geneid | 79800 |
---|---|
ensemblid | ENSG00000138380.18 |
hgncid | 14435 |
symbol | CARF |
name | calcium responsive transcription factor |
refseq_nuc | NM_024744.17 |
refseq_prot | NP_079020.13 |
ensembl_nuc | ENST00000438828.4 |
ensembl_prot | ENSP00000414644.1 |
mane_status | MANE Select |
chr | chr2 |
start | 202912275 |
end | 202988263 |
strand | + |
ver | v1.2 |
region | chr2:202912275-202988263 |
region5000 | chr2:202907275-202993263 |
regionname0 | CARF_chr2_202912275_202988263 |
regionname5000 | CARF_chr2_202907275_202993263 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 725 | 285 | 62 | 51 | 134 | 6 | 30 | 99 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0002 | 0/0 | 725 | 23 | 19 | 4 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0003 | 0/0 | 725 | 14 | 1 | 5 | 4 | 4 | 0 | 3 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0004 | 0/0 | 725 | 8 | 0 | 0 | 8 | 0 | 0 | 6 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0005 | 0/0 | 725 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0006 | 0/0 | 725 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 2178 | 277 | 55 | 51 | 133 | 6 | 30 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
c0002 | 0/0 | 2178 | 22 | 19 | 3 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
c0003 | 0/0 | 2178 | 9 | 0 | 5 | 0 | 4 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
c0004 | 0/0 | 2178 | 8 | 0 | 0 | 8 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
c0005 | 0/0 | 2178 | 5 | 5 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
c0006 | 0/0 | 2178 | 3 | 3 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
c0007 | 0/0 | 2178 | 2 | 0 | 0 | 2 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
c0008 | 0/0 | 2178 | 2 | 2 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
c0009 | 0/0 | 2178 | 2 | 0 | 0 | 2 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
c0010 | 0/0 | 2178 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
c0011 | 0/0 | 2178 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
c0012 | 0/0 | 2178 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
c0013 | 0/0 | 2178 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 5792 | 24 | 2 | 5 | 13 | 0 | 4 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
t0002 | 0/0 | 5850 | 22 | 1 | 2 | 17 | 0 | 2 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
t0003 | 0/0 | 5794 | 18 | 3 | 2 | 9 | 0 | 4 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
t0004 | 0/0 | 5800 | 18 | 0 | 3 | 12 | 1 | 2 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
t0005 | 0/0 | 5852 | 14 | 0 | 5 | 5 | 1 | 3 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
t0006 | 0/0 | 5798 | 14 | 2 | 2 | 9 | 0 | 1 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
t0007 | 0/0 | 5796 | 11 | 4 | 2 | 5 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
t0008 | 0/1 | 5856 | 9 | 1 | 4 | 1 | 0 | 2 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
t0009 | 0/0 | 5790 | 9 | 0 | 4 | 3 | 0 | 2 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
t0010 | 1/0 | 5797 | 7 | 4 | 1 | 0 | 0 | 1 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
t0011 | 0/0 | 5802 | 6 | 0 | 1 | 4 | 1 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
t0012 | 0/0 | 5800 | 6 | 4 | 2 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
t0013 | 0/0 | 5799 | 5 | 1 | 3 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
t0014 | 0/0 | 5850 | 5 | 0 | 0 | 4 | 0 | 1 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
t0015 | 0/0 | 5798 | 5 | 5 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
t0016 | 0/0 | 5793 | 5 | 0 | 2 | 1 | 2 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
t0017 | 0/0 | 5791 | 4 | 4 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
t0018 | 0/0 | 5793 | 4 | 4 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
t0019 | 0/0 | 5799 | 4 | 0 | 0 | 3 | 0 | 1 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
t0020 | 0/0 | 5801 | 4 | 0 | 1 | 3 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
t0021 | 0/0 | 5854 | 4 | 0 | 3 | 0 | 0 | 1 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
t0022 | 0/0 | 5794 | 4 | 4 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
t0023 | 0/0 | 5802 | 4 | 3 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
t0024 | 0/0 | 5862 | 3 | 0 | 0 | 3 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
t0025 | 0/0 | 5850 | 3 | 1 | 0 | 1 | 0 | 1 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
t0026 | 0/0 | 5848 | 3 | 0 | 0 | 2 | 0 | 1 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
t0027 | 0/0 | 5856 | 3 | 3 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
t0028 | 0/0 | 5852 | 3 | 0 | 0 | 3 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
t0029 | 0/0 | 5780 | 3 | 2 | 0 | 0 | 0 | 1 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
t0030 | 0/0 | 5798 | 3 | 0 | 0 | 3 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
t0031 | 0/0 | 5771 | 2 | 2 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
t0032 | 0/0 | 5795 | 2 | 2 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
t0033 | 0/0 | 5797 | 2 | 0 | 1 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
t0034 | 0/0 | 5799 | 2 | 0 | 0 | 2 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
t0035 | 0/0 | 5808 | 2 | 0 | 0 | 2 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
t0036 | 0/0 | 5854 | 2 | 2 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
t0037 | 0/0 | 5878 | 2 | 0 | 2 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
t0038 | 0/0 | 5854 | 2 | 0 | 1 | 0 | 1 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
t0039 | 0/0 | 5856 | 2 | 0 | 0 | 0 | 2 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
t0040 | 0/0 | 5808 | 2 | 2 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
t0041 | 0/0 | 5774 | 2 | 0 | 0 | 2 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
t0042 | 0/0 | 5792 | 2 | 2 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
t0043 | 0/0 | 5794 | 2 | 0 | 0 | 2 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
t0044 | 0/0 | 5804 | 2 | 1 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
t0045 | 0/0 | 5824 | 2 | 2 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
t0046 | 0/0 | 5796 | 2 | 1 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
t0047 | 0/0 | 5789 | 2 | 0 | 0 | 0 | 2 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
t0048 | 0/0 | 5797 | 2 | 0 | 1 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
t0049 | 0/0 | 5793 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
t0050 | 0/0 | 5793 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
t0051 | 0/0 | 5795 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
t0052 | 0/0 | 5799 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
t0053 | 0/0 | 5809 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
t0054 | 0/0 | 5797 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
t0055 | 0/0 | 5799 | 1 | 0 | 0 | 0 | 0 | 1 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
t0056 | 0/0 | 5803 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
t0057 | 0/0 | 5797 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
t0058 | 0/0 | 5799 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
t0059 | 0/0 | 5804 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
t0060 | 0/0 | 5808 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
t0061 | 0/0 | 5850 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
t0062 | 0/0 | 5848 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
t0063 | 0/0 | 5874 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
t0064 | 0/0 | 5846 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
t0065 | 0/0 | 5850 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
t0066 | 0/0 | 5852 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
t0067 | 0/0 | 5876 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
t0068 | 0/0 | 5878 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
t0069 | 0/0 | 5848 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
t0070 | 0/0 | 5852 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
t0071 | 0/0 | 5876 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
t0072 | 0/0 | 5850 | 1 | 0 | 0 | 0 | 0 | 1 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
t0073 | 0/0 | 5868 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
t0074 | 0/0 | 5848 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
t0075 | 0/0 | 5852 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
t0076 | 0/0 | 5852 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
t0077 | 0/0 | 5852 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
t0078 | 0/0 | 5884 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
t0079 | 0/0 | 5850 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
t0080 | 0/0 | 5852 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
t0081 | 0/0 | 5854 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
t0082 | 0/0 | 5854 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
t0083 | 0/0 | 5856 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
t0084 | 0/0 | 5858 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
t0085 | 0/0 | 5882 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
t0086 | 0/0 | 5856 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
t0087 | 0/0 | 5858 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
t0088 | 0/0 | 5846 | 1 | 0 | 0 | 0 | 0 | 1 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
t0089 | 0/0 | 5854 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
t0090 | 0/0 | 5856 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
t0091 | 0/0 | 5814 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
t0092 | 0/0 | 5850 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
t0093 | 0/0 | 5788 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
t0094 | 0/0 | 5796 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
t0095 | 0/0 | 5796 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
t0096 | 0/0 | 5802 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
t0097 | 0/0 | 5804 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
t0098 | 0/0 | 5810 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
t0099 | 0/0 | 5814 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
t0100 | 0/0 | 5812 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
t0101 | 0/0 | 5816 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
t0102 | 0/0 | 5804 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
t0103 | 0/0 | 5798 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
t0104 | 0/0 | 5796 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
t0105 | 0/0 | 5800 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
t0106 | 0/0 | 5794 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
t0107 | 0/0 | 5850 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
t0108 | 0/0 | 5796 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
t0109 | 0/0 | 5788 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
t0110 | 0/0 | 5796 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
t0111 | 0/0 | 5802 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
t0112 | 0/0 | 5798 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
t0113 | 0/0 | 5796 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
t0114 | 0/0 | 5856 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
t0115 | 0/0 | 5783 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
t0116 | 0/0 | 5789 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
t0117 | 0/0 | 5791 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
t0118 | 0/0 | 5795 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
t0119 | 0/0 | 5788 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0002 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0004 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0006 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0017 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0117 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0293 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 2178 | 277 | 55 | 51 | 133 | 6 | 30 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0001c0005 | 0/0 | 2178 | 5 | 5 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0001c0008 | 0/0 | 2178 | 2 | 2 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0001c0011 | 0/0 | 2178 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0002c0002 | 0/0 | 2178 | 22 | 19 | 3 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0002c0012 | 0/0 | 2178 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0003c0003 | 0/0 | 2178 | 9 | 0 | 5 | 0 | 4 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0003c0007 | 0/0 | 2178 | 2 | 0 | 0 | 2 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0003c0009 | 0/0 | 2178 | 2 | 0 | 0 | 2 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0003c0013 | 0/0 | 2178 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0004c0004 | 0/0 | 2178 | 8 | 0 | 0 | 8 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0005c0006 | 0/0 | 2178 | 3 | 3 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0006c0010 | 0/0 | 2178 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 7969 | 24 | 2 | 5 | 13 | 0 | 4 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0001c0001t0002 | 0/0 | 8027 | 22 | 1 | 2 | 17 | 0 | 2 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0001c0001t0003 | 0/0 | 7971 | 18 | 3 | 2 | 9 | 0 | 4 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0001c0001t0004 | 0/0 | 7977 | 17 | 0 | 3 | 11 | 1 | 2 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0001c0001t0005 | 0/0 | 8029 | 14 | 0 | 5 | 5 | 1 | 3 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0001c0001t0006 | 0/0 | 7975 | 14 | 2 | 2 | 9 | 0 | 1 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0001c0001t0007 | 0/0 | 7973 | 11 | 4 | 2 | 5 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0001c0001t0008 | 0/1 | 8033 | 9 | 1 | 4 | 1 | 0 | 2 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0001c0001t0009 | 0/0 | 7967 | 9 | 0 | 4 | 3 | 0 | 2 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0001c0001t0010 | 1/0 | 7974 | 7 | 4 | 1 | 0 | 0 | 1 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0001c0001t0011 | 0/0 | 7979 | 6 | 0 | 1 | 4 | 1 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0001c0001t0013 | 0/0 | 7976 | 5 | 1 | 3 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0001c0001t0014 | 0/0 | 8027 | 5 | 0 | 0 | 4 | 0 | 1 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0001c0001t0015 | 0/0 | 7975 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0001c0001t0017 | 0/0 | 7968 | 3 | 3 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0001c0001t0018 | 0/0 | 7970 | 4 | 4 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0001c0001t0019 | 0/0 | 7976 | 1 | 0 | 0 | 0 | 0 | 1 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0001c0001t0020 | 0/0 | 7978 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0001c0001t0021 | 0/0 | 8031 | 4 | 0 | 3 | 0 | 0 | 1 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0001c0001t0024 | 0/0 | 8039 | 3 | 0 | 0 | 3 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0001c0001t0025 | 0/0 | 8027 | 3 | 1 | 0 | 1 | 0 | 1 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0001c0001t0026 | 0/0 | 8025 | 3 | 0 | 0 | 2 | 0 | 1 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0001c0001t0027 | 0/0 | 8033 | 3 | 3 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0001c0001t0028 | 0/0 | 8029 | 3 | 0 | 0 | 3 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0001c0001t0029 | 0/0 | 7957 | 3 | 2 | 0 | 0 | 0 | 1 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0001c0001t0030 | 0/0 | 7975 | 3 | 0 | 0 | 3 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0001c0001t0031 | 0/0 | 7948 | 2 | 2 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0001c0001t0032 | 0/0 | 7972 | 2 | 2 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0001c0001t0033 | 0/0 | 7974 | 2 | 0 | 1 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0001c0001t0034 | 0/0 | 7976 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0001c0001t0035 | 0/0 | 7985 | 2 | 0 | 0 | 2 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0001c0001t0036 | 0/0 | 8031 | 2 | 2 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0001c0001t0037 | 0/0 | 8055 | 2 | 0 | 2 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0001c0001t0038 | 0/0 | 8031 | 2 | 0 | 1 | 0 | 1 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0001c0001t0039 | 0/0 | 8033 | 2 | 0 | 0 | 0 | 2 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0001c0001t0041 | 0/0 | 7951 | 2 | 0 | 0 | 2 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0001c0001t0042 | 0/0 | 7969 | 2 | 2 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0001c0001t0043 | 0/0 | 7971 | 2 | 0 | 0 | 2 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0001c0001t0044 | 0/0 | 7981 | 2 | 1 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0001c0001t0045 | 0/0 | 8001 | 2 | 2 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0001c0001t0049 | 0/0 | 7970 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0001c0001t0050 | 0/0 | 7970 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0001c0001t0051 | 0/0 | 7972 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0001c0001t0052 | 0/0 | 7976 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0001c0001t0053 | 0/0 | 7986 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0001c0001t0055 | 0/0 | 7976 | 1 | 0 | 0 | 0 | 0 | 1 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0001c0001t0056 | 0/0 | 7980 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0001c0001t0061 | 0/0 | 8027 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0001c0001t0062 | 0/0 | 8025 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0001c0001t0063 | 0/0 | 8051 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0001c0001t0064 | 0/0 | 8023 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0001c0001t0065 | 0/0 | 8027 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0001c0001t0066 | 0/0 | 8029 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0001c0001t0067 | 0/0 | 8053 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0001c0001t0068 | 0/0 | 8055 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0001c0001t0069 | 0/0 | 8025 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0001c0001t0070 | 0/0 | 8029 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0001c0001t0071 | 0/0 | 8053 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0001c0001t0072 | 0/0 | 8027 | 1 | 0 | 0 | 0 | 0 | 1 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0001c0001t0073 | 0/0 | 8045 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0001c0001t0074 | 0/0 | 8025 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0001c0001t0075 | 0/0 | 8029 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0001c0001t0076 | 0/0 | 8029 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0001c0001t0077 | 0/0 | 8029 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0001c0001t0078 | 0/0 | 8061 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0001c0001t0079 | 0/0 | 8027 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0001c0001t0080 | 0/0 | 8029 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0001c0001t0081 | 0/0 | 8031 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0001c0001t0082 | 0/0 | 8031 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0001c0001t0083 | 0/0 | 8033 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0001c0001t0084 | 0/0 | 8035 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0001c0001t0085 | 0/0 | 8059 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0001c0001t0086 | 0/0 | 8033 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0001c0001t0087 | 0/0 | 8035 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0001c0001t0088 | 0/0 | 8023 | 1 | 0 | 0 | 0 | 0 | 1 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0001c0001t0089 | 0/0 | 8031 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0001c0001t0090 | 0/0 | 8033 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0001c0001t0093 | 0/0 | 7965 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0001c0001t0094 | 0/0 | 7973 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0001c0001t0095 | 0/0 | 7973 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0001c0001t0096 | 0/0 | 7979 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0001c0001t0100 | 0/0 | 7989 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0001c0001t0101 | 0/0 | 7993 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0001c0001t0102 | 0/0 | 7981 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0001c0001t0103 | 0/0 | 7975 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0001c0001t0104 | 0/0 | 7973 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0001c0001t0106 | 0/0 | 7971 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0001c0001t0108 | 0/0 | 7973 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0001c0001t0109 | 0/0 | 7965 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0001c0001t0110 | 0/0 | 7973 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0001c0001t0111 | 0/0 | 7979 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0001c0001t0112 | 0/0 | 7975 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0001c0001t0113 | 0/0 | 7973 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0001c0001t0114 | 0/0 | 8033 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0001c0005t0040 | 0/0 | 7985 | 2 | 2 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0001c0005t0060 | 0/0 | 7985 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0001c0005t0091 | 0/0 | 7991 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0001c0005t0092 | 0/0 | 8027 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0001c0008t0015 | 0/0 | 7975 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0001c0008t0022 | 0/0 | 7971 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0001c0011t0004 | 0/0 | 7977 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0002c0002t0012 | 0/0 | 7977 | 5 | 4 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0002c0002t0015 | 0/0 | 7975 | 3 | 3 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0002c0002t0022 | 0/0 | 7971 | 3 | 3 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0002c0002t0023 | 0/0 | 7979 | 4 | 3 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0002c0002t0046 | 0/0 | 7973 | 2 | 1 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0002c0002t0059 | 0/0 | 7981 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0002c0002t0097 | 0/0 | 7981 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0002c0002t0098 | 0/0 | 7987 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0002c0002t0099 | 0/0 | 7991 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0002c0002t0105 | 0/0 | 7977 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0002c0012t0012 | 0/0 | 7977 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0003c0003t0016 | 0/0 | 7970 | 4 | 0 | 2 | 0 | 2 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0003c0003t0047 | 0/0 | 7966 | 2 | 0 | 0 | 0 | 2 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0003c0003t0048 | 0/0 | 7974 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0003c0003t0115 | 0/0 | 7960 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0003c0003t0116 | 0/0 | 7966 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0003c0007t0048 | 0/0 | 7974 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0003c0007t0118 | 0/0 | 7972 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0003c0009t0016 | 0/0 | 7970 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0003c0009t0117 | 0/0 | 7968 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0003c0013t0119 | 0/0 | 7965 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0004c0004t0019 | 0/0 | 7976 | 3 | 0 | 0 | 3 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0004c0004t0020 | 0/0 | 7978 | 3 | 0 | 0 | 3 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0004c0004t0034 | 0/0 | 7976 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0004c0004t0054 | 0/0 | 7974 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0005c0006t0017 | 0/0 | 7968 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0005c0006t0057 | 0/0 | 7974 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0005c0006t0058 | 0/0 | 7976 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
a0006c0010t0107 | 0/0 | 8027 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | copy fasta | chr2 | 202907275 | 202993263 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0002g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0002g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0002g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0003g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0003g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0003g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0003g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0003g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0003g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0003g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0003g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0003g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0003g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0003g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0003g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0003g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0003g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0003g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0003g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0003g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0004g0006 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0004g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0004g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0004g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0004g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0004g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0004g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0004g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0004g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0004g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0004g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0004g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0004g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0004g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0004g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0004g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0005g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0005g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0005g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0005g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0005g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0005g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0005g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0005g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0005g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0005g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0005g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0005g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0005g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0005g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0006g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0006g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0006g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0006g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0006g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0006g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0006g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0006g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0006g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0006g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0006g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0006g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0006g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0006g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0007g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0007g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0007g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0007g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0007g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0007g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0007g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0007g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0007g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0007g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0007g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0008g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0008g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0008g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0008g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0008g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0008g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0008g0117 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0008g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0008g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0009g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0009g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0009g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0009g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0009g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0009g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0009g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0009g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0009g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0010g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0010g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0010g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0010g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0010g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0010g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0010g0293 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0011g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0011g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0011g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0011g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0011g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0011g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0013g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0013g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0013g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0013g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0013g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0014g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0014g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0014g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0014g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0014g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0015g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0017g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0017g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0017g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0018g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0018g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0018g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0018g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0019g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0020g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0021g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0021g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0021g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0024g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0024g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0024g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0025g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0025g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0025g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0026g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0026g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0026g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0027g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0027g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0027g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0028g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0028g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0028g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0029g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0029g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0029g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0030g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0030g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0030g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0031g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0031g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0032g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0032g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0033g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0033g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0034g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0035g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0035g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0036g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0036g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0037g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0037g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0038g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0038g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0039g0004 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0041g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0041g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0042g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0042g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0043g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0043g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0044g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0044g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0045g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0045g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0049g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0050g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0051g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0052g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0053g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0055g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0056g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0061g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0062g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0063g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0064g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0065g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0066g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0067g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0068g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0069g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0070g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0071g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0072g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0073g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0074g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0075g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0076g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0077g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0078g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0079g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0080g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0081g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0082g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0083g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0084g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0085g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0086g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0087g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0088g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0089g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0090g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0093g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0094g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0095g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0096g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0100g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0101g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0102g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0103g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0104g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0106g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0108g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0109g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0110g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0111g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0112g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0113g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0001t0114g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0005t0040g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0005t0040g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0005t0060g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0005t0091g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0005t0092g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0008t0015g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0008t0022g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0001c0011t0004g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0002c0002t0012g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0002c0002t0012g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0002c0002t0012g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0002c0002t0012g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0002c0002t0012g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0002c0002t0015g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0002c0002t0015g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0002c0002t0015g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0002c0002t0022g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0002c0002t0022g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0002c0002t0022g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0002c0002t0023g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0002c0002t0023g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0002c0002t0023g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0002c0002t0023g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0002c0002t0046g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0002c0002t0046g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0002c0002t0059g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0002c0002t0097g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0002c0002t0098g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0002c0002t0099g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0002c0002t0105g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0002c0012t0012g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0003c0003t0016g0002 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0003c0003t0016g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0003c0003t0016g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0003c0003t0016g0017 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0003c0003t0047g0001 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0003c0003t0048g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0003c0003t0115g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0003c0003t0116g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0003c0007t0048g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0003c0007t0118g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0003c0009t0016g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0003c0009t0117g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0003c0013t0119g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0004c0004t0019g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0004c0004t0019g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0004c0004t0019g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0004c0004t0020g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0004c0004t0020g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0004c0004t0020g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0004c0004t0034g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0004c0004t0054g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0005c0006t0017g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0005c0006t0057g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0005c0006t0058g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
a0006c0010t0107g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00323 | hp1 | a0001 | c0001 | t0005 | g0141 | EUR | FIN | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG00323 | hp2 | a0001 | c0001 | t0011 | g0219 | EUR | FIN | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG00408 | hp1 | a0001 | c0001 | t0006 | g0196 | EAS | CHS | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG00408 | hp2 | a0001 | c0001 | t0065 | g0032 | EAS | CHS | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG00423 | hp2 | a0001 | c0001 | t0026 | g0086 | EAS | CHS | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG00438 | hp1 | a0001 | c0001 | t0074 | g0057 | EAS | CHS | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG00438 | hp2 | a0003 | c0009 | t0117 | g0019 | EAS | CHS | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG00544 | hp1 | a0001 | c0001 | t0087 | g0079 | EAS | CHS | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | CHS | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG00597 | hp1 | a0001 | c0001 | t0004 | g0229 | EAS | CHS | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG00597 | hp2 | a0001 | c0001 | t0014 | g0104 | EAS | CHS | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG00609 | hp1 | a0001 | c0001 | t0003 | g0008 | EAS | CHS | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG00609 | hp2 | a0001 | c0001 | t0002 | g0139 | EAS | CHS | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG00621 | hp1 | a0001 | c0001 | t0006 | g0060 | EAS | CHS | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | CHS | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG00642 | hp1 | a0001 | c0001 | t0009 | g0212 | AMR | PUR | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG00642 | hp2 | a0001 | c0001 | t0089 | g0099 | AMR | PUR | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG00673 | hp1 | a0001 | c0001 | t0079 | g0071 | EAS | CHS | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG00673 | hp2 | a0001 | c0001 | t0096 | g0097 | EAS | CHS | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG00733 | hp1 | a0001 | c0001 | t0114 | g0116 | AMR | PUR | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG00733 | hp2 | a0002 | c0002 | t0046 | g0303 | AMR | PUR | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG00735 | hp1 | a0003 | c0003 | t0116 | g0002 | AMR | PUR | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG00735 | hp2 | a0001 | c0001 | t0008 | g0077 | AMR | PUR | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG00738 | hp1 | a0001 | c0001 | t0020 | g0285 | AMR | PUR | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG00738 | hp2 | a0003 | c0003 | t0115 | g0018 | AMR | PUR | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG00741 | hp1 | a0001 | c0001 | t0008 | g0076 | AMR | PUR | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG00741 | hp2 | a0001 | c0001 | t0003 | g0176 | AMR | PUR | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG01081 | hp1 | a0001 | c0001 | t0085 | g0020 | AMR | PUR | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG01081 | hp2 | a0001 | c0001 | t0011 | g0227 | AMR | PUR | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG01099 | hp1 | a0001 | c0001 | t0002 | g0140 | AMR | PUR | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG01099 | hp2 | a0003 | c0003 | t0016 | g0014 | AMR | PUR | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG01106 | hp1 | a0001 | c0001 | t0008 | g0115 | AMR | PUR | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG01106 | hp2 | a0001 | c0001 | t0005 | g0142 | AMR | PUR | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG01109 | hp1 | a0001 | c0001 | t0005 | g0055 | AMR | PUR | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG01109 | hp2 | a0002 | c0012 | t0012 | g0310 | AMR | PUR | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG01167 | hp1 | a0003 | c0003 | t0048 | g0011 | AMR | PUR | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG01167 | hp2 | a0001 | c0001 | t0005 | g0143 | AMR | PUR | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG01168 | hp1 | a0001 | c0001 | t0004 | g0291 | AMR | PUR | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG01168 | hp2 | a0002 | c0002 | t0023 | g0306 | AMR | PUR | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG01169 | hp1 | a0002 | c0002 | t0012 | g0307 | AMR | PUR | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG01169 | hp2 | a0001 | c0001 | t0005 | g0144 | AMR | PUR | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG01175 | hp1 | a0001 | c0001 | t0004 | g0180 | AMR | PUR | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG01175 | hp2 | a0001 | c0001 | t0005 | g0069 | AMR | PUR | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG01192 | hp2 | a0001 | c0001 | t0090 | g0064 | AMR | PUR | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0213 | AMR | CLM | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG01255 | hp2 | a0001 | c0001 | t0002 | g0112 | AMR | CLM | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG01256 | hp1 | a0001 | c0001 | t0021 | g0003 | AMR | CLM | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0205 | AMR | CLM | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG01257 | hp1 | a0001 | c0001 | t0013 | g0265 | AMR | CLM | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG01257 | hp2 | a0001 | c0001 | t0006 | g0153 | AMR | CLM | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG01258 | hp1 | a0001 | c0001 | t0006 | g0152 | AMR | CLM | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG01258 | hp2 | a0001 | c0001 | t0021 | g0003 | AMR | CLM | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG01346 | hp1 | a0001 | c0001 | t0008 | g0080 | AMR | CLM | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG01346 | hp2 | a0001 | c0001 | t0076 | g0037 | AMR | CLM | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | CLM | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG01358 | hp2 | a0001 | c0001 | t0070 | g0067 | AMR | CLM | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG01361 | hp1 | a0001 | c0001 | t0003 | g0167 | AMR | CLM | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG01361 | hp2 | a0001 | c0001 | t0071 | g0039 | AMR | CLM | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG01496 | hp1 | a0001 | c0001 | t0038 | g0075 | AMR | CLM | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG01496 | hp2 | a0003 | c0003 | t0016 | g0013 | AMR | CLM | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG01515 | hp1 | a0003 | c0003 | t0016 | g0017 | EUR | IBS | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG01515 | hp2 | a0001 | c0001 | t0039 | g0004 | EUR | IBS | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG01516 | hp1 | a0003 | c0003 | t0047 | g0001 | EUR | IBS | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG01516 | hp2 | a0001 | c0001 | t0004 | g0290 | EUR | IBS | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG01517 | hp1 | a0001 | c0001 | t0039 | g0004 | EUR | IBS | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG01517 | hp2 | a0003 | c0003 | t0047 | g0001 | EUR | IBS | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG01884 | hp1 | a0002 | c0002 | t0012 | g0317 | AFR | ACB | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG01884 | hp2 | a0003 | c0013 | t0119 | g0010 | AFR | ACB | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG01943 | hp1 | a0001 | c0001 | t0033 | g0286 | AMR | PEL | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG01943 | hp2 | a0001 | c0001 | t0007 | g0218 | AMR | PEL | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG01952 | hp1 | a0001 | c0001 | t0013 | g0251 | AMR | PEL | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG01952 | hp2 | a0001 | c0001 | t0009 | g0179 | AMR | PEL | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG01975 | hp1 | a0001 | c0001 | t0112 | g0220 | AMR | PEL | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG01975 | hp2 | a0001 | c0001 | t0013 | g0280 | AMR | PEL | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG01981 | hp1 | a0001 | c0001 | t0021 | g0021 | AMR | PEL | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG01981 | hp2 | a0001 | c0001 | t0009 | g0215 | AMR | PEL | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG02040 | hp1 | a0001 | c0001 | t0006 | g0235 | EAS | KHV | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG02040 | hp2 | a0001 | c0001 | t0003 | g0155 | EAS | KHV | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG02055 | hp1 | a0006 | c0010 | t0107 | g0026 | AFR | ACB | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG02055 | hp2 | a0001 | c0001 | t0003 | g0214 | AFR | ACB | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG02056 | hp1 | a0001 | c0001 | t0008 | g0035 | EAS | KHV | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG02056 | hp2 | a0001 | c0001 | t0011 | g0162 | EAS | KHV | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG02071 | hp1 | a0001 | c0001 | t0066 | g0044 | EAS | KHV | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG02071 | hp2 | a0001 | c0001 | t0028 | g0040 | EAS | KHV | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG02080 | hp1 | a0001 | c0001 | t0093 | g0148 | EAS | KHV | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG02080 | hp2 | a0001 | c0001 | t0077 | g0042 | EAS | KHV | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG02083 | hp1 | a0001 | c0001 | t0007 | g0241 | EAS | KHV | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG02083 | hp2 | a0001 | c0001 | t0028 | g0131 | EAS | KHV | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG02129 | hp1 | a0001 | c0001 | t0004 | g0226 | EAS | KHV | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG02129 | hp2 | a0004 | c0004 | t0054 | g0278 | EAS | KHV | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG02132 | hp1 | a0004 | c0004 | t0034 | g0276 | EAS | KHV | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG02132 | hp2 | a0001 | c0001 | t0075 | g0137 | EAS | KHV | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG02135 | hp1 | a0001 | c0001 | t0006 | g0244 | EAS | KHV | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG02135 | hp2 | a0001 | c0001 | t0003 | g0201 | EAS | KHV | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG02145 | hp1 | a0001 | c0005 | t0060 | g0145 | AFR | ACB | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG02145 | hp2 | a0001 | c0001 | t0013 | g0253 | AFR | ACB | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG02148 | hp1 | a0001 | c0001 | t0053 | g0256 | AMR | PEL | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG02148 | hp2 | a0001 | c0001 | t0009 | g0169 | AMR | PEL | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG02155 | hp1 | a0001 | c0001 | t0006 | g0007 | EAS | CDX | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG02155 | hp2 | a0001 | c0001 | t0006 | g0149 | EAS | CDX | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG02165 | hp1 | a0001 | c0001 | t0005 | g0107 | EAS | CDX | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CDX | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG02257 | hp1 | a0001 | c0001 | t0032 | g0255 | AFR | ACB | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG02257 | hp2 | a0005 | c0006 | t0058 | g0248 | AFR | ACB | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG02258 | hp1 | a0002 | c0002 | t0012 | g0314 | AFR | ACB | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG02258 | hp2 | a0001 | c0001 | t0042 | g0298 | AFR | ACB | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0216 | AMR | PEL | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG02273 | hp2 | a0001 | c0001 | t0037 | g0084 | AMR | PEL | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG02280 | hp1 | a0001 | c0001 | t0006 | g0236 | AFR | ACB | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG02280 | hp2 | a0001 | c0001 | t0084 | g0046 | AFR | ACB | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG02293 | hp1 | a0001 | c0001 | t0010 | g0267 | AMR | PEL | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG02293 | hp2 | a0001 | c0001 | t0007 | g0158 | AMR | PEL | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG02300 | hp1 | a0001 | c0001 | t0037 | g0135 | AMR | PEL | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG02300 | hp2 | a0001 | c0001 | t0004 | g0156 | AMR | PEL | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG02451 | hp1 | a0001 | c0005 | t0040 | g0325 | AFR | ACB | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG02451 | hp2 | a0001 | c0001 | t0007 | g0031 | AFR | ACB | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG02572 | hp1 | a0001 | c0001 | t0007 | g0165 | AFR | GWD | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG02572 | hp2 | a0002 | c0002 | t0015 | g0316 | AFR | GWD | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG02602 | hp1 | a0001 | c0001 | t0014 | g0113 | SAS | PJL | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG02602 | hp2 | a0001 | c0001 | t0003 | g0160 | SAS | PJL | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG02615 | hp1 | a0001 | c0001 | t0010 | g0257 | AFR | GWD | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG02615 | hp2 | a0001 | c0001 | t0010 | g0250 | AFR | GWD | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG02622 | hp1 | a0005 | c0006 | t0017 | g0245 | AFR | GWD | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG02622 | hp2 | a0001 | c0001 | t0010 | g0252 | AFR | GWD | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG02630 | hp1 | a0001 | c0001 | t0027 | g0048 | AFR | GWD | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG02630 | hp2 | a0001 | c0001 | t0018 | g0269 | AFR | GWD | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG02717 | hp1 | a0002 | c0002 | t0012 | g0312 | AFR | GWD | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG02717 | hp2 | a0001 | c0005 | t0040 | g0147 | AFR | GWD | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG02723 | hp1 | a0001 | c0001 | t0006 | g0206 | AFR | GWD | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG02723 | hp2 | a0001 | c0001 | t0017 | g0271 | AFR | GWD | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | GWD | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG02809 | hp2 | a0001 | c0001 | t0050 | g0281 | AFR | GWD | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG02818 | hp1 | a0002 | c0002 | t0015 | g0311 | AFR | GWD | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG02818 | hp2 | a0001 | c0001 | t0027 | g0045 | AFR | GWD | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG02886 | hp1 | a0001 | c0001 | t0007 | g0208 | AFR | GWD | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG02886 | hp2 | a0001 | c0001 | t0018 | g0283 | AFR | GWD | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG02895 | hp1 | a0002 | c0002 | t0023 | g0302 | AFR | GWD | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG02895 | hp2 | a0001 | c0005 | t0092 | g0146 | AFR | GWD | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG02896 | hp1 | a0001 | c0001 | t0029 | g0300 | AFR | GWD | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG02896 | hp2 | a0002 | c0002 | t0105 | g0321 | AFR | GWD | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG02897 | hp1 | a0001 | c0001 | t0029 | g0301 | AFR | GWD | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG02897 | hp2 | a0002 | c0002 | t0023 | g0305 | AFR | GWD | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG02970 | hp1 | a0001 | c0008 | t0015 | g0243 | AFR | ESN | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG02970 | hp2 | a0001 | c0001 | t0017 | g0261 | AFR | ESN | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG02976 | hp1 | a0001 | c0001 | t0044 | g0207 | AFR | ESN | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG02976 | hp2 | a0001 | c0001 | t0101 | g0240 | AFR | ESN | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG03041 | hp1 | a0002 | c0002 | t0022 | g0304 | AFR | GWD | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG03041 | hp2 | a0001 | c0001 | t0027 | g0050 | AFR | GWD | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG03098 | hp1 | a0001 | c0001 | t0051 | g0246 | AFR | MSL | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG03098 | hp2 | a0002 | c0002 | t0099 | g0322 | AFR | MSL | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG03130 | hp1 | a0002 | c0002 | t0098 | g0318 | AFR | ESN | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG03130 | hp2 | a0001 | c0001 | t0031 | g0264 | AFR | ESN | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG03139 | hp1 | a0001 | c0001 | t0100 | g0009 | AFR | ESN | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG03139 | hp2 | a0005 | c0006 | t0057 | g0259 | AFR | ESN | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG03195 | hp1 | a0001 | c0001 | t0031 | g0263 | AFR | ESN | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG03195 | hp2 | a0002 | c0002 | t0097 | g0320 | AFR | ESN | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG03209 | hp1 | a0001 | c0001 | t0083 | g0049 | AFR | MSL | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG03209 | hp2 | a0001 | c0001 | t0018 | g0270 | AFR | MSL | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG03225 | hp1 | a0002 | c0002 | t0012 | g0319 | AFR | MSL | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG03225 | hp2 | a0001 | c0001 | t0045 | g0098 | AFR | MSL | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG03239 | hp1 | a0001 | c0001 | t0021 | g0022 | SAS | PJL | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG03239 | hp2 | a0001 | c0001 | t0055 | g0274 | SAS | PJL | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG03453 | hp1 | a0001 | c0001 | t0008 | g0078 | AFR | MSL | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG03453 | hp2 | a0001 | c0001 | t0045 | g0063 | AFR | MSL | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG03490 | hp1 | a0001 | c0001 | t0026 | g0106 | SAS | PJL | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG03490 | hp2 | a0001 | c0001 | t0004 | g0006 | SAS | PJL | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG03491 | hp1 | a0001 | c0001 | t0008 | g0296 | SAS | PJL | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG03491 | hp2 | a0001 | c0001 | t0003 | g0183 | SAS | PJL | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG03492 | hp1 | a0001 | c0001 | t0004 | g0006 | SAS | PJL | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG03492 | hp2 | a0001 | c0001 | t0008 | g0297 | SAS | PJL | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG03516 | hp1 | a0001 | c0001 | t0003 | g0189 | AFR | ESN | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG03516 | hp2 | a0002 | c0002 | t0015 | g0323 | AFR | ESN | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG03540 | hp1 | a0002 | c0002 | t0022 | g0309 | AFR | GWD | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG03540 | hp2 | a0001 | c0001 | t0010 | g0268 | AFR | GWD | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG03579 | hp1 | a0001 | c0001 | t0007 | g0288 | AFR | MSL | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG03579 | hp2 | a0001 | c0005 | t0091 | g0043 | AFR | MSL | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG03669 | hp1 | a0001 | c0001 | t0010 | g0273 | SAS | PJL | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG03669 | hp2 | a0001 | c0001 | t0003 | g0166 | SAS | PJL | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG03688 | hp1 | a0001 | c0001 | t0005 | g0068 | SAS | STU | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG03688 | hp2 | a0001 | c0001 | t0006 | g0168 | SAS | STU | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG03704 | hp1 | a0001 | c0001 | t0005 | g0110 | SAS | PJL | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG03704 | hp2 | a0001 | c0001 | t0072 | g0119 | SAS | PJL | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG03710 | hp1 | a0001 | c0001 | t0019 | g0295 | SAS | PJL | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG03710 | hp2 | a0001 | c0001 | t0009 | g0191 | SAS | PJL | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0199 | SAS | BEB | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG03831 | hp2 | a0001 | c0001 | t0025 | g0074 | SAS | BEB | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG03834 | hp1 | a0001 | c0001 | t0029 | g0217 | SAS | BEB | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG03834 | hp2 | a0001 | c0001 | t0002 | g0111 | SAS | BEB | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0095 | SAS | BEB | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG03942 | hp2 | a0001 | c0001 | t0002 | g0108 | SAS | BEB | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG04115 | hp1 | a0001 | c0001 | t0009 | g0182 | SAS | STU | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG04115 | hp2 | a0001 | c0001 | t0005 | g0058 | SAS | STU | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG04204 | hp1 | a0001 | c0001 | t0003 | g0209 | SAS | STU | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0289 | SAS | STU | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG04228 | hp1 | a0001 | c0001 | t0088 | g0065 | SAS | STU | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0120 | SAS | STU | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
NA18747 | hp1 | a0001 | c0001 | t0003 | g0150 | EAS | CHB | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
NA18747 | hp2 | a0001 | c0001 | t0067 | g0124 | EAS | CHB | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
NA18906 | hp1 | a0001 | c0001 | t0036 | g0033 | AFR | YRI | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
NA18906 | hp2 | a0001 | c0001 | t0018 | g0249 | AFR | YRI | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
NA18939 | hp1 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
NA18940 | hp1 | a0001 | c0001 | t0024 | g0038 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
NA18940 | hp2 | a0001 | c0001 | t0003 | g0062 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
NA18945 | hp1 | a0001 | c0001 | t0011 | g0027 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
NA18945 | hp2 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
NA18946 | hp1 | a0001 | c0001 | t0095 | g0225 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
NA18946 | hp2 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
NA18948 | hp1 | a0001 | c0011 | t0004 | g0233 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
NA18948 | hp2 | a0001 | c0001 | t0056 | g0260 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
NA18951 | hp1 | a0001 | c0001 | t0030 | g0195 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
NA18951 | hp2 | a0001 | c0001 | t0028 | g0092 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
NA18952 | hp1 | a0003 | c0007 | t0118 | g0016 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
NA18954 | hp1 | a0001 | c0001 | t0007 | g0028 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
NA18954 | hp2 | a0001 | c0001 | t0005 | g0100 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
NA18959 | hp1 | a0001 | c0001 | t0044 | g0210 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
NA18959 | hp2 | a0001 | c0001 | t0005 | g0294 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
NA18960 | hp2 | a0001 | c0001 | t0003 | g0232 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
NA18962 | hp1 | a0001 | c0001 | t0041 | g0185 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
NA18962 | hp2 | a0001 | c0001 | t0007 | g0202 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
NA18965 | hp1 | a0001 | c0001 | t0004 | g0151 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
NA18965 | hp2 | a0001 | c0001 | t0081 | g0041 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
NA18966 | hp1 | a0004 | c0004 | t0020 | g0275 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
NA18966 | hp2 | a0003 | c0007 | t0048 | g0012 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
NA18968 | hp1 | a0001 | c0001 | t0030 | g0194 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
NA18968 | hp2 | a0004 | c0004 | t0019 | g0277 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
NA18969 | hp1 | a0001 | c0001 | t0004 | g0238 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
NA18969 | hp2 | a0004 | c0004 | t0019 | g0279 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
NA18970 | hp1 | a0001 | c0001 | t0003 | g0231 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
NA18970 | hp2 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
NA18972 | hp1 | a0001 | c0001 | t0102 | g0174 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
NA18972 | hp2 | a0004 | c0004 | t0020 | g0247 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
NA18974 | hp1 | a0001 | c0001 | t0002 | g0121 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
NA18974 | hp2 | a0001 | c0001 | t0007 | g0237 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
NA18977 | hp1 | a0001 | c0001 | t0080 | g0052 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
NA18977 | hp2 | a0001 | c0001 | t0003 | g0059 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
NA18978 | hp1 | a0001 | c0001 | t0035 | g0101 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
NA18978 | hp2 | a0001 | c0001 | t0006 | g0159 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
NA18980 | hp1 | a0001 | c0001 | t0006 | g0239 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
NA18980 | hp2 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
NA18981 | hp1 | a0001 | c0001 | t0026 | g0089 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
NA18981 | hp2 | a0001 | c0001 | t0004 | g0053 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
NA18982 | hp1 | a0001 | c0001 | t0004 | g0204 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
NA18982 | hp2 | a0001 | c0001 | t0035 | g0105 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
NA18984 | hp1 | a0001 | c0001 | t0009 | g0234 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
NA18984 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
NA18986 | hp1 | a0001 | c0001 | t0002 | g0138 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
NA18986 | hp2 | a0001 | c0001 | t0041 | g0186 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
NA18988 | hp1 | a0001 | c0001 | t0104 | g0173 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
NA18988 | hp2 | a0001 | c0001 | t0034 | g0284 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
NA18991 | hp1 | a0001 | c0001 | t0006 | g0230 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
NA18991 | hp2 | a0001 | c0001 | t0024 | g0126 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
NA18993 | hp1 | a0001 | c0001 | t0005 | g0070 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
NA18993 | hp2 | a0001 | c0001 | t0110 | g0163 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
NA18994 | hp1 | a0001 | c0001 | t0004 | g0172 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
NA18994 | hp2 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
NA18995 | hp1 | a0001 | c0001 | t0025 | g0091 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
NA18995 | hp2 | a0001 | c0001 | t0007 | g0061 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
NA18998 | hp1 | a0001 | c0001 | t0014 | g0102 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
NA18999 | hp1 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
NA18999 | hp2 | a0001 | c0001 | t0043 | g0023 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
NA19001 | hp1 | a0001 | c0001 | t0078 | g0072 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
NA19001 | hp2 | a0001 | c0001 | t0003 | g0171 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
NA19003 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
NA19003 | hp2 | a0001 | c0001 | t0011 | g0203 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
NA19004 | hp1 | a0001 | c0001 | t0004 | g0221 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
NA19004 | hp2 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
NA19009 | hp1 | a0001 | c0001 | t0004 | g0178 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
NA19009 | hp2 | a0001 | c0001 | t0073 | g0083 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
NA19010 | hp1 | a0001 | c0001 | t0111 | g0193 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
NA19010 | hp2 | a0001 | c0001 | t0069 | g0128 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
NA19030 | hp1 | a0001 | c0001 | t0002 | g0036 | AFR | LWK | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
NA19030 | hp2 | a0001 | c0001 | t0003 | g0181 | AFR | LWK | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
NA19043 | hp1 | a0002 | c0002 | t0022 | g0308 | AFR | LWK | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
NA19043 | hp2 | a0001 | c0001 | t0032 | g0254 | AFR | LWK | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
NA19057 | hp1 | a0001 | c0001 | t0014 | g0103 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
NA19057 | hp2 | a0001 | c0001 | t0094 | g0024 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
NA19062 | hp1 | a0001 | c0001 | t0109 | g0093 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
NA19062 | hp2 | a0001 | c0001 | t0024 | g0134 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
NA19064 | hp1 | a0001 | c0001 | t0011 | g0224 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
NA19064 | hp2 | a0004 | c0004 | t0020 | g0258 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
NA19065 | hp1 | a0001 | c0001 | t0005 | g0109 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
NA19065 | hp2 | a0001 | c0001 | t0009 | g0157 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
NA19066 | hp1 | a0001 | c0001 | t0082 | g0114 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
NA19066 | hp2 | a0001 | c0001 | t0108 | g0190 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
NA19070 | hp1 | a0001 | c0001 | t0068 | g0123 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
NA19070 | hp2 | a0001 | c0001 | t0004 | g0228 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
NA19077 | hp1 | a0001 | c0001 | t0013 | g0272 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
NA19077 | hp2 | a0001 | c0001 | t0014 | g0073 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
NA19078 | hp1 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
NA19078 | hp2 | a0001 | c0001 | t0113 | g0188 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
NA19081 | hp2 | a0001 | c0001 | t0030 | g0192 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
NA19083 | hp1 | a0001 | c0001 | t0106 | g0096 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
NA19083 | hp2 | a0001 | c0001 | t0002 | g0130 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
NA19084 | hp1 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
NA19084 | hp2 | a0004 | c0004 | t0019 | g0287 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
NA19085 | hp2 | a0003 | c0009 | t0016 | g0015 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
NA19086 | hp1 | a0001 | c0001 | t0062 | g0122 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
NA19086 | hp2 | a0001 | c0001 | t0043 | g0025 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
NA19087 | hp1 | a0001 | c0001 | t0009 | g0184 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
NA19088 | hp1 | a0001 | c0001 | t0033 | g0051 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
NA19088 | hp2 | a0001 | c0001 | t0064 | g0081 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
NA19091 | hp1 | a0001 | c0001 | t0004 | g0029 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
NA19091 | hp2 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | YRI | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
NA19240 | hp2 | a0001 | c0001 | t0042 | g0299 | AFR | YRI | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
NA20129 | hp1 | a0001 | c0001 | t0017 | g0262 | AFR | ASW | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
NA20129 | hp2 | a0002 | c0002 | t0046 | g0315 | AFR | ASW | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
NA20752 | hp1 | a0001 | c0001 | t0038 | g0056 | EUR | TSI | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
NA20752 | hp2 | a0003 | c0003 | t0016 | g0002 | EUR | TSI | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG02109 | hp1 | a0001 | c0001 | t0103 | g0292 | AFR | ACB | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG02109 | hp2 | a0001 | c0001 | t0049 | g0282 | AFR | ACB | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG02486 | hp1 | a0001 | c0001 | t0025 | g0047 | AFR | ACB | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG02486 | hp2 | a0001 | c0008 | t0022 | g0242 | AFR | ACB | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG02559 | hp1 | a0002 | c0002 | t0059 | g0324 | AFR | ACB | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG02559 | hp2 | a0001 | c0001 | t0063 | g0034 | AFR | ACB | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG06807 | hp1 | a0001 | c0001 | t0036 | g0066 | AFR | USA | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
HG06807 | hp2 | a0002 | c0002 | t0023 | g0313 | AFR | USA | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
NA20300 | hp1 | a0001 | c0001 | t0015 | g0009 | AFR | USA | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
NA20300 | hp2 | a0001 | c0001 | t0061 | g0223 | AFR | USA | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
NA21309 | hp1 | a0001 | c0001 | t0086 | g0118 | AFR | LWK | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
NA21309 | hp2 | a0001 | c0001 | t0052 | g0266 | AFR | LWK | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0008 | g0117 | REF | REF | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0010 | g0293 | REF | REF | CARF_chr2_202907275_202993263 | CARF | chr2 | 202907275 | 202993263 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:202942892
|
A | T | 1 | a0002 | 23 | HG00733.hp2 HG01109.hp2 HG01168.hp2 others(20): Show |
missense_variant | MODERATE | c.231A>T | p.Gln77His | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/17 | 1388/7974 | 231/2178 | 77/725 | chr2 | 202942892 | ||
chr2:202954047
|
T | C | 1 | a0006 | 1 | HG02055.hp1 | missense_variant | MODERATE | c.470T>C | p.Val157Ala | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 7/17 | 1627/7974 | 470/2178 | 157/725 | chr2 | 202954047 | ||
chr2:202982094
|
A | T | 1 | a0003 | 14 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(11): Show |
missense_variant | MODERATE | c.1712A>T | p.Tyr571Phe | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 16/17 | 2869/7974 | 1712/2178 | 571/725 | chr2 | 202982094 | ||
chr2:202982142
|
C | T | 1 | a0004 | 8 | HG02129.hp2 HG02132.hp1 NA18966.hp1 others(5): Show |
missense_variant | MODERATE | c.1760C>T | p.Pro587Leu | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 16/17 | 2917/7974 | 1760/2178 | 587/725 | chr2 | 202982142 | ||
chr2:202983619
|
A | G | 1 | a0005 | 3 | HG02257.hp2 HG02622.hp1 HG03139.hp2 |
missense_variant | MODERATE | c.2173A>G | p.Thr725Ala | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3330/7974 | 2173/2178 | 725/725 | chr2 | 202983619 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:202942805
|
C | G | 1 | a0003c0013 | 1 | HG01884.hp2 | synonymous_variant | LOW | c.144C>G | p.Pro48Pro | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/17 | 1301/7974 | 144/2178 | 48/725 | chr2 | 202942805 | ||
chr2:202952621
|
A | G | 1 | a0001c0011 | 1 | NA18948.hp1 | synonymous_variant | LOW | c.369A>G | p.Thr123Thr | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 6/17 | 1526/7974 | 369/2178 | 123/725 | chr2 | 202952621 | ||
chr2:202954132
|
C | T | 1 | a0003c0009 | 2 | HG00438.hp2 NA19085.hp2 |
splice_region_variant&synonymous_variant | LOW | c.555C>T | p.Thr185Thr | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 7/17 | 1712/7974 | 555/2178 | 185/725 | chr2 | 202954132 | ||
chr2:202955716
|
T | C | 1 | a0003c0007 | 2 | NA18952.hp1 NA18966.hp2 |
synonymous_variant | LOW | c.600T>C | p.Ser200Ser | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 8/17 | 1757/7974 | 600/2178 | 200/725 | chr2 | 202955716 | ||
chr2:202971577
|
A | C | 1 | a0002c0012 | 1 | HG01109.hp2 | synonymous_variant | LOW | c.1170A>C | p.Ser390Ser | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 12/17 | 2327/7974 | 1170/2178 | 390/725 | chr2 | 202971577 | ||
chr2:202974364
|
C | T | 1 | a0001c0005 | 5 | HG02145.hp1 HG02451.hp1 HG02717.hp2 others(2): Show |
synonymous_variant | LOW | c.1362C>T | p.Pro454Pro | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 13/17 | 2519/7974 | 1362/2178 | 454/725 | chr2 | 202974364 | ||
chr2:202977292
|
G | A | 1 | a0001c0008 | 2 | HG02486.hp2 HG02970.hp1 |
synonymous_variant | LOW | c.1518G>A | p.Gly506Gly | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 14/17 | 2675/7974 | 1518/2178 | 506/725 | chr2 | 202977292 | ||
chr2:202982401
|
G | A | 2 | a0002c0002a0002c0012 | 23 | HG00733.hp2 HG01109.hp2 HG01168.hp2 others(20): Show |
synonymous_variant | LOW | c.2019G>A | p.Gln673Gln | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 16/17 | 3176/7974 | 2019/2178 | 673/725 | chr2 | 202982401 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:202912476
|
C | CT | 106 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(103): Show | 288 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(285): Show |
5_prime_UTR_variant | MODIFIER | c.-956_-955insT | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 1/17 | 29426 | chr2 | 202912476 | |||||
chr2:202912503
|
C | T | 10 | a0003c0003t0016a0003c0003t0047a0003c0003t0048others(7): Show | 14 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(11): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-929C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 1/17 | chr2 | 202912503 | ||||||
chr2:202912527
|
T | G | 1 | a0002c0002t0059 | 1 | HG02559.hp1 | 5_prime_UTR_variant | MODIFIER | c.-905T>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 1/17 | 29376 | chr2 | 202912527 | |||||
chr2:202913019
|
A | G | 1 | a0003c0013t0119 | 1 | HG01884.hp2 | 5_prime_UTR_variant | MODIFIER | c.-413A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 1/17 | 28884 | chr2 | 202913019 | |||||
chr2:202913085
|
A | C | 1 | a0001c0001t0114 | 1 | HG00733.hp1 | 5_prime_UTR_variant | MODIFIER | c.-347A>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 1/17 | 28818 | chr2 | 202913085 | |||||
chr2:202917993
|
G | T | 2 | a0005c0006t0057a0005c0006t0058 | 2 | HG02257.hp2 HG03139.hp2 |
5_prime_UTR_variant | MODIFIER | c.-213G>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 2/17 | 23910 | chr2 | 202917993 | |||||
chr2:202924409
|
G | A | 1 | a0001c0005t0060 | 1 | HG02145.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-50G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/17 | chr2 | 202924409 | ||||||
chr2:202983679
|
G | A | 10 | a0003c0003t0016a0003c0003t0047a0003c0003t0048others(7): Show | 14 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*55G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 55 | chr2 | 202983679 | |||||
chr2:202983711
|
G | A | 1 | a0001c0001t0061 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*87G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 87 | chr2 | 202983711 | |||||
chr2:202983945
|
A | C | 1 | a0001c0001t0113 | 1 | NA19078.hp2 | 3_prime_UTR_variant | MODIFIER | c.*321A>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 321 | chr2 | 202983945 | |||||
chr2:202984001
|
G | A | 45 | a0001c0001t0002a0001c0001t0005a0001c0001t0008others(42): Show | 109 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(106): Show |
3_prime_UTR_variant | MODIFIER | c.*377G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 377 | chr2 | 202984001 | |||||
chr2:202984605
|
T | C | 2 | a0001c0001t0049a0001c0001t0050 | 2 | HG02109.hp2 HG02809.hp2 |
3_prime_UTR_variant | MODIFIER | c.*981T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 981 | chr2 | 202984605 | |||||
chr2:202984690
|
A | C | 1 | a0001c0001t0112 | 1 | HG01975.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1066A>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 1066 | chr2 | 202984690 | |||||
chr2:202984800
|
A | T | 4 | a0001c0001t0030a0001c0001t0109a0001c0001t0110others(1): Show | 6 | NA18951.hp1 NA18968.hp1 NA18993.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1176A>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 1176 | chr2 | 202984800 | |||||
chr2:202984813
|
T | C | 4 | a0001c0005t0040a0001c0005t0060a0001c0005t0091others(1): Show | 5 | HG02145.hp1 HG02451.hp1 HG02717.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1189T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 1189 | chr2 | 202984813 | |||||
chr2:202984857
|
A | C | 1 | a0001c0001t0108 | 1 | NA19066.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1233A>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 1233 | chr2 | 202984857 | |||||
chr2:202984930
|
C | T | 1 | a0006c0010t0107 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1306C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 1306 | chr2 | 202984930 | |||||
chr2:202985005
|
G | A | 1 | a0003c0003t0047 | 2 | HG01516.hp1 HG01517.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1381G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 1381 | chr2 | 202985005 | |||||
chr2:202985025
|
C | T | 1 | a0001c0001t0106 | 1 | NA19083.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1401C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 1401 | chr2 | 202985025 | |||||
chr2:202985059
|
A | C | 1 | a0002c0002t0105 | 1 | HG02896.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1435A>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 1435 | chr2 | 202985059 | |||||
chr2:202985116
|
C | T | 1 | a0001c0001t0104 | 1 | NA18988.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1492C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 1492 | chr2 | 202985116 | |||||
chr2:202985190
|
A | G | 1 | a0001c0001t0050 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1566A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 1566 | chr2 | 202985190 | |||||
chr2:202985288
|
C | G | 10 | a0003c0003t0016a0003c0003t0047a0003c0003t0048others(7): Show | 14 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1664C>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 1664 | chr2 | 202985288 | |||||
chr2:202985744
|
G | C | 107 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(104): Show | 289 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(286): Show |
3_prime_UTR_variant | MODIFIER | c.*2120G>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 2120 | chr2 | 202985744 | |||||
chr2:202985785
|
G | A | 107 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(104): Show | 289 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(286): Show |
3_prime_UTR_variant | MODIFIER | c.*2161G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 2161 | chr2 | 202985785 | |||||
chr2:202986013
|
A | T | 2 | a0001c0001t0089a0001c0001t0090 | 2 | HG00642.hp2 HG01192.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2389A>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 2389 | chr2 | 202986013 | |||||
chr2:202986419
|
G | T | 1 | a0001c0001t0102 | 1 | NA18972.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2795G>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 2795 | chr2 | 202986419 | |||||
chr2:202986568
|
A | G | 10 | a0001c0001t0019a0001c0001t0020a0001c0001t0033others(7): Show | 15 | HG00738.hp1 HG01943.hp1 HG02129.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*2944A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 2944 | chr2 | 202986568 | |||||
chr2:202986615
|
CAGTT | C | 9 | a0003c0003t0016a0003c0003t0047a0003c0003t0048others(6): Show | 13 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*2995_*2998delTAGT | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 2995 | INFO_REALIGN_3_PRIME | chr2 | 202986615 | ||||
chr2:202986621
|
G | A | 1 | a0001c0001t0104 | 1 | NA18988.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2997G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 2997 | chr2 | 202986621 | |||||
chr2:202986867
|
C | CAT | 4 | a0001c0001t0004a0001c0011t0004a0003c0003t0048others(1): Show | 20 | HG00597.hp1 HG01167.hp1 HG01168.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*3243_*3244insAT | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3244 | chr2 | 202986867 | |||||
chr2:202986867
|
C | CATAT | 3 | a0001c0001t0011a0001c0001t0096a0001c0001t0111 | 8 | HG00323.hp2 HG00673.hp2 HG01081.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3243_*3244insATAT | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3244 | chr2 | 202986867 | |||||
chr2:202986867
|
C | CATATAT | 2 | a0001c0001t0044a0001c0001t0102 | 3 | HG02976.hp1 NA18959.hp1 NA18972.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3243_*3244insATAT others(2): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3244 | chr2 | 202986867 | |||||
chr2:202986867
|
CGT | C | 10 | a0001c0001t0007a0001c0001t0051a0001c0001t0094others(7): Show | 23 | HG01099.hp2 HG01496.hp2 HG01515.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*3244_*3245delGT | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3244 | chr2 | 202986867 | |||||
chr2:202986867
|
CGTAT | C | 6 | a0001c0001t0003a0001c0001t0043a0001c0001t0049others(3): Show | 24 | HG00438.hp2 HG00609.hp1 HG00741.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*3244_*3247delGTAT | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3244 | chr2 | 202986867 | |||||
chr2:202986867
|
CGTATAT | C | 4 | a0001c0001t0001a0001c0001t0042a0003c0003t0047others(1): Show | 29 | HG00423.hp1 HG00544.hp2 HG00621.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*3244_*3249delGTAT others(2): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3244 | chr2 | 202986867 | |||||
chr2:202986867
|
CGTATATA others(1): Show |
C | 1 | a0001c0001t0009 | 9 | HG00642.hp1 HG01952.hp2 HG01981.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3244_*3251delGTAT others(4): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3244 | chr2 | 202986867 | |||||
chr2:202986867
|
CGTATATA others(3): Show |
C | 2 | a0001c0001t0093a0001c0001t0109 | 2 | HG02080.hp1 NA19062.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3244_*3253delGTAT others(6): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3244 | chr2 | 202986867 | |||||
chr2:202986867
|
CGTATATA others(5): Show |
C | 1 | a0003c0003t0115 | 1 | HG00738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3244_*3255delGTAT others(8): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3244 | chr2 | 202986867 | |||||
chr2:202986867
|
CGTATATA others(11): Show |
C | 1 | a0001c0001t0029 | 3 | HG02896.hp1 HG02897.hp1 HG03834.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3244_*3261delGTAT others(14): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3244 | chr2 | 202986867 | |||||
chr2:202986867
|
CGTATATA others(17): Show |
C | 1 | a0001c0001t0041 | 2 | NA18962.hp1 NA18986.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3244_*3267delGTAT others(20): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3244 | chr2 | 202986867 | |||||
chr2:202986868
|
G | A | 14 | a0001c0001t0004a0001c0001t0006a0001c0001t0011others(11): Show | 51 | HG00323.hp2 HG00408.hp1 HG00597.hp1 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*3244G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3244 | chr2 | 202986868 | |||||
chr2:202986868
|
G | GTA | 11 | a0001c0001t0013a0001c0001t0019a0001c0001t0034others(8): Show | 21 | HG01109.hp2 HG01169.hp1 HG01257.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*3283_*3284dupTA | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3285 | INFO_REALIGN_3_PRIME | chr2 | 202986868 | ||||
chr2:202986868
|
G | GTATA | 3 | a0001c0001t0020a0002c0002t0023a0004c0004t0020 | 8 | HG00738.hp1 HG01168.hp2 HG02895.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3281_*3284dupTATA | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3285 | INFO_REALIGN_3_PRIME | chr2 | 202986868 | ||||
chr2:202986868
|
G | GTATATA | 3 | a0001c0001t0056a0002c0002t0059a0002c0002t0097 | 3 | HG02559.hp1 HG03195.hp2 NA18948.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3279_*3284dupTATA others(2): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3285 | INFO_REALIGN_3_PRIME | chr2 | 202986868 | ||||
chr2:202986868
|
G | GTATATAT others(3): Show |
1 | a0001c0001t0035 | 2 | NA18978.hp1 NA18982.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3252_*3253insCATA others(6): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3253 | INFO_REALIGN_3_PRIME | chr2 | 202986868 | ||||
chr2:202986868
|
G | GTATATAT others(5): Show |
2 | a0001c0001t0053a0002c0002t0098 | 2 | HG02148.hp1 HG03130.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3273_*3284dupTATA others(8): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3285 | INFO_REALIGN_3_PRIME | chr2 | 202986868 | ||||
chr2:202986868
|
G | GTATATAT others(9): Show |
1 | a0002c0002t0099 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3269_*3284dupTATA others(12): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3285 | INFO_REALIGN_3_PRIME | chr2 | 202986868 | ||||
chr2:202986868
|
G | GTATGTAT others(7): Show |
1 | a0001c0001t0100 | 1 | HG03139.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3247_*3248insGTAT others(10): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3248 | INFO_REALIGN_3_PRIME | chr2 | 202986868 | ||||
chr2:202986868
|
G | GTATGTAT others(11): Show |
1 | a0001c0001t0101 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3247_*3248insGTAT others(14): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3248 | INFO_REALIGN_3_PRIME | chr2 | 202986868 | ||||
chr2:202986868
|
GTA | G | 2 | a0001c0001t0032a0002c0002t0046 | 4 | HG00733.hp2 HG02257.hp1 NA19043.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3283_*3284delTA | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3283 | INFO_REALIGN_3_PRIME | chr2 | 202986868 | ||||
chr2:202986868
|
GTATA | G | 3 | a0001c0001t0018a0001c0008t0022a0002c0002t0022 | 8 | HG02486.hp2 HG02630.hp2 HG02886.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3281_*3284delTATA | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3281 | INFO_REALIGN_3_PRIME | chr2 | 202986868 | ||||
chr2:202986868
|
GTATATA | G | 2 | a0001c0001t0017a0005c0006t0017 | 4 | HG02622.hp1 HG02723.hp2 HG02970.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3279_*3284delTATA others(2): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3279 | INFO_REALIGN_3_PRIME | chr2 | 202986868 | ||||
chr2:202986868
|
GTATATAT others(3): Show |
G | 1 | a0003c0013t0119 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3275_*3284delTATA others(6): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3275 | INFO_REALIGN_3_PRIME | chr2 | 202986868 | ||||
chr2:202986868
|
GTATATAT others(19): Show |
G | 1 | a0001c0001t0031 | 2 | HG03130.hp2 HG03195.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3259_*3284delTATA others(22): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3259 | INFO_REALIGN_3_PRIME | chr2 | 202986868 | ||||
chr2:202986871
|
T | TATATATA others(9): Show |
1 | a0001c0005t0091 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3262_*3263insCATA others(12): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3263 | INFO_REALIGN_3_PRIME | chr2 | 202986871 | ||||
chr2:202986877
|
T | TATATATA others(3): Show |
2 | a0001c0005t0040a0001c0005t0060 | 3 | HG02145.hp1 HG02451.hp1 HG02717.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3262_*3263insCATA others(6): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3263 | INFO_REALIGN_3_PRIME | chr2 | 202986877 | ||||
chr2:202986881
|
T | TATATATA others(49): Show |
1 | a0001c0001t0036 | 2 | HG06807.hp1 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3266_*3267insCATA others(52): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3267 | INFO_REALIGN_3_PRIME | chr2 | 202986881 | ||||
chr2:202986881
|
T | TATATATA others(51): Show |
1 | a0001c0001t0027 | 3 | HG02630.hp1 HG02818.hp2 HG03041.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3266_*3267insCATA others(54): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3267 | INFO_REALIGN_3_PRIME | chr2 | 202986881 | ||||
chr2:202986881
|
T | TATATATA others(53): Show |
1 | a0001c0001t0084 | 1 | HG02280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3268_*3269insCATA others(56): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3269 | INFO_REALIGN_3_PRIME | chr2 | 202986881 | ||||
chr2:202986883
|
T | TATACATA others(19): Show |
1 | a0001c0001t0045 | 2 | HG03225.hp2 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3262_*3263insCATA others(22): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3263 | INFO_REALIGN_3_PRIME | chr2 | 202986883 | ||||
chr2:202986883
|
T | TATACGTA others(45): Show |
1 | a0006c0010t0107 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3262_*3263insCGTA others(48): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3263 | INFO_REALIGN_3_PRIME | chr2 | 202986883 | ||||
chr2:202986883
|
T | TATATATA others(47): Show |
1 | a0001c0001t0070 | 1 | HG01358.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3266_*3267insCATA others(50): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3267 | INFO_REALIGN_3_PRIME | chr2 | 202986883 | ||||
chr2:202986883
|
T | TATATATA others(49): Show |
1 | a0001c0001t0081 | 1 | NA18965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3268_*3269insCATA others(52): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3269 | INFO_REALIGN_3_PRIME | chr2 | 202986883 | ||||
chr2:202986883
|
T | TATATATA others(51): Show |
1 | a0001c0001t0083 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3268_*3269insCATA others(54): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3269 | INFO_REALIGN_3_PRIME | chr2 | 202986883 | ||||
chr2:202986884
|
A | ATATATAT others(51): Show |
1 | a0001c0001t0090 | 1 | HG01192.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3270_*3271insCATA others(54): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3271 | INFO_REALIGN_3_PRIME | chr2 | 202986884 | ||||
chr2:202986885
|
T | C | 1 | a0001c0001t0035 | 2 | NA18978.hp1 NA18982.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3261T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3261 | chr2 | 202986885 | |||||
chr2:202986885
|
T | TATATACA others(41): Show |
1 | a0001c0001t0064 | 1 | NA19088.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3266_*3267insCATA others(44): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3267 | INFO_REALIGN_3_PRIME | chr2 | 202986885 | ||||
chr2:202986885
|
T | TATATACA others(47): Show |
1 | a0001c0001t0066 | 1 | HG02071.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3266_*3267insCATA others(50): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3267 | INFO_REALIGN_3_PRIME | chr2 | 202986885 | ||||
chr2:202986885
|
T | TATATACA others(45): Show |
1 | a0001c0001t0025 | 3 | HG02486.hp1 HG03831.hp2 NA18995.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3266_*3267insCATA others(48): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3267 | INFO_REALIGN_3_PRIME | chr2 | 202986885 | ||||
chr2:202986885
|
T | TATATACA others(45): Show |
2 | a0001c0001t0014a0001c0001t0072 | 6 | HG00597.hp2 HG02602.hp1 HG03704.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3266_*3267insCATA others(48): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3267 | INFO_REALIGN_3_PRIME | chr2 | 202986885 | ||||
chr2:202986885
|
T | TATATACA others(47): Show |
1 | a0001c0001t0005 | 14 | HG00323.hp1 HG01106.hp2 HG01109.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*3266_*3267insCATA others(50): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3267 | INFO_REALIGN_3_PRIME | chr2 | 202986885 | ||||
chr2:202986885
|
T | TATATACA others(47): Show |
1 | a0001c0001t0076 | 1 | HG01346.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3266_*3267insCATA others(50): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3267 | INFO_REALIGN_3_PRIME | chr2 | 202986885 | ||||
chr2:202986885
|
T | TATATATA others(79): Show |
1 | a0001c0001t0078 | 1 | NA19001.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3268_*3269insCATA others(82): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3269 | INFO_REALIGN_3_PRIME | chr2 | 202986885 | ||||
chr2:202986885
|
T | TATATATA others(47): Show |
1 | a0001c0001t0080 | 1 | NA18977.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3268_*3269insCATA others(50): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3269 | INFO_REALIGN_3_PRIME | chr2 | 202986885 | ||||
chr2:202986885
|
T | TATATATA others(49): Show |
1 | a0001c0001t0082 | 1 | NA19066.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3268_*3269insCATA others(52): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3269 | INFO_REALIGN_3_PRIME | chr2 | 202986885 | ||||
chr2:202986885
|
T | TATATATA others(41): Show |
1 | a0001c0001t0088 | 1 | HG04228.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3274_*3275insCATA others(44): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3275 | INFO_REALIGN_3_PRIME | chr2 | 202986885 | ||||
chr2:202986885
|
T | TGTATATA others(51): Show |
1 | a0001c0001t0039 | 2 | HG01515.hp2 HG01517.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3261_*3262insGTAT others(54): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3262 | chr2 | 202986885 | |||||
chr2:202986886
|
A | ATATATAT others(77): Show |
1 | a0001c0001t0085 | 1 | HG01081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3270_*3271insCATA others(80): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3271 | INFO_REALIGN_3_PRIME | chr2 | 202986886 | ||||
chr2:202986886
|
A | ATATATAT others(49): Show |
2 | a0001c0001t0021a0001c0001t0089 | 5 | HG00642.hp2 HG01256.hp1 HG01258.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3270_*3271insCATA others(52): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3271 | INFO_REALIGN_3_PRIME | chr2 | 202986886 | ||||
chr2:202986886
|
A | ATATATAT others(51): Show |
1 | a0001c0001t0008 | 9 | HG00735.hp2 HG00741.hp1 HG01106.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3270_*3271insCATA others(54): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3271 | INFO_REALIGN_3_PRIME | chr2 | 202986886 | ||||
chr2:202986886
|
A | ATATATAT others(49): Show |
1 | a0001c0001t0038 | 2 | HG01496.hp1 NA20752.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3270_*3271insCGTA others(52): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3271 | INFO_REALIGN_3_PRIME | chr2 | 202986886 | ||||
chr2:202986886
|
A | ATATATAT others(51): Show |
2 | a0001c0001t0086a0001c0001t0114 | 2 | HG00733.hp1 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3272_*3273insCATA others(54): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3273 | INFO_REALIGN_3_PRIME | chr2 | 202986886 | ||||
chr2:202986886
|
A | ATATATAT others(53): Show |
1 | a0001c0001t0087 | 1 | HG00544.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3272_*3273insCATA others(56): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3273 | INFO_REALIGN_3_PRIME | chr2 | 202986886 | ||||
chr2:202986886
|
A | G | 1 | a0001c0001t0039 | 2 | HG01515.hp2 HG01517.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3262A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3262 | chr2 | 202986886 | |||||
chr2:202986887
|
T | TACATATA others(43): Show |
1 | a0001c0001t0062 | 1 | NA19086.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3264_*3265insCATA others(46): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3265 | INFO_REALIGN_3_PRIME | chr2 | 202986887 | ||||
chr2:202986887
|
T | TATACATA others(57): Show |
1 | a0001c0001t0024 | 3 | NA18940.hp1 NA18991.hp2 NA19062.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3266_*3267insCATA others(60): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3267 | INFO_REALIGN_3_PRIME | chr2 | 202986887 | ||||
chr2:202986887
|
T | TATACATA others(69): Show |
1 | a0001c0001t0063 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3266_*3267insCATA others(72): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3267 | INFO_REALIGN_3_PRIME | chr2 | 202986887 | ||||
chr2:202986887
|
T | TATACATA others(45): Show |
1 | a0001c0001t0065 | 1 | HG00408.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3266_*3267insCATA others(48): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3267 | INFO_REALIGN_3_PRIME | chr2 | 202986887 | ||||
chr2:202986887
|
T | TATACATA others(71): Show |
1 | a0001c0001t0067 | 1 | NA18747.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3266_*3267insCATA others(74): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3267 | INFO_REALIGN_3_PRIME | chr2 | 202986887 | ||||
chr2:202986887
|
T | TATACATA others(73): Show |
1 | a0001c0001t0068 | 1 | NA19070.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3266_*3267insCATA others(76): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3267 | INFO_REALIGN_3_PRIME | chr2 | 202986887 | ||||
chr2:202986887
|
T | TATACATA others(43): Show |
1 | a0001c0001t0069 | 1 | NA19010.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3266_*3267insCATA others(46): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3267 | INFO_REALIGN_3_PRIME | chr2 | 202986887 | ||||
chr2:202986887
|
T | TATACATA others(73): Show |
1 | a0001c0001t0037 | 2 | HG02273.hp2 HG02300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3266_*3267insCATA others(76): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3267 | INFO_REALIGN_3_PRIME | chr2 | 202986887 | ||||
chr2:202986887
|
T | TATACATA others(43): Show |
1 | a0001c0001t0026 | 3 | HG00423.hp2 HG03490.hp1 NA18981.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3266_*3267insCATA others(46): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3267 | INFO_REALIGN_3_PRIME | chr2 | 202986887 | ||||
chr2:202986887
|
T | TATACATA others(45): Show |
3 | a0001c0001t0002a0001c0001t0061a0001c0005t0092 | 24 | HG00609.hp2 HG01099.hp1 HG01255.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*3266_*3267insCATA others(48): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3267 | INFO_REALIGN_3_PRIME | chr2 | 202986887 | ||||
chr2:202986887
|
T | TATACATA others(63): Show |
1 | a0001c0001t0073 | 1 | NA19009.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3266_*3267insCATA others(66): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3267 | INFO_REALIGN_3_PRIME | chr2 | 202986887 | ||||
chr2:202986887
|
T | TATACATA others(47): Show |
1 | a0001c0001t0075 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3266_*3267insCATA others(50): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3267 | INFO_REALIGN_3_PRIME | chr2 | 202986887 | ||||
chr2:202986887
|
T | TATACATA others(47): Show |
1 | a0001c0001t0077 | 1 | HG02080.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3266_*3267insCATA others(50): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3267 | INFO_REALIGN_3_PRIME | chr2 | 202986887 | ||||
chr2:202986887
|
T | TATATACA others(45): Show |
1 | a0001c0001t0079 | 1 | HG00673.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3268_*3269insCATA others(48): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3269 | INFO_REALIGN_3_PRIME | chr2 | 202986887 | ||||
chr2:202986887
|
T | TATATACA others(47): Show |
1 | a0001c0001t0028 | 3 | HG02071.hp2 HG02083.hp2 NA18951.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3268_*3269insCATA others(50): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3269 | INFO_REALIGN_3_PRIME | chr2 | 202986887 | ||||
chr2:202986889
|
T | TACATATA others(71): Show |
1 | a0001c0001t0071 | 1 | HG01361.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3266_*3267insCATA others(74): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3267 | INFO_REALIGN_3_PRIME | chr2 | 202986889 | ||||
chr2:202986889
|
T | TACATATA others(43): Show |
1 | a0001c0001t0074 | 1 | HG00438.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3266_*3267insCATA others(46): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3267 | INFO_REALIGN_3_PRIME | chr2 | 202986889 | ||||
chr2:202986964
|
C | CT | 9 | a0003c0003t0016a0003c0003t0047a0003c0003t0048others(6): Show | 13 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*3349dupT | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 3350 | INFO_REALIGN_3_PRIME | chr2 | 202986964 | ||||
chr2:202987706
|
G | A | 1 | a0001c0001t0113 | 1 | NA19078.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4082G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 4082 | chr2 | 202987706 | |||||
chr2:202987864
|
A | C | 109 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(106): Show | 291 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(288): Show |
3_prime_UTR_variant | MODIFIER | c.*4240A>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 4240 | chr2 | 202987864 | |||||
chr2:202987905
|
G | C | 108 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(105): Show | 292 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(289): Show |
3_prime_UTR_variant | MODIFIER | c.*4281G>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 4281 | chr2 | 202987905 | |||||
chr2:202988007
|
A | C | 3 | a0001c0001t0043a0001c0001t0094a0001c0001t0102 | 4 | NA18972.hp1 NA18999.hp2 NA19057.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4383A>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 4383 | chr2 | 202988007 | |||||
chr2:202988089
|
C | T | 1 | a0001c0001t0042 | 2 | HG02258.hp2 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4465C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 17/17 | 4465 | chr2 | 202988089 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:202913175
|
C | T | 1 | a0001c0005t0040g0325 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-330+73C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 1/16 | chr2 | 202913175 | ||||||
chr2:202913180
|
G | A | 13 | a0003c0003t0016g0002a0003c0003t0016g0013a0003c0003t0016g0014others(10): Show | 14 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.-330+78G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 1/16 | chr2 | 202913180 | ||||||
chr2:202913264
|
A | G | 23 | a0002c0002t0012g0307a0002c0002t0012g0312a0002c0002t0012g0314others(20): Show | 23 | HG00733.hp2 HG01109.hp2 HG01168.hp2 others(20): Show |
intron_variant | MODIFIER | c.-330+162A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 1/16 | chr2 | 202913264 | ||||||
chr2:202913477
|
A | T | 12 | a0003c0003t0016g0002a0003c0003t0016g0013a0003c0003t0016g0014others(9): Show | 13 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.-330+375A>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 1/16 | chr2 | 202913477 | ||||||
chr2:202913522
|
T | C | 4 | a0001c0001t0021g0003a0001c0001t0021g0021a0001c0001t0021g0022others(1): Show | 5 | HG01081.hp1 HG01256.hp1 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.-330+420T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 1/16 | chr2 | 202913522 | ||||||
chr2:202913772
|
C | T | 2 | a0001c0001t0029g0300a0001c0001t0029g0301 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-330+670C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 1/16 | chr2 | 202913772 | ||||||
chr2:202913882
|
A | G | 2 | a0001c0001t0042g0298a0001c0001t0042g0299 | 2 | HG02258.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-330+780A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 1/16 | chr2 | 202913882 | ||||||
chr2:202913956
|
A | T | 2 | a0001c0001t0029g0300a0001c0001t0029g0301 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-330+854A>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 1/16 | chr2 | 202913956 | ||||||
chr2:202913957
|
CT | C | 3 | a0001c0001t0043g0023a0001c0001t0043g0025a0001c0001t0094g0024 | 3 | NA18999.hp2 NA19057.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.-330+859delT | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 202913957 | |||||
chr2:202914099
|
G | A | 1 | a0006c0010t0107g0026 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-330+997G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 1/16 | chr2 | 202914099 | ||||||
chr2:202914283
|
A | G | 2 | a0001c0001t0008g0296a0001c0001t0008g0297 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.-330+1181A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 1/16 | chr2 | 202914283 | ||||||
chr2:202914553
|
T | C | 13 | a0003c0003t0016g0002a0003c0003t0016g0013a0003c0003t0016g0014others(10): Show | 14 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.-330+1451T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 1/16 | chr2 | 202914553 | ||||||
chr2:202914736
|
G | A | 4 | a0001c0001t0001g0030a0001c0001t0004g0029a0001c0001t0007g0028others(1): Show | 4 | NA18945.hp1 NA18954.hp1 NA19074.hp2 others(1): Show |
intron_variant | MODIFIER | c.-330+1634G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 1/16 | chr2 | 202914736 | ||||||
chr2:202914779
|
C | CA | 44 | a0001c0001t0002g0036a0001c0001t0007g0031a0001c0001t0008g0035others(41): Show | 45 | HG00408.hp2 HG00438.hp2 HG00733.hp2 others(42): Show |
intron_variant | MODIFIER | c.-330+1689dupA | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 202914779 | |||||
chr2:202914788
|
A | C | 1 | a0001c0001t0019g0295 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-330+1686A>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 1/16 | chr2 | 202914788 | ||||||
chr2:202914791
|
AC | A | 119 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0030others(116): Show | 121 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(118): Show |
intron_variant | MODIFIER | c.-330+1690delC | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 1/16 | chr2 | 202914791 | ||||||
chr2:202914792
|
C | A | 203 | a0001c0001t0001g0054a0001c0001t0001g0094a0001c0001t0001g0095others(200): Show | 206 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(203): Show |
intron_variant | MODIFIER | c.-330+1690C>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 1/16 | chr2 | 202914792 | ||||||
chr2:202914796
|
C | A | 282 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0030others(279): Show | 287 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(284): Show |
intron_variant | MODIFIER | c.-330+1694C>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 1/16 | chr2 | 202914796 | ||||||
chr2:202914826
|
T | C | 1 | a0001c0001t0103g0292 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-330+1724T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 1/16 | chr2 | 202914826 | ||||||
chr2:202914952
|
T | A | 1 | a0001c0005t0091g0043 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-330+1850T>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 1/16 | chr2 | 202914952 | ||||||
chr2:202914957
|
T | A | 1 | a0001c0001t0007g0031 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-330+1855T>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 1/16 | chr2 | 202914957 | ||||||
chr2:202915103
|
G | A | 1 | a0005c0006t0017g0245 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-330+2001G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 1/16 | chr2 | 202915103 | ||||||
chr2:202915120
|
G | A | 2 | a0001c0001t0065g0032a0001c0001t0066g0044 | 2 | HG00408.hp2 HG02071.hp1 |
intron_variant | MODIFIER | c.-330+2018G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 1/16 | chr2 | 202915120 | ||||||
chr2:202915236
|
C | T | 1 | a0002c0002t0105g0321 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-330+2134C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 1/16 | chr2 | 202915236 | ||||||
chr2:202915241
|
C | G | 1 | a0001c0001t0103g0292 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-330+2139C>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 1/16 | chr2 | 202915241 | ||||||
chr2:202915381
|
T | G | 7 | a0001c0001t0025g0047a0001c0001t0027g0045a0001c0001t0027g0048others(4): Show | 7 | HG02280.hp2 HG02486.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.-330+2279T>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 1/16 | chr2 | 202915381 | ||||||
chr2:202915390
|
G | C | 1 | a0001c0001t0093g0148 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-330+2288G>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 1/16 | chr2 | 202915390 | ||||||
chr2:202915496
|
A | G | 5 | a0001c0005t0040g0147a0001c0005t0040g0325a0001c0005t0060g0145others(2): Show | 5 | HG02145.hp1 HG02451.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.-329-2381A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 1/16 | chr2 | 202915496 | ||||||
chr2:202915756
|
T | C | 13 | a0003c0003t0016g0002a0003c0003t0016g0013a0003c0003t0016g0014others(10): Show | 14 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.-329-2121T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 1/16 | chr2 | 202915756 | ||||||
chr2:202915792
|
A | G | 13 | a0003c0003t0016g0002a0003c0003t0016g0013a0003c0003t0016g0014others(10): Show | 14 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.-329-2085A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 1/16 | chr2 | 202915792 | ||||||
chr2:202915873
|
G | A | 1 | a0001c0001t0007g0288 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-329-2004G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 1/16 | chr2 | 202915873 | ||||||
chr2:202916095
|
G | T | 1 | a0001c0001t0007g0031 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-329-1782G>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 1/16 | chr2 | 202916095 | ||||||
chr2:202916112
|
C | A | 1 | a0001c0001t0103g0292 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-329-1765C>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 1/16 | chr2 | 202916112 | ||||||
chr2:202916162
|
T | TTTTA | 4 | a0001c0001t0051g0246a0002c0002t0012g0319a0002c0002t0059g0324others(1): Show | 4 | HG02559.hp1 HG03098.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-329-1683_-329-168 others(8): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 202916162 | |||||
chr2:202916162
|
T | TTTTATTT others(1): Show |
13 | a0002c0002t0012g0312a0002c0002t0012g0314a0002c0002t0012g0317others(10): Show | 13 | HG01109.hp2 HG01884.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.-329-1687_-329-168 others(12): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 202916162 | |||||
chr2:202916162
|
T | TTTTATTT others(5): Show |
7 | a0002c0002t0012g0307a0002c0002t0022g0304a0002c0002t0022g0308others(4): Show | 7 | HG00733.hp2 HG01168.hp2 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.-329-1691_-329-168 others(16): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 202916162 | |||||
chr2:202916162
|
TTTTA | T | 244 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0030others(241): Show | 248 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(245): Show |
intron_variant | MODIFIER | c.-329-1683_-329-168 others(8): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 202916162 | |||||
chr2:202916162
|
TTTTATTT others(1): Show |
T | 3 | a0001c0001t0005g0143a0001c0001t0005g0144a0001c0001t0006g0244 | 3 | HG01167.hp2 HG01169.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.-329-1687_-329-168 others(12): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 202916162 | |||||
chr2:202916288
|
C | T | 7 | a0001c0001t0025g0047a0001c0001t0027g0045a0001c0001t0027g0048others(4): Show | 7 | HG02280.hp2 HG02486.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.-329-1589C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 1/16 | chr2 | 202916288 | ||||||
chr2:202916348
|
C | T | 279 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0030others(276): Show | 284 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(281): Show |
intron_variant | MODIFIER | c.-329-1529C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 1/16 | chr2 | 202916348 | ||||||
chr2:202916397
|
G | T | 2 | a0001c0008t0015g0243a0001c0008t0022g0242 | 2 | HG02486.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-329-1480G>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 1/16 | chr2 | 202916397 | ||||||
chr2:202916449
|
G | A | 1 | a0001c0001t0080g0052 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.-329-1428G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 1/16 | chr2 | 202916449 | ||||||
chr2:202916482
|
G | A | 1 | a0001c0001t0051g0246 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-329-1395G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 1/16 | chr2 | 202916482 | ||||||
chr2:202916517
|
C | T | 1 | a0001c0001t0005g0142 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-329-1360C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 1/16 | chr2 | 202916517 | ||||||
chr2:202916549
|
C | T | 2 | a0001c0001t0020g0285a0001c0001t0033g0286 | 2 | HG00738.hp1 HG01943.hp1 |
intron_variant | MODIFIER | c.-329-1328C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 1/16 | chr2 | 202916549 | ||||||
chr2:202916699
|
A | T | 2 | a0001c0008t0015g0243a0001c0008t0022g0242 | 2 | HG02486.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-329-1178A>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 1/16 | chr2 | 202916699 | ||||||
chr2:202916806
|
GGCCCAAG others(16): Show |
G | 9 | a0001c0001t0001g0154a0001c0001t0003g0155a0001c0001t0004g0053others(6): Show | 9 | HG01257.hp2 HG01258.hp1 HG02040.hp2 others(6): Show |
intron_variant | MODIFIER | c.-329-1069_-329-104 others(27): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 202916806 | |||||
chr2:202916833
|
A | C | 9 | a0001c0001t0001g0154a0001c0001t0003g0155a0001c0001t0004g0053others(6): Show | 9 | HG01257.hp2 HG01258.hp1 HG02040.hp2 others(6): Show |
intron_variant | MODIFIER | c.-329-1044A>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 1/16 | chr2 | 202916833 | ||||||
chr2:202917017
|
C | T | 1 | a0003c0013t0119g0010 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-329-860C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 1/16 | chr2 | 202917017 | ||||||
chr2:202917018
|
G | A | 12 | a0003c0003t0016g0002a0003c0003t0016g0013a0003c0003t0016g0014others(9): Show | 13 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.-329-859G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 1/16 | chr2 | 202917018 | ||||||
chr2:202917026
|
C | T | 1 | a0001c0001t0034g0284 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.-329-851C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 1/16 | chr2 | 202917026 | ||||||
chr2:202917103
|
T | C | 1 | a0001c0001t0007g0031 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-329-774T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 1/16 | chr2 | 202917103 | ||||||
chr2:202917210
|
C | CA | 176 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0030others(173): Show | 180 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(177): Show |
intron_variant | MODIFIER | c.-329-641dupA | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 202917210 | |||||
chr2:202917210
|
C | CAA | 82 | a0001c0001t0001g0154a0001c0001t0001g0164a0001c0001t0001g0170others(79): Show | 82 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.-329-642_-329-641d others(4): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 202917210 | |||||
chr2:202917210
|
C | CAAA | 15 | a0001c0001t0001g0054a0001c0001t0001g0161a0001c0001t0003g0160others(12): Show | 15 | HG00438.hp1 HG00621.hp2 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.-329-643_-329-641d others(5): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 202917210 | |||||
chr2:202917210
|
C | CAAAAAAA others(3): Show |
1 | a0003c0003t0047g0001 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.-329-650_-329-641d others(12): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 202917210 | |||||
chr2:202917237
|
G | T | 1 | a0001c0001t0007g0031 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-329-640G>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 1/16 | chr2 | 202917237 | ||||||
chr2:202917238
|
C | T | 1 | a0001c0001t0007g0031 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-329-639C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 1/16 | chr2 | 202917238 | ||||||
chr2:202917247
|
G | T | 2 | a0001c0008t0015g0243a0001c0008t0022g0242 | 2 | HG02486.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-329-630G>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 1/16 | chr2 | 202917247 | ||||||
chr2:202917652
|
T | A | 1 | a0001c0001t0003g0183 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-329-225T>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 1/16 | chr2 | 202917652 | ||||||
chr2:202917657
|
A | G | 1 | a0001c0001t0003g0183 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-329-220A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 1/16 | chr2 | 202917657 | ||||||
chr2:202918286
|
C | T | 315 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0030others(312): Show | 319 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(316): Show |
intron_variant | MODIFIER | c.-163+243C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 2/16 | chr2 | 202918286 | ||||||
chr2:202918336
|
C | T | 1 | a0001c0001t0025g0091 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.-163+293C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 2/16 | chr2 | 202918336 | ||||||
chr2:202918337
|
G | C | 1 | a0001c0001t0028g0092 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.-163+294G>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 2/16 | chr2 | 202918337 | ||||||
chr2:202918347
|
C | T | 3 | a0001c0001t0015g0009a0001c0001t0100g0009a0001c0001t0101g0240 | 3 | HG02976.hp2 HG03139.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-163+304C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 2/16 | chr2 | 202918347 | ||||||
chr2:202918373
|
T | C | 1 | a0001c0001t0008g0035 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-163+330T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 2/16 | chr2 | 202918373 | ||||||
chr2:202918486
|
T | C | 282 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0030others(279): Show | 287 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(284): Show |
intron_variant | MODIFIER | c.-163+443T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 2/16 | chr2 | 202918486 | ||||||
chr2:202918525
|
C | T | 1 | a0003c0013t0119g0010 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-163+482C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 2/16 | chr2 | 202918525 | ||||||
chr2:202918545
|
C | CA | 8 | a0001c0001t0001g0187a0001c0001t0003g0189a0001c0001t0005g0058others(5): Show | 8 | HG03516.hp1 HG04115.hp2 NA18962.hp1 others(5): Show |
intron_variant | MODIFIER | c.-163+510dupA | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 202918545 | |||||
chr2:202918591
|
T | G | 1 | a0001c0001t0003g0160 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-163+548T>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 2/16 | chr2 | 202918591 | ||||||
chr2:202918622
|
A | G | 2 | a0001c0001t0004g0238a0001c0001t0006g0239 | 2 | NA18969.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.-163+579A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 2/16 | chr2 | 202918622 | ||||||
chr2:202918761
|
G | A | 13 | a0003c0003t0016g0002a0003c0003t0016g0013a0003c0003t0016g0014others(10): Show | 14 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.-163+718G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 2/16 | chr2 | 202918761 | ||||||
chr2:202918843
|
G | C | 3 | a0001c0001t0033g0051a0001c0001t0034g0284a0001c0001t0056g0260 | 3 | NA18948.hp2 NA18988.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.-163+800G>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 2/16 | chr2 | 202918843 | ||||||
chr2:202919404
|
G | C | 2 | a0001c0001t0015g0009a0001c0001t0100g0009 | 2 | HG03139.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-163+1361G>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 2/16 | chr2 | 202919404 | ||||||
chr2:202919479
|
A | G | 107 | a0001c0001t0001g0120a0001c0001t0002g0005a0001c0001t0002g0036others(104): Show | 110 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.-163+1436A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 2/16 | chr2 | 202919479 | ||||||
chr2:202919577
|
T | G | 1 | a0001c0001t0009g0191 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-163+1534T>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 2/16 | chr2 | 202919577 | ||||||
chr2:202919638
|
G | T | 1 | a0001c0001t0007g0237 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-163+1595G>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 2/16 | chr2 | 202919638 | ||||||
chr2:202919676
|
C | A | 1 | a0003c0013t0119g0010 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-163+1633C>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 2/16 | chr2 | 202919676 | ||||||
chr2:202919721
|
G | A | 2 | a0001c0001t0029g0300a0001c0001t0029g0301 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-163+1678G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 2/16 | chr2 | 202919721 | ||||||
chr2:202919855
|
T | G | 6 | a0001c0001t0030g0192a0001c0001t0030g0194a0001c0001t0030g0195others(3): Show | 6 | NA18951.hp1 NA18968.hp1 NA18993.hp2 others(3): Show |
intron_variant | MODIFIER | c.-163+1812T>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 2/16 | chr2 | 202919855 | ||||||
chr2:202919870
|
A | G | 1 | a0003c0013t0119g0010 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-163+1827A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 2/16 | chr2 | 202919870 | ||||||
chr2:202919910
|
AAAAGGGT others(1): Show |
A | 36 | a0001c0001t0002g0005a0001c0001t0002g0082a0001c0001t0002g0085others(33): Show | 37 | HG00423.hp2 HG00438.hp1 HG00609.hp2 others(34): Show |
intron_variant | MODIFIER | c.-163+1871_-163+187 others(12): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 202919910 | |||||
chr2:202920149
|
T | C | 2 | a0001c0001t0001g0161a0001c0001t0001g0164 | 2 | HG02809.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-163+2106T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 2/16 | chr2 | 202920149 | ||||||
chr2:202920177
|
C | T | 7 | a0001c0001t0002g0090a0001c0001t0002g0138a0001c0001t0002g0139others(4): Show | 7 | HG00438.hp1 HG00609.hp2 HG02071.hp2 others(4): Show |
intron_variant | MODIFIER | c.-163+2134C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 2/16 | chr2 | 202920177 | ||||||
chr2:202920311
|
C | G | 1 | a0001c0001t0002g0136 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.-163+2268C>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 2/16 | chr2 | 202920311 | ||||||
chr2:202920353
|
C | T | 3 | a0001c0001t0015g0009a0001c0001t0100g0009a0001c0001t0101g0240 | 3 | HG02976.hp2 HG03139.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-163+2310C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 2/16 | chr2 | 202920353 | ||||||
chr2:202920851
|
G | A | 1 | a0002c0002t0012g0319 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-163+2808G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 2/16 | chr2 | 202920851 | ||||||
chr2:202920852
|
C | A | 1 | a0002c0002t0012g0319 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-163+2809C>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 2/16 | chr2 | 202920852 | ||||||
chr2:202921071
|
G | A | 1 | a0001c0001t0006g0196 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-163+3028G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 2/16 | chr2 | 202921071 | ||||||
chr2:202921168
|
A | T | 1 | a0001c0001t0037g0135 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-163+3125A>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 2/16 | chr2 | 202921168 | ||||||
chr2:202921244
|
G | T | 2 | a0001c0001t0045g0063a0001c0001t0045g0098 | 2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-162-3053G>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 2/16 | chr2 | 202921244 | ||||||
chr2:202921551
|
A | G | 102 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0030others(99): Show | 103 | HG00323.hp2 HG00423.hp1 HG00597.hp1 others(100): Show |
intron_variant | MODIFIER | c.-162-2746A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 2/16 | chr2 | 202921551 | ||||||
chr2:202921710
|
G | A | 1 | a0001c0001t0011g0203 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.-162-2587G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 2/16 | chr2 | 202921710 | ||||||
chr2:202921879
|
G | T | 1 | a0001c0001t0018g0283 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-162-2418G>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 2/16 | chr2 | 202921879 | ||||||
chr2:202922076
|
A | G | 1 | a0001c0001t0007g0031 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-162-2221A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 2/16 | chr2 | 202922076 | ||||||
chr2:202922088
|
C | A | 23 | a0002c0002t0012g0307a0002c0002t0012g0312a0002c0002t0012g0314others(20): Show | 23 | HG00733.hp2 HG01109.hp2 HG01168.hp2 others(20): Show |
intron_variant | MODIFIER | c.-162-2209C>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 2/16 | chr2 | 202922088 | ||||||
chr2:202922089
|
A | G | 13 | a0003c0003t0016g0002a0003c0003t0016g0013a0003c0003t0016g0014others(10): Show | 14 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.-162-2208A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 2/16 | chr2 | 202922089 | ||||||
chr2:202922397
|
A | G | 13 | a0003c0003t0016g0002a0003c0003t0016g0013a0003c0003t0016g0014others(10): Show | 14 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.-162-1900A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 2/16 | chr2 | 202922397 | ||||||
chr2:202922538
|
C | A | 1 | a0001c0001t0074g0057 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-162-1759C>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 2/16 | chr2 | 202922538 | ||||||
chr2:202922682
|
A | G | 12 | a0003c0003t0016g0002a0003c0003t0016g0013a0003c0003t0016g0014others(9): Show | 13 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.-162-1615A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 2/16 | chr2 | 202922682 | ||||||
chr2:202922802
|
C | T | 3 | a0001c0001t0049g0282a0001c0001t0050g0281a0001c0001t0051g0246 | 3 | HG02109.hp2 HG02809.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-162-1495C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 2/16 | chr2 | 202922802 | ||||||
chr2:202923048
|
C | T | 1 | a0003c0013t0119g0010 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-162-1249C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 2/16 | chr2 | 202923048 | ||||||
chr2:202923082
|
A | C | 1 | a0001c0001t0109g0093 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-162-1215A>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 2/16 | chr2 | 202923082 | ||||||
chr2:202923190
|
G | A | 2 | a0001c0001t0089g0099a0001c0001t0090g0064 | 2 | HG00642.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.-162-1107G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 2/16 | chr2 | 202923190 | ||||||
chr2:202923197
|
C | T | 1 | a0002c0002t0097g0320 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-162-1100C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 2/16 | chr2 | 202923197 | ||||||
chr2:202923244
|
A | G | 1 | a0001c0001t0009g0182 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-162-1053A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 2/16 | chr2 | 202923244 | ||||||
chr2:202923685
|
G | A | 1 | a0001c0001t0002g0140 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-162-612G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 2/16 | chr2 | 202923685 | ||||||
chr2:202923726
|
A | G | 1 | a0001c0001t0103g0292 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-162-571A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 2/16 | chr2 | 202923726 | ||||||
chr2:202923918
|
G | A | 1 | a0001c0001t0004g0204 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.-162-379G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 2/16 | chr2 | 202923918 | ||||||
chr2:202924205
|
T | G | 4 | a0001c0001t0010g0250a0001c0001t0017g0261a0001c0001t0017g0262others(1): Show | 4 | HG02615.hp2 HG02970.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.-162-92T>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 2/16 | chr2 | 202924205 | ||||||
chr2:202924227
|
T | C | 13 | a0003c0003t0016g0002a0003c0003t0016g0013a0003c0003t0016g0014others(10): Show | 14 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.-162-70T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 2/16 | chr2 | 202924227 | ||||||
chr2:202924956
|
C | T | 13 | a0003c0003t0016g0002a0003c0003t0016g0013a0003c0003t0016g0014others(10): Show | 14 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.-44+541C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202924956 | ||||||
chr2:202924969
|
C | G | 2 | a0001c0001t0049g0282a0001c0001t0050g0281 | 2 | HG02109.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.-44+554C>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202924969 | ||||||
chr2:202925003
|
A | G | 1 | a0001c0001t0013g0280 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-44+588A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202925003 | ||||||
chr2:202925080
|
A | G | 1 | a0001c0001t0072g0119 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-44+665A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202925080 | ||||||
chr2:202925379
|
T | C | 1 | a0001c0001t0051g0246 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-44+964T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202925379 | ||||||
chr2:202925558
|
A | G | 1 | a0005c0006t0017g0245 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-44+1143A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202925558 | ||||||
chr2:202925588
|
C | T | 1 | a0002c0002t0022g0308 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-44+1173C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202925588 | ||||||
chr2:202925975
|
C | A | 23 | a0002c0002t0012g0307a0002c0002t0012g0312a0002c0002t0012g0314others(20): Show | 23 | HG00733.hp2 HG01109.hp2 HG01168.hp2 others(20): Show |
intron_variant | MODIFIER | c.-44+1560C>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202925975 | ||||||
chr2:202926166
|
T | C | 13 | a0003c0003t0016g0002a0003c0003t0016g0013a0003c0003t0016g0014others(10): Show | 14 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.-44+1751T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202926166 | ||||||
chr2:202926240
|
T | C | 1 | a0001c0001t0088g0065 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-44+1825T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202926240 | ||||||
chr2:202926482
|
A | G | 1 | a0001c0001t0108g0190 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-44+2067A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202926482 | ||||||
chr2:202926596
|
C | T | 23 | a0002c0002t0012g0307a0002c0002t0012g0312a0002c0002t0012g0314others(20): Show | 23 | HG00733.hp2 HG01109.hp2 HG01168.hp2 others(20): Show |
intron_variant | MODIFIER | c.-44+2181C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202926596 | ||||||
chr2:202926610
|
G | A | 13 | a0003c0003t0016g0002a0003c0003t0016g0013a0003c0003t0016g0014others(10): Show | 14 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.-44+2195G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202926610 | ||||||
chr2:202926846
|
A | G | 2 | a0001c0001t0003g0189a0001c0001t0006g0236 | 2 | HG02280.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-44+2431A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202926846 | ||||||
chr2:202927024
|
G | T | 1 | a0001c0001t0051g0246 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-44+2609G>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202927024 | ||||||
chr2:202927189
|
G | A | 13 | a0003c0003t0016g0002a0003c0003t0016g0013a0003c0003t0016g0014others(10): Show | 14 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.-44+2774G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202927189 | ||||||
chr2:202927323
|
CTTTT | C | 12 | a0003c0003t0016g0002a0003c0003t0016g0013a0003c0003t0016g0014others(9): Show | 13 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.-44+2915_-44+2918d others(6): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 202927323 | |||||
chr2:202927326
|
T | C | 23 | a0002c0002t0012g0307a0002c0002t0012g0312a0002c0002t0012g0314others(20): Show | 23 | HG00733.hp2 HG01109.hp2 HG01168.hp2 others(20): Show |
intron_variant | MODIFIER | c.-44+2911T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202927326 | ||||||
chr2:202927370
|
C | A | 2 | a0001c0001t0029g0300a0001c0001t0029g0301 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-44+2955C>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202927370 | ||||||
chr2:202927408
|
T | G | 20 | a0002c0002t0012g0307a0002c0002t0012g0312a0002c0002t0012g0314others(17): Show | 20 | HG00733.hp2 HG01109.hp2 HG01168.hp2 others(17): Show |
intron_variant | MODIFIER | c.-44+2993T>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202927408 | ||||||
chr2:202927521
|
A | G | 1 | a0001c0001t0003g0181 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-44+3106A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202927521 | ||||||
chr2:202927905
|
A | G | 13 | a0003c0003t0016g0002a0003c0003t0016g0013a0003c0003t0016g0014others(10): Show | 14 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.-44+3490A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202927905 | ||||||
chr2:202928053
|
G | C | 1 | a0001c0001t0103g0292 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-44+3638G>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202928053 | ||||||
chr2:202928084
|
T | C | 2 | a0001c0001t0001g0161a0001c0001t0001g0164 | 2 | HG02809.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-44+3669T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202928084 | ||||||
chr2:202928093
|
C | T | 281 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0030others(278): Show | 286 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(283): Show |
intron_variant | MODIFIER | c.-44+3678C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202928093 | ||||||
chr2:202928364
|
G | C | 3 | a0001c0001t0015g0009a0001c0001t0100g0009a0001c0001t0101g0240 | 3 | HG02976.hp2 HG03139.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-44+3949G>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202928364 | ||||||
chr2:202928377
|
C | T | 1 | a0003c0009t0117g0019 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-44+3962C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202928377 | ||||||
chr2:202928378
|
G | A | 1 | a0001c0001t0001g0030 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.-44+3963G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202928378 | ||||||
chr2:202928478
|
G | A | 3 | a0001c0001t0003g0059a0001c0001t0007g0237a0001c0001t0106g0096 | 3 | NA18974.hp2 NA18977.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.-44+4063G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202928478 | ||||||
chr2:202928582
|
C | T | 1 | a0001c0001t0071g0039 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-44+4167C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202928582 | ||||||
chr2:202928591
|
A | G | 2 | a0001c0001t0006g0235a0001c0001t0009g0234 | 2 | HG02040.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.-44+4176A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202928591 | ||||||
chr2:202928653
|
C | A | 131 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0030others(128): Show | 132 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(129): Show |
intron_variant | MODIFIER | c.-44+4238C>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202928653 | ||||||
chr2:202928664
|
G | A | 23 | a0002c0002t0012g0307a0002c0002t0012g0312a0002c0002t0012g0314others(20): Show | 23 | HG00733.hp2 HG01109.hp2 HG01168.hp2 others(20): Show |
intron_variant | MODIFIER | c.-44+4249G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202928664 | ||||||
chr2:202928753
|
G | A | 2 | a0001c0001t0045g0063a0001c0001t0045g0098 | 2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-44+4338G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202928753 | ||||||
chr2:202928786
|
A | G | 2 | a0001c0001t0049g0282a0001c0001t0050g0281 | 2 | HG02109.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.-44+4371A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202928786 | ||||||
chr2:202928899
|
T | G | 1 | a0003c0013t0119g0010 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-44+4484T>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202928899 | ||||||
chr2:202928992
|
A | G | 1 | a0001c0001t0034g0284 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.-44+4577A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202928992 | ||||||
chr2:202929020
|
AC | A | 114 | a0001c0001t0002g0005a0001c0001t0002g0036a0001c0001t0002g0082others(111): Show | 117 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.-44+4606delC | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202929020 | ||||||
chr2:202929539
|
T | C | 12 | a0003c0003t0016g0002a0003c0003t0016g0013a0003c0003t0016g0014others(9): Show | 13 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.-44+5124T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202929539 | ||||||
chr2:202929595
|
T | C | 1 | a0001c0001t0013g0251 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-44+5180T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202929595 | ||||||
chr2:202929716
|
G | A | 13 | a0003c0003t0016g0002a0003c0003t0016g0013a0003c0003t0016g0014others(10): Show | 14 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.-44+5301G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202929716 | ||||||
chr2:202929757
|
T | C | 4 | a0001c0001t0010g0252a0001c0001t0013g0253a0001c0001t0032g0254others(1): Show | 4 | HG02145.hp2 HG02257.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.-44+5342T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202929757 | ||||||
chr2:202929910
|
G | A | 1 | a0001c0001t0005g0100 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.-44+5495G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202929910 | ||||||
chr2:202930061
|
G | C | 2 | a0001c0001t0049g0282a0001c0001t0050g0281 | 2 | HG02109.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.-44+5646G>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202930061 | ||||||
chr2:202930349
|
G | A | 2 | a0001c0001t0049g0282a0001c0001t0050g0281 | 2 | HG02109.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.-44+5934G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202930349 | ||||||
chr2:202930906
|
G | A | 1 | a0002c0002t0012g0319 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-44+6491G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202930906 | ||||||
chr2:202930962
|
T | C | 1 | a0001c0001t0045g0098 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-44+6547T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202930962 | ||||||
chr2:202930968
|
C | CT | 22 | a0001c0001t0001g0095a0001c0001t0002g0088a0001c0001t0002g0139others(19): Show | 22 | HG00609.hp2 HG00733.hp2 HG01175.hp1 others(19): Show |
intron_variant | MODIFIER | c.-44+6575dupT | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 202930968 | |||||
chr2:202930968
|
CT | C | 6 | a0001c0001t0001g0205a0001c0001t0002g0121a0001c0001t0005g0143others(3): Show | 6 | HG01167.hp2 HG01256.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.-44+6575delT | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 202930968 | |||||
chr2:202930994
|
A | G | 13 | a0003c0003t0016g0002a0003c0003t0016g0013a0003c0003t0016g0014others(10): Show | 14 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.-44+6579A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202930994 | ||||||
chr2:202930998
|
G | A | 1 | a0001c0001t0103g0292 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-44+6583G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202930998 | ||||||
chr2:202931039
|
G | A | 13 | a0003c0003t0016g0002a0003c0003t0016g0013a0003c0003t0016g0014others(10): Show | 14 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.-44+6624G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202931039 | ||||||
chr2:202931215
|
G | A | 2 | a0001c0001t0031g0263a0001c0001t0031g0264 | 2 | HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-44+6800G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202931215 | ||||||
chr2:202931264
|
T | G | 13 | a0003c0003t0016g0002a0003c0003t0016g0013a0003c0003t0016g0014others(10): Show | 14 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.-44+6849T>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202931264 | ||||||
chr2:202931267
|
C | T | 19 | a0001c0001t0008g0035a0001c0001t0008g0076a0001c0001t0008g0077others(16): Show | 21 | HG00544.hp1 HG00733.hp1 HG00735.hp2 others(18): Show |
intron_variant | MODIFIER | c.-44+6852C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202931267 | ||||||
chr2:202931520
|
C | T | 1 | a0001c0001t0103g0292 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-44+7105C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202931520 | ||||||
chr2:202931655
|
G | A | 1 | a0001c0001t0071g0039 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-44+7240G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202931655 | ||||||
chr2:202931727
|
GCAATAAC others(35): Show |
G | 5 | a0001c0005t0040g0147a0001c0005t0040g0325a0001c0005t0060g0145others(2): Show | 5 | HG02145.hp1 HG02451.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.-44+7340_-44+7381d others(44): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 202931727 | |||||
chr2:202932091
|
C | G | 16 | a0001c0001t0015g0009a0001c0001t0100g0009a0001c0001t0101g0240others(13): Show | 17 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(14): Show |
intron_variant | MODIFIER | c.-44+7676C>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202932091 | ||||||
chr2:202932131
|
T | C | 23 | a0002c0002t0012g0307a0002c0002t0012g0312a0002c0002t0012g0314others(20): Show | 23 | HG00733.hp2 HG01109.hp2 HG01168.hp2 others(20): Show |
intron_variant | MODIFIER | c.-44+7716T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202932131 | ||||||
chr2:202932265
|
C | T | 21 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0197others(18): Show | 21 | HG00544.hp2 HG00738.hp1 HG01943.hp1 others(18): Show |
intron_variant | MODIFIER | c.-44+7850C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202932265 | ||||||
chr2:202932288
|
TCA | T | 3 | a0001c0001t0013g0251a0001c0001t0013g0265a0001c0001t0053g0256 | 3 | HG01257.hp1 HG01952.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.-44+7876_-44+7877d others(4): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 202932288 | |||||
chr2:202932318
|
G | T | 1 | a0001c0001t0025g0074 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-44+7903G>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202932318 | ||||||
chr2:202932472
|
G | A | 1 | a0001c0001t0072g0119 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-44+8057G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202932472 | ||||||
chr2:202932612
|
G | A | 1 | a0001c0001t0051g0246 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-44+8197G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202932612 | ||||||
chr2:202932735
|
T | C | 1 | a0001c0001t0002g0139 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-44+8320T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202932735 | ||||||
chr2:202932824
|
A | G | 1 | a0006c0010t0107g0026 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-44+8409A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202932824 | ||||||
chr2:202932831
|
T | G | 1 | a0005c0006t0017g0245 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-44+8416T>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202932831 | ||||||
chr2:202932842
|
G | A | 1 | a0003c0003t0048g0011 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-44+8427G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202932842 | ||||||
chr2:202933451
|
G | A | 1 | a0001c0001t0007g0031 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-43-8409G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202933451 | ||||||
chr2:202933484
|
T | G | 2 | a0001c0008t0015g0243a0001c0008t0022g0242 | 2 | HG02486.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-43-8376T>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202933484 | ||||||
chr2:202933531
|
C | G | 1 | a0005c0006t0057g0259 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-43-8329C>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202933531 | ||||||
chr2:202933595
|
C | T | 13 | a0003c0003t0016g0002a0003c0003t0016g0013a0003c0003t0016g0014others(10): Show | 14 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.-43-8265C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202933595 | ||||||
chr2:202933642
|
TC | T | 12 | a0003c0003t0016g0002a0003c0003t0016g0013a0003c0003t0016g0014others(9): Show | 13 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.-43-8217delC | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202933642 | ||||||
chr2:202933862
|
C | T | 13 | a0003c0003t0016g0002a0003c0003t0016g0013a0003c0003t0016g0014others(10): Show | 14 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.-43-7998C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202933862 | ||||||
chr2:202933862
|
CTTTCTTT others(3): Show |
C | 106 | a0001c0001t0002g0005a0001c0001t0002g0036a0001c0001t0002g0082others(103): Show | 109 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.-43-7984_-43-7975d others(12): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 202933862 | |||||
chr2:202933924
|
CTTTCTTT others(13): Show |
C | 1 | a0001c0001t0062g0122 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-43-7932_-43-7913d others(22): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 202933924 | |||||
chr2:202934057
|
T | A | 1 | a0001c0001t0004g0053 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.-43-7803T>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202934057 | ||||||
chr2:202934179
|
A | T | 1 | a0001c0001t0082g0114 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-43-7681A>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202934179 | ||||||
chr2:202934256
|
A | G | 1 | a0001c0001t0026g0089 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.-43-7604A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202934256 | ||||||
chr2:202934290
|
C | T | 1 | a0001c0001t0001g0199 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-43-7570C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202934290 | ||||||
chr2:202934632
|
G | A | 6 | a0001c0001t0021g0003a0001c0001t0021g0021a0001c0001t0021g0022others(3): Show | 7 | HG01081.hp1 HG01256.hp1 HG01258.hp2 others(4): Show |
intron_variant | MODIFIER | c.-43-7228G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202934632 | ||||||
chr2:202934665
|
G | A | 8 | a0001c0001t0025g0047a0001c0001t0027g0045a0001c0001t0027g0048others(5): Show | 8 | HG02280.hp2 HG02486.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.-43-7195G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202934665 | ||||||
chr2:202934670
|
G | A | 1 | a0001c0001t0005g0055 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-43-7190G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202934670 | ||||||
chr2:202934905
|
A | G | 1 | a0001c0001t0017g0262 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-43-6955A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202934905 | ||||||
chr2:202935023
|
G | A | 1 | a0003c0007t0048g0012 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.-43-6837G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202935023 | ||||||
chr2:202935024
|
T | C | 1 | a0001c0001t0005g0058 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-43-6836T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202935024 | ||||||
chr2:202935101
|
A | AATATATA others(3): Show |
1 | a0001c0001t0003g0232 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.-43-6746_-43-6737d others(12): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 202935101 | |||||
chr2:202935101
|
A | AATATATA others(13): Show |
128 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0030others(125): Show | 129 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(126): Show |
intron_variant | MODIFIER | c.-43-6756_-43-6737d others(22): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 202935101 | |||||
chr2:202935324
|
TTATA | T | 273 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0030others(270): Show | 278 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(275): Show |
intron_variant | MODIFIER | c.-43-6520_-43-6517d others(6): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 202935324 | |||||
chr2:202935324
|
TTATATA | T | 8 | a0001c0001t0025g0047a0001c0001t0027g0045a0001c0001t0027g0048others(5): Show | 8 | HG02280.hp2 HG02486.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.-43-6522_-43-6517d others(8): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 202935324 | |||||
chr2:202935367
|
G | A | 1 | a0002c0002t0015g0311 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-43-6493G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202935367 | ||||||
chr2:202935660
|
G | A | 1 | a0001c0001t0001g0094 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-43-6200G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202935660 | ||||||
chr2:202935666
|
C | T | 1 | a0001c0001t0018g0283 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-43-6194C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202935666 | ||||||
chr2:202935708
|
A | G | 3 | a0001c0001t0003g0231a0001c0001t0004g0178a0001c0001t0006g0230 | 3 | NA18970.hp1 NA18991.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.-43-6152A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202935708 | ||||||
chr2:202935730
|
T | C | 24 | a0001c0001t0001g0054a0001c0001t0001g0094a0001c0001t0001g0095others(21): Show | 24 | HG00408.hp1 HG00544.hp2 HG00621.hp2 others(21): Show |
intron_variant | MODIFIER | c.-43-6130T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202935730 | ||||||
chr2:202935800
|
TC | T | 5 | a0001c0001t0003g0181a0001c0001t0006g0206a0001c0001t0007g0165others(2): Show | 5 | HG02572.hp1 HG02723.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.-43-6059delC | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202935800 | ||||||
chr2:202936212
|
T | G | 1 | a0001c0001t0001g0200 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.-43-5648T>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202936212 | ||||||
chr2:202936276
|
T | G | 1 | a0001c0001t0007g0031 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-43-5584T>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202936276 | ||||||
chr2:202936503
|
T | G | 13 | a0003c0003t0016g0002a0003c0003t0016g0013a0003c0003t0016g0014others(10): Show | 14 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.-43-5357T>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202936503 | ||||||
chr2:202936538
|
G | C | 2 | a0001c0001t0065g0032a0001c0001t0066g0044 | 2 | HG00408.hp2 HG02071.hp1 |
intron_variant | MODIFIER | c.-43-5322G>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202936538 | ||||||
chr2:202936980
|
A | G | 1 | a0001c0001t0004g0029 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.-43-4880A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202936980 | ||||||
chr2:202937108
|
G | A | 1 | a0006c0010t0107g0026 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-43-4752G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202937108 | ||||||
chr2:202937172
|
G | A | 1 | a0001c0001t0005g0100 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.-43-4688G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202937172 | ||||||
chr2:202937356
|
CAG | C | 9 | a0001c0001t0001g0154a0001c0001t0003g0155a0001c0001t0004g0053others(6): Show | 9 | HG01257.hp2 HG01258.hp1 HG02040.hp2 others(6): Show |
intron_variant | MODIFIER | c.-43-4501_-43-4500d others(4): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 202937356 | |||||
chr2:202937458
|
TA | T | 23 | a0001c0001t0007g0031a0002c0002t0012g0307a0002c0002t0012g0312others(20): Show | 23 | HG00733.hp2 HG01109.hp2 HG01168.hp2 others(20): Show |
intron_variant | MODIFIER | c.-43-4401delA | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202937458 | ||||||
chr2:202937459
|
A | T | 1 | a0002c0002t0097g0320 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-43-4401A>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202937459 | ||||||
chr2:202937465
|
T | G | 1 | a0001c0001t0001g0200 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.-43-4395T>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202937465 | ||||||
chr2:202937636
|
T | G | 1 | a0001c0001t0055g0274 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-43-4224T>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202937636 | ||||||
chr2:202937796
|
T | C | 1 | a0001c0001t0001g0289 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-43-4064T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202937796 | ||||||
chr2:202937815
|
G | A | 1 | a0001c0001t0031g0263 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-43-4045G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202937815 | ||||||
chr2:202937903
|
G | A | 3 | a0001c0001t0003g0166a0001c0001t0003g0183a0001c0001t0003g0209 | 3 | HG03491.hp2 HG03669.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.-43-3957G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202937903 | ||||||
chr2:202937930
|
T | TA | 10 | a0001c0001t0004g0290a0001c0001t0009g0182a0001c0001t0009g0184others(7): Show | 11 | HG00438.hp2 HG00735.hp1 HG01099.hp2 others(8): Show |
intron_variant | MODIFIER | c.-43-3914dupA | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 202937930 | |||||
chr2:202937930
|
TA | T | 108 | a0001c0001t0002g0005a0001c0001t0002g0036a0001c0001t0002g0082others(105): Show | 110 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.-43-3914delA | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 202937930 | |||||
chr2:202937946
|
AT | A | 5 | a0001c0001t0003g0181a0001c0001t0006g0206a0001c0001t0007g0165others(2): Show | 5 | HG02572.hp1 HG02723.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.-43-3913delT | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202937946 | ||||||
chr2:202937964
|
T | G | 1 | a0001c0001t0001g0200 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.-43-3896T>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202937964 | ||||||
chr2:202938057
|
G | A | 1 | a0001c0001t0007g0031 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-43-3803G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202938057 | ||||||
chr2:202938060
|
T | G | 1 | a0001c0001t0001g0200 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.-43-3800T>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202938060 | ||||||
chr2:202938144
|
T | A | 3 | a0001c0001t0015g0009a0001c0001t0100g0009a0001c0001t0101g0240 | 3 | HG02976.hp2 HG03139.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-43-3716T>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202938144 | ||||||
chr2:202938209
|
A | G | 1 | a0001c0001t0056g0260 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-43-3651A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202938209 | ||||||
chr2:202938315
|
C | T | 1 | a0001c0001t0002g0088 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.-43-3545C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202938315 | ||||||
chr2:202938353
|
A | G | 1 | a0002c0002t0059g0324 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-43-3507A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202938353 | ||||||
chr2:202938432
|
T | A | 1 | a0001c0001t0007g0031 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-43-3428T>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202938432 | ||||||
chr2:202938515
|
C | T | 1 | a0001c0001t0004g0151 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.-43-3345C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202938515 | ||||||
chr2:202938612
|
T | C | 1 | a0001c0001t0034g0284 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.-43-3248T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202938612 | ||||||
chr2:202938651
|
T | G | 129 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0030others(126): Show | 131 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(128): Show |
intron_variant | MODIFIER | c.-43-3209T>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202938651 | ||||||
chr2:202938652
|
T | G | 2 | a0001c0001t0006g0060a0001c0008t0022g0242 | 2 | HG00621.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.-43-3208T>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202938652 | ||||||
chr2:202938659
|
GT | G | 124 | a0001c0001t0002g0005a0001c0001t0002g0036a0001c0001t0002g0082others(121): Show | 127 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(124): Show |
intron_variant | MODIFIER | c.-43-3191delT | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 202938659 | |||||
chr2:202938778
|
G | A | 3 | a0001c0001t0001g0094a0001c0001t0001g0197a0001c0001t0001g0198 | 3 | HG00544.hp2 NA18998.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.-43-3082G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202938778 | ||||||
chr2:202938906
|
C | T | 1 | a0001c0001t0008g0035 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-43-2954C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202938906 | ||||||
chr2:202939198
|
T | G | 3 | a0001c0001t0015g0009a0001c0001t0100g0009a0001c0001t0101g0240 | 3 | HG02976.hp2 HG03139.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-43-2662T>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202939198 | ||||||
chr2:202939566
|
C | T | 13 | a0003c0003t0016g0002a0003c0003t0016g0013a0003c0003t0016g0014others(10): Show | 14 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.-43-2294C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202939566 | ||||||
chr2:202939682
|
TTTC | T | 11 | a0003c0003t0016g0002a0003c0003t0016g0013a0003c0003t0016g0014others(8): Show | 12 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(9): Show |
intron_variant | MODIFIER | c.-43-2175_-43-2173d others(5): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 202939682 | |||||
chr2:202939685
|
C | CT | 22 | a0001c0001t0001g0054a0001c0001t0001g0177a0001c0001t0003g0231others(19): Show | 22 | HG00621.hp2 HG01257.hp1 HG01346.hp1 others(19): Show |
intron_variant | MODIFIER | c.-43-2154dupT | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 202939685 | |||||
chr2:202939685
|
CT | C | 6 | a0001c0001t0001g0197a0001c0001t0001g0211a0001c0001t0029g0300others(3): Show | 6 | HG01496.hp1 HG02896.hp1 NA18939.hp2 others(3): Show |
intron_variant | MODIFIER | c.-43-2154delT | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 202939685 | |||||
chr2:202939685
|
CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0008g0035 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-43-2164_-43-2154d others(13): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 202939685 | |||||
chr2:202939689
|
T | C | 3 | a0001c0001t0003g0167a0001c0001t0049g0282a0001c0001t0050g0281 | 3 | HG01361.hp1 HG02109.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.-43-2171T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202939689 | ||||||
chr2:202939690
|
T | C | 1 | a0002c0002t0012g0317 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-43-2170T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202939690 | ||||||
chr2:202939691
|
T | C | 1 | a0001c0001t0003g0232 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.-43-2169T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202939691 | ||||||
chr2:202939970
|
A | G | 1 | a0001c0001t0024g0134 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-43-1890A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202939970 | ||||||
chr2:202940023
|
C | G | 11 | a0001c0001t0001g0154a0001c0001t0001g0161a0001c0001t0001g0164others(8): Show | 11 | HG01257.hp2 HG01258.hp1 HG02040.hp2 others(8): Show |
intron_variant | MODIFIER | c.-43-1837C>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202940023 | ||||||
chr2:202940115
|
C | G | 1 | a0001c0001t0001g0199 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-43-1745C>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202940115 | ||||||
chr2:202940180
|
T | A | 1 | a0001c0001t0103g0292 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-43-1680T>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202940180 | ||||||
chr2:202940195
|
A | C | 1 | a0001c0001t0003g0232 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.-43-1665A>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202940195 | ||||||
chr2:202940311
|
A | G | 290 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0030others(287): Show | 295 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(292): Show |
intron_variant | MODIFIER | c.-43-1549A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202940311 | ||||||
chr2:202940485
|
ATGG | A | 4 | a0001c0001t0014g0073a0001c0001t0014g0102a0001c0001t0014g0103others(1): Show | 4 | HG00597.hp2 NA18998.hp1 NA19057.hp1 others(1): Show |
intron_variant | MODIFIER | c.-43-1371_-43-1369d others(5): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 202940485 | |||||
chr2:202940722
|
T | C | 1 | a0006c0010t0107g0026 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-43-1138T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202940722 | ||||||
chr2:202940741
|
T | C | 24 | a0001c0001t0001g0054a0001c0001t0001g0094a0001c0001t0001g0095others(21): Show | 24 | HG00408.hp1 HG00544.hp2 HG00621.hp2 others(21): Show |
intron_variant | MODIFIER | c.-43-1119T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202940741 | ||||||
chr2:202940817
|
G | C | 1 | a0001c0005t0092g0146 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-43-1043G>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202940817 | ||||||
chr2:202940829
|
G | A | 13 | a0003c0003t0016g0002a0003c0003t0016g0013a0003c0003t0016g0014others(10): Show | 14 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.-43-1031G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202940829 | ||||||
chr2:202941085
|
A | T | 1 | a0001c0001t0082g0114 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-43-775A>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202941085 | ||||||
chr2:202941206
|
C | G | 13 | a0003c0003t0016g0002a0003c0003t0016g0013a0003c0003t0016g0014others(10): Show | 14 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.-43-654C>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202941206 | ||||||
chr2:202941206
|
C | T | 1 | a0001c0001t0045g0098 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-43-654C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202941206 | ||||||
chr2:202941216
|
T | C | 133 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0030others(130): Show | 134 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.-43-644T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202941216 | ||||||
chr2:202941328
|
T | A | 1 | a0001c0001t0025g0074 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-43-532T>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202941328 | ||||||
chr2:202941351
|
A | T | 282 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0030others(279): Show | 287 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(284): Show |
intron_variant | MODIFIER | c.-43-509A>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202941351 | ||||||
chr2:202941626
|
T | C | 1 | a0001c0001t0035g0105 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.-43-234T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202941626 | ||||||
chr2:202941639
|
G | A | 1 | a0001c0001t0063g0034 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-43-221G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | chr2 | 202941639 | ||||||
chr2:202941714
|
GTTAATTT others(1): Show |
G | 13 | a0003c0003t0016g0002a0003c0003t0016g0013a0003c0003t0016g0014others(10): Show | 14 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.-43-140_-43-133del others(8): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 202941714 | |||||
chr2:202942001
|
C | T | 13 | a0003c0003t0016g0002a0003c0003t0016g0013a0003c0003t0016g0014others(10): Show | 14 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.78+21C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 4/16 | chr2 | 202942001 | ||||||
chr2:202942082
|
A | C | 2 | a0001c0001t0008g0296a0001c0001t0008g0297 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.78+102A>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 4/16 | chr2 | 202942082 | ||||||
chr2:202942105
|
G | A | 2 | a0001c0001t0067g0124a0001c0001t0068g0123 | 2 | NA18747.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.78+125G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 4/16 | chr2 | 202942105 | ||||||
chr2:202942144
|
C | T | 2 | a0001c0001t0014g0113a0001c0001t0088g0065 | 2 | HG02602.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.78+164C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 4/16 | chr2 | 202942144 | ||||||
chr2:202942235
|
G | A | 1 | a0005c0006t0017g0245 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.78+255G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 4/16 | chr2 | 202942235 | ||||||
chr2:202942291
|
G | A | 3 | a0001c0001t0015g0009a0001c0001t0100g0009a0001c0001t0101g0240 | 3 | HG02976.hp2 HG03139.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.78+311G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 4/16 | chr2 | 202942291 | ||||||
chr2:202942360
|
A | T | 13 | a0003c0003t0016g0002a0003c0003t0016g0013a0003c0003t0016g0014others(10): Show | 14 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.78+380A>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 4/16 | chr2 | 202942360 | ||||||
chr2:202942710
|
C | T | 1 | a0001c0001t0007g0031 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.79-30C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 4/16 | chr2 | 202942710 | ||||||
chr2:202943417
|
T | C | 4 | a0001c0001t0030g0192a0001c0001t0030g0194a0001c0001t0030g0195others(1): Show | 4 | NA18951.hp1 NA18968.hp1 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.306+450T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | chr2 | 202943417 | ||||||
chr2:202943587
|
T | TAC | 71 | a0001c0001t0001g0030a0001c0001t0001g0177a0001c0001t0002g0005others(68): Show | 73 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.306+662_306+663dup others(2): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 202943587 | |||||
chr2:202943587
|
T | TACAC | 40 | a0001c0001t0001g0187a0001c0001t0001g0199a0001c0001t0002g0085others(37): Show | 40 | HG00642.hp2 HG01496.hp1 HG02071.hp2 others(37): Show |
intron_variant | MODIFIER | c.306+660_306+663dup others(4): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 202943587 | |||||
chr2:202943587
|
T | TACACAC | 42 | a0001c0001t0001g0120a0001c0001t0001g0154a0001c0001t0001g0170others(39): Show | 43 | HG00642.hp1 HG00673.hp1 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.306+658_306+663dup others(6): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 202943587 | |||||
chr2:202943587
|
T | TACACACA others(1): Show |
38 | a0001c0001t0001g0289a0001c0001t0002g0036a0001c0001t0002g0088others(35): Show | 38 | HG00408.hp1 HG00408.hp2 HG00733.hp1 others(35): Show |
intron_variant | MODIFIER | c.306+656_306+663dup others(8): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 202943587 | |||||
chr2:202943587
|
T | TACACACA others(3): Show |
25 | a0001c0001t0001g0054a0001c0001t0001g0094a0001c0001t0001g0095others(22): Show | 26 | HG00323.hp1 HG00544.hp2 HG00621.hp2 others(23): Show |
intron_variant | MODIFIER | c.306+654_306+663dup others(10): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 202943587 | |||||
chr2:202943587
|
T | TACACACA others(5): Show |
13 | a0001c0001t0002g0082a0001c0001t0003g0189a0001c0001t0004g0156others(10): Show | 13 | HG01109.hp1 HG01358.hp2 HG02300.hp2 others(10): Show |
intron_variant | MODIFIER | c.306+652_306+663dup others(12): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 202943587 | |||||
chr2:202943587
|
T | TACACACA others(7): Show |
6 | a0001c0001t0005g0144a0001c0001t0006g0236a0001c0001t0007g0165others(3): Show | 6 | HG01169.hp2 HG02258.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.306+650_306+663dup others(14): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 202943587 | |||||
chr2:202943587
|
T | TACACACA others(9): Show |
3 | a0001c0001t0003g0155a0001c0001t0003g0181a0001c0001t0005g0143 | 3 | HG01167.hp2 HG02040.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.306+648_306+663dup others(16): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 202943587 | |||||
chr2:202943587
|
T | TCACACAC others(12): Show |
1 | a0001c0001t0001g0197 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.306+620_306+621ins others(19): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | chr2 | 202943587 | ||||||
chr2:202943587
|
TAC | T | 22 | a0001c0001t0001g0205a0001c0001t0004g0229a0001c0001t0017g0271others(19): Show | 22 | HG00597.hp1 HG00733.hp2 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.306+662_306+663del others(2): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 202943587 | |||||
chr2:202943587
|
TACAC | T | 3 | a0001c0001t0049g0282a0001c0001t0050g0281a0002c0002t0059g0324 | 3 | HG02109.hp2 HG02559.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.306+660_306+663del others(4): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 202943587 | |||||
chr2:202943587
|
TACACACA others(5): Show |
T | 2 | a0001c0001t0001g0161a0001c0001t0001g0164 | 2 | HG02809.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.306+652_306+663del others(12): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 202943587 | |||||
chr2:202943617
|
CACACACA others(7): Show |
C | 12 | a0003c0003t0016g0002a0003c0003t0016g0013a0003c0003t0016g0014others(9): Show | 13 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.306+652_306+665del others(14): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 202943617 | |||||
chr2:202943619
|
CACACACA others(5): Show |
C | 1 | a0003c0013t0119g0010 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.306+654_306+665del others(12): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 202943619 | |||||
chr2:202943631
|
T | C | 108 | a0001c0001t0001g0154a0001c0001t0002g0005a0001c0001t0002g0036others(105): Show | 111 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.306+664T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | chr2 | 202943631 | ||||||
chr2:202943633
|
T | C | 1 | a0001c0001t0002g0132 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.306+666T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | chr2 | 202943633 | ||||||
chr2:202943652
|
G | GT | 107 | a0001c0001t0002g0005a0001c0001t0002g0036a0001c0001t0002g0082others(104): Show | 110 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.306+696dupT | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 202943652 | |||||
chr2:202943686
|
C | T | 1 | a0006c0010t0107g0026 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.306+719C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | chr2 | 202943686 | ||||||
chr2:202943809
|
G | A | 29 | a0001c0001t0018g0249a0001c0001t0019g0295a0001c0001t0020g0285others(26): Show | 30 | HG00438.hp2 HG00735.hp1 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.306+842G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | chr2 | 202943809 | ||||||
chr2:202944032
|
A | T | 1 | a0001c0001t0051g0246 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.306+1065A>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | chr2 | 202944032 | ||||||
chr2:202944064
|
G | A | 2 | a0001c0001t0001g0211a0001c0001t0006g0060 | 2 | HG00621.hp1 NA18939.hp2 |
intron_variant | MODIFIER | c.306+1097G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | chr2 | 202944064 | ||||||
chr2:202944112
|
G | A | 12 | a0003c0003t0016g0002a0003c0003t0016g0013a0003c0003t0016g0014others(9): Show | 13 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.306+1145G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | chr2 | 202944112 | ||||||
chr2:202944151
|
T | C | 1 | a0001c0001t0087g0079 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.306+1184T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | chr2 | 202944151 | ||||||
chr2:202944332
|
C | T | 2 | a0001c0008t0015g0243a0001c0008t0022g0242 | 2 | HG02486.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.306+1365C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | chr2 | 202944332 | ||||||
chr2:202944394
|
T | G | 1 | a0001c0001t0076g0037 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.306+1427T>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | chr2 | 202944394 | ||||||
chr2:202944555
|
A | G | 1 | a0001c0001t0007g0288 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.306+1588A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | chr2 | 202944555 | ||||||
chr2:202944650
|
C | T | 5 | a0001c0005t0040g0147a0001c0005t0040g0325a0001c0005t0060g0145others(2): Show | 5 | HG02145.hp1 HG02451.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.306+1683C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | chr2 | 202944650 | ||||||
chr2:202944661
|
A | G | 1 | a0001c0001t0007g0288 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.306+1694A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | chr2 | 202944661 | ||||||
chr2:202944807
|
A | AC | 283 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0030others(280): Show | 288 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(285): Show |
intron_variant | MODIFIER | c.306+1840_306+1841i others(3): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | chr2 | 202944807 | ||||||
chr2:202945116
|
C | G | 1 | a0001c0001t0001g0289 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.306+2149C>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | chr2 | 202945116 | ||||||
chr2:202945307
|
A | T | 1 | a0001c0001t0030g0195 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.306+2340A>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | chr2 | 202945307 | ||||||
chr2:202945410
|
C | G | 1 | a0001c0001t0001g0095 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.306+2443C>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | chr2 | 202945410 | ||||||
chr2:202945411
|
C | T | 4 | a0001c0001t0010g0250a0001c0001t0017g0261a0001c0001t0017g0262others(1): Show | 4 | HG02615.hp2 HG02970.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.306+2444C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | chr2 | 202945411 | ||||||
chr2:202945644
|
G | T | 1 | a0001c0001t0045g0098 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.306+2677G>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | chr2 | 202945644 | ||||||
chr2:202945672
|
G | A | 2 | a0003c0007t0048g0012a0003c0007t0118g0016 | 2 | NA18952.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.306+2705G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | chr2 | 202945672 | ||||||
chr2:202945915
|
T | C | 2 | a0001c0008t0015g0243a0001c0008t0022g0242 | 2 | HG02486.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.306+2948T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | chr2 | 202945915 | ||||||
chr2:202946590
|
G | A | 2 | a0001c0001t0045g0063a0001c0001t0045g0098 | 2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.306+3623G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | chr2 | 202946590 | ||||||
chr2:202946692
|
A | G | 1 | a0001c0001t0004g0291 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.306+3725A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | chr2 | 202946692 | ||||||
chr2:202946866
|
C | A | 1 | a0001c0001t0078g0072 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.306+3899C>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | chr2 | 202946866 | ||||||
chr2:202946905
|
G | A | 13 | a0003c0003t0016g0002a0003c0003t0016g0013a0003c0003t0016g0014others(10): Show | 14 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.306+3938G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | chr2 | 202946905 | ||||||
chr2:202946920
|
G | A | 3 | a0001c0001t0002g0036a0001c0001t0005g0109a0001c0001t0063g0034 | 3 | HG02559.hp2 NA19030.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.306+3953G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | chr2 | 202946920 | ||||||
chr2:202947124
|
T | C | 283 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0030others(280): Show | 288 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(285): Show |
intron_variant | MODIFIER | c.306+4157T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | chr2 | 202947124 | ||||||
chr2:202947179
|
A | T | 13 | a0003c0003t0016g0002a0003c0003t0016g0013a0003c0003t0016g0014others(10): Show | 14 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.306+4212A>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | chr2 | 202947179 | ||||||
chr2:202947189
|
A | C | 13 | a0003c0003t0016g0002a0003c0003t0016g0013a0003c0003t0016g0014others(10): Show | 14 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.306+4222A>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | chr2 | 202947189 | ||||||
chr2:202947325
|
A | C | 3 | a0001c0001t0002g0005a0001c0001t0002g0087a0001c0001t0002g0121 | 4 | NA18974.hp1 NA18984.hp2 NA19003.hp1 others(1): Show |
intron_variant | MODIFIER | c.306+4358A>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | chr2 | 202947325 | ||||||
chr2:202948200
|
C | A | 132 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0030others(129): Show | 133 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.307-4359C>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | chr2 | 202948200 | ||||||
chr2:202948344
|
T | G | 1 | a0003c0013t0119g0010 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.307-4215T>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | chr2 | 202948344 | ||||||
chr2:202948783
|
C | T | 1 | a0001c0001t0007g0031 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.307-3776C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | chr2 | 202948783 | ||||||
chr2:202948784
|
G | A | 1 | a0005c0006t0057g0259 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.307-3775G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | chr2 | 202948784 | ||||||
chr2:202948808
|
T | A | 1 | a0001c0001t0003g0059 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.307-3751T>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | chr2 | 202948808 | ||||||
chr2:202948912
|
CT | C | 7 | a0001c0001t0025g0047a0001c0001t0027g0045a0001c0001t0027g0048others(4): Show | 7 | HG02280.hp2 HG02486.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.307-3643delT | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 202948912 | |||||
chr2:202949132
|
G | A | 1 | a0001c0001t0010g0252 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.307-3427G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | chr2 | 202949132 | ||||||
chr2:202949342
|
C | CA | 23 | a0001c0001t0001g0054a0001c0001t0001g0094a0001c0001t0001g0095others(20): Show | 23 | HG00408.hp1 HG00544.hp2 HG00621.hp2 others(20): Show |
intron_variant | MODIFIER | c.307-3202dupA | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 202949342 | |||||
chr2:202949342
|
CA | C | 14 | a0003c0003t0016g0002a0003c0003t0016g0013a0003c0003t0016g0014others(11): Show | 15 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.307-3202delA | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 202949342 | |||||
chr2:202949486
|
C | CT | 14 | a0001c0001t0103g0292a0003c0003t0016g0002a0003c0003t0016g0013others(11): Show | 15 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.307-3066dupT | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 202949486 | |||||
chr2:202949515
|
A | ATTT | 36 | a0001c0001t0001g0198a0001c0001t0002g0085a0001c0001t0002g0088others(33): Show | 36 | HG00323.hp1 HG00408.hp2 HG00544.hp1 others(33): Show |
intron_variant | MODIFIER | c.307-3043_307-3041d others(5): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 202949515 | |||||
chr2:202949516
|
T | TTTTTTA | 7 | a0001c0001t0005g0058a0001c0001t0008g0296a0001c0001t0008g0297others(4): Show | 7 | HG02630.hp1 HG02818.hp2 HG03491.hp1 others(4): Show |
intron_variant | MODIFIER | c.307-3041_307-3040i others(8): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 202949516 | |||||
chr2:202949516
|
TTTA | T | 104 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0030others(101): Show | 106 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.307-2995_307-2993d others(5): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 202949516 | |||||
chr2:202949516
|
TTTATTA | T | 44 | a0001c0001t0001g0095a0001c0001t0001g0154a0001c0001t0001g0197others(41): Show | 44 | HG00642.hp1 HG00733.hp2 HG01109.hp2 others(41): Show |
intron_variant | MODIFIER | c.307-2998_307-2993d others(8): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 202949516 | |||||
chr2:202949516
|
TTTATTAT others(2): Show |
T | 15 | a0001c0001t0001g0170a0001c0001t0001g0213a0001c0001t0001g0216others(12): Show | 15 | HG01255.hp1 HG01358.hp1 HG01981.hp2 others(12): Show |
intron_variant | MODIFIER | c.307-3001_307-2993d others(11): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 202949516 | |||||
chr2:202949516
|
TTTATTAT others(5): Show |
T | 3 | a0001c0001t0002g0125a0001c0001t0007g0031a0001c0001t0009g0179 | 3 | HG01952.hp2 HG02451.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.307-3004_307-2993d others(14): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 202949516 | |||||
chr2:202949519
|
A | T | 86 | a0001c0001t0001g0094a0001c0001t0001g0120a0001c0001t0001g0161others(83): Show | 88 | HG00544.hp2 HG00597.hp2 HG00642.hp2 others(85): Show |
intron_variant | MODIFIER | c.307-3040A>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | chr2 | 202949519 | ||||||
chr2:202949522
|
A | T | 68 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0030others(65): Show | 69 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.307-3037A>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | chr2 | 202949522 | ||||||
chr2:202949525
|
A | T | 18 | a0001c0001t0001g0095a0001c0001t0001g0154a0001c0001t0001g0197others(15): Show | 18 | HG00733.hp2 HG01168.hp2 HG01169.hp1 others(15): Show |
intron_variant | MODIFIER | c.307-3034A>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | chr2 | 202949525 | ||||||
chr2:202949528
|
A | T | 2 | a0001c0001t0042g0298a0001c0008t0022g0242 | 2 | HG02258.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.307-3031A>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | chr2 | 202949528 | ||||||
chr2:202949531
|
A | T | 2 | a0001c0001t0002g0125a0001c0001t0007g0031 | 2 | HG02451.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.307-3028A>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | chr2 | 202949531 | ||||||
chr2:202949608
|
T | C | 2 | a0001c0001t0006g0152a0001c0001t0006g0153 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.307-2951T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | chr2 | 202949608 | ||||||
chr2:202949619
|
C | G | 20 | a0002c0002t0012g0312a0002c0002t0012g0314a0002c0002t0012g0317others(17): Show | 20 | HG01109.hp2 HG01884.hp1 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.307-2940C>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | chr2 | 202949619 | ||||||
chr2:202949684
|
G | A | 1 | a0001c0001t0103g0292 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.307-2875G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | chr2 | 202949684 | ||||||
chr2:202949971
|
A | T | 13 | a0003c0003t0016g0002a0003c0003t0016g0013a0003c0003t0016g0014others(10): Show | 14 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.307-2588A>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | chr2 | 202949971 | ||||||
chr2:202950092
|
A | C | 1 | a0005c0006t0058g0248 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.307-2467A>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | chr2 | 202950092 | ||||||
chr2:202950324
|
T | G | 1 | a0001c0001t0019g0295 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.307-2235T>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | chr2 | 202950324 | ||||||
chr2:202950745
|
A | G | 8 | a0001c0001t0025g0047a0001c0001t0027g0045a0001c0001t0027g0048others(5): Show | 8 | HG02280.hp2 HG02486.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.307-1814A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | chr2 | 202950745 | ||||||
chr2:202951011
|
A | T | 4 | a0001c0001t0003g0231a0001c0001t0004g0178a0001c0001t0006g0230others(1): Show | 4 | HG03834.hp1 NA18970.hp1 NA18991.hp1 others(1): Show |
intron_variant | MODIFIER | c.307-1548A>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | chr2 | 202951011 | ||||||
chr2:202951017
|
T | A | 13 | a0003c0003t0016g0002a0003c0003t0016g0013a0003c0003t0016g0014others(10): Show | 14 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.307-1542T>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | chr2 | 202951017 | ||||||
chr2:202951073
|
G | A | 1 | a0001c0001t0103g0292 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.307-1486G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | chr2 | 202951073 | ||||||
chr2:202951131
|
T | C | 282 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0030others(279): Show | 287 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(284): Show |
intron_variant | MODIFIER | c.307-1428T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | chr2 | 202951131 | ||||||
chr2:202951252
|
A | G | 1 | a0001c0001t0028g0092 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.307-1307A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | chr2 | 202951252 | ||||||
chr2:202951259
|
T | C | 1 | a0001c0001t0009g0212 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.307-1300T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | chr2 | 202951259 | ||||||
chr2:202951686
|
T | G | 1 | a0001c0001t0076g0037 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.307-873T>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | chr2 | 202951686 | ||||||
chr2:202951771
|
G | A | 13 | a0003c0003t0016g0002a0003c0003t0016g0013a0003c0003t0016g0014others(10): Show | 14 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.307-788G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | chr2 | 202951771 | ||||||
chr2:202951836
|
C | CT | 14 | a0001c0001t0026g0089a0003c0003t0016g0002a0003c0003t0016g0013others(11): Show | 15 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.307-709dupT | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 202951836 | |||||
chr2:202951872
|
G | A | 1 | a0001c0001t0004g0226 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.307-687G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | chr2 | 202951872 | ||||||
chr2:202951979
|
C | T | 1 | a0001c0001t0005g0068 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.307-580C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | chr2 | 202951979 | ||||||
chr2:202952035
|
G | A | 2 | a0003c0007t0048g0012a0003c0007t0118g0016 | 2 | NA18952.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.307-524G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | chr2 | 202952035 | ||||||
chr2:202952534
|
A | AT | 13 | a0003c0003t0016g0002a0003c0003t0016g0013a0003c0003t0016g0014others(10): Show | 14 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.307-13dupT | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 202952534 | |||||
chr2:202952699
|
A | C | 2 | a0001c0001t0008g0077a0001c0001t0008g0115 | 2 | HG00735.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.427+20A>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 6/16 | chr2 | 202952699 | ||||||
chr2:202952758
|
C | A | 1 | a0001c0001t0007g0031 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.427+79C>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 6/16 | chr2 | 202952758 | ||||||
chr2:202952816
|
C | T | 1 | a0001c0001t0055g0274 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.427+137C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 6/16 | chr2 | 202952816 | ||||||
chr2:202953498
|
G | GT | 137 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0030others(134): Show | 138 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(135): Show |
intron_variant | MODIFIER | c.428-488dupT | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | 202953498 | |||||
chr2:202953498
|
G | GTT | 57 | a0001c0001t0001g0120a0001c0001t0001g0161a0001c0001t0001g0177others(54): Show | 57 | HG00621.hp1 HG00642.hp1 HG00673.hp2 others(54): Show |
intron_variant | MODIFIER | c.428-489_428-488dup others(2): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | 202953498 | |||||
chr2:202953498
|
G | GTTT | 101 | a0001c0001t0002g0005a0001c0001t0002g0036a0001c0001t0002g0082others(98): Show | 104 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.428-490_428-488dup others(3): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | 202953498 | |||||
chr2:202953498
|
G | GTTTT | 23 | a0001c0001t0002g0132a0001c0001t0005g0055a0001c0001t0005g0058others(20): Show | 24 | HG00438.hp2 HG00673.hp1 HG00733.hp1 others(21): Show |
intron_variant | MODIFIER | c.428-491_428-488dup others(4): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | 202953498 | |||||
chr2:202953498
|
G | T | 1 | a0001c0001t0051g0246 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.428-507G>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 6/16 | chr2 | 202953498 | ||||||
chr2:202953576
|
A | T | 13 | a0003c0003t0016g0002a0003c0003t0016g0013a0003c0003t0016g0014others(10): Show | 14 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.428-429A>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 6/16 | chr2 | 202953576 | ||||||
chr2:202953577
|
T | C | 3 | a0001c0001t0015g0009a0001c0001t0100g0009a0001c0001t0101g0240 | 3 | HG02976.hp2 HG03139.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.428-428T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 6/16 | chr2 | 202953577 | ||||||
chr2:202953852
|
A | G | 283 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0030others(280): Show | 288 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(285): Show |
intron_variant | MODIFIER | c.428-153A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 6/16 | chr2 | 202953852 | ||||||
chr2:202953971
|
T | C | 2 | a0001c0008t0015g0243a0001c0008t0022g0242 | 2 | HG02486.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.428-34T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 6/16 | chr2 | 202953971 | ||||||
chr2:202954431
|
A | G | 1 | a0001c0001t0028g0131 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.557+297A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 7/16 | chr2 | 202954431 | ||||||
chr2:202954689
|
G | T | 1 | a0001c0001t0010g0257 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.557+555G>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 7/16 | chr2 | 202954689 | ||||||
chr2:202954710
|
TA | T | 18 | a0001c0001t0001g0170a0001c0001t0001g0200a0001c0001t0001g0213others(15): Show | 18 | HG00323.hp2 HG00642.hp1 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.557+593delA | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 202954710 | |||||
chr2:202954748
|
A | G | 13 | a0003c0003t0016g0002a0003c0003t0016g0013a0003c0003t0016g0014others(10): Show | 14 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.557+614A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 7/16 | chr2 | 202954748 | ||||||
chr2:202954764
|
C | T | 1 | a0001c0001t0027g0050 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.557+630C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 7/16 | chr2 | 202954764 | ||||||
chr2:202954800
|
G | A | 1 | a0001c0001t0001g0213 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.557+666G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 7/16 | chr2 | 202954800 | ||||||
chr2:202954826
|
G | A | 1 | a0002c0002t0105g0321 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.557+692G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 7/16 | chr2 | 202954826 | ||||||
chr2:202954963
|
G | A | 1 | a0003c0013t0119g0010 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.558-711G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 7/16 | chr2 | 202954963 | ||||||
chr2:202955052
|
A | T | 282 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0030others(279): Show | 287 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(284): Show |
intron_variant | MODIFIER | c.558-622A>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 7/16 | chr2 | 202955052 | ||||||
chr2:202955054
|
ATTTGT | A | 7 | a0004c0004t0019g0277a0004c0004t0019g0279a0004c0004t0019g0287others(4): Show | 7 | HG02129.hp2 HG02132.hp1 NA18968.hp2 others(4): Show |
intron_variant | MODIFIER | c.558-616_558-612del others(5): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 202955054 | |||||
chr2:202955296
|
A | G | 3 | a0001c0001t0041g0185a0001c0001t0041g0186a0001c0001t0108g0190 | 3 | NA18962.hp1 NA18986.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.558-378A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 7/16 | chr2 | 202955296 | ||||||
chr2:202955476
|
T | C | 24 | a0001c0001t0001g0054a0001c0001t0001g0094a0001c0001t0001g0095others(21): Show | 24 | HG00408.hp1 HG00544.hp2 HG00621.hp2 others(21): Show |
intron_variant | MODIFIER | c.558-198T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 7/16 | chr2 | 202955476 | ||||||
chr2:202955552
|
T | C | 114 | a0001c0001t0002g0005a0001c0001t0002g0036a0001c0001t0002g0082others(111): Show | 117 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.558-122T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 7/16 | chr2 | 202955552 | ||||||
chr2:202955574
|
A | T | 1 | a0001c0001t0005g0110 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.558-100A>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 7/16 | chr2 | 202955574 | ||||||
chr2:202955825
|
C | G | 4 | a0001c0001t0004g0156a0001c0001t0006g0152a0001c0001t0006g0153others(1): Show | 4 | HG01257.hp2 HG01258.hp1 HG02293.hp2 others(1): Show |
intron_variant | MODIFIER | c.642+67C>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 8/16 | chr2 | 202955825 | ||||||
chr2:202955863
|
T | C | 1 | a0001c0001t0003g0231 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.642+105T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 8/16 | chr2 | 202955863 | ||||||
chr2:202955901
|
T | C | 1 | a0001c0005t0092g0146 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.642+143T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 8/16 | chr2 | 202955901 | ||||||
chr2:202956200
|
T | C | 4 | a0003c0003t0016g0002a0003c0003t0016g0013a0003c0003t0016g0014others(1): Show | 4 | HG00735.hp1 HG01099.hp2 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.642+442T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 8/16 | chr2 | 202956200 | ||||||
chr2:202956261
|
T | G | 6 | a0001c0001t0030g0192a0001c0001t0030g0194a0001c0001t0030g0195others(3): Show | 6 | NA18951.hp1 NA18968.hp1 NA18993.hp2 others(3): Show |
intron_variant | MODIFIER | c.642+503T>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 8/16 | chr2 | 202956261 | ||||||
chr2:202956539
|
C | T | 2 | a0001c0001t0001g0211a0001c0001t0006g0060 | 2 | HG00621.hp1 NA18939.hp2 |
intron_variant | MODIFIER | c.642+781C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 8/16 | chr2 | 202956539 | ||||||
chr2:202956542
|
C | T | 4 | a0001c0001t0010g0252a0001c0001t0013g0253a0001c0001t0032g0254others(1): Show | 4 | HG02145.hp2 HG02257.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.642+784C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 8/16 | chr2 | 202956542 | ||||||
chr2:202957017
|
G | A | 1 | a0001c0001t0009g0182 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.642+1259G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 8/16 | chr2 | 202957017 | ||||||
chr2:202957070
|
T | C | 12 | a0003c0003t0016g0002a0003c0003t0016g0013a0003c0003t0016g0014others(9): Show | 13 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.642+1312T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 8/16 | chr2 | 202957070 | ||||||
chr2:202957166
|
T | G | 23 | a0002c0002t0012g0307a0002c0002t0012g0312a0002c0002t0012g0314others(20): Show | 23 | HG00733.hp2 HG01109.hp2 HG01168.hp2 others(20): Show |
intron_variant | MODIFIER | c.642+1408T>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 8/16 | chr2 | 202957166 | ||||||
chr2:202957289
|
G | T | 1 | a0001c0001t0003g0232 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.642+1531G>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 8/16 | chr2 | 202957289 | ||||||
chr2:202957472
|
G | A | 3 | a0001c0001t0001g0094a0001c0001t0001g0197a0001c0001t0001g0198 | 3 | HG00544.hp2 NA18998.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.642+1714G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 8/16 | chr2 | 202957472 | ||||||
chr2:202957775
|
C | T | 3 | a0001c0001t0049g0282a0001c0001t0050g0281a0001c0001t0051g0246 | 3 | HG02109.hp2 HG02809.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.642+2017C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 8/16 | chr2 | 202957775 | ||||||
chr2:202957984
|
G | T | 2 | a0001c0001t0045g0063a0001c0001t0045g0098 | 2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.642+2226G>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 8/16 | chr2 | 202957984 | ||||||
chr2:202958168
|
C | G | 13 | a0003c0003t0016g0002a0003c0003t0016g0013a0003c0003t0016g0014others(10): Show | 14 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.642+2410C>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 8/16 | chr2 | 202958168 | ||||||
chr2:202958247
|
A | ATGTG | 5 | a0001c0005t0040g0147a0001c0005t0040g0325a0001c0005t0060g0145others(2): Show | 5 | HG02145.hp1 HG02451.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.642+2490_642+2491i others(6): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr2 | 202958247 | |||||
chr2:202958247
|
A | ATGTGTGT others(9): Show |
1 | a0001c0001t0035g0105 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.642+2490_642+2491i others(18): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr2 | 202958247 | |||||
chr2:202958249
|
A | ATGTG | 4 | a0001c0001t0015g0009a0001c0001t0100g0009a0001c0001t0101g0240others(1): Show | 4 | HG01884.hp2 HG02976.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.642+2519_642+2522d others(6): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr2 | 202958249 | |||||
chr2:202958249
|
A | ATGTGTG | 21 | a0001c0001t0001g0054a0001c0001t0001g0154a0001c0001t0001g0161others(18): Show | 22 | HG00621.hp2 HG00735.hp1 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.642+2517_642+2522d others(8): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr2 | 202958249 | |||||
chr2:202958249
|
A | ATGTGTGT others(1): Show |
119 | a0001c0001t0001g0007a0001c0001t0001g0094a0001c0001t0001g0095others(116): Show | 120 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(117): Show |
intron_variant | MODIFIER | c.642+2515_642+2522d others(10): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr2 | 202958249 | |||||
chr2:202958249
|
A | ATGTGTGT others(3): Show |
46 | a0001c0001t0001g0030a0001c0001t0001g0120a0001c0001t0001g0187others(43): Show | 46 | HG00323.hp2 HG00733.hp2 HG00741.hp2 others(43): Show |
intron_variant | MODIFIER | c.642+2513_642+2522d others(12): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr2 | 202958249 | |||||
chr2:202958249
|
A | ATGTGTGT others(5): Show |
21 | a0001c0001t0001g0008a0001c0001t0001g0222a0001c0001t0002g0108others(18): Show | 21 | HG00423.hp1 HG00609.hp1 HG00673.hp2 others(18): Show |
intron_variant | MODIFIER | c.642+2511_642+2522d others(14): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr2 | 202958249 | |||||
chr2:202958249
|
A | ATGTGTGT others(7): Show |
11 | a0001c0001t0002g0036a0001c0001t0002g0111a0001c0001t0005g0141others(8): Show | 11 | HG00323.hp1 HG01081.hp1 HG02148.hp1 others(8): Show |
intron_variant | MODIFIER | c.642+2509_642+2522d others(16): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr2 | 202958249 | |||||
chr2:202958249
|
A | ATGTGTGT others(9): Show |
82 | a0001c0001t0002g0005a0001c0001t0002g0082a0001c0001t0002g0085others(79): Show | 85 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.642+2507_642+2522d others(18): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr2 | 202958249 | |||||
chr2:202958249
|
A | ATGTGTGT others(11): Show |
11 | a0001c0001t0005g0055a0001c0001t0005g0068a0001c0001t0005g0070others(8): Show | 11 | HG01109.hp1 HG01346.hp1 HG01496.hp1 others(8): Show |
intron_variant | MODIFIER | c.642+2505_642+2522d others(20): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr2 | 202958249 | |||||
chr2:202958249
|
A | ATGTGTGT others(13): Show |
4 | a0001c0001t0002g0112a0001c0001t0002g0132a0001c0001t0008g0076others(1): Show | 4 | HG00741.hp1 HG01255.hp2 NA18945.hp2 others(1): Show |
intron_variant | MODIFIER | c.642+2503_642+2522d others(22): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr2 | 202958249 | |||||
chr2:202958249
|
A | G | 6 | a0001c0001t0035g0105a0001c0005t0040g0147a0001c0005t0040g0325others(3): Show | 6 | HG02145.hp1 HG02451.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.642+2491A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 8/16 | chr2 | 202958249 | ||||||
chr2:202958249
|
ATGTG | A | 3 | a0001c0001t0007g0218a0001c0001t0112g0220a0005c0006t0017g0245 | 3 | HG01943.hp2 HG01975.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.642+2519_642+2522d others(6): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr2 | 202958249 | |||||
chr2:202958350
|
G | A | 2 | a0001c0001t0001g0161a0001c0001t0001g0164 | 2 | HG02809.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.642+2592G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 8/16 | chr2 | 202958350 | ||||||
chr2:202958387
|
A | G | 1 | a0003c0013t0119g0010 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.642+2629A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 8/16 | chr2 | 202958387 | ||||||
chr2:202958677
|
C | T | 13 | a0003c0003t0016g0002a0003c0003t0016g0013a0003c0003t0016g0014others(10): Show | 14 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.643-2560C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 8/16 | chr2 | 202958677 | ||||||
chr2:202958723
|
GGTAAAAC others(3): Show |
G | 2 | a0001c0001t0003g0189a0001c0001t0006g0236 | 2 | HG02280.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.643-2511_643-2502d others(12): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr2 | 202958723 | |||||
chr2:202958819
|
C | T | 1 | a0001c0001t0009g0184 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.643-2418C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 8/16 | chr2 | 202958819 | ||||||
chr2:202958903
|
C | CA | 102 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0030others(99): Show | 103 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.643-2313dupA | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr2 | 202958903 | |||||
chr2:202958903
|
C | CAA | 6 | a0001c0001t0003g0167a0001c0001t0003g0214a0001c0001t0006g0168others(3): Show | 6 | HG01361.hp1 HG02055.hp2 HG02135.hp1 others(3): Show |
intron_variant | MODIFIER | c.643-2314_643-2313d others(4): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr2 | 202958903 | |||||
chr2:202958903
|
CA | C | 19 | a0001c0001t0001g0198a0001c0001t0005g0143a0001c0005t0040g0147others(16): Show | 20 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(17): Show |
intron_variant | MODIFIER | c.643-2313delA | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr2 | 202958903 | |||||
chr2:202958984
|
CTT | C | 115 | a0001c0001t0002g0005a0001c0001t0002g0036a0001c0001t0002g0082others(112): Show | 118 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.643-2250_643-2249d others(4): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr2 | 202958984 | |||||
chr2:202958994
|
T | C | 4 | a0001c0001t0003g0201a0001c0001t0006g0196a0001c0001t0007g0202others(1): Show | 4 | HG00408.hp1 HG02083.hp1 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.643-2243T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 8/16 | chr2 | 202958994 | ||||||
chr2:202959191
|
G | A | 2 | a0001c0001t0089g0099a0001c0001t0090g0064 | 2 | HG00642.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.643-2046G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 8/16 | chr2 | 202959191 | ||||||
chr2:202959236
|
T | TAA | 157 | a0001c0001t0002g0005a0001c0001t0002g0036a0001c0001t0002g0082others(154): Show | 161 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(158): Show |
intron_variant | MODIFIER | c.643-2000_643-1999i others(4): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr2 | 202959236 | |||||
chr2:202959533
|
C | T | 1 | a0001c0001t0006g0168 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.643-1704C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 8/16 | chr2 | 202959533 | ||||||
chr2:202959608
|
C | G | 1 | a0001c0005t0060g0145 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.643-1629C>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 8/16 | chr2 | 202959608 | ||||||
chr2:202959815
|
CA | C | 272 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0030others(269): Show | 276 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(273): Show |
intron_variant | MODIFIER | c.643-1408delA | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr2 | 202959815 | |||||
chr2:202959815
|
CAA | C | 14 | a0002c0002t0022g0304a0003c0003t0016g0002a0003c0003t0016g0013others(11): Show | 15 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.643-1409_643-1408d others(4): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr2 | 202959815 | |||||
chr2:202960051
|
A | C | 4 | a0001c0001t0030g0192a0001c0001t0030g0194a0001c0001t0030g0195others(1): Show | 4 | NA18951.hp1 NA18968.hp1 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.643-1186A>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 8/16 | chr2 | 202960051 | ||||||
chr2:202960075
|
T | C | 2 | a0001c0001t0002g0140a0001c0001t0005g0141 | 2 | HG00323.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.643-1162T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 8/16 | chr2 | 202960075 | ||||||
chr2:202960320
|
A | G | 1 | a0005c0006t0017g0245 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.643-917A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 8/16 | chr2 | 202960320 | ||||||
chr2:202960335
|
C | T | 1 | a0001c0001t0007g0031 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.643-902C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 8/16 | chr2 | 202960335 | ||||||
chr2:202960383
|
A | G | 13 | a0003c0003t0016g0002a0003c0003t0016g0013a0003c0003t0016g0014others(10): Show | 14 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.643-854A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 8/16 | chr2 | 202960383 | ||||||
chr2:202960704
|
ACCTTCCC others(1): Show |
A | 15 | a0001c0001t0049g0282a0001c0001t0050g0281a0003c0003t0016g0002others(12): Show | 16 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(13): Show |
intron_variant | MODIFIER | c.643-517_643-510del others(8): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr2 | 202960704 | |||||
chr2:202960728
|
A | G | 2 | a0001c0001t0005g0142a0001c0001t0070g0067 | 2 | HG01106.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.643-509A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 8/16 | chr2 | 202960728 | ||||||
chr2:202960779
|
T | TTCCCTCC others(1): Show |
13 | a0003c0003t0016g0002a0003c0003t0016g0013a0003c0003t0016g0014others(10): Show | 14 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.643-450_643-443dup others(8): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr2 | 202960779 | |||||
chr2:202961510
|
T | G | 1 | a0001c0001t0109g0093 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.832+84T>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 9/16 | chr2 | 202961510 | ||||||
chr2:202961673
|
G | A | 13 | a0003c0003t0016g0002a0003c0003t0016g0013a0003c0003t0016g0014others(10): Show | 14 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.832+247G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 9/16 | chr2 | 202961673 | ||||||
chr2:202961691
|
A | G | 1 | a0001c0001t0044g0207 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.832+265A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 9/16 | chr2 | 202961691 | ||||||
chr2:202961730
|
T | C | 3 | a0001c0001t0015g0009a0001c0001t0100g0009a0001c0001t0101g0240 | 3 | HG02976.hp2 HG03139.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.832+304T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 9/16 | chr2 | 202961730 | ||||||
chr2:202961825
|
T | G | 1 | a0001c0001t0017g0261 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.832+399T>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 9/16 | chr2 | 202961825 | ||||||
chr2:202962267
|
G | A | 1 | a0001c0001t0013g0272 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.832+841G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 9/16 | chr2 | 202962267 | ||||||
chr2:202962357
|
G | A | 1 | a0003c0013t0119g0010 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.832+931G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 9/16 | chr2 | 202962357 | ||||||
chr2:202962709
|
A | G | 13 | a0003c0003t0016g0002a0003c0003t0016g0013a0003c0003t0016g0014others(10): Show | 14 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.832+1283A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 9/16 | chr2 | 202962709 | ||||||
chr2:202962711
|
G | A | 1 | a0001c0001t0009g0169 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.832+1285G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 9/16 | chr2 | 202962711 | ||||||
chr2:202962712
|
T | TTTACTTT others(48): Show |
1 | a0001c0001t0009g0169 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.832+1286_832+1287i others(57): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 9/16 | chr2 | 202962712 | ||||||
chr2:202962714
|
G | A | 1 | a0001c0001t0009g0169 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.832+1288G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 9/16 | chr2 | 202962714 | ||||||
chr2:202962757
|
T | C | 13 | a0003c0003t0016g0002a0003c0003t0016g0013a0003c0003t0016g0014others(10): Show | 14 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.832+1331T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 9/16 | chr2 | 202962757 | ||||||
chr2:202962926
|
T | C | 286 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0030others(283): Show | 291 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(288): Show |
intron_variant | MODIFIER | c.832+1500T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 9/16 | chr2 | 202962926 | ||||||
chr2:202962952
|
C | G | 13 | a0003c0003t0016g0002a0003c0003t0016g0013a0003c0003t0016g0014others(10): Show | 14 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.832+1526C>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 9/16 | chr2 | 202962952 | ||||||
chr2:202962967
|
T | TA | 13 | a0003c0003t0016g0002a0003c0003t0016g0013a0003c0003t0016g0014others(10): Show | 14 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.832+1544dupA | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr2 | 202962967 | |||||
chr2:202963280
|
T | C | 1 | a0006c0010t0107g0026 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.832+1854T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 9/16 | chr2 | 202963280 | ||||||
chr2:202963315
|
CA | C | 251 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0030others(248): Show | 256 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(253): Show |
intron_variant | MODIFIER | c.832+1907delA | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr2 | 202963315 | |||||
chr2:202963416
|
G | T | 1 | a0002c0002t0059g0324 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.832+1990G>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 9/16 | chr2 | 202963416 | ||||||
chr2:202963469
|
G | A | 12 | a0003c0003t0016g0002a0003c0003t0016g0013a0003c0003t0016g0014others(9): Show | 13 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.832+2043G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 9/16 | chr2 | 202963469 | ||||||
chr2:202963905
|
C | T | 1 | a0001c0001t0003g0167 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.832+2479C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 9/16 | chr2 | 202963905 | ||||||
chr2:202964074
|
T | TATAA | 13 | a0003c0003t0016g0002a0003c0003t0016g0013a0003c0003t0016g0014others(10): Show | 14 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.832+2649_832+2652d others(6): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr2 | 202964074 | |||||
chr2:202964138
|
A | C | 1 | a0001c0001t0002g0125 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.832+2712A>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 9/16 | chr2 | 202964138 | ||||||
chr2:202964175
|
T | C | 1 | a0001c0001t0079g0071 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.832+2749T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 9/16 | chr2 | 202964175 | ||||||
chr2:202964183
|
A | G | 5 | a0001c0001t0009g0184a0001c0001t0041g0185a0001c0001t0041g0186others(2): Show | 5 | NA18962.hp1 NA18986.hp2 NA19066.hp2 others(2): Show |
intron_variant | MODIFIER | c.832+2757A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 9/16 | chr2 | 202964183 | ||||||
chr2:202964210
|
G | A | 5 | a0001c0005t0040g0147a0001c0005t0040g0325a0001c0005t0060g0145others(2): Show | 5 | HG02145.hp1 HG02451.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.833-2768G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 9/16 | chr2 | 202964210 | ||||||
chr2:202964270
|
C | CTTTG | 23 | a0002c0002t0012g0307a0002c0002t0012g0312a0002c0002t0012g0314others(20): Show | 23 | HG00733.hp2 HG01109.hp2 HG01168.hp2 others(20): Show |
intron_variant | MODIFIER | c.833-2688_833-2685d others(6): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr2 | 202964270 | |||||
chr2:202964294
|
T | G | 2 | a0001c0008t0015g0243a0001c0008t0022g0242 | 2 | HG02486.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.833-2684T>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 9/16 | chr2 | 202964294 | ||||||
chr2:202964301
|
T | A | 285 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0030others(282): Show | 290 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(287): Show |
intron_variant | MODIFIER | c.833-2677T>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 9/16 | chr2 | 202964301 | ||||||
chr2:202964303
|
G | A | 1 | a0001c0001t0035g0101 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.833-2675G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 9/16 | chr2 | 202964303 | ||||||
chr2:202964502
|
A | C | 13 | a0003c0003t0016g0002a0003c0003t0016g0013a0003c0003t0016g0014others(10): Show | 14 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.833-2476A>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 9/16 | chr2 | 202964502 | ||||||
chr2:202964561
|
A | G | 13 | a0003c0003t0016g0002a0003c0003t0016g0013a0003c0003t0016g0014others(10): Show | 14 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.833-2417A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 9/16 | chr2 | 202964561 | ||||||
chr2:202964601
|
C | A | 2 | a0001c0001t0045g0063a0001c0001t0045g0098 | 2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.833-2377C>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 9/16 | chr2 | 202964601 | ||||||
chr2:202964859
|
T | TTA | 17 | a0001c0001t0010g0252a0001c0001t0013g0253a0001c0001t0032g0254others(14): Show | 18 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(15): Show |
intron_variant | MODIFIER | c.833-2106_833-2105d others(4): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr2 | 202964859 | |||||
chr2:202964883
|
G | GTA | 29 | a0001c0001t0001g0030a0001c0001t0001g0187a0001c0001t0002g0140others(26): Show | 31 | HG00323.hp1 HG00438.hp2 HG00735.hp1 others(28): Show |
intron_variant | MODIFIER | c.833-2078_833-2077d others(4): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr2 | 202964883 | |||||
chr2:202964883
|
G | GTATA | 94 | a0001c0001t0002g0005a0001c0001t0002g0036a0001c0001t0002g0082others(91): Show | 96 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.833-2080_833-2077d others(6): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr2 | 202964883 | |||||
chr2:202964883
|
G | GTATATA | 3 | a0001c0001t0002g0127a0001c0001t0077g0042a0001c0001t0085g0020 | 3 | HG01081.hp1 HG02080.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.833-2082_833-2077d others(8): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr2 | 202964883 | |||||
chr2:202964883
|
GTA | G | 24 | a0001c0001t0045g0098a0002c0002t0012g0307a0002c0002t0012g0312others(21): Show | 24 | HG00733.hp2 HG01109.hp2 HG01168.hp2 others(21): Show |
intron_variant | MODIFIER | c.833-2078_833-2077d others(4): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr2 | 202964883 | |||||
chr2:202964885
|
A | G | 1 | a0001c0001t0011g0203 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.833-2093A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 9/16 | chr2 | 202964885 | ||||||
chr2:202964900
|
T | C | 3 | a0005c0006t0017g0245a0005c0006t0057g0259a0005c0006t0058g0248 | 3 | HG02257.hp2 HG02622.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.833-2078T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 9/16 | chr2 | 202964900 | ||||||
chr2:202964900
|
T | TATAC | 6 | a0001c0001t0037g0084a0001c0001t0037g0135a0001c0001t0067g0124others(3): Show | 6 | HG01361.hp2 HG02055.hp1 HG02273.hp2 others(3): Show |
intron_variant | MODIFIER | c.833-2077_833-2076i others(6): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr2 | 202964900 | |||||
chr2:202964902
|
C | T | 3 | a0001c0001t0001g0211a0001c0001t0006g0060a0003c0013t0119g0010 | 3 | HG00621.hp1 HG01884.hp2 NA18939.hp2 |
intron_variant | MODIFIER | c.833-2076C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 9/16 | chr2 | 202964902 | ||||||
chr2:202964950
|
A | G | 1 | a0001c0001t0005g0055 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.833-2028A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 9/16 | chr2 | 202964950 | ||||||
chr2:202965505
|
T | C | 13 | a0003c0003t0016g0002a0003c0003t0016g0013a0003c0003t0016g0014others(10): Show | 14 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.833-1473T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 9/16 | chr2 | 202965505 | ||||||
chr2:202965666
|
G | A | 1 | a0001c0001t0076g0037 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.833-1312G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 9/16 | chr2 | 202965666 | ||||||
chr2:202965921
|
A | G | 1 | a0006c0010t0107g0026 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.833-1057A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 9/16 | chr2 | 202965921 | ||||||
chr2:202966073
|
A | C | 289 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0030others(286): Show | 294 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(291): Show |
intron_variant | MODIFIER | c.833-905A>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 9/16 | chr2 | 202966073 | ||||||
chr2:202966104
|
A | G | 1 | a0001c0001t0013g0251 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.833-874A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 9/16 | chr2 | 202966104 | ||||||
chr2:202966128
|
A | G | 13 | a0003c0003t0016g0002a0003c0003t0016g0013a0003c0003t0016g0014others(10): Show | 14 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.833-850A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 9/16 | chr2 | 202966128 | ||||||
chr2:202966253
|
T | C | 3 | a0003c0003t0016g0002a0003c0003t0016g0014a0003c0003t0116g0002 | 3 | HG00735.hp1 HG01099.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.833-725T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 9/16 | chr2 | 202966253 | ||||||
chr2:202966299
|
G | A | 1 | a0001c0001t0006g0244 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.833-679G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 9/16 | chr2 | 202966299 | ||||||
chr2:202966442
|
G | T | 1 | a0001c0001t0072g0119 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.833-536G>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 9/16 | chr2 | 202966442 | ||||||
chr2:202966489
|
T | A | 13 | a0003c0003t0016g0002a0003c0003t0016g0013a0003c0003t0016g0014others(10): Show | 14 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.833-489T>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 9/16 | chr2 | 202966489 | ||||||
chr2:202966529
|
A | T | 13 | a0003c0003t0016g0002a0003c0003t0016g0013a0003c0003t0016g0014others(10): Show | 14 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.833-449A>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 9/16 | chr2 | 202966529 | ||||||
chr2:202966629
|
G | A | 125 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0030others(122): Show | 126 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(123): Show |
intron_variant | MODIFIER | c.833-349G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 9/16 | chr2 | 202966629 | ||||||
chr2:202966692
|
A | T | 1 | a0002c0002t0012g0319 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.833-286A>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 9/16 | chr2 | 202966692 | ||||||
chr2:202966723
|
T | A | 2 | a0001c0001t0049g0282a0001c0001t0050g0281 | 2 | HG02109.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.833-255T>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 9/16 | chr2 | 202966723 | ||||||
chr2:202966918
|
T | C | 5 | a0001c0005t0040g0147a0001c0005t0040g0325a0001c0005t0060g0145others(2): Show | 5 | HG02145.hp1 HG02451.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.833-60T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 9/16 | chr2 | 202966918 | ||||||
chr2:202967397
|
A | G | 8 | a0003c0003t0016g0002a0003c0003t0016g0013a0003c0003t0016g0014others(5): Show | 9 | HG00735.hp1 HG00738.hp2 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.953+299A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 10/16 | chr2 | 202967397 | ||||||
chr2:202967563
|
A | G | 3 | a0001c0001t0015g0009a0001c0001t0100g0009a0001c0001t0101g0240 | 3 | HG02976.hp2 HG03139.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.953+465A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 10/16 | chr2 | 202967563 | ||||||
chr2:202967850
|
T | C | 286 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0030others(283): Show | 291 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(288): Show |
intron_variant | MODIFIER | c.953+752T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 10/16 | chr2 | 202967850 | ||||||
chr2:202967851
|
G | A | 23 | a0002c0002t0012g0307a0002c0002t0012g0312a0002c0002t0012g0314others(20): Show | 23 | HG00733.hp2 HG01109.hp2 HG01168.hp2 others(20): Show |
intron_variant | MODIFIER | c.953+753G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 10/16 | chr2 | 202967851 | ||||||
chr2:202968102
|
A | G | 1 | a0001c0005t0092g0146 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.953+1004A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 10/16 | chr2 | 202968102 | ||||||
chr2:202968144
|
C | T | 4 | a0003c0003t0016g0002a0003c0003t0016g0013a0003c0003t0016g0014others(1): Show | 4 | HG00735.hp1 HG01099.hp2 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.953+1046C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 10/16 | chr2 | 202968144 | ||||||
chr2:202968158
|
C | G | 1 | a0001c0001t0077g0042 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.953+1060C>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 10/16 | chr2 | 202968158 | ||||||
chr2:202968160
|
T | C | 1 | a0001c0001t0051g0246 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.953+1062T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 10/16 | chr2 | 202968160 | ||||||
chr2:202968178
|
C | T | 1 | a0001c0001t0080g0052 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.953+1080C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 10/16 | chr2 | 202968178 | ||||||
chr2:202968179
|
G | A | 1 | a0001c0001t0003g0059 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.953+1081G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 10/16 | chr2 | 202968179 | ||||||
chr2:202968246
|
C | T | 1 | a0004c0004t0019g0277 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.953+1148C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 10/16 | chr2 | 202968246 | ||||||
chr2:202968295
|
G | A | 12 | a0003c0003t0016g0002a0003c0003t0016g0013a0003c0003t0016g0014others(9): Show | 13 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.953+1197G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 10/16 | chr2 | 202968295 | ||||||
chr2:202968767
|
C | T | 2 | a0005c0006t0057g0259a0005c0006t0058g0248 | 2 | HG02257.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.954-1152C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 10/16 | chr2 | 202968767 | ||||||
chr2:202969110
|
T | G | 2 | a0001c0001t0029g0300a0001c0001t0029g0301 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.954-809T>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 10/16 | chr2 | 202969110 | ||||||
chr2:202969116
|
C | G | 1 | a0001c0001t0104g0173 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.954-803C>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 10/16 | chr2 | 202969116 | ||||||
chr2:202969154
|
A | G | 13 | a0003c0003t0016g0002a0003c0003t0016g0013a0003c0003t0016g0014others(10): Show | 14 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.954-765A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 10/16 | chr2 | 202969154 | ||||||
chr2:202969250
|
G | T | 1 | a0001c0001t0010g0267 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.954-669G>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 10/16 | chr2 | 202969250 | ||||||
chr2:202969578
|
A | AAAAT | 3 | a0002c0002t0022g0308a0002c0002t0059g0324a0002c0002t0097g0320 | 3 | HG02559.hp1 HG03195.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.954-302_954-299dup others(4): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr2 | 202969578 | |||||
chr2:202969578
|
AAAAT | A | 272 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0030others(269): Show | 276 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(273): Show |
intron_variant | MODIFIER | c.954-302_954-299del others(4): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr2 | 202969578 | |||||
chr2:202969578
|
AAAATAAA others(9): Show |
A | 19 | a0002c0002t0012g0307a0002c0002t0012g0312a0002c0002t0012g0314others(16): Show | 19 | HG00733.hp2 HG01109.hp2 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.954-314_954-299del others(16): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr2 | 202969578 | |||||
chr2:202969578
|
AAAATAAA others(13): Show |
A | 9 | a0001c0001t0001g0154a0001c0001t0003g0155a0001c0001t0004g0053others(6): Show | 9 | HG01257.hp2 HG01258.hp1 HG02040.hp2 others(6): Show |
intron_variant | MODIFIER | c.954-318_954-299del others(20): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr2 | 202969578 | |||||
chr2:202969578
|
AAAATAAA others(17): Show |
A | 2 | a0001c0001t0078g0072a0001c0001t0082g0114 | 2 | NA19001.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.954-322_954-299del others(24): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr2 | 202969578 | |||||
chr2:202969617
|
A | G | 7 | a0001c0001t0002g0090a0001c0001t0002g0138a0001c0001t0002g0139others(4): Show | 7 | HG00438.hp1 HG00609.hp2 HG02071.hp1 others(4): Show |
intron_variant | MODIFIER | c.954-302A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 10/16 | chr2 | 202969617 | ||||||
chr2:202969673
|
A | C | 23 | a0002c0002t0012g0307a0002c0002t0012g0312a0002c0002t0012g0314others(20): Show | 23 | HG00733.hp2 HG01109.hp2 HG01168.hp2 others(20): Show |
intron_variant | MODIFIER | c.954-246A>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 10/16 | chr2 | 202969673 | ||||||
chr2:202969678
|
C | G | 285 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0030others(282): Show | 290 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(287): Show |
intron_variant | MODIFIER | c.954-241C>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 10/16 | chr2 | 202969678 | ||||||
chr2:202969913
|
A | T | 2 | a0001c0001t0001g0161a0001c0001t0001g0164 | 2 | HG02809.hp1 NA19240.hp1 |
splice_region_variant&intron_variant | LOW | c.954-6A>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 10/16 | chr2 | 202969913 | ||||||
chr2:202970346
|
A | G | 1 | a0003c0013t0119g0010 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1097+284A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 11/16 | chr2 | 202970346 | ||||||
chr2:202970421
|
C | T | 1 | a0001c0001t0013g0272 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1097+359C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 11/16 | chr2 | 202970421 | ||||||
chr2:202970454
|
A | C | 12 | a0003c0003t0016g0002a0003c0003t0016g0013a0003c0003t0016g0014others(9): Show | 13 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.1097+392A>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 11/16 | chr2 | 202970454 | ||||||
chr2:202970624
|
G | A | 1 | a0001c0001t0001g0289 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1097+562G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 11/16 | chr2 | 202970624 | ||||||
chr2:202970723
|
A | G | 1 | a0001c0001t0072g0119 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1097+661A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 11/16 | chr2 | 202970723 | ||||||
chr2:202970892
|
T | A | 24 | a0001c0001t0001g0054a0001c0001t0001g0094a0001c0001t0001g0095others(21): Show | 24 | HG00408.hp1 HG00544.hp2 HG00621.hp2 others(21): Show |
intron_variant | MODIFIER | c.1098-613T>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 11/16 | chr2 | 202970892 | ||||||
chr2:202971067
|
C | T | 1 | a0001c0001t0038g0056 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1098-438C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 11/16 | chr2 | 202971067 | ||||||
chr2:202971187
|
T | C | 2 | a0001c0001t0002g0139a0001c0001t0075g0137 | 2 | HG00609.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.1098-318T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 11/16 | chr2 | 202971187 | ||||||
chr2:202971745
|
T | C | 3 | a0001c0001t0015g0009a0001c0001t0100g0009a0001c0001t0101g0240 | 3 | HG02976.hp2 HG03139.hp1 NA20300.hp1 |
splice_region_variant&intron_variant | LOW | c.1331+7T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 12/16 | chr2 | 202971745 | ||||||
chr2:202971784
|
G | C | 12 | a0003c0003t0016g0002a0003c0003t0016g0013a0003c0003t0016g0014others(9): Show | 13 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.1331+46G>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 12/16 | chr2 | 202971784 | ||||||
chr2:202971914
|
C | T | 2 | a0001c0001t0004g0238a0001c0001t0006g0239 | 2 | NA18969.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.1331+176C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 12/16 | chr2 | 202971914 | ||||||
chr2:202972474
|
C | G | 1 | a0001c0001t0002g0108 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1331+736C>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 12/16 | chr2 | 202972474 | ||||||
chr2:202972475
|
G | A | 1 | a0001c0001t0103g0292 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1331+737G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 12/16 | chr2 | 202972475 | ||||||
chr2:202972674
|
T | TA | 14 | a0001c0001t0001g0198a0001c0001t0001g0200a0001c0001t0004g0053others(11): Show | 14 | HG01109.hp2 HG01168.hp2 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.1331+957dupA | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr2 | 202972674 | |||||
chr2:202972674
|
T | TAA | 98 | a0001c0001t0001g0164a0001c0001t0001g0177a0001c0001t0002g0005others(95): Show | 101 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.1331+956_1331+957d others(4): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr2 | 202972674 | |||||
chr2:202972674
|
T | TAAA | 103 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0030others(100): Show | 104 | HG00323.hp2 HG00423.hp1 HG00597.hp1 others(101): Show |
intron_variant | MODIFIER | c.1331+955_1331+957d others(5): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr2 | 202972674 | |||||
chr2:202972674
|
T | TAAAA | 6 | a0001c0001t0001g0222a0001c0001t0003g0181a0001c0001t0003g0214others(3): Show | 6 | HG02055.hp2 HG02056.hp2 HG03688.hp2 others(3): Show |
intron_variant | MODIFIER | c.1331+954_1331+957d others(6): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr2 | 202972674 | |||||
chr2:202972674
|
TA | T | 13 | a0003c0003t0016g0002a0003c0003t0016g0013a0003c0003t0016g0014others(10): Show | 14 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.1331+957delA | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr2 | 202972674 | |||||
chr2:202972674
|
TAAAAAAA others(5): Show |
T | 2 | a0001c0001t0014g0113a0001c0001t0088g0065 | 2 | HG02602.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1331+946_1331+957d others(14): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr2 | 202972674 | |||||
chr2:202972850
|
G | T | 13 | a0003c0003t0016g0002a0003c0003t0016g0013a0003c0003t0016g0014others(10): Show | 14 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.1331+1112G>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 12/16 | chr2 | 202972850 | ||||||
chr2:202972896
|
T | A | 1 | a0006c0010t0107g0026 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1331+1158T>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 12/16 | chr2 | 202972896 | ||||||
chr2:202972945
|
A | T | 1 | a0004c0004t0034g0276 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1331+1207A>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 12/16 | chr2 | 202972945 | ||||||
chr2:202972951
|
T | C | 2 | a0001c0001t0045g0063a0001c0001t0045g0098 | 2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1331+1213T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 12/16 | chr2 | 202972951 | ||||||
chr2:202973022
|
C | G | 2 | a0001c0001t0089g0099a0001c0001t0090g0064 | 2 | HG00642.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.1331+1284C>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 12/16 | chr2 | 202973022 | ||||||
chr2:202973452
|
A | G | 4 | a0001c0001t0008g0076a0001c0001t0008g0077a0001c0001t0008g0080others(1): Show | 4 | HG00735.hp2 HG00741.hp1 HG01106.hp1 others(1): Show |
intron_variant | MODIFIER | c.1332-882A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 12/16 | chr2 | 202973452 | ||||||
chr2:202973579
|
T | C | 2 | a0001c0001t0045g0063a0001c0001t0045g0098 | 2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1332-755T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 12/16 | chr2 | 202973579 | ||||||
chr2:202973669
|
A | G | 1 | a0001c0001t0007g0031 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1332-665A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 12/16 | chr2 | 202973669 | ||||||
chr2:202973825
|
C | T | 3 | a0001c0001t0015g0009a0001c0001t0100g0009a0001c0001t0101g0240 | 3 | HG02976.hp2 HG03139.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1332-509C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 12/16 | chr2 | 202973825 | ||||||
chr2:202973859
|
G | A | 19 | a0002c0002t0012g0307a0002c0002t0012g0312a0002c0002t0012g0314others(16): Show | 19 | HG00733.hp2 HG01109.hp2 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.1332-475G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 12/16 | chr2 | 202973859 | ||||||
chr2:202974238
|
T | C | 13 | a0003c0003t0016g0002a0003c0003t0016g0013a0003c0003t0016g0014others(10): Show | 14 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.1332-96T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 12/16 | chr2 | 202974238 | ||||||
chr2:202974685
|
G | A | 1 | a0001c0001t0002g0111 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1494+189G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 13/16 | chr2 | 202974685 | ||||||
chr2:202974886
|
G | A | 2 | a0001c0001t0031g0263a0001c0001t0031g0264 | 2 | HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1494+390G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 13/16 | chr2 | 202974886 | ||||||
chr2:202974903
|
A | AAT | 5 | a0001c0001t0005g0069a0001c0001t0005g0142a0001c0001t0005g0143others(2): Show | 5 | HG01106.hp2 HG01167.hp2 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.1494+419_1494+420d others(4): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr2 | 202974903 | |||||
chr2:202974905
|
T | A | 13 | a0003c0003t0016g0002a0003c0003t0016g0013a0003c0003t0016g0014others(10): Show | 14 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.1494+409T>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 13/16 | chr2 | 202974905 | ||||||
chr2:202974918
|
C | T | 1 | a0001c0001t0001g0175 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1494+422C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 13/16 | chr2 | 202974918 | ||||||
chr2:202975076
|
C | T | 23 | a0002c0002t0012g0307a0002c0002t0012g0312a0002c0002t0012g0314others(20): Show | 23 | HG00733.hp2 HG01109.hp2 HG01168.hp2 others(20): Show |
intron_variant | MODIFIER | c.1494+580C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 13/16 | chr2 | 202975076 | ||||||
chr2:202975300
|
C | T | 3 | a0002c0002t0012g0307a0002c0002t0023g0306a0002c0002t0046g0303 | 3 | HG00733.hp2 HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1494+804C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 13/16 | chr2 | 202975300 | ||||||
chr2:202975477
|
C | T | 5 | a0002c0002t0012g0307a0002c0002t0022g0304a0002c0002t0023g0306others(2): Show | 5 | HG00733.hp2 HG01109.hp2 HG01168.hp2 others(2): Show |
intron_variant | MODIFIER | c.1494+981C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 13/16 | chr2 | 202975477 | ||||||
chr2:202975842
|
C | T | 13 | a0003c0003t0016g0002a0003c0003t0016g0013a0003c0003t0016g0014others(10): Show | 14 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.1494+1346C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 13/16 | chr2 | 202975842 | ||||||
chr2:202975853
|
T | C | 1 | a0001c0001t0001g0197 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1494+1357T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 13/16 | chr2 | 202975853 | ||||||
chr2:202976028
|
G | A | 286 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0030others(283): Show | 291 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(288): Show |
intron_variant | MODIFIER | c.1495-1241G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 13/16 | chr2 | 202976028 | ||||||
chr2:202976087
|
A | C | 285 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0030others(282): Show | 290 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(287): Show |
intron_variant | MODIFIER | c.1495-1182A>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 13/16 | chr2 | 202976087 | ||||||
chr2:202976091
|
A | C | 107 | a0001c0001t0002g0005a0001c0001t0002g0036a0001c0001t0002g0082others(104): Show | 110 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.1495-1178A>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 13/16 | chr2 | 202976091 | ||||||
chr2:202976095
|
A | C | 107 | a0001c0001t0002g0005a0001c0001t0002g0036a0001c0001t0002g0082others(104): Show | 110 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.1495-1174A>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 13/16 | chr2 | 202976095 | ||||||
chr2:202976099
|
A | C | 107 | a0001c0001t0002g0005a0001c0001t0002g0036a0001c0001t0002g0082others(104): Show | 110 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.1495-1170A>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 13/16 | chr2 | 202976099 | ||||||
chr2:202976250
|
G | T | 15 | a0001c0008t0015g0243a0001c0008t0022g0242a0003c0003t0016g0002others(12): Show | 16 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(13): Show |
intron_variant | MODIFIER | c.1495-1019G>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 13/16 | chr2 | 202976250 | ||||||
chr2:202976335
|
C | T | 9 | a0001c0001t0010g0257a0001c0001t0010g0267a0001c0001t0010g0273others(6): Show | 9 | HG01257.hp1 HG01884.hp2 HG01952.hp1 others(6): Show |
intron_variant | MODIFIER | c.1495-934C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 13/16 | chr2 | 202976335 | ||||||
chr2:202976388
|
G | A | 1 | a0001c0005t0091g0043 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1495-881G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 13/16 | chr2 | 202976388 | ||||||
chr2:202976477
|
A | G | 1 | a0001c0001t0052g0266 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1495-792A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 13/16 | chr2 | 202976477 | ||||||
chr2:202976716
|
C | CT | 320 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0030others(317): Show | 325 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(322): Show |
intron_variant | MODIFIER | c.1495-538dupT | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr2 | 202976716 | |||||
chr2:202977006
|
T | A | 1 | a0001c0001t0013g0272 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1495-263T>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 13/16 | chr2 | 202977006 | ||||||
chr2:202977805
|
G | A | 1 | a0001c0001t0006g0168 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1558+473G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 14/16 | chr2 | 202977805 | ||||||
chr2:202977823
|
C | G | 1 | a0001c0001t0110g0163 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1558+491C>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 14/16 | chr2 | 202977823 | ||||||
chr2:202977938
|
C | T | 13 | a0003c0003t0016g0002a0003c0003t0016g0013a0003c0003t0016g0014others(10): Show | 14 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.1558+606C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 14/16 | chr2 | 202977938 | ||||||
chr2:202977990
|
C | T | 1 | a0001c0001t0051g0246 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1558+658C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 14/16 | chr2 | 202977990 | ||||||
chr2:202978410
|
G | T | 114 | a0001c0001t0002g0005a0001c0001t0002g0036a0001c0001t0002g0082others(111): Show | 117 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.1558+1078G>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 14/16 | chr2 | 202978410 | ||||||
chr2:202978562
|
A | G | 3 | a0001c0001t0037g0084a0001c0001t0037g0135a0001c0001t0071g0039 | 3 | HG01361.hp2 HG02273.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.1558+1230A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 14/16 | chr2 | 202978562 | ||||||
chr2:202978624
|
C | A | 1 | a0001c0001t0013g0280 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1558+1292C>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 14/16 | chr2 | 202978624 | ||||||
chr2:202979449
|
G | A | 1 | a0001c0001t0003g0189 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1559-2106G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 14/16 | chr2 | 202979449 | ||||||
chr2:202979757
|
C | T | 13 | a0003c0003t0016g0002a0003c0003t0016g0013a0003c0003t0016g0014others(10): Show | 14 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.1559-1798C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 14/16 | chr2 | 202979757 | ||||||
chr2:202979758
|
G | A | 1 | a0001c0001t0018g0283 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1559-1797G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 14/16 | chr2 | 202979758 | ||||||
chr2:202980164
|
C | T | 24 | a0001c0001t0001g0054a0001c0001t0001g0094a0001c0001t0001g0095others(21): Show | 24 | HG00408.hp1 HG00544.hp2 HG00621.hp2 others(21): Show |
intron_variant | MODIFIER | c.1559-1391C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 14/16 | chr2 | 202980164 | ||||||
chr2:202980250
|
G | C | 2 | a0005c0006t0057g0259a0005c0006t0058g0248 | 2 | HG02257.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1559-1305G>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 14/16 | chr2 | 202980250 | ||||||
chr2:202980578
|
A | C | 100 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0030others(97): Show | 101 | HG00323.hp2 HG00423.hp1 HG00597.hp1 others(98): Show |
intron_variant | MODIFIER | c.1559-977A>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 14/16 | chr2 | 202980578 | ||||||
chr2:202980616
|
G | GTA | 14 | a0001c0001t0004g0053a0001c0001t0005g0058a0001c0001t0010g0252others(11): Show | 14 | HG01109.hp2 HG01361.hp2 HG01952.hp1 others(11): Show |
intron_variant | MODIFIER | c.1559-894_1559-893d others(4): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr2 | 202980616 | |||||
chr2:202980616
|
G | GTATA | 15 | a0001c0001t0001g0199a0001c0001t0001g0216a0001c0001t0002g0125others(12): Show | 16 | HG00738.hp1 HG01109.hp1 HG01256.hp1 others(13): Show |
intron_variant | MODIFIER | c.1559-896_1559-893d others(6): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr2 | 202980616 | |||||
chr2:202980616
|
G | GTATATA | 34 | a0001c0001t0001g0120a0001c0001t0001g0154a0001c0001t0001g0198others(31): Show | 34 | HG00423.hp2 HG00733.hp1 HG01168.hp2 others(31): Show |
intron_variant | MODIFIER | c.1559-898_1559-893d others(8): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr2 | 202980616 | |||||
chr2:202980616
|
G | GTATATAT others(1): Show |
41 | a0001c0001t0001g0054a0001c0001t0001g0095a0001c0001t0001g0200others(38): Show | 41 | HG00408.hp2 HG00621.hp2 HG00673.hp1 others(38): Show |
intron_variant | MODIFIER | c.1559-900_1559-893d others(10): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr2 | 202980616 | |||||
chr2:202980616
|
G | GTATATAT others(3): Show |
32 | a0001c0001t0001g0197a0001c0001t0002g0108a0001c0001t0002g0139others(29): Show | 32 | HG00544.hp1 HG00609.hp2 HG00733.hp2 others(29): Show |
intron_variant | MODIFIER | c.1559-902_1559-893d others(12): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr2 | 202980616 | |||||
chr2:202980616
|
G | GTATATAT others(5): Show |
22 | a0001c0001t0001g0289a0001c0001t0002g0090a0001c0001t0002g0111others(19): Show | 22 | HG01167.hp2 HG01169.hp2 HG01358.hp2 others(19): Show |
intron_variant | MODIFIER | c.1559-904_1559-893d others(14): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr2 | 202980616 | |||||
chr2:202980616
|
G | GTATATAT others(7): Show |
11 | a0001c0001t0002g0088a0001c0001t0006g0196a0001c0001t0008g0296others(8): Show | 11 | HG00408.hp1 HG00642.hp2 HG02148.hp2 others(8): Show |
intron_variant | MODIFIER | c.1559-906_1559-893d others(16): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr2 | 202980616 | |||||
chr2:202980616
|
G | GTATATAT others(9): Show |
3 | a0001c0001t0001g0094a0001c0001t0064g0081a0001c0001t0074g0057 | 3 | HG00438.hp1 HG00544.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.1559-908_1559-893d others(18): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr2 | 202980616 | |||||
chr2:202980616
|
G | GTATATAT others(11): Show |
6 | a0001c0001t0003g0214a0001c0001t0005g0069a0001c0001t0006g0236others(3): Show | 6 | HG01175.hp2 HG02055.hp2 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.1559-910_1559-893d others(20): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr2 | 202980616 | |||||
chr2:202980616
|
G | GTATATAT others(13): Show |
4 | a0001c0001t0002g0138a0001c0001t0003g0189a0001c0001t0009g0157others(1): Show | 4 | HG03516.hp1 NA18948.hp2 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.1559-912_1559-893d others(22): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr2 | 202980616 | |||||
chr2:202980616
|
G | GTATATAT others(15): Show |
1 | a0001c0001t0009g0182 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1559-914_1559-893d others(24): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr2 | 202980616 | |||||
chr2:202980616
|
G | GTATATAT others(47): Show |
1 | a0001c0001t0045g0063 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1559-893_1559-892i others(56): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr2 | 202980616 | |||||
chr2:202980616
|
GTA | G | 8 | a0001c0001t0001g0161a0001c0001t0001g0164a0001c0001t0009g0215others(5): Show | 8 | HG01981.hp2 HG02602.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.1559-894_1559-893d others(4): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr2 | 202980616 | |||||
chr2:202980616
|
GTATA | G | 10 | a0001c0001t0002g0036a0001c0001t0029g0300a0001c0001t0029g0301others(7): Show | 11 | HG01515.hp2 HG01517.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.1559-896_1559-893d others(6): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr2 | 202980616 | |||||
chr2:202980616
|
GTATATAT others(1): Show |
G | 3 | a0001c0001t0002g0133a0001c0001t0009g0212a0002c0002t0015g0323 | 3 | HG00642.hp1 HG03516.hp2 NA18939.hp1 |
intron_variant | MODIFIER | c.1559-900_1559-893d others(10): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr2 | 202980616 | |||||
chr2:202980616
|
GTATATAT others(3): Show |
G | 3 | a0001c0001t0001g0170a0001c0001t0002g0112a0001c0001t0076g0037 | 3 | HG01255.hp2 HG01346.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.1559-902_1559-893d others(12): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr2 | 202980616 | |||||
chr2:202980616
|
GTATATAT others(5): Show |
G | 7 | a0001c0001t0002g0005a0001c0001t0002g0087a0001c0001t0002g0129others(4): Show | 8 | HG00438.hp2 HG02083.hp2 NA18984.hp2 others(5): Show |
intron_variant | MODIFIER | c.1559-904_1559-893d others(14): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr2 | 202980616 | |||||
chr2:202980616
|
GTATATAT others(7): Show |
G | 2 | a0001c0001t0002g0121a0001c0001t0013g0280 | 2 | HG01975.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.1559-906_1559-893d others(16): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr2 | 202980616 | |||||
chr2:202980616
|
GTATATAT others(9): Show |
G | 5 | a0001c0001t0015g0009a0001c0001t0100g0009a0001c0001t0101g0240others(2): Show | 5 | HG02572.hp2 HG02976.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1559-908_1559-893d others(18): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr2 | 202980616 | |||||
chr2:202980616
|
GTATATAT others(11): Show |
G | 13 | a0001c0001t0002g0085a0001c0001t0002g0127a0003c0003t0016g0002others(10): Show | 14 | HG00735.hp1 HG00738.hp2 HG01099.hp2 others(11): Show |
intron_variant | MODIFIER | c.1559-910_1559-893d others(20): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr2 | 202980616 | |||||
chr2:202980616
|
GTATATAT others(15): Show |
G | 2 | a0001c0001t0042g0298a0001c0001t0042g0299 | 2 | HG02258.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1559-914_1559-893d others(24): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr2 | 202980616 | |||||
chr2:202980616
|
GTATATAT others(19): Show |
G | 1 | a0001c0001t0002g0140 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1559-918_1559-893d others(28): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr2 | 202980616 | |||||
chr2:202980616
|
GTATATAT others(21): Show |
G | 74 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0030others(71): Show | 75 | HG00323.hp2 HG00423.hp1 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.1559-920_1559-893d others(30): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr2 | 202980616 | |||||
chr2:202980616
|
GTATATAT others(23): Show |
G | 2 | a0001c0001t0095g0225a0001c0001t0096g0097 | 2 | HG00673.hp2 NA18946.hp1 |
intron_variant | MODIFIER | c.1559-922_1559-893d others(32): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr2 | 202980616 | |||||
chr2:202980616
|
GTATATAT others(29): Show |
G | 1 | a0006c0010t0107g0026 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1559-928_1559-893d others(38): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr2 | 202980616 | |||||
chr2:202980623
|
T | TATATATA others(4): Show |
1 | a0001c0001t0006g0159 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1559-931_1559-921d others(13): Show |
CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr2 | 202980623 | |||||
chr2:202980629
|
T | G | 2 | a0003c0009t0016g0015a0003c0009t0117g0019 | 2 | HG00438.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.1559-926T>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 14/16 | chr2 | 202980629 | ||||||
chr2:202980630
|
A | T | 2 | a0003c0009t0016g0015a0003c0009t0117g0019 | 2 | HG00438.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.1559-925A>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 14/16 | chr2 | 202980630 | ||||||
chr2:202980631
|
T | G | 1 | a0001c0001t0013g0280 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1559-924T>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 14/16 | chr2 | 202980631 | ||||||
chr2:202980632
|
A | T | 1 | a0001c0001t0013g0280 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1559-923A>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 14/16 | chr2 | 202980632 | ||||||
chr2:202980635
|
T | G | 11 | a0003c0003t0016g0002a0003c0003t0016g0013a0003c0003t0016g0014others(8): Show | 12 | HG00735.hp1 HG00738.hp2 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.1559-920T>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 14/16 | chr2 | 202980635 | ||||||
chr2:202980636
|
A | T | 11 | a0003c0003t0016g0002a0003c0003t0016g0013a0003c0003t0016g0014others(8): Show | 12 | HG00735.hp1 HG00738.hp2 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.1559-919A>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 14/16 | chr2 | 202980636 | ||||||
chr2:202980661
|
T | C | 1 | a0005c0006t0057g0259 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1559-894T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 14/16 | chr2 | 202980661 | ||||||
chr2:202980808
|
T | G | 2 | a0001c0001t0042g0298a0001c0001t0042g0299 | 2 | HG02258.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1559-747T>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 14/16 | chr2 | 202980808 | ||||||
chr2:202980923
|
T | C | 284 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0030others(281): Show | 289 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(286): Show |
intron_variant | MODIFIER | c.1559-632T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 14/16 | chr2 | 202980923 | ||||||
chr2:202981105
|
A | G | 13 | a0003c0003t0016g0002a0003c0003t0016g0013a0003c0003t0016g0014others(10): Show | 14 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.1559-450A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 14/16 | chr2 | 202981105 | ||||||
chr2:202981210
|
C | A | 1 | a0001c0001t0005g0058 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1559-345C>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 14/16 | chr2 | 202981210 | ||||||
chr2:202981213
|
C | T | 1 | a0001c0001t0005g0058 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1559-342C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 14/16 | chr2 | 202981213 | ||||||
chr2:202981273
|
T | C | 13 | a0003c0003t0016g0002a0003c0003t0016g0013a0003c0003t0016g0014others(10): Show | 14 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.1559-282T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 14/16 | chr2 | 202981273 | ||||||
chr2:202981291
|
G | A | 1 | a0001c0001t0024g0038 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1559-264G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 14/16 | chr2 | 202981291 | ||||||
chr2:202981396
|
G | A | 1 | a0001c0001t0010g0257 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1559-159G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 14/16 | chr2 | 202981396 | ||||||
chr2:202981453
|
A | T | 1 | a0001c0001t0011g0227 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1559-102A>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 14/16 | chr2 | 202981453 | ||||||
chr2:202981509
|
T | C | 5 | a0001c0005t0040g0147a0001c0005t0040g0325a0001c0005t0060g0145others(2): Show | 5 | HG02145.hp1 HG02451.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1559-46T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 14/16 | chr2 | 202981509 | ||||||
chr2:202981779
|
G | A | 1 | a0001c0001t0003g0183 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1689+94G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 15/16 | chr2 | 202981779 | ||||||
chr2:202981801
|
T | C | 1 | a0003c0013t0119g0010 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1689+116T>C | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 15/16 | chr2 | 202981801 | ||||||
chr2:202981820
|
C | T | 1 | a0001c0001t0006g0196 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1689+135C>T | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 15/16 | chr2 | 202981820 | ||||||
chr2:202982051
|
G | A | 1 | a0001c0001t0045g0098 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1690-21G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 15/16 | chr2 | 202982051 | ||||||
chr2:202982602
|
C | G | 13 | a0003c0003t0016g0002a0003c0003t0016g0013a0003c0003t0016g0014others(10): Show | 14 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.2059+161C>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 16/16 | chr2 | 202982602 | ||||||
chr2:202982626
|
T | A | 1 | a0001c0001t0004g0228 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.2059+185T>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 16/16 | chr2 | 202982626 | ||||||
chr2:202982659
|
G | A | 13 | a0003c0003t0016g0002a0003c0003t0016g0013a0003c0003t0016g0014others(10): Show | 14 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.2059+218G>A | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 16/16 | chr2 | 202982659 | ||||||
chr2:202982694
|
A | G | 13 | a0003c0003t0016g0002a0003c0003t0016g0013a0003c0003t0016g0014others(10): Show | 14 | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.2059+253A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 16/16 | chr2 | 202982694 | ||||||
chr2:202983180
|
A | G | 1 | a0001c0001t0002g0132 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.2060-326A>G | CARF | ENSG00000138380.18 | transcript | ENST00000438828.4 | protein_coding | 16/16 | chr2 | 202983180 |