geneid | 26136 |
---|---|
ensemblid | ENSG00000135269.18 |
hgncid | 14620 |
symbol | TES |
name | testin LIM domain protein |
refseq_nuc | NM_015641.4 |
refseq_prot | NP_056456.1 |
ensembl_nuc | ENST00000358204.9 |
ensembl_prot | ENSP00000350937.4 |
mane_status | MANE Select |
chr | chr7 |
start | 116210539 |
end | 116258783 |
strand | + |
ver | v1.2 |
region | chr7:116210539-116258783 |
region5000 | chr7:116205539-116263783 |
regionname0 | TES_chr7_116210539_116258783 |
regionname5000 | TES_chr7_116205539_116263783 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 421 | 372 | 78 | 67 | 174 | 14 | 37 | 134 | TES_chr7_116205539_116263783 | TES | copy fasta | chr7 | 116205539 | 116263783 |
a0002 | 0/0 | 421 | 10 | 0 | 0 | 10 | 0 | 0 | 10 | TES_chr7_116205539_116263783 | TES | copy fasta | chr7 | 116205539 | 116263783 |
a0003 | 0/0 | 421 | 3 | 0 | 0 | 0 | 0 | 3 | 0 | TES_chr7_116205539_116263783 | TES | copy fasta | chr7 | 116205539 | 116263783 |
a0004 | 0/0 | 421 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | copy fasta | chr7 | 116205539 | 116263783 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1266 | 199 | 37 | 43 | 83 | 8 | 26 | TES_chr7_116205539_116263783 | TES | copy fasta | chr7 | 116205539 | 116263783 |
c0002 | 0/0 | 1266 | 172 | 40 | 24 | 91 | 6 | 11 | TES_chr7_116205539_116263783 | TES | copy fasta | chr7 | 116205539 | 116263783 |
c0003 | 0/0 | 1266 | 10 | 0 | 0 | 10 | 0 | 0 | TES_chr7_116205539_116263783 | TES | copy fasta | chr7 | 116205539 | 116263783 |
c0004 | 0/0 | 1266 | 3 | 0 | 0 | 0 | 0 | 3 | TES_chr7_116205539_116263783 | TES | copy fasta | chr7 | 116205539 | 116263783 |
c0005 | 0/0 | 1266 | 1 | 0 | 1 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | copy fasta | chr7 | 116205539 | 116263783 |
c0006 | 0/0 | 1266 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | copy fasta | chr7 | 116205539 | 116263783 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 1466 | 99 | 13 | 10 | 68 | 4 | 4 | TES_chr7_116205539_116263783 | TES | copy fasta | chr7 | 116205539 | 116263783 |
t0002 | 0/0 | 1471 | 71 | 0 | 16 | 48 | 1 | 6 | TES_chr7_116205539_116263783 | TES | copy fasta | chr7 | 116205539 | 116263783 |
t0003 | 0/0 | 1470 | 67 | 10 | 14 | 27 | 5 | 11 | TES_chr7_116205539_116263783 | TES | copy fasta | chr7 | 116205539 | 116263783 |
t0004 | 0/0 | 1468 | 64 | 10 | 11 | 31 | 2 | 10 | TES_chr7_116205539_116263783 | TES | copy fasta | chr7 | 116205539 | 116263783 |
t0005 | 1/1 | 1471 | 58 | 23 | 14 | 8 | 2 | 9 | TES_chr7_116205539_116263783 | TES | copy fasta | chr7 | 116205539 | 116263783 |
t0006 | 0/0 | 1469 | 15 | 15 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | copy fasta | chr7 | 116205539 | 116263783 |
t0007 | 0/0 | 1471 | 4 | 4 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | copy fasta | chr7 | 116205539 | 116263783 |
t0008 | 0/0 | 1466 | 4 | 1 | 2 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | copy fasta | chr7 | 116205539 | 116263783 |
t0009 | 0/0 | 1466 | 2 | 2 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | copy fasta | chr7 | 116205539 | 116263783 |
t0010 | 0/0 | 1466 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | copy fasta | chr7 | 116205539 | 116263783 |
t0011 | 0/0 | 1466 | 1 | 0 | 1 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | copy fasta | chr7 | 116205539 | 116263783 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0002 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0003 | 0/0 | 5 | 0 | 2 | 0 | 1 | 2 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0004 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0005 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0006 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0008 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0012 | 0/0 | 4 | 0 | 2 | 0 | 2 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0014 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0019 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0020 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0030 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0043 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0044 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0047 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0048 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0049 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0050 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0051 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0052 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0267 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0272 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0285 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0286 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1266 | 199 | 37 | 43 | 83 | 8 | 26 | TES_chr7_116205539_116263783 | TES | copy fasta | chr7 | 116205539 | 116263783 |
a0001c0002 | 0/0 | 1266 | 172 | 40 | 24 | 91 | 6 | 11 | TES_chr7_116205539_116263783 | TES | copy fasta | chr7 | 116205539 | 116263783 |
a0001c0006 | 0/0 | 1266 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | copy fasta | chr7 | 116205539 | 116263783 |
a0002c0003 | 0/0 | 1266 | 10 | 0 | 0 | 10 | 0 | 0 | TES_chr7_116205539_116263783 | TES | copy fasta | chr7 | 116205539 | 116263783 |
a0003c0004 | 0/0 | 1266 | 3 | 0 | 0 | 0 | 0 | 3 | TES_chr7_116205539_116263783 | TES | copy fasta | chr7 | 116205539 | 116263783 |
a0004c0005 | 0/0 | 1266 | 1 | 0 | 1 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | copy fasta | chr7 | 116205539 | 116263783 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002 | 0/0 | 2736 | 71 | 0 | 16 | 48 | 1 | 6 | TES_chr7_116205539_116263783 | TES | copy fasta | chr7 | 116205539 | 116263783 |
a0001c0001t0003 | 0/0 | 2735 | 67 | 10 | 14 | 27 | 5 | 11 | TES_chr7_116205539_116263783 | TES | copy fasta | chr7 | 116205539 | 116263783 |
a0001c0001t0005 | 1/1 | 2736 | 57 | 23 | 13 | 8 | 2 | 9 | TES_chr7_116205539_116263783 | TES | copy fasta | chr7 | 116205539 | 116263783 |
a0001c0001t0007 | 0/0 | 2736 | 4 | 4 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | copy fasta | chr7 | 116205539 | 116263783 |
a0001c0002t0001 | 0/0 | 2731 | 88 | 12 | 10 | 58 | 4 | 4 | TES_chr7_116205539_116263783 | TES | copy fasta | chr7 | 116205539 | 116263783 |
a0001c0002t0004 | 0/0 | 2733 | 61 | 10 | 11 | 31 | 2 | 7 | TES_chr7_116205539_116263783 | TES | copy fasta | chr7 | 116205539 | 116263783 |
a0001c0002t0006 | 0/0 | 2734 | 15 | 15 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | copy fasta | chr7 | 116205539 | 116263783 |
a0001c0002t0008 | 0/0 | 2731 | 4 | 1 | 2 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | copy fasta | chr7 | 116205539 | 116263783 |
a0001c0002t0009 | 0/0 | 2731 | 2 | 2 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | copy fasta | chr7 | 116205539 | 116263783 |
a0001c0002t0010 | 0/0 | 2731 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | copy fasta | chr7 | 116205539 | 116263783 |
a0001c0002t0011 | 0/0 | 2731 | 1 | 0 | 1 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | copy fasta | chr7 | 116205539 | 116263783 |
a0001c0006t0001 | 0/0 | 2731 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | copy fasta | chr7 | 116205539 | 116263783 |
a0002c0003t0001 | 0/0 | 2731 | 10 | 0 | 0 | 10 | 0 | 0 | TES_chr7_116205539_116263783 | TES | copy fasta | chr7 | 116205539 | 116263783 |
a0003c0004t0004 | 0/0 | 2733 | 3 | 0 | 0 | 0 | 0 | 3 | TES_chr7_116205539_116263783 | TES | copy fasta | chr7 | 116205539 | 116263783 |
a0004c0005t0005 | 0/0 | 2736 | 1 | 0 | 1 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | copy fasta | chr7 | 116205539 | 116263783 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002g0001 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0002g0003 | 0/0 | 5 | 0 | 2 | 0 | 1 | 2 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0002g0004 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0002g0008 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0002g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0002g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0002g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0002g0030 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0002g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0002g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0002g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0002g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0002g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0002g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0002g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0002g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0002g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0002g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0002g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0003g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0003g0012 | 0/0 | 4 | 0 | 2 | 0 | 2 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0003g0014 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0003g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0003g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0003g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0003g0047 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0003g0048 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0003g0049 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0003g0050 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0003g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0003g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0003g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0003g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0003g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0003g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0003g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0003g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0003g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0003g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0003g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0003g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0003g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0003g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0003g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0003g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0003g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0003g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0003g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0003g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0003g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0003g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0003g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0003g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0003g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0003g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0003g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0003g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0003g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0003g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0003g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0003g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0003g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0003g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0003g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0003g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0003g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0003g0267 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0003g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0003g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0003g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0003g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0005g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0005g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0005g0043 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0005g0044 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0005g0051 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0005g0052 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0005g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0005g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0005g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0005g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0005g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0005g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0005g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0005g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0005g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0005g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0005g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0005g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0005g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0005g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0005g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0005g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0005g0272 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0005g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0005g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0005g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0005g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0005g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0005g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0005g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0005g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0005g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0005g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0005g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0005g0285 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0005g0286 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0005g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0005g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0005g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0005g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0005g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0005g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0005g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0005g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0005g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0005g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0005g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0005g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0005g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0005g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0007g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0007g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0001t0007g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0001g0005 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0001g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0004g0002 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0004g0006 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0004g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0004g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0004g0019 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0004g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0004g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0004g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0004g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0004g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0004g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0004g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0004g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0004g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0004g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0004g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0004g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0004g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0004g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0004g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0004g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0004g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0004g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0004g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0004g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0004g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0004g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0004g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0004g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0004g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0004g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0004g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0004g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0004g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0004g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0004g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0004g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0004g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0004g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0004g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0004g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0004g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0004g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0004g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0006g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0006g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0006g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0006g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0006g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0006g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0006g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0006g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0006g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0006g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0006g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0006g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0006g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0006g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0008g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0008g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0008g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0009g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0010g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0002t0011g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0001c0006t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0002c0003t0001g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0002c0003t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0002c0003t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0002c0003t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0002c0003t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0002c0003t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0002c0003t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0002c0003t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0003c0004t0004g0020 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0003c0004t0004g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
a0004c0005t0005g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0002 | t0004 | g0070 | EUR | GBR | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG00140 | hp2 | a0001 | c0001 | t0003 | g0243 | EUR | GBR | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG00280 | hp1 | a0001 | c0002 | t0001 | g0204 | EUR | FIN | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG00280 | hp2 | a0001 | c0001 | t0005 | g0286 | EUR | FIN | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG00408 | hp1 | a0001 | c0002 | t0001 | g0156 | EAS | CHS | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG00408 | hp2 | a0001 | c0002 | t0004 | g0002 | EAS | CHS | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG00423 | hp1 | a0001 | c0001 | t0002 | g0120 | EAS | CHS | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG00423 | hp2 | a0001 | c0002 | t0001 | g0038 | EAS | CHS | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG00438 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG00438 | hp2 | a0001 | c0002 | t0004 | g0002 | EAS | CHS | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG00544 | hp1 | a0001 | c0002 | t0001 | g0214 | EAS | CHS | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG00544 | hp2 | a0001 | c0002 | t0001 | g0170 | EAS | CHS | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG00558 | hp1 | a0001 | c0002 | t0001 | g0149 | EAS | CHS | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG00558 | hp2 | a0001 | c0001 | t0003 | g0262 | EAS | CHS | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG00609 | hp1 | a0001 | c0001 | t0002 | g0123 | EAS | CHS | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG00609 | hp2 | a0001 | c0002 | t0001 | g0160 | EAS | CHS | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG00621 | hp1 | a0001 | c0001 | t0003 | g0011 | EAS | CHS | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG00621 | hp2 | a0001 | c0001 | t0002 | g0125 | EAS | CHS | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG00639 | hp1 | a0001 | c0002 | t0001 | g0196 | AMR | PUR | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG00639 | hp2 | a0001 | c0001 | t0002 | g0032 | AMR | PUR | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG00642 | hp1 | a0001 | c0001 | t0005 | g0233 | AMR | PUR | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG00642 | hp2 | a0001 | c0001 | t0005 | g0227 | AMR | PUR | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG00733 | hp1 | a0001 | c0002 | t0011 | g0210 | AMR | PUR | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG00733 | hp2 | a0001 | c0001 | t0002 | g0137 | AMR | PUR | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG00735 | hp1 | a0001 | c0001 | t0005 | g0283 | AMR | PUR | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG00735 | hp2 | a0001 | c0001 | t0003 | g0218 | AMR | PUR | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG00738 | hp1 | a0001 | c0002 | t0004 | g0073 | AMR | PUR | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG00738 | hp2 | a0001 | c0001 | t0003 | g0050 | AMR | PUR | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG00741 | hp1 | a0001 | c0001 | t0002 | g0136 | AMR | PUR | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG00741 | hp2 | a0001 | c0001 | t0003 | g0065 | AMR | PUR | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG01069 | hp1 | a0001 | c0001 | t0005 | g0043 | AMR | PUR | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG01069 | hp2 | a0001 | c0002 | t0001 | g0016 | AMR | PUR | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG01070 | hp1 | a0001 | c0001 | t0005 | g0042 | AMR | PUR | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG01070 | hp2 | a0001 | c0002 | t0008 | g0034 | AMR | PUR | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG01071 | hp1 | a0001 | c0002 | t0008 | g0034 | AMR | PUR | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG01071 | hp2 | a0001 | c0002 | t0001 | g0016 | AMR | PUR | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG01081 | hp1 | a0001 | c0002 | t0004 | g0084 | AMR | PUR | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG01081 | hp2 | a0001 | c0001 | t0005 | g0044 | AMR | PUR | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG01099 | hp1 | a0001 | c0001 | t0002 | g0032 | AMR | PUR | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG01099 | hp2 | a0001 | c0002 | t0001 | g0187 | AMR | PUR | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG01106 | hp1 | a0001 | c0001 | t0005 | g0236 | AMR | PUR | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG01106 | hp2 | a0001 | c0001 | t0003 | g0050 | AMR | PUR | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG01109 | hp1 | a0001 | c0001 | t0003 | g0244 | AMR | PUR | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG01109 | hp2 | a0001 | c0002 | t0004 | g0006 | AMR | PUR | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG01167 | hp1 | a0001 | c0001 | t0002 | g0017 | AMR | PUR | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG01167 | hp2 | a0001 | c0001 | t0003 | g0047 | AMR | PUR | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG01168 | hp1 | a0001 | c0002 | t0004 | g0086 | AMR | PUR | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG01168 | hp2 | a0001 | c0001 | t0005 | g0044 | AMR | PUR | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG01169 | hp1 | a0001 | c0001 | t0002 | g0017 | AMR | PUR | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG01169 | hp2 | a0001 | c0001 | t0005 | g0235 | AMR | PUR | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG01175 | hp1 | a0001 | c0002 | t0001 | g0152 | AMR | PUR | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG01175 | hp2 | a0001 | c0001 | t0003 | g0012 | AMR | PUR | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG01243 | hp1 | a0004 | c0005 | t0005 | g0273 | AMR | PUR | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG01243 | hp2 | a0001 | c0001 | t0003 | g0264 | AMR | PUR | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG01255 | hp1 | a0001 | c0001 | t0005 | g0282 | AMR | CLM | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG01255 | hp2 | a0001 | c0001 | t0003 | g0219 | AMR | CLM | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG01256 | hp1 | a0001 | c0002 | t0001 | g0201 | AMR | CLM | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG01256 | hp2 | a0001 | c0002 | t0004 | g0006 | AMR | CLM | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG01257 | hp1 | a0001 | c0002 | t0004 | g0006 | AMR | CLM | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG01257 | hp2 | a0001 | c0001 | t0003 | g0014 | AMR | CLM | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG01258 | hp1 | a0001 | c0001 | t0003 | g0014 | AMR | CLM | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG01258 | hp2 | a0001 | c0002 | t0004 | g0006 | AMR | CLM | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG01346 | hp1 | a0001 | c0002 | t0001 | g0153 | AMR | CLM | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG01346 | hp2 | a0001 | c0001 | t0002 | g0138 | AMR | CLM | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG01358 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG01358 | hp2 | a0001 | c0002 | t0004 | g0089 | AMR | CLM | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG01433 | hp1 | a0001 | c0001 | t0005 | g0230 | AMR | CLM | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG01433 | hp2 | a0001 | c0002 | t0001 | g0106 | AMR | CLM | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG01496 | hp1 | a0001 | c0001 | t0005 | g0042 | AMR | CLM | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0135 | AMR | CLM | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG01515 | hp1 | a0001 | c0002 | t0001 | g0161 | EUR | IBS | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG01515 | hp2 | a0001 | c0001 | t0003 | g0266 | EUR | IBS | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG01516 | hp1 | a0001 | c0001 | t0002 | g0003 | EUR | IBS | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG01516 | hp2 | a0001 | c0001 | t0003 | g0012 | EUR | IBS | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG01517 | hp1 | a0001 | c0002 | t0001 | g0191 | EUR | IBS | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG01517 | hp2 | a0001 | c0001 | t0003 | g0012 | EUR | IBS | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG01891 | hp1 | a0001 | c0001 | t0005 | g0043 | AFR | ACB | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG01891 | hp2 | a0001 | c0001 | t0005 | g0229 | AFR | ACB | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG01928 | hp1 | a0001 | c0001 | t0002 | g0147 | AMR | PEL | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG01928 | hp2 | a0001 | c0002 | t0004 | g0079 | AMR | PEL | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG01934 | hp1 | a0001 | c0001 | t0002 | g0008 | AMR | PEL | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG01934 | hp2 | a0001 | c0002 | t0001 | g0200 | AMR | PEL | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG01943 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG01943 | hp2 | a0001 | c0002 | t0004 | g0066 | AMR | PEL | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG01952 | hp1 | a0001 | c0002 | t0001 | g0207 | AMR | PEL | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG01952 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | PEL | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG01978 | hp1 | a0001 | c0001 | t0005 | g0237 | AMR | PEL | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG01978 | hp2 | a0001 | c0001 | t0003 | g0014 | AMR | PEL | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG01993 | hp1 | a0001 | c0001 | t0002 | g0121 | AMR | PEL | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG01993 | hp2 | a0001 | c0001 | t0003 | g0012 | AMR | PEL | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG02015 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | KHV | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG02015 | hp2 | a0001 | c0001 | t0005 | g0290 | EAS | KHV | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG02027 | hp1 | a0001 | c0001 | t0003 | g0269 | EAS | KHV | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG02027 | hp2 | a0001 | c0002 | t0001 | g0169 | EAS | KHV | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG02040 | hp1 | a0001 | c0002 | t0004 | g0088 | EAS | KHV | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG02040 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | KHV | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG02055 | hp1 | a0001 | c0002 | t0006 | g0108 | AFR | ACB | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG02055 | hp2 | a0001 | c0001 | t0005 | g0287 | AFR | ACB | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG02071 | hp1 | a0001 | c0002 | t0001 | g0054 | EAS | KHV | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG02071 | hp2 | a0001 | c0001 | t0005 | g0298 | EAS | KHV | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG02074 | hp1 | a0001 | c0002 | t0001 | g0183 | EAS | KHV | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG02074 | hp2 | a0001 | c0001 | t0003 | g0255 | EAS | KHV | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG02083 | hp1 | a0001 | c0001 | t0003 | g0249 | EAS | KHV | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG02083 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | KHV | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG02129 | hp1 | a0001 | c0001 | t0002 | g0118 | EAS | KHV | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG02129 | hp2 | a0001 | c0002 | t0001 | g0185 | EAS | KHV | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG02132 | hp1 | a0001 | c0002 | t0001 | g0116 | EAS | KHV | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG02132 | hp2 | a0001 | c0001 | t0003 | g0047 | EAS | KHV | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG02155 | hp1 | a0001 | c0002 | t0004 | g0083 | EAS | CDX | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG02155 | hp2 | a0001 | c0002 | t0001 | g0176 | EAS | CDX | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG02165 | hp1 | a0001 | c0002 | t0001 | g0195 | EAS | CDX | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0035 | EAS | CDX | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG02257 | hp1 | a0001 | c0001 | t0003 | g0221 | AFR | ACB | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG02257 | hp2 | a0001 | c0001 | t0005 | g0231 | AFR | ACB | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG02258 | hp1 | a0001 | c0001 | t0005 | g0296 | AFR | ACB | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG02258 | hp2 | a0001 | c0002 | t0006 | g0102 | AFR | ACB | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG02273 | hp1 | a0001 | c0001 | t0002 | g0008 | AMR | PEL | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG02273 | hp2 | a0001 | c0001 | t0003 | g0246 | AMR | PEL | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG02280 | hp1 | a0001 | c0002 | t0006 | g0057 | AFR | ACB | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG02280 | hp2 | a0001 | c0001 | t0005 | g0232 | AFR | ACB | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG02300 | hp1 | a0001 | c0002 | t0004 | g0069 | AMR | PEL | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG02300 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | PEL | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG02523 | hp1 | a0001 | c0002 | t0001 | g0208 | EAS | KHV | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG02523 | hp2 | a0001 | c0002 | t0001 | g0209 | EAS | KHV | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG02602 | hp1 | a0001 | c0001 | t0003 | g0048 | SAS | PJL | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG02615 | hp1 | a0001 | c0002 | t0001 | g0110 | AFR | GWD | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG02615 | hp2 | a0001 | c0001 | t0005 | g0052 | AFR | GWD | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG02622 | hp1 | a0001 | c0002 | t0001 | g0113 | AFR | GWD | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG02622 | hp2 | a0001 | c0002 | t0006 | g0100 | AFR | GWD | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG02630 | hp1 | a0001 | c0001 | t0005 | g0274 | AFR | GWD | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG02630 | hp2 | a0001 | c0002 | t0001 | g0114 | AFR | GWD | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG02647 | hp1 | a0001 | c0001 | t0003 | g0041 | AFR | GWD | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG02647 | hp2 | a0001 | c0002 | t0001 | g0105 | AFR | GWD | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG02683 | hp1 | a0001 | c0001 | t0005 | g0277 | SAS | PJL | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG02683 | hp2 | a0001 | c0001 | t0005 | g0224 | SAS | PJL | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG02735 | hp1 | a0001 | c0001 | t0005 | g0228 | SAS | PJL | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG02735 | hp2 | a0001 | c0002 | t0004 | g0080 | SAS | PJL | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG02738 | hp1 | a0001 | c0002 | t0004 | g0019 | SAS | PJL | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG02738 | hp2 | a0001 | c0001 | t0003 | g0049 | SAS | PJL | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG02809 | hp1 | a0001 | c0002 | t0004 | g0024 | AFR | GWD | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG02809 | hp2 | a0001 | c0002 | t0006 | g0060 | AFR | GWD | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG02818 | hp1 | a0001 | c0002 | t0001 | g0111 | AFR | GWD | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG02818 | hp2 | a0001 | c0001 | t0005 | g0284 | AFR | GWD | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG02886 | hp1 | a0001 | c0001 | t0003 | g0239 | AFR | GWD | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG02886 | hp2 | a0001 | c0002 | t0004 | g0071 | AFR | GWD | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG02895 | hp1 | a0001 | c0002 | t0009 | g0028 | AFR | GWD | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG02895 | hp2 | a0001 | c0001 | t0005 | g0280 | AFR | GWD | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG02896 | hp1 | a0001 | c0002 | t0009 | g0028 | AFR | GWD | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG02896 | hp2 | a0001 | c0001 | t0003 | g0041 | AFR | GWD | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG02965 | hp1 | a0001 | c0002 | t0001 | g0194 | AFR | ESN | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG02965 | hp2 | a0001 | c0001 | t0005 | g0051 | AFR | ESN | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG02970 | hp1 | a0001 | c0002 | t0004 | g0095 | AFR | ESN | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG02970 | hp2 | a0001 | c0001 | t0005 | g0294 | AFR | ESN | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG02976 | hp1 | a0001 | c0001 | t0005 | g0293 | AFR | ESN | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG02976 | hp2 | a0001 | c0002 | t0006 | g0058 | AFR | ESN | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG03098 | hp1 | a0001 | c0002 | t0004 | g0098 | AFR | MSL | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG03098 | hp2 | a0001 | c0002 | t0001 | g0166 | AFR | MSL | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG03130 | hp1 | a0001 | c0002 | t0004 | g0097 | AFR | ESN | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG03130 | hp2 | a0001 | c0001 | t0005 | g0300 | AFR | ESN | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG03139 | hp1 | a0001 | c0001 | t0003 | g0260 | AFR | ESN | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG03139 | hp2 | a0001 | c0001 | t0005 | g0225 | AFR | ESN | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG03195 | hp1 | a0001 | c0002 | t0006 | g0026 | AFR | ESN | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG03195 | hp2 | a0001 | c0001 | t0007 | g0040 | AFR | ESN | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG03209 | hp1 | a0001 | c0002 | t0004 | g0024 | AFR | MSL | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG03209 | hp2 | a0001 | c0002 | t0006 | g0109 | AFR | MSL | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG03239 | hp1 | a0001 | c0001 | t0003 | g0265 | SAS | PJL | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG03239 | hp2 | a0001 | c0001 | t0005 | g0234 | SAS | PJL | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG03453 | hp1 | a0001 | c0002 | t0006 | g0026 | AFR | MSL | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG03453 | hp2 | a0001 | c0002 | t0001 | g0027 | AFR | MSL | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG03486 | hp1 | a0001 | c0002 | t0006 | g0056 | AFR | MSL | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG03486 | hp2 | a0001 | c0002 | t0001 | g0029 | AFR | MSL | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG03491 | hp1 | a0003 | c0004 | t0004 | g0020 | SAS | PJL | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG03491 | hp2 | a0001 | c0001 | t0005 | g0297 | SAS | PJL | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG03492 | hp1 | a0003 | c0004 | t0004 | g0020 | SAS | PJL | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG03492 | hp2 | a0001 | c0001 | t0002 | g0131 | SAS | PJL | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG03516 | hp1 | a0001 | c0001 | t0003 | g0259 | AFR | ESN | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG03516 | hp2 | a0001 | c0002 | t0006 | g0101 | AFR | ESN | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG03540 | hp1 | a0001 | c0001 | t0005 | g0288 | AFR | GWD | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG03540 | hp2 | a0001 | c0001 | t0005 | g0275 | AFR | GWD | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG03579 | hp1 | a0001 | c0001 | t0005 | g0061 | AFR | MSL | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG03579 | hp2 | a0001 | c0002 | t0004 | g0023 | AFR | MSL | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG03669 | hp1 | a0001 | c0002 | t0001 | g0175 | SAS | PJL | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG03669 | hp2 | a0001 | c0001 | t0003 | g0049 | SAS | PJL | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG03688 | hp1 | a0001 | c0001 | t0005 | g0279 | SAS | STU | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG03688 | hp2 | a0001 | c0001 | t0003 | g0270 | SAS | STU | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG03704 | hp1 | a0001 | c0001 | t0005 | g0278 | SAS | PJL | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG03704 | hp2 | a0001 | c0001 | t0002 | g0117 | SAS | PJL | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG03710 | hp1 | a0001 | c0001 | t0003 | g0048 | SAS | PJL | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG03710 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG03834 | hp1 | a0001 | c0001 | t0002 | g0030 | SAS | BEB | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG03834 | hp2 | a0001 | c0001 | t0003 | g0261 | SAS | BEB | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG03927 | hp1 | a0001 | c0002 | t0001 | g0055 | SAS | BEB | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG03927 | hp2 | a0001 | c0002 | t0004 | g0019 | SAS | BEB | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG03942 | hp1 | a0003 | c0004 | t0004 | g0078 | SAS | BEB | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG03942 | hp2 | a0001 | c0001 | t0003 | g0258 | SAS | BEB | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG04115 | hp1 | a0001 | c0002 | t0001 | g0104 | SAS | STU | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG04115 | hp2 | a0001 | c0001 | t0005 | g0295 | SAS | STU | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG04184 | hp1 | a0001 | c0002 | t0001 | g0155 | SAS | BEB | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG04184 | hp2 | a0001 | c0001 | t0003 | g0254 | SAS | BEB | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG04199 | hp1 | a0001 | c0002 | t0004 | g0081 | SAS | STU | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG04199 | hp2 | a0001 | c0001 | t0002 | g0030 | SAS | STU | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG04204 | hp1 | a0001 | c0002 | t0004 | g0067 | SAS | STU | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG04204 | hp2 | a0001 | c0001 | t0005 | g0289 | SAS | STU | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG04228 | hp1 | a0001 | c0001 | t0003 | g0220 | SAS | STU | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG04228 | hp2 | a0001 | c0002 | t0004 | g0076 | SAS | STU | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA18522 | hp1 | a0001 | c0006 | t0001 | g0027 | AFR | YRI | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA18522 | hp2 | a0001 | c0002 | t0004 | g0096 | AFR | YRI | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA18612 | hp1 | a0001 | c0001 | t0003 | g0271 | EAS | CHB | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA18612 | hp2 | a0001 | c0002 | t0004 | g0007 | EAS | CHB | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA18747 | hp1 | a0001 | c0001 | t0005 | g0291 | EAS | CHB | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA18747 | hp2 | a0001 | c0001 | t0003 | g0053 | EAS | CHB | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA18906 | hp1 | a0001 | c0002 | t0006 | g0301 | AFR | YRI | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA18906 | hp2 | a0001 | c0002 | t0001 | g0112 | AFR | YRI | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA18939 | hp1 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA18939 | hp2 | a0001 | c0002 | t0004 | g0092 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA18940 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA18940 | hp2 | a0001 | c0002 | t0001 | g0174 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA18941 | hp1 | a0001 | c0002 | t0001 | g0177 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA18941 | hp2 | a0001 | c0001 | t0003 | g0251 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA18942 | hp1 | a0001 | c0002 | t0004 | g0090 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA18942 | hp2 | a0001 | c0002 | t0001 | g0037 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA18943 | hp1 | a0001 | c0002 | t0004 | g0085 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA18943 | hp2 | a0001 | c0002 | t0001 | g0168 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA18944 | hp1 | a0001 | c0001 | t0002 | g0140 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA18944 | hp2 | a0001 | c0002 | t0001 | g0180 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA18945 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA18945 | hp2 | a0001 | c0001 | t0005 | g0299 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA18946 | hp1 | a0001 | c0001 | t0003 | g0240 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA18946 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA18949 | hp1 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA18949 | hp2 | a0001 | c0002 | t0001 | g0159 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA18951 | hp1 | a0001 | c0002 | t0001 | g0182 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA18951 | hp2 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA18953 | hp1 | a0001 | c0001 | t0003 | g0046 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA18953 | hp2 | a0002 | c0003 | t0001 | g0205 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA18954 | hp1 | a0001 | c0002 | t0004 | g0082 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA18954 | hp2 | a0001 | c0002 | t0001 | g0198 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA18956 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA18956 | hp2 | a0001 | c0002 | t0004 | g0074 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA18957 | hp1 | a0001 | c0002 | t0004 | g0002 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA18957 | hp2 | a0002 | c0003 | t0001 | g0193 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA18959 | hp1 | a0001 | c0002 | t0004 | g0007 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA18959 | hp2 | a0001 | c0002 | t0001 | g0172 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA18960 | hp1 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA18960 | hp2 | a0001 | c0002 | t0004 | g0087 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA18961 | hp1 | a0001 | c0001 | t0003 | g0241 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA18961 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA18962 | hp1 | a0001 | c0001 | t0002 | g0145 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA18962 | hp2 | a0001 | c0002 | t0001 | g0211 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA18964 | hp1 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA18964 | hp2 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA18965 | hp1 | a0001 | c0001 | t0005 | g0015 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA18965 | hp2 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA18966 | hp1 | a0001 | c0002 | t0001 | g0197 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA18966 | hp2 | a0001 | c0001 | t0003 | g0247 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA18968 | hp1 | a0001 | c0002 | t0004 | g0025 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA18968 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA18970 | hp1 | a0001 | c0002 | t0004 | g0007 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA18970 | hp2 | a0001 | c0001 | t0003 | g0045 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA18971 | hp1 | a0001 | c0001 | t0003 | g0250 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA18971 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA18973 | hp1 | a0001 | c0002 | t0001 | g0203 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA18973 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA18975 | hp1 | a0001 | c0002 | t0001 | g0212 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA18975 | hp2 | a0001 | c0002 | t0004 | g0022 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA18977 | hp1 | a0001 | c0001 | t0002 | g0134 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA18977 | hp2 | a0001 | c0002 | t0001 | g0039 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA18978 | hp1 | a0001 | c0002 | t0004 | g0091 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA18978 | hp2 | a0001 | c0002 | t0001 | g0164 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA18981 | hp1 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA18981 | hp2 | a0001 | c0002 | t0001 | g0157 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA18983 | hp1 | a0001 | c0002 | t0001 | g0181 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA18983 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA18984 | hp1 | a0001 | c0002 | t0001 | g0188 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA18984 | hp2 | a0001 | c0001 | t0003 | g0253 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA18988 | hp1 | a0001 | c0002 | t0004 | g0077 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA18988 | hp2 | a0001 | c0001 | t0002 | g0128 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA18989 | hp1 | a0001 | c0001 | t0005 | g0015 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA18989 | hp2 | a0002 | c0003 | t0001 | g0013 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA18990 | hp1 | a0001 | c0002 | t0008 | g0139 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA18990 | hp2 | a0001 | c0001 | t0002 | g0142 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA18992 | hp1 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA18992 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA18993 | hp1 | a0001 | c0002 | t0001 | g0115 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA18993 | hp2 | a0001 | c0001 | t0005 | g0015 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA18994 | hp1 | a0001 | c0002 | t0001 | g0199 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA18994 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA18995 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA18995 | hp2 | a0001 | c0002 | t0001 | g0154 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA18997 | hp1 | a0001 | c0001 | t0005 | g0292 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA18997 | hp2 | a0001 | c0002 | t0001 | g0148 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA18998 | hp1 | a0001 | c0001 | t0002 | g0141 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA18998 | hp2 | a0001 | c0001 | t0003 | g0045 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA18999 | hp1 | a0001 | c0002 | t0004 | g0021 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA18999 | hp2 | a0002 | c0003 | t0001 | g0202 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA19000 | hp1 | a0001 | c0002 | t0001 | g0173 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA19000 | hp2 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA19001 | hp1 | a0001 | c0001 | t0003 | g0248 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA19001 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA19002 | hp1 | a0001 | c0002 | t0001 | g0192 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA19002 | hp2 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA19003 | hp1 | a0002 | c0003 | t0001 | g0013 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA19003 | hp2 | a0001 | c0001 | t0002 | g0143 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA19006 | hp1 | a0002 | c0003 | t0001 | g0150 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA19006 | hp2 | a0001 | c0001 | t0002 | g0124 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA19007 | hp1 | a0001 | c0002 | t0010 | g0215 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA19007 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA19010 | hp1 | a0001 | c0001 | t0002 | g0146 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA19010 | hp2 | a0001 | c0002 | t0001 | g0213 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA19011 | hp1 | a0001 | c0001 | t0003 | g0268 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA19011 | hp2 | a0002 | c0003 | t0001 | g0038 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA19012 | hp1 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA19012 | hp2 | a0001 | c0002 | t0001 | g0039 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA19030 | hp1 | a0001 | c0002 | t0001 | g0107 | AFR | LWK | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA19030 | hp2 | a0001 | c0001 | t0005 | g0051 | AFR | LWK | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA19043 | hp1 | a0001 | c0001 | t0003 | g0238 | AFR | LWK | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA19043 | hp2 | a0001 | c0001 | t0007 | g0217 | AFR | LWK | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA19056 | hp1 | a0001 | c0001 | t0003 | g0242 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA19056 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA19057 | hp1 | a0001 | c0002 | t0001 | g0206 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA19057 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA19058 | hp1 | a0001 | c0002 | t0004 | g0018 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA19058 | hp2 | a0002 | c0003 | t0001 | g0013 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA19063 | hp1 | a0001 | c0002 | t0001 | g0179 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA19063 | hp2 | a0001 | c0002 | t0004 | g0018 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA19064 | hp1 | a0001 | c0002 | t0004 | g0002 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA19064 | hp2 | a0001 | c0002 | t0001 | g0158 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA19065 | hp1 | a0001 | c0002 | t0001 | g0186 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA19065 | hp2 | a0001 | c0002 | t0004 | g0025 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA19066 | hp1 | a0001 | c0002 | t0004 | g0022 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA19066 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA19068 | hp1 | a0001 | c0002 | t0001 | g0190 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA19068 | hp2 | a0001 | c0002 | t0004 | g0021 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA19070 | hp1 | a0001 | c0002 | t0004 | g0007 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA19070 | hp2 | a0002 | c0003 | t0001 | g0189 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA19072 | hp1 | a0001 | c0001 | t0003 | g0216 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA19072 | hp2 | a0001 | c0002 | t0004 | g0063 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA19074 | hp1 | a0001 | c0002 | t0004 | g0094 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA19074 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA19075 | hp1 | a0001 | c0002 | t0004 | g0002 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA19075 | hp2 | a0001 | c0002 | t0001 | g0037 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA19078 | hp1 | a0001 | c0001 | t0003 | g0046 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA19078 | hp2 | a0001 | c0002 | t0001 | g0167 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA19081 | hp1 | a0001 | c0002 | t0001 | g0163 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA19081 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA19084 | hp1 | a0001 | c0001 | t0002 | g0122 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA19084 | hp2 | a0001 | c0001 | t0003 | g0252 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA19086 | hp1 | a0001 | c0001 | t0002 | g0144 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA19086 | hp2 | a0001 | c0002 | t0001 | g0162 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA19087 | hp1 | a0001 | c0001 | t0003 | g0263 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA19087 | hp2 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA19088 | hp1 | a0001 | c0002 | t0001 | g0184 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA19088 | hp2 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA19089 | hp1 | a0001 | c0002 | t0004 | g0075 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA19089 | hp2 | a0001 | c0002 | t0001 | g0178 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA19090 | hp1 | a0001 | c0002 | t0004 | g0093 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA19090 | hp2 | a0002 | c0003 | t0001 | g0165 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA19091 | hp1 | a0001 | c0002 | t0001 | g0171 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA19091 | hp2 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA19240 | hp1 | a0001 | c0001 | t0005 | g0052 | AFR | YRI | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA19240 | hp2 | a0001 | c0002 | t0006 | g0099 | AFR | YRI | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA20129 | hp1 | a0001 | c0001 | t0007 | g0062 | AFR | ASW | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA20129 | hp2 | a0001 | c0002 | t0004 | g0023 | AFR | ASW | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA20752 | hp1 | a0001 | c0002 | t0004 | g0064 | EUR | TSI | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA20752 | hp2 | a0001 | c0001 | t0003 | g0267 | EUR | TSI | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA20805 | hp1 | a0001 | c0002 | t0001 | g0151 | EUR | TSI | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA20805 | hp2 | a0001 | c0001 | t0005 | g0223 | EUR | TSI | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA20905 | hp1 | a0001 | c0001 | t0003 | g0256 | SAS | GIH | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA20905 | hp2 | a0001 | c0002 | t0004 | g0068 | SAS | GIH | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG02109 | hp1 | a0001 | c0001 | t0005 | g0276 | AFR | ACB | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG02109 | hp2 | a0001 | c0001 | t0005 | g0226 | AFR | ACB | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG02486 | hp1 | a0001 | c0002 | t0004 | g0072 | AFR | ACB | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG02486 | hp2 | a0001 | c0002 | t0006 | g0059 | AFR | ACB | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG02559 | hp1 | a0001 | c0001 | t0003 | g0245 | AFR | ACB | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG02559 | hp2 | a0001 | c0001 | t0007 | g0040 | AFR | ACB | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG03471 | hp1 | a0001 | c0001 | t0005 | g0281 | AFR | MSL | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
HG03471 | hp2 | a0001 | c0001 | t0003 | g0222 | AFR | MSL | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA18955 | hp1 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA18955 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA20300 | hp1 | a0001 | c0002 | t0008 | g0130 | AFR | USA | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA20300 | hp2 | a0001 | c0002 | t0001 | g0029 | AFR | USA | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA21309 | hp1 | a0001 | c0001 | t0003 | g0257 | AFR | LWK | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
NA21309 | hp2 | a0001 | c0002 | t0006 | g0103 | AFR | LWK | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0005 | g0285 | REF | REF | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0005 | g0272 | REF | REF | TES_chr7_116205539_116263783 | TES | chr7 | 116205539 | 116263783 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:116234536
|
G | A | 1 | a0004 | 1 | HG01243.hp1 | missense_variant&splice_region_variant | MODERATE | c.30G>A | p.Met10Ile | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/7 | 199/2736 | 30/1266 | 10/421 | chr7 | 116234536 | ||
chr7:116250456
|
C | T | 1 | a0002 | 10 | NA18953.hp2 NA18957.hp2 NA18989.hp2 others(7): Show |
missense_variant | MODERATE | c.662C>T | p.Ala221Val | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 4/7 | 831/2736 | 662/1266 | 221/421 | chr7 | 116250456 | ||
chr7:116257352
|
A | G | 1 | a0003 | 3 | HG03491.hp1 HG03492.hp1 HG03942.hp1 |
missense_variant | MODERATE | c.1136A>G | p.Asn379Ser | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 7/7 | 1305/2736 | 1136/1266 | 379/421 | chr7 | 116257352 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:116257338
|
G | C | 3 | a0001c0002a0002c0003a0003c0004 | 185 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(182): Show |
synonymous_variant | LOW | c.1122G>C | p.Arg374Arg | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 7/7 | 1291/2736 | 1122/1266 | 374/421 | chr7 | 116257338 | ||
chr7:116257338
|
G | T | 1 | a0001c0006 | 1 | NA18522.hp1 | synonymous_variant | LOW | c.1122G>T | p.Arg374Arg | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 7/7 | 1291/2736 | 1122/1266 | 374/421 | chr7 | 116257338 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:116210588
|
G | C | 1 | a0001c0002t0009 | 2 | HG02895.hp1 HG02896.hp1 |
5_prime_UTR_variant | MODIFIER | c.-120G>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/7 | 120 | chr7 | 116210588 | |||||
chr7:116210621
|
C | T | 2 | a0001c0001t0002a0001c0002t0008 | 75 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(72): Show |
5_prime_UTR_variant | MODIFIER | c.-87C>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/7 | 87 | chr7 | 116210621 | |||||
chr7:116257569
|
G | A | 1 | a0001c0002t0010 | 1 | NA19007.hp1 | 3_prime_UTR_variant | MODIFIER | c.*87G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 7/7 | 87 | chr7 | 116257569 | |||||
chr7:116257638
|
AT | A | 10 | a0001c0002t0001a0001c0002t0004a0001c0002t0006others(7): Show | 186 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(183): Show |
3_prime_UTR_variant | MODIFIER | c.*164delT | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 7/7 | 164 | INFO_REALIGN_3_PRIME | chr7 | 116257638 | ||||
chr7:116257738
|
T | TAG | 10 | a0001c0002t0001a0001c0002t0004a0001c0002t0006others(7): Show | 186 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(183): Show |
3_prime_UTR_variant | MODIFIER | c.*256_*257insAG | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 7/7 | 257 | chr7 | 116257738 | |||||
chr7:116257817
|
A | G | 10 | a0001c0002t0001a0001c0002t0004a0001c0002t0006others(7): Show | 186 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(183): Show |
3_prime_UTR_variant | MODIFIER | c.*335A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 7/7 | 335 | chr7 | 116257817 | |||||
chr7:116257830
|
C | T | 10 | a0001c0002t0001a0001c0002t0004a0001c0002t0006others(7): Show | 186 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(183): Show |
3_prime_UTR_variant | MODIFIER | c.*348C>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 7/7 | 348 | chr7 | 116257830 | |||||
chr7:116257872
|
AAAG | A | 7 | a0001c0002t0001a0001c0002t0008a0001c0002t0009others(4): Show | 107 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(104): Show |
3_prime_UTR_variant | MODIFIER | c.*393_*395delGAA | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 7/7 | 393 | INFO_REALIGN_3_PRIME | chr7 | 116257872 | ||||
chr7:116257915
|
T | G | 1 | a0001c0002t0011 | 1 | HG00733.hp1 | 3_prime_UTR_variant | MODIFIER | c.*433T>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 7/7 | 433 | chr7 | 116257915 | |||||
chr7:116258123
|
G | C | 10 | a0001c0002t0001a0001c0002t0004a0001c0002t0006others(7): Show | 186 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(183): Show |
3_prime_UTR_variant | MODIFIER | c.*641G>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 7/7 | 641 | chr7 | 116258123 | |||||
chr7:116258190
|
AT | A | 1 | a0001c0001t0003 | 67 | HG00140.hp2 HG00558.hp2 HG00621.hp1 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*721delT | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 7/7 | 721 | INFO_REALIGN_3_PRIME | chr7 | 116258190 | ||||
chr7:116258190
|
ATT | A | 8 | a0001c0002t0001a0001c0002t0006a0001c0002t0008others(5): Show | 122 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(119): Show |
3_prime_UTR_variant | MODIFIER | c.*720_*721delTT | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 7/7 | 720 | INFO_REALIGN_3_PRIME | chr7 | 116258190 | ||||
chr7:116258190
|
ATTT | A | 2 | a0001c0002t0004a0003c0004t0004 | 64 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(61): Show |
3_prime_UTR_variant | MODIFIER | c.*719_*721delTTT | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 7/7 | 719 | INFO_REALIGN_3_PRIME | chr7 | 116258190 | ||||
chr7:116258388
|
G | C | 10 | a0001c0002t0001a0001c0002t0004a0001c0002t0006others(7): Show | 186 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(183): Show |
3_prime_UTR_variant | MODIFIER | c.*906G>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 7/7 | 906 | chr7 | 116258388 | |||||
chr7:116258514
|
G | T | 1 | a0001c0001t0007 | 4 | HG02559.hp2 HG03195.hp2 NA19043.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1032G>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 7/7 | 1032 | chr7 | 116258514 | |||||
chr7:116258561
|
AT | A | 10 | a0001c0002t0001a0001c0002t0004a0001c0002t0006others(7): Show | 186 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(183): Show |
3_prime_UTR_variant | MODIFIER | c.*1087delT | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 7/7 | 1087 | INFO_REALIGN_3_PRIME | chr7 | 116258561 | ||||
chr7:116258656
|
A | G | 1 | a0001c0001t0003 | 67 | HG00140.hp2 HG00558.hp2 HG00621.hp1 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*1174A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 7/7 | 1174 | chr7 | 116258656 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:116210756
|
G | A | 1 | a0001c0002t0001g0016 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.27+22G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116210756 | ||||||
chr7:116210764
|
T | C | 1 | a0001c0001t0003g0053 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.27+30T>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116210764 | ||||||
chr7:116210779
|
G | C | 1 | a0001c0002t0001g0054 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.27+45G>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116210779 | ||||||
chr7:116210861
|
C | T | 1 | a0001c0002t0006g0301 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.27+127C>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116210861 | ||||||
chr7:116210883
|
T | A | 1 | a0001c0002t0001g0055 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.27+149T>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116210883 | ||||||
chr7:116210883
|
T | C | 202 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0004others(199): Show | 263 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(260): Show |
intron_variant | MODIFIER | c.27+149T>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116210883 | ||||||
chr7:116210983
|
C | G | 2 | a0001c0001t0007g0040a0001c0001t0007g0217 | 3 | HG02559.hp2 HG03195.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.27+249C>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116210983 | ||||||
chr7:116211123
|
G | A | 1 | a0001c0001t0002g0017 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.27+389G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116211123 | ||||||
chr7:116211433
|
T | C | 202 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0004others(199): Show | 263 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(260): Show |
intron_variant | MODIFIER | c.27+699T>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116211433 | ||||||
chr7:116211437
|
C | A | 4 | a0001c0002t0006g0056a0001c0002t0006g0057a0001c0002t0006g0058others(1): Show | 4 | HG02280.hp1 HG02486.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.27+703C>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116211437 | ||||||
chr7:116211649
|
G | C | 5 | a0001c0001t0005g0061a0001c0001t0007g0040a0001c0001t0007g0062others(2): Show | 6 | HG02559.hp2 HG02809.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.27+915G>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116211649 | ||||||
chr7:116211809
|
GA | G | 150 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0004others(147): Show | 192 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(189): Show |
intron_variant | MODIFIER | c.27+1079delA | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 116211809 | |||||
chr7:116211927
|
G | A | 271 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0004others(268): Show | 350 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(347): Show |
intron_variant | MODIFIER | c.27+1193G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116211927 | ||||||
chr7:116212077
|
C | T | 139 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0004others(136): Show | 180 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(177): Show |
intron_variant | MODIFIER | c.27+1343C>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116212077 | ||||||
chr7:116212106
|
C | G | 202 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0004others(199): Show | 263 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(260): Show |
intron_variant | MODIFIER | c.27+1372C>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116212106 | ||||||
chr7:116212459
|
A | T | 1 | a0001c0001t0005g0300 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.27+1725A>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116212459 | ||||||
chr7:116212727
|
T | C | 1 | a0001c0002t0001g0104 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.27+1993T>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116212727 | ||||||
chr7:116212792
|
A | G | 125 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0004others(122): Show | 164 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(161): Show |
intron_variant | MODIFIER | c.27+2058A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116212792 | ||||||
chr7:116212915
|
T | C | 1 | a0001c0001t0003g0218 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.27+2181T>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116212915 | ||||||
chr7:116212971
|
A | G | 1 | a0001c0002t0010g0215 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.27+2237A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116212971 | ||||||
chr7:116213012
|
C | T | 150 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0004others(147): Show | 192 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(189): Show |
intron_variant | MODIFIER | c.27+2278C>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116213012 | ||||||
chr7:116213046
|
T | C | 52 | a0001c0001t0003g0065a0001c0001t0005g0061a0001c0001t0007g0040others(49): Show | 71 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.27+2312T>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116213046 | ||||||
chr7:116213055
|
T | A | 1 | a0001c0002t0001g0115 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.27+2321T>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116213055 | ||||||
chr7:116213214
|
C | T | 1 | a0001c0002t0006g0301 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.27+2480C>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116213214 | ||||||
chr7:116213449
|
A | C | 202 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0004others(199): Show | 263 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(260): Show |
intron_variant | MODIFIER | c.27+2715A>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116213449 | ||||||
chr7:116213537
|
A | C | 1 | a0001c0002t0001g0214 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.27+2803A>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116213537 | ||||||
chr7:116213565
|
C | T | 4 | a0001c0001t0005g0061a0001c0001t0007g0040a0001c0001t0007g0062others(1): Show | 5 | HG02559.hp2 HG03195.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.27+2831C>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116213565 | ||||||
chr7:116213916
|
T | A | 1 | a0001c0002t0001g0116 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.27+3182T>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116213916 | ||||||
chr7:116214261
|
A | G | 1 | a0001c0001t0005g0300 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.27+3527A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116214261 | ||||||
chr7:116214418
|
A | T | 4 | a0001c0002t0006g0056a0001c0002t0006g0057a0001c0002t0006g0058others(1): Show | 4 | HG02280.hp1 HG02486.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.27+3684A>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116214418 | ||||||
chr7:116214635
|
A | C | 3 | a0001c0001t0007g0040a0001c0001t0007g0062a0001c0001t0007g0217 | 4 | HG02559.hp2 HG03195.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.27+3901A>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116214635 | ||||||
chr7:116214667
|
A | G | 1 | a0001c0001t0003g0271 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.27+3933A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116214667 | ||||||
chr7:116214802
|
C | G | 1 | a0001c0002t0006g0301 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.27+4068C>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116214802 | ||||||
chr7:116214969
|
C | T | 94 | a0001c0002t0001g0005a0001c0002t0001g0016a0001c0002t0001g0027others(91): Show | 105 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.27+4235C>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116214969 | ||||||
chr7:116215155
|
G | A | 1 | a0001c0002t0006g0060 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.27+4421G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116215155 | ||||||
chr7:116215226
|
G | A | 1 | a0001c0001t0003g0219 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.27+4492G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116215226 | ||||||
chr7:116215737
|
C | T | 105 | a0001c0002t0001g0005a0001c0002t0001g0016a0001c0002t0001g0027others(102): Show | 117 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.27+5003C>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116215737 | ||||||
chr7:116215798
|
G | A | 1 | a0001c0002t0001g0104 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.27+5064G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116215798 | ||||||
chr7:116215964
|
C | G | 1 | a0001c0001t0003g0270 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.27+5230C>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116215964 | ||||||
chr7:116216403
|
C | T | 1 | a0001c0002t0006g0103 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.27+5669C>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116216403 | ||||||
chr7:116216482
|
G | A | 3 | a0001c0001t0007g0040a0001c0001t0007g0062a0001c0001t0007g0217 | 4 | HG02559.hp2 HG03195.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.27+5748G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116216482 | ||||||
chr7:116216548
|
T | C | 226 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0014others(223): Show | 275 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.27+5814T>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116216548 | ||||||
chr7:116216627
|
T | C | 157 | a0001c0001t0003g0065a0001c0001t0005g0061a0001c0001t0007g0040others(154): Show | 188 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.27+5893T>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116216627 | ||||||
chr7:116216970
|
G | C | 1 | a0001c0001t0003g0220 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.27+6236G>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116216970 | ||||||
chr7:116217039
|
C | G | 3 | a0001c0002t0006g0101a0001c0002t0006g0102a0001c0002t0006g0103 | 3 | HG02258.hp2 HG03516.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.27+6305C>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116217039 | ||||||
chr7:116217113
|
T | C | 1 | a0001c0001t0002g0117 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.27+6379T>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116217113 | ||||||
chr7:116217116
|
A | G | 157 | a0001c0001t0003g0065a0001c0001t0005g0061a0001c0001t0007g0040others(154): Show | 188 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.27+6382A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116217116 | ||||||
chr7:116217155
|
C | T | 3 | a0001c0002t0006g0101a0001c0002t0006g0102a0001c0002t0006g0103 | 3 | HG02258.hp2 HG03516.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.27+6421C>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116217155 | ||||||
chr7:116217321
|
A | G | 47 | a0001c0001t0003g0065a0001c0002t0004g0002a0001c0002t0004g0006others(44): Show | 65 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.27+6587A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116217321 | ||||||
chr7:116217516
|
T | C | 1 | a0001c0001t0002g0118 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.27+6782T>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116217516 | ||||||
chr7:116217516
|
T | G | 1 | a0001c0002t0004g0063 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.27+6782T>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116217516 | ||||||
chr7:116217689
|
T | G | 1 | a0001c0001t0002g0017 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.27+6955T>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116217689 | ||||||
chr7:116217800
|
C | T | 1 | a0001c0001t0002g0147 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.27+7066C>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116217800 | ||||||
chr7:116218061
|
A | G | 1 | a0001c0002t0006g0060 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.27+7327A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116218061 | ||||||
chr7:116218236
|
T | C | 1 | a0001c0002t0001g0148 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.27+7502T>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116218236 | ||||||
chr7:116218310
|
A | T | 1 | a0001c0001t0003g0271 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.27+7576A>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116218310 | ||||||
chr7:116218311
|
T | TG | 302 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0004others(299): Show | 385 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(382): Show |
intron_variant | MODIFIER | c.27+7579dupG | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 116218311 | |||||
chr7:116218593
|
G | A | 4 | a0001c0001t0003g0041a0001c0001t0003g0221a0001c0001t0003g0222others(1): Show | 5 | HG02257.hp1 HG02647.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.27+7859G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116218593 | ||||||
chr7:116218681
|
AT | A | 47 | a0001c0001t0003g0065a0001c0002t0004g0002a0001c0002t0004g0006others(44): Show | 65 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.27+7948delT | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116218681 | ||||||
chr7:116218689
|
T | A | 6 | a0001c0001t0003g0065a0001c0002t0004g0006a0001c0002t0004g0064others(3): Show | 9 | HG00741.hp2 HG01109.hp2 HG01256.hp2 others(6): Show |
intron_variant | MODIFIER | c.27+7955T>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116218689 | ||||||
chr7:116218715
|
A | G | 1 | a0001c0001t0005g0299 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.27+7981A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116218715 | ||||||
chr7:116219011
|
C | G | 297 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0004others(294): Show | 379 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(376): Show |
intron_variant | MODIFIER | c.27+8277C>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116219011 | ||||||
chr7:116219022
|
G | A | 1 | a0001c0002t0001g0149 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.27+8288G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116219022 | ||||||
chr7:116219103
|
G | T | 2 | a0001c0001t0007g0040a0001c0001t0007g0217 | 3 | HG02559.hp2 HG03195.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.27+8369G>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116219103 | ||||||
chr7:116219108
|
G | T | 2 | a0001c0001t0007g0040a0001c0001t0007g0217 | 3 | HG02559.hp2 HG03195.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.27+8374G>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116219108 | ||||||
chr7:116219113
|
C | G | 226 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0014others(223): Show | 275 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.27+8379C>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116219113 | ||||||
chr7:116219347
|
GAGCTAGT others(3): Show |
G | 1 | a0001c0001t0005g0061 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.27+8616_27+8625del others(10): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 116219347 | |||||
chr7:116219540
|
A | G | 47 | a0001c0001t0003g0065a0001c0002t0004g0002a0001c0002t0004g0006others(44): Show | 65 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.27+8806A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116219540 | ||||||
chr7:116220225
|
G | A | 1 | a0002c0003t0001g0150 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.27+9491G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116220225 | ||||||
chr7:116220516
|
G | A | 1 | a0001c0001t0005g0223 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.27+9782G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116220516 | ||||||
chr7:116220719
|
C | A | 1 | a0001c0002t0006g0060 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.27+9985C>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116220719 | ||||||
chr7:116220729
|
A | T | 157 | a0001c0001t0003g0065a0001c0001t0005g0061a0001c0001t0007g0040others(154): Show | 188 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.27+9995A>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116220729 | ||||||
chr7:116220771
|
G | A | 3 | a0001c0001t0005g0277a0001c0001t0005g0278a0001c0001t0005g0279 | 3 | HG02683.hp1 HG03688.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.27+10037G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116220771 | ||||||
chr7:116220880
|
A | G | 52 | a0001c0001t0003g0065a0001c0001t0005g0061a0001c0001t0007g0040others(49): Show | 71 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.27+10146A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116220880 | ||||||
chr7:116220910
|
A | G | 105 | a0001c0002t0001g0005a0001c0002t0001g0016a0001c0002t0001g0027others(102): Show | 117 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.27+10176A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116220910 | ||||||
chr7:116220933
|
C | T | 6 | a0001c0001t0003g0065a0001c0002t0004g0006a0001c0002t0004g0064others(3): Show | 9 | HG00741.hp2 HG01109.hp2 HG01256.hp2 others(6): Show |
intron_variant | MODIFIER | c.27+10199C>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116220933 | ||||||
chr7:116221156
|
A | G | 1 | a0001c0002t0006g0060 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.27+10422A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116221156 | ||||||
chr7:116221348
|
G | A | 1 | a0001c0002t0004g0069 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.27+10614G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116221348 | ||||||
chr7:116221592
|
T | C | 5 | a0001c0001t0005g0061a0001c0001t0007g0040a0001c0001t0007g0062others(2): Show | 6 | HG02559.hp2 HG02809.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.27+10858T>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116221592 | ||||||
chr7:116221606
|
T | C | 157 | a0001c0001t0003g0065a0001c0001t0005g0061a0001c0001t0007g0040others(154): Show | 188 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.27+10872T>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116221606 | ||||||
chr7:116221631
|
A | T | 1 | a0001c0001t0003g0220 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.27+10897A>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116221631 | ||||||
chr7:116221718
|
C | T | 1 | a0001c0001t0005g0298 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.27+10984C>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116221718 | ||||||
chr7:116221792
|
G | T | 9 | a0001c0001t0002g0001a0001c0001t0002g0009a0001c0001t0002g0010others(6): Show | 21 | HG00438.hp1 HG02040.hp2 HG02083.hp2 others(18): Show |
intron_variant | MODIFIER | c.27+11058G>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116221792 | ||||||
chr7:116222238
|
G | A | 1 | a0001c0002t0001g0151 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.27+11504G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116222238 | ||||||
chr7:116222242
|
A | T | 157 | a0001c0001t0003g0065a0001c0001t0005g0061a0001c0001t0007g0040others(154): Show | 188 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.27+11508A>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116222242 | ||||||
chr7:116222281
|
C | T | 1 | a0001c0001t0002g0141 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.27+11547C>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116222281 | ||||||
chr7:116222286
|
T | C | 1 | a0001c0002t0006g0301 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.27+11552T>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116222286 | ||||||
chr7:116222350
|
C | T | 1 | a0001c0002t0004g0025 | 2 | NA18968.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.27+11616C>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116222350 | ||||||
chr7:116222848
|
A | G | 157 | a0001c0001t0003g0065a0001c0001t0005g0061a0001c0001t0007g0040others(154): Show | 188 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.28-11686A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116222848 | ||||||
chr7:116222917
|
C | T | 1 | a0001c0002t0001g0213 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.28-11617C>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116222917 | ||||||
chr7:116222920
|
A | G | 3 | a0001c0001t0003g0053a0001c0001t0003g0268a0001c0001t0003g0269 | 3 | HG02027.hp1 NA18747.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.28-11614A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116222920 | ||||||
chr7:116222981
|
G | A | 2 | a0001c0001t0007g0040a0001c0001t0007g0217 | 3 | HG02559.hp2 HG03195.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.28-11553G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116222981 | ||||||
chr7:116223260
|
T | C | 105 | a0001c0002t0001g0005a0001c0002t0001g0016a0001c0002t0001g0027others(102): Show | 117 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.28-11274T>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116223260 | ||||||
chr7:116223340
|
C | T | 47 | a0001c0001t0003g0065a0001c0002t0004g0002a0001c0002t0004g0006others(44): Show | 65 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.28-11194C>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116223340 | ||||||
chr7:116223387
|
A | G | 105 | a0001c0002t0001g0005a0001c0002t0001g0016a0001c0002t0001g0027others(102): Show | 117 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.28-11147A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116223387 | ||||||
chr7:116223392
|
G | A | 157 | a0001c0001t0003g0065a0001c0001t0005g0061a0001c0001t0007g0040others(154): Show | 188 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.28-11142G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116223392 | ||||||
chr7:116223416
|
T | C | 3 | a0001c0002t0006g0101a0001c0002t0006g0102a0001c0002t0006g0103 | 3 | HG02258.hp2 HG03516.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.28-11118T>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116223416 | ||||||
chr7:116223569
|
G | A | 2 | a0001c0002t0001g0152a0001c0002t0001g0153 | 2 | HG01175.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.28-10965G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116223569 | ||||||
chr7:116223571
|
G | A | 1 | a0001c0001t0003g0041 | 2 | HG02647.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.28-10963G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116223571 | ||||||
chr7:116223949
|
T | C | 1 | a0001c0002t0006g0060 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.28-10585T>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116223949 | ||||||
chr7:116224156
|
G | A | 47 | a0001c0001t0003g0065a0001c0002t0004g0002a0001c0002t0004g0006others(44): Show | 65 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.28-10378G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116224156 | ||||||
chr7:116224158
|
G | A | 35 | a0001c0002t0004g0002a0001c0002t0004g0007a0001c0002t0004g0018others(32): Show | 48 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(45): Show |
intron_variant | MODIFIER | c.28-10376G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116224158 | ||||||
chr7:116224278
|
A | G | 47 | a0001c0001t0003g0065a0001c0002t0004g0002a0001c0002t0004g0006others(44): Show | 65 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.28-10256A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116224278 | ||||||
chr7:116224331
|
A | G | 3 | a0001c0001t0003g0012a0001c0001t0003g0266a0001c0001t0003g0267 | 6 | HG01175.hp2 HG01515.hp2 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.28-10203A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116224331 | ||||||
chr7:116224342
|
A | G | 47 | a0001c0001t0003g0065a0001c0002t0004g0002a0001c0002t0004g0006others(44): Show | 65 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.28-10192A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116224342 | ||||||
chr7:116224469
|
G | A | 226 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0014others(223): Show | 275 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.28-10065G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116224469 | ||||||
chr7:116224692
|
G | A | 102 | a0001c0002t0001g0005a0001c0002t0001g0016a0001c0002t0001g0027others(99): Show | 114 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(111): Show |
intron_variant | MODIFIER | c.28-9842G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116224692 | ||||||
chr7:116224696
|
T | C | 1 | a0001c0002t0004g0070 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.28-9838T>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116224696 | ||||||
chr7:116224828
|
C | T | 3 | a0001c0002t0006g0101a0001c0002t0006g0102a0001c0002t0006g0103 | 3 | HG02258.hp2 HG03516.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.28-9706C>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116224828 | ||||||
chr7:116224835
|
C | A | 157 | a0001c0001t0003g0065a0001c0001t0005g0061a0001c0001t0007g0040others(154): Show | 188 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.28-9699C>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116224835 | ||||||
chr7:116224869
|
G | A | 2 | a0001c0001t0005g0280a0001c0001t0005g0281 | 2 | HG02895.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.28-9665G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116224869 | ||||||
chr7:116224870
|
GA | G | 208 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0014others(205): Show | 254 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.28-9655delA | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 116224870 | |||||
chr7:116224987
|
A | G | 1 | a0001c0001t0003g0265 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.28-9547A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116224987 | ||||||
chr7:116225121
|
A | T | 4 | a0001c0002t0001g0111a0001c0002t0001g0112a0001c0002t0001g0113others(1): Show | 4 | HG02622.hp1 HG02630.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.28-9413A>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116225121 | ||||||
chr7:116225172
|
T | TAAAAACA others(313): Show |
1 | a0001c0002t0001g0154 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.28-9353_28-9352ins others(320): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 116225172 | |||||
chr7:116225172
|
T | TAAAAACA others(302): Show |
1 | a0001c0002t0006g0301 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.28-9353_28-9352ins others(309): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 116225172 | |||||
chr7:116225172
|
T | TAAAAACA others(311): Show |
1 | a0001c0002t0006g0101 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.28-9353_28-9352ins others(318): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 116225172 | |||||
chr7:116225172
|
T | TAAAAACA others(310): Show |
2 | a0001c0002t0006g0102a0001c0002t0006g0103 | 2 | HG02258.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.28-9353_28-9352ins others(317): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 116225172 | |||||
chr7:116225172
|
T | TAAAAACA others(314): Show |
17 | a0001c0002t0001g0105a0001c0002t0001g0115a0001c0002t0001g0155others(14): Show | 17 | HG00408.hp1 HG00609.hp2 HG01515.hp1 others(14): Show |
intron_variant | MODIFIER | c.28-9353_28-9352ins others(321): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 116225172 | |||||
chr7:116225172
|
T | TAAAAACA others(313): Show |
73 | a0001c0002t0001g0005a0001c0002t0001g0016a0001c0002t0001g0027others(70): Show | 84 | HG00280.hp1 HG00423.hp2 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.28-9353_28-9352ins others(320): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 116225172 | |||||
chr7:116225172
|
T | TAAAAACA others(312): Show |
6 | a0001c0002t0001g0211a0001c0002t0006g0026a0001c0002t0006g0057others(3): Show | 7 | HG02280.hp1 HG02486.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.28-9353_28-9352ins others(319): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 116225172 | |||||
chr7:116225172
|
T | TAAAAACA others(314): Show |
1 | a0001c0002t0001g0152 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.28-9353_28-9352ins others(321): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 116225172 | |||||
chr7:116225172
|
T | TAAAAACA others(313): Show |
1 | a0001c0002t0001g0153 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.28-9353_28-9352ins others(320): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 116225172 | |||||
chr7:116225172
|
T | TAAAAACA others(313): Show |
1 | a0001c0002t0001g0212 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.28-9353_28-9352ins others(320): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 116225172 | |||||
chr7:116225172
|
T | TAAAAACA others(314): Show |
1 | a0001c0002t0001g0113 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.28-9353_28-9352ins others(321): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 116225172 | |||||
chr7:116225196
|
C | A | 3 | a0001c0001t0003g0219a0001c0001t0003g0238a0001c0001t0003g0239 | 3 | HG01255.hp2 HG02886.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.28-9338C>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116225196 | ||||||
chr7:116225458
|
G | C | 226 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0014others(223): Show | 275 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.28-9076G>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116225458 | ||||||
chr7:116225537
|
A | G | 1 | a0001c0002t0001g0169 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.28-8997A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116225537 | ||||||
chr7:116225569
|
C | T | 1 | a0001c0001t0002g0140 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.28-8965C>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116225569 | ||||||
chr7:116225684
|
A | G | 1 | a0001c0002t0001g0113 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.28-8850A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116225684 | ||||||
chr7:116225794
|
G | A | 3 | a0001c0002t0006g0101a0001c0002t0006g0102a0001c0002t0006g0103 | 3 | HG02258.hp2 HG03516.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.28-8740G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116225794 | ||||||
chr7:116226300
|
A | G | 157 | a0001c0001t0003g0065a0001c0001t0005g0061a0001c0001t0007g0040others(154): Show | 188 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.28-8234A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116226300 | ||||||
chr7:116226480
|
A | G | 2 | a0001c0001t0002g0035a0001c0002t0008g0139 | 3 | HG02165.hp2 NA18960.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.28-8054A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116226480 | ||||||
chr7:116226502
|
G | A | 1 | a0001c0001t0002g0017 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.28-8032G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116226502 | ||||||
chr7:116226517
|
C | T | 1 | a0001c0001t0003g0264 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.28-8017C>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116226517 | ||||||
chr7:116226518
|
G | A | 1 | a0001c0001t0002g0119 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.28-8016G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116226518 | ||||||
chr7:116226734
|
G | A | 47 | a0001c0001t0003g0065a0001c0002t0004g0002a0001c0002t0004g0006others(44): Show | 65 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.28-7800G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116226734 | ||||||
chr7:116226768
|
C | A | 1 | a0001c0001t0002g0030 | 2 | HG03834.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.28-7766C>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116226768 | ||||||
chr7:116226820
|
G | T | 1 | a0001c0001t0003g0263 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.28-7714G>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116226820 | ||||||
chr7:116226826
|
A | G | 80 | a0001c0002t0001g0005a0001c0002t0001g0016a0001c0002t0001g0037others(77): Show | 89 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.28-7708A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116226826 | ||||||
chr7:116226944
|
G | A | 1 | a0001c0002t0001g0170 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.28-7590G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116226944 | ||||||
chr7:116227088
|
T | TTTTA | 7 | a0001c0001t0005g0044a0001c0001t0005g0232a0001c0001t0005g0233others(4): Show | 8 | HG00642.hp1 HG01081.hp2 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.28-7403_28-7400dup others(4): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 116227088 | |||||
chr7:116227088
|
TTTTA | T | 69 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0004others(66): Show | 101 | HG00280.hp2 HG00438.hp1 HG00609.hp1 others(98): Show |
intron_variant | MODIFIER | c.28-7403_28-7400del others(4): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 116227088 | |||||
chr7:116227088
|
TTTTATTT others(1): Show |
T | 10 | a0001c0001t0002g0120a0001c0001t0003g0271a0001c0002t0001g0055others(7): Show | 11 | HG00423.hp1 HG00733.hp1 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.28-7407_28-7400del others(8): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 116227088 | |||||
chr7:116227088
|
TTTTATTT others(5): Show |
T | 197 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0014others(194): Show | 242 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.28-7411_28-7400del others(12): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 116227088 | |||||
chr7:116227088
|
TTTTATTT others(9): Show |
T | 1 | a0001c0001t0003g0238 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.28-7415_28-7400del others(16): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 116227088 | |||||
chr7:116227088
|
TTTTATTT others(13): Show |
T | 2 | a0001c0001t0003g0219a0001c0002t0001g0171 | 2 | HG01255.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.28-7419_28-7400del others(20): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 116227088 | |||||
chr7:116227241
|
C | T | 104 | a0001c0002t0001g0005a0001c0002t0001g0016a0001c0002t0001g0027others(101): Show | 116 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(113): Show |
intron_variant | MODIFIER | c.28-7293C>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116227241 | ||||||
chr7:116227272
|
G | A | 2 | a0001c0002t0004g0071a0001c0002t0004g0072 | 2 | HG02486.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.28-7262G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116227272 | ||||||
chr7:116227318
|
T | G | 1 | a0001c0001t0002g0121 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.28-7216T>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116227318 | ||||||
chr7:116227446
|
A | G | 1 | a0001c0001t0005g0061 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.28-7088A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116227446 | ||||||
chr7:116227485
|
C | T | 6 | a0001c0002t0004g0002a0001c0002t0004g0090a0001c0002t0004g0091others(3): Show | 10 | HG00408.hp2 HG00438.hp2 NA18939.hp2 others(7): Show |
intron_variant | MODIFIER | c.28-7049C>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116227485 | ||||||
chr7:116227486
|
G | A | 1 | a0001c0002t0004g0073 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.28-7048G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116227486 | ||||||
chr7:116227693
|
A | G | 2 | a0001c0002t0004g0067a0001c0002t0004g0068 | 2 | HG04204.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.28-6841A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116227693 | ||||||
chr7:116227703
|
A | G | 47 | a0001c0001t0003g0065a0001c0002t0004g0002a0001c0002t0004g0006others(44): Show | 65 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.28-6831A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116227703 | ||||||
chr7:116227728
|
A | G | 3 | a0001c0002t0006g0026a0001c0002t0006g0099a0001c0002t0006g0100 | 4 | HG02622.hp2 HG03195.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.28-6806A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116227728 | ||||||
chr7:116227839
|
G | A | 47 | a0001c0001t0003g0065a0001c0002t0004g0002a0001c0002t0004g0006others(44): Show | 65 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.28-6695G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116227839 | ||||||
chr7:116227999
|
C | CT | 47 | a0001c0001t0003g0065a0001c0001t0005g0061a0001c0002t0004g0002others(44): Show | 65 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.28-6527dupT | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 116227999 | |||||
chr7:116227999
|
CTTTTTTT others(7): Show |
C | 1 | a0001c0001t0003g0266 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.28-6516_28-6503del others(14): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 116227999 | |||||
chr7:116228008
|
G | GT | 20 | a0001c0001t0003g0050a0001c0001t0005g0042a0001c0001t0005g0043others(17): Show | 24 | HG00642.hp1 HG00642.hp2 HG00738.hp2 others(21): Show |
intron_variant | MODIFIER | c.28-6513dupT | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 116228008 | |||||
chr7:116228008
|
G | T | 5 | a0001c0001t0007g0040a0001c0001t0007g0062a0001c0001t0007g0217others(2): Show | 6 | HG01358.hp2 HG02559.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.28-6526G>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116228008 | ||||||
chr7:116228019
|
T | G | 1 | a0001c0002t0004g0074 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.28-6515T>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116228019 | ||||||
chr7:116228021
|
T | G | 1 | a0001c0002t0001g0172 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.28-6513T>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116228021 | ||||||
chr7:116228022
|
G | GT | 104 | a0001c0002t0001g0005a0001c0002t0001g0016a0001c0002t0001g0027others(101): Show | 116 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(113): Show |
intron_variant | MODIFIER | c.28-6503dupT | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 116228022 | |||||
chr7:116228022
|
G | T | 1 | a0001c0002t0001g0172 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.28-6512G>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116228022 | ||||||
chr7:116228255
|
A | G | 10 | a0001c0001t0005g0044a0001c0001t0005g0223a0001c0001t0005g0229others(7): Show | 11 | HG00642.hp1 HG01081.hp2 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.28-6279A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116228255 | ||||||
chr7:116228318
|
A | G | 1 | a0001c0001t0005g0294 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.28-6216A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116228318 | ||||||
chr7:116228663
|
T | G | 1 | a0001c0002t0006g0060 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.28-5871T>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116228663 | ||||||
chr7:116228744
|
T | C | 157 | a0001c0001t0003g0065a0001c0001t0005g0061a0001c0001t0007g0040others(154): Show | 188 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.28-5790T>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116228744 | ||||||
chr7:116228779
|
T | G | 1 | a0001c0001t0005g0061 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.28-5755T>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116228779 | ||||||
chr7:116228861
|
C | A | 5 | a0001c0001t0005g0061a0001c0001t0007g0040a0001c0001t0007g0062others(2): Show | 6 | HG02559.hp2 HG02809.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.28-5673C>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116228861 | ||||||
chr7:116228885
|
A | G | 47 | a0001c0001t0003g0065a0001c0002t0004g0002a0001c0002t0004g0006others(44): Show | 65 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.28-5649A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116228885 | ||||||
chr7:116228917
|
C | T | 1 | a0001c0001t0005g0293 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.28-5617C>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116228917 | ||||||
chr7:116228998
|
C | CTATATAT others(3): Show |
1 | a0001c0001t0007g0062 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.28-5509_28-5500dup others(10): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 116228998 | |||||
chr7:116228998
|
C | CTATATAT others(9): Show |
1 | a0002c0003t0001g0013 | 3 | NA18989.hp2 NA19003.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.28-5515_28-5500dup others(16): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 116228998 | |||||
chr7:116228998
|
C | CTATATAT others(11): Show |
5 | a0001c0001t0005g0061a0001c0001t0007g0040a0001c0002t0001g0038others(2): Show | 6 | HG00423.hp2 HG02559.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.28-5517_28-5500dup others(18): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 116228998 | |||||
chr7:116228998
|
C | CTATATAT others(13): Show |
1 | a0001c0001t0007g0217 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.28-5519_28-5500dup others(20): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 116228998 | |||||
chr7:116228998
|
C | CTATATAT others(15): Show |
1 | a0002c0003t0001g0193 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.28-5521_28-5500dup others(22): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 116228998 | |||||
chr7:116228998
|
C | CTATATAT others(19): Show |
4 | a0001c0002t0006g0109a0002c0003t0001g0150a0002c0003t0001g0165others(1): Show | 4 | HG03209.hp2 NA18999.hp2 NA19006.hp1 others(1): Show |
intron_variant | MODIFIER | c.28-5525_28-5500dup others(26): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 116228998 | |||||
chr7:116228998
|
C | CTATATAT others(21): Show |
1 | a0002c0003t0001g0205 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.28-5527_28-5500dup others(28): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 116228998 | |||||
chr7:116228998
|
CTA | C | 8 | a0001c0001t0002g0008a0001c0001t0002g0121a0001c0001t0002g0136others(5): Show | 12 | HG00733.hp2 HG00741.hp1 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.28-5501_28-5500del others(2): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 116228998 | |||||
chr7:116228998
|
CTATA | C | 23 | a0001c0001t0002g0118a0001c0001t0002g0133a0001c0001t0002g0134others(20): Show | 28 | HG00280.hp2 HG00738.hp2 HG01070.hp2 others(25): Show |
intron_variant | MODIFIER | c.28-5503_28-5500del others(4): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 116228998 | |||||
chr7:116228998
|
CTATATA | C | 74 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0004others(71): Show | 107 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.28-5505_28-5500del others(6): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 116228998 | |||||
chr7:116228998
|
CTATATAT others(1): Show |
C | 69 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0045others(66): Show | 94 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(91): Show |
intron_variant | MODIFIER | c.28-5507_28-5500del others(8): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 116228998 | |||||
chr7:116228998
|
CTATATAT others(3): Show |
C | 20 | a0001c0001t0005g0042a0001c0001t0005g0043a0001c0001t0005g0044others(17): Show | 23 | HG00642.hp1 HG00642.hp2 HG01069.hp1 others(20): Show |
intron_variant | MODIFIER | c.28-5509_28-5500del others(10): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 116228998 | |||||
chr7:116228998
|
CTATATAT others(13): Show |
C | 1 | a0001c0002t0001g0155 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.28-5519_28-5500del others(20): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 116228998 | |||||
chr7:116229025
|
TATATATA others(3): Show |
T | 1 | a0001c0002t0006g0060 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.28-5508_28-5499del others(10): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116229025 | ||||||
chr7:116229033
|
T | A | 10 | a0001c0001t0005g0051a0001c0002t0001g0055a0001c0002t0001g0115others(7): Show | 11 | HG00408.hp1 HG02155.hp2 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.28-5501T>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116229033 | ||||||
chr7:116229033
|
T | TAA | 5 | a0001c0002t0006g0026a0001c0002t0006g0099a0001c0002t0006g0101others(2): Show | 6 | HG02258.hp2 HG03195.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.28-5500_28-5499dup others(2): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 116229033 | |||||
chr7:116229033
|
T | TATATATA others(1): Show |
12 | a0001c0002t0001g0005a0001c0002t0001g0104a0001c0002t0001g0157others(9): Show | 16 | HG00544.hp1 HG02015.hp1 HG02027.hp2 others(13): Show |
intron_variant | MODIFIER | c.28-5500_28-5499ins others(8): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 116229033 | |||||
chr7:116229033
|
T | TATATATA others(3): Show |
4 | a0001c0002t0001g0054a0001c0002t0001g0180a0001c0002t0001g0212others(1): Show | 4 | HG02071.hp1 NA18906.hp1 NA18944.hp2 others(1): Show |
intron_variant | MODIFIER | c.28-5500_28-5499ins others(10): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 116229033 | |||||
chr7:116229033
|
T | TATATATA others(5): Show |
7 | a0001c0002t0001g0027a0001c0002t0001g0160a0001c0002t0001g0170others(4): Show | 7 | HG00544.hp2 HG00609.hp2 HG03453.hp2 others(4): Show |
intron_variant | MODIFIER | c.28-5500_28-5499ins others(12): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 116229033 | |||||
chr7:116229033
|
T | TATATATA others(7): Show |
6 | a0001c0002t0001g0149a0001c0002t0001g0171a0001c0002t0001g0183others(3): Show | 6 | HG00558.hp1 HG02074.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.28-5500_28-5499ins others(14): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 116229033 | |||||
chr7:116229033
|
T | TATATATA others(9): Show |
1 | a0001c0002t0001g0184 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.28-5500_28-5499ins others(16): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 116229033 | |||||
chr7:116229033
|
T | TATATATA others(11): Show |
5 | a0001c0002t0001g0106a0001c0002t0001g0111a0001c0002t0001g0185others(2): Show | 5 | HG01433.hp2 HG02129.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.28-5500_28-5499ins others(18): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 116229033 | |||||
chr7:116229033
|
T | TATATATA others(13): Show |
5 | a0001c0002t0001g0037a0001c0002t0001g0187a0001c0002t0001g0188others(2): Show | 7 | HG00733.hp1 HG01099.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.28-5500_28-5499ins others(20): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 116229033 | |||||
chr7:116229033
|
T | TATATATA others(15): Show |
6 | a0001c0002t0001g0029a0001c0002t0001g0107a0001c0002t0001g0152others(3): Show | 7 | HG01175.hp1 HG01515.hp1 HG01517.hp1 others(4): Show |
intron_variant | MODIFIER | c.28-5500_28-5499ins others(22): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 116229033 | |||||
chr7:116229033
|
T | TATATATA others(17): Show |
5 | a0001c0002t0001g0105a0001c0002t0001g0151a0001c0002t0001g0162others(2): Show | 5 | HG02055.hp1 HG02647.hp2 NA19002.hp1 others(2): Show |
intron_variant | MODIFIER | c.28-5500_28-5499ins others(24): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 116229033 | |||||
chr7:116229033
|
T | TATATATA others(18): Show |
1 | a0001c0002t0001g0197 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.28-5500_28-5499ins others(25): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 116229033 | |||||
chr7:116229033
|
T | TATATATA others(19): Show |
8 | a0001c0002t0001g0112a0001c0002t0001g0113a0001c0002t0001g0116others(5): Show | 8 | HG00639.hp1 HG02132.hp1 HG02165.hp1 others(5): Show |
intron_variant | MODIFIER | c.28-5500_28-5499ins others(26): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 116229033 | |||||
chr7:116229033
|
T | TATATATA others(21): Show |
7 | a0001c0002t0001g0039a0001c0002t0001g0114a0001c0002t0001g0164others(4): Show | 8 | HG01256.hp1 HG01934.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.28-5500_28-5499ins others(28): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 116229033 | |||||
chr7:116229033
|
T | TATATATA others(23): Show |
5 | a0001c0002t0001g0154a0001c0002t0001g0166a0001c0002t0001g0168others(2): Show | 5 | HG00280.hp1 HG03098.hp2 NA18943.hp2 others(2): Show |
intron_variant | MODIFIER | c.28-5500_28-5499ins others(30): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 116229033 | |||||
chr7:116229033
|
T | TATATATA others(25): Show |
3 | a0001c0002t0001g0016a0001c0002t0001g0153a0001c0002t0001g0206 | 4 | HG01069.hp2 HG01071.hp2 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.28-5500_28-5499ins others(32): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 116229033 | |||||
chr7:116229033
|
T | TATATATA others(27): Show |
2 | a0001c0002t0001g0207a0001c0002t0010g0215 | 2 | HG01952.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.28-5500_28-5499ins others(34): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 116229033 | |||||
chr7:116229033
|
T | TATATATA others(29): Show |
1 | a0001c0002t0001g0167 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.28-5500_28-5499ins others(36): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 116229033 | |||||
chr7:116229033
|
T | TATATATA others(31): Show |
1 | a0001c0002t0001g0110 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.28-5500_28-5499ins others(38): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 116229033 | |||||
chr7:116229034
|
A | ATATATAT others(28): Show |
2 | a0001c0002t0001g0208a0001c0002t0001g0209 | 2 | HG02523.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.28-5500_28-5499ins others(35): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116229034 | ||||||
chr7:116229145
|
T | G | 1 | a0001c0002t0006g0103 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.28-5389T>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116229145 | ||||||
chr7:116229155
|
T | C | 1 | a0001c0001t0005g0296 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.28-5379T>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116229155 | ||||||
chr7:116229179
|
C | A | 1 | a0001c0001t0003g0240 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.28-5355C>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116229179 | ||||||
chr7:116229205
|
G | A | 1 | a0001c0001t0002g0030 | 2 | HG03834.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.28-5329G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116229205 | ||||||
chr7:116229274
|
A | G | 47 | a0001c0001t0003g0065a0001c0002t0004g0002a0001c0002t0004g0006others(44): Show | 65 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.28-5260A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116229274 | ||||||
chr7:116229323
|
C | G | 1 | a0001c0001t0005g0061 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.28-5211C>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116229323 | ||||||
chr7:116229374
|
G | C | 3 | a0001c0002t0006g0101a0001c0002t0006g0102a0001c0002t0006g0103 | 3 | HG02258.hp2 HG03516.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.28-5160G>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116229374 | ||||||
chr7:116229589
|
T | C | 35 | a0001c0002t0004g0002a0001c0002t0004g0007a0001c0002t0004g0018others(32): Show | 48 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(45): Show |
intron_variant | MODIFIER | c.28-4945T>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116229589 | ||||||
chr7:116229806
|
A | G | 2 | a0001c0002t0006g0108a0001c0002t0006g0109 | 2 | HG02055.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.28-4728A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116229806 | ||||||
chr7:116229948
|
T | C | 4 | a0001c0002t0001g0157a0001c0002t0001g0177a0001c0002t0001g0178others(1): Show | 4 | NA18941.hp1 NA18944.hp2 NA18981.hp2 others(1): Show |
intron_variant | MODIFIER | c.28-4586T>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116229948 | ||||||
chr7:116229956
|
A | C | 2 | a0001c0001t0007g0040a0001c0001t0007g0217 | 3 | HG02559.hp2 HG03195.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.28-4578A>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116229956 | ||||||
chr7:116230002
|
A | G | 5 | a0001c0002t0006g0101a0001c0002t0006g0102a0001c0002t0006g0103others(2): Show | 5 | HG02055.hp1 HG02258.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.28-4532A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116230002 | ||||||
chr7:116230074
|
T | C | 1 | a0001c0002t0001g0190 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.28-4460T>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116230074 | ||||||
chr7:116230079
|
C | G | 1 | a0001c0001t0002g0121 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.28-4455C>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116230079 | ||||||
chr7:116230083
|
A | G | 1 | a0002c0003t0001g0165 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.28-4451A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116230083 | ||||||
chr7:116230211
|
C | T | 18 | a0001c0001t0005g0042a0001c0001t0005g0043a0001c0001t0005g0044others(15): Show | 21 | HG00642.hp1 HG00642.hp2 HG01069.hp1 others(18): Show |
intron_variant | MODIFIER | c.28-4323C>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116230211 | ||||||
chr7:116230788
|
TC | T | 47 | a0001c0001t0003g0065a0001c0002t0004g0002a0001c0002t0004g0006others(44): Show | 65 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.28-3744delC | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 116230788 | |||||
chr7:116230904
|
C | T | 1 | a0001c0002t0001g0196 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.28-3630C>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116230904 | ||||||
chr7:116230907
|
C | T | 1 | a0001c0001t0003g0261 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.28-3627C>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116230907 | ||||||
chr7:116231355
|
A | T | 1 | a0001c0002t0009g0028 | 2 | HG02895.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.28-3179A>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116231355 | ||||||
chr7:116231480
|
A | T | 1 | a0001c0002t0001g0174 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.28-3054A>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116231480 | ||||||
chr7:116231490
|
C | CAGAGATG others(2): Show |
157 | a0001c0001t0003g0065a0001c0001t0005g0061a0001c0001t0007g0040others(154): Show | 188 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.28-3041_28-3040ins others(9): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 116231490 | |||||
chr7:116231498
|
C | T | 2 | a0001c0002t0001g0201a0001c0002t0001g0207 | 2 | HG01256.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.28-3036C>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116231498 | ||||||
chr7:116231821
|
A | G | 1 | a0001c0002t0004g0068 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.28-2713A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116231821 | ||||||
chr7:116232027
|
C | T | 3 | a0001c0002t0006g0101a0001c0002t0006g0102a0001c0002t0006g0103 | 3 | HG02258.hp2 HG03516.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.28-2507C>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116232027 | ||||||
chr7:116232351
|
T | C | 18 | a0001c0001t0005g0042a0001c0001t0005g0043a0001c0001t0005g0044others(15): Show | 21 | HG00642.hp1 HG00642.hp2 HG01069.hp1 others(18): Show |
intron_variant | MODIFIER | c.28-2183T>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116232351 | ||||||
chr7:116232354
|
A | G | 1 | a0001c0001t0003g0254 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.28-2180A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116232354 | ||||||
chr7:116232556
|
A | AAC | 157 | a0001c0001t0003g0065a0001c0001t0005g0061a0001c0001t0007g0040others(154): Show | 188 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.28-1977_28-1976dup others(2): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 116232556 | |||||
chr7:116232666
|
C | G | 1 | a0001c0002t0006g0301 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.28-1868C>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116232666 | ||||||
chr7:116232715
|
CAATTT | C | 3 | a0001c0001t0005g0282a0001c0001t0005g0283a0001c0001t0005g0297 | 3 | HG00735.hp1 HG01255.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.28-1814_28-1810del others(5): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | 116232715 | |||||
chr7:116232816
|
G | A | 1 | a0001c0001t0002g0122 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.28-1718G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116232816 | ||||||
chr7:116233066
|
A | G | 1 | a0001c0001t0005g0289 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.28-1468A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116233066 | ||||||
chr7:116233098
|
G | A | 3 | a0001c0002t0006g0101a0001c0002t0006g0102a0001c0002t0006g0103 | 3 | HG02258.hp2 HG03516.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.28-1436G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116233098 | ||||||
chr7:116233116
|
T | A | 1 | a0001c0002t0006g0060 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.28-1418T>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116233116 | ||||||
chr7:116233228
|
T | C | 3 | a0001c0001t0003g0219a0001c0001t0003g0238a0001c0001t0003g0239 | 3 | HG01255.hp2 HG02886.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.28-1306T>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116233228 | ||||||
chr7:116233231
|
A | G | 2 | a0001c0002t0004g0025a0001c0002t0004g0088 | 3 | HG02040.hp1 NA18968.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.28-1303A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116233231 | ||||||
chr7:116233347
|
A | G | 1 | a0001c0001t0005g0061 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.28-1187A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116233347 | ||||||
chr7:116233614
|
A | G | 1 | a0001c0002t0001g0182 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.28-920A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116233614 | ||||||
chr7:116233644
|
G | A | 4 | a0001c0001t0002g0035a0001c0001t0002g0119a0001c0001t0002g0133others(1): Show | 5 | HG02165.hp2 NA18960.hp1 NA18990.hp1 others(2): Show |
intron_variant | MODIFIER | c.28-890G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116233644 | ||||||
chr7:116234037
|
A | T | 47 | a0001c0001t0003g0065a0001c0002t0004g0002a0001c0002t0004g0006others(44): Show | 65 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.28-497A>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116234037 | ||||||
chr7:116234261
|
T | A | 4 | a0001c0002t0006g0056a0001c0002t0006g0057a0001c0002t0006g0058others(1): Show | 4 | HG02280.hp1 HG02486.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.28-273T>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116234261 | ||||||
chr7:116234356
|
G | A | 1 | a0001c0001t0005g0232 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.28-178G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116234356 | ||||||
chr7:116234381
|
T | C | 2 | a0001c0002t0006g0026a0001c0002t0006g0099 | 3 | HG03195.hp1 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.28-153T>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116234381 | ||||||
chr7:116234412
|
T | C | 157 | a0001c0001t0003g0065a0001c0001t0005g0061a0001c0001t0007g0040others(154): Show | 188 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.28-122T>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116234412 | ||||||
chr7:116234506
|
C | T | 157 | a0001c0001t0003g0065a0001c0001t0005g0061a0001c0001t0007g0040others(154): Show | 188 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.28-28C>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 1/6 | chr7 | 116234506 | ||||||
chr7:116234668
|
A | G | 1 | a0001c0002t0001g0110 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.113+49A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116234668 | ||||||
chr7:116234675
|
C | T | 1 | a0001c0002t0010g0215 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.113+56C>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116234675 | ||||||
chr7:116234755
|
A | C | 1 | a0001c0001t0002g0145 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.113+136A>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116234755 | ||||||
chr7:116234763
|
TAA | T | 226 | a0001c0001t0002g0132a0001c0001t0003g0011a0001c0001t0003g0012others(223): Show | 275 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.113+148_113+149del others(2): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr7 | 116234763 | |||||
chr7:116234953
|
C | CT | 47 | a0001c0001t0003g0065a0001c0002t0004g0002a0001c0002t0004g0006others(44): Show | 65 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.113+343dupT | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr7 | 116234953 | |||||
chr7:116235046
|
C | T | 1 | a0001c0001t0003g0253 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.113+427C>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116235046 | ||||||
chr7:116235098
|
G | A | 2 | a0001c0001t0007g0062a0001c0002t0006g0301 | 2 | NA18906.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.113+479G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116235098 | ||||||
chr7:116235107
|
C | CTAAT | 2 | a0001c0001t0007g0040a0001c0001t0007g0217 | 3 | HG02559.hp2 HG03195.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.113+490_113+493dup others(4): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr7 | 116235107 | |||||
chr7:116235305
|
G | C | 157 | a0001c0001t0003g0065a0001c0001t0005g0061a0001c0001t0007g0040others(154): Show | 188 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.113+686G>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116235305 | ||||||
chr7:116235317
|
C | T | 2 | a0001c0002t0001g0200a0001c0002t0001g0206 | 2 | HG01934.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.113+698C>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116235317 | ||||||
chr7:116235578
|
T | G | 1 | a0001c0001t0007g0062 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.113+959T>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116235578 | ||||||
chr7:116235637
|
A | ATAGTGGT others(11): Show |
1 | a0001c0002t0004g0081 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.113+1019_113+1036d others(20): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr7 | 116235637 | |||||
chr7:116235678
|
G | C | 1 | a0001c0001t0005g0282 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.113+1059G>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116235678 | ||||||
chr7:116235714
|
TGGCAGCT others(9): Show |
T | 2 | a0001c0001t0002g0036a0001c0001t0002g0142 | 3 | NA18981.hp1 NA18990.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.113+1098_113+1113d others(18): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr7 | 116235714 | |||||
chr7:116235887
|
T | C | 16 | a0001c0001t0005g0015a0001c0001t0005g0277a0001c0001t0005g0278others(13): Show | 18 | HG00280.hp2 HG00735.hp1 HG01255.hp1 others(15): Show |
intron_variant | MODIFIER | c.113+1268T>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116235887 | ||||||
chr7:116236050
|
G | T | 1 | a0001c0002t0006g0100 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.113+1431G>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116236050 | ||||||
chr7:116236084
|
A | G | 47 | a0001c0001t0003g0065a0001c0002t0004g0002a0001c0002t0004g0006others(44): Show | 65 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.113+1465A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116236084 | ||||||
chr7:116236283
|
C | T | 1 | a0001c0001t0002g0144 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.113+1664C>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116236283 | ||||||
chr7:116236311
|
C | T | 157 | a0001c0001t0003g0065a0001c0001t0005g0061a0001c0001t0007g0040others(154): Show | 188 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.113+1692C>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116236311 | ||||||
chr7:116236381
|
T | C | 47 | a0001c0001t0003g0065a0001c0002t0004g0002a0001c0002t0004g0006others(44): Show | 65 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.113+1762T>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116236381 | ||||||
chr7:116236425
|
A | G | 1 | a0001c0001t0005g0228 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.113+1806A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116236425 | ||||||
chr7:116236501
|
T | G | 1 | a0001c0001t0003g0041 | 2 | HG02647.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.113+1882T>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116236501 | ||||||
chr7:116236580
|
A | G | 226 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0014others(223): Show | 275 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.113+1961A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116236580 | ||||||
chr7:116236627
|
A | G | 1 | a0001c0001t0003g0260 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.113+2008A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116236627 | ||||||
chr7:116236648
|
C | T | 1 | a0001c0001t0005g0061 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.113+2029C>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116236648 | ||||||
chr7:116236649
|
G | A | 1 | a0001c0002t0001g0192 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.113+2030G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116236649 | ||||||
chr7:116236665
|
C | T | 18 | a0001c0001t0005g0042a0001c0001t0005g0043a0001c0001t0005g0044others(15): Show | 21 | HG00642.hp1 HG00642.hp2 HG01069.hp1 others(18): Show |
intron_variant | MODIFIER | c.113+2046C>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116236665 | ||||||
chr7:116237231
|
G | T | 4 | a0001c0001t0005g0061a0001c0001t0007g0040a0001c0001t0007g0062others(1): Show | 5 | HG02559.hp2 HG03195.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.113+2612G>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116237231 | ||||||
chr7:116237379
|
C | A | 1 | a0001c0002t0004g0075 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.113+2760C>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116237379 | ||||||
chr7:116237524
|
T | G | 1 | a0001c0001t0002g0031 | 2 | NA18949.hp1 NA18955.hp1 |
intron_variant | MODIFIER | c.113+2905T>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116237524 | ||||||
chr7:116237606
|
A | G | 94 | a0001c0002t0001g0005a0001c0002t0001g0016a0001c0002t0001g0027others(91): Show | 105 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.113+2987A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116237606 | ||||||
chr7:116237747
|
GCCAACAT others(53): Show |
G | 1 | a0001c0002t0004g0085 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.113+3132_113+3191d others(62): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr7 | 116237747 | |||||
chr7:116237750
|
A | G | 3 | a0001c0001t0007g0040a0001c0001t0007g0062a0001c0001t0007g0217 | 4 | HG02559.hp2 HG03195.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.113+3131A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116237750 | ||||||
chr7:116237812
|
G | T | 1 | a0001c0002t0004g0085 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.113+3193G>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116237812 | ||||||
chr7:116237813
|
T | A | 1 | a0001c0002t0004g0085 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.113+3194T>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116237813 | ||||||
chr7:116237815
|
C | A | 1 | a0001c0002t0004g0085 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.113+3196C>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116237815 | ||||||
chr7:116237816
|
T | A | 1 | a0001c0002t0004g0085 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.113+3197T>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116237816 | ||||||
chr7:116237819
|
C | T | 1 | a0001c0002t0004g0085 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.113+3200C>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116237819 | ||||||
chr7:116237820
|
A | G | 46 | a0001c0001t0003g0065a0001c0002t0004g0002a0001c0002t0004g0006others(43): Show | 64 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.113+3201A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116237820 | ||||||
chr7:116237824
|
C | T | 1 | a0001c0002t0004g0085 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.113+3205C>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116237824 | ||||||
chr7:116237825
|
C | T | 1 | a0001c0002t0004g0085 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.113+3206C>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116237825 | ||||||
chr7:116237826
|
T | A | 1 | a0001c0002t0004g0085 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.113+3207T>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116237826 | ||||||
chr7:116237830
|
C | CAACCTTT others(53): Show |
1 | a0001c0002t0004g0085 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.113+3211_113+3212i others(62): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116237830 | ||||||
chr7:116237831
|
T | G | 1 | a0001c0002t0004g0085 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.113+3212T>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116237831 | ||||||
chr7:116237833
|
G | A | 1 | a0001c0002t0004g0085 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.113+3214G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116237833 | ||||||
chr7:116237843
|
G | GGT | 156 | a0001c0001t0003g0065a0001c0001t0005g0061a0001c0001t0007g0040others(153): Show | 187 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(184): Show |
intron_variant | MODIFIER | c.113+3239_113+3240d others(4): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr7 | 116237843 | |||||
chr7:116238066
|
C | G | 1 | a0001c0002t0006g0060 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.113+3447C>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116238066 | ||||||
chr7:116238177
|
C | G | 1 | a0001c0002t0004g0080 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.113+3558C>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116238177 | ||||||
chr7:116238268
|
A | G | 3 | a0001c0001t0002g0008a0001c0001t0002g0121a0001c0001t0002g0138 | 6 | HG01346.hp2 HG01934.hp1 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.113+3649A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116238268 | ||||||
chr7:116238438
|
T | G | 1 | a0001c0001t0003g0255 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.113+3819T>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116238438 | ||||||
chr7:116238458
|
A | G | 94 | a0001c0002t0001g0005a0001c0002t0001g0016a0001c0002t0001g0027others(91): Show | 105 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.113+3839A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116238458 | ||||||
chr7:116238468
|
G | A | 1 | a0001c0002t0001g0170 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.113+3849G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116238468 | ||||||
chr7:116238479
|
CTA | C | 47 | a0001c0001t0003g0065a0001c0002t0004g0002a0001c0002t0004g0006others(44): Show | 65 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.113+3862_113+3863d others(4): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr7 | 116238479 | |||||
chr7:116238585
|
C | CATCATTA others(5): Show |
4 | a0001c0002t0006g0056a0001c0002t0006g0057a0001c0002t0006g0058others(1): Show | 4 | HG02280.hp1 HG02486.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.113+3968_113+3969i others(14): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr7 | 116238585 | |||||
chr7:116238585
|
C | CATT | 5 | a0001c0001t0002g0123a0001c0001t0003g0219a0001c0001t0003g0238others(2): Show | 5 | HG00609.hp1 HG01255.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.113+3994_113+3996d others(5): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr7 | 116238585 | |||||
chr7:116238585
|
C | CATTATT | 40 | a0001c0001t0003g0065a0001c0001t0003g0259a0001c0001t0005g0287others(37): Show | 55 | HG00408.hp2 HG00438.hp2 HG00738.hp1 others(52): Show |
intron_variant | MODIFIER | c.113+3991_113+3996d others(8): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr7 | 116238585 | |||||
chr7:116238585
|
C | CATTATTA others(2): Show |
42 | a0001c0001t0003g0012a0001c0001t0003g0014a0001c0001t0003g0041others(39): Show | 54 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(51): Show |
intron_variant | MODIFIER | c.113+3988_113+3996d others(11): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr7 | 116238585 | |||||
chr7:116238585
|
C | CATTATTA others(5): Show |
37 | a0001c0001t0003g0220a0001c0001t0003g0255a0001c0001t0003g0271others(34): Show | 42 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(39): Show |
intron_variant | MODIFIER | c.113+3985_113+3996d others(14): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr7 | 116238585 | |||||
chr7:116238585
|
C | CATTATTA others(8): Show |
60 | a0001c0001t0003g0242a0001c0002t0001g0005a0001c0002t0001g0027others(57): Show | 67 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.113+3982_113+3996d others(17): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr7 | 116238585 | |||||
chr7:116238585
|
C | CATTATTA others(11): Show |
3 | a0001c0002t0001g0039a0001c0002t0001g0195a0001c0002t0001g0213 | 4 | HG02165.hp1 NA18977.hp2 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.113+3979_113+3996d others(20): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr7 | 116238585 | |||||
chr7:116238585
|
C | CATTATTA others(14): Show |
2 | a0001c0002t0001g0194a0001c0002t0001g0196 | 2 | HG00639.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.113+3976_113+3996d others(23): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr7 | 116238585 | |||||
chr7:116238588
|
T | C | 6 | a0001c0002t0004g0023a0001c0002t0004g0024a0001c0002t0004g0095others(3): Show | 8 | HG02809.hp1 HG02970.hp1 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.113+3969T>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116238588 | ||||||
chr7:116238596
|
T | TTATTATT others(7): Show |
1 | a0001c0002t0006g0060 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.113+3979_113+3992d others(16): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr7 | 116238596 | |||||
chr7:116238616
|
T | A | 50 | a0001c0001t0003g0065a0001c0001t0007g0040a0001c0001t0007g0217others(47): Show | 69 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.113+3997T>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116238616 | ||||||
chr7:116238756
|
C | T | 105 | a0001c0002t0001g0005a0001c0002t0001g0016a0001c0002t0001g0027others(102): Show | 117 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.113+4137C>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116238756 | ||||||
chr7:116238775
|
A | C | 4 | a0001c0001t0005g0061a0001c0001t0007g0040a0001c0001t0007g0062others(1): Show | 5 | HG02559.hp2 HG03195.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.113+4156A>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116238775 | ||||||
chr7:116239113
|
T | C | 1 | a0001c0002t0006g0301 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.113+4494T>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116239113 | ||||||
chr7:116239386
|
A | G | 2 | a0001c0002t0001g0161a0001c0002t0001g0191 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.113+4767A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116239386 | ||||||
chr7:116239478
|
G | A | 1 | a0001c0002t0001g0174 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.113+4859G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116239478 | ||||||
chr7:116239511
|
C | G | 1 | a0001c0001t0005g0061 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.113+4892C>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116239511 | ||||||
chr7:116239648
|
G | A | 1 | a0001c0001t0005g0226 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.113+5029G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116239648 | ||||||
chr7:116239754
|
G | A | 1 | a0001c0002t0006g0060 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.113+5135G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116239754 | ||||||
chr7:116239884
|
A | T | 47 | a0001c0001t0003g0065a0001c0002t0004g0002a0001c0002t0004g0006others(44): Show | 65 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.113+5265A>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116239884 | ||||||
chr7:116239885
|
G | GT | 47 | a0001c0001t0003g0065a0001c0002t0004g0002a0001c0002t0004g0006others(44): Show | 65 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.113+5268dupT | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr7 | 116239885 | |||||
chr7:116239920
|
C | T | 2 | a0001c0002t0001g0164a0001c0002t0001g0199 | 2 | NA18978.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.113+5301C>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116239920 | ||||||
chr7:116240223
|
G | A | 157 | a0001c0001t0003g0065a0001c0001t0005g0061a0001c0001t0007g0040others(154): Show | 188 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.113+5604G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116240223 | ||||||
chr7:116240315
|
G | A | 1 | a0001c0002t0006g0100 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.113+5696G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116240315 | ||||||
chr7:116240386
|
T | C | 7 | a0001c0002t0006g0026a0001c0002t0006g0056a0001c0002t0006g0057others(4): Show | 8 | HG02280.hp1 HG02486.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.113+5767T>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116240386 | ||||||
chr7:116240434
|
G | T | 3 | a0001c0002t0006g0101a0001c0002t0006g0102a0001c0002t0006g0103 | 3 | HG02258.hp2 HG03516.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.113+5815G>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116240434 | ||||||
chr7:116240465
|
C | A | 1 | a0001c0001t0003g0045 | 2 | NA18970.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.113+5846C>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116240465 | ||||||
chr7:116240484
|
G | A | 4 | a0001c0001t0005g0061a0001c0001t0007g0040a0001c0001t0007g0062others(1): Show | 5 | HG02559.hp2 HG03195.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.113+5865G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116240484 | ||||||
chr7:116240723
|
C | G | 4 | a0001c0001t0002g0004a0001c0001t0002g0033a0001c0001t0002g0140others(1): Show | 9 | NA18944.hp1 NA18946.hp2 NA18956.hp1 others(6): Show |
intron_variant | MODIFIER | c.113+6104C>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116240723 | ||||||
chr7:116241105
|
G | A | 157 | a0001c0001t0003g0065a0001c0001t0005g0061a0001c0001t0007g0040others(154): Show | 188 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.113+6486G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116241105 | ||||||
chr7:116241218
|
G | A | 1 | a0001c0001t0005g0229 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.113+6599G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116241218 | ||||||
chr7:116241351
|
T | C | 3 | a0001c0001t0003g0011a0001c0001t0003g0240a0001c0001t0003g0252 | 6 | HG00621.hp1 NA18946.hp1 NA18965.hp2 others(3): Show |
intron_variant | MODIFIER | c.113+6732T>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116241351 | ||||||
chr7:116241386
|
T | A | 1 | a0001c0001t0005g0233 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.113+6767T>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116241386 | ||||||
chr7:116241404
|
A | G | 157 | a0001c0001t0003g0065a0001c0001t0005g0061a0001c0001t0007g0040others(154): Show | 188 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.113+6785A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116241404 | ||||||
chr7:116241482
|
G | A | 4 | a0001c0002t0006g0056a0001c0002t0006g0057a0001c0002t0006g0058others(1): Show | 4 | HG02280.hp1 HG02486.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.113+6863G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116241482 | ||||||
chr7:116241625
|
A | G | 226 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0014others(223): Show | 275 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.113+7006A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116241625 | ||||||
chr7:116241653
|
G | A | 1 | a0001c0002t0006g0057 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.113+7034G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116241653 | ||||||
chr7:116241686
|
T | A | 105 | a0001c0002t0001g0005a0001c0002t0001g0016a0001c0002t0001g0027others(102): Show | 117 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.113+7067T>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116241686 | ||||||
chr7:116241689
|
G | GTA | 105 | a0001c0002t0001g0005a0001c0002t0001g0016a0001c0002t0001g0027others(102): Show | 117 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.113+7070_113+7071i others(4): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116241689 | ||||||
chr7:116241690
|
G | T | 105 | a0001c0002t0001g0005a0001c0002t0001g0016a0001c0002t0001g0027others(102): Show | 117 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.113+7071G>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116241690 | ||||||
chr7:116241691
|
T | G | 105 | a0001c0002t0001g0005a0001c0002t0001g0016a0001c0002t0001g0027others(102): Show | 117 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.113+7072T>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116241691 | ||||||
chr7:116241881
|
T | C | 1 | a0001c0001t0005g0232 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.114-7139T>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116241881 | ||||||
chr7:116242269
|
G | A | 157 | a0001c0001t0003g0065a0001c0001t0005g0061a0001c0001t0007g0040others(154): Show | 188 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.114-6751G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116242269 | ||||||
chr7:116242469
|
A | G | 1 | a0001c0002t0006g0301 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.114-6551A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116242469 | ||||||
chr7:116242507
|
A | ATC | 15 | a0001c0001t0002g0032a0001c0001t0002g0035a0001c0001t0002g0117others(12): Show | 17 | HG00423.hp1 HG00639.hp2 HG01099.hp1 others(14): Show |
intron_variant | MODIFIER | c.114-6483_114-6482d others(4): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr7 | 116242507 | |||||
chr7:116242507
|
ATCTC | A | 63 | a0001c0001t0003g0065a0001c0001t0005g0042a0001c0001t0005g0043others(60): Show | 84 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.114-6485_114-6482d others(6): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr7 | 116242507 | |||||
chr7:116242507
|
ATCTCTC | A | 4 | a0001c0001t0005g0061a0001c0001t0007g0040a0001c0001t0007g0062others(1): Show | 5 | HG02559.hp2 HG03195.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.114-6487_114-6482d others(8): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr7 | 116242507 | |||||
chr7:116242525
|
CTCTCTCT others(13): Show |
C | 101 | a0001c0002t0001g0005a0001c0002t0001g0016a0001c0002t0001g0027others(98): Show | 112 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.114-6490_114-6471d others(22): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr7 | 116242525 | |||||
chr7:116242527
|
C | G | 1 | a0001c0001t0003g0262 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.114-6493C>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116242527 | ||||||
chr7:116242527
|
CTCTCTCT others(11): Show |
C | 4 | a0001c0002t0001g0029a0001c0002t0001g0105a0001c0002t0001g0107others(1): Show | 5 | HG02615.hp1 HG02647.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.114-6488_114-6471d others(20): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr7 | 116242527 | |||||
chr7:116242529
|
CTCTCTCT others(3): Show |
C | 42 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0041others(39): Show | 54 | HG00558.hp2 HG00621.hp1 HG00738.hp2 others(51): Show |
intron_variant | MODIFIER | c.114-6485_114-6476d others(12): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr7 | 116242529 | |||||
chr7:116242531
|
CTCTCTCT others(7): Show |
C | 1 | a0001c0002t0006g0060 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.114-6484_114-6471d others(16): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr7 | 116242531 | |||||
chr7:116242533
|
CTCTCTG | C | 9 | a0001c0001t0003g0014a0001c0001t0003g0049a0001c0001t0003g0218others(6): Show | 12 | HG00140.hp2 HG00735.hp2 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.114-6476_114-6471d others(8): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr7 | 116242533 | |||||
chr7:116242542
|
T | C | 1 | a0001c0001t0002g0134 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.114-6478T>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116242542 | ||||||
chr7:116242545
|
G | C | 51 | a0001c0001t0003g0065a0001c0001t0005g0061a0001c0001t0007g0040others(48): Show | 70 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.114-6475G>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116242545 | ||||||
chr7:116243399
|
T | G | 157 | a0001c0001t0003g0065a0001c0001t0005g0061a0001c0001t0007g0040others(154): Show | 188 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.114-5621T>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116243399 | ||||||
chr7:116243477
|
T | C | 1 | a0001c0002t0001g0151 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.114-5543T>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116243477 | ||||||
chr7:116243531
|
C | T | 18 | a0001c0001t0005g0042a0001c0001t0005g0043a0001c0001t0005g0044others(15): Show | 21 | HG00642.hp1 HG00642.hp2 HG01069.hp1 others(18): Show |
intron_variant | MODIFIER | c.114-5489C>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116243531 | ||||||
chr7:116243753
|
A | G | 3 | a0001c0002t0006g0101a0001c0002t0006g0102a0001c0002t0006g0103 | 3 | HG02258.hp2 HG03516.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.114-5267A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116243753 | ||||||
chr7:116243878
|
A | C | 2 | a0001c0001t0005g0285a0001c0001t0005g0286 | 2 | HG00280.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.114-5142A>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116243878 | ||||||
chr7:116244024
|
G | C | 225 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0014others(222): Show | 274 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(271): Show |
intron_variant | MODIFIER | c.114-4996G>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116244024 | ||||||
chr7:116244255
|
C | T | 1 | a0001c0002t0001g0213 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.114-4765C>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116244255 | ||||||
chr7:116244265
|
C | A | 157 | a0001c0001t0003g0065a0001c0001t0005g0061a0001c0001t0007g0040others(154): Show | 188 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.114-4755C>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116244265 | ||||||
chr7:116244427
|
A | G | 1 | a0001c0002t0001g0186 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.114-4593A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116244427 | ||||||
chr7:116244544
|
G | C | 51 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0014others(48): Show | 66 | HG00140.hp2 HG00558.hp2 HG00621.hp1 others(63): Show |
intron_variant | MODIFIER | c.114-4476G>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116244544 | ||||||
chr7:116244575
|
C | T | 47 | a0001c0001t0003g0065a0001c0002t0004g0002a0001c0002t0004g0006others(44): Show | 65 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.114-4445C>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116244575 | ||||||
chr7:116244728
|
A | T | 35 | a0001c0002t0004g0002a0001c0002t0004g0007a0001c0002t0004g0018others(32): Show | 48 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(45): Show |
intron_variant | MODIFIER | c.114-4292A>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116244728 | ||||||
chr7:116244747
|
A | T | 1 | a0001c0002t0004g0098 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.114-4273A>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116244747 | ||||||
chr7:116244873
|
C | T | 1 | a0001c0001t0003g0245 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.114-4147C>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116244873 | ||||||
chr7:116245031
|
C | T | 1 | a0001c0002t0004g0080 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.114-3989C>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116245031 | ||||||
chr7:116245038
|
A | G | 1 | a0001c0001t0005g0237 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.114-3982A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116245038 | ||||||
chr7:116245142
|
G | A | 1 | a0001c0001t0005g0061 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.114-3878G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116245142 | ||||||
chr7:116245251
|
T | C | 2 | a0002c0003t0001g0189a0002c0003t0001g0193 | 2 | NA18957.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.114-3769T>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116245251 | ||||||
chr7:116245256
|
C | T | 2 | a0001c0001t0007g0040a0001c0001t0007g0217 | 3 | HG02559.hp2 HG03195.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.114-3764C>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116245256 | ||||||
chr7:116245270
|
T | C | 2 | a0001c0002t0001g0152a0001c0002t0001g0153 | 2 | HG01175.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.114-3750T>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116245270 | ||||||
chr7:116245298
|
C | A | 47 | a0001c0001t0003g0065a0001c0002t0004g0002a0001c0002t0004g0006others(44): Show | 65 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.114-3722C>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116245298 | ||||||
chr7:116245380
|
C | A | 3 | a0001c0001t0002g0008a0001c0001t0002g0121a0001c0001t0002g0138 | 6 | HG01346.hp2 HG01934.hp1 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.114-3640C>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116245380 | ||||||
chr7:116245566
|
C | T | 2 | a0001c0002t0004g0069a0001c0002t0004g0079 | 2 | HG01928.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.114-3454C>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116245566 | ||||||
chr7:116245622
|
C | G | 1 | a0001c0002t0001g0155 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.114-3398C>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116245622 | ||||||
chr7:116245656
|
T | G | 3 | a0001c0001t0002g0008a0001c0001t0002g0121a0001c0001t0002g0138 | 6 | HG01346.hp2 HG01934.hp1 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.114-3364T>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116245656 | ||||||
chr7:116245953
|
A | C | 226 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0014others(223): Show | 275 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.114-3067A>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116245953 | ||||||
chr7:116245955
|
C | G | 101 | a0001c0002t0001g0005a0001c0002t0001g0016a0001c0002t0001g0027others(98): Show | 113 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.114-3065C>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116245955 | ||||||
chr7:116246025
|
A | G | 157 | a0001c0001t0003g0065a0001c0001t0005g0061a0001c0001t0007g0040others(154): Show | 188 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.114-2995A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116246025 | ||||||
chr7:116246053
|
TC | T | 47 | a0001c0001t0003g0065a0001c0002t0004g0002a0001c0002t0004g0006others(44): Show | 65 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.114-2966delC | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116246053 | ||||||
chr7:116246340
|
T | C | 1 | a0001c0002t0001g0114 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.114-2680T>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116246340 | ||||||
chr7:116246497
|
C | G | 1 | a0001c0001t0005g0061 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.114-2523C>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116246497 | ||||||
chr7:116246511
|
A | G | 1 | a0001c0002t0001g0159 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.114-2509A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116246511 | ||||||
chr7:116246553
|
C | A | 3 | a0001c0001t0007g0040a0001c0001t0007g0062a0001c0001t0007g0217 | 4 | HG02559.hp2 HG03195.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.114-2467C>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116246553 | ||||||
chr7:116246748
|
G | A | 6 | a0001c0001t0003g0065a0001c0002t0004g0006a0001c0002t0004g0064others(3): Show | 9 | HG00741.hp2 HG01109.hp2 HG01256.hp2 others(6): Show |
intron_variant | MODIFIER | c.114-2272G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116246748 | ||||||
chr7:116246766
|
A | C | 1 | a0001c0001t0002g0131 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.114-2254A>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116246766 | ||||||
chr7:116246779
|
A | G | 1 | a0001c0001t0002g0140 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.114-2241A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116246779 | ||||||
chr7:116246797
|
G | C | 1 | a0001c0002t0011g0210 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.114-2223G>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116246797 | ||||||
chr7:116246805
|
A | G | 1 | a0001c0001t0002g0131 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.114-2215A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116246805 | ||||||
chr7:116246868
|
C | CTGTG | 153 | a0001c0001t0003g0065a0001c0002t0001g0005a0001c0002t0001g0016others(150): Show | 183 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(180): Show |
intron_variant | MODIFIER | c.114-2150_114-2147d others(6): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr7 | 116246868 | |||||
chr7:116246872
|
G | GTGTGTA | 4 | a0001c0001t0005g0061a0001c0001t0007g0040a0001c0001t0007g0062others(1): Show | 5 | HG02559.hp2 HG03195.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.114-2147_114-2146i others(8): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr7 | 116246872 | |||||
chr7:116246874
|
A | G | 3 | a0001c0001t0007g0040a0001c0001t0007g0062a0001c0001t0007g0217 | 4 | HG02559.hp2 HG03195.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.114-2146A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116246874 | ||||||
chr7:116246874
|
A | T | 1 | a0001c0001t0005g0061 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.114-2146A>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116246874 | ||||||
chr7:116246877
|
T | G | 2 | a0001c0002t0006g0108a0001c0002t0006g0109 | 2 | HG02055.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.114-2143T>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116246877 | ||||||
chr7:116246911
|
C | T | 1 | a0001c0001t0003g0267 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.114-2109C>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116246911 | ||||||
chr7:116246913
|
A | C | 1 | a0001c0001t0003g0267 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.114-2107A>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116246913 | ||||||
chr7:116246914
|
G | C | 1 | a0001c0001t0003g0267 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.114-2106G>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116246914 | ||||||
chr7:116246939
|
C | G | 105 | a0001c0002t0001g0005a0001c0002t0001g0016a0001c0002t0001g0027others(102): Show | 117 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.114-2081C>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116246939 | ||||||
chr7:116246946
|
C | CT | 83 | a0001c0002t0001g0005a0001c0002t0001g0016a0001c0002t0001g0027others(80): Show | 93 | HG00280.hp1 HG00423.hp2 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.114-2074_114-2073i others(3): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116246946 | ||||||
chr7:116246946
|
C | CTT | 19 | a0001c0001t0005g0061a0001c0002t0001g0156a0001c0002t0001g0157others(16): Show | 20 | HG00140.hp1 HG00408.hp1 HG01943.hp2 others(17): Show |
intron_variant | MODIFIER | c.114-2074_114-2073i others(4): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116246946 | ||||||
chr7:116246946
|
C | CTTT | 42 | a0001c0002t0001g0173a0001c0002t0004g0002a0001c0002t0004g0006others(39): Show | 60 | HG00408.hp2 HG00438.hp2 HG00738.hp1 others(57): Show |
intron_variant | MODIFIER | c.114-2074_114-2073i others(5): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116246946 | ||||||
chr7:116246947
|
C | CT | 15 | a0001c0001t0002g0137a0001c0001t0005g0043a0001c0001t0005g0223others(12): Show | 16 | HG00642.hp1 HG00642.hp2 HG00733.hp2 others(13): Show |
intron_variant | MODIFIER | c.114-2053dupT | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr7 | 116246947 | |||||
chr7:116246947
|
C | T | 152 | a0001c0001t0003g0065a0001c0001t0005g0061a0001c0002t0001g0005others(149): Show | 181 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(178): Show |
intron_variant | MODIFIER | c.114-2073C>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116246947 | ||||||
chr7:116246947
|
CT | C | 51 | a0001c0001t0002g0017a0001c0001t0002g0125a0001c0001t0003g0011others(48): Show | 67 | HG00140.hp2 HG00558.hp2 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.114-2053delT | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr7 | 116246947 | |||||
chr7:116246970
|
G | A | 1 | a0001c0001t0003g0270 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.114-2050G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116246970 | ||||||
chr7:116247016
|
G | A | 52 | a0001c0001t0003g0065a0001c0001t0005g0061a0001c0001t0007g0040others(49): Show | 71 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.114-2004G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116247016 | ||||||
chr7:116247144
|
A | C | 2 | a0001c0001t0003g0249a0001c0001t0003g0271 | 2 | HG02083.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.114-1876A>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116247144 | ||||||
chr7:116247172
|
G | A | 1 | a0001c0001t0002g0126 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.114-1848G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116247172 | ||||||
chr7:116247173
|
A | G | 47 | a0001c0001t0003g0065a0001c0002t0004g0002a0001c0002t0004g0006others(44): Show | 65 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.114-1847A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116247173 | ||||||
chr7:116247254
|
A | G | 302 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0004others(299): Show | 385 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(382): Show |
intron_variant | MODIFIER | c.114-1766A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116247254 | ||||||
chr7:116247268
|
A | T | 1 | a0001c0002t0001g0204 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.114-1752A>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116247268 | ||||||
chr7:116247415
|
T | C | 1 | a0001c0002t0006g0060 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.114-1605T>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116247415 | ||||||
chr7:116247416
|
ATTAT | A | 2 | a0001c0001t0007g0040a0001c0001t0007g0217 | 3 | HG02559.hp2 HG03195.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.114-1597_114-1594d others(6): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr7 | 116247416 | |||||
chr7:116247532
|
T | C | 2 | a0001c0002t0004g0019a0001c0002t0004g0076 | 3 | HG02738.hp1 HG03927.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.114-1488T>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116247532 | ||||||
chr7:116247756
|
G | T | 3 | a0001c0001t0007g0040a0001c0001t0007g0062a0001c0001t0007g0217 | 4 | HG02559.hp2 HG03195.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.114-1264G>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116247756 | ||||||
chr7:116247777
|
T | G | 1 | a0001c0001t0005g0288 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.114-1243T>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116247777 | ||||||
chr7:116247864
|
A | G | 47 | a0001c0001t0003g0065a0001c0002t0004g0002a0001c0002t0004g0006others(44): Show | 65 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.114-1156A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116247864 | ||||||
chr7:116248014
|
G | T | 105 | a0001c0002t0001g0005a0001c0002t0001g0016a0001c0002t0001g0027others(102): Show | 117 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.114-1006G>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116248014 | ||||||
chr7:116248041
|
C | G | 4 | a0001c0002t0004g0090a0001c0002t0004g0091a0001c0002t0004g0093others(1): Show | 4 | NA18942.hp1 NA18978.hp1 NA19074.hp1 others(1): Show |
intron_variant | MODIFIER | c.114-979C>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116248041 | ||||||
chr7:116248061
|
T | G | 1 | a0001c0002t0001g0151 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.114-959T>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116248061 | ||||||
chr7:116248108
|
A | G | 157 | a0001c0001t0003g0065a0001c0001t0005g0061a0001c0001t0007g0040others(154): Show | 188 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.114-912A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116248108 | ||||||
chr7:116248145
|
T | A | 47 | a0001c0001t0003g0065a0001c0002t0004g0002a0001c0002t0004g0006others(44): Show | 65 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.114-875T>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116248145 | ||||||
chr7:116248264
|
T | G | 2 | a0001c0002t0006g0101a0001c0002t0006g0102 | 2 | HG02258.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.114-756T>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116248264 | ||||||
chr7:116248285
|
G | A | 157 | a0001c0001t0003g0065a0001c0001t0005g0061a0001c0001t0007g0040others(154): Show | 188 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.114-735G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116248285 | ||||||
chr7:116248491
|
GA | G | 2 | a0001c0001t0007g0040a0001c0001t0007g0217 | 3 | HG02559.hp2 HG03195.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.114-527delA | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr7 | 116248491 | |||||
chr7:116248510
|
C | T | 1 | a0001c0001t0002g0001 | 6 | HG00438.hp1 NA18940.hp1 NA18945.hp1 others(3): Show |
intron_variant | MODIFIER | c.114-510C>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116248510 | ||||||
chr7:116248602
|
G | T | 1 | a0001c0001t0005g0278 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.114-418G>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116248602 | ||||||
chr7:116248665
|
A | T | 1 | a0001c0001t0005g0061 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.114-355A>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 2/6 | chr7 | 116248665 | ||||||
chr7:116249315
|
G | T | 3 | a0001c0002t0001g0156a0001c0002t0001g0173a0001c0002t0001g0174 | 3 | HG00408.hp1 NA18940.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.366+43G>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 3/6 | chr7 | 116249315 | ||||||
chr7:116249382
|
T | A | 1 | a0001c0001t0003g0046 | 2 | NA18953.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.366+110T>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 3/6 | chr7 | 116249382 | ||||||
chr7:116249859
|
A | G | 52 | a0001c0001t0003g0065a0001c0001t0005g0061a0001c0001t0007g0040others(49): Show | 71 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.367-302A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 3/6 | chr7 | 116249859 | ||||||
chr7:116249945
|
T | C | 4 | a0001c0001t0005g0061a0001c0001t0007g0040a0001c0001t0007g0062others(1): Show | 5 | HG02559.hp2 HG03195.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.367-216T>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 3/6 | chr7 | 116249945 | ||||||
chr7:116250002
|
C | T | 5 | a0002c0003t0001g0150a0002c0003t0001g0165a0002c0003t0001g0189others(2): Show | 5 | NA18957.hp2 NA18999.hp2 NA19006.hp1 others(2): Show |
intron_variant | MODIFIER | c.367-159C>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 3/6 | chr7 | 116250002 | ||||||
chr7:116250056
|
A | G | 1 | a0001c0002t0001g0151 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.367-105A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 3/6 | chr7 | 116250056 | ||||||
chr7:116250086
|
C | T | 2 | a0001c0001t0007g0040a0001c0001t0007g0217 | 3 | HG02559.hp2 HG03195.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.367-75C>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 3/6 | chr7 | 116250086 | ||||||
chr7:116250103
|
G | A | 61 | a0001c0001t0005g0061a0001c0001t0007g0040a0001c0001t0007g0062others(58): Show | 81 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.367-58G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 3/6 | chr7 | 116250103 | ||||||
chr7:116250133
|
A | G | 57 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0014others(54): Show | 72 | HG00140.hp2 HG00558.hp2 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.367-28A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 3/6 | chr7 | 116250133 | ||||||
chr7:116250780
|
A | G | 195 | a0001c0001t0002g0032a0001c0001t0003g0011a0001c0001t0003g0012others(192): Show | 233 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(230): Show |
intron_variant | MODIFIER | c.702+284A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 4/6 | chr7 | 116250780 | ||||||
chr7:116251067
|
T | C | 1 | a0001c0002t0004g0076 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.702+571T>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 4/6 | chr7 | 116251067 | ||||||
chr7:116251091
|
G | T | 1 | a0001c0002t0001g0175 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.702+595G>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 4/6 | chr7 | 116251091 | ||||||
chr7:116251274
|
C | T | 11 | a0001c0002t0004g0006a0001c0002t0004g0023a0001c0002t0004g0024others(8): Show | 16 | HG01109.hp2 HG01256.hp2 HG01257.hp1 others(13): Show |
intron_variant | MODIFIER | c.703-486C>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 4/6 | chr7 | 116251274 | ||||||
chr7:116251421
|
G | A | 102 | a0001c0002t0001g0005a0001c0002t0001g0016a0001c0002t0001g0027others(99): Show | 115 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.703-339G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 4/6 | chr7 | 116251421 | ||||||
chr7:116251459
|
A | G | 123 | a0001c0001t0005g0061a0001c0001t0007g0040a0001c0001t0007g0062others(120): Show | 142 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.703-301A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 4/6 | chr7 | 116251459 | ||||||
chr7:116251552
|
A | G | 1 | a0001c0001t0002g0030 | 2 | HG03834.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.703-208A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 4/6 | chr7 | 116251552 | ||||||
chr7:116251573
|
C | G | 1 | a0001c0002t0004g0086 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.703-187C>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 4/6 | chr7 | 116251573 | ||||||
chr7:116251587
|
G | A | 123 | a0001c0001t0005g0061a0001c0001t0007g0040a0001c0001t0007g0062others(120): Show | 142 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.703-173G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 4/6 | chr7 | 116251587 | ||||||
chr7:116251593
|
G | A | 1 | a0001c0001t0003g0050 | 2 | HG00738.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.703-167G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 4/6 | chr7 | 116251593 | ||||||
chr7:116251632
|
G | A | 123 | a0001c0001t0005g0061a0001c0001t0007g0040a0001c0001t0007g0062others(120): Show | 142 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.703-128G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 4/6 | chr7 | 116251632 | ||||||
chr7:116251692
|
AAAAG | A | 107 | a0001c0001t0003g0257a0001c0002t0001g0005a0001c0002t0001g0016others(104): Show | 120 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.703-56_703-53delGA others(2): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr7 | 116251692 | |||||
chr7:116251723
|
C | T | 1 | a0001c0002t0001g0105 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.703-37C>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 4/6 | chr7 | 116251723 | ||||||
chr7:116252106
|
A | G | 1 | a0001c0002t0006g0060 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.918+131A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 5/6 | chr7 | 116252106 | ||||||
chr7:116252224
|
C | T | 9 | a0001c0002t0004g0002a0001c0002t0004g0021a0001c0002t0004g0063others(6): Show | 14 | HG00408.hp2 HG00438.hp2 NA18939.hp2 others(11): Show |
intron_variant | MODIFIER | c.919-94C>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 5/6 | chr7 | 116252224 | ||||||
chr7:116252241
|
C | A | 107 | a0001c0002t0001g0005a0001c0002t0001g0016a0001c0002t0001g0027others(104): Show | 120 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.919-77C>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 5/6 | chr7 | 116252241 | ||||||
chr7:116252291
|
C | A | 1 | a0001c0001t0005g0298 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.919-27C>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 5/6 | chr7 | 116252291 | ||||||
chr7:116252541
|
T | C | 3 | a0001c0002t0004g0007a0001c0002t0004g0018a0001c0002t0004g0077 | 7 | NA18612.hp2 NA18959.hp1 NA18970.hp1 others(4): Show |
intron_variant | MODIFIER | c.1077+65T>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116252541 | ||||||
chr7:116252596
|
T | G | 158 | a0001c0001t0005g0061a0001c0001t0007g0040a0001c0001t0007g0062others(155): Show | 190 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(187): Show |
intron_variant | MODIFIER | c.1077+120T>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116252596 | ||||||
chr7:116252641
|
A | G | 1 | a0001c0001t0003g0255 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1077+165A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116252641 | ||||||
chr7:116252675
|
A | G | 1 | a0001c0002t0006g0060 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1077+199A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116252675 | ||||||
chr7:116252684
|
A | G | 158 | a0001c0001t0005g0061a0001c0001t0007g0040a0001c0001t0007g0062others(155): Show | 190 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(187): Show |
intron_variant | MODIFIER | c.1077+208A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116252684 | ||||||
chr7:116252703
|
G | A | 106 | a0001c0002t0001g0005a0001c0002t0001g0016a0001c0002t0001g0027others(103): Show | 119 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.1077+227G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116252703 | ||||||
chr7:116252872
|
C | A | 2 | a0001c0002t0006g0108a0001c0002t0006g0109 | 2 | HG02055.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1077+396C>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116252872 | ||||||
chr7:116252969
|
A | G | 1 | a0001c0002t0001g0207 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1077+493A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116252969 | ||||||
chr7:116252991
|
A | G | 107 | a0001c0002t0001g0005a0001c0002t0001g0016a0001c0002t0001g0027others(104): Show | 120 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.1077+515A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116252991 | ||||||
chr7:116253039
|
A | C | 2 | a0001c0001t0007g0040a0001c0001t0007g0217 | 3 | HG02559.hp2 HG03195.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1077+563A>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116253039 | ||||||
chr7:116253143
|
A | G | 1 | a0001c0001t0007g0062 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1077+667A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116253143 | ||||||
chr7:116253308
|
A | G | 111 | a0001c0001t0005g0061a0001c0001t0007g0040a0001c0001t0007g0062others(108): Show | 125 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.1077+832A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116253308 | ||||||
chr7:116253353
|
A | T | 154 | a0001c0002t0001g0005a0001c0002t0001g0016a0001c0002t0001g0027others(151): Show | 185 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(182): Show |
intron_variant | MODIFIER | c.1077+877A>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116253353 | ||||||
chr7:116253428
|
T | G | 1 | a0001c0002t0001g0196 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1077+952T>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116253428 | ||||||
chr7:116253593
|
A | G | 158 | a0001c0001t0005g0061a0001c0001t0007g0040a0001c0001t0007g0062others(155): Show | 190 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(187): Show |
intron_variant | MODIFIER | c.1077+1117A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116253593 | ||||||
chr7:116253697
|
G | A | 1 | a0001c0001t0002g0033 | 2 | NA18964.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.1077+1221G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116253697 | ||||||
chr7:116253791
|
A | C | 154 | a0001c0002t0001g0005a0001c0002t0001g0016a0001c0002t0001g0027others(151): Show | 185 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(182): Show |
intron_variant | MODIFIER | c.1077+1315A>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116253791 | ||||||
chr7:116253822
|
C | A | 1 | a0001c0001t0005g0282 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1077+1346C>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116253822 | ||||||
chr7:116253837
|
A | G | 1 | a0001c0002t0006g0108 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1077+1361A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116253837 | ||||||
chr7:116253843
|
T | C | 154 | a0001c0002t0001g0005a0001c0002t0001g0016a0001c0002t0001g0027others(151): Show | 185 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(182): Show |
intron_variant | MODIFIER | c.1077+1367T>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116253843 | ||||||
chr7:116253965
|
T | C | 5 | a0001c0002t0004g0006a0001c0002t0004g0064a0001c0002t0004g0066others(2): Show | 8 | HG01109.hp2 HG01256.hp2 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.1077+1489T>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116253965 | ||||||
chr7:116254055
|
ACAAGACG others(1): Show |
A | 52 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0014others(49): Show | 67 | HG00140.hp2 HG00558.hp2 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.1077+1583_1077+159 others(12): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr7 | 116254055 | |||||
chr7:116254322
|
T | C | 154 | a0001c0002t0001g0005a0001c0002t0001g0016a0001c0002t0001g0027others(151): Show | 185 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(182): Show |
intron_variant | MODIFIER | c.1077+1846T>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116254322 | ||||||
chr7:116254324
|
C | CT | 154 | a0001c0002t0001g0005a0001c0002t0001g0016a0001c0002t0001g0027others(151): Show | 185 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(182): Show |
intron_variant | MODIFIER | c.1077+1855dupT | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr7 | 116254324 | |||||
chr7:116254349
|
C | G | 154 | a0001c0002t0001g0005a0001c0002t0001g0016a0001c0002t0001g0027others(151): Show | 185 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(182): Show |
intron_variant | MODIFIER | c.1077+1873C>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116254349 | ||||||
chr7:116254462
|
A | G | 1 | a0001c0002t0001g0209 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1077+1986A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116254462 | ||||||
chr7:116254473
|
C | T | 108 | a0001c0002t0001g0005a0001c0002t0001g0016a0001c0002t0001g0027others(105): Show | 121 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.1077+1997C>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116254473 | ||||||
chr7:116254474
|
G | A | 108 | a0001c0002t0001g0005a0001c0002t0001g0016a0001c0002t0001g0027others(105): Show | 121 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.1077+1998G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116254474 | ||||||
chr7:116254504
|
G | A | 18 | a0001c0001t0005g0042a0001c0001t0005g0043a0001c0001t0005g0044others(15): Show | 21 | HG00642.hp1 HG00642.hp2 HG01069.hp1 others(18): Show |
intron_variant | MODIFIER | c.1077+2028G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116254504 | ||||||
chr7:116254510
|
C | T | 1 | a0001c0001t0003g0050 | 2 | HG00738.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.1077+2034C>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116254510 | ||||||
chr7:116254511
|
G | A | 1 | a0001c0002t0001g0195 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1077+2035G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116254511 | ||||||
chr7:116254529
|
T | G | 1 | a0001c0002t0006g0060 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1077+2053T>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116254529 | ||||||
chr7:116254535
|
A | T | 157 | a0001c0001t0005g0277a0001c0001t0007g0062a0001c0002t0001g0005others(154): Show | 188 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.1077+2059A>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116254535 | ||||||
chr7:116254546
|
C | T | 1 | a0001c0001t0005g0291 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1077+2070C>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116254546 | ||||||
chr7:116254585
|
A | C | 1 | a0001c0002t0001g0195 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1077+2109A>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116254585 | ||||||
chr7:116254611
|
C | G | 1 | a0001c0001t0003g0220 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1077+2135C>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116254611 | ||||||
chr7:116254735
|
C | T | 1 | a0001c0001t0005g0282 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1077+2259C>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116254735 | ||||||
chr7:116254740
|
CA | C | 8 | a0001c0002t0004g0022a0001c0002t0004g0024a0001c0002t0004g0064others(5): Show | 10 | HG02040.hp1 HG02809.hp1 HG02970.hp1 others(7): Show |
intron_variant | MODIFIER | c.1077+2272delA | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr7 | 116254740 | |||||
chr7:116254746
|
AAAT | A | 105 | a0001c0002t0001g0016a0001c0002t0001g0027a0001c0002t0001g0029others(102): Show | 124 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(121): Show |
intron_variant | MODIFIER | c.1077+2272_1077+227 others(7): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr7 | 116254746 | |||||
chr7:116254746
|
AAATAT | A | 20 | a0001c0002t0001g0005a0001c0002t0001g0037a0001c0002t0001g0112others(17): Show | 27 | HG00408.hp1 HG00609.hp2 HG01928.hp2 others(24): Show |
intron_variant | MODIFIER | c.1077+2272_1077+227 others(9): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr7 | 116254746 | |||||
chr7:116254747
|
A | AT | 15 | a0001c0002t0004g0019a0001c0002t0004g0025a0001c0002t0004g0067others(12): Show | 17 | HG00140.hp1 HG00738.hp1 HG01358.hp2 others(14): Show |
intron_variant | MODIFIER | c.1077+2271_1077+227 others(5): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116254747 | ||||||
chr7:116254747
|
A | ATAT | 6 | a0001c0002t0001g0162a0001c0002t0004g0072a0001c0002t0004g0080others(3): Show | 7 | HG01081.hp1 HG02486.hp1 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.1077+2271_1077+227 others(7): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116254747 | ||||||
chr7:116254747
|
A | T | 2 | a0001c0001t0002g0129a0001c0001t0002g0134 | 2 | NA18951.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.1077+2271A>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116254747 | ||||||
chr7:116254747
|
AAT | A | 9 | a0001c0001t0002g0117a0001c0001t0002g0136a0001c0001t0003g0046others(6): Show | 10 | HG00741.hp1 HG01255.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.1077+2282_1077+228 others(6): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr7 | 116254747 | |||||
chr7:116254749
|
T | A | 1 | a0001c0001t0005g0274 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1077+2273T>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116254749 | ||||||
chr7:116254752
|
A | G | 5 | a0001c0002t0004g0072a0001c0002t0004g0080a0001c0002t0004g0084others(2): Show | 6 | HG01081.hp1 HG02486.hp1 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.1077+2276A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116254752 | ||||||
chr7:116254754
|
A | G | 20 | a0001c0002t0001g0162a0001c0002t0004g0019a0001c0002t0004g0025others(17): Show | 23 | HG00140.hp1 HG00738.hp1 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.1077+2278A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116254754 | ||||||
chr7:116254756
|
A | ATG | 21 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0047others(18): Show | 30 | HG00621.hp1 HG00735.hp2 HG01069.hp1 others(27): Show |
intron_variant | MODIFIER | c.1077+2281_1077+228 others(6): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr7 | 116254756 | |||||
chr7:116254756
|
A | ATGTG | 14 | a0001c0001t0003g0048a0001c0001t0003g0065a0001c0001t0003g0222others(11): Show | 16 | HG00140.hp2 HG00642.hp1 HG00642.hp2 others(13): Show |
intron_variant | MODIFIER | c.1077+2281_1077+228 others(8): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr7 | 116254756 | |||||
chr7:116254756
|
A | ATGTGTG | 4 | a0001c0001t0003g0050a0001c0001t0003g0244a0001c0001t0005g0231others(1): Show | 5 | HG00738.hp2 HG01106.hp2 HG01109.hp1 others(2): Show |
intron_variant | MODIFIER | c.1077+2281_1077+228 others(10): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr7 | 116254756 | |||||
chr7:116254756
|
A | G | 34 | a0001c0001t0003g0252a0001c0001t0003g0256a0001c0001t0003g0271others(31): Show | 39 | HG00140.hp1 HG00738.hp1 HG01081.hp1 others(36): Show |
intron_variant | MODIFIER | c.1077+2280A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116254756 | ||||||
chr7:116254756
|
ATATGTGT others(7): Show |
A | 1 | a0001c0001t0003g0245 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1077+2282_1077+229 others(18): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr7 | 116254756 | |||||
chr7:116254758
|
A | ATG | 13 | a0001c0001t0002g0121a0001c0001t0002g0122a0001c0001t0002g0123others(10): Show | 13 | HG00280.hp2 HG00609.hp1 HG00621.hp2 others(10): Show |
intron_variant | MODIFIER | c.1077+2320_1077+232 others(6): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr7 | 116254758 | |||||
chr7:116254758
|
A | G | 113 | a0001c0001t0002g0001a0001c0001t0002g0010a0001c0001t0002g0144others(110): Show | 157 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.1077+2282A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116254758 | ||||||
chr7:116254758
|
ATG | A | 4 | a0001c0001t0002g0127a0001c0001t0005g0061a0001c0001t0005g0297others(1): Show | 4 | HG03491.hp2 HG03579.hp1 NA18939.hp1 others(1): Show |
intron_variant | MODIFIER | c.1077+2320_1077+232 others(6): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr7 | 116254758 | |||||
chr7:116254758
|
ATGTG | A | 70 | a0001c0001t0005g0278a0001c0002t0001g0016a0001c0002t0001g0038others(67): Show | 75 | HG00280.hp1 HG00423.hp2 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.1077+2318_1077+232 others(8): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr7 | 116254758 | |||||
chr7:116254758
|
ATGTGTG | A | 6 | a0001c0002t0001g0027a0001c0002t0001g0113a0001c0002t0001g0115others(3): Show | 6 | HG02622.hp1 HG03453.hp2 NA18522.hp1 others(3): Show |
intron_variant | MODIFIER | c.1077+2316_1077+232 others(10): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr7 | 116254758 | |||||
chr7:116254758
|
ATGTGTGT others(1): Show |
A | 12 | a0001c0002t0001g0029a0001c0002t0001g0105a0001c0002t0006g0026others(9): Show | 14 | HG02258.hp2 HG02280.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.1077+2314_1077+232 others(12): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr7 | 116254758 | |||||
chr7:116254758
|
ATGTGTGT others(3): Show |
A | 1 | a0001c0002t0006g0301 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1077+2312_1077+232 others(14): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr7 | 116254758 | |||||
chr7:116254760
|
G | A | 19 | a0001c0001t0007g0040a0001c0001t0007g0217a0001c0002t0001g0005others(16): Show | 26 | HG00408.hp1 HG00609.hp2 HG01934.hp2 others(23): Show |
intron_variant | MODIFIER | c.1077+2284G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116254760 | ||||||
chr7:116254762
|
G | A | 1 | a0001c0001t0005g0061 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1077+2286G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116254762 | ||||||
chr7:116254764
|
G | A | 1 | a0001c0001t0005g0061 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1077+2288G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116254764 | ||||||
chr7:116254932
|
T | C | 1 | a0001c0002t0001g0163 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1078-2362T>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116254932 | ||||||
chr7:116254956
|
G | T | 155 | a0001c0002t0001g0005a0001c0002t0001g0016a0001c0002t0001g0027others(152): Show | 186 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.1078-2338G>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116254956 | ||||||
chr7:116254974
|
T | A | 1 | a0001c0002t0001g0170 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1078-2320T>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116254974 | ||||||
chr7:116255001
|
A | AAGAG | 155 | a0001c0002t0001g0005a0001c0002t0001g0016a0001c0002t0001g0027others(152): Show | 186 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.1078-2289_1078-228 others(8): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr7 | 116255001 | |||||
chr7:116255181
|
T | C | 155 | a0001c0002t0001g0005a0001c0002t0001g0016a0001c0002t0001g0027others(152): Show | 186 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.1078-2113T>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116255181 | ||||||
chr7:116255379
|
T | C | 155 | a0001c0002t0001g0005a0001c0002t0001g0016a0001c0002t0001g0027others(152): Show | 186 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.1078-1915T>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116255379 | ||||||
chr7:116255382
|
C | T | 52 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0014others(49): Show | 67 | HG00140.hp2 HG00558.hp2 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.1078-1912C>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116255382 | ||||||
chr7:116255461
|
T | C | 46 | a0001c0002t0004g0002a0001c0002t0004g0006a0001c0002t0004g0007others(43): Show | 64 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.1078-1833T>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116255461 | ||||||
chr7:116255538
|
C | T | 1 | a0001c0001t0005g0228 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1078-1756C>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116255538 | ||||||
chr7:116255664
|
A | G | 155 | a0001c0002t0001g0005a0001c0002t0001g0016a0001c0002t0001g0027others(152): Show | 186 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.1078-1630A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116255664 | ||||||
chr7:116255697
|
A | G | 52 | a0001c0001t0003g0011a0001c0001t0003g0012a0001c0001t0003g0014others(49): Show | 67 | HG00140.hp2 HG00558.hp2 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.1078-1597A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116255697 | ||||||
chr7:116255768
|
T | C | 1 | a0001c0001t0003g0252 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1078-1526T>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116255768 | ||||||
chr7:116255834
|
A | G | 1 | a0001c0002t0006g0060 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1078-1460A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116255834 | ||||||
chr7:116255941
|
G | GACA | 155 | a0001c0002t0001g0005a0001c0002t0001g0016a0001c0002t0001g0027others(152): Show | 186 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.1078-1352_1078-135 others(7): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr7 | 116255941 | |||||
chr7:116255995
|
G | A | 155 | a0001c0002t0001g0005a0001c0002t0001g0016a0001c0002t0001g0027others(152): Show | 186 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.1078-1299G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116255995 | ||||||
chr7:116256037
|
C | T | 47 | a0001c0002t0004g0002a0001c0002t0004g0006a0001c0002t0004g0007others(44): Show | 65 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.1078-1257C>T | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116256037 | ||||||
chr7:116256074
|
C | CAAAG | 155 | a0001c0002t0001g0005a0001c0002t0001g0016a0001c0002t0001g0027others(152): Show | 186 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.1078-1217_1078-121 others(8): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr7 | 116256074 | |||||
chr7:116256139
|
A | G | 1 | a0001c0001t0003g0053 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1078-1155A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116256139 | ||||||
chr7:116256198
|
C | A | 1 | a0001c0002t0006g0060 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1078-1096C>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116256198 | ||||||
chr7:116256312
|
CT | C | 108 | a0001c0002t0001g0005a0001c0002t0001g0016a0001c0002t0001g0027others(105): Show | 121 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.1078-980delT | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr7 | 116256312 | |||||
chr7:116256353
|
A | G | 1 | a0001c0001t0005g0233 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1078-941A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116256353 | ||||||
chr7:116256399
|
T | A | 1 | a0001c0002t0006g0301 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1078-895T>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116256399 | ||||||
chr7:116256652
|
AAC | A | 5 | a0001c0001t0005g0061a0001c0001t0007g0040a0001c0001t0007g0062others(2): Show | 6 | HG02559.hp2 HG02809.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.1078-638_1078-637d others(4): Show |
TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr7 | 116256652 | |||||
chr7:116256662
|
G | A | 155 | a0001c0002t0001g0005a0001c0002t0001g0016a0001c0002t0001g0027others(152): Show | 186 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.1078-632G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116256662 | ||||||
chr7:116256690
|
G | A | 2 | a0001c0001t0005g0282a0001c0001t0005g0283 | 2 | HG00735.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.1078-604G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116256690 | ||||||
chr7:116257042
|
T | C | 155 | a0001c0002t0001g0005a0001c0002t0001g0016a0001c0002t0001g0027others(152): Show | 186 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.1078-252T>C | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116257042 | ||||||
chr7:116257168
|
A | G | 173 | a0001c0001t0005g0042a0001c0001t0005g0043a0001c0001t0005g0044others(170): Show | 207 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(204): Show |
intron_variant | MODIFIER | c.1078-126A>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116257168 | ||||||
chr7:116257181
|
G | A | 3 | a0001c0001t0007g0040a0001c0001t0007g0062a0001c0001t0007g0217 | 4 | HG02559.hp2 HG03195.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.1078-113G>A | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116257181 | ||||||
chr7:116257188
|
T | G | 173 | a0001c0001t0005g0042a0001c0001t0005g0043a0001c0001t0005g0044others(170): Show | 207 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(204): Show |
intron_variant | MODIFIER | c.1078-106T>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116257188 | ||||||
chr7:116257233
|
T | G | 47 | a0001c0002t0004g0002a0001c0002t0004g0006a0001c0002t0004g0007others(44): Show | 65 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.1078-61T>G | TES | ENSG00000135269.18 | transcript | ENST00000358204.9 | protein_coding | 6/6 | chr7 | 116257233 |