geneid | 5229 |
---|---|
ensemblid | ENSG00000164219.10 |
hgncid | 8895 |
symbol | PGGT1B |
name | protein geranylgeranyltransferase type I subunit beta |
refseq_nuc | NM_005023.4 |
refseq_prot | NP_005014.2 |
ensembl_nuc | ENST00000419445.6 |
ensembl_prot | ENSP00000404676.1 |
mane_status | MANE Select |
chr | chr5 |
start | 115204012 |
end | 115262877 |
strand | - |
ver | v1.2 |
region | chr5:115204012-115262877 |
region5000 | chr5:115199012-115267877 |
regionname0 | PGGT1B_chr5_115204012_115262877 |
regionname5000 | PGGT1B_chr5_115199012_115267877 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 377 | 367 | 85 | 74 | 150 | 16 | 40 | 118 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0002 | 0/0 | 377 | 4 | 3 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0003 | 0/0 | 377 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1134 | 349 | 85 | 73 | 134 | 16 | 39 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
c0002 | 0/0 | 1134 | 16 | 0 | 1 | 15 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
c0003 | 0/0 | 1134 | 4 | 3 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
c0004 | 0/0 | 1134 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
c0005 | 0/0 | 1134 | 1 | 0 | 0 | 0 | 0 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
c0006 | 0/0 | 1134 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 8409 | 54 | 5 | 8 | 36 | 2 | 3 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
t0002 | 1/0 | 8417 | 24 | 0 | 7 | 11 | 2 | 3 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
t0003 | 0/0 | 8422 | 18 | 0 | 7 | 7 | 0 | 4 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
t0004 | 0/0 | 8435 | 12 | 0 | 0 | 11 | 1 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
t0005 | 0/0 | 8408 | 11 | 0 | 0 | 11 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
t0006 | 0/0 | 8419 | 11 | 1 | 0 | 7 | 0 | 3 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
t0007 | 0/0 | 8437 | 9 | 2 | 0 | 5 | 1 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
t0008 | 0/0 | 8409 | 9 | 0 | 0 | 9 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
t0009 | 0/0 | 8421 | 9 | 0 | 3 | 2 | 3 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
t0010 | 0/0 | 8439 | 8 | 0 | 4 | 2 | 0 | 2 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
t0011 | 0/0 | 8433 | 6 | 0 | 0 | 5 | 0 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
t0012 | 0/0 | 8441 | 5 | 0 | 2 | 3 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
t0013 | 0/0 | 8424 | 5 | 1 | 4 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
t0014 | 0/0 | 8433 | 4 | 4 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
t0015 | 0/0 | 8436 | 4 | 0 | 1 | 2 | 1 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
t0016 | 0/0 | 8418 | 4 | 0 | 3 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
t0017 | 0/0 | 8424 | 3 | 3 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
t0018 | 0/0 | 8431 | 3 | 0 | 2 | 0 | 0 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
t0019 | 0/0 | 8447 | 3 | 0 | 1 | 2 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
t0020 | 0/0 | 8443 | 3 | 0 | 1 | 1 | 0 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
t0021 | 0/0 | 8433 | 3 | 0 | 1 | 0 | 1 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
t0022 | 0/0 | 8429 | 3 | 0 | 1 | 1 | 1 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
t0023 | 0/1 | 8432 | 3 | 0 | 1 | 0 | 1 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
t0024 | 0/0 | 8410 | 3 | 1 | 0 | 1 | 0 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
t0025 | 0/0 | 8433 | 3 | 2 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
t0026 | 0/0 | 8438 | 3 | 2 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
t0027 | 0/0 | 8436 | 3 | 2 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
t0028 | 0/0 | 8434 | 3 | 0 | 1 | 0 | 0 | 2 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
t0029 | 0/0 | 8430 | 3 | 1 | 0 | 0 | 0 | 2 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
t0030 | 0/0 | 8420 | 3 | 0 | 0 | 3 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
t0031 | 0/0 | 8423 | 3 | 0 | 0 | 3 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
t0032 | 0/0 | 8422 | 3 | 1 | 0 | 0 | 0 | 2 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
t0033 | 0/0 | 8423 | 3 | 0 | 1 | 2 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
t0034 | 0/0 | 8433 | 2 | 2 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
t0035 | 0/0 | 8431 | 2 | 1 | 0 | 0 | 0 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
t0036 | 0/0 | 8409 | 2 | 2 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
t0037 | 0/0 | 8431 | 2 | 0 | 0 | 2 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
t0038 | 0/0 | 8429 | 2 | 2 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
t0039 | 0/0 | 8425 | 2 | 2 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
t0040 | 0/0 | 8437 | 2 | 2 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
t0041 | 0/0 | 8410 | 2 | 2 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
t0042 | 0/0 | 8428 | 2 | 2 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
t0043 | 0/0 | 8409 | 2 | 0 | 0 | 0 | 0 | 2 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
t0044 | 0/0 | 8438 | 2 | 0 | 1 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
t0045 | 0/0 | 8433 | 2 | 2 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
t0046 | 0/0 | 8437 | 2 | 2 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
t0047 | 0/0 | 8418 | 2 | 0 | 0 | 2 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
t0048 | 0/0 | 8434 | 2 | 2 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
t0049 | 0/0 | 8442 | 2 | 2 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
t0050 | 0/0 | 8432 | 2 | 0 | 1 | 0 | 0 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
t0051 | 0/0 | 8411 | 2 | 2 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
t0052 | 0/0 | 8421 | 2 | 0 | 0 | 2 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
t0053 | 0/0 | 8426 | 2 | 0 | 1 | 0 | 1 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
t0054 | 0/0 | 8434 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
t0055 | 0/0 | 8412 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
t0056 | 0/0 | 8412 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
t0057 | 0/0 | 8437 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
t0058 | 0/0 | 8431 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
t0059 | 0/0 | 8431 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
t0060 | 0/0 | 8448 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
t0061 | 0/0 | 8438 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
t0062 | 0/0 | 8424 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
t0063 | 0/0 | 8428 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
t0064 | 0/0 | 8429 | 1 | 0 | 0 | 0 | 0 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
t0065 | 0/0 | 8439 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
t0066 | 0/0 | 8439 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
t0067 | 0/0 | 8433 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
t0068 | 0/0 | 8445 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
t0069 | 0/0 | 8441 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
t0070 | 0/0 | 8433 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
t0071 | 0/0 | 8449 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
t0072 | 0/0 | 8445 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
t0073 | 0/0 | 8443 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
t0074 | 0/0 | 8441 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
t0075 | 0/0 | 8439 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
t0076 | 0/0 | 8437 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
t0077 | 0/0 | 8435 | 1 | 0 | 0 | 0 | 0 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
t0078 | 0/0 | 8431 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
t0079 | 0/0 | 8425 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
t0080 | 0/0 | 8419 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
t0081 | 0/0 | 8439 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
t0082 | 0/0 | 8411 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
t0083 | 0/0 | 8431 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
t0084 | 0/0 | 8429 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
t0085 | 0/0 | 8427 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
t0086 | 0/0 | 8425 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
t0087 | 0/0 | 8437 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
t0088 | 0/0 | 8435 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
t0089 | 0/0 | 8432 | 1 | 0 | 0 | 0 | 0 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
t0090 | 0/0 | 8432 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
t0091 | 0/0 | 8439 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
t0092 | 0/0 | 8445 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
t0093 | 0/0 | 8443 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
t0094 | 0/0 | 8441 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
t0095 | 0/0 | 8439 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
t0096 | 0/0 | 8433 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
t0097 | 0/0 | 8409 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
t0098 | 0/0 | 8408 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
t0099 | 0/0 | 8411 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
t0100 | 0/0 | 8409 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
t0101 | 0/0 | 8409 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
t0102 | 0/0 | 8410 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
t0103 | 0/0 | 8447 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
t0104 | 0/0 | 8443 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
t0105 | 0/0 | 8439 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
t0106 | 0/0 | 8422 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
t0107 | 0/0 | 8450 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
t0108 | 0/0 | 8446 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
t0109 | 0/0 | 8442 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
t0110 | 0/0 | 8434 | 1 | 0 | 0 | 0 | 1 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
t0111 | 0/0 | 8409 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
t0112 | 0/0 | 8410 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
t0113 | 0/0 | 8444 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
t0114 | 0/0 | 8438 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
t0115 | 0/0 | 8410 | 1 | 0 | 0 | 0 | 0 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
t0116 | 0/0 | 8414 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
t0117 | 0/0 | 8445 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
t0118 | 0/0 | 8441 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
t0119 | 0/0 | 8435 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
t0120 | 0/0 | 8429 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
t0121 | 0/0 | 8411 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
t0122 | 0/0 | 8420 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
t0123 | 0/0 | 8416 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
t0124 | 0/0 | 8437 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
t0125 | 0/0 | 8436 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
t0126 | 0/0 | 8432 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
t0127 | 0/0 | 8444 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
t0128 | 0/0 | 8440 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
t0129 | 0/0 | 8428 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
t0130 | 0/0 | 8417 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
t0131 | 0/0 | 8432 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
t0132 | 0/0 | 8425 | 1 | 0 | 0 | 0 | 0 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
t0133 | 0/0 | 8423 | 1 | 0 | 0 | 0 | 0 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
t0134 | 0/0 | 8428 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
t0135 | 0/0 | 8422 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
t0136 | 0/0 | 8412 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
t0137 | 0/0 | 8417 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
t0138 | 0/0 | 8425 | 1 | 0 | 0 | 0 | 0 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
t0139 | 0/0 | 8425 | 1 | 0 | 0 | 0 | 1 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
t0140 | 0/0 | 8419 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
t0141 | 0/0 | 8422 | 1 | 0 | 0 | 0 | 0 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0003 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0004 | 0/0 | 3 | 0 | 0 | 0 | 2 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0007 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0012 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0015 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0016 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0075 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0319 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0324 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0341 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1134 | 349 | 85 | 73 | 134 | 16 | 39 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0002 | 0/0 | 1134 | 16 | 0 | 1 | 15 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0005 | 0/0 | 1134 | 1 | 0 | 0 | 0 | 0 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0006 | 0/0 | 1134 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0002c0003 | 0/0 | 1134 | 4 | 3 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0003c0004 | 0/0 | 1134 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 9542 | 53 | 5 | 7 | 36 | 2 | 3 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0001t0002 | 1/0 | 9550 | 23 | 0 | 7 | 10 | 2 | 3 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0001t0003 | 0/0 | 9555 | 18 | 0 | 7 | 7 | 0 | 4 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0001t0004 | 0/0 | 9568 | 3 | 0 | 0 | 2 | 1 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0001t0005 | 0/0 | 9541 | 10 | 0 | 0 | 10 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0001t0006 | 0/0 | 9552 | 11 | 1 | 0 | 7 | 0 | 3 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0001t0007 | 0/0 | 9570 | 9 | 2 | 0 | 5 | 1 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0001t0008 | 0/0 | 9542 | 9 | 0 | 0 | 9 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0001t0009 | 0/0 | 9554 | 9 | 0 | 3 | 2 | 3 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0001t0010 | 0/0 | 9572 | 8 | 0 | 4 | 2 | 0 | 2 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0001t0011 | 0/0 | 9566 | 5 | 0 | 0 | 4 | 0 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0001t0012 | 0/0 | 9574 | 4 | 0 | 2 | 2 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0001t0013 | 0/0 | 9557 | 5 | 1 | 4 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0001t0014 | 0/0 | 9566 | 4 | 4 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0001t0015 | 0/0 | 9569 | 2 | 0 | 0 | 1 | 1 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0001t0016 | 0/0 | 9551 | 4 | 0 | 3 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0001t0017 | 0/0 | 9557 | 3 | 3 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0001t0018 | 0/0 | 9564 | 3 | 0 | 2 | 0 | 0 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0001t0019 | 0/0 | 9580 | 2 | 0 | 1 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0001t0020 | 0/0 | 9576 | 3 | 0 | 1 | 1 | 0 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0001t0021 | 0/0 | 9566 | 3 | 0 | 1 | 0 | 1 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0001t0022 | 0/0 | 9562 | 3 | 0 | 1 | 1 | 1 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0001t0023 | 0/1 | 9565 | 3 | 0 | 1 | 0 | 1 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0001t0024 | 0/0 | 9543 | 3 | 1 | 0 | 1 | 0 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0001t0025 | 0/0 | 9566 | 3 | 2 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0001t0026 | 0/0 | 9571 | 3 | 2 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0001t0027 | 0/0 | 9569 | 3 | 2 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0001t0028 | 0/0 | 9567 | 3 | 0 | 1 | 0 | 0 | 2 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0001t0029 | 0/0 | 9563 | 3 | 1 | 0 | 0 | 0 | 2 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0001t0030 | 0/0 | 9553 | 3 | 0 | 0 | 3 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0001t0031 | 0/0 | 9556 | 3 | 0 | 0 | 3 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0001t0032 | 0/0 | 9555 | 3 | 1 | 0 | 0 | 0 | 2 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0001t0033 | 0/0 | 9556 | 3 | 0 | 1 | 2 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0001t0035 | 0/0 | 9564 | 2 | 1 | 0 | 0 | 0 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0001t0036 | 0/0 | 9542 | 2 | 2 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0001t0037 | 0/0 | 9564 | 2 | 0 | 0 | 2 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0001t0038 | 0/0 | 9562 | 2 | 2 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0001t0039 | 0/0 | 9558 | 2 | 2 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0001t0040 | 0/0 | 9570 | 2 | 2 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0001t0041 | 0/0 | 9543 | 2 | 2 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0001t0042 | 0/0 | 9561 | 2 | 2 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0001t0043 | 0/0 | 9542 | 2 | 0 | 0 | 0 | 0 | 2 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0001t0044 | 0/0 | 9571 | 2 | 0 | 1 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0001t0045 | 0/0 | 9566 | 2 | 2 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0001t0046 | 0/0 | 9570 | 2 | 2 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0001t0047 | 0/0 | 9551 | 2 | 0 | 0 | 2 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0001t0048 | 0/0 | 9567 | 2 | 2 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0001t0049 | 0/0 | 9575 | 2 | 2 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0001t0050 | 0/0 | 9565 | 2 | 0 | 1 | 0 | 0 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0001t0051 | 0/0 | 9544 | 2 | 2 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0001t0052 | 0/0 | 9554 | 2 | 0 | 0 | 2 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0001t0053 | 0/0 | 9559 | 2 | 0 | 1 | 0 | 1 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0001t0054 | 0/0 | 9567 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0001t0055 | 0/0 | 9545 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0001t0056 | 0/0 | 9545 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0001t0059 | 0/0 | 9564 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0001t0060 | 0/0 | 9581 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0001t0061 | 0/0 | 9571 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0001t0062 | 0/0 | 9557 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0001t0063 | 0/0 | 9561 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0001t0064 | 0/0 | 9562 | 1 | 0 | 0 | 0 | 0 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0001t0065 | 0/0 | 9572 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0001t0066 | 0/0 | 9572 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0001t0067 | 0/0 | 9566 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0001t0068 | 0/0 | 9578 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0001t0069 | 0/0 | 9574 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0001t0071 | 0/0 | 9582 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0001t0072 | 0/0 | 9578 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0001t0073 | 0/0 | 9576 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0001t0074 | 0/0 | 9574 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0001t0075 | 0/0 | 9572 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0001t0076 | 0/0 | 9570 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0001t0077 | 0/0 | 9568 | 1 | 0 | 0 | 0 | 0 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0001t0078 | 0/0 | 9564 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0001t0079 | 0/0 | 9558 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0001t0080 | 0/0 | 9552 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0001t0081 | 0/0 | 9572 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0001t0082 | 0/0 | 9544 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0001t0083 | 0/0 | 9564 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0001t0084 | 0/0 | 9562 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0001t0085 | 0/0 | 9560 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0001t0086 | 0/0 | 9558 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0001t0087 | 0/0 | 9570 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0001t0088 | 0/0 | 9568 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0001t0089 | 0/0 | 9565 | 1 | 0 | 0 | 0 | 0 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0001t0090 | 0/0 | 9565 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0001t0091 | 0/0 | 9572 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0001t0092 | 0/0 | 9578 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0001t0093 | 0/0 | 9576 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0001t0094 | 0/0 | 9574 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0001t0095 | 0/0 | 9572 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0001t0096 | 0/0 | 9566 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0001t0097 | 0/0 | 9542 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0001t0098 | 0/0 | 9541 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0001t0099 | 0/0 | 9544 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0001t0100 | 0/0 | 9542 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0001t0101 | 0/0 | 9542 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0001t0102 | 0/0 | 9543 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0001t0103 | 0/0 | 9580 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0001t0104 | 0/0 | 9576 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0001t0105 | 0/0 | 9572 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0001t0106 | 0/0 | 9555 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0001t0107 | 0/0 | 9583 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0001t0108 | 0/0 | 9579 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0001t0109 | 0/0 | 9575 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0001t0110 | 0/0 | 9567 | 1 | 0 | 0 | 0 | 1 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0001t0111 | 0/0 | 9542 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0001t0112 | 0/0 | 9543 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0001t0113 | 0/0 | 9577 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0001t0114 | 0/0 | 9571 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0001t0115 | 0/0 | 9543 | 1 | 0 | 0 | 0 | 0 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0001t0116 | 0/0 | 9547 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0001t0117 | 0/0 | 9578 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0001t0118 | 0/0 | 9574 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0001t0119 | 0/0 | 9568 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0001t0120 | 0/0 | 9562 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0001t0121 | 0/0 | 9544 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0001t0122 | 0/0 | 9553 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0001t0123 | 0/0 | 9549 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0001t0124 | 0/0 | 9570 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0001t0125 | 0/0 | 9569 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0001t0126 | 0/0 | 9565 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0001t0127 | 0/0 | 9577 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0001t0128 | 0/0 | 9573 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0001t0129 | 0/0 | 9561 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0001t0130 | 0/0 | 9550 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0001t0131 | 0/0 | 9565 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0001t0132 | 0/0 | 9558 | 1 | 0 | 0 | 0 | 0 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0001t0134 | 0/0 | 9561 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0001t0135 | 0/0 | 9555 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0001t0136 | 0/0 | 9545 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0001t0137 | 0/0 | 9550 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0001t0138 | 0/0 | 9558 | 1 | 0 | 0 | 0 | 0 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0001t0139 | 0/0 | 9558 | 1 | 0 | 0 | 0 | 1 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0001t0140 | 0/0 | 9552 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0001t0141 | 0/0 | 9555 | 1 | 0 | 0 | 0 | 0 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0002t0004 | 0/0 | 9568 | 9 | 0 | 0 | 9 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0002t0005 | 0/0 | 9541 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0002t0011 | 0/0 | 9566 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0002t0012 | 0/0 | 9574 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0002t0015 | 0/0 | 9569 | 2 | 0 | 1 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0002t0019 | 0/0 | 9580 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0002t0070 | 0/0 | 9566 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0005t0133 | 0/0 | 9556 | 1 | 0 | 0 | 0 | 0 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0001c0006t0002 | 0/0 | 9550 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0002c0003t0034 | 0/0 | 9566 | 2 | 2 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0002c0003t0057 | 0/0 | 9570 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0002c0003t0058 | 0/0 | 9564 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
a0003c0004t0001 | 0/0 | 9542 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | copy fasta | chr5 | 115199012 | 115267877 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0002g0004 | 0/0 | 3 | 0 | 0 | 0 | 2 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0002g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0002g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0002g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0002g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0002g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0002g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0002g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0002g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0002g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0002g0324 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0002g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0002g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0002g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0002g0341 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0002g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0003g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0003g0003 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0003g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0003g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0003g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0003g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0003g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0003g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0003g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0003g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0003g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0003g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0003g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0003g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0004g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0004g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0004g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0005g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0005g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0005g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0005g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0005g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0005g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0005g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0005g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0005g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0006g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0006g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0006g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0006g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0006g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0006g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0006g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0006g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0006g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0007g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0007g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0007g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0007g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0007g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0007g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0007g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0007g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0007g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0008g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0008g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0008g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0008g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0008g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0008g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0008g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0009g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0009g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0009g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0009g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0009g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0009g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0009g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0009g0319 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0009g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0010g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0010g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0010g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0010g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0010g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0010g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0010g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0010g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0011g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0011g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0011g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0011g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0011g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0012g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0012g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0012g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0012g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0013g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0013g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0013g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0013g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0014g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0014g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0014g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0014g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0015g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0015g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0016g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0016g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0016g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0017g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0017g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0017g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0018g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0018g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0018g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0019g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0019g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0020g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0020g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0020g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0021g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0021g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0021g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0022g0007 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0022g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0023g0075 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0023g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0023g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0024g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0024g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0024g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0025g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0025g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0025g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0026g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0026g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0026g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0027g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0027g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0027g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0028g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0028g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0028g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0029g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0029g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0029g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0030g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0030g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0030g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0031g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0031g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0031g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0032g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0032g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0032g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0033g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0033g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0033g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0035g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0035g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0036g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0036g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0037g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0037g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0038g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0038g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0039g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0039g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0040g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0041g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0041g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0042g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0042g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0043g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0043g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0044g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0044g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0045g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0045g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0046g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0046g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0047g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0047g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0048g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0048g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0049g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0049g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0050g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0050g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0051g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0051g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0052g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0052g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0053g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0053g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0054g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0055g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0056g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0059g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0060g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0061g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0062g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0063g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0064g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0065g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0066g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0067g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0068g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0069g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0071g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0072g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0073g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0074g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0075g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0076g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0077g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0078g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0079g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0080g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0081g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0082g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0083g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0084g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0085g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0086g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0087g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0088g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0089g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0090g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0091g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0092g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0093g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0094g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0095g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0096g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0097g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0098g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0099g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0100g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0101g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0102g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0103g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0104g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0105g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0106g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0107g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0108g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0109g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0110g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0111g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0112g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0113g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0114g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0115g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0116g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0117g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0118g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0119g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0120g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0121g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0122g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0123g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0124g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0125g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0126g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0127g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0128g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0129g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0130g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0131g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0132g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0134g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0135g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0136g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0137g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0138g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0139g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0140g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0141g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0002t0004g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0002t0004g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0002t0004g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0002t0004g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0002t0004g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0002t0004g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0002t0004g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0002t0005g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0002t0011g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0002t0012g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0002t0015g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0002t0015g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0002t0019g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0002t0070g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0005t0133g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0006t0002g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0002c0003t0034g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0002c0003t0034g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0002c0003t0057g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0002c0003t0058g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0003c0004t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0009 | g0319 | EUR | GBR | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG00099 | hp2 | a0001 | c0001 | t0015 | g0079 | EUR | GBR | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG00140 | hp1 | a0001 | c0001 | t0004 | g0068 | EUR | GBR | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG00140 | hp2 | a0001 | c0001 | t0009 | g0248 | EUR | GBR | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG00280 | hp1 | a0001 | c0001 | t0023 | g0103 | EUR | FIN | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG00280 | hp2 | a0001 | c0001 | t0009 | g0238 | EUR | FIN | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG00323 | hp1 | a0001 | c0001 | t0139 | g0233 | EUR | FIN | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG00323 | hp2 | a0001 | c0001 | t0110 | g0074 | EUR | FIN | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG00408 | hp1 | a0001 | c0002 | t0005 | g0090 | EAS | CHS | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | CHS | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG00558 | hp1 | a0001 | c0001 | t0076 | g0073 | EAS | CHS | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | CHS | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG00609 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | CHS | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG00609 | hp2 | a0001 | c0001 | t0075 | g0072 | EAS | CHS | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | CHS | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG00621 | hp2 | a0001 | c0001 | t0022 | g0099 | EAS | CHS | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG00642 | hp1 | a0001 | c0001 | t0018 | g0046 | AMR | PUR | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG00642 | hp2 | a0001 | c0001 | t0073 | g0055 | AMR | PUR | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG00673 | hp1 | a0001 | c0001 | t0005 | g0093 | EAS | CHS | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG00673 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | CHS | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG00733 | hp1 | a0001 | c0001 | t0021 | g0054 | AMR | PUR | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG00733 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | PUR | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG00735 | hp1 | a0001 | c0001 | t0044 | g0085 | AMR | PUR | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG00735 | hp2 | a0001 | c0001 | t0009 | g0316 | AMR | PUR | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG00738 | hp1 | a0001 | c0001 | t0023 | g0098 | AMR | PUR | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG00738 | hp2 | a0001 | c0001 | t0002 | g0321 | AMR | PUR | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG00741 | hp1 | a0001 | c0001 | t0009 | g0247 | AMR | PUR | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0207 | AMR | PUR | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG01069 | hp1 | a0001 | c0001 | t0016 | g0304 | AMR | PUR | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG01069 | hp2 | a0001 | c0001 | t0003 | g0242 | AMR | PUR | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG01070 | hp1 | a0001 | c0001 | t0060 | g0109 | AMR | PUR | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG01070 | hp2 | a0001 | c0001 | t0013 | g0292 | AMR | PUR | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG01071 | hp1 | a0001 | c0001 | t0016 | g0018 | AMR | PUR | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG01071 | hp2 | a0001 | c0001 | t0071 | g0110 | AMR | PUR | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG01074 | hp1 | a0002 | c0003 | t0058 | g0150 | AMR | PUR | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG01074 | hp2 | a0001 | c0001 | t0018 | g0047 | AMR | PUR | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG01081 | hp1 | a0001 | c0001 | t0003 | g0251 | AMR | PUR | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG01081 | hp2 | a0001 | c0001 | t0010 | g0107 | AMR | PUR | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG01099 | hp1 | a0001 | c0001 | t0003 | g0230 | AMR | PUR | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG01099 | hp2 | a0001 | c0001 | t0022 | g0007 | AMR | PUR | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG01109 | hp1 | a0001 | c0001 | t0069 | g0202 | AMR | PUR | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG01109 | hp2 | a0001 | c0001 | t0016 | g0018 | AMR | PUR | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG01167 | hp2 | a0001 | c0001 | t0009 | g0234 | AMR | PUR | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG01168 | hp1 | a0001 | c0001 | t0068 | g0033 | AMR | PUR | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG01168 | hp2 | a0001 | c0001 | t0122 | g0243 | AMR | PUR | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG01192 | hp1 | a0001 | c0001 | t0027 | g0289 | AMR | PUR | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG01192 | hp2 | a0001 | c0001 | t0107 | g0197 | AMR | PUR | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG01243 | hp1 | a0001 | c0001 | t0025 | g0194 | AMR | PUR | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG01243 | hp2 | a0001 | c0001 | t0136 | g0266 | AMR | PUR | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG01256 | hp1 | a0001 | c0001 | t0010 | g0071 | AMR | CLM | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG01256 | hp2 | a0001 | c0001 | t0053 | g0250 | AMR | CLM | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG01257 | hp1 | a0001 | c0001 | t0019 | g0106 | AMR | CLM | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG01257 | hp2 | a0001 | c0001 | t0013 | g0017 | AMR | CLM | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG01258 | hp1 | a0001 | c0001 | t0010 | g0200 | AMR | CLM | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG01258 | hp2 | a0001 | c0001 | t0013 | g0017 | AMR | CLM | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG01261 | hp1 | a0001 | c0001 | t0065 | g0045 | AMR | CLM | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG01261 | hp2 | a0001 | c0001 | t0111 | g0144 | AMR | CLM | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG01346 | hp1 | a0001 | c0001 | t0003 | g0320 | AMR | CLM | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG01346 | hp2 | a0001 | c0001 | t0137 | g0254 | AMR | CLM | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG01361 | hp1 | a0001 | c0001 | t0010 | g0112 | AMR | CLM | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG01361 | hp2 | a0001 | c0001 | t0003 | g0258 | AMR | CLM | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG01433 | hp1 | a0001 | c0001 | t0072 | g0111 | AMR | CLM | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG01433 | hp2 | a0001 | c0001 | t0002 | g0331 | AMR | CLM | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG01496 | hp1 | a0001 | c0001 | t0120 | g0139 | AMR | CLM | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG01496 | hp2 | a0001 | c0001 | t0055 | g0295 | AMR | CLM | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0179 | EUR | IBS | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG01515 | hp2 | a0001 | c0001 | t0053 | g0244 | EUR | IBS | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG01516 | hp1 | a0001 | c0001 | t0002 | g0004 | EUR | IBS | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG01516 | hp2 | a0001 | c0001 | t0007 | g0064 | EUR | IBS | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG01517 | hp1 | a0001 | c0001 | t0002 | g0004 | EUR | IBS | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0015 | EUR | IBS | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG01884 | hp1 | a0001 | c0001 | t0036 | g0157 | AFR | ACB | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG01884 | hp2 | a0001 | c0001 | t0017 | g0186 | AFR | ACB | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | ACB | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG01891 | hp2 | a0001 | c0001 | t0129 | g0030 | AFR | ACB | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG01928 | hp1 | a0001 | c0001 | t0002 | g0311 | AMR | PEL | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG01928 | hp2 | a0001 | c0001 | t0012 | g0229 | AMR | PEL | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG01934 | hp1 | a0001 | c0001 | t0026 | g0277 | AMR | PEL | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG01943 | hp1 | a0001 | c0001 | t0123 | g0329 | AMR | PEL | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG01943 | hp2 | a0001 | c0001 | t0081 | g0065 | AMR | PEL | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | PEL | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG01952 | hp2 | a0001 | c0001 | t0002 | g0330 | AMR | PEL | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG01975 | hp1 | a0001 | c0001 | t0103 | g0191 | AMR | PEL | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG01975 | hp2 | a0003 | c0004 | t0001 | g0021 | AMR | PEL | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG01978 | hp1 | a0001 | c0001 | t0002 | g0344 | AMR | PEL | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG01978 | hp2 | a0001 | c0001 | t0033 | g0235 | AMR | PEL | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG01981 | hp1 | a0001 | c0001 | t0028 | g0267 | AMR | PEL | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG01993 | hp1 | a0001 | c0001 | t0013 | g0237 | AMR | PEL | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG01993 | hp2 | a0001 | c0001 | t0012 | g0226 | AMR | PEL | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG02004 | hp1 | a0001 | c0001 | t0134 | g0180 | AMR | PEL | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | PEL | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG02015 | hp1 | a0001 | c0001 | t0005 | g0300 | EAS | KHV | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | KHV | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG02040 | hp1 | a0001 | c0001 | t0009 | g0310 | EAS | KHV | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG02040 | hp2 | a0001 | c0001 | t0005 | g0301 | EAS | KHV | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG02055 | hp1 | a0001 | c0001 | t0085 | g0218 | AFR | ACB | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG02055 | hp2 | a0001 | c0001 | t0092 | g0025 | AFR | ACB | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG02056 | hp1 | a0001 | c0001 | t0002 | g0314 | EAS | KHV | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG02056 | hp2 | a0001 | c0001 | t0080 | g0100 | EAS | KHV | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG02071 | hp1 | a0001 | c0002 | t0070 | g0061 | EAS | KHV | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG02071 | hp2 | a0001 | c0001 | t0020 | g0087 | EAS | KHV | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG02074 | hp1 | a0001 | c0001 | t0019 | g0081 | EAS | KHV | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | KHV | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | KHV | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG02080 | hp2 | a0001 | c0001 | t0037 | g0094 | EAS | KHV | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG02083 | hp1 | a0001 | c0001 | t0099 | g0154 | EAS | KHV | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG02083 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | KHV | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG02129 | hp1 | a0001 | c0001 | t0007 | g0108 | EAS | KHV | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG02129 | hp2 | a0001 | c0001 | t0002 | g0305 | EAS | KHV | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | KHV | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG02132 | hp2 | a0001 | c0001 | t0104 | g0190 | EAS | KHV | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG02145 | hp1 | a0001 | c0001 | t0013 | g0256 | AFR | ACB | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG02145 | hp2 | a0001 | c0001 | t0014 | g0203 | AFR | ACB | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | PEL | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG02148 | hp2 | a0001 | c0002 | t0015 | g0132 | AMR | PEL | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG02257 | hp1 | a0001 | c0001 | t0054 | g0279 | AFR | ACB | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG02257 | hp2 | a0001 | c0001 | t0006 | g0332 | AFR | ACB | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG02258 | hp1 | a0001 | c0001 | t0042 | g0346 | AFR | ACB | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG02258 | hp2 | a0001 | c0001 | t0128 | g0276 | AFR | ACB | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG02273 | hp1 | a0001 | c0001 | t0050 | g0268 | AMR | PEL | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG02273 | hp2 | a0001 | c0001 | t0002 | g0312 | AMR | PEL | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG02280 | hp1 | a0001 | c0001 | t0121 | g0146 | AFR | ACB | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG02280 | hp2 | a0001 | c0001 | t0017 | g0214 | AFR | ACB | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG02293 | hp1 | a0001 | c0001 | t0131 | g0196 | AMR | PEL | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG02293 | hp2 | a0001 | c0001 | t0020 | g0105 | AMR | PEL | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG02300 | hp1 | a0001 | c0001 | t0002 | g0340 | AMR | PEL | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG02300 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | PEL | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG02451 | hp1 | a0001 | c0001 | t0039 | g0199 | AFR | ACB | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG02451 | hp2 | a0001 | c0001 | t0048 | g0282 | AFR | ACB | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG02572 | hp1 | a0001 | c0001 | t0014 | g0095 | AFR | GWD | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | GWD | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0052 | SAS | PJL | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG02602 | hp2 | a0001 | c0001 | t0077 | g0134 | SAS | PJL | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG02615 | hp1 | a0001 | c0001 | t0036 | g0156 | AFR | GWD | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG02615 | hp2 | a0001 | c0001 | t0094 | g0024 | AFR | GWD | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG02622 | hp1 | a0001 | c0001 | t0041 | g0261 | AFR | GWD | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG02622 | hp2 | a0001 | c0001 | t0029 | g0286 | AFR | GWD | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG02647 | hp1 | a0001 | c0001 | t0014 | g0096 | AFR | GWD | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG02647 | hp2 | a0001 | c0001 | t0062 | g0294 | AFR | GWD | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG02683 | hp1 | a0001 | c0001 | t0002 | g0004 | SAS | PJL | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG02683 | hp2 | a0001 | c0001 | t0141 | g0035 | SAS | PJL | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG02698 | hp1 | a0001 | c0001 | t0115 | g0163 | SAS | PJL | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG02698 | hp2 | a0001 | c0001 | t0002 | g0322 | SAS | PJL | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG02717 | hp1 | a0001 | c0001 | t0024 | g0149 | AFR | GWD | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG02717 | hp2 | a0001 | c0001 | t0119 | g0298 | AFR | GWD | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG02738 | hp1 | a0001 | c0001 | t0021 | g0053 | SAS | PJL | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG02738 | hp2 | a0001 | c0001 | t0003 | g0257 | SAS | PJL | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG02809 | hp1 | a0001 | c0001 | t0091 | g0027 | AFR | GWD | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG02809 | hp2 | a0001 | c0001 | t0048 | g0284 | AFR | GWD | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG02818 | hp1 | a0001 | c0001 | t0027 | g0280 | AFR | GWD | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG02818 | hp2 | a0001 | c0001 | t0117 | g0299 | AFR | GWD | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG02886 | hp1 | a0001 | c0001 | t0096 | g0023 | AFR | GWD | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG02886 | hp2 | a0001 | c0001 | t0118 | g0297 | AFR | GWD | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG02895 | hp1 | a0001 | c0001 | t0084 | g0062 | AFR | GWD | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG02895 | hp2 | a0001 | c0001 | t0045 | g0032 | AFR | GWD | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG02896 | hp1 | a0001 | c0001 | t0106 | g0345 | AFR | GWD | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG02896 | hp2 | a0001 | c0001 | t0040 | g0008 | AFR | GWD | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG02897 | hp1 | a0001 | c0001 | t0040 | g0008 | AFR | GWD | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG02897 | hp2 | a0001 | c0001 | t0045 | g0031 | AFR | GWD | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG02965 | hp1 | a0001 | c0001 | t0066 | g0041 | AFR | ESN | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG02965 | hp2 | a0001 | c0001 | t0140 | g0278 | AFR | ESN | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG02970 | hp1 | a0001 | c0001 | t0127 | g0273 | AFR | ESN | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG02970 | hp2 | a0001 | c0001 | t0017 | g0070 | AFR | ESN | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG03017 | hp1 | a0001 | c0001 | t0003 | g0003 | SAS | PJL | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG03017 | hp2 | a0001 | c0001 | t0010 | g0078 | SAS | PJL | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG03041 | hp1 | a0001 | c0001 | t0090 | g0044 | AFR | GWD | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG03041 | hp2 | a0001 | c0001 | t0095 | g0028 | AFR | GWD | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG03098 | hp1 | a0002 | c0003 | t0034 | g0151 | AFR | MSL | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG03098 | hp2 | a0001 | c0001 | t0114 | g0022 | AFR | MSL | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG03130 | hp1 | a0001 | c0001 | t0056 | g0034 | AFR | ESN | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG03130 | hp2 | a0001 | c0001 | t0046 | g0140 | AFR | ESN | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG03139 | hp1 | a0001 | c0001 | t0087 | g0201 | AFR | ESN | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG03139 | hp2 | a0001 | c0001 | t0038 | g0216 | AFR | ESN | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG03195 | hp1 | a0001 | c0001 | t0035 | g0043 | AFR | ESN | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG03195 | hp2 | a0001 | c0001 | t0026 | g0290 | AFR | ESN | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG03209 | hp1 | a0001 | c0001 | t0027 | g0270 | AFR | MSL | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | MSL | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG03225 | hp1 | a0001 | c0001 | t0039 | g0069 | AFR | MSL | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG03225 | hp2 | a0001 | c0001 | t0067 | g0042 | AFR | MSL | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG03453 | hp1 | a0001 | c0001 | t0124 | g0291 | AFR | MSL | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG03453 | hp2 | a0001 | c0001 | t0049 | g0269 | AFR | MSL | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG03490 | hp1 | a0001 | c0001 | t0138 | g0240 | SAS | PJL | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG03490 | hp2 | a0001 | c0001 | t0029 | g0271 | SAS | PJL | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG03491 | hp1 | a0001 | c0001 | t0018 | g0050 | SAS | PJL | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG03491 | hp2 | a0001 | c0001 | t0043 | g0155 | SAS | PJL | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG03492 | hp1 | a0001 | c0001 | t0029 | g0275 | SAS | PJL | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG03492 | hp2 | a0001 | c0001 | t0043 | g0185 | SAS | PJL | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG03516 | hp1 | a0002 | c0003 | t0034 | g0152 | AFR | ESN | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG03516 | hp2 | a0001 | c0001 | t0038 | g0219 | AFR | ESN | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG03540 | hp1 | a0001 | c0001 | t0049 | g0274 | AFR | GWD | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG03540 | hp2 | a0001 | c0001 | t0102 | g0189 | AFR | GWD | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG03579 | hp1 | a0001 | c0001 | t0126 | g0283 | AFR | MSL | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG03579 | hp2 | a0001 | c0001 | t0086 | g0077 | AFR | MSL | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG03654 | hp1 | a0001 | c0001 | t0032 | g0241 | SAS | PJL | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG03654 | hp2 | a0001 | c0001 | t0132 | g0315 | SAS | PJL | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG03669 | hp1 | a0001 | c0001 | t0089 | g0049 | SAS | PJL | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG03669 | hp2 | a0001 | c0001 | t0006 | g0309 | SAS | PJL | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG03688 | hp1 | a0001 | c0001 | t0007 | g0123 | SAS | STU | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG03688 | hp2 | a0001 | c0001 | t0003 | g0255 | SAS | STU | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG03704 | hp1 | a0001 | c0001 | t0028 | g0287 | SAS | PJL | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG03704 | hp2 | a0001 | c0001 | t0006 | g0318 | SAS | PJL | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG03710 | hp1 | a0001 | c0001 | t0010 | g0086 | SAS | PJL | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG03710 | hp2 | a0001 | c0001 | t0035 | g0048 | SAS | PJL | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG03831 | hp1 | a0001 | c0001 | t0009 | g0249 | SAS | BEB | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0036 | SAS | BEB | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG03834 | hp1 | a0001 | c0001 | t0003 | g0236 | SAS | BEB | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG03834 | hp2 | a0001 | c0005 | t0133 | g0323 | SAS | BEB | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG03927 | hp1 | a0001 | c0001 | t0006 | g0343 | SAS | BEB | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG03927 | hp2 | a0001 | c0001 | t0028 | g0285 | SAS | BEB | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG04115 | hp1 | a0001 | c0001 | t0064 | g0051 | SAS | STU | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG04115 | hp2 | a0001 | c0001 | t0002 | g0341 | SAS | STU | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG04184 | hp1 | a0001 | c0001 | t0032 | g0246 | SAS | BEB | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG04184 | hp2 | a0001 | c0001 | t0011 | g0204 | SAS | BEB | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG04199 | hp1 | a0001 | c0001 | t0024 | g0060 | SAS | STU | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG04199 | hp2 | a0001 | c0001 | t0020 | g0101 | SAS | STU | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA18522 | hp1 | a0001 | c0001 | t0041 | g0262 | AFR | YRI | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA18522 | hp2 | a0001 | c0001 | t0025 | g0195 | AFR | YRI | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | CHB | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA18612 | hp2 | a0001 | c0001 | t0008 | g0135 | EAS | CHB | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA18747 | hp1 | a0001 | c0001 | t0005 | g0302 | EAS | CHB | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA18906 | hp1 | a0001 | c0001 | t0093 | g0026 | AFR | YRI | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA18906 | hp2 | a0001 | c0001 | t0042 | g0259 | AFR | YRI | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA18940 | hp1 | a0001 | c0001 | t0004 | g0136 | EAS | JPT | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA18941 | hp2 | a0001 | c0002 | t0004 | g0063 | EAS | JPT | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA18943 | hp2 | a0001 | c0001 | t0130 | g0327 | EAS | JPT | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA18944 | hp2 | a0001 | c0001 | t0008 | g0038 | EAS | JPT | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA18945 | hp2 | a0001 | c0001 | t0010 | g0225 | EAS | JPT | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA18946 | hp1 | a0001 | c0001 | t0074 | g0263 | EAS | JPT | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA18946 | hp2 | a0001 | c0001 | t0011 | g0067 | EAS | JPT | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA18947 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA18947 | hp2 | a0001 | c0001 | t0008 | g0010 | EAS | JPT | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA18948 | hp1 | a0001 | c0001 | t0006 | g0307 | EAS | JPT | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA18948 | hp2 | a0001 | c0001 | t0011 | g0083 | EAS | JPT | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA18949 | hp1 | a0001 | c0001 | t0005 | g0303 | EAS | JPT | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA18949 | hp2 | a0001 | c0001 | t0047 | g0325 | EAS | JPT | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA18951 | hp1 | a0001 | c0001 | t0006 | g0005 | EAS | JPT | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA18951 | hp2 | a0001 | c0002 | t0004 | g0013 | EAS | JPT | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA18952 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA18952 | hp2 | a0001 | c0001 | t0002 | g0308 | EAS | JPT | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA18957 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA18962 | hp1 | a0001 | c0002 | t0011 | g0126 | EAS | JPT | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA18962 | hp2 | a0001 | c0006 | t0002 | g0339 | EAS | JPT | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA18964 | hp1 | a0001 | c0001 | t0052 | g0175 | EAS | JPT | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA18968 | hp2 | a0001 | c0002 | t0004 | g0128 | EAS | JPT | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA18969 | hp1 | a0001 | c0002 | t0004 | g0013 | EAS | JPT | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA18969 | hp2 | a0001 | c0001 | t0008 | g0006 | EAS | JPT | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA18970 | hp1 | a0001 | c0002 | t0004 | g0014 | EAS | JPT | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA18970 | hp2 | a0001 | c0001 | t0031 | g0183 | EAS | JPT | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA18971 | hp1 | a0001 | c0001 | t0100 | g0115 | EAS | JPT | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA18971 | hp2 | a0001 | c0001 | t0108 | g0084 | EAS | JPT | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA18972 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA18972 | hp2 | a0001 | c0001 | t0097 | g0118 | EAS | JPT | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA18973 | hp1 | a0001 | c0001 | t0061 | g0228 | EAS | JPT | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA18973 | hp2 | a0001 | c0001 | t0002 | g0313 | EAS | JPT | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA18975 | hp1 | a0001 | c0002 | t0004 | g0209 | EAS | JPT | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA18975 | hp2 | a0001 | c0001 | t0006 | g0005 | EAS | JPT | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA18977 | hp1 | a0001 | c0001 | t0012 | g0223 | EAS | JPT | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA18978 | hp1 | a0001 | c0001 | t0024 | g0141 | EAS | JPT | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA18978 | hp2 | a0001 | c0001 | t0015 | g0097 | EAS | JPT | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA18979 | hp1 | a0001 | c0001 | t0044 | g0124 | EAS | JPT | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA18979 | hp2 | a0001 | c0001 | t0005 | g0089 | EAS | JPT | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA18980 | hp1 | a0001 | c0001 | t0006 | g0005 | EAS | JPT | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA18981 | hp1 | a0001 | c0001 | t0079 | g0113 | EAS | JPT | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA18981 | hp2 | a0001 | c0001 | t0030 | g0335 | EAS | JPT | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA18982 | hp2 | a0001 | c0001 | t0105 | g0188 | EAS | JPT | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA18986 | hp1 | a0001 | c0002 | t0004 | g0014 | EAS | JPT | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA18986 | hp2 | a0001 | c0001 | t0006 | g0333 | EAS | JPT | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA18989 | hp1 | a0001 | c0001 | t0009 | g0336 | EAS | JPT | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA18989 | hp2 | a0001 | c0001 | t0008 | g0039 | EAS | JPT | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA18990 | hp1 | a0001 | c0001 | t0005 | g0009 | EAS | JPT | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA18990 | hp2 | a0001 | c0001 | t0052 | g0184 | EAS | JPT | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA18991 | hp1 | a0001 | c0001 | t0008 | g0037 | EAS | JPT | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA18991 | hp2 | a0001 | c0001 | t0033 | g0231 | EAS | JPT | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA18992 | hp1 | a0001 | c0001 | t0007 | g0224 | EAS | JPT | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA18993 | hp1 | a0001 | c0001 | t0007 | g0125 | EAS | JPT | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA18998 | hp2 | a0001 | c0001 | t0007 | g0221 | EAS | JPT | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA18999 | hp2 | a0001 | c0001 | t0008 | g0121 | EAS | JPT | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA19000 | hp1 | a0001 | c0001 | t0031 | g0176 | EAS | JPT | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA19000 | hp2 | a0001 | c0001 | t0098 | g0206 | EAS | JPT | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA19002 | hp2 | a0001 | c0001 | t0006 | g0338 | EAS | JPT | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA19003 | hp2 | a0001 | c0001 | t0002 | g0317 | EAS | JPT | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA19005 | hp2 | a0001 | c0001 | t0003 | g0213 | EAS | JPT | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA19006 | hp2 | a0001 | c0001 | t0033 | g0253 | EAS | JPT | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA19007 | hp1 | a0001 | c0001 | t0005 | g0009 | EAS | JPT | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA19007 | hp2 | a0001 | c0001 | t0003 | g0252 | EAS | JPT | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA19009 | hp1 | a0001 | c0001 | t0011 | g0080 | EAS | JPT | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA19009 | hp2 | a0001 | c0001 | t0101 | g0120 | EAS | JPT | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA19010 | hp1 | a0001 | c0001 | t0012 | g0222 | EAS | JPT | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA19010 | hp2 | a0001 | c0001 | t0030 | g0337 | EAS | JPT | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA19011 | hp2 | a0001 | c0001 | t0047 | g0326 | EAS | JPT | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | LWK | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA19043 | hp2 | a0001 | c0001 | t0046 | g0192 | AFR | LWK | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA19058 | hp1 | a0001 | c0001 | t0031 | g0177 | EAS | JPT | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA19058 | hp2 | a0001 | c0001 | t0010 | g0082 | EAS | JPT | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA19060 | hp1 | a0001 | c0002 | t0015 | g0133 | EAS | JPT | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA19060 | hp2 | a0001 | c0001 | t0002 | g0306 | EAS | JPT | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA19063 | hp1 | a0001 | c0001 | t0008 | g0010 | EAS | JPT | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA19063 | hp2 | a0001 | c0001 | t0005 | g0091 | EAS | JPT | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA19064 | hp1 | a0001 | c0001 | t0005 | g0137 | EAS | JPT | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA19064 | hp2 | a0001 | c0001 | t0088 | g0187 | EAS | JPT | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA19070 | hp2 | a0001 | c0001 | t0003 | g0182 | EAS | JPT | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA19076 | hp1 | a0001 | c0001 | t0007 | g0220 | EAS | JPT | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA19076 | hp2 | a0001 | c0001 | t0006 | g0342 | EAS | JPT | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA19078 | hp2 | a0001 | c0002 | t0019 | g0127 | EAS | JPT | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA19080 | hp1 | a0001 | c0002 | t0004 | g0130 | EAS | JPT | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA19080 | hp2 | a0001 | c0001 | t0003 | g0232 | EAS | JPT | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA19082 | hp1 | a0001 | c0002 | t0004 | g0131 | EAS | JPT | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA19084 | hp1 | a0001 | c0001 | t0004 | g0088 | EAS | JPT | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA19085 | hp1 | a0001 | c0002 | t0012 | g0129 | EAS | JPT | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA19085 | hp2 | a0001 | c0001 | t0008 | g0006 | EAS | JPT | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA19086 | hp1 | a0001 | c0001 | t0037 | g0205 | EAS | JPT | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA19086 | hp2 | a0001 | c0001 | t0030 | g0334 | EAS | JPT | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA19087 | hp2 | a0001 | c0001 | t0011 | g0102 | EAS | JPT | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA19090 | hp1 | a0001 | c0001 | t0112 | g0116 | EAS | JPT | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA19090 | hp2 | a0001 | c0001 | t0016 | g0328 | EAS | JPT | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA19240 | hp1 | a0001 | c0001 | t0078 | g0215 | AFR | YRI | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA19240 | hp2 | a0001 | c0001 | t0113 | g0029 | AFR | YRI | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA20129 | hp1 | a0001 | c0001 | t0025 | g0193 | AFR | ASW | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA20129 | hp2 | a0001 | c0001 | t0116 | g0040 | AFR | ASW | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA20805 | hp1 | a0001 | c0001 | t0021 | g0056 | EUR | TSI | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA20805 | hp2 | a0001 | c0001 | t0022 | g0007 | EUR | TSI | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0162 | SAS | GIH | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA20905 | hp2 | a0001 | c0001 | t0050 | g0272 | SAS | GIH | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG01123 | hp1 | a0001 | c0001 | t0135 | g0239 | AMR | CLM | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG01123 | hp2 | a0001 | c0001 | t0109 | g0198 | AMR | CLM | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG02109 | hp1 | a0001 | c0001 | t0032 | g0245 | AFR | ACB | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG02109 | hp2 | a0001 | c0001 | t0007 | g0104 | AFR | ACB | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG02486 | hp1 | a0001 | c0001 | t0063 | g0217 | AFR | ACB | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | ACB | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG02559 | hp1 | a0001 | c0001 | t0014 | g0076 | AFR | ACB | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG02559 | hp2 | a0001 | c0001 | t0051 | g0265 | AFR | ACB | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG03471 | hp1 | a0001 | c0001 | t0125 | g0281 | AFR | MSL | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG03471 | hp2 | a0001 | c0001 | t0083 | g0092 | AFR | MSL | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG06807 | hp1 | a0002 | c0003 | t0057 | g0153 | AFR | USA | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG06807 | hp2 | a0001 | c0001 | t0007 | g0066 | AFR | USA | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA20300 | hp1 | a0001 | c0001 | t0082 | g0227 | AFR | USA | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA20300 | hp2 | a0001 | c0001 | t0059 | g0296 | AFR | USA | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA21309 | hp1 | a0001 | c0001 | t0026 | g0288 | AFR | LWK | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA21309 | hp2 | a0001 | c0001 | t0051 | g0264 | AFR | LWK | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0023 | g0075 | REF | REF | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0324 | REF | REF | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:115241559
|
T | C | 1 | a0002 | 4 | HG01074.hp1 HG03098.hp1 HG03516.hp1 others(1): Show |
missense_variant | MODERATE | c.307A>G | p.Ile103Val | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 3/9 | 333/9550 | 307/1134 | 103/377 | chr5 | 115241559 | ||
chr5:115262845
|
C | T | 1 | a0003 | 1 | HG01975.hp2 | missense_variant | MODERATE | c.7G>A | p.Ala3Thr | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 1/9 | 33/9550 | 7/1134 | 3/377 | chr5 | 115262845 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:115237905
|
T | C | 1 | a0001c0002 | 16 | HG00408.hp1 HG02071.hp1 HG02148.hp2 others(13): Show |
synonymous_variant | LOW | c.432A>G | p.Lys144Lys | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 4/9 | 458/9550 | 432/1134 | 144/377 | chr5 | 115237905 | ||
chr5:115237926
|
G | A | 1 | a0001c0005 | 1 | HG03834.hp2 | synonymous_variant | LOW | c.411C>T | p.Asp137Asp | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 4/9 | 437/9550 | 411/1134 | 137/377 | chr5 | 115237926 | ||
chr5:115253228
|
G | A | 1 | a0001c0006 | 1 | NA18962.hp2 | synonymous_variant | LOW | c.168C>T | p.Ser56Ser | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 2/9 | 194/9550 | 168/1134 | 56/377 | chr5 | 115253228 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:115204047
|
G | C | 8 | a0001c0001t0091a0001c0001t0092a0001c0001t0093others(5): Show | 8 | HG02055.hp2 HG02615.hp2 HG02809.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*8355C>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 9/9 | 8355 | chr5 | 115204047 | |||||
chr5:115204352
|
G | A | 1 | a0001c0001t0077 | 1 | HG02602.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8050C>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 9/9 | 8050 | chr5 | 115204352 | |||||
chr5:115204766
|
T | C | 38 | a0001c0001t0004a0001c0001t0005a0001c0001t0007others(35): Show | 90 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(87): Show |
3_prime_UTR_variant | MODIFIER | c.*7636A>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 9/9 | 7636 | chr5 | 115204766 | |||||
chr5:115204831
|
T | C | 1 | a0001c0001t0106 | 1 | HG02896.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7571A>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 9/9 | 7571 | chr5 | 115204831 | |||||
chr5:115204967
|
G | A | 2 | a0001c0001t0017a0001c0001t0062 | 4 | HG01884.hp2 HG02280.hp2 HG02647.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*7435C>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 9/9 | 7435 | chr5 | 115204967 | |||||
chr5:115205069
|
T | G | 1 | a0001c0001t0073 | 1 | HG00642.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7333A>C | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 9/9 | 7333 | chr5 | 115205069 | |||||
chr5:115205102
|
C | T | 1 | a0001c0001t0065 | 1 | HG01261.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7300G>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 9/9 | 7300 | chr5 | 115205102 | |||||
chr5:115205137
|
T | G | 1 | a0001c0001t0062 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7265A>C | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 9/9 | 7265 | chr5 | 115205137 | |||||
chr5:115205405
|
G | C | 1 | a0001c0001t0042 | 2 | HG02258.hp1 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6997C>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 9/9 | 6997 | chr5 | 115205405 | |||||
chr5:115205484
|
C | T | 5 | a0001c0001t0036a0001c0001t0041a0001c0001t0051others(2): Show | 8 | HG01243.hp2 HG01884.hp1 HG02559.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*6918G>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 9/9 | 6918 | chr5 | 115205484 | |||||
chr5:115205490
|
T | TA | 25 | a0001c0001t0001a0001c0001t0008a0001c0001t0024others(22): Show | 91 | HG00408.hp2 HG00558.hp2 HG00621.hp1 others(88): Show |
3_prime_UTR_variant | MODIFIER | c.*6911dupT | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 9/9 | 6911 | chr5 | 115205490 | |||||
chr5:115205579
|
A | T | 1 | a0001c0001t0100 | 1 | NA18971.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6823T>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 9/9 | 6823 | chr5 | 115205579 | |||||
chr5:115205668
|
C | T | 3 | a0001c0001t0074a0001c0001t0075a0001c0001t0076 | 3 | HG00558.hp1 HG00609.hp2 NA18946.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6734G>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 9/9 | 6734 | chr5 | 115205668 | |||||
chr5:115205872
|
G | A | 1 | a0001c0001t0068 | 1 | HG01168.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6530C>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 9/9 | 6530 | chr5 | 115205872 | |||||
chr5:115205936
|
T | TTAAATA | 124 | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(121): Show | 272 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(269): Show |
3_prime_UTR_variant | MODIFIER | c.*6465_*6466insTATT others(2): Show |
PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 9/9 | 6465 | chr5 | 115205936 | |||||
chr5:115205940
|
T | C | 1 | a0001c0001t0036 | 2 | HG01884.hp1 HG02615.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6462A>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 9/9 | 6462 | chr5 | 115205940 | |||||
chr5:115206012
|
C | T | 1 | a0001c0001t0041 | 2 | HG02622.hp1 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6390G>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 9/9 | 6390 | chr5 | 115206012 | |||||
chr5:115206041
|
C | T | 8 | a0001c0001t0091a0001c0001t0092a0001c0001t0093others(5): Show | 8 | HG02055.hp2 HG02615.hp2 HG02809.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*6361G>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 9/9 | 6361 | chr5 | 115206041 | |||||
chr5:115206190
|
T | G | 79 | a0001c0001t0004a0001c0001t0005a0001c0001t0007others(76): Show | 157 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(154): Show |
3_prime_UTR_variant | MODIFIER | c.*6212A>C | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 9/9 | 6212 | chr5 | 115206190 | |||||
chr5:115206211
|
C | T | 124 | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(121): Show | 272 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(269): Show |
3_prime_UTR_variant | MODIFIER | c.*6191G>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 9/9 | 6191 | chr5 | 115206211 | |||||
chr5:115206278
|
A | G | 1 | a0001c0001t0098 | 1 | NA19000.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6124T>C | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 9/9 | 6124 | chr5 | 115206278 | |||||
chr5:115206282
|
T | C | 8 | a0001c0001t0091a0001c0001t0092a0001c0001t0093others(5): Show | 8 | HG02055.hp2 HG02615.hp2 HG02809.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*6120A>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 9/9 | 6120 | chr5 | 115206282 | |||||
chr5:115206411
|
T | A | 58 | a0001c0001t0004a0001c0001t0005a0001c0001t0007others(55): Show | 122 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(119): Show |
3_prime_UTR_variant | MODIFIER | c.*5991A>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 9/9 | 5991 | chr5 | 115206411 | |||||
chr5:115206549
|
C | T | 1 | a0001c0001t0079 | 1 | NA18981.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5853G>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 9/9 | 5853 | chr5 | 115206549 | |||||
chr5:115206589
|
A | G | 1 | a0001c0001t0141 | 1 | HG02683.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5813T>C | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 9/9 | 5813 | chr5 | 115206589 | |||||
chr5:115206754
|
A | AGAT | 8 | a0001c0001t0091a0001c0001t0092a0001c0001t0093others(5): Show | 8 | HG02055.hp2 HG02615.hp2 HG02809.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*5645_*5647dupATC | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 9/9 | 5647 | chr5 | 115206754 | |||||
chr5:115206987
|
A | G | 1 | a0001c0001t0059 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5415T>C | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 9/9 | 5415 | chr5 | 115206987 | |||||
chr5:115207029
|
T | C | 2 | a0001c0001t0068a0001c0001t0069 | 2 | HG01109.hp1 HG01168.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5373A>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 9/9 | 5373 | chr5 | 115207029 | |||||
chr5:115207030
|
T | A | 2 | a0001c0001t0068a0001c0001t0069 | 2 | HG01109.hp1 HG01168.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5372A>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 9/9 | 5372 | chr5 | 115207030 | |||||
chr5:115207067
|
A | G | 8 | a0001c0001t0091a0001c0001t0092a0001c0001t0093others(5): Show | 8 | HG02055.hp2 HG02615.hp2 HG02809.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*5335T>C | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 9/9 | 5335 | chr5 | 115207067 | |||||
chr5:115207180
|
C | CAT | 5 | a0001c0001t0006a0001c0001t0030a0001c0001t0047others(2): Show | 18 | HG02257.hp2 HG02896.hp1 HG02965.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*5220_*5221dupAT | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 9/9 | 5221 | chr5 | 115207180 | |||||
chr5:115207180
|
C | CATAT | 9 | a0001c0001t0003a0001c0001t0009a0001c0001t0032others(6): Show | 39 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*5218_*5221dupATAT | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 9/9 | 5221 | chr5 | 115207180 | |||||
chr5:115207180
|
C | CATATAT | 9 | a0001c0001t0013a0001c0001t0017a0001c0001t0031others(6): Show | 18 | HG01070.hp2 HG01257.hp2 HG01258.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*5216_*5221dupATAT others(2): Show |
PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 9/9 | 5221 | chr5 | 115207180 | |||||
chr5:115207180
|
C | CATATATA others(1): Show |
9 | a0001c0001t0029a0001c0001t0042a0001c0001t0053others(6): Show | 13 | HG00323.hp1 HG01256.hp2 HG01496.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*5214_*5221dupATAT others(4): Show |
PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 9/9 | 5221 | chr5 | 115207180 | |||||
chr5:115207180
|
C | CATATATA others(3): Show |
9 | a0001c0001t0022a0001c0001t0038a0001c0001t0050others(6): Show | 13 | HG00621.hp2 HG01074.hp1 HG01099.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*5212_*5221dupATAT others(6): Show |
PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 9/9 | 5221 | chr5 | 115207180 | |||||
chr5:115207180
|
C | CATATATA others(5): Show |
15 | a0001c0001t0018a0001c0001t0023a0001c0001t0025others(12): Show | 28 | HG00280.hp1 HG00642.hp1 HG00738.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*5210_*5221dupATAT others(8): Show |
PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 9/9 | 5221 | chr5 | 115207180 | |||||
chr5:115207180
|
C | CATATATA others(7): Show |
12 | a0001c0001t0011a0001c0001t0014a0001c0001t0021others(9): Show | 23 | HG00323.hp2 HG00733.hp1 HG01192.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*5208_*5221dupATAT others(10): Show |
PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 9/9 | 5221 | chr5 | 115207180 | |||||
chr5:115207180
|
C | CATATATA others(9): Show |
11 | a0001c0001t0004a0001c0001t0015a0001c0001t0026others(8): Show | 26 | HG00099.hp2 HG00140.hp1 HG01934.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*5206_*5221dupATAT others(12): Show |
PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 9/9 | 5221 | chr5 | 115207180 | |||||
chr5:115207180
|
C | CATATATA others(11): Show |
8 | a0001c0001t0007a0001c0001t0040a0001c0001t0044others(5): Show | 18 | HG00558.hp1 HG00735.hp1 HG01516.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*5204_*5221dupATAT others(14): Show |
PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 9/9 | 5221 | chr5 | 115207180 | |||||
chr5:115207180
|
C | CATATATA others(13): Show |
9 | a0001c0001t0010a0001c0001t0049a0001c0001t0061others(6): Show | 17 | HG00609.hp2 HG01081.hp2 HG01256.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*5202_*5221dupATAT others(16): Show |
PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 9/9 | 5221 | chr5 | 115207180 | |||||
chr5:115207180
|
C | CATATATA others(15): Show |
8 | a0001c0001t0012a0001c0001t0069a0001c0001t0074others(5): Show | 11 | HG01109.hp1 HG01123.hp2 HG01928.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*5200_*5221dupATAT others(18): Show |
PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 9/9 | 5221 | chr5 | 115207180 | |||||
chr5:115207180
|
C | CATATATA others(17): Show |
3 | a0001c0001t0020a0001c0001t0073a0001c0001t0117 | 5 | HG00642.hp2 HG02071.hp2 HG02293.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*5198_*5221dupATAT others(20): Show |
PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 9/9 | 5221 | chr5 | 115207180 | |||||
chr5:115207180
|
C | CATATATA others(19): Show |
4 | a0001c0001t0068a0001c0001t0072a0001c0001t0103others(1): Show | 4 | HG01168.hp1 HG01433.hp1 HG01975.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5196_*5221dupATAT others(22): Show |
PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 9/9 | 5221 | chr5 | 115207180 | |||||
chr5:115207180
|
C | CATATATA others(21): Show |
2 | a0001c0001t0019a0001c0002t0019 | 3 | HG01257.hp1 HG02074.hp1 NA19078.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5221_*5222insATAT others(24): Show |
PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 9/9 | 5221 | chr5 | 115207180 | |||||
chr5:115207180
|
C | CATATATA others(23): Show |
3 | a0001c0001t0060a0001c0001t0071a0001c0001t0107 | 3 | HG01070.hp1 HG01071.hp2 HG01192.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5221_*5222insATAT others(26): Show |
PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 9/9 | 5221 | chr5 | 115207180 | |||||
chr5:115207180
|
CATATATA others(1): Show |
C | 4 | a0001c0001t0055a0001c0001t0056a0001c0001t0082others(1): Show | 4 | HG01496.hp2 HG03130.hp1 NA20129.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5214_*5221delATAT others(4): Show |
PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 9/9 | 5214 | chr5 | 115207180 | |||||
chr5:115207180
|
CATATATA others(3): Show |
C | 1 | a0001c0001t0099 | 1 | HG02083.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5212_*5221delATAT others(6): Show |
PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 9/9 | 5212 | chr5 | 115207180 | |||||
chr5:115207180
|
CATATATA others(5): Show |
C | 20 | a0001c0001t0001a0001c0001t0005a0001c0001t0008others(17): Show | 95 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(92): Show |
3_prime_UTR_variant | MODIFIER | c.*5210_*5221delATAT others(8): Show |
PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 9/9 | 5210 | chr5 | 115207180 | |||||
chr5:115207186
|
T | TATATATA others(13): Show |
1 | a0001c0001t0081 | 1 | HG01943.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5215_*5216insGTAT others(16): Show |
PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 9/9 | 5215 | chr5 | 115207186 | |||||
chr5:115207192
|
T | C | 2 | a0001c0001t0055a0001c0001t0056 | 2 | HG01496.hp2 HG03130.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5210A>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 9/9 | 5210 | chr5 | 115207192 | |||||
chr5:115207213
|
G | A | 1 | a0001c0001t0056 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5189C>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 9/9 | 5189 | chr5 | 115207213 | |||||
chr5:115207493
|
T | C | 1 | a0001c0001t0063 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4909A>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 9/9 | 4909 | chr5 | 115207493 | |||||
chr5:115207553
|
A | C | 1 | a0001c0001t0106 | 1 | HG02896.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4849T>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 9/9 | 4849 | chr5 | 115207553 | |||||
chr5:115207624
|
T | C | 55 | a0001c0001t0004a0001c0001t0007a0001c0001t0010others(52): Show | 109 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(106): Show |
3_prime_UTR_variant | MODIFIER | c.*4778A>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 9/9 | 4778 | chr5 | 115207624 | |||||
chr5:115207661
|
G | A | 1 | a0001c0001t0042 | 2 | HG02258.hp1 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4741C>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 9/9 | 4741 | chr5 | 115207661 | |||||
chr5:115207664
|
C | A | 2 | a0001c0001t0068a0001c0001t0069 | 2 | HG01109.hp1 HG01168.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4738G>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 9/9 | 4738 | chr5 | 115207664 | |||||
chr5:115207869
|
T | C | 1 | a0001c0001t0124 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4533A>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 9/9 | 4533 | chr5 | 115207869 | |||||
chr5:115208132
|
C | CT | 5 | a0001c0001t0036a0001c0001t0041a0001c0001t0051others(2): Show | 8 | HG01243.hp2 HG01884.hp1 HG02559.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*4269dupA | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 9/9 | 4269 | chr5 | 115208132 | |||||
chr5:115208202
|
A | C | 59 | a0001c0001t0004a0001c0001t0005a0001c0001t0007others(56): Show | 123 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(120): Show |
3_prime_UTR_variant | MODIFIER | c.*4200T>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 9/9 | 4200 | chr5 | 115208202 | |||||
chr5:115208459
|
T | G | 6 | a0001c0001t0025a0001c0001t0046a0001c0001t0117others(3): Show | 9 | HG01243.hp1 HG01496.hp1 HG02717.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3943A>C | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 9/9 | 3943 | chr5 | 115208459 | |||||
chr5:115208490
|
C | T | 3 | a0001c0001t0048a0001c0001t0125a0001c0001t0126 | 4 | HG02451.hp2 HG02809.hp2 HG03471.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3912G>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 9/9 | 3912 | chr5 | 115208490 | |||||
chr5:115208616
|
A | G | 1 | a0001c0002t0070 | 1 | HG02071.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3786T>C | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 9/9 | 3786 | chr5 | 115208616 | |||||
chr5:115208691
|
T | C | 1 | a0001c0001t0101 | 1 | NA19009.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3711A>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 9/9 | 3711 | chr5 | 115208691 | |||||
chr5:115208831
|
T | C | 1 | a0001c0001t0136 | 1 | HG01243.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3571A>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 9/9 | 3571 | chr5 | 115208831 | |||||
chr5:115209090
|
G | A | 1 | a0001c0001t0115 | 1 | HG02698.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3312C>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 9/9 | 3312 | chr5 | 115209090 | |||||
chr5:115209178
|
A | G | 3 | a0001c0001t0018a0001c0001t0064a0001c0001t0089 | 5 | HG00642.hp1 HG01074.hp2 HG03491.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3224T>C | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 9/9 | 3224 | chr5 | 115209178 | |||||
chr5:115209296
|
A | G | 1 | a0001c0001t0097 | 1 | NA18972.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3106T>C | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 9/9 | 3106 | chr5 | 115209296 | |||||
chr5:115209307
|
C | G | 1 | a0001c0001t0102 | 1 | HG03540.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3095G>C | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 9/9 | 3095 | chr5 | 115209307 | |||||
chr5:115209312
|
A | T | 123 | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(120): Show | 273 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(270): Show |
3_prime_UTR_variant | MODIFIER | c.*3090T>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 9/9 | 3090 | chr5 | 115209312 | |||||
chr5:115209423
|
C | T | 2 | a0001c0001t0055a0001c0001t0056 | 2 | HG01496.hp2 HG03130.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2979G>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 9/9 | 2979 | chr5 | 115209423 | |||||
chr5:115209473
|
G | A | 51 | a0001c0001t0004a0001c0001t0007a0001c0001t0010others(48): Show | 105 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(102): Show |
3_prime_UTR_variant | MODIFIER | c.*2929C>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 9/9 | 2929 | chr5 | 115209473 | |||||
chr5:115209682
|
G | T | 1 | a0001c0001t0121 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2720C>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 9/9 | 2720 | chr5 | 115209682 | |||||
chr5:115209814
|
A | G | 16 | a0001c0001t0001a0001c0001t0005a0001c0001t0008others(13): Show | 87 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(84): Show |
3_prime_UTR_variant | MODIFIER | c.*2588T>C | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 9/9 | 2588 | chr5 | 115209814 | |||||
chr5:115209869
|
C | T | 1 | a0001c0001t0041 | 2 | HG02622.hp1 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2533G>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 9/9 | 2533 | chr5 | 115209869 | |||||
chr5:115209940
|
C | T | 8 | a0001c0001t0091a0001c0001t0092a0001c0001t0093others(5): Show | 8 | HG02055.hp2 HG02615.hp2 HG02809.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2462G>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 9/9 | 2462 | chr5 | 115209940 | |||||
chr5:115210061
|
T | G | 7 | a0001c0001t0014a0001c0001t0040a0001c0001t0083others(4): Show | 11 | HG02055.hp1 HG02145.hp2 HG02559.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2341A>C | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 9/9 | 2341 | chr5 | 115210061 | |||||
chr5:115210219
|
G | A | 1 | a0001c0001t0087 | 1 | HG03139.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2183C>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 9/9 | 2183 | chr5 | 115210219 | |||||
chr5:115210302
|
T | C | 2 | a0001c0001t0055a0001c0001t0056 | 2 | HG01496.hp2 HG03130.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2100A>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 9/9 | 2100 | chr5 | 115210302 | |||||
chr5:115210332
|
G | T | 2 | a0001c0001t0055a0001c0001t0056 | 2 | HG01496.hp2 HG03130.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2070C>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 9/9 | 2070 | chr5 | 115210332 | |||||
chr5:115210408
|
A | G | 1 | a0001c0001t0138 | 1 | HG03490.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1994T>C | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 9/9 | 1994 | chr5 | 115210408 | |||||
chr5:115210415
|
C | A | 2 | a0001c0001t0055a0001c0001t0056 | 2 | HG01496.hp2 HG03130.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1987G>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 9/9 | 1987 | chr5 | 115210415 | |||||
chr5:115210419
|
G | C | 8 | a0001c0001t0091a0001c0001t0092a0001c0001t0093others(5): Show | 8 | HG02055.hp2 HG02615.hp2 HG02809.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1983C>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 9/9 | 1983 | chr5 | 115210419 | |||||
chr5:115210437
|
A | G | 1 | a0001c0001t0130 | 1 | NA18943.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1965T>C | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 9/9 | 1965 | chr5 | 115210437 | |||||
chr5:115210554
|
C | A | 122 | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(119): Show | 270 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(267): Show |
3_prime_UTR_variant | MODIFIER | c.*1848G>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 9/9 | 1848 | chr5 | 115210554 | |||||
chr5:115210696
|
T | C | 1 | a0001c0001t0111 | 1 | HG01261.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1706A>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 9/9 | 1706 | chr5 | 115210696 | |||||
chr5:115210720
|
A | T | 1 | a0001c0001t0068 | 1 | HG01168.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1682T>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 9/9 | 1682 | chr5 | 115210720 | |||||
chr5:115210725
|
A | G | 1 | a0001c0001t0091 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1677T>C | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 9/9 | 1677 | chr5 | 115210725 | |||||
chr5:115210800
|
G | A | 1 | a0001c0001t0116 | 1 | NA20129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1602C>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 9/9 | 1602 | chr5 | 115210800 | |||||
chr5:115210851
|
T | C | 1 | a0001c0001t0088 | 1 | NA19064.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1551A>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 9/9 | 1551 | chr5 | 115210851 | |||||
chr5:115210937
|
T | G | 8 | a0001c0001t0091a0001c0001t0092a0001c0001t0093others(5): Show | 8 | HG02055.hp2 HG02615.hp2 HG02809.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1465A>C | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 9/9 | 1465 | chr5 | 115210937 | |||||
chr5:115211006
|
C | T | 8 | a0001c0001t0091a0001c0001t0092a0001c0001t0093others(5): Show | 8 | HG02055.hp2 HG02615.hp2 HG02809.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1396G>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 9/9 | 1396 | chr5 | 115211006 | |||||
chr5:115211008
|
C | T | 2 | a0001c0001t0008a0001c0001t0112 | 10 | NA18612.hp2 NA18944.hp2 NA18947.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1394G>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 9/9 | 1394 | chr5 | 115211008 | |||||
chr5:115211209
|
C | T | 122 | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(119): Show | 270 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(267): Show |
3_prime_UTR_variant | MODIFIER | c.*1193G>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 9/9 | 1193 | chr5 | 115211209 | |||||
chr5:115211342
|
C | T | 8 | a0001c0001t0018a0001c0001t0035a0001c0001t0064others(5): Show | 11 | HG00642.hp1 HG01074.hp2 HG01261.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1060G>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 9/9 | 1060 | chr5 | 115211342 | |||||
chr5:115211389
|
T | C | 1 | a0001c0001t0059 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1013A>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 9/9 | 1013 | chr5 | 115211389 | |||||
chr5:115211437
|
T | C | 21 | a0001c0001t0025a0001c0001t0026a0001c0001t0027others(18): Show | 36 | HG01192.hp1 HG01243.hp1 HG01496.hp1 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*965A>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 9/9 | 965 | chr5 | 115211437 | |||||
chr5:115211598
|
C | CA | 4 | a0001c0001t0016a0001c0001t0030a0001c0001t0033others(1): Show | 11 | HG01069.hp1 HG01071.hp1 HG01109.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*803dupT | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 9/9 | 803 | chr5 | 115211598 | |||||
chr5:115211598
|
CA | C | 24 | a0001c0001t0026a0001c0001t0027a0001c0001t0028others(21): Show | 39 | HG00323.hp1 HG01168.hp2 HG01192.hp1 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*803delT | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 9/9 | 803 | chr5 | 115211598 | |||||
chr5:115211598
|
CAA | C | 14 | a0001c0001t0024a0001c0001t0025a0001c0001t0045others(11): Show | 21 | HG01243.hp1 HG01496.hp1 HG02559.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*802_*803delTT | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 9/9 | 802 | chr5 | 115211598 | |||||
chr5:115211598
|
CAAA | C | 37 | a0001c0001t0001a0001c0001t0005a0001c0001t0008others(34): Show | 114 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(111): Show |
3_prime_UTR_variant | MODIFIER | c.*801_*803delTTT | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 9/9 | 801 | chr5 | 115211598 | |||||
chr5:115211598
|
CAAAA | C | 47 | a0001c0001t0004a0001c0001t0007a0001c0001t0010others(44): Show | 97 | HG00140.hp1 HG00558.hp1 HG00609.hp2 others(94): Show |
3_prime_UTR_variant | MODIFIER | c.*800_*803delTTTT | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 9/9 | 800 | chr5 | 115211598 | |||||
chr5:115211598
|
CAAAAA | C | 5 | a0001c0001t0017a0001c0001t0060a0001c0001t0061others(2): Show | 7 | HG01070.hp1 HG01884.hp2 HG02280.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*799_*803delTTTTT | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 9/9 | 799 | chr5 | 115211598 | |||||
chr5:115211697
|
T | C | 3 | a0002c0003t0034a0002c0003t0057a0002c0003t0058 | 4 | HG01074.hp1 HG03098.hp1 HG03516.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*705A>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 9/9 | 705 | chr5 | 115211697 | |||||
chr5:115211984
|
C | T | 1 | a0001c0001t0059 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*418G>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 9/9 | 418 | chr5 | 115211984 | |||||
chr5:115212007
|
T | C | 2 | a0001c0001t0051a0001c0001t0136 | 3 | HG01243.hp2 HG02559.hp2 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*395A>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 9/9 | 395 | chr5 | 115212007 | |||||
chr5:115212083
|
TAA | T | 3 | a0002c0003t0034a0002c0003t0057a0002c0003t0058 | 4 | HG01074.hp1 HG03098.hp1 HG03516.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*317_*318delTT | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 9/9 | 317 | chr5 | 115212083 | |||||
chr5:115212122
|
C | A | 1 | a0001c0001t0137 | 1 | HG01346.hp2 | 3_prime_UTR_variant | MODIFIER | c.*280G>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 9/9 | 280 | chr5 | 115212122 | |||||
chr5:115212237
|
G | T | 2 | a0001c0001t0055a0001c0001t0056 | 2 | HG01496.hp2 HG03130.hp1 |
3_prime_UTR_variant | MODIFIER | c.*165C>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 9/9 | 165 | chr5 | 115212237 | |||||
chr5:115212369
|
A | G | 1 | a0001c0001t0054 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*33T>C | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 9/9 | 33 | chr5 | 115212369 | |||||
chr5:115212374
|
T | TC | 11 | a0001c0001t0003a0001c0001t0013a0001c0001t0031others(8): Show | 40 | HG00323.hp1 HG00733.hp2 HG01069.hp2 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*27dupG | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 9/9 | 27 | chr5 | 115212374 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:115212750
|
T | TA | 8 | a0001c0001t0091g0027a0001c0001t0092g0025a0001c0001t0093g0026others(5): Show | 8 | HG02055.hp2 HG02615.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.953-168dupT | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 8/8 | chr5 | 115212750 | ||||||
chr5:115212875
|
A | C | 1 | a0001c0001t0002g0317 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.953-292T>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 8/8 | chr5 | 115212875 | ||||||
chr5:115212901
|
A | G | 1 | a0001c0002t0004g0063 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.953-318T>C | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 8/8 | chr5 | 115212901 | ||||||
chr5:115212945
|
G | A | 4 | a0001c0001t0017g0070a0001c0001t0017g0186a0001c0001t0017g0214others(1): Show | 4 | HG01884.hp2 HG02280.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.953-362C>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 8/8 | chr5 | 115212945 | ||||||
chr5:115213238
|
C | T | 9 | a0001c0001t0036g0156a0001c0001t0036g0157a0001c0001t0041g0261others(6): Show | 9 | HG01243.hp2 HG01884.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.953-655G>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 8/8 | chr5 | 115213238 | ||||||
chr5:115213255
|
C | T | 7 | a0001c0001t0014g0076a0001c0001t0014g0095a0001c0001t0014g0096others(4): Show | 8 | HG02145.hp2 HG02559.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.953-672G>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 8/8 | chr5 | 115213255 | ||||||
chr5:115213390
|
T | C | 43 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0182others(40): Show | 48 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(45): Show |
intron_variant | MODIFIER | c.953-807A>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 8/8 | chr5 | 115213390 | ||||||
chr5:115213534
|
G | A | 1 | a0001c0001t0015g0097 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.953-951C>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 8/8 | chr5 | 115213534 | ||||||
chr5:115213588
|
A | G | 4 | a0001c0001t0006g0309a0001c0001t0006g0318a0001c0001t0006g0332others(1): Show | 4 | HG02257.hp2 HG03669.hp2 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.953-1005T>C | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 8/8 | chr5 | 115213588 | ||||||
chr5:115213619
|
A | G | 1 | a0001c0001t0055g0295 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.953-1036T>C | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 8/8 | chr5 | 115213619 | ||||||
chr5:115213624
|
T | A | 2 | a0001c0001t0001g0161a0001c0001t0001g0166 | 2 | HG02486.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.953-1041A>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 8/8 | chr5 | 115213624 | ||||||
chr5:115213702
|
G | A | 1 | a0001c0001t0007g0224 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.953-1119C>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 8/8 | chr5 | 115213702 | ||||||
chr5:115214025
|
A | G | 3 | a0001c0001t0010g0071a0001c0001t0010g0078a0001c0001t0010g0200 | 3 | HG01256.hp1 HG01258.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.953-1442T>C | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 8/8 | chr5 | 115214025 | ||||||
chr5:115214088
|
A | C | 2 | a0001c0001t0023g0075a0001c0001t0110g0074 | 2 | HG00323.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.953-1505T>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 8/8 | chr5 | 115214088 | ||||||
chr5:115214155
|
T | A | 1 | a0001c0001t0023g0098 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.953-1572A>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 8/8 | chr5 | 115214155 | ||||||
chr5:115214303
|
T | TA | 83 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(80): Show | 93 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.953-1721dupT | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 8/8 | chr5 | 115214303 | ||||||
chr5:115214398
|
A | G | 8 | a0001c0001t0091g0027a0001c0001t0092g0025a0001c0001t0093g0026others(5): Show | 8 | HG02055.hp2 HG02615.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.953-1815T>C | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 8/8 | chr5 | 115214398 | ||||||
chr5:115214579
|
A | T | 3 | a0001c0001t0051g0264a0001c0001t0051g0265a0001c0001t0136g0266 | 3 | HG01243.hp2 HG02559.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.953-1996T>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 8/8 | chr5 | 115214579 | ||||||
chr5:115214803
|
C | T | 1 | a0001c0001t0042g0259 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.952+2062G>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 8/8 | chr5 | 115214803 | ||||||
chr5:115214885
|
T | C | 1 | a0001c0001t0033g0235 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.952+1980A>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 8/8 | chr5 | 115214885 | ||||||
chr5:115215011
|
T | C | 98 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(95): Show | 108 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.952+1854A>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 8/8 | chr5 | 115215011 | ||||||
chr5:115215029
|
C | T | 3 | a0001c0001t0021g0053a0001c0001t0021g0054a0001c0001t0021g0056 | 3 | HG00733.hp1 HG02738.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.952+1836G>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 8/8 | chr5 | 115215029 | ||||||
chr5:115215150
|
C | T | 8 | a0001c0001t0091g0027a0001c0001t0092g0025a0001c0001t0093g0026others(5): Show | 8 | HG02055.hp2 HG02615.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.952+1715G>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 8/8 | chr5 | 115215150 | ||||||
chr5:115215154
|
A | G | 28 | a0001c0001t0026g0277a0001c0001t0026g0288a0001c0001t0026g0290others(25): Show | 28 | HG01192.hp1 HG01891.hp2 HG01934.hp1 others(25): Show |
intron_variant | MODIFIER | c.952+1711T>C | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 8/8 | chr5 | 115215154 | ||||||
chr5:115215187
|
G | A | 1 | a0001c0001t0059g0296 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.952+1678C>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 8/8 | chr5 | 115215187 | ||||||
chr5:115215246
|
C | G | 1 | a0001c0001t0001g0059 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.952+1619G>C | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 8/8 | chr5 | 115215246 | ||||||
chr5:115215293
|
G | A | 5 | a0001c0001t0009g0234a0001c0001t0009g0238a0001c0001t0009g0247others(2): Show | 5 | HG00140.hp2 HG00280.hp2 HG00741.hp1 others(2): Show |
intron_variant | MODIFIER | c.952+1572C>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 8/8 | chr5 | 115215293 | ||||||
chr5:115215300
|
A | G | 2 | a0001c0001t0055g0295a0001c0001t0056g0034 | 2 | HG01496.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.952+1565T>C | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 8/8 | chr5 | 115215300 | ||||||
chr5:115215391
|
C | G | 1 | a0001c0001t0024g0149 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.952+1474G>C | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 8/8 | chr5 | 115215391 | ||||||
chr5:115215410
|
T | C | 1 | a0001c0001t0042g0346 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.952+1455A>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 8/8 | chr5 | 115215410 | ||||||
chr5:115215577
|
C | A | 2 | a0001c0001t0042g0259a0001c0001t0042g0346 | 2 | HG02258.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.952+1288G>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 8/8 | chr5 | 115215577 | ||||||
chr5:115215637
|
G | A | 1 | a0001c0001t0042g0346 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.952+1228C>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 8/8 | chr5 | 115215637 | ||||||
chr5:115215640
|
T | C | 1 | a0001c0001t0017g0070 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.952+1225A>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 8/8 | chr5 | 115215640 | ||||||
chr5:115215655
|
G | C | 1 | a0001c0001t0059g0296 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.952+1210C>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 8/8 | chr5 | 115215655 | ||||||
chr5:115215675
|
T | C | 5 | a0001c0001t0002g0311a0001c0001t0002g0312a0001c0001t0016g0018others(2): Show | 6 | HG01069.hp1 HG01071.hp1 HG01109.hp2 others(3): Show |
intron_variant | MODIFIER | c.952+1190A>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 8/8 | chr5 | 115215675 | ||||||
chr5:115215789
|
C | T | 1 | a0001c0001t0102g0189 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.952+1076G>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 8/8 | chr5 | 115215789 | ||||||
chr5:115216112
|
T | A | 1 | a0001c0001t0068g0033 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.952+753A>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 8/8 | chr5 | 115216112 | ||||||
chr5:115216172
|
C | T | 1 | a0001c0001t0059g0296 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.952+693G>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 8/8 | chr5 | 115216172 | ||||||
chr5:115216305
|
G | A | 256 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(253): Show | 270 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.952+560C>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 8/8 | chr5 | 115216305 | ||||||
chr5:115216341
|
C | T | 1 | a0001c0001t0002g0306 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.952+524G>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 8/8 | chr5 | 115216341 | ||||||
chr5:115216534
|
C | T | 1 | a0001c0001t0110g0074 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.952+331G>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 8/8 | chr5 | 115216534 | ||||||
chr5:115216653
|
T | C | 195 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(192): Show | 209 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.952+212A>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 8/8 | chr5 | 115216653 | ||||||
chr5:115216690
|
T | C | 4 | a0001c0001t0025g0193a0001c0001t0025g0194a0001c0001t0025g0195others(1): Show | 4 | HG01243.hp1 NA18522.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.952+175A>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 8/8 | chr5 | 115216690 | ||||||
chr5:115216731
|
T | C | 1 | a0001c0001t0044g0085 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.952+134A>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 8/8 | chr5 | 115216731 | ||||||
chr5:115217024
|
C | T | 1 | a0001c0001t0020g0087 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.844-51G>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 7/8 | chr5 | 115217024 | ||||||
chr5:115217045
|
C | T | 2 | a0001c0001t0042g0259a0001c0001t0042g0346 | 2 | HG02258.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.844-72G>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 7/8 | chr5 | 115217045 | ||||||
chr5:115217137
|
T | C | 2 | a0001c0001t0041g0261a0001c0001t0041g0262 | 2 | HG02622.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.844-164A>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 7/8 | chr5 | 115217137 | ||||||
chr5:115217310
|
ACTCTTAT others(6): Show |
A | 73 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(70): Show | 83 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(80): Show |
intron_variant | MODIFIER | c.844-350_844-338del others(13): Show |
PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 7/8 | chr5 | 115217310 | ||||||
chr5:115217376
|
TA | T | 73 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(70): Show | 83 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(80): Show |
intron_variant | MODIFIER | c.844-404delT | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 7/8 | chr5 | 115217376 | ||||||
chr5:115217396
|
A | T | 1 | a0001c0001t0025g0195 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.844-423T>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 7/8 | chr5 | 115217396 | ||||||
chr5:115217398
|
T | A | 1 | a0001c0001t0025g0195 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.844-425A>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 7/8 | chr5 | 115217398 | ||||||
chr5:115217451
|
T | C | 1 | a0001c0001t0001g0117 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.844-478A>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 7/8 | chr5 | 115217451 | ||||||
chr5:115217680
|
G | C | 1 | a0001c0001t0039g0069 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.844-707C>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 7/8 | chr5 | 115217680 | ||||||
chr5:115217681
|
C | T | 1 | a0001c0001t0037g0205 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.844-708G>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 7/8 | chr5 | 115217681 | ||||||
chr5:115218006
|
G | A | 2 | a0001c0001t0041g0261a0001c0001t0041g0262 | 2 | HG02622.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.844-1033C>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 7/8 | chr5 | 115218006 | ||||||
chr5:115218090
|
G | A | 4 | a0001c0001t0003g0242a0001c0001t0003g0257a0001c0001t0013g0292others(1): Show | 4 | HG01069.hp2 HG01070.hp2 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.844-1117C>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 7/8 | chr5 | 115218090 | ||||||
chr5:115218204
|
T | A | 1 | a0001c0001t0069g0202 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.844-1231A>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 7/8 | chr5 | 115218204 | ||||||
chr5:115218301
|
C | T | 11 | a0001c0001t0018g0046a0001c0001t0018g0047a0001c0001t0018g0050others(8): Show | 11 | HG00642.hp1 HG01074.hp2 HG01261.hp1 others(8): Show |
intron_variant | MODIFIER | c.844-1328G>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 7/8 | chr5 | 115218301 | ||||||
chr5:115218397
|
G | GTA | 58 | a0001c0001t0003g0003a0001c0001t0003g0230a0001c0001t0003g0232others(55): Show | 61 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(58): Show |
intron_variant | MODIFIER | c.844-1426_844-1425d others(4): Show |
PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 7/8 | chr5 | 115218397 | ||||||
chr5:115218397
|
G | GTATA | 11 | a0001c0001t0003g0002a0001c0001t0003g0182a0001c0001t0003g0213others(8): Show | 13 | HG01243.hp1 HG01496.hp1 HG02004.hp1 others(10): Show |
intron_variant | MODIFIER | c.844-1428_844-1425d others(6): Show |
PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 7/8 | chr5 | 115218397 | ||||||
chr5:115218397
|
GTA | G | 44 | a0001c0001t0007g0104a0001c0001t0014g0095a0001c0001t0018g0046others(41): Show | 44 | HG00642.hp1 HG01074.hp2 HG01168.hp1 others(41): Show |
intron_variant | MODIFIER | c.844-1426_844-1425d others(4): Show |
PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 7/8 | chr5 | 115218397 | ||||||
chr5:115218491
|
C | CA | 29 | a0001c0001t0001g0138a0001c0001t0001g0167a0001c0001t0001g0172others(26): Show | 29 | HG00642.hp1 HG00741.hp2 HG01074.hp1 others(26): Show |
intron_variant | MODIFIER | c.844-1519dupT | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 7/8 | chr5 | 115218491 | ||||||
chr5:115218491
|
CA | C | 129 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0002g0313others(126): Show | 133 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.844-1519delT | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 7/8 | chr5 | 115218491 | ||||||
chr5:115218491
|
CAA | C | 15 | a0001c0001t0007g0221a0001c0001t0017g0070a0001c0001t0017g0186others(12): Show | 15 | HG00733.hp1 HG01884.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.844-1520_844-1519d others(4): Show |
PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 7/8 | chr5 | 115218491 | ||||||
chr5:115218561
|
G | A | 2 | a0001c0001t0055g0295a0001c0001t0056g0034 | 2 | HG01496.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.844-1588C>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 7/8 | chr5 | 115218561 | ||||||
chr5:115218606
|
A | G | 1 | a0001c0001t0008g0121 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.844-1633T>C | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 7/8 | chr5 | 115218606 | ||||||
chr5:115218638
|
T | C | 1 | a0001c0001t0042g0346 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.844-1665A>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 7/8 | chr5 | 115218638 | ||||||
chr5:115218815
|
C | T | 3 | a0001c0001t0051g0264a0001c0001t0051g0265a0001c0001t0136g0266 | 3 | HG01243.hp2 HG02559.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.844-1842G>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 7/8 | chr5 | 115218815 | ||||||
chr5:115218843
|
T | G | 2 | a0001c0001t0068g0033a0001c0001t0069g0202 | 2 | HG01109.hp1 HG01168.hp1 |
intron_variant | MODIFIER | c.844-1870A>C | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 7/8 | chr5 | 115218843 | ||||||
chr5:115218862
|
G | A | 256 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(253): Show | 270 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.844-1889C>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 7/8 | chr5 | 115218862 | ||||||
chr5:115218884
|
T | G | 1 | a0001c0001t0059g0296 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.844-1911A>C | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 7/8 | chr5 | 115218884 | ||||||
chr5:115218980
|
T | C | 2 | a0001c0001t0001g0210a0001c0001t0001g0211 | 2 | NA18943.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.844-2007A>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 7/8 | chr5 | 115218980 | ||||||
chr5:115218988
|
T | A | 1 | a0001c0001t0001g0168 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.844-2015A>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 7/8 | chr5 | 115218988 | ||||||
chr5:115219049
|
A | G | 13 | a0001c0001t0025g0193a0001c0001t0025g0194a0001c0001t0025g0195others(10): Show | 13 | HG01074.hp1 HG01243.hp1 HG01496.hp1 others(10): Show |
intron_variant | MODIFIER | c.844-2076T>C | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 7/8 | chr5 | 115219049 | ||||||
chr5:115219057
|
C | G | 1 | a0001c0001t0006g0332 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.844-2084G>C | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 7/8 | chr5 | 115219057 | ||||||
chr5:115219277
|
C | A | 256 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(253): Show | 270 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.844-2304G>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 7/8 | chr5 | 115219277 | ||||||
chr5:115219308
|
C | G | 2 | a0001c0001t0068g0033a0001c0001t0069g0202 | 2 | HG01109.hp1 HG01168.hp1 |
intron_variant | MODIFIER | c.844-2335G>C | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 7/8 | chr5 | 115219308 | ||||||
chr5:115219346
|
G | A | 1 | a0001c0001t0002g0306 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.844-2373C>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 7/8 | chr5 | 115219346 | ||||||
chr5:115219682
|
G | C | 1 | a0001c0001t0001g0052 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.843+2142C>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 7/8 | chr5 | 115219682 | ||||||
chr5:115219700
|
A | G | 1 | a0001c0001t0027g0270 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.843+2124T>C | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 7/8 | chr5 | 115219700 | ||||||
chr5:115219918
|
T | C | 4 | a0001c0001t0009g0249a0001c0001t0013g0256a0001c0001t0053g0244others(1): Show | 4 | HG01168.hp2 HG01515.hp2 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.843+1906A>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 7/8 | chr5 | 115219918 | ||||||
chr5:115220223
|
G | T | 1 | a0001c0001t0009g0248 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.843+1601C>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 7/8 | chr5 | 115220223 | ||||||
chr5:115220440
|
C | T | 1 | a0001c0001t0050g0272 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.843+1384G>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 7/8 | chr5 | 115220440 | ||||||
chr5:115220496
|
G | A | 101 | a0001c0001t0004g0068a0001c0001t0004g0088a0001c0001t0004g0136others(98): Show | 105 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.843+1328C>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 7/8 | chr5 | 115220496 | ||||||
chr5:115220526
|
C | T | 1 | a0001c0001t0001g0052 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.843+1298G>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 7/8 | chr5 | 115220526 | ||||||
chr5:115220667
|
C | T | 1 | a0001c0001t0132g0315 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.843+1157G>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 7/8 | chr5 | 115220667 | ||||||
chr5:115220695
|
C | T | 1 | a0001c0001t0001g0208 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.843+1129G>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 7/8 | chr5 | 115220695 | ||||||
chr5:115220696
|
G | A | 1 | a0001c0001t0082g0227 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.843+1128C>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 7/8 | chr5 | 115220696 | ||||||
chr5:115220938
|
G | C | 1 | a0001c0001t0001g0122 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.843+886C>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 7/8 | chr5 | 115220938 | ||||||
chr5:115221097
|
T | A | 1 | a0001c0001t0001g0057 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.843+727A>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 7/8 | chr5 | 115221097 | ||||||
chr5:115221197
|
A | T | 1 | a0001c0001t0059g0296 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.843+627T>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 7/8 | chr5 | 115221197 | ||||||
chr5:115221218
|
G | GT | 11 | a0001c0001t0018g0046a0001c0001t0018g0047a0001c0001t0018g0050others(8): Show | 11 | HG00642.hp1 HG01074.hp2 HG01261.hp1 others(8): Show |
intron_variant | MODIFIER | c.843+605dupA | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 7/8 | chr5 | 115221218 | ||||||
chr5:115221271
|
T | C | 1 | a0001c0001t0001g0293 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.843+553A>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 7/8 | chr5 | 115221271 | ||||||
chr5:115221352
|
T | A | 1 | a0001c0001t0029g0286 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.843+472A>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 7/8 | chr5 | 115221352 | ||||||
chr5:115221402
|
T | C | 1 | a0001c0001t0025g0193 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.843+422A>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 7/8 | chr5 | 115221402 | ||||||
chr5:115221418
|
G | A | 1 | a0001c0001t0068g0033 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.843+406C>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 7/8 | chr5 | 115221418 | ||||||
chr5:115221427
|
T | C | 26 | a0001c0001t0026g0277a0001c0001t0026g0288a0001c0001t0026g0290others(23): Show | 26 | HG01192.hp1 HG01891.hp2 HG01934.hp1 others(23): Show |
intron_variant | MODIFIER | c.843+397A>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 7/8 | chr5 | 115221427 | ||||||
chr5:115221615
|
T | C | 3 | a0001c0001t0051g0264a0001c0001t0051g0265a0001c0001t0136g0266 | 3 | HG01243.hp2 HG02559.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.843+209A>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 7/8 | chr5 | 115221615 | ||||||
chr5:115221627
|
G | T | 5 | a0001c0001t0009g0234a0001c0001t0009g0238a0001c0001t0009g0247others(2): Show | 5 | HG00140.hp2 HG00280.hp2 HG00741.hp1 others(2): Show |
intron_variant | MODIFIER | c.843+197C>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 7/8 | chr5 | 115221627 | ||||||
chr5:115221756
|
C | T | 3 | a0001c0001t0042g0259a0001c0001t0042g0346a0001c0001t0106g0345 | 3 | HG02258.hp1 HG02896.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.843+68G>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 7/8 | chr5 | 115221756 | ||||||
chr5:115222030
|
C | T | 26 | a0001c0001t0026g0277a0001c0001t0026g0288a0001c0001t0026g0290others(23): Show | 26 | HG01192.hp1 HG01891.hp2 HG01934.hp1 others(23): Show |
intron_variant | MODIFIER | c.659-22G>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 6/8 | chr5 | 115222030 | ||||||
chr5:115222197
|
T | C | 1 | a0001c0001t0003g0255 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.659-189A>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 6/8 | chr5 | 115222197 | ||||||
chr5:115222216
|
T | G | 1 | a0001c0001t0116g0040 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.659-208A>C | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 6/8 | chr5 | 115222216 | ||||||
chr5:115222431
|
G | C | 257 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(254): Show | 271 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.659-423C>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 6/8 | chr5 | 115222431 | ||||||
chr5:115222561
|
G | C | 4 | a0002c0003t0034g0151a0002c0003t0034g0152a0002c0003t0057g0153others(1): Show | 4 | HG01074.hp1 HG03098.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.659-553C>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 6/8 | chr5 | 115222561 | ||||||
chr5:115222762
|
C | T | 1 | a0001c0001t0013g0237 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.659-754G>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 6/8 | chr5 | 115222762 | ||||||
chr5:115222780
|
A | C | 8 | a0001c0001t0091g0027a0001c0001t0092g0025a0001c0001t0093g0026others(5): Show | 8 | HG02055.hp2 HG02615.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.659-772T>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 6/8 | chr5 | 115222780 | ||||||
chr5:115222831
|
A | G | 1 | a0001c0001t0116g0040 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.659-823T>C | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 6/8 | chr5 | 115222831 | ||||||
chr5:115223024
|
G | A | 1 | a0001c0001t0012g0226 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.659-1016C>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 6/8 | chr5 | 115223024 | ||||||
chr5:115223130
|
T | C | 2 | a0001c0001t0068g0033a0001c0001t0069g0202 | 2 | HG01109.hp1 HG01168.hp1 |
intron_variant | MODIFIER | c.659-1122A>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 6/8 | chr5 | 115223130 | ||||||
chr5:115223167
|
T | C | 1 | a0001c0001t0117g0299 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.659-1159A>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 6/8 | chr5 | 115223167 | ||||||
chr5:115223328
|
G | C | 2 | a0001c0001t0117g0299a0001c0001t0118g0297 | 2 | HG02818.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.659-1320C>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 6/8 | chr5 | 115223328 | ||||||
chr5:115223341
|
G | A | 8 | a0001c0001t0091g0027a0001c0001t0092g0025a0001c0001t0093g0026others(5): Show | 8 | HG02055.hp2 HG02615.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.659-1333C>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 6/8 | chr5 | 115223341 | ||||||
chr5:115223359
|
T | A | 1 | a0001c0001t0001g0057 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.659-1351A>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 6/8 | chr5 | 115223359 | ||||||
chr5:115223408
|
A | G | 1 | a0001c0001t0027g0270 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.659-1400T>C | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 6/8 | chr5 | 115223408 | ||||||
chr5:115223434
|
AAC | A | 8 | a0001c0001t0091g0027a0001c0001t0092g0025a0001c0001t0093g0026others(5): Show | 8 | HG02055.hp2 HG02615.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.659-1428_659-1427d others(4): Show |
PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 6/8 | chr5 | 115223434 | ||||||
chr5:115223483
|
G | A | 1 | a0001c0001t0027g0289 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.659-1475C>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 6/8 | chr5 | 115223483 | ||||||
chr5:115223552
|
G | C | 1 | a0001c0001t0059g0296 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.659-1544C>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 6/8 | chr5 | 115223552 | ||||||
chr5:115223566
|
G | A | 2 | a0001c0001t0038g0216a0001c0001t0038g0219 | 2 | HG03139.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.659-1558C>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 6/8 | chr5 | 115223566 | ||||||
chr5:115223673
|
C | T | 258 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(255): Show | 272 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.659-1665G>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 6/8 | chr5 | 115223673 | ||||||
chr5:115223811
|
C | A | 2 | a0001c0001t0045g0031a0001c0001t0045g0032 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.659-1803G>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 6/8 | chr5 | 115223811 | ||||||
chr5:115223883
|
T | C | 9 | a0001c0001t0025g0193a0001c0001t0025g0194a0001c0001t0025g0195others(6): Show | 9 | HG01243.hp1 HG01496.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.659-1875A>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 6/8 | chr5 | 115223883 | ||||||
chr5:115224008
|
C | G | 26 | a0001c0001t0026g0277a0001c0001t0026g0288a0001c0001t0026g0290others(23): Show | 26 | HG01192.hp1 HG01891.hp2 HG01934.hp1 others(23): Show |
intron_variant | MODIFIER | c.659-2000G>C | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 6/8 | chr5 | 115224008 | ||||||
chr5:115224014
|
G | A | 7 | a0001c0001t0004g0068a0001c0001t0007g0066a0001c0001t0007g0123others(4): Show | 7 | HG00140.hp1 HG03688.hp1 HG03710.hp1 others(4): Show |
intron_variant | MODIFIER | c.659-2006C>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 6/8 | chr5 | 115224014 | ||||||
chr5:115224035
|
T | C | 1 | a0001c0001t0028g0285 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.659-2027A>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 6/8 | chr5 | 115224035 | ||||||
chr5:115224107
|
A | G | 13 | a0001c0001t0025g0193a0001c0001t0025g0194a0001c0001t0025g0195others(10): Show | 13 | HG01074.hp1 HG01243.hp1 HG01496.hp1 others(10): Show |
intron_variant | MODIFIER | c.659-2099T>C | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 6/8 | chr5 | 115224107 | ||||||
chr5:115224115
|
T | TA | 257 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(254): Show | 271 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.659-2108dupT | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 6/8 | chr5 | 115224115 | ||||||
chr5:115224126
|
T | C | 1 | a0001c0001t0002g0321 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.659-2118A>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 6/8 | chr5 | 115224126 | ||||||
chr5:115224128
|
A | G | 35 | a0001c0001t0026g0277a0001c0001t0026g0288a0001c0001t0026g0290others(32): Show | 35 | HG01192.hp1 HG01891.hp2 HG01934.hp1 others(32): Show |
intron_variant | MODIFIER | c.659-2120T>C | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 6/8 | chr5 | 115224128 | ||||||
chr5:115224143
|
A | G | 2 | a0001c0001t0042g0259a0001c0001t0042g0346 | 2 | HG02258.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.659-2135T>C | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 6/8 | chr5 | 115224143 | ||||||
chr5:115224226
|
T | C | 1 | a0001c0001t0004g0088 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.659-2218A>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 6/8 | chr5 | 115224226 | ||||||
chr5:115224291
|
C | A | 2 | a0001c0001t0042g0259a0001c0001t0042g0346 | 2 | HG02258.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.659-2283G>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 6/8 | chr5 | 115224291 | ||||||
chr5:115224421
|
G | A | 1 | a0001c0001t0020g0087 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.659-2413C>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 6/8 | chr5 | 115224421 | ||||||
chr5:115224550
|
A | T | 1 | a0001c0001t0002g0344 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.659-2542T>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 6/8 | chr5 | 115224550 | ||||||
chr5:115224566
|
T | G | 2 | a0001c0001t0042g0259a0001c0001t0042g0346 | 2 | HG02258.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.659-2558A>C | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 6/8 | chr5 | 115224566 | ||||||
chr5:115224681
|
G | A | 80 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(77): Show | 91 | HG00408.hp2 HG00558.hp2 HG00609.hp1 others(88): Show |
intron_variant | MODIFIER | c.659-2673C>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 6/8 | chr5 | 115224681 | ||||||
chr5:115224699
|
G | A | 3 | a0001c0001t0004g0088a0001c0001t0004g0136a0001c0001t0015g0097 | 3 | NA18940.hp1 NA18978.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.659-2691C>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 6/8 | chr5 | 115224699 | ||||||
chr5:115224755
|
T | C | 88 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(85): Show | 99 | HG00408.hp2 HG00558.hp2 HG00609.hp1 others(96): Show |
intron_variant | MODIFIER | c.659-2747A>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 6/8 | chr5 | 115224755 | ||||||
chr5:115224833
|
C | CA | 26 | a0001c0001t0001g0012a0001c0001t0001g0036a0001c0001t0001g0117others(23): Show | 27 | HG00642.hp1 HG00741.hp2 HG01074.hp2 others(24): Show |
intron_variant | MODIFIER | c.659-2826dupT | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 6/8 | chr5 | 115224833 | ||||||
chr5:115224947
|
A | T | 3 | a0001c0001t0042g0259a0001c0001t0042g0346a0001c0001t0106g0345 | 3 | HG02258.hp1 HG02896.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.659-2939T>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 6/8 | chr5 | 115224947 | ||||||
chr5:115225250
|
C | T | 4 | a0001c0001t0017g0070a0001c0001t0017g0186a0001c0001t0017g0214others(1): Show | 4 | HG01884.hp2 HG02280.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.659-3242G>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 6/8 | chr5 | 115225250 | ||||||
chr5:115225333
|
G | A | 1 | a0001c0001t0062g0294 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.659-3325C>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 6/8 | chr5 | 115225333 | ||||||
chr5:115225349
|
A | G | 1 | a0001c0001t0025g0193 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.659-3341T>C | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 6/8 | chr5 | 115225349 | ||||||
chr5:115225401
|
G | GT | 118 | a0001c0001t0004g0068a0001c0001t0004g0088a0001c0001t0004g0136others(115): Show | 123 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.659-3394dupA | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 6/8 | chr5 | 115225401 | ||||||
chr5:115225592
|
G | T | 1 | a0001c0001t0116g0040 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.659-3584C>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 6/8 | chr5 | 115225592 | ||||||
chr5:115225609
|
T | C | 1 | a0001c0001t0039g0069 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.659-3601A>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 6/8 | chr5 | 115225609 | ||||||
chr5:115225649
|
A | AT | 20 | a0001c0001t0003g0255a0001c0001t0010g0071a0001c0001t0010g0078others(17): Show | 20 | HG01074.hp1 HG01256.hp1 HG01258.hp1 others(17): Show |
intron_variant | MODIFIER | c.659-3642dupA | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 6/8 | chr5 | 115225649 | ||||||
chr5:115225649
|
AT | A | 17 | a0001c0001t0001g0159a0001c0001t0001g0162a0001c0001t0001g0178others(14): Show | 17 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(14): Show |
intron_variant | MODIFIER | c.659-3642delA | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 6/8 | chr5 | 115225649 | ||||||
chr5:115225688
|
C | T | 1 | a0001c0001t0077g0134 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.659-3680G>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 6/8 | chr5 | 115225688 | ||||||
chr5:115225753
|
C | T | 1 | a0001c0001t0001g0164 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.659-3745G>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 6/8 | chr5 | 115225753 | ||||||
chr5:115225782
|
A | G | 1 | a0001c0001t0059g0296 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.659-3774T>C | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 6/8 | chr5 | 115225782 | ||||||
chr5:115225791
|
G | A | 4 | a0002c0003t0034g0151a0002c0003t0034g0152a0002c0003t0057g0153others(1): Show | 4 | HG01074.hp1 HG03098.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.659-3783C>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 6/8 | chr5 | 115225791 | ||||||
chr5:115225900
|
C | T | 1 | a0001c0001t0028g0287 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.659-3892G>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 6/8 | chr5 | 115225900 | ||||||
chr5:115226057
|
C | T | 1 | a0001c0001t0115g0163 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.659-4049G>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 6/8 | chr5 | 115226057 | ||||||
chr5:115226088
|
G | A | 2 | a0001c0001t0046g0140a0001c0001t0120g0139 | 2 | HG01496.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.659-4080C>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 6/8 | chr5 | 115226088 | ||||||
chr5:115226260
|
T | G | 1 | a0001c0001t0086g0077 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.659-4252A>C | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 6/8 | chr5 | 115226260 | ||||||
chr5:115226388
|
C | T | 2 | a0001c0001t0003g0236a0001c0001t0013g0017 | 3 | HG01257.hp2 HG01258.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.659-4380G>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 6/8 | chr5 | 115226388 | ||||||
chr5:115226547
|
TATATATA others(2): Show |
T | 35 | a0001c0001t0025g0193a0001c0001t0025g0194a0001c0001t0025g0195others(32): Show | 35 | HG01192.hp1 HG01243.hp1 HG01496.hp1 others(32): Show |
intron_variant | MODIFIER | c.658+4420_658+4428d others(11): Show |
PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 6/8 | chr5 | 115226547 | ||||||
chr5:115226553
|
T | A | 3 | a0001c0001t0042g0259a0001c0001t0042g0346a0001c0001t0106g0345 | 3 | HG02258.hp1 HG02896.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.658+4423A>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 6/8 | chr5 | 115226553 | ||||||
chr5:115226558
|
T | C | 1 | a0001c0001t0116g0040 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.658+4418A>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 6/8 | chr5 | 115226558 | ||||||
chr5:115226572
|
G | A | 1 | a0001c0001t0124g0291 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.658+4404C>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 6/8 | chr5 | 115226572 | ||||||
chr5:115226703
|
T | C | 4 | a0002c0003t0034g0151a0002c0003t0034g0152a0002c0003t0057g0153others(1): Show | 4 | HG01074.hp1 HG03098.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.658+4273A>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 6/8 | chr5 | 115226703 | ||||||
chr5:115226886
|
C | T | 3 | a0001c0001t0042g0259a0001c0001t0042g0346a0001c0001t0106g0345 | 3 | HG02258.hp1 HG02896.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.658+4090G>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 6/8 | chr5 | 115226886 | ||||||
chr5:115226890
|
A | C | 4 | a0002c0003t0034g0151a0002c0003t0034g0152a0002c0003t0057g0153others(1): Show | 4 | HG01074.hp1 HG03098.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.658+4086T>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 6/8 | chr5 | 115226890 | ||||||
chr5:115226979
|
G | A | 1 | a0001c0001t0068g0033 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.658+3997C>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 6/8 | chr5 | 115226979 | ||||||
chr5:115227007
|
T | A | 1 | a0001c0001t0059g0296 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.658+3969A>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 6/8 | chr5 | 115227007 | ||||||
chr5:115227033
|
G | A | 1 | a0001c0001t0013g0292 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.658+3943C>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 6/8 | chr5 | 115227033 | ||||||
chr5:115227077
|
A | C | 23 | a0001c0001t0026g0277a0001c0001t0026g0288a0001c0001t0026g0290others(20): Show | 23 | HG01192.hp1 HG01891.hp2 HG01934.hp1 others(20): Show |
intron_variant | MODIFIER | c.658+3899T>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 6/8 | chr5 | 115227077 | ||||||
chr5:115227194
|
A | G | 35 | a0001c0001t0025g0193a0001c0001t0025g0194a0001c0001t0025g0195others(32): Show | 35 | HG01192.hp1 HG01243.hp1 HG01496.hp1 others(32): Show |
intron_variant | MODIFIER | c.658+3782T>C | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 6/8 | chr5 | 115227194 | ||||||
chr5:115227429
|
T | C | 106 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(103): Show | 120 | HG00408.hp2 HG00558.hp2 HG00609.hp1 others(117): Show |
intron_variant | MODIFIER | c.658+3547A>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 6/8 | chr5 | 115227429 | ||||||
chr5:115227493
|
C | G | 1 | a0001c0001t0011g0067 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.658+3483G>C | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 6/8 | chr5 | 115227493 | ||||||
chr5:115227724
|
A | C | 88 | a0001c0001t0004g0068a0001c0001t0004g0088a0001c0001t0004g0136others(85): Show | 92 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(89): Show |
intron_variant | MODIFIER | c.658+3252T>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 6/8 | chr5 | 115227724 | ||||||
chr5:115227751
|
A | C | 102 | a0001c0001t0004g0068a0001c0001t0004g0088a0001c0001t0004g0136others(99): Show | 106 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.658+3225T>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 6/8 | chr5 | 115227751 | ||||||
chr5:115227753
|
T | C | 105 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(102): Show | 117 | HG00408.hp2 HG00558.hp2 HG00621.hp1 others(114): Show |
intron_variant | MODIFIER | c.658+3223A>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 6/8 | chr5 | 115227753 | ||||||
chr5:115228426
|
T | C | 2 | a0001c0001t0008g0010a0001c0001t0008g0121 | 3 | NA18947.hp2 NA18999.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.658+2550A>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 6/8 | chr5 | 115228426 | ||||||
chr5:115228523
|
G | C | 82 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(79): Show | 93 | HG00408.hp2 HG00558.hp2 HG00621.hp1 others(90): Show |
intron_variant | MODIFIER | c.658+2453C>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 6/8 | chr5 | 115228523 | ||||||
chr5:115228531
|
T | G | 4 | a0001c0001t0014g0076a0001c0001t0014g0095a0001c0001t0014g0096others(1): Show | 5 | HG02559.hp1 HG02572.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.658+2445A>C | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 6/8 | chr5 | 115228531 | ||||||
chr5:115228681
|
A | T | 35 | a0001c0001t0025g0193a0001c0001t0025g0194a0001c0001t0025g0195others(32): Show | 35 | HG01192.hp1 HG01243.hp1 HG01496.hp1 others(32): Show |
intron_variant | MODIFIER | c.658+2295T>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 6/8 | chr5 | 115228681 | ||||||
chr5:115228699
|
G | A | 1 | a0001c0001t0140g0278 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.658+2277C>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 6/8 | chr5 | 115228699 | ||||||
chr5:115228703
|
A | G | 82 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(79): Show | 93 | HG00408.hp2 HG00558.hp2 HG00621.hp1 others(90): Show |
intron_variant | MODIFIER | c.658+2273T>C | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 6/8 | chr5 | 115228703 | ||||||
chr5:115228726
|
G | A | 1 | a0001c0001t0001g0212 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.658+2250C>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 6/8 | chr5 | 115228726 | ||||||
chr5:115228745
|
C | G | 258 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(255): Show | 274 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(271): Show |
intron_variant | MODIFIER | c.658+2231G>C | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 6/8 | chr5 | 115228745 | ||||||
chr5:115228856
|
T | C | 2 | a0001c0001t0055g0295a0001c0001t0056g0034 | 2 | HG01496.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.658+2120A>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 6/8 | chr5 | 115228856 | ||||||
chr5:115228871
|
A | T | 3 | a0001c0001t0008g0006a0001c0001t0008g0038a0001c0001t0008g0039 | 4 | NA18944.hp2 NA18969.hp2 NA18989.hp2 others(1): Show |
intron_variant | MODIFIER | c.658+2105T>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 6/8 | chr5 | 115228871 | ||||||
chr5:115228933
|
C | T | 1 | a0001c0001t0028g0267 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.658+2043G>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 6/8 | chr5 | 115228933 | ||||||
chr5:115229011
|
A | G | 1 | a0001c0001t0029g0286 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.658+1965T>C | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 6/8 | chr5 | 115229011 | ||||||
chr5:115229045
|
C | T | 264 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(261): Show | 280 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(277): Show |
intron_variant | MODIFIER | c.658+1931G>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 6/8 | chr5 | 115229045 | ||||||
chr5:115229086
|
T | G | 1 | a0001c0002t0004g0063 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.658+1890A>C | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 6/8 | chr5 | 115229086 | ||||||
chr5:115229249
|
C | G | 127 | a0001c0001t0004g0068a0001c0001t0004g0088a0001c0001t0004g0136others(124): Show | 132 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.658+1727G>C | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 6/8 | chr5 | 115229249 | ||||||
chr5:115229381
|
T | C | 2 | a0001c0001t0060g0109a0001c0001t0071g0110 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.658+1595A>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 6/8 | chr5 | 115229381 | ||||||
chr5:115229419
|
G | A | 2 | a0001c0001t0045g0031a0001c0001t0045g0032 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.658+1557C>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 6/8 | chr5 | 115229419 | ||||||
chr5:115229596
|
G | T | 1 | a0001c0001t0129g0030 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.658+1380C>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 6/8 | chr5 | 115229596 | ||||||
chr5:115229803
|
T | C | 5 | a0001c0001t0001g0142a0001c0001t0001g0148a0001c0001t0024g0149others(2): Show | 5 | HG01891.hp1 HG02280.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.658+1173A>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 6/8 | chr5 | 115229803 | ||||||
chr5:115230144
|
A | G | 1 | a0001c0001t0083g0092 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.658+832T>C | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 6/8 | chr5 | 115230144 | ||||||
chr5:115230203
|
G | A | 2 | a0001c0001t0042g0259a0001c0001t0042g0346 | 2 | HG02258.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.658+773C>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 6/8 | chr5 | 115230203 | ||||||
chr5:115230219
|
A | G | 8 | a0001c0001t0091g0027a0001c0001t0092g0025a0001c0001t0093g0026others(5): Show | 8 | HG02055.hp2 HG02615.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.658+757T>C | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 6/8 | chr5 | 115230219 | ||||||
chr5:115230286
|
T | C | 1 | a0001c0001t0029g0286 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.658+690A>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 6/8 | chr5 | 115230286 | ||||||
chr5:115230353
|
C | T | 1 | a0001c0001t0052g0175 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.658+623G>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 6/8 | chr5 | 115230353 | ||||||
chr5:115230555
|
T | C | 2 | a0001c0001t0039g0069a0001c0001t0039g0199 | 2 | HG02451.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.658+421A>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 6/8 | chr5 | 115230555 | ||||||
chr5:115230916
|
C | T | 2 | a0001c0001t0055g0295a0001c0001t0056g0034 | 2 | HG01496.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.658+60G>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 6/8 | chr5 | 115230916 | ||||||
chr5:115231177
|
A | T | 110 | a0001c0001t0004g0068a0001c0001t0004g0088a0001c0001t0004g0136others(107): Show | 115 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.613-156T>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 5/8 | chr5 | 115231177 | ||||||
chr5:115231205
|
C | T | 1 | a0001c0001t0068g0033 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.613-184G>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 5/8 | chr5 | 115231205 | ||||||
chr5:115231251
|
C | T | 4 | a0002c0003t0034g0151a0002c0003t0034g0152a0002c0003t0057g0153others(1): Show | 4 | HG01074.hp1 HG03098.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.613-230G>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 5/8 | chr5 | 115231251 | ||||||
chr5:115231330
|
C | T | 94 | a0001c0001t0004g0068a0001c0001t0004g0088a0001c0001t0004g0136others(91): Show | 99 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.613-309G>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 5/8 | chr5 | 115231330 | ||||||
chr5:115231349
|
C | T | 172 | a0001c0001t0004g0068a0001c0001t0004g0088a0001c0001t0004g0136others(169): Show | 177 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.613-328G>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 5/8 | chr5 | 115231349 | ||||||
chr5:115231482
|
C | T | 1 | a0001c0001t0011g0204 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.613-461G>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 5/8 | chr5 | 115231482 | ||||||
chr5:115231483
|
A | G | 1 | a0001c0001t0001g0162 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.613-462T>C | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 5/8 | chr5 | 115231483 | ||||||
chr5:115231582
|
A | T | 1 | a0001c0001t0026g0288 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.613-561T>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 5/8 | chr5 | 115231582 | ||||||
chr5:115231610
|
G | A | 5 | a0001c0001t0036g0156a0001c0001t0036g0157a0001c0001t0041g0261others(2): Show | 5 | HG01884.hp1 HG02615.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.613-589C>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 5/8 | chr5 | 115231610 | ||||||
chr5:115231689
|
G | A | 1 | a0001c0001t0059g0296 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.613-668C>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 5/8 | chr5 | 115231689 | ||||||
chr5:115231691
|
T | A | 1 | a0001c0001t0011g0080 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.613-670A>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 5/8 | chr5 | 115231691 | ||||||
chr5:115231732
|
C | G | 1 | a0001c0001t0033g0235 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.613-711G>C | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 5/8 | chr5 | 115231732 | ||||||
chr5:115231929
|
G | A | 1 | a0001c0001t0129g0030 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.613-908C>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 5/8 | chr5 | 115231929 | ||||||
chr5:115231930
|
C | T | 1 | a0001c0001t0011g0080 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.613-909G>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 5/8 | chr5 | 115231930 | ||||||
chr5:115231931
|
G | A | 4 | a0002c0003t0034g0151a0002c0003t0034g0152a0002c0003t0057g0153others(1): Show | 4 | HG01074.hp1 HG03098.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.613-910C>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 5/8 | chr5 | 115231931 | ||||||
chr5:115232104
|
A | C | 107 | a0001c0001t0004g0068a0001c0001t0004g0088a0001c0001t0004g0136others(104): Show | 111 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.613-1083T>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 5/8 | chr5 | 115232104 | ||||||
chr5:115232170
|
G | C | 89 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(86): Show | 99 | HG00408.hp2 HG00558.hp2 HG00621.hp1 others(96): Show |
intron_variant | MODIFIER | c.613-1149C>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 5/8 | chr5 | 115232170 | ||||||
chr5:115232242
|
A | C | 2 | a0001c0001t0042g0259a0001c0001t0042g0346 | 2 | HG02258.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.613-1221T>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 5/8 | chr5 | 115232242 | ||||||
chr5:115232386
|
C | T | 1 | a0001c0001t0001g0058 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.613-1365G>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 5/8 | chr5 | 115232386 | ||||||
chr5:115232387
|
G | A | 1 | a0001c0001t0041g0262 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.613-1366C>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 5/8 | chr5 | 115232387 | ||||||
chr5:115232665
|
T | C | 2 | a0001c0001t0002g0322a0001c0001t0009g0310 | 2 | HG02040.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.613-1644A>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 5/8 | chr5 | 115232665 | ||||||
chr5:115232744
|
T | C | 11 | a0001c0001t0018g0046a0001c0001t0018g0047a0001c0001t0018g0050others(8): Show | 11 | HG00642.hp1 HG01074.hp2 HG01261.hp1 others(8): Show |
intron_variant | MODIFIER | c.613-1723A>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 5/8 | chr5 | 115232744 | ||||||
chr5:115232768
|
T | C | 1 | a0001c0001t0140g0278 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.613-1747A>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 5/8 | chr5 | 115232768 | ||||||
chr5:115232808
|
G | A | 1 | a0001c0001t0128g0276 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.613-1787C>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 5/8 | chr5 | 115232808 | ||||||
chr5:115232949
|
C | A | 94 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(91): Show | 106 | HG00408.hp2 HG00558.hp2 HG00621.hp1 others(103): Show |
intron_variant | MODIFIER | c.613-1928G>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 5/8 | chr5 | 115232949 | ||||||
chr5:115232960
|
T | C | 266 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(263): Show | 282 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(279): Show |
intron_variant | MODIFIER | c.613-1939A>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 5/8 | chr5 | 115232960 | ||||||
chr5:115232989
|
CAAAAAAA others(10): Show |
C | 109 | a0001c0001t0004g0068a0001c0001t0004g0088a0001c0001t0004g0136others(106): Show | 113 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.613-1985_613-1969d others(19): Show |
PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 5/8 | chr5 | 115232989 | ||||||
chr5:115233106
|
G | A | 2 | a0001c0001t0045g0031a0001c0001t0045g0032 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.613-2085C>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 5/8 | chr5 | 115233106 | ||||||
chr5:115233230
|
A | C | 2 | a0001c0001t0068g0033a0001c0001t0069g0202 | 2 | HG01109.hp1 HG01168.hp1 |
intron_variant | MODIFIER | c.613-2209T>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 5/8 | chr5 | 115233230 | ||||||
chr5:115233252
|
C | T | 2 | a0001c0001t0015g0079a0001c0001t0023g0098 | 2 | HG00099.hp2 HG00738.hp1 |
intron_variant | MODIFIER | c.613-2231G>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 5/8 | chr5 | 115233252 | ||||||
chr5:115233278
|
A | C | 1 | a0001c0001t0100g0115 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.613-2257T>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 5/8 | chr5 | 115233278 | ||||||
chr5:115233306
|
G | C | 1 | a0001c0001t0025g0195 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.613-2285C>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 5/8 | chr5 | 115233306 | ||||||
chr5:115233466
|
G | T | 4 | a0001c0001t0025g0193a0001c0001t0025g0194a0001c0001t0025g0195others(1): Show | 4 | HG01243.hp1 NA18522.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.613-2445C>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 5/8 | chr5 | 115233466 | ||||||
chr5:115233545
|
GA | G | 81 | a0001c0001t0004g0068a0001c0001t0004g0088a0001c0001t0004g0136others(78): Show | 84 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(81): Show |
intron_variant | MODIFIER | c.613-2525delT | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 5/8 | chr5 | 115233545 | ||||||
chr5:115233546
|
A | G | 1 | a0001c0001t0001g0212 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.613-2525T>C | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 5/8 | chr5 | 115233546 | ||||||
chr5:115233580
|
A | G | 1 | a0001c0001t0063g0217 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.613-2559T>C | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 5/8 | chr5 | 115233580 | ||||||
chr5:115233582
|
A | C | 1 | a0001c0001t0056g0034 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.613-2561T>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 5/8 | chr5 | 115233582 | ||||||
chr5:115233612
|
A | C | 1 | a0001c0001t0001g0159 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.613-2591T>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 5/8 | chr5 | 115233612 | ||||||
chr5:115233613
|
C | G | 1 | a0001c0001t0103g0191 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.613-2592G>C | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 5/8 | chr5 | 115233613 | ||||||
chr5:115233661
|
T | A | 99 | a0001c0001t0004g0068a0001c0001t0004g0088a0001c0001t0004g0136others(96): Show | 102 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.613-2640A>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 5/8 | chr5 | 115233661 | ||||||
chr5:115233682
|
G | T | 8 | a0001c0001t0091g0027a0001c0001t0092g0025a0001c0001t0093g0026others(5): Show | 8 | HG02055.hp2 HG02615.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.613-2661C>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 5/8 | chr5 | 115233682 | ||||||
chr5:115233755
|
A | G | 3 | a0001c0001t0117g0299a0001c0001t0118g0297a0001c0001t0119g0298 | 3 | HG02717.hp2 HG02818.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.612+2635T>C | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 5/8 | chr5 | 115233755 | ||||||
chr5:115233829
|
T | C | 257 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(254): Show | 271 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.612+2561A>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 5/8 | chr5 | 115233829 | ||||||
chr5:115233832
|
T | C | 1 | a0001c0001t0102g0189 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.612+2558A>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 5/8 | chr5 | 115233832 | ||||||
chr5:115233833
|
A | G | 1 | a0001c0001t0106g0345 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.612+2557T>C | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 5/8 | chr5 | 115233833 | ||||||
chr5:115234005
|
A | T | 3 | a0001c0001t0045g0031a0001c0001t0045g0032a0001c0001t0129g0030 | 3 | HG01891.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.612+2385T>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 5/8 | chr5 | 115234005 | ||||||
chr5:115234166
|
GT | G | 257 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(254): Show | 271 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.612+2223delA | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 5/8 | chr5 | 115234166 | ||||||
chr5:115234208
|
CAA | C | 8 | a0001c0001t0036g0156a0001c0001t0036g0157a0001c0001t0041g0261others(5): Show | 8 | HG01243.hp2 HG01884.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.612+2180_612+2181d others(4): Show |
PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 5/8 | chr5 | 115234208 | ||||||
chr5:115234215
|
CA | C | 256 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(253): Show | 270 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.612+2174delT | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 5/8 | chr5 | 115234215 | ||||||
chr5:115234220
|
A | G | 4 | a0002c0003t0034g0151a0002c0003t0034g0152a0002c0003t0057g0153others(1): Show | 4 | HG01074.hp1 HG03098.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.612+2170T>C | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 5/8 | chr5 | 115234220 | ||||||
chr5:115234232
|
T | C | 4 | a0002c0003t0034g0151a0002c0003t0034g0152a0002c0003t0057g0153others(1): Show | 4 | HG01074.hp1 HG03098.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.612+2158A>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 5/8 | chr5 | 115234232 | ||||||
chr5:115234299
|
G | A | 72 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(69): Show | 82 | HG00408.hp2 HG00558.hp2 HG00621.hp1 others(79): Show |
intron_variant | MODIFIER | c.612+2091C>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 5/8 | chr5 | 115234299 | ||||||
chr5:115234337
|
C | T | 6 | a0001c0001t0003g0182a0001c0001t0031g0176a0001c0001t0031g0177others(3): Show | 6 | NA18964.hp1 NA18970.hp2 NA18990.hp2 others(3): Show |
intron_variant | MODIFIER | c.612+2053G>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 5/8 | chr5 | 115234337 | ||||||
chr5:115234365
|
A | G | 86 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(83): Show | 97 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(94): Show |
intron_variant | MODIFIER | c.612+2025T>C | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 5/8 | chr5 | 115234365 | ||||||
chr5:115234442
|
T | G | 2 | a0001c0001t0117g0299a0001c0001t0118g0297 | 2 | HG02818.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.612+1948A>C | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 5/8 | chr5 | 115234442 | ||||||
chr5:115234444
|
T | G | 11 | a0001c0001t0018g0046a0001c0001t0018g0047a0001c0001t0018g0050others(8): Show | 11 | HG00642.hp1 HG01074.hp2 HG01261.hp1 others(8): Show |
intron_variant | MODIFIER | c.612+1946A>C | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 5/8 | chr5 | 115234444 | ||||||
chr5:115234607
|
T | A | 82 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(79): Show | 92 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(89): Show |
intron_variant | MODIFIER | c.612+1783A>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 5/8 | chr5 | 115234607 | ||||||
chr5:115234910
|
T | G | 11 | a0001c0001t0018g0046a0001c0001t0018g0047a0001c0001t0018g0050others(8): Show | 11 | HG00642.hp1 HG01074.hp2 HG01261.hp1 others(8): Show |
intron_variant | MODIFIER | c.612+1480A>C | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 5/8 | chr5 | 115234910 | ||||||
chr5:115235068
|
T | G | 5 | a0001c0001t0038g0216a0001c0001t0038g0219a0001c0001t0063g0217others(2): Show | 5 | HG02055.hp1 HG02486.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.612+1322A>C | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 5/8 | chr5 | 115235068 | ||||||
chr5:115235394
|
G | T | 1 | a0001c0001t0068g0033 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.612+996C>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 5/8 | chr5 | 115235394 | ||||||
chr5:115235413
|
G | T | 3 | a0001c0001t0042g0259a0001c0001t0042g0346a0001c0001t0106g0345 | 3 | HG02258.hp1 HG02896.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.612+977C>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 5/8 | chr5 | 115235413 | ||||||
chr5:115235420
|
T | C | 4 | a0002c0003t0034g0151a0002c0003t0034g0152a0002c0003t0057g0153others(1): Show | 4 | HG01074.hp1 HG03098.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.612+970A>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 5/8 | chr5 | 115235420 | ||||||
chr5:115235561
|
C | T | 34 | a0001c0001t0025g0193a0001c0001t0025g0194a0001c0001t0025g0195others(31): Show | 34 | HG01192.hp1 HG01243.hp1 HG01496.hp1 others(31): Show |
intron_variant | MODIFIER | c.612+829G>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 5/8 | chr5 | 115235561 | ||||||
chr5:115235796
|
G | C | 8 | a0001c0001t0091g0027a0001c0001t0092g0025a0001c0001t0093g0026others(5): Show | 8 | HG02055.hp2 HG02615.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.612+594C>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 5/8 | chr5 | 115235796 | ||||||
chr5:115235842
|
C | T | 34 | a0001c0001t0025g0193a0001c0001t0025g0194a0001c0001t0025g0195others(31): Show | 34 | HG01192.hp1 HG01243.hp1 HG01496.hp1 others(31): Show |
intron_variant | MODIFIER | c.612+548G>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 5/8 | chr5 | 115235842 | ||||||
chr5:115235859
|
C | A | 2 | a0001c0001t0041g0261a0001c0001t0041g0262 | 2 | HG02622.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.612+531G>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 5/8 | chr5 | 115235859 | ||||||
chr5:115235994
|
C | T | 1 | a0001c0001t0059g0296 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.612+396G>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 5/8 | chr5 | 115235994 | ||||||
chr5:115236061
|
G | T | 256 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(253): Show | 270 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.612+329C>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 5/8 | chr5 | 115236061 | ||||||
chr5:115236088
|
T | C | 8 | a0001c0001t0091g0027a0001c0001t0092g0025a0001c0001t0093g0026others(5): Show | 8 | HG02055.hp2 HG02615.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.612+302A>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 5/8 | chr5 | 115236088 | ||||||
chr5:115236283
|
C | A | 7 | a0001c0001t0001g0012a0001c0001t0001g0117a0001c0001t0001g0119others(4): Show | 8 | HG00741.hp2 HG01934.hp2 HG01975.hp2 others(5): Show |
intron_variant | MODIFIER | c.612+107G>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 5/8 | chr5 | 115236283 | ||||||
chr5:115236554
|
T | C | 2 | a0001c0001t0068g0033a0001c0001t0069g0202 | 2 | HG01109.hp1 HG01168.hp1 |
intron_variant | MODIFIER | c.480-32A>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 4/8 | chr5 | 115236554 | ||||||
chr5:115236749
|
T | A | 26 | a0001c0001t0026g0277a0001c0001t0026g0288a0001c0001t0026g0290others(23): Show | 26 | HG01192.hp1 HG01891.hp2 HG01934.hp1 others(23): Show |
intron_variant | MODIFIER | c.480-227A>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 4/8 | chr5 | 115236749 | ||||||
chr5:115236765
|
C | T | 10 | a0001c0001t0036g0156a0001c0001t0036g0157a0001c0001t0041g0261others(7): Show | 10 | HG01243.hp2 HG01496.hp2 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.480-243G>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 4/8 | chr5 | 115236765 | ||||||
chr5:115236861
|
A | T | 1 | a0001c0001t0002g0308 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.480-339T>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 4/8 | chr5 | 115236861 | ||||||
chr5:115236862
|
A | T | 1 | a0001c0001t0002g0308 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.480-340T>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 4/8 | chr5 | 115236862 | ||||||
chr5:115236863
|
A | T | 1 | a0001c0001t0002g0308 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.480-341T>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 4/8 | chr5 | 115236863 | ||||||
chr5:115236864
|
A | T | 1 | a0001c0001t0002g0308 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.480-342T>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 4/8 | chr5 | 115236864 | ||||||
chr5:115237154
|
A | G | 35 | a0001c0001t0025g0193a0001c0001t0025g0194a0001c0001t0025g0195others(32): Show | 35 | HG01192.hp1 HG01243.hp1 HG01496.hp1 others(32): Show |
intron_variant | MODIFIER | c.480-632T>C | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 4/8 | chr5 | 115237154 | ||||||
chr5:115237465
|
C | T | 3 | a0001c0002t0004g0128a0001c0002t0004g0209a0001c0002t0015g0133 | 3 | NA18968.hp2 NA18975.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.479+393G>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 4/8 | chr5 | 115237465 | ||||||
chr5:115237567
|
G | T | 1 | a0001c0001t0010g0078 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.479+291C>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 4/8 | chr5 | 115237567 | ||||||
chr5:115238159
|
C | T | 1 | a0001c0001t0086g0077 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.328-150G>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 3/8 | chr5 | 115238159 | ||||||
chr5:115238176
|
A | T | 114 | a0001c0001t0004g0068a0001c0001t0004g0088a0001c0001t0004g0136others(111): Show | 119 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(116): Show |
intron_variant | MODIFIER | c.328-167T>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 3/8 | chr5 | 115238176 | ||||||
chr5:115238291
|
A | AT | 87 | a0001c0001t0001g0173a0001c0001t0001g0179a0001c0001t0002g0004others(84): Show | 95 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(92): Show |
intron_variant | MODIFIER | c.328-283dupA | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 3/8 | chr5 | 115238291 | ||||||
chr5:115238291
|
A | ATT | 95 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(92): Show | 109 | HG00408.hp2 HG00558.hp2 HG00609.hp1 others(106): Show |
intron_variant | MODIFIER | c.328-284_328-283dup others(2): Show |
PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 3/8 | chr5 | 115238291 | ||||||
chr5:115238291
|
A | ATTT | 40 | a0001c0001t0001g0114a0001c0001t0001g0119a0001c0001t0001g0142others(37): Show | 40 | HG00621.hp1 HG00673.hp1 HG00741.hp2 others(37): Show |
intron_variant | MODIFIER | c.328-285_328-283dup others(3): Show |
PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 3/8 | chr5 | 115238291 | ||||||
chr5:115238291
|
A | ATTTTTTT others(3): Show |
5 | a0001c0001t0018g0047a0001c0001t0051g0265a0001c0001t0064g0051others(2): Show | 5 | HG01074.hp2 HG01243.hp2 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.328-292_328-283dup others(10): Show |
PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 3/8 | chr5 | 115238291 | ||||||
chr5:115238291
|
A | ATTTTTTT others(4): Show |
2 | a0001c0001t0018g0046a0001c0001t0027g0270 | 2 | HG00642.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.328-293_328-283dup others(11): Show |
PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 3/8 | chr5 | 115238291 | ||||||
chr5:115238291
|
A | ATTTTTTT others(7): Show |
3 | a0001c0001t0049g0269a0001c0001t0051g0264a0001c0001t0127g0273 | 3 | HG02970.hp1 HG03453.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.328-296_328-283dup others(14): Show |
PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 3/8 | chr5 | 115238291 | ||||||
chr5:115238291
|
A | ATTTTTTT others(9): Show |
2 | a0001c0001t0055g0295a0001c0001t0056g0034 | 2 | HG01496.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.328-298_328-283dup others(16): Show |
PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 3/8 | chr5 | 115238291 | ||||||
chr5:115238291
|
A | ATTTTTTT others(13): Show |
3 | a0001c0001t0028g0287a0001c0001t0029g0271a0001c0001t0029g0275 | 3 | HG03490.hp2 HG03492.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.328-302_328-283dup others(20): Show |
PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 3/8 | chr5 | 115238291 | ||||||
chr5:115238291
|
A | ATTTTTTT others(14): Show |
2 | a0001c0001t0050g0268a0001c0001t0050g0272 | 2 | HG02273.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.328-303_328-283dup others(21): Show |
PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 3/8 | chr5 | 115238291 | ||||||
chr5:115238291
|
A | ATTTTTTT others(15): Show |
3 | a0001c0001t0026g0277a0001c0001t0029g0286a0001c0001t0049g0274 | 3 | HG01934.hp1 HG02622.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.328-304_328-283dup others(22): Show |
PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 3/8 | chr5 | 115238291 | ||||||
chr5:115238291
|
A | ATTTTTTT others(16): Show |
1 | a0001c0001t0054g0279 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.328-305_328-283dup others(23): Show |
PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 3/8 | chr5 | 115238291 | ||||||
chr5:115238291
|
A | ATTTTTTT others(19): Show |
1 | a0001c0001t0027g0289 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.328-308_328-283dup others(26): Show |
PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 3/8 | chr5 | 115238291 | ||||||
chr5:115238291
|
A | ATTTTTTT others(20): Show |
1 | a0001c0001t0026g0290 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.328-309_328-283dup others(27): Show |
PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 3/8 | chr5 | 115238291 | ||||||
chr5:115238291
|
A | ATTTTTTT others(21): Show |
1 | a0001c0001t0124g0291 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.328-310_328-283dup others(28): Show |
PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 3/8 | chr5 | 115238291 | ||||||
chr5:115238291
|
A | ATTTTTTT others(22): Show |
2 | a0001c0001t0028g0285a0001c0001t0129g0030 | 2 | HG01891.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.328-311_328-283dup others(29): Show |
PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 3/8 | chr5 | 115238291 | ||||||
chr5:115238291
|
ATTTTTTT others(3): Show |
A | 9 | a0001c0001t0025g0193a0001c0001t0025g0194a0001c0001t0025g0195others(6): Show | 9 | HG01243.hp1 HG01496.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.328-292_328-283del others(10): Show |
PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 3/8 | chr5 | 115238291 | ||||||
chr5:115238414
|
C | T | 1 | a0001c0001t0106g0345 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.328-405G>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 3/8 | chr5 | 115238414 | ||||||
chr5:115239034
|
C | G | 33 | a0001c0001t0003g0003a0001c0001t0003g0230a0001c0001t0003g0232others(30): Show | 36 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(33): Show |
intron_variant | MODIFIER | c.328-1025G>C | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 3/8 | chr5 | 115239034 | ||||||
chr5:115239123
|
C | T | 5 | a0001c0001t0002g0311a0001c0001t0002g0312a0001c0001t0016g0018others(2): Show | 6 | HG01069.hp1 HG01071.hp1 HG01109.hp2 others(3): Show |
intron_variant | MODIFIER | c.328-1114G>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 3/8 | chr5 | 115239123 | ||||||
chr5:115239125
|
C | T | 34 | a0001c0001t0025g0193a0001c0001t0025g0194a0001c0001t0025g0195others(31): Show | 34 | HG01192.hp1 HG01243.hp1 HG01496.hp1 others(31): Show |
intron_variant | MODIFIER | c.328-1116G>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 3/8 | chr5 | 115239125 | ||||||
chr5:115239269
|
C | T | 8 | a0001c0001t0091g0027a0001c0001t0092g0025a0001c0001t0093g0026others(5): Show | 8 | HG02055.hp2 HG02615.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.328-1260G>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 3/8 | chr5 | 115239269 | ||||||
chr5:115239313
|
G | C | 96 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(93): Show | 108 | HG00408.hp2 HG00558.hp2 HG00621.hp1 others(105): Show |
intron_variant | MODIFIER | c.328-1304C>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 3/8 | chr5 | 115239313 | ||||||
chr5:115239390
|
T | A | 2 | a0001c0001t0036g0156a0001c0001t0036g0157 | 2 | HG01884.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.328-1381A>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 3/8 | chr5 | 115239390 | ||||||
chr5:115239440
|
G | C | 1 | a0001c0001t0021g0054 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.328-1431C>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 3/8 | chr5 | 115239440 | ||||||
chr5:115239487
|
T | A | 1 | a0001c0001t0001g0058 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.328-1478A>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 3/8 | chr5 | 115239487 | ||||||
chr5:115239521
|
T | G | 2 | a0001c0001t0055g0295a0001c0001t0056g0034 | 2 | HG01496.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.328-1512A>C | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 3/8 | chr5 | 115239521 | ||||||
chr5:115239674
|
A | G | 8 | a0001c0001t0091g0027a0001c0001t0092g0025a0001c0001t0093g0026others(5): Show | 8 | HG02055.hp2 HG02615.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.328-1665T>C | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 3/8 | chr5 | 115239674 | ||||||
chr5:115239702
|
C | G | 1 | a0001c0001t0003g0255 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.328-1693G>C | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 3/8 | chr5 | 115239702 | ||||||
chr5:115239800
|
C | A | 36 | a0001c0001t0025g0193a0001c0001t0025g0194a0001c0001t0025g0195others(33): Show | 36 | HG01192.hp1 HG01243.hp1 HG01496.hp1 others(33): Show |
intron_variant | MODIFIER | c.327+1739G>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 3/8 | chr5 | 115239800 | ||||||
chr5:115239814
|
G | A | 1 | a0001c0001t0068g0033 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.327+1725C>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 3/8 | chr5 | 115239814 | ||||||
chr5:115239819
|
T | C | 8 | a0001c0001t0091g0027a0001c0001t0092g0025a0001c0001t0093g0026others(5): Show | 8 | HG02055.hp2 HG02615.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.327+1720A>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 3/8 | chr5 | 115239819 | ||||||
chr5:115239924
|
A | G | 1 | a0001c0001t0024g0060 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.327+1615T>C | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 3/8 | chr5 | 115239924 | ||||||
chr5:115240081
|
T | C | 1 | a0001c0001t0042g0346 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.327+1458A>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 3/8 | chr5 | 115240081 | ||||||
chr5:115240169
|
G | A | 1 | a0001c0001t0116g0040 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.327+1370C>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 3/8 | chr5 | 115240169 | ||||||
chr5:115240235
|
G | A | 9 | a0001c0002t0004g0014a0001c0002t0004g0063a0001c0002t0004g0128others(6): Show | 10 | HG02071.hp1 HG02148.hp2 NA18941.hp2 others(7): Show |
intron_variant | MODIFIER | c.327+1304C>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 3/8 | chr5 | 115240235 | ||||||
chr5:115240313
|
C | G | 1 | a0001c0001t0116g0040 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.327+1226G>C | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 3/8 | chr5 | 115240313 | ||||||
chr5:115240456
|
T | A | 8 | a0001c0001t0091g0027a0001c0001t0092g0025a0001c0001t0093g0026others(5): Show | 8 | HG02055.hp2 HG02615.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.327+1083A>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 3/8 | chr5 | 115240456 | ||||||
chr5:115240901
|
T | C | 139 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(136): Show | 151 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(148): Show |
intron_variant | MODIFIER | c.327+638A>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 3/8 | chr5 | 115240901 | ||||||
chr5:115241091
|
C | A | 1 | a0001c0001t0121g0146 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.327+448G>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 3/8 | chr5 | 115241091 | ||||||
chr5:115241113
|
T | C | 4 | a0001c0001t0021g0053a0001c0001t0021g0054a0001c0001t0021g0056others(1): Show | 4 | HG00642.hp2 HG00733.hp1 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.327+426A>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 3/8 | chr5 | 115241113 | ||||||
chr5:115241405
|
T | C | 1 | a0001c0001t0116g0040 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.327+134A>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 3/8 | chr5 | 115241405 | ||||||
chr5:115241498
|
C | A | 1 | a0001c0001t0005g0091 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.327+41G>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 3/8 | chr5 | 115241498 | ||||||
chr5:115241779
|
T | C | 2 | a0001c0001t0055g0295a0001c0001t0056g0034 | 2 | HG01496.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.260-173A>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 2/8 | chr5 | 115241779 | ||||||
chr5:115241849
|
C | T | 2 | a0001c0001t0010g0071a0001c0001t0010g0200 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.260-243G>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 2/8 | chr5 | 115241849 | ||||||
chr5:115241914
|
G | A | 10 | a0001c0001t0032g0245a0001c0001t0032g0246a0001c0001t0091g0027others(7): Show | 10 | HG02055.hp2 HG02109.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.260-308C>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 2/8 | chr5 | 115241914 | ||||||
chr5:115242022
|
C | T | 1 | a0001c0001t0120g0139 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.260-416G>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 2/8 | chr5 | 115242022 | ||||||
chr5:115242032
|
G | A | 1 | a0001c0001t0020g0101 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.260-426C>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 2/8 | chr5 | 115242032 | ||||||
chr5:115242049
|
T | C | 4 | a0001c0001t0005g0302a0001c0001t0025g0193a0001c0001t0025g0194others(1): Show | 4 | HG01243.hp1 NA18522.hp2 NA18747.hp1 others(1): Show |
intron_variant | MODIFIER | c.260-443A>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 2/8 | chr5 | 115242049 | ||||||
chr5:115242154
|
T | C | 1 | a0001c0001t0042g0259 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.260-548A>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 2/8 | chr5 | 115242154 | ||||||
chr5:115242162
|
G | C | 2 | a0001c0001t0043g0155a0001c0001t0043g0185 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.260-556C>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 2/8 | chr5 | 115242162 | ||||||
chr5:115242207
|
C | T | 2 | a0001c0001t0017g0070a0001c0001t0017g0214 | 2 | HG02280.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.260-601G>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 2/8 | chr5 | 115242207 | ||||||
chr5:115242253
|
C | G | 1 | a0001c0001t0059g0296 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.260-647G>C | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 2/8 | chr5 | 115242253 | ||||||
chr5:115242277
|
A | G | 1 | a0001c0001t0030g0337 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.260-671T>C | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 2/8 | chr5 | 115242277 | ||||||
chr5:115242522
|
C | T | 1 | a0001c0001t0140g0278 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.260-916G>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 2/8 | chr5 | 115242522 | ||||||
chr5:115242534
|
T | C | 1 | a0001c0001t0134g0180 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.260-928A>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 2/8 | chr5 | 115242534 | ||||||
chr5:115242582
|
T | C | 1 | a0001c0001t0089g0049 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.260-976A>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 2/8 | chr5 | 115242582 | ||||||
chr5:115242740
|
G | A | 3 | a0001c0001t0027g0270a0001c0001t0049g0269a0001c0001t0127g0273 | 3 | HG02970.hp1 HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.260-1134C>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 2/8 | chr5 | 115242740 | ||||||
chr5:115242760
|
A | G | 8 | a0001c0001t0091g0027a0001c0001t0092g0025a0001c0001t0093g0026others(5): Show | 8 | HG02055.hp2 HG02615.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.260-1154T>C | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 2/8 | chr5 | 115242760 | ||||||
chr5:115242804
|
T | C | 8 | a0001c0001t0091g0027a0001c0001t0092g0025a0001c0001t0093g0026others(5): Show | 8 | HG02055.hp2 HG02615.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.260-1198A>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 2/8 | chr5 | 115242804 | ||||||
chr5:115242897
|
G | A | 1 | a0001c0001t0001g0174 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.260-1291C>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 2/8 | chr5 | 115242897 | ||||||
chr5:115242913
|
G | A | 3 | a0001c0001t0045g0031a0001c0001t0045g0032a0001c0001t0129g0030 | 3 | HG01891.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.260-1307C>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 2/8 | chr5 | 115242913 | ||||||
chr5:115242965
|
GAA | G | 98 | a0001c0001t0004g0068a0001c0001t0004g0088a0001c0001t0004g0136others(95): Show | 102 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.260-1361_260-1360d others(4): Show |
PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 2/8 | chr5 | 115242965 | ||||||
chr5:115242995
|
T | C | 11 | a0001c0001t0018g0046a0001c0001t0018g0047a0001c0001t0018g0050others(8): Show | 11 | HG00642.hp1 HG01074.hp2 HG01261.hp1 others(8): Show |
intron_variant | MODIFIER | c.260-1389A>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 2/8 | chr5 | 115242995 | ||||||
chr5:115243219
|
A | T | 5 | a0001c0001t0005g0093a0001c0001t0005g0300a0001c0001t0005g0301others(2): Show | 5 | HG00673.hp1 HG02015.hp1 HG02040.hp2 others(2): Show |
intron_variant | MODIFIER | c.260-1613T>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 2/8 | chr5 | 115243219 | ||||||
chr5:115243311
|
G | A | 1 | a0001c0001t0116g0040 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.260-1705C>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 2/8 | chr5 | 115243311 | ||||||
chr5:115243384
|
T | C | 1 | a0001c0001t0116g0040 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.260-1778A>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 2/8 | chr5 | 115243384 | ||||||
chr5:115243713
|
T | C | 1 | a0001c0001t0011g0102 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.260-2107A>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 2/8 | chr5 | 115243713 | ||||||
chr5:115244090
|
C | A | 8 | a0001c0001t0091g0027a0001c0001t0092g0025a0001c0001t0093g0026others(5): Show | 8 | HG02055.hp2 HG02615.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.260-2484G>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 2/8 | chr5 | 115244090 | ||||||
chr5:115244135
|
C | T | 2 | a0001c0001t0068g0033a0001c0001t0069g0202 | 2 | HG01109.hp1 HG01168.hp1 |
intron_variant | MODIFIER | c.260-2529G>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 2/8 | chr5 | 115244135 | ||||||
chr5:115244281
|
C | A | 53 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0036others(50): Show | 57 | HG00408.hp2 HG00558.hp2 HG01167.hp1 others(54): Show |
intron_variant | MODIFIER | c.260-2675G>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 2/8 | chr5 | 115244281 | ||||||
chr5:115244357
|
C | T | 1 | a0001c0001t0059g0296 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.260-2751G>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 2/8 | chr5 | 115244357 | ||||||
chr5:115244397
|
G | A | 45 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0036others(42): Show | 47 | HG00408.hp2 HG00558.hp2 HG01167.hp1 others(44): Show |
intron_variant | MODIFIER | c.260-2791C>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 2/8 | chr5 | 115244397 | ||||||
chr5:115244413
|
T | C | 8 | a0001c0001t0091g0027a0001c0001t0092g0025a0001c0001t0093g0026others(5): Show | 8 | HG02055.hp2 HG02615.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.260-2807A>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 2/8 | chr5 | 115244413 | ||||||
chr5:115244452
|
G | A | 1 | a0001c0002t0004g0130 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.260-2846C>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 2/8 | chr5 | 115244452 | ||||||
chr5:115244455
|
ACT | A | 5 | a0001c0001t0091g0027a0001c0001t0094g0024a0001c0001t0095g0028others(2): Show | 5 | HG02615.hp2 HG02809.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.260-2851_260-2850d others(4): Show |
PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 2/8 | chr5 | 115244455 | ||||||
chr5:115244458
|
C | G | 3 | a0001c0001t0092g0025a0001c0001t0093g0026a0001c0001t0096g0023 | 3 | HG02055.hp2 HG02886.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.260-2852G>C | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 2/8 | chr5 | 115244458 | ||||||
chr5:115244460
|
G | C | 3 | a0001c0001t0092g0025a0001c0001t0093g0026a0001c0001t0096g0023 | 3 | HG02055.hp2 HG02886.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.260-2854C>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 2/8 | chr5 | 115244460 | ||||||
chr5:115244463
|
T | A | 3 | a0001c0001t0092g0025a0001c0001t0093g0026a0001c0001t0096g0023 | 3 | HG02055.hp2 HG02886.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.260-2857A>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 2/8 | chr5 | 115244463 | ||||||
chr5:115244466
|
C | A | 3 | a0001c0001t0092g0025a0001c0001t0093g0026a0001c0001t0096g0023 | 3 | HG02055.hp2 HG02886.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.260-2860G>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 2/8 | chr5 | 115244466 | ||||||
chr5:115244466
|
C | CA | 157 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0052others(154): Show | 168 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.260-2861dupT | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 2/8 | chr5 | 115244466 | ||||||
chr5:115244466
|
C | CAA | 65 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0016others(62): Show | 69 | HG00621.hp2 HG00642.hp2 HG00673.hp1 others(66): Show |
intron_variant | MODIFIER | c.260-2862_260-2861d others(4): Show |
PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 2/8 | chr5 | 115244466 | ||||||
chr5:115244480
|
A | AAG | 34 | a0001c0001t0025g0193a0001c0001t0025g0194a0001c0001t0026g0277others(31): Show | 34 | HG01192.hp1 HG01243.hp1 HG01496.hp1 others(31): Show |
intron_variant | MODIFIER | c.260-2875_260-2874i others(4): Show |
PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 2/8 | chr5 | 115244480 | ||||||
chr5:115244510
|
C | T | 1 | a0001c0001t0059g0296 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.260-2904G>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 2/8 | chr5 | 115244510 | ||||||
chr5:115244534
|
A | G | 1 | a0001c0001t0006g0333 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.260-2928T>C | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 2/8 | chr5 | 115244534 | ||||||
chr5:115244643
|
C | G | 268 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(265): Show | 284 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(281): Show |
intron_variant | MODIFIER | c.260-3037G>C | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 2/8 | chr5 | 115244643 | ||||||
chr5:115244682
|
G | C | 8 | a0001c0001t0091g0027a0001c0001t0092g0025a0001c0001t0093g0026others(5): Show | 8 | HG02055.hp2 HG02615.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.260-3076C>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 2/8 | chr5 | 115244682 | ||||||
chr5:115244685
|
G | A | 1 | a0001c0001t0123g0329 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.260-3079C>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 2/8 | chr5 | 115244685 | ||||||
chr5:115244840
|
C | T | 2 | a0001c0001t0011g0067a0001c0001t0088g0187 | 2 | NA18946.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.260-3234G>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 2/8 | chr5 | 115244840 | ||||||
chr5:115244955
|
G | A | 41 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0182others(38): Show | 46 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(43): Show |
intron_variant | MODIFIER | c.260-3349C>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 2/8 | chr5 | 115244955 | ||||||
chr5:115245045
|
T | C | 72 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(69): Show | 81 | HG00408.hp2 HG00558.hp2 HG00621.hp1 others(78): Show |
intron_variant | MODIFIER | c.260-3439A>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 2/8 | chr5 | 115245045 | ||||||
chr5:115245053
|
C | T | 8 | a0001c0001t0091g0027a0001c0001t0092g0025a0001c0001t0093g0026others(5): Show | 8 | HG02055.hp2 HG02615.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.260-3447G>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 2/8 | chr5 | 115245053 | ||||||
chr5:115245066
|
T | A | 2 | a0001c0001t0068g0033a0001c0001t0069g0202 | 2 | HG01109.hp1 HG01168.hp1 |
intron_variant | MODIFIER | c.260-3460A>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 2/8 | chr5 | 115245066 | ||||||
chr5:115245260
|
A | G | 2 | a0001c0001t0026g0277a0001c0001t0050g0268 | 2 | HG01934.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.260-3654T>C | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 2/8 | chr5 | 115245260 | ||||||
chr5:115245624
|
A | C | 1 | a0001c0001t0001g0260 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.260-4018T>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 2/8 | chr5 | 115245624 | ||||||
chr5:115245787
|
G | A | 8 | a0001c0001t0091g0027a0001c0001t0092g0025a0001c0001t0093g0026others(5): Show | 8 | HG02055.hp2 HG02615.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.260-4181C>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 2/8 | chr5 | 115245787 | ||||||
chr5:115245814
|
A | G | 39 | a0001c0001t0025g0193a0001c0001t0025g0194a0001c0001t0025g0195others(36): Show | 39 | HG01192.hp1 HG01243.hp1 HG01496.hp1 others(36): Show |
intron_variant | MODIFIER | c.260-4208T>C | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 2/8 | chr5 | 115245814 | ||||||
chr5:115246028
|
A | T | 1 | a0001c0001t0001g0160 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.260-4422T>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 2/8 | chr5 | 115246028 | ||||||
chr5:115246212
|
C | T | 2 | a0001c0001t0001g0159a0001c0001t0001g0171 | 2 | HG00558.hp2 NA18940.hp2 |
intron_variant | MODIFIER | c.260-4606G>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 2/8 | chr5 | 115246212 | ||||||
chr5:115246312
|
C | T | 1 | a0001c0001t0116g0040 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.260-4706G>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 2/8 | chr5 | 115246312 | ||||||
chr5:115246313
|
G | A | 122 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(119): Show | 134 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.260-4707C>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 2/8 | chr5 | 115246313 | ||||||
chr5:115246345
|
T | C | 54 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0036others(51): Show | 56 | HG00408.hp2 HG00558.hp2 HG01167.hp1 others(53): Show |
intron_variant | MODIFIER | c.260-4739A>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 2/8 | chr5 | 115246345 | ||||||
chr5:115246355
|
CA | C | 13 | a0001c0001t0001g0158a0001c0001t0004g0068a0001c0001t0007g0221others(10): Show | 13 | HG00140.hp1 HG02040.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.260-4750delT | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 2/8 | chr5 | 115246355 | ||||||
chr5:115246380
|
T | C | 1 | a0001c0001t0141g0035 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.260-4774A>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 2/8 | chr5 | 115246380 | ||||||
chr5:115246397
|
G | A | 3 | a0001c0001t0035g0043a0001c0001t0066g0041a0001c0001t0090g0044 | 3 | HG02965.hp1 HG03041.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.260-4791C>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 2/8 | chr5 | 115246397 | ||||||
chr5:115246409
|
G | A | 1 | a0001c0006t0002g0339 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.260-4803C>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 2/8 | chr5 | 115246409 | ||||||
chr5:115246603
|
C | G | 1 | a0001c0001t0107g0197 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.260-4997G>C | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 2/8 | chr5 | 115246603 | ||||||
chr5:115246720
|
G | A | 8 | a0001c0001t0091g0027a0001c0001t0092g0025a0001c0001t0093g0026others(5): Show | 8 | HG02055.hp2 HG02615.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.260-5114C>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 2/8 | chr5 | 115246720 | ||||||
chr5:115246842
|
G | A | 2 | a0001c0001t0025g0194a0001c0001t0025g0195 | 2 | HG01243.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.260-5236C>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 2/8 | chr5 | 115246842 | ||||||
chr5:115246991
|
G | A | 68 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(65): Show | 77 | HG00408.hp2 HG00558.hp2 HG00621.hp1 others(74): Show |
intron_variant | MODIFIER | c.260-5385C>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 2/8 | chr5 | 115246991 | ||||||
chr5:115247017
|
G | A | 8 | a0001c0001t0091g0027a0001c0001t0092g0025a0001c0001t0093g0026others(5): Show | 8 | HG02055.hp2 HG02615.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.260-5411C>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 2/8 | chr5 | 115247017 | ||||||
chr5:115247413
|
T | C | 2 | a0001c0001t0053g0250a0001c0001t0139g0233 | 2 | HG00323.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.259+5724A>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 2/8 | chr5 | 115247413 | ||||||
chr5:115247486
|
C | G | 2 | a0001c0001t0096g0023a0001c0001t0114g0022 | 2 | HG02886.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.259+5651G>C | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 2/8 | chr5 | 115247486 | ||||||
chr5:115247516
|
C | T | 1 | a0001c0001t0141g0035 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.259+5621G>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 2/8 | chr5 | 115247516 | ||||||
chr5:115248007
|
T | A | 1 | a0001c0001t0024g0149 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.259+5130A>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 2/8 | chr5 | 115248007 | ||||||
chr5:115248171
|
T | G | 2 | a0001c0001t0055g0295a0001c0001t0056g0034 | 2 | HG01496.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.259+4966A>C | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 2/8 | chr5 | 115248171 | ||||||
chr5:115248213
|
T | C | 8 | a0001c0001t0091g0027a0001c0001t0092g0025a0001c0001t0093g0026others(5): Show | 8 | HG02055.hp2 HG02615.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.259+4924A>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 2/8 | chr5 | 115248213 | ||||||
chr5:115248222
|
T | C | 3 | a0001c0001t0002g0330a0001c0001t0002g0331a0001c0001t0002g0340 | 3 | HG01433.hp2 HG01952.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.259+4915A>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 2/8 | chr5 | 115248222 | ||||||
chr5:115248340
|
T | C | 11 | a0001c0001t0018g0046a0001c0001t0018g0047a0001c0001t0018g0050others(8): Show | 11 | HG00642.hp1 HG01074.hp2 HG01261.hp1 others(8): Show |
intron_variant | MODIFIER | c.259+4797A>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 2/8 | chr5 | 115248340 | ||||||
chr5:115248723
|
T | C | 2 | a0001c0001t0014g0203a0001c0001t0084g0062 | 2 | HG02145.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.259+4414A>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 2/8 | chr5 | 115248723 | ||||||
chr5:115248814
|
C | T | 8 | a0001c0001t0091g0027a0001c0001t0092g0025a0001c0001t0093g0026others(5): Show | 8 | HG02055.hp2 HG02615.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.259+4323G>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 2/8 | chr5 | 115248814 | ||||||
chr5:115248815
|
G | A | 1 | a0001c0001t0119g0298 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.259+4322C>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 2/8 | chr5 | 115248815 | ||||||
chr5:115248863
|
C | G | 11 | a0001c0001t0008g0006a0001c0001t0008g0037a0001c0001t0008g0038others(8): Show | 12 | HG00642.hp1 HG01074.hp2 HG01261.hp1 others(9): Show |
intron_variant | MODIFIER | c.259+4274G>C | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 2/8 | chr5 | 115248863 | ||||||
chr5:115248905
|
T | C | 1 | a0001c0001t0068g0033 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.259+4232A>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 2/8 | chr5 | 115248905 | ||||||
chr5:115248987
|
T | G | 1 | a0001c0001t0001g0171 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.259+4150A>C | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 2/8 | chr5 | 115248987 | ||||||
chr5:115249210
|
T | G | 1 | a0001c0002t0070g0061 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.259+3927A>C | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 2/8 | chr5 | 115249210 | ||||||
chr5:115249301
|
A | G | 1 | a0001c0001t0004g0068 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.259+3836T>C | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 2/8 | chr5 | 115249301 | ||||||
chr5:115249429
|
G | A | 8 | a0001c0001t0091g0027a0001c0001t0092g0025a0001c0001t0093g0026others(5): Show | 8 | HG02055.hp2 HG02615.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.259+3708C>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 2/8 | chr5 | 115249429 | ||||||
chr5:115249545
|
C | G | 1 | a0001c0001t0011g0067 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.259+3592G>C | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 2/8 | chr5 | 115249545 | ||||||
chr5:115249610
|
T | C | 8 | a0001c0001t0091g0027a0001c0001t0092g0025a0001c0001t0093g0026others(5): Show | 8 | HG02055.hp2 HG02615.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.259+3527A>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 2/8 | chr5 | 115249610 | ||||||
chr5:115249663
|
C | T | 260 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(257): Show | 274 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(271): Show |
intron_variant | MODIFIER | c.259+3474G>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 2/8 | chr5 | 115249663 | ||||||
chr5:115249808
|
T | G | 8 | a0001c0001t0091g0027a0001c0001t0092g0025a0001c0001t0093g0026others(5): Show | 8 | HG02055.hp2 HG02615.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.259+3329A>C | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 2/8 | chr5 | 115249808 | ||||||
chr5:115250079
|
A | T | 1 | a0001c0001t0099g0154 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.259+3058T>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 2/8 | chr5 | 115250079 | ||||||
chr5:115250249
|
T | A | 1 | a0001c0001t0003g0251 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.259+2888A>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 2/8 | chr5 | 115250249 | ||||||
chr5:115250268
|
C | T | 1 | a0001c0001t0067g0042 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.259+2869G>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 2/8 | chr5 | 115250268 | ||||||
chr5:115250287
|
T | C | 2 | a0001c0001t0117g0299a0001c0001t0118g0297 | 2 | HG02818.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.259+2850A>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 2/8 | chr5 | 115250287 | ||||||
chr5:115250368
|
G | C | 2 | a0001c0001t0117g0299a0001c0001t0118g0297 | 2 | HG02818.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.259+2769C>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 2/8 | chr5 | 115250368 | ||||||
chr5:115250382
|
G | C | 2 | a0001c0001t0055g0295a0001c0001t0056g0034 | 2 | HG01496.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.259+2755C>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 2/8 | chr5 | 115250382 | ||||||
chr5:115250714
|
T | C | 1 | a0001c0001t0023g0103 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.259+2423A>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 2/8 | chr5 | 115250714 | ||||||
chr5:115250752
|
C | T | 1 | a0001c0001t0007g0066 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.259+2385G>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 2/8 | chr5 | 115250752 | ||||||
chr5:115251115
|
G | T | 8 | a0001c0001t0091g0027a0001c0001t0092g0025a0001c0001t0093g0026others(5): Show | 8 | HG02055.hp2 HG02615.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.259+2022C>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 2/8 | chr5 | 115251115 | ||||||
chr5:115251253
|
C | A | 260 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(257): Show | 274 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(271): Show |
intron_variant | MODIFIER | c.259+1884G>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 2/8 | chr5 | 115251253 | ||||||
chr5:115251316
|
T | C | 8 | a0001c0001t0006g0005a0001c0001t0006g0307a0001c0001t0006g0333others(5): Show | 10 | NA18948.hp1 NA18951.hp1 NA18975.hp2 others(7): Show |
intron_variant | MODIFIER | c.259+1821A>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 2/8 | chr5 | 115251316 | ||||||
chr5:115251343
|
T | A | 4 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0001t0001g0174others(1): Show | 4 | NA18980.hp2 NA18999.hp1 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.259+1794A>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 2/8 | chr5 | 115251343 | ||||||
chr5:115251397
|
C | T | 1 | a0001c0001t0081g0065 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.259+1740G>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 2/8 | chr5 | 115251397 | ||||||
chr5:115251414
|
C | T | 1 | a0001c0001t0102g0189 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.259+1723G>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 2/8 | chr5 | 115251414 | ||||||
chr5:115251446
|
G | T | 2 | a0001c0001t0007g0104a0001c0001t0020g0105 | 2 | HG02109.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.259+1691C>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 2/8 | chr5 | 115251446 | ||||||
chr5:115251452
|
G | A | 35 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(32): Show | 42 | HG00621.hp1 HG00741.hp2 HG01070.hp1 others(39): Show |
intron_variant | MODIFIER | c.259+1685C>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 2/8 | chr5 | 115251452 | ||||||
chr5:115251494
|
A | G | 28 | a0001c0001t0026g0277a0001c0001t0026g0288a0001c0001t0026g0290others(25): Show | 28 | HG01192.hp1 HG01891.hp2 HG01934.hp1 others(25): Show |
intron_variant | MODIFIER | c.259+1643T>C | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 2/8 | chr5 | 115251494 | ||||||
chr5:115251499
|
G | A | 3 | a0001c0001t0007g0123a0001c0001t0007g0125a0001c0001t0044g0124 | 3 | HG03688.hp1 NA18979.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.259+1638C>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 2/8 | chr5 | 115251499 | ||||||
chr5:115251524
|
T | C | 1 | a0001c0001t0103g0191 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.259+1613A>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 2/8 | chr5 | 115251524 | ||||||
chr5:115251561
|
A | T | 1 | a0001c0001t0006g0309 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.259+1576T>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 2/8 | chr5 | 115251561 | ||||||
chr5:115251596
|
A | G | 8 | a0001c0001t0036g0156a0001c0001t0036g0157a0001c0001t0041g0261others(5): Show | 8 | HG01243.hp2 HG01884.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.259+1541T>C | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 2/8 | chr5 | 115251596 | ||||||
chr5:115251657
|
C | G | 8 | a0001c0001t0091g0027a0001c0001t0092g0025a0001c0001t0093g0026others(5): Show | 8 | HG02055.hp2 HG02615.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.259+1480G>C | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 2/8 | chr5 | 115251657 | ||||||
chr5:115251676
|
C | T | 8 | a0001c0001t0091g0027a0001c0001t0092g0025a0001c0001t0093g0026others(5): Show | 8 | HG02055.hp2 HG02615.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.259+1461G>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 2/8 | chr5 | 115251676 | ||||||
chr5:115251724
|
G | A | 13 | a0001c0002t0004g0013a0001c0002t0004g0014a0001c0002t0004g0063others(10): Show | 15 | HG02071.hp1 HG02148.hp2 NA18941.hp2 others(12): Show |
intron_variant | MODIFIER | c.259+1413C>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 2/8 | chr5 | 115251724 | ||||||
chr5:115251792
|
A | G | 8 | a0001c0001t0091g0027a0001c0001t0092g0025a0001c0001t0093g0026others(5): Show | 8 | HG02055.hp2 HG02615.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.259+1345T>C | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 2/8 | chr5 | 115251792 | ||||||
chr5:115251814
|
G | A | 1 | a0001c0001t0028g0285 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.259+1323C>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 2/8 | chr5 | 115251814 | ||||||
chr5:115251831
|
TA | T | 7 | a0001c0001t0018g0046a0001c0001t0018g0047a0001c0001t0018g0050others(4): Show | 7 | HG00642.hp1 HG01074.hp2 HG01261.hp1 others(4): Show |
intron_variant | MODIFIER | c.259+1305delT | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 2/8 | chr5 | 115251831 | ||||||
chr5:115252001
|
C | T | 1 | a0001c0001t0007g0064 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.259+1136G>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 2/8 | chr5 | 115252001 | ||||||
chr5:115252159
|
T | C | 8 | a0001c0001t0003g0002a0001c0001t0003g0182a0001c0001t0003g0213others(5): Show | 10 | NA18947.hp1 NA18952.hp1 NA18957.hp2 others(7): Show |
intron_variant | MODIFIER | c.259+978A>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 2/8 | chr5 | 115252159 | ||||||
chr5:115252263
|
G | T | 5 | a0001c0001t0036g0156a0001c0001t0036g0157a0001c0001t0041g0261others(2): Show | 5 | HG01884.hp1 HG02615.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.259+874C>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 2/8 | chr5 | 115252263 | ||||||
chr5:115252455
|
A | G | 8 | a0001c0001t0091g0027a0001c0001t0092g0025a0001c0001t0093g0026others(5): Show | 8 | HG02055.hp2 HG02615.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.259+682T>C | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 2/8 | chr5 | 115252455 | ||||||
chr5:115252588
|
G | A | 1 | a0001c0001t0042g0259 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.259+549C>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 2/8 | chr5 | 115252588 | ||||||
chr5:115252608
|
T | C | 2 | a0001c0001t0018g0050a0001c0001t0064g0051 | 2 | HG03491.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.259+529A>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 2/8 | chr5 | 115252608 | ||||||
chr5:115252936
|
A | G | 7 | a0001c0001t0026g0290a0001c0001t0028g0287a0001c0001t0029g0271others(4): Show | 7 | HG02258.hp2 HG03195.hp2 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.259+201T>C | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 2/8 | chr5 | 115252936 | ||||||
chr5:115253052
|
C | CAAGT | 23 | a0001c0001t0018g0046a0001c0001t0018g0047a0001c0001t0018g0050others(20): Show | 23 | HG00642.hp1 HG01074.hp1 HG01074.hp2 others(20): Show |
intron_variant | MODIFIER | c.259+81_259+84dupAC others(2): Show |
PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 2/8 | chr5 | 115253052 | ||||||
chr5:115253455
|
A | G | 20 | a0001c0001t0001g0058a0001c0001t0018g0046a0001c0001t0018g0047others(17): Show | 20 | HG00642.hp1 HG01074.hp2 HG01261.hp1 others(17): Show |
intron_variant | MODIFIER | c.141-200T>C | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 1/8 | chr5 | 115253455 | ||||||
chr5:115253516
|
T | C | 2 | a0001c0001t0055g0295a0001c0001t0056g0034 | 2 | HG01496.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.141-261A>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 1/8 | chr5 | 115253516 | ||||||
chr5:115253521
|
C | A | 1 | a0001c0001t0029g0286 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.141-266G>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 1/8 | chr5 | 115253521 | ||||||
chr5:115253647
|
A | G | 1 | a0001c0001t0033g0235 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.141-392T>C | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 1/8 | chr5 | 115253647 | ||||||
chr5:115253681
|
G | A | 2 | a0001c0001t0041g0261a0001c0001t0041g0262 | 2 | HG02622.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.141-426C>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 1/8 | chr5 | 115253681 | ||||||
chr5:115253805
|
G | A | 1 | a0001c0001t0021g0056 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.141-550C>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 1/8 | chr5 | 115253805 | ||||||
chr5:115253836
|
T | C | 2 | a0001c0001t0131g0196a0001c0001t0134g0180 | 2 | HG02004.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.141-581A>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 1/8 | chr5 | 115253836 | ||||||
chr5:115254056
|
T | C | 1 | a0001c0001t0059g0296 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.141-801A>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 1/8 | chr5 | 115254056 | ||||||
chr5:115254154
|
A | C | 1 | a0001c0001t0068g0033 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.141-899T>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 1/8 | chr5 | 115254154 | ||||||
chr5:115254196
|
T | C | 1 | a0001c0001t0006g0309 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.141-941A>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 1/8 | chr5 | 115254196 | ||||||
chr5:115254211
|
G | A | 267 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(264): Show | 283 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(280): Show |
intron_variant | MODIFIER | c.141-956C>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 1/8 | chr5 | 115254211 | ||||||
chr5:115254450
|
T | C | 1 | a0001c0001t0077g0134 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.141-1195A>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 1/8 | chr5 | 115254450 | ||||||
chr5:115254526
|
T | C | 11 | a0001c0001t0018g0046a0001c0001t0018g0047a0001c0001t0018g0050others(8): Show | 11 | HG00642.hp1 HG01074.hp2 HG01261.hp1 others(8): Show |
intron_variant | MODIFIER | c.141-1271A>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 1/8 | chr5 | 115254526 | ||||||
chr5:115254601
|
C | CT | 256 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(253): Show | 272 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.141-1347dupA | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 1/8 | chr5 | 115254601 | ||||||
chr5:115254616
|
A | T | 4 | a0001c0001t0025g0193a0001c0001t0025g0194a0001c0001t0025g0195others(1): Show | 4 | HG01243.hp1 NA18522.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.141-1361T>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 1/8 | chr5 | 115254616 | ||||||
chr5:115254646
|
G | A | 138 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(135): Show | 150 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(147): Show |
intron_variant | MODIFIER | c.141-1391C>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 1/8 | chr5 | 115254646 | ||||||
chr5:115254896
|
T | C | 1 | a0001c0001t0056g0034 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.141-1641A>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 1/8 | chr5 | 115254896 | ||||||
chr5:115254904
|
A | G | 2 | a0001c0001t0001g0210a0001c0001t0001g0211 | 2 | NA18943.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.141-1649T>C | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 1/8 | chr5 | 115254904 | ||||||
chr5:115254958
|
T | C | 19 | a0001c0001t0018g0046a0001c0001t0018g0047a0001c0001t0018g0050others(16): Show | 19 | HG00642.hp1 HG01074.hp2 HG01261.hp1 others(16): Show |
intron_variant | MODIFIER | c.141-1703A>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 1/8 | chr5 | 115254958 | ||||||
chr5:115255194
|
G | T | 68 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0036others(65): Show | 72 | HG00408.hp2 HG00558.hp2 HG01074.hp1 others(69): Show |
intron_variant | MODIFIER | c.141-1939C>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 1/8 | chr5 | 115255194 | ||||||
chr5:115255230
|
G | A | 1 | a0001c0001t0028g0287 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.141-1975C>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 1/8 | chr5 | 115255230 | ||||||
chr5:115255556
|
A | C | 8 | a0001c0001t0091g0027a0001c0001t0092g0025a0001c0001t0093g0026others(5): Show | 8 | HG02055.hp2 HG02615.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.141-2301T>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 1/8 | chr5 | 115255556 | ||||||
chr5:115255665
|
T | C | 1 | a0001c0001t0002g0340 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.141-2410A>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 1/8 | chr5 | 115255665 | ||||||
chr5:115255755
|
T | C | 1 | a0001c0001t0068g0033 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.141-2500A>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 1/8 | chr5 | 115255755 | ||||||
chr5:115255942
|
C | T | 2 | a0001c0001t0036g0156a0001c0001t0036g0157 | 2 | HG01884.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.141-2687G>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 1/8 | chr5 | 115255942 | ||||||
chr5:115256029
|
C | G | 198 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(195): Show | 210 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.141-2774G>C | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 1/8 | chr5 | 115256029 | ||||||
chr5:115256134
|
A | G | 1 | a0001c0001t0006g0309 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.141-2879T>C | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 1/8 | chr5 | 115256134 | ||||||
chr5:115256156
|
T | C | 25 | a0001c0001t0026g0277a0001c0001t0026g0288a0001c0001t0026g0290others(22): Show | 25 | HG01192.hp1 HG01891.hp2 HG01934.hp1 others(22): Show |
intron_variant | MODIFIER | c.141-2901A>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 1/8 | chr5 | 115256156 | ||||||
chr5:115256271
|
C | T | 1 | a0001c0001t0002g0308 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.141-3016G>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 1/8 | chr5 | 115256271 | ||||||
chr5:115256291
|
A | C | 3 | a0001c0001t0092g0025a0001c0001t0093g0026a0001c0001t0094g0024 | 3 | HG02055.hp2 HG02615.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.141-3036T>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 1/8 | chr5 | 115256291 | ||||||
chr5:115256803
|
T | C | 2 | a0001c0001t0003g0252a0001c0001t0033g0253 | 2 | NA19006.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.141-3548A>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 1/8 | chr5 | 115256803 | ||||||
chr5:115256817
|
G | A | 1 | a0001c0001t0129g0030 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.141-3562C>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 1/8 | chr5 | 115256817 | ||||||
chr5:115256866
|
T | C | 2 | a0001c0001t0001g0181a0001c0001t0099g0154 | 2 | HG02083.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.141-3611A>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 1/8 | chr5 | 115256866 | ||||||
chr5:115257192
|
G | GA | 268 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(265): Show | 284 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(281): Show |
intron_variant | MODIFIER | c.141-3938dupT | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 1/8 | chr5 | 115257192 | ||||||
chr5:115257332
|
A | G | 300 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(297): Show | 319 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(316): Show |
intron_variant | MODIFIER | c.141-4077T>C | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 1/8 | chr5 | 115257332 | ||||||
chr5:115257368
|
G | GC | 3 | a0001c0001t0003g0182a0001c0001t0031g0183a0001c0001t0052g0184 | 3 | NA18970.hp2 NA18990.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.141-4114dupG | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 1/8 | chr5 | 115257368 | ||||||
chr5:115257529
|
T | A | 1 | a0001c0001t0106g0345 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.141-4274A>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 1/8 | chr5 | 115257529 | ||||||
chr5:115257530
|
C | CA | 172 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(169): Show | 183 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.141-4276dupT | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 1/8 | chr5 | 115257530 | ||||||
chr5:115257530
|
C | CAA | 6 | a0001c0001t0001g0208a0001c0001t0004g0136a0001c0001t0005g0137others(3): Show | 6 | HG01975.hp1 HG02132.hp2 NA18940.hp1 others(3): Show |
intron_variant | MODIFIER | c.141-4277_141-4276d others(4): Show |
PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 1/8 | chr5 | 115257530 | ||||||
chr5:115257530
|
CA | C | 22 | a0001c0001t0001g0057a0001c0001t0001g0142a0001c0001t0001g0143others(19): Show | 22 | HG00323.hp1 HG01074.hp1 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.141-4276delT | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 1/8 | chr5 | 115257530 | ||||||
chr5:115257629
|
C | G | 2 | a0001c0001t0096g0023a0001c0001t0114g0022 | 2 | HG02886.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.141-4374G>C | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 1/8 | chr5 | 115257629 | ||||||
chr5:115257638
|
G | A | 33 | a0001c0001t0025g0193a0001c0001t0025g0194a0001c0001t0025g0195others(30): Show | 33 | HG01192.hp1 HG01243.hp1 HG01496.hp1 others(30): Show |
intron_variant | MODIFIER | c.141-4383C>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 1/8 | chr5 | 115257638 | ||||||
chr5:115257780
|
A | T | 1 | a0001c0001t0139g0233 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.141-4525T>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 1/8 | chr5 | 115257780 | ||||||
chr5:115257822
|
A | G | 1 | a0001c0001t0068g0033 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.141-4567T>C | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 1/8 | chr5 | 115257822 | ||||||
chr5:115257932
|
T | G | 1 | a0001c0001t0050g0272 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.141-4677A>C | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 1/8 | chr5 | 115257932 | ||||||
chr5:115257965
|
A | T | 2 | a0001c0001t0046g0140a0001c0001t0120g0139 | 2 | HG01496.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.141-4710T>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 1/8 | chr5 | 115257965 | ||||||
chr5:115257997
|
T | C | 1 | a0001c0001t0042g0259 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.140+4715A>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 1/8 | chr5 | 115257997 | ||||||
chr5:115258120
|
C | A | 1 | a0001c0001t0131g0196 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.140+4592G>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 1/8 | chr5 | 115258120 | ||||||
chr5:115258213
|
A | G | 15 | a0001c0001t0008g0006a0001c0001t0008g0037a0001c0001t0008g0038others(12): Show | 16 | HG00642.hp1 HG01074.hp2 HG01261.hp1 others(13): Show |
intron_variant | MODIFIER | c.140+4499T>C | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 1/8 | chr5 | 115258213 | ||||||
chr5:115258312
|
C | G | 1 | a0001c0002t0070g0061 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.140+4400G>C | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 1/8 | chr5 | 115258312 | ||||||
chr5:115258418
|
G | T | 131 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(128): Show | 142 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.140+4294C>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 1/8 | chr5 | 115258418 | ||||||
chr5:115258423
|
T | C | 8 | a0001c0001t0091g0027a0001c0001t0092g0025a0001c0001t0093g0026others(5): Show | 8 | HG02055.hp2 HG02615.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.140+4289A>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 1/8 | chr5 | 115258423 | ||||||
chr5:115258442
|
C | T | 128 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(125): Show | 139 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.140+4270G>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 1/8 | chr5 | 115258442 | ||||||
chr5:115258845
|
G | A | 2 | a0001c0001t0107g0197a0001c0001t0109g0198 | 2 | HG01123.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.140+3867C>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 1/8 | chr5 | 115258845 | ||||||
chr5:115258916
|
G | C | 8 | a0001c0001t0091g0027a0001c0001t0092g0025a0001c0001t0093g0026others(5): Show | 8 | HG02055.hp2 HG02615.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.140+3796C>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 1/8 | chr5 | 115258916 | ||||||
chr5:115258947
|
C | G | 1 | a0001c0001t0139g0233 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.140+3765G>C | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 1/8 | chr5 | 115258947 | ||||||
chr5:115258961
|
T | C | 1 | a0001c0001t0068g0033 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.140+3751A>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 1/8 | chr5 | 115258961 | ||||||
chr5:115259310
|
G | A | 1 | a0001c0001t0027g0289 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.140+3402C>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 1/8 | chr5 | 115259310 | ||||||
chr5:115259417
|
C | T | 8 | a0001c0001t0091g0027a0001c0001t0092g0025a0001c0001t0093g0026others(5): Show | 8 | HG02055.hp2 HG02615.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.140+3295G>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 1/8 | chr5 | 115259417 | ||||||
chr5:115259612
|
C | T | 2 | a0001c0001t0003g0232a0001c0001t0033g0231 | 2 | NA18991.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.140+3100G>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 1/8 | chr5 | 115259612 | ||||||
chr5:115259620
|
C | T | 1 | a0001c0001t0024g0060 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.140+3092G>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 1/8 | chr5 | 115259620 | ||||||
chr5:115259685
|
C | CA | 54 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0001g0210others(51): Show | 55 | HG00642.hp1 HG00741.hp2 HG01074.hp2 others(52): Show |
intron_variant | MODIFIER | c.140+3026dupT | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 1/8 | chr5 | 115259685 | ||||||
chr5:115259685
|
C | CAA | 19 | a0001c0001t0008g0039a0001c0001t0017g0214a0001c0001t0021g0053others(16): Show | 19 | HG00642.hp2 HG00733.hp1 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.140+3025_140+3026d others(4): Show |
PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 1/8 | chr5 | 115259685 | ||||||
chr5:115259685
|
CA | C | 16 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(13): Show | 16 | HG01069.hp1 HG01070.hp2 HG01099.hp1 others(13): Show |
intron_variant | MODIFIER | c.140+3026delT | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 1/8 | chr5 | 115259685 | ||||||
chr5:115259743
|
G | A | 8 | a0001c0001t0091g0027a0001c0001t0092g0025a0001c0001t0093g0026others(5): Show | 8 | HG02055.hp2 HG02615.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.140+2969C>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 1/8 | chr5 | 115259743 | ||||||
chr5:115259752
|
G | A | 10 | a0001c0001t0007g0220a0001c0001t0007g0221a0001c0001t0007g0224others(7): Show | 10 | HG01928.hp2 HG01993.hp2 NA18945.hp2 others(7): Show |
intron_variant | MODIFIER | c.140+2960C>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 1/8 | chr5 | 115259752 | ||||||
chr5:115259757
|
A | G | 4 | a0001c0001t0021g0053a0001c0001t0021g0054a0001c0001t0021g0056others(1): Show | 4 | HG00642.hp2 HG00733.hp1 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.140+2955T>C | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 1/8 | chr5 | 115259757 | ||||||
chr5:115259949
|
T | C | 15 | a0001c0001t0008g0006a0001c0001t0008g0037a0001c0001t0008g0038others(12): Show | 16 | HG00642.hp1 HG01074.hp2 HG01261.hp1 others(13): Show |
intron_variant | MODIFIER | c.140+2763A>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 1/8 | chr5 | 115259949 | ||||||
chr5:115260158
|
G | A | 1 | a0001c0001t0056g0034 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.140+2554C>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 1/8 | chr5 | 115260158 | ||||||
chr5:115260213
|
A | G | 267 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(264): Show | 283 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(280): Show |
intron_variant | MODIFIER | c.140+2499T>C | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 1/8 | chr5 | 115260213 | ||||||
chr5:115260260
|
T | G | 2 | a0001c0001t0042g0259a0001c0001t0042g0346 | 2 | HG02258.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.140+2452A>C | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 1/8 | chr5 | 115260260 | ||||||
chr5:115260303
|
T | A | 1 | a0001c0001t0055g0295 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.140+2409A>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 1/8 | chr5 | 115260303 | ||||||
chr5:115260434
|
T | C | 1 | a0001c0001t0001g0260 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.140+2278A>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 1/8 | chr5 | 115260434 | ||||||
chr5:115260627
|
A | G | 1 | a0001c0001t0001g0052 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.140+2085T>C | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 1/8 | chr5 | 115260627 | ||||||
chr5:115260701
|
C | A | 1 | a0001c0001t0106g0345 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.140+2011G>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 1/8 | chr5 | 115260701 | ||||||
chr5:115260743
|
GC | G | 3 | a0001c0001t0117g0299a0001c0001t0118g0297a0001c0001t0119g0298 | 3 | HG02717.hp2 HG02818.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.140+1968delG | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 1/8 | chr5 | 115260743 | ||||||
chr5:115260995
|
A | G | 16 | a0001c0001t0008g0006a0001c0001t0008g0037a0001c0001t0008g0038others(13): Show | 17 | HG00642.hp1 HG01074.hp2 HG01261.hp1 others(14): Show |
intron_variant | MODIFIER | c.140+1717T>C | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 1/8 | chr5 | 115260995 | ||||||
chr5:115261028
|
T | C | 2 | a0001c0001t0041g0261a0001c0001t0041g0262 | 2 | HG02622.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.140+1684A>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 1/8 | chr5 | 115261028 | ||||||
chr5:115261047
|
C | T | 4 | a0001c0001t0008g0006a0001c0001t0008g0037a0001c0001t0008g0038others(1): Show | 5 | NA18944.hp2 NA18969.hp2 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.140+1665G>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 1/8 | chr5 | 115261047 | ||||||
chr5:115261066
|
A | G | 1 | a0001c0001t0001g0036 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.140+1646T>C | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 1/8 | chr5 | 115261066 | ||||||
chr5:115261095
|
C | T | 1 | a0001c0001t0141g0035 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.140+1617G>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 1/8 | chr5 | 115261095 | ||||||
chr5:115261313
|
T | C | 1 | a0001c0001t0074g0263 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.140+1399A>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 1/8 | chr5 | 115261313 | ||||||
chr5:115261419
|
A | C | 1 | a0001c0001t0055g0295 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.140+1293T>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 1/8 | chr5 | 115261419 | ||||||
chr5:115261449
|
T | C | 32 | a0001c0001t0013g0292a0001c0001t0026g0277a0001c0001t0026g0288others(29): Show | 32 | HG01070.hp2 HG01192.hp1 HG01243.hp2 others(29): Show |
intron_variant | MODIFIER | c.140+1263A>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 1/8 | chr5 | 115261449 | ||||||
chr5:115261456
|
A | G | 1 | a0001c0001t0056g0034 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.140+1256T>C | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 1/8 | chr5 | 115261456 | ||||||
chr5:115261517
|
T | A | 1 | a0001c0001t0001g0293 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.140+1195A>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 1/8 | chr5 | 115261517 | ||||||
chr5:115261636
|
A | G | 1 | a0001c0001t0059g0296 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.140+1076T>C | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 1/8 | chr5 | 115261636 | ||||||
chr5:115261722
|
T | C | 1 | a0001c0001t0062g0294 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.140+990A>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 1/8 | chr5 | 115261722 | ||||||
chr5:115261881
|
A | T | 1 | a0001c0001t0055g0295 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.140+831T>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 1/8 | chr5 | 115261881 | ||||||
chr5:115262042
|
A | G | 1 | a0001c0001t0068g0033 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.140+670T>C | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 1/8 | chr5 | 115262042 | ||||||
chr5:115262088
|
G | A | 1 | a0001c0001t0055g0295 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.140+624C>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 1/8 | chr5 | 115262088 | ||||||
chr5:115262166
|
C | T | 3 | a0001c0001t0045g0031a0001c0001t0045g0032a0001c0001t0129g0030 | 3 | HG01891.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.140+546G>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 1/8 | chr5 | 115262166 | ||||||
chr5:115262260
|
G | C | 4 | a0001c0001t0059g0296a0001c0001t0117g0299a0001c0001t0118g0297others(1): Show | 4 | HG02717.hp2 HG02818.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.140+452C>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 1/8 | chr5 | 115262260 | ||||||
chr5:115262265
|
T | C | 4 | a0001c0001t0005g0300a0001c0001t0005g0301a0001c0001t0005g0302others(1): Show | 4 | HG02015.hp1 HG02040.hp2 NA18747.hp1 others(1): Show |
intron_variant | MODIFIER | c.140+447A>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 1/8 | chr5 | 115262265 | ||||||
chr5:115262507
|
C | T | 291 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(288): Show | 310 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(307): Show |
intron_variant | MODIFIER | c.140+205G>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 1/8 | chr5 | 115262507 | ||||||
chr5:115262600
|
C | G | 8 | a0001c0001t0091g0027a0001c0001t0092g0025a0001c0001t0093g0026others(5): Show | 8 | HG02055.hp2 HG02615.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.140+112G>C | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 1/8 | chr5 | 115262600 | ||||||
chr5:115262671
|
C | A | 1 | a0001c0001t0042g0346 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.140+41G>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 1/8 | chr5 | 115262671 |