Item | Value |
---|---|
geneid | 217 |
ensemblid | ENSG00000111275.13 |
hgncid | 404 |
symbol | ALDH2 |
name | aldehyde dehydrogenase 2 family member |
refseq_nuc | NM_000690.4 |
refseq_prot | NP_000681.2 |
ensembl_nuc | ENST00000261733.7 |
ensembl_prot | ENSP00000261733.2 |
mane_status | MANE Select |
chr | chr12 |
start | 111766933 |
end | 111817532 |
strand | + |
ver | v1.2 |
region | chr12:111766933-111817532 |
region5000 | chr12:111761933-111822532 |
regionname0 | ALDH2_chr12_111766933_111817532 |
regionname5000 | ALDH2_chr12_111761933_111822532 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 517 | 311 | 87 | 52 | 128 | 6 | 36 | 99 | ALDH2_chr12_111761933_111822532 | ALDH2 | MLRAA others(512): Show |
chr12 | 111761933 | 111822532 |
a0002 | 0/0 | 517 | 25 | 0 | 0 | 25 | 0 | 0 | 21 | ALDH2_chr12_111761933_111822532 | ALDH2 | MLRAA others(512): Show |
chr12 | 111761933 | 111822532 |
a0003 | 0/0 | 517 | 4 | 0 | 0 | 0 | 0 | 4 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | MLRAA others(512): Show |
chr12 | 111761933 | 111822532 |
a0004 | 0/0 | 517 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | MLRAA others(512): Show |
chr12 | 111761933 | 111822532 |
a0005 | 0/0 | 517 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | MLRAA others(512): Show |
chr12 | 111761933 | 111822532 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1551 | 305 | 84 | 52 | 125 | 6 | 36 | ALDH2_chr12_111761933_111822532 | ALDH2 | ATGTT others(1546): Show |
chr12 | 111761933 | 111822532 | ||
a0001c0004 | 0/0 | 1551 | 3 | 0 | 0 | 3 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | ATGTT others(1546): Show |
chr12 | 111761933 | 111822532 | ||
a0001c0006 | 0/0 | 1551 | 1 | 1 | 0 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | ATGTT others(1546): Show |
chr12 | 111761933 | 111822532 | ||
a0001c0007 | 0/0 | 1551 | 1 | 1 | 0 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | ATGTT others(1546): Show |
chr12 | 111761933 | 111822532 | ||
a0001c0009 | 0/0 | 1551 | 1 | 1 | 0 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | ATGTT others(1546): Show |
chr12 | 111761933 | 111822532 | ||
a0002c0002 | 0/0 | 1551 | 25 | 0 | 0 | 25 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | ATGTT others(1546): Show |
chr12 | 111761933 | 111822532 | ||
a0003c0003 | 0/0 | 1551 | 4 | 0 | 0 | 0 | 0 | 4 | ALDH2_chr12_111761933_111822532 | ALDH2 | ATGTT others(1546): Show |
chr12 | 111761933 | 111822532 | ||
a0004c0005 | 0/0 | 1551 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | ATGTT others(1546): Show |
chr12 | 111761933 | 111822532 | ||
a0005c0008 | 0/0 | 1551 | 1 | 1 | 0 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | ATGTT others(1546): Show |
chr12 | 111761933 | 111822532 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 9562 | 29 | 0 | 5 | 22 | 0 | 2 | ALDH2_chr12_111761933_111822532 | ALDH2 | GAGAC others(9557): Show |
chr12 | 111761933 | 111822532 |
a0001c0001t0002 | 1/1 | 9561 | 37 | 7 | 16 | 8 | 1 | 3 | ALDH2_chr12_111761933_111822532 | ALDH2 | GAGAC others(9556): Show |
chr12 | 111761933 | 111822532 |
a0001c0001t0003 | 0/0 | 9561 | 21 | 7 | 1 | 12 | 0 | 1 | ALDH2_chr12_111761933_111822532 | ALDH2 | GAGAC others(9556): Show |
chr12 | 111761933 | 111822532 |
a0001c0001t0004 | 0/0 | 9562 | 14 | 1 | 6 | 7 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | GAGAC others(9557): Show |
chr12 | 111761933 | 111822532 |
a0001c0001t0005 | 0/0 | 9562 | 10 | 0 | 1 | 7 | 0 | 2 | ALDH2_chr12_111761933_111822532 | ALDH2 | GAGAC others(9557): Show |
chr12 | 111761933 | 111822532 |
a0001c0001t0006 | 0/0 | 9562 | 10 | 4 | 2 | 2 | 0 | 2 | ALDH2_chr12_111761933_111822532 | ALDH2 | GAGAC others(9557): Show |
chr12 | 111761933 | 111822532 |
a0001c0001t0007 | 0/0 | 9562 | 9 | 0 | 1 | 2 | 2 | 4 | ALDH2_chr12_111761933_111822532 | ALDH2 | GAGAC others(9557): Show |
chr12 | 111761933 | 111822532 |
a0001c0001t0008 | 0/0 | 9561 | 7 | 0 | 0 | 7 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | GAGAC others(9556): Show |
chr12 | 111761933 | 111822532 |
a0001c0001t0009 | 0/0 | 9561 | 2 | 0 | 0 | 2 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | GAGAC others(9556): Show |
chr12 | 111761933 | 111822532 |
a0001c0001t0010 | 0/0 | 9562 | 6 | 0 | 3 | 0 | 0 | 3 | ALDH2_chr12_111761933_111822532 | ALDH2 | GAGAC others(9557): Show |
chr12 | 111761933 | 111822532 |
a0001c0001t0011 | 0/0 | 9563 | 6 | 4 | 2 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | GAGAC others(9558): Show |
chr12 | 111761933 | 111822532 |
a0001c0001t0012 | 0/0 | 9561 | 6 | 4 | 1 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | GAGAC others(9556): Show |
chr12 | 111761933 | 111822532 |
a0001c0001t0013 | 0/0 | 9561 | 6 | 0 | 0 | 6 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | GAGAC others(9556): Show |
chr12 | 111761933 | 111822532 |
a0001c0001t0014 | 0/0 | 9559 | 6 | 6 | 0 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | GAGAC others(9554): Show |
chr12 | 111761933 | 111822532 |
a0001c0001t0015 | 0/0 | 9562 | 4 | 0 | 0 | 4 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | GAGAC others(9557): Show |
chr12 | 111761933 | 111822532 |
a0001c0001t0016 | 0/0 | 9563 | 4 | 0 | 1 | 2 | 0 | 1 | ALDH2_chr12_111761933_111822532 | ALDH2 | GAGAC others(9558): Show |
chr12 | 111761933 | 111822532 |
a0001c0001t0017 | 0/0 | 9560 | 2 | 2 | 0 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | GAGAC others(9555): Show |
chr12 | 111761933 | 111822532 |
a0001c0001t0018 | 0/0 | 9561 | 3 | 0 | 0 | 1 | 0 | 2 | ALDH2_chr12_111761933_111822532 | ALDH2 | GAGAC others(9556): Show |
chr12 | 111761933 | 111822532 |
a0001c0001t0019 | 0/0 | 9562 | 3 | 3 | 0 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | GAGAC others(9557): Show |
chr12 | 111761933 | 111822532 |
a0001c0001t0020 | 0/0 | 9562 | 3 | 0 | 0 | 3 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | GAGAC others(9557): Show |
chr12 | 111761933 | 111822532 |
a0001c0001t0021 | 0/0 | 9562 | 3 | 2 | 0 | 0 | 0 | 1 | ALDH2_chr12_111761933_111822532 | ALDH2 | GAGAC others(9557): Show |
chr12 | 111761933 | 111822532 |
a0001c0001t0022 | 0/0 | 9560 | 3 | 0 | 0 | 3 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | GAGAC others(9555): Show |
chr12 | 111761933 | 111822532 |
a0001c0001t0023 | 0/0 | 9559 | 3 | 3 | 0 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | GAGAC others(9554): Show |
chr12 | 111761933 | 111822532 |
a0001c0001t0024 | 0/0 | 9559 | 3 | 1 | 1 | 0 | 1 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | GAGAC others(9554): Show |
chr12 | 111761933 | 111822532 |
a0001c0001t0025 | 0/0 | 9560 | 2 | 2 | 0 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | GAGAC others(9555): Show |
chr12 | 111761933 | 111822532 |
a0001c0001t0026 | 0/0 | 9563 | 2 | 2 | 0 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | GAGAC others(9558): Show |
chr12 | 111761933 | 111822532 |
a0001c0001t0028 | 0/0 | 9562 | 2 | 0 | 2 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | GAGAC others(9557): Show |
chr12 | 111761933 | 111822532 |
a0001c0001t0029 | 0/0 | 9563 | 2 | 2 | 0 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | GAGAC others(9558): Show |
chr12 | 111761933 | 111822532 |
a0001c0001t0030 | 0/0 | 9563 | 2 | 2 | 0 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | GAGAC others(9558): Show |
chr12 | 111761933 | 111822532 |
a0001c0001t0031 | 0/0 | 9562 | 2 | 0 | 0 | 2 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | GAGAC others(9557): Show |
chr12 | 111761933 | 111822532 |
a0001c0001t0032 | 0/0 | 9561 | 2 | 0 | 0 | 2 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | GAGAC others(9556): Show |
chr12 | 111761933 | 111822532 |
a0001c0001t0033 | 0/0 | 9559 | 2 | 0 | 0 | 2 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | GAGAC others(9554): Show |
chr12 | 111761933 | 111822532 |
a0001c0001t0034 | 0/0 | 9562 | 1 | 1 | 0 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | GAGAC others(9557): Show |
chr12 | 111761933 | 111822532 |
a0001c0001t0035 | 0/0 | 9561 | 2 | 2 | 0 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | GAGAC others(9556): Show |
chr12 | 111761933 | 111822532 |
a0001c0001t0036 | 0/0 | 9562 | 2 | 0 | 0 | 2 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | GAGAC others(9557): Show |
chr12 | 111761933 | 111822532 |
a0001c0001t0037 | 0/0 | 9562 | 1 | 0 | 0 | 0 | 0 | 1 | ALDH2_chr12_111761933_111822532 | ALDH2 | GAGAC others(9557): Show |
chr12 | 111761933 | 111822532 |
a0001c0001t0038 | 0/0 | 9561 | 1 | 1 | 0 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | GAGAC others(9556): Show |
chr12 | 111761933 | 111822532 |
a0001c0001t0039 | 0/0 | 9561 | 1 | 1 | 0 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | GAGAC others(9556): Show |
chr12 | 111761933 | 111822532 |
a0001c0001t0040 | 0/0 | 9560 | 1 | 0 | 1 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | GAGAC others(9555): Show |
chr12 | 111761933 | 111822532 |
a0001c0001t0041 | 0/0 | 9561 | 1 | 1 | 0 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | GAGAC others(9556): Show |
chr12 | 111761933 | 111822532 |
a0001c0001t0042 | 0/0 | 9561 | 1 | 0 | 0 | 0 | 0 | 1 | ALDH2_chr12_111761933_111822532 | ALDH2 | GAGAC others(9556): Show |
chr12 | 111761933 | 111822532 |
a0001c0001t0043 | 0/0 | 9561 | 1 | 0 | 0 | 0 | 0 | 1 | ALDH2_chr12_111761933_111822532 | ALDH2 | GAGAC others(9556): Show |
chr12 | 111761933 | 111822532 |
a0001c0001t0044 | 0/0 | 9564 | 1 | 1 | 0 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | GAGAC others(9559): Show |
chr12 | 111761933 | 111822532 |
a0001c0001t0045 | 0/0 | 9562 | 1 | 0 | 0 | 0 | 0 | 1 | ALDH2_chr12_111761933_111822532 | ALDH2 | GAGAC others(9557): Show |
chr12 | 111761933 | 111822532 |
a0001c0001t0046 | 0/0 | 9563 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | GAGAC others(9558): Show |
chr12 | 111761933 | 111822532 |
a0001c0001t0047 | 0/0 | 9562 | 1 | 0 | 1 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | GAGAC others(9557): Show |
chr12 | 111761933 | 111822532 |
a0001c0001t0048 | 0/0 | 9563 | 1 | 0 | 0 | 0 | 0 | 1 | ALDH2_chr12_111761933_111822532 | ALDH2 | GAGAC others(9558): Show |
chr12 | 111761933 | 111822532 |
a0001c0001t0049 | 0/0 | 9565 | 1 | 1 | 0 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | GAGAC others(9560): Show |
chr12 | 111761933 | 111822532 |
a0001c0001t0050 | 0/0 | 9561 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | GAGAC others(9556): Show |
chr12 | 111761933 | 111822532 |
a0001c0001t0051 | 0/0 | 9561 | 1 | 1 | 0 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | GAGAC others(9556): Show |
chr12 | 111761933 | 111822532 |
a0001c0001t0052 | 0/0 | 9562 | 1 | 1 | 0 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | GAGAC others(9557): Show |
chr12 | 111761933 | 111822532 |
a0001c0001t0053 | 0/0 | 9562 | 1 | 1 | 0 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | GAGAC others(9557): Show |
chr12 | 111761933 | 111822532 |
a0001c0001t0054 | 0/0 | 9562 | 1 | 1 | 0 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | GAGAC others(9557): Show |
chr12 | 111761933 | 111822532 |
a0001c0001t0055 | 0/0 | 9563 | 1 | 1 | 0 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | GAGAC others(9558): Show |
chr12 | 111761933 | 111822532 |
a0001c0001t0056 | 0/0 | 9563 | 1 | 1 | 0 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | GAGAC others(9558): Show |
chr12 | 111761933 | 111822532 |
a0001c0001t0057 | 0/0 | 9562 | 1 | 1 | 0 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | GAGAC others(9557): Show |
chr12 | 111761933 | 111822532 |
a0001c0001t0058 | 0/0 | 9561 | 1 | 1 | 0 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | GAGAC others(9556): Show |
chr12 | 111761933 | 111822532 |
a0001c0001t0059 | 0/0 | 9565 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | GAGAC others(9560): Show |
chr12 | 111761933 | 111822532 |
a0001c0001t0060 | 0/0 | 9561 | 1 | 0 | 1 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | GAGAC others(9556): Show |
chr12 | 111761933 | 111822532 |
a0001c0001t0061 | 0/0 | 9562 | 1 | 0 | 0 | 0 | 0 | 1 | ALDH2_chr12_111761933_111822532 | ALDH2 | GAGAC others(9557): Show |
chr12 | 111761933 | 111822532 |
a0001c0001t0063 | 0/0 | 9562 | 1 | 0 | 0 | 0 | 0 | 1 | ALDH2_chr12_111761933_111822532 | ALDH2 | GAGAC others(9557): Show |
chr12 | 111761933 | 111822532 |
a0001c0001t0064 | 0/0 | 9562 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | GAGAC others(9557): Show |
chr12 | 111761933 | 111822532 |
a0001c0001t0065 | 0/0 | 9561 | 1 | 0 | 0 | 0 | 0 | 1 | ALDH2_chr12_111761933_111822532 | ALDH2 | GAGAC others(9556): Show |
chr12 | 111761933 | 111822532 |
a0001c0001t0067 | 0/0 | 9561 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | GAGAC others(9556): Show |
chr12 | 111761933 | 111822532 |
a0001c0001t0068 | 0/0 | 9561 | 1 | 0 | 0 | 0 | 1 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | GAGAC others(9556): Show |
chr12 | 111761933 | 111822532 |
a0001c0001t0069 | 0/0 | 9562 | 1 | 0 | 1 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | GAGAC others(9557): Show |
chr12 | 111761933 | 111822532 |
a0001c0001t0070 | 0/0 | 9560 | 1 | 0 | 0 | 0 | 0 | 1 | ALDH2_chr12_111761933_111822532 | ALDH2 | GAGAC others(9555): Show |
chr12 | 111761933 | 111822532 |
a0001c0001t0071 | 0/0 | 9561 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | GAGAC others(9556): Show |
chr12 | 111761933 | 111822532 |
a0001c0001t0072 | 0/0 | 9560 | 1 | 0 | 1 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | GAGAC others(9555): Show |
chr12 | 111761933 | 111822532 |
a0001c0001t0073 | 0/0 | 9563 | 1 | 0 | 1 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | GAGAC others(9558): Show |
chr12 | 111761933 | 111822532 |
a0001c0001t0074 | 0/0 | 9562 | 1 | 0 | 0 | 0 | 0 | 1 | ALDH2_chr12_111761933_111822532 | ALDH2 | GAGAC others(9557): Show |
chr12 | 111761933 | 111822532 |
a0001c0001t0075 | 0/0 | 9563 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | GAGAC others(9558): Show |
chr12 | 111761933 | 111822532 |
a0001c0001t0076 | 0/0 | 9564 | 1 | 1 | 0 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | GAGAC others(9559): Show |
chr12 | 111761933 | 111822532 |
a0001c0001t0077 | 0/0 | 9563 | 1 | 1 | 0 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | GAGAC others(9558): Show |
chr12 | 111761933 | 111822532 |
a0001c0001t0078 | 0/0 | 9564 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | GAGAC others(9559): Show |
chr12 | 111761933 | 111822532 |
a0001c0001t0079 | 0/0 | 9562 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | GAGAC others(9557): Show |
chr12 | 111761933 | 111822532 |
a0001c0001t0080 | 0/0 | 9562 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | GAGAC others(9557): Show |
chr12 | 111761933 | 111822532 |
a0001c0001t0081 | 0/0 | 9568 | 1 | 0 | 0 | 0 | 0 | 1 | ALDH2_chr12_111761933_111822532 | ALDH2 | GAGAC others(9563): Show |
chr12 | 111761933 | 111822532 |
a0001c0001t0082 | 0/0 | 9563 | 1 | 0 | 1 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | GAGAC others(9558): Show |
chr12 | 111761933 | 111822532 |
a0001c0001t0083 | 0/0 | 9563 | 1 | 1 | 0 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | GAGAC others(9558): Show |
chr12 | 111761933 | 111822532 |
a0001c0001t0084 | 0/0 | 9558 | 1 | 1 | 0 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | GAGAC others(9553): Show |
chr12 | 111761933 | 111822532 |
a0001c0001t0085 | 0/0 | 9560 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | GAGAC others(9555): Show |
chr12 | 111761933 | 111822532 |
a0001c0001t0086 | 0/0 | 9560 | 1 | 1 | 0 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | GAGAC others(9555): Show |
chr12 | 111761933 | 111822532 |
a0001c0001t0087 | 0/0 | 9559 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | GAGAC others(9554): Show |
chr12 | 111761933 | 111822532 |
a0001c0001t0088 | 0/0 | 9558 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | GAGAC others(9553): Show |
chr12 | 111761933 | 111822532 |
a0001c0001t0089 | 0/0 | 9558 | 1 | 1 | 0 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | GAGAC others(9553): Show |
chr12 | 111761933 | 111822532 |
a0001c0001t0090 | 0/0 | 9559 | 1 | 1 | 0 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | GAGAC others(9554): Show |
chr12 | 111761933 | 111822532 |
a0001c0001t0091 | 0/0 | 9559 | 1 | 1 | 0 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | GAGAC others(9554): Show |
chr12 | 111761933 | 111822532 |
a0001c0001t0092 | 0/0 | 9562 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | GAGAC others(9557): Show |
chr12 | 111761933 | 111822532 |
a0001c0001t0093 | 0/0 | 9564 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | GAGAC others(9559): Show |
chr12 | 111761933 | 111822532 |
a0001c0001t0094 | 0/0 | 9562 | 1 | 0 | 0 | 0 | 0 | 1 | ALDH2_chr12_111761933_111822532 | ALDH2 | GAGAC others(9557): Show |
chr12 | 111761933 | 111822532 |
a0001c0001t0095 | 0/0 | 9560 | 1 | 1 | 0 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | GAGAC others(9555): Show |
chr12 | 111761933 | 111822532 |
a0001c0001t0096 | 0/0 | 9560 | 1 | 0 | 1 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | GAGAC others(9555): Show |
chr12 | 111761933 | 111822532 |
a0001c0001t0097 | 0/0 | 9562 | 1 | 1 | 0 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | GAGAC others(9557): Show |
chr12 | 111761933 | 111822532 |
a0001c0001t0098 | 0/0 | 9562 | 1 | 1 | 0 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | GAGAC others(9557): Show |
chr12 | 111761933 | 111822532 |
a0001c0001t0099 | 0/0 | 9561 | 1 | 0 | 0 | 0 | 1 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | GAGAC others(9556): Show |
chr12 | 111761933 | 111822532 |
a0001c0001t0100 | 0/0 | 9561 | 1 | 0 | 0 | 0 | 0 | 1 | ALDH2_chr12_111761933_111822532 | ALDH2 | GAGAC others(9556): Show |
chr12 | 111761933 | 111822532 |
a0001c0001t0101 | 0/0 | 9562 | 1 | 0 | 0 | 0 | 0 | 1 | ALDH2_chr12_111761933_111822532 | ALDH2 | GAGAC others(9557): Show |
chr12 | 111761933 | 111822532 |
a0001c0001t0102 | 0/0 | 9560 | 1 | 1 | 0 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | GAGAC others(9555): Show |
chr12 | 111761933 | 111822532 |
a0001c0001t0104 | 0/0 | 9559 | 1 | 0 | 1 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | GAGAC others(9554): Show |
chr12 | 111761933 | 111822532 |
a0001c0001t0105 | 0/0 | 9560 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | GAGAC others(9555): Show |
chr12 | 111761933 | 111822532 |
a0001c0001t0106 | 0/0 | 9561 | 1 | 0 | 0 | 0 | 0 | 1 | ALDH2_chr12_111761933_111822532 | ALDH2 | GAGAC others(9556): Show |
chr12 | 111761933 | 111822532 |
a0001c0001t0107 | 0/0 | 9561 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | GAGAC others(9556): Show |
chr12 | 111761933 | 111822532 |
a0001c0001t0108 | 0/0 | 9561 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | GAGAC others(9556): Show |
chr12 | 111761933 | 111822532 |
a0001c0001t0109 | 0/0 | 9559 | 1 | 1 | 0 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | GAGAC others(9554): Show |
chr12 | 111761933 | 111822532 |
a0001c0001t0110 | 0/0 | 9563 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | GAGAC others(9558): Show |
chr12 | 111761933 | 111822532 |
a0001c0001t0111 | 0/0 | 9562 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | GAGAC others(9557): Show |
chr12 | 111761933 | 111822532 |
a0001c0001t0112 | 0/0 | 9561 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | GAGAC others(9556): Show |
chr12 | 111761933 | 111822532 |
a0001c0001t0113 | 0/0 | 9562 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | GAGAC others(9557): Show |
chr12 | 111761933 | 111822532 |
a0001c0001t0114 | 0/0 | 9560 | 1 | 1 | 0 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | GAGAC others(9555): Show |
chr12 | 111761933 | 111822532 |
a0001c0001t0116 | 0/0 | 9558 | 1 | 1 | 0 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | GAGAC others(9553): Show |
chr12 | 111761933 | 111822532 |
a0001c0001t0118 | 0/0 | 9558 | 1 | 0 | 1 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | GAGAC others(9553): Show |
chr12 | 111761933 | 111822532 |
a0001c0001t0120 | 0/0 | 9561 | 1 | 1 | 0 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | GAGAC others(9556): Show |
chr12 | 111761933 | 111822532 |
a0001c0001t0121 | 0/0 | 9562 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | GAGAC others(9557): Show |
chr12 | 111761933 | 111822532 |
a0001c0001t0122 | 0/0 | 9562 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | GAGAC others(9557): Show |
chr12 | 111761933 | 111822532 |
a0001c0001t0123 | 0/0 | 9564 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | GAGAC others(9559): Show |
chr12 | 111761933 | 111822532 |
a0001c0001t0124 | 0/0 | 9563 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | GAGAC others(9558): Show |
chr12 | 111761933 | 111822532 |
a0001c0001t0125 | 0/0 | 9561 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | GAGAC others(9556): Show |
chr12 | 111761933 | 111822532 |
a0001c0001t0126 | 0/0 | 9562 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | GAGAC others(9557): Show |
chr12 | 111761933 | 111822532 |
a0001c0004t0001 | 0/0 | 9562 | 2 | 0 | 0 | 2 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | GAGAC others(9557): Show |
chr12 | 111761933 | 111822532 |
a0001c0004t0009 | 0/0 | 9561 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | GAGAC others(9556): Show |
chr12 | 111761933 | 111822532 |
a0001c0006t0127 | 0/0 | 9561 | 1 | 1 | 0 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | GAGAC others(9556): Show |
chr12 | 111761933 | 111822532 |
a0001c0007t0017 | 0/0 | 9560 | 1 | 1 | 0 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | GAGAC others(9555): Show |
chr12 | 111761933 | 111822532 |
a0001c0009t0103 | 0/0 | 9562 | 1 | 1 | 0 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | GAGAC others(9557): Show |
chr12 | 111761933 | 111822532 |
a0002c0002t0001 | 0/0 | 9562 | 17 | 0 | 0 | 17 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | GAGAC others(9557): Show |
chr12 | 111761933 | 111822532 |
a0002c0002t0004 | 0/0 | 9562 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | GAGAC others(9557): Show |
chr12 | 111761933 | 111822532 |
a0002c0002t0009 | 0/0 | 9561 | 4 | 0 | 0 | 4 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | GAGAC others(9556): Show |
chr12 | 111761933 | 111822532 |
a0002c0002t0115 | 0/0 | 9561 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | GAGAC others(9556): Show |
chr12 | 111761933 | 111822532 |
a0002c0002t0117 | 0/0 | 9562 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | GAGAC others(9557): Show |
chr12 | 111761933 | 111822532 |
a0002c0002t0119 | 0/0 | 9562 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | GAGAC others(9557): Show |
chr12 | 111761933 | 111822532 |
a0003c0003t0005 | 0/0 | 9562 | 1 | 0 | 0 | 0 | 0 | 1 | ALDH2_chr12_111761933_111822532 | ALDH2 | GAGAC others(9557): Show |
chr12 | 111761933 | 111822532 |
a0003c0003t0027 | 0/0 | 9562 | 2 | 0 | 0 | 0 | 0 | 2 | ALDH2_chr12_111761933_111822532 | ALDH2 | GAGAC others(9557): Show |
chr12 | 111761933 | 111822532 |
a0003c0003t0062 | 0/0 | 9563 | 1 | 0 | 0 | 0 | 0 | 1 | ALDH2_chr12_111761933_111822532 | ALDH2 | GAGAC others(9558): Show |
chr12 | 111761933 | 111822532 |
a0004c0005t0066 | 0/0 | 9563 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | GAGAC others(9558): Show |
chr12 | 111761933 | 111822532 |
a0005c0008t0034 | 0/0 | 9562 | 1 | 1 | 0 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | GAGAC others(9557): Show |
chr12 | 111761933 | 111822532 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0004 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0001g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0002g0001 | 1/0 | 10 | 1 | 7 | 0 | 1 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0002g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0002g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0002g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0002g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0002g0144 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0002g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0002g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0002g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0002g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0002g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0002g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0002g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0002g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0002g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0003g0002 | 0/0 | 6 | 2 | 0 | 4 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0003g0009 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0003g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0003g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0003g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0003g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0003g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0003g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0003g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0004g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0004g0006 | 0/0 | 4 | 1 | 3 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0004g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0004g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0004g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0004g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0004g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0004g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0004g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0005g0021 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0005g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0005g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0005g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0005g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0005g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0005g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0005g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0005g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0006g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0006g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0006g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0006g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0006g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0006g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0006g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0006g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0006g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0007g0011 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0007g0020 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0007g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0007g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0007g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0007g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0007g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0008g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0008g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0008g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0008g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0008g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0008g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0008g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0009g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0009g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0010g0001 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0010g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0010g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0010g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0011g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0011g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0011g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0011g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0012g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0012g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0012g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0012g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0012g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0013g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0013g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0013g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0013g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0013g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0014g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0014g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0014g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0014g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0014g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0014g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0015g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0015g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0015g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0015g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0016g0004 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0016g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0017g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0017g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0018g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0018g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0018g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0019g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0019g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0019g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0020g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0020g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0020g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0021g0002 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0021g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0022g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0022g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0023g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0023g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0023g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0024g0018 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0024g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0025g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0025g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0026g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0026g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0028g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0028g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0029g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0029g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0030g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0030g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0031g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0031g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0032g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0032g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0033g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0033g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0034g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0035g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0035g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0036g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0036g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0037g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0038g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0039g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0040g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0041g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0042g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0043g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0044g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0045g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0046g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0047g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0048g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0049g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0050g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0051g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0052g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0053g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0054g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0055g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0056g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0057g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0058g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0059g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0060g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0061g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0063g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0064g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0065g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0067g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0068g0001 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0069g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0070g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0071g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0072g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0073g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0074g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0075g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0076g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0077g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0078g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0079g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0080g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0081g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0082g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0083g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0084g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0085g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0086g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0087g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0088g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0089g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0090g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0091g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0092g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0093g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0094g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0095g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0096g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0097g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0098g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0099g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0100g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0101g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0102g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0104g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0105g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0106g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0107g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0108g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0109g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0110g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0111g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0112g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0113g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0114g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0116g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0118g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0120g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0121g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0122g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0123g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0124g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0125g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0001t0126g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0004t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0004t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0004t0009g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0006t0127g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0007t0017g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0001c0009t0103g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0002c0002t0001g0003 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0002c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0002c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0002c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0002c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0002c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0002c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0002c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0002c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0002c0002t0004g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0002c0002t0009g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0002c0002t0009g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0002c0002t0009g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0002c0002t0115g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0002c0002t0117g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0002c0002t0119g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0003c0003t0005g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0003c0003t0027g0019 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0003c0003t0062g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0004c0005t0066g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
a0005c0008t0034g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0002 | g0001 | EUR | GBR | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG00099 | hp2 | a0001 | c0001 | t0024 | g0018 | EUR | GBR | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG00140 | hp1 | a0001 | c0001 | t0068 | g0001 | EUR | GBR | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG00140 | hp2 | a0001 | c0001 | t0007 | g0011 | EUR | GBR | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG00408 | hp1 | a0001 | c0001 | t0107 | g0017 | EAS | CHS | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | CHS | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG00438 | hp1 | a0002 | c0002 | t0119 | g0003 | EAS | CHS | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | CHS | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG00544 | hp1 | a0001 | c0001 | t0067 | g0167 | EAS | CHS | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG00544 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | CHS | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG00597 | hp1 | a0001 | c0001 | t0122 | g0203 | EAS | CHS | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG00597 | hp2 | a0001 | c0001 | t0108 | g0075 | EAS | CHS | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG00609 | hp1 | a0001 | c0001 | t0075 | g0070 | EAS | CHS | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG00609 | hp2 | a0001 | c0001 | t0032 | g0138 | EAS | CHS | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG00673 | hp1 | a0001 | c0001 | t0004 | g0226 | EAS | CHS | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG00673 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | CHS | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | PUR | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG00735 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG00738 | hp1 | a0001 | c0001 | t0002 | g0152 | AMR | PUR | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG00738 | hp2 | a0001 | c0001 | t0007 | g0011 | AMR | PUR | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG01071 | hp1 | a0001 | c0001 | t0002 | g0154 | AMR | PUR | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG01099 | hp1 | a0001 | c0001 | t0003 | g0009 | AMR | PUR | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG01099 | hp2 | a0001 | c0001 | t0006 | g0125 | AMR | PUR | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG01106 | hp1 | a0001 | c0001 | t0073 | g0011 | AMR | PUR | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG01106 | hp2 | a0001 | c0001 | t0060 | g0165 | AMR | PUR | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG01109 | hp1 | a0001 | c0001 | t0002 | g0024 | AMR | PUR | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG01109 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG01167 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG01167 | hp2 | a0001 | c0001 | t0012 | g0033 | AMR | PUR | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG01168 | hp1 | a0001 | c0001 | t0011 | g0031 | AMR | PUR | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG01168 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG01169 | hp1 | a0001 | c0001 | t0002 | g0025 | AMR | PUR | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG01169 | hp2 | a0001 | c0001 | t0011 | g0031 | AMR | PUR | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG01175 | hp1 | a0001 | c0001 | t0024 | g0018 | AMR | PUR | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG01175 | hp2 | a0001 | c0001 | t0006 | g0126 | AMR | PUR | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG01192 | hp1 | a0001 | c0001 | t0002 | g0155 | AMR | PUR | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG01192 | hp2 | a0001 | c0001 | t0002 | g0160 | AMR | PUR | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG01243 | hp1 | a0001 | c0001 | t0104 | g0010 | AMR | PUR | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG01243 | hp2 | a0001 | c0001 | t0082 | g0240 | AMR | PUR | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG01256 | hp1 | a0001 | c0001 | t0002 | g0145 | AMR | CLM | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG01256 | hp2 | a0001 | c0001 | t0004 | g0182 | AMR | CLM | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG01257 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG01257 | hp2 | a0001 | c0001 | t0028 | g0001 | AMR | CLM | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG01258 | hp1 | a0001 | c0001 | t0004 | g0185 | AMR | CLM | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG01258 | hp2 | a0001 | c0001 | t0028 | g0148 | AMR | CLM | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG01361 | hp1 | a0001 | c0001 | t0047 | g0146 | AMR | CLM | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG01361 | hp2 | a0001 | c0001 | t0096 | g0076 | AMR | CLM | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG01433 | hp1 | a0001 | c0001 | t0069 | g0001 | AMR | CLM | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG01433 | hp2 | a0001 | c0001 | t0016 | g0189 | AMR | CLM | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG01496 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | CLM | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG01884 | hp1 | a0001 | c0001 | t0029 | g0122 | AFR | ACB | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG01884 | hp2 | a0001 | c0001 | t0014 | g0179 | AFR | ACB | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG01891 | hp1 | a0001 | c0001 | t0102 | g0123 | AFR | ACB | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG01891 | hp2 | a0001 | c0009 | t0103 | g0231 | AFR | ACB | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG01928 | hp1 | a0001 | c0001 | t0010 | g0001 | AMR | PEL | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG01928 | hp2 | a0001 | c0001 | t0004 | g0006 | AMR | PEL | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | PEL | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG01934 | hp2 | a0001 | c0001 | t0010 | g0012 | AMR | PEL | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG01943 | hp1 | a0001 | c0001 | t0002 | g0025 | AMR | PEL | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG01943 | hp2 | a0001 | c0001 | t0040 | g0042 | AMR | PEL | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG01952 | hp1 | a0001 | c0001 | t0072 | g0001 | AMR | PEL | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG01952 | hp2 | a0001 | c0001 | t0004 | g0006 | AMR | PEL | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG01993 | hp1 | a0001 | c0001 | t0005 | g0111 | AMR | PEL | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG01993 | hp2 | a0001 | c0001 | t0004 | g0204 | AMR | PEL | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG02027 | hp1 | a0001 | c0001 | t0031 | g0086 | EAS | KHV | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | KHV | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG02040 | hp1 | a0001 | c0001 | t0121 | g0068 | EAS | KHV | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG02040 | hp2 | a0001 | c0001 | t0036 | g0171 | EAS | KHV | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG02055 | hp1 | a0001 | c0001 | t0097 | g0084 | AFR | ACB | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG02055 | hp2 | a0001 | c0001 | t0011 | g0230 | AFR | ACB | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG02056 | hp1 | a0001 | c0001 | t0008 | g0074 | EAS | KHV | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG02056 | hp2 | a0001 | c0001 | t0002 | g0157 | EAS | KHV | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG02071 | hp1 | a0001 | c0001 | t0008 | g0017 | EAS | KHV | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG02071 | hp2 | a0001 | c0001 | t0016 | g0004 | EAS | KHV | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG02074 | hp1 | a0004 | c0005 | t0066 | g0097 | EAS | KHV | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG02074 | hp2 | a0001 | c0001 | t0004 | g0202 | EAS | KHV | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG02080 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | KHV | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG02080 | hp2 | a0001 | c0004 | t0001 | g0243 | EAS | KHV | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG02129 | hp2 | a0001 | c0001 | t0008 | g0091 | EAS | KHV | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG02132 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | KHV | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG02132 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | KHV | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | KHV | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG02135 | hp2 | a0001 | c0001 | t0080 | g0112 | EAS | KHV | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG02145 | hp1 | a0001 | c0001 | t0014 | g0177 | AFR | ACB | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG02145 | hp2 | a0001 | c0001 | t0021 | g0002 | AFR | ACB | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG02148 | hp1 | a0001 | c0001 | t0010 | g0161 | AMR | PEL | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG02148 | hp2 | a0001 | c0001 | t0004 | g0006 | AMR | PEL | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG02165 | hp1 | a0001 | c0001 | t0020 | g0065 | EAS | CDX | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CDX | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG02257 | hp1 | a0001 | c0001 | t0035 | g0005 | AFR | ACB | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG02257 | hp2 | a0001 | c0001 | t0039 | g0041 | AFR | ACB | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG02258 | hp1 | a0001 | c0001 | t0002 | g0217 | AFR | ACB | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG02258 | hp2 | a0001 | c0001 | t0014 | g0085 | AFR | ACB | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG02273 | hp1 | a0001 | c0001 | t0118 | g0210 | AMR | PEL | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG02273 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG02280 | hp1 | a0001 | c0001 | t0019 | g0233 | AFR | ACB | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG02280 | hp2 | a0001 | c0001 | t0011 | g0007 | AFR | ACB | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG02451 | hp1 | a0001 | c0001 | t0002 | g0147 | AFR | ACB | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG02451 | hp2 | a0001 | c0001 | t0089 | g0172 | AFR | ACB | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG02523 | hp1 | a0001 | c0001 | t0031 | g0066 | EAS | KHV | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG02523 | hp2 | a0001 | c0001 | t0020 | g0153 | EAS | KHV | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG02572 | hp1 | a0001 | c0001 | t0002 | g0133 | AFR | GWD | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG02572 | hp2 | a0001 | c0001 | t0076 | g0007 | AFR | GWD | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG02602 | hp1 | a0003 | c0003 | t0005 | g0094 | SAS | PJL | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG02602 | hp2 | a0001 | c0001 | t0005 | g0021 | SAS | PJL | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG02622 | hp1 | a0001 | c0001 | t0091 | g0027 | AFR | GWD | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG02622 | hp2 | a0001 | c0001 | t0014 | g0178 | AFR | GWD | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG02630 | hp1 | a0001 | c0001 | t0019 | g0015 | AFR | GWD | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG02630 | hp2 | a0001 | c0001 | t0002 | g0130 | AFR | GWD | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG02683 | hp1 | a0001 | c0001 | t0065 | g0026 | SAS | PJL | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG02683 | hp2 | a0001 | c0001 | t0021 | g0002 | SAS | PJL | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG02717 | hp1 | a0005 | c0008 | t0034 | g0005 | AFR | GWD | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG02717 | hp2 | a0001 | c0001 | t0017 | g0038 | AFR | GWD | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG02723 | hp1 | a0001 | c0001 | t0023 | g0175 | AFR | GWD | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG02723 | hp2 | a0001 | c0001 | t0012 | g0008 | AFR | GWD | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG02735 | hp1 | a0001 | c0001 | t0043 | g0105 | SAS | PJL | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG02735 | hp2 | a0001 | c0001 | t0042 | g0229 | SAS | PJL | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG02738 | hp1 | a0001 | c0001 | t0003 | g0077 | SAS | PJL | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG02738 | hp2 | a0001 | c0001 | t0002 | g0026 | SAS | PJL | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG02809 | hp1 | a0001 | c0001 | t0025 | g0036 | AFR | GWD | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG02809 | hp2 | a0001 | c0001 | t0034 | g0005 | AFR | GWD | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG02818 | hp1 | a0001 | c0001 | t0095 | g0174 | AFR | GWD | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG02818 | hp2 | a0001 | c0001 | t0012 | g0034 | AFR | GWD | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG02886 | hp1 | a0001 | c0001 | t0026 | g0236 | AFR | GWD | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG02886 | hp2 | a0001 | c0001 | t0003 | g0009 | AFR | GWD | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG02896 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | GWD | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG02896 | hp2 | a0001 | c0001 | t0014 | g0044 | AFR | GWD | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG02897 | hp1 | a0001 | c0001 | t0014 | g0045 | AFR | GWD | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG02897 | hp2 | a0001 | c0001 | t0084 | g0027 | AFR | GWD | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG02965 | hp1 | a0001 | c0001 | t0006 | g0108 | AFR | ESN | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG02965 | hp2 | a0001 | c0001 | t0017 | g0035 | AFR | ESN | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG02970 | hp1 | a0001 | c0001 | t0006 | g0109 | AFR | ESN | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG02970 | hp2 | a0001 | c0001 | t0056 | g0053 | AFR | ESN | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG02976 | hp1 | a0001 | c0001 | t0052 | g0168 | AFR | ESN | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG02976 | hp2 | a0001 | c0006 | t0127 | g0170 | AFR | ESN | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0206 | SAS | PJL | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG03017 | hp2 | a0001 | c0001 | t0007 | g0100 | SAS | PJL | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG03041 | hp1 | a0001 | c0001 | t0041 | g0024 | AFR | GWD | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG03041 | hp2 | a0001 | c0001 | t0114 | g0005 | AFR | GWD | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG03098 | hp1 | a0001 | c0001 | t0006 | g0022 | AFR | MSL | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG03098 | hp2 | a0001 | c0001 | t0058 | g0117 | AFR | MSL | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG03130 | hp1 | a0001 | c0007 | t0017 | g0040 | AFR | ESN | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG03130 | hp2 | a0001 | c0001 | t0044 | g0054 | AFR | ESN | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG03139 | hp1 | a0001 | c0001 | t0024 | g0072 | AFR | ESN | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG03139 | hp2 | a0001 | c0001 | t0023 | g0176 | AFR | ESN | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG03195 | hp1 | a0001 | c0001 | t0086 | g0051 | AFR | ESN | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG03195 | hp2 | a0001 | c0001 | t0051 | g0134 | AFR | ESN | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG03209 | hp1 | a0001 | c0001 | t0002 | g0095 | AFR | MSL | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG03209 | hp2 | a0001 | c0001 | t0002 | g0163 | AFR | MSL | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG03225 | hp1 | a0001 | c0001 | t0090 | g0169 | AFR | MSL | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG03225 | hp2 | a0001 | c0001 | t0055 | g0015 | AFR | MSL | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0187 | SAS | PJL | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG03239 | hp2 | a0001 | c0001 | t0010 | g0001 | SAS | PJL | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG03453 | hp1 | a0001 | c0001 | t0011 | g0241 | AFR | MSL | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG03453 | hp2 | a0001 | c0001 | t0003 | g0002 | AFR | MSL | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG03486 | hp1 | a0001 | c0001 | t0021 | g0232 | AFR | MSL | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG03486 | hp2 | a0001 | c0001 | t0098 | g0008 | AFR | MSL | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG03491 | hp1 | a0001 | c0001 | t0063 | g0099 | SAS | PJL | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG03491 | hp2 | a0003 | c0003 | t0027 | g0019 | SAS | PJL | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG03492 | hp1 | a0001 | c0001 | t0002 | g0135 | SAS | PJL | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG03492 | hp2 | a0003 | c0003 | t0027 | g0019 | SAS | PJL | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG03516 | hp1 | a0001 | c0001 | t0003 | g0056 | AFR | ESN | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG03516 | hp2 | a0001 | c0001 | t0057 | g0023 | AFR | ESN | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG03540 | hp1 | a0001 | c0001 | t0030 | g0235 | AFR | GWD | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG03540 | hp2 | a0001 | c0001 | t0026 | g0121 | AFR | GWD | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG03579 | hp1 | a0001 | c0001 | t0012 | g0008 | AFR | MSL | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG03579 | hp2 | a0001 | c0001 | t0011 | g0007 | AFR | MSL | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG03654 | hp1 | a0001 | c0001 | t0106 | g0002 | SAS | PJL | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG03654 | hp2 | a0001 | c0001 | t0006 | g0164 | SAS | PJL | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG03669 | hp1 | a0001 | c0001 | t0010 | g0001 | SAS | PJL | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG03669 | hp2 | a0001 | c0001 | t0005 | g0215 | SAS | PJL | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG03688 | hp1 | a0001 | c0001 | t0074 | g0103 | SAS | STU | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG03688 | hp2 | a0001 | c0001 | t0100 | g0047 | SAS | STU | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG03704 | hp1 | a0001 | c0001 | t0070 | g0158 | SAS | PJL | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG03704 | hp2 | a0001 | c0001 | t0037 | g0030 | SAS | PJL | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG03710 | hp1 | a0001 | c0001 | t0018 | g0136 | SAS | PJL | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG03710 | hp2 | a0001 | c0001 | t0018 | g0124 | SAS | PJL | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG03831 | hp1 | a0001 | c0001 | t0045 | g0012 | SAS | BEB | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG03831 | hp2 | a0003 | c0003 | t0062 | g0118 | SAS | BEB | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG03927 | hp1 | a0001 | c0001 | t0101 | g0002 | SAS | BEB | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG03927 | hp2 | a0001 | c0001 | t0006 | g0142 | SAS | BEB | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG04115 | hp1 | a0001 | c0001 | t0081 | g0120 | SAS | STU | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG04115 | hp2 | a0001 | c0001 | t0094 | g0010 | SAS | STU | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG04184 | hp1 | a0001 | c0001 | t0061 | g0030 | SAS | BEB | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG04184 | hp2 | a0001 | c0001 | t0007 | g0242 | SAS | BEB | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG04204 | hp1 | a0001 | c0001 | t0016 | g0004 | SAS | STU | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG04204 | hp2 | a0001 | c0001 | t0007 | g0107 | SAS | STU | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG04228 | hp1 | a0001 | c0001 | t0048 | g0228 | SAS | STU | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG04228 | hp2 | a0001 | c0001 | t0010 | g0159 | SAS | STU | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
NA18906 | hp1 | a0001 | c0001 | t0035 | g0183 | AFR | YRI | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
NA18906 | hp2 | a0001 | c0001 | t0077 | g0007 | AFR | YRI | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
NA18942 | hp1 | a0001 | c0001 | t0064 | g0001 | EAS | JPT | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
NA18943 | hp2 | a0001 | c0001 | t0005 | g0119 | EAS | JPT | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
NA18945 | hp1 | a0001 | c0001 | t0113 | g0002 | EAS | JPT | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
NA18946 | hp1 | a0001 | c0001 | t0085 | g0092 | EAS | JPT | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
NA18946 | hp2 | a0002 | c0002 | t0009 | g0003 | EAS | JPT | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
NA18947 | hp1 | a0001 | c0001 | t0004 | g0014 | EAS | JPT | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
NA18947 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
NA18948 | hp1 | a0001 | c0001 | t0015 | g0129 | EAS | JPT | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
NA18949 | hp1 | a0001 | c0001 | t0005 | g0098 | EAS | JPT | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
NA18949 | hp2 | a0001 | c0001 | t0003 | g0071 | EAS | JPT | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
NA18950 | hp1 | a0001 | c0001 | t0111 | g0057 | EAS | JPT | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
NA18951 | hp1 | a0001 | c0001 | t0105 | g0067 | EAS | JPT | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
NA18951 | hp2 | a0002 | c0002 | t0009 | g0003 | EAS | JPT | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
NA18952 | hp1 | a0001 | c0001 | t0018 | g0104 | EAS | JPT | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
NA18952 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
NA18954 | hp1 | a0002 | c0002 | t0117 | g0003 | EAS | JPT | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
NA18954 | hp2 | a0001 | c0001 | t0079 | g0113 | EAS | JPT | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
NA18957 | hp1 | a0001 | c0001 | t0125 | g0198 | EAS | JPT | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
NA18957 | hp2 | a0001 | c0001 | t0009 | g0181 | EAS | JPT | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
NA18959 | hp1 | a0001 | c0001 | t0003 | g0082 | EAS | JPT | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
NA18959 | hp2 | a0001 | c0001 | t0123 | g0220 | EAS | JPT | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
NA18960 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
NA18960 | hp2 | a0001 | c0001 | t0004 | g0014 | EAS | JPT | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
NA18961 | hp1 | a0001 | c0004 | t0001 | g0201 | EAS | JPT | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
NA18961 | hp2 | a0001 | c0001 | t0078 | g0140 | EAS | JPT | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
NA18964 | hp1 | a0001 | c0001 | t0032 | g0002 | EAS | JPT | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
NA18965 | hp1 | a0001 | c0001 | t0008 | g0064 | EAS | JPT | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
NA18965 | hp2 | a0001 | c0001 | t0004 | g0211 | EAS | JPT | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
NA18967 | hp1 | a0001 | c0001 | t0093 | g0218 | EAS | JPT | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
NA18968 | hp1 | a0002 | c0002 | t0001 | g0190 | EAS | JPT | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
NA18968 | hp2 | a0001 | c0001 | t0088 | g0002 | EAS | JPT | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
NA18969 | hp1 | a0001 | c0001 | t0016 | g0004 | EAS | JPT | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
NA18969 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
NA18971 | hp1 | a0001 | c0001 | t0022 | g0002 | EAS | JPT | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
NA18971 | hp2 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
NA18975 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
NA18975 | hp2 | a0001 | c0001 | t0126 | g0114 | EAS | JPT | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
NA18978 | hp1 | a0001 | c0001 | t0112 | g0073 | EAS | JPT | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
NA18978 | hp2 | a0001 | c0001 | t0033 | g0197 | EAS | JPT | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
NA18979 | hp1 | a0001 | c0001 | t0006 | g0141 | EAS | JPT | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
NA18979 | hp2 | a0001 | c0001 | t0006 | g0012 | EAS | JPT | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
NA18980 | hp1 | a0001 | c0001 | t0022 | g0010 | EAS | JPT | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
NA18980 | hp2 | a0002 | c0002 | t0004 | g0193 | EAS | JPT | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
NA18981 | hp2 | a0001 | c0001 | t0013 | g0058 | EAS | JPT | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
NA18984 | hp1 | a0001 | c0001 | t0002 | g0156 | EAS | JPT | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
NA18984 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
NA18985 | hp1 | a0001 | c0001 | t0002 | g0139 | EAS | JPT | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
NA18985 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
NA18986 | hp1 | a0001 | c0001 | t0020 | g0162 | EAS | JPT | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
NA18986 | hp2 | a0002 | c0002 | t0009 | g0184 | EAS | JPT | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
NA18987 | hp1 | a0002 | c0002 | t0001 | g0192 | EAS | JPT | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
NA18987 | hp2 | a0001 | c0001 | t0013 | g0090 | EAS | JPT | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
NA18989 | hp1 | a0001 | c0001 | t0009 | g0223 | EAS | JPT | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
NA18989 | hp2 | a0001 | c0001 | t0013 | g0063 | EAS | JPT | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
NA18992 | hp1 | a0001 | c0001 | t0005 | g0021 | EAS | JPT | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
NA18992 | hp2 | a0001 | c0001 | t0003 | g0089 | EAS | JPT | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
NA18994 | hp1 | a0002 | c0002 | t0001 | g0208 | EAS | JPT | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
NA18994 | hp2 | a0001 | c0001 | t0003 | g0088 | EAS | JPT | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
NA19000 | hp1 | a0001 | c0004 | t0009 | g0004 | EAS | JPT | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
NA19000 | hp2 | a0001 | c0001 | t0008 | g0093 | EAS | JPT | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
NA19002 | hp1 | a0001 | c0001 | t0015 | g0128 | EAS | JPT | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
NA19004 | hp1 | a0002 | c0002 | t0009 | g0194 | EAS | JPT | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
NA19004 | hp2 | a0001 | c0001 | t0007 | g0131 | EAS | JPT | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
NA19007 | hp2 | a0001 | c0001 | t0046 | g0001 | EAS | JPT | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
NA19009 | hp1 | a0001 | c0001 | t0008 | g0043 | EAS | JPT | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
NA19009 | hp2 | a0001 | c0001 | t0124 | g0213 | EAS | JPT | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
NA19011 | hp1 | a0001 | c0001 | t0005 | g0106 | EAS | JPT | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
NA19011 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
NA19012 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
NA19012 | hp2 | a0001 | c0001 | t0013 | g0059 | EAS | JPT | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
NA19030 | hp1 | a0001 | c0001 | t0083 | g0110 | AFR | LWK | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
NA19030 | hp2 | a0001 | c0001 | t0038 | g0037 | AFR | LWK | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
NA19043 | hp1 | a0001 | c0001 | t0053 | g0023 | AFR | LWK | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
NA19043 | hp2 | a0001 | c0001 | t0003 | g0055 | AFR | LWK | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
NA19054 | hp1 | a0001 | c0001 | t0005 | g0188 | EAS | JPT | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
NA19054 | hp2 | a0002 | c0002 | t0001 | g0115 | EAS | JPT | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
NA19056 | hp1 | a0001 | c0001 | t0087 | g0048 | EAS | JPT | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
NA19056 | hp2 | a0001 | c0001 | t0015 | g0150 | EAS | JPT | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
NA19057 | hp1 | a0001 | c0001 | t0013 | g0016 | EAS | JPT | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
NA19057 | hp2 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
NA19063 | hp2 | a0001 | c0001 | t0007 | g0132 | EAS | JPT | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
NA19065 | hp1 | a0001 | c0001 | t0005 | g0116 | EAS | JPT | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
NA19065 | hp2 | a0001 | c0001 | t0022 | g0002 | EAS | JPT | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
NA19066 | hp2 | a0001 | c0001 | t0059 | g0101 | EAS | JPT | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
NA19067 | hp2 | a0001 | c0001 | t0002 | g0166 | EAS | JPT | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
NA19068 | hp2 | a0001 | c0001 | t0003 | g0083 | EAS | JPT | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
NA19070 | hp1 | a0001 | c0001 | t0036 | g0180 | EAS | JPT | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
NA19070 | hp2 | a0001 | c0001 | t0013 | g0016 | EAS | JPT | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
NA19074 | hp1 | a0002 | c0002 | t0115 | g0003 | EAS | JPT | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
NA19074 | hp2 | a0001 | c0001 | t0003 | g0069 | EAS | JPT | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
NA19079 | hp1 | a0001 | c0001 | t0071 | g0143 | EAS | JPT | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
NA19079 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
NA19081 | hp1 | a0002 | c0002 | t0001 | g0191 | EAS | JPT | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
NA19081 | hp2 | a0001 | c0001 | t0092 | g0049 | EAS | JPT | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
NA19082 | hp1 | a0001 | c0001 | t0033 | g0014 | EAS | JPT | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
NA19082 | hp2 | a0001 | c0001 | t0012 | g0052 | EAS | JPT | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
NA19083 | hp1 | a0001 | c0001 | t0002 | g0216 | EAS | JPT | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
NA19083 | hp2 | a0001 | c0001 | t0003 | g0087 | EAS | JPT | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
NA19084 | hp2 | a0001 | c0001 | t0008 | g0062 | EAS | JPT | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
NA19085 | hp1 | a0001 | c0001 | t0015 | g0001 | EAS | JPT | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
NA19085 | hp2 | a0002 | c0002 | t0001 | g0195 | EAS | JPT | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
NA19087 | hp1 | a0001 | c0001 | t0002 | g0137 | EAS | JPT | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
NA19087 | hp2 | a0001 | c0001 | t0003 | g0079 | EAS | JPT | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
NA19088 | hp1 | a0001 | c0001 | t0110 | g0080 | EAS | JPT | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
NA19091 | hp1 | a0002 | c0002 | t0001 | g0196 | EAS | JPT | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
NA19091 | hp2 | a0001 | c0001 | t0005 | g0102 | EAS | JPT | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
NA19240 | hp1 | a0001 | c0001 | t0023 | g0173 | AFR | YRI | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
NA19240 | hp2 | a0001 | c0001 | t0120 | g0239 | AFR | YRI | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
NA20129 | hp1 | a0001 | c0001 | t0025 | g0039 | AFR | ASW | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
NA20129 | hp2 | a0001 | c0001 | t0003 | g0002 | AFR | ASW | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
NA20752 | hp1 | a0001 | c0001 | t0099 | g0078 | EUR | TSI | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
NA20752 | hp2 | a0001 | c0001 | t0007 | g0020 | EUR | TSI | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
NA20905 | hp1 | a0001 | c0001 | t0002 | g0149 | SAS | GIH | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
NA20905 | hp2 | a0001 | c0001 | t0007 | g0020 | SAS | GIH | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG01123 | hp1 | a0001 | c0001 | t0002 | g0151 | AMR | CLM | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG02109 | hp1 | a0001 | c0001 | t0116 | g0005 | AFR | ACB | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG02109 | hp2 | a0001 | c0001 | t0019 | g0238 | AFR | ACB | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG02486 | hp1 | a0001 | c0001 | t0049 | g0032 | AFR | ACB | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG02486 | hp2 | a0001 | c0001 | t0012 | g0050 | AFR | ACB | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG02559 | hp1 | a0001 | c0001 | t0030 | g0237 | AFR | ACB | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG02559 | hp2 | a0001 | c0001 | t0109 | g0127 | AFR | ACB | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG03471 | hp1 | a0001 | c0001 | t0029 | g0096 | AFR | MSL | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
HG03471 | hp2 | a0001 | c0001 | t0003 | g0009 | AFR | MSL | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
NA18955 | hp1 | a0001 | c0001 | t0050 | g0013 | EAS | JPT | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
NA18955 | hp2 | a0002 | c0002 | t0001 | g0212 | EAS | JPT | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
NA20300 | hp1 | a0001 | c0001 | t0003 | g0081 | AFR | USA | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
NA20300 | hp2 | a0001 | c0001 | t0004 | g0006 | AFR | USA | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
NA21309 | hp1 | a0001 | c0001 | t0054 | g0234 | AFR | LWK | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
NA21309 | hp2 | a0001 | c0001 | t0006 | g0022 | AFR | LWK | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0144 | REF | REF | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0001 | REF | REF | ALDH2_chr12_111761933_111822532 | ALDH2 | chr12 | 111761933 | 111822532 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:111790546 | C | A | 1 | a0004 | 1 | HG02074.hp1 | missense_variant | MODERATE | c.665C>A | p.Ala222Asp | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 6/13 | 715/9561 | 665/1554 | 222/517 | chr12 | 111790546 | |||
chr12:111791355 | C | T | 1 | a0003 | 4 | HG02602.hp1 HG03491.hp2 HG03492.hp2 others(1): Show |
missense_variant | MODERATE | c.731C>T | p.Thr244Met | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 7/13 | 781/9561 | 731/1554 | 244/517 | chr12 | 111791355 | |||
chr12:111798121 | C | T | 1 | a0005 | 1 | HG02717.hp1 | missense_variant | MODERATE | c.1127C>T | p.Thr376Met | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 10/13 | 1177/9561 | 1127/1554 | 376/517 | chr12 | 111798121 | |||
chr12:111803962 | G | A | 1 | a0002 | 25 | HG00438.hp1 HG00544.hp2 HG00673.hp2 others(22): Show |
missense_variant | MODERATE | c.1510G>A | p.Glu504Lys | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 12/13 | 1560/9561 | 1510/1554 | 504/517 | chr12 | 111803962 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:111783251 | C | T | 1 | a0001c0004 | 3 | HG02080.hp2 NA18961.hp1 NA19000.hp1 |
synonymous_variant | LOW | c.313C>T | p.Leu105Leu | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 3/13 | 363/9561 | 313/1554 | 105/517 | chr12 | 111783251 | |||
chr12:111792115 | T | C | 1 | a0001c0006 | 1 | HG02976.hp2 | synonymous_variant | LOW | c.850T>C | p.Leu284Leu | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 8/13 | 900/9561 | 850/1554 | 284/517 | chr12 | 111792115 | |||
chr12:111792614 | A | G | 1 | a0001c0009 | 1 | HG01891.hp2 | synonymous_variant | LOW | c.915A>G | p.Glu305Glu | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 9/13 | 965/9561 | 915/1554 | 305/517 | chr12 | 111792614 | |||
chr12:111799980 | G | A | 1 | a0001c0007 | 1 | HG03130.hp1 | synonymous_variant | LOW | c.1323G>A | p.Thr441Thr | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 11/13 | 1373/9561 | 1323/1554 | 441/517 | chr12 | 111799980 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:111766952 | C | A | 1 | a0001c0001t0037 | 1 | HG03704.hp2 | 5_prime_UTR_variant | MODIFIER | c.-31C>A | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 1/13 | 31 | chr12 | 111766952 | ||||||
chr12:111809728 | T | C | 6 | a0001c0001t0017 a0001c0001t0025 a0001c0001t0038 others(3): Show |
8 | HG01943.hp2 HG02257.hp2 HG02717.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*153T>C | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 13/13 | 153 | chr12 | 111809728 | ||||||
chr12:111809867 | C | T | 1 | a0001c0006t0127 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*292C>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 13/13 | 292 | chr12 | 111809867 | ||||||
chr12:111810040 | C | T | 1 | a0001c0001t0126 | 1 | NA18975.hp2 | 3_prime_UTR_variant | MODIFIER | c.*465C>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 13/13 | 465 | chr12 | 111810040 | ||||||
chr12:111810388 | C | T | 26 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0009 others(23): Show |
94 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(91): Show |
3_prime_UTR_variant | MODIFIER | c.*813C>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 13/13 | 813 | chr12 | 111810388 | ||||||
chr12:111810408 | TTC | T | 41 | a0001c0001t0003 a0001c0001t0008 a0001c0001t0012 others(38): Show |
92 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(89): Show |
3_prime_UTR_variant | MODIFIER | c.*835_*836delCT | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 13/13 | 835 | INFO_REALIGN_3_PRIME | chr12 | 111810408 | |||||
chr12:111810465 | T | G | 32 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0009 others(29): Show |
102 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(99): Show |
3_prime_UTR_variant | MODIFIER | c.*890T>G | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 13/13 | 890 | chr12 | 111810465 | ||||||
chr12:111810605 | A | AT | 12 | a0001c0001t0020 a0001c0001t0029 a0001c0001t0030 others(9): Show |
16 | HG01243.hp2 HG01884.hp1 HG02165.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1050dupT | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 13/13 | 1051 | INFO_REALIGN_3_PRIME | chr12 | 111810605 | |||||
chr12:111810605 | A | T | 2 | a0001c0001t0036 a0001c0001t0125 |
3 | HG02040.hp2 NA18957.hp1 NA19070.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1030A>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 13/13 | 1030 | chr12 | 111810605 | ||||||
chr12:111810605 | AT | A | 12 | a0001c0001t0018 a0001c0001t0041 a0001c0001t0042 others(9): Show |
14 | HG02451.hp2 HG02735.hp1 HG02735.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1050delT | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 13/13 | 1050 | INFO_REALIGN_3_PRIME | chr12 | 111810605 | |||||
chr12:111810670 | C | T | 1 | a0001c0001t0122 | 1 | HG00597.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1095C>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 13/13 | 1095 | chr12 | 111810670 | ||||||
chr12:111810692 | C | T | 4 | a0001c0001t0078 a0001c0001t0079 a0001c0001t0080 others(1): Show |
4 | HG02135.hp2 NA18954.hp2 NA18961.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1117C>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 13/13 | 1117 | chr12 | 111810692 | ||||||
chr12:111810836 | G | A | 3 | a0001c0001t0084 a0001c0001t0090 a0001c0001t0091 |
3 | HG02622.hp1 HG02897.hp2 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1261G>A | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 13/13 | 1261 | chr12 | 111810836 | ||||||
chr12:111811149 | C | T | 1 | a0001c0001t0032 | 2 | HG00609.hp2 NA18964.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1574C>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 13/13 | 1574 | chr12 | 111811149 | ||||||
chr12:111811182 | C | CA | 19 | a0001c0001t0010 a0001c0001t0026 a0001c0001t0031 others(16): Show |
26 | HG01361.hp1 HG01361.hp2 HG01928.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*1624dupA | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 13/13 | 1625 | INFO_REALIGN_3_PRIME | chr12 | 111811182 | |||||
chr12:111811182 | CA | C | 24 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0009 others(21): Show |
88 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(85): Show |
3_prime_UTR_variant | MODIFIER | c.*1624delA | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 13/13 | 1624 | INFO_REALIGN_3_PRIME | chr12 | 111811182 | |||||
chr12:111811336 | A | C | 32 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0009 others(29): Show |
102 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(99): Show |
3_prime_UTR_variant | MODIFIER | c.*1761A>C | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 13/13 | 1761 | chr12 | 111811336 | ||||||
chr12:111811466 | C | CT | 4 | a0001c0001t0011 a0001c0001t0049 a0001c0001t0076 others(1): Show |
9 | HG01168.hp1 HG01169.hp2 HG02055.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1902dupT | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 13/13 | 1903 | INFO_REALIGN_3_PRIME | chr12 | 111811466 | |||||
chr12:111811513 | G | A | 1 | a0001c0001t0050 | 1 | NA18955.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1938G>A | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 13/13 | 1938 | chr12 | 111811513 | ||||||
chr12:111811721 | A | G | 1 | a0001c0001t0028 | 2 | HG01257.hp2 HG01258.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2146A>G | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 13/13 | 2146 | chr12 | 111811721 | ||||||
chr12:111811919 | C | T | 1 | a0001c0001t0121 | 1 | HG02040.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2344C>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 13/13 | 2344 | chr12 | 111811919 | ||||||
chr12:111811947 | C | A | 1 | a0001c0001t0051 | 1 | HG03195.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2372C>A | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 13/13 | 2372 | chr12 | 111811947 | ||||||
chr12:111812031 | G | A | 1 | a0001c0001t0052 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2456G>A | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 13/13 | 2456 | chr12 | 111812031 | ||||||
chr12:111812080 | T | G | 92 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(89): Show |
223 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(220): Show |
3_prime_UTR_variant | MODIFIER | c.*2505T>G | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 13/13 | 2505 | chr12 | 111812080 | ||||||
chr12:111812288 | T | C | 1 | a0001c0001t0123 | 1 | NA18959.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2713T>C | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 13/13 | 2713 | chr12 | 111812288 | ||||||
chr12:111812354 | G | A | 35 | a0001c0001t0003 a0001c0001t0008 a0001c0001t0012 others(32): Show |
77 | HG00408.hp1 HG00597.hp2 HG00609.hp2 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*2779G>A | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 13/13 | 2779 | chr12 | 111812354 | ||||||
chr12:111812396 | G | A | 6 | a0001c0001t0014 a0001c0001t0023 a0001c0001t0024 others(3): Show |
15 | HG00099.hp2 HG01175.hp1 HG01361.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*2821G>A | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 13/13 | 2821 | chr12 | 111812396 | ||||||
chr12:111812545 | T | C | 5 | a0001c0001t0012 a0001c0001t0086 a0001c0001t0092 others(2): Show |
10 | HG01167.hp2 HG02055.hp1 HG02486.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2970T>C | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 13/13 | 2970 | chr12 | 111812545 | ||||||
chr12:111812548 | A | G | 6 | a0001c0001t0014 a0001c0001t0023 a0001c0001t0024 others(3): Show |
15 | HG00099.hp2 HG01175.hp1 HG01361.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*2973A>G | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 13/13 | 2973 | chr12 | 111812548 | ||||||
chr12:111812631 | T | C | 31 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0009 others(28): Show |
101 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(98): Show |
3_prime_UTR_variant | MODIFIER | c.*3056T>C | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 13/13 | 3056 | chr12 | 111812631 | ||||||
chr12:111812669 | G | C | 1 | a0001c0001t0060 | 1 | HG01106.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3094G>C | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 13/13 | 3094 | chr12 | 111812669 | ||||||
chr12:111812822 | G | A | 1 | a0001c0001t0099 | 1 | NA20752.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3247G>A | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 13/13 | 3247 | chr12 | 111812822 | ||||||
chr12:111812850 | C | G | 1 | a0001c0001t0109 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3275C>G | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 13/13 | 3275 | chr12 | 111812850 | ||||||
chr12:111813097 | A | T | 1 | a0001c0001t0082 | 1 | HG01243.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3522A>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 13/13 | 3522 | chr12 | 111813097 | ||||||
chr12:111813255 | A | G | 1 | a0001c0001t0043 | 1 | HG02735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3680A>G | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 13/13 | 3680 | chr12 | 111813255 | ||||||
chr12:111813286 | C | G | 3 | a0001c0001t0008 a0001c0001t0075 a0001c0001t0108 |
9 | HG00597.hp2 HG00609.hp1 HG02056.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3711C>G | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 13/13 | 3711 | chr12 | 111813286 | ||||||
chr12:111813339 | G | A | 2 | a0001c0001t0037 a0001c0001t0061 |
2 | HG03704.hp2 HG04184.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3764G>A | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 13/13 | 3764 | chr12 | 111813339 | ||||||
chr12:111813393 | A | G | 22 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0009 others(19): Show |
89 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(86): Show |
3_prime_UTR_variant | MODIFIER | c.*3818A>G | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 13/13 | 3818 | chr12 | 111813393 | ||||||
chr12:111813558 | C | T | 7 | a0001c0001t0007 a0001c0001t0037 a0001c0001t0042 others(4): Show |
15 | HG00140.hp2 HG00738.hp2 HG01106.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*3983C>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 13/13 | 3983 | chr12 | 111813558 | ||||||
chr12:111814143 | C | A | 1 | a0001c0001t0100 | 1 | HG03688.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4568C>A | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 13/13 | 4568 | chr12 | 111814143 | ||||||
chr12:111814248 | A | G | 4 | a0001c0001t0094 a0001c0001t0099 a0001c0001t0100 others(1): Show |
4 | HG03654.hp1 HG03688.hp2 HG04115.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4673A>G | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 13/13 | 4673 | chr12 | 111814248 | ||||||
chr12:111814279 | G | A | 1 | a0001c0006t0127 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4704G>A | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 13/13 | 4704 | chr12 | 111814279 | ||||||
chr12:111814522 | A | G | 1 | a0001c0001t0108 | 1 | HG00597.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4947A>G | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 13/13 | 4947 | chr12 | 111814522 | ||||||
chr12:111814526 | C | T | 26 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0009 others(23): Show |
94 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(91): Show |
3_prime_UTR_variant | MODIFIER | c.*4951C>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 13/13 | 4951 | chr12 | 111814526 | ||||||
chr12:111814537 | C | CA | 9 | a0001c0001t0028 a0001c0001t0041 a0001c0001t0049 others(6): Show |
10 | HG01106.hp1 HG01257.hp2 HG01258.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*4982dupA | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 13/13 | 4983 | INFO_REALIGN_3_PRIME | chr12 | 111814537 | |||||
chr12:111814537 | CA | C | 34 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0009 others(31): Show |
104 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(101): Show |
3_prime_UTR_variant | MODIFIER | c.*4982delA | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 13/13 | 4982 | INFO_REALIGN_3_PRIME | chr12 | 111814537 | |||||
chr12:111814615 | C | T | 6 | a0001c0001t0017 a0001c0001t0025 a0001c0001t0038 others(3): Show |
8 | HG01943.hp2 HG02257.hp2 HG02717.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*5040C>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 13/13 | 5040 | chr12 | 111814615 | ||||||
chr12:111814673 | C | T | 1 | a0001c0001t0040 | 1 | HG01943.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5098C>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 13/13 | 5098 | chr12 | 111814673 | ||||||
chr12:111814689 | A | G | 1 | a0001c0001t0057 | 1 | HG03516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5114A>G | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 13/13 | 5114 | chr12 | 111814689 | ||||||
chr12:111814753 | G | A | 4 | a0001c0001t0013 a0001c0001t0085 a0001c0001t0105 others(1): Show |
9 | NA18946.hp1 NA18950.hp1 NA18951.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*5178G>A | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 13/13 | 5178 | chr12 | 111814753 | ||||||
chr12:111814762 | T | C | 2 | a0001c0001t0053 a0001c0001t0057 |
2 | HG03516.hp2 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5187T>C | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 13/13 | 5187 | chr12 | 111814762 | ||||||
chr12:111814779 | G | A | 1 | a0001c0001t0063 | 1 | HG03491.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5204G>A | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 13/13 | 5204 | chr12 | 111814779 | ||||||
chr12:111814806 | C | A | 2 | a0001c0001t0029 a0001c0001t0052 |
3 | HG01884.hp1 HG02976.hp1 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5231C>A | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 13/13 | 5231 | chr12 | 111814806 | ||||||
chr12:111814834 | C | CA | 7 | a0001c0001t0015 a0001c0001t0064 a0001c0001t0071 others(4): Show |
10 | HG02055.hp1 HG02572.hp2 HG04115.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*5277dupA | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 13/13 | 5278 | INFO_REALIGN_3_PRIME | chr12 | 111814834 | |||||
chr12:111814834 | CA | C | 33 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0009 others(30): Show |
103 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(100): Show |
3_prime_UTR_variant | MODIFIER | c.*5277delA | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 13/13 | 5277 | INFO_REALIGN_3_PRIME | chr12 | 111814834 | |||||
chr12:111814845 | A | G | 32 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0009 others(29): Show |
102 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(99): Show |
3_prime_UTR_variant | MODIFIER | c.*5270A>G | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 13/13 | 5270 | chr12 | 111814845 | ||||||
chr12:111815236 | G | A | 1 | a0001c0006t0127 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5661G>A | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 13/13 | 5661 | chr12 | 111815236 | ||||||
chr12:111815704 | G | T | 1 | a0001c0001t0081 | 1 | HG04115.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6129G>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 13/13 | 6129 | chr12 | 111815704 | ||||||
chr12:111815768 | C | CAT | 26 | a0001c0001t0003 a0001c0001t0008 a0001c0001t0012 others(23): Show |
64 | HG00597.hp2 HG00609.hp1 HG00609.hp2 others(61): Show |
3_prime_UTR_variant | MODIFIER | c.*6206_*6207dupAT | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 13/13 | 6208 | INFO_REALIGN_3_PRIME | chr12 | 111815768 | |||||
chr12:111815781 | A | AT | 6 | a0001c0001t0017 a0001c0001t0038 a0001c0001t0040 others(3): Show |
7 | HG01433.hp1 HG01943.hp2 HG02717.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*6221dupT | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 13/13 | 6222 | INFO_REALIGN_3_PRIME | chr12 | 111815781 | |||||
chr12:111815781 | A | T | 20 | a0001c0001t0001 a0001c0001t0009 a0001c0001t0016 others(17): Show |
76 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(73): Show |
3_prime_UTR_variant | MODIFIER | c.*6206A>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 13/13 | 6206 | chr12 | 111815781 | ||||||
chr12:111815782 | T | TA | 41 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0007 others(38): Show |
83 | HG00140.hp2 HG00738.hp2 HG01099.hp2 others(80): Show |
3_prime_UTR_variant | MODIFIER | c.*6207_*6208insA | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 13/13 | 6208 | chr12 | 111815782 | ||||||
chr12:111815782 | T | TATA | 4 | a0001c0001t0021 a0001c0001t0081 a0001c0001t0098 others(1): Show |
6 | HG01891.hp2 HG02145.hp2 HG02683.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*6207_*6208insATA | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 13/13 | 6208 | chr12 | 111815782 | ||||||
chr12:111815783 | T | A | 16 | a0001c0001t0008 a0001c0001t0015 a0001c0001t0023 others(13): Show |
27 | HG00597.hp2 HG02056.hp1 HG02071.hp1 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*6208T>A | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 13/13 | 6208 | chr12 | 111815783 | ||||||
chr12:111815784 | T | A | 21 | a0001c0001t0005 a0001c0001t0007 a0001c0001t0018 others(18): Show |
41 | HG00140.hp2 HG00738.hp2 HG01106.hp1 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*6209T>A | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 13/13 | 6209 | chr12 | 111815784 | ||||||
chr12:111815785 | T | A | 2 | a0001c0001t0084 a0001c0001t0090 |
2 | HG02897.hp2 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6210T>A | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 13/13 | 6210 | chr12 | 111815785 | ||||||
chr12:111815786 | T | A | 2 | a0003c0003t0027 a0003c0003t0062 |
3 | HG03491.hp2 HG03492.hp2 HG03831.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6211T>A | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 13/13 | 6211 | chr12 | 111815786 | ||||||
chr12:111815795 | T | G | 1 | a0001c0001t0116 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6220T>G | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 13/13 | 6220 | chr12 | 111815795 | ||||||
chr12:111815796 | T | A | 1 | a0001c0001t0116 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6221T>A | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 13/13 | 6221 | chr12 | 111815796 | ||||||
chr12:111815796 | T | TTGA | 7 | a0001c0001t0009 a0001c0001t0035 a0001c0001t0114 others(4): Show |
12 | HG02257.hp1 HG03041.hp2 NA18906.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*6221_*6222insTGA | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 13/13 | 6222 | chr12 | 111815796 | ||||||
chr12:111815796 | T | TTTGA | 17 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0016 others(14): Show |
79 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(76): Show |
3_prime_UTR_variant | MODIFIER | c.*6221_*6222insTTGA | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 13/13 | 6222 | chr12 | 111815796 | ||||||
chr12:111815837 | G | A | 1 | a0002c0002t0119 | 1 | HG00438.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6262G>A | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 13/13 | 6262 | chr12 | 111815837 | ||||||
chr12:111815860 | C | T | 1 | a0001c0001t0071 | 1 | NA19079.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6285C>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 13/13 | 6285 | chr12 | 111815860 | ||||||
chr12:111815958 | G | A | 1 | a0001c0001t0067 | 1 | HG00544.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6383G>A | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 13/13 | 6383 | chr12 | 111815958 | ||||||
chr12:111816413 | C | T | 1 | a0001c0001t0064 | 1 | NA18942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6838C>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 13/13 | 6838 | chr12 | 111816413 | ||||||
chr12:111816515 | T | C | 6 | a0001c0001t0017 a0001c0001t0025 a0001c0001t0038 others(3): Show |
8 | HG01943.hp2 HG02257.hp2 HG02717.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*6940T>C | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 13/13 | 6940 | chr12 | 111816515 | ||||||
chr12:111816590 | C | T | 1 | a0001c0009t0103 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7015C>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 13/13 | 7015 | chr12 | 111816590 | ||||||
chr12:111816885 | T | C | 3 | a0001c0001t0053 a0001c0001t0057 a0001c0001t0058 |
3 | HG03098.hp2 HG03516.hp2 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*7310T>C | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 13/13 | 7310 | chr12 | 111816885 | ||||||
chr12:111817058 | C | T | 1 | a0001c0001t0068 | 1 | HG00140.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7483C>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 13/13 | 7483 | chr12 | 111817058 | ||||||
chr12:111817127 | G | A | 1 | a0001c0001t0039 | 1 | HG02257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7552G>A | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 13/13 | 7552 | chr12 | 111817127 | ||||||
chr12:111817137 | C | T | 21 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0009 others(18): Show |
88 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(85): Show |
3_prime_UTR_variant | MODIFIER | c.*7562C>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 13/13 | 7562 | chr12 | 111817137 | ||||||
chr12:111817371 | C | A | 1 | a0001c0001t0010 | 6 | HG01928.hp1 HG01934.hp2 HG02148.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*7796C>A | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 13/13 | 7796 | chr12 | 111817371 | ||||||
chr12:111817456 | A | G | 2 | a0001c0001t0044 a0001c0001t0056 |
2 | HG02970.hp2 HG03130.hp2 |
3_prime_UTR_variant | MODIFIER | c.*7881A>G | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 13/13 | 7881 | chr12 | 111817456 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:111767246 | C | T | 1 | a0001c0004t0001g0243 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.114+150C>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 1/12 | chr12 | 111767246 | |||||||
chr12:111767307 | T | A | 1 | a0001c0001t0049g0032 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.114+211T>A | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 1/12 | chr12 | 111767307 | |||||||
chr12:111767420 | C | A | 4 | a0001c0001t0012g0008 a0001c0001t0012g0033 a0001c0001t0012g0034 others(1): Show |
5 | HG01167.hp2 HG02723.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.114+324C>A | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 1/12 | chr12 | 111767420 | |||||||
chr12:111767646 | C | T | 1 | a0001c0001t0007g0242 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.114+550C>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 1/12 | chr12 | 111767646 | |||||||
chr12:111767658 | C | A | 2 | a0001c0001t0019g0015 a0001c0001t0055g0015 |
2 | HG02630.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.114+562C>A | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 1/12 | chr12 | 111767658 | |||||||
chr12:111767740 | C | G | 19 | a0001c0001t0011g0007 a0001c0001t0011g0031 a0001c0001t0011g0230 others(16): Show |
21 | HG01168.hp1 HG01169.hp2 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.114+644C>G | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 1/12 | chr12 | 111767740 | |||||||
chr12:111767837 | G | A | 8 | a0001c0001t0017g0035 a0001c0001t0017g0038 a0001c0001t0025g0036 others(5): Show |
8 | HG01943.hp2 HG02257.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.114+741G>A | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 1/12 | chr12 | 111767837 | |||||||
chr12:111767843 | A | G | 4 | a0001c0001t0037g0030 a0001c0001t0042g0229 a0001c0001t0048g0228 others(1): Show |
4 | HG02735.hp2 HG03704.hp2 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.114+747A>G | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 1/12 | chr12 | 111767843 | |||||||
chr12:111768255 | C | T | 10 | a0001c0001t0001g0029 a0001c0001t0001g0219 a0001c0001t0001g0221 others(7): Show |
11 | HG00408.hp2 HG00438.hp2 HG00673.hp1 others(8): Show |
intron_variant | MODIFIER | c.114+1159C>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 1/12 | chr12 | 111768255 | |||||||
chr12:111768256 | G | A | 1 | a0001c0001t0008g0043 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.114+1160G>A | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 1/12 | chr12 | 111768256 | |||||||
chr12:111768390 | C | G | 1 | a0001c0001t0002g0217 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.114+1294C>G | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 1/12 | chr12 | 111768390 | |||||||
chr12:111768390 | C | T | 1 | a0001c0001t0093g0218 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.114+1294C>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 1/12 | chr12 | 111768390 | |||||||
chr12:111768456 | C | A | 2 | a0001c0001t0014g0044 a0001c0001t0014g0045 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.114+1360C>A | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 1/12 | chr12 | 111768456 | |||||||
chr12:111768706 | C | T | 1 | a0001c0001t0002g0216 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.114+1610C>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 1/12 | chr12 | 111768706 | |||||||
chr12:111768846 | C | T | 9 | a0001c0001t0005g0215 a0001c0001t0017g0035 a0001c0001t0017g0038 others(6): Show |
9 | HG01943.hp2 HG02257.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.114+1750C>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 1/12 | chr12 | 111768846 | |||||||
chr12:111768881 | G | A | 70 | a0001c0001t0001g0046 a0001c0001t0001g0060 a0001c0001t0001g0061 others(67): Show |
82 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.114+1785G>A | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 1/12 | chr12 | 111768881 | |||||||
chr12:111769091 | A | G | 158 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0028 others(155): Show |
193 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(190): Show |
intron_variant | MODIFIER | c.114+1995A>G | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 1/12 | chr12 | 111769091 | |||||||
chr12:111769456 | A | G | 8 | a0001c0001t0017g0035 a0001c0001t0017g0038 a0001c0001t0025g0036 others(5): Show |
8 | HG01943.hp2 HG02257.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.114+2360A>G | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 1/12 | chr12 | 111769456 | |||||||
chr12:111769496 | T | A | 73 | a0001c0001t0001g0046 a0001c0001t0001g0060 a0001c0001t0001g0061 others(70): Show |
85 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(82): Show |
intron_variant | MODIFIER | c.114+2400T>A | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 1/12 | chr12 | 111769496 | |||||||
chr12:111769498 | T | C | 8 | a0001c0001t0017g0035 a0001c0001t0017g0038 a0001c0001t0025g0036 others(5): Show |
8 | HG01943.hp2 HG02257.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.114+2402T>C | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 1/12 | chr12 | 111769498 | |||||||
chr12:111769505 | G | A | 1 | a0001c0006t0127g0170 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.114+2409G>A | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 1/12 | chr12 | 111769505 | |||||||
chr12:111769572 | C | CT | 75 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0028 others(72): Show |
98 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.114+2490dupT | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 111769572 | ||||||
chr12:111769625 | G | C | 8 | a0001c0001t0017g0035 a0001c0001t0017g0038 a0001c0001t0025g0036 others(5): Show |
8 | HG01943.hp2 HG02257.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.114+2529G>C | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 1/12 | chr12 | 111769625 | |||||||
chr12:111769695 | G | C | 8 | a0001c0001t0017g0035 a0001c0001t0017g0038 a0001c0001t0025g0036 others(5): Show |
8 | HG01943.hp2 HG02257.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.114+2599G>C | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 1/12 | chr12 | 111769695 | |||||||
chr12:111769713 | C | T | 1 | a0001c0001t0052g0168 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.114+2617C>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 1/12 | chr12 | 111769713 | |||||||
chr12:111770143 | C | CA | 221 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0028 others(218): Show |
263 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(260): Show |
intron_variant | MODIFIER | c.114+3062dupA | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 111770143 | ||||||
chr12:111770258 | G | T | 1 | a0001c0001t0049g0032 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.114+3162G>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 1/12 | chr12 | 111770258 | |||||||
chr12:111770350 | A | T | 1 | a0001c0001t0001g0227 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.114+3254A>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 1/12 | chr12 | 111770350 | |||||||
chr12:111770629 | A | C | 1 | a0001c0001t0109g0127 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.114+3533A>C | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 1/12 | chr12 | 111770629 | |||||||
chr12:111770655 | A | T | 1 | a0001c0001t0067g0167 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.114+3559A>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 1/12 | chr12 | 111770655 | |||||||
chr12:111770722 | C | G | 8 | a0001c0001t0017g0035 a0001c0001t0017g0038 a0001c0001t0025g0036 others(5): Show |
8 | HG01943.hp2 HG02257.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.114+3626C>G | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 1/12 | chr12 | 111770722 | |||||||
chr12:111770723 | T | C | 8 | a0001c0001t0017g0035 a0001c0001t0017g0038 a0001c0001t0025g0036 others(5): Show |
8 | HG01943.hp2 HG02257.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.114+3627T>C | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 1/12 | chr12 | 111770723 | |||||||
chr12:111770796 | C | G | 1 | a0001c0006t0127g0170 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.114+3700C>G | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 1/12 | chr12 | 111770796 | |||||||
chr12:111771034 | C | G | 73 | a0001c0001t0001g0046 a0001c0001t0001g0060 a0001c0001t0001g0061 others(70): Show |
85 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(82): Show |
intron_variant | MODIFIER | c.114+3938C>G | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 1/12 | chr12 | 111771034 | |||||||
chr12:111771193 | C | T | 66 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0028 others(63): Show |
89 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.114+4097C>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 1/12 | chr12 | 111771193 | |||||||
chr12:111771463 | G | A | 2 | a0001c0001t0002g0095 a0003c0003t0005g0094 |
2 | HG02602.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.114+4367G>A | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 1/12 | chr12 | 111771463 | |||||||
chr12:111771537 | C | T | 66 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0028 others(63): Show |
89 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.114+4441C>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 1/12 | chr12 | 111771537 | |||||||
chr12:111771581 | A | C | 1 | a0001c0001t0040g0042 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.114+4485A>C | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 1/12 | chr12 | 111771581 | |||||||
chr12:111771827 | G | A | 1 | a0001c0001t0029g0096 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.114+4731G>A | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 1/12 | chr12 | 111771827 | |||||||
chr12:111771875 | G | A | 2 | a0001c0001t0009g0181 a0001c0001t0036g0180 |
2 | NA18957.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.114+4779G>A | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 1/12 | chr12 | 111771875 | |||||||
chr12:111771895 | TCGAGACC others(3): Show |
T | 2 | a0001c0001t0006g0125 a0001c0001t0006g0126 |
2 | HG01099.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.114+4801_114+4810d others(12): Show |
ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 111771895 | ||||||
chr12:111771948 | A | C | 1 | a0001c0001t0040g0042 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.114+4852A>C | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 1/12 | chr12 | 111771948 | |||||||
chr12:111772047 | C | T | 1 | a0001c0001t0042g0229 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.114+4951C>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 1/12 | chr12 | 111772047 | |||||||
chr12:111772089 | A | G | 1 | a0001c0001t0018g0124 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.114+4993A>G | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 1/12 | chr12 | 111772089 | |||||||
chr12:111772147 | A | G | 1 | a0001c0006t0127g0170 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.114+5051A>G | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 1/12 | chr12 | 111772147 | |||||||
chr12:111772168 | A | T | 1 | a0001c0006t0127g0170 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.114+5072A>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 1/12 | chr12 | 111772168 | |||||||
chr12:111772172 | T | C | 1 | a0001c0001t0001g0046 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.114+5076T>C | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 1/12 | chr12 | 111772172 | |||||||
chr12:111772216 | C | T | 1 | a0001c0001t0090g0169 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.114+5120C>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 1/12 | chr12 | 111772216 | |||||||
chr12:111772234 | A | T | 1 | a0001c0001t0002g0095 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.114+5138A>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 1/12 | chr12 | 111772234 | |||||||
chr12:111772330 | T | C | 2 | a0001c0001t0015g0128 a0001c0001t0015g0129 |
2 | NA18948.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.114+5234T>C | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 1/12 | chr12 | 111772330 | |||||||
chr12:111772388 | G | A | 1 | a0004c0005t0066g0097 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.114+5292G>A | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 1/12 | chr12 | 111772388 | |||||||
chr12:111772674 | G | GT | 134 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0028 others(131): Show |
168 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(165): Show |
intron_variant | MODIFIER | c.114+5595dupT | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 111772674 | ||||||
chr12:111772674 | G | GTT | 16 | a0001c0001t0001g0046 a0001c0001t0001g0214 a0001c0001t0003g0087 others(13): Show |
17 | HG00673.hp1 HG01934.hp1 HG02027.hp1 others(14): Show |
intron_variant | MODIFIER | c.114+5594_114+5595d others(4): Show |
ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 111772674 | ||||||
chr12:111772674 | G | T | 1 | a0001c0001t0008g0091 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.114+5578G>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 1/12 | chr12 | 111772674 | |||||||
chr12:111772674 | GTT | G | 7 | a0001c0001t0017g0035 a0001c0001t0017g0038 a0001c0001t0025g0036 others(4): Show |
7 | HG01943.hp2 HG02717.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.114+5594_114+5595d others(4): Show |
ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 111772674 | ||||||
chr12:111772730 | A | G | 8 | a0001c0001t0017g0035 a0001c0001t0017g0038 a0001c0001t0025g0036 others(5): Show |
8 | HG01943.hp2 HG02257.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.114+5634A>G | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 1/12 | chr12 | 111772730 | |||||||
chr12:111772942 | CA | C | 149 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0028 others(146): Show |
184 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(181): Show |
intron_variant | MODIFIER | c.114+5858delA | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 111772942 | ||||||
chr12:111773024 | C | T | 2 | a0001c0001t0102g0123 a0001c0001t0109g0127 |
2 | HG01891.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.114+5928C>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 1/12 | chr12 | 111773024 | |||||||
chr12:111773070 | A | T | 1 | a0001c0001t0042g0229 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.114+5974A>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 1/12 | chr12 | 111773070 | |||||||
chr12:111773353 | A | G | 8 | a0001c0001t0017g0035 a0001c0001t0017g0038 a0001c0001t0025g0036 others(5): Show |
8 | HG01943.hp2 HG02257.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.114+6257A>G | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 1/12 | chr12 | 111773353 | |||||||
chr12:111773404 | C | T | 8 | a0001c0001t0017g0035 a0001c0001t0017g0038 a0001c0001t0025g0036 others(5): Show |
8 | HG01943.hp2 HG02257.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.114+6308C>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 1/12 | chr12 | 111773404 | |||||||
chr12:111773454 | C | T | 1 | a0001c0001t0003g0083 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.114+6358C>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 1/12 | chr12 | 111773454 | |||||||
chr12:111773617 | A | G | 1 | a0001c0001t0040g0042 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.114+6521A>G | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 1/12 | chr12 | 111773617 | |||||||
chr12:111774005 | C | T | 8 | a0001c0001t0017g0035 a0001c0001t0017g0038 a0001c0001t0025g0036 others(5): Show |
8 | HG01943.hp2 HG02257.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.114+6909C>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 1/12 | chr12 | 111774005 | |||||||
chr12:111774029 | T | C | 243 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0028 others(240): Show |
285 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(282): Show |
intron_variant | MODIFIER | c.114+6933T>C | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 1/12 | chr12 | 111774029 | |||||||
chr12:111774070 | G | C | 1 | a0001c0001t0036g0180 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.114+6974G>C | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 1/12 | chr12 | 111774070 | |||||||
chr12:111774109 | A | G | 1 | a0001c0001t0011g0241 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.114+7013A>G | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 1/12 | chr12 | 111774109 | |||||||
chr12:111774173 | T | C | 3 | a0001c0001t0084g0027 a0001c0001t0090g0169 a0001c0001t0091g0027 |
3 | HG02622.hp1 HG02897.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.114+7077T>C | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 1/12 | chr12 | 111774173 | |||||||
chr12:111774271 | A | G | 8 | a0001c0001t0017g0035 a0001c0001t0017g0038 a0001c0001t0025g0036 others(5): Show |
8 | HG01943.hp2 HG02257.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.114+7175A>G | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 1/12 | chr12 | 111774271 | |||||||
chr12:111774477 | G | A | 1 | a0001c0001t0071g0143 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.114+7381G>A | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 1/12 | chr12 | 111774477 | |||||||
chr12:111774769 | G | A | 1 | a0001c0001t0005g0098 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.115-7149G>A | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 1/12 | chr12 | 111774769 | |||||||
chr12:111774830 | G | A | 1 | a0001c0001t0058g0117 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.115-7088G>A | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 1/12 | chr12 | 111774830 | |||||||
chr12:111774833 | C | T | 1 | a0001c0001t0012g0033 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.115-7085C>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 1/12 | chr12 | 111774833 | |||||||
chr12:111775247 | A | G | 8 | a0001c0001t0017g0035 a0001c0001t0017g0038 a0001c0001t0025g0036 others(5): Show |
8 | HG01943.hp2 HG02257.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.115-6671A>G | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 1/12 | chr12 | 111775247 | |||||||
chr12:111775519 | T | C | 9 | a0001c0001t0017g0035 a0001c0001t0017g0038 a0001c0001t0025g0036 others(6): Show |
9 | HG01943.hp2 HG02257.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.115-6399T>C | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 1/12 | chr12 | 111775519 | |||||||
chr12:111775557 | G | A | 10 | a0001c0001t0014g0044 a0001c0001t0014g0045 a0001c0001t0014g0177 others(7): Show |
10 | HG01884.hp2 HG02145.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.115-6361G>A | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 1/12 | chr12 | 111775557 | |||||||
chr12:111775775 | T | C | 1 | a0002c0002t0009g0184 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.115-6143T>C | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 1/12 | chr12 | 111775775 | |||||||
chr12:111775870 | C | A | 4 | a0001c0001t0063g0099 a0003c0003t0005g0094 a0003c0003t0027g0019 others(1): Show |
5 | HG02602.hp1 HG03491.hp1 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.115-6048C>A | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 1/12 | chr12 | 111775870 | |||||||
chr12:111776161 | C | G | 8 | a0001c0001t0017g0035 a0001c0001t0017g0038 a0001c0001t0025g0036 others(5): Show |
8 | HG01943.hp2 HG02257.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.115-5757C>G | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 1/12 | chr12 | 111776161 | |||||||
chr12:111776490 | G | A | 1 | a0001c0006t0127g0170 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.115-5428G>A | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 1/12 | chr12 | 111776490 | |||||||
chr12:111776496 | C | G | 8 | a0001c0001t0017g0035 a0001c0001t0017g0038 a0001c0001t0025g0036 others(5): Show |
8 | HG01943.hp2 HG02257.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.115-5422C>G | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 1/12 | chr12 | 111776496 | |||||||
chr12:111776655 | G | T | 73 | a0001c0001t0001g0046 a0001c0001t0001g0060 a0001c0001t0001g0061 others(70): Show |
85 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(82): Show |
intron_variant | MODIFIER | c.115-5263G>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 1/12 | chr12 | 111776655 | |||||||
chr12:111776698 | A | AT | 6 | a0001c0001t0005g0116 a0001c0001t0013g0090 a0001c0001t0084g0027 others(3): Show |
6 | HG02622.hp1 HG02897.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.115-5206dupT | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 111776698 | ||||||
chr12:111776698 | AT | A | 14 | a0001c0001t0004g0211 a0001c0001t0012g0008 a0001c0001t0012g0033 others(11): Show |
15 | HG01167.hp2 HG02055.hp1 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.115-5206delT | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 111776698 | ||||||
chr12:111776699 | T | A | 1 | a0001c0001t0003g0077 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.115-5219T>A | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 1/12 | chr12 | 111776699 | |||||||
chr12:111776771 | A | G | 10 | a0001c0001t0014g0044 a0001c0001t0014g0045 a0001c0001t0014g0177 others(7): Show |
10 | HG01884.hp2 HG02145.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.115-5147A>G | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 1/12 | chr12 | 111776771 | |||||||
chr12:111776888 | T | C | 6 | a0001c0001t0011g0007 a0001c0001t0011g0031 a0001c0001t0011g0230 others(3): Show |
8 | HG01168.hp1 HG01169.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.115-5030T>C | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 1/12 | chr12 | 111776888 | |||||||
chr12:111776964 | G | T | 3 | a0001c0001t0084g0027 a0001c0001t0090g0169 a0001c0001t0091g0027 |
3 | HG02622.hp1 HG02897.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.115-4954G>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 1/12 | chr12 | 111776964 | |||||||
chr12:111777107 | T | TGGAAGAA others(4): Show |
9 | a0001c0001t0017g0035 a0001c0001t0017g0038 a0001c0001t0025g0036 others(6): Show |
9 | HG01943.hp2 HG02257.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.115-4809_115-4808i others(13): Show |
ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 111777107 | ||||||
chr12:111777287 | C | G | 1 | a0001c0001t0003g0082 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.115-4631C>G | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 1/12 | chr12 | 111777287 | |||||||
chr12:111777573 | T | C | 8 | a0001c0001t0017g0035 a0001c0001t0017g0038 a0001c0001t0025g0036 others(5): Show |
8 | HG01943.hp2 HG02257.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.115-4345T>C | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 1/12 | chr12 | 111777573 | |||||||
chr12:111777603 | C | G | 1 | a0001c0001t0007g0242 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.115-4315C>G | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 1/12 | chr12 | 111777603 | |||||||
chr12:111777603 | C | T | 2 | a0001c0001t0002g0166 a0001c0001t0020g0162 |
2 | NA18986.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.115-4315C>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 1/12 | chr12 | 111777603 | |||||||
chr12:111777759 | A | G | 1 | a0001c0001t0118g0210 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.115-4159A>G | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 1/12 | chr12 | 111777759 | |||||||
chr12:111777974 | A | G | 8 | a0001c0001t0017g0035 a0001c0001t0017g0038 a0001c0001t0025g0036 others(5): Show |
8 | HG01943.hp2 HG02257.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.115-3944A>G | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 1/12 | chr12 | 111777974 | |||||||
chr12:111778001 | C | T | 1 | a0001c0001t0042g0229 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.115-3917C>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 1/12 | chr12 | 111778001 | |||||||
chr12:111778052 | C | T | 2 | a0003c0003t0027g0019 a0003c0003t0062g0118 |
3 | HG03491.hp2 HG03492.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.115-3866C>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 1/12 | chr12 | 111778052 | |||||||
chr12:111778099 | G | A | 8 | a0001c0001t0017g0035 a0001c0001t0017g0038 a0001c0001t0025g0036 others(5): Show |
8 | HG01943.hp2 HG02257.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.115-3819G>A | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 1/12 | chr12 | 111778099 | |||||||
chr12:111778262 | C | T | 1 | a0001c0001t0006g0142 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.115-3656C>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 1/12 | chr12 | 111778262 | |||||||
chr12:111778321 | G | A | 2 | a0001c0001t0004g0182 a0001c0001t0004g0185 |
2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.115-3597G>A | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 1/12 | chr12 | 111778321 | |||||||
chr12:111778493 | C | T | 1 | a0001c0001t0087g0048 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.115-3425C>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 1/12 | chr12 | 111778493 | |||||||
chr12:111778555 | A | G | 1 | a0001c0001t0003g0081 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.115-3363A>G | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 1/12 | chr12 | 111778555 | |||||||
chr12:111778566 | C | G | 1 | a0001c0001t0049g0032 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.115-3352C>G | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 1/12 | chr12 | 111778566 | |||||||
chr12:111778690 | C | T | 1 | a0001c0001t0049g0032 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.115-3228C>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 1/12 | chr12 | 111778690 | |||||||
chr12:111778691 | G | A | 1 | a0001c0001t0002g0145 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.115-3227G>A | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 1/12 | chr12 | 111778691 | |||||||
chr12:111778789 | C | T | 1 | a0001c0001t0014g0179 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.115-3129C>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 1/12 | chr12 | 111778789 | |||||||
chr12:111778835 | GA | G | 19 | a0001c0001t0011g0007 a0001c0001t0011g0031 a0001c0001t0011g0230 others(16): Show |
21 | HG01168.hp1 HG01169.hp2 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.115-3071delA | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 111778835 | ||||||
chr12:111778982 | C | G | 1 | a0001c0001t0010g0161 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.115-2936C>G | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 1/12 | chr12 | 111778982 | |||||||
chr12:111779103 | A | C | 8 | a0001c0001t0017g0035 a0001c0001t0017g0038 a0001c0001t0025g0036 others(5): Show |
8 | HG01943.hp2 HG02257.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.115-2815A>C | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 1/12 | chr12 | 111779103 | |||||||
chr12:111779334 | C | T | 65 | a0001c0001t0001g0046 a0001c0001t0001g0060 a0001c0001t0001g0061 others(62): Show |
75 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(72): Show |
intron_variant | MODIFIER | c.115-2584C>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 1/12 | chr12 | 111779334 | |||||||
chr12:111779404 | G | A | 70 | a0001c0001t0001g0046 a0001c0001t0001g0060 a0001c0001t0001g0061 others(67): Show |
82 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.115-2514G>A | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 1/12 | chr12 | 111779404 | |||||||
chr12:111779538 | T | G | 1 | a0001c0001t0018g0124 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.115-2380T>G | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 1/12 | chr12 | 111779538 | |||||||
chr12:111779572 | C | T | 1 | a0001c0001t0052g0168 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.115-2346C>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 1/12 | chr12 | 111779572 | |||||||
chr12:111779772 | G | A | 2 | a0001c0001t0002g0024 a0001c0001t0041g0024 |
2 | HG01109.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.115-2146G>A | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 1/12 | chr12 | 111779772 | |||||||
chr12:111780135 | C | T | 1 | a0001c0001t0012g0033 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.115-1783C>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 1/12 | chr12 | 111780135 | |||||||
chr12:111780136 | G | A | 1 | a0001c0006t0127g0170 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.115-1782G>A | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 1/12 | chr12 | 111780136 | |||||||
chr12:111780358 | G | A | 5 | a0001c0001t0013g0016 a0001c0001t0013g0058 a0001c0001t0013g0059 others(2): Show |
6 | NA18946.hp1 NA18950.hp1 NA18981.hp2 others(3): Show |
intron_variant | MODIFIER | c.115-1560G>A | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 1/12 | chr12 | 111780358 | |||||||
chr12:111780455 | A | G | 1 | a0001c0001t0006g0141 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.115-1463A>G | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 1/12 | chr12 | 111780455 | |||||||
chr12:111780476 | C | A | 1 | a0001c0001t0010g0161 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.115-1442C>A | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 1/12 | chr12 | 111780476 | |||||||
chr12:111780552 | C | T | 1 | a0001c0001t0082g0240 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.115-1366C>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 1/12 | chr12 | 111780552 | |||||||
chr12:111780553 | G | A | 3 | a0001c0001t0001g0046 a0001c0001t0001g0060 a0001c0001t0001g0061 |
3 | HG00735.hp1 HG01496.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.115-1365G>A | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 1/12 | chr12 | 111780553 | |||||||
chr12:111780602 | G | A | 2 | a0001c0001t0021g0232 a0001c0009t0103g0231 |
2 | HG01891.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.115-1316G>A | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 1/12 | chr12 | 111780602 | |||||||
chr12:111780662 | C | T | 1 | a0001c0001t0035g0183 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.115-1256C>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 1/12 | chr12 | 111780662 | |||||||
chr12:111780773 | T | G | 8 | a0001c0001t0017g0035 a0001c0001t0017g0038 a0001c0001t0025g0036 others(5): Show |
8 | HG01943.hp2 HG02257.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.115-1145T>G | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 1/12 | chr12 | 111780773 | |||||||
chr12:111780837 | C | T | 19 | a0001c0001t0011g0007 a0001c0001t0011g0031 a0001c0001t0011g0230 others(16): Show |
21 | HG01168.hp1 HG01169.hp2 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.115-1081C>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 1/12 | chr12 | 111780837 | |||||||
chr12:111781034 | A | T | 1 | a0002c0002t0009g0184 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.115-884A>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 1/12 | chr12 | 111781034 | |||||||
chr12:111781094 | G | A | 8 | a0001c0001t0017g0035 a0001c0001t0017g0038 a0001c0001t0025g0036 others(5): Show |
8 | HG01943.hp2 HG02257.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.115-824G>A | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 1/12 | chr12 | 111781094 | |||||||
chr12:111781124 | C | A | 1 | a0001c0001t0002g0130 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.115-794C>A | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 1/12 | chr12 | 111781124 | |||||||
chr12:111781218 | A | G | 1 | a0001c0001t0120g0239 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.115-700A>G | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 1/12 | chr12 | 111781218 | |||||||
chr12:111781235 | C | G | 1 | a0001c0001t0012g0034 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.115-683C>G | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 1/12 | chr12 | 111781235 | |||||||
chr12:111781602 | A | G | 2 | a0001c0001t0102g0123 a0001c0001t0109g0127 |
2 | HG01891.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.115-316A>G | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 1/12 | chr12 | 111781602 | |||||||
chr12:111781780 | G | A | 1 | a0001c0006t0127g0170 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.115-138G>A | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 1/12 | chr12 | 111781780 | |||||||
chr12:111781803 | C | A | 2 | a0001c0001t0025g0036 a0001c0001t0038g0037 |
2 | HG02809.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.115-115C>A | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 1/12 | chr12 | 111781803 | |||||||
chr12:111781837 | G | GT | 10 | a0001c0001t0002g0095 a0001c0001t0026g0121 a0001c0001t0029g0096 others(7): Show |
10 | HG01884.hp1 HG02976.hp1 HG02976.hp2 others(7): Show |
intron_variant | MODIFIER | c.115-70dupT | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 111781837 | ||||||
chr12:111781892 | G | A | 2 | a0001c0001t0015g0128 a0001c0001t0015g0129 |
2 | NA18948.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.115-26G>A | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 1/12 | chr12 | 111781892 | |||||||
chr12:111782373 | G | A | 29 | a0001c0001t0002g0095 a0001c0001t0011g0007 a0001c0001t0011g0031 others(26): Show |
31 | HG01168.hp1 HG01169.hp2 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.219+351G>A | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 2/12 | chr12 | 111782373 | |||||||
chr12:111782442 | G | C | 1 | a0001c0001t0001g0186 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.219+420G>C | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 2/12 | chr12 | 111782442 | |||||||
chr12:111782446 | G | T | 1 | a0001c0006t0127g0170 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.219+424G>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 2/12 | chr12 | 111782446 | |||||||
chr12:111782610 | C | T | 1 | a0001c0001t0024g0018 | 2 | HG00099.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.220-548C>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 2/12 | chr12 | 111782610 | |||||||
chr12:111782611 | G | A | 8 | a0001c0001t0017g0035 a0001c0001t0017g0038 a0001c0001t0025g0036 others(5): Show |
8 | HG01943.hp2 HG02257.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.220-547G>A | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 2/12 | chr12 | 111782611 | |||||||
chr12:111782661 | G | C | 1 | a0001c0001t0025g0036 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.220-497G>C | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 2/12 | chr12 | 111782661 | |||||||
chr12:111782896 | A | AAAAAAAA others(1): Show |
8 | a0001c0001t0017g0035 a0001c0001t0017g0038 a0001c0001t0025g0036 others(5): Show |
8 | HG01943.hp2 HG02257.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.220-257_220-250dup others(8): Show |
ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr12 | 111782896 | ||||||
chr12:111782919 | A | G | 8 | a0001c0001t0017g0035 a0001c0001t0017g0038 a0001c0001t0025g0036 others(5): Show |
8 | HG01943.hp2 HG02257.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.220-239A>G | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 2/12 | chr12 | 111782919 | |||||||
chr12:111782983 | T | C | 1 | a0001c0001t0102g0123 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.220-175T>C | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 2/12 | chr12 | 111782983 | |||||||
chr12:111783092 | G | C | 3 | a0001c0001t0084g0027 a0001c0001t0090g0169 a0001c0001t0091g0027 |
3 | HG02622.hp1 HG02897.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.220-66G>C | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 2/12 | chr12 | 111783092 | |||||||
chr12:111783496 | T | C | 1 | a0001c0001t0001g0187 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.360+198T>C | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 3/12 | chr12 | 111783496 | |||||||
chr12:111783549 | G | A | 73 | a0001c0001t0001g0046 a0001c0001t0001g0060 a0001c0001t0001g0061 others(70): Show |
85 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(82): Show |
intron_variant | MODIFIER | c.360+251G>A | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 3/12 | chr12 | 111783549 | |||||||
chr12:111783734 | C | T | 8 | a0001c0001t0017g0035 a0001c0001t0017g0038 a0001c0001t0025g0036 others(5): Show |
8 | HG01943.hp2 HG02257.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.360+436C>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 3/12 | chr12 | 111783734 | |||||||
chr12:111783799 | C | T | 19 | a0001c0001t0011g0007 a0001c0001t0011g0031 a0001c0001t0011g0230 others(16): Show |
21 | HG01168.hp1 HG01169.hp2 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.360+501C>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 3/12 | chr12 | 111783799 | |||||||
chr12:111783808 | C | T | 1 | a0001c0001t0035g0183 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.360+510C>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 3/12 | chr12 | 111783808 | |||||||
chr12:111784101 | C | T | 1 | a0001c0001t0011g0031 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.360+803C>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 3/12 | chr12 | 111784101 | |||||||
chr12:111784278 | C | T | 1 | a0001c0001t0002g0160 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.360+980C>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 3/12 | chr12 | 111784278 | |||||||
chr12:111784624 | A | G | 1 | a0001c0001t0025g0039 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.361-643A>G | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 3/12 | chr12 | 111784624 | |||||||
chr12:111784705 | C | T | 1 | a0001c0001t0010g0159 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.361-562C>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 3/12 | chr12 | 111784705 | |||||||
chr12:111784966 | C | T | 1 | a0001c0001t0081g0120 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.361-301C>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 3/12 | chr12 | 111784966 | |||||||
chr12:111784984 | C | T | 73 | a0001c0001t0001g0046 a0001c0001t0001g0060 a0001c0001t0001g0061 others(70): Show |
85 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(82): Show |
intron_variant | MODIFIER | c.361-283C>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 3/12 | chr12 | 111784984 | |||||||
chr12:111785062 | GC | G | 66 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0028 others(63): Show |
89 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.361-203delC | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr12 | 111785062 | ||||||
chr12:111785069 | C | G | 1 | a0001c0006t0127g0170 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.361-198C>G | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 3/12 | chr12 | 111785069 | |||||||
chr12:111785093 | T | C | 1 | a0001c0001t0109g0127 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.361-174T>C | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 3/12 | chr12 | 111785093 | |||||||
chr12:111785136 | G | GC | 9 | a0001c0001t0017g0035 a0001c0001t0017g0038 a0001c0001t0025g0036 others(6): Show |
9 | HG01943.hp2 HG02257.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.361-131_361-130ins others(1): Show |
ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 3/12 | chr12 | 111785136 | |||||||
chr12:111785137 | G | A | 1 | a0001c0006t0127g0170 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.361-130G>A | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 3/12 | chr12 | 111785137 | |||||||
chr12:111785169 | C | T | 1 | a0001c0001t0025g0039 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.361-98C>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 3/12 | chr12 | 111785169 | |||||||
chr12:111785450 | G | A | 1 | a0001c0001t0056g0053 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.440+104G>A | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 4/12 | chr12 | 111785450 | |||||||
chr12:111786044 | C | G | 1 | a0001c0001t0056g0053 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.440+698C>G | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 4/12 | chr12 | 111786044 | |||||||
chr12:111786142 | G | C | 9 | a0001c0001t0017g0035 a0001c0001t0017g0038 a0001c0001t0025g0036 others(6): Show |
9 | HG01943.hp2 HG02257.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.440+796G>C | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 4/12 | chr12 | 111786142 | |||||||
chr12:111786263 | G | T | 1 | a0001c0006t0127g0170 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.440+917G>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 4/12 | chr12 | 111786263 | |||||||
chr12:111786268 | G | A | 2 | a0001c0001t0007g0131 a0001c0001t0007g0132 |
2 | NA19004.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.440+922G>A | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 4/12 | chr12 | 111786268 | |||||||
chr12:111786292 | A | G | 8 | a0001c0001t0017g0035 a0001c0001t0017g0038 a0001c0001t0025g0036 others(5): Show |
8 | HG01943.hp2 HG02257.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.440+946A>G | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 4/12 | chr12 | 111786292 | |||||||
chr12:111786386 | G | A | 1 | a0001c0001t0026g0121 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.440+1040G>A | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 4/12 | chr12 | 111786386 | |||||||
chr12:111786418 | A | C | 1 | a0001c0001t0093g0218 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.440+1072A>C | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 4/12 | chr12 | 111786418 | |||||||
chr12:111787067 | G | A | 1 | a0001c0001t0016g0189 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.440+1721G>A | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 4/12 | chr12 | 111787067 | |||||||
chr12:111787160 | C | T | 1 | a0001c0001t0001g0225 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.440+1814C>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 4/12 | chr12 | 111787160 | |||||||
chr12:111787441 | A | T | 2 | a0001c0001t0014g0177 a0001c0001t0014g0178 |
2 | HG02145.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.440+2095A>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 4/12 | chr12 | 111787441 | |||||||
chr12:111787500 | C | G | 6 | a0001c0001t0011g0007 a0001c0001t0011g0031 a0001c0001t0011g0230 others(3): Show |
8 | HG01168.hp1 HG01169.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.440+2154C>G | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 4/12 | chr12 | 111787500 | |||||||
chr12:111787709 | A | T | 1 | a0001c0006t0127g0170 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.441-2114A>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 4/12 | chr12 | 111787709 | |||||||
chr12:111787756 | G | A | 1 | a0001c0001t0047g0146 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.441-2067G>A | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 4/12 | chr12 | 111787756 | |||||||
chr12:111787932 | A | G | 9 | a0001c0001t0017g0035 a0001c0001t0017g0038 a0001c0001t0025g0036 others(6): Show |
9 | HG01943.hp2 HG02257.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.441-1891A>G | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 4/12 | chr12 | 111787932 | |||||||
chr12:111787995 | C | T | 7 | a0001c0001t0005g0098 a0001c0001t0005g0119 a0001c0001t0078g0140 others(4): Show |
7 | HG02074.hp1 HG02135.hp2 NA18943.hp2 others(4): Show |
intron_variant | MODIFIER | c.441-1828C>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 4/12 | chr12 | 111787995 | |||||||
chr12:111788082 | G | A | 4 | a0001c0001t0007g0011 a0001c0001t0007g0020 a0001c0001t0007g0100 others(1): Show |
6 | HG00140.hp2 HG00738.hp2 HG01106.hp1 others(3): Show |
intron_variant | MODIFIER | c.441-1741G>A | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 4/12 | chr12 | 111788082 | |||||||
chr12:111788123 | C | T | 158 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0028 others(155): Show |
193 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(190): Show |
intron_variant | MODIFIER | c.441-1700C>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 4/12 | chr12 | 111788123 | |||||||
chr12:111788124 | C | T | 1 | a0001c0001t0110g0080 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.441-1699C>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 4/12 | chr12 | 111788124 | |||||||
chr12:111788240 | C | T | 2 | a0001c0001t0002g0013 a0001c0001t0050g0013 |
3 | HG02080.hp1 NA18955.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.441-1583C>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 4/12 | chr12 | 111788240 | |||||||
chr12:111788330 | G | A | 10 | a0001c0001t0002g0095 a0001c0001t0026g0121 a0001c0001t0029g0096 others(7): Show |
10 | HG01884.hp1 HG01891.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.441-1493G>A | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 4/12 | chr12 | 111788330 | |||||||
chr12:111788440 | G | A | 9 | a0001c0001t0017g0035 a0001c0001t0017g0038 a0001c0001t0025g0036 others(6): Show |
9 | HG01943.hp2 HG02257.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.441-1383G>A | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 4/12 | chr12 | 111788440 | |||||||
chr12:111788629 | G | A | 67 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0028 others(64): Show |
90 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.441-1194G>A | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 4/12 | chr12 | 111788629 | |||||||
chr12:111788652 | A | G | 1 | a0001c0001t0093g0218 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.441-1171A>G | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 4/12 | chr12 | 111788652 | |||||||
chr12:111788688 | G | T | 1 | a0001c0006t0127g0170 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.441-1135G>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 4/12 | chr12 | 111788688 | |||||||
chr12:111788831 | C | T | 1 | a0001c0001t0001g0046 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.441-992C>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 4/12 | chr12 | 111788831 | |||||||
chr12:111789017 | C | CT | 12 | a0001c0001t0001g0061 a0001c0001t0001g0209 a0001c0001t0001g0224 others(9): Show |
12 | HG00735.hp1 HG01993.hp1 HG03704.hp2 others(9): Show |
intron_variant | MODIFIER | c.441-788dupT | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 111789017 | ||||||
chr12:111789017 | CT | C | 11 | a0001c0001t0002g0216 a0001c0001t0017g0035 a0001c0001t0017g0038 others(8): Show |
11 | HG01943.hp2 HG02257.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.441-788delT | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 111789017 | ||||||
chr12:111789048 | C | T | 1 | a0001c0001t0070g0158 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.441-775C>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 4/12 | chr12 | 111789048 | |||||||
chr12:111789386 | G | T | 4 | a0001c0001t0006g0022 a0001c0001t0006g0108 a0001c0001t0006g0109 others(1): Show |
5 | HG02965.hp1 HG02970.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.441-437G>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 4/12 | chr12 | 111789386 | |||||||
chr12:111789491 | C | CA | 58 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0028 others(55): Show |
81 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.441-319dupA | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 111789491 | ||||||
chr12:111789498 | A | T | 4 | a0001c0001t0002g0137 a0001c0001t0002g0139 a0001c0001t0006g0141 others(1): Show |
4 | HG00609.hp2 NA18979.hp1 NA18985.hp1 others(1): Show |
intron_variant | MODIFIER | c.441-325A>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 4/12 | chr12 | 111789498 | |||||||
chr12:111789510 | G | C | 1 | a0001c0001t0054g0234 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.441-313G>C | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 4/12 | chr12 | 111789510 | |||||||
chr12:111789523 | A | G | 8 | a0001c0001t0017g0035 a0001c0001t0017g0038 a0001c0001t0025g0036 others(5): Show |
8 | HG02257.hp2 HG02717.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.441-300A>G | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 4/12 | chr12 | 111789523 | |||||||
chr12:111789524 | A | G | 1 | a0001c0001t0040g0042 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.441-299A>G | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 4/12 | chr12 | 111789524 | |||||||
chr12:111789993 | A | G | 8 | a0001c0001t0017g0035 a0001c0001t0017g0038 a0001c0001t0025g0036 others(5): Show |
8 | HG01943.hp2 HG02257.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.552+59A>G | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 5/12 | chr12 | 111789993 | |||||||
chr12:111790161 | G | A | 1 | a0001c0001t0004g0226 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.552+227G>A | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 5/12 | chr12 | 111790161 | |||||||
chr12:111790217 | A | T | 8 | a0001c0001t0017g0035 a0001c0001t0017g0038 a0001c0001t0025g0036 others(5): Show |
8 | HG01943.hp2 HG02257.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.553-217A>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 5/12 | chr12 | 111790217 | |||||||
chr12:111790691 | A | C | 1 | a0001c0001t0003g0083 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.681+129A>C | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 6/12 | chr12 | 111790691 | |||||||
chr12:111790897 | A | G | 1 | a0001c0006t0127g0170 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.681+335A>G | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 6/12 | chr12 | 111790897 | |||||||
chr12:111790910 | T | C | 70 | a0001c0001t0001g0046 a0001c0001t0001g0060 a0001c0001t0001g0061 others(67): Show |
82 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.681+348T>C | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 6/12 | chr12 | 111790910 | |||||||
chr12:111791045 | T | C | 73 | a0001c0001t0001g0046 a0001c0001t0001g0060 a0001c0001t0001g0061 others(70): Show |
85 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(82): Show |
intron_variant | MODIFIER | c.682-261T>C | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 6/12 | chr12 | 111791045 | |||||||
chr12:111791068 | A | G | 1 | a0001c0001t0002g0157 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.682-238A>G | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 6/12 | chr12 | 111791068 | |||||||
chr12:111791091 | T | C | 1 | a0001c0001t0019g0233 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.682-215T>C | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 6/12 | chr12 | 111791091 | |||||||
chr12:111791124 | C | T | 1 | a0001c0006t0127g0170 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.682-182C>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 6/12 | chr12 | 111791124 | |||||||
chr12:111791277 | C | T | 8 | a0001c0001t0017g0035 a0001c0001t0017g0038 a0001c0001t0025g0036 others(5): Show |
8 | HG01943.hp2 HG02257.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.682-29C>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 6/12 | chr12 | 111791277 | |||||||
chr12:111791533 | C | T | 4 | a0001c0001t0003g0079 a0001c0001t0003g0082 a0001c0001t0003g0088 others(1): Show |
4 | NA18959.hp1 NA18992.hp2 NA18994.hp2 others(1): Show |
intron_variant | MODIFIER | c.795+114C>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 7/12 | chr12 | 111791533 | |||||||
chr12:111791597 | A | G | 2 | a0001c0001t0037g0030 a0001c0001t0061g0030 |
2 | HG03704.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.795+178A>G | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 7/12 | chr12 | 111791597 | |||||||
chr12:111791735 | T | A | 8 | a0001c0001t0017g0035 a0001c0001t0017g0038 a0001c0001t0025g0036 others(5): Show |
8 | HG01943.hp2 HG02257.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.795+316T>A | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 7/12 | chr12 | 111791735 | |||||||
chr12:111792026 | A | G | 1 | a0001c0001t0007g0107 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.796-35A>G | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 7/12 | chr12 | 111792026 | |||||||
chr12:111792211 | A | G | 9 | a0001c0001t0017g0035 a0001c0001t0017g0038 a0001c0001t0025g0036 others(6): Show |
9 | HG01943.hp2 HG02257.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.898+48A>G | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 8/12 | chr12 | 111792211 | |||||||
chr12:111792215 | G | C | 16 | a0002c0002t0001g0003 a0002c0002t0001g0115 a0002c0002t0001g0190 others(13): Show |
25 | HG00438.hp1 HG00544.hp2 HG00673.hp2 others(22): Show |
intron_variant | MODIFIER | c.898+52G>C | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 8/12 | chr12 | 111792215 | |||||||
chr12:111792232 | G | A | 70 | a0001c0001t0001g0046 a0001c0001t0001g0060 a0001c0001t0001g0061 others(67): Show |
82 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.898+69G>A | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 8/12 | chr12 | 111792232 | |||||||
chr12:111792415 | C | T | 8 | a0001c0001t0017g0035 a0001c0001t0017g0038 a0001c0001t0025g0036 others(5): Show |
8 | HG01943.hp2 HG02257.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.899-183C>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 8/12 | chr12 | 111792415 | |||||||
chr12:111792790 | A | T | 1 | a0001c0001t0099g0078 | 1 | NA20752.hp1 | splice_region_variant&intron_variant | LOW | c.1083+8A>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 9/12 | chr12 | 111792790 | |||||||
chr12:111793010 | G | T | 1 | a0001c0001t0029g0096 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1083+228G>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 9/12 | chr12 | 111793010 | |||||||
chr12:111793177 | T | G | 2 | a0001c0001t0102g0123 a0001c0001t0109g0127 |
2 | HG01891.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.1083+395T>G | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 9/12 | chr12 | 111793177 | |||||||
chr12:111793202 | T | TTTTA | 7 | a0001c0001t0014g0177 a0001c0001t0014g0178 a0001c0001t0023g0173 others(4): Show |
7 | HG02145.hp1 HG02451.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1083+437_1083+440d others(6): Show |
ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr12 | 111793202 | ||||||
chr12:111793585 | G | GT | 70 | a0001c0001t0001g0046 a0001c0001t0001g0060 a0001c0001t0001g0061 others(67): Show |
82 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.1083+814dupT | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr12 | 111793585 | ||||||
chr12:111793585 | GT | G | 8 | a0001c0001t0017g0035 a0001c0001t0017g0038 a0001c0001t0025g0036 others(5): Show |
8 | HG01943.hp2 HG02257.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1083+814delT | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr12 | 111793585 | ||||||
chr12:111793848 | C | T | 2 | a0001c0001t0014g0044 a0001c0001t0014g0045 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1083+1066C>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 9/12 | chr12 | 111793848 | |||||||
chr12:111794014 | A | AT | 50 | a0001c0001t0001g0006 a0001c0001t0001g0028 a0001c0001t0001g0205 others(47): Show |
55 | HG00140.hp2 HG00597.hp2 HG00738.hp2 others(52): Show |
intron_variant | MODIFIER | c.1083+1255dupT | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr12 | 111794014 | ||||||
chr12:111794014 | AT | A | 9 | a0001c0001t0002g0147 a0001c0001t0008g0062 a0001c0001t0020g0162 others(6): Show |
9 | HG01258.hp2 HG02257.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.1083+1255delT | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr12 | 111794014 | ||||||
chr12:111794329 | T | C | 1 | a0001c0001t0002g0137 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1083+1547T>C | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 9/12 | chr12 | 111794329 | |||||||
chr12:111794330 | G | A | 1 | a0001c0001t0126g0114 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1083+1548G>A | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 9/12 | chr12 | 111794330 | |||||||
chr12:111794366 | C | T | 1 | a0001c0001t0020g0162 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1083+1584C>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 9/12 | chr12 | 111794366 | |||||||
chr12:111794432 | C | T | 3 | a0001c0001t0006g0022 a0001c0001t0006g0108 a0001c0001t0083g0110 |
4 | HG02965.hp1 HG03098.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.1083+1650C>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 9/12 | chr12 | 111794432 | |||||||
chr12:111794552 | G | C | 4 | a0001c0001t0003g0009 a0001c0001t0003g0056 a0001c0001t0044g0054 others(1): Show |
6 | HG01099.hp1 HG02886.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1083+1770G>C | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 9/12 | chr12 | 111794552 | |||||||
chr12:111795064 | A | T | 1 | a0001c0001t0006g0126 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1083+2282A>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 9/12 | chr12 | 111795064 | |||||||
chr12:111795214 | T | C | 243 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0028 others(240): Show |
285 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(282): Show |
intron_variant | MODIFIER | c.1083+2432T>C | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 9/12 | chr12 | 111795214 | |||||||
chr12:111795294 | C | T | 1 | a0001c0001t0001g0224 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1083+2512C>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 9/12 | chr12 | 111795294 | |||||||
chr12:111795370 | C | T | 1 | a0001c0001t0003g0087 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1083+2588C>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 9/12 | chr12 | 111795370 | |||||||
chr12:111795431 | C | T | 2 | a0001c0001t0012g0052 a0001c0001t0092g0049 |
2 | NA19081.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.1084-2647C>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 9/12 | chr12 | 111795431 | |||||||
chr12:111795439 | C | T | 1 | a0001c0001t0012g0052 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1084-2639C>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 9/12 | chr12 | 111795439 | |||||||
chr12:111795596 | C | CT | 147 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0028 others(144): Show |
182 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(179): Show |
intron_variant | MODIFIER | c.1084-2468dupT | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr12 | 111795596 | ||||||
chr12:111795660 | C | T | 1 | a0001c0006t0127g0170 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1084-2418C>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 9/12 | chr12 | 111795660 | |||||||
chr12:111795677 | C | T | 9 | a0001c0001t0007g0107 a0001c0001t0017g0035 a0001c0001t0017g0038 others(6): Show |
9 | HG01943.hp2 HG02257.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.1084-2401C>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 9/12 | chr12 | 111795677 | |||||||
chr12:111795691 | G | A | 70 | a0001c0001t0001g0046 a0001c0001t0001g0060 a0001c0001t0001g0061 others(67): Show |
82 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.1084-2387G>A | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 9/12 | chr12 | 111795691 | |||||||
chr12:111795714 | C | A | 1 | a0001c0001t0002g0149 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1084-2364C>A | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 9/12 | chr12 | 111795714 | |||||||
chr12:111795887 | G | A | 1 | a0001c0001t0071g0143 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1084-2191G>A | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 9/12 | chr12 | 111795887 | |||||||
chr12:111796191 | G | A | 43 | a0001c0001t0002g0024 a0001c0001t0005g0021 a0001c0001t0005g0098 others(40): Show |
48 | HG00140.hp2 HG00738.hp2 HG01099.hp2 others(45): Show |
intron_variant | MODIFIER | c.1084-1887G>A | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 9/12 | chr12 | 111796191 | |||||||
chr12:111796312 | A | G | 8 | a0001c0001t0017g0035 a0001c0001t0017g0038 a0001c0001t0025g0036 others(5): Show |
8 | HG01943.hp2 HG02257.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1084-1766A>G | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 9/12 | chr12 | 111796312 | |||||||
chr12:111796344 | T | A | 1 | a0001c0001t0033g0197 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1084-1734T>A | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 9/12 | chr12 | 111796344 | |||||||
chr12:111796345 | A | T | 8 | a0001c0001t0017g0035 a0001c0001t0017g0038 a0001c0001t0025g0036 others(5): Show |
8 | HG01943.hp2 HG02257.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1084-1733A>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 9/12 | chr12 | 111796345 | |||||||
chr12:111796515 | G | T | 1 | a0001c0006t0127g0170 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1084-1563G>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 9/12 | chr12 | 111796515 | |||||||
chr12:111796631 | G | A | 8 | a0001c0001t0017g0035 a0001c0001t0017g0038 a0001c0001t0025g0036 others(5): Show |
8 | HG01943.hp2 HG02257.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1084-1447G>A | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 9/12 | chr12 | 111796631 | |||||||
chr12:111796645 | G | A | 2 | a0001c0001t0001g0029 a0001c0001t0001g0224 |
3 | HG00438.hp2 NA18981.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.1084-1433G>A | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 9/12 | chr12 | 111796645 | |||||||
chr12:111796718 | C | A | 1 | a0001c0006t0127g0170 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1084-1360C>A | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 9/12 | chr12 | 111796718 | |||||||
chr12:111796904 | C | A | 8 | a0001c0001t0002g0095 a0001c0001t0026g0121 a0001c0001t0029g0096 others(5): Show |
8 | HG01884.hp1 HG02976.hp1 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.1084-1174C>A | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 9/12 | chr12 | 111796904 | |||||||
chr12:111796921 | A | G | 1 | a0001c0001t0043g0105 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1084-1157A>G | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 9/12 | chr12 | 111796921 | |||||||
chr12:111796964 | CT | C | 8 | a0001c0001t0008g0064 a0001c0001t0014g0044 a0001c0001t0089g0172 others(5): Show |
8 | HG01891.hp1 HG02451.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1084-1097delT | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr12 | 111796964 | ||||||
chr12:111796986 | C | T | 8 | a0001c0001t0002g0095 a0001c0001t0026g0121 a0001c0001t0029g0096 others(5): Show |
8 | HG01884.hp1 HG02976.hp1 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.1084-1092C>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 9/12 | chr12 | 111796986 | |||||||
chr12:111797272 | T | C | 1 | a0001c0006t0127g0170 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1084-806T>C | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 9/12 | chr12 | 111797272 | |||||||
chr12:111797456 | C | T | 1 | a0001c0006t0127g0170 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1084-622C>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 9/12 | chr12 | 111797456 | |||||||
chr12:111797511 | G | C | 1 | a0001c0001t0001g0225 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1084-567G>C | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 9/12 | chr12 | 111797511 | |||||||
chr12:111797614 | CA | C | 83 | a0001c0001t0001g0046 a0001c0001t0001g0060 a0001c0001t0001g0061 others(80): Show |
95 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(92): Show |
intron_variant | MODIFIER | c.1084-451delA | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr12 | 111797614 | ||||||
chr12:111797614 | CAA | C | 77 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0028 others(74): Show |
100 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.1084-452_1084-451d others(4): Show |
ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr12 | 111797614 | ||||||
chr12:111797979 | C | A | 73 | a0001c0001t0001g0046 a0001c0001t0001g0060 a0001c0001t0001g0061 others(70): Show |
85 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(82): Show |
intron_variant | MODIFIER | c.1084-99C>A | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 9/12 | chr12 | 111797979 | |||||||
chr12:111798411 | G | T | 1 | a0001c0001t0001g0214 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1248+169G>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 10/12 | chr12 | 111798411 | |||||||
chr12:111798412 | T | G | 1 | a0001c0001t0001g0214 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1248+170T>G | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 10/12 | chr12 | 111798412 | |||||||
chr12:111798413 | C | T | 1 | a0001c0001t0001g0214 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1248+171C>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 10/12 | chr12 | 111798413 | |||||||
chr12:111798592 | TG | T | 8 | a0001c0001t0017g0035 a0001c0001t0017g0038 a0001c0001t0025g0036 others(5): Show |
8 | HG01943.hp2 HG02257.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1248+352delG | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr12 | 111798592 | ||||||
chr12:111798805 | G | A | 2 | a0001c0001t0003g0009 a0001c0001t0003g0056 |
4 | HG01099.hp1 HG02886.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1248+563G>A | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 10/12 | chr12 | 111798805 | |||||||
chr12:111798966 | G | A | 1 | a0001c0001t0017g0038 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1248+724G>A | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 10/12 | chr12 | 111798966 | |||||||
chr12:111799021 | C | T | 6 | a0001c0001t0034g0005 a0001c0001t0035g0005 a0001c0001t0035g0183 others(3): Show |
6 | HG02109.hp1 HG02257.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1248+779C>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 10/12 | chr12 | 111799021 | |||||||
chr12:111799079 | A | G | 1 | a0001c0001t0122g0203 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1249-827A>G | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 10/12 | chr12 | 111799079 | |||||||
chr12:111799164 | A | G | 2 | a0001c0001t0001g0205 a0001c0001t0004g0202 |
2 | HG02074.hp2 NA18950.hp2 |
intron_variant | MODIFIER | c.1249-742A>G | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 10/12 | chr12 | 111799164 | |||||||
chr12:111799331 | A | G | 8 | a0001c0001t0017g0035 a0001c0001t0017g0038 a0001c0001t0025g0036 others(5): Show |
8 | HG01943.hp2 HG02257.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1249-575A>G | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 10/12 | chr12 | 111799331 | |||||||
chr12:111799348 | G | T | 1 | a0001c0001t0054g0234 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1249-558G>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 10/12 | chr12 | 111799348 | |||||||
chr12:111799352 | A | T | 1 | a0001c0001t0054g0234 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1249-554A>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 10/12 | chr12 | 111799352 | |||||||
chr12:111799471 | A | AT | 8 | a0001c0001t0003g0071 a0001c0001t0006g0126 a0001c0001t0007g0100 others(5): Show |
8 | HG01175.hp2 HG02027.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1249-419dupT | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr12 | 111799471 | ||||||
chr12:111799471 | AT | A | 9 | a0001c0001t0002g0095 a0001c0001t0017g0035 a0001c0001t0017g0038 others(6): Show |
9 | HG01943.hp2 HG02257.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.1249-419delT | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr12 | 111799471 | ||||||
chr12:111799472 | T | A | 1 | a0001c0006t0127g0170 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1249-434T>A | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 10/12 | chr12 | 111799472 | |||||||
chr12:111799535 | C | A | 8 | a0001c0001t0017g0035 a0001c0001t0017g0038 a0001c0001t0025g0036 others(5): Show |
8 | HG01943.hp2 HG02257.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1249-371C>A | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 10/12 | chr12 | 111799535 | |||||||
chr12:111799643 | C | T | 3 | a0001c0001t0002g0156 a0001c0001t0002g0166 a0001c0001t0020g0162 |
3 | NA18984.hp1 NA18986.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.1249-263C>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 10/12 | chr12 | 111799643 | |||||||
chr12:111799644 | G | A | 1 | a0001c0001t0019g0233 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1249-262G>A | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 10/12 | chr12 | 111799644 | |||||||
chr12:111799705 | C | T | 8 | a0001c0001t0017g0035 a0001c0001t0017g0038 a0001c0001t0025g0036 others(5): Show |
8 | HG01943.hp2 HG02257.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1249-201C>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 10/12 | chr12 | 111799705 | |||||||
chr12:111799772 | G | A | 1 | a0002c0002t0004g0193 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1249-134G>A | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 10/12 | chr12 | 111799772 | |||||||
chr12:111799814 | C | T | 1 | a0001c0001t0109g0127 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1249-92C>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 10/12 | chr12 | 111799814 | |||||||
chr12:111799825 | A | C | 1 | a0001c0001t0018g0104 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1249-81A>C | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 10/12 | chr12 | 111799825 | |||||||
chr12:111799849 | C | T | 3 | a0001c0001t0014g0177 a0001c0001t0014g0178 a0001c0001t0023g0175 |
3 | HG02145.hp1 HG02622.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1249-57C>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 10/12 | chr12 | 111799849 | |||||||
chr12:111799851 | C | T | 1 | a0001c0001t0002g0155 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1249-55C>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 10/12 | chr12 | 111799851 | |||||||
chr12:111800102 | A | T | 1 | a0001c0001t0054g0234 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1406+39A>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 11/12 | chr12 | 111800102 | |||||||
chr12:111800177 | T | C | 2 | a0001c0001t0036g0180 a0001c0001t0125g0198 |
2 | NA18957.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.1406+114T>C | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 11/12 | chr12 | 111800177 | |||||||
chr12:111800182 | C | T | 2 | a0001c0001t0019g0015 a0001c0001t0055g0015 |
2 | HG02630.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1406+119C>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 11/12 | chr12 | 111800182 | |||||||
chr12:111800195 | C | T | 1 | a0001c0001t0063g0099 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1406+132C>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 11/12 | chr12 | 111800195 | |||||||
chr12:111800244 | T | C | 8 | a0001c0001t0017g0035 a0001c0001t0017g0038 a0001c0001t0025g0036 others(5): Show |
8 | HG01943.hp2 HG02257.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1406+181T>C | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 11/12 | chr12 | 111800244 | |||||||
chr12:111800446 | C | G | 1 | a0001c0001t0075g0070 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1406+383C>G | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 11/12 | chr12 | 111800446 | |||||||
chr12:111800460 | C | T | 1 | a0001c0001t0086g0051 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1406+397C>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 11/12 | chr12 | 111800460 | |||||||
chr12:111800580 | A | G | 8 | a0001c0001t0017g0035 a0001c0001t0017g0038 a0001c0001t0025g0036 others(5): Show |
8 | HG01943.hp2 HG02257.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1406+517A>G | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 11/12 | chr12 | 111800580 | |||||||
chr12:111800629 | C | T | 3 | a0001c0001t0001g0046 a0001c0001t0001g0060 a0001c0001t0001g0061 |
3 | HG00735.hp1 HG01496.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.1406+566C>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 11/12 | chr12 | 111800629 | |||||||
chr12:111800801 | A | G | 1 | a0001c0001t0025g0036 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1406+738A>G | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 11/12 | chr12 | 111800801 | |||||||
chr12:111800927 | G | A | 2 | a0001c0001t0012g0050 a0001c0001t0097g0084 |
2 | HG02055.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.1406+864G>A | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 11/12 | chr12 | 111800927 | |||||||
chr12:111801209 | G | A | 1 | a0001c0009t0103g0231 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1406+1146G>A | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 11/12 | chr12 | 111801209 | |||||||
chr12:111801289 | G | A | 19 | a0001c0001t0011g0007 a0001c0001t0011g0031 a0001c0001t0011g0230 others(16): Show |
21 | HG01168.hp1 HG01169.hp2 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.1406+1226G>A | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 11/12 | chr12 | 111801289 | |||||||
chr12:111801317 | A | G | 1 | a0001c0006t0127g0170 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1406+1254A>G | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 11/12 | chr12 | 111801317 | |||||||
chr12:111801337 | A | C | 79 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0028 others(76): Show |
102 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.1406+1274A>C | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 11/12 | chr12 | 111801337 | |||||||
chr12:111801592 | G | A | 2 | a0001c0001t0001g0219 a0001c0001t0001g0225 |
2 | NA18942.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.1406+1529G>A | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 11/12 | chr12 | 111801592 | |||||||
chr12:111801658 | C | G | 1 | a0001c0001t0003g0077 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1406+1595C>G | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 11/12 | chr12 | 111801658 | |||||||
chr12:111801693 | C | CA | 13 | a0001c0001t0008g0017 a0001c0001t0008g0043 a0001c0001t0008g0062 others(10): Show |
13 | HG00408.hp1 HG00597.hp2 HG00609.hp1 others(10): Show |
intron_variant | MODIFIER | c.1406+1645dupA | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 111801693 | ||||||
chr12:111801693 | CA | C | 16 | a0001c0001t0002g0137 a0001c0001t0011g0007 a0001c0001t0011g0031 others(13): Show |
18 | HG01168.hp1 HG01169.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.1406+1645delA | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 111801693 | ||||||
chr12:111802068 | T | C | 189 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0028 others(186): Show |
226 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(223): Show |
intron_variant | MODIFIER | c.1407-1791T>C | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 11/12 | chr12 | 111802068 | |||||||
chr12:111802336 | C | T | 1 | a0001c0001t0002g0157 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1407-1523C>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 11/12 | chr12 | 111802336 | |||||||
chr12:111802337 | G | A | 1 | a0001c0001t0002g0137 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1407-1522G>A | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 11/12 | chr12 | 111802337 | |||||||
chr12:111802388 | G | A | 63 | a0001c0001t0003g0002 a0001c0001t0003g0009 a0001c0001t0003g0055 others(60): Show |
74 | HG00408.hp1 HG00597.hp2 HG00609.hp1 others(71): Show |
intron_variant | MODIFIER | c.1407-1471G>A | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 11/12 | chr12 | 111802388 | |||||||
chr12:111802411 | C | CA | 5 | a0001c0001t0002g0156 a0001c0001t0006g0022 a0001c0001t0006g0109 others(2): Show |
6 | HG02135.hp2 HG02970.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.1407-1428dupA | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 111802411 | ||||||
chr12:111802411 | CA | C | 147 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0028 others(144): Show |
181 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(178): Show |
intron_variant | MODIFIER | c.1407-1428delA | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 111802411 | ||||||
chr12:111802411 | CAA | C | 20 | a0001c0001t0003g0069 a0001c0001t0004g0182 a0001c0001t0014g0044 others(17): Show |
21 | HG00099.hp2 HG01175.hp1 HG01256.hp2 others(18): Show |
intron_variant | MODIFIER | c.1407-1429_1407-142 others(6): Show |
ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 111802411 | ||||||
chr12:111802478 | G | C | 1 | a0001c0006t0127g0170 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1407-1381G>C | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 11/12 | chr12 | 111802478 | |||||||
chr12:111802619 | A | G | 32 | a0001c0001t0002g0135 a0001c0001t0002g0137 a0001c0001t0002g0139 others(29): Show |
35 | HG00140.hp2 HG00738.hp2 HG01099.hp2 others(32): Show |
intron_variant | MODIFIER | c.1407-1240A>G | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 11/12 | chr12 | 111802619 | |||||||
chr12:111802646 | C | T | 1 | a0001c0001t0040g0042 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1407-1213C>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 11/12 | chr12 | 111802646 | |||||||
chr12:111802647 | A | G | 1 | a0001c0001t0040g0042 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1407-1212A>G | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 11/12 | chr12 | 111802647 | |||||||
chr12:111802662 | C | T | 6 | a0001c0001t0011g0007 a0001c0001t0011g0031 a0001c0001t0011g0230 others(3): Show |
8 | HG01168.hp1 HG01169.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.1407-1197C>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 11/12 | chr12 | 111802662 | |||||||
chr12:111802691 | T | C | 1 | a0001c0001t0070g0158 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1407-1168T>C | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 11/12 | chr12 | 111802691 | |||||||
chr12:111802697 | A | G | 1 | a0001c0001t0002g0154 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1407-1162A>G | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 11/12 | chr12 | 111802697 | |||||||
chr12:111802753 | A | G | 2 | a0001c0001t0053g0023 a0001c0001t0057g0023 |
2 | HG03516.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1407-1106A>G | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 11/12 | chr12 | 111802753 | |||||||
chr12:111802858 | C | T | 1 | a0001c0001t0109g0127 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1407-1001C>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 11/12 | chr12 | 111802858 | |||||||
chr12:111802875 | G | A | 78 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0028 others(75): Show |
101 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.1407-984G>A | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 11/12 | chr12 | 111802875 | |||||||
chr12:111802892 | A | AAAAAG | 75 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0028 others(72): Show |
98 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.1407-962_1407-958d others(7): Show |
ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 111802892 | ||||||
chr12:111803084 | G | A | 78 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0028 others(75): Show |
101 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.1407-775G>A | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 11/12 | chr12 | 111803084 | |||||||
chr12:111803175 | A | G | 1 | a0001c0001t0020g0153 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1407-684A>G | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 11/12 | chr12 | 111803175 | |||||||
chr12:111803281 | CA | C | 14 | a0001c0001t0011g0007 a0001c0001t0011g0031 a0001c0001t0011g0230 others(11): Show |
16 | HG01168.hp1 HG01169.hp2 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.1407-566delA | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 111803281 | ||||||
chr12:111803314 | C | T | 1 | a0001c0006t0127g0170 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1407-545C>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 11/12 | chr12 | 111803314 | |||||||
chr12:111803415 | T | C | 8 | a0001c0001t0017g0035 a0001c0001t0017g0038 a0001c0001t0025g0036 others(5): Show |
8 | HG01943.hp2 HG02257.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1407-444T>C | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 11/12 | chr12 | 111803415 | |||||||
chr12:111803585 | T | A | 14 | a0001c0001t0014g0044 a0001c0001t0014g0045 a0001c0001t0014g0085 others(11): Show |
15 | HG00099.hp2 HG01175.hp1 HG01361.hp2 others(12): Show |
intron_variant | MODIFIER | c.1407-274T>A | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 11/12 | chr12 | 111803585 | |||||||
chr12:111803598 | G | A | 70 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0028 others(67): Show |
93 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.1407-261G>A | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 11/12 | chr12 | 111803598 | |||||||
chr12:111803655 | G | T | 1 | a0001c0001t0071g0143 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1407-204G>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 11/12 | chr12 | 111803655 | |||||||
chr12:111803668 | G | A | 14 | a0001c0001t0014g0044 a0001c0001t0014g0045 a0001c0001t0014g0085 others(11): Show |
15 | HG00099.hp2 HG01175.hp1 HG01361.hp2 others(12): Show |
intron_variant | MODIFIER | c.1407-191G>A | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 11/12 | chr12 | 111803668 | |||||||
chr12:111803684 | C | T | 1 | a0002c0002t0001g0196 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1407-175C>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 11/12 | chr12 | 111803684 | |||||||
chr12:111803748 | T | A | 93 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0028 others(90): Show |
117 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.1407-111T>A | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 11/12 | chr12 | 111803748 | |||||||
chr12:111803793 | G | C | 3 | a0001c0001t0002g0130 a0001c0001t0002g0133 a0001c0001t0002g0163 |
3 | HG02572.hp1 HG02630.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1407-66G>C | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 11/12 | chr12 | 111803793 | |||||||
chr12:111803991 | T | C | 1 | a0001c0006t0127g0170 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1521+18T>C | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 12/12 | chr12 | 111803991 | |||||||
chr12:111804338 | T | A | 1 | a0001c0001t0017g0038 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1521+365T>A | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 12/12 | chr12 | 111804338 | |||||||
chr12:111804355 | C | T | 1 | a0001c0001t0044g0054 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1521+382C>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 12/12 | chr12 | 111804355 | |||||||
chr12:111804401 | G | A | 78 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0028 others(75): Show |
101 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.1521+428G>A | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 12/12 | chr12 | 111804401 | |||||||
chr12:111804619 | C | T | 2 | a0001c0001t0014g0044 a0001c0001t0014g0045 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1521+646C>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 12/12 | chr12 | 111804619 | |||||||
chr12:111804662 | G | A | 1 | a0001c0001t0008g0064 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1521+689G>A | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 12/12 | chr12 | 111804662 | |||||||
chr12:111804746 | C | CA | 9 | a0001c0001t0017g0035 a0001c0001t0017g0038 a0001c0001t0025g0036 others(6): Show |
9 | HG01943.hp2 HG02257.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.1521+789dupA | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr12 | 111804746 | ||||||
chr12:111804746 | CA | C | 7 | a0001c0001t0002g0025 a0001c0001t0003g0082 a0001c0001t0004g0182 others(4): Show |
8 | HG01169.hp1 HG01256.hp2 HG01943.hp1 others(5): Show |
intron_variant | MODIFIER | c.1521+789delA | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr12 | 111804746 | ||||||
chr12:111804876 | C | T | 1 | a0001c0001t0109g0127 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1521+903C>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 12/12 | chr12 | 111804876 | |||||||
chr12:111804914 | G | A | 1 | a0001c0001t0003g0088 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1521+941G>A | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 12/12 | chr12 | 111804914 | |||||||
chr12:111804932 | A | G | 1 | a0001c0001t0002g0152 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1521+959A>G | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 12/12 | chr12 | 111804932 | |||||||
chr12:111804959 | G | A | 3 | a0003c0003t0005g0094 a0003c0003t0027g0019 a0003c0003t0062g0118 |
4 | HG02602.hp1 HG03491.hp2 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.1521+986G>A | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 12/12 | chr12 | 111804959 | |||||||
chr12:111805098 | T | C | 1 | a0001c0007t0017g0040 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1521+1125T>C | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 12/12 | chr12 | 111805098 | |||||||
chr12:111805165 | A | G | 1 | a0001c0001t0108g0075 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1521+1192A>G | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 12/12 | chr12 | 111805165 | |||||||
chr12:111805751 | G | A | 1 | a0001c0001t0026g0121 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1521+1778G>A | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 12/12 | chr12 | 111805751 | |||||||
chr12:111805765 | G | A | 1 | a0001c0001t0002g0139 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1521+1792G>A | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 12/12 | chr12 | 111805765 | |||||||
chr12:111805947 | C | T | 1 | a0001c0006t0127g0170 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1521+1974C>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 12/12 | chr12 | 111805947 | |||||||
chr12:111805983 | A | G | 1 | a0001c0001t0026g0121 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1521+2010A>G | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 12/12 | chr12 | 111805983 | |||||||
chr12:111806025 | A | C | 77 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0028 others(74): Show |
100 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.1521+2052A>C | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 12/12 | chr12 | 111806025 | |||||||
chr12:111806122 | G | C | 1 | a0001c0006t0127g0170 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1521+2149G>C | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 12/12 | chr12 | 111806122 | |||||||
chr12:111806222 | C | T | 1 | a0001c0001t0004g0204 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1521+2249C>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 12/12 | chr12 | 111806222 | |||||||
chr12:111806223 | G | C | 1 | a0001c0001t0019g0233 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1521+2250G>C | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 12/12 | chr12 | 111806223 | |||||||
chr12:111806249 | G | A | 63 | a0001c0001t0003g0002 a0001c0001t0003g0009 a0001c0001t0003g0055 others(60): Show |
74 | HG00408.hp1 HG00597.hp2 HG00609.hp1 others(71): Show |
intron_variant | MODIFIER | c.1521+2276G>A | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 12/12 | chr12 | 111806249 | |||||||
chr12:111806336 | AAAAC | A | 81 | a0001c0001t0003g0002 a0001c0001t0003g0009 a0001c0001t0003g0055 others(78): Show |
93 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(90): Show |
intron_variant | MODIFIER | c.1521+2373_1521+237 others(8): Show |
ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr12 | 111806336 | ||||||
chr12:111806337 | A | G | 1 | a0001c0001t0111g0057 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1521+2364A>G | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 12/12 | chr12 | 111806337 | |||||||
chr12:111806340 | C | A | 1 | a0001c0001t0111g0057 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1521+2367C>A | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 12/12 | chr12 | 111806340 | |||||||
chr12:111806502 | C | T | 1 | a0001c0001t0026g0121 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1521+2529C>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 12/12 | chr12 | 111806502 | |||||||
chr12:111806609 | C | T | 14 | a0001c0001t0014g0044 a0001c0001t0014g0045 a0001c0001t0014g0085 others(11): Show |
15 | HG00099.hp2 HG01175.hp1 HG01361.hp2 others(12): Show |
intron_variant | MODIFIER | c.1521+2636C>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 12/12 | chr12 | 111806609 | |||||||
chr12:111806843 | T | C | 2 | a0001c0001t0015g0150 a0001c0001t0071g0143 |
2 | NA19056.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.1522-2700T>C | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 12/12 | chr12 | 111806843 | |||||||
chr12:111806925 | C | T | 3 | a0001c0001t0015g0150 a0001c0001t0039g0041 a0001c0001t0071g0143 |
3 | HG02257.hp2 NA19056.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.1522-2618C>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 12/12 | chr12 | 111806925 | |||||||
chr12:111807112 | A | C | 1 | a0001c0006t0127g0170 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1522-2431A>C | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 12/12 | chr12 | 111807112 | |||||||
chr12:111807235 | C | T | 5 | a0001c0001t0002g0013 a0001c0001t0002g0156 a0001c0001t0002g0166 others(2): Show |
6 | HG02080.hp1 NA18955.hp1 NA18975.hp1 others(3): Show |
intron_variant | MODIFIER | c.1522-2308C>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 12/12 | chr12 | 111807235 | |||||||
chr12:111807284 | G | A | 14 | a0001c0001t0014g0044 a0001c0001t0014g0045 a0001c0001t0014g0085 others(11): Show |
15 | HG00099.hp2 HG01175.hp1 HG01361.hp2 others(12): Show |
intron_variant | MODIFIER | c.1522-2259G>A | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 12/12 | chr12 | 111807284 | |||||||
chr12:111807285 | G | GA | 10 | a0001c0001t0005g0102 a0001c0001t0009g0223 a0001c0001t0011g0230 others(7): Show |
10 | HG02055.hp2 HG02080.hp2 HG02523.hp1 others(7): Show |
intron_variant | MODIFIER | c.1522-2247dupA | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr12 | 111807285 | ||||||
chr12:111807366 | A | C | 226 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0028 others(223): Show |
268 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(265): Show |
intron_variant | MODIFIER | c.1522-2177A>C | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 12/12 | chr12 | 111807366 | |||||||
chr12:111807416 | G | A | 1 | a0001c0001t0003g0081 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1522-2127G>A | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 12/12 | chr12 | 111807416 | |||||||
chr12:111807539 | T | C | 1 | a0001c0001t0001g0046 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1522-2004T>C | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 12/12 | chr12 | 111807539 | |||||||
chr12:111807701 | C | T | 1 | a0001c0001t0095g0174 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1522-1842C>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 12/12 | chr12 | 111807701 | |||||||
chr12:111807833 | T | G | 41 | a0001c0001t0005g0021 a0001c0001t0005g0098 a0001c0001t0005g0102 others(38): Show |
46 | HG00140.hp2 HG00738.hp2 HG01099.hp2 others(43): Show |
intron_variant | MODIFIER | c.1522-1710T>G | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 12/12 | chr12 | 111807833 | |||||||
chr12:111807875 | AT | A | 83 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0028 others(80): Show |
106 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(103): Show |
intron_variant | MODIFIER | c.1522-1651delT | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr12 | 111807875 | ||||||
chr12:111807969 | C | T | 2 | a0001c0001t0014g0044 a0001c0001t0014g0045 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1522-1574C>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 12/12 | chr12 | 111807969 | |||||||
chr12:111808150 | C | T | 1 | a0001c0006t0127g0170 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1522-1393C>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 12/12 | chr12 | 111808150 | |||||||
chr12:111808287 | T | C | 1 | a0001c0001t0002g0135 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1522-1256T>C | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 12/12 | chr12 | 111808287 | |||||||
chr12:111808380 | A | C | 1 | a0001c0006t0127g0170 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1522-1163A>C | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 12/12 | chr12 | 111808380 | |||||||
chr12:111808397 | A | G | 78 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0028 others(75): Show |
101 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.1522-1146A>G | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 12/12 | chr12 | 111808397 | |||||||
chr12:111808423 | G | A | 1 | a0001c0006t0127g0170 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1522-1120G>A | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 12/12 | chr12 | 111808423 | |||||||
chr12:111808479 | T | C | 3 | a0001c0001t0019g0233 a0001c0001t0054g0234 a0001c0001t0082g0240 |
3 | HG01243.hp2 HG02280.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1522-1064T>C | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 12/12 | chr12 | 111808479 | |||||||
chr12:111808573 | C | T | 1 | a0001c0001t0002g0151 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1522-970C>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 12/12 | chr12 | 111808573 | |||||||
chr12:111808653 | C | T | 8 | a0001c0001t0017g0035 a0001c0001t0017g0038 a0001c0001t0025g0036 others(5): Show |
8 | HG01943.hp2 HG02257.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1522-890C>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 12/12 | chr12 | 111808653 | |||||||
chr12:111808662 | G | A | 1 | a0001c0001t0013g0058 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1522-881G>A | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 12/12 | chr12 | 111808662 | |||||||
chr12:111808832 | G | A | 1 | a0001c0001t0083g0110 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1522-711G>A | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 12/12 | chr12 | 111808832 | |||||||
chr12:111809150 | C | G | 186 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0028 others(183): Show |
223 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(220): Show |
intron_variant | MODIFIER | c.1522-393C>G | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 12/12 | chr12 | 111809150 | |||||||
chr12:111809296 | AT | A | 6 | a0001c0001t0001g0006 a0001c0001t0004g0006 a0001c0001t0004g0182 others(3): Show |
9 | HG01071.hp2 HG01256.hp2 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1522-246delT | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 12/12 | chr12 | 111809296 | |||||||
chr12:111809299 | C | T | 1 | a0001c0001t0002g0149 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1522-244C>T | ALDH2 | ENSG00000111275.13 | transcript | ENST00000261733.7 | protein_coding | 12/12 | chr12 | 111809299 |