geneid | 54677 |
---|---|
ensemblid | ENSG00000005469.12 |
hgncid | 2366 |
symbol | CROT |
name | carnitine O-octanoyltransferase |
refseq_nuc | NM_021151.4 |
refseq_prot | NP_066974.2 |
ensembl_nuc | ENST00000331536.8 |
ensembl_prot | ENSP00000331981.4 |
mane_status | MANE Select |
chr | chr7 |
start | 87345664 |
end | 87399794 |
strand | + |
ver | v1.2 |
region | chr7:87345664-87399794 |
region5000 | chr7:87340664-87404794 |
regionname0 | CROT_chr7_87345664_87399794 |
regionname5000 | CROT_chr7_87340664_87404794 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 612 | 251 | 77 | 41 | 106 | 9 | 16 | 77 | CROT_chr7_87340664_87404794 | CROT | copy fasta | chr7 | 87340664 | 87404794 |
a0002 | 0/0 | 612 | 22 | 10 | 2 | 0 | 2 | 8 | 0 | CROT_chr7_87340664_87404794 | CROT | copy fasta | chr7 | 87340664 | 87404794 |
a0003 | 0/0 | 612 | 3 | 0 | 3 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | copy fasta | chr7 | 87340664 | 87404794 |
a0004 | 0/0 | 612 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CROT_chr7_87340664_87404794 | CROT | copy fasta | chr7 | 87340664 | 87404794 |
a0005 | 0/0 | 612 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CROT_chr7_87340664_87404794 | CROT | copy fasta | chr7 | 87340664 | 87404794 |
a0006 | 0/0 | 612 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | copy fasta | chr7 | 87340664 | 87404794 |
a0007 | 0/0 | 612 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CROT_chr7_87340664_87404794 | CROT | copy fasta | chr7 | 87340664 | 87404794 |
a0008 | 0/0 | 612 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | copy fasta | chr7 | 87340664 | 87404794 |
a0009 | 0/0 | 612 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | copy fasta | chr7 | 87340664 | 87404794 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1839 | 251 | 77 | 41 | 106 | 9 | 16 | CROT_chr7_87340664_87404794 | CROT | copy fasta | chr7 | 87340664 | 87404794 |
c0002 | 0/0 | 1839 | 22 | 10 | 2 | 0 | 2 | 8 | CROT_chr7_87340664_87404794 | CROT | copy fasta | chr7 | 87340664 | 87404794 |
c0003 | 0/0 | 1839 | 3 | 0 | 3 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | copy fasta | chr7 | 87340664 | 87404794 |
c0004 | 0/0 | 1839 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | copy fasta | chr7 | 87340664 | 87404794 |
c0005 | 0/0 | 1839 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | copy fasta | chr7 | 87340664 | 87404794 |
c0006 | 0/0 | 1839 | 1 | 0 | 0 | 0 | 1 | 0 | CROT_chr7_87340664_87404794 | CROT | copy fasta | chr7 | 87340664 | 87404794 |
c0007 | 0/0 | 1839 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | copy fasta | chr7 | 87340664 | 87404794 |
c0008 | 0/0 | 1839 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | copy fasta | chr7 | 87340664 | 87404794 |
c0009 | 0/0 | 1839 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | copy fasta | chr7 | 87340664 | 87404794 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 1367 | 233 | 66 | 40 | 99 | 10 | 16 | CROT_chr7_87340664_87404794 | CROT | copy fasta | chr7 | 87340664 | 87404794 |
t0002 | 0/0 | 1367 | 18 | 3 | 5 | 0 | 2 | 8 | CROT_chr7_87340664_87404794 | CROT | copy fasta | chr7 | 87340664 | 87404794 |
t0003 | 0/0 | 1376 | 16 | 15 | 1 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | copy fasta | chr7 | 87340664 | 87404794 |
t0004 | 0/0 | 1367 | 5 | 0 | 0 | 5 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | copy fasta | chr7 | 87340664 | 87404794 |
t0005 | 0/0 | 1367 | 3 | 0 | 0 | 3 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | copy fasta | chr7 | 87340664 | 87404794 |
t0006 | 0/0 | 1367 | 2 | 0 | 0 | 2 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | copy fasta | chr7 | 87340664 | 87404794 |
t0007 | 0/0 | 1367 | 2 | 2 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | copy fasta | chr7 | 87340664 | 87404794 |
t0008 | 0/0 | 1367 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | copy fasta | chr7 | 87340664 | 87404794 |
t0009 | 0/0 | 1367 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | copy fasta | chr7 | 87340664 | 87404794 |
t0010 | 0/0 | 1376 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | copy fasta | chr7 | 87340664 | 87404794 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 11 | 0 | 2 | 9 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0002 | 0/0 | 9 | 0 | 1 | 6 | 0 | 2 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0003 | 0/0 | 7 | 1 | 4 | 0 | 0 | 2 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0004 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0005 | 0/0 | 5 | 0 | 3 | 0 | 1 | 1 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0006 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0007 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0009 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0021 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0079 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0165 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1839 | 251 | 77 | 41 | 106 | 9 | 16 | CROT_chr7_87340664_87404794 | CROT | copy fasta | chr7 | 87340664 | 87404794 |
a0002c0002 | 0/0 | 1839 | 22 | 10 | 2 | 0 | 2 | 8 | CROT_chr7_87340664_87404794 | CROT | copy fasta | chr7 | 87340664 | 87404794 |
a0003c0003 | 0/0 | 1839 | 3 | 0 | 3 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | copy fasta | chr7 | 87340664 | 87404794 |
a0004c0004 | 0/0 | 1839 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | copy fasta | chr7 | 87340664 | 87404794 |
a0005c0009 | 0/0 | 1839 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | copy fasta | chr7 | 87340664 | 87404794 |
a0006c0005 | 0/0 | 1839 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | copy fasta | chr7 | 87340664 | 87404794 |
a0007c0007 | 0/0 | 1839 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | copy fasta | chr7 | 87340664 | 87404794 |
a0008c0006 | 0/0 | 1839 | 1 | 0 | 0 | 0 | 1 | 0 | CROT_chr7_87340664_87404794 | CROT | copy fasta | chr7 | 87340664 | 87404794 |
a0009c0008 | 0/0 | 1839 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | copy fasta | chr7 | 87340664 | 87404794 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 3205 | 220 | 58 | 40 | 95 | 9 | 16 | CROT_chr7_87340664_87404794 | CROT | copy fasta | chr7 | 87340664 | 87404794 |
a0001c0001t0003 | 0/0 | 3214 | 16 | 15 | 1 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | copy fasta | chr7 | 87340664 | 87404794 |
a0001c0001t0004 | 0/0 | 3205 | 5 | 0 | 0 | 5 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | copy fasta | chr7 | 87340664 | 87404794 |
a0001c0001t0005 | 0/0 | 3205 | 3 | 0 | 0 | 3 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | copy fasta | chr7 | 87340664 | 87404794 |
a0001c0001t0006 | 0/0 | 3205 | 2 | 0 | 0 | 2 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | copy fasta | chr7 | 87340664 | 87404794 |
a0001c0001t0007 | 0/0 | 3205 | 2 | 2 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | copy fasta | chr7 | 87340664 | 87404794 |
a0001c0001t0008 | 0/0 | 3205 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | copy fasta | chr7 | 87340664 | 87404794 |
a0001c0001t0009 | 0/0 | 3205 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | copy fasta | chr7 | 87340664 | 87404794 |
a0001c0001t0010 | 0/0 | 3214 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | copy fasta | chr7 | 87340664 | 87404794 |
a0002c0002t0001 | 0/0 | 3205 | 7 | 7 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | copy fasta | chr7 | 87340664 | 87404794 |
a0002c0002t0002 | 0/0 | 3205 | 15 | 3 | 2 | 0 | 2 | 8 | CROT_chr7_87340664_87404794 | CROT | copy fasta | chr7 | 87340664 | 87404794 |
a0003c0003t0002 | 0/0 | 3205 | 3 | 0 | 3 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | copy fasta | chr7 | 87340664 | 87404794 |
a0004c0004t0001 | 0/0 | 3205 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | copy fasta | chr7 | 87340664 | 87404794 |
a0005c0009t0001 | 0/0 | 3205 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | copy fasta | chr7 | 87340664 | 87404794 |
a0006c0005t0001 | 0/0 | 3205 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | copy fasta | chr7 | 87340664 | 87404794 |
a0007c0007t0001 | 0/0 | 3205 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | copy fasta | chr7 | 87340664 | 87404794 |
a0008c0006t0001 | 0/0 | 3205 | 1 | 0 | 0 | 0 | 1 | 0 | CROT_chr7_87340664_87404794 | CROT | copy fasta | chr7 | 87340664 | 87404794 |
a0009c0008t0001 | 0/0 | 3205 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | copy fasta | chr7 | 87340664 | 87404794 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 11 | 0 | 2 | 9 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0002 | 0/0 | 7 | 0 | 1 | 4 | 0 | 2 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0004 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0005 | 0/0 | 5 | 0 | 3 | 0 | 1 | 1 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0007 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0079 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0165 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0003g0006 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0003g0009 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0003g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0003g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0003g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0003g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0003g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0003g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0003g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0003g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0003g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0004g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0004g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0004g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0005g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0005g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0005g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0006g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0007g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0008g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0009g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0001c0001t0010g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0002c0002t0001g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0002c0002t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0002c0002t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0002c0002t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0002c0002t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0002c0002t0002g0003 | 0/0 | 4 | 1 | 1 | 0 | 0 | 2 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0002c0002t0002g0021 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0002c0002t0002g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0002c0002t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0002c0002t0002g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0002c0002t0002g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0002c0002t0002g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0002c0002t0002g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0002c0002t0002g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0002c0002t0002g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0002c0002t0002g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0003c0003t0002g0003 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0004c0004t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0005c0009t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0006c0005t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0007c0007t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0008c0006t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
a0009c0008t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0046 | EUR | GBR | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0184 | EUR | GBR | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0102 | EUR | GBR | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG00140 | hp2 | a0002 | c0002 | t0002 | g0021 | EUR | GBR | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | FIN | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0121 | EUR | FIN | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG00323 | hp1 | a0002 | c0002 | t0002 | g0073 | EUR | FIN | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0056 | EUR | FIN | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | CHS | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG00423 | hp1 | a0001 | c0001 | t0008 | g0023 | EAS | CHS | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG00423 | hp2 | a0001 | c0001 | t0006 | g0028 | EAS | CHS | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | CHS | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG00544 | hp2 | a0006 | c0005 | t0001 | g0002 | EAS | CHS | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | CHS | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | CHS | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | CHS | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | CHS | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | CHS | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | CHS | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | PUR | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG00735 | hp1 | a0002 | c0002 | t0002 | g0003 | AMR | PUR | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0199 | AMR | PUR | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0198 | AMR | PUR | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG01192 | hp1 | a0002 | c0002 | t0002 | g0071 | AMR | PUR | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG01243 | hp1 | a0001 | c0001 | t0003 | g0006 | AMR | PUR | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0080 | AMR | PUR | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | CLM | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0182 | AMR | CLM | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | CLM | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | CLM | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0209 | AMR | CLM | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | ACB | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | ACB | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0197 | AMR | PEL | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0205 | AMR | PEL | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG01943 | hp1 | a0003 | c0003 | t0002 | g0003 | AMR | PEL | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0047 | AMR | PEL | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | PEL | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | PEL | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG02004 | hp1 | a0003 | c0003 | t0002 | g0003 | AMR | PEL | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | PEL | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG02040 | hp1 | a0001 | c0001 | t0005 | g0202 | EAS | KHV | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | KHV | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | ACB | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG02055 | hp2 | a0001 | c0001 | t0003 | g0031 | AFR | ACB | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | KHV | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | KHV | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | KHV | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG02080 | hp2 | a0001 | c0001 | t0004 | g0011 | EAS | KHV | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | KHV | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | KHV | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | KHV | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | KHV | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | KHV | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | ACB | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | ACB | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG02148 | hp1 | a0003 | c0003 | t0002 | g0003 | AMR | PEL | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | PEL | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | CDX | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | CDX | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG02257 | hp1 | a0001 | c0001 | t0003 | g0009 | AFR | ACB | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | ACB | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | ACB | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG02451 | hp2 | a0001 | c0001 | t0003 | g0009 | AFR | ACB | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG02572 | hp1 | a0002 | c0002 | t0002 | g0212 | AFR | GWD | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0193 | AFR | GWD | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | GWD | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG02615 | hp2 | a0002 | c0002 | t0001 | g0210 | AFR | GWD | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0214 | AFR | GWD | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | GWD | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG02630 | hp2 | a0002 | c0002 | t0002 | g0003 | AFR | GWD | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG02647 | hp1 | a0001 | c0001 | t0003 | g0032 | AFR | GWD | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | GWD | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG02683 | hp2 | a0002 | c0002 | t0002 | g0170 | SAS | PJL | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG02717 | hp1 | a0001 | c0001 | t0009 | g0203 | AFR | GWD | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG02717 | hp2 | a0001 | c0001 | t0003 | g0009 | AFR | GWD | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG02723 | hp1 | a0001 | c0001 | t0003 | g0039 | AFR | GWD | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | GWD | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0137 | SAS | PJL | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0104 | SAS | PJL | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | GWD | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG02818 | hp2 | a0009 | c0008 | t0001 | g0159 | AFR | GWD | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG02886 | hp1 | a0001 | c0001 | t0007 | g0015 | AFR | GWD | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG02886 | hp2 | a0002 | c0002 | t0002 | g0070 | AFR | GWD | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | GWD | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG02896 | hp1 | a0001 | c0001 | t0003 | g0030 | AFR | GWD | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | GWD | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | GWD | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | ESN | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG02922 | hp2 | a0001 | c0001 | t0003 | g0006 | AFR | ESN | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | ESN | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG02965 | hp2 | a0002 | c0002 | t0001 | g0014 | AFR | ESN | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG02970 | hp1 | a0001 | c0001 | t0003 | g0006 | AFR | ESN | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | ESN | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | ESN | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG03017 | hp1 | a0002 | c0002 | t0002 | g0185 | SAS | PJL | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG03041 | hp1 | a0001 | c0001 | t0010 | g0035 | AFR | GWD | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | GWD | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | ESN | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG03130 | hp2 | a0001 | c0001 | t0003 | g0037 | AFR | ESN | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | ESN | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | ESN | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | ESN | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG03195 | hp2 | a0002 | c0002 | t0001 | g0058 | AFR | ESN | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0204 | AFR | MSL | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | MSL | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | MSL | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | MSL | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0146 | SAS | PJL | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0194 | SAS | PJL | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0078 | SAS | PJL | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG03516 | hp1 | a0001 | c0001 | t0003 | g0006 | AFR | ESN | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG03516 | hp2 | a0002 | c0002 | t0001 | g0057 | AFR | ESN | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG03540 | hp1 | a0001 | c0001 | t0003 | g0034 | AFR | GWD | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | GWD | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | MSL | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | MSL | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG03654 | hp1 | a0002 | c0002 | t0002 | g0003 | SAS | PJL | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0160 | SAS | PJL | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG03669 | hp1 | a0002 | c0002 | t0002 | g0072 | SAS | PJL | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0136 | SAS | PJL | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0151 | SAS | BEB | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0176 | SAS | BEB | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG03927 | hp1 | a0002 | c0002 | t0002 | g0021 | SAS | BEB | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0168 | SAS | BEB | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG03942 | hp1 | a0002 | c0002 | t0002 | g0003 | SAS | BEB | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0208 | SAS | BEB | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0144 | SAS | STU | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG04115 | hp2 | a0002 | c0002 | t0002 | g0075 | SAS | STU | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG04199 | hp1 | a0002 | c0002 | t0002 | g0171 | SAS | STU | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0084 | SAS | STU | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | CHB | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | CHB | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | CHB | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | CHB | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | YRI | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | YRI | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
NA18942 | hp2 | a0001 | c0001 | t0004 | g0077 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
NA18966 | hp2 | a0001 | c0001 | t0004 | g0101 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
NA18969 | hp1 | a0004 | c0004 | t0001 | g0164 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
NA18984 | hp1 | a0007 | c0007 | t0001 | g0002 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
NA18984 | hp2 | a0001 | c0001 | t0004 | g0011 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
NA18990 | hp2 | a0001 | c0001 | t0006 | g0028 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
NA19005 | hp1 | a0005 | c0009 | t0001 | g0213 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
NA19011 | hp1 | a0001 | c0001 | t0005 | g0201 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | LWK | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | LWK | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | LWK | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | LWK | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
NA19065 | hp2 | a0001 | c0001 | t0005 | g0200 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
NA19068 | hp2 | a0001 | c0001 | t0004 | g0011 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
NA19072 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | YRI | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | YRI | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ASW | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
NA20129 | hp2 | a0001 | c0001 | t0003 | g0038 | AFR | ASW | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0099 | EUR | TSI | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
NA20752 | hp2 | a0008 | c0006 | t0001 | g0085 | EUR | TSI | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0074 | EUR | TSI | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0161 | EUR | TSI | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | CLM | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | CLM | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG02109 | hp1 | a0001 | c0001 | t0007 | g0015 | AFR | ACB | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG02109 | hp2 | a0002 | c0002 | t0001 | g0014 | AFR | ACB | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG02486 | hp2 | a0001 | c0001 | t0003 | g0036 | AFR | ACB | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | ACB | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | MSL | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | USA | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
HG06807 | hp2 | a0001 | c0001 | t0003 | g0033 | AFR | USA | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
NA20300 | hp1 | a0002 | c0002 | t0001 | g0211 | AFR | USA | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0172 | AFR | USA | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
NA21309 | hp1 | a0002 | c0002 | t0001 | g0014 | AFR | LWK | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | LWK | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0079 | REF | REF | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0165 | REF | REF | CROT_chr7_87340664_87404794 | CROT | chr7 | 87340664 | 87404794 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:87349142
|
T | C | 1 | a0003 | 3 | HG01943.hp1 HG02004.hp1 HG02148.hp1 |
missense_variant | MODERATE | c.74T>C | p.Val25Ala | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/18 | 290/3205 | 74/1839 | 25/612 | chr7 | 87349142 | ||
chr7:87361430
|
G | A | 1 | a0004 | 1 | NA18969.hp1 | missense_variant | MODERATE | c.281G>A | p.Arg94His | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 5/18 | 497/3205 | 281/1839 | 94/612 | chr7 | 87361430 | ||
chr7:87361507
|
A | G | 1 | a0005 | 1 | NA19005.hp1 | missense_variant | MODERATE | c.358A>G | p.Thr120Ala | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 5/18 | 574/3205 | 358/1839 | 120/612 | chr7 | 87361507 | ||
chr7:87391707
|
G | C | 2 | a0002a0003 | 25 | HG00140.hp2 HG00323.hp1 HG00735.hp1 others(22): Show |
missense_variant | MODERATE | c.1420G>C | p.Val474Leu | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 14/18 | 1636/3205 | 1420/1839 | 474/612 | chr7 | 87391707 | ||
chr7:87392810
|
C | G | 1 | a0009 | 1 | HG02818.hp2 | missense_variant | MODERATE | c.1585C>G | p.Leu529Val | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 16/18 | 1801/3205 | 1585/1839 | 529/612 | chr7 | 87392810 | ||
chr7:87392948
|
C | A | 1 | a0006 | 1 | HG00544.hp2 | missense_variant&splice_region_variant | MODERATE | c.1599C>A | p.Ser533Arg | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 17/18 | 1815/3205 | 1599/1839 | 533/612 | chr7 | 87392948 | ||
chr7:87392992
|
A | G | 1 | a0007 | 1 | NA18984.hp1 | missense_variant | MODERATE | c.1643A>G | p.Tyr548Cys | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 17/18 | 1859/3205 | 1643/1839 | 548/612 | chr7 | 87392992 | ||
chr7:87393031
|
A | G | 1 | a0008 | 1 | NA20752.hp2 | missense_variant | MODERATE | c.1682A>G | p.Asn561Ser | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 17/18 | 1898/3205 | 1682/1839 | 561/612 | chr7 | 87393031 |
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 |
---|
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:87345679
|
C | T | 1 | a0001c0001t0004 | 5 | HG02080.hp2 NA18942.hp2 NA18966.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-201C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 1/18 | 3390 | chr7 | 87345679 | |||||
chr7:87345694
|
G | C | 1 | a0001c0001t0005 | 3 | HG02040.hp1 NA19011.hp1 NA19065.hp2 |
5_prime_UTR_variant | MODIFIER | c.-186G>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 1/18 | 3375 | chr7 | 87345694 | |||||
chr7:87345709
|
G | T | 2 | a0001c0001t0003a0001c0001t0010 | 17 | HG01243.hp1 HG02055.hp2 HG02257.hp1 others(14): Show |
5_prime_UTR_variant | MODIFIER | c.-171G>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 1/18 | 3360 | chr7 | 87345709 | |||||
chr7:87345714
|
T | C | 1 | a0001c0001t0006 | 2 | HG00423.hp2 NA18990.hp2 |
5_prime_UTR_variant | MODIFIER | c.-166T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 1/18 | 3355 | chr7 | 87345714 | |||||
chr7:87345727
|
T | TGCGGCAG others(2): Show |
2 | a0001c0001t0003a0001c0001t0010 | 17 | HG01243.hp1 HG02055.hp2 HG02257.hp1 others(14): Show |
5_prime_UTR_variant | MODIFIER | c.-147_-139dupAGAGGC others(3): Show |
CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 1/18 | 3327 | INFO_REALIGN_3_PRIME | chr7 | 87345727 | ||||
chr7:87398843
|
C | T | 2 | a0002c0002t0002a0003c0003t0002 | 18 | HG00140.hp2 HG00323.hp1 HG00735.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*199C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 18/18 | 199 | chr7 | 87398843 | |||||
chr7:87399104
|
C | A | 1 | a0001c0001t0008 | 1 | HG00423.hp1 | 3_prime_UTR_variant | MODIFIER | c.*460C>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 18/18 | 460 | chr7 | 87399104 | |||||
chr7:87399342
|
G | A | 1 | a0001c0001t0007 | 2 | HG02109.hp1 HG02886.hp1 |
3_prime_UTR_variant | MODIFIER | c.*698G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 18/18 | 698 | chr7 | 87399342 | |||||
chr7:87399521
|
A | T | 1 | a0001c0001t0010 | 1 | HG03041.hp1 | 3_prime_UTR_variant | MODIFIER | c.*877A>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 18/18 | 877 | chr7 | 87399521 | |||||
chr7:87399710
|
T | A | 1 | a0001c0001t0009 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1066T>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 18/18 | 1066 | chr7 | 87399710 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:87345827
|
T | TTAAGTCG others(13): Show |
12 | a0001c0001t0003g0006a0001c0001t0003g0009a0001c0001t0003g0030others(9): Show | 17 | HG01243.hp1 HG02055.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.-113+75_-113+76ins others(20): Show |
CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 87345827 | |||||
chr7:87345916
|
T | C | 12 | a0001c0001t0003g0006a0001c0001t0003g0009a0001c0001t0003g0030others(9): Show | 17 | HG01243.hp1 HG02055.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.-113+149T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 1/17 | chr7 | 87345916 | ||||||
chr7:87345920
|
G | A | 6 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(3): Show | 7 | HG02109.hp1 HG02145.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.-113+153G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 1/17 | chr7 | 87345920 | ||||||
chr7:87345950
|
G | A | 12 | a0001c0001t0003g0006a0001c0001t0003g0009a0001c0001t0003g0030others(9): Show | 17 | HG01243.hp1 HG02055.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.-113+183G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 1/17 | chr7 | 87345950 | ||||||
chr7:87346030
|
G | T | 1 | a0001c0001t0001g0044 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-113+263G>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 1/17 | chr7 | 87346030 | ||||||
chr7:87346031
|
C | A | 1 | a0001c0001t0001g0044 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-113+264C>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 1/17 | chr7 | 87346031 | ||||||
chr7:87346107
|
C | A | 3 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0044 | 3 | HG02145.hp2 HG02630.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-112-233C>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 1/17 | chr7 | 87346107 | ||||||
chr7:87346120
|
T | C | 12 | a0001c0001t0003g0006a0001c0001t0003g0009a0001c0001t0003g0030others(9): Show | 17 | HG01243.hp1 HG02055.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.-112-220T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 1/17 | chr7 | 87346120 | ||||||
chr7:87346198
|
CGT | C | 12 | a0001c0001t0003g0006a0001c0001t0003g0009a0001c0001t0003g0030others(9): Show | 17 | HG01243.hp1 HG02055.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.-112-137_-112-136d others(4): Show |
CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 87346198 | |||||
chr7:87346245
|
C | G | 1 | a0001c0001t0001g0214 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-112-95C>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 1/17 | chr7 | 87346245 | ||||||
chr7:87346248
|
C | G | 12 | a0001c0001t0003g0006a0001c0001t0003g0009a0001c0001t0003g0030others(9): Show | 17 | HG01243.hp1 HG02055.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.-112-92C>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 1/17 | chr7 | 87346248 | ||||||
chr7:87346252
|
T | A | 12 | a0001c0001t0003g0006a0001c0001t0003g0009a0001c0001t0003g0030others(9): Show | 17 | HG01243.hp1 HG02055.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.-112-88T>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 1/17 | chr7 | 87346252 | ||||||
chr7:87346730
|
A | G | 12 | a0001c0001t0003g0006a0001c0001t0003g0009a0001c0001t0003g0030others(9): Show | 17 | HG01243.hp1 HG02055.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.-22+300A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 2/17 | chr7 | 87346730 | ||||||
chr7:87346900
|
C | T | 6 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(3): Show | 7 | HG02109.hp1 HG02145.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.-22+470C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 2/17 | chr7 | 87346900 | ||||||
chr7:87347145
|
G | A | 12 | a0001c0001t0003g0006a0001c0001t0003g0009a0001c0001t0003g0030others(9): Show | 17 | HG01243.hp1 HG02055.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.-22+715G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 2/17 | chr7 | 87347145 | ||||||
chr7:87347276
|
A | G | 7 | a0001c0001t0003g0006a0001c0001t0003g0009a0001c0001t0003g0036others(4): Show | 12 | HG01243.hp1 HG02257.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.-22+846A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 2/17 | chr7 | 87347276 | ||||||
chr7:87347281
|
G | C | 1 | a0001c0001t0001g0045 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-22+851G>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 2/17 | chr7 | 87347281 | ||||||
chr7:87347494
|
C | T | 1 | a0005c0009t0001g0213 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.-22+1064C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 2/17 | chr7 | 87347494 | ||||||
chr7:87347615
|
A | G | 1 | a0002c0002t0002g0212 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-22+1185A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 2/17 | chr7 | 87347615 | ||||||
chr7:87347697
|
G | GT | 12 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(9): Show | 15 | HG01496.hp1 HG02109.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.-22+1278dupT | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 87347697 | |||||
chr7:87348065
|
T | C | 1 | a0001c0001t0001g0046 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-21-983T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 2/17 | chr7 | 87348065 | ||||||
chr7:87348067
|
T | A | 1 | a0001c0001t0001g0046 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-21-981T>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 2/17 | chr7 | 87348067 | ||||||
chr7:87348109
|
A | G | 12 | a0001c0001t0003g0006a0001c0001t0003g0009a0001c0001t0003g0030others(9): Show | 17 | HG01243.hp1 HG02055.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.-21-939A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 2/17 | chr7 | 87348109 | ||||||
chr7:87348149
|
C | G | 1 | a0001c0001t0001g0206 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-21-899C>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 2/17 | chr7 | 87348149 | ||||||
chr7:87348179
|
C | T | 12 | a0001c0001t0003g0006a0001c0001t0003g0009a0001c0001t0003g0030others(9): Show | 17 | HG01243.hp1 HG02055.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.-21-869C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 2/17 | chr7 | 87348179 | ||||||
chr7:87348222
|
T | A | 7 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0047others(4): Show | 18 | HG01358.hp1 HG01496.hp2 HG01943.hp2 others(15): Show |
intron_variant | MODIFIER | c.-21-826T>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 2/17 | chr7 | 87348222 | ||||||
chr7:87348252
|
C | T | 12 | a0001c0001t0003g0006a0001c0001t0003g0009a0001c0001t0003g0030others(9): Show | 17 | HG01243.hp1 HG02055.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.-21-796C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 2/17 | chr7 | 87348252 | ||||||
chr7:87348270
|
A | G | 3 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0044 | 3 | HG02145.hp2 HG02630.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-21-778A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 2/17 | chr7 | 87348270 | ||||||
chr7:87348332
|
A | G | 12 | a0001c0001t0003g0006a0001c0001t0003g0009a0001c0001t0003g0030others(9): Show | 17 | HG01243.hp1 HG02055.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.-21-716A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 2/17 | chr7 | 87348332 | ||||||
chr7:87348386
|
G | C | 12 | a0001c0001t0003g0006a0001c0001t0003g0009a0001c0001t0003g0030others(9): Show | 17 | HG01243.hp1 HG02055.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.-21-662G>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 2/17 | chr7 | 87348386 | ||||||
chr7:87348393
|
G | A | 13 | a0001c0001t0001g0045a0001c0001t0003g0006a0001c0001t0003g0009others(10): Show | 18 | HG01243.hp1 HG02055.hp2 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.-21-655G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 2/17 | chr7 | 87348393 | ||||||
chr7:87348435
|
A | G | 1 | a0001c0001t0001g0205 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-21-613A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 2/17 | chr7 | 87348435 | ||||||
chr7:87348526
|
T | C | 1 | a0001c0001t0001g0052 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-21-522T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 2/17 | chr7 | 87348526 | ||||||
chr7:87348531
|
T | C | 1 | a0001c0001t0001g0053 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-21-517T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 2/17 | chr7 | 87348531 | ||||||
chr7:87348571
|
G | C | 2 | a0001c0001t0001g0054a0001c0001t0001g0055 | 2 | HG01978.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.-21-477G>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 2/17 | chr7 | 87348571 | ||||||
chr7:87348578
|
T | C | 26 | a0001c0001t0001g0017a0001c0001t0001g0040a0001c0001t0001g0041others(23): Show | 33 | HG00323.hp2 HG00639.hp1 HG01175.hp1 others(30): Show |
intron_variant | MODIFIER | c.-21-470T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 2/17 | chr7 | 87348578 | ||||||
chr7:87348602
|
T | C | 1 | a0001c0001t0001g0045 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-21-446T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 2/17 | chr7 | 87348602 | ||||||
chr7:87348698
|
T | A | 1 | a0001c0001t0001g0056 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-21-350T>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 2/17 | chr7 | 87348698 | ||||||
chr7:87348928
|
A | G | 1 | a0001c0001t0001g0204 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-21-120A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 2/17 | chr7 | 87348928 | ||||||
chr7:87348931
|
A | G | 1 | a0001c0001t0009g0203 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-21-117A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 2/17 | chr7 | 87348931 | ||||||
chr7:87348945
|
C | T | 1 | a0001c0001t0003g0039 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-21-103C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 2/17 | chr7 | 87348945 | ||||||
chr7:87349031
|
C | A | 157 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(154): Show | 208 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(205): Show |
intron_variant | MODIFIER | c.-21-17C>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 2/17 | chr7 | 87349031 | ||||||
chr7:87349238
|
T | C | 12 | a0001c0001t0003g0006a0001c0001t0003g0009a0001c0001t0003g0030others(9): Show | 17 | HG01243.hp1 HG02055.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.115+55T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87349238 | ||||||
chr7:87349319
|
C | T | 1 | a0001c0001t0009g0203 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.115+136C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87349319 | ||||||
chr7:87349413
|
T | G | 12 | a0001c0001t0003g0006a0001c0001t0003g0009a0001c0001t0003g0030others(9): Show | 17 | HG01243.hp1 HG02055.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.115+230T>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87349413 | ||||||
chr7:87349462
|
C | T | 12 | a0001c0001t0003g0006a0001c0001t0003g0009a0001c0001t0003g0030others(9): Show | 17 | HG01243.hp1 HG02055.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.115+279C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87349462 | ||||||
chr7:87349523
|
A | G | 12 | a0001c0001t0003g0006a0001c0001t0003g0009a0001c0001t0003g0030others(9): Show | 17 | HG01243.hp1 HG02055.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.115+340A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87349523 | ||||||
chr7:87349526
|
C | A | 1 | a0001c0001t0001g0062 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.115+343C>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87349526 | ||||||
chr7:87349545
|
G | GAATACAT others(2): Show |
3 | a0001c0001t0005g0200a0001c0001t0005g0201a0001c0001t0005g0202 | 3 | HG02040.hp1 NA19011.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.115+365_115+373dup others(9): Show |
CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 87349545 | |||||
chr7:87349613
|
C | A | 8 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0063others(5): Show | 10 | HG01884.hp1 HG02145.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.115+430C>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87349613 | ||||||
chr7:87349618
|
T | C | 12 | a0001c0001t0003g0006a0001c0001t0003g0009a0001c0001t0003g0030others(9): Show | 17 | HG01243.hp1 HG02055.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.115+435T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87349618 | ||||||
chr7:87349639
|
T | C | 1 | a0001c0001t0001g0151 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.115+456T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87349639 | ||||||
chr7:87349773
|
T | C | 2 | a0001c0001t0001g0020a0001c0001t0001g0069 | 3 | NA18948.hp2 NA18974.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.115+590T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87349773 | ||||||
chr7:87349796
|
T | C | 6 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(3): Show | 7 | HG02109.hp1 HG02145.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.115+613T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87349796 | ||||||
chr7:87350007
|
A | G | 1 | a0001c0001t0001g0045 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.115+824A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87350007 | ||||||
chr7:87350026
|
A | G | 12 | a0001c0001t0003g0006a0001c0001t0003g0009a0001c0001t0003g0030others(9): Show | 17 | HG01243.hp1 HG02055.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.115+843A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87350026 | ||||||
chr7:87350146
|
G | C | 1 | a0001c0001t0001g0017 | 2 | HG01175.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.115+963G>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87350146 | ||||||
chr7:87350148
|
T | C | 1 | a0001c0001t0001g0045 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.115+965T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87350148 | ||||||
chr7:87350203
|
A | G | 115 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(112): Show | 151 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(148): Show |
intron_variant | MODIFIER | c.115+1020A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87350203 | ||||||
chr7:87350388
|
G | A | 1 | a0001c0001t0001g0152 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.115+1205G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87350388 | ||||||
chr7:87350544
|
G | A | 11 | a0001c0001t0003g0006a0001c0001t0003g0009a0001c0001t0003g0030others(8): Show | 16 | HG01243.hp1 HG02055.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.115+1361G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87350544 | ||||||
chr7:87350736
|
G | C | 1 | a0001c0001t0009g0203 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.115+1553G>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87350736 | ||||||
chr7:87350881
|
C | T | 4 | a0001c0001t0003g0031a0001c0001t0003g0032a0001c0001t0003g0033others(1): Show | 4 | HG02055.hp2 HG02647.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.115+1698C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87350881 | ||||||
chr7:87350935
|
T | A | 2 | a0001c0001t0004g0011a0001c0001t0004g0077 | 4 | HG02080.hp2 NA18942.hp2 NA18984.hp2 others(1): Show |
intron_variant | MODIFIER | c.115+1752T>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87350935 | ||||||
chr7:87350992
|
T | C | 1 | a0001c0001t0001g0012 | 3 | NA18963.hp1 NA18974.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.115+1809T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87350992 | ||||||
chr7:87351022
|
A | AG | 18 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(15): Show | 24 | HG01243.hp1 HG02055.hp2 HG02109.hp1 others(21): Show |
intron_variant | MODIFIER | c.115+1839_115+1840i others(3): Show |
CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87351022 | ||||||
chr7:87351034
|
T | C | 3 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0007g0015 | 4 | HG02109.hp1 HG02615.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.115+1851T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87351034 | ||||||
chr7:87351080
|
A | G | 3 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0007g0015 | 4 | HG02109.hp1 HG02615.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.115+1897A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87351080 | ||||||
chr7:87351113
|
C | A | 1 | a0001c0001t0001g0153 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.115+1930C>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87351113 | ||||||
chr7:87351136
|
G | A | 1 | a0001c0001t0001g0045 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.115+1953G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87351136 | ||||||
chr7:87351183
|
C | A | 3 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0007g0015 | 4 | HG02109.hp1 HG02615.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.115+2000C>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87351183 | ||||||
chr7:87351186
|
G | T | 3 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0007g0015 | 4 | HG02109.hp1 HG02615.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.115+2003G>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87351186 | ||||||
chr7:87351308
|
CA | C | 111 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(108): Show | 148 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(145): Show |
intron_variant | MODIFIER | c.115+2149delA | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 87351308 | |||||
chr7:87351308
|
CAA | C | 25 | a0001c0001t0001g0010a0001c0001t0001g0018a0001c0001t0001g0019others(22): Show | 36 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(33): Show |
intron_variant | MODIFIER | c.115+2148_115+2149d others(4): Show |
CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 87351308 | |||||
chr7:87351324
|
A | G | 3 | a0001c0001t0001g0197a0001c0001t0001g0198a0001c0001t0001g0199 | 3 | HG00741.hp1 HG01109.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.115+2141A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87351324 | ||||||
chr7:87351327
|
A | G | 2 | a0001c0001t0001g0149a0001c0001t0001g0150 | 2 | NA18962.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.115+2144A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87351327 | ||||||
chr7:87351339
|
G | A | 3 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0007g0015 | 4 | HG02109.hp1 HG02615.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.115+2156G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87351339 | ||||||
chr7:87351513
|
A | ATTAGCTC others(336): Show |
1 | a0001c0001t0001g0042 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.115+2344_115+2345i others(345): Show |
CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 87351513 | |||||
chr7:87351513
|
A | ATTAGCTC others(337): Show |
1 | a0001c0001t0001g0043 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.115+2344_115+2345i others(346): Show |
CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 87351513 | |||||
chr7:87351513
|
A | ATTAGCTC others(341): Show |
1 | a0001c0001t0007g0015 | 2 | HG02109.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.115+2344_115+2345i others(350): Show |
CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 87351513 | |||||
chr7:87351699
|
G | A | 3 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0007g0015 | 4 | HG02109.hp1 HG02615.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.115+2516G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87351699 | ||||||
chr7:87351940
|
A | G | 3 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0007g0015 | 4 | HG02109.hp1 HG02615.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.115+2757A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87351940 | ||||||
chr7:87352092
|
T | C | 1 | a0001c0001t0003g0039 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.115+2909T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87352092 | ||||||
chr7:87352207
|
T | G | 115 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(112): Show | 151 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(148): Show |
intron_variant | MODIFIER | c.115+3024T>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87352207 | ||||||
chr7:87352485
|
G | C | 157 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(154): Show | 208 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(205): Show |
intron_variant | MODIFIER | c.115+3302G>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87352485 | ||||||
chr7:87352487
|
C | T | 3 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0007g0015 | 4 | HG02109.hp1 HG02615.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.115+3304C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87352487 | ||||||
chr7:87352488
|
G | A | 1 | a0001c0001t0001g0197 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.115+3305G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87352488 | ||||||
chr7:87352684
|
A | G | 3 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0007g0015 | 4 | HG02109.hp1 HG02615.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.115+3501A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87352684 | ||||||
chr7:87352708
|
A | G | 3 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0007g0015 | 4 | HG02109.hp1 HG02615.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.115+3525A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87352708 | ||||||
chr7:87352753
|
C | A | 3 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0007g0015 | 4 | HG02109.hp1 HG02615.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.115+3570C>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87352753 | ||||||
chr7:87352799
|
C | T | 3 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0007g0015 | 4 | HG02109.hp1 HG02615.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.115+3616C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87352799 | ||||||
chr7:87352875
|
A | G | 15 | a0001c0001t0001g0010a0001c0001t0001g0046a0001c0001t0001g0052others(12): Show | 23 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(20): Show |
intron_variant | MODIFIER | c.115+3692A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87352875 | ||||||
chr7:87353007
|
A | T | 2 | a0001c0001t0001g0192a0001c0001t0001g0193 | 2 | HG02572.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.115+3824A>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87353007 | ||||||
chr7:87353117
|
G | C | 15 | a0001c0001t0001g0010a0001c0001t0001g0046a0001c0001t0001g0052others(12): Show | 23 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(20): Show |
intron_variant | MODIFIER | c.115+3934G>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87353117 | ||||||
chr7:87353133
|
G | A | 1 | a0001c0001t0001g0154 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.115+3950G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87353133 | ||||||
chr7:87353149
|
A | C | 2 | a0001c0001t0001g0143a0001c0001t0001g0144 | 2 | HG01167.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.115+3966A>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87353149 | ||||||
chr7:87353155
|
C | A | 157 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(154): Show | 208 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(205): Show |
intron_variant | MODIFIER | c.115+3972C>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87353155 | ||||||
chr7:87353172
|
T | A | 1 | a0001c0001t0001g0214 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.115+3989T>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87353172 | ||||||
chr7:87353173
|
G | A | 2 | a0001c0001t0001g0086a0001c0001t0001g0087 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.115+3990G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87353173 | ||||||
chr7:87353348
|
C | T | 1 | a0001c0001t0001g0055 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.115+4165C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87353348 | ||||||
chr7:87353391
|
C | T | 1 | a0008c0006t0001g0085 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.115+4208C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87353391 | ||||||
chr7:87353406
|
C | T | 3 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0007g0015 | 4 | HG02109.hp1 HG02615.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.115+4223C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87353406 | ||||||
chr7:87353541
|
G | A | 157 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(154): Show | 208 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(205): Show |
intron_variant | MODIFIER | c.115+4358G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87353541 | ||||||
chr7:87353549
|
A | G | 6 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0001g0209others(3): Show | 8 | HG01496.hp1 HG02109.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.115+4366A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87353549 | ||||||
chr7:87353621
|
G | T | 157 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(154): Show | 208 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(205): Show |
intron_variant | MODIFIER | c.115+4438G>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87353621 | ||||||
chr7:87353768
|
G | GA | 3 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0007g0015 | 4 | HG02109.hp1 HG02615.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.115+4587dupA | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 87353768 | |||||
chr7:87353790
|
G | A | 1 | a0001c0001t0009g0203 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.115+4607G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87353790 | ||||||
chr7:87353800
|
G | A | 3 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0007g0015 | 4 | HG02109.hp1 HG02615.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.115+4617G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87353800 | ||||||
chr7:87353949
|
G | A | 3 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0007g0015 | 4 | HG02109.hp1 HG02615.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.115+4766G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87353949 | ||||||
chr7:87354012
|
C | T | 3 | a0001c0001t0001g0017a0001c0001t0001g0056a0001c0001t0001g0061 | 4 | HG00323.hp2 HG01175.hp1 HG01255.hp2 others(1): Show |
intron_variant | MODIFIER | c.115+4829C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87354012 | ||||||
chr7:87354232
|
G | T | 1 | a0001c0001t0001g0052 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.116-4974G>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87354232 | ||||||
chr7:87354250
|
T | C | 3 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0007g0015 | 4 | HG02109.hp1 HG02615.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.116-4956T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87354250 | ||||||
chr7:87354258
|
G | C | 3 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0007g0015 | 4 | HG02109.hp1 HG02615.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.116-4948G>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87354258 | ||||||
chr7:87354336
|
G | C | 3 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0007g0015 | 4 | HG02109.hp1 HG02615.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.116-4870G>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87354336 | ||||||
chr7:87354399
|
A | G | 131 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(128): Show | 175 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.116-4807A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87354399 | ||||||
chr7:87354434
|
T | G | 3 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0007g0015 | 4 | HG02109.hp1 HG02615.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.116-4772T>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87354434 | ||||||
chr7:87354703
|
C | T | 3 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0007g0015 | 4 | HG02109.hp1 HG02615.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.116-4503C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87354703 | ||||||
chr7:87354767
|
A | T | 2 | a0001c0001t0001g0191a0001c0001t0001g0196 | 2 | NA18942.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.116-4439A>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87354767 | ||||||
chr7:87354769
|
T | A | 1 | a0001c0001t0001g0088 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.116-4437T>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87354769 | ||||||
chr7:87354951
|
T | C | 3 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0007g0015 | 4 | HG02109.hp1 HG02615.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.116-4255T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87354951 | ||||||
chr7:87354952
|
C | G | 10 | a0001c0001t0001g0186a0001c0001t0001g0187a0001c0001t0001g0188others(7): Show | 11 | HG00423.hp2 HG02040.hp1 NA18747.hp2 others(8): Show |
intron_variant | MODIFIER | c.116-4254C>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87354952 | ||||||
chr7:87355103
|
AT | A | 137 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(134): Show | 179 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.116-4089delT | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 87355103 | |||||
chr7:87355130
|
C | T | 1 | a0002c0002t0002g0185 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.116-4076C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87355130 | ||||||
chr7:87355214
|
C | T | 3 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0007g0015 | 4 | HG02109.hp1 HG02615.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.116-3992C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87355214 | ||||||
chr7:87355349
|
C | T | 109 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(106): Show | 143 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.116-3857C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87355349 | ||||||
chr7:87355559
|
T | C | 1 | a0001c0001t0010g0035 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.116-3647T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87355559 | ||||||
chr7:87355576
|
C | G | 2 | a0001c0001t0001g0042a0001c0001t0001g0043 | 2 | HG02615.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.116-3630C>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87355576 | ||||||
chr7:87355723
|
GA | G | 3 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0007g0015 | 4 | HG02109.hp1 HG02615.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.116-3482delA | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87355723 | ||||||
chr7:87355806
|
C | T | 3 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0007g0015 | 4 | HG02109.hp1 HG02615.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.116-3400C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87355806 | ||||||
chr7:87355816
|
G | GAGTATAT others(5): Show |
1 | a0002c0002t0002g0071 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.116-3378_116-3367d others(14): Show |
CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 87355816 | |||||
chr7:87355827
|
A | G | 3 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0007g0015 | 4 | HG02109.hp1 HG02615.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.116-3379A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87355827 | ||||||
chr7:87355850
|
G | A | 3 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0007g0015 | 4 | HG02109.hp1 HG02615.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.116-3356G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87355850 | ||||||
chr7:87355866
|
T | A | 3 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0007g0015 | 4 | HG02109.hp1 HG02615.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.116-3340T>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87355866 | ||||||
chr7:87355912
|
T | G | 1 | a0001c0001t0007g0015 | 2 | HG02109.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.116-3294T>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87355912 | ||||||
chr7:87355977
|
AATTTT | A | 3 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0007g0015 | 4 | HG02109.hp1 HG02615.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.116-3213_116-3209d others(7): Show |
CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 87355977 | |||||
chr7:87356115
|
A | G | 3 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0007g0015 | 4 | HG02109.hp1 HG02615.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.116-3091A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87356115 | ||||||
chr7:87356121
|
C | T | 2 | a0001c0001t0001g0029a0001c0001t0001g0184 | 3 | HG00099.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.116-3085C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87356121 | ||||||
chr7:87356252
|
T | C | 157 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(154): Show | 208 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(205): Show |
intron_variant | MODIFIER | c.116-2954T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87356252 | ||||||
chr7:87356257
|
T | C | 3 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0007g0015 | 4 | HG02109.hp1 HG02615.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.116-2949T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87356257 | ||||||
chr7:87356403
|
C | T | 5 | a0001c0001t0001g0017a0001c0001t0001g0056a0001c0001t0001g0059others(2): Show | 6 | HG00323.hp2 HG00639.hp1 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.116-2803C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87356403 | ||||||
chr7:87356828
|
C | T | 4 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0136others(1): Show | 4 | HG01978.hp2 HG02148.hp2 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.116-2378C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87356828 | ||||||
chr7:87357000
|
T | C | 34 | a0001c0001t0001g0010a0001c0001t0001g0040a0001c0001t0001g0041others(31): Show | 48 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(45): Show |
intron_variant | MODIFIER | c.116-2206T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87357000 | ||||||
chr7:87357060
|
G | C | 2 | a0001c0001t0001g0156a0001c0001t0001g0157 | 2 | NA18990.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.116-2146G>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87357060 | ||||||
chr7:87357105
|
G | A | 3 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0007g0015 | 4 | HG02109.hp1 HG02615.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.116-2101G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87357105 | ||||||
chr7:87357182
|
T | G | 4 | a0001c0001t0001g0025a0001c0001t0001g0154a0001c0001t0001g0158others(1): Show | 5 | HG02055.hp1 HG02451.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.116-2024T>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87357182 | ||||||
chr7:87357207
|
G | A | 3 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0007g0015 | 4 | HG02109.hp1 HG02615.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.116-1999G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87357207 | ||||||
chr7:87357316
|
C | T | 7 | a0001c0001t0001g0017a0001c0001t0001g0056a0001c0001t0001g0059others(4): Show | 8 | HG00323.hp2 HG00639.hp1 HG01175.hp1 others(5): Show |
intron_variant | MODIFIER | c.116-1890C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87357316 | ||||||
chr7:87357380
|
C | A | 1 | a0001c0001t0001g0089 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.116-1826C>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87357380 | ||||||
chr7:87357547
|
T | C | 4 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0003g0039others(1): Show | 5 | HG02109.hp1 HG02615.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.116-1659T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87357547 | ||||||
chr7:87357655
|
G | A | 3 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0160 | 3 | HG02615.hp1 HG02976.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.116-1551G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87357655 | ||||||
chr7:87357680
|
G | C | 1 | a0001c0001t0001g0161 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.116-1526G>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87357680 | ||||||
chr7:87357746
|
C | T | 3 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0007g0015 | 4 | HG02109.hp1 HG02615.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.116-1460C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87357746 | ||||||
chr7:87357828
|
T | A | 1 | a0001c0001t0001g0143 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.116-1378T>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87357828 | ||||||
chr7:87357881
|
G | C | 3 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0007g0015 | 4 | HG02109.hp1 HG02615.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.116-1325G>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87357881 | ||||||
chr7:87357936
|
G | A | 3 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0007g0015 | 4 | HG02109.hp1 HG02615.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.116-1270G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87357936 | ||||||
chr7:87357939
|
G | C | 1 | a0001c0001t0001g0090 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.116-1267G>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87357939 | ||||||
chr7:87357940
|
G | T | 4 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0136others(1): Show | 4 | HG01978.hp2 HG02148.hp2 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.116-1266G>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87357940 | ||||||
chr7:87358072
|
C | A | 3 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0007g0015 | 4 | HG02109.hp1 HG02615.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.116-1134C>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87358072 | ||||||
chr7:87358203
|
C | T | 1 | a0001c0001t0001g0150 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.116-1003C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87358203 | ||||||
chr7:87358242
|
C | T | 4 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0045others(1): Show | 5 | HG02109.hp1 HG02615.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.116-964C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87358242 | ||||||
chr7:87358252
|
T | C | 3 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0007g0015 | 4 | HG02109.hp1 HG02615.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.116-954T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87358252 | ||||||
chr7:87358339
|
A | G | 187 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(184): Show | 241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.116-867A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87358339 | ||||||
chr7:87358438
|
C | T | 5 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0007g0015others(2): Show | 6 | HG02109.hp1 HG02615.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.116-768C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87358438 | ||||||
chr7:87358446
|
C | A | 5 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0007g0015others(2): Show | 6 | HG02109.hp1 HG02615.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.116-760C>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87358446 | ||||||
chr7:87358481
|
C | CA | 145 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(142): Show | 184 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(181): Show |
intron_variant | MODIFIER | c.116-706dupA | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 87358481 | |||||
chr7:87358481
|
C | CAA | 6 | a0001c0001t0001g0091a0001c0001t0001g0197a0001c0001t0003g0006others(3): Show | 9 | HG01243.hp1 HG01934.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.116-707_116-706dup others(2): Show |
CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 87358481 | |||||
chr7:87358481
|
CAAA | C | 5 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0007g0015others(2): Show | 6 | HG02109.hp1 HG02615.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.116-708_116-706del others(3): Show |
CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 87358481 | |||||
chr7:87358551
|
A | C | 1 | a0001c0001t0001g0157 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.116-655A>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87358551 | ||||||
chr7:87358552
|
A | T | 5 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0007g0015others(2): Show | 6 | HG02109.hp1 HG02615.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.116-654A>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87358552 | ||||||
chr7:87358630
|
GA | G | 7 | a0001c0001t0001g0054a0001c0001t0001g0207a0001c0001t0001g0208others(4): Show | 9 | HG01496.hp1 HG02109.hp2 HG02148.hp2 others(6): Show |
intron_variant | MODIFIER | c.116-571delA | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 87358630 | |||||
chr7:87358702
|
T | C | 2 | a0001c0001t0001g0193a0001c0001t0003g0039 | 2 | HG02572.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.116-504T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87358702 | ||||||
chr7:87358848
|
G | A | 4 | a0001c0001t0001g0042a0001c0001t0001g0043a0002c0002t0001g0057others(1): Show | 4 | HG02615.hp1 HG02976.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.116-358G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87358848 | ||||||
chr7:87358887
|
T | G | 5 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0007g0015others(2): Show | 6 | HG02109.hp1 HG02615.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.116-319T>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87358887 | ||||||
chr7:87358928
|
G | A | 5 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0007g0015others(2): Show | 6 | HG02109.hp1 HG02615.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.116-278G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87358928 | ||||||
chr7:87359040
|
C | T | 14 | a0001c0001t0001g0025a0001c0001t0001g0042a0001c0001t0001g0043others(11): Show | 16 | HG02055.hp1 HG02055.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.116-166C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87359040 | ||||||
chr7:87359051
|
T | C | 5 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0007g0015others(2): Show | 6 | HG02109.hp1 HG02615.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.116-155T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87359051 | ||||||
chr7:87359177
|
A | G | 1 | a0001c0001t0001g0130 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.116-29A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 3/17 | chr7 | 87359177 | ||||||
chr7:87359347
|
T | C | 1 | a0001c0001t0001g0149 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.240+17T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 4/17 | chr7 | 87359347 | ||||||
chr7:87359354
|
A | AT | 5 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0007g0015others(2): Show | 6 | HG02109.hp1 HG02615.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.240+25dupT | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr7 | 87359354 | |||||
chr7:87359723
|
G | A | 33 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0045others(30): Show | 44 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(41): Show |
intron_variant | MODIFIER | c.240+393G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 4/17 | chr7 | 87359723 | ||||||
chr7:87359731
|
A | G | 2 | a0001c0001t0001g0089a0001c0001t0001g0129 | 2 | HG00741.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.240+401A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 4/17 | chr7 | 87359731 | ||||||
chr7:87359847
|
C | T | 4 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0094others(1): Show | 4 | HG02896.hp2 HG02897.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.240+517C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 4/17 | chr7 | 87359847 | ||||||
chr7:87360039
|
A | T | 1 | a0001c0001t0001g0056 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.240+709A>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 4/17 | chr7 | 87360039 | ||||||
chr7:87360159
|
G | A | 2 | a0001c0001t0001g0042a0001c0001t0001g0043 | 2 | HG02615.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.240+829G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 4/17 | chr7 | 87360159 | ||||||
chr7:87360334
|
A | G | 10 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0016others(7): Show | 24 | HG00408.hp2 HG01358.hp1 HG01496.hp2 others(21): Show |
intron_variant | MODIFIER | c.240+1004A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 4/17 | chr7 | 87360334 | ||||||
chr7:87360378
|
T | C | 5 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0007g0015others(2): Show | 6 | HG02109.hp1 HG02615.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.241-1012T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 4/17 | chr7 | 87360378 | ||||||
chr7:87360616
|
C | T | 2 | a0001c0001t0001g0059a0001c0001t0001g0060 | 2 | HG00639.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.241-774C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 4/17 | chr7 | 87360616 | ||||||
chr7:87360720
|
T | C | 2 | a0001c0001t0001g0096a0001c0001t0001g0097 | 2 | HG02965.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.241-670T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 4/17 | chr7 | 87360720 | ||||||
chr7:87360894
|
T | C | 5 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0007g0015others(2): Show | 6 | HG02109.hp1 HG02615.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.241-496T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 4/17 | chr7 | 87360894 | ||||||
chr7:87361073
|
G | A | 5 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0007g0015others(2): Show | 6 | HG02109.hp1 HG02615.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.241-317G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 4/17 | chr7 | 87361073 | ||||||
chr7:87361146
|
A | G | 1 | a0001c0001t0001g0027 | 2 | HG02155.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.241-244A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 4/17 | chr7 | 87361146 | ||||||
chr7:87361179
|
C | A | 5 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0100others(2): Show | 5 | HG01109.hp1 HG01167.hp1 HG01175.hp2 others(2): Show |
intron_variant | MODIFIER | c.241-211C>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 4/17 | chr7 | 87361179 | ||||||
chr7:87361201
|
G | C | 5 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0007g0015others(2): Show | 6 | HG02109.hp1 HG02615.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.241-189G>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 4/17 | chr7 | 87361201 | ||||||
chr7:87361718
|
T | C | 5 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0007g0015others(2): Show | 6 | HG02109.hp1 HG02615.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.423-10T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 5/17 | chr7 | 87361718 | ||||||
chr7:87362026
|
G | A | 5 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0007g0015others(2): Show | 6 | HG02109.hp1 HG02615.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.547+174G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | chr7 | 87362026 | ||||||
chr7:87362209
|
A | G | 1 | a0001c0001t0001g0148 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.547+357A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | chr7 | 87362209 | ||||||
chr7:87362280
|
G | A | 5 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0007g0015others(2): Show | 6 | HG02109.hp1 HG02615.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.547+428G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | chr7 | 87362280 | ||||||
chr7:87362304
|
C | CT | 6 | a0001c0001t0001g0084a0001c0001t0001g0100a0001c0001t0001g0126others(3): Show | 7 | HG01175.hp2 HG02109.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.547+471dupT | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr7 | 87362304 | |||||
chr7:87362304
|
CT | C | 26 | a0001c0001t0001g0017a0001c0001t0001g0040a0001c0001t0001g0041others(23): Show | 33 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(30): Show |
intron_variant | MODIFIER | c.547+471delT | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr7 | 87362304 | |||||
chr7:87362304
|
CTT | C | 2 | a0001c0001t0001g0005a0001c0001t0001g0161 | 6 | HG00280.hp1 HG01070.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.547+470_547+471del others(2): Show |
CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr7 | 87362304 | |||||
chr7:87362304
|
CTTTT | C | 6 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0001g0209others(3): Show | 8 | HG01496.hp1 HG02109.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.547+468_547+471del others(4): Show |
CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr7 | 87362304 | |||||
chr7:87362324
|
G | T | 1 | a0001c0001t0001g0043 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.547+472G>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | chr7 | 87362324 | ||||||
chr7:87362359
|
C | T | 37 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0040others(34): Show | 48 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(45): Show |
intron_variant | MODIFIER | c.547+507C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | chr7 | 87362359 | ||||||
chr7:87362362
|
C | T | 5 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0007g0015others(2): Show | 6 | HG02109.hp1 HG02615.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.547+510C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | chr7 | 87362362 | ||||||
chr7:87362404
|
T | C | 42 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0040others(39): Show | 54 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(51): Show |
intron_variant | MODIFIER | c.547+552T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | chr7 | 87362404 | ||||||
chr7:87362408
|
T | C | 4 | a0001c0001t0001g0138a0001c0001t0004g0011a0001c0001t0004g0077others(1): Show | 6 | HG02080.hp2 NA18942.hp2 NA18966.hp2 others(3): Show |
intron_variant | MODIFIER | c.547+556T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | chr7 | 87362408 | ||||||
chr7:87362429
|
T | C | 2 | a0001c0001t0001g0102a0001c0001t0001g0194 | 2 | HG00140.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.547+577T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | chr7 | 87362429 | ||||||
chr7:87362542
|
C | T | 5 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0007g0015others(2): Show | 6 | HG02109.hp1 HG02615.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.547+690C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | chr7 | 87362542 | ||||||
chr7:87362579
|
G | A | 3 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0044 | 3 | HG02145.hp2 HG02630.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.547+727G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | chr7 | 87362579 | ||||||
chr7:87362631
|
T | C | 1 | a0001c0001t0001g0103 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.547+779T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | chr7 | 87362631 | ||||||
chr7:87362642
|
AT | A | 6 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0003g0030others(3): Show | 7 | HG02109.hp1 HG02615.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.547+801delT | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr7 | 87362642 | |||||
chr7:87362729
|
GT | G | 5 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0084others(2): Show | 5 | HG02735.hp2 HG03491.hp1 HG04199.hp2 others(2): Show |
intron_variant | MODIFIER | c.547+884delT | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr7 | 87362729 | |||||
chr7:87363009
|
C | A | 1 | a0001c0001t0004g0101 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.547+1157C>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | chr7 | 87363009 | ||||||
chr7:87363131
|
C | T | 1 | a0001c0001t0001g0183 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.547+1279C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | chr7 | 87363131 | ||||||
chr7:87363369
|
A | T | 5 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0007g0015others(2): Show | 6 | HG02109.hp1 HG02615.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.547+1517A>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | chr7 | 87363369 | ||||||
chr7:87363489
|
T | G | 5 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0007g0015others(2): Show | 6 | HG02109.hp1 HG02615.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.547+1637T>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | chr7 | 87363489 | ||||||
chr7:87363654
|
G | A | 5 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0007g0015others(2): Show | 6 | HG02109.hp1 HG02615.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.547+1802G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | chr7 | 87363654 | ||||||
chr7:87363855
|
T | G | 1 | a0001c0001t0001g0139 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.547+2003T>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | chr7 | 87363855 | ||||||
chr7:87364127
|
A | G | 5 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0007g0015others(2): Show | 6 | HG02109.hp1 HG02615.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.547+2275A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | chr7 | 87364127 | ||||||
chr7:87364221
|
C | T | 5 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0007g0015others(2): Show | 6 | HG02109.hp1 HG02615.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.547+2369C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | chr7 | 87364221 | ||||||
chr7:87364235
|
C | G | 42 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0040others(39): Show | 54 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(51): Show |
intron_variant | MODIFIER | c.547+2383C>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | chr7 | 87364235 | ||||||
chr7:87364487
|
C | A | 1 | a0001c0001t0001g0105 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.547+2635C>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | chr7 | 87364487 | ||||||
chr7:87364578
|
G | A | 1 | a0001c0001t0001g0150 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.547+2726G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | chr7 | 87364578 | ||||||
chr7:87364599
|
G | A | 1 | a0001c0001t0001g0172 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.547+2747G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | chr7 | 87364599 | ||||||
chr7:87365070
|
A | G | 1 | a0001c0001t0001g0017 | 2 | HG01175.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.547+3218A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | chr7 | 87365070 | ||||||
chr7:87365147
|
T | G | 2 | a0002c0002t0001g0057a0002c0002t0001g0058 | 2 | HG03195.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.547+3295T>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | chr7 | 87365147 | ||||||
chr7:87365191
|
T | C | 5 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0007g0015others(2): Show | 6 | HG02109.hp1 HG02615.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.547+3339T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | chr7 | 87365191 | ||||||
chr7:87365214
|
C | G | 5 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0007g0015others(2): Show | 6 | HG02109.hp1 HG02615.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.547+3362C>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | chr7 | 87365214 | ||||||
chr7:87365232
|
T | G | 1 | a0001c0001t0001g0103 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.547+3380T>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | chr7 | 87365232 | ||||||
chr7:87365243
|
C | T | 1 | a0001c0001t0001g0182 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.547+3391C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | chr7 | 87365243 | ||||||
chr7:87365292
|
C | T | 5 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0007g0015others(2): Show | 6 | HG02109.hp1 HG02615.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.547+3440C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | chr7 | 87365292 | ||||||
chr7:87365381
|
G | A | 1 | a0001c0001t0009g0203 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.547+3529G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | chr7 | 87365381 | ||||||
chr7:87365444
|
C | T | 1 | a0001c0001t0010g0035 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.547+3592C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | chr7 | 87365444 | ||||||
chr7:87365459
|
C | T | 34 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0017others(31): Show | 48 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(45): Show |
intron_variant | MODIFIER | c.547+3607C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | chr7 | 87365459 | ||||||
chr7:87365489
|
C | CA | 35 | a0001c0001t0001g0004a0001c0001t0001g0017a0001c0001t0001g0042others(32): Show | 47 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(44): Show |
intron_variant | MODIFIER | c.547+3650dupA | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr7 | 87365489 | |||||
chr7:87365612
|
TTTTG | T | 22 | a0001c0001t0001g0025a0001c0001t0001g0154a0001c0001t0001g0158others(19): Show | 30 | HG01243.hp1 HG01496.hp1 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.548-3758_548-3755d others(6): Show |
CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr7 | 87365612 | |||||
chr7:87365618
|
T | C | 1 | a0001c0001t0001g0193 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.548-3758T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | chr7 | 87365618 | ||||||
chr7:87365622
|
C | CT | 6 | a0001c0001t0001g0041a0001c0001t0001g0053a0001c0001t0001g0067others(3): Show | 6 | HG01934.hp1 HG02145.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.548-3738dupT | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr7 | 87365622 | |||||
chr7:87365622
|
C | CTT | 5 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0007g0015others(2): Show | 6 | HG02109.hp1 HG02615.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.548-3739_548-3738d others(4): Show |
CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr7 | 87365622 | |||||
chr7:87365664
|
G | A | 1 | a0001c0001t0001g0063 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.548-3712G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | chr7 | 87365664 | ||||||
chr7:87365709
|
A | G | 5 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0007g0015others(2): Show | 6 | HG02109.hp1 HG02615.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.548-3667A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | chr7 | 87365709 | ||||||
chr7:87365710
|
C | T | 36 | a0001c0001t0001g0007a0001c0001t0001g0024a0001c0001t0001g0026others(33): Show | 43 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(40): Show |
intron_variant | MODIFIER | c.548-3666C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | chr7 | 87365710 | ||||||
chr7:87365797
|
A | G | 7 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0192others(4): Show | 8 | HG02109.hp1 HG02572.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.548-3579A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | chr7 | 87365797 | ||||||
chr7:87365812
|
C | T | 1 | a0001c0001t0001g0097 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.548-3564C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | chr7 | 87365812 | ||||||
chr7:87365854
|
C | T | 2 | a0001c0001t0001g0042a0001c0001t0001g0043 | 2 | HG02615.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.548-3522C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | chr7 | 87365854 | ||||||
chr7:87365883
|
G | A | 1 | a0001c0001t0001g0064 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.548-3493G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | chr7 | 87365883 | ||||||
chr7:87366097
|
C | T | 1 | a0001c0001t0003g0030 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.548-3279C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | chr7 | 87366097 | ||||||
chr7:87366242
|
A | AT | 14 | a0001c0001t0001g0025a0001c0001t0001g0059a0001c0001t0001g0060others(11): Show | 19 | HG00639.hp1 HG01243.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.548-3124dupT | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr7 | 87366242 | |||||
chr7:87366331
|
G | T | 22 | a0001c0001t0001g0004a0001c0001t0001g0040a0001c0001t0001g0041others(19): Show | 27 | HG00639.hp1 HG01884.hp2 HG02109.hp1 others(24): Show |
intron_variant | MODIFIER | c.548-3045G>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | chr7 | 87366331 | ||||||
chr7:87366606
|
T | C | 33 | a0001c0001t0001g0025a0001c0001t0001g0040a0001c0001t0001g0041others(30): Show | 45 | HG00140.hp2 HG00323.hp1 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.548-2770T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | chr7 | 87366606 | ||||||
chr7:87366635
|
C | G | 33 | a0001c0001t0001g0025a0001c0001t0001g0040a0001c0001t0001g0041others(30): Show | 45 | HG00140.hp2 HG00323.hp1 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.548-2741C>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | chr7 | 87366635 | ||||||
chr7:87366643
|
A | G | 1 | a0001c0001t0007g0015 | 2 | HG02109.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.548-2733A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | chr7 | 87366643 | ||||||
chr7:87366665
|
G | A | 1 | a0001c0001t0007g0015 | 2 | HG02109.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.548-2711G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | chr7 | 87366665 | ||||||
chr7:87366683
|
T | C | 130 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(127): Show | 153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): Show |
intron_variant | MODIFIER | c.548-2693T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | chr7 | 87366683 | ||||||
chr7:87366766
|
C | T | 11 | a0001c0001t0001g0004a0001c0001t0001g0045a0001c0001t0001g0086others(8): Show | 15 | HG02258.hp1 HG02559.hp1 HG02895.hp2 others(12): Show |
intron_variant | MODIFIER | c.548-2610C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | chr7 | 87366766 | ||||||
chr7:87366783
|
G | A | 4 | a0001c0001t0001g0192a0001c0001t0001g0193a0001c0001t0003g0039others(1): Show | 4 | HG02572.hp2 HG02723.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.548-2593G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | chr7 | 87366783 | ||||||
chr7:87366895
|
G | A | 30 | a0001c0001t0001g0025a0001c0001t0001g0040a0001c0001t0001g0041others(27): Show | 42 | HG00140.hp2 HG00323.hp1 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.548-2481G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | chr7 | 87366895 | ||||||
chr7:87367033
|
A | G | 1 | a0001c0001t0003g0039 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.548-2343A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | chr7 | 87367033 | ||||||
chr7:87367091
|
G | C | 2 | a0001c0001t0001g0059a0001c0001t0001g0060 | 2 | HG00639.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.548-2285G>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | chr7 | 87367091 | ||||||
chr7:87367107
|
T | G | 2 | a0001c0001t0001g0059a0001c0001t0001g0060 | 2 | HG00639.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.548-2269T>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | chr7 | 87367107 | ||||||
chr7:87367173
|
A | G | 185 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(182): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.548-2203A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | chr7 | 87367173 | ||||||
chr7:87367760
|
C | G | 1 | a0001c0001t0007g0015 | 2 | HG02109.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.548-1616C>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | chr7 | 87367760 | ||||||
chr7:87367847
|
T | C | 184 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(181): Show | 225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.548-1529T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | chr7 | 87367847 | ||||||
chr7:87367895
|
C | T | 3 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0044 | 3 | HG02145.hp2 HG02630.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.548-1481C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | chr7 | 87367895 | ||||||
chr7:87368092
|
G | A | 2 | a0001c0001t0003g0009a0001c0001t0003g0038 | 4 | HG02257.hp1 HG02451.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.548-1284G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | chr7 | 87368092 | ||||||
chr7:87368187
|
C | T | 1 | a0001c0001t0003g0038 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.548-1189C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | chr7 | 87368187 | ||||||
chr7:87368193
|
T | C | 2 | a0001c0001t0001g0106a0001c0001t0001g0150 | 2 | HG00597.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.548-1183T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | chr7 | 87368193 | ||||||
chr7:87368202
|
C | T | 1 | a0001c0001t0003g0037 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.548-1174C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | chr7 | 87368202 | ||||||
chr7:87368378
|
C | A | 133 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(130): Show | 156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.548-998C>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | chr7 | 87368378 | ||||||
chr7:87368400
|
G | A | 12 | a0001c0001t0001g0004a0001c0001t0001g0045a0001c0001t0001g0086others(9): Show | 16 | HG02258.hp1 HG02559.hp1 HG02717.hp1 others(13): Show |
intron_variant | MODIFIER | c.548-976G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | chr7 | 87368400 | ||||||
chr7:87368490
|
C | T | 1 | a0008c0006t0001g0085 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.548-886C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | chr7 | 87368490 | ||||||
chr7:87368927
|
T | A | 3 | a0001c0001t0001g0192a0001c0001t0001g0193a0001c0001t0010g0035 | 3 | HG02572.hp2 HG03041.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.548-449T>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | chr7 | 87368927 | ||||||
chr7:87369007
|
C | T | 1 | a0001c0001t0001g0052 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.548-369C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | chr7 | 87369007 | ||||||
chr7:87369019
|
C | T | 133 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(130): Show | 156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.548-357C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 6/17 | chr7 | 87369019 | ||||||
chr7:87369526
|
G | A | 124 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(121): Show | 146 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.656+42G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 7/17 | chr7 | 87369526 | ||||||
chr7:87369547
|
A | G | 12 | a0001c0001t0001g0004a0001c0001t0001g0045a0001c0001t0001g0086others(9): Show | 16 | HG02258.hp1 HG02559.hp1 HG02717.hp1 others(13): Show |
intron_variant | MODIFIER | c.656+63A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 7/17 | chr7 | 87369547 | ||||||
chr7:87369593
|
A | T | 1 | a0001c0001t0001g0124 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.656+109A>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 7/17 | chr7 | 87369593 | ||||||
chr7:87369612
|
A | T | 1 | a0001c0001t0001g0019 | 2 | HG02976.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.656+128A>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 7/17 | chr7 | 87369612 | ||||||
chr7:87369620
|
AT | A | 129 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(126): Show | 152 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(149): Show |
intron_variant | MODIFIER | c.656+137delT | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 7/17 | chr7 | 87369620 | ||||||
chr7:87369621
|
T | A | 1 | a0001c0001t0001g0100 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.656+137T>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 7/17 | chr7 | 87369621 | ||||||
chr7:87369828
|
T | C | 1 | a0001c0001t0001g0138 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.656+344T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 7/17 | chr7 | 87369828 | ||||||
chr7:87369874
|
C | T | 170 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(167): Show | 205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.656+390C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 7/17 | chr7 | 87369874 | ||||||
chr7:87370222
|
G | C | 3 | a0001c0001t0001g0078a0001c0001t0001g0084a0001c0001t0001g0104 | 3 | HG02735.hp2 HG03491.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.656+738G>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 7/17 | chr7 | 87370222 | ||||||
chr7:87370395
|
C | G | 1 | a0001c0001t0001g0130 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.656+911C>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 7/17 | chr7 | 87370395 | ||||||
chr7:87370398
|
G | A | 12 | a0002c0002t0002g0003a0002c0002t0002g0021a0002c0002t0002g0070others(9): Show | 18 | HG00140.hp2 HG00323.hp1 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.656+914G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 7/17 | chr7 | 87370398 | ||||||
chr7:87370528
|
A | C | 12 | a0002c0002t0002g0003a0002c0002t0002g0021a0002c0002t0002g0070others(9): Show | 18 | HG00140.hp2 HG00323.hp1 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.656+1044A>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 7/17 | chr7 | 87370528 | ||||||
chr7:87370549
|
T | C | 20 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0052others(17): Show | 28 | HG00140.hp2 HG00323.hp1 HG00735.hp1 others(25): Show |
intron_variant | MODIFIER | c.656+1065T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 7/17 | chr7 | 87370549 | ||||||
chr7:87370711
|
C | A | 2 | a0001c0001t0001g0059a0001c0001t0001g0060 | 2 | HG00639.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.656+1227C>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 7/17 | chr7 | 87370711 | ||||||
chr7:87371007
|
A | G | 3 | a0001c0001t0001g0192a0001c0001t0001g0193a0001c0001t0010g0035 | 3 | HG02572.hp2 HG03041.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.656+1523A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 7/17 | chr7 | 87371007 | ||||||
chr7:87371022
|
T | C | 3 | a0001c0001t0001g0192a0001c0001t0001g0193a0001c0001t0010g0035 | 3 | HG02572.hp2 HG03041.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.656+1538T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 7/17 | chr7 | 87371022 | ||||||
chr7:87371040
|
A | G | 12 | a0001c0001t0001g0025a0001c0001t0001g0154a0001c0001t0001g0158others(9): Show | 16 | HG01243.hp1 HG02055.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.656+1556A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 7/17 | chr7 | 87371040 | ||||||
chr7:87371509
|
T | G | 168 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(165): Show | 203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.656+2025T>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 7/17 | chr7 | 87371509 | ||||||
chr7:87371957
|
G | A | 1 | a0001c0001t0001g0107 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.656+2473G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 7/17 | chr7 | 87371957 | ||||||
chr7:87372006
|
A | C | 2 | a0001c0001t0003g0009a0001c0001t0003g0038 | 4 | HG02257.hp1 HG02451.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.656+2522A>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 7/17 | chr7 | 87372006 | ||||||
chr7:87372007
|
C | A | 10 | a0001c0001t0001g0067a0001c0001t0001g0098a0001c0001t0001g0099others(7): Show | 10 | HG01109.hp1 HG01123.hp2 HG01167.hp1 others(7): Show |
intron_variant | MODIFIER | c.656+2523C>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 7/17 | chr7 | 87372007 | ||||||
chr7:87372007
|
C | CA | 6 | a0001c0001t0001g0163a0001c0001t0001g0169a0001c0001t0001g0187others(3): Show | 8 | HG02257.hp1 HG02451.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.656+2536dupA | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr7 | 87372007 | |||||
chr7:87372007
|
CA | C | 93 | a0001c0001t0001g0002a0001c0001t0001g0017a0001c0001t0001g0018others(90): Show | 112 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.656+2536delA | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr7 | 87372007 | |||||
chr7:87372008
|
A | C | 9 | a0001c0001t0001g0067a0001c0001t0001g0099a0001c0001t0001g0100others(6): Show | 9 | HG01123.hp2 HG01167.hp1 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.656+2524A>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 7/17 | chr7 | 87372008 | ||||||
chr7:87372019
|
A | C | 2 | a0001c0001t0001g0059a0001c0001t0001g0060 | 2 | HG00639.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.656+2535A>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 7/17 | chr7 | 87372019 | ||||||
chr7:87372235
|
A | T | 7 | a0001c0001t0001g0008a0001c0001t0001g0026a0001c0001t0001g0048others(4): Show | 11 | HG00408.hp1 HG00408.hp2 HG00621.hp2 others(8): Show |
intron_variant | MODIFIER | c.656+2751A>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 7/17 | chr7 | 87372235 | ||||||
chr7:87372360
|
T | C | 1 | a0001c0001t0009g0203 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.656+2876T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 7/17 | chr7 | 87372360 | ||||||
chr7:87372440
|
A | C | 2 | a0001c0001t0001g0066a0001c0001t0001g0067 | 2 | HG02145.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.656+2956A>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 7/17 | chr7 | 87372440 | ||||||
chr7:87372763
|
G | A | 1 | a0001c0001t0001g0125 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.657-2869G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 7/17 | chr7 | 87372763 | ||||||
chr7:87372816
|
A | G | 1 | a0001c0001t0001g0063 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.657-2816A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 7/17 | chr7 | 87372816 | ||||||
chr7:87372825
|
A | G | 2 | a0001c0001t0001g0052a0001c0001t0003g0037 | 2 | HG02723.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.657-2807A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 7/17 | chr7 | 87372825 | ||||||
chr7:87372933
|
G | A | 1 | a0001c0001t0001g0148 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.657-2699G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 7/17 | chr7 | 87372933 | ||||||
chr7:87373047
|
T | C | 1 | a0001c0001t0001g0113 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.657-2585T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 7/17 | chr7 | 87373047 | ||||||
chr7:87373074
|
G | T | 2 | a0001c0001t0001g0059a0001c0001t0001g0060 | 2 | HG00639.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.657-2558G>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 7/17 | chr7 | 87373074 | ||||||
chr7:87373086
|
T | A | 1 | a0001c0001t0001g0136 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.657-2546T>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 7/17 | chr7 | 87373086 | ||||||
chr7:87373218
|
T | C | 1 | a0001c0001t0001g0134 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.657-2414T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 7/17 | chr7 | 87373218 | ||||||
chr7:87373418
|
G | A | 164 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(161): Show | 198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
intron_variant | MODIFIER | c.657-2214G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 7/17 | chr7 | 87373418 | ||||||
chr7:87373458
|
C | G | 8 | a0001c0001t0001g0023a0001c0001t0001g0055a0001c0001t0001g0105others(5): Show | 8 | HG00423.hp1 HG01978.hp2 HG02004.hp2 others(5): Show |
intron_variant | MODIFIER | c.657-2174C>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 7/17 | chr7 | 87373458 | ||||||
chr7:87373499
|
C | A | 1 | a0001c0001t0001g0080 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.657-2133C>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 7/17 | chr7 | 87373499 | ||||||
chr7:87373547
|
A | T | 1 | a0001c0001t0001g0209 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.657-2085A>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 7/17 | chr7 | 87373547 | ||||||
chr7:87373750
|
C | T | 127 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(124): Show | 149 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(146): Show |
intron_variant | MODIFIER | c.657-1882C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 7/17 | chr7 | 87373750 | ||||||
chr7:87373896
|
C | A | 5 | a0002c0002t0001g0014a0002c0002t0001g0057a0002c0002t0001g0058others(2): Show | 7 | HG02109.hp2 HG02615.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.657-1736C>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 7/17 | chr7 | 87373896 | ||||||
chr7:87374114
|
A | C | 2 | a0001c0001t0001g0059a0001c0001t0001g0060 | 2 | HG00639.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.657-1518A>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 7/17 | chr7 | 87374114 | ||||||
chr7:87374606
|
A | G | 217 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(214): Show | 281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.657-1026A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 7/17 | chr7 | 87374606 | ||||||
chr7:87374608
|
C | G | 1 | a0001c0001t0003g0039 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.657-1024C>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 7/17 | chr7 | 87374608 | ||||||
chr7:87374965
|
T | G | 165 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(162): Show | 199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.657-667T>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 7/17 | chr7 | 87374965 | ||||||
chr7:87375063
|
G | A | 1 | a0001c0001t0001g0114 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.657-569G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 7/17 | chr7 | 87375063 | ||||||
chr7:87375166
|
T | A | 1 | a0001c0001t0007g0015 | 2 | HG02109.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.657-466T>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 7/17 | chr7 | 87375166 | ||||||
chr7:87375285
|
A | G | 5 | a0002c0002t0001g0014a0002c0002t0001g0057a0002c0002t0001g0058others(2): Show | 7 | HG02109.hp2 HG02615.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.657-347A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 7/17 | chr7 | 87375285 | ||||||
chr7:87375311
|
G | T | 1 | a0001c0001t0003g0036 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.657-321G>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 7/17 | chr7 | 87375311 | ||||||
chr7:87375480
|
T | A | 5 | a0001c0001t0001g0024a0001c0001t0001g0174a0001c0001t0004g0011others(2): Show | 8 | HG02040.hp2 HG02080.hp2 NA18942.hp2 others(5): Show |
intron_variant | MODIFIER | c.657-152T>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 7/17 | chr7 | 87375480 | ||||||
chr7:87375594
|
C | G | 1 | a0001c0001t0003g0039 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.657-38C>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 7/17 | chr7 | 87375594 | ||||||
chr7:87375749
|
C | T | 1 | a0001c0001t0001g0060 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.750+24C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 8/17 | chr7 | 87375749 | ||||||
chr7:87375775
|
T | C | 2 | a0001c0001t0001g0098a0001c0001t0001g0099 | 2 | HG01109.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.750+50T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 8/17 | chr7 | 87375775 | ||||||
chr7:87375971
|
C | CT | 122 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(119): Show | 143 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.876+29dupT | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr7 | 87375971 | |||||
chr7:87376157
|
G | A | 1 | a0001c0001t0001g0183 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.876+204G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 9/17 | chr7 | 87376157 | ||||||
chr7:87376368
|
C | T | 1 | a0001c0001t0001g0083 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.876+415C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 9/17 | chr7 | 87376368 | ||||||
chr7:87376633
|
A | AT | 18 | a0001c0001t0001g0025a0001c0001t0001g0052a0001c0001t0001g0122others(15): Show | 22 | HG01243.hp1 HG02055.hp1 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.876+695dupT | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr7 | 87376633 | |||||
chr7:87376718
|
C | G | 17 | a0002c0002t0001g0014a0002c0002t0001g0057a0002c0002t0001g0058others(14): Show | 25 | HG00140.hp2 HG00323.hp1 HG00735.hp1 others(22): Show |
intron_variant | MODIFIER | c.877-631C>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 9/17 | chr7 | 87376718 | ||||||
chr7:87376777
|
A | G | 1 | a0001c0001t0009g0203 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.877-572A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 9/17 | chr7 | 87376777 | ||||||
chr7:87376815
|
C | A | 1 | a0001c0001t0003g0039 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.877-534C>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 9/17 | chr7 | 87376815 | ||||||
chr7:87376970
|
G | A | 1 | a0001c0001t0007g0015 | 2 | HG02109.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.877-379G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 9/17 | chr7 | 87376970 | ||||||
chr7:87376971
|
A | G | 7 | a0001c0001t0001g0017a0001c0001t0001g0046a0001c0001t0001g0056others(4): Show | 8 | HG00099.hp1 HG00323.hp2 HG01175.hp1 others(5): Show |
intron_variant | MODIFIER | c.877-378A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 9/17 | chr7 | 87376971 | ||||||
chr7:87377198
|
A | G | 1 | a0001c0001t0001g0102 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.877-151A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 9/17 | chr7 | 87377198 | ||||||
chr7:87377251
|
G | C | 164 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(161): Show | 198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
intron_variant | MODIFIER | c.877-98G>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 9/17 | chr7 | 87377251 | ||||||
chr7:87377292
|
A | G | 1 | a0001c0001t0001g0169 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.877-57A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 9/17 | chr7 | 87377292 | ||||||
chr7:87377536
|
G | C | 2 | a0001c0001t0001g0005a0001c0001t0001g0161 | 6 | HG00280.hp1 HG01070.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.978+86G>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 10/17 | chr7 | 87377536 | ||||||
chr7:87377576
|
A | G | 3 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0044 | 3 | HG02145.hp2 HG02630.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.978+126A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 10/17 | chr7 | 87377576 | ||||||
chr7:87377829
|
G | C | 1 | a0001c0001t0001g0022 | 2 | HG01071.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.978+379G>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 10/17 | chr7 | 87377829 | ||||||
chr7:87377863
|
A | G | 164 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(161): Show | 198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
intron_variant | MODIFIER | c.978+413A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 10/17 | chr7 | 87377863 | ||||||
chr7:87378287
|
A | G | 1 | a0001c0001t0001g0045 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.978+837A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 10/17 | chr7 | 87378287 | ||||||
chr7:87378293
|
C | T | 2 | a0001c0001t0001g0191a0001c0001t0001g0196 | 2 | NA18942.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.978+843C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 10/17 | chr7 | 87378293 | ||||||
chr7:87378294
|
A | G | 164 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(161): Show | 198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
intron_variant | MODIFIER | c.978+844A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 10/17 | chr7 | 87378294 | ||||||
chr7:87378306
|
A | G | 1 | a0001c0001t0001g0136 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.978+856A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 10/17 | chr7 | 87378306 | ||||||
chr7:87378340
|
C | T | 164 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(161): Show | 198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
intron_variant | MODIFIER | c.978+890C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 10/17 | chr7 | 87378340 | ||||||
chr7:87378341
|
G | A | 1 | a0001c0001t0001g0186 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.978+891G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 10/17 | chr7 | 87378341 | ||||||
chr7:87378346
|
C | CA | 31 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0049others(28): Show | 43 | HG00621.hp2 HG00735.hp1 HG01243.hp1 others(40): Show |
intron_variant | MODIFIER | c.978+912dupA | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr7 | 87378346 | |||||
chr7:87378346
|
C | CAA | 114 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(111): Show | 135 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(132): Show |
intron_variant | MODIFIER | c.978+911_978+912dup others(2): Show |
CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr7 | 87378346 | |||||
chr7:87378346
|
C | CAAA | 10 | a0001c0001t0001g0023a0001c0001t0001g0055a0001c0001t0001g0064others(7): Show | 10 | HG00423.hp1 HG01978.hp2 HG02004.hp2 others(7): Show |
intron_variant | MODIFIER | c.978+910_978+912dup others(3): Show |
CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr7 | 87378346 | |||||
chr7:87378428
|
T | C | 5 | a0001c0001t0001g0017a0001c0001t0001g0046a0001c0001t0001g0056others(2): Show | 6 | HG00099.hp1 HG00323.hp2 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.978+978T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 10/17 | chr7 | 87378428 | ||||||
chr7:87378487
|
A | G | 1 | a0001c0001t0001g0208 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.978+1037A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 10/17 | chr7 | 87378487 | ||||||
chr7:87378492
|
C | G | 1 | a0001c0001t0001g0208 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.978+1042C>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 10/17 | chr7 | 87378492 | ||||||
chr7:87378573
|
A | G | 1 | a0001c0001t0001g0155 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.978+1123A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 10/17 | chr7 | 87378573 | ||||||
chr7:87378639
|
T | C | 181 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(178): Show | 222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.978+1189T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 10/17 | chr7 | 87378639 | ||||||
chr7:87378907
|
C | T | 6 | a0001c0001t0001g0017a0001c0001t0001g0046a0001c0001t0001g0056others(3): Show | 7 | HG00099.hp1 HG00323.hp2 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.978+1457C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 10/17 | chr7 | 87378907 | ||||||
chr7:87378962
|
T | G | 2 | a0001c0001t0001g0191a0001c0001t0001g0196 | 2 | NA18942.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.978+1512T>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 10/17 | chr7 | 87378962 | ||||||
chr7:87379045
|
C | G | 4 | a0001c0001t0003g0031a0001c0001t0003g0032a0001c0001t0003g0033others(1): Show | 4 | HG02055.hp2 HG02647.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.978+1595C>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 10/17 | chr7 | 87379045 | ||||||
chr7:87379092
|
T | C | 1 | a0001c0001t0001g0050 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.978+1642T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 10/17 | chr7 | 87379092 | ||||||
chr7:87379134
|
C | T | 1 | a0005c0009t0001g0213 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.978+1684C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 10/17 | chr7 | 87379134 | ||||||
chr7:87379420
|
T | A | 1 | a0001c0001t0001g0208 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.978+1970T>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 10/17 | chr7 | 87379420 | ||||||
chr7:87379478
|
C | A | 1 | a0001c0001t0001g0116 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.978+2028C>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 10/17 | chr7 | 87379478 | ||||||
chr7:87379697
|
C | A | 1 | a0002c0002t0002g0075 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.979-2213C>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 10/17 | chr7 | 87379697 | ||||||
chr7:87379879
|
G | A | 3 | a0001c0001t0001g0163a0001c0001t0001g0169a0004c0004t0001g0164 | 3 | NA18969.hp1 NA18998.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.979-2031G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 10/17 | chr7 | 87379879 | ||||||
chr7:87380122
|
T | G | 5 | a0001c0001t0001g0022a0001c0001t0001g0108a0001c0001t0001g0130others(2): Show | 6 | HG01070.hp2 HG01071.hp1 HG01074.hp1 others(3): Show |
intron_variant | MODIFIER | c.979-1788T>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 10/17 | chr7 | 87380122 | ||||||
chr7:87380141
|
A | T | 1 | a0001c0001t0001g0121 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.979-1769A>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 10/17 | chr7 | 87380141 | ||||||
chr7:87380245
|
T | TCCTATTT others(143): Show |
1 | a0001c0001t0001g0117 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.979-1652_979-1651i others(152): Show |
CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr7 | 87380245 | |||||
chr7:87380245
|
T | TCCTATTT others(143): Show |
1 | a0001c0001t0001g0127 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.979-1604_979-1603i others(152): Show |
CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr7 | 87380245 | |||||
chr7:87380245
|
T | TCCTATTT others(143): Show |
122 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(119): Show | 144 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(141): Show |
intron_variant | MODIFIER | c.979-1664_979-1515d others(152): Show |
CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr7 | 87380245 | |||||
chr7:87380353
|
A | C | 1 | a0001c0001t0001g0161 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.979-1557A>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 10/17 | chr7 | 87380353 | ||||||
chr7:87380405
|
T | A | 1 | a0001c0001t0001g0118 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.979-1505T>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 10/17 | chr7 | 87380405 | ||||||
chr7:87380888
|
G | A | 162 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(159): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.979-1022G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 10/17 | chr7 | 87380888 | ||||||
chr7:87380974
|
G | A | 2 | a0001c0001t0003g0009a0001c0001t0003g0038 | 4 | HG02257.hp1 HG02451.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.979-936G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 10/17 | chr7 | 87380974 | ||||||
chr7:87381370
|
C | T | 2 | a0001c0001t0001g0059a0001c0001t0001g0060 | 2 | HG00639.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.979-540C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 10/17 | chr7 | 87381370 | ||||||
chr7:87381390
|
T | C | 2 | a0001c0001t0001g0198a0001c0001t0001g0199 | 2 | HG00741.hp1 HG01109.hp2 |
intron_variant | MODIFIER | c.979-520T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 10/17 | chr7 | 87381390 | ||||||
chr7:87381391
|
G | A | 1 | a0001c0001t0001g0208 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.979-519G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 10/17 | chr7 | 87381391 | ||||||
chr7:87381531
|
T | A | 2 | a0001c0001t0001g0026a0001c0001t0001g0081 | 3 | HG00621.hp2 HG02080.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.979-379T>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 10/17 | chr7 | 87381531 | ||||||
chr7:87381572
|
G | A | 162 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(159): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.979-338G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 10/17 | chr7 | 87381572 | ||||||
chr7:87381727
|
T | G | 2 | a0001c0001t0001g0107a0001c0001t0001g0109 | 2 | HG00738.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.979-183T>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 10/17 | chr7 | 87381727 | ||||||
chr7:87381751
|
T | C | 13 | a0001c0001t0001g0004a0001c0001t0001g0045a0001c0001t0001g0086others(10): Show | 17 | HG02258.hp1 HG02559.hp1 HG02717.hp1 others(14): Show |
intron_variant | MODIFIER | c.979-159T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 10/17 | chr7 | 87381751 | ||||||
chr7:87382033
|
G | A | 162 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(159): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.1062+40G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 11/17 | chr7 | 87382033 | ||||||
chr7:87382228
|
AC | A | 13 | a0001c0001t0001g0004a0001c0001t0001g0045a0001c0001t0001g0086others(10): Show | 17 | HG02258.hp1 HG02559.hp1 HG02717.hp1 others(14): Show |
intron_variant | MODIFIER | c.1170+48delC | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 12/17 | chr7 | 87382228 | ||||||
chr7:87382388
|
G | A | 17 | a0001c0001t0001g0025a0001c0001t0001g0040a0001c0001t0001g0041others(14): Show | 21 | HG01243.hp1 HG02055.hp1 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.1171-25G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 12/17 | chr7 | 87382388 | ||||||
chr7:87382393
|
C | T | 13 | a0001c0001t0001g0004a0001c0001t0001g0045a0001c0001t0001g0086others(10): Show | 17 | HG02258.hp1 HG02559.hp1 HG02717.hp1 others(14): Show |
intron_variant | MODIFIER | c.1171-20C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 12/17 | chr7 | 87382393 | ||||||
chr7:87382591
|
A | G | 1 | a0001c0001t0005g0202 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1301+48A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87382591 | ||||||
chr7:87382668
|
A | G | 2 | a0001c0001t0003g0009a0001c0001t0003g0038 | 4 | HG02257.hp1 HG02451.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1301+125A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87382668 | ||||||
chr7:87382793
|
T | C | 8 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0063others(5): Show | 10 | HG01884.hp1 HG02145.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.1301+250T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87382793 | ||||||
chr7:87382817
|
G | A | 2 | a0001c0001t0001g0059a0001c0001t0001g0060 | 2 | HG00639.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.1301+274G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87382817 | ||||||
chr7:87382911
|
C | T | 1 | a0002c0002t0001g0210 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1301+368C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87382911 | ||||||
chr7:87383003
|
A | G | 17 | a0001c0001t0001g0025a0001c0001t0001g0040a0001c0001t0001g0041others(14): Show | 21 | HG01243.hp1 HG02055.hp1 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.1301+460A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87383003 | ||||||
chr7:87383006
|
T | A | 2 | a0001c0001t0001g0026a0001c0001t0001g0081 | 3 | HG00621.hp2 HG02080.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.1301+463T>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87383006 | ||||||
chr7:87383099
|
C | T | 162 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(159): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.1301+556C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87383099 | ||||||
chr7:87383106
|
G | A | 2 | a0001c0001t0001g0059a0001c0001t0001g0060 | 2 | HG00639.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.1301+563G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87383106 | ||||||
chr7:87383147
|
A | G | 12 | a0002c0002t0002g0003a0002c0002t0002g0021a0002c0002t0002g0070others(9): Show | 18 | HG00140.hp2 HG00323.hp1 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.1301+604A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87383147 | ||||||
chr7:87383154
|
A | G | 14 | a0001c0001t0001g0025a0001c0001t0001g0052a0001c0001t0001g0154others(11): Show | 18 | HG01243.hp1 HG02055.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.1301+611A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87383154 | ||||||
chr7:87383267
|
C | G | 2 | a0001c0001t0003g0009a0001c0001t0003g0038 | 4 | HG02257.hp1 HG02451.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1301+724C>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87383267 | ||||||
chr7:87383315
|
C | T | 17 | a0001c0001t0001g0025a0001c0001t0001g0040a0001c0001t0001g0041others(14): Show | 21 | HG01243.hp1 HG02055.hp1 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.1301+772C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87383315 | ||||||
chr7:87383367
|
T | C | 1 | a0001c0001t0001g0179 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1301+824T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87383367 | ||||||
chr7:87383382
|
A | C | 162 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(159): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.1301+839A>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87383382 | ||||||
chr7:87383497
|
CT | C | 134 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(131): Show | 158 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(155): Show |
intron_variant | MODIFIER | c.1301+970delT | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr7 | 87383497 | |||||
chr7:87383742
|
G | A | 1 | a0001c0001t0001g0083 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1301+1199G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87383742 | ||||||
chr7:87383790
|
C | T | 1 | a0001c0001t0007g0015 | 2 | HG02109.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1301+1247C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87383790 | ||||||
chr7:87383792
|
C | T | 1 | a0001c0001t0001g0160 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1301+1249C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87383792 | ||||||
chr7:87384000
|
T | G | 2 | a0001c0001t0001g0029a0001c0001t0001g0184 | 3 | HG00099.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1301+1457T>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87384000 | ||||||
chr7:87384004
|
C | T | 13 | a0001c0001t0001g0004a0001c0001t0001g0045a0001c0001t0001g0086others(10): Show | 17 | HG02258.hp1 HG02559.hp1 HG02717.hp1 others(14): Show |
intron_variant | MODIFIER | c.1301+1461C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87384004 | ||||||
chr7:87384005
|
G | A | 4 | a0001c0001t0001g0173a0001c0001t0001g0187a0001c0001t0001g0188others(1): Show | 4 | HG00544.hp1 NA18747.hp2 NA18957.hp1 others(1): Show |
intron_variant | MODIFIER | c.1301+1462G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87384005 | ||||||
chr7:87384164
|
C | T | 14 | a0001c0001t0001g0025a0001c0001t0001g0052a0001c0001t0001g0154others(11): Show | 18 | HG01243.hp1 HG02055.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.1301+1621C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87384164 | ||||||
chr7:87384261
|
A | T | 3 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0044 | 3 | HG02145.hp2 HG02630.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1301+1718A>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87384261 | ||||||
chr7:87384367
|
A | T | 2 | a0001c0001t0001g0020a0001c0001t0001g0069 | 3 | NA18948.hp2 NA18974.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.1301+1824A>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87384367 | ||||||
chr7:87384376
|
A | G | 1 | a0001c0001t0001g0144 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1301+1833A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87384376 | ||||||
chr7:87384439
|
C | A | 1 | a0001c0001t0001g0177 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1301+1896C>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87384439 | ||||||
chr7:87384472
|
C | T | 1 | a0001c0001t0001g0052 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1301+1929C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87384472 | ||||||
chr7:87384764
|
G | T | 13 | a0001c0001t0001g0004a0001c0001t0001g0045a0001c0001t0001g0086others(10): Show | 17 | HG02258.hp1 HG02559.hp1 HG02717.hp1 others(14): Show |
intron_variant | MODIFIER | c.1301+2221G>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87384764 | ||||||
chr7:87385039
|
C | T | 17 | a0002c0002t0001g0014a0002c0002t0001g0057a0002c0002t0001g0058others(14): Show | 25 | HG00140.hp2 HG00323.hp1 HG00735.hp1 others(22): Show |
intron_variant | MODIFIER | c.1301+2496C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87385039 | ||||||
chr7:87385117
|
T | C | 163 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(160): Show | 198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
intron_variant | MODIFIER | c.1301+2574T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87385117 | ||||||
chr7:87385149
|
T | C | 2 | a0001c0001t0001g0059a0001c0001t0001g0060 | 2 | HG00639.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.1301+2606T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87385149 | ||||||
chr7:87385613
|
G | A | 12 | a0002c0002t0002g0003a0002c0002t0002g0021a0002c0002t0002g0070others(9): Show | 18 | HG00140.hp2 HG00323.hp1 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.1301+3070G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87385613 | ||||||
chr7:87385816
|
G | T | 1 | a0001c0001t0001g0208 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1301+3273G>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87385816 | ||||||
chr7:87385869
|
T | C | 2 | a0001c0001t0001g0010a0001c0001t0001g0205 | 4 | HG01934.hp2 HG02083.hp2 NA18955.hp1 others(1): Show |
intron_variant | MODIFIER | c.1301+3326T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87385869 | ||||||
chr7:87385914
|
C | G | 2 | a0001c0001t0001g0059a0001c0001t0001g0060 | 2 | HG00639.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.1301+3371C>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87385914 | ||||||
chr7:87386396
|
T | C | 1 | a0009c0008t0001g0159 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1301+3853T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87386396 | ||||||
chr7:87386570
|
T | C | 1 | a0001c0001t0001g0083 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1301+4027T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87386570 | ||||||
chr7:87386617
|
T | C | 2 | a0001c0001t0001g0059a0001c0001t0001g0060 | 2 | HG00639.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.1301+4074T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87386617 | ||||||
chr7:87386670
|
G | A | 3 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0044 | 3 | HG02145.hp2 HG02630.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1301+4127G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87386670 | ||||||
chr7:87386683
|
T | C | 2 | a0001c0001t0001g0059a0001c0001t0001g0060 | 2 | HG00639.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.1301+4140T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87386683 | ||||||
chr7:87386744
|
G | A | 1 | a0001c0001t0001g0137 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1301+4201G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87386744 | ||||||
chr7:87386892
|
G | C | 12 | a0001c0001t0001g0025a0001c0001t0001g0154a0001c0001t0001g0158others(9): Show | 16 | HG01243.hp1 HG02055.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.1301+4349G>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87386892 | ||||||
chr7:87387148
|
A | G | 1 | a0001c0001t0001g0044 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1302-4441A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87387148 | ||||||
chr7:87387173
|
G | A | 12 | a0001c0001t0001g0025a0001c0001t0001g0154a0001c0001t0001g0158others(9): Show | 16 | HG01243.hp1 HG02055.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.1302-4416G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87387173 | ||||||
chr7:87387182
|
T | C | 1 | a0001c0001t0003g0039 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1302-4407T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87387182 | ||||||
chr7:87387311
|
T | C | 3 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0044 | 3 | HG02145.hp2 HG02630.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1302-4278T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87387311 | ||||||
chr7:87387517
|
G | A | 17 | a0002c0002t0001g0014a0002c0002t0001g0057a0002c0002t0001g0058others(14): Show | 25 | HG00140.hp2 HG00323.hp1 HG00735.hp1 others(22): Show |
intron_variant | MODIFIER | c.1302-4072G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87387517 | ||||||
chr7:87387520
|
C | T | 124 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(121): Show | 146 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(143): Show |
intron_variant | MODIFIER | c.1302-4069C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87387520 | ||||||
chr7:87387526
|
G | A | 1 | a0001c0001t0003g0037 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1302-4063G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87387526 | ||||||
chr7:87388218
|
C | T | 2 | a0001c0001t0001g0191a0001c0001t0001g0196 | 2 | NA18942.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.1302-3371C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87388218 | ||||||
chr7:87388225
|
A | C | 14 | a0001c0001t0001g0025a0001c0001t0001g0052a0001c0001t0001g0154others(11): Show | 18 | HG01243.hp1 HG02055.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.1302-3364A>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87388225 | ||||||
chr7:87388547
|
C | T | 162 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(159): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.1302-3042C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87388547 | ||||||
chr7:87388759
|
A | G | 7 | a0001c0001t0001g0025a0001c0001t0001g0154a0001c0001t0001g0158others(4): Show | 11 | HG01243.hp1 HG02055.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.1302-2830A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87388759 | ||||||
chr7:87388805
|
A | G | 1 | a0002c0002t0002g0075 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1302-2784A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87388805 | ||||||
chr7:87388954
|
T | C | 2 | a0001c0001t0001g0042a0001c0001t0001g0043 | 2 | HG02615.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1302-2635T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87388954 | ||||||
chr7:87388996
|
T | C | 1 | a0001c0001t0010g0035 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1302-2593T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87388996 | ||||||
chr7:87389215
|
C | T | 124 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(121): Show | 146 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(143): Show |
intron_variant | MODIFIER | c.1302-2374C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87389215 | ||||||
chr7:87389263
|
C | G | 1 | a0001c0001t0001g0129 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1302-2326C>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87389263 | ||||||
chr7:87389280
|
C | A | 3 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0044 | 3 | HG02145.hp2 HG02630.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1302-2309C>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87389280 | ||||||
chr7:87389423
|
C | A | 1 | a0001c0001t0010g0035 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1302-2166C>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87389423 | ||||||
chr7:87389436
|
T | C | 5 | a0002c0002t0001g0014a0002c0002t0001g0057a0002c0002t0001g0058others(2): Show | 7 | HG02109.hp2 HG02615.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.1302-2153T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87389436 | ||||||
chr7:87389449
|
G | A | 125 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(122): Show | 147 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(144): Show |
intron_variant | MODIFIER | c.1302-2140G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87389449 | ||||||
chr7:87389480
|
G | T | 14 | a0001c0001t0001g0025a0001c0001t0001g0052a0001c0001t0001g0154others(11): Show | 18 | HG01243.hp1 HG02055.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.1302-2109G>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87389480 | ||||||
chr7:87389507
|
A | G | 7 | a0001c0001t0001g0025a0001c0001t0001g0154a0001c0001t0001g0158others(4): Show | 11 | HG01243.hp1 HG02055.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.1302-2082A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87389507 | ||||||
chr7:87389827
|
GTTGTTCC | G | 124 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(121): Show | 146 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(143): Show |
intron_variant | MODIFIER | c.1302-1760_1302-175 others(11): Show |
CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr7 | 87389827 | |||||
chr7:87389860
|
A | G | 163 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(160): Show | 198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
intron_variant | MODIFIER | c.1302-1729A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87389860 | ||||||
chr7:87389896
|
G | A | 2 | a0001c0001t0001g0059a0001c0001t0001g0060 | 2 | HG00639.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.1302-1693G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87389896 | ||||||
chr7:87390081
|
C | T | 3 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0044 | 3 | HG02145.hp2 HG02630.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1302-1508C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87390081 | ||||||
chr7:87390237
|
C | A | 1 | a0001c0001t0001g0175 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1302-1352C>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87390237 | ||||||
chr7:87390323
|
C | T | 1 | a0001c0001t0010g0035 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1302-1266C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87390323 | ||||||
chr7:87390699
|
A | G | 1 | a0001c0001t0010g0035 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1302-890A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87390699 | ||||||
chr7:87390812
|
T | G | 2 | a0001c0001t0001g0059a0001c0001t0001g0060 | 2 | HG00639.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.1302-777T>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87390812 | ||||||
chr7:87390858
|
C | T | 2 | a0001c0001t0003g0009a0001c0001t0003g0038 | 4 | HG02257.hp1 HG02451.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1302-731C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87390858 | ||||||
chr7:87390986
|
G | C | 1 | a0001c0001t0001g0198 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1302-603G>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87390986 | ||||||
chr7:87390988
|
T | G | 2 | a0001c0001t0003g0009a0001c0001t0003g0038 | 4 | HG02257.hp1 HG02451.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1302-601T>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87390988 | ||||||
chr7:87391471
|
C | T | 2 | a0001c0001t0001g0102a0001c0001t0001g0194 | 2 | HG00140.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.1302-118C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 13/17 | chr7 | 87391471 | ||||||
chr7:87392016
|
G | C | 2 | a0001c0001t0001g0059a0001c0001t0001g0060 | 2 | HG00639.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.1425+304G>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 14/17 | chr7 | 87392016 | ||||||
chr7:87392129
|
T | C | 14 | a0001c0001t0001g0025a0001c0001t0001g0052a0001c0001t0001g0154others(11): Show | 18 | HG01243.hp1 HG02055.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.1425+417T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 14/17 | chr7 | 87392129 | ||||||
chr7:87392208
|
G | A | 12 | a0002c0002t0002g0003a0002c0002t0002g0021a0002c0002t0002g0070others(9): Show | 18 | HG00140.hp2 HG00323.hp1 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.1426-358G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 14/17 | chr7 | 87392208 | ||||||
chr7:87392397
|
T | C | 12 | a0001c0001t0001g0025a0001c0001t0001g0154a0001c0001t0001g0158others(9): Show | 16 | HG01243.hp1 HG02055.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.1426-169T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 14/17 | chr7 | 87392397 | ||||||
chr7:87392401
|
C | T | 3 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0044 | 3 | HG02145.hp2 HG02630.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1426-165C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 14/17 | chr7 | 87392401 | ||||||
chr7:87392423
|
A | T | 5 | a0001c0001t0001g0150a0001c0001t0001g0167a0001c0001t0004g0011others(2): Show | 7 | HG02071.hp1 HG02080.hp2 NA18942.hp2 others(4): Show |
intron_variant | MODIFIER | c.1426-143A>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 14/17 | chr7 | 87392423 | ||||||
chr7:87392489
|
T | A | 1 | a0001c0001t0001g0076 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1426-77T>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 14/17 | chr7 | 87392489 | ||||||
chr7:87392708
|
G | C | 162 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(159): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.1505-22G>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 15/17 | chr7 | 87392708 | ||||||
chr7:87393280
|
T | C | 126 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(123): Show | 148 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(145): Show |
intron_variant | MODIFIER | c.1718+213T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 17/17 | chr7 | 87393280 | ||||||
chr7:87393307
|
C | T | 12 | a0001c0001t0001g0025a0001c0001t0001g0154a0001c0001t0001g0158others(9): Show | 16 | HG01243.hp1 HG02055.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.1718+240C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 17/17 | chr7 | 87393307 | ||||||
chr7:87393518
|
G | A | 1 | a0001c0001t0001g0188 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1718+451G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 17/17 | chr7 | 87393518 | ||||||
chr7:87393665
|
T | C | 178 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(175): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.1718+598T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 17/17 | chr7 | 87393665 | ||||||
chr7:87393788
|
G | A | 6 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0186others(3): Show | 6 | NA18948.hp1 NA18985.hp2 NA18990.hp1 others(3): Show |
intron_variant | MODIFIER | c.1718+721G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 17/17 | chr7 | 87393788 | ||||||
chr7:87393879
|
A | T | 124 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(121): Show | 146 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(143): Show |
intron_variant | MODIFIER | c.1718+812A>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 17/17 | chr7 | 87393879 | ||||||
chr7:87393949
|
A | C | 1 | a0001c0001t0010g0035 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1718+882A>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 17/17 | chr7 | 87393949 | ||||||
chr7:87394003
|
C | A | 3 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0044 | 3 | HG02145.hp2 HG02630.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1718+936C>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 17/17 | chr7 | 87394003 | ||||||
chr7:87394220
|
G | A | 1 | a0001c0001t0003g0033 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1718+1153G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 17/17 | chr7 | 87394220 | ||||||
chr7:87394321
|
G | A | 1 | a0001c0001t0001g0063 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1718+1254G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 17/17 | chr7 | 87394321 | ||||||
chr7:87394553
|
T | C | 1 | a0001c0001t0001g0045 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1718+1486T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 17/17 | chr7 | 87394553 | ||||||
chr7:87394555
|
T | TA | 143 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(140): Show | 170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): Show |
intron_variant | MODIFIER | c.1718+1499dupA | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr7 | 87394555 | |||||
chr7:87394555
|
T | TAA | 31 | a0001c0001t0001g0004a0001c0001t0001g0045a0001c0001t0001g0086others(28): Show | 43 | HG00140.hp2 HG00323.hp1 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.1718+1498_1718+149 others(6): Show |
CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr7 | 87394555 | |||||
chr7:87394556
|
A | T | 1 | a0001c0001t0001g0173 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1718+1489A>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 17/17 | chr7 | 87394556 | ||||||
chr7:87394650
|
A | T | 2 | a0001c0001t0001g0172a0001c0001t0001g0183 | 2 | NA19003.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1718+1583A>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 17/17 | chr7 | 87394650 | ||||||
chr7:87394676
|
A | G | 5 | a0002c0002t0001g0014a0002c0002t0001g0057a0002c0002t0001g0058others(2): Show | 7 | HG02109.hp2 HG02615.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.1718+1609A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 17/17 | chr7 | 87394676 | ||||||
chr7:87394713
|
A | G | 1 | a0001c0001t0001g0208 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1718+1646A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 17/17 | chr7 | 87394713 | ||||||
chr7:87394803
|
G | A | 1 | a0001c0001t0003g0039 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1718+1736G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 17/17 | chr7 | 87394803 | ||||||
chr7:87394987
|
G | GA | 19 | a0001c0001t0001g0025a0001c0001t0001g0052a0001c0001t0001g0059others(16): Show | 23 | HG00140.hp1 HG00639.hp1 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.1718+1930dupA | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr7 | 87394987 | |||||
chr7:87395038
|
T | C | 1 | a0001c0001t0003g0039 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1718+1971T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 17/17 | chr7 | 87395038 | ||||||
chr7:87395203
|
G | C | 2 | a0001c0001t0001g0059a0001c0001t0001g0060 | 2 | HG00639.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.1718+2136G>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 17/17 | chr7 | 87395203 | ||||||
chr7:87395270
|
G | GT | 122 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(119): Show | 144 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(141): Show |
intron_variant | MODIFIER | c.1718+2208dupT | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr7 | 87395270 | |||||
chr7:87395270
|
G | GTT | 3 | a0001c0001t0001g0062a0001c0001t0001g0193a0001c0001t0005g0200 | 3 | HG02572.hp2 HG03225.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.1718+2207_1718+220 others(6): Show |
CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr7 | 87395270 | |||||
chr7:87395294
|
G | T | 1 | a0001c0001t0001g0093 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1718+2227G>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 17/17 | chr7 | 87395294 | ||||||
chr7:87395336
|
C | G | 14 | a0001c0001t0001g0025a0001c0001t0001g0052a0001c0001t0001g0154others(11): Show | 18 | HG01243.hp1 HG02055.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.1718+2269C>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 17/17 | chr7 | 87395336 | ||||||
chr7:87395369
|
A | G | 124 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(121): Show | 146 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(143): Show |
intron_variant | MODIFIER | c.1718+2302A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 17/17 | chr7 | 87395369 | ||||||
chr7:87395402
|
C | T | 1 | a0001c0001t0007g0015 | 2 | HG02109.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1718+2335C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 17/17 | chr7 | 87395402 | ||||||
chr7:87395517
|
T | G | 1 | a0001c0001t0001g0065 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1718+2450T>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 17/17 | chr7 | 87395517 | ||||||
chr7:87395636
|
C | A | 1 | a0001c0001t0001g0016 | 2 | HG01358.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.1718+2569C>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 17/17 | chr7 | 87395636 | ||||||
chr7:87395789
|
A | G | 1 | a0001c0001t0001g0095 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1718+2722A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 17/17 | chr7 | 87395789 | ||||||
chr7:87395811
|
A | G | 1 | a0001c0001t0001g0214 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1719-2713A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 17/17 | chr7 | 87395811 | ||||||
chr7:87396030
|
T | A | 1 | a0001c0001t0007g0015 | 2 | HG02109.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1719-2494T>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 17/17 | chr7 | 87396030 | ||||||
chr7:87396031
|
C | T | 1 | a0001c0001t0001g0026 | 2 | HG00621.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.1719-2493C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 17/17 | chr7 | 87396031 | ||||||
chr7:87396134
|
G | A | 1 | a0001c0001t0001g0178 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1719-2390G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 17/17 | chr7 | 87396134 | ||||||
chr7:87396451
|
G | T | 1 | a0001c0001t0001g0120 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1719-2073G>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 17/17 | chr7 | 87396451 | ||||||
chr7:87396501
|
C | T | 1 | a0001c0001t0007g0015 | 2 | HG02109.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1719-2023C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 17/17 | chr7 | 87396501 | ||||||
chr7:87396626
|
CTT | C | 12 | a0002c0002t0002g0003a0002c0002t0002g0021a0002c0002t0002g0070others(9): Show | 18 | HG00140.hp2 HG00323.hp1 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.1719-1897_1719-189 others(6): Show |
CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 17/17 | chr7 | 87396626 | ||||||
chr7:87396690
|
T | TA | 143 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(140): Show | 171 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(168): Show |
intron_variant | MODIFIER | c.1719-1822dupA | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr7 | 87396690 | |||||
chr7:87396690
|
T | TAA | 17 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0044others(14): Show | 23 | HG00140.hp2 HG00323.hp1 HG00735.hp1 others(20): Show |
intron_variant | MODIFIER | c.1719-1823_1719-182 others(6): Show |
CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr7 | 87396690 | |||||
chr7:87396741
|
T | C | 1 | a0001c0001t0010g0035 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1719-1783T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 17/17 | chr7 | 87396741 | ||||||
chr7:87396858
|
G | A | 14 | a0001c0001t0001g0025a0001c0001t0001g0052a0001c0001t0001g0154others(11): Show | 18 | HG01243.hp1 HG02055.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.1719-1666G>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 17/17 | chr7 | 87396858 | ||||||
chr7:87396952
|
T | A | 1 | a0001c0001t0001g0119 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1719-1572T>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 17/17 | chr7 | 87396952 | ||||||
chr7:87397133
|
C | T | 2 | a0001c0001t0001g0059a0001c0001t0001g0060 | 2 | HG00639.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.1719-1391C>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 17/17 | chr7 | 87397133 | ||||||
chr7:87397217
|
A | G | 178 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(175): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.1719-1307A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 17/17 | chr7 | 87397217 | ||||||
chr7:87397257
|
A | G | 20 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0044others(17): Show | 28 | HG00140.hp2 HG00323.hp1 HG00735.hp1 others(25): Show |
intron_variant | MODIFIER | c.1719-1267A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 17/17 | chr7 | 87397257 | ||||||
chr7:87397349
|
T | C | 1 | a0001c0001t0001g0064 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1719-1175T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 17/17 | chr7 | 87397349 | ||||||
chr7:87397350
|
C | A | 1 | a0001c0001t0001g0064 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1719-1174C>A | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 17/17 | chr7 | 87397350 | ||||||
chr7:87397350
|
C | CA | 172 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(169): Show | 213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
intron_variant | MODIFIER | c.1719-1161dupA | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr7 | 87397350 | |||||
chr7:87397478
|
T | C | 1 | a0001c0001t0001g0163 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1719-1046T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 17/17 | chr7 | 87397478 | ||||||
chr7:87397519
|
A | T | 1 | a0002c0002t0002g0171 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1719-1005A>T | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 17/17 | chr7 | 87397519 | ||||||
chr7:87398000
|
T | C | 1 | a0001c0001t0001g0125 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1719-524T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 17/17 | chr7 | 87398000 | ||||||
chr7:87398103
|
C | CT | 116 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(113): Show | 138 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.1719-408dupT | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr7 | 87398103 | |||||
chr7:87398103
|
CT | C | 16 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0044others(13): Show | 22 | HG00140.hp2 HG00323.hp1 HG00735.hp1 others(19): Show |
intron_variant | MODIFIER | c.1719-408delT | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr7 | 87398103 | |||||
chr7:87398126
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T | C | 1 | a0001c0001t0001g0208 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1719-398T>C | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 17/17 | chr7 | 87398126 | ||||||
chr7:87398520
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A | G | 1 | a0002c0002t0001g0057 | 1 | HG03516.hp2 | splice_region_variant&intron_variant | LOW | c.1719-4A>G | CROT | ENSG00000005469.12 | transcript | ENST00000331536.8 | protein_coding | 17/17 | chr7 | 87398520 |