Item | Value |
---|---|
geneid | 55858 |
ensemblid | ENSG00000134851.13 |
hgncid | 30760 |
symbol | TMEM165 |
name | transmembrane protein 165 |
refseq_nuc | NM_018475.5 |
refseq_prot | NP_060945.2 |
ensembl_nuc | ENST00000381334.10 |
ensembl_prot | ENSP00000370736.5 |
mane_status | MANE Select |
chr | chr4 |
start | 55395957 |
end | 55426175 |
strand | + |
ver | v1.2 |
region | chr4:55395957-55426175 |
region5000 | chr4:55390957-55431175 |
regionname0 | TMEM165_chr4_55395957_55426175 |
regionname5000 | TMEM165_chr4_55390957_55431175 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 324 | 380 | 93 | 72 | 158 | 15 | 40 | 124 | TMEM165_chr4_55390957_55431175 | TMEM165 | copy fasta | chr4 | 55390957 | 55431175 |
a0002 | 0/0 | 324 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | copy fasta | chr4 | 55390957 | 55431175 |
a0003 | 0/0 | 324 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | copy fasta | chr4 | 55390957 | 55431175 |
chapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/0 | 975 | 275 | 83 | 50 | 105 | 8 | 29 | TMEM165_chr4_55390957_55431175 | TMEM165 | copy fasta | chr4 | 55390957 | 55431175 | |
c0002 | 1/1 | 975 | 103 | 10 | 20 | 53 | 7 | 11 | TMEM165_chr4_55390957_55431175 | TMEM165 | copy fasta | chr4 | 55390957 | 55431175 | |
c0003 | 0/0 | 975 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | copy fasta | chr4 | 55390957 | 55431175 | |
c0004 | 0/0 | 975 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | copy fasta | chr4 | 55390957 | 55431175 | |
c0005 | 0/0 | 975 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | copy fasta | chr4 | 55390957 | 55431175 | |
c0006 | 0/0 | 975 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | copy fasta | chr4 | 55390957 | 55431175 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 957 | 140 | 48 | 21 | 51 | 6 | 12 | TMEM165_chr4_55390957_55431175 | TMEM165 | copy fasta | chr4 | 55390957 | 55431175 |
t0002 | 0/0 | 955 | 128 | 17 | 31 | 68 | 2 | 10 | TMEM165_chr4_55390957_55431175 | TMEM165 | copy fasta | chr4 | 55390957 | 55431175 |
t0003 | 0/0 | 957 | 80 | 4 | 15 | 36 | 7 | 18 | TMEM165_chr4_55390957_55431175 | TMEM165 | copy fasta | chr4 | 55390957 | 55431175 |
t0004 | 0/0 | 957 | 9 | 9 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | copy fasta | chr4 | 55390957 | 55431175 |
t0005 | 0/0 | 957 | 7 | 7 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | copy fasta | chr4 | 55390957 | 55431175 |
t0006 | 0/0 | 957 | 4 | 4 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | copy fasta | chr4 | 55390957 | 55431175 |
t0007 | 0/0 | 957 | 4 | 1 | 2 | 0 | 1 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | copy fasta | chr4 | 55390957 | 55431175 |
t0008 | 0/0 | 957 | 2 | 1 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | copy fasta | chr4 | 55390957 | 55431175 |
t0009 | 0/0 | 957 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | copy fasta | chr4 | 55390957 | 55431175 |
t0010 | 0/0 | 989 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | copy fasta | chr4 | 55390957 | 55431175 |
t0011 | 0/0 | 957 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | copy fasta | chr4 | 55390957 | 55431175 |
t0012 | 0/0 | 957 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | copy fasta | chr4 | 55390957 | 55431175 |
t0013 | 0/0 | 955 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | copy fasta | chr4 | 55390957 | 55431175 |
t0014 | 0/0 | 955 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | copy fasta | chr4 | 55390957 | 55431175 |
t0015 | 0/0 | 957 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | copy fasta | chr4 | 55390957 | 55431175 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0004 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0006 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0007 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0009 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0015 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0018 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0171 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0172 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0301 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0329 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0335 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0353 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0354 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0357 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0360 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0361 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 975 | 275 | 83 | 50 | 105 | 8 | 29 | TMEM165_chr4_55390957_55431175 | TMEM165 | copy fasta | chr4 | 55390957 | 55431175 | |
a0001c0002 | 1/1 | 975 | 103 | 10 | 20 | 53 | 7 | 11 | TMEM165_chr4_55390957_55431175 | TMEM165 | copy fasta | chr4 | 55390957 | 55431175 | |
a0001c0003 | 0/0 | 975 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | copy fasta | chr4 | 55390957 | 55431175 | |
a0001c0005 | 0/0 | 975 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | copy fasta | chr4 | 55390957 | 55431175 | |
a0002c0004 | 0/0 | 975 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | copy fasta | chr4 | 55390957 | 55431175 | |
a0003c0006 | 0/0 | 975 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | copy fasta | chr4 | 55390957 | 55431175 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 1931 | 42 | 39 | 2 | 0 | 0 | 1 | TMEM165_chr4_55390957_55431175 | TMEM165 | copy fasta | chr4 | 55390957 | 55431175 |
a0001c0001t0002 | 0/0 | 1929 | 127 | 17 | 30 | 68 | 2 | 10 | TMEM165_chr4_55390957_55431175 | TMEM165 | copy fasta | chr4 | 55390957 | 55431175 |
a0001c0001t0003 | 0/0 | 1931 | 79 | 4 | 15 | 36 | 6 | 18 | TMEM165_chr4_55390957_55431175 | TMEM165 | copy fasta | chr4 | 55390957 | 55431175 |
a0001c0001t0004 | 0/0 | 1931 | 9 | 9 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | copy fasta | chr4 | 55390957 | 55431175 |
a0001c0001t0005 | 0/0 | 1931 | 7 | 7 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | copy fasta | chr4 | 55390957 | 55431175 |
a0001c0001t0006 | 0/0 | 1931 | 4 | 4 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | copy fasta | chr4 | 55390957 | 55431175 |
a0001c0001t0008 | 0/0 | 1931 | 2 | 1 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | copy fasta | chr4 | 55390957 | 55431175 |
a0001c0001t0009 | 0/0 | 1931 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | copy fasta | chr4 | 55390957 | 55431175 |
a0001c0001t0012 | 0/0 | 1931 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | copy fasta | chr4 | 55390957 | 55431175 |
a0001c0001t0013 | 0/0 | 1929 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | copy fasta | chr4 | 55390957 | 55431175 |
a0001c0001t0014 | 0/0 | 1929 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | copy fasta | chr4 | 55390957 | 55431175 |
a0001c0002t0001 | 1/1 | 1931 | 97 | 9 | 18 | 51 | 6 | 11 | TMEM165_chr4_55390957_55431175 | TMEM165 | copy fasta | chr4 | 55390957 | 55431175 |
a0001c0002t0007 | 0/0 | 1931 | 4 | 1 | 2 | 0 | 1 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | copy fasta | chr4 | 55390957 | 55431175 |
a0001c0002t0010 | 0/0 | 1963 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | copy fasta | chr4 | 55390957 | 55431175 |
a0001c0002t0011 | 0/0 | 1931 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | copy fasta | chr4 | 55390957 | 55431175 |
a0001c0003t0001 | 0/0 | 1931 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | copy fasta | chr4 | 55390957 | 55431175 |
a0001c0005t0002 | 0/0 | 1929 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | copy fasta | chr4 | 55390957 | 55431175 |
a0002c0004t0003 | 0/0 | 1931 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | copy fasta | chr4 | 55390957 | 55431175 |
a0003c0006t0015 | 0/0 | 1931 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | copy fasta | chr4 | 55390957 | 55431175 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0001g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0001g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0001g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0001g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0001g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0001g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0001g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0001g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0001g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0002g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0002g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0002g0006 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0002g0007 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0002g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0002g0009 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0002g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0002g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0002g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0002g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0002g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0002g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0002g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0002g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0002g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0002g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0002g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0002g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0002g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0002g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0002g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0002g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0002g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0002g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0002g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0002g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0002g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0002g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0002g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0002g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0002g0354 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0003g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0003g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0003g0018 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0003g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0003g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0003g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0003g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0003g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0003g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0003g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0003g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0003g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0003g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0003g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0003g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0003g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0003g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0003g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0003g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0003g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0003g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0003g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0003g0301 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0003g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0003g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0003g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0003g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0003g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0003g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0003g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0003g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0003g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0003g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0003g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0003g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0003g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0003g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0003g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0003g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0003g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0003g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0003g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0003g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0003g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0003g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0003g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0003g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0003g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0003g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0003g0329 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0003g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0003g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0003g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0003g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0003g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0003g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0003g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0003g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0003g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0003g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0003g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0003g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0003g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0003g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0003g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0003g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0003g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0003g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0003g0353 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0003g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0003g0357 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0003g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0003g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0003g0360 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0003g0361 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0004g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0004g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0004g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0004g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0004g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0004g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0004g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0004g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0004g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0005g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0005g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0005g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0005g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0005g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0005g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0005g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0006g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0006g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0006g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0006g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0008g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0008g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0009g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0009g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0012g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0013g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0001t0014g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0002t0001g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0002t0001g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0002t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0002t0001g0015 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0002t0001g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0002t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0002t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0002t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0002t0001g0171 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0002t0001g0172 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0002t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0002t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0002t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0002t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0002t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0002t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0002t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0002t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0002t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0002t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0002t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0002t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0002t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0002t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0002t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0002t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0002t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0002t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0002t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0002t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0002t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0002t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0002t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0002t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0002t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0002t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0002t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0002t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0002t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0002t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0002t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0002t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0002t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0002t0007g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0002t0007g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0002t0007g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0002t0007g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0002t0010g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0002t0011g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0003t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0001c0005t0002g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0002c0004t0003g0335 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
a0003c0006t0015g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0002 | t0001 | g0175 | EUR | GBR | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG00099 | hp2 | a0001 | c0001 | t0002 | g0074 | EUR | GBR | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG00140 | hp1 | a0001 | c0001 | t0003 | g0361 | EUR | GBR | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG00140 | hp2 | a0001 | c0001 | t0003 | g0329 | EUR | GBR | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG00280 | hp1 | a0001 | c0001 | t0002 | g0077 | EUR | FIN | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG00280 | hp2 | a0001 | c0001 | t0003 | g0301 | EUR | FIN | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG00323 | hp1 | a0001 | c0002 | t0001 | g0174 | EUR | FIN | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG00323 | hp2 | a0002 | c0004 | t0003 | g0335 | EUR | FIN | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG00438 | hp1 | a0001 | c0001 | t0002 | g0098 | EAS | CHS | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG00438 | hp2 | a0001 | c0002 | t0001 | g0231 | EAS | CHS | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG00544 | hp1 | a0001 | c0001 | t0002 | g0095 | EAS | CHS | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG00544 | hp2 | a0001 | c0002 | t0001 | g0194 | EAS | CHS | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG00558 | hp1 | a0001 | c0002 | t0001 | g0229 | EAS | CHS | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG00558 | hp2 | a0001 | c0001 | t0002 | g0131 | EAS | CHS | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG00597 | hp1 | a0001 | c0002 | t0001 | g0248 | EAS | CHS | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG00597 | hp2 | a0001 | c0001 | t0003 | g0313 | EAS | CHS | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG00609 | hp1 | a0001 | c0002 | t0001 | g0256 | EAS | CHS | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG00609 | hp2 | a0001 | c0001 | t0002 | g0123 | EAS | CHS | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG00621 | hp1 | a0001 | c0001 | t0002 | g0069 | EAS | CHS | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG00621 | hp2 | a0001 | c0002 | t0001 | g0227 | EAS | CHS | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG00642 | hp1 | a0001 | c0002 | t0001 | g0263 | AMR | PUR | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG00642 | hp2 | a0001 | c0001 | t0003 | g0338 | AMR | PUR | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG00673 | hp1 | a0001 | c0001 | t0002 | g0067 | EAS | CHS | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG00673 | hp2 | a0001 | c0001 | t0003 | g0325 | EAS | CHS | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG00733 | hp1 | a0001 | c0001 | t0014 | g0055 | AMR | PUR | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG00733 | hp2 | a0001 | c0002 | t0001 | g0261 | AMR | PUR | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG00735 | hp1 | a0001 | c0001 | t0002 | g0138 | AMR | PUR | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG00735 | hp2 | a0001 | c0002 | t0001 | g0264 | AMR | PUR | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG00738 | hp1 | a0001 | c0002 | t0001 | g0238 | AMR | PUR | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG00738 | hp2 | a0001 | c0001 | t0002 | g0026 | AMR | PUR | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG01069 | hp1 | a0001 | c0001 | t0003 | g0290 | AMR | PUR | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG01069 | hp2 | a0001 | c0002 | t0001 | g0020 | AMR | PUR | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG01070 | hp1 | a0001 | c0001 | t0002 | g0075 | AMR | PUR | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG01070 | hp2 | a0001 | c0001 | t0003 | g0302 | AMR | PUR | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG01071 | hp1 | a0001 | c0002 | t0001 | g0021 | AMR | PUR | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG01071 | hp2 | a0001 | c0001 | t0002 | g0078 | AMR | PUR | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG01074 | hp1 | a0001 | c0001 | t0003 | g0327 | AMR | PUR | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG01074 | hp2 | a0001 | c0001 | t0002 | g0136 | AMR | PUR | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG01081 | hp1 | a0001 | c0001 | t0002 | g0084 | AMR | PUR | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG01081 | hp2 | a0001 | c0003 | t0001 | g0255 | AMR | PUR | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG01099 | hp1 | a0001 | c0001 | t0003 | g0320 | AMR | PUR | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG01167 | hp1 | a0001 | c0001 | t0003 | g0353 | AMR | PUR | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG01167 | hp2 | a0001 | c0001 | t0002 | g0059 | AMR | PUR | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG01168 | hp1 | a0001 | c0002 | t0001 | g0203 | AMR | PUR | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG01168 | hp2 | a0001 | c0001 | t0012 | g0284 | AMR | PUR | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG01169 | hp1 | a0001 | c0002 | t0001 | g0204 | AMR | PUR | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG01169 | hp2 | a0001 | c0001 | t0003 | g0352 | AMR | PUR | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG01175 | hp1 | a0001 | c0001 | t0003 | g0349 | AMR | PUR | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG01175 | hp2 | a0001 | c0001 | t0002 | g0043 | AMR | PUR | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG01192 | hp1 | a0001 | c0002 | t0007 | g0259 | AMR | PUR | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG01192 | hp2 | a0001 | c0001 | t0003 | g0282 | AMR | PUR | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG01243 | hp1 | a0001 | c0002 | t0001 | g0239 | AMR | PUR | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG01243 | hp2 | a0001 | c0001 | t0008 | g0164 | AMR | PUR | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG01255 | hp1 | a0001 | c0005 | t0002 | g0004 | AMR | CLM | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG01255 | hp2 | a0001 | c0002 | t0001 | g0217 | AMR | CLM | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG01256 | hp1 | a0001 | c0002 | t0007 | g0180 | AMR | CLM | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG01256 | hp2 | a0001 | c0001 | t0002 | g0079 | AMR | CLM | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG01257 | hp1 | a0001 | c0002 | t0001 | g0016 | AMR | CLM | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG01257 | hp2 | a0001 | c0001 | t0002 | g0073 | AMR | CLM | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG01258 | hp1 | a0001 | c0001 | t0002 | g0083 | AMR | CLM | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG01258 | hp2 | a0001 | c0002 | t0001 | g0016 | AMR | CLM | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | CLM | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG01261 | hp2 | a0001 | c0001 | t0003 | g0351 | AMR | CLM | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG01346 | hp1 | a0001 | c0001 | t0002 | g0046 | AMR | CLM | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG01346 | hp2 | a0001 | c0002 | t0001 | g0176 | AMR | CLM | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG01358 | hp1 | a0001 | c0001 | t0002 | g0093 | AMR | CLM | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG01358 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | CLM | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG01361 | hp1 | a0001 | c0001 | t0003 | g0307 | AMR | CLM | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG01361 | hp2 | a0001 | c0001 | t0002 | g0092 | AMR | CLM | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG01433 | hp1 | a0001 | c0002 | t0001 | g0211 | AMR | CLM | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG01433 | hp2 | a0001 | c0001 | t0002 | g0139 | AMR | CLM | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG01496 | hp1 | a0001 | c0001 | t0002 | g0085 | AMR | CLM | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0111 | AMR | CLM | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG01515 | hp1 | a0001 | c0001 | t0003 | g0018 | EUR | IBS | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG01515 | hp2 | a0001 | c0002 | t0007 | g0177 | EUR | IBS | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG01517 | hp1 | a0001 | c0001 | t0003 | g0018 | EUR | IBS | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG01517 | hp2 | a0001 | c0001 | t0003 | g0357 | EUR | IBS | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG01884 | hp1 | a0001 | c0001 | t0009 | g0023 | AFR | ACB | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG01884 | hp2 | a0001 | c0001 | t0004 | g0279 | AFR | ACB | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG01891 | hp1 | a0001 | c0001 | t0002 | g0141 | AFR | ACB | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG01891 | hp2 | a0001 | c0001 | t0005 | g0270 | AFR | ACB | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG01928 | hp1 | a0001 | c0001 | t0002 | g0041 | AMR | PEL | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG01928 | hp2 | a0001 | c0001 | t0002 | g0112 | AMR | PEL | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG01943 | hp1 | a0001 | c0001 | t0003 | g0339 | AMR | PEL | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG01943 | hp2 | a0001 | c0001 | t0002 | g0107 | AMR | PEL | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG01952 | hp1 | a0001 | c0001 | t0002 | g0125 | AMR | PEL | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG01952 | hp2 | a0001 | c0001 | t0002 | g0135 | AMR | PEL | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG01978 | hp1 | a0001 | c0001 | t0002 | g0035 | AMR | PEL | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG01978 | hp2 | a0001 | c0002 | t0001 | g0012 | AMR | PEL | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG01981 | hp1 | a0001 | c0001 | t0003 | g0323 | AMR | PEL | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG01981 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | PEL | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG02015 | hp1 | a0001 | c0001 | t0002 | g0040 | EAS | KHV | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG02015 | hp2 | a0001 | c0002 | t0001 | g0192 | EAS | KHV | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG02027 | hp1 | a0001 | c0002 | t0001 | g0195 | EAS | KHV | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG02027 | hp2 | a0001 | c0002 | t0001 | g0221 | EAS | KHV | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | ACB | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG02055 | hp2 | a0001 | c0002 | t0001 | g0169 | AFR | ACB | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG02074 | hp1 | a0001 | c0001 | t0002 | g0126 | EAS | KHV | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG02074 | hp2 | a0001 | c0002 | t0001 | g0240 | EAS | KHV | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG02083 | hp1 | a0001 | c0002 | t0001 | g0252 | EAS | KHV | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG02083 | hp2 | a0001 | c0001 | t0002 | g0089 | EAS | KHV | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG02129 | hp1 | a0001 | c0001 | t0002 | g0110 | EAS | KHV | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG02129 | hp2 | a0001 | c0002 | t0001 | g0220 | EAS | KHV | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG02132 | hp1 | a0001 | c0002 | t0001 | g0216 | EAS | KHV | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG02132 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | KHV | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG02135 | hp1 | a0001 | c0002 | t0001 | g0014 | EAS | KHV | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG02135 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | KHV | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG02145 | hp1 | a0001 | c0001 | t0003 | g0359 | AFR | ACB | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | ACB | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG02148 | hp1 | a0001 | c0001 | t0002 | g0130 | AMR | PEL | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG02148 | hp2 | a0001 | c0001 | t0002 | g0137 | AMR | PEL | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG02257 | hp1 | a0001 | c0001 | t0002 | g0053 | AFR | ACB | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0355 | AFR | ACB | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | ACB | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | ACB | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG02273 | hp1 | a0001 | c0001 | t0002 | g0044 | AMR | PEL | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG02273 | hp2 | a0001 | c0001 | t0002 | g0007 | AMR | PEL | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | ACB | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG02280 | hp2 | a0001 | c0001 | t0003 | g0266 | AFR | ACB | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG02293 | hp1 | a0001 | c0001 | t0002 | g0009 | AMR | PEL | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG02293 | hp2 | a0001 | c0002 | t0001 | g0012 | AMR | PEL | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG02300 | hp1 | a0001 | c0002 | t0001 | g0246 | AMR | PEL | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG02300 | hp2 | a0001 | c0001 | t0003 | g0287 | AMR | PEL | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG02451 | hp1 | a0001 | c0001 | t0004 | g0185 | AFR | ACB | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG02451 | hp2 | a0001 | c0001 | t0003 | g0308 | AFR | ACB | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG02523 | hp1 | a0001 | c0001 | t0002 | g0113 | EAS | KHV | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG02523 | hp2 | a0001 | c0002 | t0001 | g0014 | EAS | KHV | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | GWD | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG02572 | hp2 | a0001 | c0001 | t0004 | g0281 | AFR | GWD | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG02602 | hp1 | a0001 | c0001 | t0002 | g0019 | SAS | PJL | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG02602 | hp2 | a0001 | c0002 | t0001 | g0260 | SAS | PJL | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG02615 | hp1 | a0001 | c0002 | t0001 | g0198 | AFR | GWD | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG02615 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | GWD | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | GWD | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG02647 | hp1 | a0001 | c0001 | t0006 | g0258 | AFR | GWD | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG02698 | hp1 | a0001 | c0001 | t0003 | g0319 | SAS | PJL | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG02698 | hp2 | a0001 | c0002 | t0001 | g0247 | SAS | PJL | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG02717 | hp1 | a0001 | c0001 | t0004 | g0280 | AFR | GWD | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG02717 | hp2 | a0001 | c0001 | t0002 | g0076 | AFR | GWD | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | GWD | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG02809 | hp2 | a0001 | c0001 | t0002 | g0058 | AFR | GWD | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0265 | AFR | GWD | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG02886 | hp1 | a0001 | c0001 | t0005 | g0269 | AFR | GWD | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG02886 | hp2 | a0001 | c0001 | t0005 | g0271 | AFR | GWD | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0342 | AFR | GWD | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG02895 | hp2 | a0001 | c0001 | t0002 | g0051 | AFR | GWD | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0312 | AFR | GWD | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG02896 | hp2 | a0001 | c0001 | t0004 | g0278 | AFR | GWD | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0345 | AFR | GWD | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG02897 | hp2 | a0001 | c0001 | t0004 | g0276 | AFR | GWD | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | ESN | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG02965 | hp2 | a0001 | c0002 | t0001 | g0250 | AFR | ESN | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | ESN | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | ESN | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | ESN | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG02976 | hp2 | a0001 | c0001 | t0005 | g0275 | AFR | ESN | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG03017 | hp1 | a0001 | c0001 | t0003 | g0304 | SAS | PJL | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG03017 | hp2 | a0001 | c0002 | t0001 | g0201 | SAS | PJL | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG03041 | hp1 | a0001 | c0001 | t0002 | g0052 | AFR | GWD | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | GWD | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG03130 | hp1 | a0001 | c0001 | t0002 | g0049 | AFR | ESN | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | ESN | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG03139 | hp1 | a0001 | c0001 | t0004 | g0186 | AFR | ESN | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG03139 | hp2 | a0001 | c0001 | t0002 | g0047 | AFR | ESN | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | ESN | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG03195 | hp2 | a0001 | c0001 | t0002 | g0060 | AFR | ESN | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | MSL | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG03209 | hp2 | a0001 | c0002 | t0001 | g0215 | AFR | MSL | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG03225 | hp1 | a0001 | c0002 | t0001 | g0001 | AFR | MSL | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG03239 | hp1 | a0001 | c0001 | t0003 | g0303 | SAS | PJL | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG03239 | hp2 | a0001 | c0001 | t0002 | g0082 | SAS | PJL | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG03453 | hp1 | a0001 | c0001 | t0002 | g0056 | AFR | MSL | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG03453 | hp2 | a0001 | c0002 | t0001 | g0214 | AFR | MSL | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | MSL | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG03486 | hp2 | a0001 | c0001 | t0005 | g0274 | AFR | MSL | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG03490 | hp1 | a0001 | c0001 | t0002 | g0006 | SAS | PJL | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG03490 | hp2 | a0001 | c0002 | t0001 | g0226 | SAS | PJL | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG03491 | hp1 | a0001 | c0002 | t0001 | g0015 | SAS | PJL | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG03491 | hp2 | a0001 | c0001 | t0003 | g0292 | SAS | PJL | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG03492 | hp1 | a0001 | c0002 | t0001 | g0015 | SAS | PJL | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG03492 | hp2 | a0001 | c0001 | t0002 | g0006 | SAS | PJL | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG03516 | hp1 | a0001 | c0001 | t0006 | g0163 | AFR | ESN | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0168 | AFR | ESN | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | GWD | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG03540 | hp2 | a0001 | c0002 | t0001 | g0001 | AFR | GWD | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG03579 | hp1 | a0001 | c0001 | t0002 | g0057 | AFR | MSL | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | MSL | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG03654 | hp1 | a0001 | c0002 | t0001 | g0209 | SAS | PJL | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG03654 | hp2 | a0001 | c0001 | t0003 | g0298 | SAS | PJL | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG03669 | hp1 | a0001 | c0002 | t0001 | g0200 | SAS | PJL | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG03669 | hp2 | a0001 | c0001 | t0003 | g0346 | SAS | PJL | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG03688 | hp1 | a0001 | c0001 | t0003 | g0310 | SAS | STU | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG03688 | hp2 | a0001 | c0001 | t0003 | g0306 | SAS | STU | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG03710 | hp1 | a0001 | c0001 | t0003 | g0332 | SAS | PJL | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG03710 | hp2 | a0001 | c0002 | t0001 | g0213 | SAS | PJL | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG03831 | hp1 | a0001 | c0001 | t0003 | g0293 | SAS | BEB | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG03831 | hp2 | a0001 | c0001 | t0003 | g0311 | SAS | BEB | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG03834 | hp1 | a0001 | c0002 | t0001 | g0190 | SAS | BEB | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG03834 | hp2 | a0001 | c0001 | t0002 | g0097 | SAS | BEB | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG03927 | hp1 | a0001 | c0001 | t0002 | g0038 | SAS | BEB | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG03927 | hp2 | a0001 | c0001 | t0003 | g0296 | SAS | BEB | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG03942 | hp1 | a0001 | c0001 | t0003 | g0291 | SAS | BEB | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0029 | SAS | BEB | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG04115 | hp1 | a0001 | c0001 | t0002 | g0034 | SAS | STU | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG04115 | hp2 | a0001 | c0001 | t0003 | g0360 | SAS | STU | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG04184 | hp1 | a0001 | c0002 | t0001 | g0208 | SAS | BEB | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG04184 | hp2 | a0001 | c0001 | t0002 | g0039 | SAS | BEB | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG04204 | hp1 | a0001 | c0001 | t0003 | g0297 | SAS | STU | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG04204 | hp2 | a0001 | c0001 | t0002 | g0285 | SAS | STU | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG04228 | hp1 | a0001 | c0001 | t0003 | g0295 | SAS | STU | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG04228 | hp2 | a0001 | c0001 | t0003 | g0318 | SAS | STU | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA18522 | hp1 | a0001 | c0001 | t0008 | g0162 | AFR | YRI | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA18522 | hp2 | a0001 | c0001 | t0002 | g0048 | AFR | YRI | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA18612 | hp1 | a0001 | c0002 | t0011 | g0233 | EAS | CHB | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA18612 | hp2 | a0001 | c0001 | t0003 | g0305 | EAS | CHB | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA18747 | hp1 | a0001 | c0002 | t0001 | g0193 | EAS | CHB | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA18747 | hp2 | a0001 | c0001 | t0002 | g0115 | EAS | CHB | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | YRI | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA18906 | hp2 | a0001 | c0001 | t0006 | g0161 | AFR | YRI | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA18939 | hp1 | a0001 | c0001 | t0003 | g0336 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA18939 | hp2 | a0001 | c0001 | t0002 | g0117 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA18942 | hp1 | a0001 | c0001 | t0003 | g0321 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA18942 | hp2 | a0001 | c0001 | t0002 | g0114 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA18943 | hp1 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA18943 | hp2 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA18947 | hp1 | a0001 | c0001 | t0002 | g0140 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA18947 | hp2 | a0001 | c0001 | t0003 | g0343 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA18948 | hp1 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA18948 | hp2 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA18949 | hp1 | a0001 | c0001 | t0002 | g0101 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA18949 | hp2 | a0001 | c0002 | t0001 | g0210 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA18950 | hp1 | a0001 | c0001 | t0002 | g0124 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA18950 | hp2 | a0001 | c0002 | t0001 | g0257 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA18954 | hp1 | a0001 | c0002 | t0010 | g0228 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA18954 | hp2 | a0001 | c0001 | t0002 | g0142 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA18959 | hp1 | a0001 | c0002 | t0001 | g0234 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA18959 | hp2 | a0001 | c0001 | t0003 | g0337 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA18961 | hp1 | a0001 | c0001 | t0003 | g0331 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA18961 | hp2 | a0001 | c0002 | t0001 | g0225 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA18962 | hp1 | a0001 | c0002 | t0001 | g0157 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA18962 | hp2 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA18964 | hp1 | a0001 | c0001 | t0003 | g0317 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA18964 | hp2 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA18965 | hp1 | a0001 | c0001 | t0003 | g0288 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA18965 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA18968 | hp1 | a0001 | c0001 | t0003 | g0324 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA18968 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA18969 | hp1 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA18969 | hp2 | a0001 | c0001 | t0003 | g0358 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA18970 | hp1 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA18970 | hp2 | a0001 | c0002 | t0001 | g0235 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA18971 | hp1 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA18971 | hp2 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA18972 | hp1 | a0001 | c0001 | t0002 | g0134 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA18972 | hp2 | a0001 | c0002 | t0001 | g0237 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA18974 | hp1 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA18974 | hp2 | a0001 | c0001 | t0003 | g0309 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA18978 | hp1 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA18978 | hp2 | a0001 | c0001 | t0003 | g0326 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA18979 | hp1 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA18979 | hp2 | a0001 | c0002 | t0001 | g0242 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA18981 | hp1 | a0001 | c0001 | t0002 | g0122 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA18981 | hp2 | a0001 | c0001 | t0003 | g0328 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA18983 | hp1 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA18983 | hp2 | a0001 | c0002 | t0001 | g0244 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA18984 | hp1 | a0001 | c0002 | t0001 | g0223 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA18984 | hp2 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA18986 | hp1 | a0001 | c0002 | t0001 | g0232 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA18986 | hp2 | a0001 | c0001 | t0002 | g0120 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA18987 | hp1 | a0001 | c0001 | t0003 | g0289 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA18987 | hp2 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA18988 | hp1 | a0001 | c0001 | t0003 | g0314 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA18988 | hp2 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA18990 | hp1 | a0001 | c0001 | t0002 | g0118 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA18990 | hp2 | a0001 | c0001 | t0003 | g0330 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA18995 | hp1 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA18995 | hp2 | a0001 | c0002 | t0001 | g0245 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA18998 | hp1 | a0001 | c0002 | t0001 | g0224 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA18998 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA18999 | hp1 | a0001 | c0002 | t0001 | g0254 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA18999 | hp2 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA19000 | hp1 | a0001 | c0002 | t0001 | g0199 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA19000 | hp2 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA19001 | hp1 | a0001 | c0001 | t0002 | g0128 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA19001 | hp2 | a0001 | c0001 | t0003 | g0322 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA19002 | hp1 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA19002 | hp2 | a0001 | c0001 | t0003 | g0299 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA19004 | hp1 | a0001 | c0001 | t0002 | g0121 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA19004 | hp2 | a0001 | c0001 | t0003 | g0316 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA19005 | hp1 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA19005 | hp2 | a0001 | c0002 | t0001 | g0251 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA19009 | hp1 | a0001 | c0001 | t0003 | g0017 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA19009 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA19010 | hp1 | a0001 | c0002 | t0001 | g0191 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA19010 | hp2 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA19011 | hp1 | a0001 | c0002 | t0001 | g0241 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA19011 | hp2 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA19012 | hp1 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA19012 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA19030 | hp1 | a0001 | c0001 | t0004 | g0159 | AFR | LWK | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA19030 | hp2 | a0001 | c0001 | t0005 | g0272 | AFR | LWK | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | LWK | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA19043 | hp2 | a0001 | c0002 | t0007 | g0179 | AFR | LWK | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA19054 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA19054 | hp2 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA19057 | hp1 | a0001 | c0001 | t0003 | g0283 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA19057 | hp2 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA19058 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA19058 | hp2 | a0001 | c0002 | t0001 | g0253 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA19059 | hp1 | a0001 | c0002 | t0001 | g0158 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA19059 | hp2 | a0001 | c0001 | t0003 | g0356 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA19062 | hp1 | a0001 | c0001 | t0003 | g0348 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA19062 | hp2 | a0001 | c0002 | t0001 | g0196 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA19064 | hp1 | a0001 | c0002 | t0001 | g0182 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA19064 | hp2 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA19065 | hp1 | a0001 | c0001 | t0002 | g0099 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA19065 | hp2 | a0001 | c0002 | t0001 | g0206 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA19067 | hp1 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA19067 | hp2 | a0001 | c0002 | t0001 | g0188 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA19068 | hp1 | a0001 | c0001 | t0002 | g0109 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA19068 | hp2 | a0001 | c0001 | t0003 | g0315 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA19070 | hp1 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA19070 | hp2 | a0001 | c0001 | t0003 | g0334 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA19074 | hp1 | a0001 | c0002 | t0001 | g0207 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA19074 | hp2 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA19077 | hp1 | a0001 | c0002 | t0001 | g0236 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA19077 | hp2 | a0001 | c0001 | t0003 | g0286 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA19079 | hp1 | a0001 | c0002 | t0001 | g0243 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA19079 | hp2 | a0001 | c0002 | t0001 | g0178 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA19080 | hp1 | a0001 | c0001 | t0003 | g0333 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA19080 | hp2 | a0001 | c0002 | t0001 | g0230 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA19081 | hp1 | a0001 | c0002 | t0001 | g0219 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA19081 | hp2 | a0001 | c0001 | t0002 | g0143 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA19083 | hp1 | a0001 | c0002 | t0001 | g0262 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA19083 | hp2 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA19084 | hp1 | a0001 | c0002 | t0001 | g0197 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA19084 | hp2 | a0001 | c0001 | t0003 | g0300 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA19086 | hp1 | a0001 | c0002 | t0001 | g0205 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA19086 | hp2 | a0001 | c0001 | t0003 | g0347 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA19087 | hp1 | a0001 | c0002 | t0001 | g0189 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA19087 | hp2 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA19089 | hp1 | a0001 | c0001 | t0003 | g0017 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA19089 | hp2 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA19090 | hp1 | a0001 | c0002 | t0001 | g0222 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA19090 | hp2 | a0001 | c0001 | t0013 | g0144 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA19240 | hp1 | a0001 | c0001 | t0009 | g0022 | AFR | YRI | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA19240 | hp2 | a0001 | c0001 | t0003 | g0267 | AFR | YRI | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA20129 | hp1 | a0001 | c0001 | t0004 | g0277 | AFR | ASW | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0362 | AFR | ASW | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA20752 | hp1 | a0001 | c0002 | t0001 | g0173 | EUR | TSI | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA20752 | hp2 | a0001 | c0002 | t0001 | g0218 | EUR | TSI | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA20805 | hp1 | a0001 | c0002 | t0001 | g0170 | EUR | TSI | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA20805 | hp2 | a0001 | c0002 | t0001 | g0249 | EUR | TSI | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA20905 | hp1 | a0001 | c0001 | t0003 | g0294 | SAS | GIH | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA20905 | hp2 | a0001 | c0001 | t0002 | g0354 | SAS | GIH | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG01123 | hp1 | a0001 | c0002 | t0001 | g0212 | AMR | CLM | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG01123 | hp2 | a0001 | c0001 | t0003 | g0350 | AMR | CLM | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | ACB | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG02109 | hp2 | a0001 | c0001 | t0002 | g0050 | AFR | ACB | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG02486 | hp1 | a0001 | c0001 | t0005 | g0273 | AFR | ACB | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG02486 | hp2 | a0001 | c0001 | t0002 | g0054 | AFR | ACB | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0344 | AFR | ACB | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | ACB | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG03471 | hp1 | a0001 | c0001 | t0002 | g0036 | AFR | MSL | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG03471 | hp2 | a0001 | c0001 | t0006 | g0160 | AFR | MSL | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG06807 | hp1 | a0001 | c0002 | t0001 | g0202 | AFR | USA | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0341 | AFR | USA | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA18955 | hp1 | a0001 | c0001 | t0003 | g0340 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA18955 | hp2 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA20300 | hp1 | a0001 | c0001 | t0002 | g0045 | AFR | USA | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | USA | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA21309 | hp1 | a0001 | c0002 | t0001 | g0181 | AFR | LWK | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
NA21309 | hp2 | a0003 | c0006 | t0015 | g0268 | AFR | LWK | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0001 | g0172 | REF | REF | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
homoSapiens_grch38 | hp1 | a0001 | c0002 | t0001 | g0171 | REF | REF | TMEM165_chr4_55390957_55431175 | TMEM165 | chr4 | 55390957 | 55431175 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:55396365 | C | G | 1 | a0003 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.176C>G | p.Ala59Gly | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/6 | 409/1931 | 176/975 | 59/324 | chr4 | 55396365 | ||
chr4:55411728 | G | A | 1 | a0002 | 1 | HG00323.hp2 | missense_variant | MODERATE | c.322G>A | p.Glu108Lys | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 2/6 | 555/1931 | 322/975 | 108/324 | chr4 | 55411728 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:55396207 | A | G | 4 | a0001c0001a0001c0005a0002c0004others(1): Show | 278 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(275): Show |
synonymous_variant | LOW | c.18A>G | p.Pro6Pro | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/6 | 251/1931 | 18/975 | 6/324 | chr4 | 55396207 | ||
chr4:55411700 | C | T | 1 | a0001c0003 | 1 | HG01081.hp2 | synonymous_variant | LOW | c.294C>T | p.Val98Val | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 2/6 | 527/1931 | 294/975 | 98/324 | chr4 | 55411700 | ||
chr4:55411790 | C | T | 1 | a0001c0005 | 1 | HG01255.hp1 | synonymous_variant | LOW | c.384C>T | p.Thr128Thr | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 2/6 | 617/1931 | 384/975 | 128/324 | chr4 | 55411790 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:55396043 | T | C | 1 | a0001c0001t0005 | 7 | HG01891.hp2 HG02486.hp1 HG02886.hp1 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-147T>C | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/6 | 147 | chr4 | 55396043 | |||||
chr4:55396160 | C | T | 1 | a0003c0006t0015 | 1 | NA21309.hp2 | 5_prime_UTR_variant | MODIFIER | c.-30C>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/6 | 30 | chr4 | 55396160 | |||||
chr4:55425453 | CAA | C | 4 | a0001c0001t0002a0001c0001t0013a0001c0001t0014others(1): Show | 130 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(127): Show |
3_prime_UTR_variant | MODIFIER | c.*2_*3delAA | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 6/6 | 2 | chr4 | 55425453 | |||||
chr4:55425556 | A | G | 1 | a0001c0001t0014 | 1 | HG00733.hp1 | 3_prime_UTR_variant | MODIFIER | c.*104A>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 6/6 | 104 | chr4 | 55425556 | |||||
chr4:55425578 | C | CCCATTAT others(25): Show |
1 | a0001c0002t0010 | 1 | NA18954.hp1 | 3_prime_UTR_variant | MODIFIER | c.*128_*159dupCATTAT others(26): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 6/6 | 160 | INFO_REALIGN_3_PRIME | chr4 | 55425578 | ||||
chr4:55425584 | A | C | 1 | a0001c0002t0007 | 4 | HG01192.hp1 HG01256.hp1 HG01515.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*132A>C | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 6/6 | 132 | chr4 | 55425584 | |||||
chr4:55425605 | T | C | 2 | a0001c0001t0006a0001c0001t0008 | 6 | HG01243.hp2 HG02647.hp1 HG03471.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*153T>C | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 6/6 | 153 | chr4 | 55425605 | |||||
chr4:55425688 | A | G | 1 | a0001c0001t0012 | 1 | HG01168.hp2 | 3_prime_UTR_variant | MODIFIER | c.*236A>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 6/6 | 236 | chr4 | 55425688 | |||||
chr4:55425704 | T | C | 1 | a0001c0001t0008 | 2 | HG01243.hp2 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*252T>C | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 6/6 | 252 | chr4 | 55425704 | |||||
chr4:55425725 | T | G | 1 | a0001c0002t0011 | 1 | NA18612.hp1 | 3_prime_UTR_variant | MODIFIER | c.*273T>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 6/6 | 273 | chr4 | 55425725 | |||||
chr4:55425934 | A | T | 3 | a0001c0001t0003a0001c0001t0012a0002c0004t0003 | 81 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(78): Show |
3_prime_UTR_variant | MODIFIER | c.*482A>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 6/6 | 482 | chr4 | 55425934 | |||||
chr4:55425946 | T | C | 1 | a0001c0001t0004 | 9 | HG01884.hp2 HG02451.hp1 HG02572.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*494T>C | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 6/6 | 494 | chr4 | 55425946 | |||||
chr4:55425957 | T | A | 1 | a0001c0001t0009 | 2 | HG01884.hp1 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*505T>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 6/6 | 505 | chr4 | 55425957 | |||||
chr4:55426079 | A | C | 1 | a0001c0001t0013 | 1 | NA19090.hp2 | 3_prime_UTR_variant | MODIFIER | c.*627A>C | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 6/6 | 627 | chr4 | 55426079 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:55396435 | C | T | 1 | a0001c0001t0001g0362 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.207+39C>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55396435 | ||||||
chr4:55396457 | C | G | 1 | a0001c0001t0003g0361 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.207+61C>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55396457 | ||||||
chr4:55396472 | C | T | 1 | a0001c0001t0003g0360 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.207+76C>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55396472 | ||||||
chr4:55396574 | C | G | 83 | a0001c0001t0001g0312a0001c0001t0001g0341a0001c0001t0001g0342others(80): Show | 87 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.207+178C>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55396574 | ||||||
chr4:55396635 | C | T | 6 | a0001c0001t0004g0276a0001c0001t0004g0277a0001c0001t0004g0278others(3): Show | 6 | HG01884.hp2 HG02572.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.207+239C>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55396635 | ||||||
chr4:55396697 | C | G | 7 | a0001c0001t0005g0269a0001c0001t0005g0270a0001c0001t0005g0271others(4): Show | 7 | HG01891.hp2 HG02486.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.207+301C>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55396697 | ||||||
chr4:55396945 | C | A | 1 | a0001c0001t0003g0282 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.207+549C>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55396945 | ||||||
chr4:55396960 | G | A | 7 | a0001c0001t0005g0269a0001c0001t0005g0270a0001c0001t0005g0271others(4): Show | 7 | HG01891.hp2 HG02486.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.207+564G>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55396960 | ||||||
chr4:55396966 | G | C | 1 | a0001c0001t0002g0019 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.207+570G>C | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55396966 | ||||||
chr4:55396968 | G | T | 1 | a0003c0006t0015g0268 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.207+572G>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55396968 | ||||||
chr4:55397213 | A | G | 2 | a0001c0001t0003g0266a0001c0001t0003g0267 | 2 | HG02280.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.207+817A>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55397213 | ||||||
chr4:55397236 | G | C | 2 | a0001c0002t0001g0020a0001c0002t0001g0021 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.207+840G>C | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55397236 | ||||||
chr4:55397267 | C | T | 1 | a0003c0006t0015g0268 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.207+871C>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55397267 | ||||||
chr4:55397376 | T | G | 2 | a0001c0001t0009g0022a0001c0001t0009g0023 | 2 | HG01884.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.207+980T>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55397376 | ||||||
chr4:55397463 | C | T | 1 | a0001c0001t0003g0359 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.207+1067C>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55397463 | ||||||
chr4:55397494 | GA | G | 8 | a0001c0001t0003g0357a0001c0001t0003g0358a0001c0001t0004g0276others(5): Show | 8 | HG01517.hp2 HG01884.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.207+1111delA | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55397494 | |||||
chr4:55397562 | T | C | 2 | a0001c0001t0001g0024a0001c0001t0001g0025 | 2 | HG02647.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.207+1166T>C | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55397562 | ||||||
chr4:55397836 | T | C | 1 | a0001c0001t0003g0283 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.207+1440T>C | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55397836 | ||||||
chr4:55397910 | A | AT | 9 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0265others(6): Show | 9 | HG00642.hp1 HG00733.hp2 HG00735.hp2 others(6): Show |
intron_variant | MODIFIER | c.207+1528dupT | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55397910 | |||||
chr4:55397910 | AT | A | 17 | a0001c0001t0001g0011a0001c0001t0001g0145a0001c0001t0001g0146others(14): Show | 18 | HG02145.hp2 HG02257.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.207+1528delT | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55397910 | |||||
chr4:55397910 | ATTT | A | 213 | a0001c0001t0001g0003a0001c0001t0001g0027a0001c0001t0001g0028others(210): Show | 224 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.207+1526_207+1528d others(5): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55397910 | |||||
chr4:55398026 | G | A | 1 | a0001c0001t0004g0159 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.207+1630G>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55398026 | ||||||
chr4:55398040 | G | C | 1 | a0001c0001t0001g0145 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.207+1644G>C | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55398040 | ||||||
chr4:55398049 | G | T | 1 | a0001c0001t0006g0258 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.207+1653G>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55398049 | ||||||
chr4:55398161 | C | T | 1 | a0001c0001t0001g0265 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.207+1765C>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55398161 | ||||||
chr4:55398328 | T | C | 2 | a0001c0001t0002g0285a0001c0001t0012g0284 | 2 | HG01168.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.207+1932T>C | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55398328 | ||||||
chr4:55398348 | ACAACAG | A | 6 | a0001c0001t0005g0270a0001c0001t0005g0271a0001c0001t0005g0272others(3): Show | 6 | HG01891.hp2 HG02486.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.207+1955_207+1960d others(8): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55398348 | |||||
chr4:55398505 | T | C | 1 | a0001c0001t0002g0026 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.207+2109T>C | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55398505 | ||||||
chr4:55398586 | C | G | 205 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0006others(202): Show | 214 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(211): Show |
intron_variant | MODIFIER | c.207+2190C>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55398586 | ||||||
chr4:55398599 | A | G | 1 | a0001c0001t0001g0032 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.207+2203A>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55398599 | ||||||
chr4:55398612 | A | G | 3 | a0001c0001t0002g0142a0001c0001t0002g0143a0001c0001t0013g0144 | 3 | NA18954.hp2 NA19081.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.207+2216A>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55398612 | ||||||
chr4:55398729 | A | G | 6 | a0001c0001t0005g0270a0001c0001t0005g0271a0001c0001t0005g0272others(3): Show | 6 | HG01891.hp2 HG02486.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.207+2333A>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55398729 | ||||||
chr4:55398774 | C | G | 213 | a0001c0001t0001g0003a0001c0001t0001g0027a0001c0001t0001g0028others(210): Show | 224 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.207+2378C>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55398774 | ||||||
chr4:55398887 | AAC | A | 200 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(197): Show | 210 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.207+2493_207+2494d others(4): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55398887 | |||||
chr4:55398888 | AC | A | 9 | a0001c0001t0002g0033a0001c0001t0002g0034a0001c0001t0002g0035others(6): Show | 9 | HG01978.hp1 HG02280.hp2 HG02300.hp2 others(6): Show |
intron_variant | MODIFIER | c.207+2493delC | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55398888 | ||||||
chr4:55398920 | A | G | 2 | a0001c0001t0001g0029a0001c0001t0001g0032 | 2 | HG01261.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.207+2524A>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55398920 | ||||||
chr4:55399130 | T | G | 1 | a0001c0002t0001g0188 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.207+2734T>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55399130 | ||||||
chr4:55399327 | C | G | 2 | a0001c0001t0002g0036a0001c0001t0002g0141 | 2 | HG01891.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.207+2931C>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55399327 | ||||||
chr4:55399400 | T | G | 20 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0001g0167others(17): Show | 20 | HG01243.hp2 HG01884.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.207+3004T>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55399400 | ||||||
chr4:55399494 | T | C | 2 | a0001c0001t0001g0027a0001c0001t0001g0028 | 2 | HG02809.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.207+3098T>C | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55399494 | ||||||
chr4:55400013 | CT | C | 6 | a0001c0001t0003g0289a0001c0001t0003g0290a0001c0001t0004g0276others(3): Show | 6 | HG01069.hp1 HG01069.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.207+3631delT | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55400013 | |||||
chr4:55400045 | A | G | 16 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0145others(13): Show | 18 | HG02145.hp2 HG02257.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.207+3649A>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55400045 | ||||||
chr4:55400131 | C | T | 86 | a0001c0001t0001g0003a0001c0001t0001g0027a0001c0001t0001g0028others(83): Show | 91 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.207+3735C>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55400131 | ||||||
chr4:55400167 | A | G | 86 | a0001c0001t0001g0003a0001c0001t0001g0027a0001c0001t0001g0028others(83): Show | 91 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.207+3771A>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55400167 | ||||||
chr4:55400172 | A | T | 1 | a0001c0001t0003g0288 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.207+3776A>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55400172 | ||||||
chr4:55400182 | A | T | 1 | a0001c0001t0003g0288 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.207+3786A>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55400182 | ||||||
chr4:55400184 | A | T | 1 | a0001c0001t0003g0288 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.207+3788A>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55400184 | ||||||
chr4:55400184 | AAT | A | 12 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0001g0167others(9): Show | 12 | HG01243.hp2 HG01884.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.207+3790_207+3791d others(4): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55400184 | |||||
chr4:55400187 | A | T | 1 | a0001c0001t0003g0288 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.207+3791A>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55400187 | ||||||
chr4:55400221 | T | TATTA | 343 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0013others(340): Show | 359 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(356): Show |
intron_variant | MODIFIER | c.207+3828_207+3831d others(6): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55400221 | |||||
chr4:55400223 | T | A | 1 | a0001c0001t0003g0288 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.207+3827T>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55400223 | ||||||
chr4:55400226 | A | T | 1 | a0001c0001t0003g0288 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.207+3830A>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55400226 | ||||||
chr4:55400236 | G | A | 1 | a0001c0001t0003g0288 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.207+3840G>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55400236 | ||||||
chr4:55400243 | A | ATAT | 53 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0013others(50): Show | 57 | HG00099.hp1 HG00323.hp1 HG01069.hp2 others(54): Show |
intron_variant | MODIFIER | c.207+3851_207+3853d others(5): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55400243 | |||||
chr4:55400244 | T | TATAATA | 8 | a0001c0001t0003g0291a0001c0001t0003g0292a0001c0001t0003g0293others(5): Show | 8 | HG01168.hp2 HG03491.hp2 HG03831.hp1 others(5): Show |
intron_variant | MODIFIER | c.207+3850_207+3851i others(8): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55400244 | |||||
chr4:55400244 | T | TATTATAA others(2): Show |
285 | a0001c0001t0001g0003a0001c0001t0001g0027a0001c0001t0001g0028others(282): Show | 299 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(296): Show |
intron_variant | MODIFIER | c.207+3854_207+3855i others(11): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55400244 | |||||
chr4:55400246 | T | TTA | 3 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0148 | 3 | HG02145.hp2 HG02976.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.207+3854_207+3855d others(4): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55400246 | |||||
chr4:55400256 | TTAATATA | T | 3 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0003g0298 | 3 | HG02809.hp1 HG03130.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.207+3875_207+3881d others(9): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55400256 | |||||
chr4:55400258 | A | AATATATA others(24): Show |
2 | a0001c0001t0001g0024a0001c0001t0001g0025 | 2 | HG02647.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.207+3874_207+3904d others(33): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55400258 | |||||
chr4:55400258 | A | T | 1 | a0001c0001t0003g0288 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.207+3862A>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55400258 | ||||||
chr4:55400265 | A | AATATATA others(17): Show |
1 | a0001c0001t0003g0300 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.207+3881_207+3904d others(26): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55400265 | |||||
chr4:55400265 | A | AATATATA others(48): Show |
4 | a0001c0001t0002g0043a0001c0001t0002g0044a0001c0001t0002g0045others(1): Show | 4 | HG01175.hp2 HG01346.hp1 HG02273.hp1 others(1): Show |
intron_variant | MODIFIER | c.207+3918_207+3919i others(57): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55400265 | |||||
chr4:55400265 | A | T | 1 | a0001c0001t0003g0288 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.207+3869A>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55400265 | ||||||
chr4:55400272 | A | AATATAAT others(24): Show |
1 | a0001c0001t0002g0037 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.207+3892_207+3893i others(33): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55400272 | |||||
chr4:55400272 | A | AATATAAT others(12): Show |
1 | a0001c0002t0001g0257 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.207+3893_207+3911d others(21): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55400272 | |||||
chr4:55400272 | A | AATATAAT others(21): Show |
1 | a0001c0001t0002g0038 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.207+3877_207+3904d others(30): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55400272 | |||||
chr4:55400272 | A | AATATAAT others(55): Show |
2 | a0001c0001t0002g0036a0001c0001t0002g0141 | 2 | HG01891.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.207+3904_207+3905i others(64): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55400272 | |||||
chr4:55400272 | A | AATATAAT others(24): Show |
184 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0006others(181): Show | 192 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(189): Show |
intron_variant | MODIFIER | c.207+3888_207+3918d others(33): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55400272 | |||||
chr4:55400272 | A | AATATAAT others(36): Show |
1 | a0001c0001t0002g0035 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.207+3911_207+3912i others(45): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55400272 | |||||
chr4:55400273 | A | G | 7 | a0001c0001t0001g0011a0001c0001t0001g0145a0001c0001t0001g0146others(4): Show | 8 | HG02145.hp2 HG02257.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.207+3877A>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55400273 | ||||||
chr4:55400277 | A | T | 1 | a0003c0006t0015g0268 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.207+3881A>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55400277 | ||||||
chr4:55400278 | ATAT | A | 25 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0146others(22): Show | 27 | HG01884.hp2 HG02145.hp2 HG02257.hp2 others(24): Show |
intron_variant | MODIFIER | c.207+3886_207+3888d others(5): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55400278 | |||||
chr4:55400281 | T | TTATATAT others(21): Show |
2 | a0001c0001t0002g0039a0001c0001t0002g0040 | 2 | HG02015.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.207+3889_207+3916d others(30): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55400281 | |||||
chr4:55400284 | T | TATATTAT others(5): Show |
1 | a0001c0001t0002g0042 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.207+3907_207+3918d others(14): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55400284 | |||||
chr4:55400284 | TATATTAT others(5): Show |
T | 10 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0001g0167others(7): Show | 10 | HG01243.hp2 HG02109.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.207+3907_207+3918d others(14): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55400284 | |||||
chr4:55400289 | TATATATA others(12): Show |
T | 4 | a0001c0001t0003g0350a0001c0001t0003g0351a0001c0001t0003g0352others(1): Show | 4 | HG01123.hp2 HG01167.hp1 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.207+3898_207+3916d others(21): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55400289 | |||||
chr4:55400296 | A | AATATTAT others(24): Show |
9 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0005g0269others(6): Show | 9 | HG01891.hp2 HG02486.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.207+3916_207+3917i others(33): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55400296 | |||||
chr4:55400297 | ATAT | A | 3 | a0001c0001t0001g0265a0001c0001t0003g0266a0001c0001t0003g0267 | 3 | HG02280.hp2 HG02818.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.207+3905_207+3907d others(5): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55400297 | |||||
chr4:55400309 | A | ATATTATA others(24): Show |
1 | a0001c0001t0002g0140 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.207+3918_207+3919i others(33): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55400309 | |||||
chr4:55400319 | T | C | 86 | a0001c0001t0001g0003a0001c0001t0001g0027a0001c0001t0001g0028others(83): Show | 91 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.207+3923T>C | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55400319 | ||||||
chr4:55400323 | TTA | T | 7 | a0001c0001t0001g0011a0001c0001t0001g0145a0001c0001t0001g0146others(4): Show | 8 | HG02145.hp2 HG02257.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.207+3934_207+3935d others(4): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55400323 | |||||
chr4:55400333 | TATA | T | 76 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0312others(73): Show | 80 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(77): Show |
intron_variant | MODIFIER | c.207+3941_207+3943d others(5): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55400333 | |||||
chr4:55400337 | A | T | 4 | a0001c0001t0003g0282a0001c0001t0003g0298a0001c0001t0003g0301others(1): Show | 4 | HG00280.hp2 HG01192.hp2 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.207+3941A>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55400337 | ||||||
chr4:55400339 | ATTAATTA others(1): Show |
A | 4 | a0001c0001t0003g0282a0001c0001t0003g0298a0001c0001t0003g0301others(1): Show | 4 | HG00280.hp2 HG01192.hp2 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.207+3944_207+3951d others(10): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55400339 | ||||||
chr4:55400376 | TATA | T | 296 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0025others(293): Show | 310 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(307): Show |
intron_variant | MODIFIER | c.207+3991_207+3993d others(5): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55400376 | |||||
chr4:55400458 | T | A | 1 | a0001c0001t0003g0302 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.207+4062T>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55400458 | ||||||
chr4:55400534 | CTCACGCC others(2347): Show |
C | 16 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0145others(13): Show | 18 | HG02145.hp2 HG02257.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.207+4156_207+6509d others(2): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55400534 | |||||
chr4:55400557 | C | T | 205 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0006others(202): Show | 214 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(211): Show |
intron_variant | MODIFIER | c.207+4161C>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55400557 | ||||||
chr4:55400627 | C | T | 1 | a0001c0001t0001g0362 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.207+4231C>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55400627 | ||||||
chr4:55400636 | A | G | 1 | a0001c0001t0003g0287 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.207+4240A>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55400636 | ||||||
chr4:55400715 | A | C | 316 | a0001c0001t0001g0003a0001c0001t0001g0027a0001c0001t0001g0028others(313): Show | 330 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(327): Show |
intron_variant | MODIFIER | c.207+4319A>C | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55400715 | ||||||
chr4:55400844 | A | G | 1 | a0001c0001t0003g0359 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.207+4448A>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55400844 | ||||||
chr4:55401015 | T | C | 2 | a0001c0001t0001g0029a0001c0001t0001g0032 | 2 | HG01261.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.207+4619T>C | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55401015 | ||||||
chr4:55401060 | GAGGGGGG others(6): Show |
G | 1 | a0001c0001t0003g0356 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.207+4665_207+4677d others(15): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55401060 | ||||||
chr4:55401234 | T | C | 1 | a0003c0006t0015g0268 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.207+4838T>C | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55401234 | ||||||
chr4:55401306 | C | T | 105 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(102): Show | 111 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.207+4910C>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55401306 | ||||||
chr4:55401656 | C | T | 5 | a0001c0001t0002g0135a0001c0001t0002g0136a0001c0001t0002g0137others(2): Show | 5 | HG00735.hp1 HG01074.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.207+5260C>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55401656 | ||||||
chr4:55401720 | C | T | 1 | a0003c0006t0015g0268 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.207+5324C>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55401720 | ||||||
chr4:55401732 | C | T | 3 | a0001c0002t0001g0157a0001c0002t0001g0256a0001c0002t0001g0257 | 3 | HG00609.hp1 NA18950.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.207+5336C>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55401732 | ||||||
chr4:55401839 | G | C | 1 | a0001c0002t0001g0194 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.207+5443G>C | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55401839 | ||||||
chr4:55401854 | C | T | 1 | a0001c0001t0003g0301 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.207+5458C>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55401854 | ||||||
chr4:55401882 | C | T | 1 | a0001c0003t0001g0255 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.207+5486C>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55401882 | ||||||
chr4:55402119 | C | CAAAAA | 15 | a0001c0001t0001g0029a0001c0001t0001g0183a0001c0001t0001g0184others(12): Show | 15 | HG00558.hp2 HG02015.hp1 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.207+5731_207+5735d others(7): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402119 | |||||
chr4:55402119 | C | CAAAAAA | 200 | a0001c0001t0001g0003a0001c0001t0001g0027a0001c0001t0001g0028others(197): Show | 211 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(208): Show |
intron_variant | MODIFIER | c.207+5730_207+5735d others(8): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402119 | |||||
chr4:55402119 | C | CAAAAAAA | 10 | a0001c0001t0001g0167a0001c0001t0002g0033a0001c0001t0002g0043others(7): Show | 10 | HG01175.hp2 HG02723.hp2 HG03130.hp1 others(7): Show |
intron_variant | MODIFIER | c.207+5729_207+5735d others(9): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402119 | |||||
chr4:55402119 | C | CAAAAAAA others(1): Show |
14 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0004g0186others(11): Show | 14 | HG01243.hp2 HG01884.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.207+5728_207+5735d others(10): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402119 | |||||
chr4:55402119 | C | CAAAAAAA others(9): Show |
1 | a0001c0001t0001g0025 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.207+5735_207+5736i others(18): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402119 | |||||
chr4:55402119 | C | CAAAAAAA others(10): Show |
1 | a0001c0001t0001g0024 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.207+5735_207+5736i others(19): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402119 | |||||
chr4:55402119 | C | CAAAAAAA others(11): Show |
2 | a0001c0001t0004g0277a0001c0001t0009g0023 | 2 | HG01884.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.207+5735_207+5736i others(20): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402119 | |||||
chr4:55402119 | C | CAAAAAAA others(12): Show |
2 | a0001c0001t0001g0265a0001c0001t0009g0022 | 2 | HG02818.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.207+5735_207+5736i others(21): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402119 | |||||
chr4:55402124 | A | AAAAAAAA others(36): Show |
1 | a0001c0001t0004g0185 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.207+5735_207+5736i others(45): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402124 | |||||
chr4:55402173 | T | A | 2 | a0001c0001t0001g0027a0001c0001t0001g0028 | 2 | HG02809.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.207+5777T>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55402173 | ||||||
chr4:55402243 | A | G | 1 | a0001c0001t0002g0019 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.207+5847A>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55402243 | ||||||
chr4:55402268 | TAAC | T | 214 | a0001c0001t0001g0003a0001c0001t0001g0027a0001c0001t0001g0028others(211): Show | 225 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(222): Show |
intron_variant | MODIFIER | c.207+5875_207+5877d others(5): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402268 | |||||
chr4:55402340 | T | C | 214 | a0001c0001t0001g0003a0001c0001t0001g0027a0001c0001t0001g0028others(211): Show | 225 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(222): Show |
intron_variant | MODIFIER | c.207+5944T>C | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55402340 | ||||||
chr4:55402388 | C | CGTGT | 7 | a0001c0001t0001g0166a0001c0001t0006g0258a0001c0001t0008g0162others(4): Show | 7 | HG02109.hp1 HG02647.hp1 NA18522.hp1 others(4): Show |
intron_variant | MODIFIER | c.207+6005_207+6008d others(6): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402388 | |||||
chr4:55402388 | CGTGT | C | 3 | a0001c0001t0003g0266a0001c0001t0003g0267a0001c0001t0003g0346 | 3 | HG02280.hp2 HG03669.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.207+6005_207+6008d others(6): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402388 | |||||
chr4:55402397 | GTGTGTGT others(11): Show |
G | 2 | a0001c0001t0001g0029a0001c0001t0001g0032 | 2 | HG01261.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.207+6003_207+6020d others(20): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402397 | |||||
chr4:55402399 | GTGTGTAT others(1): Show |
G | 11 | a0001c0001t0001g0312a0001c0001t0003g0303a0001c0001t0003g0304others(8): Show | 11 | HG01361.hp1 HG02145.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.207+6005_207+6012d others(10): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402399 | |||||
chr4:55402399 | GTGTGTAT others(3): Show |
G | 44 | a0001c0001t0003g0002a0001c0001t0003g0017a0001c0001t0003g0018others(41): Show | 48 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(45): Show |
intron_variant | MODIFIER | c.207+6005_207+6014d others(12): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402399 | |||||
chr4:55402399 | GTGTGTAT others(5): Show |
G | 18 | a0001c0001t0001g0027a0001c0001t0001g0341a0001c0001t0001g0342others(15): Show | 18 | HG00140.hp1 HG01069.hp1 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.207+6005_207+6016d others(14): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402399 | |||||
chr4:55402399 | GTGTGTAT others(7): Show |
G | 4 | a0001c0001t0001g0003a0001c0001t0001g0028a0001c0001t0001g0030others(1): Show | 5 | HG02055.hp1 HG02622.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.207+6005_207+6018d others(16): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402399 | |||||
chr4:55402403 | G | A | 131 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0006others(128): Show | 136 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.207+6007G>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55402403 | ||||||
chr4:55402403 | G | GTGTATA | 3 | a0001c0002t0001g0188a0001c0002t0001g0190a0001c0002t0001g0213 | 3 | HG03710.hp2 HG03834.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.207+6008_207+6009i others(8): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402403 | |||||
chr4:55402403 | G | GTGTATAT others(3): Show |
2 | a0001c0002t0001g0207a0001c0002t0001g0208 | 2 | HG04184.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.207+6008_207+6009i others(12): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402403 | |||||
chr4:55402403 | G | GTGTATAT others(5): Show |
2 | a0001c0002t0001g0203a0001c0002t0001g0204 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.207+6008_207+6009i others(14): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402403 | |||||
chr4:55402403 | G | GTGTATAT others(7): Show |
1 | a0001c0002t0001g0205 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.207+6008_207+6009i others(16): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402403 | |||||
chr4:55402403 | G | GTGTGTA | 11 | a0001c0001t0006g0160a0001c0001t0006g0161a0001c0001t0006g0163others(8): Show | 11 | HG00558.hp1 HG00738.hp1 HG01081.hp2 others(8): Show |
intron_variant | MODIFIER | c.207+6008_207+6009i others(8): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402403 | |||||
chr4:55402403 | G | GTGTGTAT others(1): Show |
10 | a0001c0002t0001g0158a0001c0002t0001g0225a0001c0002t0001g0231others(7): Show | 10 | HG00438.hp2 HG00642.hp1 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.207+6008_207+6009i others(10): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402403 | |||||
chr4:55402403 | G | GTGTGTAT others(3): Show |
8 | a0001c0002t0001g0226a0001c0002t0001g0234a0001c0002t0001g0235others(5): Show | 8 | HG00597.hp1 HG02698.hp2 HG03490.hp2 others(5): Show |
intron_variant | MODIFIER | c.207+6008_207+6009i others(12): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402403 | |||||
chr4:55402403 | G | GTGTGTAT others(5): Show |
6 | a0001c0002t0001g0157a0001c0002t0001g0221a0001c0002t0001g0222others(3): Show | 6 | HG00621.hp2 HG02027.hp2 NA18962.hp1 others(3): Show |
intron_variant | MODIFIER | c.207+6008_207+6009i others(14): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402403 | |||||
chr4:55402403 | G | GTGTGTAT others(7): Show |
2 | a0001c0002t0001g0220a0001c0002t0010g0228 | 2 | HG02129.hp2 NA18954.hp1 |
intron_variant | MODIFIER | c.207+6008_207+6009i others(16): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402403 | |||||
chr4:55402403 | G | GTGTGTAT others(9): Show |
2 | a0001c0002t0001g0219a0001c0002t0001g0224 | 2 | NA18998.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.207+6008_207+6009i others(18): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402403 | |||||
chr4:55402403 | G | GTGTGTGT others(1): Show |
3 | a0001c0002t0001g0252a0001c0002t0001g0253a0001c0002t0001g0264 | 3 | HG00735.hp2 HG02083.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.207+6008_207+6009i others(10): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402403 | |||||
chr4:55402403 | G | GTGTGTGT others(3): Show |
1 | a0001c0002t0001g0251 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.207+6008_207+6009i others(12): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402403 | |||||
chr4:55402403 | G | GTGTGTGT others(7): Show |
1 | a0001c0001t0008g0164 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.207+6008_207+6009i others(16): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402403 | |||||
chr4:55402403 | G | GTGTGTGT others(3): Show |
1 | a0001c0002t0001g0254 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.207+6008_207+6009i others(12): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402403 | |||||
chr4:55402403 | G | GTGTGTGT others(5): Show |
1 | a0001c0002t0001g0194 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.207+6008_207+6009i others(14): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402403 | |||||
chr4:55402403 | GTA | G | 5 | a0001c0001t0001g0165a0001c0001t0001g0167a0001c0001t0005g0272others(2): Show | 5 | HG02258.hp2 HG02486.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.207+6037_207+6038d others(4): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402403 | |||||
chr4:55402403 | GTATA | G | 4 | a0001c0001t0001g0362a0001c0001t0004g0281a0001c0001t0005g0275others(1): Show | 4 | HG02572.hp2 HG02976.hp2 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.207+6035_207+6038d others(6): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402403 | |||||
chr4:55402405 | A | G | 39 | a0001c0001t0001g0024a0001c0001t0001g0166a0001c0001t0001g0168others(36): Show | 42 | HG00609.hp1 HG01123.hp1 HG01255.hp2 others(39): Show |
intron_variant | MODIFIER | c.207+6009A>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55402405 | ||||||
chr4:55402407 | A | G | 11 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0001g0167others(8): Show | 11 | HG00609.hp1 HG02109.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.207+6011A>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55402407 | ||||||
chr4:55402409 | A | G | 5 | a0001c0001t0001g0165a0001c0001t0001g0167a0001c0001t0001g0168others(2): Show | 5 | HG02258.hp2 HG02572.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.207+6013A>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55402409 | ||||||
chr4:55402411 | A | G | 3 | a0001c0001t0001g0165a0001c0001t0001g0167a0001c0001t0004g0281 | 3 | HG02258.hp2 HG02572.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.207+6015A>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55402411 | ||||||
chr4:55402417 | ATATATAT others(14): Show |
A | 1 | a0001c0001t0002g0130 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.207+6023_207+6043d others(23): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402417 | |||||
chr4:55402419 | ATATATAT others(10): Show |
A | 1 | a0001c0002t0001g0181 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.207+6025_207+6041d others(19): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402419 | |||||
chr4:55402419 | ATATATAT others(11): Show |
A | 1 | a0001c0001t0002g0037 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.207+6025_207+6042d others(20): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402419 | |||||
chr4:55402419 | ATATATAT others(13): Show |
A | 10 | a0001c0001t0002g0043a0001c0001t0002g0061a0001c0001t0002g0122others(7): Show | 10 | HG00609.hp2 HG01175.hp2 HG01952.hp1 others(7): Show |
intron_variant | MODIFIER | c.207+6025_207+6044d others(22): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402419 | |||||
chr4:55402419 | ATATATAT others(14): Show |
A | 35 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0009others(32): Show | 39 | HG01167.hp2 HG01346.hp1 HG01358.hp2 others(36): Show |
intron_variant | MODIFIER | c.207+6025_207+6045d others(23): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402419 | |||||
chr4:55402419 | ATATATAT others(15): Show |
A | 1 | a0001c0001t0002g0103 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.207+6025_207+6046d others(24): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402419 | |||||
chr4:55402421 | ATATATAT others(10): Show |
A | 1 | a0001c0002t0001g0256 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.207+6027_207+6043d others(19): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402421 | |||||
chr4:55402421 | ATATATAT others(11): Show |
A | 1 | a0001c0001t0002g0285 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.207+6027_207+6044d others(20): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402421 | |||||
chr4:55402421 | ATATATAT others(13): Show |
A | 10 | a0001c0001t0002g0034a0001c0001t0002g0036a0001c0001t0002g0039others(7): Show | 10 | HG01433.hp2 HG02809.hp2 HG03471.hp1 others(7): Show |
intron_variant | MODIFIER | c.207+6027_207+6046d others(22): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402421 | |||||
chr4:55402421 | ATATATAT others(14): Show |
A | 43 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0006others(40): Show | 45 | HG00438.hp1 HG00544.hp1 HG00733.hp1 others(42): Show |
intron_variant | MODIFIER | c.207+6027_207+6047d others(23): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402421 | |||||
chr4:55402421 | ATATATAT others(15): Show |
A | 9 | a0001c0001t0002g0040a0001c0001t0002g0051a0001c0001t0002g0074others(6): Show | 9 | HG00099.hp2 HG00280.hp1 HG01070.hp1 others(6): Show |
intron_variant | MODIFIER | c.207+6027_207+6048d others(24): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402421 | |||||
chr4:55402421 | ATATATAT others(16): Show |
A | 2 | a0001c0001t0002g0073a0001c0001t0003g0346 | 2 | HG01257.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.207+6027_207+6049d others(25): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402421 | |||||
chr4:55402423 | ATATATAT others(11): Show |
A | 1 | a0001c0001t0002g0050 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.207+6029_207+6046d others(20): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402423 | |||||
chr4:55402423 | ATATATAT others(12): Show |
A | 1 | a0001c0001t0002g0072 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.207+6029_207+6047d others(21): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402423 | |||||
chr4:55402423 | ATATATAT others(13): Show |
A | 4 | a0001c0001t0002g0070a0001c0001t0002g0071a0001c0001t0002g0131others(1): Show | 4 | HG00558.hp2 HG01261.hp2 NA18943.hp2 others(1): Show |
intron_variant | MODIFIER | c.207+6029_207+6048d others(22): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402423 | |||||
chr4:55402423 | ATATATAT others(14): Show |
A | 8 | a0001c0001t0002g0064a0001c0001t0002g0065a0001c0001t0002g0066others(5): Show | 8 | HG00621.hp1 HG00673.hp1 HG01123.hp2 others(5): Show |
intron_variant | MODIFIER | c.207+6029_207+6049d others(23): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402423 | |||||
chr4:55402423 | ATATATAT others(15): Show |
A | 2 | a0001c0001t0002g0063a0001c0001t0003g0347 | 2 | NA18948.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.207+6029_207+6050d others(24): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402423 | |||||
chr4:55402425 | ATATATAT others(10): Show |
A | 1 | a0001c0001t0002g0038 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.207+6031_207+6047d others(19): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402425 | |||||
chr4:55402425 | ATATATAT others(12): Show |
A | 1 | a0001c0001t0002g0062 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.207+6031_207+6049d others(21): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402425 | |||||
chr4:55402427 | ATATATAT others(6): Show |
A | 1 | a0001c0001t0005g0269 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.207+6033_207+6045d others(15): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402427 | |||||
chr4:55402429 | ATATATTT others(4): Show |
A | 1 | a0001c0001t0001g0265 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.207+6035_207+6045d others(13): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402429 | |||||
chr4:55402431 | A | T | 2 | a0001c0001t0005g0274a0001c0001t0005g0275 | 2 | HG02976.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.207+6035A>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55402431 | ||||||
chr4:55402433 | A | T | 9 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0004g0186others(6): Show | 9 | HG00597.hp1 HG01884.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.207+6037A>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55402433 | ||||||
chr4:55402433 | ATTTTTTT others(2): Show |
A | 10 | a0001c0001t0001g0312a0001c0001t0001g0341a0001c0001t0001g0342others(7): Show | 10 | HG01168.hp2 HG02559.hp1 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.207+6063_207+6071d others(11): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402433 | |||||
chr4:55402433 | ATTTTTTT others(3): Show |
A | 5 | a0001c0001t0003g0291a0001c0001t0003g0302a0001c0001t0003g0311others(2): Show | 5 | HG00642.hp2 HG01070.hp2 HG01943.hp1 others(2): Show |
intron_variant | MODIFIER | c.207+6062_207+6071d others(12): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402433 | |||||
chr4:55402433 | ATTTTTTT others(4): Show |
A | 47 | a0001c0001t0003g0002a0001c0001t0003g0018a0001c0001t0003g0282others(44): Show | 50 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(47): Show |
intron_variant | MODIFIER | c.207+6061_207+6071d others(13): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402433 | |||||
chr4:55402433 | ATTTTTTT others(5): Show |
A | 3 | a0001c0001t0003g0017a0001c0001t0003g0306a0001c0001t0003g0307 | 4 | HG01361.hp1 HG03688.hp2 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.207+6060_207+6071d others(14): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402433 | |||||
chr4:55402433 | ATTTTTTT others(6): Show |
A | 6 | a0001c0001t0003g0267a0001c0001t0003g0303a0001c0001t0003g0304others(3): Show | 6 | HG01175.hp1 HG03017.hp1 HG03239.hp1 others(3): Show |
intron_variant | MODIFIER | c.207+6059_207+6071d others(15): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402433 | |||||
chr4:55402433 | ATTTTTTT others(7): Show |
A | 1 | a0001c0001t0003g0266 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.207+6058_207+6071d others(16): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402433 | |||||
chr4:55402434 | T | TA | 33 | a0001c0001t0006g0160a0001c0001t0006g0161a0001c0001t0006g0258others(30): Show | 33 | HG00438.hp2 HG00733.hp2 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.207+6038_207+6039i others(3): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55402434 | ||||||
chr4:55402434 | T | TATATA | 9 | a0001c0002t0001g0012a0001c0002t0001g0014a0001c0002t0001g0015others(6): Show | 12 | HG00099.hp1 HG01123.hp1 HG01433.hp1 others(9): Show |
intron_variant | MODIFIER | c.207+6038_207+6039i others(7): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55402434 | ||||||
chr4:55402434 | T | TATATATA others(4): Show |
3 | a0001c0002t0001g0020a0001c0002t0001g0021a0001c0002t0001g0202 | 3 | HG01069.hp2 HG01071.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.207+6038_207+6039i others(13): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55402434 | ||||||
chr4:55402434 | T | TATATATA others(6): Show |
1 | a0001c0002t0001g0201 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.207+6038_207+6039i others(15): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55402434 | ||||||
chr4:55402434 | T | TATATATA others(8): Show |
1 | a0001c0002t0001g0206 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.207+6038_207+6039i others(17): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55402434 | ||||||
chr4:55402434 | T | TATATATA others(10): Show |
1 | a0001c0002t0001g0200 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.207+6038_207+6039i others(19): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55402434 | ||||||
chr4:55402434 | T | TATATATA others(16): Show |
1 | a0001c0002t0001g0199 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.207+6038_207+6039i others(25): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55402434 | ||||||
chr4:55402435 | T | A | 23 | a0001c0001t0001g0166a0001c0001t0006g0163a0001c0001t0008g0164others(20): Show | 23 | HG00558.hp1 HG00621.hp2 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.207+6039T>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55402435 | ||||||
chr4:55402436 | T | A | 41 | a0001c0001t0006g0160a0001c0001t0006g0161a0001c0001t0006g0258others(38): Show | 44 | HG00438.hp2 HG00738.hp1 HG01069.hp2 others(41): Show |
intron_variant | MODIFIER | c.207+6040T>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55402436 | ||||||
chr4:55402437 | T | A | 4 | a0001c0002t0001g0203a0001c0002t0001g0204a0001c0002t0001g0229others(1): Show | 4 | HG00558.hp1 HG01168.hp1 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.207+6041T>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55402437 | ||||||
chr4:55402438 | T | A | 13 | a0001c0002t0001g0191a0001c0002t0001g0201a0001c0002t0001g0202others(10): Show | 13 | HG02027.hp2 HG02129.hp2 HG02965.hp2 others(10): Show |
intron_variant | MODIFIER | c.207+6042T>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55402438 | ||||||
chr4:55402439 | T | A | 3 | a0001c0001t0001g0183a0001c0002t0001g0229a0001c0002t0001g0254 | 3 | HG00558.hp1 HG02622.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.207+6043T>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55402439 | ||||||
chr4:55402440 | T | A | 1 | a0001c0002t0001g0219 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.207+6044T>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55402440 | ||||||
chr4:55402534 | G | C | 2 | a0001c0001t0001g0165a0001c0001t0001g0167 | 2 | HG02258.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.207+6138G>C | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55402534 | ||||||
chr4:55402552 | A | G | 1 | a0001c0001t0002g0098 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.207+6156A>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55402552 | ||||||
chr4:55402681 | C | T | 1 | a0001c0001t0003g0290 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.207+6285C>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55402681 | ||||||
chr4:55402699 | C | T | 1 | a0001c0002t0001g0181 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.207+6303C>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55402699 | ||||||
chr4:55402795 | C | CTTTTTTT others(1): Show |
6 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0006g0160others(3): Show | 6 | HG01243.hp2 HG02109.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.207+6406_207+6413d others(10): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402795 | |||||
chr4:55402795 | C | CTTTTTTT others(2): Show |
16 | a0001c0001t0001g0165a0001c0001t0001g0168a0001c0001t0001g0183others(13): Show | 16 | HG01884.hp1 HG01891.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.207+6405_207+6413d others(11): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402795 | |||||
chr4:55402795 | C | CTTTTTTT others(3): Show |
2 | a0001c0001t0001g0032a0001c0001t0005g0273 | 2 | HG01261.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.207+6404_207+6413d others(12): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402795 | |||||
chr4:55402795 | C | CTTTTTTT others(4): Show |
1 | a0001c0001t0001g0029 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.207+6403_207+6413d others(13): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402795 | |||||
chr4:55402795 | C | CTTTTTTT others(6): Show |
10 | a0001c0001t0001g0003a0001c0001t0001g0027a0001c0001t0001g0028others(7): Show | 11 | HG01168.hp2 HG02055.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.207+6401_207+6413d others(15): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402795 | |||||
chr4:55402795 | C | CTTTTTTT others(7): Show |
50 | a0001c0001t0001g0312a0001c0001t0001g0341a0001c0001t0001g0342others(47): Show | 53 | HG00140.hp1 HG00280.hp2 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.207+6400_207+6413d others(16): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402795 | |||||
chr4:55402795 | C | CTTTTTTT others(8): Show |
94 | a0001c0001t0001g0344a0001c0001t0002g0004a0001c0001t0002g0005others(91): Show | 100 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.207+6413_207+6414i others(17): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402795 | |||||
chr4:55402795 | C | CTTTTTTT others(9): Show |
47 | a0001c0001t0002g0033a0001c0001t0002g0034a0001c0001t0002g0035others(44): Show | 47 | HG00438.hp1 HG00544.hp1 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.207+6413_207+6414i others(18): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402795 | |||||
chr4:55402795 | C | CTTTTTTT others(10): Show |
7 | a0001c0001t0002g0038a0001c0001t0002g0056a0001c0001t0002g0057others(4): Show | 7 | HG00323.hp2 HG03453.hp1 HG03579.hp1 others(4): Show |
intron_variant | MODIFIER | c.207+6413_207+6414i others(19): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402795 | |||||
chr4:55402795 | C | CTTTTTTT others(14): Show |
1 | a0001c0001t0003g0266 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.207+6413_207+6414i others(23): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402795 | |||||
chr4:55402795 | C | CTTTTTTT others(15): Show |
1 | a0001c0001t0003g0267 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.207+6413_207+6414i others(24): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402795 | |||||
chr4:55402795 | C | CTTTTTTT others(16): Show |
1 | a0001c0001t0002g0010 | 2 | HG02132.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.207+6413_207+6414i others(25): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55402795 | |||||
chr4:55402875 | T | G | 2 | a0001c0001t0003g0266a0001c0001t0003g0267 | 2 | HG02280.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.207+6479T>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55402875 | ||||||
chr4:55402892 | C | T | 1 | a0001c0001t0001g0156 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.207+6496C>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55402892 | ||||||
chr4:55402912 | C | T | 1 | a0001c0001t0003g0294 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.207+6516C>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55402912 | ||||||
chr4:55403178 | A | C | 1 | a0001c0001t0005g0269 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.207+6782A>C | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55403178 | ||||||
chr4:55403210 | G | A | 1 | a0001c0002t0001g0237 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.207+6814G>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55403210 | ||||||
chr4:55403335 | G | GCAGGTAT others(325): Show |
12 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0001g0167others(9): Show | 12 | HG01891.hp2 HG02109.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.207+6959_207+6960i others(334): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55403335 | |||||
chr4:55403335 | G | GCAGGTAT others(326): Show |
10 | a0001c0001t0001g0265a0001c0001t0005g0275a0001c0001t0006g0160others(7): Show | 10 | HG01243.hp2 HG01884.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.207+6959_207+6960i others(335): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55403335 | |||||
chr4:55403389 | G | T | 1 | a0001c0001t0002g0010 | 2 | HG02132.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.207+6993G>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55403389 | ||||||
chr4:55403492 | C | CT | 276 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0024others(273): Show | 291 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(288): Show |
intron_variant | MODIFIER | c.207+7101dupT | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55403492 | |||||
chr4:55403492 | C | CTT | 15 | a0001c0001t0001g0265a0001c0001t0002g0135a0001c0001t0002g0136others(12): Show | 15 | HG00280.hp2 HG00558.hp1 HG00735.hp1 others(12): Show |
intron_variant | MODIFIER | c.207+7100_207+7101d others(4): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55403492 | |||||
chr4:55403496 | T | C | 1 | a0003c0006t0015g0268 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.207+7100T>C | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55403496 | ||||||
chr4:55403497 | TC | T | 8 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0005g0269others(5): Show | 8 | HG02559.hp2 HG02622.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.207+7102delC | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55403497 | ||||||
chr4:55403498 | C | T | 323 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0013others(320): Show | 339 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(336): Show |
intron_variant | MODIFIER | c.207+7102C>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55403498 | ||||||
chr4:55403516 | A | C | 204 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0006others(201): Show | 213 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(210): Show |
intron_variant | MODIFIER | c.207+7120A>C | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55403516 | ||||||
chr4:55403518 | T | C | 1 | a0001c0001t0002g0054 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.207+7122T>C | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55403518 | ||||||
chr4:55403576 | T | A | 5 | a0001c0001t0003g0302a0001c0001t0006g0160a0001c0001t0006g0161others(2): Show | 5 | HG01070.hp2 HG02647.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.207+7180T>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55403576 | ||||||
chr4:55403576 | T | TA | 292 | a0001c0001t0001g0003a0001c0001t0001g0027a0001c0001t0001g0028others(289): Show | 306 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(303): Show |
intron_variant | MODIFIER | c.207+7187dupA | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55403576 | |||||
chr4:55403706 | C | T | 1 | a0001c0001t0002g0118 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.207+7310C>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55403706 | ||||||
chr4:55403812 | A | G | 79 | a0001c0001t0001g0312a0001c0001t0001g0341a0001c0001t0001g0342others(76): Show | 83 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.207+7416A>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55403812 | ||||||
chr4:55403830 | T | G | 1 | a0001c0002t0001g0208 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.207+7434T>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55403830 | ||||||
chr4:55403985 | TCTTAA | T | 205 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0006others(202): Show | 214 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(211): Show |
intron_variant | MODIFIER | c.207+7593_207+7597d others(7): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55403985 | |||||
chr4:55403998 | A | G | 1 | a0001c0001t0001g0032 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.207+7602A>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55403998 | ||||||
chr4:55404045 | C | CT | 7 | a0001c0001t0004g0159a0001c0001t0004g0186a0001c0001t0004g0277others(4): Show | 7 | HG01884.hp2 HG02572.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.208-7552dupT | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55404045 | |||||
chr4:55404045 | CT | C | 14 | a0001c0001t0001g0146a0001c0001t0001g0165a0001c0001t0001g0166others(11): Show | 14 | HG01243.hp2 HG01884.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.208-7552delT | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55404045 | |||||
chr4:55404045 | CTT | C | 12 | a0001c0001t0001g0032a0001c0001t0001g0156a0001c0001t0001g0183others(9): Show | 12 | HG01261.hp1 HG01891.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.208-7553_208-7552d others(4): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55404045 | |||||
chr4:55404045 | CTTT | C | 292 | a0001c0001t0001g0003a0001c0001t0001g0027a0001c0001t0001g0028others(289): Show | 306 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(303): Show |
intron_variant | MODIFIER | c.208-7554_208-7552d others(5): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55404045 | |||||
chr4:55404050 | T | C | 13 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0001g0167others(10): Show | 13 | HG01243.hp2 HG01884.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.208-7564T>C | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55404050 | ||||||
chr4:55404160 | C | T | 2 | a0001c0001t0001g0152a0001c0001t0001g0153 | 2 | HG02572.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.208-7454C>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55404160 | ||||||
chr4:55404177 | A | AT | 14 | a0001c0001t0001g0013a0001c0001t0001g0029a0001c0001t0001g0032others(11): Show | 15 | HG01261.hp1 HG01943.hp1 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.208-7425dupT | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55404177 | |||||
chr4:55404200 | T | C | 1 | a0001c0001t0002g0104 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.208-7414T>C | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55404200 | ||||||
chr4:55404206 | T | C | 331 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0013others(328): Show | 347 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(344): Show |
intron_variant | MODIFIER | c.208-7408T>C | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55404206 | ||||||
chr4:55404206 | T | G | 1 | a0001c0001t0002g0129 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.208-7408T>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55404206 | ||||||
chr4:55404253 | G | A | 2 | a0001c0001t0001g0029a0001c0001t0001g0032 | 2 | HG01261.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.208-7361G>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55404253 | ||||||
chr4:55404305 | A | G | 292 | a0001c0001t0001g0003a0001c0001t0001g0027a0001c0001t0001g0028others(289): Show | 306 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(303): Show |
intron_variant | MODIFIER | c.208-7309A>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55404305 | ||||||
chr4:55404464 | C | T | 1 | a0001c0001t0003g0302 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.208-7150C>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55404464 | ||||||
chr4:55404606 | AT | A | 39 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0145others(36): Show | 41 | HG01243.hp2 HG01884.hp1 HG01891.hp2 others(38): Show |
intron_variant | MODIFIER | c.208-6996delT | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55404606 | |||||
chr4:55404606 | ATTTTT | A | 10 | a0001c0001t0002g0004a0001c0001t0002g0047a0001c0001t0002g0048others(7): Show | 10 | HG01255.hp1 HG02615.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.208-7000_208-6996d others(7): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55404606 | |||||
chr4:55404611 | T | A | 284 | a0001c0001t0001g0003a0001c0001t0001g0027a0001c0001t0001g0028others(281): Show | 298 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(295): Show |
intron_variant | MODIFIER | c.208-7003T>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55404611 | ||||||
chr4:55404617 | T | G | 4 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0001g0167others(1): Show | 4 | HG02109.hp1 HG02258.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.208-6997T>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55404617 | ||||||
chr4:55404689 | C | T | 1 | a0001c0002t0001g0221 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.208-6925C>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55404689 | ||||||
chr4:55404832 | T | A | 12 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0001g0167others(9): Show | 12 | HG01243.hp2 HG01884.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.208-6782T>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55404832 | ||||||
chr4:55404896 | A | G | 1 | a0001c0001t0004g0281 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.208-6718A>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55404896 | ||||||
chr4:55404924 | T | G | 1 | a0001c0001t0003g0313 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.208-6690T>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55404924 | ||||||
chr4:55404977 | GCACCC | G | 4 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0001g0167others(1): Show | 4 | HG02109.hp1 HG02258.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.208-6634_208-6630d others(7): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55404977 | |||||
chr4:55405086 | C | T | 10 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0001g0167others(7): Show | 10 | HG01243.hp2 HG02109.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.208-6528C>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55405086 | ||||||
chr4:55405250 | G | C | 12 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0001g0167others(9): Show | 12 | HG01243.hp2 HG01884.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.208-6364G>C | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55405250 | ||||||
chr4:55405498 | A | G | 2 | a0001c0001t0002g0061a0001c0001t0002g0116 | 2 | NA18971.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.208-6116A>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55405498 | ||||||
chr4:55405562 | A | G | 1 | a0001c0001t0002g0097 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.208-6052A>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55405562 | ||||||
chr4:55405566 | A | G | 9 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0005g0269others(6): Show | 9 | HG01891.hp2 HG02486.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.208-6048A>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55405566 | ||||||
chr4:55405775 | G | T | 9 | a0001c0001t0004g0159a0001c0001t0004g0185a0001c0001t0004g0186others(6): Show | 9 | HG01884.hp2 HG02451.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.208-5839G>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55405775 | ||||||
chr4:55405894 | C | G | 13 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0001g0167others(10): Show | 13 | HG01243.hp2 HG01884.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.208-5720C>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55405894 | ||||||
chr4:55405959 | T | G | 1 | a0001c0001t0003g0300 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.208-5655T>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55405959 | ||||||
chr4:55406129 | C | T | 1 | a0001c0001t0005g0269 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.208-5485C>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55406129 | ||||||
chr4:55406236 | C | G | 1 | a0001c0001t0001g0155 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.208-5378C>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55406236 | ||||||
chr4:55406483 | C | T | 9 | a0001c0001t0004g0159a0001c0001t0004g0185a0001c0001t0004g0186others(6): Show | 9 | HG01884.hp2 HG02451.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.208-5131C>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55406483 | ||||||
chr4:55406487 | A | G | 1 | a0001c0001t0004g0159 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.208-5127A>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55406487 | ||||||
chr4:55406507 | A | G | 1 | a0001c0001t0005g0269 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.208-5107A>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55406507 | ||||||
chr4:55406520 | T | C | 1 | a0001c0001t0002g0094 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.208-5094T>C | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55406520 | ||||||
chr4:55406559 | G | A | 2 | a0001c0001t0001g0024a0001c0001t0001g0025 | 2 | HG02647.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.208-5055G>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55406559 | ||||||
chr4:55406696 | G | C | 80 | a0001c0001t0001g0312a0001c0001t0001g0341a0001c0001t0001g0342others(77): Show | 84 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.208-4918G>C | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55406696 | ||||||
chr4:55406845 | A | G | 2 | a0001c0001t0001g0029a0001c0001t0001g0032 | 2 | HG01261.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.208-4769A>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55406845 | ||||||
chr4:55406955 | C | T | 1 | a0001c0001t0002g0046 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.208-4659C>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55406955 | ||||||
chr4:55406979 | T | C | 1 | a0001c0001t0005g0273 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.208-4635T>C | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55406979 | ||||||
chr4:55407119 | G | A | 2 | a0001c0001t0002g0104a0001c0001t0002g0105 | 2 | NA18948.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.208-4495G>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55407119 | ||||||
chr4:55407120 | G | C | 62 | a0001c0001t0003g0002a0001c0001t0003g0017a0001c0001t0003g0018others(59): Show | 66 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(63): Show |
intron_variant | MODIFIER | c.208-4494G>C | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55407120 | ||||||
chr4:55407142 | A | C | 1 | a0001c0001t0002g0058 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.208-4472A>C | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55407142 | ||||||
chr4:55407285 | T | C | 2 | a0001c0001t0002g0004a0001c0005t0002g0004 | 2 | HG01255.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.208-4329T>C | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55407285 | ||||||
chr4:55407625 | T | C | 1 | a0001c0001t0001g0355 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.208-3989T>C | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55407625 | ||||||
chr4:55407721 | G | C | 2 | a0001c0001t0001g0024a0001c0001t0001g0025 | 2 | HG02647.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.208-3893G>C | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55407721 | ||||||
chr4:55407928 | T | A | 1 | a0001c0001t0004g0186 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.208-3686T>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55407928 | ||||||
chr4:55407965 | G | A | 124 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0006others(121): Show | 130 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.208-3649G>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55407965 | ||||||
chr4:55408140 | G | A | 214 | a0001c0001t0001g0003a0001c0001t0001g0027a0001c0001t0001g0028others(211): Show | 225 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(222): Show |
intron_variant | MODIFIER | c.208-3474G>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55408140 | ||||||
chr4:55408163 | C | T | 213 | a0001c0001t0001g0003a0001c0001t0001g0027a0001c0001t0001g0028others(210): Show | 224 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.208-3451C>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55408163 | ||||||
chr4:55408164 | G | A | 2 | a0001c0001t0001g0024a0001c0001t0001g0025 | 2 | HG02647.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.208-3450G>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55408164 | ||||||
chr4:55408174 | G | A | 9 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0005g0269others(6): Show | 9 | HG01891.hp2 HG02486.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.208-3440G>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55408174 | ||||||
chr4:55408304 | G | A | 2 | a0001c0001t0001g0029a0001c0001t0001g0032 | 2 | HG01261.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.208-3310G>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55408304 | ||||||
chr4:55408506 | A | G | 16 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0145others(13): Show | 18 | HG02145.hp2 HG02257.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.208-3108A>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55408506 | ||||||
chr4:55408533 | T | TAAAAAAT others(3): Show |
1 | a0001c0001t0003g0356 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.208-3080_208-3071d others(12): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55408533 | |||||
chr4:55408597 | T | A | 294 | a0001c0001t0001g0003a0001c0001t0001g0027a0001c0001t0001g0028others(291): Show | 308 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(305): Show |
intron_variant | MODIFIER | c.208-3017T>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55408597 | ||||||
chr4:55408862 | C | T | 2 | a0001c0001t0001g0024a0001c0001t0001g0025 | 2 | HG02647.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.208-2752C>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55408862 | ||||||
chr4:55408922 | C | CT | 285 | a0001c0001t0001g0003a0001c0001t0001g0027a0001c0001t0001g0028others(282): Show | 299 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(296): Show |
intron_variant | MODIFIER | c.208-2678dupT | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55408922 | |||||
chr4:55408998 | T | C | 2 | a0001c0001t0009g0022a0001c0001t0009g0023 | 2 | HG01884.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.208-2616T>C | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55408998 | ||||||
chr4:55409053 | G | A | 6 | a0001c0001t0006g0160a0001c0001t0006g0161a0001c0001t0006g0163others(3): Show | 6 | HG01243.hp2 HG02647.hp1 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.208-2561G>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55409053 | ||||||
chr4:55409063 | G | T | 124 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0006others(121): Show | 130 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.208-2551G>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55409063 | ||||||
chr4:55409067 | G | A | 5 | a0001c0001t0001g0312a0001c0001t0001g0341a0001c0001t0001g0342others(2): Show | 5 | HG02559.hp1 HG02895.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.208-2547G>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55409067 | ||||||
chr4:55409197 | T | C | 2 | a0001c0001t0002g0034a0001c0001t0002g0082 | 2 | HG03239.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.208-2417T>C | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55409197 | ||||||
chr4:55409567 | T | C | 1 | a0001c0002t0001g0169 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.208-2047T>C | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55409567 | ||||||
chr4:55409574 | T | C | 1 | a0001c0001t0001g0152 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.208-2040T>C | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55409574 | ||||||
chr4:55409590 | T | G | 1 | a0001c0001t0002g0050 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.208-2024T>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55409590 | ||||||
chr4:55409658 | G | A | 2 | a0001c0001t0001g0183a0001c0001t0001g0184 | 2 | HG02559.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.208-1956G>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55409658 | ||||||
chr4:55409694 | G | A | 1 | a0001c0002t0001g0193 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.208-1920G>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55409694 | ||||||
chr4:55409780 | A | T | 2 | a0001c0001t0001g0027a0001c0001t0001g0028 | 2 | HG02809.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.208-1834A>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55409780 | ||||||
chr4:55409901 | G | A | 5 | a0001c0001t0001g0312a0001c0001t0001g0341a0001c0001t0001g0342others(2): Show | 5 | HG02559.hp1 HG02895.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.208-1713G>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55409901 | ||||||
chr4:55409961 | C | T | 1 | a0001c0001t0001g0355 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.208-1653C>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55409961 | ||||||
chr4:55410167 | T | C | 204 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0006others(201): Show | 213 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(210): Show |
intron_variant | MODIFIER | c.208-1447T>C | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55410167 | ||||||
chr4:55410311 | C | T | 82 | a0001c0001t0001g0312a0001c0001t0001g0341a0001c0001t0001g0342others(79): Show | 86 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(83): Show |
intron_variant | MODIFIER | c.208-1303C>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55410311 | ||||||
chr4:55410372 | AATGACAG others(18): Show |
A | 1 | a0001c0001t0003g0356 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.208-1241_208-1217d others(27): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55410372 | ||||||
chr4:55410464 | A | G | 1 | a0003c0006t0015g0268 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.208-1150A>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55410464 | ||||||
chr4:55410466 | G | A | 1 | a0003c0006t0015g0268 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.208-1148G>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55410466 | ||||||
chr4:55410551 | G | A | 1 | a0001c0001t0009g0022 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.208-1063G>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55410551 | ||||||
chr4:55410602 | G | A | 1 | a0001c0001t0001g0156 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.208-1012G>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55410602 | ||||||
chr4:55410608 | C | T | 2 | a0001c0001t0009g0022a0001c0001t0009g0023 | 2 | HG01884.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.208-1006C>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55410608 | ||||||
chr4:55410701 | G | A | 1 | a0001c0001t0002g0074 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.208-913G>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55410701 | ||||||
chr4:55410728 | C | T | 82 | a0001c0001t0001g0312a0001c0001t0001g0341a0001c0001t0001g0342others(79): Show | 86 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(83): Show |
intron_variant | MODIFIER | c.208-886C>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55410728 | ||||||
chr4:55410759 | G | A | 1 | a0001c0002t0001g0209 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.208-855G>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55410759 | ||||||
chr4:55410859 | G | A | 2 | a0001c0001t0003g0266a0001c0001t0003g0267 | 2 | HG02280.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.208-755G>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55410859 | ||||||
chr4:55411044 | A | C | 10 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0001g0167others(7): Show | 10 | HG01243.hp2 HG02109.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.208-570A>C | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55411044 | ||||||
chr4:55411064 | G | A | 1 | a0001c0001t0002g0044 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.208-550G>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55411064 | ||||||
chr4:55411130 | G | A | 2 | a0001c0001t0002g0052a0001c0001t0002g0058 | 2 | HG02809.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.208-484G>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55411130 | ||||||
chr4:55411134 | C | CA | 8 | a0001c0001t0002g0035a0001c0001t0002g0043a0001c0001t0002g0050others(5): Show | 8 | HG01175.hp2 HG01978.hp1 HG02074.hp2 others(5): Show |
intron_variant | MODIFIER | c.208-463dupA | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55411134 | |||||
chr4:55411134 | CA | C | 8 | a0001c0001t0001g0029a0001c0001t0001g0032a0001c0001t0001g0154others(5): Show | 8 | HG01261.hp1 HG02886.hp1 HG03942.hp2 others(5): Show |
intron_variant | MODIFIER | c.208-463delA | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr4 | 55411134 | |||||
chr4:55411151 | A | G | 2 | a0001c0001t0001g0029a0001c0001t0001g0032 | 2 | HG01261.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.208-463A>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55411151 | ||||||
chr4:55411179 | G | A | 1 | a0001c0001t0001g0355 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.208-435G>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55411179 | ||||||
chr4:55411384 | C | T | 1 | a0001c0001t0003g0359 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.208-230C>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55411384 | ||||||
chr4:55411449 | C | T | 1 | a0001c0002t0001g0213 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.208-165C>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55411449 | ||||||
chr4:55411554 | G | A | 1 | a0001c0002t0001g0217 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.208-60G>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 1/5 | chr4 | 55411554 | ||||||
chr4:55411868 | C | T | 1 | a0001c0001t0001g0156 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.433+29C>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 2/5 | chr4 | 55411868 | ||||||
chr4:55411967 | A | G | 1 | a0001c0001t0003g0301 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.433+128A>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 2/5 | chr4 | 55411967 | ||||||
chr4:55411970 | TTTTCCTT others(8): Show |
T | 2 | a0001c0001t0001g0029a0001c0001t0001g0032 | 2 | HG01261.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.433+148_433+162del others(15): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 55411970 | |||||
chr4:55412132 | C | T | 1 | a0001c0001t0002g0051 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.433+293C>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 2/5 | chr4 | 55412132 | ||||||
chr4:55412161 | G | A | 1 | a0001c0002t0001g0221 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.433+322G>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 2/5 | chr4 | 55412161 | ||||||
chr4:55412221 | G | A | 2 | a0001c0001t0002g0075a0001c0001t0002g0078 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.433+382G>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 2/5 | chr4 | 55412221 | ||||||
chr4:55412332 | T | C | 2 | a0001c0001t0002g0079a0001c0001t0002g0083 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.433+493T>C | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 2/5 | chr4 | 55412332 | ||||||
chr4:55412349 | G | A | 2 | a0001c0001t0001g0029a0001c0001t0001g0032 | 2 | HG01261.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.433+510G>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 2/5 | chr4 | 55412349 | ||||||
chr4:55412393 | C | CA | 14 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0001g0167others(11): Show | 14 | HG01884.hp2 HG02109.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.433+578dupA | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 55412393 | |||||
chr4:55412393 | C | CAAA | 13 | a0001c0001t0001g0342a0001c0001t0002g0004a0001c0001t0002g0043others(10): Show | 13 | HG01175.hp2 HG01255.hp1 HG01346.hp1 others(10): Show |
intron_variant | MODIFIER | c.433+576_433+578dup others(3): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 55412393 | |||||
chr4:55412393 | C | CAAAA | 171 | a0001c0001t0001g0032a0001c0001t0001g0312a0001c0001t0001g0344others(168): Show | 180 | HG00099.hp2 HG00280.hp1 HG00438.hp2 others(177): Show |
intron_variant | MODIFIER | c.433+575_433+578dup others(4): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 55412393 | |||||
chr4:55412393 | C | CAAAAA | 82 | a0001c0001t0001g0029a0001c0001t0001g0341a0001c0001t0002g0036others(79): Show | 86 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(83): Show |
intron_variant | MODIFIER | c.433+574_433+578dup others(5): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 55412393 | |||||
chr4:55412393 | C | CAAAAAA | 16 | a0001c0001t0002g0101a0001c0001t0003g0287a0001c0001t0003g0289others(13): Show | 16 | HG00642.hp2 HG01175.hp1 HG01361.hp1 others(13): Show |
intron_variant | MODIFIER | c.433+573_433+578dup others(6): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 55412393 | |||||
chr4:55412393 | C | CAAAAAAA others(3): Show |
1 | a0001c0001t0001g0030 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.433+569_433+578dup others(10): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 55412393 | |||||
chr4:55412393 | C | CAAAAAAA others(5): Show |
2 | a0001c0001t0001g0027a0001c0001t0001g0028 | 2 | HG02809.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.433+567_433+578dup others(12): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 55412393 | |||||
chr4:55412393 | CA | C | 18 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0024others(15): Show | 20 | HG02145.hp2 HG02257.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.433+578delA | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 55412393 | |||||
chr4:55412714 | C | G | 2 | a0001c0001t0001g0183a0001c0001t0001g0184 | 2 | HG02559.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.433+875C>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 2/5 | chr4 | 55412714 | ||||||
chr4:55412983 | A | T | 4 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0001g0167others(1): Show | 4 | HG02109.hp1 HG02258.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.433+1144A>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 2/5 | chr4 | 55412983 | ||||||
chr4:55412987 | A | T | 14 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0001g0167others(11): Show | 14 | HG01243.hp2 HG01884.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.433+1148A>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 2/5 | chr4 | 55412987 | ||||||
chr4:55412991 | T | A | 87 | a0001c0001t0001g0003a0001c0001t0001g0027a0001c0001t0001g0028others(84): Show | 92 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(89): Show |
intron_variant | MODIFIER | c.433+1152T>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 2/5 | chr4 | 55412991 | ||||||
chr4:55413170 | G | A | 5 | a0001c0001t0001g0312a0001c0001t0001g0341a0001c0001t0001g0342others(2): Show | 5 | HG02559.hp1 HG02895.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.433+1331G>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 2/5 | chr4 | 55413170 | ||||||
chr4:55413302 | ATTTTTAT others(9): Show |
A | 2 | a0001c0001t0001g0183a0001c0001t0001g0184 | 2 | HG02559.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.433+1477_433+1492d others(18): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 55413302 | |||||
chr4:55413318 | C | CT | 6 | a0001c0001t0006g0160a0001c0001t0006g0161a0001c0001t0006g0163others(3): Show | 6 | HG01243.hp2 HG02647.hp1 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.433+1484dupT | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 55413318 | |||||
chr4:55413357 | C | A | 2 | a0001c0001t0001g0024a0001c0001t0001g0025 | 2 | HG02647.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.433+1518C>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 2/5 | chr4 | 55413357 | ||||||
chr4:55413363 | G | A | 30 | a0001c0001t0003g0002a0001c0001t0003g0282a0001c0001t0003g0287others(27): Show | 32 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(29): Show |
intron_variant | MODIFIER | c.433+1524G>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 2/5 | chr4 | 55413363 | ||||||
chr4:55413385 | A | G | 294 | a0001c0001t0001g0003a0001c0001t0001g0027a0001c0001t0001g0028others(291): Show | 308 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(305): Show |
intron_variant | MODIFIER | c.433+1546A>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 2/5 | chr4 | 55413385 | ||||||
chr4:55413522 | G | A | 1 | a0001c0001t0002g0354 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.433+1683G>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 2/5 | chr4 | 55413522 | ||||||
chr4:55413561 | C | T | 2 | a0001c0001t0002g0092a0001c0001t0002g0093 | 2 | HG01358.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.433+1722C>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 2/5 | chr4 | 55413561 | ||||||
chr4:55413708 | A | G | 105 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(102): Show | 111 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.433+1869A>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 2/5 | chr4 | 55413708 | ||||||
chr4:55413774 | A | T | 10 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0001g0167others(7): Show | 10 | HG01243.hp2 HG02109.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.433+1935A>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 2/5 | chr4 | 55413774 | ||||||
chr4:55413804 | A | T | 1 | a0003c0006t0015g0268 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.433+1965A>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 2/5 | chr4 | 55413804 | ||||||
chr4:55413805 | C | G | 1 | a0003c0006t0015g0268 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.433+1966C>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 2/5 | chr4 | 55413805 | ||||||
chr4:55413861 | T | C | 1 | a0001c0002t0001g0201 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.433+2022T>C | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 2/5 | chr4 | 55413861 | ||||||
chr4:55413993 | G | A | 1 | a0001c0001t0002g0084 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.433+2154G>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 2/5 | chr4 | 55413993 | ||||||
chr4:55414021 | C | T | 2 | a0001c0001t0001g0027a0001c0001t0001g0028 | 2 | HG02809.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.433+2182C>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 2/5 | chr4 | 55414021 | ||||||
chr4:55414066 | A | T | 291 | a0001c0001t0001g0003a0001c0001t0001g0027a0001c0001t0001g0028others(288): Show | 305 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(302): Show |
intron_variant | MODIFIER | c.433+2227A>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 2/5 | chr4 | 55414066 | ||||||
chr4:55414095 | C | T | 1 | a0001c0001t0001g0166 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.433+2256C>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 2/5 | chr4 | 55414095 | ||||||
chr4:55414104 | T | G | 2 | a0001c0002t0001g0207a0001c0002t0001g0210 | 2 | NA18949.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.433+2265T>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 2/5 | chr4 | 55414104 | ||||||
chr4:55414121 | C | A | 9 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0005g0269others(6): Show | 9 | HG01891.hp2 HG02486.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.433+2282C>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 2/5 | chr4 | 55414121 | ||||||
chr4:55414224 | T | C | 334 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0013others(331): Show | 350 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(347): Show |
intron_variant | MODIFIER | c.433+2385T>C | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 2/5 | chr4 | 55414224 | ||||||
chr4:55414296 | T | TA | 294 | a0001c0001t0001g0003a0001c0001t0001g0027a0001c0001t0001g0028others(291): Show | 308 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(305): Show |
intron_variant | MODIFIER | c.433+2457_433+2458i others(3): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 2/5 | chr4 | 55414296 | ||||||
chr4:55414306 | T | A | 1 | a0001c0001t0001g0265 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.433+2467T>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 2/5 | chr4 | 55414306 | ||||||
chr4:55414432 | A | T | 2 | a0001c0001t0002g0051a0001c0001t0002g0057 | 2 | HG02895.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.433+2593A>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 2/5 | chr4 | 55414432 | ||||||
chr4:55414504 | G | A | 1 | a0001c0001t0002g0019 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.434-2568G>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 2/5 | chr4 | 55414504 | ||||||
chr4:55414750 | A | G | 1 | a0001c0001t0002g0125 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.434-2322A>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 2/5 | chr4 | 55414750 | ||||||
chr4:55414991 | T | A | 1 | a0001c0002t0001g0170 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.434-2081T>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 2/5 | chr4 | 55414991 | ||||||
chr4:55415082 | T | C | 1 | a0001c0002t0001g0247 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.434-1990T>C | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 2/5 | chr4 | 55415082 | ||||||
chr4:55415153 | A | G | 105 | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(102): Show | 111 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.434-1919A>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 2/5 | chr4 | 55415153 | ||||||
chr4:55415172 | C | G | 2 | a0001c0002t0007g0179a0001c0002t0007g0180 | 2 | HG01256.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.434-1900C>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 2/5 | chr4 | 55415172 | ||||||
chr4:55415290 | T | G | 3 | a0001c0001t0003g0314a0001c0001t0003g0321a0001c0001t0003g0328 | 3 | NA18942.hp1 NA18981.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.434-1782T>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 2/5 | chr4 | 55415290 | ||||||
chr4:55415317 | G | A | 87 | a0001c0001t0001g0003a0001c0001t0001g0027a0001c0001t0001g0028others(84): Show | 92 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(89): Show |
intron_variant | MODIFIER | c.434-1755G>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 2/5 | chr4 | 55415317 | ||||||
chr4:55415398 | C | G | 1 | a0001c0001t0001g0362 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.434-1674C>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 2/5 | chr4 | 55415398 | ||||||
chr4:55415454 | C | G | 9 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0005g0269others(6): Show | 9 | HG01891.hp2 HG02486.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.434-1618C>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 2/5 | chr4 | 55415454 | ||||||
chr4:55415466 | C | T | 2 | a0001c0001t0001g0029a0001c0001t0001g0032 | 2 | HG01261.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.434-1606C>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 2/5 | chr4 | 55415466 | ||||||
chr4:55415468 | G | A | 1 | a0001c0001t0001g0362 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.434-1604G>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 2/5 | chr4 | 55415468 | ||||||
chr4:55415602 | C | T | 18 | a0001c0001t0001g0001a0001c0002t0001g0001a0001c0002t0001g0012others(15): Show | 20 | HG00099.hp1 HG00323.hp1 HG01069.hp2 others(17): Show |
intron_variant | MODIFIER | c.434-1470C>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 2/5 | chr4 | 55415602 | ||||||
chr4:55415847 | TTTTC | T | 7 | a0001c0001t0004g0185a0001c0001t0004g0276a0001c0001t0004g0277others(4): Show | 7 | HG01884.hp2 HG02451.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.434-1213_434-1210d others(6): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 55415847 | |||||
chr4:55415863 | T | C | 1 | a0001c0001t0002g0095 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.434-1209T>C | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 2/5 | chr4 | 55415863 | ||||||
chr4:55416135 | A | G | 3 | a0001c0001t0001g0265a0001c0001t0009g0022a0001c0001t0009g0023 | 3 | HG01884.hp1 HG02818.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.434-937A>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 2/5 | chr4 | 55416135 | ||||||
chr4:55416280 | A | G | 1 | a0001c0002t0007g0180 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.434-792A>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 2/5 | chr4 | 55416280 | ||||||
chr4:55416330 | G | A | 1 | a0001c0001t0001g0362 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.434-742G>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 2/5 | chr4 | 55416330 | ||||||
chr4:55416485 | T | G | 1 | a0003c0006t0015g0268 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.434-587T>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 2/5 | chr4 | 55416485 | ||||||
chr4:55416507 | T | A | 1 | a0001c0002t0001g0015 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.434-565T>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 2/5 | chr4 | 55416507 | ||||||
chr4:55416823 | AGGAAGAT others(15): Show |
A | 4 | a0001c0001t0002g0109a0001c0001t0002g0115a0001c0001t0002g0124others(1): Show | 4 | NA18747.hp2 NA18950.hp1 NA18962.hp2 others(1): Show |
intron_variant | MODIFIER | c.434-245_434-224del others(22): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr4 | 55416823 | |||||
chr4:55416918 | G | T | 7 | a0001c0001t0001g0011a0001c0001t0001g0145a0001c0001t0001g0146others(4): Show | 8 | HG02145.hp2 HG02257.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.434-154G>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 2/5 | chr4 | 55416918 | ||||||
chr4:55417534 | T | C | 1 | a0001c0001t0002g0063 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.610-269T>C | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 3/5 | chr4 | 55417534 | ||||||
chr4:55417584 | G | C | 1 | a0001c0002t0001g0208 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.610-219G>C | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 3/5 | chr4 | 55417584 | ||||||
chr4:55417739 | T | C | 2 | a0001c0001t0001g0183a0001c0001t0001g0184 | 2 | HG02559.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.610-64T>C | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 3/5 | chr4 | 55417739 | ||||||
chr4:55418436 | A | T | 1 | a0001c0001t0001g0145 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.792+451A>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55418436 | ||||||
chr4:55418462 | T | G | 1 | a0001c0001t0002g0019 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.792+477T>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55418462 | ||||||
chr4:55418464 | C | T | 222 | a0001c0001t0001g0003a0001c0001t0001g0027a0001c0001t0001g0028others(219): Show | 233 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.792+479C>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55418464 | ||||||
chr4:55418479 | G | A | 1 | a0001c0001t0003g0303 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.792+494G>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55418479 | ||||||
chr4:55418521 | GA | G | 6 | a0001c0001t0002g0142a0001c0001t0003g0266a0001c0001t0003g0267others(3): Show | 6 | HG01169.hp1 HG01891.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.792+550delA | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55418521 | |||||
chr4:55418608 | C | G | 1 | a0001c0001t0001g0362 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.792+623C>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55418608 | ||||||
chr4:55418683 | C | G | 1 | a0001c0001t0001g0156 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.792+698C>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55418683 | ||||||
chr4:55418768 | C | T | 1 | a0001c0001t0001g0151 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.792+783C>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55418768 | ||||||
chr4:55418891 | A | C | 1 | a0001c0001t0002g0285 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.792+906A>C | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55418891 | ||||||
chr4:55418915 | C | G | 62 | a0001c0001t0003g0002a0001c0001t0003g0017a0001c0001t0003g0018others(59): Show | 66 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(63): Show |
intron_variant | MODIFIER | c.792+930C>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55418915 | ||||||
chr4:55418999 | T | G | 297 | a0001c0001t0001g0003a0001c0001t0001g0027a0001c0001t0001g0028others(294): Show | 311 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(308): Show |
intron_variant | MODIFIER | c.792+1014T>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55418999 | ||||||
chr4:55419010 | A | G | 5 | a0001c0001t0001g0003a0001c0001t0001g0027a0001c0001t0001g0028others(2): Show | 6 | HG02055.hp1 HG02622.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.792+1025A>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55419010 | ||||||
chr4:55419059 | A | G | 2 | a0001c0001t0001g0029a0001c0001t0001g0032 | 2 | HG01261.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.792+1074A>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55419059 | ||||||
chr4:55419138 | C | T | 297 | a0001c0001t0001g0003a0001c0001t0001g0027a0001c0001t0001g0028others(294): Show | 311 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(308): Show |
intron_variant | MODIFIER | c.792+1153C>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55419138 | ||||||
chr4:55419239 | A | T | 1 | a0001c0001t0002g0114 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.792+1254A>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55419239 | ||||||
chr4:55419598 | A | G | 1 | a0001c0001t0001g0265 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.792+1613A>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55419598 | ||||||
chr4:55419710 | T | G | 13 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0001g0167others(10): Show | 13 | HG01243.hp2 HG01884.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.792+1725T>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55419710 | ||||||
chr4:55419723 | G | C | 2 | a0001c0002t0001g0202a0001c0002t0001g0214 | 2 | HG03453.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.792+1738G>C | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55419723 | ||||||
chr4:55419957 | G | A | 1 | a0001c0001t0002g0354 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.792+1972G>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55419957 | ||||||
chr4:55420021 | G | T | 124 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0006others(121): Show | 130 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.792+2036G>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55420021 | ||||||
chr4:55420062 | C | T | 1 | a0001c0002t0007g0259 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.792+2077C>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55420062 | ||||||
chr4:55420098 | G | GA | 44 | a0001c0001t0002g0052a0001c0001t0003g0002a0001c0001t0003g0018others(41): Show | 47 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(44): Show |
intron_variant | MODIFIER | c.792+2122dupA | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420098 | |||||
chr4:55420098 | G | GAAAAA | 14 | a0001c0001t0002g0004a0001c0001t0002g0117a0001c0001t0003g0017others(11): Show | 15 | HG01255.hp1 HG02615.hp2 NA18939.hp1 others(12): Show |
intron_variant | MODIFIER | c.792+2118_792+2122d others(7): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420098 | |||||
chr4:55420098 | G | GAAAAAAA others(1): Show |
14 | a0001c0001t0002g0005a0001c0001t0002g0009a0001c0001t0002g0035others(11): Show | 16 | HG01175.hp2 HG01346.hp1 HG01928.hp1 others(13): Show |
intron_variant | MODIFIER | c.792+2115_792+2122d others(10): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420098 | |||||
chr4:55420098 | G | GAAAAAAA others(2): Show |
8 | a0001c0001t0002g0007a0001c0001t0002g0033a0001c0001t0002g0042others(5): Show | 9 | HG02273.hp2 NA18955.hp2 NA18962.hp2 others(6): Show |
intron_variant | MODIFIER | c.792+2114_792+2122d others(11): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420098 | |||||
chr4:55420098 | G | GAAAAAAA others(4): Show |
7 | a0001c0001t0002g0063a0001c0001t0002g0066a0001c0001t0002g0067others(4): Show | 7 | HG00673.hp1 HG04204.hp2 NA18943.hp2 others(4): Show |
intron_variant | MODIFIER | c.792+2122_792+2123i others(13): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420098 | |||||
chr4:55420098 | G | GAAAAAAA others(6): Show |
2 | a0001c0001t0002g0065a0001c0001t0002g0133 | 2 | NA18971.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.792+2122_792+2123i others(15): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420098 | |||||
chr4:55420098 | G | GAAAAAAA others(11): Show |
1 | a0001c0001t0002g0059 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.792+2122_792+2123i others(20): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420098 | |||||
chr4:55420098 | GAA | G | 10 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0148others(7): Show | 10 | HG02145.hp2 HG02257.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.792+2121_792+2122d others(4): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420098 | |||||
chr4:55420106 | A | AAAAAAAA others(13): Show |
1 | a0001c0001t0002g0099 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.792+2122_792+2123i others(22): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420106 | |||||
chr4:55420106 | A | AAAAAAAA others(12): Show |
1 | a0001c0001t0002g0053 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.792+2122_792+2123i others(21): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420106 | |||||
chr4:55420106 | A | AAAAAAAA others(14): Show |
1 | a0001c0001t0002g0019 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.792+2122_792+2123i others(23): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420106 | |||||
chr4:55420106 | A | AAAAAAAA others(11): Show |
1 | a0001c0001t0002g0134 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.792+2122_792+2123i others(20): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420106 | |||||
chr4:55420106 | A | AAAAAAAA others(13): Show |
2 | a0001c0001t0002g0054a0001c0002t0001g0194 | 2 | HG00544.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.792+2122_792+2123i others(22): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420106 | |||||
chr4:55420106 | A | AAAAAAAA others(15): Show |
2 | a0001c0002t0001g0211a0001c0002t0001g0218 | 2 | HG01433.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.792+2122_792+2123i others(24): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420106 | |||||
chr4:55420106 | A | AAAAAAAA others(8): Show |
2 | a0001c0001t0002g0060a0001c0002t0001g0208 | 2 | HG03195.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.792+2122_792+2123i others(17): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420106 | |||||
chr4:55420106 | A | AAAAAAAA others(12): Show |
2 | a0001c0001t0002g0131a0001c0002t0001g0216 | 2 | HG00558.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.792+2122_792+2123i others(21): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420106 | |||||
chr4:55420106 | A | AAAAAAAA others(14): Show |
1 | a0001c0002t0001g0200 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.792+2122_792+2123i others(23): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420106 | |||||
chr4:55420106 | A | AAAAAAAA others(16): Show |
1 | a0001c0002t0001g0203 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.792+2122_792+2123i others(25): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420106 | |||||
chr4:55420106 | A | AAAAAAAA others(18): Show |
1 | a0001c0001t0002g0132 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.792+2122_792+2123i others(27): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420106 | |||||
chr4:55420106 | A | AAAAAAAA others(20): Show |
1 | a0001c0002t0001g0264 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.792+2122_792+2123i others(29): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420106 | |||||
chr4:55420106 | A | AAAAAAAA others(9): Show |
1 | a0001c0002t0001g0157 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.792+2122_792+2123i others(18): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420106 | |||||
chr4:55420106 | A | AAAAAAAA others(11): Show |
1 | a0001c0002t0001g0229 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.792+2122_792+2123i others(20): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420106 | |||||
chr4:55420106 | A | AAAAAAAA others(13): Show |
1 | a0001c0002t0001g0252 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.792+2122_792+2123i others(22): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420106 | |||||
chr4:55420106 | A | AAAAAAAA others(15): Show |
1 | a0001c0002t0001g0204 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.792+2122_792+2123i others(24): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420106 | |||||
chr4:55420106 | A | AAAAAAAA others(17): Show |
1 | a0001c0002t0001g0246 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.792+2122_792+2123i others(26): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420106 | |||||
chr4:55420106 | A | AAAAAAAA others(6): Show |
4 | a0001c0001t0002g0026a0001c0001t0002g0036a0001c0001t0002g0064others(1): Show | 4 | HG00738.hp2 HG02129.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.792+2122_792+2123i others(15): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420106 | |||||
chr4:55420106 | A | AAAAAAAA others(8): Show |
3 | a0001c0001t0002g0037a0001c0001t0002g0120a0001c0002t0001g0213 | 3 | HG03710.hp2 NA18986.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.792+2122_792+2123i others(17): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420106 | |||||
chr4:55420106 | A | AAAAAAAA others(10): Show |
3 | a0001c0001t0002g0123a0001c0002t0001g0220a0001c0002t0001g0247 | 3 | HG00609.hp2 HG02129.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.792+2122_792+2123i others(19): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420106 | |||||
chr4:55420106 | A | AAAAAAAA others(12): Show |
2 | a0001c0001t0002g0100a0001c0002t0001g0195 | 2 | HG02027.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.792+2122_792+2123i others(21): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420106 | |||||
chr4:55420106 | A | AAAAAAAA others(14): Show |
4 | a0001c0001t0002g0095a0001c0002t0001g0189a0001c0002t0001g0244others(1): Show | 4 | HG00544.hp1 NA18983.hp2 NA18995.hp2 others(1): Show |
intron_variant | MODIFIER | c.792+2122_792+2123i others(23): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420106 | |||||
chr4:55420106 | A | AAAAAAAA others(16): Show |
1 | a0001c0001t0014g0055 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.792+2122_792+2123i others(25): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420106 | |||||
chr4:55420106 | A | AAAAAAAA others(18): Show |
1 | a0001c0002t0001g0188 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.792+2122_792+2123i others(27): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420106 | |||||
chr4:55420106 | A | AAAAAAAA others(5): Show |
2 | a0001c0001t0002g0034a0001c0001t0002g0141 | 2 | HG01891.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.792+2122_792+2123i others(14): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420106 | |||||
chr4:55420106 | A | AAAAAAAA others(7): Show |
2 | a0001c0001t0002g0010a0001c0002t0001g0238 | 3 | HG00738.hp1 HG02132.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.792+2122_792+2123i others(16): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420106 | |||||
chr4:55420106 | A | AAAAAAAA others(9): Show |
2 | a0001c0001t0002g0135a0001c0002t0001g0190 | 2 | HG01952.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.792+2122_792+2123i others(18): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420106 | |||||
chr4:55420106 | A | AAAAAAAA others(11): Show |
4 | a0001c0002t0001g0016a0001c0002t0001g0209a0001c0002t0001g0239others(1): Show | 5 | HG00609.hp1 HG01243.hp1 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.792+2122_792+2123i others(20): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420106 | |||||
chr4:55420106 | A | AAAAAAAA others(13): Show |
2 | a0001c0002t0001g0249a0001c0002t0001g0260 | 2 | HG02602.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.792+2122_792+2123i others(22): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420106 | |||||
chr4:55420106 | A | AAAAAAAA others(15): Show |
2 | a0001c0002t0001g0212a0001c0002t0001g0254 | 2 | HG01123.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.792+2122_792+2123i others(24): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420106 | |||||
chr4:55420106 | A | AAAAAAAA others(17): Show |
1 | a0001c0002t0001g0015 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.792+2122_792+2123i others(26): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420106 | |||||
chr4:55420106 | A | AAAAAAAA others(19): Show |
1 | a0001c0003t0001g0255 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.792+2122_792+2123i others(28): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420106 | |||||
chr4:55420106 | A | AAAAAAAA others(4): Show |
9 | a0001c0001t0002g0074a0001c0001t0002g0075a0001c0001t0002g0078others(6): Show | 9 | HG00099.hp2 HG01070.hp1 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.792+2122_792+2123i others(13): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420106 | |||||
chr4:55420106 | A | AAAAAAAA others(6): Show |
12 | a0001c0001t0002g0082a0001c0001t0002g0084a0001c0001t0002g0092others(9): Show | 12 | HG00438.hp2 HG01081.hp1 HG01361.hp2 others(9): Show |
intron_variant | MODIFIER | c.792+2122_792+2123i others(15): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420106 | |||||
chr4:55420106 | A | AAAAAAAA others(8): Show |
4 | a0001c0001t0002g0098a0001c0001t0002g0140a0001c0002t0001g0191others(1): Show | 4 | HG00438.hp1 NA18947.hp1 NA18954.hp1 others(1): Show |
intron_variant | MODIFIER | c.792+2122_792+2123i others(17): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420106 | |||||
chr4:55420106 | A | AAAAAAAA others(10): Show |
6 | a0001c0001t0002g0086a0001c0002t0001g0014a0001c0002t0001g0192others(3): Show | 7 | HG00621.hp2 HG02015.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.792+2122_792+2123i others(19): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420106 | |||||
chr4:55420106 | A | AAAAAAAA others(12): Show |
7 | a0001c0001t0002g0050a0001c0002t0001g0196a0001c0002t0001g0202others(4): Show | 7 | HG02109.hp2 HG03453.hp2 HG03490.hp2 others(4): Show |
intron_variant | MODIFIER | c.792+2122_792+2123i others(21): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420106 | |||||
chr4:55420106 | A | AAAAAAAA others(14): Show |
2 | a0001c0002t0001g0210a0001c0002t0001g0224 | 2 | NA18949.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.792+2122_792+2123i others(23): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420106 | |||||
chr4:55420106 | A | AAAAAAAA others(18): Show |
1 | a0001c0002t0001g0222 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.792+2122_792+2123i others(27): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420106 | |||||
chr4:55420106 | A | AAAAAAAA others(3): Show |
5 | a0001c0001t0002g0008a0001c0001t0002g0106a0001c0001t0002g0111others(2): Show | 6 | HG00280.hp2 HG01358.hp2 HG01496.hp2 others(3): Show |
intron_variant | MODIFIER | c.792+2122_792+2123i others(12): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420106 | |||||
chr4:55420106 | A | AAAAAAAA others(5): Show |
1 | a0001c0001t0002g0087 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.792+2122_792+2123i others(14): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420106 | |||||
chr4:55420106 | A | AAAAAAAA others(7): Show |
2 | a0001c0001t0002g0057a0001c0001t0002g0073 | 2 | HG01257.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.792+2122_792+2123i others(16): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420106 | |||||
chr4:55420106 | A | AAAAAAAA others(9): Show |
1 | a0001c0002t0001g0250 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.792+2122_792+2123i others(18): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420106 | |||||
chr4:55420106 | A | AAAAAAAA others(11): Show |
3 | a0001c0001t0002g0051a0001c0002t0001g0205a0001c0002t0001g0225 | 3 | HG02895.hp2 NA18961.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.792+2122_792+2123i others(20): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420106 | |||||
chr4:55420106 | A | AAAAAAAA others(15): Show |
1 | a0001c0002t0001g0261 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.792+2122_792+2123i others(24): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420106 | |||||
chr4:55420106 | A | AAAAAAAA others(4): Show |
9 | a0001c0001t0002g0056a0001c0001t0002g0058a0001c0001t0002g0062others(6): Show | 9 | HG00280.hp1 HG00621.hp1 HG01256.hp2 others(6): Show |
intron_variant | MODIFIER | c.792+2122_792+2123i others(13): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420106 | |||||
chr4:55420106 | A | AAAAAAAA others(6): Show |
4 | a0001c0001t0002g0006a0001c0001t0002g0089a0001c0002t0001g0158others(1): Show | 5 | HG02083.hp2 HG03490.hp1 HG03492.hp2 others(2): Show |
intron_variant | MODIFIER | c.792+2122_792+2123i others(15): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420106 | |||||
chr4:55420106 | A | AAAAAAAA others(8): Show |
1 | a0001c0001t0002g0040 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.792+2122_792+2123i others(17): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420106 | |||||
chr4:55420106 | A | AAAAAAAA others(10): Show |
6 | a0001c0001t0002g0039a0001c0001t0013g0144a0001c0002t0001g0223others(3): Show | 6 | HG04184.hp2 NA18959.hp1 NA18984.hp1 others(3): Show |
intron_variant | MODIFIER | c.792+2122_792+2123i others(19): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420106 | |||||
chr4:55420106 | A | AAAAAAAA others(12): Show |
3 | a0001c0001t0002g0076a0001c0002t0001g0236a0001c0002t0001g0240 | 3 | HG02074.hp2 HG02717.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.792+2122_792+2123i others(21): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420106 | |||||
chr4:55420106 | A | AAAAAAAA others(14): Show |
3 | a0001c0001t0003g0332a0001c0002t0001g0242a0001c0002t0001g0263 | 3 | HG00642.hp1 HG03710.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.792+2122_792+2123i others(23): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420106 | |||||
chr4:55420106 | A | AAAAAAAA others(16): Show |
2 | a0001c0002t0001g0221a0001c0002t0001g0232 | 2 | HG02027.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.792+2122_792+2123i others(25): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420106 | |||||
chr4:55420106 | A | AAAAAAAA others(22): Show |
1 | a0001c0002t0001g0206 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.792+2122_792+2123i others(31): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420106 | |||||
chr4:55420106 | A | AAAAAAAA others(3): Show |
2 | a0001c0001t0002g0061a0001c0001t0002g0109 | 2 | NA19068.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.792+2122_792+2123i others(12): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420106 | |||||
chr4:55420106 | A | AAAAAAAA others(13): Show |
1 | a0001c0002t0001g0248 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.792+2122_792+2123i others(22): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420106 | |||||
chr4:55420106 | A | AAAAAAAA others(17): Show |
1 | a0001c0001t0002g0138 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.792+2122_792+2123i others(26): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420106 | |||||
chr4:55420106 | A | AAAAAAAT others(4): Show |
2 | a0001c0001t0002g0090a0001c0001t0002g0102 | 2 | NA18943.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.792+2122_792+2123i others(13): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420106 | |||||
chr4:55420106 | A | AAAAAAAT others(8): Show |
1 | a0001c0002t0001g0199 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.792+2122_792+2123i others(17): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420106 | |||||
chr4:55420106 | A | AAAAAAAT others(14): Show |
1 | a0001c0001t0002g0136 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.792+2122_792+2123i others(23): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420106 | |||||
chr4:55420106 | A | AAAAAATA others(11): Show |
1 | a0001c0001t0002g0139 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.792+2122_792+2123i others(20): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420106 | |||||
chr4:55420106 | A | AAATATAT others(12): Show |
1 | a0001c0001t0003g0320 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.792+2122_792+2123i others(21): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420106 | |||||
chr4:55420106 | A | T | 2 | a0001c0001t0001g0145a0001c0001t0001g0149 | 2 | HG02258.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.792+2121A>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55420106 | ||||||
chr4:55420107 | AT | A | 33 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0031others(30): Show | 34 | HG01070.hp2 HG01167.hp1 HG01168.hp2 others(31): Show |
intron_variant | MODIFIER | c.792+2123delT | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55420107 | ||||||
chr4:55420107 | ATAT | A | 5 | a0001c0001t0003g0266a0001c0001t0003g0267a0001c0001t0003g0310others(2): Show | 5 | HG02145.hp1 HG02280.hp2 HG03688.hp1 others(2): Show |
intron_variant | MODIFIER | c.792+2123_792+2125d others(5): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55420107 | ||||||
chr4:55420108 | T | A | 84 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(81): Show | 87 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(84): Show |
intron_variant | MODIFIER | c.792+2123T>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55420108 | ||||||
chr4:55420110 | T | A | 94 | a0001c0001t0001g0003a0001c0001t0001g0027a0001c0001t0001g0029others(91): Show | 98 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.792+2125T>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55420110 | ||||||
chr4:55420112 | T | A | 52 | a0001c0001t0001g0003a0001c0001t0001g0027a0001c0001t0001g0030others(49): Show | 56 | HG01069.hp1 HG01070.hp2 HG01074.hp1 others(53): Show |
intron_variant | MODIFIER | c.792+2127T>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55420112 | ||||||
chr4:55420114 | T | A | 16 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0002g0038others(13): Show | 16 | HG01255.hp2 HG02055.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.792+2129T>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55420114 | ||||||
chr4:55420116 | T | A | 3 | a0001c0001t0002g0038a0001c0001t0002g0052a0001c0002t0001g0257 | 3 | HG03041.hp1 HG03927.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.792+2131T>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55420116 | ||||||
chr4:55420118 | T | A | 1 | a0001c0002t0001g0257 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.792+2133T>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55420118 | ||||||
chr4:55420119 | A | T | 1 | a0001c0001t0001g0155 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.792+2134A>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55420119 | ||||||
chr4:55420120 | TAC | T | 3 | a0001c0001t0001g0011a0001c0001t0003g0350a0001c0001t0006g0163 | 4 | HG01123.hp2 HG03225.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.792+2137_792+2138d others(4): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420120 | |||||
chr4:55420122 | C | T | 323 | a0001c0001t0001g0003a0001c0001t0001g0013a0001c0001t0001g0027others(320): Show | 338 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(335): Show |
intron_variant | MODIFIER | c.792+2137C>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55420122 | ||||||
chr4:55420123 | A | T | 10 | a0001c0001t0001g0145a0001c0001t0001g0149a0001c0001t0001g0150others(7): Show | 10 | HG02257.hp2 HG02258.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.792+2138A>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55420123 | ||||||
chr4:55420127 | A | T | 22 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0145others(19): Show | 24 | HG01243.hp2 HG02145.hp2 HG02257.hp2 others(21): Show |
intron_variant | MODIFIER | c.792+2142A>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55420127 | ||||||
chr4:55420131 | T | A | 286 | a0001c0001t0001g0003a0001c0001t0001g0027a0001c0001t0001g0028others(283): Show | 300 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(297): Show |
intron_variant | MODIFIER | c.792+2146T>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55420131 | ||||||
chr4:55420134 | TTTATTTA others(4): Show |
T | 1 | a0001c0001t0002g0038 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.792+2152_792+2162d others(13): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420134 | |||||
chr4:55420135 | T | A | 282 | a0001c0001t0001g0003a0001c0001t0001g0027a0001c0001t0001g0028others(279): Show | 296 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(293): Show |
intron_variant | MODIFIER | c.792+2150T>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55420135 | ||||||
chr4:55420139 | T | A | 209 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(206): Show | 218 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(215): Show |
intron_variant | MODIFIER | c.792+2154T>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55420139 | ||||||
chr4:55420141 | ATTTAT | A | 9 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0001g0167others(6): Show | 9 | HG01884.hp1 HG02109.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.792+2164_792+2168d others(7): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420141 | |||||
chr4:55420142 | TTTA | T | 6 | a0001c0001t0003g0292a0001c0001t0003g0293a0001c0001t0003g0294others(3): Show | 6 | HG01168.hp2 HG03491.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.792+2160_792+2162d others(5): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420142 | |||||
chr4:55420143 | T | A | 122 | a0001c0001t0001g0029a0001c0001t0001g0032a0001c0001t0002g0004others(119): Show | 127 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.792+2158T>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55420143 | ||||||
chr4:55420145 | AT | A | 219 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0013others(216): Show | 232 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(229): Show |
intron_variant | MODIFIER | c.792+2164delT | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420145 | |||||
chr4:55420146 | T | A | 8 | a0001c0001t0002g0038a0001c0001t0002g0137a0001c0001t0003g0292others(5): Show | 8 | HG01168.hp2 HG02148.hp2 HG03491.hp2 others(5): Show |
intron_variant | MODIFIER | c.792+2161T>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55420146 | ||||||
chr4:55420146 | T | TA | 96 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0010others(93): Show | 99 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(96): Show |
intron_variant | MODIFIER | c.792+2161_792+2162i others(3): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55420146 | ||||||
chr4:55420146 | T | TTTA | 7 | a0001c0001t0001g0312a0001c0001t0001g0341a0001c0001t0001g0342others(4): Show | 7 | HG02559.hp1 HG02895.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.792+2163_792+2164i others(5): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420146 | |||||
chr4:55420146 | T | TTTATTTA others(4): Show |
3 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0005g0269 | 3 | HG02647.hp2 HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.792+2163_792+2164i others(13): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55420146 | |||||
chr4:55420148 | T | A | 7 | a0001c0001t0002g0064a0001c0001t0002g0066a0001c0001t0002g0069others(4): Show | 7 | HG00621.hp1 HG04204.hp2 NA18747.hp2 others(4): Show |
intron_variant | MODIFIER | c.792+2163T>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55420148 | ||||||
chr4:55420172 | C | T | 1 | a0001c0001t0005g0271 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.792+2187C>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55420172 | ||||||
chr4:55420215 | T | C | 1 | a0001c0001t0002g0052 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.792+2230T>C | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55420215 | ||||||
chr4:55420258 | G | T | 11 | a0001c0001t0001g0029a0001c0001t0001g0032a0001c0001t0001g0183others(8): Show | 11 | HG01261.hp1 HG01891.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.792+2273G>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55420258 | ||||||
chr4:55420306 | C | T | 1 | a0001c0002t0001g0214 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.792+2321C>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55420306 | ||||||
chr4:55420329 | ATAGACTC others(25): Show |
A | 1 | a0001c0002t0010g0228 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.792+2345_792+2376d others(34): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55420329 | ||||||
chr4:55420394 | T | G | 2 | a0001c0002t0001g0020a0001c0002t0001g0021 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.792+2409T>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55420394 | ||||||
chr4:55420446 | A | T | 297 | a0001c0001t0001g0003a0001c0001t0001g0027a0001c0001t0001g0028others(294): Show | 311 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(308): Show |
intron_variant | MODIFIER | c.792+2461A>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55420446 | ||||||
chr4:55420533 | A | G | 2 | a0001c0001t0003g0307a0001c0001t0003g0338 | 2 | HG00642.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.792+2548A>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55420533 | ||||||
chr4:55420550 | T | C | 344 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0013others(341): Show | 360 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(357): Show |
intron_variant | MODIFIER | c.792+2565T>C | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55420550 | ||||||
chr4:55420568 | A | G | 11 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0001g0167others(8): Show | 11 | HG01243.hp2 HG02109.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.792+2583A>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55420568 | ||||||
chr4:55420701 | A | G | 1 | a0001c0001t0002g0111 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.792+2716A>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55420701 | ||||||
chr4:55420769 | C | T | 9 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0001g0187others(6): Show | 9 | HG01891.hp2 HG02280.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.792+2784C>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55420769 | ||||||
chr4:55420911 | A | T | 9 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0001g0187others(6): Show | 9 | HG01891.hp2 HG02280.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.792+2926A>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55420911 | ||||||
chr4:55421145 | C | T | 16 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0145others(13): Show | 18 | HG02145.hp2 HG02257.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.792+3160C>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55421145 | ||||||
chr4:55421166 | C | CA | 21 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0145others(18): Show | 21 | HG00642.hp2 HG01175.hp1 HG01981.hp1 others(18): Show |
intron_variant | MODIFIER | c.792+3203dupA | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55421166 | |||||
chr4:55421166 | C | CAA | 5 | a0001c0001t0001g0001a0001c0001t0001g0265a0001c0001t0003g0314others(2): Show | 6 | HG00673.hp2 HG01099.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.792+3202_792+3203d others(4): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55421166 | |||||
chr4:55421166 | CA | C | 27 | a0001c0001t0001g0003a0001c0001t0001g0027a0001c0001t0001g0028others(24): Show | 28 | HG01123.hp2 HG01167.hp1 HG01168.hp2 others(25): Show |
intron_variant | MODIFIER | c.792+3203delA | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55421166 | |||||
chr4:55421166 | CAAAAA | C | 195 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0006others(192): Show | 204 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(201): Show |
intron_variant | MODIFIER | c.792+3199_792+3203d others(7): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55421166 | |||||
chr4:55421284 | A | G | 4 | a0001c0002t0001g0195a0001c0002t0001g0196a0001c0002t0001g0197others(1): Show | 4 | HG02027.hp1 NA19062.hp2 NA19084.hp1 others(1): Show |
intron_variant | MODIFIER | c.793-3254A>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55421284 | ||||||
chr4:55421297 | C | CT | 36 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0032others(33): Show | 37 | HG00140.hp2 HG00621.hp2 HG00673.hp2 others(34): Show |
intron_variant | MODIFIER | c.793-3220dupT | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55421297 | |||||
chr4:55421297 | C | CTT | 15 | a0001c0001t0003g0017a0001c0001t0003g0286a0001c0001t0003g0299others(12): Show | 16 | NA18612.hp1 NA18939.hp1 NA18959.hp2 others(13): Show |
intron_variant | MODIFIER | c.793-3221_793-3220d others(4): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55421297 | |||||
chr4:55421297 | CT | C | 36 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0024others(33): Show | 38 | HG01070.hp2 HG01099.hp1 HG01884.hp2 others(35): Show |
intron_variant | MODIFIER | c.793-3220delT | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55421297 | |||||
chr4:55421297 | CTT | C | 11 | a0001c0001t0001g0165a0001c0001t0001g0167a0001c0001t0001g0168others(8): Show | 11 | HG01243.hp2 HG01884.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.793-3221_793-3220d others(4): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55421297 | |||||
chr4:55421300 | T | C | 4 | a0001c0002t0001g0202a0001c0002t0001g0214a0001c0002t0001g0215others(1): Show | 4 | HG02965.hp2 HG03209.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.793-3238T>C | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55421300 | ||||||
chr4:55421301 | T | C | 1 | a0001c0002t0001g0198 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.793-3237T>C | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55421301 | ||||||
chr4:55421391 | C | T | 1 | a0001c0001t0003g0348 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.793-3147C>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55421391 | ||||||
chr4:55421522 | T | A | 1 | a0001c0001t0001g0355 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.793-3016T>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55421522 | ||||||
chr4:55421709 | C | T | 1 | a0001c0001t0001g0145 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.793-2829C>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55421709 | ||||||
chr4:55421876 | A | G | 1 | a0001c0001t0012g0284 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.793-2662A>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55421876 | ||||||
chr4:55421915 | GA | G | 351 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0011others(348): Show | 369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.793-2612delA | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55421915 | |||||
chr4:55421958 | A | C | 217 | a0001c0001t0001g0003a0001c0001t0001g0027a0001c0001t0001g0028others(214): Show | 228 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(225): Show |
intron_variant | MODIFIER | c.793-2580A>C | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55421958 | ||||||
chr4:55422317 | G | A | 5 | a0001c0002t0001g0222a0001c0002t0001g0225a0001c0002t0001g0234others(2): Show | 5 | NA18954.hp1 NA18959.hp1 NA18961.hp2 others(2): Show |
intron_variant | MODIFIER | c.793-2221G>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55422317 | ||||||
chr4:55422361 | G | A | 1 | a0001c0001t0001g0265 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.793-2177G>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55422361 | ||||||
chr4:55422363 | T | G | 1 | a0001c0001t0002g0102 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.793-2175T>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55422363 | ||||||
chr4:55422510 | G | A | 2 | a0001c0001t0001g0029a0001c0001t0001g0032 | 2 | HG01261.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.793-2028G>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55422510 | ||||||
chr4:55422576 | C | G | 77 | a0001c0001t0003g0002a0001c0001t0003g0017a0001c0001t0003g0018others(74): Show | 81 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(78): Show |
intron_variant | MODIFIER | c.793-1962C>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55422576 | ||||||
chr4:55422656 | A | AT | 13 | a0001c0001t0001g0011a0001c0001t0001g0145a0001c0001t0001g0146others(10): Show | 14 | HG01243.hp2 HG02145.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.793-1872dupT | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55422656 | |||||
chr4:55422656 | A | T | 1 | a0001c0001t0001g0265 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.793-1882A>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55422656 | ||||||
chr4:55422660 | T | A | 2 | a0001c0001t0009g0022a0001c0001t0009g0023 | 2 | HG01884.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.793-1878T>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55422660 | ||||||
chr4:55422915 | C | T | 7 | a0001c0002t0001g0195a0001c0002t0001g0196a0001c0002t0001g0197others(4): Show | 7 | HG02027.hp1 HG02132.hp1 NA18949.hp2 others(4): Show |
intron_variant | MODIFIER | c.793-1623C>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55422915 | ||||||
chr4:55423200 | G | T | 2 | a0001c0001t0004g0159a0001c0001t0004g0186 | 2 | HG03139.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.793-1338G>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55423200 | ||||||
chr4:55423212 | C | A | 326 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0013others(323): Show | 342 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(339): Show |
intron_variant | MODIFIER | c.793-1326C>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55423212 | ||||||
chr4:55423233 | C | G | 9 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0001g0187others(6): Show | 9 | HG01891.hp2 HG02280.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.793-1305C>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55423233 | ||||||
chr4:55423339 | G | A | 22 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0001g0167others(19): Show | 22 | HG01243.hp2 HG01884.hp1 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.793-1199G>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55423339 | ||||||
chr4:55423344 | G | A | 1 | a0001c0001t0002g0038 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.793-1194G>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55423344 | ||||||
chr4:55423425 | T | TAAAG | 8 | a0001c0001t0001g0013a0001c0001t0001g0149a0001c0001t0001g0150others(5): Show | 9 | HG02572.hp1 HG02818.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.793-1113_793-1112i others(6): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55423425 | ||||||
chr4:55423426 | C | T | 8 | a0001c0001t0001g0013a0001c0001t0001g0149a0001c0001t0001g0150others(5): Show | 9 | HG02572.hp1 HG02818.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.793-1112C>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55423426 | ||||||
chr4:55423569 | C | T | 4 | a0001c0001t0003g0018a0001c0001t0003g0290a0001c0001t0003g0327others(1): Show | 5 | HG00140.hp2 HG01069.hp1 HG01074.hp1 others(2): Show |
intron_variant | MODIFIER | c.793-969C>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55423569 | ||||||
chr4:55423611 | C | T | 206 | a0001c0001t0001g0029a0001c0001t0001g0032a0001c0001t0002g0004others(203): Show | 215 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(212): Show |
intron_variant | MODIFIER | c.793-927C>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55423611 | ||||||
chr4:55423612 | A | G | 304 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0013others(301): Show | 320 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(317): Show |
intron_variant | MODIFIER | c.793-926A>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55423612 | ||||||
chr4:55423618 | T | C | 204 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0006others(201): Show | 213 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(210): Show |
intron_variant | MODIFIER | c.793-920T>C | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55423618 | ||||||
chr4:55423619 | C | T | 1 | a0001c0002t0001g0257 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.793-919C>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55423619 | ||||||
chr4:55423662 | A | G | 2 | a0001c0001t0009g0022a0001c0001t0009g0023 | 2 | HG01884.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.793-876A>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55423662 | ||||||
chr4:55423832 | A | G | 326 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0013others(323): Show | 342 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(339): Show |
intron_variant | MODIFIER | c.793-706A>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55423832 | ||||||
chr4:55423885 | CTGGT | C | 14 | a0001c0001t0002g0086a0001c0001t0002g0090a0001c0001t0002g0094others(11): Show | 14 | HG00438.hp1 HG00544.hp1 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.793-650_793-647del others(4): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr4 | 55423885 | |||||
chr4:55423890 | T | A | 14 | a0001c0001t0002g0086a0001c0001t0002g0090a0001c0001t0002g0094others(11): Show | 14 | HG00438.hp1 HG00544.hp1 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.793-648T>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55423890 | ||||||
chr4:55424053 | A | G | 326 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0013others(323): Show | 342 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(339): Show |
intron_variant | MODIFIER | c.793-485A>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55424053 | ||||||
chr4:55424134 | G | T | 2 | a0001c0001t0002g0004a0001c0005t0002g0004 | 2 | HG01255.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.793-404G>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55424134 | ||||||
chr4:55424270 | T | C | 206 | a0001c0001t0001g0029a0001c0001t0001g0032a0001c0001t0002g0004others(203): Show | 215 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(212): Show |
intron_variant | MODIFIER | c.793-268T>C | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55424270 | ||||||
chr4:55424329 | C | T | 206 | a0001c0001t0001g0029a0001c0001t0001g0032a0001c0001t0002g0004others(203): Show | 215 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(212): Show |
intron_variant | MODIFIER | c.793-209C>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55424329 | ||||||
chr4:55424391 | C | T | 206 | a0001c0001t0001g0029a0001c0001t0001g0032a0001c0001t0002g0004others(203): Show | 215 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(212): Show |
intron_variant | MODIFIER | c.793-147C>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55424391 | ||||||
chr4:55424406 | T | C | 204 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0006others(201): Show | 213 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(210): Show |
intron_variant | MODIFIER | c.793-132T>C | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55424406 | ||||||
chr4:55424463 | C | T | 3 | a0001c0001t0003g0291a0001c0001t0003g0292a0001c0001t0003g0297 | 3 | HG03491.hp2 HG03942.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.793-75C>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 4/5 | chr4 | 55424463 | ||||||
chr4:55424773 | T | TAATA | 206 | a0001c0001t0001g0029a0001c0001t0001g0032a0001c0001t0002g0004others(203): Show | 215 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(212): Show |
intron_variant | MODIFIER | c.898+131_898+132ins others(4): Show |
TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr4 | 55424773 | |||||
chr4:55424948 | A | G | 1 | a0001c0001t0003g0311 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.898+305A>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 5/5 | chr4 | 55424948 | ||||||
chr4:55424957 | A | G | 9 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0001g0187others(6): Show | 9 | HG01891.hp2 HG02280.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.898+314A>G | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 5/5 | chr4 | 55424957 | ||||||
chr4:55424989 | G | A | 2 | a0001c0001t0002g0104a0001c0001t0002g0105 | 2 | NA18948.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.898+346G>A | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 5/5 | chr4 | 55424989 | ||||||
chr4:55425281 | G | T | 1 | a0001c0001t0002g0037 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.899-95G>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 5/5 | chr4 | 55425281 | ||||||
chr4:55425312 | C | T | 126 | a0001c0001t0001g0029a0001c0001t0001g0032a0001c0001t0002g0004others(123): Show | 132 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.899-64C>T | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 5/5 | chr4 | 55425312 | ||||||
chr4:55425361 | T | C | 126 | a0001c0001t0001g0029a0001c0001t0001g0032a0001c0001t0002g0004others(123): Show | 132 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.899-15T>C | TMEM165 | ENSG00000134851.13 | transcript | ENST00000381334.10 | protein_coding | 5/5 | chr4 | 55425361 |