Item | Value |
---|---|
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 | MAATE others(372): Show |
chr5 | 115199012 | 115267877 |
a0002 | 0/0 | 377 | 4 | 3 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | MAATE others(372): Show |
chr5 | 115199012 | 115267877 |
a0003 | 0/0 | 377 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | MATTE others(372): Show |
chr5 | 115199012 | 115267877 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1131 | 349 | 85 | 73 | 134 | 16 | 39 | PGGT1B_chr5_115199012_115267877 | PGGT1B | ATGGC others(1126): Show |
chr5 | 115199012 | 115267877 | ||
a0001c0002 | 0/0 | 1131 | 16 | 0 | 1 | 15 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | ATGGC others(1126): Show |
chr5 | 115199012 | 115267877 | ||
a0001c0005 | 0/0 | 1131 | 1 | 0 | 0 | 0 | 0 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | ATGGC others(1126): Show |
chr5 | 115199012 | 115267877 | ||
a0001c0006 | 0/0 | 1131 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | ATGGC others(1126): Show |
chr5 | 115199012 | 115267877 | ||
a0002c0003 | 0/0 | 1131 | 4 | 3 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | ATGGC others(1126): Show |
chr5 | 115199012 | 115267877 | ||
a0003c0004 | 0/0 | 1131 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | ATGGC others(1126): Show |
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 | GCGGC others(9537): Show |
chr5 | 115199012 | 115267877 |
a0001c0001t0002 | 1/0 | 9550 | 23 | 0 | 7 | 10 | 2 | 3 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9545): Show |
chr5 | 115199012 | 115267877 |
a0001c0001t0003 | 0/0 | 9555 | 18 | 0 | 7 | 7 | 0 | 4 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9550): Show |
chr5 | 115199012 | 115267877 |
a0001c0001t0004 | 0/0 | 9568 | 3 | 0 | 0 | 2 | 1 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9563): Show |
chr5 | 115199012 | 115267877 |
a0001c0001t0005 | 0/0 | 9541 | 10 | 0 | 0 | 10 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9536): Show |
chr5 | 115199012 | 115267877 |
a0001c0001t0006 | 0/0 | 9552 | 11 | 1 | 0 | 7 | 0 | 3 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9547): Show |
chr5 | 115199012 | 115267877 |
a0001c0001t0007 | 0/0 | 9570 | 9 | 2 | 0 | 5 | 1 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9565): Show |
chr5 | 115199012 | 115267877 |
a0001c0001t0008 | 0/0 | 9542 | 9 | 0 | 0 | 9 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9537): Show |
chr5 | 115199012 | 115267877 |
a0001c0001t0009 | 0/0 | 9554 | 9 | 0 | 3 | 2 | 3 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9549): Show |
chr5 | 115199012 | 115267877 |
a0001c0001t0010 | 0/0 | 9572 | 8 | 0 | 4 | 2 | 0 | 2 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9567): Show |
chr5 | 115199012 | 115267877 |
a0001c0001t0011 | 0/0 | 9566 | 5 | 0 | 0 | 4 | 0 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9561): Show |
chr5 | 115199012 | 115267877 |
a0001c0001t0012 | 0/0 | 9574 | 4 | 0 | 2 | 2 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9569): Show |
chr5 | 115199012 | 115267877 |
a0001c0001t0013 | 0/0 | 9557 | 5 | 1 | 4 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9552): Show |
chr5 | 115199012 | 115267877 |
a0001c0001t0014 | 0/0 | 9566 | 4 | 4 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9561): Show |
chr5 | 115199012 | 115267877 |
a0001c0001t0015 | 0/0 | 9569 | 2 | 0 | 0 | 1 | 1 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9564): Show |
chr5 | 115199012 | 115267877 |
a0001c0001t0016 | 0/0 | 9551 | 4 | 0 | 3 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9546): Show |
chr5 | 115199012 | 115267877 |
a0001c0001t0017 | 0/0 | 9557 | 3 | 3 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9552): Show |
chr5 | 115199012 | 115267877 |
a0001c0001t0018 | 0/0 | 9564 | 3 | 0 | 2 | 0 | 0 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9559): Show |
chr5 | 115199012 | 115267877 |
a0001c0001t0019 | 0/0 | 9580 | 2 | 0 | 1 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9575): Show |
chr5 | 115199012 | 115267877 |
a0001c0001t0020 | 0/0 | 9576 | 3 | 0 | 1 | 1 | 0 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9571): Show |
chr5 | 115199012 | 115267877 |
a0001c0001t0021 | 0/0 | 9566 | 3 | 0 | 1 | 0 | 1 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9561): Show |
chr5 | 115199012 | 115267877 |
a0001c0001t0022 | 0/0 | 9562 | 3 | 0 | 1 | 1 | 1 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9557): Show |
chr5 | 115199012 | 115267877 |
a0001c0001t0023 | 0/1 | 9565 | 3 | 0 | 1 | 0 | 1 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9560): Show |
chr5 | 115199012 | 115267877 |
a0001c0001t0024 | 0/0 | 9543 | 3 | 1 | 0 | 1 | 0 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9538): Show |
chr5 | 115199012 | 115267877 |
a0001c0001t0025 | 0/0 | 9566 | 3 | 2 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9561): Show |
chr5 | 115199012 | 115267877 |
a0001c0001t0026 | 0/0 | 9571 | 3 | 2 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9566): Show |
chr5 | 115199012 | 115267877 |
a0001c0001t0027 | 0/0 | 9569 | 3 | 2 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9564): Show |
chr5 | 115199012 | 115267877 |
a0001c0001t0028 | 0/0 | 9567 | 3 | 0 | 1 | 0 | 0 | 2 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9562): Show |
chr5 | 115199012 | 115267877 |
a0001c0001t0029 | 0/0 | 9563 | 3 | 1 | 0 | 0 | 0 | 2 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9558): Show |
chr5 | 115199012 | 115267877 |
a0001c0001t0030 | 0/0 | 9553 | 3 | 0 | 0 | 3 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9548): Show |
chr5 | 115199012 | 115267877 |
a0001c0001t0031 | 0/0 | 9556 | 3 | 0 | 0 | 3 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9551): Show |
chr5 | 115199012 | 115267877 |
a0001c0001t0032 | 0/0 | 9555 | 3 | 1 | 0 | 0 | 0 | 2 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9550): Show |
chr5 | 115199012 | 115267877 |
a0001c0001t0033 | 0/0 | 9556 | 3 | 0 | 1 | 2 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9551): Show |
chr5 | 115199012 | 115267877 |
a0001c0001t0035 | 0/0 | 9564 | 2 | 1 | 0 | 0 | 0 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9559): Show |
chr5 | 115199012 | 115267877 |
a0001c0001t0036 | 0/0 | 9542 | 2 | 2 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9537): Show |
chr5 | 115199012 | 115267877 |
a0001c0001t0037 | 0/0 | 9564 | 2 | 0 | 0 | 2 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9559): Show |
chr5 | 115199012 | 115267877 |
a0001c0001t0038 | 0/0 | 9562 | 2 | 2 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9557): Show |
chr5 | 115199012 | 115267877 |
a0001c0001t0039 | 0/0 | 9558 | 2 | 2 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9553): Show |
chr5 | 115199012 | 115267877 |
a0001c0001t0040 | 0/0 | 9552 | 2 | 0 | 1 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9547): Show |
chr5 | 115199012 | 115267877 |
a0001c0001t0041 | 0/0 | 9570 | 2 | 2 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9565): Show |
chr5 | 115199012 | 115267877 |
a0001c0001t0042 | 0/0 | 9543 | 2 | 2 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9538): Show |
chr5 | 115199012 | 115267877 |
a0001c0001t0043 | 0/0 | 9561 | 2 | 2 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9556): Show |
chr5 | 115199012 | 115267877 |
a0001c0001t0044 | 0/0 | 9542 | 2 | 0 | 0 | 0 | 0 | 2 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9537): Show |
chr5 | 115199012 | 115267877 |
a0001c0001t0045 | 0/0 | 9571 | 2 | 0 | 1 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9566): Show |
chr5 | 115199012 | 115267877 |
a0001c0001t0046 | 0/0 | 9566 | 2 | 2 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9561): Show |
chr5 | 115199012 | 115267877 |
a0001c0001t0047 | 0/0 | 9570 | 2 | 2 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9565): Show |
chr5 | 115199012 | 115267877 |
a0001c0001t0048 | 0/0 | 9551 | 2 | 0 | 0 | 2 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9546): Show |
chr5 | 115199012 | 115267877 |
a0001c0001t0049 | 0/0 | 9567 | 2 | 2 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9562): Show |
chr5 | 115199012 | 115267877 |
a0001c0001t0050 | 0/0 | 9575 | 2 | 2 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9570): Show |
chr5 | 115199012 | 115267877 |
a0001c0001t0051 | 0/0 | 9565 | 2 | 0 | 1 | 0 | 0 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9560): Show |
chr5 | 115199012 | 115267877 |
a0001c0001t0052 | 0/0 | 9544 | 2 | 2 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9539): Show |
chr5 | 115199012 | 115267877 |
a0001c0001t0053 | 0/0 | 9554 | 2 | 0 | 0 | 2 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9549): Show |
chr5 | 115199012 | 115267877 |
a0001c0001t0054 | 0/0 | 9559 | 2 | 0 | 1 | 0 | 1 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9554): Show |
chr5 | 115199012 | 115267877 |
a0001c0001t0055 | 0/0 | 9567 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9562): Show |
chr5 | 115199012 | 115267877 |
a0001c0001t0056 | 0/0 | 9545 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9540): Show |
chr5 | 115199012 | 115267877 |
a0001c0001t0057 | 0/0 | 9545 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9540): Show |
chr5 | 115199012 | 115267877 |
a0001c0001t0060 | 0/0 | 9564 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9559): Show |
chr5 | 115199012 | 115267877 |
a0001c0001t0061 | 0/0 | 9581 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9576): Show |
chr5 | 115199012 | 115267877 |
a0001c0001t0062 | 0/0 | 9571 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9566): Show |
chr5 | 115199012 | 115267877 |
a0001c0001t0063 | 0/0 | 9557 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9552): Show |
chr5 | 115199012 | 115267877 |
a0001c0001t0064 | 0/0 | 9561 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9556): Show |
chr5 | 115199012 | 115267877 |
a0001c0001t0065 | 0/0 | 9562 | 1 | 0 | 0 | 0 | 0 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9557): Show |
chr5 | 115199012 | 115267877 |
a0001c0001t0066 | 0/0 | 9572 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9567): Show |
chr5 | 115199012 | 115267877 |
a0001c0001t0067 | 0/0 | 9572 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9567): Show |
chr5 | 115199012 | 115267877 |
a0001c0001t0068 | 0/0 | 9566 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9561): Show |
chr5 | 115199012 | 115267877 |
a0001c0001t0069 | 0/0 | 9578 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9573): Show |
chr5 | 115199012 | 115267877 |
a0001c0001t0070 | 0/0 | 9574 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9569): Show |
chr5 | 115199012 | 115267877 |
a0001c0001t0072 | 0/0 | 9582 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9577): Show |
chr5 | 115199012 | 115267877 |
a0001c0001t0073 | 0/0 | 9578 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9573): Show |
chr5 | 115199012 | 115267877 |
a0001c0001t0074 | 0/0 | 9576 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9571): Show |
chr5 | 115199012 | 115267877 |
a0001c0001t0075 | 0/0 | 9574 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9569): Show |
chr5 | 115199012 | 115267877 |
a0001c0001t0076 | 0/0 | 9572 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9567): Show |
chr5 | 115199012 | 115267877 |
a0001c0001t0077 | 0/0 | 9570 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9565): Show |
chr5 | 115199012 | 115267877 |
a0001c0001t0078 | 0/0 | 9568 | 1 | 0 | 0 | 0 | 0 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9563): Show |
chr5 | 115199012 | 115267877 |
a0001c0001t0079 | 0/0 | 9564 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9559): Show |
chr5 | 115199012 | 115267877 |
a0001c0001t0080 | 0/0 | 9558 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9553): Show |
chr5 | 115199012 | 115267877 |
a0001c0001t0081 | 0/0 | 9544 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9539): Show |
chr5 | 115199012 | 115267877 |
a0001c0001t0082 | 0/0 | 9564 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9559): Show |
chr5 | 115199012 | 115267877 |
a0001c0001t0083 | 0/0 | 9562 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9557): Show |
chr5 | 115199012 | 115267877 |
a0001c0001t0084 | 0/0 | 9560 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9555): Show |
chr5 | 115199012 | 115267877 |
a0001c0001t0085 | 0/0 | 9558 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9553): Show |
chr5 | 115199012 | 115267877 |
a0001c0001t0086 | 0/0 | 9570 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9565): Show |
chr5 | 115199012 | 115267877 |
a0001c0001t0087 | 0/0 | 9568 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9563): Show |
chr5 | 115199012 | 115267877 |
a0001c0001t0088 | 0/0 | 9565 | 1 | 0 | 0 | 0 | 0 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9560): Show |
chr5 | 115199012 | 115267877 |
a0001c0001t0089 | 0/0 | 9565 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9560): Show |
chr5 | 115199012 | 115267877 |
a0001c0001t0090 | 0/0 | 9572 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9567): Show |
chr5 | 115199012 | 115267877 |
a0001c0001t0091 | 0/0 | 9578 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9573): Show |
chr5 | 115199012 | 115267877 |
a0001c0001t0092 | 0/0 | 9576 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9571): Show |
chr5 | 115199012 | 115267877 |
a0001c0001t0093 | 0/0 | 9574 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9569): Show |
chr5 | 115199012 | 115267877 |
a0001c0001t0094 | 0/0 | 9572 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9567): Show |
chr5 | 115199012 | 115267877 |
a0001c0001t0095 | 0/0 | 9566 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9561): Show |
chr5 | 115199012 | 115267877 |
a0001c0001t0096 | 0/0 | 9542 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9537): Show |
chr5 | 115199012 | 115267877 |
a0001c0001t0097 | 0/0 | 9541 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9536): Show |
chr5 | 115199012 | 115267877 |
a0001c0001t0098 | 0/0 | 9544 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9539): Show |
chr5 | 115199012 | 115267877 |
a0001c0001t0099 | 0/0 | 9542 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9537): Show |
chr5 | 115199012 | 115267877 |
a0001c0001t0100 | 0/0 | 9542 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9537): Show |
chr5 | 115199012 | 115267877 |
a0001c0001t0101 | 0/0 | 9543 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9538): Show |
chr5 | 115199012 | 115267877 |
a0001c0001t0102 | 0/0 | 9580 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9575): Show |
chr5 | 115199012 | 115267877 |
a0001c0001t0103 | 0/0 | 9576 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9571): Show |
chr5 | 115199012 | 115267877 |
a0001c0001t0104 | 0/0 | 9572 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9567): Show |
chr5 | 115199012 | 115267877 |
a0001c0001t0105 | 0/0 | 9555 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9550): Show |
chr5 | 115199012 | 115267877 |
a0001c0001t0106 | 0/0 | 9583 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9578): Show |
chr5 | 115199012 | 115267877 |
a0001c0001t0107 | 0/0 | 9579 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9574): Show |
chr5 | 115199012 | 115267877 |
a0001c0001t0108 | 0/0 | 9575 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9570): Show |
chr5 | 115199012 | 115267877 |
a0001c0001t0109 | 0/0 | 9567 | 1 | 0 | 0 | 0 | 1 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9562): Show |
chr5 | 115199012 | 115267877 |
a0001c0001t0110 | 0/0 | 9542 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9537): Show |
chr5 | 115199012 | 115267877 |
a0001c0001t0111 | 0/0 | 9543 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9538): Show |
chr5 | 115199012 | 115267877 |
a0001c0001t0112 | 0/0 | 9577 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9572): Show |
chr5 | 115199012 | 115267877 |
a0001c0001t0113 | 0/0 | 9571 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9566): Show |
chr5 | 115199012 | 115267877 |
a0001c0001t0114 | 0/0 | 9543 | 1 | 0 | 0 | 0 | 0 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9538): Show |
chr5 | 115199012 | 115267877 |
a0001c0001t0115 | 0/0 | 9547 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9542): Show |
chr5 | 115199012 | 115267877 |
a0001c0001t0116 | 0/0 | 9578 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9573): Show |
chr5 | 115199012 | 115267877 |
a0001c0001t0117 | 0/0 | 9574 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9569): Show |
chr5 | 115199012 | 115267877 |
a0001c0001t0118 | 0/0 | 9568 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9563): Show |
chr5 | 115199012 | 115267877 |
a0001c0001t0119 | 0/0 | 9562 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9557): Show |
chr5 | 115199012 | 115267877 |
a0001c0001t0120 | 0/0 | 9544 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9539): Show |
chr5 | 115199012 | 115267877 |
a0001c0001t0121 | 0/0 | 9553 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9548): Show |
chr5 | 115199012 | 115267877 |
a0001c0001t0122 | 0/0 | 9549 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9544): Show |
chr5 | 115199012 | 115267877 |
a0001c0001t0123 | 0/0 | 9570 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9565): Show |
chr5 | 115199012 | 115267877 |
a0001c0001t0124 | 0/0 | 9569 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9564): Show |
chr5 | 115199012 | 115267877 |
a0001c0001t0125 | 0/0 | 9565 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9560): Show |
chr5 | 115199012 | 115267877 |
a0001c0001t0126 | 0/0 | 9577 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9572): Show |
chr5 | 115199012 | 115267877 |
a0001c0001t0127 | 0/0 | 9573 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9568): Show |
chr5 | 115199012 | 115267877 |
a0001c0001t0128 | 0/0 | 9561 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9556): Show |
chr5 | 115199012 | 115267877 |
a0001c0001t0129 | 0/0 | 9550 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9545): Show |
chr5 | 115199012 | 115267877 |
a0001c0001t0130 | 0/0 | 9565 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9560): Show |
chr5 | 115199012 | 115267877 |
a0001c0001t0131 | 0/0 | 9558 | 1 | 0 | 0 | 0 | 0 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9553): Show |
chr5 | 115199012 | 115267877 |
a0001c0001t0133 | 0/0 | 9561 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9556): Show |
chr5 | 115199012 | 115267877 |
a0001c0001t0134 | 0/0 | 9555 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9550): Show |
chr5 | 115199012 | 115267877 |
a0001c0001t0135 | 0/0 | 9545 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9540): Show |
chr5 | 115199012 | 115267877 |
a0001c0001t0136 | 0/0 | 9550 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9545): Show |
chr5 | 115199012 | 115267877 |
a0001c0001t0137 | 0/0 | 9558 | 1 | 0 | 0 | 0 | 0 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9553): Show |
chr5 | 115199012 | 115267877 |
a0001c0001t0138 | 0/0 | 9558 | 1 | 0 | 0 | 0 | 1 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9553): Show |
chr5 | 115199012 | 115267877 |
a0001c0001t0139 | 0/0 | 9552 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9547): Show |
chr5 | 115199012 | 115267877 |
a0001c0001t0140 | 0/0 | 9555 | 1 | 0 | 0 | 0 | 0 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9550): Show |
chr5 | 115199012 | 115267877 |
a0001c0002t0004 | 0/0 | 9568 | 9 | 0 | 0 | 9 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9563): Show |
chr5 | 115199012 | 115267877 |
a0001c0002t0005 | 0/0 | 9541 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9536): Show |
chr5 | 115199012 | 115267877 |
a0001c0002t0011 | 0/0 | 9566 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9561): Show |
chr5 | 115199012 | 115267877 |
a0001c0002t0012 | 0/0 | 9574 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9569): Show |
chr5 | 115199012 | 115267877 |
a0001c0002t0015 | 0/0 | 9569 | 2 | 0 | 1 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9564): Show |
chr5 | 115199012 | 115267877 |
a0001c0002t0019 | 0/0 | 9580 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9575): Show |
chr5 | 115199012 | 115267877 |
a0001c0002t0071 | 0/0 | 9566 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9561): Show |
chr5 | 115199012 | 115267877 |
a0001c0005t0132 | 0/0 | 9556 | 1 | 0 | 0 | 0 | 0 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9551): Show |
chr5 | 115199012 | 115267877 |
a0001c0006t0002 | 0/0 | 9550 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9545): Show |
chr5 | 115199012 | 115267877 |
a0002c0003t0034 | 0/0 | 9566 | 2 | 2 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9561): Show |
chr5 | 115199012 | 115267877 |
a0002c0003t0058 | 0/0 | 9570 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9565): Show |
chr5 | 115199012 | 115267877 |
a0002c0003t0059 | 0/0 | 9564 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9559): Show |
chr5 | 115199012 | 115267877 |
a0003c0004t0001 | 0/0 | 9542 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | GCGGC others(9537): Show |
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 |
a0001c0001t0040g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0040g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0041g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0042g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0042g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0043g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0043g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0044g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0044g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0045g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0045g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0046g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0046g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0047g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0047g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0048g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0048g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0049g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0049g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0050g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0050g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0051g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0051g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0052g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0052g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0053g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0053g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0054g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0054g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0055g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0056g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0057g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0060g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0061g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0062g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0063g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0064g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0065g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0066g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0067g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0068g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0069g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0070g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0072g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0073g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0074g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0075g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0076g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0077g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0078g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0079g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0080g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0081g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0082g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0083g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0084g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0085g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0086g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0087g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0088g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0089g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0090g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0091g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0092g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0093g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0094g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0095g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0096g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0097g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0098g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0099g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0100g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0101g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0102g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0103g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0104g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0105g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0106g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0107g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0108g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0109g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0110g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0111g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0112g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0113g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0114g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0115g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0116g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0117g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0118g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0119g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0120g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0121g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0122g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0123g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0124g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0125g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0126g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0127g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0128g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0129g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0130g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0131g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0133g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0134g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0135g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0136g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0137g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0138g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0139g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0001t0140g0035 | 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 |
a0001c0002t0071g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0001c0005t0132g0323 | 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 |
a0002c0003t0058g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
a0002c0003t0059g0150 | 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 | t0138 | g0233 | EUR | FIN | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG00323 | hp2 | a0001 | c0001 | t0109 | 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 | t0077 | 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 | t0076 | 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 | t0074 | 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 | t0045 | 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 | t0061 | 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 | t0072 | g0110 | AMR | PUR | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG01074 | hp1 | a0002 | c0003 | t0059 | 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 | t0070 | 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 | t0069 | g0033 | AMR | PUR | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG01168 | hp2 | a0001 | c0001 | t0121 | 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 | t0106 | 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 | t0135 | 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 | t0054 | 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 | t0066 | g0045 | AMR | CLM | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG01261 | hp2 | a0001 | c0001 | t0110 | 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 | t0136 | 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 | t0073 | 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 | t0119 | g0139 | AMR | CLM | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG01496 | hp2 | a0001 | c0001 | t0056 | 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 | t0054 | 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 | t0128 | 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 | t0122 | g0329 | AMR | PEL | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG01943 | hp2 | a0001 | c0001 | t0040 | 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 | t0102 | 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 | t0133 | 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 | t0084 | g0218 | AFR | ACB | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG02055 | hp2 | a0001 | c0001 | t0091 | 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 | t0040 | g0100 | EAS | KHV | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG02071 | hp1 | a0001 | c0002 | t0071 | 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 | t0098 | 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 | t0103 | 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 | t0055 | 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 | t0043 | g0346 | AFR | ACB | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG02258 | hp2 | a0001 | c0001 | t0127 | g0276 | AFR | ACB | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG02273 | hp1 | a0001 | c0001 | t0051 | 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 | t0120 | 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 | t0130 | 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 | t0049 | 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 | t0078 | 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 | t0093 | g0024 | AFR | GWD | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG02622 | hp1 | a0001 | c0001 | t0042 | 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 | t0063 | 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 | t0140 | g0035 | SAS | PJL | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG02698 | hp1 | a0001 | c0001 | t0114 | 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 | t0118 | 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 | t0090 | g0027 | AFR | GWD | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG02809 | hp2 | a0001 | c0001 | t0049 | 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 | t0116 | g0299 | AFR | GWD | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG02886 | hp1 | a0001 | c0001 | t0095 | g0023 | AFR | GWD | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG02886 | hp2 | a0001 | c0001 | t0117 | g0297 | AFR | GWD | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG02895 | hp1 | a0001 | c0001 | t0083 | g0062 | AFR | GWD | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG02895 | hp2 | a0001 | c0001 | t0046 | g0032 | AFR | GWD | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG02896 | hp1 | a0001 | c0001 | t0105 | g0345 | AFR | GWD | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG02896 | hp2 | a0001 | c0001 | t0041 | g0008 | AFR | GWD | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG02897 | hp1 | a0001 | c0001 | t0041 | g0008 | AFR | GWD | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG02897 | hp2 | a0001 | c0001 | t0046 | g0031 | AFR | GWD | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG02965 | hp1 | a0001 | c0001 | t0067 | g0041 | AFR | ESN | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG02965 | hp2 | a0001 | c0001 | t0139 | g0278 | AFR | ESN | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG02970 | hp1 | a0001 | c0001 | t0126 | 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 | t0089 | g0044 | AFR | GWD | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG03041 | hp2 | a0001 | c0001 | t0094 | 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 | t0113 | g0022 | AFR | MSL | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG03130 | hp1 | a0001 | c0001 | t0057 | g0034 | AFR | ESN | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG03130 | hp2 | a0001 | c0001 | t0047 | g0140 | AFR | ESN | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG03139 | hp1 | a0001 | c0001 | t0086 | 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 | t0068 | g0042 | AFR | MSL | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG03453 | hp1 | a0001 | c0001 | t0123 | g0291 | AFR | MSL | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG03453 | hp2 | a0001 | c0001 | t0050 | g0269 | AFR | MSL | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG03490 | hp1 | a0001 | c0001 | t0137 | 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 | t0044 | 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 | t0044 | 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 | t0050 | g0274 | AFR | GWD | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG03540 | hp2 | a0001 | c0001 | t0101 | g0189 | AFR | GWD | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG03579 | hp1 | a0001 | c0001 | t0125 | g0283 | AFR | MSL | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG03579 | hp2 | a0001 | c0001 | t0085 | 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 | t0131 | g0315 | SAS | PJL | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG03669 | hp1 | a0001 | c0001 | t0088 | 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 | t0132 | 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 | t0065 | 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 | t0042 | 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 | t0092 | g0026 | AFR | YRI | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA18906 | hp2 | a0001 | c0001 | t0043 | 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 | t0129 | 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 | t0075 | 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 | t0048 | 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 | t0053 | 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 | t0099 | g0115 | EAS | JPT | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA18971 | hp2 | a0001 | c0001 | t0107 | 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 | t0096 | g0118 | EAS | JPT | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA18973 | hp1 | a0001 | c0001 | t0062 | 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 | t0045 | 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 | t0080 | 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 | t0104 | 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 | t0053 | 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 | t0097 | 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 | t0100 | 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 | t0048 | 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 | t0047 | 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 | t0087 | 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 | t0111 | 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 | t0079 | g0215 | AFR | YRI | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA19240 | hp2 | a0001 | c0001 | t0112 | 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 | t0115 | 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 | t0051 | g0272 | SAS | GIH | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG01123 | hp1 | a0001 | c0001 | t0134 | g0239 | AMR | CLM | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG01123 | hp2 | a0001 | c0001 | t0108 | 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 | t0064 | 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 | t0052 | g0265 | AFR | ACB | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG03471 | hp1 | a0001 | c0001 | t0124 | g0281 | AFR | MSL | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG03471 | hp2 | a0001 | c0001 | t0082 | g0092 | AFR | MSL | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
HG06807 | hp1 | a0002 | c0003 | t0058 | 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 | t0081 | g0227 | AFR | USA | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
NA20300 | hp2 | a0001 | c0001 | t0060 | 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 | t0052 | g0264 | AFR | LWK | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
homoSapiens | chm13v2 | a0001 | c0001 | t0023 | g0075 | REF | REF | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0324 | REF | REF | PGGT1B_chr5_115199012_115267877 | PGGT1B | chr5 | 115199012 | 115267877 |
view | 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 |
view | 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 |
view | 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 | a0001c0001t0090 a0001c0001t0091 a0001c0001t0092 others(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 | a0001c0001t0078 | 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 | 37 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0007 others(34): Show |
89 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(86): 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 | a0001c0001t0105 | 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 | a0001c0001t0017 a0001c0001t0063 |
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 | a0001c0001t0074 | 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 | a0001c0001t0066 | 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 | a0001c0001t0063 | 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 | a0001c0001t0043 | 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 | a0001c0001t0036 a0001c0001t0042 a0001c0001t0052 others(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 | a0001c0001t0001 a0001c0001t0008 a0001c0001t0024 others(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 | a0001c0001t0099 | 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 | a0001c0001t0075 a0001c0001t0076 a0001c0001t0077 |
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 | a0001c0001t0069 | 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 | 123 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(120): Show |
271 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(268): 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 | a0001c0001t0042 | 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 | a0001c0001t0090 a0001c0001t0091 a0001c0001t0092 others(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 | 78 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0007 others(75): Show |
156 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(153): 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 | 123 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(120): Show |
271 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(268): 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 | a0001c0001t0097 | 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 | a0001c0001t0090 a0001c0001t0091 a0001c0001t0092 others(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 | 57 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0007 others(54): Show |
121 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(118): 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 | a0001c0001t0080 | 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 | a0001c0001t0140 | 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 | a0001c0001t0090 a0001c0001t0091 a0001c0001t0092 others(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 | a0001c0001t0060 | 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 | a0001c0001t0069 a0001c0001t0070 |
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 | a0001c0001t0069 a0001c0001t0070 |
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 | a0001c0001t0090 a0001c0001t0091 a0001c0001t0092 others(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 | a0001c0001t0006 a0001c0001t0030 a0001c0001t0048 others(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 | a0001c0001t0003 a0001c0001t0009 a0001c0001t0032 others(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 | a0001c0001t0013 a0001c0001t0017 a0001c0001t0031 others(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 | a0001c0001t0029 a0001c0001t0043 a0001c0001t0054 others(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 | a0001c0001t0022 a0001c0001t0038 a0001c0001t0051 others(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 | a0001c0001t0018 a0001c0001t0023 a0001c0001t0025 others(12): Show |
27 | HG00280.hp1 HG00642.hp1 HG00738.hp1 others(24): 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 | a0001c0001t0011 a0001c0001t0014 a0001c0001t0021 others(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 | a0001c0001t0004 a0001c0001t0015 a0001c0001t0026 others(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 | a0001c0001t0007 a0001c0001t0041 a0001c0001t0045 others(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 | a0001c0001t0010 a0001c0001t0050 a0001c0001t0062 others(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 | a0001c0001t0012 a0001c0001t0070 a0001c0001t0075 others(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 | a0001c0001t0020 a0001c0001t0074 a0001c0001t0116 |
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 | a0001c0001t0069 a0001c0001t0073 a0001c0001t0102 others(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 | a0001c0001t0019 a0001c0002t0019 |
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 | a0001c0001t0061 a0001c0001t0072 a0001c0001t0106 |
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 | a0001c0001t0056 a0001c0001t0057 a0001c0001t0081 others(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 | a0001c0001t0098 | 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 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0008 others(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 | a0001c0001t0040 | 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 | a0001c0001t0056 a0001c0001t0057 |
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 | a0001c0001t0057 | 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 | a0001c0001t0064 | 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 | a0001c0001t0105 | 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 | 54 | a0001c0001t0004 a0001c0001t0007 a0001c0001t0010 others(51): Show |
108 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(105): 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 | a0001c0001t0043 | 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 | a0001c0001t0069 a0001c0001t0070 |
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 | a0001c0001t0123 | 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 | a0001c0001t0036 a0001c0001t0042 a0001c0001t0052 others(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 | 58 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0007 others(55): Show |
122 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(119): 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 | a0001c0001t0025 a0001c0001t0047 a0001c0001t0116 others(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 | a0001c0001t0049 a0001c0001t0124 a0001c0001t0125 |
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 | a0001c0002t0071 | 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 | a0001c0001t0100 | 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 | a0001c0001t0135 | 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 | a0001c0001t0114 | 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 | a0001c0001t0018 a0001c0001t0065 a0001c0001t0088 |
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 | a0001c0001t0096 | 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 | a0001c0001t0101 | 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 | 122 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(119): Show |
272 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(269): 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 | a0001c0001t0056 a0001c0001t0057 |
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 | 50 | a0001c0001t0004 a0001c0001t0007 a0001c0001t0010 others(47): Show |
104 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(101): 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 | a0001c0001t0120 | 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 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0008 others(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 | a0001c0001t0042 | 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 | a0001c0001t0090 a0001c0001t0091 a0001c0001t0092 others(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 | a0001c0001t0014 a0001c0001t0041 a0001c0001t0082 others(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 | a0001c0001t0086 | 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 | a0001c0001t0056 a0001c0001t0057 |
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 | a0001c0001t0056 a0001c0001t0057 |
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 | a0001c0001t0137 | 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 | a0001c0001t0056 a0001c0001t0057 |
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 | a0001c0001t0090 a0001c0001t0091 a0001c0001t0092 others(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 | a0001c0001t0129 | 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 | 121 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(118): Show |
269 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(266): 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 | a0001c0001t0110 | 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 | a0001c0001t0069 | 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 | a0001c0001t0090 | 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 | a0001c0001t0115 | 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 | a0001c0001t0087 | 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 | a0001c0001t0090 a0001c0001t0091 a0001c0001t0092 others(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 | a0001c0001t0090 a0001c0001t0091 a0001c0001t0092 others(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 | a0001c0001t0008 a0001c0001t0111 |
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 | 121 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(118): Show |
269 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(266): 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 | a0001c0001t0018 a0001c0001t0035 a0001c0001t0065 others(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 | a0001c0001t0060 | 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 | a0001c0001t0025 a0001c0001t0026 a0001c0001t0027 others(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 | a0001c0001t0016 a0001c0001t0030 a0001c0001t0033 others(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 | a0001c0001t0026 a0001c0001t0027 a0001c0001t0028 others(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 | a0001c0001t0024 a0001c0001t0025 a0001c0001t0046 others(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 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0008 others(34): Show |
113 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(110): 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 | 46 | a0001c0001t0004 a0001c0001t0007 a0001c0001t0010 others(43): 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 | a0001c0001t0017 a0001c0001t0061 a0001c0001t0062 others(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 | a0002c0003t0034 a0002c0003t0058 a0002c0003t0059 |
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 | a0001c0001t0060 | 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 | a0001c0001t0052 a0001c0001t0135 |
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 | a0002c0003t0034 a0002c0003t0058 a0002c0003t0059 |
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 | a0001c0001t0136 | 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 | a0001c0001t0056 a0001c0001t0057 |
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 | a0001c0001t0055 | 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 | a0001c0001t0003 a0001c0001t0013 a0001c0001t0031 others(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 |
view | 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 | a0001c0001t0090g0027 a0001c0001t0091g0025 a0001c0001t0092g0026 others(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 | a0001c0001t0017g0070 a0001c0001t0017g0186 a0001c0001t0017g0214 others(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 | a0001c0001t0036g0156 a0001c0001t0036g0157 a0001c0001t0042g0261 others(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 | a0001c0001t0014g0076 a0001c0001t0014g0095 a0001c0001t0014g0096 others(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 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0182 others(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 | a0001c0001t0006g0309 a0001c0001t0006g0318 a0001c0001t0006g0332 others(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 | a0001c0001t0056g0295 | 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 | a0001c0001t0001g0161 a0001c0001t0001g0166 |
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 | a0001c0001t0010g0071 a0001c0001t0010g0078 a0001c0001t0010g0200 |
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 | 1 | a0001c0001t0109g0074 | 1 | HG00323.hp2 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(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 | a0001c0001t0090g0027 a0001c0001t0091g0025 a0001c0001t0092g0026 others(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 | a0001c0001t0052g0264 a0001c0001t0052g0265 a0001c0001t0135g0266 |
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 | a0001c0001t0043g0259 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(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 | a0001c0001t0021g0053 a0001c0001t0021g0054 a0001c0001t0021g0056 |
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 | a0001c0001t0090g0027 a0001c0001t0091g0025 a0001c0001t0092g0026 others(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 | a0001c0001t0026g0277 a0001c0001t0026g0288 a0001c0001t0026g0290 others(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 | a0001c0001t0060g0296 | 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 | a0001c0001t0009g0234 a0001c0001t0009g0238 a0001c0001t0009g0247 others(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 | a0001c0001t0056g0295 a0001c0001t0057g0034 |
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 | a0001c0001t0043g0346 | 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 | a0001c0001t0043g0259 a0001c0001t0043g0346 |
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 | a0001c0001t0043g0346 | 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 | a0001c0001t0060g0296 | 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 | a0001c0001t0002g0311 a0001c0001t0002g0312 a0001c0001t0016g0018 others(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 | a0001c0001t0101g0189 | 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 | a0001c0001t0069g0033 | 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 | a0001c0001t0060g0296 | 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 | 255 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(252): Show |
269 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(266): 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 | a0001c0001t0109g0074 | 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 | 194 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(191): Show |
208 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(205): 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 | a0001c0001t0025g0193 a0001c0001t0025g0194 a0001c0001t0025g0195 others(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 | a0001c0001t0045g0085 | 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 | a0001c0001t0043g0259 a0001c0001t0043g0346 |
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 | a0001c0001t0042g0261 a0001c0001t0042g0262 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(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 | a0001c0001t0042g0261 a0001c0001t0042g0262 |
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 | a0001c0001t0003g0242 a0001c0001t0003g0257 a0001c0001t0013g0292 others(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 | a0001c0001t0070g0202 | 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 | a0001c0001t0018g0046 a0001c0001t0018g0047 a0001c0001t0018g0050 others(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 | a0001c0001t0003g0003 a0001c0001t0003g0230 a0001c0001t0003g0232 others(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 | a0001c0001t0003g0002 a0001c0001t0003g0182 a0001c0001t0003g0213 others(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 | a0001c0001t0007g0104 a0001c0001t0014g0095 a0001c0001t0018g0046 others(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 | a0001c0001t0001g0138 a0001c0001t0001g0167 a0001c0001t0001g0172 others(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 | 128 | a0001c0001t0001g0160 a0001c0001t0001g0165 a0001c0001t0002g0313 others(125): Show |
132 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.844-1519delT | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 7/8 | chr5 | 115218491 | |||||||
chr5:115218491 | CAA | C | 15 | a0001c0001t0007g0221 a0001c0001t0017g0070 a0001c0001t0017g0186 others(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 | a0001c0001t0056g0295 a0001c0001t0057g0034 |
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 | a0001c0001t0043g0346 | 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 | a0001c0001t0052g0264 a0001c0001t0052g0265 a0001c0001t0135g0266 |
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 | a0001c0001t0069g0033 a0001c0001t0070g0202 |
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 | 255 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(252): Show |
269 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(266): 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 | a0001c0001t0060g0296 | 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 | a0001c0001t0001g0210 a0001c0001t0001g0211 |
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 | a0001c0001t0025g0193 a0001c0001t0025g0194 a0001c0001t0025g0195 others(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 | 255 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(252): Show |
269 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(266): 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 | a0001c0001t0069g0033 a0001c0001t0070g0202 |
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 | a0001c0001t0009g0249 a0001c0001t0013g0256 a0001c0001t0054g0244 others(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 | a0001c0001t0051g0272 | 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 | 100 | a0001c0001t0004g0068 a0001c0001t0004g0088 a0001c0001t0004g0136 others(97): Show |
104 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(101): 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 | a0001c0001t0131g0315 | 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 | a0001c0001t0081g0227 | 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 | a0001c0001t0060g0296 | 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 | a0001c0001t0018g0046 a0001c0001t0018g0047 a0001c0001t0018g0050 others(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 | a0001c0001t0069g0033 | 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 | a0001c0001t0026g0277 a0001c0001t0026g0288 a0001c0001t0026g0290 others(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 | a0001c0001t0052g0264 a0001c0001t0052g0265 a0001c0001t0135g0266 |
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 | a0001c0001t0009g0234 a0001c0001t0009g0238 a0001c0001t0009g0247 others(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 | a0001c0001t0043g0259 a0001c0001t0043g0346 a0001c0001t0105g0345 |
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 | a0001c0001t0026g0277 a0001c0001t0026g0288 a0001c0001t0026g0290 others(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 | a0001c0001t0115g0040 | 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 | 256 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(253): Show |
270 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(267): 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 | a0002c0003t0034g0151 a0002c0003t0034g0152 a0002c0003t0058g0153 others(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 | a0001c0001t0090g0027 a0001c0001t0091g0025 a0001c0001t0092g0026 others(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 | a0001c0001t0115g0040 | 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 | a0001c0001t0069g0033 a0001c0001t0070g0202 |
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 | a0001c0001t0116g0299 | 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 | a0001c0001t0116g0299 a0001c0001t0117g0297 |
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 | a0001c0001t0090g0027 a0001c0001t0091g0025 a0001c0001t0092g0026 others(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 | a0001c0001t0090g0027 a0001c0001t0091g0025 a0001c0001t0092g0026 others(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 | a0001c0001t0060g0296 | 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 | a0001c0001t0038g0216 a0001c0001t0038g0219 |
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 | 257 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(254): Show |
271 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(268): 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 | a0001c0001t0046g0031 a0001c0001t0046g0032 |
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 | a0001c0001t0025g0193 a0001c0001t0025g0194 a0001c0001t0025g0195 others(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 | a0001c0001t0026g0277 a0001c0001t0026g0288 a0001c0001t0026g0290 others(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 | a0001c0001t0004g0068 a0001c0001t0007g0066 a0001c0001t0007g0123 others(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 | a0001c0001t0025g0193 a0001c0001t0025g0194 a0001c0001t0025g0195 others(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 | 256 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(253): Show |
270 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(267): 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 | a0001c0001t0026g0277 a0001c0001t0026g0288 a0001c0001t0026g0290 others(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 | a0001c0001t0043g0259 a0001c0001t0043g0346 |
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 | a0001c0001t0043g0259 a0001c0001t0043g0346 |
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 | a0001c0001t0043g0259 a0001c0001t0043g0346 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(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 | a0001c0001t0004g0088 a0001c0001t0004g0136 a0001c0001t0015g0097 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(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 | a0001c0001t0001g0012 a0001c0001t0001g0036 a0001c0001t0001g0117 others(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 | a0001c0001t0043g0259 a0001c0001t0043g0346 a0001c0001t0105g0345 |
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 | a0001c0001t0017g0070 a0001c0001t0017g0186 a0001c0001t0017g0214 others(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 | a0001c0001t0063g0294 | 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 | 117 | a0001c0001t0004g0068 a0001c0001t0004g0088 a0001c0001t0004g0136 others(114): Show |
122 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.659-3394dupA | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 6/8 | chr5 | 115225401 | |||||||
chr5:115225592 | G | T | 1 | a0001c0001t0115g0040 | 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 | a0001c0001t0003g0255 a0001c0001t0010g0071 a0001c0001t0010g0078 others(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 | 16 | a0001c0001t0001g0159 a0001c0001t0001g0162 a0001c0001t0001g0178 others(13): Show |
16 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(13): Show |
intron_variant | MODIFIER | c.659-3642delA | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 6/8 | chr5 | 115225649 | |||||||
chr5:115225688 | C | T | 1 | a0001c0001t0078g0134 | 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 | a0001c0001t0060g0296 | 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 | a0002c0003t0034g0151 a0002c0003t0034g0152 a0002c0003t0058g0153 others(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 | a0001c0001t0114g0163 | 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 | a0001c0001t0047g0140 a0001c0001t0119g0139 |
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 | a0001c0001t0085g0077 | 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 | a0001c0001t0003g0236 a0001c0001t0013g0017 |
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 | a0001c0001t0025g0193 a0001c0001t0025g0194 a0001c0001t0025g0195 others(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 | a0001c0001t0043g0259 a0001c0001t0043g0346 a0001c0001t0105g0345 |
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 | a0001c0001t0115g0040 | 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 | a0001c0001t0123g0291 | 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 | a0002c0003t0034g0151 a0002c0003t0034g0152 a0002c0003t0058g0153 others(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 | a0001c0001t0043g0259 a0001c0001t0043g0346 a0001c0001t0105g0345 |
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 | a0002c0003t0034g0151 a0002c0003t0034g0152 a0002c0003t0058g0153 others(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 | a0001c0001t0069g0033 | 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 | a0001c0001t0060g0296 | 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 | a0001c0001t0026g0277 a0001c0001t0026g0288 a0001c0001t0026g0290 others(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 | a0001c0001t0025g0193 a0001c0001t0025g0194 a0001c0001t0025g0195 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(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 | 87 | a0001c0001t0004g0068 a0001c0001t0004g0088 a0001c0001t0004g0136 others(84): Show |
91 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.658+3252T>G | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 6/8 | chr5 | 115227724 | |||||||
chr5:115227751 | A | C | 101 | a0001c0001t0004g0068 a0001c0001t0004g0088 a0001c0001t0004g0136 others(98): Show |
105 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(102): 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 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(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 | a0001c0001t0008g0010 a0001c0001t0008g0121 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(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 | a0001c0001t0014g0076 a0001c0001t0014g0095 a0001c0001t0014g0096 others(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 | a0001c0001t0025g0193 a0001c0001t0025g0194 a0001c0001t0025g0195 others(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 | a0001c0001t0139g0278 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(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 | 257 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(254): Show |
273 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(270): 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 | a0001c0001t0056g0295 a0001c0001t0057g0034 |
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 | a0001c0001t0008g0006 a0001c0001t0008g0038 a0001c0001t0008g0039 |
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 | 263 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(260): Show |
279 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(276): 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 | 126 | a0001c0001t0004g0068 a0001c0001t0004g0088 a0001c0001t0004g0136 others(123): Show |
131 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(128): 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 | a0001c0001t0061g0109 a0001c0001t0072g0110 |
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 | a0001c0001t0046g0031 a0001c0001t0046g0032 |
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 | a0001c0001t0128g0030 | 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 | a0001c0001t0001g0142 a0001c0001t0001g0148 a0001c0001t0024g0149 others(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 | a0001c0001t0082g0092 | 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 | a0001c0001t0043g0259 a0001c0001t0043g0346 |
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 | a0001c0001t0090g0027 a0001c0001t0091g0025 a0001c0001t0092g0026 others(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 | a0001c0001t0053g0175 | 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 | a0001c0001t0039g0069 a0001c0001t0039g0199 |
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 | a0001c0001t0056g0295 a0001c0001t0057g0034 |
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 | 109 | a0001c0001t0004g0068 a0001c0001t0004g0088 a0001c0001t0004g0136 others(106): Show |
114 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(111): 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 | a0001c0001t0069g0033 | 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 | a0002c0003t0034g0151 a0002c0003t0034g0152 a0002c0003t0058g0153 others(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 | 93 | a0001c0001t0004g0068 a0001c0001t0004g0088 a0001c0001t0004g0136 others(90): Show |
98 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(95): Show |
intron_variant | MODIFIER | c.613-309G>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 5/8 | chr5 | 115231330 | |||||||
chr5:115231349 | C | T | 171 | a0001c0001t0004g0068 a0001c0001t0004g0088 a0001c0001t0004g0136 others(168): Show |
176 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(173): 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 | a0001c0001t0036g0156 a0001c0001t0036g0157 a0001c0001t0042g0261 others(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 | a0001c0001t0060g0296 | 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 | a0001c0001t0128g0030 | 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 | a0002c0003t0034g0151 a0002c0003t0034g0152 a0002c0003t0058g0153 others(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 | 106 | a0001c0001t0004g0068 a0001c0001t0004g0088 a0001c0001t0004g0136 others(103): Show |
110 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(107): 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 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(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 | a0001c0001t0043g0259 a0001c0001t0043g0346 |
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 | a0001c0001t0042g0262 | 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 | a0001c0001t0002g0322 a0001c0001t0009g0310 |
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 | a0001c0001t0018g0046 a0001c0001t0018g0047 a0001c0001t0018g0050 others(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 | a0001c0001t0139g0278 | 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 | a0001c0001t0127g0276 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(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 | 265 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(262): Show |
281 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(278): 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 | 108 | a0001c0001t0004g0068 a0001c0001t0004g0088 a0001c0001t0004g0136 others(105): Show |
112 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(109): 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 | a0001c0001t0046g0031 a0001c0001t0046g0032 |
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 | a0001c0001t0069g0033 a0001c0001t0070g0202 |
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 | a0001c0001t0015g0079 a0001c0001t0023g0098 |
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 | a0001c0001t0099g0115 | 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 | a0001c0001t0025g0193 a0001c0001t0025g0194 a0001c0001t0025g0195 others(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 | 80 | a0001c0001t0004g0068 a0001c0001t0004g0088 a0001c0001t0004g0136 others(77): Show |
83 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(80): 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 | a0001c0001t0064g0217 | 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 | a0001c0001t0057g0034 | 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 | a0001c0001t0102g0191 | 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 | 98 | a0001c0001t0004g0068 a0001c0001t0004g0088 a0001c0001t0004g0136 others(95): Show |
101 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(98): 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 | a0001c0001t0090g0027 a0001c0001t0091g0025 a0001c0001t0092g0026 others(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 | a0001c0001t0116g0299 a0001c0001t0117g0297 a0001c0001t0118g0298 |
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 | 256 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(253): Show |
270 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(267): 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 | a0001c0001t0101g0189 | 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 | a0001c0001t0105g0345 | 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 | a0001c0001t0046g0031 a0001c0001t0046g0032 a0001c0001t0128g0030 |
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 | 256 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(253): Show |
270 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.612+2223delA | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 5/8 | chr5 | 115234166 | |||||||
chr5:115234208 | CAA | C | 8 | a0001c0001t0036g0156 a0001c0001t0036g0157 a0001c0001t0042g0261 others(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 | 255 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(252): Show |
269 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(266): Show |
intron_variant | MODIFIER | c.612+2174delT | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 5/8 | chr5 | 115234215 | |||||||
chr5:115234220 | A | G | 4 | a0002c0003t0034g0151 a0002c0003t0034g0152 a0002c0003t0058g0153 others(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 | a0002c0003t0034g0151 a0002c0003t0034g0152 a0002c0003t0058g0153 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(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 | a0001c0001t0003g0182 a0001c0001t0031g0176 a0001c0001t0031g0177 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(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 | a0001c0001t0116g0299 a0001c0001t0117g0297 |
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 | a0001c0001t0018g0046 a0001c0001t0018g0047 a0001c0001t0018g0050 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(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 | a0001c0001t0018g0046 a0001c0001t0018g0047 a0001c0001t0018g0050 others(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 | a0001c0001t0038g0216 a0001c0001t0038g0219 a0001c0001t0064g0217 others(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 | a0001c0001t0069g0033 | 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 | a0001c0001t0043g0259 a0001c0001t0043g0346 a0001c0001t0105g0345 |
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 | a0002c0003t0034g0151 a0002c0003t0034g0152 a0002c0003t0058g0153 others(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 | a0001c0001t0025g0193 a0001c0001t0025g0194 a0001c0001t0025g0195 others(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 | a0001c0001t0090g0027 a0001c0001t0091g0025 a0001c0001t0092g0026 others(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 | a0001c0001t0025g0193 a0001c0001t0025g0194 a0001c0001t0025g0195 others(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 | a0001c0001t0042g0261 a0001c0001t0042g0262 |
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 | a0001c0001t0060g0296 | 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 | 255 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(252): Show |
269 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(266): 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 | a0001c0001t0090g0027 a0001c0001t0091g0025 a0001c0001t0092g0026 others(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 | a0001c0001t0001g0012 a0001c0001t0001g0117 a0001c0001t0001g0119 others(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 | a0001c0001t0069g0033 a0001c0001t0070g0202 |
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 | a0001c0001t0026g0277 a0001c0001t0026g0288 a0001c0001t0026g0290 others(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 | a0001c0001t0036g0156 a0001c0001t0036g0157 a0001c0001t0042g0261 others(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 | a0001c0001t0025g0193 a0001c0001t0025g0194 a0001c0001t0025g0195 others(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 | a0001c0002t0004g0128 a0001c0002t0004g0209 a0001c0002t0015g0133 |
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 | a0001c0001t0085g0077 | 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 | 113 | a0001c0001t0004g0068 a0001c0001t0004g0088 a0001c0001t0004g0136 others(110): Show |
118 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.328-167T>A | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 3/8 | chr5 | 115238176 | |||||||
chr5:115238291 | A | AT | 86 | a0001c0001t0001g0173 a0001c0001t0001g0179 a0001c0001t0002g0004 others(83): Show |
94 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.328-283dupA | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 3/8 | chr5 | 115238291 | |||||||
chr5:115238291 | A | ATT | 95 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(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 | a0001c0001t0001g0114 a0001c0001t0001g0119 a0001c0001t0001g0142 others(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 | a0001c0001t0018g0047 a0001c0001t0052g0265 a0001c0001t0065g0051 others(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 | a0001c0001t0018g0046 a0001c0001t0027g0270 |
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 | a0001c0001t0050g0269 a0001c0001t0052g0264 a0001c0001t0126g0273 |
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 | a0001c0001t0056g0295 a0001c0001t0057g0034 |
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 | a0001c0001t0028g0287 a0001c0001t0029g0271 a0001c0001t0029g0275 |
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 | a0001c0001t0051g0268 a0001c0001t0051g0272 |
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 | a0001c0001t0026g0277 a0001c0001t0029g0286 a0001c0001t0050g0274 |
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 | a0001c0001t0055g0279 | 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 | a0001c0001t0123g0291 | 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 | a0001c0001t0028g0285 a0001c0001t0128g0030 |
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 | a0001c0001t0025g0193 a0001c0001t0025g0194 a0001c0001t0025g0195 others(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 | a0001c0001t0105g0345 | 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 | a0001c0001t0003g0003 a0001c0001t0003g0230 a0001c0001t0003g0232 others(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 | a0001c0001t0002g0311 a0001c0001t0002g0312 a0001c0001t0016g0018 others(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 | a0001c0001t0025g0193 a0001c0001t0025g0194 a0001c0001t0025g0195 others(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 | a0001c0001t0090g0027 a0001c0001t0091g0025 a0001c0001t0092g0026 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(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 | a0001c0001t0036g0156 a0001c0001t0036g0157 |
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 | a0001c0001t0056g0295 a0001c0001t0057g0034 |
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 | a0001c0001t0090g0027 a0001c0001t0091g0025 a0001c0001t0092g0026 others(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 | a0001c0001t0025g0193 a0001c0001t0025g0194 a0001c0001t0025g0195 others(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 | a0001c0001t0069g0033 | 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 | a0001c0001t0090g0027 a0001c0001t0091g0025 a0001c0001t0092g0026 others(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 | a0001c0001t0043g0346 | 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 | a0001c0001t0115g0040 | 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 | a0001c0002t0004g0014 a0001c0002t0004g0063 a0001c0002t0004g0128 others(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 | a0001c0001t0115g0040 | 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 | a0001c0001t0090g0027 a0001c0001t0091g0025 a0001c0001t0092g0026 others(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 | 138 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(135): Show |
150 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(147): 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 | a0001c0001t0120g0146 | 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 | a0001c0001t0021g0053 a0001c0001t0021g0054 a0001c0001t0021g0056 others(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 | a0001c0001t0115g0040 | 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 | a0001c0001t0056g0295 a0001c0001t0057g0034 |
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 | a0001c0001t0010g0071 a0001c0001t0010g0200 |
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 | a0001c0001t0032g0245 a0001c0001t0032g0246 a0001c0001t0090g0027 others(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 | a0001c0001t0119g0139 | 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 | a0001c0001t0005g0302 a0001c0001t0025g0193 a0001c0001t0025g0194 others(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 | a0001c0001t0043g0259 | 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 | a0001c0001t0044g0155 a0001c0001t0044g0185 |
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 | a0001c0001t0017g0070 a0001c0001t0017g0214 |
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 | a0001c0001t0060g0296 | 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 | a0001c0001t0139g0278 | 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 | a0001c0001t0133g0180 | 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 | a0001c0001t0088g0049 | 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 | a0001c0001t0027g0270 a0001c0001t0050g0269 a0001c0001t0126g0273 |
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 | a0001c0001t0090g0027 a0001c0001t0091g0025 a0001c0001t0092g0026 others(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 | a0001c0001t0090g0027 a0001c0001t0091g0025 a0001c0001t0092g0026 others(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 | a0001c0001t0046g0031 a0001c0001t0046g0032 a0001c0001t0128g0030 |
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 | 97 | a0001c0001t0004g0068 a0001c0001t0004g0088 a0001c0001t0004g0136 others(94): Show |
101 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(98): 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 | a0001c0001t0018g0046 a0001c0001t0018g0047 a0001c0001t0018g0050 others(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 | a0001c0001t0005g0093 a0001c0001t0005g0300 a0001c0001t0005g0301 others(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 | a0001c0001t0115g0040 | 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 | a0001c0001t0115g0040 | 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 | a0001c0001t0090g0027 a0001c0001t0091g0025 a0001c0001t0092g0026 others(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 | a0001c0001t0069g0033 a0001c0001t0070g0202 |
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 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0036 others(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 | a0001c0001t0060g0296 | 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 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0036 others(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 | a0001c0001t0090g0027 a0001c0001t0091g0025 a0001c0001t0092g0026 others(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 | a0001c0001t0090g0027 a0001c0001t0093g0024 a0001c0001t0094g0028 others(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 | a0001c0001t0091g0025 a0001c0001t0092g0026 a0001c0001t0095g0023 |
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 | a0001c0001t0091g0025 a0001c0001t0092g0026 a0001c0001t0095g0023 |
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 | a0001c0001t0091g0025 a0001c0001t0092g0026 a0001c0001t0095g0023 |
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 | a0001c0001t0091g0025 a0001c0001t0092g0026 a0001c0001t0095g0023 |
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 | 156 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0052 others(153): Show |
167 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.260-2861dupT | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 2/8 | chr5 | 115244466 | |||||||
chr5:115244466 | C | CAA | 65 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0016 others(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 | a0001c0001t0025g0193 a0001c0001t0025g0194 a0001c0001t0026g0277 others(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 | a0001c0001t0060g0296 | 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 | 267 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(264): Show |
283 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(280): 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 | a0001c0001t0090g0027 a0001c0001t0091g0025 a0001c0001t0092g0026 others(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 | a0001c0001t0122g0329 | 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 | a0001c0001t0011g0067 a0001c0001t0087g0187 |
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 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0182 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(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 | a0001c0001t0090g0027 a0001c0001t0091g0025 a0001c0001t0092g0026 others(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 | a0001c0001t0069g0033 a0001c0001t0070g0202 |
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 | a0001c0001t0026g0277 a0001c0001t0051g0268 |
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 | a0001c0001t0090g0027 a0001c0001t0091g0025 a0001c0001t0092g0026 others(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 | a0001c0001t0025g0193 a0001c0001t0025g0194 a0001c0001t0025g0195 others(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 | a0001c0001t0001g0159 a0001c0001t0001g0171 |
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 | a0001c0001t0115g0040 | 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 | 121 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(118): Show |
133 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(130): 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 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0036 others(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 | a0001c0001t0001g0158 a0001c0001t0004g0068 a0001c0001t0007g0221 others(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 | a0001c0001t0140g0035 | 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 | a0001c0001t0035g0043 a0001c0001t0067g0041 a0001c0001t0089g0044 |
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 | a0001c0001t0106g0197 | 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 | a0001c0001t0090g0027 a0001c0001t0091g0025 a0001c0001t0092g0026 others(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 | a0001c0001t0025g0194 a0001c0001t0025g0195 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(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 | a0001c0001t0090g0027 a0001c0001t0091g0025 a0001c0001t0092g0026 others(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 | a0001c0001t0054g0250 a0001c0001t0138g0233 |
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 | a0001c0001t0095g0023 a0001c0001t0113g0022 |
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 | a0001c0001t0140g0035 | 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 | a0001c0001t0056g0295 a0001c0001t0057g0034 |
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 | a0001c0001t0090g0027 a0001c0001t0091g0025 a0001c0001t0092g0026 others(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 | a0001c0001t0002g0330 a0001c0001t0002g0331 a0001c0001t0002g0340 |
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 | a0001c0001t0018g0046 a0001c0001t0018g0047 a0001c0001t0018g0050 others(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 | a0001c0001t0014g0203 a0001c0001t0083g0062 |
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 | a0001c0001t0090g0027 a0001c0001t0091g0025 a0001c0001t0092g0026 others(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 | a0001c0001t0118g0298 | 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 | a0001c0001t0008g0006 a0001c0001t0008g0037 a0001c0001t0008g0038 others(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 | a0001c0001t0069g0033 | 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 | a0001c0002t0071g0061 | 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 | a0001c0001t0090g0027 a0001c0001t0091g0025 a0001c0001t0092g0026 others(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 | a0001c0001t0090g0027 a0001c0001t0091g0025 a0001c0001t0092g0026 others(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 | 259 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(256): Show |
273 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(270): 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 | a0001c0001t0090g0027 a0001c0001t0091g0025 a0001c0001t0092g0026 others(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 | a0001c0001t0098g0154 | 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 | a0001c0001t0068g0042 | 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 | a0001c0001t0116g0299 a0001c0001t0117g0297 |
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 | a0001c0001t0116g0299 a0001c0001t0117g0297 |
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 | a0001c0001t0056g0295 a0001c0001t0057g0034 |
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 | a0001c0001t0090g0027 a0001c0001t0091g0025 a0001c0001t0092g0026 others(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 | 259 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(256): Show |
273 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(270): 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 | a0001c0001t0006g0005 a0001c0001t0006g0307 a0001c0001t0006g0333 others(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 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0174 others(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 | a0001c0001t0040g0065 | 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 | a0001c0001t0101g0189 | 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 | a0001c0001t0007g0104 a0001c0001t0020g0105 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(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 | a0001c0001t0026g0277 a0001c0001t0026g0288 a0001c0001t0026g0290 others(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 | a0001c0001t0007g0123 a0001c0001t0007g0125 a0001c0001t0045g0124 |
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 | a0001c0001t0102g0191 | 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 | a0001c0001t0036g0156 a0001c0001t0036g0157 a0001c0001t0042g0261 others(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 | a0001c0001t0090g0027 a0001c0001t0091g0025 a0001c0001t0092g0026 others(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 | a0001c0001t0090g0027 a0001c0001t0091g0025 a0001c0001t0092g0026 others(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 | a0001c0002t0004g0013 a0001c0002t0004g0014 a0001c0002t0004g0063 others(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 | a0001c0001t0090g0027 a0001c0001t0091g0025 a0001c0001t0092g0026 others(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 | a0001c0001t0018g0046 a0001c0001t0018g0047 a0001c0001t0018g0050 others(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 | a0001c0001t0003g0002 a0001c0001t0003g0182 a0001c0001t0003g0213 others(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 | a0001c0001t0036g0156 a0001c0001t0036g0157 a0001c0001t0042g0261 others(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 | a0001c0001t0090g0027 a0001c0001t0091g0025 a0001c0001t0092g0026 others(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 | a0001c0001t0043g0259 | 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 | a0001c0001t0018g0050 a0001c0001t0065g0051 |
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 | a0001c0001t0026g0290 a0001c0001t0028g0287 a0001c0001t0029g0271 others(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 | a0001c0001t0018g0046 a0001c0001t0018g0047 a0001c0001t0018g0050 others(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 | a0001c0001t0001g0058 a0001c0001t0018g0046 a0001c0001t0018g0047 others(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 | a0001c0001t0056g0295 a0001c0001t0057g0034 |
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 | a0001c0001t0042g0261 a0001c0001t0042g0262 |
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 | a0001c0001t0130g0196 a0001c0001t0133g0180 |
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 | a0001c0001t0060g0296 | 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 | a0001c0001t0069g0033 | 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 | 266 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(263): Show |
282 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(279): 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 | a0001c0001t0078g0134 | 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 | a0001c0001t0018g0046 a0001c0001t0018g0047 a0001c0001t0018g0050 others(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 | 255 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(252): Show |
271 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.141-1347dupA | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 1/8 | chr5 | 115254601 | |||||||
chr5:115254616 | A | T | 4 | a0001c0001t0025g0193 a0001c0001t0025g0194 a0001c0001t0025g0195 others(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 | 137 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(134): Show |
149 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(146): 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 | a0001c0001t0057g0034 | 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 | a0001c0001t0001g0210 a0001c0001t0001g0211 |
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 | a0001c0001t0018g0046 a0001c0001t0018g0047 a0001c0001t0018g0050 others(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 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0036 others(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 | a0001c0001t0090g0027 a0001c0001t0091g0025 a0001c0001t0092g0026 others(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 | a0001c0001t0069g0033 | 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 | a0001c0001t0036g0156 a0001c0001t0036g0157 |
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 | 197 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(194): Show |
209 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(206): 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 | a0001c0001t0026g0277 a0001c0001t0026g0288 a0001c0001t0026g0290 others(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 | a0001c0001t0091g0025 a0001c0001t0092g0026 a0001c0001t0093g0024 |
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 | a0001c0001t0003g0252 a0001c0001t0033g0253 |
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 | a0001c0001t0128g0030 | 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 | a0001c0001t0001g0181 a0001c0001t0098g0154 |
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 | 267 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(264): Show |
283 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(280): Show |
intron_variant | MODIFIER | c.141-3938dupT | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 1/8 | chr5 | 115257192 | |||||||
chr5:115257332 | A | G | 299 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(296): Show |
318 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(315): 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 | a0001c0001t0003g0182 a0001c0001t0031g0183 a0001c0001t0053g0184 |
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 | a0001c0001t0105g0345 | 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 | 171 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(168): Show |
182 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.141-4276dupT | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 1/8 | chr5 | 115257530 | |||||||
chr5:115257530 | C | CAA | 6 | a0001c0001t0001g0208 a0001c0001t0004g0136 a0001c0001t0005g0137 others(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 | a0001c0001t0001g0057 a0001c0001t0001g0142 a0001c0001t0001g0143 others(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 | a0001c0001t0095g0023 a0001c0001t0113g0022 |
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 | a0001c0001t0025g0193 a0001c0001t0025g0194 a0001c0001t0025g0195 others(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 | a0001c0001t0138g0233 | 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 | a0001c0001t0069g0033 | 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 | a0001c0001t0051g0272 | 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 | a0001c0001t0047g0140 a0001c0001t0119g0139 |
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 | a0001c0001t0043g0259 | 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 | a0001c0001t0130g0196 | 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 | a0001c0001t0008g0006 a0001c0001t0008g0037 a0001c0001t0008g0038 others(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 | a0001c0002t0071g0061 | 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 | 130 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(127): Show |
141 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(138): 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 | a0001c0001t0090g0027 a0001c0001t0091g0025 a0001c0001t0092g0026 others(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 | 127 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(124): Show |
138 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(135): 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 | a0001c0001t0106g0197 a0001c0001t0108g0198 |
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 | a0001c0001t0090g0027 a0001c0001t0091g0025 a0001c0001t0092g0026 others(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 | a0001c0001t0138g0233 | 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 | a0001c0001t0069g0033 | 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 | a0001c0001t0090g0027 a0001c0001t0091g0025 a0001c0001t0092g0026 others(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 | a0001c0001t0003g0232 a0001c0001t0033g0231 |
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 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0210 others(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 | a0001c0001t0008g0039 a0001c0001t0017g0214 a0001c0001t0021g0053 others(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 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0059 others(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 | a0001c0001t0090g0027 a0001c0001t0091g0025 a0001c0001t0092g0026 others(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 | a0001c0001t0007g0220 a0001c0001t0007g0221 a0001c0001t0007g0224 others(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 | a0001c0001t0021g0053 a0001c0001t0021g0054 a0001c0001t0021g0056 others(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 | a0001c0001t0008g0006 a0001c0001t0008g0037 a0001c0001t0008g0038 others(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 | a0001c0001t0057g0034 | 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 | 266 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(263): Show |
282 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(279): 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 | a0001c0001t0043g0259 a0001c0001t0043g0346 |
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 | a0001c0001t0056g0295 | 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 | a0001c0001t0105g0345 | 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 | a0001c0001t0116g0299 a0001c0001t0117g0297 a0001c0001t0118g0298 |
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 | a0001c0001t0008g0006 a0001c0001t0008g0037 a0001c0001t0008g0038 others(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 | a0001c0001t0042g0261 a0001c0001t0042g0262 |
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 | a0001c0001t0008g0006 a0001c0001t0008g0037 a0001c0001t0008g0038 others(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 | a0001c0001t0140g0035 | 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 | a0001c0001t0075g0263 | 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 | a0001c0001t0056g0295 | 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 | a0001c0001t0013g0292 a0001c0001t0026g0277 a0001c0001t0026g0288 others(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 | a0001c0001t0057g0034 | 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 | a0001c0001t0060g0296 | 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 | a0001c0001t0063g0294 | 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 | a0001c0001t0056g0295 | 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 | a0001c0001t0069g0033 | 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 | a0001c0001t0056g0295 | 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 | a0001c0001t0046g0031 a0001c0001t0046g0032 a0001c0001t0128g0030 |
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 | a0001c0001t0060g0296 a0001c0001t0116g0299 a0001c0001t0117g0297 others(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 | a0001c0001t0005g0300 a0001c0001t0005g0301 a0001c0001t0005g0302 others(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 | 290 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(287): Show |
309 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(306): 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 | a0001c0001t0090g0027 a0001c0001t0091g0025 a0001c0001t0092g0026 others(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 | a0001c0001t0043g0346 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.140+41G>T | PGGT1B | ENSG00000164219.10 | transcript | ENST00000419445.6 | protein_coding | 1/8 | chr5 | 115262671 |