geneid | 90390 |
---|---|
ensemblid | ENSG00000164758.7 |
hgncid | 23032 |
symbol | MED30 |
name | mediator complex subunit 30 |
refseq_nuc | NM_080651.4 |
refseq_prot | NP_542382.1 |
ensembl_nuc | ENST00000297347.7 |
ensembl_prot | ENSP00000297347.3 |
mane_status | MANE Select |
chr | chr8 |
start | 117520713 |
end | 117540262 |
strand | + |
ver | v1.2 |
region | chr8:117520713-117540262 |
region5000 | chr8:117515713-117545262 |
regionname0 | MED30_chr8_117520713_117540262 |
regionname5000 | MED30_chr8_117515713_117545262 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 178 | 342 | 80 | 72 | 146 | 14 | 28 | 116 | MED30_chr8_117515713_117545262 | MED30 | copy fasta | chr8 | 117515713 | 117545262 |
a0002 | 0/0 | 178 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | copy fasta | chr8 | 117515713 | 117545262 |
a0003 | 0/0 | 178 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | copy fasta | chr8 | 117515713 | 117545262 |
a0004 | 0/0 | 178 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | copy fasta | chr8 | 117515713 | 117545262 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 537 | 341 | 80 | 71 | 146 | 14 | 28 | MED30_chr8_117515713_117545262 | MED30 | copy fasta | chr8 | 117515713 | 117545262 |
c0002 | 0/0 | 537 | 3 | 3 | 0 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | copy fasta | chr8 | 117515713 | 117545262 |
c0003 | 0/0 | 537 | 2 | 2 | 0 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | copy fasta | chr8 | 117515713 | 117545262 |
c0004 | 0/0 | 537 | 1 | 1 | 0 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | copy fasta | chr8 | 117515713 | 117545262 |
c0005 | 0/0 | 537 | 1 | 0 | 1 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | copy fasta | chr8 | 117515713 | 117545262 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/0 | 449 | 160 | 26 | 32 | 82 | 4 | 15 | MED30_chr8_117515713_117545262 | MED30 | copy fasta | chr8 | 117515713 | 117545262 |
t0002 | 0/1 | 449 | 85 | 27 | 13 | 33 | 2 | 9 | MED30_chr8_117515713_117545262 | MED30 | copy fasta | chr8 | 117515713 | 117545262 |
t0003 | 0/0 | 448 | 43 | 5 | 9 | 22 | 3 | 4 | MED30_chr8_117515713_117545262 | MED30 | copy fasta | chr8 | 117515713 | 117545262 |
t0004 | 0/0 | 448 | 39 | 11 | 16 | 7 | 5 | 0 | MED30_chr8_117515713_117545262 | MED30 | copy fasta | chr8 | 117515713 | 117545262 |
t0005 | 0/0 | 449 | 14 | 12 | 2 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | copy fasta | chr8 | 117515713 | 117545262 |
t0006 | 0/0 | 453 | 4 | 4 | 0 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | copy fasta | chr8 | 117515713 | 117545262 |
t0007 | 0/0 | 449 | 1 | 0 | 0 | 1 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | copy fasta | chr8 | 117515713 | 117545262 |
t0008 | 0/0 | 449 | 1 | 0 | 0 | 1 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | copy fasta | chr8 | 117515713 | 117545262 |
t0009 | 0/0 | 449 | 1 | 1 | 0 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | copy fasta | chr8 | 117515713 | 117545262 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 1/0 | 66 | 11 | 14 | 33 | 3 | 4 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0002 | 0/0 | 30 | 4 | 6 | 15 | 1 | 4 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0003 | 0/0 | 22 | 4 | 4 | 12 | 0 | 2 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0004 | 0/0 | 14 | 2 | 6 | 5 | 1 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0005 | 0/0 | 13 | 0 | 1 | 12 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0006 | 0/1 | 6 | 1 | 0 | 3 | 0 | 1 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0007 | 0/0 | 6 | 0 | 4 | 0 | 1 | 1 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0008 | 0/0 | 6 | 0 | 1 | 4 | 0 | 1 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0009 | 0/0 | 5 | 0 | 2 | 1 | 0 | 2 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0010 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0011 | 0/0 | 4 | 0 | 1 | 0 | 1 | 2 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0012 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0013 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0014 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0021 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0022 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0027 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0032 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0038 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 537 | 341 | 80 | 71 | 146 | 14 | 28 | MED30_chr8_117515713_117545262 | MED30 | copy fasta | chr8 | 117515713 | 117545262 |
a0001c0005 | 0/0 | 537 | 1 | 0 | 1 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | copy fasta | chr8 | 117515713 | 117545262 |
a0002c0002 | 0/0 | 537 | 3 | 3 | 0 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | copy fasta | chr8 | 117515713 | 117545262 |
a0003c0003 | 0/0 | 537 | 2 | 2 | 0 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | copy fasta | chr8 | 117515713 | 117545262 |
a0004c0004 | 0/0 | 537 | 1 | 1 | 0 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | copy fasta | chr8 | 117515713 | 117545262 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 985 | 159 | 26 | 31 | 82 | 4 | 15 | MED30_chr8_117515713_117545262 | MED30 | copy fasta | chr8 | 117515713 | 117545262 |
a0001c0001t0002 | 0/1 | 985 | 80 | 22 | 13 | 33 | 2 | 9 | MED30_chr8_117515713_117545262 | MED30 | copy fasta | chr8 | 117515713 | 117545262 |
a0001c0001t0003 | 0/0 | 984 | 42 | 4 | 9 | 22 | 3 | 4 | MED30_chr8_117515713_117545262 | MED30 | copy fasta | chr8 | 117515713 | 117545262 |
a0001c0001t0004 | 0/0 | 984 | 39 | 11 | 16 | 7 | 5 | 0 | MED30_chr8_117515713_117545262 | MED30 | copy fasta | chr8 | 117515713 | 117545262 |
a0001c0001t0005 | 0/0 | 985 | 14 | 12 | 2 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | copy fasta | chr8 | 117515713 | 117545262 |
a0001c0001t0006 | 0/0 | 989 | 4 | 4 | 0 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | copy fasta | chr8 | 117515713 | 117545262 |
a0001c0001t0007 | 0/0 | 985 | 1 | 0 | 0 | 1 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | copy fasta | chr8 | 117515713 | 117545262 |
a0001c0001t0008 | 0/0 | 985 | 1 | 0 | 0 | 1 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | copy fasta | chr8 | 117515713 | 117545262 |
a0001c0001t0009 | 0/0 | 985 | 1 | 1 | 0 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | copy fasta | chr8 | 117515713 | 117545262 |
a0001c0005t0001 | 0/0 | 985 | 1 | 0 | 1 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | copy fasta | chr8 | 117515713 | 117545262 |
a0002c0002t0002 | 0/0 | 985 | 3 | 3 | 0 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | copy fasta | chr8 | 117515713 | 117545262 |
a0003c0003t0002 | 0/0 | 985 | 2 | 2 | 0 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | copy fasta | chr8 | 117515713 | 117545262 |
a0004c0004t0003 | 0/0 | 984 | 1 | 1 | 0 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | copy fasta | chr8 | 117515713 | 117545262 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 1/0 | 63 | 10 | 13 | 32 | 3 | 4 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0001g0003 | 0/0 | 21 | 4 | 4 | 11 | 0 | 2 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0001g0008 | 0/0 | 6 | 0 | 1 | 4 | 0 | 1 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0001g0009 | 0/0 | 5 | 0 | 2 | 1 | 0 | 2 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0001g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0002g0002 | 0/0 | 27 | 2 | 5 | 15 | 1 | 4 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0002g0006 | 0/1 | 6 | 1 | 0 | 3 | 0 | 1 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0002g0012 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0002g0014 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0002g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0002g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0002g0022 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0002g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0002g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0002g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0002g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0002g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0002g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0003g0005 | 0/0 | 13 | 0 | 1 | 12 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0003g0007 | 0/0 | 6 | 0 | 4 | 0 | 1 | 1 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0003g0011 | 0/0 | 4 | 0 | 1 | 0 | 1 | 2 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0003g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0003g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0003g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0003g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0003g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0003g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0003g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0003g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0003g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0003g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0003g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0003g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0004g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0004g0004 | 0/0 | 14 | 2 | 6 | 5 | 1 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0004g0013 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0004g0021 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0004g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0004g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0004g0038 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0004g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0004g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0004g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0004g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0004g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0004g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0004g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0004g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0004g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0004g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0004g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0005g0010 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0005g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0005g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0005g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0005g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0005g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0005g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0006g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0006g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0007g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0008g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0001t0009g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0001c0005t0001g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0002c0002t0002g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0003c0003t0002g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
a0004c0004t0003g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0003 | g0011 | EUR | GBR | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG00140 | hp1 | a0001 | c0001 | t0004 | g0038 | EUR | GBR | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG00140 | hp2 | a0001 | c0001 | t0003 | g0007 | EUR | GBR | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG00280 | hp1 | a0001 | c0001 | t0002 | g0002 | EUR | FIN | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG00323 | hp1 | a0001 | c0001 | t0003 | g0060 | EUR | FIN | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0122 | EUR | FIN | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG00438 | hp1 | a0001 | c0001 | t0004 | g0141 | EAS | CHS | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG00544 | hp1 | a0001 | c0001 | t0002 | g0125 | EAS | CHS | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | CHS | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG00558 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | CHS | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | CHS | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | CHS | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG00639 | hp1 | a0001 | c0001 | t0005 | g0136 | AMR | PUR | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG00639 | hp2 | a0001 | c0001 | t0004 | g0129 | AMR | PUR | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG00642 | hp1 | a0001 | c0001 | t0004 | g0004 | AMR | PUR | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG00642 | hp2 | a0001 | c0001 | t0003 | g0061 | AMR | PUR | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG00733 | hp1 | a0001 | c0001 | t0002 | g0044 | AMR | PUR | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG00733 | hp2 | a0001 | c0001 | t0004 | g0130 | AMR | PUR | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG00735 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG00735 | hp2 | a0001 | c0001 | t0004 | g0037 | AMR | PUR | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG00738 | hp1 | a0001 | c0001 | t0003 | g0026 | AMR | PUR | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG00741 | hp2 | a0001 | c0001 | t0002 | g0047 | AMR | PUR | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG01070 | hp1 | a0001 | c0001 | t0004 | g0138 | AMR | PUR | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG01081 | hp1 | a0001 | c0001 | t0004 | g0037 | AMR | PUR | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG01106 | hp2 | a0001 | c0001 | t0004 | g0002 | AMR | PUR | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG01109 | hp1 | a0001 | c0001 | t0002 | g0012 | AMR | PUR | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG01109 | hp2 | a0001 | c0001 | t0004 | g0004 | AMR | PUR | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG01167 | hp1 | a0001 | c0001 | t0004 | g0143 | AMR | PUR | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG01175 | hp2 | a0001 | c0001 | t0002 | g0022 | AMR | PUR | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG01192 | hp2 | a0001 | c0001 | t0004 | g0038 | AMR | PUR | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG01243 | hp1 | a0001 | c0001 | t0005 | g0010 | AMR | PUR | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG01255 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | CLM | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG01256 | hp1 | a0001 | c0001 | t0003 | g0005 | AMR | CLM | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG01257 | hp1 | a0001 | c0001 | t0002 | g0023 | AMR | CLM | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG01258 | hp1 | a0001 | c0001 | t0002 | g0023 | AMR | CLM | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG01261 | hp1 | a0001 | c0001 | t0004 | g0021 | AMR | CLM | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0071 | AMR | CLM | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG01346 | hp2 | a0001 | c0001 | t0003 | g0007 | AMR | CLM | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG01361 | hp2 | a0001 | c0001 | t0003 | g0026 | AMR | CLM | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | CLM | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG01496 | hp1 | a0001 | c0001 | t0003 | g0011 | AMR | CLM | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG01515 | hp1 | a0001 | c0001 | t0004 | g0131 | EUR | IBS | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG01515 | hp2 | a0001 | c0001 | t0004 | g0139 | EUR | IBS | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG01517 | hp1 | a0001 | c0001 | t0004 | g0132 | EUR | IBS | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG01884 | hp1 | a0001 | c0001 | t0002 | g0064 | AFR | ACB | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG01884 | hp2 | a0001 | c0001 | t0005 | g0036 | AFR | ACB | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG01891 | hp1 | a0001 | c0001 | t0002 | g0018 | AFR | ACB | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG01891 | hp2 | a0001 | c0001 | t0005 | g0134 | AFR | ACB | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG01928 | hp2 | a0001 | c0001 | t0003 | g0007 | AMR | PEL | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG01934 | hp1 | a0001 | c0001 | t0003 | g0007 | AMR | PEL | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG01934 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG01943 | hp2 | a0001 | c0001 | t0004 | g0004 | AMR | PEL | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG01952 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PEL | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG01975 | hp1 | a0001 | c0005 | t0001 | g0001 | AMR | PEL | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG01975 | hp2 | a0001 | c0001 | t0004 | g0004 | AMR | PEL | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | PEL | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG01981 | hp1 | a0001 | c0001 | t0004 | g0004 | AMR | PEL | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | PEL | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG01993 | hp2 | a0001 | c0001 | t0004 | g0004 | AMR | PEL | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG02004 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG02027 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG02055 | hp1 | a0001 | c0001 | t0002 | g0006 | AFR | ACB | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | KHV | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | KHV | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | KHV | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | KHV | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG02132 | hp1 | a0001 | c0001 | t0002 | g0049 | EAS | KHV | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG02132 | hp2 | a0001 | c0001 | t0002 | g0034 | EAS | KHV | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | KHV | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG02145 | hp1 | a0001 | c0001 | t0005 | g0020 | AFR | ACB | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG02145 | hp2 | a0001 | c0001 | t0004 | g0021 | AFR | ACB | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | CDX | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | CDX | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG02257 | hp1 | a0001 | c0001 | t0002 | g0055 | AFR | ACB | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG02273 | hp2 | a0001 | c0001 | t0003 | g0007 | AMR | PEL | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG02280 | hp1 | a0001 | c0001 | t0005 | g0135 | AFR | ACB | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | ACB | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG02293 | hp2 | a0001 | c0001 | t0002 | g0051 | AMR | PEL | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | PEL | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG02300 | hp2 | a0001 | c0001 | t0004 | g0142 | AMR | PEL | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG02451 | hp1 | a0001 | c0001 | t0004 | g0004 | AFR | ACB | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | ACB | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG02523 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG02572 | hp1 | a0001 | c0001 | t0006 | g0133 | AFR | GWD | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0032 | SAS | PJL | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG02615 | hp1 | a0001 | c0001 | t0002 | g0126 | AFR | GWD | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG02622 | hp1 | a0001 | c0001 | t0003 | g0025 | AFR | GWD | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | GWD | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG02630 | hp1 | a0002 | c0002 | t0002 | g0017 | AFR | GWD | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG02647 | hp1 | a0001 | c0001 | t0006 | g0019 | AFR | GWD | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG02647 | hp2 | a0001 | c0001 | t0005 | g0010 | AFR | GWD | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0106 | SAS | PJL | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0104 | SAS | PJL | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG02717 | hp1 | a0001 | c0001 | t0006 | g0019 | AFR | GWD | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG02717 | hp2 | a0001 | c0001 | t0002 | g0012 | AFR | GWD | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG02723 | hp2 | a0001 | c0001 | t0004 | g0013 | AFR | GWD | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG02738 | hp1 | a0001 | c0001 | t0003 | g0027 | SAS | PJL | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG02738 | hp2 | a0001 | c0001 | t0002 | g0045 | SAS | PJL | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG02809 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | GWD | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG02809 | hp2 | a0001 | c0001 | t0003 | g0057 | AFR | GWD | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG02818 | hp1 | a0001 | c0001 | t0002 | g0012 | AFR | GWD | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG02818 | hp2 | a0001 | c0001 | t0006 | g0019 | AFR | GWD | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG02886 | hp1 | a0001 | c0001 | t0002 | g0029 | AFR | GWD | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG02895 | hp1 | a0001 | c0001 | t0002 | g0068 | AFR | GWD | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG02895 | hp2 | a0001 | c0001 | t0002 | g0028 | AFR | GWD | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG02896 | hp1 | a0001 | c0001 | t0002 | g0018 | AFR | GWD | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | GWD | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG02922 | hp1 | a0001 | c0001 | t0002 | g0028 | AFR | ESN | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | ESN | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG02965 | hp1 | a0001 | c0001 | t0004 | g0035 | AFR | ESN | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG02965 | hp2 | a0003 | c0003 | t0002 | g0002 | AFR | ESN | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG02970 | hp1 | a0001 | c0001 | t0003 | g0062 | AFR | ESN | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG02970 | hp2 | a0001 | c0001 | t0004 | g0021 | AFR | ESN | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG02976 | hp1 | a0001 | c0001 | t0004 | g0013 | AFR | ESN | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0107 | SAS | PJL | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG03017 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | GWD | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG03098 | hp1 | a0004 | c0004 | t0003 | g0027 | AFR | MSL | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG03098 | hp2 | a0001 | c0001 | t0004 | g0128 | AFR | MSL | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG03130 | hp1 | a0002 | c0002 | t0002 | g0017 | AFR | ESN | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG03130 | hp2 | a0001 | c0001 | t0005 | g0010 | AFR | ESN | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG03139 | hp1 | a0001 | c0001 | t0002 | g0018 | AFR | ESN | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG03139 | hp2 | a0001 | c0001 | t0005 | g0010 | AFR | ESN | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG03195 | hp1 | a0001 | c0001 | t0004 | g0013 | AFR | ESN | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG03195 | hp2 | a0001 | c0001 | t0009 | g0001 | AFR | ESN | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | MSL | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | MSL | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG03453 | hp1 | a0001 | c0001 | t0004 | g0013 | AFR | MSL | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG03453 | hp2 | a0001 | c0001 | t0002 | g0052 | AFR | MSL | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG03486 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | MSL | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG03492 | hp1 | a0001 | c0001 | t0002 | g0014 | SAS | PJL | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | ESN | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG03540 | hp1 | a0001 | c0001 | t0002 | g0069 | AFR | GWD | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG03540 | hp2 | a0001 | c0001 | t0005 | g0020 | AFR | GWD | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG03654 | hp2 | a0001 | c0001 | t0002 | g0048 | SAS | PJL | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG03669 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG03831 | hp1 | a0001 | c0001 | t0003 | g0007 | SAS | BEB | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0032 | SAS | BEB | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG03834 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | BEB | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG04184 | hp1 | a0001 | c0001 | t0003 | g0011 | SAS | BEB | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG04184 | hp2 | a0001 | c0001 | t0002 | g0006 | SAS | BEB | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | STU | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG04199 | hp2 | a0001 | c0001 | t0003 | g0011 | SAS | STU | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0110 | SAS | STU | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | YRI | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
NA18522 | hp2 | a0001 | c0001 | t0002 | g0012 | AFR | YRI | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | CHB | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
NA18612 | hp2 | a0001 | c0001 | t0004 | g0004 | EAS | CHB | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | YRI | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
NA18906 | hp2 | a0001 | c0001 | t0004 | g0035 | AFR | YRI | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
NA18941 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
NA18942 | hp1 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
NA18943 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
NA18944 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
NA18945 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
NA18947 | hp2 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
NA18949 | hp1 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
NA18950 | hp1 | a0001 | c0001 | t0003 | g0059 | EAS | JPT | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
NA18952 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
NA18953 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
NA18954 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
NA18957 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
NA18963 | hp2 | a0001 | c0001 | t0003 | g0024 | EAS | JPT | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
NA18964 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
NA18968 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
NA18971 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
NA18972 | hp2 | a0001 | c0001 | t0003 | g0024 | EAS | JPT | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
NA18974 | hp1 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
NA18974 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
NA18975 | hp2 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
NA18978 | hp2 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
NA18981 | hp1 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
NA18981 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
NA18982 | hp2 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
NA18983 | hp1 | a0001 | c0001 | t0007 | g0003 | EAS | JPT | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
NA18983 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
NA18984 | hp1 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
NA18986 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
NA18988 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
NA18988 | hp2 | a0001 | c0001 | t0003 | g0058 | EAS | JPT | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
NA18989 | hp2 | a0001 | c0001 | t0004 | g0140 | EAS | JPT | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
NA18990 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
NA18992 | hp1 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
NA18997 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
NA19000 | hp2 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
NA19002 | hp1 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
NA19005 | hp2 | a0001 | c0001 | t0003 | g0066 | EAS | JPT | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
NA19009 | hp1 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
NA19010 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
NA19011 | hp1 | a0001 | c0001 | t0008 | g0001 | EAS | JPT | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
NA19011 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
NA19012 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
NA19043 | hp1 | a0001 | c0001 | t0002 | g0067 | AFR | LWK | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
NA19043 | hp2 | a0001 | c0001 | t0005 | g0036 | AFR | LWK | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
NA19057 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
NA19058 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
NA19060 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
NA19064 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
NA19067 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
NA19070 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
NA19072 | hp1 | a0001 | c0001 | t0003 | g0063 | EAS | JPT | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
NA19072 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
NA19078 | hp2 | a0001 | c0001 | t0003 | g0040 | EAS | JPT | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
NA19080 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
NA19081 | hp1 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
NA19084 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
NA19089 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
NA19090 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | YRI | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
NA20129 | hp1 | a0001 | c0001 | t0003 | g0025 | AFR | ASW | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
NA20129 | hp2 | a0001 | c0001 | t0005 | g0010 | AFR | ASW | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
NA20752 | hp1 | a0001 | c0001 | t0004 | g0004 | EUR | TSI | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
NA20752 | hp2 | a0001 | c0001 | t0002 | g0054 | EUR | TSI | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
NA20905 | hp1 | a0001 | c0001 | t0002 | g0065 | SAS | GIH | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG01123 | hp1 | a0001 | c0001 | t0002 | g0042 | AMR | CLM | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG02109 | hp1 | a0003 | c0003 | t0002 | g0002 | AFR | ACB | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG02109 | hp2 | a0001 | c0001 | t0002 | g0029 | AFR | ACB | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG02559 | hp2 | a0001 | c0001 | t0002 | g0050 | AFR | ACB | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG06807 | hp1 | a0001 | c0001 | t0005 | g0137 | AFR | USA | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
HG06807 | hp2 | a0001 | c0001 | t0002 | g0022 | AFR | USA | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
NA18955 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | USA | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
NA20300 | hp2 | a0001 | c0001 | t0005 | g0020 | AFR | USA | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
NA21309 | hp1 | a0002 | c0002 | t0002 | g0017 | AFR | LWK | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
NA21309 | hp2 | a0001 | c0001 | t0004 | g0004 | AFR | LWK | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0006 | REF | REF | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0001 | REF | REF | MED30_chr8_117515713_117545262 | MED30 | chr8 | 117515713 | 117545262 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:117520905
|
G | T | 1 | a0003 | 2 | HG02109.hp1 HG02965.hp2 |
missense_variant | MODERATE | c.29G>T | p.Gly10Val | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 1/4 | 193/985 | 29/537 | 10/178 | chr8 | 117520905 | ||
chr8:117520949
|
G | T | 1 | a0002 | 3 | HG02630.hp1 HG03130.hp1 NA21309.hp1 |
missense_variant | MODERATE | c.73G>T | p.Ala25Ser | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 1/4 | 237/985 | 73/537 | 25/178 | chr8 | 117520949 | ||
chr8:117528792
|
G | T | 1 | a0004 | 1 | HG03098.hp1 | missense_variant | MODERATE | c.319G>T | p.Asp107Tyr | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 2/4 | 483/985 | 319/537 | 107/178 | chr8 | 117528792 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:117520927
|
C | T | 1 | a0001c0005 | 1 | HG01975.hp1 | synonymous_variant | LOW | c.51C>T | p.Ala17Ala | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 1/4 | 215/985 | 51/537 | 17/178 | chr8 | 117520927 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:117520714
|
TG | T | 1 | a0001c0001t0004 | 39 | HG00140.hp1 HG00438.hp1 HG00639.hp2 others(36): Show |
5_prime_UTR_variant | MODIFIER | c.-162delG | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 1/4 | 162 | chr8 | 117520714 | |||||
chr8:117520725
|
A | G | 8 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(5): Show | 185 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(182): Show |
5_prime_UTR_variant | MODIFIER | c.-152A>G | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 1/4 | 152 | chr8 | 117520725 | |||||
chr8:117520791
|
C | T | 1 | a0001c0001t0009 | 1 | HG03195.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-86C>T | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 1/4 | chr8 | 117520791 | ||||||
chr8:117520792
|
G | A | 1 | a0001c0001t0007 | 1 | NA18983.hp1 | 5_prime_UTR_variant | MODIFIER | c.-85G>A | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 1/4 | 85 | chr8 | 117520792 | |||||
chr8:117520822
|
C | G | 1 | a0001c0001t0005 | 14 | HG00639.hp1 HG01243.hp1 HG01884.hp2 others(11): Show |
5_prime_UTR_variant | MODIFIER | c.-55C>G | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 1/4 | 55 | chr8 | 117520822 | |||||
chr8:117520827
|
C | A | 1 | a0001c0001t0005 | 14 | HG00639.hp1 HG01243.hp1 HG01884.hp2 others(11): Show |
5_prime_UTR_variant | MODIFIER | c.-50C>A | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 1/4 | 50 | chr8 | 117520827 | |||||
chr8:117520829
|
C | T | 1 | a0001c0001t0008 | 1 | NA19011.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-48C>T | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 1/4 | chr8 | 117520829 | ||||||
chr8:117540098
|
T | G | 1 | a0001c0001t0006 | 4 | HG02572.hp1 HG02647.hp1 HG02717.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*120T>G | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 4/4 | 120 | chr8 | 117540098 | |||||
chr8:117540135
|
CT | C | 2 | a0001c0001t0003a0004c0004t0003 | 43 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*164delT | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 4/4 | 164 | INFO_REALIGN_3_PRIME | chr8 | 117540135 | ||||
chr8:117540148
|
T | TATTA | 1 | a0001c0001t0006 | 4 | HG02572.hp1 HG02647.hp1 HG02717.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*173_*174insAATT | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 4/4 | 174 | INFO_REALIGN_3_PRIME | chr8 | 117540148 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:117521073
|
A | G | 30 | a0001c0001t0002g0034a0001c0001t0002g0125a0001c0001t0002g0126others(27): Show | 61 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(58): Show |
intron_variant | MODIFIER | c.177+20A>G | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 1/3 | chr8 | 117521073 | ||||||
chr8:117521143
|
T | A | 83 | a0001c0001t0001g0039a0001c0001t0002g0002a0001c0001t0002g0006others(80): Show | 186 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(183): Show |
intron_variant | MODIFIER | c.177+90T>A | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 1/3 | chr8 | 117521143 | ||||||
chr8:117521205
|
C | T | 11 | a0001c0001t0004g0004a0001c0001t0004g0013a0001c0001t0004g0021others(8): Show | 31 | HG00140.hp1 HG00438.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.177+152C>T | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 1/3 | chr8 | 117521205 | ||||||
chr8:117521266
|
A | G | 1 | a0001c0001t0001g0124 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.177+213A>G | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 1/3 | chr8 | 117521266 | ||||||
chr8:117521314
|
C | G | 1 | a0001c0001t0003g0007 | 6 | HG00140.hp2 HG01346.hp2 HG01928.hp2 others(3): Show |
intron_variant | MODIFIER | c.177+261C>G | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 1/3 | chr8 | 117521314 | ||||||
chr8:117521421
|
A | AT | 6 | a0001c0001t0002g0012a0001c0001t0002g0018a0001c0001t0002g0029others(3): Show | 12 | HG01109.hp1 HG01891.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.177+376dupT | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 117521421 | |||||
chr8:117521429
|
T | A | 1 | a0001c0001t0001g0070 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.177+376T>A | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 1/3 | chr8 | 117521429 | ||||||
chr8:117521436
|
AC | A | 9 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0071others(6): Show | 11 | HG01175.hp1 HG01346.hp1 HG01952.hp2 others(8): Show |
intron_variant | MODIFIER | c.177+384delC | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 1/3 | chr8 | 117521436 | ||||||
chr8:117521604
|
C | T | 1 | a0001c0001t0001g0123 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.177+551C>T | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 1/3 | chr8 | 117521604 | ||||||
chr8:117521685
|
C | T | 2 | a0001c0001t0001g0121a0001c0001t0001g0122 | 2 | HG00323.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.177+632C>T | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 1/3 | chr8 | 117521685 | ||||||
chr8:117521687
|
G | T | 2 | a0001c0001t0002g0028a0002c0002t0002g0017 | 5 | HG02630.hp1 HG02895.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.177+634G>T | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 1/3 | chr8 | 117521687 | ||||||
chr8:117521705
|
C | CT | 9 | a0001c0001t0002g0012a0001c0001t0002g0018a0001c0001t0002g0029others(6): Show | 17 | HG00639.hp1 HG01109.hp1 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.177+662dupT | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 117521705 | |||||
chr8:117521725
|
C | G | 1 | a0001c0001t0001g0120 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.177+672C>G | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 1/3 | chr8 | 117521725 | ||||||
chr8:117521795
|
C | T | 1 | a0001c0001t0001g0119 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.177+742C>T | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 1/3 | chr8 | 117521795 | ||||||
chr8:117521868
|
C | T | 1 | a0001c0001t0003g0066 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.177+815C>T | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 1/3 | chr8 | 117521868 | ||||||
chr8:117522053
|
A | G | 7 | a0001c0001t0005g0010a0001c0001t0005g0020a0001c0001t0005g0036others(4): Show | 14 | HG00639.hp1 HG01243.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.177+1000A>G | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 1/3 | chr8 | 117522053 | ||||||
chr8:117522363
|
A | G | 1 | a0001c0001t0002g0065 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.177+1310A>G | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 1/3 | chr8 | 117522363 | ||||||
chr8:117522367
|
A | G | 1 | a0001c0001t0001g0118 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.177+1314A>G | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 1/3 | chr8 | 117522367 | ||||||
chr8:117522412
|
T | C | 4 | a0001c0001t0002g0034a0001c0001t0002g0125a0001c0001t0002g0126others(1): Show | 5 | HG00544.hp1 HG02132.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.177+1359T>C | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 1/3 | chr8 | 117522412 | ||||||
chr8:117522635
|
C | T | 2 | a0001c0001t0004g0013a0001c0001t0004g0021 | 7 | HG01261.hp1 HG02145.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.177+1582C>T | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 1/3 | chr8 | 117522635 | ||||||
chr8:117522635
|
CT | C | 5 | a0001c0001t0004g0035a0001c0001t0004g0128a0001c0001t0004g0138others(2): Show | 8 | HG01070.hp1 HG02572.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.177+1595delT | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 117522635 | |||||
chr8:117522636
|
T | C | 20 | a0001c0001t0004g0004a0001c0001t0004g0013a0001c0001t0004g0021others(17): Show | 47 | HG00140.hp1 HG00438.hp1 HG00639.hp1 others(44): Show |
intron_variant | MODIFIER | c.177+1583T>C | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 1/3 | chr8 | 117522636 | ||||||
chr8:117522637
|
T | C | 4 | a0001c0001t0004g0035a0001c0001t0004g0128a0001c0001t0004g0138others(1): Show | 5 | HG01070.hp1 HG01167.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.177+1584T>C | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 1/3 | chr8 | 117522637 | ||||||
chr8:117522701
|
T | TGGAAATT others(326): Show |
1 | a0001c0001t0004g0131 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.177+1658_177+1659i others(335): Show |
MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 117522701 | |||||
chr8:117522701
|
T | TGGAAATT others(327): Show |
1 | a0001c0001t0004g0132 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.177+1658_177+1659i others(336): Show |
MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 117522701 | |||||
chr8:117522755
|
A | G | 2 | a0001c0001t0004g0035a0001c0001t0004g0128 | 3 | HG02965.hp1 HG03098.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.177+1702A>G | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 1/3 | chr8 | 117522755 | ||||||
chr8:117522815
|
T | G | 11 | a0001c0001t0002g0034a0001c0001t0002g0125a0001c0001t0002g0126others(8): Show | 19 | HG00544.hp1 HG00639.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.177+1762T>G | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 1/3 | chr8 | 117522815 | ||||||
chr8:117522948
|
T | G | 1 | a0001c0001t0001g0039 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.177+1895T>G | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 1/3 | chr8 | 117522948 | ||||||
chr8:117522981
|
A | G | 6 | a0001c0001t0001g0008a0001c0001t0001g0113a0001c0001t0001g0114others(3): Show | 11 | HG00558.hp1 HG00673.hp1 HG00738.hp2 others(8): Show |
intron_variant | MODIFIER | c.177+1928A>G | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 1/3 | chr8 | 117522981 | ||||||
chr8:117522998
|
T | C | 83 | a0001c0001t0001g0039a0001c0001t0002g0002a0001c0001t0002g0006others(80): Show | 186 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(183): Show |
intron_variant | MODIFIER | c.177+1945T>C | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 1/3 | chr8 | 117522998 | ||||||
chr8:117522999
|
G | A | 2 | a0001c0001t0006g0019a0001c0001t0006g0133 | 4 | HG02572.hp1 HG02647.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.177+1946G>A | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 1/3 | chr8 | 117522999 | ||||||
chr8:117523010
|
T | A | 1 | a0001c0001t0001g0078 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.177+1957T>A | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 1/3 | chr8 | 117523010 | ||||||
chr8:117523139
|
C | T | 1 | a0001c0001t0005g0135 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.177+2086C>T | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 1/3 | chr8 | 117523139 | ||||||
chr8:117523159
|
T | A | 44 | a0001c0001t0002g0002a0001c0001t0002g0006a0001c0001t0002g0014others(41): Show | 107 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.177+2106T>A | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 1/3 | chr8 | 117523159 | ||||||
chr8:117523195
|
CT | C | 34 | a0001c0001t0001g0039a0001c0001t0001g0079a0001c0001t0001g0080others(31): Show | 75 | HG00280.hp1 HG00558.hp2 HG00639.hp1 others(72): Show |
intron_variant | MODIFIER | c.177+2154delT | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 117523195 | |||||
chr8:117523210
|
GT | G | 16 | a0001c0001t0002g0041a0001c0001t0002g0055a0001c0001t0002g0056others(13): Show | 37 | HG01243.hp1 HG01256.hp1 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.177+2169delT | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 117523210 | |||||
chr8:117523272
|
T | G | 1 | a0001c0001t0001g0071 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.177+2219T>G | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 1/3 | chr8 | 117523272 | ||||||
chr8:117523386
|
A | G | 2 | a0001c0001t0003g0058a0001c0001t0003g0059 | 2 | NA18950.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.177+2333A>G | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 1/3 | chr8 | 117523386 | ||||||
chr8:117523478
|
G | A | 1 | a0001c0001t0001g0082 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.177+2425G>A | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 1/3 | chr8 | 117523478 | ||||||
chr8:117523482
|
G | T | 2 | a0001c0001t0002g0012a0001c0001t0002g0029 | 6 | HG01109.hp1 HG02109.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.177+2429G>T | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 1/3 | chr8 | 117523482 | ||||||
chr8:117523643
|
C | T | 1 | a0001c0001t0002g0054 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.177+2590C>T | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 1/3 | chr8 | 117523643 | ||||||
chr8:117523816
|
A | G | 47 | a0001c0001t0001g0033a0001c0001t0002g0002a0001c0001t0002g0006others(44): Show | 113 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.177+2763A>G | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 1/3 | chr8 | 117523816 | ||||||
chr8:117523823
|
AT | A | 2 | a0001c0001t0004g0035a0001c0001t0004g0128 | 3 | HG02965.hp1 HG03098.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.177+2771delT | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 1/3 | chr8 | 117523823 | ||||||
chr8:117523843
|
C | G | 1 | a0001c0001t0002g0053 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.177+2790C>G | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 1/3 | chr8 | 117523843 | ||||||
chr8:117523931
|
C | A | 2 | a0001c0001t0006g0019a0001c0001t0006g0133 | 4 | HG02572.hp1 HG02647.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.177+2878C>A | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 1/3 | chr8 | 117523931 | ||||||
chr8:117523945
|
G | T | 12 | a0001c0001t0004g0035a0001c0001t0004g0128a0001c0001t0004g0129others(9): Show | 20 | HG00639.hp2 HG00733.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.177+2892G>T | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 1/3 | chr8 | 117523945 | ||||||
chr8:117524160
|
G | A | 16 | a0001c0001t0002g0034a0001c0001t0002g0125a0001c0001t0002g0126others(13): Show | 25 | HG00544.hp1 HG00639.hp2 HG00733.hp2 others(22): Show |
intron_variant | MODIFIER | c.177+3107G>A | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 1/3 | chr8 | 117524160 | ||||||
chr8:117524202
|
T | G | 19 | a0001c0001t0002g0056a0001c0001t0003g0005a0001c0001t0003g0007others(16): Show | 44 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(41): Show |
intron_variant | MODIFIER | c.177+3149T>G | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 1/3 | chr8 | 117524202 | ||||||
chr8:117524526
|
C | G | 1 | a0001c0001t0002g0028 | 2 | HG02895.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.177+3473C>G | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 1/3 | chr8 | 117524526 | ||||||
chr8:117524600
|
T | C | 1 | a0001c0001t0002g0042 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.177+3547T>C | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 1/3 | chr8 | 117524600 | ||||||
chr8:117524658
|
AG | A | 2 | a0001c0001t0002g0028a0002c0002t0002g0017 | 5 | HG02630.hp1 HG02895.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.177+3606delG | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 1/3 | chr8 | 117524658 | ||||||
chr8:117524688
|
A | G | 1 | a0001c0001t0001g0039 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.177+3635A>G | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 1/3 | chr8 | 117524688 | ||||||
chr8:117524777
|
GCAT | G | 17 | a0001c0001t0002g0012a0001c0001t0002g0018a0001c0001t0002g0029others(14): Show | 43 | HG00140.hp1 HG00438.hp1 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.177+3725_177+3727d others(5): Show |
MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 1/3 | chr8 | 117524777 | ||||||
chr8:117524849
|
C | T | 16 | a0001c0001t0002g0034a0001c0001t0002g0125a0001c0001t0002g0126others(13): Show | 25 | HG00544.hp1 HG00639.hp2 HG00733.hp2 others(22): Show |
intron_variant | MODIFIER | c.177+3796C>T | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 1/3 | chr8 | 117524849 | ||||||
chr8:117524923
|
T | C | 1 | a0001c0001t0002g0043 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.178-3728T>C | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 1/3 | chr8 | 117524923 | ||||||
chr8:117525061
|
C | T | 1 | a0001c0001t0001g0077 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.178-3590C>T | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 1/3 | chr8 | 117525061 | ||||||
chr8:117525166
|
C | CT | 10 | a0001c0001t0004g0035a0001c0001t0004g0128a0001c0001t0004g0129others(7): Show | 16 | HG00639.hp2 HG00733.hp2 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.178-3484dupT | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 117525166 | |||||
chr8:117525170
|
G | C | 1 | a0001c0001t0001g0039 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.178-3481G>C | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 1/3 | chr8 | 117525170 | ||||||
chr8:117525178
|
C | A | 1 | a0001c0001t0001g0039 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.178-3473C>A | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 1/3 | chr8 | 117525178 | ||||||
chr8:117525216
|
T | C | 2 | a0001c0001t0002g0028a0002c0002t0002g0017 | 5 | HG02630.hp1 HG02895.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.178-3435T>C | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 1/3 | chr8 | 117525216 | ||||||
chr8:117525230
|
A | G | 1 | a0001c0001t0002g0028 | 2 | HG02895.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.178-3421A>G | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 1/3 | chr8 | 117525230 | ||||||
chr8:117525343
|
C | CT | 5 | a0001c0001t0001g0112a0001c0001t0002g0028a0001c0001t0004g0035others(2): Show | 9 | HG02630.hp1 HG02895.hp2 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.178-3295dupT | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 117525343 | |||||
chr8:117525356
|
T | C | 2 | a0001c0001t0006g0019a0001c0001t0006g0133 | 4 | HG02572.hp1 HG02647.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.178-3295T>C | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 1/3 | chr8 | 117525356 | ||||||
chr8:117525393
|
A | G | 47 | a0001c0001t0001g0111a0001c0001t0002g0002a0001c0001t0002g0006others(44): Show | 112 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.178-3258A>G | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 1/3 | chr8 | 117525393 | ||||||
chr8:117525417
|
C | T | 4 | a0001c0001t0002g0034a0001c0001t0002g0125a0001c0001t0002g0126others(1): Show | 5 | HG00544.hp1 HG02132.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.178-3234C>T | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 1/3 | chr8 | 117525417 | ||||||
chr8:117525422
|
T | C | 1 | a0001c0001t0001g0083 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.178-3229T>C | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 1/3 | chr8 | 117525422 | ||||||
chr8:117525439
|
A | AT | 2 | a0001c0001t0006g0019a0001c0001t0006g0133 | 4 | HG02572.hp1 HG02647.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.178-3205dupT | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 117525439 | |||||
chr8:117525450
|
T | C | 82 | a0001c0001t0001g0111a0001c0001t0002g0002a0001c0001t0002g0006others(79): Show | 185 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.178-3201T>C | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 1/3 | chr8 | 117525450 | ||||||
chr8:117525489
|
A | G | 4 | a0001c0001t0005g0010a0001c0001t0005g0036a0001c0001t0005g0134others(1): Show | 9 | HG01243.hp1 HG01884.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.178-3162A>G | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 1/3 | chr8 | 117525489 | ||||||
chr8:117525628
|
A | T | 1 | a0001c0001t0003g0063 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.178-3023A>T | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 1/3 | chr8 | 117525628 | ||||||
chr8:117525767
|
T | C | 4 | a0001c0001t0002g0034a0001c0001t0002g0125a0001c0001t0002g0126others(1): Show | 5 | HG00544.hp1 HG02132.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.178-2884T>C | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 1/3 | chr8 | 117525767 | ||||||
chr8:117525956
|
G | A | 2 | a0001c0001t0006g0019a0001c0001t0006g0133 | 4 | HG02572.hp1 HG02647.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.178-2695G>A | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 1/3 | chr8 | 117525956 | ||||||
chr8:117526012
|
A | G | 1 | a0001c0001t0001g0110 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.178-2639A>G | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 1/3 | chr8 | 117526012 | ||||||
chr8:117526094
|
TTA | T | 3 | a0001c0001t0004g0013a0001c0001t0004g0021a0001c0001t0004g0143 | 8 | HG01167.hp1 HG01261.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.178-2555_178-2554d others(4): Show |
MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 117526094 | |||||
chr8:117526289
|
C | G | 8 | a0001c0001t0004g0004a0001c0001t0004g0037a0001c0001t0004g0038others(5): Show | 23 | HG00140.hp1 HG00438.hp1 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.178-2362C>G | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 1/3 | chr8 | 117526289 | ||||||
chr8:117526298
|
C | G | 1 | a0001c0001t0001g0032 | 2 | HG02602.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.178-2353C>G | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 1/3 | chr8 | 117526298 | ||||||
chr8:117526418
|
A | G | 28 | a0001c0001t0001g0111a0001c0001t0002g0002a0001c0001t0002g0006others(25): Show | 68 | HG00280.hp1 HG00558.hp2 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.178-2233A>G | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 1/3 | chr8 | 117526418 | ||||||
chr8:117526444
|
T | C | 6 | a0001c0001t0002g0012a0001c0001t0002g0018a0001c0001t0002g0029others(3): Show | 12 | HG01109.hp1 HG01891.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.178-2207T>C | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 1/3 | chr8 | 117526444 | ||||||
chr8:117526444
|
T | G | 28 | a0001c0001t0001g0111a0001c0001t0002g0002a0001c0001t0002g0006others(25): Show | 68 | HG00280.hp1 HG00558.hp2 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.178-2207T>G | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 1/3 | chr8 | 117526444 | ||||||
chr8:117526519
|
A | T | 1 | a0002c0002t0002g0017 | 3 | HG02630.hp1 HG03130.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.178-2132A>T | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 1/3 | chr8 | 117526519 | ||||||
chr8:117526544
|
G | A | 1 | a0001c0001t0004g0128 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.178-2107G>A | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 1/3 | chr8 | 117526544 | ||||||
chr8:117526623
|
G | A | 1 | a0001c0001t0002g0053 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.178-2028G>A | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 1/3 | chr8 | 117526623 | ||||||
chr8:117526657
|
C | T | 4 | a0001c0001t0005g0010a0001c0001t0005g0036a0001c0001t0005g0134others(1): Show | 9 | HG01243.hp1 HG01884.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.178-1994C>T | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 1/3 | chr8 | 117526657 | ||||||
chr8:117526658
|
G | A | 1 | a0001c0001t0001g0084 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.178-1993G>A | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 1/3 | chr8 | 117526658 | ||||||
chr8:117526809
|
A | G | 2 | a0001c0001t0004g0035a0001c0001t0004g0128 | 3 | HG02965.hp1 HG03098.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.178-1842A>G | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 1/3 | chr8 | 117526809 | ||||||
chr8:117526964
|
G | A | 3 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0045 | 5 | HG01175.hp2 HG01257.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.178-1687G>A | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 1/3 | chr8 | 117526964 | ||||||
chr8:117527006
|
A | G | 2 | a0001c0001t0006g0019a0001c0001t0006g0133 | 4 | HG02572.hp1 HG02647.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.178-1645A>G | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 1/3 | chr8 | 117527006 | ||||||
chr8:117527007
|
T | C | 11 | a0001c0001t0004g0004a0001c0001t0004g0013a0001c0001t0004g0021others(8): Show | 31 | HG00140.hp1 HG00438.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.178-1644T>C | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 1/3 | chr8 | 117527007 | ||||||
chr8:117527111
|
C | G | 1 | a0001c0001t0001g0076 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.178-1540C>G | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 1/3 | chr8 | 117527111 | ||||||
chr8:117527342
|
T | G | 1 | a0001c0001t0001g0113 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.178-1309T>G | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 1/3 | chr8 | 117527342 | ||||||
chr8:117527616
|
A | G | 2 | a0001c0001t0006g0019a0001c0001t0006g0133 | 4 | HG02572.hp1 HG02647.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.178-1035A>G | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 1/3 | chr8 | 117527616 | ||||||
chr8:117527636
|
CT | C | 32 | a0001c0001t0001g0039a0001c0001t0001g0087a0001c0001t0001g0088others(29): Show | 65 | HG00438.hp1 HG00558.hp1 HG00639.hp2 others(62): Show |
intron_variant | MODIFIER | c.178-997delT | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 117527636 | |||||
chr8:117527636
|
CTT | C | 9 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0071others(6): Show | 11 | HG01175.hp1 HG01346.hp1 HG01952.hp2 others(8): Show |
intron_variant | MODIFIER | c.178-998_178-997del others(2): Show |
MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 117527636 | |||||
chr8:117527636
|
CTTTTTTT | C | 49 | a0001c0001t0001g0085a0001c0001t0001g0111a0001c0001t0002g0002others(46): Show | 114 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.178-1003_178-997de others(8): Show |
MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 117527636 | |||||
chr8:117527767
|
G | A | 1 | a0001c0001t0002g0125 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.178-884G>A | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 1/3 | chr8 | 117527767 | ||||||
chr8:117527780
|
C | T | 4 | a0001c0001t0005g0010a0001c0001t0005g0036a0001c0001t0005g0134others(1): Show | 9 | HG01243.hp1 HG01884.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.178-871C>T | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 1/3 | chr8 | 117527780 | ||||||
chr8:117527797
|
A | C | 1 | a0001c0001t0001g0109 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.178-854A>C | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 1/3 | chr8 | 117527797 | ||||||
chr8:117527812
|
A | T | 1 | a0001c0001t0001g0039 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.178-839A>T | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 1/3 | chr8 | 117527812 | ||||||
chr8:117527883
|
A | C | 8 | a0001c0001t0004g0004a0001c0001t0004g0037a0001c0001t0004g0038others(5): Show | 23 | HG00140.hp1 HG00438.hp1 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.178-768A>C | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 1/3 | chr8 | 117527883 | ||||||
chr8:117528101
|
CCTG | C | 4 | a0001c0001t0005g0010a0001c0001t0005g0036a0001c0001t0005g0134others(1): Show | 9 | HG01243.hp1 HG01884.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.178-547_178-545del others(3): Show |
MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | 117528101 | |||||
chr8:117528345
|
T | G | 1 | a0001c0001t0001g0039 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.178-306T>G | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 1/3 | chr8 | 117528345 | ||||||
chr8:117528459
|
A | C | 2 | a0001c0001t0004g0035a0001c0001t0004g0128 | 3 | HG02965.hp1 HG03098.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.178-192A>C | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 1/3 | chr8 | 117528459 | ||||||
chr8:117528459
|
A | G | 2 | a0001c0001t0006g0019a0001c0001t0006g0133 | 4 | HG02572.hp1 HG02647.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.178-192A>G | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 1/3 | chr8 | 117528459 | ||||||
chr8:117528548
|
A | G | 2 | a0001c0001t0006g0019a0001c0001t0006g0133 | 4 | HG02572.hp1 HG02647.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.178-103A>G | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 1/3 | chr8 | 117528548 | ||||||
chr8:117528593
|
A | G | 1 | a0001c0001t0001g0039 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.178-58A>G | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 1/3 | chr8 | 117528593 | ||||||
chr8:117528624
|
T | C | 19 | a0001c0001t0002g0056a0001c0001t0003g0005a0001c0001t0003g0007others(16): Show | 44 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(41): Show |
intron_variant | MODIFIER | c.178-27T>C | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 1/3 | chr8 | 117528624 | ||||||
chr8:117528818
|
T | C | 4 | a0001c0001t0002g0034a0001c0001t0002g0125a0001c0001t0002g0126others(1): Show | 5 | HG00544.hp1 HG02132.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.336+9T>C | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 2/3 | chr8 | 117528818 | ||||||
chr8:117529413
|
G | A | 7 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0071others(4): Show | 9 | HG01175.hp1 HG01346.hp1 HG01952.hp2 others(6): Show |
intron_variant | MODIFIER | c.336+604G>A | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 2/3 | chr8 | 117529413 | ||||||
chr8:117529496
|
A | C | 1 | a0001c0001t0001g0108 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.336+687A>C | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 2/3 | chr8 | 117529496 | ||||||
chr8:117529598
|
T | G | 17 | a0001c0001t0002g0012a0001c0001t0002g0018a0001c0001t0002g0029others(14): Show | 43 | HG00140.hp1 HG00438.hp1 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.336+789T>G | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 2/3 | chr8 | 117529598 | ||||||
chr8:117529624
|
G | A | 4 | a0001c0001t0004g0129a0001c0001t0004g0130a0001c0001t0004g0131others(1): Show | 4 | HG00639.hp2 HG00733.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.336+815G>A | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 2/3 | chr8 | 117529624 | ||||||
chr8:117529627
|
A | C | 4 | a0001c0001t0001g0031a0001c0001t0001g0071a0001c0001t0001g0073others(1): Show | 5 | HG01175.hp1 HG01346.hp1 HG01952.hp2 others(2): Show |
intron_variant | MODIFIER | c.336+818A>C | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 2/3 | chr8 | 117529627 | ||||||
chr8:117529680
|
T | C | 1 | a0001c0001t0002g0046 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.336+871T>C | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 2/3 | chr8 | 117529680 | ||||||
chr8:117529791
|
G | A | 1 | a0001c0001t0001g0115 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.337-932G>A | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 2/3 | chr8 | 117529791 | ||||||
chr8:117530048
|
G | A | 1 | a0001c0001t0001g0090 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.337-675G>A | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 2/3 | chr8 | 117530048 | ||||||
chr8:117530181
|
G | A | 16 | a0001c0001t0002g0034a0001c0001t0002g0125a0001c0001t0002g0126others(13): Show | 25 | HG00544.hp1 HG00639.hp2 HG00733.hp2 others(22): Show |
intron_variant | MODIFIER | c.337-542G>A | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 2/3 | chr8 | 117530181 | ||||||
chr8:117530218
|
A | G | 1 | a0001c0001t0001g0107 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.337-505A>G | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 2/3 | chr8 | 117530218 | ||||||
chr8:117530262
|
G | T | 1 | a0001c0001t0002g0052 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.337-461G>T | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 2/3 | chr8 | 117530262 | ||||||
chr8:117530423
|
T | C | 9 | a0001c0001t0002g0056a0001c0001t0003g0005a0001c0001t0003g0016others(6): Show | 24 | HG01256.hp1 NA18941.hp1 NA18944.hp2 others(21): Show |
intron_variant | MODIFIER | c.337-300T>C | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 2/3 | chr8 | 117530423 | ||||||
chr8:117530496
|
C | A | 17 | a0001c0001t0002g0012a0001c0001t0002g0018a0001c0001t0002g0029others(14): Show | 43 | HG00140.hp1 HG00438.hp1 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.337-227C>A | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 2/3 | chr8 | 117530496 | ||||||
chr8:117530602
|
G | A | 6 | a0001c0001t0002g0012a0001c0001t0002g0018a0001c0001t0002g0029others(3): Show | 12 | HG01109.hp1 HG01891.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.337-121G>A | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 2/3 | chr8 | 117530602 | ||||||
chr8:117530983
|
AG | A | 2 | a0001c0001t0003g0025a0001c0001t0003g0062 | 3 | HG02622.hp1 HG02970.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.441+158delG | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 117530983 | |||||
chr8:117531087
|
T | A | 9 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0071others(6): Show | 11 | HG01175.hp1 HG01346.hp1 HG01952.hp2 others(8): Show |
intron_variant | MODIFIER | c.441+260T>A | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 3/3 | chr8 | 117531087 | ||||||
chr8:117531333
|
T | G | 1 | a0001c0001t0003g0057 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.441+506T>G | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 3/3 | chr8 | 117531333 | ||||||
chr8:117531431
|
C | T | 4 | a0001c0001t0004g0129a0001c0001t0004g0130a0001c0001t0004g0131others(1): Show | 4 | HG00639.hp2 HG00733.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.441+604C>T | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 3/3 | chr8 | 117531431 | ||||||
chr8:117531703
|
T | A | 1 | a0001c0001t0002g0067 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.441+876T>A | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 3/3 | chr8 | 117531703 | ||||||
chr8:117531704
|
A | T | 1 | a0001c0001t0002g0054 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.441+877A>T | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 3/3 | chr8 | 117531704 | ||||||
chr8:117531772
|
A | C | 1 | a0001c0001t0001g0106 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.441+945A>C | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 3/3 | chr8 | 117531772 | ||||||
chr8:117531829
|
A | T | 47 | a0001c0001t0001g0111a0001c0001t0002g0002a0001c0001t0002g0006others(44): Show | 112 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.441+1002A>T | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 3/3 | chr8 | 117531829 | ||||||
chr8:117532130
|
A | G | 3 | a0001c0001t0005g0020a0001c0001t0005g0136a0001c0001t0005g0137 | 5 | HG00639.hp1 HG02145.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.441+1303A>G | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 3/3 | chr8 | 117532130 | ||||||
chr8:117532206
|
A | G | 8 | a0001c0001t0004g0004a0001c0001t0004g0037a0001c0001t0004g0038others(5): Show | 23 | HG00140.hp1 HG00438.hp1 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.441+1379A>G | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 3/3 | chr8 | 117532206 | ||||||
chr8:117532443
|
G | T | 2 | a0001c0001t0001g0070a0001c0001t0001g0105 | 2 | HG02083.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.441+1616G>T | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 3/3 | chr8 | 117532443 | ||||||
chr8:117532558
|
G | A | 1 | a0001c0001t0001g0091 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.441+1731G>A | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 3/3 | chr8 | 117532558 | ||||||
chr8:117532562
|
G | A | 1 | a0001c0001t0002g0047 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.441+1735G>A | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 3/3 | chr8 | 117532562 | ||||||
chr8:117532575
|
C | G | 1 | a0001c0001t0003g0057 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.441+1748C>G | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 3/3 | chr8 | 117532575 | ||||||
chr8:117532649
|
T | G | 17 | a0001c0001t0002g0012a0001c0001t0002g0018a0001c0001t0002g0029others(14): Show | 43 | HG00140.hp1 HG00438.hp1 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.441+1822T>G | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 3/3 | chr8 | 117532649 | ||||||
chr8:117532691
|
A | C | 1 | a0001c0001t0004g0142 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.441+1864A>C | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 3/3 | chr8 | 117532691 | ||||||
chr8:117532715
|
G | A | 3 | a0001c0001t0005g0020a0001c0001t0005g0136a0001c0001t0005g0137 | 5 | HG00639.hp1 HG02145.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.441+1888G>A | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 3/3 | chr8 | 117532715 | ||||||
chr8:117532943
|
T | C | 1 | a0001c0001t0001g0115 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.441+2116T>C | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 3/3 | chr8 | 117532943 | ||||||
chr8:117533113
|
A | G | 1 | a0001c0001t0001g0104 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.441+2286A>G | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 3/3 | chr8 | 117533113 | ||||||
chr8:117533337
|
G | A | 6 | a0001c0001t0002g0012a0001c0001t0002g0018a0001c0001t0002g0029others(3): Show | 12 | HG01109.hp1 HG01891.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.441+2510G>A | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 3/3 | chr8 | 117533337 | ||||||
chr8:117533363
|
A | G | 1 | a0001c0001t0002g0045 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.441+2536A>G | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 3/3 | chr8 | 117533363 | ||||||
chr8:117533371
|
T | C | 1 | a0001c0001t0003g0007 | 6 | HG00140.hp2 HG01346.hp2 HG01928.hp2 others(3): Show |
intron_variant | MODIFIER | c.441+2544T>C | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 3/3 | chr8 | 117533371 | ||||||
chr8:117533414
|
T | A | 1 | a0001c0001t0001g0110 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.441+2587T>A | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 3/3 | chr8 | 117533414 | ||||||
chr8:117533550
|
A | G | 4 | a0001c0001t0005g0010a0001c0001t0005g0036a0001c0001t0005g0134others(1): Show | 9 | HG01243.hp1 HG01884.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.441+2723A>G | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 3/3 | chr8 | 117533550 | ||||||
chr8:117533555
|
G | A | 1 | a0001c0001t0001g0092 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.441+2728G>A | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 3/3 | chr8 | 117533555 | ||||||
chr8:117533625
|
T | TTTAA | 47 | a0001c0001t0001g0111a0001c0001t0002g0002a0001c0001t0002g0006others(44): Show | 112 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.441+2801_441+2804d others(6): Show |
MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 117533625 | |||||
chr8:117533852
|
A | C | 2 | a0001c0001t0002g0034a0001c0001t0002g0127 | 3 | HG02132.hp2 NA18975.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.441+3025A>C | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 3/3 | chr8 | 117533852 | ||||||
chr8:117534174
|
C | A | 2 | a0001c0001t0001g0079a0001c0001t0001g0093 | 2 | NA18960.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.441+3347C>A | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 3/3 | chr8 | 117534174 | ||||||
chr8:117534174
|
C | T | 2 | a0001c0001t0006g0019a0001c0001t0006g0133 | 4 | HG02572.hp1 HG02647.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.441+3347C>T | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 3/3 | chr8 | 117534174 | ||||||
chr8:117534512
|
G | A | 28 | a0001c0001t0001g0111a0001c0001t0002g0002a0001c0001t0002g0006others(25): Show | 68 | HG00280.hp1 HG00558.hp2 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.441+3685G>A | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 3/3 | chr8 | 117534512 | ||||||
chr8:117534523
|
C | CTGA | 28 | a0001c0001t0001g0111a0001c0001t0002g0002a0001c0001t0002g0006others(25): Show | 68 | HG00280.hp1 HG00558.hp2 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.441+3699_441+3701d others(5): Show |
MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 117534523 | |||||
chr8:117534571
|
G | A | 1 | a0001c0001t0001g0094 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.441+3744G>A | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 3/3 | chr8 | 117534571 | ||||||
chr8:117534586
|
C | G | 1 | a0001c0001t0002g0125 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.441+3759C>G | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 3/3 | chr8 | 117534586 | ||||||
chr8:117534624
|
A | G | 1 | a0001c0001t0001g0089 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.441+3797A>G | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 3/3 | chr8 | 117534624 | ||||||
chr8:117534727
|
A | G | 4 | a0001c0001t0002g0034a0001c0001t0002g0125a0001c0001t0002g0126others(1): Show | 5 | HG00544.hp1 HG02132.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.441+3900A>G | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 3/3 | chr8 | 117534727 | ||||||
chr8:117534827
|
A | G | 1 | a0001c0001t0001g0103 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.441+4000A>G | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 3/3 | chr8 | 117534827 | ||||||
chr8:117534850
|
G | GT | 13 | a0001c0001t0001g0003a0001c0001t0001g0078a0001c0001t0001g0081others(10): Show | 33 | HG00609.hp1 HG00609.hp2 HG00621.hp1 others(30): Show |
intron_variant | MODIFIER | c.441+4041dupT | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 117534850 | |||||
chr8:117534850
|
G | GTTT | 4 | a0001c0001t0002g0028a0001c0001t0002g0048a0001c0001t0005g0010others(1): Show | 9 | HG01243.hp1 HG02280.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.441+4039_441+4041d others(5): Show |
MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 117534850 | |||||
chr8:117534850
|
G | GTTTT | 14 | a0001c0001t0002g0056a0001c0001t0003g0005a0001c0001t0003g0016others(11): Show | 32 | HG01256.hp1 HG01884.hp2 HG01891.hp2 others(29): Show |
intron_variant | MODIFIER | c.441+4038_441+4041d others(6): Show |
MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 117534850 | |||||
chr8:117534850
|
G | GTTTTT | 11 | a0001c0001t0002g0034a0001c0001t0002g0068a0001c0001t0002g0125others(8): Show | 22 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(19): Show |
intron_variant | MODIFIER | c.441+4037_441+4041d others(7): Show |
MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 117534850 | |||||
chr8:117534850
|
G | GTTTTTT | 11 | a0001c0001t0001g0072a0001c0001t0002g0014a0001c0001t0002g0018others(8): Show | 17 | HG00558.hp2 HG00642.hp2 HG01261.hp1 others(14): Show |
intron_variant | MODIFIER | c.441+4036_441+4041d others(8): Show |
MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 117534850 | |||||
chr8:117534850
|
G | GTTTTTTT | 37 | a0001c0001t0001g0030a0001c0001t0001g0039a0001c0001t0001g0071others(34): Show | 88 | HG00140.hp1 HG00280.hp1 HG00639.hp1 others(85): Show |
intron_variant | MODIFIER | c.441+4035_441+4041d others(9): Show |
MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 117534850 | |||||
chr8:117534850
|
G | GTTTTTTT others(1): Show |
9 | a0001c0001t0001g0031a0001c0001t0001g0111a0001c0001t0002g0006others(6): Show | 17 | HG00438.hp1 HG00733.hp2 HG01175.hp1 others(14): Show |
intron_variant | MODIFIER | c.441+4034_441+4041d others(10): Show |
MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 117534850 | |||||
chr8:117534850
|
G | GTTTTTTT others(3): Show |
2 | a0001c0001t0004g0035a0001c0001t0004g0128 | 3 | HG02965.hp1 HG03098.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.441+4032_441+4041d others(12): Show |
MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 117534850 | |||||
chr8:117534850
|
G | T | 1 | a0001c0001t0004g0013 | 4 | HG02723.hp2 HG02976.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.441+4023G>T | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 3/3 | chr8 | 117534850 | ||||||
chr8:117535008
|
T | A | 28 | a0001c0001t0001g0111a0001c0001t0002g0002a0001c0001t0002g0006others(25): Show | 68 | HG00280.hp1 HG00558.hp2 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.441+4181T>A | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 3/3 | chr8 | 117535008 | ||||||
chr8:117535218
|
T | C | 1 | a0001c0001t0001g0094 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.441+4391T>C | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 3/3 | chr8 | 117535218 | ||||||
chr8:117535239
|
C | CT | 12 | a0001c0001t0001g0009a0001c0001t0001g0086a0001c0001t0001g0089others(9): Show | 21 | HG00140.hp1 HG00438.hp1 HG01192.hp2 others(18): Show |
intron_variant | MODIFIER | c.441+4433dupT | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 117535239 | |||||
chr8:117535239
|
CT | C | 26 | a0001c0001t0001g0095a0001c0001t0002g0012a0001c0001t0002g0018others(23): Show | 50 | HG00323.hp1 HG00544.hp1 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.441+4433delT | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 117535239 | |||||
chr8:117535282
|
T | C | 1 | a0001c0001t0002g0047 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.441+4455T>C | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 3/3 | chr8 | 117535282 | ||||||
chr8:117535284
|
AC | A | 4 | a0001c0001t0002g0034a0001c0001t0002g0125a0001c0001t0002g0126others(1): Show | 5 | HG00544.hp1 HG02132.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.441+4460delC | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 117535284 | |||||
chr8:117535307
|
C | T | 2 | a0001c0001t0001g0111a0001c0001t0002g0064 | 2 | HG01884.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.441+4480C>T | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 3/3 | chr8 | 117535307 | ||||||
chr8:117535365
|
G | T | 11 | a0001c0001t0003g0005a0001c0001t0003g0016a0001c0001t0003g0024others(8): Show | 27 | HG01256.hp1 HG02622.hp1 HG02809.hp2 others(24): Show |
intron_variant | MODIFIER | c.442-4518G>T | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 3/3 | chr8 | 117535365 | ||||||
chr8:117535535
|
C | CT | 4 | a0001c0001t0001g0113a0001c0001t0001g0116a0001c0001t0006g0019others(1): Show | 6 | HG02165.hp1 HG02165.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.442-4337dupT | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 117535535 | |||||
chr8:117535566
|
C | T | 2 | a0001c0001t0006g0019a0001c0001t0006g0133 | 4 | HG02572.hp1 HG02647.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.442-4317C>T | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 3/3 | chr8 | 117535566 | ||||||
chr8:117535569
|
G | A | 15 | a0001c0001t0004g0004a0001c0001t0004g0013a0001c0001t0004g0021others(12): Show | 40 | HG00140.hp1 HG00438.hp1 HG00642.hp1 others(37): Show |
intron_variant | MODIFIER | c.442-4314G>A | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 3/3 | chr8 | 117535569 | ||||||
chr8:117535579
|
C | T | 6 | a0001c0001t0001g0070a0001c0001t0001g0099a0001c0001t0001g0100others(3): Show | 6 | HG02083.hp2 NA18946.hp1 NA18956.hp1 others(3): Show |
intron_variant | MODIFIER | c.442-4304C>T | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 3/3 | chr8 | 117535579 | ||||||
chr8:117535677
|
A | G | 28 | a0001c0001t0001g0111a0001c0001t0002g0002a0001c0001t0002g0006others(25): Show | 68 | HG00280.hp1 HG00558.hp2 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.442-4206A>G | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 3/3 | chr8 | 117535677 | ||||||
chr8:117535781
|
T | G | 6 | a0001c0001t0002g0034a0001c0001t0002g0125a0001c0001t0002g0126others(3): Show | 9 | HG00544.hp1 HG02132.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.442-4102T>G | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 3/3 | chr8 | 117535781 | ||||||
chr8:117535801
|
T | C | 1 | a0001c0001t0002g0049 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.442-4082T>C | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 3/3 | chr8 | 117535801 | ||||||
chr8:117536058
|
A | G | 2 | a0001c0001t0006g0019a0001c0001t0006g0133 | 4 | HG02572.hp1 HG02647.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.442-3825A>G | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 3/3 | chr8 | 117536058 | ||||||
chr8:117536123
|
T | C | 1 | a0001c0001t0002g0050 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.442-3760T>C | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 3/3 | chr8 | 117536123 | ||||||
chr8:117536585
|
T | C | 1 | a0001c0001t0001g0099 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.442-3298T>C | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 3/3 | chr8 | 117536585 | ||||||
chr8:117536700
|
C | T | 1 | a0001c0001t0001g0088 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.442-3183C>T | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 3/3 | chr8 | 117536700 | ||||||
chr8:117536711
|
T | C | 1 | a0001c0001t0001g0100 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.442-3172T>C | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 3/3 | chr8 | 117536711 | ||||||
chr8:117536767
|
T | G | 8 | a0001c0001t0002g0034a0001c0001t0002g0125a0001c0001t0002g0126others(5): Show | 14 | HG00544.hp1 HG01243.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.442-3116T>G | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 3/3 | chr8 | 117536767 | ||||||
chr8:117537072
|
C | T | 1 | a0001c0001t0002g0069 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.442-2811C>T | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 3/3 | chr8 | 117537072 | ||||||
chr8:117537073
|
G | A | 1 | a0001c0001t0001g0070 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.442-2810G>A | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 3/3 | chr8 | 117537073 | ||||||
chr8:117537137
|
T | C | 19 | a0001c0001t0002g0056a0001c0001t0003g0005a0001c0001t0003g0007others(16): Show | 44 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(41): Show |
intron_variant | MODIFIER | c.442-2746T>C | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 3/3 | chr8 | 117537137 | ||||||
chr8:117537208
|
A | G | 10 | a0001c0001t0002g0034a0001c0001t0002g0125a0001c0001t0002g0126others(7): Show | 18 | HG00544.hp1 HG01243.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.442-2675A>G | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 3/3 | chr8 | 117537208 | ||||||
chr8:117537271
|
G | A | 2 | a0001c0001t0006g0019a0001c0001t0006g0133 | 4 | HG02572.hp1 HG02647.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.442-2612G>A | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 3/3 | chr8 | 117537271 | ||||||
chr8:117537572
|
A | C | 1 | a0001c0001t0001g0098 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.442-2311A>C | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 3/3 | chr8 | 117537572 | ||||||
chr8:117537759
|
G | A | 1 | a0001c0001t0003g0058 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.442-2124G>A | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 3/3 | chr8 | 117537759 | ||||||
chr8:117537788
|
G | GT | 9 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0071others(6): Show | 11 | HG01175.hp1 HG01346.hp1 HG01952.hp2 others(8): Show |
intron_variant | MODIFIER | c.442-2090dupT | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 117537788 | |||||
chr8:117537889
|
GAA | G | 2 | a0001c0001t0002g0028a0002c0002t0002g0017 | 5 | HG02630.hp1 HG02895.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.442-1991_442-1990d others(4): Show |
MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 117537889 | |||||
chr8:117538651
|
T | C | 29 | a0001c0001t0001g0096a0001c0001t0001g0111a0001c0001t0002g0002others(26): Show | 69 | HG00280.hp1 HG00558.hp2 HG00639.hp1 others(66): Show |
intron_variant | MODIFIER | c.442-1232T>C | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 3/3 | chr8 | 117538651 | ||||||
chr8:117538663
|
A | T | 7 | a0001c0001t0003g0007a0001c0001t0003g0011a0001c0001t0003g0026others(4): Show | 16 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(13): Show |
intron_variant | MODIFIER | c.442-1220A>T | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 3/3 | chr8 | 117538663 | ||||||
chr8:117538990
|
A | C | 6 | a0001c0001t0002g0034a0001c0001t0002g0125a0001c0001t0002g0126others(3): Show | 9 | HG00544.hp1 HG02132.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.442-893A>C | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 3/3 | chr8 | 117538990 | ||||||
chr8:117539015
|
T | TAACA | 4 | a0001c0001t0005g0010a0001c0001t0005g0036a0001c0001t0005g0134others(1): Show | 9 | HG01243.hp1 HG01884.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.442-867_442-864dup others(4): Show |
MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 117539015 | |||||
chr8:117539019
|
A | G | 1 | a0001c0001t0001g0039 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.442-864A>G | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 3/3 | chr8 | 117539019 | ||||||
chr8:117539066
|
A | G | 29 | a0001c0001t0001g0096a0001c0001t0001g0111a0001c0001t0002g0002others(26): Show | 69 | HG00280.hp1 HG00558.hp2 HG00639.hp1 others(66): Show |
intron_variant | MODIFIER | c.442-817A>G | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 3/3 | chr8 | 117539066 | ||||||
chr8:117539162
|
G | A | 1 | a0001c0001t0001g0102 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.442-721G>A | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 3/3 | chr8 | 117539162 | ||||||
chr8:117539199
|
T | C | 6 | a0001c0001t0002g0034a0001c0001t0002g0125a0001c0001t0002g0126others(3): Show | 9 | HG00544.hp1 HG02132.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.442-684T>C | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 3/3 | chr8 | 117539199 | ||||||
chr8:117539217
|
G | A | 1 | a0001c0001t0002g0069 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.442-666G>A | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 3/3 | chr8 | 117539217 | ||||||
chr8:117539364
|
C | T | 4 | a0001c0001t0004g0129a0001c0001t0004g0130a0001c0001t0004g0131others(1): Show | 4 | HG00639.hp2 HG00733.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.442-519C>T | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 3/3 | chr8 | 117539364 | ||||||
chr8:117539374
|
T | C | 92 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0039others(89): Show | 197 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(194): Show |
intron_variant | MODIFIER | c.442-509T>C | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 3/3 | chr8 | 117539374 | ||||||
chr8:117539467
|
GA | G | 7 | a0001c0001t0001g0097a0001c0001t0004g0035a0001c0001t0004g0128others(4): Show | 13 | HG01243.hp1 HG01884.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.442-402delA | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 117539467 | |||||
chr8:117539575
|
T | C | 1 | a0001c0001t0001g0109 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.442-308T>C | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 3/3 | chr8 | 117539575 | ||||||
chr8:117539603
|
T | C | 7 | a0001c0001t0003g0007a0001c0001t0003g0011a0001c0001t0003g0026others(4): Show | 16 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(13): Show |
intron_variant | MODIFIER | c.442-280T>C | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 3/3 | chr8 | 117539603 | ||||||
chr8:117539661
|
G | A | 11 | a0001c0001t0003g0005a0001c0001t0003g0016a0001c0001t0003g0024others(8): Show | 27 | HG01256.hp1 HG02622.hp1 HG02809.hp2 others(24): Show |
intron_variant | MODIFIER | c.442-222G>A | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 3/3 | chr8 | 117539661 | ||||||
chr8:117539748
|
AC | A | 2 | a0001c0001t0006g0019a0001c0001t0006g0133 | 4 | HG02572.hp1 HG02647.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.442-133delC | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr8 | 117539748 | |||||
chr8:117539793
|
A | G | 3 | a0001c0001t0003g0026a0001c0001t0003g0060a0001c0001t0003g0061 | 4 | HG00323.hp1 HG00642.hp2 HG00738.hp1 others(1): Show |
intron_variant | MODIFIER | c.442-90A>G | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 3/3 | chr8 | 117539793 | ||||||
chr8:117539829
|
C | T | 1 | a0001c0001t0002g0028 | 2 | HG02895.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.442-54C>T | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 3/3 | chr8 | 117539829 | ||||||
chr8:117539853
|
C | T | 1 | a0001c0001t0001g0122 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.442-30C>T | MED30 | ENSG00000164758.7 | transcript | ENST00000297347.7 | protein_coding | 3/3 | chr8 | 117539853 |