Item | Value |
---|---|
geneid | 4258 |
ensemblid | ENSG00000085871.9 |
hgncid | 7063 |
symbol | MGST2 |
name | microsomal glutathione S-transferase 2 |
refseq_nuc | NM_002413.5 |
refseq_prot | NP_002404.1 |
ensembl_nuc | ENST00000265498.6 |
ensembl_prot | ENSP00000265498.1 |
mane_status | MANE Select |
chr | chr4 |
start | 139665819 |
end | 139704243 |
strand | + |
ver | v1.2 |
region | chr4:139665819-139704243 |
region5000 | chr4:139660819-139709243 |
regionname0 | MGST2_chr4_139665819_139704243 |
regionname5000 | MGST2_chr4_139660819_139709243 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 147 | 439 | 92 | 82 | 204 | 16 | 43 | 166 | MGST2_chr4_139660819_139709243 | MGST2 | MAGNS others(142): Show |
chr4 | 139660819 | 139709243 |
a0002 | 0/0 | 147 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | MAGNS others(142): Show |
chr4 | 139660819 | 139709243 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 441 | 435 | 92 | 80 | 204 | 14 | 43 | MGST2_chr4_139660819_139709243 | MGST2 | ATGGC others(436): Show |
chr4 | 139660819 | 139709243 | ||
a0001c0002 | 0/0 | 441 | 3 | 0 | 1 | 0 | 2 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | ATGGC others(436): Show |
chr4 | 139660819 | 139709243 | ||
a0001c0004 | 0/0 | 441 | 1 | 0 | 1 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | ATGGC others(436): Show |
chr4 | 139660819 | 139709243 | ||
a0002c0003 | 0/0 | 441 | 1 | 0 | 0 | 0 | 0 | 1 | MGST2_chr4_139660819_139709243 | MGST2 | ATGGC others(436): Show |
chr4 | 139660819 | 139709243 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 740 | 335 | 63 | 72 | 153 | 14 | 32 | MGST2_chr4_139660819_139709243 | MGST2 | ATAAA others(735): Show |
chr4 | 139660819 | 139709243 |
a0001c0001t0002 | 0/0 | 740 | 92 | 25 | 7 | 51 | 0 | 9 | MGST2_chr4_139660819_139709243 | MGST2 | ATAAA others(735): Show |
chr4 | 139660819 | 139709243 |
a0001c0001t0003 | 0/0 | 740 | 4 | 3 | 1 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | ATAAA others(735): Show |
chr4 | 139660819 | 139709243 |
a0001c0001t0004 | 0/0 | 740 | 2 | 0 | 0 | 0 | 0 | 2 | MGST2_chr4_139660819_139709243 | MGST2 | ATAAA others(735): Show |
chr4 | 139660819 | 139709243 |
a0001c0001t0005 | 1/0 | 740 | 1 | 0 | 0 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | ATAAA others(735): Show |
chr4 | 139660819 | 139709243 |
a0001c0001t0006 | 0/0 | 740 | 1 | 1 | 0 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | ATAAA others(735): Show |
chr4 | 139660819 | 139709243 |
a0001c0002t0001 | 0/0 | 740 | 3 | 0 | 1 | 0 | 2 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | ATAAA others(735): Show |
chr4 | 139660819 | 139709243 |
a0001c0004t0001 | 0/0 | 740 | 1 | 0 | 1 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | ATAAA others(735): Show |
chr4 | 139660819 | 139709243 |
a0002c0003t0001 | 0/0 | 740 | 1 | 0 | 0 | 0 | 0 | 1 | MGST2_chr4_139660819_139709243 | MGST2 | ATAAA others(735): Show |
chr4 | 139660819 | 139709243 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 8 | 0 | 2 | 6 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0006 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0010 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0240 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0383 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0384 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0385 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0386 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0387 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0388 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0389 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0390 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0391 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0001g0392 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0002g0002 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0002g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0002g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0002g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0002g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0002g0018 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0002g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0002g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0002g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0002g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0002g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0002g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0002g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0002g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0002g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0002g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0002g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0002g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0002g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0002g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0002g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0002g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0002g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0002g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0002g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0002g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0002g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0002g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0002g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0002g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0002g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0002g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0002g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0002g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0002g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0002g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0002g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0002g0359 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0002g0360 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0002g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0002g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0002g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0002g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0002g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0002g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0002g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0002g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0002g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0002g0370 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0002g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0002g0372 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0002g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0002g0374 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0002g0375 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0002g0376 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0002g0377 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0002g0378 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0002g0379 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0002g0380 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0002g0381 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0002g0382 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0003g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0003g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0003g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0003g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0004g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0004g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0005g0213 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0001t0006g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0002t0001g0011 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0002t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0001c0004t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
a0002c0003t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0339 | EUR | GBR | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0208 | EUR | GBR | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0191 | EUR | GBR | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0096 | EUR | GBR | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0215 | EUR | FIN | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0183 | EUR | FIN | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | CHS | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | CHS | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG00438 | hp1 | a0001 | c0001 | t0002 | g0367 | EAS | CHS | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | CHS | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | CHS | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0316 | EAS | CHS | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0319 | EAS | CHS | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | CHS | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0308 | EAS | CHS | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG00597 | hp2 | a0001 | c0001 | t0002 | g0148 | EAS | CHS | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | CHS | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | CHS | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0187 | AMR | PUR | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG00639 | hp2 | a0001 | c0001 | t0002 | g0241 | AMR | PUR | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0260 | AMR | PUR | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG00642 | hp2 | a0001 | c0002 | t0001 | g0100 | AMR | PUR | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG00673 | hp1 | a0001 | c0001 | t0002 | g0374 | EAS | CHS | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | CHS | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0196 | AMR | PUR | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0258 | AMR | PUR | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0204 | AMR | PUR | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0198 | AMR | PUR | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0261 | AMR | PUR | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0280 | AMR | PUR | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0243 | AMR | PUR | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG01069 | hp2 | a0001 | c0001 | t0003 | g0162 | AMR | PUR | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0244 | AMR | PUR | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0182 | AMR | PUR | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0224 | AMR | PUR | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0327 | AMR | PUR | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0305 | AMR | PUR | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0222 | AMR | PUR | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0290 | AMR | PUR | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0201 | AMR | PUR | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG01168 | hp1 | a0001 | c0001 | t0002 | g0147 | AMR | PUR | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0088 | AMR | PUR | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG01169 | hp1 | a0001 | c0001 | t0002 | g0146 | AMR | PUR | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG01175 | hp1 | a0001 | c0001 | t0002 | g0156 | AMR | PUR | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0256 | AMR | PUR | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0227 | AMR | PUR | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG01192 | hp2 | a0001 | c0001 | t0002 | g0344 | AMR | PUR | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0294 | AMR | PUR | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | CLM | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0106 | AMR | CLM | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | CLM | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG01257 | hp1 | a0001 | c0001 | t0002 | g0380 | AMR | CLM | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG01258 | hp2 | a0001 | c0001 | t0002 | g0377 | AMR | CLM | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | CLM | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0178 | AMR | CLM | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0281 | AMR | CLM | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0298 | AMR | CLM | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0279 | AMR | CLM | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | CLM | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0181 | AMR | CLM | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | CLM | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | CLM | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0214 | AMR | CLM | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0304 | AMR | CLM | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG01496 | hp2 | a0001 | c0004 | t0001 | g0262 | AMR | CLM | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0236 | EUR | IBS | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0216 | EUR | IBS | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0023 | EUR | IBS | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG01516 | hp2 | a0001 | c0002 | t0001 | g0011 | EUR | IBS | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG01517 | hp1 | a0001 | c0002 | t0001 | g0011 | EUR | IBS | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0237 | EUR | IBS | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | ACB | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG01884 | hp2 | a0001 | c0001 | t0003 | g0235 | AFR | ACB | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0282 | AFR | ACB | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | ACB | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0203 | AMR | PEL | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PEL | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0199 | AMR | PEL | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PEL | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0264 | AMR | PEL | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0200 | AMR | PEL | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0277 | AMR | PEL | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0205 | AMR | PEL | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0323 | AMR | PEL | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PEL | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0287 | AMR | PEL | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0173 | AMR | PEL | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | KHV | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | KHV | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | KHV | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | KHV | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG02055 | hp1 | a0001 | c0001 | t0002 | g0155 | AFR | ACB | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | ACB | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | KHV | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | KHV | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | KHV | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | KHV | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | KHV | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | KHV | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG02083 | hp1 | a0001 | c0001 | t0002 | g0368 | EAS | KHV | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | KHV | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0303 | EAS | KHV | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG02129 | hp2 | a0001 | c0001 | t0002 | g0373 | EAS | KHV | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0314 | EAS | KHV | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | KHV | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | ACB | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | ACB | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0270 | AMR | PEL | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0188 | AMR | PEL | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | CDX | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG02155 | hp2 | a0001 | c0001 | t0002 | g0142 | EAS | CDX | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | CDX | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | CDX | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0232 | AFR | ACB | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0209 | AFR | ACB | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | ACB | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | ACB | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0295 | AMR | PEL | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0202 | AMR | PEL | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0238 | AFR | ACB | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0386 | AFR | ACB | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | PEL | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0197 | AMR | PEL | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | KHV | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | KHV | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0218 | AFR | GWD | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0341 | AFR | GWD | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0206 | SAS | PJL | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | GWD | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG02622 | hp1 | a0001 | c0001 | t0002 | g0134 | AFR | GWD | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG02622 | hp2 | a0001 | c0001 | t0002 | g0143 | AFR | GWD | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0233 | AFR | GWD | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | GWD | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | GWD | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG02647 | hp2 | a0001 | c0001 | t0002 | g0355 | AFR | GWD | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0242 | SAS | PJL | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0051 | SAS | PJL | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG02717 | hp1 | a0001 | c0001 | t0002 | g0019 | AFR | GWD | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | GWD | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0340 | AFR | GWD | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0278 | AFR | GWD | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0077 | SAS | PJL | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG02735 | hp2 | a0002 | c0003 | t0001 | g0259 | SAS | PJL | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0228 | SAS | PJL | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0037 | SAS | PJL | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG02809 | hp1 | a0001 | c0001 | t0002 | g0361 | AFR | GWD | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG02809 | hp2 | a0001 | c0001 | t0002 | g0015 | AFR | GWD | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0217 | AFR | GWD | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0387 | AFR | GWD | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | GWD | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG02895 | hp1 | a0001 | c0001 | t0003 | g0161 | AFR | GWD | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0186 | AFR | GWD | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG02896 | hp2 | a0001 | c0001 | t0002 | g0351 | AFR | GWD | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG02897 | hp2 | a0001 | c0001 | t0003 | g0163 | AFR | GWD | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG02922 | hp1 | a0001 | c0001 | t0002 | g0133 | AFR | ESN | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG02922 | hp2 | a0001 | c0001 | t0002 | g0342 | AFR | ESN | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG02965 | hp1 | a0001 | c0001 | t0002 | g0347 | AFR | ESN | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG02965 | hp2 | a0001 | c0001 | t0002 | g0349 | AFR | ESN | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0392 | AFR | ESN | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | ESN | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0330 | AFR | ESN | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG02976 | hp2 | a0001 | c0001 | t0002 | g0158 | AFR | ESN | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0207 | SAS | PJL | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0038 | SAS | PJL | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG03041 | hp1 | a0001 | c0001 | t0002 | g0157 | AFR | GWD | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | GWD | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0388 | AFR | MSL | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG03098 | hp2 | a0001 | c0001 | t0002 | g0345 | AFR | MSL | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG03139 | hp1 | a0001 | c0001 | t0002 | g0346 | AFR | ESN | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | ESN | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | ESN | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0251 | AFR | ESN | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | MSL | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG03209 | hp2 | a0001 | c0001 | t0002 | g0379 | AFR | MSL | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | MSL | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0234 | AFR | MSL | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0136 | SAS | PJL | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0087 | SAS | PJL | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG03453 | hp1 | a0001 | c0001 | t0002 | g0135 | AFR | MSL | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | MSL | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | MSL | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG03486 | hp2 | a0001 | c0001 | t0002 | g0350 | AFR | MSL | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG03490 | hp1 | a0001 | c0001 | t0002 | g0141 | SAS | PJL | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0212 | SAS | PJL | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0090 | SAS | PJL | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0229 | SAS | PJL | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG03492 | hp1 | a0001 | c0001 | t0002 | g0018 | SAS | PJL | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0230 | SAS | PJL | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0383 | AFR | ESN | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0250 | AFR | ESN | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG03579 | hp1 | a0001 | c0001 | t0002 | g0015 | AFR | MSL | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG03579 | hp2 | a0001 | c0001 | t0002 | g0343 | AFR | MSL | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0190 | SAS | PJL | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0221 | SAS | PJL | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG03669 | hp1 | a0001 | c0001 | t0002 | g0359 | SAS | PJL | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0078 | SAS | PJL | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0223 | SAS | STU | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0231 | SAS | STU | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0084 | SAS | PJL | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0058 | SAS | PJL | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0089 | SAS | PJL | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0045 | SAS | BEB | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0189 | SAS | BEB | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG03834 | hp1 | a0001 | c0001 | t0002 | g0372 | SAS | BEB | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG03834 | hp2 | a0001 | c0001 | t0002 | g0165 | SAS | BEB | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0068 | SAS | BEB | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0263 | SAS | BEB | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | BEB | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0070 | SAS | BEB | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0192 | SAS | BEB | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG04184 | hp2 | a0001 | c0001 | t0002 | g0360 | SAS | BEB | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG04199 | hp1 | a0001 | c0001 | t0004 | g0273 | SAS | STU | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0220 | SAS | STU | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0219 | SAS | STU | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG04204 | hp2 | a0001 | c0001 | t0002 | g0370 | SAS | STU | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG04228 | hp1 | a0001 | c0001 | t0002 | g0018 | SAS | STU | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG04228 | hp2 | a0001 | c0001 | t0004 | g0272 | SAS | STU | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA18522 | hp1 | a0001 | c0001 | t0006 | g0160 | AFR | YRI | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | YRI | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA18747 | hp1 | a0001 | c0001 | t0002 | g0371 | EAS | CHB | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | CHB | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA18906 | hp1 | a0001 | c0001 | t0002 | g0354 | AFR | YRI | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0391 | AFR | YRI | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA18939 | hp2 | a0001 | c0001 | t0002 | g0376 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA18943 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA18943 | hp2 | a0001 | c0001 | t0002 | g0144 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA18944 | hp1 | a0001 | c0001 | t0002 | g0151 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA18945 | hp2 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA18947 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA18948 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA18949 | hp2 | a0001 | c0001 | t0002 | g0366 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0328 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0322 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA18957 | hp1 | a0001 | c0001 | t0002 | g0381 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA18959 | hp1 | a0001 | c0001 | t0002 | g0378 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA18959 | hp2 | a0001 | c0001 | t0002 | g0153 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0334 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA18964 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA18966 | hp1 | a0001 | c0001 | t0002 | g0131 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0321 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA18972 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0324 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0338 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA18977 | hp1 | a0001 | c0001 | t0002 | g0364 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA18982 | hp2 | a0001 | c0001 | t0002 | g0149 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA18984 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA18985 | hp1 | a0001 | c0001 | t0002 | g0150 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA18986 | hp1 | a0001 | c0001 | t0002 | g0357 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA18988 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA18992 | hp1 | a0001 | c0001 | t0002 | g0152 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0335 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA18993 | hp2 | a0001 | c0001 | t0002 | g0356 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA18998 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA18999 | hp2 | a0001 | c0001 | t0002 | g0369 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA19000 | hp1 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA19001 | hp2 | a0001 | c0001 | t0002 | g0145 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA19002 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA19003 | hp2 | a0001 | c0001 | t0002 | g0137 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0325 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0390 | AFR | LWK | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0246 | AFR | LWK | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0385 | AFR | LWK | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0389 | AFR | LWK | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0329 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA19054 | hp2 | a0001 | c0001 | t0002 | g0353 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA19056 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA19057 | hp2 | a0001 | c0001 | t0002 | g0362 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA19058 | hp2 | a0001 | c0001 | t0002 | g0382 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0336 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA19067 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA19068 | hp1 | a0001 | c0001 | t0002 | g0352 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0326 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA19070 | hp2 | a0001 | c0001 | t0002 | g0140 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA19075 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA19077 | hp2 | a0001 | c0001 | t0002 | g0363 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0333 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA19080 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA19080 | hp2 | a0001 | c0001 | t0002 | g0358 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA19083 | hp1 | a0001 | c0001 | t0002 | g0375 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA19084 | hp1 | a0001 | c0001 | t0002 | g0154 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA19084 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA19085 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA19087 | hp2 | a0001 | c0001 | t0002 | g0365 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0337 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0275 | AFR | YRI | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0331 | AFR | YRI | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0225 | EUR | TSI | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0210 | EUR | TSI | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0299 | EUR | TSI | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0257 | EUR | TSI | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0052 | AMR | CLM | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0226 | AMR | CLM | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG02109 | hp1 | a0001 | c0001 | t0002 | g0348 | AFR | ACB | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG02109 | hp2 | a0001 | c0001 | t0002 | g0019 | AFR | ACB | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0332 | AFR | ACB | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | ACB | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | ACB | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | ACB | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0384 | AFR | MSL | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0253 | AFR | MSL | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | USA | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0252 | AFR | USA | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0320 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA18955 | hp2 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0267 | AFR | USA | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | USA | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA21309 | hp1 | a0001 | c0001 | t0002 | g0179 | AFR | LWK | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | LWK | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0240 | REF | REF | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
homoSapiens | grch38p0 | a0001 | c0001 | t0005 | g0213 | REF | REF | MGST2_chr4_139660819_139709243 | MGST2 | chr4 | 139660819 | 139709243 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:139703502 | T | C | 1 | a0002 | 1 | HG02735.hp2 | missense_variant | MODERATE | c.277T>C | p.Tyr93His | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 4/5 | 478/740 | 277/444 | 93/147 | chr4 | 139703502 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:139666061 | C | T | 1 | a0001c0004 | 1 | HG01496.hp2 | synonymous_variant | LOW | c.42C>T | p.Leu14Leu | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/5 | 243/740 | 42/444 | 14/147 | chr4 | 139666061 | |||
chr4:139695263 | C | T | 1 | a0001c0002 | 3 | HG00642.hp2 HG01516.hp2 HG01517.hp1 |
synonymous_variant | LOW | c.225C>T | p.Asn75Asn | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/5 | 426/740 | 225/444 | 75/147 | chr4 | 139695263 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:139665890 | A | G | 2 | a0001c0001t0003 a0001c0001t0006 |
5 | HG01069.hp2 HG01884.hp2 HG02895.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-130A>G | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/5 | 130 | chr4 | 139665890 | ||||||
chr4:139665920 | C | A | 1 | a0001c0001t0004 | 2 | HG04199.hp1 HG04228.hp2 |
5_prime_UTR_variant | MODIFIER | c.-100C>A | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/5 | 100 | chr4 | 139665920 | ||||||
chr4:139665971 | A | T | 1 | a0001c0001t0002 | 92 | HG00438.hp1 HG00597.hp2 HG00639.hp2 others(89): Show |
5_prime_UTR_variant | MODIFIER | c.-49A>T | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/5 | 49 | chr4 | 139665971 | ||||||
chr4:139704169 | A | G | 7 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(4): Show |
437 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(434): Show |
3_prime_UTR_variant | MODIFIER | c.*21A>G | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 5/5 | 21 | chr4 | 139704169 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:139666105 | T | TGCGTGTG others(7): Show |
11 | a0001c0001t0001g0031 a0001c0001t0001g0383 a0001c0001t0001g0384 others(8): Show |
12 | HG01070.hp2 HG01071.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.58+31_58+32insTGTG others(10): Show |
MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr4 | 139666105 | ||||||
chr4:139666107 | CGCGTGTG others(9): Show |
C | 43 | a0001c0001t0002g0007 a0001c0001t0002g0030 a0001c0001t0002g0342 others(40): Show |
46 | HG00438.hp1 HG00673.hp1 HG01192.hp2 others(43): Show |
intron_variant | MODIFIER | c.58+32_58+47delCGTG others(12): Show |
MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr4 | 139666107 | ||||||
chr4:139666109 | C | T | 256 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(253): Show |
295 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(292): Show |
intron_variant | MODIFIER | c.58+32C>T | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | chr4 | 139666109 | |||||||
chr4:139666111 | T | C | 11 | a0001c0001t0001g0031 a0001c0001t0001g0383 a0001c0001t0001g0384 others(8): Show |
12 | HG01070.hp2 HG01071.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.58+34T>C | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | chr4 | 139666111 | |||||||
chr4:139666113 | T | TGTGTGCG others(5): Show |
5 | a0001c0001t0001g0246 a0001c0001t0001g0250 a0001c0001t0001g0251 others(2): Show |
5 | HG03195.hp2 HG03471.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.58+39_58+40insTGCG others(8): Show |
MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr4 | 139666113 | ||||||
chr4:139666113 | T | TGTGTGCG others(7): Show |
1 | a0001c0001t0001g0282 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.58+39_58+40insTGCG others(10): Show |
MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr4 | 139666113 | ||||||
chr4:139666114 | GTGCGTGT | G | 155 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(152): Show |
181 | HG00140.hp2 HG00423.hp1 HG00597.hp2 others(178): Show |
intron_variant | MODIFIER | c.58+38_58+44delTGCG others(3): Show |
MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | chr4 | 139666114 | |||||||
chr4:139666115 | T | TGTGCGCG others(3): Show |
3 | a0001c0001t0001g0029 a0001c0001t0001g0340 a0001c0001t0001g0341 |
4 | HG02572.hp2 HG02723.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.58+39_58+40insTGCG others(6): Show |
MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr4 | 139666115 | ||||||
chr4:139666115 | T | TGTGCGCG others(5): Show |
91 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0026 others(88): Show |
103 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.58+39_58+40insTGCG others(8): Show |
MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr4 | 139666115 | ||||||
chr4:139666117 | C | CGCGCGCG others(5): Show |
1 | a0001c0004t0001g0262 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.58+41_58+42insCGCG others(8): Show |
MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr4 | 139666117 | ||||||
chr4:139666117 | C | T | 108 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0026 others(105): Show |
121 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(118): Show |
intron_variant | MODIFIER | c.58+40C>T | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | chr4 | 139666117 | |||||||
chr4:139666183 | T | C | 1 | a0001c0001t0001g0032 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.58+106T>C | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | chr4 | 139666183 | |||||||
chr4:139666260 | A | C | 146 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0026 others(143): Show |
163 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(160): Show |
intron_variant | MODIFIER | c.58+183A>C | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | chr4 | 139666260 | |||||||
chr4:139666288 | T | C | 30 | a0001c0001t0002g0030 a0001c0001t0002g0353 a0001c0001t0002g0354 others(27): Show |
31 | HG00438.hp1 HG00673.hp1 HG01257.hp1 others(28): Show |
intron_variant | MODIFIER | c.58+211T>C | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | chr4 | 139666288 | |||||||
chr4:139666294 | C | T | 2 | a0001c0001t0001g0243 a0001c0001t0001g0244 |
2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.58+217C>T | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | chr4 | 139666294 | |||||||
chr4:139666332 | G | A | 1 | a0001c0001t0001g0033 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.58+255G>A | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | chr4 | 139666332 | |||||||
chr4:139666390 | C | G | 1 | a0001c0001t0001g0242 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.58+313C>G | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | chr4 | 139666390 | |||||||
chr4:139666568 | T | G | 1 | a0001c0001t0001g0245 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.58+491T>G | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | chr4 | 139666568 | |||||||
chr4:139666590 | G | C | 11 | a0001c0001t0001g0246 a0001c0001t0002g0342 a0001c0001t0002g0343 others(8): Show |
11 | HG01192.hp2 HG02109.hp1 HG02896.hp2 others(8): Show |
intron_variant | MODIFIER | c.58+513G>C | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | chr4 | 139666590 | |||||||
chr4:139666801 | T | C | 11 | a0001c0001t0001g0246 a0001c0001t0002g0342 a0001c0001t0002g0343 others(8): Show |
11 | HG01192.hp2 HG02109.hp1 HG02896.hp2 others(8): Show |
intron_variant | MODIFIER | c.58+724T>C | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | chr4 | 139666801 | |||||||
chr4:139666831 | G | A | 222 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(219): Show |
251 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(248): Show |
intron_variant | MODIFIER | c.58+754G>A | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | chr4 | 139666831 | |||||||
chr4:139666924 | T | C | 3 | a0001c0001t0001g0247 a0001c0001t0001g0248 a0001c0001t0001g0249 |
3 | NA18985.hp2 NA19003.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.58+847T>C | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | chr4 | 139666924 | |||||||
chr4:139667068 | T | C | 11 | a0001c0001t0001g0246 a0001c0001t0002g0342 a0001c0001t0002g0343 others(8): Show |
11 | HG01192.hp2 HG02109.hp1 HG02896.hp2 others(8): Show |
intron_variant | MODIFIER | c.58+991T>C | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | chr4 | 139667068 | |||||||
chr4:139667206 | C | T | 1 | a0001c0001t0001g0246 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.58+1129C>T | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | chr4 | 139667206 | |||||||
chr4:139667237 | T | C | 116 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(113): Show |
131 | HG00140.hp2 HG00423.hp1 HG00609.hp2 others(128): Show |
intron_variant | MODIFIER | c.58+1160T>C | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | chr4 | 139667237 | |||||||
chr4:139667258 | T | C | 308 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(305): Show |
351 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(348): Show |
intron_variant | MODIFIER | c.58+1181T>C | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | chr4 | 139667258 | |||||||
chr4:139667365 | C | T | 1 | a0001c0001t0001g0339 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.58+1288C>T | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | chr4 | 139667365 | |||||||
chr4:139667411 | A | G | 10 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0014 others(7): Show |
16 | HG02083.hp2 NA18939.hp1 NA18946.hp2 others(13): Show |
intron_variant | MODIFIER | c.58+1334A>G | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | chr4 | 139667411 | |||||||
chr4:139667536 | T | C | 1 | a0001c0001t0001g0254 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.58+1459T>C | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | chr4 | 139667536 | |||||||
chr4:139667732 | C | T | 6 | a0001c0001t0001g0333 a0001c0001t0001g0334 a0001c0001t0001g0335 others(3): Show |
6 | NA18963.hp1 NA18975.hp2 NA18992.hp2 others(3): Show |
intron_variant | MODIFIER | c.58+1655C>T | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | chr4 | 139667732 | |||||||
chr4:139667795 | T | C | 8 | a0001c0001t0001g0166 a0001c0001t0001g0167 a0001c0001t0001g0168 others(5): Show |
8 | HG02074.hp1 NA18948.hp1 NA18965.hp2 others(5): Show |
intron_variant | MODIFIER | c.58+1718T>C | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | chr4 | 139667795 | |||||||
chr4:139667799 | A | G | 307 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(304): Show |
350 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(347): Show |
intron_variant | MODIFIER | c.58+1722A>G | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | chr4 | 139667799 | |||||||
chr4:139667862 | A | G | 308 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(305): Show |
351 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(348): Show |
intron_variant | MODIFIER | c.58+1785A>G | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | chr4 | 139667862 | |||||||
chr4:139667905 | T | A | 308 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(305): Show |
351 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(348): Show |
intron_variant | MODIFIER | c.58+1828T>A | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | chr4 | 139667905 | |||||||
chr4:139667930 | A | G | 308 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(305): Show |
351 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(348): Show |
intron_variant | MODIFIER | c.58+1853A>G | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | chr4 | 139667930 | |||||||
chr4:139667938 | C | T | 1 | a0001c0001t0002g0165 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.58+1861C>T | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | chr4 | 139667938 | |||||||
chr4:139667946 | C | T | 45 | a0001c0001t0001g0029 a0001c0001t0001g0114 a0001c0001t0001g0130 others(42): Show |
47 | HG00438.hp1 HG00673.hp1 HG01192.hp2 others(44): Show |
intron_variant | MODIFIER | c.58+1869C>T | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | chr4 | 139667946 | |||||||
chr4:139668390 | T | G | 308 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(305): Show |
351 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(348): Show |
intron_variant | MODIFIER | c.58+2313T>G | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | chr4 | 139668390 | |||||||
chr4:139668507 | G | A | 308 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(305): Show |
351 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(348): Show |
intron_variant | MODIFIER | c.58+2430G>A | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | chr4 | 139668507 | |||||||
chr4:139668584 | C | A | 261 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(258): Show |
302 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(299): Show |
intron_variant | MODIFIER | c.58+2507C>A | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | chr4 | 139668584 | |||||||
chr4:139668591 | G | GAC | 117 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(114): Show |
132 | HG00140.hp2 HG00423.hp1 HG00609.hp2 others(129): Show |
intron_variant | MODIFIER | c.58+2518_58+2519dup others(2): Show |
MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr4 | 139668591 | ||||||
chr4:139668595 | C | CAG | 49 | a0001c0001t0001g0021 a0001c0001t0001g0122 a0001c0001t0001g0123 others(46): Show |
61 | HG00597.hp2 HG01106.hp2 HG01168.hp1 others(58): Show |
intron_variant | MODIFIER | c.58+2537_58+2538dup others(2): Show |
MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr4 | 139668595 | ||||||
chr4:139668595 | CAGAG | C | 93 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0026 others(90): Show |
107 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(104): Show |
intron_variant | MODIFIER | c.58+2535_58+2538del others(4): Show |
MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr4 | 139668595 | ||||||
chr4:139668601 | G | C | 7 | a0001c0001t0001g0026 a0001c0001t0001g0256 a0001c0001t0001g0257 others(4): Show |
8 | HG00642.hp1 HG00733.hp2 HG00738.hp2 others(5): Show |
intron_variant | MODIFIER | c.58+2524G>C | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | chr4 | 139668601 | |||||||
chr4:139668613 | G | C | 97 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(94): Show |
111 | HG00140.hp2 HG00423.hp1 HG00609.hp2 others(108): Show |
intron_variant | MODIFIER | c.58+2536G>C | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | chr4 | 139668613 | |||||||
chr4:139668623 | A | AG | 12 | a0001c0001t0001g0034 a0001c0001t0001g0173 a0001c0001t0001g0174 others(9): Show |
12 | HG00741.hp1 HG01952.hp1 HG02004.hp2 others(9): Show |
intron_variant | MODIFIER | c.58+2551dupG | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr4 | 139668623 | ||||||
chr4:139668626 | G | A | 2 | a0001c0001t0001g0128 a0001c0001t0001g0129 |
2 | HG03195.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.58+2549G>A | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | chr4 | 139668626 | |||||||
chr4:139668758 | G | C | 1 | a0001c0001t0001g0267 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.58+2681G>C | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | chr4 | 139668758 | |||||||
chr4:139668838 | A | G | 1 | a0001c0004t0001g0262 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.58+2761A>G | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | chr4 | 139668838 | |||||||
chr4:139668844 | A | G | 308 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(305): Show |
351 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(348): Show |
intron_variant | MODIFIER | c.58+2767A>G | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | chr4 | 139668844 | |||||||
chr4:139668853 | G | A | 2 | a0001c0001t0002g0354 a0001c0001t0002g0355 |
2 | HG02647.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.58+2776G>A | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | chr4 | 139668853 | |||||||
chr4:139668906 | G | T | 1 | a0001c0004t0001g0262 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.58+2829G>T | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | chr4 | 139668906 | |||||||
chr4:139668996 | A | C | 308 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(305): Show |
351 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(348): Show |
intron_variant | MODIFIER | c.58+2919A>C | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | chr4 | 139668996 | |||||||
chr4:139669001 | C | T | 308 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(305): Show |
351 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(348): Show |
intron_variant | MODIFIER | c.58+2924C>T | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | chr4 | 139669001 | |||||||
chr4:139669064 | A | G | 308 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(305): Show |
351 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(348): Show |
intron_variant | MODIFIER | c.58+2987A>G | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | chr4 | 139669064 | |||||||
chr4:139669131 | C | G | 1 | a0001c0001t0001g0341 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.58+3054C>G | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | chr4 | 139669131 | |||||||
chr4:139669153 | C | A | 2 | a0001c0001t0001g0268 a0001c0001t0001g0269 |
2 | HG00673.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.58+3076C>A | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | chr4 | 139669153 | |||||||
chr4:139669155 | C | T | 2 | a0001c0001t0001g0268 a0001c0001t0001g0269 |
2 | HG00673.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.58+3078C>T | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | chr4 | 139669155 | |||||||
chr4:139669370 | C | T | 2 | a0001c0001t0001g0029 a0001c0001t0001g0340 |
3 | HG02723.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.58+3293C>T | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | chr4 | 139669370 | |||||||
chr4:139669441 | G | T | 308 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(305): Show |
351 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(348): Show |
intron_variant | MODIFIER | c.58+3364G>T | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | chr4 | 139669441 | |||||||
chr4:139669544 | G | A | 308 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(305): Show |
351 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(348): Show |
intron_variant | MODIFIER | c.58+3467G>A | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | chr4 | 139669544 | |||||||
chr4:139669569 | A | G | 6 | a0001c0001t0001g0330 a0001c0001t0001g0331 a0001c0001t0001g0332 others(3): Show |
6 | HG01192.hp2 HG02486.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.58+3492A>G | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | chr4 | 139669569 | |||||||
chr4:139669581 | C | T | 49 | a0001c0001t0001g0029 a0001c0001t0001g0031 a0001c0001t0001g0114 others(46): Show |
52 | HG00438.hp1 HG00673.hp1 HG01070.hp2 others(49): Show |
intron_variant | MODIFIER | c.58+3504C>T | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | chr4 | 139669581 | |||||||
chr4:139669683 | C | G | 1 | a0001c0001t0001g0108 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.58+3606C>G | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | chr4 | 139669683 | |||||||
chr4:139669710 | C | T | 1 | a0001c0001t0001g0332 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.58+3633C>T | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | chr4 | 139669710 | |||||||
chr4:139669793 | A | G | 308 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(305): Show |
351 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(348): Show |
intron_variant | MODIFIER | c.58+3716A>G | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | chr4 | 139669793 | |||||||
chr4:139669990 | G | T | 1 | a0001c0001t0001g0107 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.58+3913G>T | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | chr4 | 139669990 | |||||||
chr4:139670003 | C | T | 1 | a0001c0001t0001g0164 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.58+3926C>T | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | chr4 | 139670003 | |||||||
chr4:139670138 | C | T | 41 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(38): Show |
52 | HG00597.hp2 HG01106.hp2 HG01168.hp1 others(49): Show |
intron_variant | MODIFIER | c.58+4061C>T | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | chr4 | 139670138 | |||||||
chr4:139670199 | A | G | 1 | a0001c0001t0002g0241 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.58+4122A>G | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | chr4 | 139670199 | |||||||
chr4:139670238 | T | C | 1 | a0001c0001t0001g0175 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.58+4161T>C | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | chr4 | 139670238 | |||||||
chr4:139670249 | G | A | 1 | a0001c0001t0001g0270 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.58+4172G>A | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | chr4 | 139670249 | |||||||
chr4:139670258 | C | CG | 55 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(52): Show |
57 | HG00140.hp1 HG00639.hp2 HG00733.hp1 others(54): Show |
intron_variant | MODIFIER | c.58+4191dupG | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr4 | 139670258 | ||||||
chr4:139670261 | G | C | 1 | a0001c0001t0001g0035 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.58+4184G>C | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | chr4 | 139670261 | |||||||
chr4:139670261 | G | T | 306 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(303): Show |
349 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(346): Show |
intron_variant | MODIFIER | c.58+4184G>T | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | chr4 | 139670261 | |||||||
chr4:139670264 | G | T | 1 | a0001c0001t0001g0035 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.58+4187G>T | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | chr4 | 139670264 | |||||||
chr4:139670266 | GGGC | G | 301 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(298): Show |
344 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(341): Show |
intron_variant | MODIFIER | c.58+4192_58+4194del others(3): Show |
MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr4 | 139670266 | ||||||
chr4:139670269 | C | G | 1 | a0001c0001t0001g0035 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.58+4192C>G | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | chr4 | 139670269 | |||||||
chr4:139670286 | A | G | 1 | a0001c0001t0002g0381 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.58+4209A>G | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | chr4 | 139670286 | |||||||
chr4:139670443 | A | G | 1 | a0001c0001t0001g0032 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.58+4366A>G | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | chr4 | 139670443 | |||||||
chr4:139670493 | G | C | 2 | a0001c0001t0004g0272 a0001c0001t0004g0273 |
2 | HG04199.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.58+4416G>C | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | chr4 | 139670493 | |||||||
chr4:139670732 | A | C | 1 | a0001c0001t0001g0239 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.58+4655A>C | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | chr4 | 139670732 | |||||||
chr4:139670904 | C | CA | 21 | a0001c0001t0001g0034 a0001c0001t0001g0128 a0001c0001t0001g0129 others(18): Show |
22 | HG01192.hp2 HG01261.hp2 HG01496.hp2 others(19): Show |
intron_variant | MODIFIER | c.58+4844dupA | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr4 | 139670904 | ||||||
chr4:139670904 | CA | C | 21 | a0001c0001t0001g0031 a0001c0001t0001g0238 a0001c0001t0001g0250 others(18): Show |
22 | HG01069.hp2 HG01070.hp2 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.58+4844delA | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr4 | 139670904 | ||||||
chr4:139670969 | C | G | 2 | a0001c0001t0001g0236 a0001c0001t0001g0237 |
2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.58+4892C>G | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | chr4 | 139670969 | |||||||
chr4:139671474 | G | A | 2 | a0001c0001t0001g0180 a0001c0001t0002g0179 |
2 | HG01884.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.58+5397G>A | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | chr4 | 139671474 | |||||||
chr4:139671487 | C | A | 206 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0020 others(203): Show |
235 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(232): Show |
intron_variant | MODIFIER | c.58+5410C>A | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | chr4 | 139671487 | |||||||
chr4:139671508 | C | CG | 95 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(92): Show |
109 | HG00140.hp2 HG00423.hp1 HG00609.hp2 others(106): Show |
intron_variant | MODIFIER | c.58+5434dupG | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr4 | 139671508 | ||||||
chr4:139671512 | C | T | 95 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(92): Show |
109 | HG00140.hp2 HG00423.hp1 HG00609.hp2 others(106): Show |
intron_variant | MODIFIER | c.58+5435C>T | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | chr4 | 139671512 | |||||||
chr4:139671525 | G | A | 8 | a0001c0001t0001g0128 a0001c0001t0001g0330 a0001c0001t0001g0331 others(5): Show |
8 | HG01192.hp2 HG01496.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.58+5448G>A | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | chr4 | 139671525 | |||||||
chr4:139671821 | T | C | 4 | a0001c0001t0001g0034 a0001c0001t0001g0039 a0001c0001t0001g0040 others(1): Show |
4 | NA18946.hp1 NA19001.hp1 NA19006.hp2 others(1): Show |
intron_variant | MODIFIER | c.58+5744T>C | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | chr4 | 139671821 | |||||||
chr4:139671921 | C | T | 41 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(38): Show |
52 | HG00597.hp2 HG01106.hp2 HG01168.hp1 others(49): Show |
intron_variant | MODIFIER | c.58+5844C>T | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | chr4 | 139671921 | |||||||
chr4:139672097 | C | T | 1 | a0001c0001t0001g0106 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.58+6020C>T | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | chr4 | 139672097 | |||||||
chr4:139672110 | T | C | 95 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(92): Show |
109 | HG00140.hp2 HG00423.hp1 HG00609.hp2 others(106): Show |
intron_variant | MODIFIER | c.58+6033T>C | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | chr4 | 139672110 | |||||||
chr4:139672154 | A | G | 315 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(312): Show |
359 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(356): Show |
intron_variant | MODIFIER | c.58+6077A>G | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | chr4 | 139672154 | |||||||
chr4:139672179 | G | T | 8 | a0001c0001t0001g0128 a0001c0001t0001g0330 a0001c0001t0001g0331 others(5): Show |
8 | HG01192.hp2 HG01496.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.58+6102G>T | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | chr4 | 139672179 | |||||||
chr4:139672247 | T | C | 1 | a0001c0001t0001g0275 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.58+6170T>C | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | chr4 | 139672247 | |||||||
chr4:139672349 | G | A | 1 | a0001c0001t0001g0129 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.59-6194G>A | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | chr4 | 139672349 | |||||||
chr4:139672435 | G | A | 15 | a0001c0001t0001g0031 a0001c0001t0001g0250 a0001c0001t0001g0251 others(12): Show |
16 | HG01070.hp2 HG01071.hp1 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.59-6108G>A | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | chr4 | 139672435 | |||||||
chr4:139672577 | C | CT | 15 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0112 others(12): Show |
16 | HG01261.hp2 HG02055.hp2 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.59-5950dupT | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr4 | 139672577 | ||||||
chr4:139672577 | CT | C | 12 | a0001c0001t0001g0042 a0001c0001t0001g0128 a0001c0001t0001g0239 others(9): Show |
12 | HG01192.hp2 HG01496.hp2 HG01975.hp1 others(9): Show |
intron_variant | MODIFIER | c.59-5950delT | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr4 | 139672577 | ||||||
chr4:139672610 | G | C | 3 | a0001c0001t0001g0020 a0001c0001t0001g0159 a0001c0001t0001g0164 |
4 | HG02258.hp1 HG02615.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.59-5933G>C | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | chr4 | 139672610 | |||||||
chr4:139672739 | C | T | 13 | a0001c0001t0001g0020 a0001c0001t0001g0024 a0001c0001t0001g0025 others(10): Show |
16 | HG01069.hp2 HG01255.hp1 HG01256.hp2 others(13): Show |
intron_variant | MODIFIER | c.59-5804C>T | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | chr4 | 139672739 | |||||||
chr4:139672791 | T | C | 95 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(92): Show |
109 | HG00140.hp2 HG00423.hp1 HG00609.hp2 others(106): Show |
intron_variant | MODIFIER | c.59-5752T>C | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | chr4 | 139672791 | |||||||
chr4:139672983 | G | C | 1 | a0001c0001t0001g0275 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.59-5560G>C | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | chr4 | 139672983 | |||||||
chr4:139673027 | A | G | 15 | a0001c0001t0001g0031 a0001c0001t0001g0250 a0001c0001t0001g0251 others(12): Show |
16 | HG01070.hp2 HG01071.hp1 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.59-5516A>G | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | chr4 | 139673027 | |||||||
chr4:139673149 | C | A | 1 | a0001c0001t0001g0239 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.59-5394C>A | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | chr4 | 139673149 | |||||||
chr4:139673150 | A | G | 1 | a0001c0001t0001g0239 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.59-5393A>G | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | chr4 | 139673150 | |||||||
chr4:139673248 | C | T | 4 | a0001c0001t0001g0025 a0001c0001t0001g0229 a0001c0001t0001g0230 others(1): Show |
5 | HG01256.hp2 HG01258.hp1 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.59-5295C>T | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | chr4 | 139673248 | |||||||
chr4:139673249 | G | A | 15 | a0001c0001t0001g0031 a0001c0001t0001g0250 a0001c0001t0001g0251 others(12): Show |
16 | HG01070.hp2 HG01071.hp1 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.59-5294G>A | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | chr4 | 139673249 | |||||||
chr4:139673262 | C | T | 2 | a0001c0001t0001g0177 a0001c0001t0001g0178 |
2 | HG01261.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.59-5281C>T | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | chr4 | 139673262 | |||||||
chr4:139673326 | C | T | 1 | a0001c0001t0001g0327 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.59-5217C>T | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | chr4 | 139673326 | |||||||
chr4:139673397 | G | T | 57 | a0001c0001t0001g0020 a0001c0001t0001g0029 a0001c0001t0001g0114 others(54): Show |
60 | HG00438.hp1 HG00673.hp1 HG01069.hp2 others(57): Show |
intron_variant | MODIFIER | c.59-5146G>T | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | chr4 | 139673397 | |||||||
chr4:139673412 | TTTA | T | 41 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(38): Show |
52 | HG00597.hp2 HG01106.hp2 HG01168.hp1 others(49): Show |
intron_variant | MODIFIER | c.59-5128_59-5126del others(3): Show |
MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr4 | 139673412 | ||||||
chr4:139673510 | G | A | 1 | a0001c0001t0002g0358 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.59-5033G>A | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | chr4 | 139673510 | |||||||
chr4:139673513 | C | T | 2 | a0001c0001t0002g0350 a0001c0001t0002g0351 |
2 | HG02896.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.59-5030C>T | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | chr4 | 139673513 | |||||||
chr4:139673606 | T | G | 102 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0020 others(99): Show |
117 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(114): Show |
intron_variant | MODIFIER | c.59-4937T>G | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | chr4 | 139673606 | |||||||
chr4:139673714 | G | C | 3 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0111 |
3 | HG02055.hp2 HG02615.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.59-4829G>C | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | chr4 | 139673714 | |||||||
chr4:139674048 | G | A | 1 | a0001c0001t0001g0129 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.59-4495G>A | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | chr4 | 139674048 | |||||||
chr4:139674245 | T | G | 140 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(137): Show |
155 | HG00140.hp2 HG00438.hp1 HG00609.hp2 others(152): Show |
intron_variant | MODIFIER | c.59-4298T>G | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | chr4 | 139674245 | |||||||
chr4:139674261 | C | T | 6 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0228 others(3): Show |
8 | HG01255.hp1 HG01256.hp2 HG01258.hp1 others(5): Show |
intron_variant | MODIFIER | c.59-4282C>T | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | chr4 | 139674261 | |||||||
chr4:139674270 | C | T | 1 | a0001c0001t0001g0326 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.59-4273C>T | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | chr4 | 139674270 | |||||||
chr4:139674438 | C | T | 1 | a0001c0001t0001g0103 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.59-4105C>T | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | chr4 | 139674438 | |||||||
chr4:139674468 | G | GT | 18 | a0001c0001t0001g0020 a0001c0001t0001g0102 a0001c0001t0001g0159 others(15): Show |
19 | HG01069.hp2 HG01192.hp1 HG01261.hp2 others(16): Show |
intron_variant | MODIFIER | c.59-4061dupT | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr4 | 139674468 | ||||||
chr4:139674497 | T | G | 307 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(304): Show |
350 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(347): Show |
intron_variant | MODIFIER | c.59-4046T>G | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | chr4 | 139674497 | |||||||
chr4:139674927 | G | A | 1 | a0001c0001t0001g0103 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.59-3616G>A | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | chr4 | 139674927 | |||||||
chr4:139675089 | T | C | 1 | a0001c0001t0001g0181 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.59-3454T>C | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | chr4 | 139675089 | |||||||
chr4:139675156 | C | G | 1 | a0001c0001t0002g0135 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.59-3387C>G | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | chr4 | 139675156 | |||||||
chr4:139675545 | A | G | 95 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0026 others(92): Show |
109 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.59-2998A>G | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | chr4 | 139675545 | |||||||
chr4:139675546 | A | G | 1 | a0001c0001t0001g0239 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.59-2997A>G | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | chr4 | 139675546 | |||||||
chr4:139675547 | G | T | 1 | a0001c0001t0001g0239 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.59-2996G>T | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | chr4 | 139675547 | |||||||
chr4:139675705 | G | A | 5 | a0001c0001t0001g0021 a0001c0001t0001g0034 a0001c0001t0001g0039 others(2): Show |
6 | HG02818.hp2 HG03225.hp1 NA18946.hp1 others(3): Show |
intron_variant | MODIFIER | c.59-2838G>A | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | chr4 | 139675705 | |||||||
chr4:139675898 | T | C | 54 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(51): Show |
62 | HG00609.hp2 HG01069.hp1 HG01071.hp2 others(59): Show |
intron_variant | MODIFIER | c.59-2645T>C | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | chr4 | 139675898 | |||||||
chr4:139676225 | G | C | 1 | a0001c0001t0001g0043 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.59-2318G>C | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | chr4 | 139676225 | |||||||
chr4:139676319 | C | A | 8 | a0001c0001t0001g0020 a0001c0001t0001g0159 a0001c0001t0001g0164 others(5): Show |
9 | HG01069.hp2 HG01496.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.59-2224C>A | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | chr4 | 139676319 | |||||||
chr4:139676365 | C | T | 1 | a0001c0001t0002g0155 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.59-2178C>T | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | chr4 | 139676365 | |||||||
chr4:139676499 | C | G | 1 | a0001c0001t0001g0129 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.59-2044C>G | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | chr4 | 139676499 | |||||||
chr4:139676516 | T | C | 8 | a0001c0001t0001g0020 a0001c0001t0001g0159 a0001c0001t0001g0164 others(5): Show |
9 | HG01069.hp2 HG01496.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.59-2027T>C | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | chr4 | 139676516 | |||||||
chr4:139676623 | A | G | 1 | a0001c0001t0003g0235 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.59-1920A>G | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | chr4 | 139676623 | |||||||
chr4:139676781 | A | C | 1 | a0001c0001t0001g0341 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.59-1762A>C | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | chr4 | 139676781 | |||||||
chr4:139676814 | C | T | 1 | a0001c0001t0001g0129 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.59-1729C>T | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | chr4 | 139676814 | |||||||
chr4:139676887 | T | C | 5 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0111 others(2): Show |
5 | HG02055.hp2 HG02615.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.59-1656T>C | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | chr4 | 139676887 | |||||||
chr4:139676907 | A | C | 1 | a0001c0001t0001g0253 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.59-1636A>C | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | chr4 | 139676907 | |||||||
chr4:139676984 | C | A | 2 | a0001c0001t0001g0182 a0001c0001t0001g0227 |
2 | HG01074.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.59-1559C>A | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | chr4 | 139676984 | |||||||
chr4:139677143 | C | T | 1 | a0001c0002t0001g0100 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.59-1400C>T | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | chr4 | 139677143 | |||||||
chr4:139677176 | A | C | 41 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(38): Show |
52 | HG00597.hp2 HG01106.hp2 HG01168.hp1 others(49): Show |
intron_variant | MODIFIER | c.59-1367A>C | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | chr4 | 139677176 | |||||||
chr4:139677231 | C | T | 1 | a0001c0001t0001g0031 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.59-1312C>T | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | chr4 | 139677231 | |||||||
chr4:139677324 | G | C | 1 | a0001c0001t0001g0074 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.59-1219G>C | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | chr4 | 139677324 | |||||||
chr4:139677398 | A | T | 8 | a0001c0001t0001g0128 a0001c0001t0001g0226 a0001c0001t0001g0330 others(5): Show |
8 | HG01123.hp2 HG01192.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.59-1145A>T | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | chr4 | 139677398 | |||||||
chr4:139677504 | A | AT | 97 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0012 others(94): Show |
113 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(110): Show |
intron_variant | MODIFIER | c.59-1025dupT | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr4 | 139677504 | ||||||
chr4:139677504 | AT | A | 20 | a0001c0001t0001g0250 a0001c0001t0001g0251 a0001c0001t0001g0252 others(17): Show |
20 | HG01884.hp2 HG02280.hp2 HG02809.hp1 others(17): Show |
intron_variant | MODIFIER | c.59-1025delT | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr4 | 139677504 | ||||||
chr4:139677595 | A | G | 1 | a0001c0001t0001g0341 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.59-948A>G | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | chr4 | 139677595 | |||||||
chr4:139677650 | C | T | 1 | a0001c0001t0002g0344 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.59-893C>T | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | chr4 | 139677650 | |||||||
chr4:139677656 | C | T | 2 | a0001c0001t0001g0071 a0001c0001t0001g0072 |
2 | NA19079.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.59-887C>T | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | chr4 | 139677656 | |||||||
chr4:139677658 | C | G | 1 | a0001c0001t0001g0070 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.59-885C>G | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | chr4 | 139677658 | |||||||
chr4:139677723 | G | A | 1 | a0001c0001t0001g0034 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.59-820G>A | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | chr4 | 139677723 | |||||||
chr4:139677749 | C | T | 1 | a0001c0001t0001g0069 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.59-794C>T | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | chr4 | 139677749 | |||||||
chr4:139677768 | G | A | 1 | a0001c0001t0001g0014 | 2 | NA18980.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.59-775G>A | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | chr4 | 139677768 | |||||||
chr4:139677845 | G | A | 97 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0012 others(94): Show |
112 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.59-698G>A | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | chr4 | 139677845 | |||||||
chr4:139677899 | A | G | 2 | a0001c0001t0001g0224 a0001c0001t0001g0225 |
2 | HG01074.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.59-644A>G | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | chr4 | 139677899 | |||||||
chr4:139678281 | T | C | 1 | a0001c0001t0002g0136 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.59-262T>C | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 1/4 | chr4 | 139678281 | |||||||
chr4:139678740 | T | C | 3 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0001t0001g0186 |
3 | HG02145.hp1 HG02895.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.158+98T>C | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139678740 | |||||||
chr4:139678741 | G | A | 11 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0001t0001g0253 others(8): Show |
11 | HG02280.hp2 HG02886.hp1 HG03098.hp1 others(8): Show |
intron_variant | MODIFIER | c.158+99G>A | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139678741 | |||||||
chr4:139678819 | G | A | 21 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0002g0015 others(18): Show |
24 | HG01069.hp2 HG01168.hp1 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.158+177G>A | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139678819 | |||||||
chr4:139678971 | T | C | 223 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(220): Show |
259 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(256): Show |
intron_variant | MODIFIER | c.158+329T>C | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139678971 | |||||||
chr4:139678977 | C | A | 276 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(273): Show |
315 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(312): Show |
intron_variant | MODIFIER | c.158+335C>A | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139678977 | |||||||
chr4:139679153 | C | T | 217 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(214): Show |
245 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(242): Show |
intron_variant | MODIFIER | c.158+511C>T | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139679153 | |||||||
chr4:139679228 | T | C | 1 | a0001c0001t0001g0029 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.158+586T>C | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139679228 | |||||||
chr4:139679243 | C | A | 254 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(251): Show |
290 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(287): Show |
intron_variant | MODIFIER | c.158+601C>A | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139679243 | |||||||
chr4:139679248 | A | G | 3 | a0001c0001t0001g0128 a0001c0001t0002g0342 a0001c0001t0002g0343 |
3 | HG02922.hp2 HG03195.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.158+606A>G | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139679248 | |||||||
chr4:139679283 | C | T | 243 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(240): Show |
276 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(273): Show |
intron_variant | MODIFIER | c.158+641C>T | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139679283 | |||||||
chr4:139679564 | G | A | 1 | a0001c0001t0001g0384 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.158+922G>A | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139679564 | |||||||
chr4:139679607 | T | C | 2 | a0001c0001t0001g0012 a0001c0001t0001g0270 |
3 | HG01167.hp2 HG01169.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.158+965T>C | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139679607 | |||||||
chr4:139679700 | C | G | 14 | a0001c0001t0001g0020 a0001c0001t0001g0032 a0001c0001t0001g0109 others(11): Show |
15 | HG01192.hp2 HG02258.hp1 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.158+1058C>G | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139679700 | |||||||
chr4:139679875 | A | AT | 13 | a0001c0001t0001g0023 a0001c0001t0001g0026 a0001c0001t0001g0204 others(10): Show |
15 | HG00642.hp1 HG00733.hp2 HG00735.hp2 others(12): Show |
intron_variant | MODIFIER | c.158+1234dupT | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr4 | 139679875 | ||||||
chr4:139679882 | A | G | 136 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(133): Show |
160 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(157): Show |
intron_variant | MODIFIER | c.158+1240A>G | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139679882 | |||||||
chr4:139679926 | C | T | 3 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0001g0238 |
3 | HG02257.hp1 HG02280.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.158+1284C>T | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139679926 | |||||||
chr4:139680207 | A | G | 74 | a0001c0001t0001g0012 a0001c0001t0001g0020 a0001c0001t0001g0021 others(71): Show |
83 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.158+1565A>G | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139680207 | |||||||
chr4:139680208 | G | A | 74 | a0001c0001t0001g0012 a0001c0001t0001g0020 a0001c0001t0001g0021 others(71): Show |
83 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.158+1566G>A | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139680208 | |||||||
chr4:139680232 | TA | T | 74 | a0001c0001t0001g0012 a0001c0001t0001g0020 a0001c0001t0001g0021 others(71): Show |
83 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.158+1592delA | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr4 | 139680232 | ||||||
chr4:139680269 | G | A | 2 | a0001c0001t0001g0251 a0001c0001t0001g0252 |
2 | HG03195.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.158+1627G>A | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139680269 | |||||||
chr4:139680443 | G | A | 1 | a0001c0001t0001g0122 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.158+1801G>A | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139680443 | |||||||
chr4:139680623 | CT | C | 75 | a0001c0001t0001g0012 a0001c0001t0001g0020 a0001c0001t0001g0021 others(72): Show |
84 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.158+1986delT | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr4 | 139680623 | ||||||
chr4:139680637 | G | A | 305 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(302): Show |
351 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(348): Show |
intron_variant | MODIFIER | c.158+1995G>A | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139680637 | |||||||
chr4:139680665 | G | A | 1 | a0001c0001t0001g0275 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.158+2023G>A | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139680665 | |||||||
chr4:139680745 | T | G | 305 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(302): Show |
351 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(348): Show |
intron_variant | MODIFIER | c.158+2103T>G | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139680745 | |||||||
chr4:139680780 | T | C | 140 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0009 others(137): Show |
158 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(155): Show |
intron_variant | MODIFIER | c.158+2138T>C | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139680780 | |||||||
chr4:139680814 | T | C | 1 | a0001c0001t0001g0284 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.158+2172T>C | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139680814 | |||||||
chr4:139680828 | A | G | 39 | a0001c0001t0001g0012 a0001c0001t0001g0021 a0001c0001t0001g0031 others(36): Show |
45 | HG00280.hp1 HG00438.hp1 HG01070.hp2 others(42): Show |
intron_variant | MODIFIER | c.158+2186A>G | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139680828 | |||||||
chr4:139681000 | C | T | 1 | a0001c0001t0001g0020 | 2 | HG02615.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.158+2358C>T | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139681000 | |||||||
chr4:139681021 | AT | A | 74 | a0001c0001t0001g0012 a0001c0001t0001g0020 a0001c0001t0001g0021 others(71): Show |
83 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.158+2389delT | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr4 | 139681021 | ||||||
chr4:139681044 | G | A | 1 | a0001c0001t0001g0029 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.158+2402G>A | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139681044 | |||||||
chr4:139681185 | A | G | 1 | a0001c0001t0001g0275 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.158+2543A>G | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139681185 | |||||||
chr4:139681229 | T | G | 75 | a0001c0001t0001g0012 a0001c0001t0001g0020 a0001c0001t0001g0021 others(72): Show |
84 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.158+2587T>G | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139681229 | |||||||
chr4:139681306 | C | T | 75 | a0001c0001t0001g0012 a0001c0001t0001g0020 a0001c0001t0001g0021 others(72): Show |
84 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.158+2664C>T | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139681306 | |||||||
chr4:139681331 | A | G | 49 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(46): Show |
57 | HG00609.hp2 HG00639.hp1 HG01123.hp1 others(54): Show |
intron_variant | MODIFIER | c.158+2689A>G | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139681331 | |||||||
chr4:139681344 | C | G | 1 | a0001c0001t0001g0254 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.158+2702C>G | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139681344 | |||||||
chr4:139681392 | C | T | 2 | a0001c0001t0001g0038 a0001c0001t0001g0242 |
2 | HG02698.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.158+2750C>T | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139681392 | |||||||
chr4:139681460 | A | T | 130 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(127): Show |
147 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(144): Show |
intron_variant | MODIFIER | c.158+2818A>T | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139681460 | |||||||
chr4:139681599 | C | T | 75 | a0001c0001t0001g0012 a0001c0001t0001g0020 a0001c0001t0001g0021 others(72): Show |
84 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.158+2957C>T | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139681599 | |||||||
chr4:139681640 | T | C | 1 | a0001c0001t0002g0179 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.158+2998T>C | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139681640 | |||||||
chr4:139681781 | C | T | 73 | a0001c0001t0001g0012 a0001c0001t0001g0020 a0001c0001t0001g0021 others(70): Show |
81 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.158+3139C>T | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139681781 | |||||||
chr4:139681818 | C | T | 74 | a0001c0001t0001g0012 a0001c0001t0001g0020 a0001c0001t0001g0021 others(71): Show |
83 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.158+3176C>T | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139681818 | |||||||
chr4:139681853 | G | C | 2 | a0001c0001t0001g0138 a0001c0001t0001g0139 |
2 | NA18952.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.158+3211G>C | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139681853 | |||||||
chr4:139682059 | G | A | 49 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(46): Show |
57 | HG00609.hp2 HG00639.hp1 HG01123.hp1 others(54): Show |
intron_variant | MODIFIER | c.158+3417G>A | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139682059 | |||||||
chr4:139682074 | C | T | 62 | a0001c0001t0001g0012 a0001c0001t0001g0020 a0001c0001t0001g0021 others(59): Show |
70 | HG00280.hp1 HG00438.hp1 HG01070.hp2 others(67): Show |
intron_variant | MODIFIER | c.158+3432C>T | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139682074 | |||||||
chr4:139682155 | C | G | 4 | a0001c0001t0001g0184 a0001c0001t0001g0330 a0001c0001t0001g0383 others(1): Show |
4 | HG02976.hp1 HG03486.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.158+3513C>G | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139682155 | |||||||
chr4:139682158 | T | G | 2 | a0001c0001t0001g0177 a0001c0001t0001g0178 |
2 | HG01261.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.158+3516T>G | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139682158 | |||||||
chr4:139682159 | A | T | 2 | a0001c0001t0001g0177 a0001c0001t0001g0178 |
2 | HG01261.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.158+3517A>T | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139682159 | |||||||
chr4:139682181 | G | A | 1 | a0001c0001t0001g0208 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.158+3539G>A | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139682181 | |||||||
chr4:139682214 | A | T | 1 | a0001c0001t0003g0162 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.158+3572A>T | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139682214 | |||||||
chr4:139682242 | TA | T | 198 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(195): Show |
228 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(225): Show |
intron_variant | MODIFIER | c.158+3614delA | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr4 | 139682242 | ||||||
chr4:139682242 | TAA | T | 52 | a0001c0001t0001g0012 a0001c0001t0001g0020 a0001c0001t0001g0021 others(49): Show |
60 | HG00280.hp1 HG00438.hp1 HG01070.hp2 others(57): Show |
intron_variant | MODIFIER | c.158+3613_158+3614d others(4): Show |
MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr4 | 139682242 | ||||||
chr4:139682251 | A | C | 101 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(98): Show |
117 | HG00280.hp1 HG00438.hp1 HG00609.hp2 others(114): Show |
intron_variant | MODIFIER | c.158+3609A>C | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139682251 | |||||||
chr4:139682265 | G | A | 155 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(152): Show |
177 | HG00280.hp1 HG00438.hp1 HG00609.hp2 others(174): Show |
intron_variant | MODIFIER | c.158+3623G>A | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139682265 | |||||||
chr4:139682322 | T | C | 1 | a0001c0001t0001g0130 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.158+3680T>C | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139682322 | |||||||
chr4:139682502 | G | A | 1 | a0001c0001t0001g0286 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.158+3860G>A | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139682502 | |||||||
chr4:139682528 | C | T | 3 | a0001c0001t0001g0384 a0001c0001t0001g0387 a0001c0001t0001g0388 |
3 | HG02886.hp1 HG03098.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.158+3886C>T | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139682528 | |||||||
chr4:139682529 | G | A | 1 | a0001c0001t0001g0331 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.158+3887G>A | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139682529 | |||||||
chr4:139682556 | C | T | 1 | a0001c0001t0001g0098 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.158+3914C>T | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139682556 | |||||||
chr4:139682822 | C | G | 1 | a0001c0001t0001g0159 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.158+4180C>G | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139682822 | |||||||
chr4:139682910 | T | A | 1 | a0001c0001t0001g0198 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.158+4268T>A | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139682910 | |||||||
chr4:139682943 | T | G | 1 | a0001c0001t0002g0362 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.158+4301T>G | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139682943 | |||||||
chr4:139683062 | T | C | 40 | a0001c0001t0001g0021 a0001c0001t0001g0031 a0001c0001t0001g0051 others(37): Show |
45 | HG00280.hp1 HG00673.hp2 HG01070.hp2 others(42): Show |
intron_variant | MODIFIER | c.158+4420T>C | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139683062 | |||||||
chr4:139683108 | G | A | 8 | a0001c0001t0001g0020 a0001c0001t0001g0029 a0001c0001t0001g0032 others(5): Show |
10 | HG01192.hp2 HG02486.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.158+4466G>A | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139683108 | |||||||
chr4:139683379 | G | A | 2 | a0001c0001t0001g0234 a0001c0001t0001g0250 |
2 | HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.158+4737G>A | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139683379 | |||||||
chr4:139683448 | A | G | 47 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(44): Show |
55 | HG00609.hp2 HG00639.hp1 HG00735.hp2 others(52): Show |
intron_variant | MODIFIER | c.158+4806A>G | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139683448 | |||||||
chr4:139683802 | T | C | 293 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(290): Show |
338 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(335): Show |
intron_variant | MODIFIER | c.158+5160T>C | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139683802 | |||||||
chr4:139683919 | G | GT | 34 | a0001c0001t0001g0023 a0001c0001t0001g0026 a0001c0001t0001g0041 others(31): Show |
36 | HG00544.hp2 HG00642.hp1 HG00673.hp1 others(33): Show |
intron_variant | MODIFIER | c.158+5300dupT | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr4 | 139683919 | ||||||
chr4:139683919 | GT | G | 95 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(92): Show |
109 | HG00609.hp2 HG00639.hp1 HG00735.hp2 others(106): Show |
intron_variant | MODIFIER | c.158+5300delT | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr4 | 139683919 | ||||||
chr4:139683919 | GTTTTT | G | 8 | a0001c0001t0001g0021 a0001c0001t0001g0110 a0001c0001t0001g0127 others(5): Show |
9 | HG00280.hp1 HG01361.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.158+5296_158+5300d others(7): Show |
MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr4 | 139683919 | ||||||
chr4:139683995 | G | A | 1 | a0001c0001t0001g0071 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.158+5353G>A | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139683995 | |||||||
chr4:139684220 | C | G | 1 | a0001c0001t0001g0311 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.158+5578C>G | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139684220 | |||||||
chr4:139684271 | G | A | 11 | a0001c0001t0001g0128 a0001c0001t0001g0177 a0001c0001t0001g0178 others(8): Show |
11 | HG01192.hp1 HG01261.hp2 HG02148.hp2 others(8): Show |
intron_variant | MODIFIER | c.158+5629G>A | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139684271 | |||||||
chr4:139684336 | A | G | 10 | a0001c0001t0001g0022 a0001c0001t0001g0106 a0001c0001t0001g0197 others(7): Show |
11 | HG00099.hp1 HG00738.hp1 HG01123.hp2 others(8): Show |
intron_variant | MODIFIER | c.158+5694A>G | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139684336 | |||||||
chr4:139684374 | A | G | 11 | a0001c0001t0001g0128 a0001c0001t0001g0177 a0001c0001t0001g0178 others(8): Show |
11 | HG01192.hp1 HG01261.hp2 HG02148.hp2 others(8): Show |
intron_variant | MODIFIER | c.158+5732A>G | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139684374 | |||||||
chr4:139684407 | C | A | 1 | a0001c0001t0001g0012 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.158+5765C>A | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139684407 | |||||||
chr4:139684530 | G | T | 12 | a0001c0001t0001g0021 a0001c0001t0001g0110 a0001c0001t0001g0111 others(9): Show |
13 | HG00280.hp1 HG01361.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.158+5888G>T | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139684530 | |||||||
chr4:139684585 | G | C | 1 | a0001c0001t0001g0288 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.158+5943G>C | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139684585 | |||||||
chr4:139684702 | G | A | 1 | a0001c0001t0002g0142 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.158+6060G>A | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139684702 | |||||||
chr4:139684811 | A | G | 1 | a0001c0001t0001g0268 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.158+6169A>G | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139684811 | |||||||
chr4:139684961 | T | C | 8 | a0001c0001t0001g0020 a0001c0001t0001g0029 a0001c0001t0001g0032 others(5): Show |
10 | HG01192.hp2 HG02486.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.158+6319T>C | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139684961 | |||||||
chr4:139685027 | C | A | 12 | a0001c0001t0001g0021 a0001c0001t0001g0110 a0001c0001t0001g0111 others(9): Show |
13 | HG00280.hp1 HG01361.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.158+6385C>A | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139685027 | |||||||
chr4:139685142 | A | G | 246 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(243): Show |
286 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(283): Show |
intron_variant | MODIFIER | c.158+6500A>G | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139685142 | |||||||
chr4:139685157 | C | T | 2 | a0001c0001t0001g0385 a0001c0001t0002g0157 |
2 | HG03041.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.158+6515C>T | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139685157 | |||||||
chr4:139685271 | G | A | 165 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(162): Show |
194 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(191): Show |
intron_variant | MODIFIER | c.158+6629G>A | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139685271 | |||||||
chr4:139685293 | G | T | 165 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(162): Show |
194 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(191): Show |
intron_variant | MODIFIER | c.158+6651G>T | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139685293 | |||||||
chr4:139685560 | T | G | 2 | a0001c0001t0001g0026 a0001c0001t0001g0256 |
3 | HG01109.hp1 HG01175.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.158+6918T>G | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139685560 | |||||||
chr4:139685713 | G | T | 164 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(161): Show |
193 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(190): Show |
intron_variant | MODIFIER | c.158+7071G>T | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139685713 | |||||||
chr4:139685728 | A | G | 4 | a0001c0001t0001g0384 a0001c0001t0001g0387 a0001c0001t0001g0388 others(1): Show |
4 | HG02886.hp1 HG03098.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.158+7086A>G | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139685728 | |||||||
chr4:139685922 | C | T | 2 | a0001c0001t0001g0064 a0001c0001t0001g0065 |
2 | NA18974.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.158+7280C>T | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139685922 | |||||||
chr4:139685929 | G | A | 12 | a0001c0001t0001g0021 a0001c0001t0001g0110 a0001c0001t0001g0111 others(9): Show |
13 | HG00280.hp1 HG01361.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.158+7287G>A | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139685929 | |||||||
chr4:139686074 | C | A | 4 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0325 others(1): Show |
4 | NA18950.hp1 NA18959.hp2 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.158+7432C>A | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139686074 | |||||||
chr4:139686088 | A | G | 62 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0013 others(59): Show |
76 | HG00140.hp2 HG00423.hp1 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.158+7446A>G | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139686088 | |||||||
chr4:139686140 | G | A | 7 | a0001c0001t0001g0020 a0001c0001t0001g0029 a0001c0001t0001g0032 others(4): Show |
9 | HG01192.hp2 HG02486.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.158+7498G>A | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139686140 | |||||||
chr4:139686143 | G | C | 14 | a0001c0001t0001g0109 a0001c0001t0001g0128 a0001c0001t0001g0177 others(11): Show |
14 | HG01192.hp1 HG01261.hp2 HG02148.hp2 others(11): Show |
intron_variant | MODIFIER | c.158+7501G>C | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139686143 | |||||||
chr4:139686302 | CTTG | C | 8 | a0001c0001t0001g0106 a0001c0001t0001g0198 a0001c0001t0001g0200 others(5): Show |
8 | HG00099.hp1 HG00738.hp1 HG01123.hp2 others(5): Show |
intron_variant | MODIFIER | c.158+7663_158+7665d others(5): Show |
MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr4 | 139686302 | ||||||
chr4:139686375 | A | G | 1 | a0001c0001t0003g0162 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.158+7733A>G | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139686375 | |||||||
chr4:139686386 | T | G | 2 | a0001c0001t0001g0184 a0001c0004t0001g0262 |
2 | HG01496.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.158+7744T>G | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139686386 | |||||||
chr4:139686390 | G | A | 2 | a0001c0001t0001g0184 a0001c0004t0001g0262 |
2 | HG01496.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.158+7748G>A | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139686390 | |||||||
chr4:139686592 | A | G | 47 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(44): Show |
55 | HG00609.hp2 HG00639.hp1 HG00735.hp2 others(52): Show |
intron_variant | MODIFIER | c.158+7950A>G | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139686592 | |||||||
chr4:139686619 | T | A | 1 | a0001c0001t0002g0137 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.158+7977T>A | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139686619 | |||||||
chr4:139686685 | T | C | 163 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(160): Show |
192 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(189): Show |
intron_variant | MODIFIER | c.158+8043T>C | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139686685 | |||||||
chr4:139686848 | G | A | 386 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(383): Show |
434 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(431): Show |
intron_variant | MODIFIER | c.158+8206G>A | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139686848 | |||||||
chr4:139686921 | T | G | 1 | a0001c0001t0001g0257 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.159-8276T>G | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139686921 | |||||||
chr4:139686993 | C | T | 1 | a0001c0001t0002g0154 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.159-8204C>T | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139686993 | |||||||
chr4:139687006 | T | C | 1 | a0001c0001t0001g0263 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.159-8191T>C | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139687006 | |||||||
chr4:139687082 | A | C | 1 | a0001c0001t0001g0212 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.159-8115A>C | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139687082 | |||||||
chr4:139687309 | C | G | 1 | a0001c0001t0003g0162 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.159-7888C>G | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139687309 | |||||||
chr4:139687416 | G | C | 3 | a0001c0001t0001g0113 a0001c0001t0001g0129 a0001c0001t0001g0340 |
3 | HG02630.hp2 HG02723.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.159-7781G>C | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139687416 | |||||||
chr4:139687420 | G | C | 1 | a0001c0001t0001g0182 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.159-7777G>C | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139687420 | |||||||
chr4:139687429 | T | C | 17 | a0001c0001t0001g0052 a0001c0001t0001g0075 a0001c0001t0001g0173 others(14): Show |
17 | HG00140.hp1 HG00280.hp2 HG00733.hp1 others(14): Show |
intron_variant | MODIFIER | c.159-7768T>C | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139687429 | |||||||
chr4:139687491 | G | T | 16 | a0001c0001t0001g0109 a0001c0001t0001g0128 a0001c0001t0001g0177 others(13): Show |
16 | HG01192.hp1 HG01261.hp2 HG01496.hp2 others(13): Show |
intron_variant | MODIFIER | c.159-7706G>T | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139687491 | |||||||
chr4:139687640 | A | G | 1 | a0001c0002t0001g0011 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.159-7557A>G | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139687640 | |||||||
chr4:139687683 | G | A | 2 | a0001c0001t0001g0020 a0001c0001t0001g0246 |
3 | HG02615.hp2 NA19030.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.159-7514G>A | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139687683 | |||||||
chr4:139687707 | A | T | 1 | a0001c0001t0001g0085 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.159-7490A>T | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139687707 | |||||||
chr4:139687714 | T | G | 4 | a0001c0001t0001g0384 a0001c0001t0001g0387 a0001c0001t0001g0388 others(1): Show |
4 | HG02886.hp1 HG03098.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.159-7483T>G | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139687714 | |||||||
chr4:139687869 | C | G | 5 | a0001c0001t0001g0333 a0001c0001t0001g0334 a0001c0001t0001g0337 others(2): Show |
5 | NA18944.hp1 NA18963.hp1 NA18975.hp2 others(2): Show |
intron_variant | MODIFIER | c.159-7328C>G | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139687869 | |||||||
chr4:139687968 | A | C | 1 | a0001c0001t0002g0344 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.159-7229A>C | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139687968 | |||||||
chr4:139687998 | G | A | 3 | a0001c0001t0001g0113 a0001c0001t0001g0129 a0001c0001t0001g0340 |
3 | HG02630.hp2 HG02723.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.159-7199G>A | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139687998 | |||||||
chr4:139688086 | A | G | 1 | a0001c0001t0001g0309 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.159-7111A>G | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139688086 | |||||||
chr4:139688171 | A | G | 47 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(44): Show |
55 | HG00609.hp2 HG00639.hp1 HG00735.hp2 others(52): Show |
intron_variant | MODIFIER | c.159-7026A>G | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139688171 | |||||||
chr4:139688457 | C | T | 2 | a0001c0001t0001g0184 a0001c0004t0001g0262 |
2 | HG01496.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.159-6740C>T | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139688457 | |||||||
chr4:139688515 | A | AT | 48 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(45): Show |
56 | HG00597.hp1 HG00609.hp2 HG00639.hp1 others(53): Show |
intron_variant | MODIFIER | c.159-6670dupT | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr4 | 139688515 | ||||||
chr4:139688515 | AT | A | 26 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0027 others(23): Show |
30 | HG01255.hp1 HG01256.hp2 HG01258.hp1 others(27): Show |
intron_variant | MODIFIER | c.159-6670delT | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr4 | 139688515 | ||||||
chr4:139688540 | C | A | 6 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0384 others(3): Show |
6 | HG02055.hp2 HG02615.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.159-6657C>A | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139688540 | |||||||
chr4:139689038 | C | T | 1 | a0001c0001t0001g0260 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.159-6159C>T | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139689038 | |||||||
chr4:139689106 | C | CA | 125 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0013 others(122): Show |
149 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(146): Show |
intron_variant | MODIFIER | c.159-6069dupA | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr4 | 139689106 | ||||||
chr4:139689106 | C | CAA | 12 | a0001c0001t0001g0032 a0001c0001t0001g0086 a0001c0001t0001g0113 others(9): Show |
12 | HG01433.hp2 HG01981.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.159-6070_159-6069d others(4): Show |
MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr4 | 139689106 | ||||||
chr4:139689106 | CA | C | 11 | a0001c0001t0001g0056 a0001c0001t0001g0110 a0001c0001t0001g0275 others(8): Show |
11 | HG02615.hp1 HG02886.hp1 HG03098.hp1 others(8): Show |
intron_variant | MODIFIER | c.159-6069delA | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr4 | 139689106 | ||||||
chr4:139689106 | CAA | C | 44 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(41): Show |
52 | HG00609.hp2 HG00639.hp1 HG00735.hp2 others(49): Show |
intron_variant | MODIFIER | c.159-6070_159-6069d others(4): Show |
MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr4 | 139689106 | ||||||
chr4:139689129 | G | A | 2 | a0001c0001t0001g0122 a0001c0001t0001g0386 |
2 | HG01891.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.159-6068G>A | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139689129 | |||||||
chr4:139689222 | G | A | 1 | a0001c0001t0001g0074 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.159-5975G>A | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139689222 | |||||||
chr4:139689324 | C | T | 1 | a0001c0001t0001g0308 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.159-5873C>T | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139689324 | |||||||
chr4:139689367 | C | T | 2 | a0001c0001t0001g0172 a0001c0001t0002g0352 |
2 | NA18948.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.159-5830C>T | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139689367 | |||||||
chr4:139689618 | C | T | 2 | a0001c0001t0001g0037 a0001c0001t0001g0174 |
2 | HG00741.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.159-5579C>T | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139689618 | |||||||
chr4:139689761 | G | A | 1 | a0001c0001t0001g0271 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.159-5436G>A | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139689761 | |||||||
chr4:139689806 | C | G | 4 | a0001c0001t0001g0384 a0001c0001t0001g0387 a0001c0001t0001g0388 others(1): Show |
4 | HG02886.hp1 HG03098.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.159-5391C>G | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139689806 | |||||||
chr4:139689829 | C | T | 2 | a0001c0001t0001g0112 a0001c0001t0002g0155 |
2 | HG02055.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.159-5368C>T | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139689829 | |||||||
chr4:139689838 | C | A | 1 | a0001c0001t0001g0190 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.159-5359C>A | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139689838 | |||||||
chr4:139689985 | C | T | 4 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0187 others(1): Show |
4 | HG00639.hp1 HG00735.hp2 HG01256.hp1 others(1): Show |
intron_variant | MODIFIER | c.159-5212C>T | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139689985 | |||||||
chr4:139690001 | A | T | 7 | a0001c0001t0001g0020 a0001c0001t0001g0029 a0001c0001t0001g0032 others(4): Show |
9 | HG01192.hp2 HG02486.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.159-5196A>T | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139690001 | |||||||
chr4:139690028 | G | C | 100 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(97): Show |
124 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(121): Show |
intron_variant | MODIFIER | c.159-5169G>C | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139690028 | |||||||
chr4:139690077 | C | T | 1 | a0001c0001t0001g0175 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.159-5120C>T | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139690077 | |||||||
chr4:139690236 | C | T | 3 | a0001c0001t0001g0075 a0001c0001t0002g0146 a0001c0001t0002g0147 |
3 | HG01070.hp1 HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.159-4961C>T | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139690236 | |||||||
chr4:139690303 | T | A | 3 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0200 |
3 | HG01952.hp2 HG02055.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.159-4894T>A | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139690303 | |||||||
chr4:139690549 | A | C | 7 | a0001c0001t0001g0020 a0001c0001t0001g0029 a0001c0001t0001g0032 others(4): Show |
9 | HG01192.hp2 HG02486.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.159-4648A>C | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139690549 | |||||||
chr4:139690648 | G | T | 1 | a0001c0001t0001g0095 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.159-4549G>T | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139690648 | |||||||
chr4:139690880 | C | T | 47 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(44): Show |
55 | HG00609.hp2 HG00639.hp1 HG00735.hp2 others(52): Show |
intron_variant | MODIFIER | c.159-4317C>T | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139690880 | |||||||
chr4:139690905 | C | T | 164 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(161): Show |
187 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(184): Show |
intron_variant | MODIFIER | c.159-4292C>T | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139690905 | |||||||
chr4:139691066 | G | C | 115 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0012 others(112): Show |
130 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(127): Show |
intron_variant | MODIFIER | c.159-4131G>C | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139691066 | |||||||
chr4:139691114 | G | A | 1 | a0001c0001t0001g0057 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.159-4083G>A | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139691114 | |||||||
chr4:139691136 | C | G | 6 | a0001c0001t0001g0184 a0001c0001t0001g0341 a0001c0001t0001g0384 others(3): Show |
6 | HG01496.hp2 HG02572.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.159-4061C>G | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139691136 | |||||||
chr4:139691158 | G | A | 1 | a0001c0001t0001g0275 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.159-4039G>A | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139691158 | |||||||
chr4:139691243 | C | T | 1 | a0001c0001t0001g0341 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.159-3954C>T | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139691243 | |||||||
chr4:139691459 | G | A | 2 | a0001c0001t0001g0217 a0001c0001t0001g0218 |
2 | HG02572.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.159-3738G>A | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139691459 | |||||||
chr4:139691466 | T | C | 5 | a0001c0001t0001g0275 a0001c0001t0001g0384 a0001c0001t0001g0387 others(2): Show |
5 | HG02886.hp1 HG03098.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.159-3731T>C | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139691466 | |||||||
chr4:139691645 | CAG | C | 50 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(47): Show |
58 | HG00609.hp2 HG00639.hp1 HG00735.hp2 others(55): Show |
intron_variant | MODIFIER | c.159-3551_159-3550d others(4): Show |
MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139691645 | |||||||
chr4:139691666 | AGAT | A | 11 | a0001c0001t0001g0070 a0001c0001t0001g0115 a0001c0001t0001g0116 others(8): Show |
11 | HG01099.hp1 HG01496.hp1 HG03669.hp1 others(8): Show |
intron_variant | MODIFIER | c.159-3500_159-3498d others(5): Show |
MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr4 | 139691666 | ||||||
chr4:139691666 | AGATGAT | A | 97 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(94): Show |
118 | HG00423.hp2 HG00597.hp1 HG00609.hp2 others(115): Show |
intron_variant | MODIFIER | c.159-3503_159-3498d others(8): Show |
MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr4 | 139691666 | ||||||
chr4:139691666 | AGATGATG others(2): Show |
A | 10 | a0001c0001t0001g0021 a0001c0001t0001g0051 a0001c0001t0001g0058 others(7): Show |
11 | HG01361.hp2 HG02698.hp2 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.159-3506_159-3498d others(11): Show |
MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr4 | 139691666 | ||||||
chr4:139691666 | AGATGATG others(5): Show |
A | 2 | a0001c0001t0001g0298 a0001c0001t0001g0327 |
2 | HG01081.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.159-3509_159-3498d others(14): Show |
MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr4 | 139691666 | ||||||
chr4:139691666 | AGATGATG others(8): Show |
A | 1 | a0001c0001t0001g0341 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.159-3512_159-3498d others(17): Show |
MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr4 | 139691666 | ||||||
chr4:139691676 | G | T | 1 | a0001c0001t0001g0275 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.159-3521G>T | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139691676 | |||||||
chr4:139691678 | TGATGATG | T | 4 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0187 others(1): Show |
4 | HG00639.hp1 HG00735.hp2 HG01256.hp1 others(1): Show |
intron_variant | MODIFIER | c.159-3518_159-3512d others(9): Show |
MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139691678 | |||||||
chr4:139691679 | G | T | 1 | a0001c0001t0001g0275 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.159-3518G>T | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139691679 | |||||||
chr4:139691682 | G | GATT | 4 | a0001c0001t0001g0020 a0001c0001t0001g0217 a0001c0001t0001g0218 others(1): Show |
4 | HG02572.hp1 HG02615.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.159-3513_159-3512i others(5): Show |
MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr4 | 139691682 | ||||||
chr4:139691682 | G | T | 11 | a0001c0001t0001g0051 a0001c0001t0001g0058 a0001c0001t0001g0115 others(8): Show |
11 | HG01361.hp2 HG02698.hp2 HG03098.hp1 others(8): Show |
intron_variant | MODIFIER | c.159-3515G>T | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139691682 | |||||||
chr4:139691685 | G | T | 41 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(38): Show |
47 | HG00609.hp2 HG01361.hp2 HG02074.hp2 others(44): Show |
intron_variant | MODIFIER | c.159-3512G>T | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139691685 | |||||||
chr4:139691688 | G | T | 79 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(76): Show |
91 | HG00609.hp2 HG00639.hp1 HG00735.hp2 others(88): Show |
intron_variant | MODIFIER | c.159-3509G>T | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139691688 | |||||||
chr4:139691691 | G | T | 97 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(94): Show |
111 | HG00280.hp1 HG00609.hp2 HG00639.hp1 others(108): Show |
intron_variant | MODIFIER | c.159-3506G>T | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139691691 | |||||||
chr4:139691694 | G | T | 159 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(156): Show |
188 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(185): Show |
intron_variant | MODIFIER | c.159-3503G>T | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139691694 | |||||||
chr4:139691694 | GATGATT | G | 3 | a0001c0001t0001g0032 a0001c0001t0001g0184 a0001c0004t0001g0262 |
3 | HG01496.hp2 HG02486.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.159-3500_159-3495d others(8): Show |
MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr4 | 139691694 | ||||||
chr4:139691697 | G | GATGATTA others(5): Show |
2 | a0001c0001t0001g0110 a0001c0001t0001g0111 |
2 | HG02055.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.159-3498_159-3497i others(14): Show |
MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr4 | 139691697 | ||||||
chr4:139691697 | G | T | 240 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(237): Show |
280 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(277): Show |
intron_variant | MODIFIER | c.159-3500G>T | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139691697 | |||||||
chr4:139691697 | GATT | G | 37 | a0001c0001t0001g0012 a0001c0001t0001g0084 a0001c0001t0001g0109 others(34): Show |
38 | HG00544.hp2 HG00609.hp1 HG01167.hp2 others(35): Show |
intron_variant | MODIFIER | c.159-3484_159-3482d others(5): Show |
MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr4 | 139691697 | ||||||
chr4:139691700 | T | G | 8 | a0001c0001t0001g0075 a0001c0001t0001g0211 a0001c0001t0001g0225 others(5): Show |
8 | HG01070.hp1 HG01168.hp1 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.159-3497T>G | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139691700 | |||||||
chr4:139691703 | T | G | 3 | a0001c0001t0001g0227 a0001c0001t0001g0385 a0001c0001t0002g0157 |
3 | HG01192.hp1 HG03041.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.159-3494T>G | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139691703 | |||||||
chr4:139691721 | C | T | 1 | a0001c0001t0001g0305 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.159-3476C>T | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139691721 | |||||||
chr4:139691815 | T | C | 11 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0051 others(8): Show |
13 | HG01361.hp2 HG02572.hp1 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.159-3382T>C | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139691815 | |||||||
chr4:139691818 | T | C | 11 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0051 others(8): Show |
13 | HG01361.hp2 HG02572.hp1 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.159-3379T>C | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139691818 | |||||||
chr4:139691915 | C | T | 1 | a0001c0001t0001g0297 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.159-3282C>T | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139691915 | |||||||
chr4:139691938 | G | T | 11 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0051 others(8): Show |
13 | HG01361.hp2 HG02572.hp1 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.159-3259G>T | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139691938 | |||||||
chr4:139691951 | C | T | 2 | a0001c0001t0001g0184 a0001c0004t0001g0262 |
2 | HG01496.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.159-3246C>T | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139691951 | |||||||
chr4:139691952 | G | A | 93 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0029 others(90): Show |
110 | HG00423.hp2 HG00438.hp1 HG00597.hp1 others(107): Show |
intron_variant | MODIFIER | c.159-3245G>A | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139691952 | |||||||
chr4:139691992 | G | A | 1 | a0001c0001t0001g0267 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.159-3205G>A | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139691992 | |||||||
chr4:139692073 | C | T | 2 | a0001c0001t0001g0110 a0001c0001t0001g0111 |
2 | HG02055.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.159-3124C>T | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139692073 | |||||||
chr4:139692372 | G | A | 2 | a0001c0001t0001g0181 a0001c0001t0001g0299 |
2 | HG01361.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.159-2825G>A | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139692372 | |||||||
chr4:139692463 | A | G | 1 | a0001c0001t0001g0296 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.159-2734A>G | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139692463 | |||||||
chr4:139692909 | G | A | 1 | a0001c0001t0001g0341 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.159-2288G>A | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139692909 | |||||||
chr4:139693126 | T | C | 1 | a0001c0001t0001g0275 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.159-2071T>C | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139693126 | |||||||
chr4:139693192 | C | T | 2 | a0001c0001t0001g0110 a0001c0001t0001g0111 |
2 | HG02055.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.159-2005C>T | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139693192 | |||||||
chr4:139693199 | C | T | 52 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0070 others(49): Show |
55 | HG00140.hp2 HG00544.hp2 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.159-1998C>T | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139693199 | |||||||
chr4:139693276 | G | A | 4 | a0001c0001t0001g0234 a0001c0001t0001g0250 a0001c0001t0001g0253 others(1): Show |
4 | HG01884.hp2 HG03225.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.159-1921G>A | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139693276 | |||||||
chr4:139693290 | A | C | 1 | a0001c0001t0001g0065 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.159-1907A>C | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139693290 | |||||||
chr4:139693291 | G | A | 1 | a0001c0001t0001g0065 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.159-1906G>A | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139693291 | |||||||
chr4:139693321 | C | T | 1 | a0001c0001t0002g0381 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.159-1876C>T | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139693321 | |||||||
chr4:139693381 | G | A | 1 | a0001c0001t0001g0341 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.159-1816G>A | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139693381 | |||||||
chr4:139693404 | C | CA | 54 | a0001c0001t0001g0012 a0001c0001t0001g0021 a0001c0001t0001g0070 others(51): Show |
56 | HG00544.hp2 HG00609.hp1 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.159-1773dupA | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr4 | 139693404 | ||||||
chr4:139693404 | CA | C | 53 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(50): Show |
61 | HG00609.hp2 HG00639.hp1 HG00735.hp2 others(58): Show |
intron_variant | MODIFIER | c.159-1773delA | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr4 | 139693404 | ||||||
chr4:139693439 | G | A | 1 | a0001c0001t0002g0347 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.159-1758G>A | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139693439 | |||||||
chr4:139693486 | G | A | 1 | a0001c0001t0002g0145 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.159-1711G>A | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139693486 | |||||||
chr4:139693529 | G | T | 1 | a0001c0001t0001g0065 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.159-1668G>T | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139693529 | |||||||
chr4:139693557 | G | A | 140 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0012 others(137): Show |
158 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(155): Show |
intron_variant | MODIFIER | c.159-1640G>A | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139693557 | |||||||
chr4:139693855 | C | T | 1 | a0001c0001t0001g0256 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.159-1342C>T | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139693855 | |||||||
chr4:139694075 | G | T | 1 | a0001c0001t0001g0295 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.159-1122G>T | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139694075 | |||||||
chr4:139694133 | T | C | 1 | a0001c0001t0001g0212 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.159-1064T>C | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139694133 | |||||||
chr4:139694183 | CT | C | 9 | a0001c0001t0001g0039 a0001c0001t0001g0091 a0001c0001t0001g0176 others(6): Show |
9 | HG01168.hp1 HG01496.hp2 HG03486.hp1 others(6): Show |
intron_variant | MODIFIER | c.159-1000delT | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr4 | 139694183 | ||||||
chr4:139694197 | T | A | 3 | a0001c0001t0001g0022 a0001c0001t0001g0197 a0001c0001t0001g0341 |
4 | HG01358.hp2 HG01928.hp2 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.159-1000T>A | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139694197 | |||||||
chr4:139694417 | T | C | 4 | a0001c0001t0001g0020 a0001c0001t0001g0217 a0001c0001t0001g0218 others(1): Show |
5 | HG02572.hp1 HG02615.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.159-780T>C | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139694417 | |||||||
chr4:139694446 | C | T | 1 | a0001c0001t0001g0225 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.159-751C>T | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139694446 | |||||||
chr4:139694674 | C | G | 1 | a0001c0001t0001g0082 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.159-523C>G | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139694674 | |||||||
chr4:139694690 | T | A | 1 | a0001c0001t0001g0065 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.159-507T>A | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139694690 | |||||||
chr4:139694691 | G | A | 2 | a0001c0001t0001g0110 a0001c0001t0001g0111 |
2 | HG02055.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.159-506G>A | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139694691 | |||||||
chr4:139694910 | A | C | 1 | a0001c0001t0001g0120 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.159-287A>C | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 2/4 | chr4 | 139694910 | |||||||
chr4:139695308 | G | A | 234 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(231): Show |
266 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(263): Show |
intron_variant | MODIFIER | c.229+41G>A | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | chr4 | 139695308 | |||||||
chr4:139695350 | G | A | 1 | a0001c0001t0001g0312 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.229+83G>A | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | chr4 | 139695350 | |||||||
chr4:139695647 | T | C | 1 | a0001c0001t0001g0060 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.229+380T>C | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | chr4 | 139695647 | |||||||
chr4:139695720 | G | A | 204 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(201): Show |
232 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(229): Show |
intron_variant | MODIFIER | c.229+453G>A | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | chr4 | 139695720 | |||||||
chr4:139695780 | C | T | 1 | a0001c0001t0001g0321 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.229+513C>T | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | chr4 | 139695780 | |||||||
chr4:139695796 | C | G | 30 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0027 others(27): Show |
34 | HG00280.hp1 HG01255.hp1 HG01256.hp2 others(31): Show |
intron_variant | MODIFIER | c.229+529C>G | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | chr4 | 139695796 | |||||||
chr4:139695808 | C | T | 1 | a0001c0001t0001g0029 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.229+541C>T | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | chr4 | 139695808 | |||||||
chr4:139695829 | A | C | 44 | a0001c0001t0001g0012 a0001c0001t0001g0070 a0001c0001t0001g0084 others(41): Show |
45 | HG00544.hp2 HG00609.hp1 HG01099.hp1 others(42): Show |
intron_variant | MODIFIER | c.229+562A>C | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | chr4 | 139695829 | |||||||
chr4:139695925 | A | T | 204 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(201): Show |
232 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(229): Show |
intron_variant | MODIFIER | c.229+658A>T | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | chr4 | 139695925 | |||||||
chr4:139695926 | A | C | 204 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(201): Show |
232 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(229): Show |
intron_variant | MODIFIER | c.229+659A>C | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | chr4 | 139695926 | |||||||
chr4:139696126 | C | G | 190 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(187): Show |
216 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(213): Show |
intron_variant | MODIFIER | c.229+859C>G | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | chr4 | 139696126 | |||||||
chr4:139696352 | G | A | 2 | a0001c0001t0001g0229 a0001c0001t0001g0230 |
2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.229+1085G>A | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | chr4 | 139696352 | |||||||
chr4:139696420 | C | A | 1 | a0001c0001t0001g0222 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.229+1153C>A | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | chr4 | 139696420 | |||||||
chr4:139696518 | C | T | 1 | a0001c0001t0001g0341 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.229+1251C>T | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | chr4 | 139696518 | |||||||
chr4:139696540 | G | A | 1 | a0001c0001t0001g0341 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.229+1273G>A | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | chr4 | 139696540 | |||||||
chr4:139696671 | A | G | 1 | a0001c0001t0001g0328 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.229+1404A>G | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | chr4 | 139696671 | |||||||
chr4:139696721 | G | T | 1 | a0001c0001t0001g0275 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.229+1454G>T | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | chr4 | 139696721 | |||||||
chr4:139696743 | C | T | 14 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0051 others(11): Show |
16 | HG01361.hp2 HG02055.hp2 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.229+1476C>T | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | chr4 | 139696743 | |||||||
chr4:139696784 | T | C | 2 | a0001c0001t0001g0109 a0001c0001t0006g0160 |
2 | HG02647.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.229+1517T>C | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | chr4 | 139696784 | |||||||
chr4:139696849 | A | G | 2 | a0001c0001t0001g0109 a0001c0001t0006g0160 |
2 | HG02647.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.229+1582A>G | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | chr4 | 139696849 | |||||||
chr4:139696853 | T | C | 4 | a0001c0001t0001g0020 a0001c0001t0001g0217 a0001c0001t0001g0218 others(1): Show |
5 | HG02572.hp1 HG02615.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.229+1586T>C | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | chr4 | 139696853 | |||||||
chr4:139697086 | G | A | 7 | a0001c0001t0001g0021 a0001c0001t0001g0051 a0001c0001t0001g0058 others(4): Show |
8 | HG01361.hp2 HG02698.hp1 HG02698.hp2 others(5): Show |
intron_variant | MODIFIER | c.229+1819G>A | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | chr4 | 139697086 | |||||||
chr4:139697302 | G | A | 1 | a0001c0001t0001g0275 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.229+2035G>A | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | chr4 | 139697302 | |||||||
chr4:139697324 | A | G | 4 | a0001c0001t0001g0020 a0001c0001t0001g0217 a0001c0001t0001g0218 others(1): Show |
5 | HG02572.hp1 HG02615.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.229+2057A>G | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | chr4 | 139697324 | |||||||
chr4:139697410 | T | C | 2 | a0001c0001t0001g0172 a0001c0001t0002g0352 |
2 | NA18948.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.229+2143T>C | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | chr4 | 139697410 | |||||||
chr4:139697431 | G | A | 1 | a0001c0001t0003g0162 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.229+2164G>A | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | chr4 | 139697431 | |||||||
chr4:139697444 | C | A | 1 | a0001c0001t0003g0162 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.229+2177C>A | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | chr4 | 139697444 | |||||||
chr4:139697451 | C | G | 13 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0051 others(10): Show |
15 | HG01361.hp2 HG02055.hp2 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.229+2184C>G | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | chr4 | 139697451 | |||||||
chr4:139697518 | TCAGCTTT others(10): Show |
T | 2 | a0001c0001t0001g0172 a0001c0001t0002g0352 |
2 | NA18948.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.229+2252_229+2268d others(19): Show |
MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | chr4 | 139697518 | |||||||
chr4:139697537 | C | T | 2 | a0001c0001t0001g0172 a0001c0001t0002g0352 |
2 | NA18948.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.229+2270C>T | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | chr4 | 139697537 | |||||||
chr4:139697581 | C | T | 1 | a0001c0001t0001g0038 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.229+2314C>T | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | chr4 | 139697581 | |||||||
chr4:139697818 | C | G | 2 | a0001c0001t0001g0190 a0001c0001t0002g0136 |
2 | HG03239.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.229+2551C>G | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | chr4 | 139697818 | |||||||
chr4:139697921 | T | C | 31 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0027 others(28): Show |
35 | HG00280.hp1 HG01255.hp1 HG01256.hp2 others(32): Show |
intron_variant | MODIFIER | c.229+2654T>C | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | chr4 | 139697921 | |||||||
chr4:139697934 | C | T | 13 | a0001c0001t0001g0023 a0001c0001t0001g0026 a0001c0001t0001g0214 others(10): Show |
15 | HG00642.hp1 HG00733.hp2 HG00741.hp2 others(12): Show |
intron_variant | MODIFIER | c.229+2667C>T | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | chr4 | 139697934 | |||||||
chr4:139698025 | A | G | 1 | a0001c0001t0001g0008 | 2 | NA18747.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.229+2758A>G | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | chr4 | 139698025 | |||||||
chr4:139698042 | C | T | 2 | a0001c0001t0001g0188 a0001c0001t0001g0227 |
2 | HG01192.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.229+2775C>T | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | chr4 | 139698042 | |||||||
chr4:139698073 | A | G | 1 | a0001c0001t0001g0029 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.229+2806A>G | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | chr4 | 139698073 | |||||||
chr4:139698098 | A | AT | 288 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(285): Show |
334 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(331): Show |
intron_variant | MODIFIER | c.229+2844dupT | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr4 | 139698098 | ||||||
chr4:139698098 | A | T | 2 | a0001c0001t0001g0184 a0001c0004t0001g0262 |
2 | HG01496.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.229+2831A>T | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | chr4 | 139698098 | |||||||
chr4:139698238 | T | C | 1 | a0001c0001t0002g0241 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.229+2971T>C | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | chr4 | 139698238 | |||||||
chr4:139698241 | A | G | 6 | a0001c0001t0001g0021 a0001c0001t0001g0051 a0001c0001t0001g0058 others(3): Show |
7 | HG02698.hp1 HG02698.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.229+2974A>G | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | chr4 | 139698241 | |||||||
chr4:139698304 | C | T | 2 | a0001c0001t0001g0031 a0001c0001t0001g0303 |
3 | HG01070.hp2 HG01071.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.229+3037C>T | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | chr4 | 139698304 | |||||||
chr4:139698318 | A | C | 1 | a0001c0001t0002g0179 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.229+3051A>C | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | chr4 | 139698318 | |||||||
chr4:139698411 | C | A | 2 | a0001c0001t0001g0037 a0001c0001t0001g0174 |
2 | HG00741.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.229+3144C>A | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | chr4 | 139698411 | |||||||
chr4:139698417 | A | C | 3 | a0001c0001t0001g0029 a0001c0001t0001g0032 a0001c0001t0002g0344 |
4 | HG01192.hp2 HG02486.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.229+3150A>C | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | chr4 | 139698417 | |||||||
chr4:139698449 | C | A | 1 | a0001c0001t0001g0308 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.229+3182C>A | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | chr4 | 139698449 | |||||||
chr4:139698449 | C | T | 1 | a0001c0001t0001g0166 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.229+3182C>T | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | chr4 | 139698449 | |||||||
chr4:139698490 | G | A | 11 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0051 others(8): Show |
13 | HG02055.hp2 HG02572.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.229+3223G>A | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | chr4 | 139698490 | |||||||
chr4:139698522 | C | T | 1 | a0001c0001t0001g0175 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.229+3255C>T | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | chr4 | 139698522 | |||||||
chr4:139698548 | G | A | 2 | a0001c0001t0001g0217 a0001c0001t0001g0218 |
2 | HG02572.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.229+3281G>A | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | chr4 | 139698548 | |||||||
chr4:139698577 | C | G | 1 | a0001c0001t0001g0327 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.229+3310C>G | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | chr4 | 139698577 | |||||||
chr4:139698603 | G | A | 1 | a0001c0001t0001g0216 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.229+3336G>A | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | chr4 | 139698603 | |||||||
chr4:139698740 | G | A | 1 | a0001c0001t0001g0186 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.229+3473G>A | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | chr4 | 139698740 | |||||||
chr4:139698740 | G | C | 1 | a0001c0001t0001g0085 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.229+3473G>C | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | chr4 | 139698740 | |||||||
chr4:139698741 | T | G | 2 | a0001c0001t0001g0071 a0001c0001t0001g0072 |
2 | NA19079.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.229+3474T>G | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | chr4 | 139698741 | |||||||
chr4:139698789 | TTTTCTTA others(8): Show |
T | 1 | a0001c0001t0001g0299 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.229+3529_229+3543d others(17): Show |
MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr4 | 139698789 | ||||||
chr4:139698824 | C | CT | 32 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0027 others(29): Show |
36 | HG00280.hp1 HG01069.hp2 HG01255.hp1 others(33): Show |
intron_variant | MODIFIER | c.229+3569dupT | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr4 | 139698824 | ||||||
chr4:139698836 | T | C | 1 | a0001c0001t0001g0245 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.229+3569T>C | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | chr4 | 139698836 | |||||||
chr4:139698912 | A | G | 3 | a0001c0001t0001g0171 a0001c0001t0001g0317 a0001c0001t0001g0321 |
3 | NA18966.hp2 NA18979.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.229+3645A>G | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | chr4 | 139698912 | |||||||
chr4:139699020 | A | G | 1 | a0001c0001t0001g0275 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.229+3753A>G | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | chr4 | 139699020 | |||||||
chr4:139699390 | T | C | 1 | a0001c0001t0001g0341 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.230-4065T>C | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | chr4 | 139699390 | |||||||
chr4:139699418 | G | A | 12 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0051 others(9): Show |
14 | HG02055.hp2 HG02572.hp1 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.230-4037G>A | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | chr4 | 139699418 | |||||||
chr4:139699446 | A | G | 1 | a0001c0001t0001g0199 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.230-4009A>G | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | chr4 | 139699446 | |||||||
chr4:139699708 | CTGAA | C | 8 | a0001c0001t0001g0106 a0001c0001t0001g0198 a0001c0001t0001g0200 others(5): Show |
8 | HG00099.hp1 HG00738.hp1 HG01123.hp2 others(5): Show |
intron_variant | MODIFIER | c.230-3746_230-3743d others(6): Show |
MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | chr4 | 139699708 | |||||||
chr4:139699814 | G | C | 1 | a0001c0001t0001g0314 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.230-3641G>C | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | chr4 | 139699814 | |||||||
chr4:139699921 | A | G | 36 | a0001c0001t0001g0012 a0001c0001t0001g0070 a0001c0001t0001g0084 others(33): Show |
37 | HG00544.hp2 HG00609.hp1 HG01099.hp1 others(34): Show |
intron_variant | MODIFIER | c.230-3534A>G | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | chr4 | 139699921 | |||||||
chr4:139700127 | C | CT | 79 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0013 others(76): Show |
97 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.230-3306dupT | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr4 | 139700127 | ||||||
chr4:139700127 | C | CTT | 14 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0087 others(11): Show |
14 | HG00642.hp1 HG00741.hp2 HG01175.hp1 others(11): Show |
intron_variant | MODIFIER | c.230-3307_230-3306d others(4): Show |
MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr4 | 139700127 | ||||||
chr4:139700127 | CT | C | 65 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(62): Show |
74 | HG00423.hp2 HG00609.hp2 HG00639.hp1 others(71): Show |
intron_variant | MODIFIER | c.230-3306delT | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr4 | 139700127 | ||||||
chr4:139700127 | CTT | C | 126 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0012 others(123): Show |
145 | HG00280.hp1 HG00544.hp2 HG00597.hp1 others(142): Show |
intron_variant | MODIFIER | c.230-3307_230-3306d others(4): Show |
MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr4 | 139700127 | ||||||
chr4:139700153 | A | G | 1 | a0001c0001t0001g0324 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.230-3302A>G | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | chr4 | 139700153 | |||||||
chr4:139700163 | G | A | 2 | a0001c0001t0001g0184 a0001c0004t0001g0262 |
2 | HG01496.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.230-3292G>A | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | chr4 | 139700163 | |||||||
chr4:139700256 | G | C | 173 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(170): Show |
197 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(194): Show |
intron_variant | MODIFIER | c.230-3199G>C | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | chr4 | 139700256 | |||||||
chr4:139700324 | T | G | 293 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(290): Show |
339 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(336): Show |
intron_variant | MODIFIER | c.230-3131T>G | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | chr4 | 139700324 | |||||||
chr4:139700382 | C | T | 4 | a0001c0001t0001g0078 a0001c0001t0001g0219 a0001c0001t0001g0220 others(1): Show |
4 | HG01358.hp1 HG03669.hp2 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.230-3073C>T | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | chr4 | 139700382 | |||||||
chr4:139700397 | C | T | 1 | a0001c0001t0002g0373 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.230-3058C>T | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | chr4 | 139700397 | |||||||
chr4:139700502 | T | G | 1 | a0001c0001t0002g0158 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.230-2953T>G | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | chr4 | 139700502 | |||||||
chr4:139700591 | A | G | 2 | a0001c0001t0002g0345 a0001c0001t0002g0346 |
2 | HG03098.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.230-2864A>G | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | chr4 | 139700591 | |||||||
chr4:139700664 | C | G | 111 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0012 others(108): Show |
125 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(122): Show |
intron_variant | MODIFIER | c.230-2791C>G | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | chr4 | 139700664 | |||||||
chr4:139700735 | A | G | 1 | a0001c0001t0001g0130 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.230-2720A>G | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | chr4 | 139700735 | |||||||
chr4:139700744 | G | C | 1 | a0001c0001t0002g0366 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.230-2711G>C | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | chr4 | 139700744 | |||||||
chr4:139701028 | T | A | 3 | a0001c0001t0001g0021 a0001c0001t0001g0130 a0001c0001t0001g0242 |
4 | HG02698.hp1 HG02818.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.230-2427T>A | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | chr4 | 139701028 | |||||||
chr4:139701226 | C | A | 2 | a0001c0001t0002g0359 a0001c0001t0002g0360 |
2 | HG03669.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.230-2229C>A | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | chr4 | 139701226 | |||||||
chr4:139701269 | TC | T | 48 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(45): Show |
56 | HG00609.hp2 HG00639.hp1 HG00735.hp2 others(53): Show |
intron_variant | MODIFIER | c.230-2184delC | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr4 | 139701269 | ||||||
chr4:139701271 | C | G | 1 | a0001c0001t0001g0119 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.230-2184C>G | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | chr4 | 139701271 | |||||||
chr4:139701510 | A | G | 1 | a0001c0001t0002g0358 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.230-1945A>G | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | chr4 | 139701510 | |||||||
chr4:139701579 | G | A | 1 | a0001c0001t0003g0162 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.230-1876G>A | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | chr4 | 139701579 | |||||||
chr4:139701622 | G | A | 1 | a0001c0001t0002g0151 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.230-1833G>A | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | chr4 | 139701622 | |||||||
chr4:139701705 | T | C | 1 | a0001c0001t0001g0070 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.230-1750T>C | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | chr4 | 139701705 | |||||||
chr4:139701789 | C | G | 2 | a0001c0001t0001g0032 a0001c0001t0002g0344 |
2 | HG01192.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.230-1666C>G | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | chr4 | 139701789 | |||||||
chr4:139701855 | T | C | 1 | a0001c0001t0001g0188 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.230-1600T>C | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | chr4 | 139701855 | |||||||
chr4:139701968 | G | GA | 264 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(261): Show |
296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.230-1475dupA | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr4 | 139701968 | ||||||
chr4:139702079 | A | G | 4 | a0001c0001t0001g0078 a0001c0001t0001g0219 a0001c0001t0001g0220 others(1): Show |
4 | HG01358.hp1 HG03669.hp2 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.230-1376A>G | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | chr4 | 139702079 | |||||||
chr4:139702132 | T | A | 2 | a0001c0001t0001g0071 a0001c0001t0001g0072 |
2 | NA19079.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.230-1323T>A | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | chr4 | 139702132 | |||||||
chr4:139702284 | C | G | 13 | a0001c0001t0001g0027 a0001c0001t0001g0104 a0001c0001t0001g0114 others(10): Show |
15 | HG01433.hp1 HG01934.hp1 HG01943.hp2 others(12): Show |
intron_variant | MODIFIER | c.230-1171C>G | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | chr4 | 139702284 | |||||||
chr4:139702326 | C | T | 1 | a0001c0001t0001g0192 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.230-1129C>T | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | chr4 | 139702326 | |||||||
chr4:139702726 | C | T | 1 | a0001c0001t0001g0341 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.230-729C>T | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | chr4 | 139702726 | |||||||
chr4:139702789 | A | G | 5 | a0001c0001t0001g0113 a0001c0001t0001g0129 a0001c0001t0001g0340 others(2): Show |
5 | HG02109.hp1 HG02630.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.230-666A>G | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | chr4 | 139702789 | |||||||
chr4:139702799 | C | T | 188 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(185): Show |
205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.230-656C>T | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | chr4 | 139702799 | |||||||
chr4:139702844 | G | GCTTTTTT others(14): Show |
1 | a0001c0001t0001g0201 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.230-611_230-610ins others(21): Show |
MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | chr4 | 139702844 | |||||||
chr4:139702844 | G | GT | 36 | a0001c0001t0001g0006 a0001c0001t0001g0039 a0001c0001t0001g0071 others(33): Show |
39 | HG00423.hp2 HG00597.hp2 HG00639.hp2 others(36): Show |
intron_variant | MODIFIER | c.230-585dupT | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr4 | 139702844 | ||||||
chr4:139702844 | G | GTT | 23 | a0001c0001t0001g0027 a0001c0001t0001g0046 a0001c0001t0001g0048 others(20): Show |
25 | HG00280.hp1 HG01168.hp1 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.230-586_230-585dup others(2): Show |
MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr4 | 139702844 | ||||||
chr4:139702844 | G | GTTT | 10 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0047 others(7): Show |
12 | HG01255.hp1 HG01256.hp2 HG01258.hp1 others(9): Show |
intron_variant | MODIFIER | c.230-587_230-585dup others(3): Show |
MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr4 | 139702844 | ||||||
chr4:139702844 | G | GTTTTTTT others(4): Show |
3 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0192 |
3 | HG02055.hp2 HG02615.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.230-595_230-585dup others(11): Show |
MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr4 | 139702844 | ||||||
chr4:139702844 | G | GTTTTTTT others(6): Show |
21 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(18): Show |
26 | HG00609.hp2 HG01192.hp1 HG02083.hp2 others(23): Show |
intron_variant | MODIFIER | c.230-597_230-585dup others(13): Show |
MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr4 | 139702844 | ||||||
chr4:139702844 | G | GTTTTTTT others(7): Show |
29 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0044 others(26): Show |
32 | HG00639.hp1 HG01256.hp1 HG01261.hp2 others(29): Show |
intron_variant | MODIFIER | c.230-598_230-585dup others(14): Show |
MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr4 | 139702844 | ||||||
chr4:139702844 | G | GTTTTTTT others(8): Show |
11 | a0001c0001t0001g0012 a0001c0001t0001g0054 a0001c0001t0001g0062 others(8): Show |
12 | HG00735.hp2 HG01081.hp1 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.230-599_230-585dup others(15): Show |
MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr4 | 139702844 | ||||||
chr4:139702844 | G | GTTTTTTT others(9): Show |
7 | a0001c0001t0001g0045 a0001c0001t0001g0057 a0001c0001t0001g0070 others(4): Show |
7 | HG01361.hp1 HG02074.hp2 HG02148.hp1 others(4): Show |
intron_variant | MODIFIER | c.230-600_230-585dup others(16): Show |
MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr4 | 139702844 | ||||||
chr4:139702844 | G | GTTTTTTT others(11): Show |
3 | a0001c0001t0001g0171 a0001c0001t0001g0288 a0001c0001t0001g0301 |
3 | NA18951.hp1 NA18979.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.230-602_230-585dup others(18): Show |
MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr4 | 139702844 | ||||||
chr4:139702844 | G | GTTTTTTT others(12): Show |
13 | a0001c0001t0001g0077 a0001c0001t0001g0189 a0001c0001t0001g0276 others(10): Show |
13 | HG00609.hp1 HG02129.hp1 HG02735.hp1 others(10): Show |
intron_variant | MODIFIER | c.230-603_230-585dup others(19): Show |
MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr4 | 139702844 | ||||||
chr4:139702844 | G | GTTTTTTT others(13): Show |
1 | a0001c0001t0001g0266 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.230-604_230-585dup others(20): Show |
MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr4 | 139702844 | ||||||
chr4:139702844 | G | GTTTTTTT others(14): Show |
2 | a0001c0001t0001g0197 a0001c0001t0001g0198 |
2 | HG00738.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.230-605_230-585dup others(21): Show |
MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr4 | 139702844 | ||||||
chr4:139702844 | G | GTTTTTTT others(15): Show |
4 | a0001c0001t0001g0022 a0001c0001t0001g0200 a0001c0001t0001g0203 others(1): Show |
5 | HG00099.hp1 HG01358.hp2 HG01928.hp1 others(2): Show |
intron_variant | MODIFIER | c.230-606_230-585dup others(22): Show |
MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr4 | 139702844 | ||||||
chr4:139702844 | G | GTTTTTTT others(16): Show |
6 | a0001c0001t0001g0075 a0001c0001t0001g0078 a0001c0001t0001g0112 others(3): Show |
6 | HG01070.hp1 HG02055.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.230-607_230-585dup others(23): Show |
MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr4 | 139702844 | ||||||
chr4:139702844 | G | GTTTTTTT others(17): Show |
4 | a0001c0001t0001g0098 a0001c0001t0001g0106 a0001c0001t0001g0159 others(1): Show |
4 | HG00544.hp2 HG01255.hp2 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.230-608_230-585dup others(24): Show |
MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr4 | 139702844 | ||||||
chr4:139702844 | G | GTTTTTTT others(18): Show |
10 | a0001c0001t0001g0038 a0001c0001t0001g0175 a0001c0001t0001g0208 others(7): Show |
10 | HG00099.hp2 HG00558.hp2 HG01257.hp1 others(7): Show |
intron_variant | MODIFIER | c.230-609_230-585dup others(25): Show |
MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr4 | 139702844 | ||||||
chr4:139702844 | G | GTTTTTTT others(19): Show |
22 | a0001c0001t0001g0036 a0001c0001t0001g0042 a0001c0001t0001g0169 others(19): Show |
23 | HG00558.hp1 HG00673.hp1 HG00741.hp1 others(20): Show |
intron_variant | MODIFIER | c.230-610_230-585dup others(26): Show |
MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr4 | 139702844 | ||||||
chr4:139702844 | G | GTTTTTTT others(20): Show |
8 | a0001c0001t0001g0052 a0001c0001t0001g0083 a0001c0001t0001g0108 others(5): Show |
8 | HG00438.hp2 HG01099.hp2 HG01123.hp1 others(5): Show |
intron_variant | MODIFIER | c.230-585_230-584ins others(27): Show |
MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr4 | 139702844 | ||||||
chr4:139702844 | G | GTTTTTTT others(21): Show |
3 | a0001c0001t0001g0068 a0001c0001t0001g0233 a0001c0001t0004g0273 |
3 | HG02630.hp1 HG03927.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.230-585_230-584ins others(28): Show |
MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr4 | 139702844 | ||||||
chr4:139702844 | G | GTTTTTTT others(22): Show |
3 | a0001c0001t0001g0037 a0001c0001t0001g0173 a0001c0001t0001g0243 |
3 | HG01069.hp1 HG02004.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.230-585_230-584ins others(29): Show |
MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr4 | 139702844 | ||||||
chr4:139702844 | G | GTTTTTTT others(23): Show |
3 | a0001c0001t0001g0210 a0001c0001t0001g0220 a0001c0001t0001g0244 |
3 | HG01071.hp2 HG04199.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.230-585_230-584ins others(30): Show |
MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr4 | 139702844 | ||||||
chr4:139702844 | G | GTTTTTTT others(24): Show |
1 | a0001c0001t0001g0033 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.230-585_230-584ins others(31): Show |
MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr4 | 139702844 | ||||||
chr4:139702844 | G | GTTTTTTT others(25): Show |
5 | a0001c0001t0001g0222 a0001c0001t0001g0274 a0001c0001t0001g0283 others(2): Show |
5 | HG00544.hp1 HG01106.hp1 HG02165.hp1 others(2): Show |
intron_variant | MODIFIER | c.230-585_230-584ins others(32): Show |
MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr4 | 139702844 | ||||||
chr4:139702844 | G | GTTTTTTT others(29): Show |
1 | a0001c0001t0001g0076 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.230-585_230-584ins others(36): Show |
MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr4 | 139702844 | ||||||
chr4:139702844 | GTTTTT | G | 17 | a0001c0001t0001g0023 a0001c0001t0001g0026 a0001c0001t0001g0182 others(14): Show |
19 | HG00642.hp1 HG00733.hp2 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.230-589_230-585del others(5): Show |
MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr4 | 139702844 | ||||||
chr4:139702844 | GTTTTTTT others(3): Show |
G | 1 | a0001c0001t0001g0021 | 2 | HG02818.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.230-594_230-585del others(10): Show |
MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr4 | 139702844 | ||||||
chr4:139702844 | GTTTTTTT others(5): Show |
G | 4 | a0001c0001t0001g0020 a0001c0001t0001g0217 a0001c0001t0001g0218 others(1): Show |
5 | HG02572.hp1 HG02615.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.230-596_230-585del others(12): Show |
MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr4 | 139702844 | ||||||
chr4:139702867 | T | C | 1 | a0001c0001t0001g0021 | 2 | HG02818.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.230-588T>C | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | chr4 | 139702867 | |||||||
chr4:139702867 | T | TTTTTTTT others(4): Show |
1 | a0001c0001t0001g0058 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.230-585_230-584ins others(11): Show |
MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr4 | 139702867 | ||||||
chr4:139702867 | T | TTTTTTTT others(6): Show |
1 | a0001c0001t0001g0051 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.230-585_230-584ins others(13): Show |
MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr4 | 139702867 | ||||||
chr4:139702867 | T | TTTTTTTT others(7): Show |
1 | a0001c0001t0001g0252 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.230-585_230-584ins others(14): Show |
MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr4 | 139702867 | ||||||
chr4:139702867 | T | TTTTTTTT others(19): Show |
1 | a0001c0001t0001g0130 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.230-585_230-584ins others(26): Show |
MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr4 | 139702867 | ||||||
chr4:139702867 | T | TTTTTTTT others(29): Show |
1 | a0001c0001t0001g0242 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.230-585_230-584ins others(36): Show |
MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr4 | 139702867 | ||||||
chr4:139702964 | C | CTCTAATA others(6): Show |
1 | a0001c0001t0002g0381 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.230-491_230-490ins others(13): Show |
MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | chr4 | 139702964 | |||||||
chr4:139702966 | C | T | 1 | a0001c0001t0002g0381 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.230-489C>T | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | chr4 | 139702966 | |||||||
chr4:139702969 | A | T | 1 | a0001c0001t0002g0381 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.230-486A>T | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | chr4 | 139702969 | |||||||
chr4:139702973 | T | C | 1 | a0001c0001t0002g0381 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.230-482T>C | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | chr4 | 139702973 | |||||||
chr4:139702974 | G | T | 1 | a0001c0001t0002g0381 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.230-481G>T | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | chr4 | 139702974 | |||||||
chr4:139702983 | T | C | 1 | a0001c0001t0002g0381 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.230-472T>C | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | chr4 | 139702983 | |||||||
chr4:139702984 | G | T | 1 | a0001c0001t0002g0381 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.230-471G>T | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | chr4 | 139702984 | |||||||
chr4:139702986 | C | G | 1 | a0001c0001t0002g0381 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.230-469C>G | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | chr4 | 139702986 | |||||||
chr4:139702993 | T | A | 1 | a0001c0001t0002g0381 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.230-462T>A | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | chr4 | 139702993 | |||||||
chr4:139702996 | G | C | 1 | a0001c0001t0002g0381 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.230-459G>C | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | chr4 | 139702996 | |||||||
chr4:139702997 | C | T | 1 | a0001c0001t0002g0381 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.230-458C>T | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | chr4 | 139702997 | |||||||
chr4:139703014 | C | A | 2 | a0001c0001t0001g0110 a0001c0001t0001g0111 |
2 | HG02055.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.230-441C>A | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | chr4 | 139703014 | |||||||
chr4:139703039 | C | A | 1 | a0001c0001t0002g0381 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.230-416C>A | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | chr4 | 139703039 | |||||||
chr4:139703040 | C | A | 1 | a0001c0001t0002g0381 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.230-415C>A | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | chr4 | 139703040 | |||||||
chr4:139703049 | C | T | 1 | a0001c0001t0002g0381 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.230-406C>T | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | chr4 | 139703049 | |||||||
chr4:139703050 | T | C | 1 | a0001c0001t0002g0381 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.230-405T>C | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | chr4 | 139703050 | |||||||
chr4:139703084 | C | A | 1 | a0001c0001t0002g0381 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.230-371C>A | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | chr4 | 139703084 | |||||||
chr4:139703120 | T | G | 1 | a0001c0001t0002g0381 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.230-335T>G | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | chr4 | 139703120 | |||||||
chr4:139703136 | G | T | 1 | a0001c0001t0002g0381 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.230-319G>T | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | chr4 | 139703136 | |||||||
chr4:139703137 | G | T | 1 | a0001c0001t0002g0381 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.230-318G>T | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | chr4 | 139703137 | |||||||
chr4:139703178 | C | T | 12 | a0001c0001t0001g0168 a0001c0001t0001g0333 a0001c0001t0001g0334 others(9): Show |
18 | HG00597.hp2 NA18943.hp1 NA18944.hp1 others(15): Show |
intron_variant | MODIFIER | c.230-277C>T | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | chr4 | 139703178 | |||||||
chr4:139703179 | G | A | 1 | a0001c0001t0003g0162 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.230-276G>A | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | chr4 | 139703179 | |||||||
chr4:139703179 | G | T | 1 | a0001c0001t0002g0381 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.230-276G>T | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | chr4 | 139703179 | |||||||
chr4:139703188 | A | C | 1 | a0001c0001t0002g0381 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.230-267A>C | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | chr4 | 139703188 | |||||||
chr4:139703197 | G | C | 1 | a0001c0001t0003g0162 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.230-258G>C | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | chr4 | 139703197 | |||||||
chr4:139703204 | G | T | 1 | a0001c0001t0002g0381 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.230-251G>T | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | chr4 | 139703204 | |||||||
chr4:139703213 | T | A | 1 | a0001c0001t0002g0381 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.230-242T>A | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | chr4 | 139703213 | |||||||
chr4:139703219 | G | T | 1 | a0001c0001t0002g0381 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.230-236G>T | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | chr4 | 139703219 | |||||||
chr4:139703223 | A | T | 1 | a0001c0001t0002g0381 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.230-232A>T | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | chr4 | 139703223 | |||||||
chr4:139703224 | G | A | 1 | a0001c0001t0002g0381 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.230-231G>A | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | chr4 | 139703224 | |||||||
chr4:139703235 | G | T | 1 | a0001c0001t0002g0381 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.230-220G>T | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | chr4 | 139703235 | |||||||
chr4:139703237 | T | A | 1 | a0001c0001t0002g0381 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.230-218T>A | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | chr4 | 139703237 | |||||||
chr4:139703238 | T | G | 1 | a0001c0001t0002g0381 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.230-217T>G | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | chr4 | 139703238 | |||||||
chr4:139703257 | T | A | 1 | a0001c0001t0002g0381 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.230-198T>A | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | chr4 | 139703257 | |||||||
chr4:139703261 | G | A | 5 | a0001c0001t0001g0113 a0001c0001t0001g0129 a0001c0001t0001g0340 others(2): Show |
5 | HG02109.hp1 HG02630.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.230-194G>A | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | chr4 | 139703261 | |||||||
chr4:139703261 | G | T | 1 | a0001c0001t0002g0381 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.230-194G>T | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | chr4 | 139703261 | |||||||
chr4:139703269 | T | A | 1 | a0001c0001t0002g0381 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.230-186T>A | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | chr4 | 139703269 | |||||||
chr4:139703287 | G | A | 1 | a0001c0001t0002g0381 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.230-168G>A | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | chr4 | 139703287 | |||||||
chr4:139703301 | T | A | 1 | a0001c0001t0002g0381 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.230-154T>A | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | chr4 | 139703301 | |||||||
chr4:139703301 | T | C | 2 | a0001c0001t0001g0110 a0001c0001t0001g0111 |
2 | HG02055.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.230-154T>C | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | chr4 | 139703301 | |||||||
chr4:139703308 | C | A | 1 | a0001c0001t0002g0381 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.230-147C>A | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | chr4 | 139703308 | |||||||
chr4:139703309 | T | A | 1 | a0001c0001t0002g0381 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.230-146T>A | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 3/4 | chr4 | 139703309 | |||||||
chr4:139703623 | A | C | 1 | a0001c0001t0002g0165 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.311+87A>C | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 4/4 | chr4 | 139703623 | |||||||
chr4:139703727 | T | C | 2 | a0001c0001t0001g0115 a0001c0001t0001g0121 |
2 | NA18962.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.311+191T>C | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 4/4 | chr4 | 139703727 | |||||||
chr4:139703781 | A | G | 2 | a0001c0001t0001g0060 a0001c0001t0001g0107 |
2 | HG00609.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.312-235A>G | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 4/4 | chr4 | 139703781 | |||||||
chr4:139703925 | A | C | 1 | a0001c0001t0001g0341 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.312-91A>C | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 4/4 | chr4 | 139703925 | |||||||
chr4:139703933 | C | T | 4 | a0001c0001t0001g0020 a0001c0001t0001g0217 a0001c0001t0001g0218 others(1): Show |
5 | HG02572.hp1 HG02615.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.312-83C>T | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 4/4 | chr4 | 139703933 | |||||||
chr4:139704002 | T | C | 1 | a0001c0001t0001g0275 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.312-14T>C | MGST2 | ENSG00000085871.9 | transcript | ENST00000265498.6 | protein_coding | 4/4 | chr4 | 139704002 |