geneid | 9685 |
---|---|
ensemblid | ENSG00000113282.14 |
hgncid | 23186 |
symbol | CLINT1 |
name | clathrin interactor 1 |
refseq_nuc | NM_014666.4 |
refseq_prot | NP_055481.1 |
ensembl_nuc | ENST00000411809.7 |
ensembl_prot | ENSP00000388340.2 |
mane_status | MANE Select |
chr | chr5 |
start | 157785747 |
end | 157859145 |
strand | - |
ver | v1.2 |
region | chr5:157785747-157859145 |
region5000 | chr5:157780747-157864145 |
regionname0 | CLINT1_chr5_157785747_157859145 |
regionname5000 | CLINT1_chr5_157780747_157864145 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 625 | 337 | 90 | 59 | 141 | 16 | 29 | 107 | CLINT1_chr5_157780747_157864145 | CLINT1 | copy fasta | chr5 | 157780747 | 157864145 |
a0002 | 0/0 | 625 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | copy fasta | chr5 | 157780747 | 157864145 |
a0003 | 0/0 | 625 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CLINT1_chr5_157780747_157864145 | CLINT1 | copy fasta | chr5 | 157780747 | 157864145 |
a0004 | 0/0 | 625 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | copy fasta | chr5 | 157780747 | 157864145 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1878 | 321 | 74 | 59 | 141 | 16 | 29 | CLINT1_chr5_157780747_157864145 | CLINT1 | copy fasta | chr5 | 157780747 | 157864145 |
c0002 | 0/0 | 1878 | 13 | 13 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | copy fasta | chr5 | 157780747 | 157864145 |
c0003 | 0/0 | 1878 | 1 | 0 | 0 | 0 | 0 | 1 | CLINT1_chr5_157780747_157864145 | CLINT1 | copy fasta | chr5 | 157780747 | 157864145 |
c0004 | 0/0 | 1878 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | copy fasta | chr5 | 157780747 | 157864145 |
c0005 | 0/0 | 1878 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | copy fasta | chr5 | 157780747 | 157864145 |
c0006 | 0/0 | 1878 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | copy fasta | chr5 | 157780747 | 157864145 |
c0007 | 0/0 | 1878 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | copy fasta | chr5 | 157780747 | 157864145 |
c0008 | 0/0 | 1878 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | copy fasta | chr5 | 157780747 | 157864145 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 2075 | 125 | 33 | 33 | 35 | 7 | 15 | CLINT1_chr5_157780747_157864145 | CLINT1 | copy fasta | chr5 | 157780747 | 157864145 |
t0002 | 0/0 | 2075 | 105 | 10 | 19 | 60 | 7 | 9 | CLINT1_chr5_157780747_157864145 | CLINT1 | copy fasta | chr5 | 157780747 | 157864145 |
t0003 | 0/0 | 2075 | 67 | 35 | 2 | 25 | 0 | 5 | CLINT1_chr5_157780747_157864145 | CLINT1 | copy fasta | chr5 | 157780747 | 157864145 |
t0004 | 0/0 | 2075 | 28 | 7 | 5 | 13 | 2 | 1 | CLINT1_chr5_157780747_157864145 | CLINT1 | copy fasta | chr5 | 157780747 | 157864145 |
t0005 | 0/0 | 2073 | 6 | 0 | 0 | 6 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | copy fasta | chr5 | 157780747 | 157864145 |
t0006 | 0/0 | 2075 | 2 | 0 | 0 | 2 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | copy fasta | chr5 | 157780747 | 157864145 |
t0007 | 0/0 | 2075 | 2 | 2 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | copy fasta | chr5 | 157780747 | 157864145 |
t0008 | 0/0 | 2075 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | copy fasta | chr5 | 157780747 | 157864145 |
t0009 | 0/0 | 2075 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | copy fasta | chr5 | 157780747 | 157864145 |
t0010 | 0/0 | 2075 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | copy fasta | chr5 | 157780747 | 157864145 |
t0011 | 0/0 | 2075 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | copy fasta | chr5 | 157780747 | 157864145 |
t0012 | 0/0 | 2075 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | copy fasta | chr5 | 157780747 | 157864145 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0006 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0173 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0222 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0287 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0301 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0302 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0311 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1878 | 321 | 74 | 59 | 141 | 16 | 29 | CLINT1_chr5_157780747_157864145 | CLINT1 | copy fasta | chr5 | 157780747 | 157864145 |
a0001c0002 | 0/0 | 1878 | 13 | 13 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | copy fasta | chr5 | 157780747 | 157864145 |
a0001c0004 | 0/0 | 1878 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | copy fasta | chr5 | 157780747 | 157864145 |
a0001c0006 | 0/0 | 1878 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | copy fasta | chr5 | 157780747 | 157864145 |
a0001c0008 | 0/0 | 1878 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | copy fasta | chr5 | 157780747 | 157864145 |
a0002c0005 | 0/0 | 1878 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | copy fasta | chr5 | 157780747 | 157864145 |
a0003c0007 | 0/0 | 1878 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | copy fasta | chr5 | 157780747 | 157864145 |
a0004c0003 | 0/0 | 1878 | 1 | 0 | 0 | 0 | 0 | 1 | CLINT1_chr5_157780747_157864145 | CLINT1 | copy fasta | chr5 | 157780747 | 157864145 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 3952 | 122 | 32 | 32 | 35 | 7 | 14 | CLINT1_chr5_157780747_157864145 | CLINT1 | copy fasta | chr5 | 157780747 | 157864145 |
a0001c0001t0002 | 0/0 | 3952 | 104 | 9 | 19 | 60 | 7 | 9 | CLINT1_chr5_157780747_157864145 | CLINT1 | copy fasta | chr5 | 157780747 | 157864145 |
a0001c0001t0003 | 0/0 | 3952 | 52 | 21 | 2 | 24 | 0 | 5 | CLINT1_chr5_157780747_157864145 | CLINT1 | copy fasta | chr5 | 157780747 | 157864145 |
a0001c0001t0004 | 0/0 | 3952 | 28 | 7 | 5 | 13 | 2 | 1 | CLINT1_chr5_157780747_157864145 | CLINT1 | copy fasta | chr5 | 157780747 | 157864145 |
a0001c0001t0005 | 0/0 | 3950 | 6 | 0 | 0 | 6 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | copy fasta | chr5 | 157780747 | 157864145 |
a0001c0001t0006 | 0/0 | 3952 | 2 | 0 | 0 | 2 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | copy fasta | chr5 | 157780747 | 157864145 |
a0001c0001t0007 | 0/0 | 3952 | 2 | 2 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | copy fasta | chr5 | 157780747 | 157864145 |
a0001c0001t0008 | 0/0 | 3952 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | copy fasta | chr5 | 157780747 | 157864145 |
a0001c0001t0009 | 0/0 | 3952 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | copy fasta | chr5 | 157780747 | 157864145 |
a0001c0001t0010 | 0/0 | 3952 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | copy fasta | chr5 | 157780747 | 157864145 |
a0001c0001t0011 | 0/0 | 3952 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | copy fasta | chr5 | 157780747 | 157864145 |
a0001c0001t0012 | 0/0 | 3952 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | copy fasta | chr5 | 157780747 | 157864145 |
a0001c0002t0003 | 0/0 | 3952 | 13 | 13 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | copy fasta | chr5 | 157780747 | 157864145 |
a0001c0004t0003 | 0/0 | 3952 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | copy fasta | chr5 | 157780747 | 157864145 |
a0001c0006t0001 | 0/0 | 3952 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | copy fasta | chr5 | 157780747 | 157864145 |
a0001c0008t0002 | 0/0 | 3952 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | copy fasta | chr5 | 157780747 | 157864145 |
a0002c0005t0001 | 0/0 | 3952 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | copy fasta | chr5 | 157780747 | 157864145 |
a0003c0007t0003 | 0/0 | 3952 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | copy fasta | chr5 | 157780747 | 157864145 |
a0004c0003t0001 | 0/0 | 3952 | 1 | 0 | 0 | 0 | 0 | 1 | CLINT1_chr5_157780747_157864145 | CLINT1 | copy fasta | chr5 | 157780747 | 157864145 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0001g0173 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0001g0222 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0001g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0001g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0001g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0001g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0001g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0001g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0001g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0001g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0001g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0002g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0002g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0002g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0002g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0002g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0002g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0002g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0002g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0002g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0002g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0002g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0002g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0002g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0002g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0002g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0002g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0002g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0002g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0002g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0002g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0002g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0002g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0002g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0002g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0002g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0002g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0002g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0002g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0002g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0002g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0003g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0003g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0003g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0003g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0003g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0003g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0003g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0003g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0003g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0003g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0003g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0003g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0003g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0003g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0003g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0003g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0003g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0003g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0003g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0003g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0003g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0003g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0003g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0003g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0003g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0003g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0003g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0003g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0003g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0003g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0003g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0003g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0003g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0003g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0003g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0003g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0003g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0003g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0003g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0003g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0003g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0003g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0003g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0003g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0003g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0003g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0003g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0004g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0004g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0004g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0004g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0004g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0004g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0004g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0004g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0004g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0004g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0004g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0004g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0004g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0004g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0004g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0004g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0004g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0004g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0004g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0004g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0004g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0004g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0004g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0004g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0004g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0004g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0004g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0005g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0005g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0005g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0005g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0005g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0005g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0006g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0006g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0007g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0007g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0008g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0009g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0010g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0011g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0001t0012g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0002t0003g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0002t0003g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0002t0003g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0002t0003g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0002t0003g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0002t0003g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0002t0003g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0002t0003g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0002t0003g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0002t0003g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0002t0003g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0002t0003g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0002t0003g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0004t0003g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0006t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0001c0008t0002g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0002c0005t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0003c0007t0003g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
a0004c0003t0001g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0301 | EUR | GBR | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0227 | EUR | GBR | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG00140 | hp1 | a0001 | c0001 | t0002 | g0040 | EUR | GBR | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG00140 | hp2 | a0001 | c0001 | t0002 | g0168 | EUR | GBR | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0006 | EUR | FIN | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG00280 | hp2 | a0001 | c0001 | t0002 | g0161 | EUR | FIN | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG00323 | hp1 | a0001 | c0001 | t0002 | g0114 | EUR | FIN | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0302 | EUR | FIN | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | CHS | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG00423 | hp2 | a0001 | c0001 | t0002 | g0185 | EAS | CHS | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | CHS | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | CHS | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | CHS | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG00544 | hp2 | a0001 | c0001 | t0002 | g0134 | EAS | CHS | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG00597 | hp1 | a0001 | c0001 | t0003 | g0067 | EAS | CHS | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG00597 | hp2 | a0001 | c0001 | t0002 | g0130 | EAS | CHS | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG00609 | hp1 | a0001 | c0001 | t0002 | g0208 | EAS | CHS | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG00609 | hp2 | a0001 | c0001 | t0008 | g0265 | EAS | CHS | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | CHS | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG00621 | hp2 | a0001 | c0001 | t0002 | g0153 | EAS | CHS | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0243 | AMR | PUR | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0253 | AMR | PUR | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG00735 | hp1 | a0001 | c0001 | t0002 | g0124 | AMR | PUR | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG00735 | hp2 | a0001 | c0001 | t0002 | g0197 | AMR | PUR | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0237 | AMR | PUR | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG00738 | hp2 | a0001 | c0001 | t0002 | g0201 | AMR | PUR | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG00741 | hp1 | a0001 | c0001 | t0004 | g0096 | AMR | PUR | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG00741 | hp2 | a0001 | c0001 | t0002 | g0127 | AMR | PUR | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0313 | AMR | PUR | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0270 | AMR | PUR | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0278 | AMR | PUR | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0314 | AMR | PUR | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG01081 | hp1 | a0001 | c0001 | t0002 | g0016 | AMR | PUR | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0244 | AMR | PUR | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG01099 | hp1 | a0001 | c0001 | t0004 | g0104 | AMR | PUR | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG01099 | hp2 | a0001 | c0001 | t0002 | g0199 | AMR | PUR | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG01106 | hp1 | a0001 | c0001 | t0004 | g0158 | AMR | PUR | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG01106 | hp2 | a0001 | c0001 | t0002 | g0013 | AMR | PUR | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG01109 | hp1 | a0001 | c0001 | t0002 | g0111 | AMR | PUR | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG01109 | hp2 | a0001 | c0001 | t0003 | g0094 | AMR | PUR | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0318 | AMR | PUR | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0264 | AMR | PUR | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0241 | AMR | PUR | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0269 | AMR | PUR | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0324 | AMR | PUR | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG01192 | hp2 | a0001 | c0001 | t0011 | g0061 | AMR | PUR | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0309 | AMR | PUR | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0306 | AMR | PUR | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG01255 | hp1 | a0001 | c0001 | t0003 | g0049 | AMR | CLM | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0218 | AMR | CLM | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0308 | AMR | CLM | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG01256 | hp2 | a0001 | c0001 | t0002 | g0178 | AMR | CLM | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG01257 | hp1 | a0001 | c0001 | t0002 | g0177 | AMR | CLM | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0223 | AMR | CLM | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0320 | AMR | CLM | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0288 | AMR | CLM | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0292 | AMR | CLM | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG01346 | hp2 | a0001 | c0001 | t0002 | g0196 | AMR | CLM | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG01358 | hp1 | a0001 | c0001 | t0002 | g0162 | AMR | CLM | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG01358 | hp2 | a0001 | c0001 | t0004 | g0102 | AMR | CLM | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG01361 | hp1 | a0001 | c0001 | t0002 | g0207 | AMR | CLM | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0319 | AMR | CLM | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG01433 | hp1 | a0002 | c0005 | t0001 | g0212 | AMR | CLM | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0323 | AMR | CLM | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0225 | AMR | CLM | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0012 | AMR | CLM | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0219 | EUR | IBS | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG01515 | hp2 | a0001 | c0001 | t0004 | g0151 | EUR | IBS | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0311 | EUR | IBS | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG01516 | hp2 | a0001 | c0001 | t0002 | g0180 | EUR | IBS | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG01517 | hp1 | a0001 | c0001 | t0002 | g0179 | EUR | IBS | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG01517 | hp2 | a0001 | c0001 | t0004 | g0145 | EUR | IBS | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0290 | AFR | ACB | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG01884 | hp2 | a0001 | c0001 | t0003 | g0023 | AFR | ACB | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0224 | AMR | PEL | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0312 | AMR | PEL | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0271 | AMR | PEL | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0317 | AMR | PEL | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG01952 | hp1 | a0001 | c0001 | t0002 | g0169 | AMR | PEL | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0226 | AMR | PEL | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0232 | AMR | PEL | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG01981 | hp2 | a0001 | c0001 | t0004 | g0101 | AMR | PEL | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0242 | AMR | PEL | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG02004 | hp2 | a0001 | c0001 | t0002 | g0011 | AMR | PEL | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG02027 | hp1 | a0001 | c0001 | t0002 | g0121 | EAS | KHV | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | KHV | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | KHV | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG02040 | hp2 | a0001 | c0001 | t0002 | g0093 | EAS | KHV | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0279 | AFR | ACB | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0251 | AFR | ACB | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG02056 | hp1 | a0001 | c0001 | t0003 | g0025 | EAS | KHV | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG02056 | hp2 | a0001 | c0001 | t0002 | g0119 | EAS | KHV | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | KHV | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG02071 | hp2 | a0001 | c0001 | t0002 | g0137 | EAS | KHV | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | KHV | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG02074 | hp2 | a0001 | c0001 | t0002 | g0109 | EAS | KHV | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | KHV | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG02129 | hp2 | a0001 | c0001 | t0003 | g0019 | EAS | KHV | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG02135 | hp1 | a0001 | c0001 | t0003 | g0089 | EAS | KHV | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG02135 | hp2 | a0001 | c0001 | t0002 | g0138 | EAS | KHV | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG02145 | hp1 | a0001 | c0001 | t0002 | g0106 | AFR | ACB | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG02145 | hp2 | a0001 | c0001 | t0003 | g0070 | AFR | ACB | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG02165 | hp1 | a0001 | c0001 | t0002 | g0090 | EAS | CDX | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0087 | EAS | CDX | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG02257 | hp1 | a0001 | c0006 | t0001 | g0327 | AFR | ACB | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0228 | AFR | ACB | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG02258 | hp1 | a0001 | c0001 | t0003 | g0069 | AFR | ACB | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0214 | AFR | ACB | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG02273 | hp1 | a0001 | c0001 | t0002 | g0175 | AMR | PEL | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG02273 | hp2 | a0001 | c0001 | t0002 | g0015 | AMR | PEL | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG02280 | hp1 | a0001 | c0001 | t0002 | g0200 | AFR | ACB | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0294 | AFR | ACB | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG02451 | hp1 | a0001 | c0001 | t0003 | g0050 | AFR | ACB | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG02451 | hp2 | a0001 | c0002 | t0003 | g0053 | AFR | ACB | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG02523 | hp1 | a0001 | c0001 | t0004 | g0082 | EAS | KHV | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG02523 | hp2 | a0001 | c0001 | t0003 | g0036 | EAS | KHV | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0304 | AFR | GWD | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG02572 | hp2 | a0001 | c0001 | t0007 | g0333 | AFR | GWD | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG02602 | hp1 | a0001 | c0001 | t0002 | g0108 | SAS | PJL | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG02602 | hp2 | a0001 | c0001 | t0003 | g0032 | SAS | PJL | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG02615 | hp1 | a0001 | c0001 | t0003 | g0077 | AFR | GWD | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG02615 | hp2 | a0001 | c0002 | t0003 | g0056 | AFR | GWD | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG02622 | hp1 | a0001 | c0001 | t0003 | g0021 | AFR | GWD | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0274 | AFR | GWD | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0272 | AFR | GWD | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0277 | AFR | GWD | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0325 | SAS | PJL | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG02683 | hp2 | a0001 | c0001 | t0002 | g0206 | SAS | PJL | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG02717 | hp1 | a0001 | c0001 | t0012 | g0296 | AFR | GWD | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG02717 | hp2 | a0001 | c0001 | t0003 | g0048 | AFR | GWD | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG02723 | hp2 | a0001 | c0001 | t0004 | g0148 | AFR | GWD | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG02735 | hp1 | a0001 | c0001 | t0003 | g0051 | SAS | PJL | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG02735 | hp2 | a0001 | c0001 | t0002 | g0205 | SAS | PJL | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0267 | SAS | PJL | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0315 | SAS | PJL | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG02809 | hp1 | a0001 | c0002 | t0003 | g0076 | AFR | GWD | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0310 | AFR | GWD | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG02818 | hp1 | a0001 | c0001 | t0004 | g0105 | AFR | GWD | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | GWD | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG02886 | hp1 | a0001 | c0002 | t0003 | g0054 | AFR | GWD | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG02886 | hp2 | a0001 | c0001 | t0003 | g0066 | AFR | GWD | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0305 | AFR | GWD | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG02895 | hp2 | a0001 | c0001 | t0004 | g0149 | AFR | GWD | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG02896 | hp1 | a0001 | c0002 | t0003 | g0052 | AFR | GWD | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG02896 | hp2 | a0001 | c0001 | t0003 | g0034 | AFR | GWD | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG02897 | hp1 | a0001 | c0002 | t0003 | g0058 | AFR | GWD | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG02897 | hp2 | a0001 | c0001 | t0004 | g0159 | AFR | GWD | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG02922 | hp1 | a0001 | c0004 | t0003 | g0072 | AFR | ESN | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG02922 | hp2 | a0001 | c0002 | t0003 | g0081 | AFR | ESN | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0299 | AFR | ESN | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG02965 | hp2 | a0001 | c0002 | t0003 | g0057 | AFR | ESN | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG02970 | hp1 | a0001 | c0001 | t0002 | g0194 | AFR | ESN | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0295 | AFR | ESN | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0298 | AFR | ESN | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG02976 | hp2 | a0001 | c0002 | t0003 | g0073 | AFR | ESN | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0289 | AFR | GWD | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0280 | AFR | GWD | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0291 | AFR | MSL | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG03098 | hp2 | a0001 | c0002 | t0003 | g0080 | AFR | MSL | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG03130 | hp1 | a0001 | c0001 | t0010 | g0332 | AFR | ESN | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG03130 | hp2 | a0001 | c0001 | t0004 | g0095 | AFR | ESN | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG03139 | hp1 | a0001 | c0001 | t0003 | g0065 | AFR | ESN | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG03139 | hp2 | a0001 | c0001 | t0002 | g0085 | AFR | ESN | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0328 | AFR | ESN | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG03195 | hp2 | a0001 | c0008 | t0002 | g0195 | AFR | ESN | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG03225 | hp1 | a0001 | c0001 | t0003 | g0063 | AFR | MSL | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0252 | AFR | MSL | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0133 | SAS | PJL | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0220 | SAS | PJL | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG03486 | hp1 | a0001 | c0001 | t0003 | g0210 | AFR | MSL | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0307 | AFR | MSL | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG03492 | hp1 | a0001 | c0001 | t0002 | g0198 | SAS | PJL | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG03516 | hp1 | a0001 | c0001 | t0003 | g0047 | AFR | ESN | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG03516 | hp2 | a0001 | c0001 | t0003 | g0064 | AFR | ESN | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG03540 | hp1 | a0001 | c0001 | t0002 | g0193 | AFR | GWD | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG03540 | hp2 | a0001 | c0001 | t0003 | g0211 | AFR | GWD | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG03579 | hp1 | a0001 | c0001 | t0004 | g0107 | AFR | MSL | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | MSL | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG03669 | hp1 | a0001 | c0001 | t0002 | g0113 | SAS | PJL | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0229 | SAS | PJL | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0285 | SAS | STU | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG03688 | hp2 | a0001 | c0001 | t0003 | g0037 | SAS | STU | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG03831 | hp1 | a0001 | c0001 | t0003 | g0039 | SAS | BEB | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG03831 | hp2 | a0001 | c0001 | t0004 | g0099 | SAS | BEB | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG03834 | hp1 | a0001 | c0001 | t0002 | g0166 | SAS | BEB | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0215 | SAS | BEB | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0283 | SAS | BEB | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0221 | SAS | BEB | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG04115 | hp1 | a0001 | c0001 | t0002 | g0204 | SAS | STU | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG04115 | hp2 | a0004 | c0003 | t0001 | g0326 | SAS | STU | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG04184 | hp1 | a0001 | c0001 | t0003 | g0046 | SAS | BEB | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0286 | SAS | BEB | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0217 | SAS | STU | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0322 | SAS | STU | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0293 | SAS | STU | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG04228 | hp2 | a0001 | c0001 | t0002 | g0202 | SAS | STU | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
NA18522 | hp1 | a0001 | c0002 | t0003 | g0074 | AFR | YRI | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0300 | AFR | YRI | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
NA18612 | hp1 | a0001 | c0001 | t0002 | g0174 | EAS | CHB | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
NA18612 | hp2 | a0001 | c0001 | t0002 | g0182 | EAS | CHB | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
NA18747 | hp1 | a0001 | c0001 | t0002 | g0176 | EAS | CHB | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | CHB | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
NA18906 | hp1 | a0001 | c0001 | t0004 | g0097 | AFR | YRI | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
NA18906 | hp2 | a0001 | c0001 | t0002 | g0088 | AFR | YRI | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
NA18939 | hp1 | a0001 | c0001 | t0002 | g0163 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
NA18940 | hp1 | a0001 | c0001 | t0003 | g0024 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
NA18940 | hp2 | a0001 | c0001 | t0004 | g0143 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
NA18941 | hp2 | a0001 | c0001 | t0002 | g0160 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
NA18942 | hp1 | a0001 | c0001 | t0002 | g0155 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
NA18942 | hp2 | a0001 | c0001 | t0004 | g0190 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
NA18943 | hp1 | a0001 | c0001 | t0002 | g0209 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
NA18943 | hp2 | a0001 | c0001 | t0004 | g0141 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
NA18944 | hp1 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
NA18944 | hp2 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
NA18945 | hp1 | a0001 | c0001 | t0004 | g0188 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
NA18945 | hp2 | a0001 | c0001 | t0003 | g0017 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
NA18950 | hp2 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
NA18951 | hp1 | a0001 | c0001 | t0003 | g0033 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
NA18951 | hp2 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
NA18953 | hp1 | a0001 | c0001 | t0003 | g0043 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
NA18954 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
NA18956 | hp1 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
NA18961 | hp1 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
NA18962 | hp1 | a0001 | c0001 | t0003 | g0020 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
NA18962 | hp2 | a0001 | c0001 | t0005 | g0098 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
NA18963 | hp1 | a0001 | c0001 | t0003 | g0059 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
NA18964 | hp1 | a0001 | c0001 | t0002 | g0118 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
NA18964 | hp2 | a0001 | c0001 | t0002 | g0123 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
NA18965 | hp1 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
NA18965 | hp2 | a0001 | c0001 | t0004 | g0186 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
NA18966 | hp1 | a0001 | c0001 | t0006 | g0007 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
NA18968 | hp1 | a0001 | c0001 | t0002 | g0316 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
NA18968 | hp2 | a0001 | c0001 | t0002 | g0152 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
NA18970 | hp1 | a0001 | c0001 | t0002 | g0117 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
NA18971 | hp1 | a0001 | c0001 | t0002 | g0172 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
NA18971 | hp2 | a0001 | c0001 | t0003 | g0018 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
NA18974 | hp2 | a0001 | c0001 | t0003 | g0029 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
NA18975 | hp1 | a0001 | c0001 | t0004 | g0084 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
NA18975 | hp2 | a0001 | c0001 | t0006 | g0008 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
NA18978 | hp1 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0329 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
NA18980 | hp1 | a0001 | c0001 | t0003 | g0068 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
NA18980 | hp2 | a0001 | c0001 | t0002 | g0128 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
NA18981 | hp1 | a0001 | c0001 | t0005 | g0100 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
NA18987 | hp2 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
NA18989 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
NA18989 | hp2 | a0001 | c0001 | t0003 | g0035 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
NA18990 | hp1 | a0001 | c0001 | t0003 | g0027 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
NA18990 | hp2 | a0001 | c0001 | t0002 | g0122 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
NA18991 | hp2 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
NA18998 | hp1 | a0001 | c0001 | t0005 | g0150 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
NA18998 | hp2 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
NA19000 | hp1 | a0001 | c0001 | t0004 | g0142 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
NA19000 | hp2 | a0001 | c0001 | t0003 | g0041 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
NA19004 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
NA19004 | hp2 | a0001 | c0001 | t0005 | g0103 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
NA19010 | hp1 | a0001 | c0001 | t0003 | g0038 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
NA19010 | hp2 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
NA19011 | hp2 | a0001 | c0001 | t0002 | g0165 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
NA19012 | hp1 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
NA19012 | hp2 | a0001 | c0001 | t0003 | g0030 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
NA19043 | hp1 | a0001 | c0001 | t0003 | g0213 | AFR | LWK | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0331 | AFR | LWK | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
NA19054 | hp2 | a0001 | c0001 | t0002 | g0192 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
NA19056 | hp1 | a0001 | c0001 | t0002 | g0154 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
NA19056 | hp2 | a0001 | c0001 | t0005 | g0146 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
NA19060 | hp1 | a0001 | c0001 | t0002 | g0144 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
NA19060 | hp2 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
NA19062 | hp1 | a0001 | c0001 | t0004 | g0140 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
NA19064 | hp1 | a0001 | c0001 | t0003 | g0028 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
NA19064 | hp2 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
NA19065 | hp1 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
NA19065 | hp2 | a0001 | c0001 | t0003 | g0026 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
NA19066 | hp1 | a0001 | c0001 | t0002 | g0157 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
NA19068 | hp1 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
NA19068 | hp2 | a0001 | c0001 | t0004 | g0189 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
NA19074 | hp1 | a0001 | c0001 | t0002 | g0164 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
NA19079 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
NA19079 | hp2 | a0001 | c0001 | t0003 | g0071 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
NA19080 | hp1 | a0001 | c0001 | t0003 | g0062 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
NA19080 | hp2 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
NA19082 | hp2 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
NA19084 | hp1 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
NA19084 | hp2 | a0003 | c0007 | t0003 | g0031 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
NA19085 | hp2 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
NA19087 | hp1 | a0001 | c0001 | t0002 | g0131 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
NA19087 | hp2 | a0001 | c0001 | t0005 | g0147 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
NA19090 | hp2 | a0001 | c0001 | t0002 | g0110 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
NA19091 | hp1 | a0001 | c0001 | t0003 | g0042 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0281 | AFR | YRI | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
NA19240 | hp2 | a0001 | c0002 | t0003 | g0055 | AFR | YRI | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
NA20129 | hp1 | a0001 | c0002 | t0003 | g0075 | AFR | ASW | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0263 | AFR | ASW | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
NA20752 | hp1 | a0001 | c0001 | t0002 | g0086 | EUR | TSI | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0287 | EUR | TSI | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG01123 | hp1 | a0001 | c0001 | t0002 | g0014 | AMR | CLM | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0321 | AMR | CLM | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG02109 | hp1 | a0001 | c0001 | t0003 | g0022 | AFR | ACB | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG02109 | hp2 | a0001 | c0001 | t0007 | g0334 | AFR | ACB | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG02486 | hp1 | a0001 | c0001 | t0003 | g0044 | AFR | ACB | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG02486 | hp2 | a0001 | c0001 | t0002 | g0203 | AFR | ACB | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG02559 | hp1 | a0001 | c0001 | t0002 | g0120 | AFR | ACB | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0266 | AFR | ACB | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0254 | AFR | MSL | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG03471 | hp2 | a0001 | c0001 | t0003 | g0045 | AFR | MSL | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0268 | AFR | USA | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
HG06807 | hp2 | a0001 | c0001 | t0003 | g0060 | AFR | USA | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
NA18955 | hp1 | a0001 | c0001 | t0002 | g0156 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
NA18955 | hp2 | a0001 | c0001 | t0004 | g0187 | EAS | JPT | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
NA20300 | hp1 | a0001 | c0001 | t0003 | g0078 | AFR | USA | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
NA20300 | hp2 | a0001 | c0001 | t0002 | g0139 | AFR | USA | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0258 | AFR | LWK | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
NA21309 | hp2 | a0001 | c0001 | t0009 | g0330 | AFR | LWK | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0222 | REF | REF | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0173 | REF | REF | CLINT1_chr5_157780747_157864145 | CLINT1 | chr5 | 157780747 | 157864145 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:157787812
|
A | G | 1 | a0002 | 1 | HG01433.hp1 | missense_variant | MODERATE | c.1712T>C | p.Met571Thr | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 12/12 | 1887/3952 | 1712/1878 | 571/625 | chr5 | 157787812 | ||
chr5:157791783
|
T | C | 1 | a0003 | 1 | NA19084.hp2 | missense_variant | MODERATE | c.1300A>G | p.Met434Val | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 10/12 | 1475/3952 | 1300/1878 | 434/625 | chr5 | 157791783 | ||
chr5:157791912
|
C | T | 1 | a0004 | 1 | HG04115.hp2 | missense_variant | MODERATE | c.1171G>A | p.Glu391Lys | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 10/12 | 1346/3952 | 1171/1878 | 391/625 | chr5 | 157791912 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:157787664
|
G | A | 1 | a0001c0006 | 1 | HG02257.hp1 | synonymous_variant | LOW | c.1860C>T | p.Phe620Phe | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 12/12 | 2035/3952 | 1860/1878 | 620/625 | chr5 | 157787664 | ||
chr5:157789370
|
C | T | 1 | a0001c0004 | 1 | HG02922.hp1 | synonymous_variant | LOW | c.1524G>A | p.Gln508Gln | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 11/12 | 1699/3952 | 1524/1878 | 508/625 | chr5 | 157789370 | ||
chr5:157809711
|
C | G | 1 | a0001c0002 | 13 | HG02451.hp2 HG02615.hp2 HG02809.hp1 others(10): Show |
synonymous_variant | LOW | c.612G>C | p.Leu204Leu | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 6/12 | 787/3952 | 612/1878 | 204/625 | chr5 | 157809711 | ||
chr5:157816791
|
G | A | 1 | a0001c0008 | 1 | HG03195.hp2 | synonymous_variant | LOW | c.186C>T | p.Asn62Asn | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 3/12 | 361/3952 | 186/1878 | 62/625 | chr5 | 157816791 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:157785918
|
G | A | 1 | a0001c0001t0011 | 1 | HG01192.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1728C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 12/12 | 1728 | chr5 | 157785918 | |||||
chr5:157786168
|
T | C | 1 | a0001c0001t0010 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1478A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 12/12 | 1478 | chr5 | 157786168 | |||||
chr5:157786366
|
A | T | 1 | a0001c0001t0010 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1280T>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 12/12 | 1280 | chr5 | 157786366 | |||||
chr5:157786380
|
CAT | C | 1 | a0001c0001t0005 | 6 | NA18962.hp2 NA18981.hp1 NA18998.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1264_*1265delAT | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 12/12 | 1264 | chr5 | 157786380 | |||||
chr5:157786489
|
A | G | 5 | a0001c0001t0002a0001c0001t0004a0001c0001t0005others(2): Show | 141 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(138): Show |
3_prime_UTR_variant | MODIFIER | c.*1157T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 12/12 | 1157 | chr5 | 157786489 | |||||
chr5:157787179
|
A | G | 2 | a0001c0001t0004a0001c0001t0005 | 34 | HG00741.hp1 HG01099.hp1 HG01106.hp1 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*467T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 12/12 | 467 | chr5 | 157787179 | |||||
chr5:157787237
|
C | T | 1 | a0001c0001t0009 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*409G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 12/12 | 409 | chr5 | 157787237 | |||||
chr5:157787345
|
C | G | 1 | a0001c0001t0008 | 1 | HG00609.hp2 | 3_prime_UTR_variant | MODIFIER | c.*301G>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 12/12 | 301 | chr5 | 157787345 | |||||
chr5:157787426
|
T | C | 5 | a0001c0001t0003a0001c0001t0011a0001c0002t0003others(2): Show | 68 | HG00597.hp1 HG01109.hp2 HG01192.hp2 others(65): Show |
3_prime_UTR_variant | MODIFIER | c.*220A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 12/12 | 220 | chr5 | 157787426 | |||||
chr5:157787460
|
T | C | 1 | a0001c0001t0012 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*186A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 12/12 | 186 | chr5 | 157787460 | |||||
chr5:157859012
|
C | T | 1 | a0001c0001t0006 | 2 | NA18966.hp1 NA18975.hp2 |
5_prime_UTR_variant | MODIFIER | c.-42G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/12 | 42 | chr5 | 157859012 | |||||
chr5:157859096
|
G | C | 1 | a0001c0001t0007 | 2 | HG02109.hp2 HG02572.hp2 |
5_prime_UTR_variant | MODIFIER | c.-126C>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/12 | 126 | chr5 | 157859096 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:157788001
|
C | T | 1 | a0001c0001t0003g0094 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1532-9G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 11/11 | chr5 | 157788001 | ||||||
chr5:157788019
|
C | T | 68 | a0001c0001t0003g0017a0001c0001t0003g0018a0001c0001t0003g0019others(65): Show | 68 | HG00597.hp1 HG01109.hp2 HG01192.hp2 others(65): Show |
intron_variant | MODIFIER | c.1532-27G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 11/11 | chr5 | 157788019 | ||||||
chr5:157788342
|
T | C | 1 | a0001c0001t0003g0210 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1532-350A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 11/11 | chr5 | 157788342 | ||||||
chr5:157788405
|
A | G | 1 | a0001c0001t0002g0093 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1532-413T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 11/11 | chr5 | 157788405 | ||||||
chr5:157788520
|
T | A | 1 | a0002c0005t0001g0212 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1532-528A>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 11/11 | chr5 | 157788520 | ||||||
chr5:157788705
|
C | T | 73 | a0001c0001t0001g0236a0001c0001t0001g0259a0001c0001t0001g0260others(70): Show | 73 | HG00544.hp1 HG00597.hp1 HG00609.hp2 others(70): Show |
intron_variant | MODIFIER | c.1531+658G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 11/11 | chr5 | 157788705 | ||||||
chr5:157788706
|
G | A | 1 | a0001c0001t0001g0272 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1531+657C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 11/11 | chr5 | 157788706 | ||||||
chr5:157788817
|
A | C | 7 | a0001c0001t0001g0079a0001c0001t0001g0274a0001c0001t0001g0289others(4): Show | 7 | HG01884.hp1 HG02572.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1531+546T>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 11/11 | chr5 | 157788817 | ||||||
chr5:157788913
|
G | A | 3 | a0001c0001t0003g0047a0001c0001t0003g0048a0001c0001t0003g0094 | 3 | HG01109.hp2 HG02717.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1531+450C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 11/11 | chr5 | 157788913 | ||||||
chr5:157788968
|
GA | G | 129 | a0001c0001t0001g0272a0001c0001t0001g0278a0001c0001t0001g0280others(126): Show | 131 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(128): Show |
intron_variant | MODIFIER | c.1531+394delT | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 11/11 | chr5 | 157788968 | ||||||
chr5:157788968
|
GAAAAAAA others(2): Show |
G | 49 | a0001c0001t0002g0040a0001c0001t0003g0017a0001c0001t0003g0018others(46): Show | 49 | HG00140.hp1 HG00597.hp1 HG01192.hp2 others(46): Show |
intron_variant | MODIFIER | c.1531+386_1531+394d others(11): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 11/11 | chr5 | 157788968 | ||||||
chr5:157788968
|
GAAAAAAA others(3): Show |
G | 20 | a0001c0001t0003g0044a0001c0001t0003g0045a0001c0001t0003g0047others(17): Show | 20 | HG01109.hp2 HG02451.hp2 HG02486.hp1 others(17): Show |
intron_variant | MODIFIER | c.1531+385_1531+394d others(12): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 11/11 | chr5 | 157788968 | ||||||
chr5:157789169
|
T | C | 1 | a0001c0001t0002g0040 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1531+194A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 11/11 | chr5 | 157789169 | ||||||
chr5:157789181
|
T | C | 48 | a0001c0001t0002g0040a0001c0001t0003g0017a0001c0001t0003g0018others(45): Show | 48 | HG00140.hp1 HG00597.hp1 HG01192.hp2 others(45): Show |
intron_variant | MODIFIER | c.1531+182A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 11/11 | chr5 | 157789181 | ||||||
chr5:157789323
|
G | A | 1 | a0001c0001t0002g0106 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1531+40C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 11/11 | chr5 | 157789323 | ||||||
chr5:157789360
|
T | C | 1 | a0001c0001t0002g0182 | 1 | NA18612.hp2 | splice_region_variant&intron_variant | LOW | c.1531+3A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 11/11 | chr5 | 157789360 | ||||||
chr5:157789927
|
G | A | 68 | a0001c0001t0003g0017a0001c0001t0003g0018a0001c0001t0003g0019others(65): Show | 68 | HG00597.hp1 HG01109.hp2 HG01192.hp2 others(65): Show |
intron_variant | MODIFIER | c.1381-414C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 10/11 | chr5 | 157789927 | ||||||
chr5:157790031
|
T | G | 13 | a0001c0002t0003g0052a0001c0002t0003g0053a0001c0002t0003g0054others(10): Show | 13 | HG02451.hp2 HG02615.hp2 HG02809.hp1 others(10): Show |
intron_variant | MODIFIER | c.1381-518A>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 10/11 | chr5 | 157790031 | ||||||
chr5:157790188
|
G | C | 2 | a0001c0001t0003g0047a0001c0001t0003g0048 | 2 | HG02717.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1381-675C>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 10/11 | chr5 | 157790188 | ||||||
chr5:157790543
|
C | A | 1 | a0001c0001t0001g0233 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1381-1030G>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 10/11 | chr5 | 157790543 | ||||||
chr5:157790546
|
A | C | 1 | a0001c0001t0002g0114 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1381-1033T>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 10/11 | chr5 | 157790546 | ||||||
chr5:157790861
|
G | A | 2 | a0001c0001t0007g0333a0001c0001t0007g0334 | 2 | HG02109.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.1380+842C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 10/11 | chr5 | 157790861 | ||||||
chr5:157790958
|
A | T | 69 | a0001c0001t0002g0040a0001c0001t0003g0017a0001c0001t0003g0018others(66): Show | 69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.1380+745T>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 10/11 | chr5 | 157790958 | ||||||
chr5:157791002
|
A | G | 69 | a0001c0001t0002g0040a0001c0001t0003g0017a0001c0001t0003g0018others(66): Show | 69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.1380+701T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 10/11 | chr5 | 157791002 | ||||||
chr5:157791032
|
G | A | 230 | a0001c0001t0001g0006a0001c0001t0001g0308a0001c0001t0001g0309others(227): Show | 234 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.1380+671C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 10/11 | chr5 | 157791032 | ||||||
chr5:157791051
|
T | G | 49 | a0001c0001t0002g0040a0001c0001t0003g0017a0001c0001t0003g0018others(46): Show | 49 | HG00140.hp1 HG00597.hp1 HG01192.hp2 others(46): Show |
intron_variant | MODIFIER | c.1380+652A>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 10/11 | chr5 | 157791051 | ||||||
chr5:157791086
|
T | C | 2 | a0001c0001t0007g0333a0001c0001t0007g0334 | 2 | HG02109.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.1380+617A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 10/11 | chr5 | 157791086 | ||||||
chr5:157791246
|
G | T | 1 | a0001c0001t0010g0332 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1380+457C>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 10/11 | chr5 | 157791246 | ||||||
chr5:157791367
|
T | C | 2 | a0001c0001t0003g0047a0001c0001t0003g0048 | 2 | HG02717.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1380+336A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 10/11 | chr5 | 157791367 | ||||||
chr5:157791371
|
T | G | 1 | a0001c0001t0003g0094 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1380+332A>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 10/11 | chr5 | 157791371 | ||||||
chr5:157791410
|
G | T | 84 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0011others(81): Show | 86 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.1380+293C>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 10/11 | chr5 | 157791410 | ||||||
chr5:157791560
|
C | T | 1 | a0001c0001t0001g0283 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1380+143G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 10/11 | chr5 | 157791560 | ||||||
chr5:157791576
|
C | A | 4 | a0001c0001t0002g0085a0001c0001t0002g0193a0001c0001t0002g0194others(1): Show | 4 | HG02970.hp1 HG03139.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1380+127G>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 10/11 | chr5 | 157791576 | ||||||
chr5:157791582
|
CAT | C | 4 | a0001c0001t0002g0085a0001c0001t0002g0193a0001c0001t0002g0194others(1): Show | 4 | HG02970.hp1 HG03139.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1380+119_1380+120d others(4): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 10/11 | chr5 | 157791582 | ||||||
chr5:157792093
|
C | T | 1 | a0001c0004t0003g0072 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1088-98G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 9/11 | chr5 | 157792093 | ||||||
chr5:157792243
|
T | C | 1 | a0001c0001t0009g0330 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1088-248A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 9/11 | chr5 | 157792243 | ||||||
chr5:157792255
|
T | TA | 69 | a0001c0001t0002g0040a0001c0001t0003g0017a0001c0001t0003g0018others(66): Show | 69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.1088-261dupT | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 9/11 | chr5 | 157792255 | ||||||
chr5:157792289
|
T | G | 1 | a0001c0001t0003g0089 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1088-294A>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 9/11 | chr5 | 157792289 | ||||||
chr5:157792314
|
G | A | 4 | a0001c0001t0001g0271a0001c0001t0001g0292a0001c0001t0001g0301others(1): Show | 4 | HG00099.hp1 HG00323.hp2 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.1088-319C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 9/11 | chr5 | 157792314 | ||||||
chr5:157792416
|
C | T | 1 | a0001c0001t0002g0144 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1088-421G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 9/11 | chr5 | 157792416 | ||||||
chr5:157792472
|
C | T | 1 | a0002c0005t0001g0212 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1088-477G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 9/11 | chr5 | 157792472 | ||||||
chr5:157792473
|
G | A | 1 | a0001c0001t0001g0286 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1088-478C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 9/11 | chr5 | 157792473 | ||||||
chr5:157792486
|
T | G | 13 | a0001c0001t0002g0086a0001c0001t0002g0196a0001c0001t0002g0197others(10): Show | 13 | HG00735.hp2 HG00738.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.1088-491A>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 9/11 | chr5 | 157792486 | ||||||
chr5:157792642
|
A | G | 13 | a0001c0002t0003g0052a0001c0002t0003g0053a0001c0002t0003g0054others(10): Show | 13 | HG02451.hp2 HG02615.hp2 HG02809.hp1 others(10): Show |
intron_variant | MODIFIER | c.1088-647T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 9/11 | chr5 | 157792642 | ||||||
chr5:157792738
|
T | C | 1 | a0001c0001t0002g0174 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1088-743A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 9/11 | chr5 | 157792738 | ||||||
chr5:157792949
|
C | T | 13 | a0001c0001t0002g0086a0001c0001t0002g0196a0001c0001t0002g0197others(10): Show | 13 | HG00735.hp2 HG00738.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.1088-954G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 9/11 | chr5 | 157792949 | ||||||
chr5:157793082
|
T | C | 69 | a0001c0001t0002g0040a0001c0001t0003g0017a0001c0001t0003g0018others(66): Show | 69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.1088-1087A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 9/11 | chr5 | 157793082 | ||||||
chr5:157793214
|
CT | C | 76 | a0001c0001t0001g0237a0001c0001t0001g0241a0001c0001t0001g0244others(73): Show | 76 | HG00140.hp1 HG00597.hp1 HG00738.hp1 others(73): Show |
intron_variant | MODIFIER | c.1088-1220delA | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 9/11 | chr5 | 157793214 | ||||||
chr5:157793405
|
T | C | 1 | a0001c0001t0003g0050 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1088-1410A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 9/11 | chr5 | 157793405 | ||||||
chr5:157793420
|
G | A | 69 | a0001c0001t0002g0040a0001c0001t0003g0017a0001c0001t0003g0018others(66): Show | 69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.1088-1425C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 9/11 | chr5 | 157793420 | ||||||
chr5:157793492
|
C | T | 2 | a0001c0001t0007g0333a0001c0001t0007g0334 | 2 | HG02109.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.1087+1406G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 9/11 | chr5 | 157793492 | ||||||
chr5:157793577
|
G | A | 2 | a0001c0001t0003g0044a0001c0001t0003g0045 | 2 | HG02486.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1087+1321C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 9/11 | chr5 | 157793577 | ||||||
chr5:157793620
|
A | T | 2 | a0001c0001t0003g0047a0001c0001t0003g0048 | 2 | HG02717.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1087+1278T>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 9/11 | chr5 | 157793620 | ||||||
chr5:157793711
|
T | C | 2 | a0001c0001t0007g0333a0001c0001t0007g0334 | 2 | HG02109.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.1087+1187A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 9/11 | chr5 | 157793711 | ||||||
chr5:157793869
|
T | G | 2 | a0001c0001t0007g0333a0001c0001t0007g0334 | 2 | HG02109.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.1087+1029A>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 9/11 | chr5 | 157793869 | ||||||
chr5:157793957
|
C | G | 3 | a0001c0001t0002g0111a0001c0001t0002g0114a0001c0001t0002g0168 | 3 | HG00140.hp2 HG00323.hp1 HG01109.hp1 |
intron_variant | MODIFIER | c.1087+941G>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 9/11 | chr5 | 157793957 | ||||||
chr5:157793963
|
C | T | 3 | a0001c0001t0001g0305a0001c0001t0001g0306a0001c0001t0001g0307 | 3 | HG01243.hp2 HG02895.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1087+935G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 9/11 | chr5 | 157793963 | ||||||
chr5:157794095
|
A | G | 1 | a0001c0001t0001g0306 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1087+803T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 9/11 | chr5 | 157794095 | ||||||
chr5:157794141
|
T | C | 2 | a0001c0001t0003g0210a0001c0001t0004g0107 | 2 | HG03486.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1087+757A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 9/11 | chr5 | 157794141 | ||||||
chr5:157794354
|
G | GT | 13 | a0001c0002t0003g0052a0001c0002t0003g0053a0001c0002t0003g0054others(10): Show | 13 | HG02451.hp2 HG02615.hp2 HG02809.hp1 others(10): Show |
intron_variant | MODIFIER | c.1087+543dupA | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 9/11 | chr5 | 157794354 | ||||||
chr5:157794481
|
A | G | 13 | a0001c0001t0002g0086a0001c0001t0002g0196a0001c0001t0002g0197others(10): Show | 13 | HG00735.hp2 HG00738.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.1087+417T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 9/11 | chr5 | 157794481 | ||||||
chr5:157794654
|
C | A | 1 | a0001c0001t0002g0206 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1087+244G>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 9/11 | chr5 | 157794654 | ||||||
chr5:157795238
|
A | G | 70 | a0001c0001t0001g0290a0001c0001t0002g0040a0001c0001t0003g0017others(67): Show | 70 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(67): Show |
intron_variant | MODIFIER | c.1013-266T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157795238 | ||||||
chr5:157795666
|
GGGGCAAA others(2): Show |
G | 13 | a0001c0001t0002g0086a0001c0001t0002g0196a0001c0001t0002g0197others(10): Show | 13 | HG00735.hp2 HG00738.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.1013-703_1013-695d others(11): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157795666 | ||||||
chr5:157795683
|
T | C | 69 | a0001c0001t0002g0040a0001c0001t0003g0017a0001c0001t0003g0018others(66): Show | 69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.1013-711A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157795683 | ||||||
chr5:157795765
|
T | C | 1 | a0001c0001t0003g0018 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1013-793A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157795765 | ||||||
chr5:157795786
|
T | C | 48 | a0001c0001t0002g0040a0001c0001t0003g0017a0001c0001t0003g0018others(45): Show | 48 | HG00140.hp1 HG00597.hp1 HG01192.hp2 others(45): Show |
intron_variant | MODIFIER | c.1013-814A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157795786 | ||||||
chr5:157795904
|
A | G | 69 | a0001c0001t0002g0040a0001c0001t0003g0017a0001c0001t0003g0018others(66): Show | 69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.1013-932T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157795904 | ||||||
chr5:157795984
|
T | C | 2 | a0001c0001t0001g0298a0001c0001t0001g0299 | 2 | HG02965.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1013-1012A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157795984 | ||||||
chr5:157796002
|
G | C | 2 | a0001c0001t0007g0333a0001c0001t0007g0334 | 2 | HG02109.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.1013-1030C>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157796002 | ||||||
chr5:157796110
|
C | T | 2 | a0001c0001t0003g0026a0001c0001t0003g0027 | 2 | NA18990.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.1013-1138G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157796110 | ||||||
chr5:157796171
|
A | G | 1 | a0001c0001t0008g0265 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1013-1199T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157796171 | ||||||
chr5:157796225
|
G | A | 69 | a0001c0001t0002g0040a0001c0001t0003g0017a0001c0001t0003g0018others(66): Show | 69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.1013-1253C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157796225 | ||||||
chr5:157796428
|
C | T | 1 | a0001c0001t0001g0221 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1013-1456G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157796428 | ||||||
chr5:157796778
|
A | G | 69 | a0001c0001t0002g0040a0001c0001t0003g0017a0001c0001t0003g0018others(66): Show | 69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.1013-1806T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157796778 | ||||||
chr5:157796795
|
A | G | 1 | a0001c0001t0001g0312 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1013-1823T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157796795 | ||||||
chr5:157796807
|
T | C | 1 | a0001c0001t0001g0304 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1013-1835A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157796807 | ||||||
chr5:157796887
|
C | CAT | 9 | a0001c0001t0002g0093a0001c0001t0002g0127a0001c0001t0002g0175others(6): Show | 9 | HG00741.hp2 HG02040.hp2 HG02273.hp1 others(6): Show |
intron_variant | MODIFIER | c.1013-1917_1013-191 others(6): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157796887 | ||||||
chr5:157796887
|
CAT | C | 28 | a0001c0001t0001g0006a0001c0001t0001g0277a0001c0001t0001g0305others(25): Show | 29 | HG00280.hp1 HG01070.hp1 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.1013-1917_1013-191 others(6): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157796887 | ||||||
chr5:157797006
|
G | A | 69 | a0001c0001t0002g0040a0001c0001t0003g0017a0001c0001t0003g0018others(66): Show | 69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.1013-2034C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157797006 | ||||||
chr5:157797170
|
T | C | 1 | a0001c0001t0001g0279 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1013-2198A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157797170 | ||||||
chr5:157797204
|
C | T | 1 | a0001c0001t0002g0087 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1013-2232G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157797204 | ||||||
chr5:157797361
|
A | G | 210 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0011others(207): Show | 213 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(210): Show |
intron_variant | MODIFIER | c.1013-2389T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157797361 | ||||||
chr5:157797472
|
G | A | 1 | a0001c0001t0002g0133 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1013-2500C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157797472 | ||||||
chr5:157797544
|
C | T | 20 | a0001c0001t0001g0006a0001c0001t0001g0308a0001c0001t0001g0309others(17): Show | 21 | HG00280.hp1 HG01070.hp1 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.1013-2572G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157797544 | ||||||
chr5:157797823
|
T | C | 1 | a0001c0001t0002g0123 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1013-2851A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157797823 | ||||||
chr5:157797872
|
T | C | 1 | a0001c0001t0010g0332 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1013-2900A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157797872 | ||||||
chr5:157798095
|
G | A | 2 | a0001c0001t0007g0333a0001c0001t0007g0334 | 2 | HG02109.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.1013-3123C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157798095 | ||||||
chr5:157798187
|
T | C | 139 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0011others(136): Show | 142 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.1013-3215A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157798187 | ||||||
chr5:157798204
|
A | G | 1 | a0001c0001t0001g0304 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1013-3232T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157798204 | ||||||
chr5:157798205
|
G | A | 1 | a0001c0001t0001g0304 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1013-3233C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157798205 | ||||||
chr5:157798206
|
C | A | 1 | a0001c0001t0001g0304 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1013-3234G>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157798206 | ||||||
chr5:157798207
|
A | G | 1 | a0001c0001t0001g0304 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1013-3235T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157798207 | ||||||
chr5:157798213
|
C | T | 1 | a0001c0001t0001g0304 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1013-3241G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157798213 | ||||||
chr5:157798214
|
C | G | 1 | a0001c0001t0001g0304 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1013-3242G>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157798214 | ||||||
chr5:157798215
|
A | G | 1 | a0001c0001t0001g0304 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1013-3243T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157798215 | ||||||
chr5:157798221
|
C | T | 1 | a0001c0001t0001g0304 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1013-3249G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157798221 | ||||||
chr5:157798222
|
T | G | 1 | a0001c0001t0001g0304 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1013-3250A>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157798222 | ||||||
chr5:157798223
|
T | C | 1 | a0001c0001t0001g0304 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1013-3251A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157798223 | ||||||
chr5:157798224
|
C | T | 1 | a0001c0001t0001g0304 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1013-3252G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157798224 | ||||||
chr5:157798478
|
G | A | 20 | a0001c0001t0001g0006a0001c0001t0001g0308a0001c0001t0001g0309others(17): Show | 21 | HG00280.hp1 HG01070.hp1 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.1013-3506C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157798478 | ||||||
chr5:157798803
|
C | T | 1 | a0001c0001t0003g0050 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1013-3831G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157798803 | ||||||
chr5:157799076
|
C | T | 5 | a0001c0001t0003g0017a0001c0001t0003g0020a0001c0001t0003g0026others(2): Show | 5 | NA18945.hp2 NA18951.hp1 NA18962.hp1 others(2): Show |
intron_variant | MODIFIER | c.1013-4104G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157799076 | ||||||
chr5:157799221
|
C | T | 86 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0011others(83): Show | 88 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.1013-4249G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157799221 | ||||||
chr5:157799405
|
G | A | 1 | a0001c0001t0002g0088 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1012+4245C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157799405 | ||||||
chr5:157799417
|
C | A | 21 | a0001c0001t0001g0006a0001c0001t0001g0308a0001c0001t0001g0309others(18): Show | 22 | HG00280.hp1 HG01070.hp1 HG01071.hp2 others(19): Show |
intron_variant | MODIFIER | c.1012+4233G>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157799417 | ||||||
chr5:157799418
|
C | T | 1 | a0001c0001t0002g0124 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1012+4232G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157799418 | ||||||
chr5:157799463
|
T | C | 5 | a0001c0001t0004g0099a0001c0001t0004g0102a0001c0001t0004g0104others(2): Show | 5 | HG01099.hp1 HG01358.hp2 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.1012+4187A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157799463 | ||||||
chr5:157799573
|
T | C | 4 | a0001c0002t0003g0054a0001c0002t0003g0055a0001c0002t0003g0057others(1): Show | 4 | HG02886.hp1 HG02965.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.1012+4077A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157799573 | ||||||
chr5:157799605
|
T | C | 2 | a0001c0001t0007g0333a0001c0001t0007g0334 | 2 | HG02109.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.1012+4045A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157799605 | ||||||
chr5:157799968
|
T | C | 1 | a0001c0001t0002g0175 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1012+3682A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157799968 | ||||||
chr5:157800009
|
T | C | 69 | a0001c0001t0002g0040a0001c0001t0003g0017a0001c0001t0003g0018others(66): Show | 69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.1012+3641A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157800009 | ||||||
chr5:157800323
|
T | G | 33 | a0001c0001t0004g0003a0001c0001t0004g0082a0001c0001t0004g0084others(30): Show | 34 | HG00741.hp1 HG01099.hp1 HG01106.hp1 others(31): Show |
intron_variant | MODIFIER | c.1012+3327A>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157800323 | ||||||
chr5:157800368
|
C | T | 2 | a0001c0001t0001g0252a0001c0001t0001g0263 | 2 | HG03225.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1012+3282G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157800368 | ||||||
chr5:157800461
|
C | T | 69 | a0001c0001t0002g0040a0001c0001t0003g0017a0001c0001t0003g0018others(66): Show | 69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.1012+3189G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157800461 | ||||||
chr5:157800715
|
T | C | 1 | a0001c0001t0001g0239 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1012+2935A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157800715 | ||||||
chr5:157800771
|
T | C | 49 | a0001c0001t0002g0040a0001c0001t0003g0017a0001c0001t0003g0018others(46): Show | 49 | HG00140.hp1 HG00597.hp1 HG01192.hp2 others(46): Show |
intron_variant | MODIFIER | c.1012+2879A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157800771 | ||||||
chr5:157801165
|
G | T | 1 | a0001c0001t0001g0221 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1012+2485C>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157801165 | ||||||
chr5:157801224
|
T | C | 69 | a0001c0001t0002g0040a0001c0001t0003g0017a0001c0001t0003g0018others(66): Show | 69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.1012+2426A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157801224 | ||||||
chr5:157801271
|
C | T | 13 | a0001c0002t0003g0052a0001c0002t0003g0053a0001c0002t0003g0054others(10): Show | 13 | HG02451.hp2 HG02615.hp2 HG02809.hp1 others(10): Show |
intron_variant | MODIFIER | c.1012+2379G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157801271 | ||||||
chr5:157801330
|
A | T | 69 | a0001c0001t0002g0040a0001c0001t0003g0017a0001c0001t0003g0018others(66): Show | 69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.1012+2320T>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157801330 | ||||||
chr5:157801504
|
C | T | 1 | a0001c0001t0001g0238 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1012+2146G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157801504 | ||||||
chr5:157801591
|
G | T | 1 | a0001c0001t0002g0137 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1012+2059C>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157801591 | ||||||
chr5:157801894
|
T | A | 2 | a0001c0001t0003g0066a0001c0001t0003g0077 | 2 | HG02615.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1012+1756A>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157801894 | ||||||
chr5:157801898
|
GT | G | 70 | a0001c0001t0001g0234a0001c0001t0001g0255a0001c0001t0002g0040others(67): Show | 70 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(67): Show |
intron_variant | MODIFIER | c.1012+1751delA | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157801898 | ||||||
chr5:157801936
|
T | C | 210 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0011others(207): Show | 213 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(210): Show |
intron_variant | MODIFIER | c.1012+1714A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157801936 | ||||||
chr5:157801983
|
C | T | 20 | a0001c0001t0001g0006a0001c0001t0001g0308a0001c0001t0001g0309others(17): Show | 21 | HG00280.hp1 HG01070.hp1 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.1012+1667G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157801983 | ||||||
chr5:157801997
|
C | T | 69 | a0001c0001t0002g0040a0001c0001t0003g0017a0001c0001t0003g0018others(66): Show | 69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.1012+1653G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157801997 | ||||||
chr5:157802086
|
G | T | 2 | a0001c0001t0003g0044a0001c0001t0003g0045 | 2 | HG02486.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1012+1564C>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157802086 | ||||||
chr5:157802542
|
CT | C | 69 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270others(66): Show | 69 | HG00140.hp1 HG00597.hp1 HG01070.hp2 others(66): Show |
intron_variant | MODIFIER | c.1012+1107delA | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157802542 | ||||||
chr5:157802544
|
T | C | 1 | a0001c0001t0002g0108 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1012+1106A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157802544 | ||||||
chr5:157802631
|
C | T | 1 | a0002c0005t0001g0212 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1012+1019G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157802631 | ||||||
chr5:157802638
|
C | T | 20 | a0001c0001t0001g0006a0001c0001t0001g0308a0001c0001t0001g0309others(17): Show | 21 | HG00280.hp1 HG01070.hp1 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.1012+1012G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157802638 | ||||||
chr5:157802653
|
C | A | 1 | a0001c0001t0004g0095 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1012+997G>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157802653 | ||||||
chr5:157802979
|
C | T | 1 | a0001c0001t0001g0079 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1012+671G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157802979 | ||||||
chr5:157803185
|
C | T | 69 | a0001c0001t0002g0040a0001c0001t0003g0017a0001c0001t0003g0018others(66): Show | 69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.1012+465G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157803185 | ||||||
chr5:157803486
|
A | C | 2 | a0001c0001t0003g0047a0001c0001t0003g0048 | 2 | HG02717.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1012+164T>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157803486 | ||||||
chr5:157803524
|
C | G | 69 | a0001c0001t0002g0040a0001c0001t0003g0017a0001c0001t0003g0018others(66): Show | 69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.1012+126G>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157803524 | ||||||
chr5:157803636
|
A | G | 1 | a0001c0001t0003g0021 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1012+14T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 8/11 | chr5 | 157803636 | ||||||
chr5:157803826
|
T | G | 1 | a0001c0001t0002g0316 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.943-107A>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 7/11 | chr5 | 157803826 | ||||||
chr5:157804037
|
T | TA | 6 | a0001c0001t0001g0252a0001c0001t0001g0257a0001c0001t0001g0263others(3): Show | 6 | HG01981.hp2 HG02738.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.943-319dupT | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 7/11 | chr5 | 157804037 | ||||||
chr5:157804037
|
TA | T | 11 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0079others(8): Show | 11 | HG02004.hp1 HG02257.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.943-319delT | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 7/11 | chr5 | 157804037 | ||||||
chr5:157804037
|
TAA | T | 125 | a0001c0001t0001g0006a0001c0001t0001g0308a0001c0001t0001g0309others(122): Show | 128 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.943-320_943-319del others(2): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 7/11 | chr5 | 157804037 | ||||||
chr5:157804037
|
TAAAAAAA others(2): Show |
T | 69 | a0001c0001t0002g0040a0001c0001t0003g0017a0001c0001t0003g0018others(66): Show | 69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.943-327_943-319del others(9): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 7/11 | chr5 | 157804037 | ||||||
chr5:157804104
|
T | C | 1 | a0001c0001t0003g0094 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.943-385A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 7/11 | chr5 | 157804104 | ||||||
chr5:157804322
|
C | A | 69 | a0001c0001t0002g0040a0001c0001t0003g0017a0001c0001t0003g0018others(66): Show | 69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.943-603G>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 7/11 | chr5 | 157804322 | ||||||
chr5:157804454
|
T | C | 12 | a0001c0001t0001g0006a0001c0001t0001g0308a0001c0001t0001g0310others(9): Show | 13 | HG00280.hp1 HG01070.hp1 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.943-735A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 7/11 | chr5 | 157804454 | ||||||
chr5:157804782
|
C | T | 1 | a0001c0001t0002g0134 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.943-1063G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 7/11 | chr5 | 157804782 | ||||||
chr5:157804806
|
A | T | 1 | a0001c0001t0004g0107 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.942+1060T>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 7/11 | chr5 | 157804806 | ||||||
chr5:157804868
|
G | A | 69 | a0001c0001t0002g0040a0001c0001t0003g0017a0001c0001t0003g0018others(66): Show | 69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.942+998C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 7/11 | chr5 | 157804868 | ||||||
chr5:157804921
|
C | A | 5 | a0001c0001t0001g0277a0001c0001t0001g0305a0001c0001t0001g0306others(2): Show | 5 | HG01243.hp2 HG02647.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.942+945G>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 7/11 | chr5 | 157804921 | ||||||
chr5:157804931
|
A | AAAAAAG | 135 | a0001c0001t0001g0257a0001c0001t0002g0001a0001c0001t0002g0002others(132): Show | 138 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.942+929_942+934dup others(6): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 7/11 | chr5 | 157804931 | ||||||
chr5:157804931
|
AAAAAAG | A | 4 | a0001c0001t0002g0085a0001c0001t0002g0193a0001c0001t0002g0194others(1): Show | 4 | HG02970.hp1 HG03139.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.942+929_942+934del others(6): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 7/11 | chr5 | 157804931 | ||||||
chr5:157805296
|
T | A | 1 | a0001c0001t0001g0267 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.942+570A>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 7/11 | chr5 | 157805296 | ||||||
chr5:157805634
|
A | G | 210 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0011others(207): Show | 213 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(210): Show |
intron_variant | MODIFIER | c.942+232T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 7/11 | chr5 | 157805634 | ||||||
chr5:157805671
|
C | G | 1 | a0001c0001t0003g0094 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.942+195G>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 7/11 | chr5 | 157805671 | ||||||
chr5:157805713
|
T | C | 1 | a0001c0001t0001g0293 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.942+153A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 7/11 | chr5 | 157805713 | ||||||
chr5:157805756
|
C | T | 69 | a0001c0001t0002g0040a0001c0001t0003g0017a0001c0001t0003g0018others(66): Show | 69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.942+110G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 7/11 | chr5 | 157805756 | ||||||
chr5:157806149
|
G | A | 1 | a0001c0001t0002g0169 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.696-37C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 6/11 | chr5 | 157806149 | ||||||
chr5:157806281
|
A | G | 283 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0010others(280): Show | 287 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(284): Show |
intron_variant | MODIFIER | c.696-169T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 6/11 | chr5 | 157806281 | ||||||
chr5:157806298
|
G | C | 1 | a0001c0001t0001g0328 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.696-186C>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 6/11 | chr5 | 157806298 | ||||||
chr5:157806365
|
T | C | 1 | a0001c0001t0003g0094 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.696-253A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 6/11 | chr5 | 157806365 | ||||||
chr5:157806398
|
T | TTTTG | 69 | a0001c0001t0002g0040a0001c0001t0003g0017a0001c0001t0003g0018others(66): Show | 69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.696-287_696-286ins others(4): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 6/11 | chr5 | 157806398 | ||||||
chr5:157806493
|
GA | G | 69 | a0001c0001t0002g0040a0001c0001t0003g0017a0001c0001t0003g0018others(66): Show | 69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.696-382delT | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 6/11 | chr5 | 157806493 | ||||||
chr5:157806513
|
C | T | 69 | a0001c0001t0002g0040a0001c0001t0003g0017a0001c0001t0003g0018others(66): Show | 69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.696-401G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 6/11 | chr5 | 157806513 | ||||||
chr5:157806530
|
T | C | 3 | a0001c0001t0001g0311a0001c0001t0001g0318a0001c0001t0001g0321 | 3 | HG01123.hp2 HG01168.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.696-418A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 6/11 | chr5 | 157806530 | ||||||
chr5:157806850
|
G | T | 7 | a0001c0002t0003g0052a0001c0002t0003g0053a0001c0002t0003g0056others(4): Show | 7 | HG02451.hp2 HG02615.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.696-738C>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 6/11 | chr5 | 157806850 | ||||||
chr5:157806963
|
G | A | 13 | a0001c0001t0002g0086a0001c0001t0002g0196a0001c0001t0002g0197others(10): Show | 13 | HG00735.hp2 HG00738.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.696-851C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 6/11 | chr5 | 157806963 | ||||||
chr5:157806963
|
GGA | G | 123 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(120): Show | 126 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(123): Show |
intron_variant | MODIFIER | c.696-853_696-852del others(2): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 6/11 | chr5 | 157806963 | ||||||
chr5:157806963
|
GGAGA | G | 4 | a0001c0001t0002g0093a0001c0001t0002g0176a0001c0001t0004g0104others(1): Show | 4 | HG01099.hp1 HG02040.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.696-855_696-852del others(4): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 6/11 | chr5 | 157806963 | ||||||
chr5:157806963
|
GGAGAGA | G | 69 | a0001c0001t0002g0040a0001c0001t0003g0017a0001c0001t0003g0018others(66): Show | 69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.696-857_696-852del others(6): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 6/11 | chr5 | 157806963 | ||||||
chr5:157807088
|
A | G | 1 | a0001c0001t0003g0022 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.696-976T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 6/11 | chr5 | 157807088 | ||||||
chr5:157807114
|
A | AACTATGA others(2): Show |
235 | a0001c0001t0001g0006a0001c0001t0001g0277a0001c0001t0001g0305others(232): Show | 239 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.696-1003_696-1002i others(11): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 6/11 | chr5 | 157807114 | ||||||
chr5:157807237
|
A | C | 52 | a0001c0001t0002g0040a0001c0001t0003g0017a0001c0001t0003g0018others(49): Show | 52 | HG00140.hp1 HG00597.hp1 HG01192.hp2 others(49): Show |
intron_variant | MODIFIER | c.696-1125T>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 6/11 | chr5 | 157807237 | ||||||
chr5:157807411
|
T | C | 1 | a0001c0001t0001g0261 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.696-1299A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 6/11 | chr5 | 157807411 | ||||||
chr5:157807415
|
C | G | 2 | a0001c0001t0003g0047a0001c0001t0003g0048 | 2 | HG02717.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.696-1303G>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 6/11 | chr5 | 157807415 | ||||||
chr5:157807469
|
G | A | 20 | a0001c0001t0001g0006a0001c0001t0001g0308a0001c0001t0001g0309others(17): Show | 21 | HG00280.hp1 HG01070.hp1 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.696-1357C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 6/11 | chr5 | 157807469 | ||||||
chr5:157807498
|
T | C | 4 | a0001c0001t0002g0085a0001c0001t0002g0193a0001c0001t0002g0194others(1): Show | 4 | HG02970.hp1 HG03139.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.696-1386A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 6/11 | chr5 | 157807498 | ||||||
chr5:157807500
|
G | A | 1 | a0001c0001t0001g0006 | 2 | HG00280.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.696-1388C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 6/11 | chr5 | 157807500 | ||||||
chr5:157807507
|
A | G | 69 | a0001c0001t0002g0040a0001c0001t0003g0017a0001c0001t0003g0018others(66): Show | 69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.696-1395T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 6/11 | chr5 | 157807507 | ||||||
chr5:157807716
|
G | C | 69 | a0001c0001t0002g0040a0001c0001t0003g0017a0001c0001t0003g0018others(66): Show | 69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.696-1604C>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 6/11 | chr5 | 157807716 | ||||||
chr5:157807742
|
G | A | 1 | a0001c0004t0003g0072 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.696-1630C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 6/11 | chr5 | 157807742 | ||||||
chr5:157807863
|
G | A | 1 | a0001c0001t0010g0332 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.696-1751C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 6/11 | chr5 | 157807863 | ||||||
chr5:157807879
|
A | G | 1 | a0001c0001t0001g0263 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.695+1749T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 6/11 | chr5 | 157807879 | ||||||
chr5:157807931
|
G | A | 1 | a0001c0001t0001g0006 | 2 | HG00280.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.695+1697C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 6/11 | chr5 | 157807931 | ||||||
chr5:157808050
|
T | C | 1 | a0001c0001t0001g0293 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.695+1578A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 6/11 | chr5 | 157808050 | ||||||
chr5:157808105
|
A | G | 1 | a0001c0001t0001g0253 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.695+1523T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 6/11 | chr5 | 157808105 | ||||||
chr5:157808108
|
C | T | 69 | a0001c0001t0002g0040a0001c0001t0003g0017a0001c0001t0003g0018others(66): Show | 69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.695+1520G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 6/11 | chr5 | 157808108 | ||||||
chr5:157808364
|
C | T | 86 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0011others(83): Show | 88 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.695+1264G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 6/11 | chr5 | 157808364 | ||||||
chr5:157808520
|
G | C | 1 | a0001c0001t0001g0268 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.695+1108C>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 6/11 | chr5 | 157808520 | ||||||
chr5:157809116
|
T | C | 70 | a0001c0001t0002g0040a0001c0001t0003g0017a0001c0001t0003g0018others(67): Show | 70 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(67): Show |
intron_variant | MODIFIER | c.695+512A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 6/11 | chr5 | 157809116 | ||||||
chr5:157809181
|
A | T | 2 | a0001c0001t0007g0333a0001c0001t0007g0334 | 2 | HG02109.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.695+447T>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 6/11 | chr5 | 157809181 | ||||||
chr5:157809214
|
A | G | 1 | a0001c0001t0003g0051 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.695+414T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 6/11 | chr5 | 157809214 | ||||||
chr5:157809228
|
G | A | 1 | a0002c0005t0001g0212 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.695+400C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 6/11 | chr5 | 157809228 | ||||||
chr5:157809497
|
T | TA | 124 | a0001c0001t0001g0278a0001c0001t0002g0001a0001c0001t0002g0002others(121): Show | 127 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.695+130dupT | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 6/11 | chr5 | 157809497 | ||||||
chr5:157809497
|
TA | T | 71 | a0001c0001t0001g0223a0001c0001t0002g0040a0001c0001t0003g0017others(68): Show | 71 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(68): Show |
intron_variant | MODIFIER | c.695+130delT | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 6/11 | chr5 | 157809497 | ||||||
chr5:157809498
|
A | T | 3 | a0001c0001t0001g0004a0001c0001t0001g0230a0001c0001t0001g0231 | 4 | NA18941.hp1 NA19062.hp2 NA19085.hp1 others(1): Show |
intron_variant | MODIFIER | c.695+130T>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 6/11 | chr5 | 157809498 | ||||||
chr5:157809574
|
G | A | 7 | a0001c0001t0001g0272a0001c0001t0001g0278a0001c0001t0001g0280others(4): Show | 7 | HG01071.hp1 HG02647.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.695+54C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 6/11 | chr5 | 157809574 | ||||||
chr5:157809605
|
C | T | 1 | a0002c0005t0001g0212 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.695+23G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 6/11 | chr5 | 157809605 | ||||||
chr5:157809841
|
G | A | 3 | a0001c0001t0003g0047a0001c0001t0003g0048a0001c0001t0003g0094 | 3 | HG01109.hp2 HG02717.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.518-36C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 5/11 | chr5 | 157809841 | ||||||
chr5:157810253
|
A | G | 13 | a0001c0001t0002g0083a0001c0001t0002g0090a0001c0001t0002g0092others(10): Show | 13 | HG01952.hp1 HG02074.hp2 HG02165.hp1 others(10): Show |
intron_variant | MODIFIER | c.518-448T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 5/11 | chr5 | 157810253 | ||||||
chr5:157810427
|
T | C | 235 | a0001c0001t0001g0006a0001c0001t0001g0277a0001c0001t0001g0305others(232): Show | 239 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.518-622A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 5/11 | chr5 | 157810427 | ||||||
chr5:157810446
|
G | C | 1 | a0001c0001t0002g0014 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.518-641C>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 5/11 | chr5 | 157810446 | ||||||
chr5:157810450
|
A | T | 69 | a0001c0001t0002g0040a0001c0001t0003g0017a0001c0001t0003g0018others(66): Show | 69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.518-645T>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 5/11 | chr5 | 157810450 | ||||||
chr5:157810515
|
G | A | 1 | a0001c0001t0010g0332 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.518-710C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 5/11 | chr5 | 157810515 | ||||||
chr5:157810633
|
T | C | 1 | a0002c0005t0001g0212 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.518-828A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 5/11 | chr5 | 157810633 | ||||||
chr5:157810633
|
T | G | 1 | a0001c0001t0002g0106 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.518-828A>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 5/11 | chr5 | 157810633 | ||||||
chr5:157810865
|
T | C | 21 | a0001c0001t0001g0006a0001c0001t0001g0308a0001c0001t0001g0309others(18): Show | 22 | HG00280.hp1 HG01070.hp1 HG01071.hp2 others(19): Show |
intron_variant | MODIFIER | c.518-1060A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 5/11 | chr5 | 157810865 | ||||||
chr5:157810878
|
T | C | 2 | a0001c0001t0002g0131a0001c0001t0010g0332 | 2 | HG03130.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.518-1073A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 5/11 | chr5 | 157810878 | ||||||
chr5:157810879
|
T | C | 1 | a0001c0001t0001g0266 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.518-1074A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 5/11 | chr5 | 157810879 | ||||||
chr5:157811049
|
A | T | 12 | a0001c0001t0002g0002a0001c0001t0002g0110a0001c0001t0002g0117others(9): Show | 13 | HG00597.hp2 HG02027.hp1 HG02056.hp2 others(10): Show |
intron_variant | MODIFIER | c.518-1244T>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 5/11 | chr5 | 157811049 | ||||||
chr5:157811073
|
T | C | 4 | a0001c0001t0004g0141a0001c0001t0004g0143a0001c0001t0004g0188others(1): Show | 4 | NA18940.hp2 NA18943.hp2 NA18945.hp1 others(1): Show |
intron_variant | MODIFIER | c.518-1268A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 5/11 | chr5 | 157811073 | ||||||
chr5:157811105
|
C | G | 4 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270others(1): Show | 4 | HG01070.hp2 HG01169.hp2 HG02055.hp1 others(1): Show |
intron_variant | MODIFIER | c.518-1300G>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 5/11 | chr5 | 157811105 | ||||||
chr5:157811105
|
C | T | 70 | a0001c0001t0002g0040a0001c0001t0003g0017a0001c0001t0003g0018others(67): Show | 70 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(67): Show |
intron_variant | MODIFIER | c.518-1300G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 5/11 | chr5 | 157811105 | ||||||
chr5:157811264
|
G | A | 1 | a0001c0001t0004g0187 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.518-1459C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 5/11 | chr5 | 157811264 | ||||||
chr5:157811388
|
C | T | 1 | a0001c0001t0001g0267 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.518-1583G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 5/11 | chr5 | 157811388 | ||||||
chr5:157811529
|
CA | C | 35 | a0001c0001t0001g0006a0001c0001t0001g0302a0001c0001t0001g0308others(32): Show | 36 | HG00280.hp1 HG00323.hp2 HG01070.hp1 others(33): Show |
intron_variant | MODIFIER | c.517+1533delT | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 5/11 | chr5 | 157811529 | ||||||
chr5:157811529
|
CAA | C | 55 | a0001c0001t0002g0040a0001c0001t0003g0017a0001c0001t0003g0018others(52): Show | 55 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(52): Show |
intron_variant | MODIFIER | c.517+1532_517+1533d others(4): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 5/11 | chr5 | 157811529 | ||||||
chr5:157811749
|
A | G | 1 | a0001c0001t0003g0213 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.517+1314T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 5/11 | chr5 | 157811749 | ||||||
chr5:157811921
|
C | T | 2 | a0001c0001t0002g0193a0001c0008t0002g0195 | 2 | HG03195.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.517+1142G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 5/11 | chr5 | 157811921 | ||||||
chr5:157811934
|
T | C | 13 | a0001c0001t0002g0086a0001c0001t0002g0196a0001c0001t0002g0197others(10): Show | 13 | HG00735.hp2 HG00738.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.517+1129A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 5/11 | chr5 | 157811934 | ||||||
chr5:157811973
|
A | T | 69 | a0001c0001t0002g0040a0001c0001t0003g0017a0001c0001t0003g0018others(66): Show | 69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.517+1090T>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 5/11 | chr5 | 157811973 | ||||||
chr5:157812023
|
T | TAAAAAAA | 64 | a0001c0001t0002g0040a0001c0001t0003g0017a0001c0001t0003g0018others(61): Show | 64 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(61): Show |
intron_variant | MODIFIER | c.517+1033_517+1039d others(9): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 5/11 | chr5 | 157812023 | ||||||
chr5:157812112
|
G | C | 1 | a0002c0005t0001g0212 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.517+951C>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 5/11 | chr5 | 157812112 | ||||||
chr5:157812149
|
A | AAGCAG | 69 | a0001c0001t0002g0040a0001c0001t0003g0017a0001c0001t0003g0018others(66): Show | 69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.517+909_517+913dup others(5): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 5/11 | chr5 | 157812149 | ||||||
chr5:157812258
|
G | C | 1 | a0001c0001t0001g0277 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.517+805C>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 5/11 | chr5 | 157812258 | ||||||
chr5:157812288
|
T | A | 5 | a0001c0002t0003g0053a0001c0002t0003g0056a0001c0002t0003g0073others(2): Show | 5 | HG02451.hp2 HG02615.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.517+775A>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 5/11 | chr5 | 157812288 | ||||||
chr5:157812289
|
G | A | 3 | a0001c0001t0001g0224a0001c0001t0001g0225a0001c0001t0001g0226 | 3 | HG01496.hp1 HG01928.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.517+774C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 5/11 | chr5 | 157812289 | ||||||
chr5:157812400
|
C | G | 2 | a0001c0001t0001g0301a0001c0001t0001g0302 | 2 | HG00099.hp1 HG00323.hp2 |
intron_variant | MODIFIER | c.517+663G>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 5/11 | chr5 | 157812400 | ||||||
chr5:157812593
|
T | A | 2 | a0001c0001t0001g0005a0001c0001t0001g0250 | 3 | HG00438.hp1 NA18970.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.517+470A>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 5/11 | chr5 | 157812593 | ||||||
chr5:157812663
|
G | C | 2 | a0001c0001t0007g0333a0001c0001t0007g0334 | 2 | HG02109.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.517+400C>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 5/11 | chr5 | 157812663 | ||||||
chr5:157812777
|
T | C | 1 | a0001c0001t0001g0223 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.517+286A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 5/11 | chr5 | 157812777 | ||||||
chr5:157813472
|
G | T | 1 | a0001c0001t0002g0184 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.353-245C>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 4/11 | chr5 | 157813472 | ||||||
chr5:157813478
|
T | G | 1 | a0002c0005t0001g0212 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.353-251A>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 4/11 | chr5 | 157813478 | ||||||
chr5:157813534
|
T | C | 1 | a0001c0001t0001g0310 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.353-307A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 4/11 | chr5 | 157813534 | ||||||
chr5:157813657
|
C | A | 69 | a0001c0001t0002g0040a0001c0001t0003g0017a0001c0001t0003g0018others(66): Show | 69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.353-430G>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 4/11 | chr5 | 157813657 | ||||||
chr5:157813663
|
G | T | 1 | a0001c0001t0002g0120 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.353-436C>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 4/11 | chr5 | 157813663 | ||||||
chr5:157813745
|
T | C | 1 | a0001c0001t0007g0333 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.352+440A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 4/11 | chr5 | 157813745 | ||||||
chr5:157813772
|
A | G | 1 | a0001c0001t0002g0091 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.352+413T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 4/11 | chr5 | 157813772 | ||||||
chr5:157814143
|
A | G | 2 | a0001c0001t0003g0210a0001c0004t0003g0072 | 2 | HG02922.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.352+42T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 4/11 | chr5 | 157814143 | ||||||
chr5:157814297
|
C | T | 69 | a0001c0001t0002g0040a0001c0001t0003g0017a0001c0001t0003g0018others(66): Show | 69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
splice_region_variant&intron_variant | LOW | c.244-4G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 3/11 | chr5 | 157814297 | ||||||
chr5:157814359
|
TA | T | 20 | a0001c0001t0001g0006a0001c0001t0001g0308a0001c0001t0001g0309others(17): Show | 21 | HG00280.hp1 HG01070.hp1 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.244-67delT | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 3/11 | chr5 | 157814359 | ||||||
chr5:157814513
|
T | C | 1 | a0001c0001t0002g0181 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.244-220A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 3/11 | chr5 | 157814513 | ||||||
chr5:157814571
|
C | T | 69 | a0001c0001t0002g0040a0001c0001t0003g0017a0001c0001t0003g0018others(66): Show | 69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.244-278G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 3/11 | chr5 | 157814571 | ||||||
chr5:157814681
|
T | C | 1 | a0001c0001t0002g0040 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.244-388A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 3/11 | chr5 | 157814681 | ||||||
chr5:157814777
|
C | G | 1 | a0001c0001t0002g0185 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.244-484G>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 3/11 | chr5 | 157814777 | ||||||
chr5:157814804
|
G | A | 137 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0011others(134): Show | 140 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.244-511C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 3/11 | chr5 | 157814804 | ||||||
chr5:157814988
|
G | A | 1 | a0001c0001t0002g0154 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.244-695C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 3/11 | chr5 | 157814988 | ||||||
chr5:157815030
|
CA | C | 7 | a0001c0001t0001g0006a0001c0001t0001g0225a0001c0001t0001g0246others(4): Show | 8 | HG00280.hp1 HG00323.hp2 HG01346.hp2 others(5): Show |
intron_variant | MODIFIER | c.244-738delT | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 3/11 | chr5 | 157815030 | ||||||
chr5:157815078
|
A | G | 20 | a0001c0001t0001g0006a0001c0001t0001g0308a0001c0001t0001g0309others(17): Show | 21 | HG00280.hp1 HG01070.hp1 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.244-785T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 3/11 | chr5 | 157815078 | ||||||
chr5:157815104
|
T | C | 5 | a0001c0001t0001g0277a0001c0001t0001g0305a0001c0001t0001g0306others(2): Show | 5 | HG01243.hp2 HG02647.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.244-811A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 3/11 | chr5 | 157815104 | ||||||
chr5:157815120
|
T | TAC | 38 | a0001c0001t0001g0224a0001c0001t0001g0234a0001c0001t0001g0255others(35): Show | 38 | HG01070.hp2 HG01081.hp1 HG01106.hp2 others(35): Show |
intron_variant | MODIFIER | c.244-829_244-828dup others(2): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 3/11 | chr5 | 157815120 | ||||||
chr5:157815120
|
T | TACAC | 4 | a0001c0001t0002g0085a0001c0001t0002g0194a0001c0002t0003g0054others(1): Show | 4 | HG02886.hp1 HG02922.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.244-831_244-828dup others(4): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 3/11 | chr5 | 157815120 | ||||||
chr5:157815120
|
T | TACACAC | 29 | a0001c0001t0002g0090a0001c0001t0002g0109a0001c0001t0002g0116others(26): Show | 30 | HG00741.hp1 HG01099.hp1 HG01106.hp1 others(27): Show |
intron_variant | MODIFIER | c.244-833_244-828dup others(6): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 3/11 | chr5 | 157815120 | ||||||
chr5:157815120
|
T | TACACACA others(1): Show |
6 | a0001c0001t0005g0098a0001c0001t0005g0100a0001c0001t0005g0103others(3): Show | 6 | NA18962.hp2 NA18981.hp1 NA18998.hp1 others(3): Show |
intron_variant | MODIFIER | c.244-835_244-828dup others(8): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 3/11 | chr5 | 157815120 | ||||||
chr5:157815120
|
T | TACACACA others(3): Show |
1 | a0001c0001t0004g0095 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.244-837_244-828dup others(10): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 3/11 | chr5 | 157815120 | ||||||
chr5:157815120
|
T | TACACACA others(5): Show |
1 | a0001c0001t0004g0105 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.244-839_244-828dup others(12): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 3/11 | chr5 | 157815120 | ||||||
chr5:157815120
|
T | TACACACA others(7): Show |
1 | a0001c0001t0004g0107 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.244-841_244-828dup others(14): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 3/11 | chr5 | 157815120 | ||||||
chr5:157815120
|
TAC | T | 13 | a0001c0001t0001g0277a0001c0001t0001g0305a0001c0001t0001g0306others(10): Show | 13 | HG01243.hp1 HG01243.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.244-829_244-828del others(2): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 3/11 | chr5 | 157815120 | ||||||
chr5:157815168
|
C | T | 1 | a0001c0001t0002g0123 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.244-875G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 3/11 | chr5 | 157815168 | ||||||
chr5:157815262
|
T | G | 1 | a0001c0001t0003g0046 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.244-969A>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 3/11 | chr5 | 157815262 | ||||||
chr5:157815297
|
T | C | 69 | a0001c0001t0002g0040a0001c0001t0003g0017a0001c0001t0003g0018others(66): Show | 69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.244-1004A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 3/11 | chr5 | 157815297 | ||||||
chr5:157815345
|
T | C | 3 | a0001c0001t0002g0135a0001c0001t0002g0182a0001c0001t0002g0183 | 3 | NA18612.hp2 NA18987.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.244-1052A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 3/11 | chr5 | 157815345 | ||||||
chr5:157815379
|
G | A | 69 | a0001c0001t0002g0040a0001c0001t0003g0017a0001c0001t0003g0018others(66): Show | 69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.244-1086C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 3/11 | chr5 | 157815379 | ||||||
chr5:157815414
|
G | GA | 137 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0011others(134): Show | 140 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.244-1122dupT | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 3/11 | chr5 | 157815414 | ||||||
chr5:157815457
|
A | G | 210 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0011others(207): Show | 213 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(210): Show |
intron_variant | MODIFIER | c.244-1164T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 3/11 | chr5 | 157815457 | ||||||
chr5:157815463
|
T | C | 2 | a0001c0001t0007g0333a0001c0001t0007g0334 | 2 | HG02109.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.244-1170A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 3/11 | chr5 | 157815463 | ||||||
chr5:157815904
|
A | C | 1 | a0001c0001t0010g0332 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.243+830T>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 3/11 | chr5 | 157815904 | ||||||
chr5:157815911
|
A | T | 275 | a0001c0001t0001g0006a0001c0001t0001g0079a0001c0001t0001g0268others(272): Show | 279 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(276): Show |
intron_variant | MODIFIER | c.243+823T>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 3/11 | chr5 | 157815911 | ||||||
chr5:157815980
|
T | C | 210 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0011others(207): Show | 213 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(210): Show |
intron_variant | MODIFIER | c.243+754A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 3/11 | chr5 | 157815980 | ||||||
chr5:157816455
|
C | G | 3 | a0001c0001t0001g0232a0001c0001t0001g0242a0001c0001t0001g0245 | 3 | HG01981.hp1 HG02004.hp1 HG02040.hp1 |
intron_variant | MODIFIER | c.243+279G>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 3/11 | chr5 | 157816455 | ||||||
chr5:157817007
|
C | T | 1 | a0001c0001t0002g0126 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.147-177G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 2/11 | chr5 | 157817007 | ||||||
chr5:157817094
|
T | C | 13 | a0001c0002t0003g0052a0001c0002t0003g0053a0001c0002t0003g0054others(10): Show | 13 | HG02451.hp2 HG02615.hp2 HG02809.hp1 others(10): Show |
intron_variant | MODIFIER | c.147-264A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 2/11 | chr5 | 157817094 | ||||||
chr5:157817132
|
T | C | 1 | a0001c0001t0003g0210 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.147-302A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 2/11 | chr5 | 157817132 | ||||||
chr5:157817341
|
T | C | 2 | a0001c0001t0001g0269a0001c0001t0001g0270 | 2 | HG01070.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.146+102A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 2/11 | chr5 | 157817341 | ||||||
chr5:157817398
|
A | T | 1 | a0001c0001t0003g0089 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.146+45T>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 2/11 | chr5 | 157817398 | ||||||
chr5:157817587
|
T | G | 1 | a0001c0001t0003g0043 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.42-40A>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157817587 | ||||||
chr5:157817592
|
T | C | 1 | a0001c0001t0003g0051 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.42-45A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157817592 | ||||||
chr5:157817613
|
A | G | 13 | a0001c0002t0003g0052a0001c0002t0003g0053a0001c0002t0003g0054others(10): Show | 13 | HG02451.hp2 HG02615.hp2 HG02809.hp1 others(10): Show |
intron_variant | MODIFIER | c.42-66T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157817613 | ||||||
chr5:157817622
|
A | G | 13 | a0001c0002t0003g0052a0001c0002t0003g0053a0001c0002t0003g0054others(10): Show | 13 | HG02451.hp2 HG02615.hp2 HG02809.hp1 others(10): Show |
intron_variant | MODIFIER | c.42-75T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157817622 | ||||||
chr5:157817747
|
T | C | 1 | a0001c0001t0003g0210 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.42-200A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157817747 | ||||||
chr5:157818161
|
G | T | 69 | a0001c0001t0002g0040a0001c0001t0003g0017a0001c0001t0003g0018others(66): Show | 69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.42-614C>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157818161 | ||||||
chr5:157818169
|
G | C | 1 | a0002c0005t0001g0212 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.42-622C>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157818169 | ||||||
chr5:157818203
|
A | G | 20 | a0001c0001t0001g0006a0001c0001t0001g0308a0001c0001t0001g0309others(17): Show | 21 | HG00280.hp1 HG01070.hp1 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.42-656T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157818203 | ||||||
chr5:157818465
|
T | C | 7 | a0001c0001t0001g0272a0001c0001t0001g0278a0001c0001t0001g0280others(4): Show | 7 | HG01071.hp1 HG02647.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.42-918A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157818465 | ||||||
chr5:157818466
|
C | CCAA | 7 | a0001c0001t0001g0272a0001c0001t0001g0278a0001c0001t0001g0280others(4): Show | 7 | HG01071.hp1 HG02647.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.42-920_42-919insTT others(1): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157818466 | ||||||
chr5:157818467
|
T | A | 7 | a0001c0001t0001g0272a0001c0001t0001g0278a0001c0001t0001g0280others(4): Show | 7 | HG01071.hp1 HG02647.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.42-920A>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157818467 | ||||||
chr5:157818467
|
T | TA | 52 | a0001c0001t0001g0079a0001c0001t0001g0224a0001c0001t0001g0225others(49): Show | 52 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(49): Show |
intron_variant | MODIFIER | c.42-921dupT | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157818467 | ||||||
chr5:157818467
|
TA | T | 13 | a0001c0001t0001g0223a0001c0001t0001g0246a0001c0001t0001g0248others(10): Show | 13 | HG01070.hp1 HG01192.hp2 HG01257.hp1 others(10): Show |
intron_variant | MODIFIER | c.42-921delT | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157818467 | ||||||
chr5:157818604
|
G | A | 11 | a0001c0001t0004g0003a0001c0001t0004g0084a0001c0001t0004g0140others(8): Show | 12 | NA18940.hp2 NA18942.hp2 NA18943.hp2 others(9): Show |
intron_variant | MODIFIER | c.42-1057C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157818604 | ||||||
chr5:157818680
|
C | G | 13 | a0001c0002t0003g0052a0001c0002t0003g0053a0001c0002t0003g0054others(10): Show | 13 | HG02451.hp2 HG02615.hp2 HG02809.hp1 others(10): Show |
intron_variant | MODIFIER | c.42-1133G>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157818680 | ||||||
chr5:157818682
|
A | G | 7 | a0001c0001t0001g0005a0001c0001t0001g0233a0001c0001t0001g0234others(4): Show | 8 | HG00438.hp1 NA18954.hp1 NA18970.hp2 others(5): Show |
intron_variant | MODIFIER | c.42-1135T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157818682 | ||||||
chr5:157818739
|
C | T | 1 | a0001c0001t0010g0332 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.42-1192G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157818739 | ||||||
chr5:157818769
|
C | T | 1 | a0001c0001t0010g0332 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.42-1222G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157818769 | ||||||
chr5:157818913
|
G | A | 1 | a0001c0001t0010g0332 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.42-1366C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157818913 | ||||||
chr5:157819034
|
G | A | 1 | a0001c0001t0003g0044 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.42-1487C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157819034 | ||||||
chr5:157819207
|
C | G | 123 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0011others(120): Show | 126 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.42-1660G>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157819207 | ||||||
chr5:157819241
|
T | C | 69 | a0001c0001t0002g0040a0001c0001t0003g0017a0001c0001t0003g0018others(66): Show | 69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.42-1694A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157819241 | ||||||
chr5:157819474
|
C | G | 69 | a0001c0001t0002g0040a0001c0001t0003g0017a0001c0001t0003g0018others(66): Show | 69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.42-1927G>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157819474 | ||||||
chr5:157819487
|
A | T | 2 | a0001c0001t0003g0210a0001c0004t0003g0072 | 2 | HG02922.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.42-1940T>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157819487 | ||||||
chr5:157819498
|
T | C | 1 | a0001c0001t0003g0050 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.42-1951A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157819498 | ||||||
chr5:157819692
|
C | T | 3 | a0001c0001t0001g0311a0001c0001t0001g0318a0001c0001t0001g0321 | 3 | HG01123.hp2 HG01168.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.42-2145G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157819692 | ||||||
chr5:157819923
|
G | A | 1 | a0001c0001t0002g0154 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.42-2376C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157819923 | ||||||
chr5:157819964
|
G | T | 33 | a0001c0001t0004g0003a0001c0001t0004g0082a0001c0001t0004g0084others(30): Show | 34 | HG00741.hp1 HG01099.hp1 HG01106.hp1 others(31): Show |
intron_variant | MODIFIER | c.42-2417C>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157819964 | ||||||
chr5:157820131
|
AC | A | 3 | a0001c0001t0003g0047a0001c0001t0003g0048a0001c0001t0003g0094 | 3 | HG01109.hp2 HG02717.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.42-2585delG | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157820131 | ||||||
chr5:157820152
|
G | A | 209 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0011others(206): Show | 212 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(209): Show |
intron_variant | MODIFIER | c.42-2605C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157820152 | ||||||
chr5:157820264
|
C | T | 1 | a0001c0001t0001g0279 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.42-2717G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157820264 | ||||||
chr5:157820301
|
T | A | 2 | a0001c0001t0007g0333a0001c0001t0007g0334 | 2 | HG02109.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.42-2754A>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157820301 | ||||||
chr5:157820333
|
C | T | 2 | a0001c0001t0001g0280a0001c0001t0001g0281 | 2 | HG03041.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.42-2786G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157820333 | ||||||
chr5:157820346
|
C | T | 1 | a0001c0004t0003g0072 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.42-2799G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157820346 | ||||||
chr5:157820504
|
A | C | 1 | a0001c0001t0002g0040 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.42-2957T>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157820504 | ||||||
chr5:157820571
|
T | G | 1 | a0001c0001t0002g0316 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.42-3024A>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157820571 | ||||||
chr5:157820779
|
T | A | 2 | a0001c0001t0001g0280a0001c0001t0001g0281 | 2 | HG03041.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.42-3232A>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157820779 | ||||||
chr5:157820856
|
C | T | 69 | a0001c0001t0002g0040a0001c0001t0003g0017a0001c0001t0003g0018others(66): Show | 69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.42-3309G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157820856 | ||||||
chr5:157820926
|
A | G | 1 | a0001c0001t0002g0090 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.42-3379T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157820926 | ||||||
chr5:157820996
|
C | A | 1 | a0001c0001t0002g0088 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.42-3449G>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157820996 | ||||||
chr5:157821070
|
G | T | 5 | a0001c0001t0001g0274a0001c0001t0001g0289a0001c0001t0001g0290others(2): Show | 5 | HG01884.hp1 HG02572.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.42-3523C>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157821070 | ||||||
chr5:157821104
|
C | A | 1 | a0001c0001t0003g0021 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.42-3557G>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157821104 | ||||||
chr5:157821187
|
AG | A | 70 | a0001c0001t0002g0040a0001c0001t0003g0017a0001c0001t0003g0018others(67): Show | 70 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(67): Show |
intron_variant | MODIFIER | c.42-3641delC | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157821187 | ||||||
chr5:157821237
|
T | C | 2 | a0001c0001t0001g0005a0001c0001t0001g0250 | 3 | HG00438.hp1 NA18970.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.42-3690A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157821237 | ||||||
chr5:157821386
|
G | GA | 210 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0011others(207): Show | 213 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(210): Show |
intron_variant | MODIFIER | c.42-3840dupT | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157821386 | ||||||
chr5:157821422
|
A | G | 69 | a0001c0001t0002g0040a0001c0001t0003g0017a0001c0001t0003g0018others(66): Show | 69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.42-3875T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157821422 | ||||||
chr5:157821492
|
A | G | 2 | a0001c0001t0003g0047a0001c0001t0003g0048 | 2 | HG02717.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.42-3945T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157821492 | ||||||
chr5:157821540
|
T | A | 13 | a0001c0001t0002g0086a0001c0001t0002g0196a0001c0001t0002g0197others(10): Show | 13 | HG00735.hp2 HG00738.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.42-3993A>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157821540 | ||||||
chr5:157821620
|
T | G | 3 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0228 | 3 | HG02257.hp2 HG02723.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.42-4073A>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157821620 | ||||||
chr5:157821681
|
T | C | 69 | a0001c0001t0002g0040a0001c0001t0003g0017a0001c0001t0003g0018others(66): Show | 69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.42-4134A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157821681 | ||||||
chr5:157821683
|
G | T | 1 | a0001c0002t0003g0073 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.42-4136C>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157821683 | ||||||
chr5:157821839
|
G | A | 18 | a0001c0001t0001g0006a0001c0001t0001g0308a0001c0001t0001g0310others(15): Show | 19 | HG00280.hp1 HG01070.hp1 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.42-4292C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157821839 | ||||||
chr5:157821999
|
T | C | 1 | a0001c0001t0001g0279 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.42-4452A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157821999 | ||||||
chr5:157822040
|
A | G | 1 | a0002c0005t0001g0212 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.42-4493T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157822040 | ||||||
chr5:157822053
|
T | C | 1 | a0001c0001t0002g0185 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.42-4506A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157822053 | ||||||
chr5:157822065
|
G | A | 23 | a0001c0001t0004g0003a0001c0001t0004g0082a0001c0001t0004g0084others(20): Show | 24 | HG01099.hp1 HG01358.hp2 HG01515.hp2 others(21): Show |
intron_variant | MODIFIER | c.42-4518C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157822065 | ||||||
chr5:157822141
|
T | A | 1 | a0001c0001t0002g0109 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.42-4594A>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157822141 | ||||||
chr5:157822156
|
C | T | 1 | a0001c0004t0003g0072 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.42-4609G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157822156 | ||||||
chr5:157822200
|
A | G | 1 | a0002c0005t0001g0212 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.42-4653T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157822200 | ||||||
chr5:157822212
|
CT | C | 70 | a0001c0001t0002g0040a0001c0001t0003g0017a0001c0001t0003g0018others(67): Show | 70 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(67): Show |
intron_variant | MODIFIER | c.42-4666delA | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157822212 | ||||||
chr5:157822336
|
T | C | 1 | a0001c0001t0002g0153 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.42-4789A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157822336 | ||||||
chr5:157822497
|
C | T | 1 | a0001c0001t0002g0106 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.42-4950G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157822497 | ||||||
chr5:157822513
|
T | C | 1 | a0001c0001t0003g0059 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.42-4966A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157822513 | ||||||
chr5:157822737
|
A | G | 69 | a0001c0001t0002g0040a0001c0001t0003g0017a0001c0001t0003g0018others(66): Show | 69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.42-5190T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157822737 | ||||||
chr5:157822770
|
C | T | 1 | a0001c0001t0002g0092 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.42-5223G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157822770 | ||||||
chr5:157823022
|
A | T | 333 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(330): Show | 339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.42-5475T>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157823022 | ||||||
chr5:157823126
|
T | C | 1 | a0003c0007t0003g0031 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.42-5579A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157823126 | ||||||
chr5:157823156
|
G | T | 1 | a0001c0001t0001g0224 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.42-5609C>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157823156 | ||||||
chr5:157823181
|
G | C | 1 | a0001c0001t0002g0316 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.42-5634C>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157823181 | ||||||
chr5:157823254
|
T | C | 69 | a0001c0001t0002g0040a0001c0001t0003g0017a0001c0001t0003g0018others(66): Show | 69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.42-5707A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157823254 | ||||||
chr5:157823418
|
T | G | 1 | a0001c0001t0003g0210 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.42-5871A>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157823418 | ||||||
chr5:157823419
|
G | A | 1 | a0001c0001t0002g0127 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.42-5872C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157823419 | ||||||
chr5:157823456
|
G | A | 69 | a0001c0001t0002g0040a0001c0001t0003g0017a0001c0001t0003g0018others(66): Show | 69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.42-5909C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157823456 | ||||||
chr5:157823549
|
T | A | 1 | a0001c0001t0003g0094 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.42-6002A>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157823549 | ||||||
chr5:157823780
|
C | T | 5 | a0001c0001t0001g0274a0001c0001t0001g0289a0001c0001t0001g0290others(2): Show | 5 | HG01884.hp1 HG02572.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.42-6233G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157823780 | ||||||
chr5:157823782
|
G | A | 1 | a0001c0001t0010g0332 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.42-6235C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157823782 | ||||||
chr5:157823841
|
C | T | 1 | a0001c0001t0002g0106 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.42-6294G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157823841 | ||||||
chr5:157823880
|
T | C | 69 | a0001c0001t0002g0040a0001c0001t0003g0017a0001c0001t0003g0018others(66): Show | 69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.42-6333A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157823880 | ||||||
chr5:157823887
|
C | T | 1 | a0002c0005t0001g0212 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.42-6340G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157823887 | ||||||
chr5:157823905
|
G | A | 1 | a0001c0001t0002g0191 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.42-6358C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157823905 | ||||||
chr5:157823918
|
C | T | 69 | a0001c0001t0002g0040a0001c0001t0003g0017a0001c0001t0003g0018others(66): Show | 69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.42-6371G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157823918 | ||||||
chr5:157823920
|
T | C | 69 | a0001c0001t0002g0040a0001c0001t0003g0017a0001c0001t0003g0018others(66): Show | 69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.42-6373A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157823920 | ||||||
chr5:157824074
|
C | T | 20 | a0001c0001t0001g0006a0001c0001t0001g0308a0001c0001t0001g0309others(17): Show | 21 | HG00280.hp1 HG01070.hp1 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.42-6527G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157824074 | ||||||
chr5:157824129
|
T | C | 1 | a0001c0001t0003g0050 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.42-6582A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157824129 | ||||||
chr5:157824293
|
G | A | 70 | a0001c0001t0002g0040a0001c0001t0003g0017a0001c0001t0003g0018others(67): Show | 70 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(67): Show |
intron_variant | MODIFIER | c.42-6746C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157824293 | ||||||
chr5:157824356
|
G | A | 1 | a0001c0001t0002g0154 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.42-6809C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157824356 | ||||||
chr5:157824410
|
C | T | 4 | a0001c0002t0003g0054a0001c0002t0003g0055a0001c0002t0003g0057others(1): Show | 4 | HG02886.hp1 HG02965.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.42-6863G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157824410 | ||||||
chr5:157824557
|
A | G | 1 | a0001c0001t0010g0332 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.42-7010T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157824557 | ||||||
chr5:157824572
|
T | C | 2 | a0001c0001t0002g0002a0001c0001t0002g0166 | 3 | HG03834.hp1 NA19004.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.42-7025A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157824572 | ||||||
chr5:157824600
|
T | C | 1 | a0001c0001t0001g0292 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.42-7053A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157824600 | ||||||
chr5:157824626
|
G | A | 69 | a0001c0001t0002g0040a0001c0001t0003g0017a0001c0001t0003g0018others(66): Show | 69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.42-7079C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157824626 | ||||||
chr5:157824652
|
T | G | 137 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0011others(134): Show | 140 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.42-7105A>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157824652 | ||||||
chr5:157824779
|
T | G | 69 | a0001c0001t0002g0040a0001c0001t0003g0017a0001c0001t0003g0018others(66): Show | 69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.42-7232A>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157824779 | ||||||
chr5:157824833
|
A | G | 137 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0011others(134): Show | 140 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.42-7286T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157824833 | ||||||
chr5:157825153
|
G | A | 1 | a0001c0001t0003g0094 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.42-7606C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157825153 | ||||||
chr5:157825205
|
A | G | 2 | a0001c0001t0003g0024a0001c0001t0003g0067 | 2 | HG00597.hp1 NA18940.hp1 |
intron_variant | MODIFIER | c.42-7658T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157825205 | ||||||
chr5:157825387
|
A | G | 3 | a0001c0001t0002g0135a0001c0001t0002g0182a0001c0001t0002g0183 | 3 | NA18612.hp2 NA18987.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.42-7840T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157825387 | ||||||
chr5:157825814
|
C | T | 5 | a0001c0001t0001g0277a0001c0001t0001g0305a0001c0001t0001g0306others(2): Show | 5 | HG01243.hp2 HG02647.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.42-8267G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157825814 | ||||||
chr5:157825931
|
T | C | 2 | a0001c0001t0007g0333a0001c0001t0007g0334 | 2 | HG02109.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.42-8384A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157825931 | ||||||
chr5:157826176
|
G | A | 1 | a0001c0002t0003g0080 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.42-8629C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157826176 | ||||||
chr5:157826326
|
T | C | 3 | a0001c0001t0002g0135a0001c0001t0002g0182a0001c0001t0002g0183 | 3 | NA18612.hp2 NA18987.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.42-8779A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157826326 | ||||||
chr5:157826395
|
T | C | 52 | a0001c0001t0002g0040a0001c0001t0003g0017a0001c0001t0003g0018others(49): Show | 52 | HG00140.hp1 HG00597.hp1 HG01192.hp2 others(49): Show |
intron_variant | MODIFIER | c.42-8848A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157826395 | ||||||
chr5:157826425
|
A | G | 1 | a0001c0001t0002g0137 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.42-8878T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157826425 | ||||||
chr5:157826515
|
A | AT | 181 | a0001c0001t0001g0006a0001c0001t0001g0257a0001c0001t0001g0277others(178): Show | 185 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.42-8969dupA | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157826515 | ||||||
chr5:157826630
|
ACATG | A | 20 | a0001c0001t0001g0006a0001c0001t0001g0308a0001c0001t0001g0309others(17): Show | 21 | HG00280.hp1 HG01070.hp1 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.42-9087_42-9084del others(4): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157826630 | ||||||
chr5:157826638
|
G | C | 1 | a0001c0001t0002g0122 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.42-9091C>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157826638 | ||||||
chr5:157826638
|
G | T | 137 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0011others(134): Show | 140 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.42-9091C>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157826638 | ||||||
chr5:157827035
|
T | C | 1 | a0001c0001t0002g0152 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.42-9488A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157827035 | ||||||
chr5:157827223
|
A | G | 1 | a0001c0001t0001g0289 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.42-9676T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157827223 | ||||||
chr5:157827266
|
C | T | 2 | a0001c0001t0002g0179a0001c0001t0002g0180 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.42-9719G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157827266 | ||||||
chr5:157827314
|
T | C | 3 | a0001c0001t0001g0252a0001c0001t0001g0263a0001c0001t0001g0266 | 3 | HG02559.hp2 HG03225.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.42-9767A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157827314 | ||||||
chr5:157827544
|
C | T | 2 | a0001c0001t0002g0161a0001c0001t0002g0162 | 2 | HG00280.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.42-9997G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157827544 | ||||||
chr5:157827562
|
A | C | 1 | a0002c0005t0001g0212 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.42-10015T>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157827562 | ||||||
chr5:157827773
|
T | G | 1 | a0001c0001t0001g0325 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.42-10226A>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157827773 | ||||||
chr5:157827797
|
A | T | 1 | a0001c0001t0010g0332 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.42-10250T>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157827797 | ||||||
chr5:157827979
|
T | C | 2 | a0001c0001t0003g0044a0001c0001t0003g0045 | 2 | HG02486.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.42-10432A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157827979 | ||||||
chr5:157827987
|
C | T | 1 | a0001c0001t0002g0134 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.42-10440G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157827987 | ||||||
chr5:157827993
|
A | G | 70 | a0001c0001t0002g0040a0001c0001t0003g0017a0001c0001t0003g0018others(67): Show | 70 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(67): Show |
intron_variant | MODIFIER | c.42-10446T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157827993 | ||||||
chr5:157828447
|
A | C | 33 | a0001c0001t0004g0003a0001c0001t0004g0082a0001c0001t0004g0084others(30): Show | 34 | HG00741.hp1 HG01099.hp1 HG01106.hp1 others(31): Show |
intron_variant | MODIFIER | c.42-10900T>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157828447 | ||||||
chr5:157828475
|
G | A | 210 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0011others(207): Show | 213 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(210): Show |
intron_variant | MODIFIER | c.42-10928C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157828475 | ||||||
chr5:157828503
|
A | G | 2 | a0001c0001t0003g0047a0001c0001t0003g0048 | 2 | HG02717.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.42-10956T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157828503 | ||||||
chr5:157828583
|
G | A | 1 | a0001c0001t0002g0106 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.42-11036C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157828583 | ||||||
chr5:157828719
|
T | C | 1 | a0001c0001t0006g0008 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.42-11172A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157828719 | ||||||
chr5:157828892
|
C | T | 69 | a0001c0001t0002g0040a0001c0001t0003g0017a0001c0001t0003g0018others(66): Show | 69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.42-11345G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157828892 | ||||||
chr5:157828927
|
T | TA | 112 | a0001c0001t0001g0009a0001c0001t0001g0079a0001c0001t0001g0217others(109): Show | 113 | HG00140.hp1 HG00597.hp1 HG00741.hp1 others(110): Show |
intron_variant | MODIFIER | c.42-11381dupT | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157828927 | ||||||
chr5:157828927
|
T | TAA | 9 | a0001c0001t0003g0041a0001c0001t0003g0044a0001c0001t0003g0045others(6): Show | 9 | HG01981.hp2 HG02145.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.42-11382_42-11381d others(4): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157828927 | ||||||
chr5:157828927
|
TA | T | 12 | a0001c0001t0001g0241a0001c0001t0001g0242a0001c0001t0001g0243others(9): Show | 12 | HG00639.hp1 HG00639.hp2 HG00738.hp2 others(9): Show |
intron_variant | MODIFIER | c.42-11381delT | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157828927 | ||||||
chr5:157829039
|
T | C | 1 | a0001c0001t0002g0171 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.42-11492A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157829039 | ||||||
chr5:157829062
|
A | G | 1 | a0002c0005t0001g0212 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.42-11515T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157829062 | ||||||
chr5:157829102
|
AAAC | A | 9 | a0001c0001t0002g0002a0001c0001t0002g0110a0001c0001t0002g0117others(6): Show | 10 | HG02027.hp1 HG02056.hp2 HG02135.hp2 others(7): Show |
intron_variant | MODIFIER | c.42-11558_42-11556d others(5): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157829102 | ||||||
chr5:157829116
|
G | C | 69 | a0001c0001t0002g0040a0001c0001t0003g0017a0001c0001t0003g0018others(66): Show | 69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.42-11569C>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157829116 | ||||||
chr5:157829618
|
G | T | 1 | a0001c0002t0003g0054 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.42-12071C>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157829618 | ||||||
chr5:157829672
|
C | T | 136 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0011others(133): Show | 139 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.42-12125G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157829672 | ||||||
chr5:157829689
|
A | AT | 21 | a0001c0001t0001g0216a0001c0001t0001g0226a0001c0001t0001g0228others(18): Show | 21 | HG00423.hp1 HG00544.hp1 HG01261.hp2 others(18): Show |
intron_variant | MODIFIER | c.42-12143dupA | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157829689 | ||||||
chr5:157829689
|
ATT | A | 12 | a0001c0001t0002g0087a0001c0001t0002g0106a0001c0001t0002g0112others(9): Show | 12 | HG01106.hp1 HG02145.hp1 HG02165.hp2 others(9): Show |
intron_variant | MODIFIER | c.42-12144_42-12143d others(4): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157829689 | ||||||
chr5:157829689
|
ATTT | A | 132 | a0001c0001t0001g0308a0001c0001t0001g0311a0001c0001t0001g0312others(129): Show | 135 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.42-12145_42-12143d others(5): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157829689 | ||||||
chr5:157829689
|
ATTTT | A | 15 | a0001c0001t0001g0006a0001c0001t0001g0310a0001c0001t0001g0313others(12): Show | 16 | HG00280.hp1 HG01070.hp1 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.42-12146_42-12143d others(6): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157829689 | ||||||
chr5:157829689
|
ATTTTTTT others(1): Show |
A | 18 | a0001c0001t0003g0021a0001c0001t0003g0039a0001c0001t0003g0210others(15): Show | 18 | HG02451.hp2 HG02615.hp2 HG02622.hp1 others(15): Show |
intron_variant | MODIFIER | c.42-12150_42-12143d others(10): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157829689 | ||||||
chr5:157829689
|
ATTTTTTT others(2): Show |
A | 49 | a0001c0001t0002g0040a0001c0001t0003g0017a0001c0001t0003g0018others(46): Show | 49 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(46): Show |
intron_variant | MODIFIER | c.42-12151_42-12143d others(11): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157829689 | ||||||
chr5:157829689
|
ATTTTTTT others(3): Show |
A | 2 | a0001c0001t0003g0029a0001c0001t0003g0030 | 2 | NA18974.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.42-12152_42-12143d others(12): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157829689 | ||||||
chr5:157829795
|
GC | G | 70 | a0001c0001t0002g0040a0001c0001t0003g0017a0001c0001t0003g0018others(67): Show | 70 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(67): Show |
intron_variant | MODIFIER | c.42-12249delG | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157829795 | ||||||
chr5:157829839
|
C | T | 1 | a0001c0001t0001g0320 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.42-12292G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157829839 | ||||||
chr5:157829873
|
A | G | 69 | a0001c0001t0002g0040a0001c0001t0003g0017a0001c0001t0003g0018others(66): Show | 69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.42-12326T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157829873 | ||||||
chr5:157830001
|
T | C | 69 | a0001c0001t0002g0040a0001c0001t0003g0017a0001c0001t0003g0018others(66): Show | 69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.42-12454A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157830001 | ||||||
chr5:157830025
|
TAC | T | 69 | a0001c0001t0002g0040a0001c0001t0003g0017a0001c0001t0003g0018others(66): Show | 69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.42-12480_42-12479d others(4): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157830025 | ||||||
chr5:157830091
|
G | A | 1 | a0001c0001t0006g0007 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.42-12544C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157830091 | ||||||
chr5:157830185
|
T | G | 2 | a0001c0001t0007g0333a0001c0001t0007g0334 | 2 | HG02109.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.42-12638A>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157830185 | ||||||
chr5:157830232
|
T | G | 69 | a0001c0001t0002g0040a0001c0001t0003g0017a0001c0001t0003g0018others(66): Show | 69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.42-12685A>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157830232 | ||||||
chr5:157830288
|
C | A | 69 | a0001c0001t0002g0040a0001c0001t0003g0017a0001c0001t0003g0018others(66): Show | 69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.42-12741G>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157830288 | ||||||
chr5:157830320
|
G | C | 1 | a0001c0001t0002g0127 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.42-12773C>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157830320 | ||||||
chr5:157830533
|
T | C | 1 | a0001c0004t0003g0072 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.42-12986A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157830533 | ||||||
chr5:157830616
|
C | T | 136 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0011others(133): Show | 139 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.42-13069G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157830616 | ||||||
chr5:157830743
|
C | CCTCCCTC others(5): Show |
2 | a0001c0001t0003g0032a0001c0001t0003g0034 | 2 | HG02602.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.42-13208_42-13197d others(14): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157830743 | ||||||
chr5:157830746
|
C | CCCTCTCT others(4): Show |
1 | a0001c0001t0003g0049 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.42-13200_42-13199i others(13): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157830746 | ||||||
chr5:157830747
|
C | CCT | 30 | a0001c0001t0001g0218a0001c0001t0001g0312a0001c0001t0001g0319others(27): Show | 30 | HG00140.hp1 HG01192.hp2 HG01255.hp2 others(27): Show |
intron_variant | MODIFIER | c.42-13202_42-13201d others(4): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157830747 | ||||||
chr5:157830747
|
C | CCTCT | 2 | a0001c0001t0001g0006a0001c0001t0001g0323 | 3 | HG00280.hp1 HG01433.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.42-13204_42-13201d others(6): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157830747 | ||||||
chr5:157830749
|
T | TCTCTCTC others(3): Show |
5 | a0001c0001t0003g0017a0001c0001t0003g0024a0001c0001t0003g0025others(2): Show | 5 | HG02056.hp1 HG03098.hp2 HG03831.hp1 others(2): Show |
intron_variant | MODIFIER | c.42-13203_42-13202i others(12): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157830749 | ||||||
chr5:157830751
|
T | C | 1 | a0001c0001t0010g0332 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.42-13204A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157830751 | ||||||
chr5:157830751
|
T | TCTCTCTC others(1): Show |
3 | a0001c0001t0003g0026a0001c0001t0003g0062a0001c0001t0003g0064 | 3 | HG03516.hp2 NA19065.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.42-13205_42-13204i others(10): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157830751 | ||||||
chr5:157830753
|
T | TCTCTCC | 6 | a0001c0001t0003g0060a0001c0001t0003g0065a0001c0001t0003g0066others(3): Show | 6 | HG01109.hp2 HG02145.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.42-13207_42-13206i others(8): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157830753 | ||||||
chr5:157830755
|
T | TCTCC | 7 | a0001c0001t0003g0021a0001c0001t0003g0027a0001c0001t0003g0077others(4): Show | 7 | HG02615.hp1 HG02622.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.42-13209_42-13208i others(6): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157830755 | ||||||
chr5:157830757
|
C | CCT | 14 | a0001c0001t0001g0215a0001c0001t0001g0249a0001c0001t0001g0250others(11): Show | 14 | HG00438.hp1 HG00621.hp1 HG00741.hp2 others(11): Show |
intron_variant | MODIFIER | c.42-13212_42-13211d others(4): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157830757 | ||||||
chr5:157830757
|
C | CCTCT | 8 | a0001c0001t0001g0247a0001c0001t0001g0248a0001c0001t0001g0256others(5): Show | 8 | HG00323.hp2 HG00423.hp1 HG01934.hp1 others(5): Show |
intron_variant | MODIFIER | c.42-13214_42-13211d others(6): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157830757 | ||||||
chr5:157830757
|
C | CT | 5 | a0001c0001t0001g0230a0001c0001t0001g0231a0001c0001t0001g0261others(2): Show | 5 | HG00609.hp1 HG02145.hp1 NA18956.hp2 others(2): Show |
intron_variant | MODIFIER | c.42-13211_42-13210i others(3): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157830757 | ||||||
chr5:157830757
|
C | CTCT | 3 | a0001c0001t0001g0225a0001c0001t0001g0291a0001c0001t0002g0180 | 3 | HG01496.hp1 HG01516.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.42-13211_42-13210i others(5): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157830757 | ||||||
chr5:157830757
|
C | T | 61 | a0001c0001t0001g0006a0001c0001t0001g0218a0001c0001t0001g0308others(58): Show | 62 | HG00280.hp1 HG00597.hp1 HG01070.hp1 others(59): Show |
intron_variant | MODIFIER | c.42-13210G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157830757 | ||||||
chr5:157830757
|
CCT | C | 22 | a0001c0001t0002g0015a0001c0001t0002g0083a0001c0001t0002g0092others(19): Show | 22 | HG00621.hp2 HG02027.hp1 HG02040.hp2 others(19): Show |
intron_variant | MODIFIER | c.42-13212_42-13211d others(4): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157830757 | ||||||
chr5:157830757
|
CCTCT | C | 14 | a0001c0001t0001g0268a0001c0001t0004g0099a0001c0001t0004g0101others(11): Show | 14 | HG01358.hp2 HG01981.hp2 HG02723.hp2 others(11): Show |
intron_variant | MODIFIER | c.42-13214_42-13211d others(6): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157830757 | ||||||
chr5:157830757
|
CCTCTCT | C | 25 | a0001c0001t0001g0269a0001c0001t0001g0270a0001c0001t0001g0288others(22): Show | 26 | HG00735.hp2 HG00738.hp2 HG01070.hp2 others(23): Show |
intron_variant | MODIFIER | c.42-13216_42-13211d others(8): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157830757 | ||||||
chr5:157830757
|
CCTCTCTC others(1): Show |
C | 5 | a0001c0001t0001g0251a0001c0001t0004g0141a0001c0001t0004g0189others(2): Show | 5 | HG02055.hp2 HG02109.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.42-13218_42-13211d others(10): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157830757 | ||||||
chr5:157830757
|
CCTCTCTC others(3): Show |
C | 7 | a0001c0001t0001g0277a0001c0001t0001g0305a0001c0001t0001g0306others(4): Show | 7 | HG00741.hp1 HG01106.hp1 HG01243.hp2 others(4): Show |
intron_variant | MODIFIER | c.42-13220_42-13211d others(12): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157830757 | ||||||
chr5:157830759
|
T | C | 16 | a0001c0001t0003g0035a0001c0001t0003g0037a0001c0001t0003g0044others(13): Show | 16 | HG00597.hp1 HG02135.hp1 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.42-13212A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157830759 | ||||||
chr5:157830761
|
T | C | 1 | a0001c0001t0003g0063 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.42-13214A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157830761 | ||||||
chr5:157830763
|
T | C | 2 | a0001c0001t0002g0193a0001c0008t0002g0195 | 2 | HG03195.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.42-13216A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157830763 | ||||||
chr5:157830780
|
CTCTCTCT others(15): Show |
C | 1 | a0002c0005t0001g0212 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.42-13255_42-13234d others(24): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157830780 | ||||||
chr5:157830782
|
CTCTCTCT others(9): Show |
C | 2 | a0001c0001t0002g0002a0001c0001t0002g0167 | 3 | NA18965.hp1 NA19004.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.42-13251_42-13236d others(18): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157830782 | ||||||
chr5:157830784
|
CTCTCTCT others(9): Show |
C | 1 | a0001c0001t0002g0166 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.42-13253_42-13238d others(18): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157830784 | ||||||
chr5:157830790
|
C | A | 6 | a0001c0001t0005g0100a0001c0001t0005g0103a0001c0001t0005g0146others(3): Show | 6 | HG02257.hp1 NA18981.hp1 NA18998.hp1 others(3): Show |
intron_variant | MODIFIER | c.42-13243G>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157830790 | ||||||
chr5:157830792
|
C | A | 25 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0216others(22): Show | 25 | HG00423.hp2 HG01168.hp1 HG01346.hp2 others(22): Show |
intron_variant | MODIFIER | c.42-13245G>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157830792 | ||||||
chr5:157830792
|
C | CTATATAT others(3): Show |
1 | a0001c0001t0003g0048 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.42-13246_42-13245i others(12): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157830792 | ||||||
chr5:157830792
|
CTCTCTA | C | 4 | a0001c0001t0002g0122a0001c0001t0002g0199a0001c0001t0002g0202others(1): Show | 4 | HG01099.hp2 HG03130.hp2 HG04228.hp2 others(1): Show |
intron_variant | MODIFIER | c.42-13251_42-13246d others(8): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157830792 | ||||||
chr5:157830794
|
C | A | 50 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0216others(47): Show | 51 | HG00423.hp2 HG00639.hp1 HG01168.hp1 others(48): Show |
intron_variant | MODIFIER | c.42-13247G>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157830794 | ||||||
chr5:157830794
|
C | CTA | 10 | a0001c0001t0001g0242a0001c0001t0001g0257a0001c0001t0001g0272others(7): Show | 10 | HG00099.hp1 HG01256.hp1 HG01934.hp2 others(7): Show |
intron_variant | MODIFIER | c.42-13248_42-13247i others(4): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157830794 | ||||||
chr5:157830794
|
C | CTATATA | 3 | a0001c0001t0002g0106a0001c0001t0003g0068a0001c0002t0003g0056 | 3 | HG02145.hp1 HG02615.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.42-13248_42-13247i others(8): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157830794 | ||||||
chr5:157830794
|
CTCTA | C | 5 | a0001c0001t0001g0222a0001c0001t0001g0254a0001c0001t0004g0104others(2): Show | 5 | HG01099.hp1 HG01515.hp2 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.42-13251_42-13248d others(6): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157830794 | ||||||
chr5:157830796
|
C | A | 109 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(106): Show | 111 | HG00099.hp1 HG00423.hp2 HG00639.hp1 others(108): Show |
intron_variant | MODIFIER | c.42-13249G>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157830796 | ||||||
chr5:157830796
|
C | CTATA | 6 | a0001c0001t0001g0275a0001c0001t0001g0287a0001c0001t0003g0067others(3): Show | 6 | HG00597.hp1 HG01192.hp2 HG02071.hp1 others(3): Show |
intron_variant | MODIFIER | c.42-13253_42-13250d others(6): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157830796 | ||||||
chr5:157830796
|
C | CTATATA | 7 | a0001c0001t0003g0018a0001c0001t0003g0030a0001c0001t0003g0042others(4): Show | 7 | HG02451.hp2 HG02809.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.42-13255_42-13250d others(8): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157830796 | ||||||
chr5:157830796
|
C | CTATATAT others(1): Show |
4 | a0001c0001t0003g0035a0001c0001t0003g0037a0001c0001t0003g0044others(1): Show | 4 | HG02135.hp1 HG02486.hp1 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.42-13257_42-13250d others(10): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157830796 | ||||||
chr5:157830796
|
C | CTATATAT others(3): Show |
3 | a0001c0001t0002g0193a0001c0001t0002g0194a0003c0007t0003g0031 | 3 | HG02970.hp1 HG03540.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.42-13259_42-13250d others(12): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157830796 | ||||||
chr5:157830796
|
C | CTCTA | 6 | a0001c0001t0001g0273a0001c0001t0001g0285a0001c0001t0001g0324others(3): Show | 6 | HG01192.hp1 HG03486.hp1 HG03688.hp1 others(3): Show |
intron_variant | MODIFIER | c.42-13250_42-13249i others(6): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157830796 | ||||||
chr5:157830796
|
C | CTCTATA | 5 | a0001c0001t0001g0252a0001c0001t0002g0040a0001c0001t0003g0028others(2): Show | 5 | HG00140.hp1 HG03225.hp2 HG04184.hp1 others(2): Show |
intron_variant | MODIFIER | c.42-13250_42-13249i others(8): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157830796 | ||||||
chr5:157830796
|
C | CTCTCTA | 6 | a0001c0001t0001g0263a0001c0001t0003g0019a0001c0001t0003g0033others(3): Show | 6 | HG02129.hp2 NA18951.hp1 NA18953.hp1 others(3): Show |
intron_variant | MODIFIER | c.42-13250_42-13249i others(8): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157830796 | ||||||
chr5:157830796
|
C | CTCTCTAT others(1): Show |
4 | a0001c0001t0001g0276a0001c0001t0001g0286a0001c0001t0003g0036others(1): Show | 4 | HG00438.hp2 HG02523.hp2 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.42-13250_42-13249i others(10): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157830796 | ||||||
chr5:157830796
|
C | CTCTCTAT others(3): Show |
1 | a0001c0008t0002g0195 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.42-13250_42-13249i others(12): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157830796 | ||||||
chr5:157830796
|
C | CTCTCTCT others(3): Show |
1 | a0001c0001t0001g0315 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.42-13250_42-13249i others(12): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157830796 | ||||||
chr5:157830796
|
C | CTCTCTCT others(5): Show |
1 | a0001c0001t0003g0041 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.42-13250_42-13249i others(14): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157830796 | ||||||
chr5:157830796
|
CTA | C | 32 | a0001c0001t0002g0001a0001c0001t0002g0011a0001c0001t0002g0013others(29): Show | 33 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(30): Show |
intron_variant | MODIFIER | c.42-13251_42-13250d others(4): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157830796 | ||||||
chr5:157830798
|
A | C | 60 | a0001c0001t0001g0079a0001c0001t0001g0217a0001c0001t0001g0220others(57): Show | 60 | HG00323.hp2 HG00423.hp1 HG00544.hp2 others(57): Show |
intron_variant | MODIFIER | c.42-13251T>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157830798 | ||||||
chr5:157830800
|
A | C | 32 | a0001c0001t0001g0217a0001c0001t0001g0248a0001c0001t0001g0249others(29): Show | 32 | HG00140.hp2 HG00280.hp2 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.42-13253T>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157830800 | ||||||
chr5:157830802
|
A | C | 6 | a0001c0001t0001g0217a0001c0001t0001g0282a0001c0001t0002g0087others(3): Show | 6 | HG02165.hp2 HG04204.hp1 NA18939.hp1 others(3): Show |
intron_variant | MODIFIER | c.42-13255T>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157830802 | ||||||
chr5:157830835
|
G | A | 1 | a0001c0002t0003g0081 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.42-13288C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157830835 | ||||||
chr5:157830852
|
T | A | 2 | a0001c0001t0002g0090a0001c0001t0002g0109 | 2 | HG02074.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.42-13305A>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157830852 | ||||||
chr5:157831047
|
AAAAC | A | 69 | a0001c0001t0002g0040a0001c0001t0003g0017a0001c0001t0003g0018others(66): Show | 69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.42-13504_42-13501d others(6): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157831047 | ||||||
chr5:157831063
|
A | C | 20 | a0001c0001t0001g0006a0001c0001t0001g0308a0001c0001t0001g0309others(17): Show | 21 | HG00280.hp1 HG01070.hp1 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.42-13516T>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157831063 | ||||||
chr5:157831065
|
A | C | 141 | a0001c0001t0001g0004a0001c0001t0001g0229a0001c0001t0001g0230others(138): Show | 145 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.42-13518T>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157831065 | ||||||
chr5:157831190
|
CT | C | 71 | a0001c0001t0002g0040a0001c0001t0003g0017a0001c0001t0003g0018others(68): Show | 71 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(68): Show |
intron_variant | MODIFIER | c.42-13644delA | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157831190 | ||||||
chr5:157831495
|
T | C | 1 | a0001c0001t0002g0196 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.42-13948A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157831495 | ||||||
chr5:157831506
|
A | G | 2 | a0001c0001t0007g0333a0001c0001t0007g0334 | 2 | HG02109.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.42-13959T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157831506 | ||||||
chr5:157831605
|
T | C | 1 | a0001c0001t0001g0291 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.42-14058A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157831605 | ||||||
chr5:157831651
|
A | C | 69 | a0001c0001t0002g0040a0001c0001t0003g0017a0001c0001t0003g0018others(66): Show | 69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.42-14104T>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157831651 | ||||||
chr5:157831693
|
C | CT | 69 | a0001c0001t0001g0224a0001c0001t0001g0237a0001c0001t0001g0252others(66): Show | 69 | HG00140.hp1 HG00597.hp1 HG00735.hp2 others(66): Show |
intron_variant | MODIFIER | c.42-14147dupA | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157831693 | ||||||
chr5:157831693
|
C | CTT | 18 | a0001c0001t0003g0022a0001c0001t0003g0046a0001c0001t0003g0051others(15): Show | 18 | HG02109.hp1 HG02109.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.42-14148_42-14147d others(4): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157831693 | ||||||
chr5:157831693
|
CT | C | 85 | a0001c0001t0001g0214a0001c0001t0001g0270a0001c0001t0001g0303others(82): Show | 87 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(84): Show |
intron_variant | MODIFIER | c.42-14147delA | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157831693 | ||||||
chr5:157831733
|
C | T | 3 | a0001c0001t0002g0123a0001c0001t0002g0153a0001c0001t0002g0154 | 3 | HG00621.hp2 NA18964.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.42-14186G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157831733 | ||||||
chr5:157831739
|
G | A | 1 | a0001c0001t0003g0045 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.42-14192C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157831739 | ||||||
chr5:157831804
|
A | G | 69 | a0001c0001t0002g0040a0001c0001t0003g0017a0001c0001t0003g0018others(66): Show | 69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.42-14257T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157831804 | ||||||
chr5:157831816
|
T | C | 69 | a0001c0001t0002g0040a0001c0001t0003g0017a0001c0001t0003g0018others(66): Show | 69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.42-14269A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157831816 | ||||||
chr5:157831881
|
G | A | 1 | a0001c0004t0003g0072 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.42-14334C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157831881 | ||||||
chr5:157832019
|
G | A | 1 | a0001c0001t0002g0125 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.42-14472C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157832019 | ||||||
chr5:157832057
|
G | A | 5 | a0001c0001t0001g0277a0001c0001t0001g0305a0001c0001t0001g0306others(2): Show | 5 | HG01243.hp2 HG02647.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.42-14510C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157832057 | ||||||
chr5:157832067
|
A | G | 1 | a0001c0006t0001g0327 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.42-14520T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157832067 | ||||||
chr5:157832505
|
T | C | 21 | a0001c0001t0001g0006a0001c0001t0001g0308a0001c0001t0001g0309others(18): Show | 22 | HG00280.hp1 HG01070.hp1 HG01071.hp2 others(19): Show |
intron_variant | MODIFIER | c.42-14958A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157832505 | ||||||
chr5:157832585
|
TATCTTCT others(8): Show |
T | 1 | a0001c0006t0001g0327 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.42-15053_42-15039d others(17): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157832585 | ||||||
chr5:157832805
|
G | A | 9 | a0001c0001t0002g0002a0001c0001t0002g0110a0001c0001t0002g0117others(6): Show | 10 | HG02027.hp1 HG02056.hp2 HG02135.hp2 others(7): Show |
intron_variant | MODIFIER | c.42-15258C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157832805 | ||||||
chr5:157832822
|
G | A | 2 | a0001c0001t0003g0044a0001c0001t0003g0045 | 2 | HG02486.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.42-15275C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157832822 | ||||||
chr5:157833007
|
G | T | 155 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0011others(152): Show | 157 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.42-15460C>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157833007 | ||||||
chr5:157833081
|
T | G | 69 | a0001c0001t0002g0040a0001c0001t0003g0017a0001c0001t0003g0018others(66): Show | 69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.42-15534A>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157833081 | ||||||
chr5:157833167
|
A | AAC | 13 | a0001c0002t0003g0052a0001c0002t0003g0053a0001c0002t0003g0054others(10): Show | 13 | HG02451.hp2 HG02615.hp2 HG02809.hp1 others(10): Show |
intron_variant | MODIFIER | c.42-15621_42-15620i others(4): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157833167 | ||||||
chr5:157833168
|
C | A | 13 | a0001c0002t0003g0052a0001c0002t0003g0053a0001c0002t0003g0054others(10): Show | 13 | HG02451.hp2 HG02615.hp2 HG02809.hp1 others(10): Show |
intron_variant | MODIFIER | c.42-15621G>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157833168 | ||||||
chr5:157833209
|
G | A | 13 | a0001c0002t0003g0052a0001c0002t0003g0053a0001c0002t0003g0054others(10): Show | 13 | HG02451.hp2 HG02615.hp2 HG02809.hp1 others(10): Show |
intron_variant | MODIFIER | c.42-15662C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157833209 | ||||||
chr5:157833248
|
A | C | 1 | a0001c0001t0004g0102 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.42-15701T>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157833248 | ||||||
chr5:157833307
|
T | C | 69 | a0001c0001t0002g0040a0001c0001t0003g0017a0001c0001t0003g0018others(66): Show | 69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.42-15760A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157833307 | ||||||
chr5:157833400
|
T | C | 1 | a0001c0001t0002g0085 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.42-15853A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157833400 | ||||||
chr5:157833569
|
T | C | 1 | a0001c0001t0010g0332 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.42-16022A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157833569 | ||||||
chr5:157833601
|
C | T | 4 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270others(1): Show | 4 | HG01070.hp2 HG01169.hp2 HG02055.hp1 others(1): Show |
intron_variant | MODIFIER | c.42-16054G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157833601 | ||||||
chr5:157833752
|
C | A | 4 | a0001c0001t0003g0022a0001c0001t0003g0023a0001c0001t0003g0063others(1): Show | 4 | HG01884.hp2 HG02109.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.42-16205G>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157833752 | ||||||
chr5:157833889
|
C | T | 1 | a0001c0002t0003g0081 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.42-16342G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157833889 | ||||||
chr5:157833895
|
T | A | 1 | a0001c0001t0003g0045 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.42-16348A>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157833895 | ||||||
chr5:157833934
|
C | T | 2 | a0001c0001t0003g0021a0001c0001t0003g0213 | 2 | HG02622.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.42-16387G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157833934 | ||||||
chr5:157834070
|
G | A | 49 | a0001c0001t0002g0040a0001c0001t0003g0017a0001c0001t0003g0018others(46): Show | 49 | HG00140.hp1 HG00597.hp1 HG01192.hp2 others(46): Show |
intron_variant | MODIFIER | c.42-16523C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157834070 | ||||||
chr5:157834162
|
G | A | 69 | a0001c0001t0002g0040a0001c0001t0003g0017a0001c0001t0003g0018others(66): Show | 69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.42-16615C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157834162 | ||||||
chr5:157834184
|
T | C | 1 | a0001c0001t0010g0332 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.42-16637A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157834184 | ||||||
chr5:157834216
|
G | A | 69 | a0001c0001t0002g0040a0001c0001t0003g0017a0001c0001t0003g0018others(66): Show | 69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.42-16669C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157834216 | ||||||
chr5:157834290
|
G | A | 3 | a0001c0001t0003g0047a0001c0001t0003g0048a0001c0001t0003g0094 | 3 | HG01109.hp2 HG02717.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.42-16743C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157834290 | ||||||
chr5:157834294
|
G | C | 69 | a0001c0001t0002g0040a0001c0001t0003g0017a0001c0001t0003g0018others(66): Show | 69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.42-16747C>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157834294 | ||||||
chr5:157834359
|
C | T | 1 | a0001c0001t0002g0106 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.42-16812G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157834359 | ||||||
chr5:157834363
|
T | TAA | 67 | a0001c0001t0002g0040a0001c0001t0003g0017a0001c0001t0003g0018others(64): Show | 67 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(64): Show |
intron_variant | MODIFIER | c.42-16818_42-16817d others(4): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157834363 | ||||||
chr5:157834454
|
A | C | 2 | a0001c0001t0007g0333a0001c0001t0007g0334 | 2 | HG02109.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.42-16907T>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157834454 | ||||||
chr5:157834650
|
T | C | 1 | a0001c0001t0010g0332 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.42-17103A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157834650 | ||||||
chr5:157834674
|
C | T | 1 | a0001c0001t0002g0091 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.42-17127G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157834674 | ||||||
chr5:157834747
|
C | A | 2 | a0001c0001t0004g0105a0001c0001t0004g0107 | 2 | HG02818.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.42-17200G>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157834747 | ||||||
chr5:157834835
|
G | A | 1 | a0001c0001t0003g0032 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.42-17288C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157834835 | ||||||
chr5:157835179
|
T | G | 69 | a0001c0001t0002g0040a0001c0001t0003g0017a0001c0001t0003g0018others(66): Show | 69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.42-17632A>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157835179 | ||||||
chr5:157835506
|
C | A | 1 | a0001c0002t0003g0081 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.42-17959G>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157835506 | ||||||
chr5:157835754
|
T | C | 4 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270others(1): Show | 4 | HG01070.hp2 HG01169.hp2 HG02055.hp1 others(1): Show |
intron_variant | MODIFIER | c.42-18207A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157835754 | ||||||
chr5:157835755
|
G | A | 2 | a0001c0001t0003g0044a0001c0001t0003g0045 | 2 | HG02486.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.42-18208C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157835755 | ||||||
chr5:157835780
|
A | G | 1 | a0002c0005t0001g0212 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.42-18233T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157835780 | ||||||
chr5:157835808
|
C | T | 1 | a0001c0001t0002g0203 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.42-18261G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157835808 | ||||||
chr5:157835949
|
A | G | 2 | a0001c0001t0001g0252a0001c0001t0001g0263 | 2 | HG03225.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.42-18402T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157835949 | ||||||
chr5:157836012
|
C | A | 5 | a0001c0001t0001g0277a0001c0001t0001g0305a0001c0001t0001g0306others(2): Show | 5 | HG01243.hp2 HG02647.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.42-18465G>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157836012 | ||||||
chr5:157836347
|
T | A | 1 | a0001c0001t0002g0106 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.42-18800A>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157836347 | ||||||
chr5:157836385
|
T | C | 19 | a0001c0001t0001g0006a0001c0001t0001g0308a0001c0001t0001g0310others(16): Show | 20 | HG00280.hp1 HG01070.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.42-18838A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157836385 | ||||||
chr5:157836909
|
T | G | 1 | a0001c0001t0010g0332 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.42-19362A>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157836909 | ||||||
chr5:157837077
|
A | G | 1 | a0001c0001t0003g0050 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.42-19530T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157837077 | ||||||
chr5:157837110
|
C | A | 30 | a0001c0001t0001g0006a0001c0001t0001g0277a0001c0001t0001g0305others(27): Show | 31 | HG00280.hp1 HG01070.hp1 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.42-19563G>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157837110 | ||||||
chr5:157837348
|
G | A | 1 | a0001c0001t0001g0293 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.42-19801C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157837348 | ||||||
chr5:157837411
|
T | TAC | 16 | a0001c0001t0001g0005a0001c0001t0001g0215a0001c0001t0001g0233others(13): Show | 17 | HG00609.hp2 HG01071.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.42-19866_42-19865d others(4): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157837411 | ||||||
chr5:157837411
|
T | TACAC | 3 | a0001c0001t0001g0250a0001c0001t0001g0276a0001c0001t0001g0300 | 3 | HG00438.hp1 HG00438.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.42-19868_42-19865d others(6): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157837411 | ||||||
chr5:157837411
|
TACAC | T | 22 | a0001c0001t0001g0006a0001c0001t0001g0308a0001c0001t0001g0309others(19): Show | 23 | HG00280.hp1 HG01070.hp1 HG01071.hp2 others(20): Show |
intron_variant | MODIFIER | c.42-19868_42-19865d others(6): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157837411 | ||||||
chr5:157837415
|
C | CAA | 4 | a0001c0001t0002g0126a0001c0001t0002g0163a0001c0001t0002g0171others(1): Show | 4 | HG03831.hp2 NA18939.hp1 NA18944.hp2 others(1): Show |
intron_variant | MODIFIER | c.42-19869_42-19868i others(4): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157837415 | ||||||
chr5:157837415
|
C | T | 1 | a0002c0005t0001g0212 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.42-19868G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157837415 | ||||||
chr5:157837417
|
C | A | 199 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0011others(196): Show | 202 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(199): Show |
intron_variant | MODIFIER | c.42-19870G>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157837417 | ||||||
chr5:157837417
|
C | T | 22 | a0001c0001t0001g0006a0001c0001t0001g0308a0001c0001t0001g0309others(19): Show | 23 | HG00280.hp1 HG01070.hp1 HG01071.hp2 others(20): Show |
intron_variant | MODIFIER | c.42-19870G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157837417 | ||||||
chr5:157837419
|
C | T | 2 | a0001c0001t0003g0047a0001c0001t0003g0048 | 2 | HG02717.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.42-19872G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157837419 | ||||||
chr5:157837499
|
G | C | 1 | a0001c0001t0001g0315 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.42-19952C>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157837499 | ||||||
chr5:157837647
|
T | C | 2 | a0001c0001t0007g0333a0001c0001t0007g0334 | 2 | HG02109.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.42-20100A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157837647 | ||||||
chr5:157837649
|
C | CTT | 14 | a0001c0001t0002g0086a0001c0001t0002g0194a0001c0001t0002g0196others(11): Show | 14 | HG00735.hp2 HG00738.hp2 HG01099.hp2 others(11): Show |
intron_variant | MODIFIER | c.42-20104_42-20103d others(4): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157837649 | ||||||
chr5:157837649
|
C | CTTT | 88 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0011others(85): Show | 90 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.42-20105_42-20103d others(5): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157837649 | ||||||
chr5:157837649
|
C | CTTTT | 34 | a0001c0001t0002g0122a0001c0001t0002g0209a0001c0001t0004g0003others(31): Show | 35 | HG00741.hp1 HG01099.hp1 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.42-20106_42-20103d others(6): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157837649 | ||||||
chr5:157837649
|
C | CTTTTTTT others(1): Show |
18 | a0001c0001t0001g0006a0001c0001t0001g0308a0001c0001t0001g0310others(15): Show | 19 | HG00280.hp1 HG01070.hp1 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.42-20110_42-20103d others(10): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157837649 | ||||||
chr5:157837649
|
C | CTTTTTTT others(2): Show |
59 | a0001c0001t0001g0309a0001c0001t0001g0324a0001c0001t0002g0040others(56): Show | 59 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(56): Show |
intron_variant | MODIFIER | c.42-20111_42-20103d others(11): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157837649 | ||||||
chr5:157837649
|
C | CTTTTTTT others(3): Show |
15 | a0001c0001t0003g0041a0001c0001t0003g0044a0001c0001t0003g0045others(12): Show | 15 | HG02145.hp2 HG02486.hp1 HG02615.hp2 others(12): Show |
intron_variant | MODIFIER | c.42-20112_42-20103d others(12): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157837649 | ||||||
chr5:157837649
|
C | CTTTTTTT others(8): Show |
1 | a0001c0001t0010g0332 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.42-20103_42-20102i others(17): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157837649 | ||||||
chr5:157837649
|
C | T | 1 | a0001c0001t0002g0106 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.42-20102G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157837649 | ||||||
chr5:157837791
|
G | A | 21 | a0001c0001t0001g0006a0001c0001t0001g0308a0001c0001t0001g0309others(18): Show | 22 | HG00280.hp1 HG01070.hp1 HG01071.hp2 others(19): Show |
intron_variant | MODIFIER | c.42-20244C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157837791 | ||||||
chr5:157837833
|
G | A | 1 | a0001c0001t0003g0048 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.42-20286C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157837833 | ||||||
chr5:157837883
|
C | T | 21 | a0001c0001t0001g0006a0001c0001t0001g0308a0001c0001t0001g0309others(18): Show | 22 | HG00280.hp1 HG01070.hp1 HG01071.hp2 others(19): Show |
intron_variant | MODIFIER | c.42-20336G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157837883 | ||||||
chr5:157837892
|
T | C | 8 | a0001c0001t0003g0060a0001c0001t0003g0064a0001c0001t0003g0065others(5): Show | 8 | HG02145.hp2 HG02258.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.42-20345A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157837892 | ||||||
chr5:157837953
|
C | T | 4 | a0001c0001t0002g0161a0001c0001t0002g0162a0001c0001t0002g0179others(1): Show | 4 | HG00280.hp2 HG01358.hp1 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.42-20406G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157837953 | ||||||
chr5:157838025
|
T | C | 1 | a0001c0001t0003g0210 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.42-20478A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157838025 | ||||||
chr5:157838026
|
A | G | 49 | a0001c0001t0002g0040a0001c0001t0003g0017a0001c0001t0003g0018others(46): Show | 49 | HG00140.hp1 HG00597.hp1 HG01192.hp2 others(46): Show |
intron_variant | MODIFIER | c.42-20479T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157838026 | ||||||
chr5:157838055
|
T | C | 2 | a0001c0001t0007g0333a0001c0001t0007g0334 | 2 | HG02109.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.42-20508A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157838055 | ||||||
chr5:157838073
|
C | T | 1 | a0001c0001t0002g0192 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.42-20526G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157838073 | ||||||
chr5:157838122
|
G | GT | 55 | a0001c0001t0001g0221a0001c0001t0001g0235a0001c0001t0001g0271others(52): Show | 56 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(53): Show |
intron_variant | MODIFIER | c.42-20576dupA | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157838122 | ||||||
chr5:157838122
|
G | T | 1 | a0001c0001t0004g0140 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.42-20575C>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157838122 | ||||||
chr5:157838122
|
GT | G | 68 | a0001c0001t0002g0040a0001c0001t0003g0017a0001c0001t0003g0018others(65): Show | 68 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(65): Show |
intron_variant | MODIFIER | c.42-20576delA | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157838122 | ||||||
chr5:157838192
|
G | A | 1 | a0001c0001t0001g0266 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.42-20645C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157838192 | ||||||
chr5:157838279
|
C | T | 1 | a0001c0001t0002g0083 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.41+20651G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157838279 | ||||||
chr5:157838324
|
C | T | 1 | a0001c0001t0004g0082 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.41+20606G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157838324 | ||||||
chr5:157838403
|
G | T | 2 | a0001c0001t0007g0333a0001c0001t0007g0334 | 2 | HG02109.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.41+20527C>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157838403 | ||||||
chr5:157838491
|
T | A | 2 | a0001c0001t0001g0298a0001c0001t0001g0299 | 2 | HG02965.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.41+20439A>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157838491 | ||||||
chr5:157838501
|
G | A | 1 | a0001c0001t0010g0332 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.41+20429C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157838501 | ||||||
chr5:157838591
|
G | C | 1 | a0001c0001t0001g0297 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.41+20339C>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157838591 | ||||||
chr5:157838599
|
A | G | 332 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(329): Show | 338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.41+20331T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157838599 | ||||||
chr5:157838677
|
A | G | 230 | a0001c0001t0001g0006a0001c0001t0001g0308a0001c0001t0001g0309others(227): Show | 234 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.41+20253T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157838677 | ||||||
chr5:157838872
|
T | C | 21 | a0001c0001t0001g0006a0001c0001t0001g0308a0001c0001t0001g0309others(18): Show | 22 | HG00280.hp1 HG01070.hp1 HG01071.hp2 others(19): Show |
intron_variant | MODIFIER | c.41+20058A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157838872 | ||||||
chr5:157838993
|
G | C | 33 | a0001c0001t0002g0040a0001c0001t0003g0017a0001c0001t0003g0018others(30): Show | 33 | HG00140.hp1 HG00597.hp1 HG01884.hp2 others(30): Show |
intron_variant | MODIFIER | c.41+19937C>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157838993 | ||||||
chr5:157839004
|
G | A | 2 | a0001c0001t0003g0047a0001c0001t0003g0048 | 2 | HG02717.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.41+19926C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157839004 | ||||||
chr5:157839107
|
T | C | 2 | a0001c0001t0001g0269a0001c0001t0001g0270 | 2 | HG01070.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.41+19823A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157839107 | ||||||
chr5:157839114
|
A | C | 1 | a0001c0001t0003g0094 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.41+19816T>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157839114 | ||||||
chr5:157839184
|
G | A | 1 | a0001c0001t0001g0079 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.41+19746C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157839184 | ||||||
chr5:157839331
|
C | T | 2 | a0001c0002t0003g0080a0001c0002t0003g0081 | 2 | HG02922.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.41+19599G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157839331 | ||||||
chr5:157839426
|
C | T | 2 | a0001c0001t0007g0333a0001c0001t0007g0334 | 2 | HG02109.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.41+19504G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157839426 | ||||||
chr5:157839427
|
C | T | 1 | a0001c0001t0002g0176 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.41+19503G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157839427 | ||||||
chr5:157839467
|
A | G | 209 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0011others(206): Show | 212 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(209): Show |
intron_variant | MODIFIER | c.41+19463T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157839467 | ||||||
chr5:157839526
|
T | C | 1 | a0001c0001t0001g0272 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.41+19404A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157839526 | ||||||
chr5:157839575
|
C | T | 209 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0011others(206): Show | 212 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(209): Show |
intron_variant | MODIFIER | c.41+19355G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157839575 | ||||||
chr5:157839588
|
G | A | 230 | a0001c0001t0001g0006a0001c0001t0001g0308a0001c0001t0001g0309others(227): Show | 234 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.41+19342C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157839588 | ||||||
chr5:157839609
|
T | TA | 54 | a0001c0001t0001g0245a0001c0001t0001g0251a0001c0001t0002g0040others(51): Show | 54 | HG00140.hp1 HG00597.hp1 HG01192.hp2 others(51): Show |
intron_variant | MODIFIER | c.41+19320dupT | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157839609 | ||||||
chr5:157839614
|
A | T | 2 | a0001c0001t0007g0333a0001c0001t0007g0334 | 2 | HG02109.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.41+19316T>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157839614 | ||||||
chr5:157839618
|
A | C | 6 | a0001c0001t0002g0087a0001c0001t0002g0174a0001c0002t0003g0053others(3): Show | 6 | HG02165.hp2 HG02451.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.41+19312T>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157839618 | ||||||
chr5:157839626
|
C | A | 6 | a0001c0001t0001g0277a0001c0001t0001g0294a0001c0001t0001g0305others(3): Show | 6 | HG01243.hp2 HG02280.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.41+19304G>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157839626 | ||||||
chr5:157839626
|
C | CA | 69 | a0001c0001t0002g0040a0001c0001t0003g0017a0001c0001t0003g0018others(66): Show | 69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.41+19303dupT | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157839626 | ||||||
chr5:157839635
|
A | C | 21 | a0001c0001t0001g0006a0001c0001t0001g0308a0001c0001t0001g0309others(18): Show | 22 | HG00280.hp1 HG01070.hp1 HG01071.hp2 others(19): Show |
intron_variant | MODIFIER | c.41+19295T>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157839635 | ||||||
chr5:157839651
|
T | C | 52 | a0001c0001t0002g0040a0001c0001t0003g0017a0001c0001t0003g0018others(49): Show | 52 | HG00140.hp1 HG00597.hp1 HG01192.hp2 others(49): Show |
intron_variant | MODIFIER | c.41+19279A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157839651 | ||||||
chr5:157839670
|
A | T | 2 | a0001c0001t0003g0047a0001c0001t0003g0048 | 2 | HG02717.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.41+19260T>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157839670 | ||||||
chr5:157839692
|
G | A | 2 | a0001c0001t0007g0333a0001c0001t0007g0334 | 2 | HG02109.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.41+19238C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157839692 | ||||||
chr5:157839720
|
A | AATCT | 61 | a0001c0001t0001g0215a0001c0001t0001g0229a0001c0001t0001g0233others(58): Show | 62 | HG00423.hp1 HG00639.hp2 HG00738.hp1 others(59): Show |
intron_variant | MODIFIER | c.41+19206_41+19209d others(6): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157839720 | ||||||
chr5:157839720
|
A | AATCTATC others(1): Show |
26 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0214others(23): Show | 26 | HG00438.hp1 HG00438.hp2 HG00609.hp2 others(23): Show |
intron_variant | MODIFIER | c.41+19202_41+19209d others(10): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157839720 | ||||||
chr5:157839720
|
A | AATCTATC others(5): Show |
8 | a0001c0001t0001g0079a0001c0001t0001g0228a0001c0001t0001g0268others(5): Show | 8 | HG02257.hp2 HG02717.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.41+19198_41+19209d others(14): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157839720 | ||||||
chr5:157839720
|
A | AATCTATC others(9): Show |
2 | a0001c0001t0001g0312a0001c0001t0007g0333 | 2 | HG01928.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.41+19194_41+19209d others(18): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157839720 | ||||||
chr5:157839720
|
A | AATCTATC others(13): Show |
1 | a0001c0001t0001g0321 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.41+19190_41+19209d others(22): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157839720 | ||||||
chr5:157839720
|
AATCT | A | 17 | a0001c0001t0001g0221a0001c0001t0001g0227a0001c0001t0001g0244others(14): Show | 17 | HG00099.hp2 HG00621.hp1 HG00738.hp2 others(14): Show |
intron_variant | MODIFIER | c.41+19206_41+19209d others(6): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157839720 | ||||||
chr5:157839720
|
AATCTATC others(1): Show |
A | 12 | a0001c0001t0002g0083a0001c0001t0002g0093a0001c0001t0002g0106others(9): Show | 12 | HG01433.hp1 HG02040.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.41+19202_41+19209d others(10): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157839720 | ||||||
chr5:157839720
|
AATCTATC others(5): Show |
A | 77 | a0001c0001t0001g0246a0001c0001t0002g0001a0001c0001t0002g0002others(74): Show | 79 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.41+19198_41+19209d others(14): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157839720 | ||||||
chr5:157839720
|
AATCTATC others(9): Show |
A | 65 | a0001c0001t0002g0040a0001c0001t0003g0017a0001c0001t0003g0018others(62): Show | 65 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(62): Show |
intron_variant | MODIFIER | c.41+19194_41+19209d others(18): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157839720 | ||||||
chr5:157839720
|
AATCTATC others(13): Show |
A | 1 | a0001c0004t0003g0072 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.41+19190_41+19209d others(22): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157839720 | ||||||
chr5:157839722
|
T | TCTAC | 3 | a0001c0001t0001g0271a0001c0001t0001g0292a0001c0001t0001g0302 | 3 | HG00323.hp2 HG01346.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.41+19207_41+19208i others(6): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157839722 | ||||||
chr5:157839960
|
C | T | 1 | a0001c0004t0003g0072 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.41+18970G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157839960 | ||||||
chr5:157840015
|
G | A | 2 | a0001c0001t0003g0094a0002c0005t0001g0212 | 2 | HG01109.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.41+18915C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157840015 | ||||||
chr5:157840019
|
C | A | 4 | a0001c0001t0001g0247a0001c0001t0001g0248a0001c0001t0001g0249others(1): Show | 4 | HG00621.hp1 NA18961.hp2 NA18963.hp2 others(1): Show |
intron_variant | MODIFIER | c.41+18911G>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157840019 | ||||||
chr5:157840073
|
T | C | 1 | a0004c0003t0001g0326 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.41+18857A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157840073 | ||||||
chr5:157840114
|
G | C | 1 | a0001c0001t0001g0291 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.41+18816C>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157840114 | ||||||
chr5:157840166
|
A | G | 209 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0011others(206): Show | 212 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(209): Show |
intron_variant | MODIFIER | c.41+18764T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157840166 | ||||||
chr5:157840176
|
C | T | 13 | a0001c0001t0002g0086a0001c0001t0002g0196a0001c0001t0002g0197others(10): Show | 13 | HG00735.hp2 HG00738.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.41+18754G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157840176 | ||||||
chr5:157840192
|
C | CA | 10 | a0001c0001t0001g0214a0001c0001t0001g0218a0001c0001t0001g0250others(7): Show | 10 | HG00438.hp1 HG00438.hp2 HG01255.hp2 others(7): Show |
intron_variant | MODIFIER | c.41+18737dupT | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157840192 | ||||||
chr5:157840192
|
C | CAAA | 107 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0011others(104): Show | 110 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.41+18735_41+18737d others(5): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157840192 | ||||||
chr5:157840192
|
C | CAAAA | 39 | a0001c0001t0002g0088a0001c0001t0002g0106a0001c0001t0002g0111others(36): Show | 39 | HG00140.hp2 HG00609.hp1 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.41+18734_41+18737d others(6): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157840192 | ||||||
chr5:157840192
|
CA | C | 27 | a0001c0001t0001g0006a0001c0001t0001g0303a0001c0001t0001g0308others(24): Show | 28 | HG00280.hp1 HG01070.hp1 HG01071.hp2 others(25): Show |
intron_variant | MODIFIER | c.41+18737delT | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157840192 | ||||||
chr5:157840192
|
CAA | C | 45 | a0001c0001t0002g0040a0001c0001t0003g0017a0001c0001t0003g0018others(42): Show | 45 | HG00140.hp1 HG00597.hp1 HG01192.hp2 others(42): Show |
intron_variant | MODIFIER | c.41+18736_41+18737d others(4): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157840192 | ||||||
chr5:157840250
|
T | TA | 35 | a0001c0001t0001g0218a0001c0001t0002g0122a0001c0001t0002g0170others(32): Show | 36 | HG00741.hp1 HG01099.hp1 HG01106.hp1 others(33): Show |
intron_variant | MODIFIER | c.41+18679dupT | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157840250 | ||||||
chr5:157840739
|
T | TA | 53 | a0001c0001t0002g0040a0001c0001t0002g0171a0001c0001t0003g0017others(50): Show | 53 | HG00140.hp1 HG00597.hp1 HG01192.hp2 others(50): Show |
intron_variant | MODIFIER | c.41+18190dupT | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157840739 | ||||||
chr5:157840835
|
G | A | 3 | a0001c0001t0001g0219a0001c0001t0001g0222a0001c0001t0001g0223 | 3 | HG01257.hp2 HG01515.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.41+18095C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157840835 | ||||||
chr5:157840953
|
T | G | 136 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0011others(133): Show | 139 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.41+17977A>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157840953 | ||||||
chr5:157841132
|
G | A | 1 | a0001c0001t0010g0332 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.41+17798C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157841132 | ||||||
chr5:157841133
|
G | A | 1 | a0001c0001t0002g0172 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.41+17797C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157841133 | ||||||
chr5:157841158
|
C | T | 1 | a0001c0001t0003g0063 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.41+17772G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157841158 | ||||||
chr5:157841250
|
A | G | 1 | a0001c0001t0002g0139 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.41+17680T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157841250 | ||||||
chr5:157841347
|
C | T | 1 | a0001c0004t0003g0072 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.41+17583G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157841347 | ||||||
chr5:157841374
|
TGGCCAAC others(42): Show |
T | 1 | a0001c0001t0007g0334 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.41+17507_41+17555d others(51): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157841374 | ||||||
chr5:157841696
|
T | C | 5 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270others(2): Show | 5 | HG01070.hp2 HG01169.hp2 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.41+17234A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157841696 | ||||||
chr5:157841786
|
T | C | 2 | a0001c0001t0003g0044a0001c0001t0003g0045 | 2 | HG02486.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.41+17144A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157841786 | ||||||
chr5:157841845
|
A | G | 7 | a0001c0001t0001g0272a0001c0001t0001g0278a0001c0001t0001g0280others(4): Show | 7 | HG01071.hp1 HG02647.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.41+17085T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157841845 | ||||||
chr5:157841909
|
C | G | 70 | a0001c0001t0002g0040a0001c0001t0003g0017a0001c0001t0003g0018others(67): Show | 70 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(67): Show |
intron_variant | MODIFIER | c.41+17021G>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157841909 | ||||||
chr5:157841931
|
G | A | 1 | a0001c0001t0001g0293 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.41+16999C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157841931 | ||||||
chr5:157842080
|
T | C | 1 | a0002c0005t0001g0212 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.41+16850A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157842080 | ||||||
chr5:157842409
|
C | A | 51 | a0001c0001t0002g0040a0001c0001t0003g0017a0001c0001t0003g0018others(48): Show | 51 | HG00140.hp1 HG00597.hp1 HG01192.hp2 others(48): Show |
intron_variant | MODIFIER | c.41+16521G>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157842409 | ||||||
chr5:157842713
|
C | A | 36 | a0001c0001t0002g0085a0001c0001t0002g0193a0001c0001t0002g0194others(33): Show | 37 | HG00741.hp1 HG01099.hp1 HG01106.hp1 others(34): Show |
intron_variant | MODIFIER | c.41+16217G>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157842713 | ||||||
chr5:157842825
|
G | A | 2 | a0001c0001t0003g0210a0001c0004t0003g0072 | 2 | HG02922.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.41+16105C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157842825 | ||||||
chr5:157842930
|
A | G | 49 | a0001c0001t0002g0040a0001c0001t0003g0017a0001c0001t0003g0018others(46): Show | 49 | HG00140.hp1 HG00597.hp1 HG01192.hp2 others(46): Show |
intron_variant | MODIFIER | c.41+16000T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157842930 | ||||||
chr5:157843575
|
G | A | 2 | a0001c0001t0003g0044a0001c0001t0003g0045 | 2 | HG02486.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.41+15355C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157843575 | ||||||
chr5:157843741
|
A | G | 18 | a0001c0001t0001g0271a0001c0001t0001g0273a0001c0001t0001g0275others(15): Show | 18 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(15): Show |
intron_variant | MODIFIER | c.41+15189T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157843741 | ||||||
chr5:157843852
|
C | T | 85 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0011others(82): Show | 87 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(84): Show |
intron_variant | MODIFIER | c.41+15078G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157843852 | ||||||
chr5:157843867
|
G | A | 1 | a0001c0001t0001g0266 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.41+15063C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157843867 | ||||||
chr5:157843902
|
T | C | 1 | a0001c0001t0001g0324 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.41+15028A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157843902 | ||||||
chr5:157844011
|
A | G | 1 | a0001c0001t0010g0332 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.41+14919T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157844011 | ||||||
chr5:157844075
|
A | C | 5 | a0001c0001t0001g0277a0001c0001t0001g0305a0001c0001t0001g0306others(2): Show | 5 | HG01243.hp2 HG02647.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.41+14855T>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157844075 | ||||||
chr5:157844132
|
T | C | 1 | a0001c0001t0010g0332 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.41+14798A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157844132 | ||||||
chr5:157844222
|
A | C | 1 | a0001c0001t0003g0062 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.41+14708T>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157844222 | ||||||
chr5:157844680
|
G | A | 1 | a0001c0001t0002g0016 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.41+14250C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157844680 | ||||||
chr5:157844825
|
T | G | 1 | a0001c0001t0002g0123 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.41+14105A>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157844825 | ||||||
chr5:157844854
|
T | C | 1 | a0001c0001t0001g0253 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.41+14076A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157844854 | ||||||
chr5:157844897
|
T | C | 69 | a0001c0001t0002g0040a0001c0001t0003g0017a0001c0001t0003g0018others(66): Show | 69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.41+14033A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157844897 | ||||||
chr5:157844927
|
C | T | 1 | a0002c0005t0001g0212 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.41+14003G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157844927 | ||||||
chr5:157845097
|
C | T | 19 | a0001c0001t0001g0006a0001c0001t0001g0308a0001c0001t0001g0310others(16): Show | 20 | HG00280.hp1 HG01070.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.41+13833G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157845097 | ||||||
chr5:157845124
|
G | A | 1 | a0001c0001t0003g0037 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.41+13806C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157845124 | ||||||
chr5:157845210
|
G | A | 69 | a0001c0001t0002g0040a0001c0001t0003g0017a0001c0001t0003g0018others(66): Show | 69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.41+13720C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157845210 | ||||||
chr5:157845266
|
T | C | 2 | a0001c0001t0007g0333a0001c0001t0007g0334 | 2 | HG02109.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.41+13664A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157845266 | ||||||
chr5:157845327
|
C | T | 69 | a0001c0001t0002g0040a0001c0001t0003g0017a0001c0001t0003g0018others(66): Show | 69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.41+13603G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157845327 | ||||||
chr5:157845328
|
G | A | 1 | a0001c0001t0003g0043 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.41+13602C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157845328 | ||||||
chr5:157845445
|
C | T | 1 | a0001c0001t0010g0332 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.41+13485G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157845445 | ||||||
chr5:157845455
|
G | A | 209 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0011others(206): Show | 212 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(209): Show |
intron_variant | MODIFIER | c.41+13475C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157845455 | ||||||
chr5:157845553
|
A | AT | 31 | a0001c0001t0001g0216a0001c0001t0001g0234a0001c0001t0001g0261others(28): Show | 31 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(28): Show |
intron_variant | MODIFIER | c.41+13376dupA | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157845553 | ||||||
chr5:157845591
|
G | A | 1 | a0001c0001t0009g0330 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.41+13339C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157845591 | ||||||
chr5:157845638
|
G | A | 1 | a0001c0001t0001g0258 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.41+13292C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157845638 | ||||||
chr5:157845741
|
A | G | 1 | a0001c0001t0001g0311 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.41+13189T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157845741 | ||||||
chr5:157845776
|
G | A | 1 | a0001c0004t0003g0072 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.41+13154C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157845776 | ||||||
chr5:157845779
|
C | T | 1 | a0001c0001t0002g0206 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.41+13151G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157845779 | ||||||
chr5:157845823
|
G | A | 1 | a0001c0001t0004g0107 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.41+13107C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157845823 | ||||||
chr5:157845845
|
T | C | 1 | a0001c0001t0003g0038 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.41+13085A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157845845 | ||||||
chr5:157845850
|
G | A | 2 | a0001c0001t0002g0194a0001c0001t0010g0332 | 2 | HG02970.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.41+13080C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157845850 | ||||||
chr5:157845852
|
C | A | 1 | a0001c0001t0002g0108 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.41+13078G>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157845852 | ||||||
chr5:157845932
|
G | A | 1 | a0001c0001t0001g0220 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.41+12998C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157845932 | ||||||
chr5:157846380
|
CACA | C | 69 | a0001c0001t0002g0040a0001c0001t0003g0017a0001c0001t0003g0018others(66): Show | 69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.41+12547_41+12549d others(5): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157846380 | ||||||
chr5:157846599
|
T | A | 1 | a0001c0001t0001g0295 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.41+12331A>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157846599 | ||||||
chr5:157846603
|
A | G | 1 | a0001c0001t0003g0094 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.41+12327T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157846603 | ||||||
chr5:157846629
|
A | G | 1 | a0001c0001t0001g0293 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.41+12301T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157846629 | ||||||
chr5:157846651
|
A | G | 1 | a0001c0002t0003g0081 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.41+12279T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157846651 | ||||||
chr5:157846653
|
C | T | 1 | a0001c0001t0002g0083 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.41+12277G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157846653 | ||||||
chr5:157846655
|
G | C | 1 | a0001c0001t0002g0087 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.41+12275C>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157846655 | ||||||
chr5:157846673
|
C | G | 1 | a0001c0001t0002g0206 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.41+12257G>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157846673 | ||||||
chr5:157846681
|
G | A | 1 | a0001c0001t0001g0221 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.41+12249C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157846681 | ||||||
chr5:157846836
|
T | C | 52 | a0001c0001t0002g0040a0001c0001t0003g0017a0001c0001t0003g0018others(49): Show | 52 | HG00140.hp1 HG00597.hp1 HG01192.hp2 others(49): Show |
intron_variant | MODIFIER | c.41+12094A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157846836 | ||||||
chr5:157846977
|
A | G | 1 | a0001c0001t0002g0040 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.41+11953T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157846977 | ||||||
chr5:157847046
|
G | A | 5 | a0001c0001t0001g0277a0001c0001t0001g0305a0001c0001t0001g0306others(2): Show | 5 | HG01243.hp2 HG02647.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.41+11884C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157847046 | ||||||
chr5:157847095
|
AT | A | 6 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(3): Show | 6 | HG01081.hp1 HG01106.hp2 HG01123.hp1 others(3): Show |
intron_variant | MODIFIER | c.41+11834delA | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157847095 | ||||||
chr5:157847180
|
C | T | 1 | a0001c0001t0001g0275 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.41+11750G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157847180 | ||||||
chr5:157847389
|
T | C | 1 | a0002c0005t0001g0212 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.41+11541A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157847389 | ||||||
chr5:157847460
|
G | A | 1 | a0002c0005t0001g0212 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.41+11470C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157847460 | ||||||
chr5:157847477
|
C | G | 1 | a0001c0001t0002g0125 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.41+11453G>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157847477 | ||||||
chr5:157847510
|
C | CA | 14 | a0001c0001t0002g0086a0001c0001t0002g0196a0001c0001t0002g0197others(11): Show | 14 | HG00735.hp2 HG00738.hp2 HG01099.hp2 others(11): Show |
intron_variant | MODIFIER | c.41+11419dupT | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157847510 | ||||||
chr5:157847562
|
T | A | 1 | a0001c0001t0011g0061 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.41+11368A>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157847562 | ||||||
chr5:157847581
|
C | T | 136 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0011others(133): Show | 139 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.41+11349G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157847581 | ||||||
chr5:157847801
|
A | G | 1 | a0001c0001t0001g0260 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.41+11129T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157847801 | ||||||
chr5:157847811
|
A | G | 1 | a0001c0001t0001g0277 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.41+11119T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157847811 | ||||||
chr5:157847906
|
G | C | 2 | a0001c0001t0001g0280a0001c0001t0001g0281 | 2 | HG03041.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.41+11024C>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157847906 | ||||||
chr5:157848063
|
T | C | 1 | a0001c0001t0002g0106 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.41+10867A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157848063 | ||||||
chr5:157848065
|
C | T | 1 | a0002c0005t0001g0212 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.41+10865G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157848065 | ||||||
chr5:157848289
|
G | C | 124 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(121): Show | 127 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.41+10641C>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157848289 | ||||||
chr5:157848348
|
C | A | 1 | a0002c0005t0001g0212 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.41+10582G>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157848348 | ||||||
chr5:157848408
|
A | T | 7 | a0001c0001t0001g0280a0001c0001t0001g0281a0001c0001t0002g0085others(4): Show | 7 | HG02109.hp2 HG02572.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.41+10522T>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157848408 | ||||||
chr5:157848411
|
T | A | 1 | a0001c0001t0002g0108 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.41+10519A>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157848411 | ||||||
chr5:157848428
|
G | A | 124 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(121): Show | 127 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.41+10502C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157848428 | ||||||
chr5:157848488
|
G | A | 1 | a0001c0001t0010g0332 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.41+10442C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157848488 | ||||||
chr5:157848597
|
G | A | 2 | a0001c0001t0001g0222a0001c0001t0001g0223 | 2 | HG01257.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.41+10333C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157848597 | ||||||
chr5:157848773
|
T | C | 2 | a0001c0001t0006g0007a0001c0001t0006g0008 | 2 | NA18966.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.41+10157A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157848773 | ||||||
chr5:157848810
|
C | T | 3 | a0001c0001t0002g0085a0001c0001t0002g0193a0001c0008t0002g0195 | 3 | HG03139.hp2 HG03195.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.41+10120G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157848810 | ||||||
chr5:157848811
|
G | A | 1 | a0001c0001t0001g0260 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.41+10119C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157848811 | ||||||
chr5:157848818
|
C | T | 1 | a0001c0001t0010g0332 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.41+10112G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157848818 | ||||||
chr5:157848848
|
G | C | 1 | a0001c0001t0002g0124 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.41+10082C>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157848848 | ||||||
chr5:157848863
|
C | T | 1 | a0001c0001t0010g0332 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.41+10067G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157848863 | ||||||
chr5:157849111
|
A | G | 1 | a0001c0001t0010g0332 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.41+9819T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157849111 | ||||||
chr5:157849159
|
TAC | T | 4 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270others(1): Show | 4 | HG01070.hp2 HG01169.hp2 HG02055.hp1 others(1): Show |
intron_variant | MODIFIER | c.41+9769_41+9770del others(2): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157849159 | ||||||
chr5:157849208
|
A | G | 1 | a0001c0001t0011g0061 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.41+9722T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157849208 | ||||||
chr5:157849362
|
G | A | 72 | a0001c0001t0002g0040a0001c0001t0003g0017a0001c0001t0003g0018others(69): Show | 72 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(69): Show |
intron_variant | MODIFIER | c.41+9568C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157849362 | ||||||
chr5:157849492
|
C | T | 1 | a0001c0001t0002g0193 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.41+9438G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157849492 | ||||||
chr5:157849537
|
C | T | 1 | a0001c0001t0001g0266 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.41+9393G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157849537 | ||||||
chr5:157849901
|
A | T | 1 | a0001c0001t0002g0083 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.41+9029T>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157849901 | ||||||
chr5:157849978
|
A | C | 1 | a0002c0005t0001g0212 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.41+8952T>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157849978 | ||||||
chr5:157849988
|
G | T | 2 | a0001c0001t0003g0047a0001c0001t0003g0048 | 2 | HG02717.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.41+8942C>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157849988 | ||||||
chr5:157849993
|
G | A | 1 | a0001c0001t0002g0085 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.41+8937C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157849993 | ||||||
chr5:157850010
|
T | C | 1 | a0001c0001t0003g0094 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.41+8920A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157850010 | ||||||
chr5:157850028
|
C | T | 1 | a0001c0001t0002g0160 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.41+8902G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157850028 | ||||||
chr5:157850043
|
A | G | 4 | a0001c0001t0001g0272a0001c0001t0001g0278a0001c0001t0001g0298others(1): Show | 4 | HG01071.hp1 HG02647.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.41+8887T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157850043 | ||||||
chr5:157850323
|
T | C | 4 | a0001c0001t0001g0224a0001c0001t0001g0225a0001c0001t0001g0226others(1): Show | 4 | HG00099.hp2 HG01496.hp1 HG01928.hp1 others(1): Show |
intron_variant | MODIFIER | c.41+8607A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157850323 | ||||||
chr5:157850344
|
A | G | 197 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(194): Show | 200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.41+8586T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157850344 | ||||||
chr5:157850440
|
G | A | 1 | a0001c0001t0001g0291 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.41+8490C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157850440 | ||||||
chr5:157850565
|
C | T | 1 | a0001c0001t0002g0106 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.41+8365G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157850565 | ||||||
chr5:157850579
|
C | T | 1 | a0001c0001t0002g0125 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.41+8351G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157850579 | ||||||
chr5:157850612
|
C | CA | 34 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0309others(31): Show | 34 | HG00597.hp2 HG00741.hp2 HG01123.hp1 others(31): Show |
intron_variant | MODIFIER | c.41+8317dupT | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157850612 | ||||||
chr5:157850612
|
CA | C | 177 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0079others(174): Show | 180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.41+8317delT | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157850612 | ||||||
chr5:157850612
|
CAA | C | 18 | a0001c0001t0001g0215a0001c0001t0001g0272a0001c0001t0001g0331others(15): Show | 18 | HG00735.hp2 HG00738.hp2 HG01099.hp2 others(15): Show |
intron_variant | MODIFIER | c.41+8316_41+8317del others(2): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157850612 | ||||||
chr5:157850650
|
A | T | 3 | a0001c0001t0002g0135a0001c0001t0002g0182a0001c0001t0002g0183 | 3 | NA18612.hp2 NA18987.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.41+8280T>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157850650 | ||||||
chr5:157850726
|
A | G | 1 | a0001c0001t0003g0051 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.41+8204T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157850726 | ||||||
chr5:157850804
|
A | T | 197 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(194): Show | 200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.41+8126T>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157850804 | ||||||
chr5:157851123
|
G | A | 1 | a0001c0001t0001g0277 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.41+7807C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157851123 | ||||||
chr5:157851138
|
GCAAA | G | 69 | a0001c0001t0002g0040a0001c0001t0003g0017a0001c0001t0003g0018others(66): Show | 69 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.41+7788_41+7791del others(4): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157851138 | ||||||
chr5:157851271
|
C | T | 1 | a0001c0004t0003g0072 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.41+7659G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157851271 | ||||||
chr5:157851279
|
C | T | 2 | a0001c0001t0003g0044a0001c0001t0003g0045 | 2 | HG02486.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.41+7651G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157851279 | ||||||
chr5:157851323
|
A | G | 2 | a0001c0001t0003g0047a0001c0001t0003g0048 | 2 | HG02717.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.41+7607T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157851323 | ||||||
chr5:157851418
|
G | A | 3 | a0001c0001t0004g0104a0001c0001t0004g0145a0001c0001t0004g0151 | 3 | HG01099.hp1 HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.41+7512C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157851418 | ||||||
chr5:157851572
|
CAGCTACT others(15): Show |
C | 49 | a0001c0001t0002g0040a0001c0001t0003g0017a0001c0001t0003g0018others(46): Show | 49 | HG00140.hp1 HG00597.hp1 HG01192.hp2 others(46): Show |
intron_variant | MODIFIER | c.41+7336_41+7357del others(22): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157851572 | ||||||
chr5:157851680
|
C | T | 124 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(121): Show | 127 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.41+7250G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157851680 | ||||||
chr5:157851686
|
C | CA | 84 | a0001c0001t0001g0010a0001c0001t0001g0267a0001c0001t0002g0040others(81): Show | 84 | HG00140.hp1 HG00544.hp2 HG00597.hp1 others(81): Show |
intron_variant | MODIFIER | c.41+7243dupT | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157851686 | ||||||
chr5:157851782
|
T | C | 4 | a0001c0001t0001g0271a0001c0001t0001g0292a0001c0001t0001g0301others(1): Show | 4 | HG00099.hp1 HG00323.hp2 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.41+7148A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157851782 | ||||||
chr5:157851832
|
G | C | 1 | a0001c0006t0001g0327 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.41+7098C>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157851832 | ||||||
chr5:157851940
|
A | G | 1 | a0001c0001t0001g0215 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.41+6990T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157851940 | ||||||
chr5:157851976
|
A | G | 1 | a0001c0001t0006g0007 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.41+6954T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157851976 | ||||||
chr5:157852047
|
G | T | 1 | a0001c0001t0010g0332 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.41+6883C>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157852047 | ||||||
chr5:157852200
|
T | A | 3 | a0001c0001t0002g0135a0001c0001t0002g0182a0001c0001t0002g0183 | 3 | NA18612.hp2 NA18987.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.41+6730A>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157852200 | ||||||
chr5:157852206
|
T | C | 2 | a0001c0001t0002g0184a0001c0001t0002g0185 | 2 | HG00423.hp2 NA18961.hp1 |
intron_variant | MODIFIER | c.41+6724A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157852206 | ||||||
chr5:157852235
|
C | A | 1 | a0001c0001t0001g0260 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.41+6695G>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157852235 | ||||||
chr5:157852471
|
T | C | 3 | a0001c0001t0001g0004a0001c0001t0001g0230a0001c0001t0001g0231 | 4 | NA18941.hp1 NA19062.hp2 NA19085.hp1 others(1): Show |
intron_variant | MODIFIER | c.41+6459A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157852471 | ||||||
chr5:157852478
|
A | G | 1 | a0001c0001t0010g0332 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.41+6452T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157852478 | ||||||
chr5:157852500
|
C | T | 2 | a0001c0001t0004g0096a0001c0001t0004g0158 | 2 | HG00741.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.41+6430G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157852500 | ||||||
chr5:157852554
|
A | C | 1 | a0001c0001t0001g0268 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.41+6376T>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157852554 | ||||||
chr5:157852561
|
A | G | 1 | a0001c0001t0001g0293 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.41+6369T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157852561 | ||||||
chr5:157852675
|
C | T | 1 | a0001c0001t0010g0332 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.41+6255G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157852675 | ||||||
chr5:157852752
|
C | G | 230 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(227): Show | 234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.41+6178G>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157852752 | ||||||
chr5:157852820
|
T | C | 33 | a0001c0001t0004g0003a0001c0001t0004g0082a0001c0001t0004g0084others(30): Show | 34 | HG00741.hp1 HG01099.hp1 HG01106.hp1 others(31): Show |
intron_variant | MODIFIER | c.41+6110A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157852820 | ||||||
chr5:157852896
|
C | T | 2 | a0001c0001t0003g0019a0001c0001t0003g0059 | 2 | HG02129.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.41+6034G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157852896 | ||||||
chr5:157853111
|
G | T | 98 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0009others(95): Show | 100 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(97): Show |
intron_variant | MODIFIER | c.41+5819C>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157853111 | ||||||
chr5:157853123
|
A | G | 249 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(246): Show | 253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.41+5807T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157853123 | ||||||
chr5:157853173
|
C | G | 2 | a0001c0001t0002g0136a0001c0001t0002g0157 | 2 | NA19066.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.41+5757G>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157853173 | ||||||
chr5:157853282
|
G | A | 1 | a0001c0001t0001g0310 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.41+5648C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157853282 | ||||||
chr5:157853353
|
GA | G | 70 | a0001c0001t0001g0293a0001c0001t0002g0040a0001c0001t0003g0017others(67): Show | 70 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(67): Show |
intron_variant | MODIFIER | c.41+5576delT | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157853353 | ||||||
chr5:157853388
|
A | G | 70 | a0001c0001t0002g0040a0001c0001t0003g0017a0001c0001t0003g0018others(67): Show | 70 | HG00140.hp1 HG00597.hp1 HG01109.hp2 others(67): Show |
intron_variant | MODIFIER | c.41+5542T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157853388 | ||||||
chr5:157853404
|
A | G | 1 | a0001c0001t0004g0105 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.41+5526T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157853404 | ||||||
chr5:157853423
|
T | C | 1 | a0001c0001t0001g0325 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.41+5507A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157853423 | ||||||
chr5:157853550
|
G | A | 1 | a0001c0001t0002g0085 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.41+5380C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157853550 | ||||||
chr5:157853722
|
A | G | 1 | a0001c0001t0003g0094 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.41+5208T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157853722 | ||||||
chr5:157853777
|
C | CA | 38 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0231others(35): Show | 39 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(36): Show |
intron_variant | MODIFIER | c.41+5152dupT | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157853777 | ||||||
chr5:157853777
|
CA | C | 114 | a0001c0001t0001g0233a0001c0001t0001g0271a0001c0001t0001g0305others(111): Show | 115 | HG00597.hp1 HG00621.hp2 HG00738.hp2 others(112): Show |
intron_variant | MODIFIER | c.41+5152delT | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157853777 | ||||||
chr5:157853777
|
CAA | C | 9 | a0001c0001t0003g0018a0001c0001t0003g0042a0001c0001t0003g0043others(6): Show | 9 | HG01517.hp2 HG02735.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.41+5151_41+5152del others(2): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157853777 | ||||||
chr5:157853777
|
CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0003g0050 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.41+5142_41+5152del others(11): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157853777 | ||||||
chr5:157853793
|
A | G | 1 | a0001c0001t0001g0232 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.41+5137T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157853793 | ||||||
chr5:157853796
|
A | G | 1 | a0001c0001t0003g0094 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.41+5134T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157853796 | ||||||
chr5:157853905
|
T | G | 11 | a0001c0001t0004g0003a0001c0001t0004g0084a0001c0001t0004g0140others(8): Show | 12 | NA18940.hp2 NA18942.hp2 NA18943.hp2 others(9): Show |
intron_variant | MODIFIER | c.41+5025A>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157853905 | ||||||
chr5:157854025
|
A | G | 1 | a0001c0001t0002g0144 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.41+4905T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157854025 | ||||||
chr5:157854050
|
A | G | 21 | a0001c0001t0001g0006a0001c0001t0001g0308a0001c0001t0001g0309others(18): Show | 22 | HG00280.hp1 HG01070.hp1 HG01071.hp2 others(19): Show |
intron_variant | MODIFIER | c.41+4880T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157854050 | ||||||
chr5:157854279
|
C | T | 1 | a0001c0001t0007g0333 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.41+4651G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157854279 | ||||||
chr5:157854313
|
A | G | 1 | a0001c0002t0003g0080 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.41+4617T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157854313 | ||||||
chr5:157854401
|
T | C | 1 | a0001c0001t0003g0049 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.41+4529A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157854401 | ||||||
chr5:157854714
|
C | T | 1 | a0001c0001t0001g0297 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.41+4216G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157854714 | ||||||
chr5:157855141
|
C | CG | 116 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(113): Show | 119 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(116): Show |
intron_variant | MODIFIER | c.41+3788dupC | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157855141 | ||||||
chr5:157855142
|
G | GGA | 8 | a0001c0001t0001g0214a0001c0001t0001g0277a0001c0001t0001g0303others(5): Show | 8 | HG01243.hp2 HG02258.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.41+3787_41+3788ins others(2): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157855142 | ||||||
chr5:157855157
|
C | CG | 89 | a0001c0001t0001g0261a0001c0001t0001g0262a0001c0001t0001g0263others(86): Show | 92 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(89): Show |
intron_variant | MODIFIER | c.41+3772dupC | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157855157 | ||||||
chr5:157855157
|
C | CGG | 75 | a0001c0001t0001g0005a0001c0001t0001g0079a0001c0001t0001g0232others(72): Show | 76 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.41+3771_41+3772dup others(2): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157855157 | ||||||
chr5:157855157
|
C | CGGG | 35 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0215others(32): Show | 36 | HG00099.hp2 HG00438.hp2 HG01255.hp1 others(33): Show |
intron_variant | MODIFIER | c.41+3770_41+3772dup others(3): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157855157 | ||||||
chr5:157855157
|
C | CGGGG | 31 | a0001c0001t0001g0009a0001c0001t0001g0214a0001c0001t0002g0040others(28): Show | 31 | HG00140.hp1 HG01884.hp2 HG02056.hp1 others(28): Show |
intron_variant | MODIFIER | c.41+3769_41+3772dup others(4): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157855157 | ||||||
chr5:157855161
|
G | GGC | 21 | a0001c0001t0001g0006a0001c0001t0001g0308a0001c0001t0001g0309others(18): Show | 22 | HG00280.hp1 HG01070.hp1 HG01071.hp2 others(19): Show |
intron_variant | MODIFIER | c.41+3768_41+3769ins others(2): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157855161 | ||||||
chr5:157855166
|
G | T | 21 | a0001c0001t0001g0006a0001c0001t0001g0308a0001c0001t0001g0309others(18): Show | 22 | HG00280.hp1 HG01070.hp1 HG01071.hp2 others(19): Show |
intron_variant | MODIFIER | c.41+3764C>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157855166 | ||||||
chr5:157855169
|
C | T | 1 | a0001c0001t0003g0017 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.41+3761G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157855169 | ||||||
chr5:157855231
|
G | A | 1 | a0001c0001t0001g0006 | 2 | HG00280.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.41+3699C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157855231 | ||||||
chr5:157855279
|
C | G | 1 | a0001c0001t0001g0271 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.41+3651G>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157855279 | ||||||
chr5:157855399
|
T | C | 3 | a0001c0001t0001g0305a0001c0001t0001g0306a0001c0001t0001g0307 | 3 | HG01243.hp2 HG02895.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.41+3531A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157855399 | ||||||
chr5:157855406
|
T | C | 1 | a0001c0006t0001g0327 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.41+3524A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157855406 | ||||||
chr5:157855495
|
C | T | 1 | a0002c0005t0001g0212 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.41+3435G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157855495 | ||||||
chr5:157855648
|
T | C | 2 | a0001c0001t0002g0191a0001c0001t0002g0192 | 2 | NA18991.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.41+3282A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157855648 | ||||||
chr5:157855928
|
C | A | 2 | a0001c0001t0007g0333a0001c0001t0007g0334 | 2 | HG02109.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.41+3002G>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157855928 | ||||||
chr5:157856144
|
C | T | 1 | a0001c0001t0002g0088 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.41+2786G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157856144 | ||||||
chr5:157856244
|
C | T | 3 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270 | 3 | HG01070.hp2 HG01169.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.41+2686G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157856244 | ||||||
chr5:157856440
|
T | C | 4 | a0001c0001t0002g0085a0001c0001t0002g0193a0001c0001t0002g0194others(1): Show | 4 | HG02970.hp1 HG03139.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.41+2490A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157856440 | ||||||
chr5:157856489
|
G | A | 2 | a0001c0001t0007g0333a0001c0001t0007g0334 | 2 | HG02109.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.41+2441C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157856489 | ||||||
chr5:157856772
|
A | G | 1 | a0001c0001t0010g0332 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.41+2158T>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157856772 | ||||||
chr5:157856868
|
G | A | 1 | a0001c0001t0010g0332 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.41+2062C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157856868 | ||||||
chr5:157857067
|
C | T | 1 | a0001c0001t0002g0087 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.41+1863G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157857067 | ||||||
chr5:157857117
|
C | T | 3 | a0001c0001t0002g0086a0001c0001t0002g0196a0001c0001t0002g0197 | 3 | HG00735.hp2 HG01346.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.41+1813G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157857117 | ||||||
chr5:157857170
|
C | A | 21 | a0001c0001t0001g0006a0001c0001t0001g0308a0001c0001t0001g0309others(18): Show | 22 | HG00280.hp1 HG01070.hp1 HG01071.hp2 others(19): Show |
intron_variant | MODIFIER | c.41+1760G>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157857170 | ||||||
chr5:157857224
|
C | CA | 14 | a0001c0001t0002g0196a0001c0001t0002g0197a0001c0001t0002g0198others(11): Show | 14 | HG00609.hp1 HG00735.hp2 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.41+1705dupT | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157857224 | ||||||
chr5:157857224
|
CA | C | 130 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(127): Show | 133 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.41+1705delT | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157857224 | ||||||
chr5:157857224
|
CAA | C | 65 | a0001c0001t0002g0040a0001c0001t0003g0017a0001c0001t0003g0018others(62): Show | 65 | HG00140.hp1 HG00597.hp1 HG01192.hp2 others(62): Show |
intron_variant | MODIFIER | c.41+1704_41+1705del others(2): Show |
CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157857224 | ||||||
chr5:157857296
|
A | C | 6 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0013others(3): Show | 6 | HG01081.hp1 HG01106.hp2 HG01123.hp1 others(3): Show |
intron_variant | MODIFIER | c.41+1634T>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157857296 | ||||||
chr5:157857323
|
G | A | 1 | a0001c0001t0003g0210 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.41+1607C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157857323 | ||||||
chr5:157857368
|
G | A | 1 | a0001c0001t0009g0330 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.41+1562C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157857368 | ||||||
chr5:157857417
|
T | C | 1 | a0001c0001t0003g0211 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.41+1513A>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157857417 | ||||||
chr5:157857598
|
T | A | 1 | a0001c0001t0001g0331 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.41+1332A>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157857598 | ||||||
chr5:157858177
|
C | A | 1 | a0002c0005t0001g0212 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.41+753G>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157858177 | ||||||
chr5:157858206
|
T | G | 1 | a0001c0001t0010g0332 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.41+724A>C | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157858206 | ||||||
chr5:157858294
|
G | C | 1 | a0001c0001t0003g0213 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.41+636C>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157858294 | ||||||
chr5:157858542
|
C | T | 58 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0009others(55): Show | 60 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(57): Show |
intron_variant | MODIFIER | c.41+388G>A | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157858542 | ||||||
chr5:157858720
|
G | A | 121 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(118): Show | 124 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.41+210C>T | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157858720 | ||||||
chr5:157858862
|
G | C | 1 | a0001c0001t0010g0332 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.41+68C>G | CLINT1 | ENSG00000113282.14 | transcript | ENST00000411809.7 | protein_coding | 1/11 | chr5 | 157858862 |