+2354_120+2355i others(12): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37347205 | ||||||
chr2:37347205
|
A | C | 6 | a0001c0001t0001g0049a0001c0001t0001g0122a0001c0001t0001g0123others(3): Show | 7 | HG00558.hp1 HG00673.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.120+2354A>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37347205 | ||||||
chr2:37347205
|
A | T | 1 | a0001c0003t0002g0232 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.120+2354A>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37347205 | ||||||
chr2:37347207
|
C | CAT | 7 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0003t0001g0128others(4): Show | 7 | HG02145.hp1 HG02257.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.120+2364_120+2365d others(4): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347207 | |||||
chr2:37347207
|
C | CATAT | 39 | a0001c0003t0001g0015a0001c0003t0001g0142a0001c0003t0001g0143others(36): Show | 44 | HG00438.hp2 HG01192.hp2 HG01975.hp2 others(41): Show |
intron_variant | MODIFIER | c.120+2362_120+2365d others(6): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347207 | |||||
chr2:37347207
|
C | CATATATA others(109): Show |
1 | a0002c0002t0002g0256 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.120+2376_120+2377i others(118): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347207 | |||||
chr2:37347207
|
C | CATATATA others(153): Show |
1 | a0002c0002t0002g0255 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.120+2376_120+2377i others(162): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347207 | |||||
chr2:37347207
|
C | CATATATA others(80): Show |
2 | a0001c0003t0001g0148a0001c0003t0001g0151 | 2 | HG02486.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.120+2376_120+2377i others(89): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347207 | |||||
chr2:37347207
|
C | CATATATA others(69): Show |
1 | a0001c0003t0001g0132 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.120+2376_120+2377i others(78): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347207 | |||||
chr2:37347207
|
C | T | 86 | a0001c0001t0001g0007a0001c0001t0001g0016a0001c0001t0001g0028others(83): Show | 111 | HG00544.hp2 HG00558.hp1 HG00621.hp2 others(108): Show |
intron_variant | MODIFIER | c.120+2356C>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37347207 | ||||||
chr2:37347220
|
T | C | 1 | a0001c0003t0002g0233 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.120+2369T>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37347220 | ||||||
chr2:37347220
|
T | TATATATA others(89): Show |
1 | a0001c0001t0001g0203 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.120+2376_120+2377i others(98): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347220 | |||||
chr2:37347224
|
T | TATAACAT others(133): Show |
4 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0109others(1): Show | 4 | HG02258.hp1 HG02572.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.120+2376_120+2377i others(142): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347224 | |||||
chr2:37347226
|
T | TAACATAT others(165): Show |
1 | a0001c0001t0001g0106 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.120+2376_120+2377i others(174): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347226 | |||||
chr2:37347229
|
A | AT | 6 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0108others(3): Show | 6 | HG02258.hp1 HG02572.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.120+2378_120+2379i others(3): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37347229 | ||||||
chr2:37347231
|
C | CAT | 13 | a0001c0001t0001g0243a0001c0001t0003g0244a0001c0003t0001g0132others(10): Show | 13 | HG01069.hp2 HG01884.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.120+2394_120+2395d others(4): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347231 | |||||
chr2:37347231
|
C | CATAT | 14 | a0001c0001t0001g0049a0001c0001t0001g0111a0001c0001t0001g0115others(11): Show | 15 | HG00558.hp1 HG00673.hp2 HG01952.hp2 others(12): Show |
intron_variant | MODIFIER | c.120+2392_120+2395d others(6): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347231 | |||||
chr2:37347231
|
C | CATATAT | 42 | a0001c0001t0001g0007a0001c0001t0001g0016a0001c0001t0001g0028others(39): Show | 49 | HG00438.hp1 HG00642.hp2 HG00741.hp1 others(46): Show |
intron_variant | MODIFIER | c.120+2390_120+2395d others(8): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347231 | |||||
chr2:37347231
|
C | CATATATA others(1): Show |
18 | a0001c0001t0001g0014a0001c0001t0001g0019a0001c0001t0001g0024others(15): Show | 24 | HG00544.hp1 HG00735.hp1 HG02074.hp1 others(21): Show |
intron_variant | MODIFIER | c.120+2388_120+2395d others(10): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347231 | |||||
chr2:37347231
|
C | CATATATA others(38): Show |
1 | a0001c0001t0001g0055 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.120+2389_120+2390i others(47): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347231 | |||||
chr2:37347231
|
C | CATATATA others(54): Show |
4 | a0001c0003t0001g0140a0004c0005t0001g0130a0004c0005t0001g0131others(1): Show | 4 | HG01891.hp2 HG03453.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.120+2389_120+2390i others(63): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347231 | |||||
chr2:37347231
|
C | CATATATA others(108): Show |
1 | a0001c0001t0001g0052 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.120+2389_120+2390i others(117): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347231 | |||||
chr2:37347231
|
C | CATATATA others(25): Show |
1 | a0001c0001t0001g0025 | 2 | HG02165.hp2 NA19006.hp2 |
intron_variant | MODIFIER | c.120+2389_120+2390i others(34): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347231 | |||||
chr2:37347231
|
C | CATATATA others(34): Show |
1 | a0001c0001t0001g0189 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.120+2389_120+2390i others(43): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347231 | |||||
chr2:37347231
|
C | CATATATA others(27): Show |
3 | a0001c0001t0001g0114a0001c0001t0001g0240a0001c0001t0001g0241 | 3 | HG00558.hp2 NA18997.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.120+2389_120+2390i others(36): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347231 | |||||
chr2:37347231
|
C | CATATATA others(36): Show |
36 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0012others(33): Show | 48 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(45): Show |
intron_variant | MODIFIER | c.120+2389_120+2390i others(45): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347231 | |||||
chr2:37347231
|
C | CATATATA others(38): Show |
28 | a0001c0001t0001g0013a0001c0001t0001g0022a0001c0001t0001g0023others(25): Show | 34 | HG00735.hp2 HG01074.hp1 HG01123.hp2 others(31): Show |
intron_variant | MODIFIER | c.120+2389_120+2390i others(47): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347231 | |||||
chr2:37347231
|
C | CATATATA others(40): Show |
11 | a0001c0001t0001g0011a0001c0001t0001g0018a0001c0001t0001g0059others(8): Show | 14 | HG01081.hp2 HG01099.hp2 HG01346.hp1 others(11): Show |
intron_variant | MODIFIER | c.120+2389_120+2390i others(49): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347231 | |||||
chr2:37347231
|
C | CATATATA others(42): Show |
2 | a0001c0001t0001g0214a0003c0004t0002g0097 | 2 | HG00597.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.120+2389_120+2390i others(51): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347231 | |||||
chr2:37347231
|
C | CATATATA others(44): Show |
1 | a0001c0001t0001g0089 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.120+2389_120+2390i others(53): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347231 | |||||
chr2:37347231
|
C | CATATATA others(55): Show |
1 | a0001c0001t0001g0124 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.120+2389_120+2390i others(64): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347231 | |||||
chr2:37347231
|
C | CATATATA others(65): Show |
1 | a0001c0001t0001g0084 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.120+2389_120+2390i others(74): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347231 | |||||
chr2:37347231
|
C | CATATATA others(47): Show |
3 | a0001c0003t0001g0145a0001c0003t0001g0156a0001c0003t0001g0158 | 3 | HG02615.hp2 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.120+2389_120+2390i others(56): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347231 | |||||
chr2:37347231
|
C | CATATATA others(31): Show |
1 | a0001c0001t0001g0100 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.120+2389_120+2390i others(40): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347231 | |||||
chr2:37347231
|
C | CATATATA others(33): Show |
3 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0103 | 3 | HG00642.hp1 HG03834.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.120+2389_120+2390i others(42): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347231 | |||||
chr2:37347231
|
C | CATATATA others(31): Show |
1 | a0001c0001t0001g0104 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.120+2389_120+2390i others(40): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347231 | |||||
chr2:37347231
|
C | CATATATA others(35): Show |
1 | a0001c0001t0001g0105 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.120+2389_120+2390i others(44): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347231 | |||||
chr2:37347231
|
C | CATATATA others(3): Show |
1 | a0001c0003t0001g0359 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.120+2386_120+2395d others(12): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347231 | |||||
chr2:37347231
|
C | CATATATA others(106): Show |
1 | a0001c0001t0001g0204 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.120+2391_120+2392i others(115): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347231 | |||||
chr2:37347231
|
C | CATATATA others(71): Show |
1 | a0001c0006t0001g0219 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.120+2391_120+2392i others(80): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347231 | |||||
chr2:37347231
|
C | CATATATA others(73): Show |
1 | a0001c0001t0001g0218 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.120+2391_120+2392i others(82): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347231 | |||||
chr2:37347231
|
C | CATATATA others(60): Show |
3 | a0001c0003t0001g0163a0001c0003t0001g0164a0001c0003t0001g0236 | 3 | HG02809.hp2 HG03486.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.120+2391_120+2392i others(69): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347231 | |||||
chr2:37347231
|
C | CATATATA others(21): Show |
1 | a0001c0003t0003g0362 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.120+2391_120+2392i others(30): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347231 | |||||
chr2:37347231
|
C | CATATATA others(75): Show |
1 | a0001c0001t0001g0168 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.120+2391_120+2392i others(84): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347231 | |||||
chr2:37347231
|
C | CATATATA others(23): Show |
11 | a0001c0003t0001g0027a0001c0003t0001g0144a0001c0003t0001g0146others(8): Show | 12 | HG00738.hp2 HG01243.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.120+2393_120+2394i others(32): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347231 | |||||
chr2:37347231
|
C | CATATATA others(25): Show |
1 | a0001c0003t0001g0360 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.120+2393_120+2394i others(34): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347231 | |||||
chr2:37347231
|
C | CATATATA others(25): Show |
2 | a0001c0003t0001g0154a0001c0003t0001g0155 | 2 | HG03130.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.120+2408_120+2409i others(34): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347231 | |||||
chr2:37347231
|
C | T | 7 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0108others(4): Show | 7 | HG01106.hp1 HG02258.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.120+2380C>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37347231 | ||||||
chr2:37347235
|
T | TATATAAC others(13): Show |
5 | a0001c0001t0001g0017a0001c0001t0001g0075a0001c0001t0001g0136others(2): Show | 7 | NA18953.hp2 NA18973.hp1 NA18979.hp2 others(4): Show |
intron_variant | MODIFIER | c.120+2389_120+2390i others(22): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37347235 | |||||
chr2:37347442
|
T | A | 1 | a0001c0001t0001g0221 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.120+2591T>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37347442 | ||||||
chr2:37347683
|
C | T | 1 | a0001c0001t0001g0303 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.120+2832C>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37347683 | ||||||
chr2:37347822
|
T | G | 65 | a0002c0002t0002g0001a0002c0002t0002g0003a0002c0002t0002g0009others(62): Show | 85 | HG00438.hp2 HG00544.hp2 HG00621.hp2 others(82): Show |
intron_variant | MODIFIER | c.120+2971T>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37347822 | ||||||
chr2:37347883
|
C | G | 294 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(291): Show | 356 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(353): Show |
intron_variant | MODIFIER | c.120+3032C>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37347883 | ||||||
chr2:37347897
|
C | A | 1 | a0001c0001t0001g0304 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.120+3046C>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37347897 | ||||||
chr2:37347954
|
A | G | 73 | a0001c0003t0001g0140a0001c0003t0001g0155a0002c0002t0002g0001others(70): Show | 93 | HG00438.hp2 HG00544.hp2 HG00621.hp2 others(90): Show |
intron_variant | MODIFIER | c.120+3103A>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37347954 | ||||||
chr2:37348038
|
A | ATCTC | 79 | a0001c0003t0001g0026a0001c0003t0001g0140a0001c0003t0001g0155others(76): Show | 102 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(99): Show |
intron_variant | MODIFIER | c.120+3197_120+3200d others(6): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37348038 | |||||
chr2:37348038
|
A | ATCTCTC | 221 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(218): Show | 260 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(257): Show |
intron_variant | MODIFIER | c.120+3195_120+3200d others(8): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37348038 | |||||
chr2:37348054
|
G | A | 1 | a0002c0002t0002g0036 | 2 | NA18941.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.120+3203G>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37348054 | ||||||
chr2:37348063
|
C | CGT | 21 | a0001c0001t0001g0040a0001c0001t0001g0304a0001c0001t0001g0307others(18): Show | 23 | HG00639.hp1 HG01261.hp2 HG01358.hp2 others(20): Show |
intron_variant | MODIFIER | c.120+3237_120+3238d others(4): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37348063 | |||||
chr2:37348063
|
C | CGTGT | 4 | a0001c0001t0002g0305a0001c0001t0002g0306a0001c0001t0002g0353others(1): Show | 4 | HG02040.hp2 HG02083.hp1 HG02129.hp2 others(1): Show |
intron_variant | MODIFIER | c.120+3235_120+3238d others(6): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37348063 | |||||
chr2:37348063
|
C | T | 2 | a0001c0001t0001g0039a0001c0001t0001g0340 | 3 | HG00099.hp1 HG03834.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.120+3212C>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37348063 | ||||||
chr2:37348063
|
CGT | C | 250 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(247): Show | 309 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(306): Show |
intron_variant | MODIFIER | c.120+3237_120+3238d others(4): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37348063 | |||||
chr2:37348064
|
G | A | 3 | a0001c0003t0001g0128a0001c0003t0001g0359a0001c0003t0003g0129 | 3 | HG02145.hp1 HG02559.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.120+3213G>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37348064 | ||||||
chr2:37348064
|
G | T | 30 | a0001c0003t0001g0027a0001c0003t0001g0132a0001c0003t0001g0143others(27): Show | 31 | HG00738.hp2 HG01243.hp1 HG01884.hp2 others(28): Show |
intron_variant | MODIFIER | c.120+3213G>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37348064 | ||||||
chr2:37348065
|
T | C | 1 | a0001c0001t0001g0113 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.120+3214T>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37348065 | ||||||
chr2:37348067
|
T | C | 2 | a0001c0003t0001g0155a0004c0005t0001g0137 | 2 | HG02559.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.120+3216T>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37348067 | ||||||
chr2:37348121
|
C | T | 5 | a0001c0003t0001g0140a0004c0005t0001g0130a0004c0005t0001g0131others(2): Show | 5 | HG01106.hp1 HG01891.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.120+3270C>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37348121 | ||||||
chr2:37348131
|
T | C | 1 | a0001c0001t0001g0107 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.120+3280T>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37348131 | ||||||
chr2:37348144
|
C | T | 290 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(287): Show | 352 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(349): Show |
intron_variant | MODIFIER | c.120+3293C>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37348144 | ||||||
chr2:37348238
|
C | G | 93 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0012others(90): Show | 118 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.120+3387C>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37348238 | ||||||
chr2:37348300
|
C | T | 1 | a0002c0002t0002g0253 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.120+3449C>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37348300 | ||||||
chr2:37348359
|
A | G | 1 | a0001c0003t0001g0153 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.120+3508A>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37348359 | ||||||
chr2:37348434
|
C | G | 75 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0016others(72): Show | 88 | HG00438.hp1 HG00597.hp2 HG00642.hp2 others(85): Show |
intron_variant | MODIFIER | c.120+3583C>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37348434 | ||||||
chr2:37348437
|
C | G | 7 | a0001c0003t0001g0360a0001c0003t0001g0363a0001c0003t0001g0366others(4): Show | 7 | HG02109.hp1 HG02451.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.120+3586C>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37348437 | ||||||
chr2:37348478
|
G | T | 1 | a0001c0001t0002g0353 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.120+3627G>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37348478 | ||||||
chr2:37348512
|
C | T | 8 | a0001c0003t0001g0145a0001c0003t0001g0147a0001c0003t0001g0150others(5): Show | 8 | HG01884.hp2 HG01891.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.120+3661C>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37348512 | ||||||
chr2:37348604
|
C | A | 5 | a0001c0001t0001g0018a0001c0001t0001g0203a0001c0001t0001g0204others(2): Show | 7 | HG01099.hp2 HG01243.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.120+3753C>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37348604 | ||||||
chr2:37348813
|
G | A | 3 | a0001c0001t0001g0023a0001c0001t0001g0086a0001c0001t0001g0087 | 4 | NA18971.hp1 NA19004.hp1 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.120+3962G>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37348813 | ||||||
chr2:37348820
|
T | C | 4 | a0001c0001t0001g0040a0001c0001t0001g0304a0001c0001t0001g0307others(1): Show | 5 | HG02572.hp1 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.120+3969T>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37348820 | ||||||
chr2:37348867
|
T | C | 3 | a0001c0003t0001g0128a0001c0003t0001g0359a0001c0003t0003g0129 | 3 | HG02145.hp1 HG02559.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.121-3922T>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37348867 | ||||||
chr2:37348993
|
A | G | 56 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0012others(53): Show | 71 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.121-3796A>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37348993 | ||||||
chr2:37349060
|
C | T | 1 | a0004c0005t0003g0139 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.121-3729C>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37349060 | ||||||
chr2:37349134
|
C | A | 4 | a0001c0003t0001g0026a0001c0003t0005g0125a0001c0003t0005g0126others(1): Show | 5 | HG00280.hp1 HG01981.hp2 HG02602.hp1 others(2): Show |
intron_variant | MODIFIER | c.121-3655C>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37349134 | ||||||
chr2:37349259
|
A | G | 1 | a0001c0003t0001g0142 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.121-3530A>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37349259 | ||||||
chr2:37349308
|
A | G | 1 | a0001c0001t0001g0083 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.121-3481A>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37349308 | ||||||
chr2:37349410
|
A | G | 303 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(300): Show | 365 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(362): Show |
intron_variant | MODIFIER | c.121-3379A>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37349410 | ||||||
chr2:37349495
|
C | T | 293 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(290): Show | 353 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(350): Show |
intron_variant | MODIFIER | c.121-3294C>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37349495 | ||||||
chr2:37349606
|
C | G | 1 | a0001c0003t0001g0245 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.121-3183C>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37349606 | ||||||
chr2:37349709
|
A | G | 289 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(286): Show | 348 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(345): Show |
intron_variant | MODIFIER | c.121-3080A>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37349709 | ||||||
chr2:37349772
|
G | C | 66 | a0002c0002t0002g0001a0002c0002t0002g0003a0002c0002t0002g0009others(63): Show | 86 | HG00438.hp2 HG00544.hp2 HG00621.hp2 others(83): Show |
intron_variant | MODIFIER | c.121-3017G>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37349772 | ||||||
chr2:37349830
|
G | GA | 292 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(289): Show | 352 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(349): Show |
intron_variant | MODIFIER | c.121-2954dupA | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37349830 | |||||
chr2:37349847
|
C | G | 9 | a0001c0003t0001g0015a0001c0003t0001g0165a0001c0003t0001g0360others(6): Show | 11 | HG02109.hp1 HG02451.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.121-2942C>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37349847 | ||||||
chr2:37349880
|
A | G | 9 | a0001c0003t0001g0015a0001c0003t0001g0165a0001c0003t0001g0360others(6): Show | 11 | HG02109.hp1 HG02451.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.121-2909A>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37349880 | ||||||
chr2:37350242
|
G | T | 10 | a0001c0003t0001g0015a0001c0003t0001g0165a0001c0003t0001g0245others(7): Show | 12 | HG02109.hp1 HG02451.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.121-2547G>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37350242 | ||||||
chr2:37350257
|
G | C | 1 | a0001c0003t0001g0142 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.121-2532G>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37350257 | ||||||
chr2:37350266
|
C | A | 23 | a0001c0003t0001g0027a0001c0003t0001g0132a0001c0003t0001g0143others(20): Show | 24 | HG00738.hp2 HG01243.hp1 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.121-2523C>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37350266 | ||||||
chr2:37350352
|
G | C | 1 | a0001c0001t0001g0303 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.121-2437G>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37350352 | ||||||
chr2:37350635
|
T | G | 3 | a0001c0003t0001g0128a0001c0003t0001g0359a0001c0003t0003g0129 | 3 | HG02145.hp1 HG02559.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.121-2154T>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37350635 | ||||||
chr2:37350776
|
A | G | 4 | a0001c0003t0001g0026a0001c0003t0005g0125a0001c0003t0005g0126others(1): Show | 5 | HG00280.hp1 HG01981.hp2 HG02602.hp1 others(2): Show |
intron_variant | MODIFIER | c.121-2013A>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37350776 | ||||||
chr2:37350907
|
A | T | 1 | a0001c0003t0002g0232 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.121-1882A>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37350907 | ||||||
chr2:37350973
|
TGCTGAGT others(6): Show |
T | 1 | a0001c0001t0001g0070 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.121-1801_121-1789d others(15): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37350973 | |||||
chr2:37350992
|
G | C | 1 | a0003c0004t0002g0308 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.121-1797G>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37350992 | ||||||
chr2:37351002
|
T | C | 1 | a0001c0001t0001g0230 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.121-1787T>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37351002 | ||||||
chr2:37351065
|
G | A | 285 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(282): Show | 345 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(342): Show |
intron_variant | MODIFIER | c.121-1724G>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37351065 | ||||||
chr2:37351079
|
T | G | 2 | a0001c0001t0001g0243a0001c0001t0003g0244 | 2 | HG02109.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.121-1710T>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37351079 | ||||||
chr2:37351160
|
G | C | 301 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(298): Show | 363 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(360): Show |
intron_variant | MODIFIER | c.121-1629G>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37351160 | ||||||
chr2:37351179
|
G | A | 1 | a0004c0005t0001g0137 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.121-1610G>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37351179 | ||||||
chr2:37351221
|
C | A | 4 | a0001c0003t0001g0026a0001c0003t0005g0125a0001c0003t0005g0126others(1): Show | 5 | HG00280.hp1 HG01981.hp2 HG02602.hp1 others(2): Show |
intron_variant | MODIFIER | c.121-1568C>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37351221 | ||||||
chr2:37351437
|
A | C | 1 | a0004c0005t0003g0139 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.121-1352A>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37351437 | ||||||
chr2:37351455
|
T | C | 1 | a0001c0001t0001g0319 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.121-1334T>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37351455 | ||||||
chr2:37351629
|
C | T | 5 | a0001c0003t0001g0140a0004c0005t0001g0130a0004c0005t0001g0131others(2): Show | 5 | HG01106.hp1 HG01891.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.121-1160C>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37351629 | ||||||
chr2:37351758
|
T | C | 2 | a0001c0003t0001g0154a0001c0003t0001g0245 | 2 | HG02976.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.121-1031T>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37351758 | ||||||
chr2:37351769
|
C | G | 1 | a0003c0004t0002g0308 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.121-1020C>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37351769 | ||||||
chr2:37351927
|
G | C | 2 | a0001c0001t0001g0169a0001c0001t0001g0181 | 2 | NA18964.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.121-862G>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37351927 | ||||||
chr2:37351930
|
T | C | 4 | a0001c0003t0001g0026a0001c0003t0005g0125a0001c0003t0005g0126others(1): Show | 5 | HG00280.hp1 HG01981.hp2 HG02602.hp1 others(2): Show |
intron_variant | MODIFIER | c.121-859T>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37351930 | ||||||
chr2:37352016
|
G | C | 74 | a0001c0003t0001g0140a0001c0003t0001g0155a0002c0002t0002g0001others(71): Show | 94 | HG00438.hp2 HG00544.hp2 HG00621.hp2 others(91): Show |
intron_variant | MODIFIER | c.121-773G>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37352016 | ||||||
chr2:37352029
|
C | CA | 6 | a0001c0001t0001g0206a0001c0003t0001g0026a0001c0003t0005g0125others(3): Show | 7 | HG00280.hp1 HG01981.hp2 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.121-746dupA | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37352029 | |||||
chr2:37352029
|
C | CAA | 72 | a0001c0003t0001g0140a0001c0003t0001g0155a0002c0002t0002g0001others(69): Show | 92 | HG00438.hp2 HG00544.hp2 HG00621.hp2 others(89): Show |
intron_variant | MODIFIER | c.121-747_121-746dup others(2): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr2 | 37352029 | |||||
chr2:37352039
|
A | T | 9 | a0001c0003t0001g0015a0001c0003t0001g0165a0001c0003t0001g0360others(6): Show | 11 | HG02109.hp1 HG02451.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.121-750A>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37352039 | ||||||
chr2:37352043
|
A | G | 1 | a0001c0001t0001g0046 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.121-746A>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37352043 | ||||||
chr2:37352049
|
T | C | 74 | a0001c0003t0001g0140a0001c0003t0001g0155a0002c0002t0002g0001others(71): Show | 94 | HG00438.hp2 HG00544.hp2 HG00621.hp2 others(91): Show |
intron_variant | MODIFIER | c.121-740T>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37352049 | ||||||
chr2:37352324
|
T | A | 4 | a0001c0003t0001g0026a0001c0003t0005g0125a0001c0003t0005g0126others(1): Show | 5 | HG00280.hp1 HG01981.hp2 HG02602.hp1 others(2): Show |
intron_variant | MODIFIER | c.121-465T>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37352324 | ||||||
chr2:37352368
|
G | A | 1 | a0001c0001t0001g0226 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.121-421G>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37352368 | ||||||
chr2:37352440
|
C | T | 3 | a0001c0001t0001g0012a0001c0001t0001g0076a0001c0001t0001g0079 | 5 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(2): Show |
intron_variant | MODIFIER | c.121-349C>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37352440 | ||||||
chr2:37352466
|
G | T | 1 | a0001c0001t0001g0339 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.121-323G>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 1/6 | chr2 | 37352466 | ||||||
chr2:37353019
|
G | T | 1 | a0001c0003t0001g0245 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.267+84G>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37353019 | ||||||
chr2:37353202
|
A | T | 1 | a0001c0001t0001g0338 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.267+267A>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37353202 | ||||||
chr2:37353323
|
G | A | 2 | a0001c0001t0001g0184a0004c0005t0001g0137 | 2 | HG02559.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.267+388G>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37353323 | ||||||
chr2:37353348
|
G | C | 1 | a0001c0001t0001g0108 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.267+413G>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37353348 | ||||||
chr2:37353430
|
A | T | 1 | a0001c0001t0001g0176 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.267+495A>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37353430 | ||||||
chr2:37353509
|
T | A | 1 | a0001c0003t0003g0361 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.267+574T>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37353509 | ||||||
chr2:37353540
|
T | C | 2 | a0001c0001t0001g0187a0001c0001t0001g0188 | 2 | HG02257.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.267+605T>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37353540 | ||||||
chr2:37353584
|
A | G | 47 | a0001c0001t0001g0303a0001c0001t0003g0244a0001c0003t0001g0015others(44): Show | 50 | HG00738.hp2 HG01243.hp1 HG01361.hp2 others(47): Show |
intron_variant | MODIFIER | c.267+649A>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37353584 | ||||||
chr2:37353603
|
T | C | 1 | a0001c0001t0001g0081 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.267+668T>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37353603 | ||||||
chr2:37353667
|
C | A | 1 | a0001c0001t0002g0320 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.267+732C>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37353667 | ||||||
chr2:37353697
|
A | G | 12 | a0001c0001t0003g0244a0001c0003t0001g0015a0001c0003t0001g0140others(9): Show | 14 | HG01891.hp2 HG02109.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.267+762A>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37353697 | ||||||
chr2:37353717
|
T | G | 51 | a0001c0001t0001g0303a0001c0001t0003g0244a0001c0003t0001g0015others(48): Show | 54 | HG00738.hp2 HG01106.hp1 HG01243.hp1 others(51): Show |
intron_variant | MODIFIER | c.267+782T>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37353717 | ||||||
chr2:37353820
|
A | C | 2 | a0001c0001t0001g0172a0001c0001t0001g0210 | 2 | HG02735.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.267+885A>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37353820 | ||||||
chr2:37353966
|
A | G | 1 | a0001c0001t0001g0318 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.267+1031A>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37353966 | ||||||
chr2:37354007
|
G | A | 2 | a0001c0003t0001g0128a0001c0003t0003g0129 | 2 | HG02145.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.267+1072G>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37354007 | ||||||
chr2:37354111
|
G | A | 64 | a0001c0003t0001g0154a0002c0002t0002g0001a0002c0002t0002g0003others(61): Show | 84 | HG00438.hp2 HG00544.hp2 HG00621.hp2 others(81): Show |
intron_variant | MODIFIER | c.267+1176G>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37354111 | ||||||
chr2:37354224
|
A | G | 66 | a0001c0001t0001g0029a0001c0001t0001g0200a0001c0001t0001g0202others(63): Show | 71 | HG00735.hp1 HG00738.hp1 HG00738.hp2 others(68): Show |
intron_variant | MODIFIER | c.267+1289A>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37354224 | ||||||
chr2:37354504
|
T | C | 4 | a0001c0001t0001g0075a0003c0004t0002g0010a0003c0004t0002g0054others(1): Show | 6 | HG02071.hp2 NA18946.hp2 NA18951.hp1 others(3): Show |
intron_variant | MODIFIER | c.267+1569T>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37354504 | ||||||
chr2:37354614
|
A | C | 1 | a0001c0001t0001g0223 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.267+1679A>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37354614 | ||||||
chr2:37354619
|
A | G | 2 | a0001c0003t0001g0155a0004c0005t0001g0137 | 2 | HG02559.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.267+1684A>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37354619 | ||||||
chr2:37354642
|
T | A | 2 | a0001c0001t0001g0043a0001c0001t0001g0191 | 2 | HG03710.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.267+1707T>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37354642 | ||||||
chr2:37354856
|
G | T | 1 | a0001c0001t0001g0169 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.267+1921G>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37354856 | ||||||
chr2:37354868
|
C | T | 1 | a0001c0001t0001g0205 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.267+1933C>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37354868 | ||||||
chr2:37354973
|
C | G | 49 | a0001c0001t0003g0244a0001c0003t0001g0015a0001c0003t0001g0027others(46): Show | 52 | HG00738.hp2 HG01106.hp1 HG01243.hp1 others(49): Show |
intron_variant | MODIFIER | c.267+2038C>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37354973 | ||||||
chr2:37355253
|
G | T | 1 | a0001c0001t0001g0081 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.267+2318G>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37355253 | ||||||
chr2:37355325
|
A | G | 7 | a0001c0003t0001g0167a0001c0003t0001g0359a0001c0003t0002g0166others(4): Show | 7 | HG01361.hp2 HG02280.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.267+2390A>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37355325 | ||||||
chr2:37355434
|
A | G | 1 | a0001c0001t0002g0353 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.267+2499A>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37355434 | ||||||
chr2:37355530
|
T | G | 1 | a0002c0002t0002g0254 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.267+2595T>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37355530 | ||||||
chr2:37355543
|
A | G | 2 | a0001c0001t0001g0044a0003c0004t0002g0045 | 2 | HG01255.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.267+2608A>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37355543 | ||||||
chr2:37355545
|
T | C | 1 | a0001c0001t0001g0079 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.267+2610T>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37355545 | ||||||
chr2:37355684
|
G | A | 1 | a0001c0001t0001g0321 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.267+2749G>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37355684 | ||||||
chr2:37355773
|
A | T | 49 | a0001c0003t0001g0015a0001c0003t0001g0027a0001c0003t0001g0132others(46): Show | 52 | HG00738.hp2 HG01106.hp1 HG01243.hp1 others(49): Show |
intron_variant | MODIFIER | c.267+2838A>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37355773 | ||||||
chr2:37355792
|
G | A | 2 | a0001c0001t0001g0133a0001c0001t0001g0195 | 2 | HG00438.hp1 NA18954.hp2 |
intron_variant | MODIFIER | c.267+2857G>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37355792 | ||||||
chr2:37355836
|
A | T | 1 | a0001c0001t0001g0340 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.267+2901A>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37355836 | ||||||
chr2:37355945
|
C | T | 1 | a0002c0002t0002g0290 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.267+3010C>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37355945 | ||||||
chr2:37356093
|
A | G | 1 | a0002c0002t0002g0253 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.267+3158A>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37356093 | ||||||
chr2:37356423
|
C | A | 1 | a0002c0002t0002g0277 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.268-3157C>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37356423 | ||||||
chr2:37356424
|
G | T | 1 | a0002c0002t0002g0277 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.268-3156G>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37356424 | ||||||
chr2:37356478
|
C | T | 52 | a0001c0001t0001g0303a0001c0003t0001g0015a0001c0003t0001g0027others(49): Show | 55 | HG00738.hp2 HG01106.hp1 HG01243.hp1 others(52): Show |
intron_variant | MODIFIER | c.268-3102C>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37356478 | ||||||
chr2:37356531
|
T | C | 1 | a0001c0001t0001g0339 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.268-3049T>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37356531 | ||||||
chr2:37356547
|
G | A | 1 | a0001c0003t0001g0359 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.268-3033G>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37356547 | ||||||
chr2:37356654
|
C | G | 52 | a0001c0001t0001g0303a0001c0003t0001g0015a0001c0003t0001g0027others(49): Show | 55 | HG00738.hp2 HG01106.hp1 HG01243.hp1 others(52): Show |
intron_variant | MODIFIER | c.268-2926C>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37356654 | ||||||
chr2:37356831
|
C | A | 1 | a0001c0001t0001g0191 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.268-2749C>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37356831 | ||||||
chr2:37356843
|
C | T | 1 | a0001c0001t0001g0184 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.268-2737C>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37356843 | ||||||
chr2:37356902
|
A | C | 1 | a0002c0002t0002g0254 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.268-2678A>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37356902 | ||||||
chr2:37356909
|
G | T | 1 | a0001c0001t0001g0113 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.268-2671G>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37356909 | ||||||
chr2:37357005
|
C | CA | 62 | a0001c0001t0001g0011a0001c0001t0001g0030a0001c0001t0001g0062others(59): Show | 67 | HG00738.hp2 HG01081.hp2 HG01106.hp1 others(64): Show |
intron_variant | MODIFIER | c.268-2558dupA | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 37357005 | |||||
chr2:37357282
|
CT | C | 52 | a0001c0001t0001g0303a0001c0003t0001g0015a0001c0003t0001g0027others(49): Show | 55 | HG00738.hp2 HG01106.hp1 HG01243.hp1 others(52): Show |
intron_variant | MODIFIER | c.268-2285delT | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 37357282 | |||||
chr2:37357315
|
A | AT | 53 | a0001c0001t0001g0062a0001c0001t0001g0303a0001c0003t0001g0015others(50): Show | 56 | HG00738.hp2 HG01106.hp1 HG01243.hp1 others(53): Show |
intron_variant | MODIFIER | c.268-2251dupT | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 37357315 | |||||
chr2:37357329
|
T | A | 1 | a0001c0003t0001g0128 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.268-2251T>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37357329 | ||||||
chr2:37357562
|
A | G | 67 | a0001c0003t0001g0154a0002c0002t0002g0001a0002c0002t0002g0003others(64): Show | 87 | HG00438.hp2 HG00544.hp2 HG00621.hp2 others(84): Show |
intron_variant | MODIFIER | c.268-2018A>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37357562 | ||||||
chr2:37357724
|
G | A | 1 | a0002c0002t0002g0280 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.268-1856G>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37357724 | ||||||
chr2:37357866
|
C | A | 4 | a0001c0003t0001g0026a0001c0003t0005g0125a0001c0003t0005g0126others(1): Show | 5 | HG00280.hp1 HG01981.hp2 HG02602.hp1 others(2): Show |
intron_variant | MODIFIER | c.268-1714C>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37357866 | ||||||
chr2:37357878
|
A | T | 37 | a0001c0003t0001g0027a0001c0003t0001g0132a0001c0003t0001g0142others(34): Show | 38 | HG00738.hp2 HG01106.hp1 HG01243.hp1 others(35): Show |
intron_variant | MODIFIER | c.268-1702A>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37357878 | ||||||
chr2:37357883
|
GA | G | 52 | a0001c0001t0001g0303a0001c0003t0001g0015a0001c0003t0001g0027others(49): Show | 55 | HG00738.hp2 HG01106.hp1 HG01243.hp1 others(52): Show |
intron_variant | MODIFIER | c.268-1687delA | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 37357883 | |||||
chr2:37357907
|
A | G | 3 | a0001c0001t0002g0041a0001c0001t0002g0199a0001c0001t0002g0317 | 4 | HG00639.hp1 HG02615.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.268-1673A>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37357907 | ||||||
chr2:37358026
|
G | T | 1 | a0001c0001t0001g0066 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.268-1554G>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37358026 | ||||||
chr2:37358108
|
G | GA | 7 | a0001c0001t0001g0062a0001c0001t0001g0206a0001c0001t0001g0350others(4): Show | 7 | HG02027.hp1 HG02717.hp1 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.268-1456dupA | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 37358108 | |||||
chr2:37358108
|
GA | G | 8 | a0001c0001t0001g0113a0001c0001t0001g0334a0002c0002t0002g0032others(5): Show | 9 | HG01255.hp1 HG01975.hp2 NA18948.hp1 others(6): Show |
intron_variant | MODIFIER | c.268-1456delA | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 37358108 | |||||
chr2:37358121
|
A | AAAAG | 11 | a0001c0003t0001g0015a0001c0003t0001g0140a0001c0003t0001g0164others(8): Show | 13 | HG01891.hp2 HG02109.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.268-1455_268-1452d others(6): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 37358121 | |||||
chr2:37358121
|
A | AAAG | 35 | a0001c0001t0001g0303a0001c0003t0001g0027a0001c0003t0001g0128others(32): Show | 36 | HG00738.hp2 HG01243.hp1 HG01361.hp2 others(33): Show |
intron_variant | MODIFIER | c.268-1457_268-1456i others(5): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 37358121 | |||||
chr2:37358121
|
A | AAG | 6 | a0001c0003t0001g0155a0004c0005t0001g0130a0004c0005t0001g0131others(3): Show | 6 | HG01106.hp1 HG02559.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.268-1458_268-1457i others(4): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 37358121 | |||||
chr2:37358121
|
A | G | 2 | a0001c0001t0001g0335a0001c0001t0005g0336 | 2 | HG00741.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.268-1459A>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37358121 | ||||||
chr2:37358126
|
A | G | 1 | a0001c0003t0001g0142 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.268-1454A>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37358126 | ||||||
chr2:37358211
|
G | C | 6 | a0001c0001t0001g0309a0001c0001t0001g0310a0001c0001t0001g0346others(3): Show | 6 | HG01884.hp1 HG02055.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.268-1369G>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37358211 | ||||||
chr2:37358264
|
A | G | 2 | a0001c0003t0002g0232a0001c0003t0003g0231 | 2 | HG01361.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.268-1316A>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37358264 | ||||||
chr2:37358267
|
A | G | 3 | a0001c0001t0001g0303a0001c0003t0001g0128a0001c0003t0003g0129 | 3 | HG02055.hp2 HG02145.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.268-1313A>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37358267 | ||||||
chr2:37358274
|
A | G | 1 | a0001c0001t0001g0070 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.268-1306A>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37358274 | ||||||
chr2:37358277
|
A | C | 2 | a0001c0003t0001g0142a0001c0003t0002g0233 | 2 | HG03209.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.268-1303A>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37358277 | ||||||
chr2:37358340
|
G | T | 1 | a0001c0001t0001g0205 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.268-1240G>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37358340 | ||||||
chr2:37358438
|
C | CAACAAAA others(3): Show |
2 | a0001c0003t0001g0015a0001c0003t0001g0165 | 4 | HG02922.hp1 HG03209.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.268-1125_268-1116d others(12): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 37358438 | |||||
chr2:37358438
|
C | CAACAAAA others(8): Show |
43 | a0001c0003t0001g0027a0001c0003t0001g0132a0001c0003t0001g0140others(40): Show | 44 | HG00738.hp2 HG01106.hp1 HG01243.hp1 others(41): Show |
intron_variant | MODIFIER | c.268-1130_268-1116d others(17): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 37358438 | |||||
chr2:37358438
|
C | CAACAAAA others(13): Show |
3 | a0001c0003t0001g0142a0001c0003t0002g0166a0004c0005t0001g0137 | 3 | HG02559.hp2 HG03942.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.268-1135_268-1116d others(22): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 37358438 | |||||
chr2:37358442
|
A | T | 2 | a0001c0001t0001g0133a0001c0001t0001g0195 | 2 | HG00438.hp1 NA18954.hp2 |
intron_variant | MODIFIER | c.268-1138A>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37358442 | ||||||
chr2:37358461
|
C | CAAAACAA others(4): Show |
1 | a0001c0003t0001g0245 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.268-1116_268-1115i others(13): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 37358461 | |||||
chr2:37358565
|
C | T | 2 | a0001c0001t0001g0343a0001c0001t0001g0344 | 2 | HG01106.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.268-1015C>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37358565 | ||||||
chr2:37358633
|
G | C | 50 | a0001c0001t0003g0244a0001c0003t0001g0015a0001c0003t0001g0027others(47): Show | 53 | HG00738.hp2 HG01106.hp1 HG01243.hp1 others(50): Show |
intron_variant | MODIFIER | c.268-947G>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37358633 | ||||||
chr2:37358814
|
C | G | 1 | a0001c0001t0002g0320 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.268-766C>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37358814 | ||||||
chr2:37358843
|
T | C | 50 | a0001c0001t0003g0244a0001c0003t0001g0015a0001c0003t0001g0027others(47): Show | 53 | HG00738.hp2 HG01106.hp1 HG01243.hp1 others(50): Show |
intron_variant | MODIFIER | c.268-737T>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37358843 | ||||||
chr2:37358853
|
C | G | 2 | a0001c0001t0001g0011a0001c0001t0007g0011 | 3 | HG01081.hp2 HG01943.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.268-727C>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37358853 | ||||||
chr2:37358866
|
G | A | 2 | a0001c0003t0001g0142a0001c0003t0002g0233 | 2 | HG03209.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.268-714G>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37358866 | ||||||
chr2:37358922
|
C | T | 1 | a0001c0001t0001g0243 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.268-658C>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37358922 | ||||||
chr2:37358929
|
A | G | 2 | a0001c0003t0001g0155a0004c0005t0001g0137 | 2 | HG02559.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.268-651A>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37358929 | ||||||
chr2:37358934
|
T | C | 4 | a0001c0003t0001g0026a0001c0003t0005g0125a0001c0003t0005g0126others(1): Show | 5 | HG00280.hp1 HG01981.hp2 HG02602.hp1 others(2): Show |
intron_variant | MODIFIER | c.268-646T>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37358934 | ||||||
chr2:37359044
|
A | G | 4 | a0001c0001t0001g0316a0001c0001t0001g0335a0001c0001t0001g0340others(1): Show | 4 | HG00741.hp2 HG03239.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.268-536A>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37359044 | ||||||
chr2:37359092
|
G | T | 50 | a0001c0001t0003g0244a0001c0003t0001g0015a0001c0003t0001g0027others(47): Show | 53 | HG00738.hp2 HG01106.hp1 HG01243.hp1 others(50): Show |
intron_variant | MODIFIER | c.268-488G>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37359092 | ||||||
chr2:37359103
|
C | T | 50 | a0001c0001t0003g0244a0001c0003t0001g0015a0001c0003t0001g0027others(47): Show | 53 | HG00738.hp2 HG01106.hp1 HG01243.hp1 others(50): Show |
intron_variant | MODIFIER | c.268-477C>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37359103 | ||||||
chr2:37359104
|
G | T | 4 | a0001c0003t0001g0026a0001c0003t0005g0125a0001c0003t0005g0126others(1): Show | 5 | HG00280.hp1 HG01981.hp2 HG02602.hp1 others(2): Show |
intron_variant | MODIFIER | c.268-476G>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37359104 | ||||||
chr2:37359194
|
T | TTCTTTTT others(300): Show |
1 | a0004c0005t0003g0139 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.268-380_268-379ins others(307): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr2 | 37359194 | |||||
chr2:37359283
|
G | A | 2 | a0001c0001t0001g0046a0001c0001t0001g0048 | 2 | NA18951.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.268-297G>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37359283 | ||||||
chr2:37359352
|
A | G | 2 | a0001c0003t0001g0128a0001c0003t0003g0129 | 2 | HG02145.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.268-228A>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37359352 | ||||||
chr2:37359359
|
G | T | 49 | a0001c0003t0001g0015a0001c0003t0001g0027a0001c0003t0001g0132others(46): Show | 52 | HG00738.hp2 HG01106.hp1 HG01243.hp1 others(49): Show |
intron_variant | MODIFIER | c.268-221G>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37359359 | ||||||
chr2:37359537
|
C | T | 45 | a0001c0001t0003g0244a0001c0003t0001g0015a0001c0003t0001g0027others(42): Show | 48 | HG00738.hp2 HG01243.hp1 HG01361.hp2 others(45): Show |
intron_variant | MODIFIER | c.268-43C>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37359537 | ||||||
chr2:37359538
|
A | G | 182 | a0001c0001t0001g0029a0001c0001t0001g0039a0001c0001t0001g0040others(179): Show | 211 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.268-42A>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 2/6 | chr2 | 37359538 | ||||||
chr2:37359897
|
C | A | 67 | a0001c0003t0001g0154a0002c0002t0002g0001a0002c0002t0002g0003others(64): Show | 87 | HG00438.hp2 HG00544.hp2 HG00621.hp2 others(84): Show |
intron_variant | MODIFIER | c.546+39C>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37359897 | ||||||
chr2:37359922
|
C | T | 34 | a0001c0001t0003g0244a0001c0003t0001g0015a0001c0003t0001g0027others(31): Show | 37 | HG00738.hp2 HG01243.hp1 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.546+64C>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37359922 | ||||||
chr2:37359989
|
C | T | 67 | a0001c0003t0001g0154a0002c0002t0002g0001a0002c0002t0002g0003others(64): Show | 87 | HG00438.hp2 HG00544.hp2 HG00621.hp2 others(84): Show |
intron_variant | MODIFIER | c.546+131C>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37359989 | ||||||
chr2:37359997
|
G | GT | 17 | a0001c0003t0001g0143a0001c0003t0001g0145a0001c0003t0001g0146others(14): Show | 17 | HG00738.hp2 HG01243.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.546+140dupT | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 37359997 | |||||
chr2:37360089
|
T | C | 1 | a0001c0003t0002g0233 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.546+231T>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37360089 | ||||||
chr2:37360253
|
C | T | 1 | a0001c0001t0001g0243 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.546+395C>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37360253 | ||||||
chr2:37360376
|
C | T | 1 | a0001c0001t0001g0028 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.546+518C>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37360376 | ||||||
chr2:37360504
|
A | G | 1 | a0001c0003t0002g0233 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.546+646A>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37360504 | ||||||
chr2:37360524
|
T | C | 1 | a0001c0001t0002g0353 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.546+666T>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37360524 | ||||||
chr2:37360746
|
G | A | 2 | a0001c0003t0001g0158a0001c0003t0001g0160 | 2 | HG01884.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.546+888G>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37360746 | ||||||
chr2:37360759
|
T | C | 1 | a0001c0003t0001g0360 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.546+901T>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37360759 | ||||||
chr2:37360864
|
G | C | 1 | a0001c0003t0001g0245 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.546+1006G>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37360864 | ||||||
chr2:37360887
|
T | C | 1 | a0001c0001t0001g0323 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.546+1029T>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37360887 | ||||||
chr2:37360904
|
A | G | 1 | a0001c0001t0001g0333 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.546+1046A>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37360904 | ||||||
chr2:37360923
|
A | T | 6 | a0001c0003t0001g0142a0001c0003t0001g0167a0001c0003t0001g0359others(3): Show | 6 | HG02559.hp1 HG02647.hp1 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.546+1065A>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37360923 | ||||||
chr2:37361063
|
G | GATTAAAA others(6): Show |
1 | a0001c0001t0001g0192 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.546+1208_546+1209i others(15): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 37361063 | |||||
chr2:37361067
|
G | T | 1 | a0001c0001t0001g0192 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.546+1209G>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37361067 | ||||||
chr2:37361068
|
G | A | 1 | a0001c0001t0001g0192 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.546+1210G>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37361068 | ||||||
chr2:37361069
|
G | A | 1 | a0001c0001t0001g0192 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.546+1211G>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37361069 | ||||||
chr2:37361070
|
G | T | 1 | a0001c0001t0001g0192 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.546+1212G>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37361070 | ||||||
chr2:37361075
|
C | A | 1 | a0001c0001t0001g0192 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.546+1217C>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37361075 | ||||||
chr2:37361145
|
G | A | 1 | a0003c0004t0002g0056 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.546+1287G>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37361145 | ||||||
chr2:37361333
|
C | T | 1 | a0001c0001t0001g0185 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.546+1475C>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37361333 | ||||||
chr2:37361353
|
C | G | 1 | a0001c0001t0001g0073 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.546+1495C>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37361353 | ||||||
chr2:37361466
|
G | C | 17 | a0001c0003t0001g0143a0001c0003t0001g0145a0001c0003t0001g0146others(14): Show | 17 | HG00738.hp2 HG01243.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.546+1608G>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37361466 | ||||||
chr2:37361550
|
G | A | 4 | a0001c0003t0001g0167a0001c0003t0002g0166a0001c0003t0002g0234others(1): Show | 4 | HG02647.hp1 HG03471.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.546+1692G>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37361550 | ||||||
chr2:37361906
|
G | A | 28 | a0001c0003t0001g0142a0001c0003t0001g0143a0001c0003t0001g0145others(25): Show | 28 | HG00738.hp2 HG01243.hp1 HG01361.hp2 others(25): Show |
intron_variant | MODIFIER | c.546+2048G>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37361906 | ||||||
chr2:37361962
|
C | A | 4 | a0001c0003t0001g0155a0001c0003t0002g0232a0001c0003t0003g0231others(1): Show | 4 | HG01361.hp2 HG02280.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.546+2104C>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37361962 | ||||||
chr2:37362075
|
G | A | 2 | a0001c0003t0002g0234a0001c0003t0002g0235 | 2 | HG03471.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.546+2217G>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37362075 | ||||||
chr2:37362133
|
T | A | 1 | a0001c0003t0001g0154 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.546+2275T>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37362133 | ||||||
chr2:37362186
|
T | C | 2 | a0001c0001t0001g0216a0001c0001t0001g0217 | 2 | HG01496.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.546+2328T>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37362186 | ||||||
chr2:37362221
|
T | C | 2 | a0001c0001t0001g0172a0001c0001t0001g0210 | 2 | HG02735.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.546+2363T>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37362221 | ||||||
chr2:37362236
|
C | T | 23 | a0001c0003t0001g0027a0001c0003t0001g0132a0001c0003t0001g0143others(20): Show | 24 | HG00738.hp2 HG01243.hp1 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.546+2378C>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37362236 | ||||||
chr2:37362345
|
C | T | 3 | a0001c0001t0001g0350a0001c0001t0001g0351a0001c0001t0001g0352 | 3 | HG01123.hp1 HG01261.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.546+2487C>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37362345 | ||||||
chr2:37362668
|
A | G | 52 | a0001c0001t0001g0303a0001c0003t0001g0015a0001c0003t0001g0027others(49): Show | 55 | HG00738.hp2 HG01106.hp1 HG01243.hp1 others(52): Show |
intron_variant | MODIFIER | c.546+2810A>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37362668 | ||||||
chr2:37362705
|
A | T | 1 | a0003c0004t0002g0355 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.546+2847A>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37362705 | ||||||
chr2:37362806
|
G | C | 1 | a0001c0003t0003g0362 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.546+2948G>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37362806 | ||||||
chr2:37362902
|
G | A | 4 | a0001c0001t0001g0040a0001c0001t0001g0304a0001c0001t0001g0307others(1): Show | 5 | HG02572.hp1 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.546+3044G>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37362902 | ||||||
chr2:37362941
|
A | AT | 53 | a0001c0001t0001g0303a0001c0001t0003g0244a0001c0003t0001g0015others(50): Show | 56 | HG00738.hp2 HG01106.hp1 HG01243.hp1 others(53): Show |
intron_variant | MODIFIER | c.546+3088dupT | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 37362941 | |||||
chr2:37363141
|
G | A | 164 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0243others(161): Show | 191 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.546+3283G>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37363141 | ||||||
chr2:37363303
|
A | G | 1 | a0001c0003t0001g0155 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.546+3445A>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37363303 | ||||||
chr2:37363459
|
C | CA | 34 | a0001c0001t0001g0071a0001c0001t0001g0113a0001c0001t0001g0116others(31): Show | 35 | HG01109.hp1 HG01109.hp2 HG01175.hp1 others(32): Show |
intron_variant | MODIFIER | c.546+3623dupA | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 37363459 | |||||
chr2:37363459
|
C | CAA | 80 | a0001c0003t0001g0143a0001c0003t0001g0145a0001c0003t0001g0146others(77): Show | 100 | HG00544.hp2 HG00621.hp2 HG00639.hp2 others(97): Show |
intron_variant | MODIFIER | c.546+3622_546+3623d others(4): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 37363459 | |||||
chr2:37363459
|
C | CAAA | 16 | a0001c0003t0001g0015a0001c0003t0001g0140a0001c0003t0001g0149others(13): Show | 18 | HG00438.hp2 HG00738.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.546+3621_546+3623d others(5): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 37363459 | |||||
chr2:37363614
|
G | A | 36 | a0001c0001t0001g0303a0001c0003t0001g0027a0001c0003t0001g0128others(33): Show | 37 | HG00738.hp2 HG01243.hp1 HG01361.hp2 others(34): Show |
intron_variant | MODIFIER | c.547-3618G>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37363614 | ||||||
chr2:37363631
|
TTAAA | T | 5 | a0001c0001t0001g0243a0001c0003t0001g0026a0001c0003t0005g0125others(2): Show | 6 | HG00280.hp1 HG01981.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.547-3590_547-3587d others(6): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 37363631 | |||||
chr2:37363659
|
T | TA | 11 | a0001c0001t0001g0043a0001c0001t0001g0062a0001c0001t0001g0071others(8): Show | 11 | HG01952.hp2 HG02055.hp1 HG02738.hp2 others(8): Show |
intron_variant | MODIFIER | c.547-3552dupA | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 37363659 | |||||
chr2:37363659
|
TA | T | 10 | a0001c0001t0001g0065a0001c0001t0001g0080a0001c0001t0001g0112others(7): Show | 10 | HG01168.hp1 HG01169.hp1 HG02897.hp2 others(7): Show |
intron_variant | MODIFIER | c.547-3552delA | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 37363659 | |||||
chr2:37363659
|
TAAA | T | 6 | a0001c0003t0001g0142a0001c0003t0001g0155a0001c0003t0002g0232others(3): Show | 6 | HG01361.hp2 HG02280.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.547-3554_547-3552d others(5): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 37363659 | |||||
chr2:37363659
|
TAAAA | T | 107 | a0001c0001t0003g0244a0001c0003t0001g0015a0001c0003t0001g0027others(104): Show | 129 | HG00438.hp2 HG00544.hp2 HG00621.hp2 others(126): Show |
intron_variant | MODIFIER | c.547-3555_547-3552d others(6): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 37363659 | |||||
chr2:37363659
|
TAAAAA | T | 6 | a0001c0001t0001g0303a0001c0003t0001g0128a0001c0003t0001g0132others(3): Show | 7 | HG02055.hp2 HG02145.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.547-3556_547-3552d others(7): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 37363659 | |||||
chr2:37363775
|
G | C | 2 | a0001c0001t0001g0243a0001c0001t0003g0244 | 2 | HG02109.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.547-3457G>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37363775 | ||||||
chr2:37363851
|
C | G | 2 | a0001c0003t0002g0232a0001c0003t0003g0231 | 2 | HG01361.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.547-3381C>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37363851 | ||||||
chr2:37363894
|
T | C | 15 | a0001c0001t0001g0029a0001c0001t0001g0077a0001c0001t0001g0081others(12): Show | 17 | HG00735.hp1 HG00735.hp2 HG00738.hp1 others(14): Show |
intron_variant | MODIFIER | c.547-3338T>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37363894 | ||||||
chr2:37363938
|
A | G | 12 | a0001c0001t0003g0244a0001c0003t0001g0015a0001c0003t0001g0140others(9): Show | 14 | HG01891.hp2 HG02109.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.547-3294A>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37363938 | ||||||
chr2:37364017
|
T | C | 1 | a0001c0001t0001g0243 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.547-3215T>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37364017 | ||||||
chr2:37364129
|
A | G | 1 | a0001c0001t0001g0310 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.547-3103A>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37364129 | ||||||
chr2:37364309
|
T | A | 1 | a0001c0003t0003g0231 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.547-2923T>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37364309 | ||||||
chr2:37364359
|
C | T | 1 | a0001c0001t0002g0353 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.547-2873C>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37364359 | ||||||
chr2:37364372
|
A | G | 1 | a0001c0001t0001g0050 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.547-2860A>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37364372 | ||||||
chr2:37364387
|
C | T | 1 | a0001c0001t0001g0339 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.547-2845C>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37364387 | ||||||
chr2:37364388
|
G | A | 1 | a0001c0001t0002g0041 | 2 | HG02615.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.547-2844G>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37364388 | ||||||
chr2:37364595
|
C | A | 50 | a0001c0001t0003g0244a0001c0003t0001g0015a0001c0003t0001g0027others(47): Show | 53 | HG00738.hp2 HG01106.hp1 HG01243.hp1 others(50): Show |
intron_variant | MODIFIER | c.547-2637C>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37364595 | ||||||
chr2:37364622
|
T | C | 1 | a0001c0003t0001g0245 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.547-2610T>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37364622 | ||||||
chr2:37364665
|
T | C | 1 | a0001c0001t0001g0328 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.547-2567T>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37364665 | ||||||
chr2:37364863
|
T | C | 44 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0019others(41): Show | 54 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.547-2369T>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37364863 | ||||||
chr2:37364981
|
A | G | 2 | a0001c0003t0001g0140a0001c0003t0001g0360 | 2 | HG01891.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.547-2251A>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37364981 | ||||||
chr2:37365001
|
A | ATAT | 66 | a0001c0003t0001g0154a0002c0002t0002g0001a0002c0002t0002g0003others(63): Show | 86 | HG00438.hp2 HG00544.hp2 HG00621.hp2 others(83): Show |
intron_variant | MODIFIER | c.547-2211_547-2209d others(5): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 37365001 | |||||
chr2:37365001
|
ATAT | A | 50 | a0001c0001t0003g0244a0001c0003t0001g0015a0001c0003t0001g0027others(47): Show | 53 | HG00738.hp2 HG01106.hp1 HG01243.hp1 others(50): Show |
intron_variant | MODIFIER | c.547-2211_547-2209d others(5): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 37365001 | |||||
chr2:37365077
|
G | GCA | 5 | a0001c0001t0001g0007a0001c0001t0001g0135a0001c0001t0001g0198others(2): Show | 8 | HG00642.hp2 HG01928.hp1 HG01943.hp1 others(5): Show |
intron_variant | MODIFIER | c.547-2136_547-2135d others(4): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 37365077 | |||||
chr2:37365077
|
GCA | G | 4 | a0004c0005t0001g0130a0004c0005t0001g0131a0004c0005t0001g0138others(1): Show | 4 | HG01106.hp1 HG03453.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.547-2136_547-2135d others(4): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 37365077 | |||||
chr2:37365192
|
C | T | 37 | a0001c0003t0001g0027a0001c0003t0001g0132a0001c0003t0001g0142others(34): Show | 38 | HG00738.hp2 HG01106.hp1 HG01243.hp1 others(35): Show |
intron_variant | MODIFIER | c.547-2040C>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37365192 | ||||||
chr2:37365330
|
T | A | 1 | a0002c0002t0002g0274 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.547-1902T>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37365330 | ||||||
chr2:37365485
|
C | T | 251 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(248): Show | 296 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(293): Show |
intron_variant | MODIFIER | c.547-1747C>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37365485 | ||||||
chr2:37365491
|
T | C | 1 | a0001c0003t0001g0144 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.547-1741T>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37365491 | ||||||
chr2:37365613
|
GGAATTAT others(6): Show |
G | 5 | a0001c0001t0001g0039a0001c0001t0001g0316a0001c0001t0001g0335others(2): Show | 6 | HG00099.hp1 HG00741.hp2 HG03239.hp2 others(3): Show |
intron_variant | MODIFIER | c.547-1616_547-1604d others(15): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 37365613 | |||||
chr2:37365639
|
T | C | 5 | a0002c0002t0002g0038a0002c0002t0002g0266a0002c0002t0002g0288others(2): Show | 6 | NA18747.hp1 NA18948.hp1 NA18961.hp2 others(3): Show |
intron_variant | MODIFIER | c.547-1593T>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37365639 | ||||||
chr2:37365693
|
A | C | 1 | a0003c0004t0005g0291 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.547-1539A>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37365693 | ||||||
chr2:37365696
|
G | A | 1 | a0002c0002t0002g0273 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.547-1536G>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37365696 | ||||||
chr2:37365848
|
A | G | 2 | a0001c0003t0001g0128a0001c0003t0003g0129 | 2 | HG02145.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.547-1384A>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37365848 | ||||||
chr2:37365875
|
A | T | 1 | a0001c0003t0002g0233 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.547-1357A>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37365875 | ||||||
chr2:37365901
|
G | A | 10 | a0001c0001t0001g0319a0001c0001t0001g0329a0001c0001t0001g0331others(7): Show | 10 | HG00140.hp1 HG01106.hp2 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.547-1331G>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37365901 | ||||||
chr2:37365995
|
G | A | 1 | a0001c0001t0001g0212 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.547-1237G>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37365995 | ||||||
chr2:37366100
|
T | C | 38 | a0001c0001t0001g0039a0001c0001t0001g0102a0001c0001t0001g0179others(35): Show | 40 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(37): Show |
intron_variant | MODIFIER | c.547-1132T>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37366100 | ||||||
chr2:37366122
|
G | A | 1 | a0001c0001t0001g0313 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.547-1110G>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37366122 | ||||||
chr2:37366155
|
A | C | 2 | a0001c0001t0001g0309a0001c0001t0001g0310 | 2 | HG01884.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.547-1077A>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37366155 | ||||||
chr2:37366163
|
AG | A | 64 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(61): Show | 80 | HG00438.hp1 HG00621.hp1 HG00642.hp2 others(77): Show |
intron_variant | MODIFIER | c.547-1065delG | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr2 | 37366163 | |||||
chr2:37366212
|
A | C | 1 | a0001c0001t0004g0322 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.547-1020A>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37366212 | ||||||
chr2:37366240
|
C | T | 1 | a0001c0001t0001g0029 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.547-992C>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37366240 | ||||||
chr2:37366261
|
T | G | 2 | a0001c0001t0001g0187a0001c0001t0001g0188 | 2 | HG02257.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.547-971T>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37366261 | ||||||
chr2:37366285
|
G | C | 6 | a0001c0001t0001g0082a0001c0001t0005g0336a0001c0003t0001g0026others(3): Show | 7 | HG00280.hp1 HG00741.hp2 HG01123.hp2 others(4): Show |
intron_variant | MODIFIER | c.547-947G>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37366285 | ||||||
chr2:37366335
|
G | A | 1 | a0001c0003t0001g0154 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.547-897G>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37366335 | ||||||
chr2:37366375
|
A | C | 1 | a0001c0001t0001g0102 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.547-857A>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37366375 | ||||||
chr2:37366504
|
T | C | 1 | a0001c0001t0001g0340 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.547-728T>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37366504 | ||||||
chr2:37366632
|
T | C | 11 | a0001c0001t0001g0303a0001c0001t0001g0318a0001c0001t0003g0244others(8): Show | 11 | HG00280.hp1 HG00741.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.547-600T>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37366632 | ||||||
chr2:37366682
|
G | A | 2 | a0001c0001t0001g0080a0001c0001t0001g0121 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.547-550G>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37366682 | ||||||
chr2:37366820
|
C | A | 1 | a0001c0003t0002g0166 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.547-412C>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37366820 | ||||||
chr2:37366875
|
C | T | 17 | a0001c0001t0003g0110a0001c0001t0003g0244a0001c0003t0001g0015others(14): Show | 19 | HG01891.hp2 HG02109.hp1 HG02280.hp1 others(16): Show |
intron_variant | MODIFIER | c.547-357C>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37366875 | ||||||
chr2:37366911
|
T | C | 1 | a0001c0003t0003g0231 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.547-321T>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37366911 | ||||||
chr2:37366974
|
G | A | 1 | a0002c0002t0002g0296 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.547-258G>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37366974 | ||||||
chr2:37367013
|
G | C | 1 | a0003c0004t0002g0061 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.547-219G>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37367013 | ||||||
chr2:37367015
|
G | T | 4 | a0001c0001t0005g0336a0001c0003t0005g0125a0001c0003t0005g0126others(1): Show | 4 | HG00280.hp1 HG00741.hp2 NA20805.hp2 others(1): Show |
intron_variant | MODIFIER | c.547-217G>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37367015 | ||||||
chr2:37367082
|
G | C | 1 | a0001c0001t0001g0328 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.547-150G>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37367082 | ||||||
chr2:37367173
|
A | G | 4 | a0001c0001t0005g0336a0001c0003t0005g0125a0001c0003t0005g0126others(1): Show | 4 | HG00280.hp1 HG00741.hp2 NA20805.hp2 others(1): Show |
intron_variant | MODIFIER | c.547-59A>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 3/6 | chr2 | 37367173 | ||||||
chr2:37367451
|
G | A | 6 | a0001c0001t0002g0186a0001c0001t0005g0336a0001c0003t0001g0143others(3): Show | 6 | HG00280.hp1 HG00741.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.723+43G>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 4/6 | chr2 | 37367451 | ||||||
chr2:37367500
|
C | T | 1 | a0001c0001t0001g0175 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.723+92C>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 4/6 | chr2 | 37367500 | ||||||
chr2:37367551
|
G | A | 6 | a0001c0001t0001g0243a0001c0001t0001g0318a0001c0003t0001g0161others(3): Show | 6 | HG02109.hp2 HG02630.hp1 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.723+143G>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 4/6 | chr2 | 37367551 | ||||||
chr2:37367598
|
T | A | 5 | a0001c0001t0002g0186a0001c0001t0005g0336a0001c0003t0005g0125others(2): Show | 5 | HG00280.hp1 HG00741.hp2 NA20805.hp2 others(2): Show |
intron_variant | MODIFIER | c.723+190T>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 4/6 | chr2 | 37367598 | ||||||
chr2:37367641
|
G | T | 6 | a0001c0001t0001g0243a0001c0001t0001g0318a0001c0003t0001g0161others(3): Show | 6 | HG02109.hp2 HG02630.hp1 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.723+233G>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 4/6 | chr2 | 37367641 | ||||||
chr2:37367700
|
C | T | 11 | a0001c0003t0001g0015a0001c0003t0001g0140a0001c0003t0001g0164others(8): Show | 14 | HG00738.hp1 HG01069.hp2 HG01255.hp2 others(11): Show |
intron_variant | MODIFIER | c.723+292C>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 4/6 | chr2 | 37367700 | ||||||
chr2:37367701
|
G | A | 1 | a0001c0001t0002g0199 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.723+293G>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 4/6 | chr2 | 37367701 | ||||||
chr2:37367738
|
G | A | 6 | a0001c0001t0001g0243a0001c0001t0001g0318a0001c0003t0001g0161others(3): Show | 6 | HG02109.hp2 HG02630.hp1 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.723+330G>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 4/6 | chr2 | 37367738 | ||||||
chr2:37367802
|
G | A | 10 | a0001c0001t0001g0040a0001c0001t0001g0122a0001c0001t0001g0124others(7): Show | 11 | HG01106.hp1 HG02572.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.723+394G>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 4/6 | chr2 | 37367802 | ||||||
chr2:37367827
|
C | G | 6 | a0001c0001t0001g0243a0001c0001t0001g0318a0001c0003t0001g0161others(3): Show | 6 | HG02109.hp2 HG02630.hp1 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.723+419C>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 4/6 | chr2 | 37367827 | ||||||
chr2:37367845
|
G | T | 1 | a0003c0004t0002g0061 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.723+437G>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 4/6 | chr2 | 37367845 | ||||||
chr2:37367951
|
T | C | 1 | a0001c0001t0001g0316 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.723+543T>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 4/6 | chr2 | 37367951 | ||||||
chr2:37368382
|
A | G | 142 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(139): Show | 175 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(172): Show |
intron_variant | MODIFIER | c.723+974A>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 4/6 | chr2 | 37368382 | ||||||
chr2:37368408
|
C | A | 1 | a0001c0001t0001g0214 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.723+1000C>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 4/6 | chr2 | 37368408 | ||||||
chr2:37368461
|
C | T | 145 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(142): Show | 174 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(171): Show |
intron_variant | MODIFIER | c.723+1053C>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 4/6 | chr2 | 37368461 | ||||||
chr2:37368553
|
A | C | 275 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(272): Show | 334 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(331): Show |
intron_variant | MODIFIER | c.724-1132A>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 4/6 | chr2 | 37368553 | ||||||
chr2:37368618
|
C | T | 6 | a0001c0003t0001g0146a0001c0003t0001g0148a0001c0003t0001g0151others(3): Show | 6 | HG01243.hp1 HG02486.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.724-1067C>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 4/6 | chr2 | 37368618 | ||||||
chr2:37368641
|
A | G | 1 | a0001c0001t0001g0135 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.724-1044A>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 4/6 | chr2 | 37368641 | ||||||
chr2:37368647
|
C | T | 1 | a0001c0001t0001g0089 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.724-1038C>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 4/6 | chr2 | 37368647 | ||||||
chr2:37368718
|
C | G | 7 | a0001c0001t0001g0243a0001c0001t0001g0318a0001c0001t0002g0186others(4): Show | 7 | HG02109.hp2 HG02630.hp1 HG03471.hp2 others(4): Show |
intron_variant | MODIFIER | c.724-967C>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 4/6 | chr2 | 37368718 | ||||||
chr2:37368731
|
G | A | 6 | a0001c0003t0001g0027a0001c0003t0001g0128a0001c0003t0001g0132others(3): Show | 7 | HG02145.hp1 HG02451.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.724-954G>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 4/6 | chr2 | 37368731 | ||||||
chr2:37368787
|
G | A | 1 | a0001c0003t0002g0233 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.724-898G>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 4/6 | chr2 | 37368787 | ||||||
chr2:37368816
|
A | G | 1 | a0001c0001t0001g0089 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.724-869A>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 4/6 | chr2 | 37368816 | ||||||
chr2:37368826
|
G | C | 1 | a0001c0001t0001g0328 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.724-859G>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 4/6 | chr2 | 37368826 | ||||||
chr2:37368934
|
T | G | 7 | a0001c0001t0001g0243a0001c0001t0001g0318a0001c0001t0002g0186others(4): Show | 7 | HG02109.hp2 HG02630.hp1 HG03471.hp2 others(4): Show |
intron_variant | MODIFIER | c.724-751T>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 4/6 | chr2 | 37368934 | ||||||
chr2:37368946
|
C | T | 286 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(283): Show | 346 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(343): Show |
intron_variant | MODIFIER | c.724-739C>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 4/6 | chr2 | 37368946 | ||||||
chr2:37368951
|
A | G | 1 | a0001c0001t0001g0185 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.724-734A>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 4/6 | chr2 | 37368951 | ||||||
chr2:37368955
|
T | A | 258 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(255): Show | 313 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(310): Show |
intron_variant | MODIFIER | c.724-730T>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 4/6 | chr2 | 37368955 | ||||||
chr2:37368955
|
T | G | 11 | a0001c0003t0001g0015a0001c0003t0001g0140a0001c0003t0001g0164others(8): Show | 14 | HG00738.hp1 HG01069.hp2 HG01255.hp2 others(11): Show |
intron_variant | MODIFIER | c.724-730T>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 4/6 | chr2 | 37368955 | ||||||
chr2:37369006
|
G | A | 1 | a0001c0001t0001g0311 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.724-679G>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 4/6 | chr2 | 37369006 | ||||||
chr2:37369198
|
A | C | 73 | a0001c0001t0001g0184a0002c0002t0002g0001a0002c0002t0002g0003others(70): Show | 98 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(95): Show |
intron_variant | MODIFIER | c.724-487A>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 4/6 | chr2 | 37369198 | ||||||
chr2:37369235
|
A | C | 88 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(85): Show | 105 | HG00438.hp1 HG00438.hp2 HG00621.hp1 others(102): Show |
intron_variant | MODIFIER | c.724-450A>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 4/6 | chr2 | 37369235 | ||||||
chr2:37369256
|
T | C | 1 | a0002c0002t0002g0299 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.724-429T>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 4/6 | chr2 | 37369256 | ||||||
chr2:37369291
|
A | G | 1 | a0001c0001t0001g0095 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.724-394A>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 4/6 | chr2 | 37369291 | ||||||
chr2:37369352
|
G | C | 2 | a0001c0003t0002g0234a0001c0003t0002g0235 | 2 | HG03471.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.724-333G>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 4/6 | chr2 | 37369352 | ||||||
chr2:37369432
|
G | A | 1 | a0001c0001t0001g0089 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.724-253G>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 4/6 | chr2 | 37369432 | ||||||
chr2:37369574
|
A | G | 2 | a0001c0003t0001g0155a0004c0005t0001g0137 | 2 | HG02559.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.724-111A>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 4/6 | chr2 | 37369574 | ||||||
chr2:37369796
|
T | C | 7 | a0001c0001t0001g0243a0001c0001t0001g0318a0001c0003t0001g0161others(4): Show | 7 | HG02109.hp2 HG02630.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.823+12T>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 5/6 | chr2 | 37369796 | ||||||
chr2:37369958
|
C | A | 6 | a0001c0003t0001g0146a0001c0003t0001g0148a0001c0003t0001g0151others(3): Show | 6 | HG01243.hp1 HG02486.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.823+174C>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 5/6 | chr2 | 37369958 | ||||||
chr2:37370242
|
T | A | 1 | a0001c0001t0001g0104 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.823+458T>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 5/6 | chr2 | 37370242 | ||||||
chr2:37370243
|
T | C | 85 | a0001c0001t0001g0095a0001c0001t0001g0184a0001c0001t0002g0041others(82): Show | 111 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(108): Show |
intron_variant | MODIFIER | c.823+459T>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 5/6 | chr2 | 37370243 | ||||||
chr2:37370246
|
CT | C | 6 | a0001c0003t0001g0146a0001c0003t0001g0148a0001c0003t0001g0151others(3): Show | 6 | HG01243.hp1 HG02486.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.823+469delT | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 37370246 | |||||
chr2:37370347
|
AAATACTA others(12): Show |
A | 1 | a0001c0003t0001g0154 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.823+564_823+582del others(19): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 5/6 | chr2 | 37370347 | ||||||
chr2:37370369
|
A | G | 1 | a0001c0001t0001g0338 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.823+585A>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 5/6 | chr2 | 37370369 | ||||||
chr2:37370545
|
G | A | 1 | a0001c0001t0001g0240 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.823+761G>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 5/6 | chr2 | 37370545 | ||||||
chr2:37370546
|
T | C | 11 | a0001c0001t0001g0040a0001c0001t0001g0122a0001c0001t0001g0123others(8): Show | 12 | HG01106.hp1 HG02572.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.823+762T>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 5/6 | chr2 | 37370546 | ||||||
chr2:37370604
|
C | G | 1 | a0001c0001t0001g0321 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.823+820C>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 5/6 | chr2 | 37370604 | ||||||
chr2:37370712
|
A | AGGTCAGG others(17): Show |
1 | a0006c0008t0006g0337 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.823+943_823+944ins others(24): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 37370712 | |||||
chr2:37370737
|
C | T | 1 | a0001c0001t0002g0186 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.823+953C>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 5/6 | chr2 | 37370737 | ||||||
chr2:37370910
|
G | T | 7 | a0001c0001t0001g0055a0001c0001t0001g0070a0001c0001t0001g0192others(4): Show | 7 | HG01074.hp1 HG01109.hp1 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.823+1126G>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 5/6 | chr2 | 37370910 | ||||||
chr2:37370947
|
C | T | 105 | a0001c0001t0001g0184a0001c0001t0001g0243a0001c0001t0001g0318others(102): Show | 131 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(128): Show |
intron_variant | MODIFIER | c.823+1163C>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 5/6 | chr2 | 37370947 | ||||||
chr2:37370975
|
T | C | 1 | a0001c0001t0001g0319 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.823+1191T>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 5/6 | chr2 | 37370975 | ||||||
chr2:37371136
|
A | G | 1 | a0001c0001t0001g0180 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.824-1220A>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 5/6 | chr2 | 37371136 | ||||||
chr2:37371258
|
C | G | 1 | a0001c0003t0003g0129 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.824-1098C>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 5/6 | chr2 | 37371258 | ||||||
chr2:37371258
|
C | T | 1 | a0006c0008t0006g0337 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.824-1098C>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 5/6 | chr2 | 37371258 | ||||||
chr2:37371278
|
T | C | 121 | a0001c0001t0001g0029a0001c0001t0001g0039a0001c0001t0001g0075others(118): Show | 151 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(148): Show |
intron_variant | MODIFIER | c.824-1078T>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 5/6 | chr2 | 37371278 | ||||||
chr2:37371328
|
T | A | 1 | a0006c0008t0006g0337 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.824-1028T>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 5/6 | chr2 | 37371328 | ||||||
chr2:37371359
|
T | G | 7 | a0001c0001t0003g0110a0001c0001t0003g0244a0001c0003t0003g0361others(4): Show | 7 | HG02451.hp2 HG02717.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.824-997T>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 5/6 | chr2 | 37371359 | ||||||
chr2:37371369
|
G | A | 100 | a0001c0001t0001g0243a0001c0001t0002g0041a0001c0001t0002g0186others(97): Show | 127 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(124): Show |
intron_variant | MODIFIER | c.824-987G>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 5/6 | chr2 | 37371369 | ||||||
chr2:37371431
|
C | CA | 186 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(183): Show | 216 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(213): Show |
intron_variant | MODIFIER | c.824-904dupA | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 37371431 | |||||
chr2:37371431
|
C | CAA | 13 | a0001c0001t0001g0098a0001c0001t0001g0114a0001c0001t0001g0176others(10): Show | 13 | HG00140.hp1 HG00280.hp1 HG00741.hp2 others(10): Show |
intron_variant | MODIFIER | c.824-905_824-904dup others(2): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 37371431 | |||||
chr2:37371431
|
C | CAAAAA | 6 | a0001c0001t0002g0306a0002c0002t0002g0262a0002c0002t0002g0281others(3): Show | 6 | HG02040.hp2 NA18956.hp1 NA18965.hp2 others(3): Show |
intron_variant | MODIFIER | c.824-908_824-904dup others(5): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 37371431 | |||||
chr2:37371431
|
C | CAAAAAA | 74 | a0001c0001t0002g0041a0001c0001t0002g0199a0001c0001t0002g0201others(71): Show | 101 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(98): Show |
intron_variant | MODIFIER | c.824-909_824-904dup others(6): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 37371431 | |||||
chr2:37371431
|
C | CAAAAAAA | 10 | a0001c0001t0001g0243a0001c0001t0002g0320a0002c0002t0002g0246others(7): Show | 10 | HG02015.hp2 HG02109.hp2 HG02135.hp2 others(7): Show |
intron_variant | MODIFIER | c.824-910_824-904dup others(7): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 37371431 | |||||
chr2:37371431
|
CAAA | C | 9 | a0001c0001t0003g0110a0001c0001t0003g0244a0001c0003t0003g0129others(6): Show | 9 | HG02280.hp1 HG02451.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.824-906_824-904del others(3): Show |
QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr2 | 37371431 | |||||
chr2:37371453
|
G | A | 1 | a0006c0008t0006g0337 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.824-903G>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 5/6 | chr2 | 37371453 | ||||||
chr2:37371454
|
A | G | 1 | a0006c0008t0006g0337 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.824-902A>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 5/6 | chr2 | 37371454 | ||||||
chr2:37371507
|
A | G | 4 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0108others(1): Show | 4 | HG02258.hp1 HG02572.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.824-849A>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 5/6 | chr2 | 37371507 | ||||||
chr2:37371531
|
G | T | 1 | a0001c0001t0001g0243 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.824-825G>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 5/6 | chr2 | 37371531 | ||||||
chr2:37371566
|
A | T | 1 | a0006c0008t0006g0337 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.824-790A>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 5/6 | chr2 | 37371566 | ||||||
chr2:37371578
|
T | C | 1 | a0001c0001t0001g0063 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.824-778T>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 5/6 | chr2 | 37371578 | ||||||
chr2:37371771
|
C | T | 13 | a0001c0001t0001g0243a0001c0001t0003g0110a0001c0001t0003g0244others(10): Show | 13 | HG02109.hp2 HG02280.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.824-585C>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 5/6 | chr2 | 37371771 | ||||||
chr2:37371855
|
A | G | 104 | a0001c0001t0001g0243a0001c0001t0002g0041a0001c0001t0002g0186others(101): Show | 131 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(128): Show |
intron_variant | MODIFIER | c.824-501A>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 5/6 | chr2 | 37371855 | ||||||
chr2:37371958
|
T | C | 5 | a0001c0001t0002g0347a0001c0001t0002g0349a0001c0003t0002g0166others(2): Show | 5 | HG02896.hp1 HG02897.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.824-398T>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 5/6 | chr2 | 37371958 | ||||||
chr2:37372052
|
C | T | 1 | a0004c0005t0001g0130 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.824-304C>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 5/6 | chr2 | 37372052 | ||||||
chr2:37372084
|
T | C | 103 | a0001c0001t0002g0041a0001c0001t0002g0186a0001c0001t0002g0199others(100): Show | 130 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(127): Show |
intron_variant | MODIFIER | c.824-272T>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 5/6 | chr2 | 37372084 | ||||||
chr2:37372147
|
G | T | 2 | a0001c0001t0001g0071a0001c0001t0001g0072 | 2 | HG02004.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.824-209G>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 5/6 | chr2 | 37372147 | ||||||
chr2:37372194
|
C | G | 103 | a0001c0001t0002g0041a0001c0001t0002g0186a0001c0001t0002g0199others(100): Show | 130 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(127): Show |
intron_variant | MODIFIER | c.824-162C>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 5/6 | chr2 | 37372194 | ||||||
chr2:37372210
|
T | C | 4 | a0001c0001t0001g0040a0001c0001t0001g0304a0001c0001t0001g0307others(1): Show | 5 | HG02572.hp1 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.824-146T>C | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 5/6 | chr2 | 37372210 | ||||||
chr2:37372510
|
G | A | 2 | a0001c0001t0001g0343a0001c0001t0001g0344 | 2 | HG01106.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.940+38G>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 6/6 | chr2 | 37372510 | ||||||
chr2:37372537
|
G | A | 6 | a0001c0001t0001g0055a0001c0001t0001g0070a0001c0001t0001g0228others(3): Show | 6 | HG01074.hp1 HG01109.hp1 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.940+65G>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 6/6 | chr2 | 37372537 | ||||||
chr2:37372545
|
A | G | 94 | a0001c0001t0002g0041a0001c0001t0002g0186a0001c0001t0002g0199others(91): Show | 121 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(118): Show |
intron_variant | MODIFIER | c.940+73A>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 6/6 | chr2 | 37372545 | ||||||
chr2:37372568
|
T | G | 5 | a0001c0001t0002g0347a0001c0001t0002g0349a0001c0003t0002g0166others(2): Show | 5 | HG02896.hp1 HG02897.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.940+96T>G | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 6/6 | chr2 | 37372568 | ||||||
chr2:37372569
|
G | A | 5 | a0001c0001t0002g0347a0001c0001t0002g0349a0001c0003t0002g0166others(2): Show | 5 | HG02896.hp1 HG02897.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.940+97G>A | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 6/6 | chr2 | 37372569 | ||||||
chr2:37372639
|
C | T | 6 | a0001c0001t0003g0110a0001c0001t0003g0244a0001c0003t0003g0361others(3): Show | 6 | HG02451.hp2 HG02976.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.941-43C>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 6/6 | chr2 | 37372639 | ||||||
chr2:37372652
|
C | T | 1 | a0001c0001t0001g0068 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.941-30C>T | QPCT | ENSG00000115828.17 | transcript | ENST00000338415.8 | protein_coding | 6/6 | chr2 | 37372652 |