geneid | 163747 |
---|---|
ensemblid | ENSG00000162398.12 |
hgncid | 26854 |
symbol | LEXM |
name | ciliary microtubule associated protein 2 |
refseq_nuc | NM_001110533.2 |
refseq_prot | NP_001104003.1 |
ensembl_nuc | ENST00000371273.4 |
ensembl_prot | ENSP00000360320.3 |
mane_status | MANE Select |
chr | chr1 |
start | 54806063 |
end | 54842252 |
strand | + |
ver | v1.2 |
region | chr1:54806063-54842252 |
region5000 | chr1:54801063-54847252 |
regionname0 | LEXM_chr1_54806063_54842252 |
regionname5000 | LEXM_chr1_54801063_54847252 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 418 | 194 | 25 | 39 | 108 | 7 | 14 | 84 | LEXM_chr1_54801063_54847252 | LEXM | copy fasta | chr1 | 54801063 | 54847252 |
a0002 | 0/1 | 418 | 145 | 35 | 26 | 49 | 9 | 25 | 33 | LEXM_chr1_54801063_54847252 | LEXM | copy fasta | chr1 | 54801063 | 54847252 |
a0003 | 0/0 | 418 | 15 | 1 | 0 | 14 | 0 | 0 | 12 | LEXM_chr1_54801063_54847252 | LEXM | copy fasta | chr1 | 54801063 | 54847252 |
a0004 | 0/0 | 418 | 11 | 6 | 0 | 5 | 0 | 0 | 4 | LEXM_chr1_54801063_54847252 | LEXM | copy fasta | chr1 | 54801063 | 54847252 |
a0005 | 0/0 | 418 | 6 | 1 | 0 | 5 | 0 | 0 | 4 | LEXM_chr1_54801063_54847252 | LEXM | copy fasta | chr1 | 54801063 | 54847252 |
a0006 | 0/0 | 418 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | copy fasta | chr1 | 54801063 | 54847252 |
a0007 | 0/0 | 418 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | copy fasta | chr1 | 54801063 | 54847252 |
a0008 | 0/0 | 418 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | LEXM_chr1_54801063_54847252 | LEXM | copy fasta | chr1 | 54801063 | 54847252 |
a0009 | 0/0 | 418 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | copy fasta | chr1 | 54801063 | 54847252 |
a0010 | 0/0 | 418 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | copy fasta | chr1 | 54801063 | 54847252 |
a0011 | 0/0 | 418 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | copy fasta | chr1 | 54801063 | 54847252 |
a0012 | 0/0 | 418 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | LEXM_chr1_54801063_54847252 | LEXM | copy fasta | chr1 | 54801063 | 54847252 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/1 | 1257 | 114 | 25 | 19 | 39 | 8 | 22 | LEXM_chr1_54801063_54847252 | LEXM | copy fasta | chr1 | 54801063 | 54847252 |
c0002 | 1/0 | 1257 | 101 | 21 | 25 | 40 | 3 | 11 | LEXM_chr1_54801063_54847252 | LEXM | copy fasta | chr1 | 54801063 | 54847252 |
c0003 | 0/0 | 1257 | 58 | 4 | 12 | 36 | 4 | 2 | LEXM_chr1_54801063_54847252 | LEXM | copy fasta | chr1 | 54801063 | 54847252 |
c0004 | 0/0 | 1257 | 29 | 0 | 2 | 27 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | copy fasta | chr1 | 54801063 | 54847252 |
c0005 | 0/0 | 1257 | 20 | 5 | 4 | 9 | 1 | 1 | LEXM_chr1_54801063_54847252 | LEXM | copy fasta | chr1 | 54801063 | 54847252 |
c0006 | 0/0 | 1257 | 14 | 1 | 0 | 13 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | copy fasta | chr1 | 54801063 | 54847252 |
c0007 | 0/0 | 1257 | 6 | 1 | 0 | 5 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | copy fasta | chr1 | 54801063 | 54847252 |
c0008 | 0/0 | 1257 | 6 | 6 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | copy fasta | chr1 | 54801063 | 54847252 |
c0009 | 0/0 | 1257 | 5 | 0 | 0 | 4 | 0 | 1 | LEXM_chr1_54801063_54847252 | LEXM | copy fasta | chr1 | 54801063 | 54847252 |
c0010 | 0/0 | 1257 | 5 | 5 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | copy fasta | chr1 | 54801063 | 54847252 |
c0011 | 0/0 | 1257 | 5 | 0 | 3 | 1 | 0 | 1 | LEXM_chr1_54801063_54847252 | LEXM | copy fasta | chr1 | 54801063 | 54847252 |
c0012 | 0/0 | 1257 | 5 | 0 | 0 | 5 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | copy fasta | chr1 | 54801063 | 54847252 |
c0013 | 0/0 | 1257 | 3 | 3 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | copy fasta | chr1 | 54801063 | 54847252 |
c0014 | 0/0 | 1257 | 3 | 3 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | copy fasta | chr1 | 54801063 | 54847252 |
c0015 | 0/0 | 1257 | 1 | 0 | 0 | 0 | 0 | 1 | LEXM_chr1_54801063_54847252 | LEXM | copy fasta | chr1 | 54801063 | 54847252 |
c0016 | 0/0 | 1257 | 1 | 0 | 0 | 0 | 0 | 1 | LEXM_chr1_54801063_54847252 | LEXM | copy fasta | chr1 | 54801063 | 54847252 |
c0017 | 0/0 | 1257 | 1 | 0 | 1 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | copy fasta | chr1 | 54801063 | 54847252 |
c0018 | 0/0 | 1257 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | copy fasta | chr1 | 54801063 | 54847252 |
c0019 | 0/0 | 1257 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | copy fasta | chr1 | 54801063 | 54847252 |
c0020 | 0/0 | 1257 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | copy fasta | chr1 | 54801063 | 54847252 |
c0021 | 0/0 | 1257 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | copy fasta | chr1 | 54801063 | 54847252 |
c0022 | 0/0 | 1257 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | copy fasta | chr1 | 54801063 | 54847252 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 434 | 143 | 36 | 21 | 54 | 7 | 24 | LEXM_chr1_54801063_54847252 | LEXM | copy fasta | chr1 | 54801063 | 54847252 |
t0002 | 1/0 | 434 | 111 | 24 | 24 | 47 | 3 | 12 | LEXM_chr1_54801063_54847252 | LEXM | copy fasta | chr1 | 54801063 | 54847252 |
t0003 | 0/0 | 434 | 88 | 7 | 13 | 62 | 4 | 2 | LEXM_chr1_54801063_54847252 | LEXM | copy fasta | chr1 | 54801063 | 54847252 |
t0004 | 0/0 | 434 | 34 | 6 | 7 | 18 | 1 | 2 | LEXM_chr1_54801063_54847252 | LEXM | copy fasta | chr1 | 54801063 | 54847252 |
t0005 | 0/0 | 434 | 2 | 2 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | copy fasta | chr1 | 54801063 | 54847252 |
t0006 | 0/0 | 434 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | copy fasta | chr1 | 54801063 | 54847252 |
t0007 | 0/0 | 434 | 1 | 0 | 0 | 0 | 1 | 0 | LEXM_chr1_54801063_54847252 | LEXM | copy fasta | chr1 | 54801063 | 54847252 |
t0008 | 0/0 | 434 | 1 | 0 | 1 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | copy fasta | chr1 | 54801063 | 54847252 |
t0009 | 0/0 | 434 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | copy fasta | chr1 | 54801063 | 54847252 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0002 | 0/0 | 5 | 0 | 1 | 1 | 0 | 3 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0003 | 0/0 | 5 | 0 | 3 | 0 | 2 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0004 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0005 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0006 | 0/0 | 4 | 0 | 1 | 2 | 1 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0007 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0009 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0010 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0016 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0018 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0019 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0020 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0021 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0023 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0024 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0035 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0037 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0040 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0043 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0044 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0046 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0047 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0049 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0050 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0051 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0052 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0150 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0262 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0002 | 1/0 | 1257 | 101 | 21 | 25 | 40 | 3 | 11 | LEXM_chr1_54801063_54847252 | LEXM | copy fasta | chr1 | 54801063 | 54847252 |
a0001c0003 | 0/0 | 1257 | 58 | 4 | 12 | 36 | 4 | 2 | LEXM_chr1_54801063_54847252 | LEXM | copy fasta | chr1 | 54801063 | 54847252 |
a0001c0004 | 0/0 | 1257 | 29 | 0 | 2 | 27 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | copy fasta | chr1 | 54801063 | 54847252 |
a0001c0009 | 0/0 | 1257 | 5 | 0 | 0 | 4 | 0 | 1 | LEXM_chr1_54801063_54847252 | LEXM | copy fasta | chr1 | 54801063 | 54847252 |
a0001c0018 | 0/0 | 1257 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | copy fasta | chr1 | 54801063 | 54847252 |
a0002c0001 | 0/1 | 1257 | 114 | 25 | 19 | 39 | 8 | 22 | LEXM_chr1_54801063_54847252 | LEXM | copy fasta | chr1 | 54801063 | 54847252 |
a0002c0005 | 0/0 | 1257 | 20 | 5 | 4 | 9 | 1 | 1 | LEXM_chr1_54801063_54847252 | LEXM | copy fasta | chr1 | 54801063 | 54847252 |
a0002c0010 | 0/0 | 1257 | 5 | 5 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | copy fasta | chr1 | 54801063 | 54847252 |
a0002c0011 | 0/0 | 1257 | 5 | 0 | 3 | 1 | 0 | 1 | LEXM_chr1_54801063_54847252 | LEXM | copy fasta | chr1 | 54801063 | 54847252 |
a0002c0015 | 0/0 | 1257 | 1 | 0 | 0 | 0 | 0 | 1 | LEXM_chr1_54801063_54847252 | LEXM | copy fasta | chr1 | 54801063 | 54847252 |
a0003c0006 | 0/0 | 1257 | 14 | 1 | 0 | 13 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | copy fasta | chr1 | 54801063 | 54847252 |
a0003c0020 | 0/0 | 1257 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | copy fasta | chr1 | 54801063 | 54847252 |
a0004c0008 | 0/0 | 1257 | 6 | 6 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | copy fasta | chr1 | 54801063 | 54847252 |
a0004c0012 | 0/0 | 1257 | 5 | 0 | 0 | 5 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | copy fasta | chr1 | 54801063 | 54847252 |
a0005c0007 | 0/0 | 1257 | 6 | 1 | 0 | 5 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | copy fasta | chr1 | 54801063 | 54847252 |
a0006c0014 | 0/0 | 1257 | 3 | 3 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | copy fasta | chr1 | 54801063 | 54847252 |
a0007c0013 | 0/0 | 1257 | 3 | 3 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | copy fasta | chr1 | 54801063 | 54847252 |
a0008c0022 | 0/0 | 1257 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | copy fasta | chr1 | 54801063 | 54847252 |
a0009c0021 | 0/0 | 1257 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | copy fasta | chr1 | 54801063 | 54847252 |
a0010c0019 | 0/0 | 1257 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | copy fasta | chr1 | 54801063 | 54847252 |
a0011c0017 | 0/0 | 1257 | 1 | 0 | 1 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | copy fasta | chr1 | 54801063 | 54847252 |
a0012c0016 | 0/0 | 1257 | 1 | 0 | 0 | 0 | 0 | 1 | LEXM_chr1_54801063_54847252 | LEXM | copy fasta | chr1 | 54801063 | 54847252 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0002t0001 | 0/0 | 1690 | 1 | 0 | 1 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | copy fasta | chr1 | 54801063 | 54847252 |
a0001c0002t0002 | 1/0 | 1690 | 97 | 19 | 24 | 39 | 3 | 11 | LEXM_chr1_54801063_54847252 | LEXM | copy fasta | chr1 | 54801063 | 54847252 |
a0001c0002t0005 | 0/0 | 1690 | 2 | 2 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | copy fasta | chr1 | 54801063 | 54847252 |
a0001c0002t0009 | 0/0 | 1690 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | copy fasta | chr1 | 54801063 | 54847252 |
a0001c0003t0003 | 0/0 | 1690 | 55 | 4 | 11 | 34 | 4 | 2 | LEXM_chr1_54801063_54847252 | LEXM | copy fasta | chr1 | 54801063 | 54847252 |
a0001c0003t0004 | 0/0 | 1690 | 2 | 0 | 0 | 2 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | copy fasta | chr1 | 54801063 | 54847252 |
a0001c0003t0008 | 0/0 | 1690 | 1 | 0 | 1 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | copy fasta | chr1 | 54801063 | 54847252 |
a0001c0004t0003 | 0/0 | 1690 | 29 | 0 | 2 | 27 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | copy fasta | chr1 | 54801063 | 54847252 |
a0001c0009t0002 | 0/0 | 1690 | 5 | 0 | 0 | 4 | 0 | 1 | LEXM_chr1_54801063_54847252 | LEXM | copy fasta | chr1 | 54801063 | 54847252 |
a0001c0018t0003 | 0/0 | 1690 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | copy fasta | chr1 | 54801063 | 54847252 |
a0002c0001t0001 | 0/1 | 1690 | 113 | 25 | 19 | 39 | 7 | 22 | LEXM_chr1_54801063_54847252 | LEXM | copy fasta | chr1 | 54801063 | 54847252 |
a0002c0001t0007 | 0/0 | 1690 | 1 | 0 | 0 | 0 | 1 | 0 | LEXM_chr1_54801063_54847252 | LEXM | copy fasta | chr1 | 54801063 | 54847252 |
a0002c0005t0004 | 0/0 | 1690 | 20 | 5 | 4 | 9 | 1 | 1 | LEXM_chr1_54801063_54847252 | LEXM | copy fasta | chr1 | 54801063 | 54847252 |
a0002c0010t0001 | 0/0 | 1690 | 5 | 5 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | copy fasta | chr1 | 54801063 | 54847252 |
a0002c0011t0004 | 0/0 | 1690 | 5 | 0 | 3 | 1 | 0 | 1 | LEXM_chr1_54801063_54847252 | LEXM | copy fasta | chr1 | 54801063 | 54847252 |
a0002c0015t0001 | 0/0 | 1690 | 1 | 0 | 0 | 0 | 0 | 1 | LEXM_chr1_54801063_54847252 | LEXM | copy fasta | chr1 | 54801063 | 54847252 |
a0003c0006t0001 | 0/0 | 1690 | 14 | 1 | 0 | 13 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | copy fasta | chr1 | 54801063 | 54847252 |
a0003c0020t0004 | 0/0 | 1690 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | copy fasta | chr1 | 54801063 | 54847252 |
a0004c0008t0001 | 0/0 | 1690 | 5 | 5 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | copy fasta | chr1 | 54801063 | 54847252 |
a0004c0008t0006 | 0/0 | 1690 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | copy fasta | chr1 | 54801063 | 54847252 |
a0004c0012t0004 | 0/0 | 1690 | 5 | 0 | 0 | 5 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | copy fasta | chr1 | 54801063 | 54847252 |
a0005c0007t0001 | 0/0 | 1690 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | copy fasta | chr1 | 54801063 | 54847252 |
a0005c0007t0002 | 0/0 | 1690 | 5 | 1 | 0 | 4 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | copy fasta | chr1 | 54801063 | 54847252 |
a0006c0014t0003 | 0/0 | 1690 | 3 | 3 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | copy fasta | chr1 | 54801063 | 54847252 |
a0007c0013t0002 | 0/0 | 1690 | 3 | 3 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | copy fasta | chr1 | 54801063 | 54847252 |
a0008c0022t0001 | 0/0 | 1690 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | copy fasta | chr1 | 54801063 | 54847252 |
a0009c0021t0004 | 0/0 | 1690 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | copy fasta | chr1 | 54801063 | 54847252 |
a0010c0019t0002 | 0/0 | 1690 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | copy fasta | chr1 | 54801063 | 54847252 |
a0011c0017t0001 | 0/0 | 1690 | 1 | 0 | 1 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | copy fasta | chr1 | 54801063 | 54847252 |
a0012c0016t0001 | 0/0 | 1690 | 1 | 0 | 0 | 0 | 0 | 1 | LEXM_chr1_54801063_54847252 | LEXM | copy fasta | chr1 | 54801063 | 54847252 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0002t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0001c0002t0002g0005 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0001c0002t0002g0009 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0001c0002t0002g0010 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0001c0002t0002g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0001c0002t0002g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0001c0002t0002g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0001c0002t0002g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0001c0002t0002g0023 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0001c0002t0002g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0001c0002t0002g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0001c0002t0002g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0001c0002t0002g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0001c0002t0002g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0001c0002t0002g0046 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0001c0002t0002g0049 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0001c0002t0002g0050 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0001c0002t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0001c0002t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0001c0002t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0001c0002t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0001c0002t0002g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0001c0002t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0001c0002t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0001c0002t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0001c0002t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0001c0002t0002g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0001c0002t0002g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0001c0002t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0001c0002t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0001c0002t0002g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0001c0002t0002g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0001c0002t0002g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0001c0002t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0001c0002t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0001c0002t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0001c0002t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0001c0002t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0001c0002t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0001c0002t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0001c0002t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0001c0002t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0001c0002t0002g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0001c0002t0002g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0001c0002t0002g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0001c0002t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0001c0002t0002g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0001c0002t0002g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0001c0002t0002g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0001c0002t0002g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0001c0002t0002g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0001c0002t0002g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0001c0002t0002g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0001c0002t0002g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0001c0002t0002g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0001c0002t0002g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0001c0002t0002g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0001c0002t0002g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0001c0002t0002g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0001c0002t0002g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0001c0002t0002g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0001c0002t0002g0262 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0001c0002t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0001c0002t0002g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0001c0002t0002g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0001c0002t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0001c0002t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0001c0002t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0001c0002t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0001c0002t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0001c0002t0002g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0001c0002t0005g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0001c0002t0005g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0001c0002t0009g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0001c0003t0003g0003 | 0/0 | 5 | 0 | 3 | 0 | 2 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0001c0003t0003g0004 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0001c0003t0003g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0001c0003t0003g0019 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0001c0003t0003g0020 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0001c0003t0003g0021 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0001c0003t0003g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0001c0003t0003g0044 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0001c0003t0003g0047 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0001c0003t0003g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0001c0003t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0001c0003t0003g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0001c0003t0003g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0001c0003t0003g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0001c0003t0003g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0001c0003t0003g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0001c0003t0003g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0001c0003t0003g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0001c0003t0003g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0001c0003t0003g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0001c0003t0003g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0001c0003t0003g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0001c0003t0003g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0001c0003t0003g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0001c0003t0003g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0001c0003t0003g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0001c0003t0003g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0001c0003t0003g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0001c0003t0003g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0001c0003t0003g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0001c0003t0003g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0001c0003t0003g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0001c0003t0003g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0001c0003t0003g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0001c0003t0004g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0001c0003t0008g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0001c0004t0003g0001 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0001c0004t0003g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0001c0004t0003g0043 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0001c0004t0003g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0001c0004t0003g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0001c0004t0003g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0001c0004t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0001c0004t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0001c0004t0003g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0001c0004t0003g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0001c0004t0003g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0001c0004t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0001c0004t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0001c0004t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0001c0004t0003g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0001c0004t0003g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0001c0004t0003g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0001c0004t0003g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0001c0004t0003g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0001c0004t0003g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0001c0004t0003g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0001c0004t0003g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0001c0004t0003g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0001c0009t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0001c0009t0002g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0001c0009t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0001c0009t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0001c0009t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0001c0018t0003g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0002c0001t0001g0002 | 0/0 | 4 | 0 | 0 | 1 | 0 | 3 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0002c0001t0001g0006 | 0/0 | 4 | 0 | 1 | 2 | 1 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0002c0001t0001g0007 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0002c0001t0001g0016 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0002c0001t0001g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0002c0001t0001g0018 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0002c0001t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0002c0001t0001g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0002c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0002c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0002c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0002c0001t0001g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0002c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0002c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0002c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0002c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0002c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0002c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0002c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0002c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0002c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0002c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0002c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0002c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0002c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0002c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0002c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0002c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0002c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0002c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0002c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0002c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0002c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0002c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0002c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0002c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0002c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0002c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0002c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0002c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0002c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0002c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0002c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0002c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0002c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0002c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0002c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0002c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0002c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0002c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0002c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0002c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0002c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0002c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0002c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0002c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0002c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0002c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0002c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0002c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0002c0001t0001g0150 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0002c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0002c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0002c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0002c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0002c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0002c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0002c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0002c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0002c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0002c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0002c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0002c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0002c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0002c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0002c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0002c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0002c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0002c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0002c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0002c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0002c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0002c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0002c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0002c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0002c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0002c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0002c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0002c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0002c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0002c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0002c0001t0007g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0002c0005t0004g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0002c0005t0004g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0002c0005t0004g0040 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0002c0005t0004g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0002c0005t0004g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0002c0005t0004g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0002c0005t0004g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0002c0005t0004g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0002c0005t0004g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0002c0005t0004g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0002c0005t0004g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0002c0005t0004g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0002c0005t0004g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0002c0005t0004g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0002c0005t0004g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0002c0005t0004g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0002c0010t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0002c0010t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0002c0010t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0002c0010t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0002c0011t0004g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0002c0011t0004g0037 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0002c0011t0004g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0002c0011t0004g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0002c0015t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0003c0006t0001g0051 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0003c0006t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0003c0006t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0003c0006t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0003c0006t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0003c0006t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0003c0006t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0003c0006t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0003c0006t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0003c0006t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0003c0006t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0003c0006t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0003c0006t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0003c0020t0004g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0004c0008t0001g0052 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0004c0008t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0004c0008t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0004c0008t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0004c0008t0006g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0004c0012t0004g0024 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0004c0012t0004g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0004c0012t0004g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0005c0007t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0005c0007t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0005c0007t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0005c0007t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0005c0007t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0005c0007t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0006c0014t0003g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0006c0014t0003g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0007c0013t0002g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0007c0013t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0008c0022t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0009c0021t0004g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0010c0019t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0011c0017t0001g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
a0012c0016t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0002 | c0001 | t0001 | g0006 | EUR | GBR | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG00099 | hp2 | a0001 | c0003 | t0003 | g0003 | EUR | GBR | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG00140 | hp1 | a0001 | c0003 | t0003 | g0044 | EUR | GBR | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG00140 | hp2 | a0002 | c0001 | t0001 | g0148 | EUR | GBR | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG00280 | hp1 | a0002 | c0001 | t0001 | g0018 | EUR | FIN | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG00280 | hp2 | a0001 | c0002 | t0002 | g0023 | EUR | FIN | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG00323 | hp1 | a0001 | c0003 | t0003 | g0216 | EUR | FIN | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG00323 | hp2 | a0002 | c0001 | t0007 | g0154 | EUR | FIN | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG00408 | hp1 | a0001 | c0002 | t0002 | g0269 | EAS | CHS | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG00408 | hp2 | a0001 | c0004 | t0003 | g0001 | EAS | CHS | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG00423 | hp1 | a0002 | c0001 | t0001 | g0165 | EAS | CHS | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG00423 | hp2 | a0001 | c0002 | t0002 | g0268 | EAS | CHS | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG00438 | hp1 | a0002 | c0001 | t0001 | g0167 | EAS | CHS | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG00438 | hp2 | a0001 | c0004 | t0003 | g0213 | EAS | CHS | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG00544 | hp1 | a0001 | c0003 | t0003 | g0227 | EAS | CHS | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG00544 | hp2 | a0002 | c0001 | t0001 | g0147 | EAS | CHS | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG00558 | hp1 | a0001 | c0002 | t0002 | g0015 | EAS | CHS | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG00558 | hp2 | a0002 | c0005 | t0004 | g0030 | EAS | CHS | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG00609 | hp1 | a0001 | c0004 | t0003 | g0194 | EAS | CHS | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG00609 | hp2 | a0001 | c0004 | t0003 | g0190 | EAS | CHS | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG00621 | hp1 | a0001 | c0002 | t0002 | g0270 | EAS | CHS | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG00621 | hp2 | a0001 | c0003 | t0003 | g0239 | EAS | CHS | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG00639 | hp1 | a0002 | c0001 | t0001 | g0157 | AMR | PUR | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG00639 | hp2 | a0001 | c0002 | t0002 | g0253 | AMR | PUR | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG00642 | hp1 | a0002 | c0001 | t0001 | g0135 | AMR | PUR | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG00642 | hp2 | a0002 | c0001 | t0001 | g0073 | AMR | PUR | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG00673 | hp1 | a0002 | c0001 | t0001 | g0036 | EAS | CHS | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG00673 | hp2 | a0001 | c0003 | t0004 | g0027 | EAS | CHS | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG00735 | hp1 | a0001 | c0003 | t0003 | g0003 | AMR | PUR | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG00735 | hp2 | a0002 | c0001 | t0001 | g0092 | AMR | PUR | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG00741 | hp1 | a0001 | c0002 | t0002 | g0023 | AMR | PUR | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG00741 | hp2 | a0011 | c0017 | t0001 | g0002 | AMR | PUR | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG01069 | hp1 | a0001 | c0002 | t0002 | g0218 | AMR | PUR | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG01069 | hp2 | a0001 | c0002 | t0002 | g0061 | AMR | PUR | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG01070 | hp1 | a0001 | c0002 | t0002 | g0252 | AMR | PUR | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG01070 | hp2 | a0001 | c0003 | t0003 | g0215 | AMR | PUR | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG01071 | hp1 | a0001 | c0002 | t0002 | g0258 | AMR | PUR | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG01071 | hp2 | a0001 | c0002 | t0002 | g0219 | AMR | PUR | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG01074 | hp1 | a0001 | c0003 | t0003 | g0223 | AMR | PUR | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG01074 | hp2 | a0002 | c0001 | t0001 | g0139 | AMR | PUR | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG01099 | hp1 | a0001 | c0002 | t0002 | g0010 | AMR | PUR | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG01099 | hp2 | a0001 | c0002 | t0002 | g0005 | AMR | PUR | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG01106 | hp1 | a0002 | c0001 | t0001 | g0116 | AMR | PUR | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG01106 | hp2 | a0001 | c0003 | t0003 | g0003 | AMR | PUR | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG01109 | hp1 | a0002 | c0001 | t0001 | g0034 | AMR | PUR | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG01109 | hp2 | a0001 | c0003 | t0003 | g0217 | AMR | PUR | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG01167 | hp1 | a0001 | c0002 | t0001 | g0078 | AMR | PUR | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG01167 | hp2 | a0001 | c0002 | t0002 | g0026 | AMR | PUR | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG01168 | hp1 | a0002 | c0001 | t0001 | g0169 | AMR | PUR | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG01168 | hp2 | a0001 | c0004 | t0003 | g0043 | AMR | PUR | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG01169 | hp1 | a0001 | c0004 | t0003 | g0043 | AMR | PUR | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG01169 | hp2 | a0001 | c0002 | t0002 | g0026 | AMR | PUR | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG01175 | hp1 | a0002 | c0001 | t0001 | g0130 | AMR | PUR | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG01175 | hp2 | a0002 | c0005 | t0004 | g0173 | AMR | PUR | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG01192 | hp1 | a0001 | c0003 | t0003 | g0003 | AMR | PUR | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG01192 | hp2 | a0002 | c0001 | t0001 | g0182 | AMR | PUR | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG01243 | hp1 | a0002 | c0001 | t0001 | g0181 | AMR | PUR | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG01243 | hp2 | a0002 | c0005 | t0004 | g0070 | AMR | PUR | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG01255 | hp1 | a0002 | c0001 | t0001 | g0110 | AMR | CLM | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG01255 | hp2 | a0001 | c0002 | t0002 | g0005 | AMR | CLM | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG01256 | hp1 | a0001 | c0003 | t0008 | g0226 | AMR | CLM | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG01256 | hp2 | a0001 | c0002 | t0002 | g0050 | AMR | CLM | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG01257 | hp1 | a0002 | c0005 | t0004 | g0040 | AMR | CLM | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG01257 | hp2 | a0001 | c0002 | t0002 | g0046 | AMR | CLM | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG01258 | hp1 | a0002 | c0005 | t0004 | g0040 | AMR | CLM | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG01258 | hp2 | a0001 | c0002 | t0002 | g0050 | AMR | CLM | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG01261 | hp1 | a0002 | c0001 | t0001 | g0006 | AMR | CLM | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG01261 | hp2 | a0002 | c0001 | t0001 | g0034 | AMR | CLM | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG01346 | hp1 | a0001 | c0002 | t0002 | g0025 | AMR | CLM | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG01346 | hp2 | a0002 | c0001 | t0001 | g0128 | AMR | CLM | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG01361 | hp1 | a0001 | c0003 | t0003 | g0021 | AMR | CLM | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG01361 | hp2 | a0001 | c0002 | t0002 | g0023 | AMR | CLM | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG01433 | hp1 | a0001 | c0003 | t0003 | g0044 | AMR | CLM | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG01433 | hp2 | a0002 | c0001 | t0001 | g0018 | AMR | CLM | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG01515 | hp1 | a0002 | c0001 | t0001 | g0035 | EUR | IBS | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG01515 | hp2 | a0001 | c0003 | t0003 | g0003 | EUR | IBS | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG01516 | hp1 | a0001 | c0002 | t0002 | g0257 | EUR | IBS | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG01516 | hp2 | a0002 | c0001 | t0001 | g0018 | EUR | IBS | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG01884 | hp1 | a0010 | c0019 | t0002 | g0067 | AFR | ACB | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG01884 | hp2 | a0004 | c0008 | t0001 | g0052 | AFR | ACB | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG01891 | hp1 | a0001 | c0002 | t0002 | g0079 | AFR | ACB | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG01891 | hp2 | a0001 | c0002 | t0002 | g0065 | AFR | ACB | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG01934 | hp1 | a0001 | c0002 | t0002 | g0260 | AMR | PEL | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG01934 | hp2 | a0001 | c0002 | t0002 | g0005 | AMR | PEL | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG01978 | hp1 | a0001 | c0002 | t0002 | g0010 | AMR | PEL | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG01978 | hp2 | a0002 | c0011 | t0004 | g0196 | AMR | PEL | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG01981 | hp1 | a0002 | c0001 | t0001 | g0127 | AMR | PEL | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG01981 | hp2 | a0001 | c0002 | t0002 | g0010 | AMR | PEL | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG01993 | hp1 | a0001 | c0002 | t0002 | g0005 | AMR | PEL | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG01993 | hp2 | a0002 | c0001 | t0001 | g0159 | AMR | PEL | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG02004 | hp1 | a0001 | c0002 | t0002 | g0010 | AMR | PEL | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG02004 | hp2 | a0001 | c0003 | t0003 | g0019 | AMR | PEL | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG02015 | hp1 | a0002 | c0001 | t0001 | g0136 | EAS | KHV | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG02015 | hp2 | a0002 | c0001 | t0001 | g0145 | EAS | KHV | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG02027 | hp1 | a0002 | c0001 | t0001 | g0016 | EAS | KHV | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG02027 | hp2 | a0001 | c0004 | t0003 | g0001 | EAS | KHV | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG02040 | hp1 | a0004 | c0012 | t0004 | g0275 | EAS | KHV | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG02040 | hp2 | a0002 | c0011 | t0004 | g0037 | EAS | KHV | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG02055 | hp1 | a0002 | c0001 | t0001 | g0016 | AFR | ACB | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG02055 | hp2 | a0002 | c0001 | t0001 | g0134 | AFR | ACB | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG02056 | hp1 | a0001 | c0002 | t0002 | g0267 | EAS | KHV | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG02056 | hp2 | a0001 | c0003 | t0003 | g0020 | EAS | KHV | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG02071 | hp1 | a0002 | c0001 | t0001 | g0109 | EAS | KHV | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG02071 | hp2 | a0001 | c0003 | t0003 | g0229 | EAS | KHV | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG02074 | hp1 | a0002 | c0001 | t0001 | g0179 | EAS | KHV | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG02074 | hp2 | a0003 | c0006 | t0001 | g0286 | EAS | KHV | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG02080 | hp1 | a0001 | c0003 | t0003 | g0237 | EAS | KHV | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG02080 | hp2 | a0001 | c0003 | t0003 | g0008 | EAS | KHV | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG02083 | hp1 | a0002 | c0005 | t0004 | g0069 | EAS | KHV | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG02083 | hp2 | a0001 | c0004 | t0003 | g0054 | EAS | KHV | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG02132 | hp1 | a0002 | c0001 | t0001 | g0166 | EAS | KHV | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG02132 | hp2 | a0001 | c0002 | t0002 | g0011 | EAS | KHV | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG02135 | hp1 | a0001 | c0003 | t0003 | g0240 | EAS | KHV | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG02135 | hp2 | a0001 | c0003 | t0003 | g0008 | EAS | KHV | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG02145 | hp1 | a0002 | c0001 | t0001 | g0168 | AFR | ACB | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG02145 | hp2 | a0002 | c0001 | t0001 | g0007 | AFR | ACB | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG02148 | hp1 | a0001 | c0003 | t0003 | g0019 | AMR | PEL | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG02148 | hp2 | a0002 | c0011 | t0004 | g0001 | AMR | PEL | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG02155 | hp1 | a0002 | c0005 | t0004 | g0129 | EAS | CDX | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG02155 | hp2 | a0001 | c0004 | t0003 | g0195 | EAS | CDX | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG02165 | hp1 | a0003 | c0006 | t0001 | g0285 | EAS | CDX | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG02165 | hp2 | a0002 | c0005 | t0004 | g0030 | EAS | CDX | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG02257 | hp1 | a0004 | c0008 | t0006 | g0288 | AFR | ACB | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG02257 | hp2 | a0002 | c0001 | t0001 | g0124 | AFR | ACB | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG02293 | hp1 | a0002 | c0011 | t0004 | g0201 | AMR | PEL | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG02293 | hp2 | a0001 | c0002 | t0002 | g0025 | AMR | PEL | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG02300 | hp1 | a0001 | c0003 | t0003 | g0019 | AMR | PEL | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG02300 | hp2 | a0002 | c0001 | t0001 | g0133 | AMR | PEL | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG02451 | hp1 | a0007 | c0013 | t0002 | g0029 | AFR | ACB | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG02451 | hp2 | a0002 | c0010 | t0001 | g0152 | AFR | ACB | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG02523 | hp1 | a0002 | c0001 | t0001 | g0036 | EAS | KHV | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG02523 | hp2 | a0001 | c0002 | t0002 | g0266 | EAS | KHV | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG02572 | hp1 | a0002 | c0001 | t0001 | g0174 | AFR | GWD | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG02572 | hp2 | a0002 | c0001 | t0001 | g0160 | AFR | GWD | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG02602 | hp1 | a0001 | c0003 | t0003 | g0228 | SAS | PJL | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG02602 | hp2 | a0002 | c0001 | t0001 | g0002 | SAS | PJL | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG02615 | hp1 | a0002 | c0005 | t0004 | g0084 | AFR | GWD | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG02615 | hp2 | a0002 | c0001 | t0001 | g0162 | AFR | GWD | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG02622 | hp1 | a0001 | c0002 | t0002 | g0053 | AFR | GWD | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG02622 | hp2 | a0001 | c0002 | t0002 | g0009 | AFR | GWD | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG02647 | hp1 | a0004 | c0008 | t0001 | g0289 | AFR | GWD | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG02647 | hp2 | a0002 | c0001 | t0001 | g0143 | AFR | GWD | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG02698 | hp1 | a0002 | c0001 | t0001 | g0113 | SAS | PJL | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG02698 | hp2 | a0001 | c0002 | t0002 | g0108 | SAS | PJL | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG02717 | hp1 | a0001 | c0002 | t0002 | g0045 | AFR | GWD | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG02717 | hp2 | a0002 | c0005 | t0004 | g0012 | AFR | GWD | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG02723 | hp1 | a0004 | c0008 | t0001 | g0052 | AFR | GWD | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG02723 | hp2 | a0007 | c0013 | t0002 | g0080 | AFR | GWD | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG02735 | hp1 | a0002 | c0015 | t0001 | g0156 | SAS | PJL | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG02735 | hp2 | a0002 | c0001 | t0001 | g0002 | SAS | PJL | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG02738 | hp1 | a0001 | c0002 | t0002 | g0255 | SAS | PJL | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG02738 | hp2 | a0002 | c0005 | t0004 | g0131 | SAS | PJL | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG02809 | hp1 | a0004 | c0008 | t0001 | g0290 | AFR | GWD | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG02809 | hp2 | a0001 | c0002 | t0002 | g0045 | AFR | GWD | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG02818 | hp1 | a0002 | c0001 | t0001 | g0171 | AFR | GWD | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG02818 | hp2 | a0001 | c0002 | t0002 | g0009 | AFR | GWD | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG02886 | hp1 | a0007 | c0013 | t0002 | g0029 | AFR | GWD | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG02886 | hp2 | a0001 | c0002 | t0002 | g0247 | AFR | GWD | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG02895 | hp1 | a0002 | c0001 | t0001 | g0132 | AFR | GWD | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG02895 | hp2 | a0001 | c0002 | t0002 | g0265 | AFR | GWD | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG02897 | hp1 | a0002 | c0001 | t0001 | g0039 | AFR | GWD | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG02897 | hp2 | a0001 | c0003 | t0003 | g0222 | AFR | GWD | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG02922 | hp1 | a0006 | c0014 | t0003 | g0048 | AFR | ESN | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG02922 | hp2 | a0002 | c0001 | t0001 | g0125 | AFR | ESN | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG02970 | hp1 | a0002 | c0005 | t0004 | g0012 | AFR | ESN | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG02970 | hp2 | a0002 | c0010 | t0001 | g0033 | AFR | ESN | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG02976 | hp1 | a0002 | c0001 | t0001 | g0028 | AFR | ESN | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG02976 | hp2 | a0001 | c0002 | t0002 | g0248 | AFR | ESN | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG03017 | hp1 | a0001 | c0002 | t0002 | g0261 | SAS | PJL | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG03017 | hp2 | a0002 | c0001 | t0001 | g0002 | SAS | PJL | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG03041 | hp1 | a0002 | c0001 | t0001 | g0028 | AFR | GWD | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG03041 | hp2 | a0002 | c0001 | t0001 | g0180 | AFR | GWD | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG03098 | hp1 | a0001 | c0002 | t0002 | g0251 | AFR | MSL | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG03098 | hp2 | a0001 | c0002 | t0002 | g0271 | AFR | MSL | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG03130 | hp1 | a0006 | c0014 | t0003 | g0233 | AFR | ESN | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG03130 | hp2 | a0002 | c0005 | t0004 | g0012 | AFR | ESN | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG03139 | hp1 | a0002 | c0005 | t0004 | g0083 | AFR | ESN | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG03139 | hp2 | a0002 | c0001 | t0001 | g0076 | AFR | ESN | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG03209 | hp1 | a0001 | c0003 | t0003 | g0020 | AFR | MSL | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG03209 | hp2 | a0002 | c0001 | t0001 | g0117 | AFR | MSL | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG03239 | hp1 | a0001 | c0002 | t0002 | g0256 | SAS | PJL | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG03239 | hp2 | a0002 | c0001 | t0001 | g0123 | SAS | PJL | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG03453 | hp1 | a0006 | c0014 | t0003 | g0048 | AFR | MSL | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG03453 | hp2 | a0001 | c0002 | t0002 | g0077 | AFR | MSL | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG03486 | hp1 | a0001 | c0002 | t0002 | g0009 | AFR | MSL | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG03486 | hp2 | a0002 | c0001 | t0001 | g0007 | AFR | MSL | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG03490 | hp1 | a0001 | c0002 | t0002 | g0254 | SAS | PJL | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG03490 | hp2 | a0001 | c0002 | t0002 | g0049 | SAS | PJL | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG03492 | hp1 | a0002 | c0001 | t0001 | g0176 | SAS | PJL | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG03492 | hp2 | a0001 | c0002 | t0002 | g0049 | SAS | PJL | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG03516 | hp1 | a0002 | c0001 | t0001 | g0185 | AFR | ESN | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG03516 | hp2 | a0003 | c0006 | t0001 | g0273 | AFR | ESN | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG03540 | hp1 | a0002 | c0010 | t0001 | g0164 | AFR | GWD | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG03540 | hp2 | a0001 | c0002 | t0002 | g0250 | AFR | GWD | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG03579 | hp1 | a0001 | c0002 | t0005 | g0064 | AFR | MSL | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG03579 | hp2 | a0002 | c0001 | t0001 | g0007 | AFR | MSL | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG03654 | hp1 | a0001 | c0003 | t0003 | g0225 | SAS | PJL | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG03654 | hp2 | a0002 | c0001 | t0001 | g0122 | SAS | PJL | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG03669 | hp1 | a0002 | c0001 | t0001 | g0186 | SAS | PJL | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG03669 | hp2 | a0001 | c0009 | t0002 | g0200 | SAS | PJL | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG03704 | hp1 | a0002 | c0001 | t0001 | g0035 | SAS | PJL | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG03704 | hp2 | a0001 | c0002 | t0002 | g0097 | SAS | PJL | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG03710 | hp1 | a0002 | c0001 | t0001 | g0111 | SAS | PJL | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG03710 | hp2 | a0002 | c0001 | t0001 | g0089 | SAS | PJL | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG03834 | hp1 | a0001 | c0002 | t0002 | g0096 | SAS | BEB | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG03834 | hp2 | a0002 | c0001 | t0001 | g0140 | SAS | BEB | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG03927 | hp1 | a0002 | c0001 | t0001 | g0183 | SAS | BEB | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG03927 | hp2 | a0001 | c0002 | t0002 | g0259 | SAS | BEB | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG03942 | hp1 | a0002 | c0001 | t0001 | g0161 | SAS | BEB | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG03942 | hp2 | a0002 | c0001 | t0001 | g0090 | SAS | BEB | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG04115 | hp1 | a0012 | c0016 | t0001 | g0197 | SAS | STU | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG04115 | hp2 | a0002 | c0001 | t0001 | g0086 | SAS | STU | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG04184 | hp1 | a0002 | c0001 | t0001 | g0087 | SAS | BEB | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG04184 | hp2 | a0002 | c0011 | t0004 | g0037 | SAS | BEB | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG04199 | hp1 | a0002 | c0001 | t0001 | g0177 | SAS | STU | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG04199 | hp2 | a0002 | c0001 | t0001 | g0088 | SAS | STU | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG04204 | hp1 | a0002 | c0001 | t0001 | g0175 | SAS | STU | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG04204 | hp2 | a0002 | c0001 | t0001 | g0141 | SAS | STU | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA18522 | hp1 | a0001 | c0002 | t0005 | g0246 | AFR | YRI | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA18522 | hp2 | a0001 | c0002 | t0002 | g0249 | AFR | YRI | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA18747 | hp1 | a0001 | c0002 | t0002 | g0060 | EAS | CHB | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA18747 | hp2 | a0005 | c0007 | t0001 | g0068 | EAS | CHB | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA18939 | hp1 | a0002 | c0001 | t0001 | g0002 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA18939 | hp2 | a0001 | c0003 | t0003 | g0008 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA18940 | hp1 | a0001 | c0002 | t0002 | g0101 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA18940 | hp2 | a0001 | c0004 | t0003 | g0207 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA18941 | hp1 | a0003 | c0006 | t0001 | g0274 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA18941 | hp2 | a0002 | c0001 | t0001 | g0112 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA18943 | hp1 | a0002 | c0005 | t0004 | g0081 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA18943 | hp2 | a0001 | c0004 | t0003 | g0199 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA18944 | hp1 | a0001 | c0002 | t0002 | g0011 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA18944 | hp2 | a0002 | c0001 | t0001 | g0074 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA18946 | hp1 | a0003 | c0006 | t0001 | g0279 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA18946 | hp2 | a0002 | c0005 | t0004 | g0082 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA18947 | hp1 | a0001 | c0002 | t0002 | g0015 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA18947 | hp2 | a0004 | c0012 | t0004 | g0024 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA18948 | hp1 | a0001 | c0003 | t0003 | g0021 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA18948 | hp2 | a0001 | c0002 | t0002 | g0098 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA18949 | hp1 | a0002 | c0001 | t0001 | g0017 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA18949 | hp2 | a0001 | c0002 | t0002 | g0014 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA18950 | hp1 | a0004 | c0012 | t0004 | g0024 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA18950 | hp2 | a0001 | c0002 | t0002 | g0103 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA18951 | hp1 | a0001 | c0002 | t0002 | g0013 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA18951 | hp2 | a0001 | c0003 | t0003 | g0236 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA18952 | hp1 | a0001 | c0004 | t0003 | g0041 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA18952 | hp2 | a0002 | c0001 | t0001 | g0075 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA18953 | hp1 | a0001 | c0003 | t0003 | g0022 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA18953 | hp2 | a0001 | c0002 | t0002 | g0032 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA18954 | hp1 | a0001 | c0002 | t0002 | g0013 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA18954 | hp2 | a0001 | c0004 | t0003 | g0041 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA18956 | hp1 | a0001 | c0003 | t0003 | g0057 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA18956 | hp2 | a0001 | c0018 | t0003 | g0210 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA18957 | hp1 | a0003 | c0006 | t0001 | g0276 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA18957 | hp2 | a0002 | c0001 | t0001 | g0006 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA18960 | hp1 | a0001 | c0002 | t0002 | g0058 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA18960 | hp2 | a0001 | c0003 | t0003 | g0004 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA18961 | hp1 | a0001 | c0004 | t0003 | g0211 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA18961 | hp2 | a0002 | c0001 | t0001 | g0042 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA18962 | hp1 | a0002 | c0005 | t0004 | g0119 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA18962 | hp2 | a0002 | c0001 | t0001 | g0126 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA18963 | hp1 | a0002 | c0001 | t0001 | g0091 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA18963 | hp2 | a0001 | c0004 | t0003 | g0055 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA18964 | hp1 | a0002 | c0001 | t0001 | g0017 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA18964 | hp2 | a0001 | c0004 | t0003 | g0212 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA18965 | hp1 | a0001 | c0009 | t0002 | g0203 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA18965 | hp2 | a0001 | c0002 | t0002 | g0011 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA18967 | hp1 | a0001 | c0004 | t0003 | g0001 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA18967 | hp2 | a0002 | c0001 | t0001 | g0178 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA18968 | hp1 | a0002 | c0001 | t0001 | g0006 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA18968 | hp2 | a0001 | c0003 | t0003 | g0224 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA18969 | hp1 | a0001 | c0002 | t0002 | g0094 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA18969 | hp2 | a0001 | c0004 | t0003 | g0209 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA18970 | hp1 | a0002 | c0001 | t0001 | g0038 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA18970 | hp2 | a0002 | c0001 | t0001 | g0072 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA18971 | hp1 | a0001 | c0009 | t0002 | g0205 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA18971 | hp2 | a0001 | c0009 | t0002 | g0202 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA18972 | hp1 | a0002 | c0005 | t0004 | g0118 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA18972 | hp2 | a0001 | c0002 | t0002 | g0014 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA18975 | hp1 | a0001 | c0002 | t0002 | g0107 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA18975 | hp2 | a0001 | c0003 | t0003 | g0106 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA18978 | hp1 | a0001 | c0002 | t0002 | g0263 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA18978 | hp2 | a0001 | c0002 | t0002 | g0102 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA18979 | hp1 | a0001 | c0004 | t0003 | g0204 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA18979 | hp2 | a0001 | c0002 | t0002 | g0031 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA18980 | hp1 | a0002 | c0001 | t0001 | g0115 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA18980 | hp2 | a0001 | c0003 | t0003 | g0021 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA18981 | hp1 | a0004 | c0012 | t0004 | g0284 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA18981 | hp2 | a0001 | c0002 | t0002 | g0059 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA18983 | hp1 | a0001 | c0002 | t0002 | g0013 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA18983 | hp2 | a0001 | c0003 | t0003 | g0245 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA18985 | hp1 | a0003 | c0006 | t0001 | g0283 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA18985 | hp2 | a0005 | c0007 | t0002 | g0231 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA18987 | hp1 | a0002 | c0001 | t0001 | g0146 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA18987 | hp2 | a0001 | c0003 | t0003 | g0020 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA18988 | hp1 | a0001 | c0003 | t0003 | g0022 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA18988 | hp2 | a0002 | c0001 | t0001 | g0038 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA18989 | hp1 | a0002 | c0001 | t0001 | g0172 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA18989 | hp2 | a0001 | c0002 | t0002 | g0105 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA18990 | hp1 | a0008 | c0022 | t0001 | g0114 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA18990 | hp2 | a0003 | c0006 | t0001 | g0281 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA18994 | hp1 | a0001 | c0002 | t0002 | g0099 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA18994 | hp2 | a0001 | c0004 | t0003 | g0193 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA18995 | hp1 | a0001 | c0004 | t0003 | g0188 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA18995 | hp2 | a0001 | c0004 | t0003 | g0191 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA18997 | hp1 | a0001 | c0002 | t0002 | g0238 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA18997 | hp2 | a0001 | c0002 | t0002 | g0032 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA18999 | hp1 | a0001 | c0003 | t0003 | g0004 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA18999 | hp2 | a0001 | c0003 | t0003 | g0234 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA19000 | hp1 | a0003 | c0006 | t0001 | g0282 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA19000 | hp2 | a0001 | c0004 | t0003 | g0198 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA19001 | hp1 | a0001 | c0003 | t0003 | g0232 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA19001 | hp2 | a0002 | c0001 | t0001 | g0155 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA19002 | hp1 | a0001 | c0009 | t0002 | g0189 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA19002 | hp2 | a0001 | c0003 | t0003 | g0004 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA19005 | hp1 | a0001 | c0002 | t0002 | g0104 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA19005 | hp2 | a0001 | c0004 | t0003 | g0206 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA19009 | hp1 | a0001 | c0004 | t0003 | g0187 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA19009 | hp2 | a0005 | c0007 | t0002 | g0056 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA19010 | hp1 | a0002 | c0001 | t0001 | g0138 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA19010 | hp2 | a0001 | c0003 | t0003 | g0242 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA19011 | hp1 | a0001 | c0004 | t0003 | g0192 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA19011 | hp2 | a0002 | c0001 | t0001 | g0017 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA19012 | hp1 | a0002 | c0001 | t0001 | g0120 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA19012 | hp2 | a0001 | c0003 | t0003 | g0022 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA19030 | hp1 | a0001 | c0002 | t0002 | g0264 | AFR | LWK | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA19030 | hp2 | a0001 | c0003 | t0003 | g0047 | AFR | LWK | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA19043 | hp1 | a0001 | c0003 | t0003 | g0221 | AFR | LWK | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA19043 | hp2 | a0002 | c0001 | t0001 | g0039 | AFR | LWK | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA19056 | hp1 | a0002 | c0001 | t0001 | g0137 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA19056 | hp2 | a0001 | c0003 | t0003 | g0004 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA19062 | hp1 | a0001 | c0002 | t0002 | g0100 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA19062 | hp2 | a0001 | c0004 | t0003 | g0208 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA19064 | hp1 | a0001 | c0003 | t0003 | g0047 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA19064 | hp2 | a0002 | c0001 | t0001 | g0016 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA19066 | hp1 | a0001 | c0002 | t0002 | g0031 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA19066 | hp2 | a0003 | c0006 | t0001 | g0051 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA19068 | hp1 | a0002 | c0001 | t0001 | g0214 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA19068 | hp2 | a0004 | c0012 | t0004 | g0024 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA19070 | hp1 | a0001 | c0002 | t0002 | g0015 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA19070 | hp2 | a0001 | c0004 | t0003 | g0001 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA19076 | hp1 | a0001 | c0003 | t0004 | g0027 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA19076 | hp2 | a0003 | c0006 | t0001 | g0278 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA19077 | hp1 | a0001 | c0003 | t0003 | g0243 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA19077 | hp2 | a0003 | c0006 | t0001 | g0280 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA19078 | hp1 | a0001 | c0002 | t0002 | g0066 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA19078 | hp2 | a0005 | c0007 | t0002 | g0241 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA19079 | hp1 | a0002 | c0001 | t0001 | g0042 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA19079 | hp2 | a0001 | c0004 | t0003 | g0001 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA19080 | hp1 | a0002 | c0001 | t0001 | g0170 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA19080 | hp2 | a0002 | c0005 | t0004 | g0121 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA19082 | hp1 | a0001 | c0003 | t0003 | g0244 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA19082 | hp2 | a0001 | c0002 | t0002 | g0085 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA19085 | hp1 | a0001 | c0003 | t0003 | g0008 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA19085 | hp2 | a0001 | c0003 | t0003 | g0004 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA19086 | hp1 | a0001 | c0003 | t0003 | g0235 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA19086 | hp2 | a0003 | c0006 | t0001 | g0051 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA19087 | hp1 | a0002 | c0001 | t0001 | g0144 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA19087 | hp2 | a0001 | c0003 | t0003 | g0220 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA19090 | hp1 | a0001 | c0002 | t0002 | g0014 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA19090 | hp2 | a0003 | c0020 | t0004 | g0287 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA19091 | hp1 | a0005 | c0007 | t0002 | g0093 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA19091 | hp2 | a0003 | c0006 | t0001 | g0277 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA19240 | hp1 | a0004 | c0008 | t0001 | g0272 | AFR | YRI | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA19240 | hp2 | a0002 | c0010 | t0001 | g0033 | AFR | YRI | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA20129 | hp1 | a0009 | c0021 | t0004 | g0291 | AFR | ASW | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA20129 | hp2 | a0005 | c0007 | t0002 | g0063 | AFR | ASW | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA20752 | hp1 | a0001 | c0002 | t0002 | g0046 | EUR | TSI | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA20752 | hp2 | a0002 | c0001 | t0001 | g0149 | EUR | TSI | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA20805 | hp1 | a0002 | c0005 | t0004 | g0163 | EUR | TSI | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA20805 | hp2 | a0002 | c0001 | t0001 | g0142 | EUR | TSI | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA20905 | hp1 | a0001 | c0002 | t0002 | g0095 | SAS | GIH | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA20905 | hp2 | a0002 | c0001 | t0001 | g0153 | SAS | GIH | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG02109 | hp1 | a0002 | c0001 | t0001 | g0158 | AFR | ACB | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG02109 | hp2 | a0001 | c0002 | t0002 | g0071 | AFR | ACB | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG02486 | hp1 | a0002 | c0001 | t0001 | g0184 | AFR | ACB | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG02486 | hp2 | a0002 | c0010 | t0001 | g0151 | AFR | ACB | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG03471 | hp1 | a0002 | c0001 | t0001 | g0007 | AFR | MSL | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
HG03471 | hp2 | a0001 | c0002 | t0002 | g0009 | AFR | MSL | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA18955 | hp1 | a0001 | c0002 | t0009 | g0230 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
NA18955 | hp2 | a0001 | c0002 | t0002 | g0062 | EAS | JPT | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
homoSapiens_chm13v2 | hp1 | a0002 | c0001 | t0001 | g0150 | REF | REF | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
homoSapiens_grch38 | hp1 | a0001 | c0002 | t0002 | g0262 | REF | REF | LEXM_chr1_54801063_54847252 | LEXM | chr1 | 54801063 | 54847252 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:54806172
|
C | T | 4 | a0003a0004a0008others(1): Show | 28 | HG01884.hp2 HG02040.hp1 HG02074.hp2 others(25): Show |
missense_variant | MODERATE | c.56C>T | p.Thr19Met | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 1/10 | 110/1690 | 56/1257 | 19/418 | chr1 | 54806172 | ||
chr1:54807061
|
C | G | 1 | a0010 | 1 | HG01884.hp1 | missense_variant | MODERATE | c.170C>G | p.Ser57Cys | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 2/10 | 224/1690 | 170/1257 | 57/418 | chr1 | 54807061 | ||
chr1:54807070
|
A | G | 1 | a0006 | 3 | HG02922.hp1 HG03130.hp1 HG03453.hp1 |
missense_variant | MODERATE | c.179A>G | p.Tyr60Cys | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 2/10 | 233/1690 | 179/1257 | 60/418 | chr1 | 54807070 | ||
chr1:54807907
|
G | T | 4 | a0002a0008a0011others(1): Show | 148 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(145): Show |
missense_variant | MODERATE | c.376G>T | p.Gly126Cys | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/10 | 430/1690 | 376/1257 | 126/418 | chr1 | 54807907 | ||
chr1:54811819
|
A | C | 1 | a0011 | 1 | HG00741.hp2 | missense_variant | MODERATE | c.506A>C | p.Tyr169Ser | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 5/10 | 560/1690 | 506/1257 | 169/418 | chr1 | 54811819 | ||
chr1:54812145
|
G | A | 1 | a0010 | 1 | HG01884.hp1 | missense_variant | MODERATE | c.718G>A | p.Gly240Ser | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 6/10 | 772/1690 | 718/1257 | 240/418 | chr1 | 54812145 | ||
chr1:54813968
|
G | T | 2 | a0007a0009 | 4 | HG02451.hp1 HG02723.hp2 HG02886.hp1 others(1): Show |
missense_variant | MODERATE | c.917G>T | p.Arg306Leu | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 7/10 | 971/1690 | 917/1257 | 306/418 | chr1 | 54813968 | ||
chr1:54815017
|
G | A | 2 | a0003a0005 | 21 | HG02074.hp2 HG02165.hp1 HG03516.hp2 others(18): Show |
missense_variant | MODERATE | c.1028G>A | p.Cys343Tyr | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 8/10 | 1082/1690 | 1028/1257 | 343/418 | chr1 | 54815017 | ||
chr1:54841851
|
A | T | 1 | a0012 | 1 | HG04115.hp1 | missense_variant | MODERATE | c.1235A>T | p.Tyr412Phe | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 10/10 | 1289/1690 | 1235/1257 | 412/418 | chr1 | 54841851 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:54807080
|
A | G | 1 | a0010c0019 | 1 | HG01884.hp1 | synonymous_variant | LOW | c.189A>G | p.Gln63Gln | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 2/10 | 243/1690 | 189/1257 | 63/418 | chr1 | 54807080 | ||
chr1:54807630
|
G | A | 1 | a0010c0019 | 1 | HG01884.hp1 | synonymous_variant | LOW | c.297G>A | p.Thr99Thr | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 3/10 | 351/1690 | 297/1257 | 99/418 | chr1 | 54807630 | ||
chr1:54807645
|
A | C | 1 | a0001c0018 | 1 | NA18956.hp2 | synonymous_variant | LOW | c.312A>C | p.Leu104Leu | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 3/10 | 366/1690 | 312/1257 | 104/418 | chr1 | 54807645 | ||
chr1:54811841
|
C | T | 5 | a0001c0004a0001c0009a0001c0018others(2): Show | 41 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(38): Show |
synonymous_variant | LOW | c.528C>T | p.Tyr176Tyr | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 5/10 | 582/1690 | 528/1257 | 176/418 | chr1 | 54811841 | ||
chr1:54811880
|
C | T | 1 | a0002c0010 | 5 | HG02451.hp2 HG02486.hp2 HG02970.hp2 others(2): Show |
synonymous_variant | LOW | c.567C>T | p.Ser189Ser | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 5/10 | 621/1690 | 567/1257 | 189/418 | chr1 | 54811880 | ||
chr1:54817048
|
G | C | 1 | a0002c0015 | 1 | HG02735.hp1 | synonymous_variant | LOW | c.1110G>C | p.Arg370Arg | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/10 | 1164/1690 | 1110/1257 | 370/418 | chr1 | 54817048 | ||
chr1:54841828
|
A | G | 9 | a0001c0003a0001c0004a0001c0018others(6): Show | 123 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(120): Show |
synonymous_variant | LOW | c.1212A>G | p.Gly404Gly | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 10/10 | 1266/1690 | 1212/1257 | 404/418 | chr1 | 54841828 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:54806071
|
C | T | 1 | a0001c0002t0009 | 1 | NA18955.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-46C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 1/10 | chr1 | 54806071 | ||||||
chr1:54806078
|
C | T | 1 | a0001c0003t0008 | 1 | HG01256.hp1 | 5_prime_UTR_variant | MODIFIER | c.-39C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 1/10 | 39 | chr1 | 54806078 | |||||
chr1:54806101
|
A | G | 18 | a0001c0002t0001a0001c0003t0004a0002c0001t0001others(15): Show | 179 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(176): Show |
5_prime_UTR_variant | MODIFIER | c.-16A>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 1/10 | 16 | chr1 | 54806101 | |||||
chr1:54841967
|
C | T | 11 | a0001c0003t0003a0001c0003t0004a0001c0003t0008others(8): Show | 123 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(120): Show |
3_prime_UTR_variant | MODIFIER | c.*94C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 10/10 | 94 | chr1 | 54841967 | |||||
chr1:54842020
|
C | A | 11 | a0001c0003t0003a0001c0003t0004a0001c0003t0008others(8): Show | 123 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(120): Show |
3_prime_UTR_variant | MODIFIER | c.*147C>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 10/10 | 147 | chr1 | 54842020 | |||||
chr1:54842059
|
C | T | 1 | a0002c0001t0007 | 1 | HG00323.hp2 | 3_prime_UTR_variant | MODIFIER | c.*186C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 10/10 | 186 | chr1 | 54842059 | |||||
chr1:54842141
|
G | C | 2 | a0001c0002t0005a0004c0008t0006 | 3 | HG02257.hp1 HG03579.hp1 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*268G>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 10/10 | 268 | chr1 | 54842141 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:54806262
|
A | G | 23 | a0003c0006t0001g0051a0003c0006t0001g0273a0003c0006t0001g0274others(20): Show | 27 | HG01884.hp2 HG02040.hp1 HG02074.hp2 others(24): Show |
intron_variant | MODIFIER | c.104+42A>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 1/9 | chr1 | 54806262 | ||||||
chr1:54806263
|
G | A | 1 | a0001c0002t0002g0053 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.104+43G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 1/9 | chr1 | 54806263 | ||||||
chr1:54806313
|
C | T | 1 | a0004c0008t0001g0052 | 2 | HG01884.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.104+93C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 1/9 | chr1 | 54806313 | ||||||
chr1:54806340
|
G | C | 1 | a0001c0004t0003g0054 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.104+120G>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 1/9 | chr1 | 54806340 | ||||||
chr1:54806399
|
C | A | 1 | a0004c0008t0001g0272 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.104+179C>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 1/9 | chr1 | 54806399 | ||||||
chr1:54806506
|
T | C | 17 | a0003c0006t0001g0051a0003c0006t0001g0273a0003c0006t0001g0274others(14): Show | 20 | HG02040.hp1 HG02074.hp2 HG02165.hp1 others(17): Show |
intron_variant | MODIFIER | c.104+286T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 1/9 | chr1 | 54806506 | ||||||
chr1:54806507
|
G | A | 6 | a0004c0008t0001g0052a0004c0008t0001g0272a0004c0008t0001g0289others(3): Show | 7 | HG01884.hp2 HG02257.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.104+287G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 1/9 | chr1 | 54806507 | ||||||
chr1:54806663
|
A | T | 15 | a0001c0002t0002g0263a0001c0002t0002g0264a0001c0002t0002g0265others(12): Show | 16 | HG00408.hp1 HG00423.hp2 HG00621.hp1 others(13): Show |
intron_variant | MODIFIER | c.105-333A>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 1/9 | chr1 | 54806663 | ||||||
chr1:54806750
|
A | G | 32 | a0001c0002t0002g0263a0001c0002t0002g0264a0001c0002t0002g0265others(29): Show | 36 | HG00408.hp1 HG00423.hp2 HG00621.hp1 others(33): Show |
intron_variant | MODIFIER | c.105-246A>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 1/9 | chr1 | 54806750 | ||||||
chr1:54806807
|
G | GCGGGT | 15 | a0001c0002t0002g0263a0001c0002t0002g0264a0001c0002t0002g0265others(12): Show | 16 | HG00408.hp1 HG00423.hp2 HG00621.hp1 others(13): Show |
intron_variant | MODIFIER | c.105-189_105-188ins others(5): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 1/9 | chr1 | 54806807 | ||||||
chr1:54806807
|
GTGGGTGG others(3): Show |
G | 1 | a0001c0004t0003g0055 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.105-188_105-179del others(10): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 1/9 | chr1 | 54806807 | ||||||
chr1:54806808
|
T | C | 276 | a0001c0002t0001g0078a0001c0002t0002g0005a0001c0002t0002g0009others(273): Show | 364 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(361): Show |
intron_variant | MODIFIER | c.105-188T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 1/9 | chr1 | 54806808 | ||||||
chr1:54806808
|
T | G | 15 | a0001c0002t0002g0263a0001c0002t0002g0264a0001c0002t0002g0265others(12): Show | 16 | HG00408.hp1 HG00423.hp2 HG00621.hp1 others(13): Show |
intron_variant | MODIFIER | c.105-188T>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 1/9 | chr1 | 54806808 | ||||||
chr1:54806818
|
G | C | 1 | a0001c0004t0003g0055 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.105-178G>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 1/9 | chr1 | 54806818 | ||||||
chr1:54806848
|
A | G | 45 | a0001c0002t0002g0010a0001c0002t0002g0023a0001c0002t0002g0050others(42): Show | 55 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(52): Show |
intron_variant | MODIFIER | c.105-148A>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 1/9 | chr1 | 54806848 | ||||||
chr1:54806905
|
C | T | 7 | a0001c0002t0002g0009a0001c0002t0002g0247a0001c0002t0002g0248others(4): Show | 10 | HG02622.hp2 HG02818.hp2 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.105-91C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 1/9 | chr1 | 54806905 | ||||||
chr1:54806970
|
C | G | 45 | a0001c0002t0002g0010a0001c0002t0002g0023a0001c0002t0002g0050others(42): Show | 55 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(52): Show |
intron_variant | MODIFIER | c.105-26C>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 1/9 | chr1 | 54806970 | ||||||
chr1:54807313
|
C | A | 1 | a0005c0007t0002g0056 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.193-213C>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 2/9 | chr1 | 54807313 | ||||||
chr1:54807344
|
G | A | 1 | a0001c0003t0003g0057 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.193-182G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 2/9 | chr1 | 54807344 | ||||||
chr1:54807486
|
C | T | 4 | a0004c0008t0001g0052a0004c0008t0001g0289a0004c0008t0001g0290others(1): Show | 5 | HG01884.hp2 HG02647.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.193-40C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 2/9 | chr1 | 54807486 | ||||||
chr1:54807713
|
T | G | 13 | a0001c0002t0002g0005a0001c0002t0002g0011a0001c0002t0002g0025others(10): Show | 20 | HG01069.hp2 HG01099.hp2 HG01167.hp2 others(17): Show |
intron_variant | MODIFIER | c.357+23T>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 3/9 | chr1 | 54807713 | ||||||
chr1:54807749
|
A | T | 46 | a0001c0002t0002g0045a0001c0002t0002g0046a0001c0002t0002g0049others(43): Show | 71 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.357+59A>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 3/9 | chr1 | 54807749 | ||||||
chr1:54807765
|
C | T | 1 | a0002c0001t0001g0214 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.357+75C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 3/9 | chr1 | 54807765 | ||||||
chr1:54808190
|
C | T | 1 | a0004c0008t0006g0288 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.480+179C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54808190 | ||||||
chr1:54808369
|
C | T | 1 | a0001c0003t0003g0245 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.480+358C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54808369 | ||||||
chr1:54808379
|
G | A | 50 | a0001c0002t0002g0045a0001c0002t0002g0046a0001c0002t0002g0049others(47): Show | 76 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(73): Show |
intron_variant | MODIFIER | c.480+368G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54808379 | ||||||
chr1:54808405
|
C | G | 280 | a0001c0002t0001g0078a0001c0002t0002g0009a0001c0002t0002g0010others(277): Show | 362 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(359): Show |
intron_variant | MODIFIER | c.480+394C>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54808405 | ||||||
chr1:54808528
|
C | T | 3 | a0004c0008t0001g0289a0004c0008t0001g0290a0009c0021t0004g0291 | 3 | HG02647.hp1 HG02809.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.480+517C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54808528 | ||||||
chr1:54808563
|
T | A | 1 | a0002c0005t0004g0070 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.480+552T>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54808563 | ||||||
chr1:54808607
|
G | A | 12 | a0001c0002t0002g0009a0001c0002t0002g0071a0001c0002t0002g0247others(9): Show | 16 | HG01884.hp2 HG02109.hp2 HG02622.hp2 others(13): Show |
intron_variant | MODIFIER | c.480+596G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54808607 | ||||||
chr1:54808611
|
C | CGGGGGG | 16 | a0001c0004t0003g0001a0001c0004t0003g0054a0001c0004t0003g0191others(13): Show | 20 | HG00408.hp2 HG00609.hp1 HG01978.hp2 others(17): Show |
intron_variant | MODIFIER | c.480+600_480+601ins others(6): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54808611 | ||||||
chr1:54808611
|
C | CGGGGGGG | 7 | a0001c0004t0003g0204a0001c0004t0003g0206a0001c0004t0003g0207others(4): Show | 7 | NA18940.hp2 NA18956.hp2 NA18969.hp2 others(4): Show |
intron_variant | MODIFIER | c.480+600_480+601ins others(7): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54808611 | ||||||
chr1:54808611
|
C | CGGGGGGG others(3): Show |
1 | a0001c0004t0003g0055 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.480+600_480+601ins others(10): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54808611 | ||||||
chr1:54808611
|
C | CGGGGGGG others(4): Show |
3 | a0001c0004t0003g0211a0001c0004t0003g0212a0001c0004t0003g0213 | 3 | HG00438.hp2 NA18961.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.480+600_480+601ins others(11): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54808611 | ||||||
chr1:54808612
|
C | CGGGGG | 26 | a0002c0001t0001g0002a0002c0001t0001g0035a0002c0001t0001g0036others(23): Show | 32 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(29): Show |
intron_variant | MODIFIER | c.480+602_480+606dup others(5): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr1 | 54808612 | |||||
chr1:54808612
|
C | CGGGGGGG | 29 | a0001c0002t0002g0066a0001c0004t0003g0041a0002c0001t0001g0007others(26): Show | 38 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(35): Show |
intron_variant | MODIFIER | c.480+606_480+607ins others(7): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr1 | 54808612 | |||||
chr1:54808612
|
C | CGGGGGGG others(3): Show |
4 | a0002c0001t0001g0178a0002c0001t0001g0179a0002c0001t0001g0180others(1): Show | 4 | HG01243.hp1 HG02074.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.480+606_480+607ins others(10): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr1 | 54808612 | |||||
chr1:54808612
|
C | CGGGGGGG others(4): Show |
2 | a0002c0001t0001g0042a0002c0001t0001g0182 | 3 | HG01192.hp2 NA18961.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.480+606_480+607ins others(11): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr1 | 54808612 | |||||
chr1:54808612
|
C | CGGGGGGG others(5): Show |
1 | a0002c0001t0001g0183 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.480+606_480+607ins others(12): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr1 | 54808612 | |||||
chr1:54808612
|
C | G | 35 | a0001c0004t0003g0001a0001c0004t0003g0043a0001c0004t0003g0054others(32): Show | 40 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.480+601C>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54808612 | ||||||
chr1:54808616
|
GGA | G | 32 | a0001c0002t0002g0013a0001c0002t0002g0014a0001c0002t0002g0015others(29): Show | 41 | HG00408.hp1 HG00423.hp2 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.480+607_480+608del others(2): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr1 | 54808616 | |||||
chr1:54808618
|
A | C | 29 | a0001c0003t0003g0022a0001c0003t0003g0243a0001c0003t0003g0244others(26): Show | 37 | HG00140.hp2 HG00544.hp2 HG00673.hp1 others(34): Show |
intron_variant | MODIFIER | c.480+607A>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54808618 | ||||||
chr1:54808618
|
A | G | 109 | a0001c0002t0002g0066a0001c0004t0003g0001a0001c0004t0003g0041others(106): Show | 133 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.480+607A>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54808618 | ||||||
chr1:54808703
|
C | T | 29 | a0001c0004t0003g0001a0001c0004t0003g0041a0001c0004t0003g0043others(26): Show | 35 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(32): Show |
intron_variant | MODIFIER | c.480+692C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54808703 | ||||||
chr1:54808719
|
T | TG | 6 | a0001c0004t0003g0187a0001c0004t0003g0204a0002c0001t0001g0086others(3): Show | 6 | HG01255.hp1 HG02109.hp1 HG04115.hp2 others(3): Show |
intron_variant | MODIFIER | c.480+713dupG | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr1 | 54808719 | |||||
chr1:54808791
|
A | C | 156 | a0001c0002t0002g0005a0001c0002t0002g0011a0001c0002t0002g0013others(153): Show | 211 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(208): Show |
intron_variant | MODIFIER | c.480+780A>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54808791 | ||||||
chr1:54808801
|
A | G | 1 | a0001c0003t0003g0242 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.480+790A>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54808801 | ||||||
chr1:54808826
|
G | T | 2 | a0007c0013t0002g0029a0007c0013t0002g0080 | 3 | HG02451.hp1 HG02723.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.480+815G>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54808826 | ||||||
chr1:54808840
|
G | T | 1 | a0005c0007t0002g0056 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.480+829G>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54808840 | ||||||
chr1:54808853
|
G | A | 1 | a0001c0003t0003g0245 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.480+842G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54808853 | ||||||
chr1:54808856
|
C | T | 2 | a0001c0002t0002g0265a0001c0002t0002g0271 | 2 | HG02895.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.480+845C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54808856 | ||||||
chr1:54808962
|
C | T | 9 | a0001c0002t0002g0264a0001c0002t0002g0265a0001c0002t0002g0266others(6): Show | 9 | HG00408.hp1 HG00423.hp2 HG00621.hp1 others(6): Show |
intron_variant | MODIFIER | c.480+951C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54808962 | ||||||
chr1:54808985
|
T | G | 230 | a0001c0002t0002g0045a0001c0002t0002g0046a0001c0002t0002g0049others(227): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.480+974T>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54808985 | ||||||
chr1:54808987
|
T | C | 230 | a0001c0002t0002g0045a0001c0002t0002g0046a0001c0002t0002g0049others(227): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.480+976T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54808987 | ||||||
chr1:54808989
|
T | C | 230 | a0001c0002t0002g0045a0001c0002t0002g0046a0001c0002t0002g0049others(227): Show | 294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.480+978T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54808989 | ||||||
chr1:54808990
|
G | GCCTACTC others(104): Show |
115 | a0001c0002t0002g0066a0001c0002t0002g0264a0001c0002t0002g0265others(112): Show | 139 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.480+979_480+980ins others(111): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54808990 | ||||||
chr1:54808990
|
G | GCCTACTC others(104): Show |
1 | a0002c0001t0001g0135 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.480+979_480+980ins others(111): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54808990 | ||||||
chr1:54808990
|
G | GCCTACTC others(104): Show |
1 | a0001c0004t0003g0188 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.480+979_480+980ins others(111): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54808990 | ||||||
chr1:54808990
|
G | GCCTACTC others(104): Show |
92 | a0001c0002t0002g0045a0001c0002t0002g0046a0001c0002t0002g0049others(89): Show | 129 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.480+979_480+980ins others(111): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54808990 | ||||||
chr1:54808990
|
G | GCCTACTC others(104): Show |
20 | a0001c0002t0002g0263a0001c0004t0003g0211a0001c0004t0003g0213others(17): Show | 23 | HG00438.hp2 HG02040.hp1 HG02074.hp2 others(20): Show |
intron_variant | MODIFIER | c.480+979_480+980ins others(111): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54808990 | ||||||
chr1:54808990
|
G | GCCTACTC others(105): Show |
1 | a0001c0018t0003g0210 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.480+979_480+980ins others(112): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54808990 | ||||||
chr1:54808997
|
C | G | 1 | a0001c0018t0003g0210 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.480+986C>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54808997 | ||||||
chr1:54809095
|
T | C | 1 | a0003c0006t0001g0273 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.480+1084T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54809095 | ||||||
chr1:54809109
|
A | G | 1 | a0001c0002t0002g0053 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.480+1098A>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54809109 | ||||||
chr1:54809160
|
A | C | 1 | a0001c0002t0002g0264 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.480+1149A>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54809160 | ||||||
chr1:54809160
|
A | G | 1 | a0009c0021t0004g0291 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.480+1149A>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54809160 | ||||||
chr1:54809161
|
T | C | 292 | a0001c0002t0001g0078a0001c0002t0002g0005a0001c0002t0002g0009others(289): Show | 381 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(378): Show |
intron_variant | MODIFIER | c.480+1150T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54809161 | ||||||
chr1:54809234
|
C | A | 57 | a0001c0002t0002g0045a0001c0002t0002g0046a0001c0002t0002g0049others(54): Show | 86 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.480+1223C>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54809234 | ||||||
chr1:54809275
|
A | G | 2 | a0002c0001t0001g0076a0002c0001t0001g0157 | 2 | HG00639.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.480+1264A>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54809275 | ||||||
chr1:54809294
|
T | C | 53 | a0001c0002t0002g0263a0001c0004t0003g0001a0001c0004t0003g0041others(50): Show | 63 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.480+1283T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54809294 | ||||||
chr1:54809434
|
C | A | 1 | a0001c0002t0002g0094 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.480+1423C>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54809434 | ||||||
chr1:54809435
|
G | A | 1 | a0001c0002t0002g0094 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.480+1424G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54809435 | ||||||
chr1:54809482
|
T | C | 290 | a0001c0002t0002g0005a0001c0002t0002g0009a0001c0002t0002g0010others(287): Show | 379 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(376): Show |
intron_variant | MODIFIER | c.480+1471T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54809482 | ||||||
chr1:54809649
|
A | C | 1 | a0001c0018t0003g0210 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.480+1638A>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54809649 | ||||||
chr1:54809669
|
G | A | 20 | a0001c0002t0002g0013a0001c0002t0002g0014a0001c0002t0002g0015others(17): Show | 28 | HG00558.hp1 HG03704.hp2 HG03834.hp1 others(25): Show |
intron_variant | MODIFIER | c.480+1658G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54809669 | ||||||
chr1:54809763
|
C | A | 1 | a0001c0003t0003g0243 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.480+1752C>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54809763 | ||||||
chr1:54809856
|
C | G | 1 | a0001c0002t0002g0107 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.480+1845C>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54809856 | ||||||
chr1:54809856
|
C | T | 1 | a0002c0001t0001g0134 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.480+1845C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54809856 | ||||||
chr1:54809875
|
G | GA | 281 | a0001c0002t0002g0005a0001c0002t0002g0009a0001c0002t0002g0010others(278): Show | 369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.480+1873dupA | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr1 | 54809875 | |||||
chr1:54809885
|
C | A | 289 | a0001c0002t0002g0005a0001c0002t0002g0009a0001c0002t0002g0010others(286): Show | 378 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(375): Show |
intron_variant | MODIFIER | c.480+1874C>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54809885 | ||||||
chr1:54809957
|
G | C | 108 | a0001c0002t0002g0066a0002c0001t0001g0002a0002c0001t0001g0006others(105): Show | 132 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.481-1837G>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54809957 | ||||||
chr1:54810095
|
C | T | 5 | a0001c0002t0002g0049a0001c0002t0002g0238a0001c0003t0003g0237others(2): Show | 6 | HG00621.hp2 HG02080.hp1 HG02135.hp1 others(3): Show |
intron_variant | MODIFIER | c.481-1699C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54810095 | ||||||
chr1:54810096
|
G | A | 1 | a0001c0003t0003g0215 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.481-1698G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54810096 | ||||||
chr1:54810158
|
T | G | 53 | a0001c0002t0002g0263a0001c0004t0003g0001a0001c0004t0003g0041others(50): Show | 63 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.481-1636T>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54810158 | ||||||
chr1:54810368
|
T | G | 1 | a0001c0003t0003g0216 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.481-1426T>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54810368 | ||||||
chr1:54810370
|
T | A | 2 | a0001c0002t0002g0266a0002c0001t0001g0109 | 2 | HG02071.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.481-1424T>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54810370 | ||||||
chr1:54810371
|
C | T | 14 | a0001c0002t0002g0005a0001c0002t0002g0011a0001c0002t0002g0025others(11): Show | 21 | HG01069.hp2 HG01099.hp2 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.481-1423C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54810371 | ||||||
chr1:54810473
|
G | A | 1 | a0001c0004t0003g0194 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.481-1321G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54810473 | ||||||
chr1:54810572
|
C | T | 1 | a0002c0015t0001g0156 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.481-1222C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54810572 | ||||||
chr1:54810615
|
T | C | 1 | a0010c0019t0002g0067 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.481-1179T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54810615 | ||||||
chr1:54810684
|
A | G | 1 | a0002c0001t0001g0177 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.481-1110A>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54810684 | ||||||
chr1:54810878
|
G | A | 3 | a0002c0001t0001g0111a0002c0001t0001g0158a0002c0001t0001g0159 | 3 | HG01993.hp2 HG02109.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.481-916G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54810878 | ||||||
chr1:54811014
|
G | A | 57 | a0001c0002t0002g0045a0001c0002t0002g0046a0001c0002t0002g0049others(54): Show | 86 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.481-780G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54811014 | ||||||
chr1:54811057
|
T | C | 1 | a0004c0008t0001g0052 | 2 | HG01884.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.481-737T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54811057 | ||||||
chr1:54811320
|
C | G | 1 | a0001c0003t0003g0236 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.481-474C>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54811320 | ||||||
chr1:54811525
|
G | A | 15 | a0001c0002t0002g0010a0001c0002t0002g0023a0001c0002t0002g0050others(12): Show | 22 | HG00280.hp2 HG00639.hp2 HG00741.hp1 others(19): Show |
intron_variant | MODIFIER | c.481-269G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54811525 | ||||||
chr1:54811582
|
C | T | 3 | a0003c0006t0001g0285a0003c0006t0001g0286a0003c0020t0004g0287 | 3 | HG02074.hp2 HG02165.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.481-212C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54811582 | ||||||
chr1:54811673
|
C | G | 3 | a0002c0001t0001g0133a0002c0001t0001g0176a0002c0005t0004g0040 | 4 | HG01257.hp1 HG01258.hp1 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.481-121C>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54811673 | ||||||
chr1:54811674
|
G | A | 1 | a0002c0001t0001g0087 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.481-120G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54811674 | ||||||
chr1:54811751
|
G | C | 1 | a0010c0019t0002g0067 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.481-43G>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54811751 | ||||||
chr1:54811757
|
T | A | 107 | a0001c0002t0002g0066a0002c0001t0001g0002a0002c0001t0001g0006others(104): Show | 131 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.481-37T>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54811757 | ||||||
chr1:54811778
|
C | T | 34 | a0001c0004t0003g0001a0001c0004t0003g0041a0001c0004t0003g0043others(31): Show | 41 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(38): Show |
intron_variant | MODIFIER | c.481-16C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54811778 | ||||||
chr1:54811784
|
C | T | 1 | a0002c0001t0001g0075 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.481-10C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | chr1 | 54811784 | ||||||
chr1:54811785
|
G | GC | 8 | a0001c0002t0002g0009a0001c0002t0002g0071a0001c0002t0002g0247others(5): Show | 11 | HG02109.hp2 HG02622.hp2 HG02818.hp2 others(8): Show |
splice_region_variant&intron_variant | LOW | c.481-5dupC | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr1 | 54811785 | |||||
chr1:54811972
|
C | T | 5 | a0002c0001t0001g0036a0002c0001t0001g0144a0002c0001t0001g0145others(2): Show | 6 | HG00544.hp2 HG00673.hp1 HG02015.hp2 others(3): Show |
intron_variant | MODIFIER | c.618+41C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 5/9 | chr1 | 54811972 | ||||||
chr1:54812008
|
G | A | 3 | a0002c0001t0001g0160a0002c0001t0001g0184a0002c0001t0001g0185 | 3 | HG02486.hp1 HG02572.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.619-38G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 5/9 | chr1 | 54812008 | ||||||
chr1:54812292
|
C | T | 1 | a0004c0008t0001g0272 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.762+103C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 6/9 | chr1 | 54812292 | ||||||
chr1:54812386
|
C | T | 1 | a0002c0001t0001g0074 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.762+197C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 6/9 | chr1 | 54812386 | ||||||
chr1:54812646
|
T | TGAGGTAG others(301): Show |
1 | a0010c0019t0002g0067 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.762+470_762+471ins others(308): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr1 | 54812646 | |||||
chr1:54812721
|
G | C | 168 | a0001c0002t0002g0005a0001c0002t0002g0009a0001c0002t0002g0011others(165): Show | 226 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(223): Show |
intron_variant | MODIFIER | c.762+532G>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 6/9 | chr1 | 54812721 | ||||||
chr1:54812766
|
C | T | 2 | a0002c0001t0001g0039a0002c0001t0001g0132 | 3 | HG02895.hp1 HG02897.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.762+577C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 6/9 | chr1 | 54812766 | ||||||
chr1:54813104
|
A | G | 7 | a0001c0002t0002g0009a0001c0002t0002g0071a0001c0002t0002g0247others(4): Show | 10 | HG02109.hp2 HG02622.hp2 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.763-710A>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 6/9 | chr1 | 54813104 | ||||||
chr1:54813117
|
C | T | 4 | a0001c0002t0002g0026a0002c0001t0001g0130a0002c0001t0001g0175others(1): Show | 5 | HG01167.hp2 HG01169.hp2 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.763-697C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 6/9 | chr1 | 54813117 | ||||||
chr1:54813141
|
CT | C | 133 | a0001c0002t0002g0005a0001c0002t0002g0009a0001c0002t0002g0011others(130): Show | 181 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(178): Show |
intron_variant | MODIFIER | c.763-660delT | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr1 | 54813141 | |||||
chr1:54813168
|
G | A | 83 | a0001c0002t0002g0005a0001c0002t0002g0009a0001c0002t0002g0011others(80): Show | 120 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.763-646G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 6/9 | chr1 | 54813168 | ||||||
chr1:54813191
|
A | G | 1 | a0001c0002t0002g0079 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.763-623A>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 6/9 | chr1 | 54813191 | ||||||
chr1:54813392
|
C | A | 3 | a0003c0006t0001g0273a0004c0008t0006g0288a0009c0021t0004g0291 | 3 | HG02257.hp1 HG03516.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.763-422C>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 6/9 | chr1 | 54813392 | ||||||
chr1:54813649
|
T | G | 41 | a0001c0002t0001g0078a0001c0002t0002g0053a0001c0003t0003g0008others(38): Show | 52 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.763-165T>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 6/9 | chr1 | 54813649 | ||||||
chr1:54813672
|
CCCGGCCT | C | 290 | a0001c0002t0001g0078a0001c0002t0002g0005a0001c0002t0002g0009others(287): Show | 379 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(376): Show |
intron_variant | MODIFIER | c.763-130_763-124del others(7): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr1 | 54813672 | |||||
chr1:54813749
|
A | G | 2 | a0001c0002t0002g0009a0001c0002t0002g0251 | 5 | HG02622.hp2 HG02818.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.763-65A>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 6/9 | chr1 | 54813749 | ||||||
chr1:54813750
|
G | C | 2 | a0001c0002t0002g0009a0001c0002t0002g0251 | 5 | HG02622.hp2 HG02818.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.763-64G>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 6/9 | chr1 | 54813750 | ||||||
chr1:54814015
|
G | A | 5 | a0001c0003t0003g0003a0001c0003t0003g0044a0001c0003t0003g0215others(2): Show | 11 | HG00099.hp2 HG00140.hp1 HG00735.hp1 others(8): Show |
intron_variant | MODIFIER | c.924+40G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 7/9 | chr1 | 54814015 | ||||||
chr1:54814071
|
G | T | 59 | a0001c0002t0001g0078a0001c0002t0002g0049a0001c0002t0002g0079others(56): Show | 86 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.924+96G>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 7/9 | chr1 | 54814071 | ||||||
chr1:54814180
|
T | C | 51 | a0001c0002t0002g0049a0001c0002t0002g0238a0001c0002t0009g0230others(48): Show | 75 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(72): Show |
intron_variant | MODIFIER | c.924+205T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 7/9 | chr1 | 54814180 | ||||||
chr1:54814225
|
A | G | 2 | a0003c0006t0001g0273a0005c0007t0002g0063 | 2 | HG03516.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.924+250A>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 7/9 | chr1 | 54814225 | ||||||
chr1:54814228
|
G | A | 1 | a0001c0003t0003g0220 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.924+253G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 7/9 | chr1 | 54814228 | ||||||
chr1:54814305
|
G | A | 1 | a0003c0006t0001g0273 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.924+330G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 7/9 | chr1 | 54814305 | ||||||
chr1:54814352
|
C | A | 1 | a0001c0002t0001g0078 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.924+377C>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 7/9 | chr1 | 54814352 | ||||||
chr1:54814376
|
CCGCCCAA others(24): Show |
C | 1 | a0001c0003t0003g0232 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.924+402_924+432del others(31): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 7/9 | chr1 | 54814376 | ||||||
chr1:54814382
|
A | C | 1 | a0001c0002t0002g0066 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.924+407A>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 7/9 | chr1 | 54814382 | ||||||
chr1:54814398
|
C | T | 3 | a0001c0002t0002g0103a0001c0002t0002g0104a0001c0002t0002g0105 | 3 | NA18950.hp2 NA18989.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.924+423C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 7/9 | chr1 | 54814398 | ||||||
chr1:54814412
|
AAGCAGGC others(14): Show |
A | 1 | a0001c0003t0003g0221 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.924+447_924+467del others(21): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr1 | 54814412 | |||||
chr1:54814463
|
G | A | 2 | a0001c0002t0002g0045a0001c0003t0003g0217 | 3 | HG01109.hp2 HG02717.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.925-451G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 7/9 | chr1 | 54814463 | ||||||
chr1:54814750
|
G | A | 1 | a0001c0004t0003g0195 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.925-164G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 7/9 | chr1 | 54814750 | ||||||
chr1:54814762
|
C | T | 2 | a0003c0006t0001g0273a0005c0007t0002g0063 | 2 | HG03516.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.925-152C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 7/9 | chr1 | 54814762 | ||||||
chr1:54814909
|
C | T | 1 | a0001c0002t0005g0246 | 1 | NA18522.hp1 | splice_region_variant&intron_variant | LOW | c.925-5C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 7/9 | chr1 | 54814909 | ||||||
chr1:54815118
|
G | A | 2 | a0002c0001t0001g0133a0002c0001t0001g0176 | 2 | HG02300.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1050+79G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 8/9 | chr1 | 54815118 | ||||||
chr1:54815124
|
C | T | 2 | a0007c0013t0002g0029a0007c0013t0002g0080 | 3 | HG02451.hp1 HG02723.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1050+85C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 8/9 | chr1 | 54815124 | ||||||
chr1:54815151
|
C | A | 1 | a0003c0006t0001g0274 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1050+112C>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 8/9 | chr1 | 54815151 | ||||||
chr1:54815257
|
T | C | 2 | a0007c0013t0002g0029a0007c0013t0002g0080 | 3 | HG02451.hp1 HG02723.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1050+218T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 8/9 | chr1 | 54815257 | ||||||
chr1:54815333
|
A | T | 19 | a0001c0002t0002g0010a0001c0002t0002g0023a0001c0002t0002g0046others(16): Show | 26 | HG00280.hp2 HG00639.hp2 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.1050+294A>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 8/9 | chr1 | 54815333 | ||||||
chr1:54815458
|
TCC | T | 132 | a0001c0002t0002g0013a0001c0002t0002g0014a0001c0002t0002g0015others(129): Show | 163 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.1050+420_1050+421d others(4): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 8/9 | chr1 | 54815458 | ||||||
chr1:54815459
|
C | T | 144 | a0001c0002t0002g0005a0001c0002t0002g0010a0001c0002t0002g0011others(141): Show | 198 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(195): Show |
intron_variant | MODIFIER | c.1050+420C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 8/9 | chr1 | 54815459 | ||||||
chr1:54815534
|
C | G | 1 | a0001c0004t0003g0209 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1050+495C>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 8/9 | chr1 | 54815534 | ||||||
chr1:54815646
|
T | A | 1 | a0001c0002t0002g0107 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1050+607T>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 8/9 | chr1 | 54815646 | ||||||
chr1:54815781
|
G | T | 2 | a0001c0002t0002g0266a0001c0002t0002g0270 | 2 | HG00621.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.1050+742G>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 8/9 | chr1 | 54815781 | ||||||
chr1:54815858
|
A | G | 164 | a0001c0002t0002g0005a0001c0002t0002g0011a0001c0002t0002g0013others(161): Show | 205 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.1050+819A>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 8/9 | chr1 | 54815858 | ||||||
chr1:54816019
|
G | C | 2 | a0007c0013t0002g0029a0007c0013t0002g0080 | 3 | HG02451.hp1 HG02723.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1051-970G>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 8/9 | chr1 | 54816019 | ||||||
chr1:54816034
|
A | G | 6 | a0001c0002t0009g0230a0001c0003t0003g0004a0001c0003t0003g0242others(3): Show | 11 | HG00558.hp2 HG02165.hp2 NA18943.hp1 others(8): Show |
intron_variant | MODIFIER | c.1051-955A>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 8/9 | chr1 | 54816034 | ||||||
chr1:54816174
|
G | A | 88 | a0001c0002t0002g0238a0001c0002t0009g0230a0001c0003t0003g0003others(85): Show | 124 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.1051-815G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 8/9 | chr1 | 54816174 | ||||||
chr1:54816236
|
C | G | 17 | a0001c0002t0002g0010a0001c0002t0002g0023a0001c0002t0002g0046others(14): Show | 24 | HG00280.hp2 HG00639.hp2 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.1051-753C>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 8/9 | chr1 | 54816236 | ||||||
chr1:54816245
|
C | T | 1 | a0001c0002t0002g0261 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1051-744C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 8/9 | chr1 | 54816245 | ||||||
chr1:54816292
|
C | T | 146 | a0001c0002t0002g0005a0001c0002t0002g0011a0001c0002t0002g0013others(143): Show | 186 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.1051-697C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 8/9 | chr1 | 54816292 | ||||||
chr1:54816318
|
A | G | 146 | a0001c0002t0001g0078a0001c0002t0002g0009a0001c0002t0002g0010others(143): Show | 195 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(192): Show |
intron_variant | MODIFIER | c.1051-671A>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 8/9 | chr1 | 54816318 | ||||||
chr1:54816341
|
C | T | 128 | a0001c0002t0001g0078a0001c0002t0002g0009a0001c0002t0002g0010others(125): Show | 176 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(173): Show |
intron_variant | MODIFIER | c.1051-648C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 8/9 | chr1 | 54816341 | ||||||
chr1:54816396
|
A | G | 2 | a0007c0013t0002g0029a0007c0013t0002g0080 | 3 | HG02451.hp1 HG02723.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1051-593A>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 8/9 | chr1 | 54816396 | ||||||
chr1:54816406
|
T | C | 292 | a0001c0002t0001g0078a0001c0002t0002g0005a0001c0002t0002g0009others(289): Show | 381 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(378): Show |
intron_variant | MODIFIER | c.1051-583T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 8/9 | chr1 | 54816406 | ||||||
chr1:54816560
|
T | A | 143 | a0001c0002t0002g0005a0001c0002t0002g0011a0001c0002t0002g0013others(140): Show | 182 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.1051-429T>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 8/9 | chr1 | 54816560 | ||||||
chr1:54816570
|
T | C | 2 | a0001c0002t0002g0095a0001c0002t0002g0096 | 2 | HG03834.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1051-419T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 8/9 | chr1 | 54816570 | ||||||
chr1:54816621
|
T | C | 9 | a0003c0006t0001g0276a0003c0006t0001g0277a0003c0006t0001g0285others(6): Show | 9 | HG02074.hp2 HG02165.hp1 NA18957.hp1 others(6): Show |
intron_variant | MODIFIER | c.1051-368T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 8/9 | chr1 | 54816621 | ||||||
chr1:54816623
|
T | C | 1 | a0001c0002t0001g0078 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1051-366T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 8/9 | chr1 | 54816623 | ||||||
chr1:54816637
|
A | G | 143 | a0001c0002t0002g0005a0001c0002t0002g0011a0001c0002t0002g0013others(140): Show | 182 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.1051-352A>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 8/9 | chr1 | 54816637 | ||||||
chr1:54816717
|
A | G | 1 | a0001c0003t0003g0232 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1051-272A>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 8/9 | chr1 | 54816717 | ||||||
chr1:54816780
|
A | T | 1 | a0001c0002t0002g0079 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1051-209A>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 8/9 | chr1 | 54816780 | ||||||
chr1:54816883
|
A | G | 143 | a0001c0002t0002g0005a0001c0002t0002g0011a0001c0002t0002g0013others(140): Show | 182 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.1051-106A>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 8/9 | chr1 | 54816883 | ||||||
chr1:54816911
|
C | G | 22 | a0003c0006t0001g0051a0003c0006t0001g0273a0003c0006t0001g0274others(19): Show | 24 | HG02074.hp2 HG02165.hp1 HG02451.hp1 others(21): Show |
intron_variant | MODIFIER | c.1051-78C>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 8/9 | chr1 | 54816911 | ||||||
chr1:54816931
|
C | T | 1 | a0002c0011t0004g0201 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1051-58C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 8/9 | chr1 | 54816931 | ||||||
chr1:54817155
|
G | A | 3 | a0001c0002t0002g0053a0004c0008t0001g0289a0004c0008t0001g0290 | 3 | HG02622.hp1 HG02647.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1184+33G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54817155 | ||||||
chr1:54817161
|
G | A | 1 | a0001c0004t0003g0043 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1184+39G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54817161 | ||||||
chr1:54817262
|
G | A | 1 | a0001c0002t0002g0079 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1184+140G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54817262 | ||||||
chr1:54817306
|
A | C | 143 | a0001c0002t0002g0005a0001c0002t0002g0011a0001c0002t0002g0013others(140): Show | 182 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.1184+184A>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54817306 | ||||||
chr1:54817403
|
T | G | 143 | a0001c0002t0002g0005a0001c0002t0002g0011a0001c0002t0002g0013others(140): Show | 182 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.1184+281T>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54817403 | ||||||
chr1:54817477
|
C | T | 1 | a0002c0001t0001g0148 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1184+355C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54817477 | ||||||
chr1:54817693
|
A | G | 1 | a0004c0008t0001g0052 | 2 | HG01884.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1184+571A>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54817693 | ||||||
chr1:54817724
|
AT | A | 254 | a0001c0002t0002g0005a0001c0002t0002g0011a0001c0002t0002g0013others(251): Show | 331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.1184+615delT | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54817724 | |||||
chr1:54817737
|
T | G | 143 | a0001c0002t0002g0005a0001c0002t0002g0011a0001c0002t0002g0013others(140): Show | 182 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.1184+615T>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54817737 | ||||||
chr1:54817755
|
ATGAGGAC others(7): Show |
A | 143 | a0001c0002t0002g0005a0001c0002t0002g0011a0001c0002t0002g0013others(140): Show | 182 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.1184+647_1184+660d others(16): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54817755 | |||||
chr1:54817762
|
C | T | 1 | a0001c0002t0001g0078 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1184+640C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54817762 | ||||||
chr1:54817955
|
T | C | 54 | a0001c0002t0002g0238a0001c0002t0009g0230a0001c0003t0003g0003others(51): Show | 80 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(77): Show |
intron_variant | MODIFIER | c.1184+833T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54817955 | ||||||
chr1:54817975
|
A | ATCAATAG others(18): Show |
1 | a0001c0003t0003g0232 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1184+856_1184+880d others(27): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54817975 | |||||
chr1:54818045
|
A | G | 143 | a0001c0002t0002g0005a0001c0002t0002g0011a0001c0002t0002g0013others(140): Show | 182 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.1184+923A>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818045 | ||||||
chr1:54818072
|
C | T | 292 | a0001c0002t0001g0078a0001c0002t0002g0005a0001c0002t0002g0009others(289): Show | 381 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(378): Show |
intron_variant | MODIFIER | c.1184+950C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818072 | ||||||
chr1:54818085
|
T | C | 149 | a0001c0002t0001g0078a0001c0002t0002g0009a0001c0002t0002g0010others(146): Show | 199 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.1184+963T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818085 | ||||||
chr1:54818086
|
A | G | 292 | a0001c0002t0001g0078a0001c0002t0002g0005a0001c0002t0002g0009others(289): Show | 381 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(378): Show |
intron_variant | MODIFIER | c.1184+964A>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818086 | ||||||
chr1:54818335
|
T | C | 18 | a0003c0006t0001g0051a0003c0006t0001g0274a0003c0006t0001g0276others(15): Show | 19 | HG02074.hp2 HG02165.hp1 NA18747.hp2 others(16): Show |
intron_variant | MODIFIER | c.1184+1213T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818335 | ||||||
chr1:54818385
|
C | T | 289 | a0001c0002t0002g0005a0001c0002t0002g0009a0001c0002t0002g0010others(286): Show | 378 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(375): Show |
intron_variant | MODIFIER | c.1184+1263C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818385 | ||||||
chr1:54818386
|
T | C | 142 | a0001c0002t0002g0005a0001c0002t0002g0011a0001c0002t0002g0013others(139): Show | 181 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.1184+1264T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818386 | ||||||
chr1:54818391
|
C | G | 13 | a0001c0002t0002g0009a0001c0002t0002g0053a0001c0002t0002g0071others(10): Show | 17 | HG01884.hp2 HG02109.hp2 HG02622.hp1 others(14): Show |
intron_variant | MODIFIER | c.1184+1269C>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818391 | ||||||
chr1:54818481
|
A | T | 144 | a0001c0002t0002g0005a0001c0002t0002g0011a0001c0002t0002g0013others(141): Show | 183 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.1184+1359A>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818481 | ||||||
chr1:54818522
|
C | T | 144 | a0001c0002t0002g0005a0001c0002t0002g0011a0001c0002t0002g0013others(141): Show | 183 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.1184+1400C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818522 | ||||||
chr1:54818588
|
G | A | 146 | a0001c0002t0002g0005a0001c0002t0002g0011a0001c0002t0002g0013others(143): Show | 185 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.1184+1466G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818588 | ||||||
chr1:54818617
|
G | A | 146 | a0001c0002t0002g0005a0001c0002t0002g0011a0001c0002t0002g0013others(143): Show | 185 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.1184+1495G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818617 | ||||||
chr1:54818628
|
G | GA | 1 | a0001c0003t0003g0019 | 3 | HG02004.hp2 HG02148.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.1184+1507dupA | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54818628 | |||||
chr1:54818732
|
C | G | 1 | a0001c0004t0003g0208 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1184+1610C>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818732 | ||||||
chr1:54818735
|
G | C | 1 | a0001c0004t0003g0208 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1184+1613G>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818735 | ||||||
chr1:54818736
|
C | T | 1 | a0001c0004t0003g0208 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1184+1614C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818736 | ||||||
chr1:54818737
|
A | T | 1 | a0001c0004t0003g0208 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1184+1615A>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818737 | ||||||
chr1:54818739
|
G | T | 1 | a0001c0004t0003g0208 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1184+1617G>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818739 | ||||||
chr1:54818740
|
C | T | 1 | a0001c0004t0003g0208 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1184+1618C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818740 | ||||||
chr1:54818741
|
A | T | 1 | a0001c0004t0003g0208 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1184+1619A>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818741 | ||||||
chr1:54818742
|
C | T | 1 | a0001c0004t0003g0208 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1184+1620C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818742 | ||||||
chr1:54818743
|
C | A | 1 | a0001c0004t0003g0208 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1184+1621C>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818743 | ||||||
chr1:54818745
|
C | T | 1 | a0001c0004t0003g0208 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1184+1623C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818745 | ||||||
chr1:54818746
|
C | G | 1 | a0001c0004t0003g0208 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1184+1624C>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818746 | ||||||
chr1:54818748
|
C | T | 1 | a0001c0004t0003g0208 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1184+1626C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818748 | ||||||
chr1:54818749
|
A | T | 1 | a0001c0004t0003g0208 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1184+1627A>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818749 | ||||||
chr1:54818750
|
C | A | 1 | a0001c0004t0003g0208 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1184+1628C>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818750 | ||||||
chr1:54818751
|
C | A | 1 | a0001c0004t0003g0208 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1184+1629C>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818751 | ||||||
chr1:54818752
|
C | A | 1 | a0001c0004t0003g0208 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1184+1630C>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818752 | ||||||
chr1:54818752
|
C | T | 1 | a0002c0001t0001g0110 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1184+1630C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818752 | ||||||
chr1:54818753
|
G | T | 1 | a0001c0004t0003g0208 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1184+1631G>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818753 | ||||||
chr1:54818754
|
G | T | 1 | a0001c0004t0003g0208 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1184+1632G>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818754 | ||||||
chr1:54818755
|
C | A | 1 | a0001c0004t0003g0208 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1184+1633C>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818755 | ||||||
chr1:54818756
|
T | A | 1 | a0001c0004t0003g0208 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1184+1634T>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818756 | ||||||
chr1:54818762
|
T | A | 1 | a0001c0004t0003g0208 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1184+1640T>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818762 | ||||||
chr1:54818763
|
T | C | 1 | a0001c0004t0003g0208 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1184+1641T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818763 | ||||||
chr1:54818764
|
G | A | 1 | a0001c0004t0003g0208 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1184+1642G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818764 | ||||||
chr1:54818764
|
GT | G | 145 | a0001c0002t0002g0005a0001c0002t0002g0011a0001c0002t0002g0013others(142): Show | 184 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.1184+1644delT | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54818764 | |||||
chr1:54818766
|
T | A | 1 | a0001c0004t0003g0208 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1184+1644T>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818766 | ||||||
chr1:54818779
|
G | T | 1 | a0001c0004t0003g0208 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1184+1657G>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818779 | ||||||
chr1:54818781
|
C | A | 1 | a0001c0004t0003g0208 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1184+1659C>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818781 | ||||||
chr1:54818789
|
T | C | 1 | a0001c0004t0003g0208 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1184+1667T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818789 | ||||||
chr1:54818790
|
G | A | 1 | a0001c0004t0003g0208 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1184+1668G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818790 | ||||||
chr1:54818796
|
T | G | 1 | a0001c0004t0003g0208 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1184+1674T>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818796 | ||||||
chr1:54818807
|
G | T | 1 | a0001c0004t0003g0208 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1184+1685G>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818807 | ||||||
chr1:54818808
|
G | T | 1 | a0001c0004t0003g0208 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1184+1686G>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818808 | ||||||
chr1:54818813
|
G | C | 1 | a0001c0004t0003g0208 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1184+1691G>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818813 | ||||||
chr1:54818818
|
C | A | 1 | a0001c0004t0003g0208 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1184+1696C>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818818 | ||||||
chr1:54818822
|
A | T | 1 | a0001c0004t0003g0208 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1184+1700A>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818822 | ||||||
chr1:54818823
|
G | T | 1 | a0001c0004t0003g0208 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1184+1701G>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818823 | ||||||
chr1:54818826
|
C | A | 1 | a0001c0004t0003g0208 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1184+1704C>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818826 | ||||||
chr1:54818829
|
G | T | 1 | a0001c0004t0003g0208 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1184+1707G>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818829 | ||||||
chr1:54818830
|
C | T | 1 | a0001c0004t0003g0208 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1184+1708C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818830 | ||||||
chr1:54818834
|
C | A | 1 | a0001c0004t0003g0208 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1184+1712C>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818834 | ||||||
chr1:54818835
|
T | A | 1 | a0001c0004t0003g0208 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1184+1713T>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818835 | ||||||
chr1:54818836
|
G | T | 1 | a0001c0004t0003g0208 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1184+1714G>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818836 | ||||||
chr1:54818837
|
C | A | 1 | a0001c0004t0003g0208 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1184+1715C>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818837 | ||||||
chr1:54818840
|
G | C | 1 | a0001c0004t0003g0208 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1184+1718G>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818840 | ||||||
chr1:54818842
|
C | T | 1 | a0001c0004t0003g0208 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1184+1720C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818842 | ||||||
chr1:54818847
|
C | G | 1 | a0001c0004t0003g0208 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1184+1725C>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818847 | ||||||
chr1:54818848
|
C | G | 1 | a0001c0004t0003g0208 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1184+1726C>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818848 | ||||||
chr1:54818850
|
C | G | 1 | a0001c0004t0003g0208 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1184+1728C>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818850 | ||||||
chr1:54818851
|
C | A | 1 | a0001c0004t0003g0208 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1184+1729C>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818851 | ||||||
chr1:54818854
|
A | G | 146 | a0001c0002t0001g0078a0001c0002t0002g0009a0001c0002t0002g0010others(143): Show | 196 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(193): Show |
intron_variant | MODIFIER | c.1184+1732A>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818854 | ||||||
chr1:54818860
|
T | C | 1 | a0001c0004t0003g0208 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1184+1738T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818860 | ||||||
chr1:54818861
|
G | A | 1 | a0001c0004t0003g0208 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1184+1739G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818861 | ||||||
chr1:54818865
|
T | A | 1 | a0001c0004t0003g0208 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1184+1743T>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818865 | ||||||
chr1:54818866
|
T | A | 1 | a0001c0004t0003g0208 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1184+1744T>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818866 | ||||||
chr1:54818868
|
C | T | 31 | a0001c0003t0003g0008a0001c0003t0003g0234a0001c0003t0003g0235others(28): Show | 40 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.1184+1746C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818868 | ||||||
chr1:54818870
|
G | A | 1 | a0001c0004t0003g0208 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1184+1748G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818870 | ||||||
chr1:54818871
|
G | A | 1 | a0001c0004t0003g0208 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1184+1749G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818871 | ||||||
chr1:54818877
|
G | A | 1 | a0001c0004t0003g0208 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1184+1755G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818877 | ||||||
chr1:54818879
|
C | A | 1 | a0001c0004t0003g0208 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1184+1757C>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818879 | ||||||
chr1:54818883
|
G | T | 1 | a0001c0004t0003g0208 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1184+1761G>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818883 | ||||||
chr1:54818885
|
G | A | 1 | a0001c0004t0003g0208 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1184+1763G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818885 | ||||||
chr1:54818886
|
G | T | 1 | a0001c0004t0003g0208 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1184+1764G>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818886 | ||||||
chr1:54818887
|
C | A | 1 | a0001c0004t0003g0208 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1184+1765C>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818887 | ||||||
chr1:54818890
|
G | T | 1 | a0001c0004t0003g0208 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1184+1768G>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818890 | ||||||
chr1:54818891
|
C | A | 1 | a0001c0004t0003g0208 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1184+1769C>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818891 | ||||||
chr1:54818894
|
C | A | 1 | a0001c0004t0003g0208 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1184+1772C>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818894 | ||||||
chr1:54818980
|
T | C | 1 | a0001c0002t0002g0102 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1184+1858T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54818980 | ||||||
chr1:54819081
|
C | A | 159 | a0001c0002t0002g0005a0001c0002t0002g0011a0001c0002t0002g0013others(156): Show | 200 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.1184+1959C>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54819081 | ||||||
chr1:54819114
|
G | T | 2 | a0007c0013t0002g0029a0007c0013t0002g0080 | 3 | HG02451.hp1 HG02723.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1184+1992G>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54819114 | ||||||
chr1:54819118
|
C | A | 1 | a0001c0002t0005g0246 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1184+1996C>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54819118 | ||||||
chr1:54819352
|
G | A | 5 | a0001c0002t0002g0011a0001c0002t0002g0058a0001c0002t0002g0059others(2): Show | 7 | HG02132.hp2 NA18747.hp1 NA18944.hp1 others(4): Show |
intron_variant | MODIFIER | c.1184+2230G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54819352 | ||||||
chr1:54819353
|
C | A | 5 | a0001c0002t0002g0011a0001c0002t0002g0058a0001c0002t0002g0059others(2): Show | 7 | HG02132.hp2 NA18747.hp1 NA18944.hp1 others(4): Show |
intron_variant | MODIFIER | c.1184+2231C>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54819353 | ||||||
chr1:54819365
|
G | A | 2 | a0002c0001t0001g0116a0002c0001t0001g0150 | 2 | HG01106.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1184+2243G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54819365 | ||||||
chr1:54819444
|
C | T | 9 | a0001c0002t0002g0013a0001c0002t0002g0014a0001c0002t0002g0015others(6): Show | 17 | HG00558.hp1 HG03490.hp2 HG03492.hp2 others(14): Show |
intron_variant | MODIFIER | c.1184+2322C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54819444 | ||||||
chr1:54819533
|
C | T | 55 | a0001c0002t0002g0238a0001c0002t0009g0230a0001c0003t0003g0003others(52): Show | 82 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.1184+2411C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54819533 | ||||||
chr1:54819570
|
T | C | 1 | a0001c0002t0002g0264 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1184+2448T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54819570 | ||||||
chr1:54819573
|
G | A | 1 | a0001c0002t0002g0254 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1184+2451G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54819573 | ||||||
chr1:54819647
|
A | C | 2 | a0007c0013t0002g0029a0007c0013t0002g0080 | 3 | HG02451.hp1 HG02723.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1184+2525A>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54819647 | ||||||
chr1:54819812
|
T | TTTTCTTT others(24): Show |
1 | a0001c0002t0002g0238 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1184+2699_1184+270 others(35): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54819812 | |||||
chr1:54819812
|
T | TTTTCTTT others(17): Show |
1 | a0001c0003t0003g0222 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1184+2699_1184+270 others(28): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54819812 | |||||
chr1:54819812
|
T | TTTTCTTT others(21): Show |
5 | a0001c0003t0003g0020a0001c0003t0003g0106a0001c0003t0003g0223others(2): Show | 9 | HG01074.hp1 HG02056.hp2 HG03209.hp1 others(6): Show |
intron_variant | MODIFIER | c.1184+2699_1184+270 others(32): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54819812 | |||||
chr1:54819812
|
T | TTTTCTTT others(25): Show |
20 | a0001c0003t0003g0003a0001c0003t0003g0004a0001c0003t0003g0019others(17): Show | 36 | HG00099.hp2 HG00558.hp2 HG00621.hp2 others(33): Show |
intron_variant | MODIFIER | c.1184+2699_1184+270 others(36): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54819812 | |||||
chr1:54819812
|
T | TTTTCTTT others(29): Show |
16 | a0001c0002t0009g0230a0001c0003t0003g0215a0001c0003t0003g0220others(13): Show | 19 | HG00544.hp1 HG00673.hp2 HG01070.hp2 others(16): Show |
intron_variant | MODIFIER | c.1184+2699_1184+270 others(40): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54819812 | |||||
chr1:54819812
|
T | TTTTCTTT others(33): Show |
5 | a0001c0003t0003g0229a0001c0004t0003g0193a0002c0005t0004g0012others(2): Show | 7 | HG02071.hp2 HG02717.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.1184+2699_1184+270 others(44): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54819812 | |||||
chr1:54819812
|
T | TTTTCTTT others(37): Show |
5 | a0001c0003t0003g0044a0001c0003t0003g0047a0001c0003t0003g0221others(2): Show | 7 | HG00140.hp1 HG01433.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1184+2699_1184+270 others(48): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54819812 | |||||
chr1:54819812
|
T | TTTTCTTT others(45): Show |
1 | a0002c0001t0001g0161 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1184+2699_1184+270 others(56): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54819812 | |||||
chr1:54819814
|
T | C | 1 | a0001c0003t0003g0216 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1184+2692T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54819814 | ||||||
chr1:54819814
|
TTCTTTCT others(3): Show |
T | 2 | a0002c0001t0001g0116a0002c0001t0001g0150 | 2 | HG01106.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1184+2704_1184+271 others(14): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54819814 | |||||
chr1:54819824
|
C | CTT | 54 | a0001c0002t0002g0238a0001c0002t0009g0230a0001c0003t0003g0003others(51): Show | 81 | HG00099.hp2 HG00140.hp1 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.1184+2703_1184+270 others(6): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54819824 | |||||
chr1:54819824
|
C | CTTTTTCT others(21): Show |
1 | a0001c0003t0003g0216 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1184+2703_1184+270 others(32): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54819824 | |||||
chr1:54819824
|
CTCTT | C | 2 | a0007c0013t0002g0029a0007c0013t0002g0080 | 3 | HG02451.hp1 HG02723.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1184+2714_1184+271 others(8): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54819824 | |||||
chr1:54819832
|
TTCTTTC | T | 31 | a0001c0002t0001g0078a0001c0002t0002g0009a0001c0002t0002g0053others(28): Show | 36 | HG00408.hp1 HG00423.hp2 HG00621.hp1 others(33): Show |
intron_variant | MODIFIER | c.1184+2718_1184+272 others(10): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54819832 | |||||
chr1:54819835
|
TTTCTCTT others(11): Show |
T | 18 | a0001c0002t0002g0010a0001c0002t0002g0023a0001c0002t0002g0046others(15): Show | 25 | HG00280.hp2 HG00639.hp2 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.1184+2717_1184+273 others(22): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54819835 | |||||
chr1:54819839
|
TCTTTCTT others(7): Show |
T | 30 | a0001c0002t0002g0247a0001c0003t0003g0008a0001c0003t0003g0234others(27): Show | 39 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(36): Show |
intron_variant | MODIFIER | c.1184+2718_1184+273 others(18): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54819839 | ||||||
chr1:54819860
|
CCTTCCT | C | 31 | a0001c0002t0001g0078a0001c0002t0002g0009a0001c0002t0002g0053others(28): Show | 36 | HG00408.hp1 HG00423.hp2 HG00621.hp1 others(33): Show |
intron_variant | MODIFIER | c.1184+2741_1184+274 others(10): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54819860 | |||||
chr1:54819864
|
CCT | C | 46 | a0001c0002t0002g0023a0001c0002t0002g0046a0001c0002t0002g0050others(43): Show | 59 | HG00280.hp2 HG00408.hp2 HG00438.hp2 others(56): Show |
intron_variant | MODIFIER | c.1184+2747_1184+274 others(6): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54819864 | |||||
chr1:54819868
|
TCTTTC | T | 2 | a0001c0002t0002g0010a0001c0002t0002g0260 | 5 | HG01099.hp1 HG01934.hp1 HG01978.hp1 others(2): Show |
intron_variant | MODIFIER | c.1184+2747_1184+275 others(9): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54819868 | ||||||
chr1:54819876
|
CCT | C | 2 | a0001c0002t0002g0010a0001c0002t0002g0260 | 5 | HG01099.hp1 HG01934.hp1 HG01978.hp1 others(2): Show |
intron_variant | MODIFIER | c.1184+2755_1184+275 others(6): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54819876 | ||||||
chr1:54819928
|
A | ATT | 78 | a0001c0002t0001g0078a0001c0002t0002g0009a0001c0002t0002g0010others(75): Show | 99 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(96): Show |
intron_variant | MODIFIER | c.1184+2807_1184+280 others(6): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54819928 | |||||
chr1:54819930
|
A | C | 78 | a0001c0002t0001g0078a0001c0002t0002g0009a0001c0002t0002g0010others(75): Show | 99 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(96): Show |
intron_variant | MODIFIER | c.1184+2808A>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54819930 | ||||||
chr1:54819934
|
C | T | 78 | a0001c0002t0001g0078a0001c0002t0002g0009a0001c0002t0002g0010others(75): Show | 99 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(96): Show |
intron_variant | MODIFIER | c.1184+2812C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54819934 | ||||||
chr1:54819935
|
T | C | 78 | a0001c0002t0001g0078a0001c0002t0002g0009a0001c0002t0002g0010others(75): Show | 99 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(96): Show |
intron_variant | MODIFIER | c.1184+2813T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54819935 | ||||||
chr1:54819945
|
G | T | 79 | a0001c0002t0001g0078a0001c0002t0002g0009a0001c0002t0002g0010others(76): Show | 100 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.1184+2823G>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54819945 | ||||||
chr1:54819948
|
C | T | 1 | a0002c0011t0004g0196 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1184+2826C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54819948 | ||||||
chr1:54819952
|
T | C | 1 | a0002c0011t0004g0196 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1184+2830T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54819952 | ||||||
chr1:54819978
|
T | C | 78 | a0001c0002t0001g0078a0001c0002t0002g0009a0001c0002t0002g0010others(75): Show | 98 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.1184+2856T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54819978 | ||||||
chr1:54819980
|
C | T | 78 | a0001c0002t0001g0078a0001c0002t0002g0009a0001c0002t0002g0010others(75): Show | 98 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.1184+2858C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54819980 | ||||||
chr1:54819982
|
C | CTTTT | 17 | a0001c0002t0002g0010a0001c0002t0002g0023a0001c0002t0002g0046others(14): Show | 24 | HG00280.hp2 HG00639.hp2 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.1184+2861_1184+286 others(8): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54819982 | |||||
chr1:54819982
|
C | T | 61 | a0001c0002t0001g0078a0001c0002t0002g0009a0001c0002t0002g0053others(58): Show | 74 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(71): Show |
intron_variant | MODIFIER | c.1184+2860C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54819982 | ||||||
chr1:54820009
|
T | C | 79 | a0001c0002t0001g0078a0001c0002t0002g0009a0001c0002t0002g0010others(76): Show | 100 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.1184+2887T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54820009 | ||||||
chr1:54820017
|
T | C | 79 | a0001c0002t0001g0078a0001c0002t0002g0009a0001c0002t0002g0010others(76): Show | 100 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.1184+2895T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54820017 | ||||||
chr1:54820017
|
T | TTTCC | 3 | a0002c0001t0001g0039a0002c0001t0001g0132a0002c0001t0001g0162 | 4 | HG02615.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1184+2911_1184+291 others(8): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54820017 | |||||
chr1:54820017
|
TTTCC | T | 55 | a0001c0002t0002g0238a0001c0002t0009g0230a0001c0003t0003g0003others(52): Show | 82 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.1184+2911_1184+291 others(8): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54820017 | |||||
chr1:54820033
|
C | A | 50 | a0001c0002t0001g0078a0001c0002t0002g0053a0001c0002t0002g0263others(47): Show | 61 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(58): Show |
intron_variant | MODIFIER | c.1184+2911C>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54820033 | ||||||
chr1:54820041
|
A | ATTCC | 19 | a0001c0002t0002g0010a0001c0002t0002g0023a0001c0002t0002g0046others(16): Show | 25 | HG00280.hp2 HG00639.hp2 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.1184+2927_1184+293 others(8): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54820041 | |||||
chr1:54820041
|
A | C | 60 | a0001c0002t0001g0078a0001c0002t0002g0009a0001c0002t0002g0050others(57): Show | 75 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(72): Show |
intron_variant | MODIFIER | c.1184+2919A>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54820041 | ||||||
chr1:54820071
|
CCCTT | C | 53 | a0001c0002t0002g0010a0001c0002t0002g0023a0001c0002t0002g0046others(50): Show | 66 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.1184+2960_1184+296 others(8): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54820071 | |||||
chr1:54820082
|
T | C | 27 | a0001c0002t0001g0078a0001c0002t0002g0009a0001c0002t0002g0053others(24): Show | 34 | HG00408.hp1 HG01167.hp1 HG01884.hp2 others(31): Show |
intron_variant | MODIFIER | c.1184+2960T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54820082 | ||||||
chr1:54820086
|
C | T | 27 | a0001c0002t0001g0078a0001c0002t0002g0009a0001c0002t0002g0053others(24): Show | 34 | HG00408.hp1 HG01167.hp1 HG01884.hp2 others(31): Show |
intron_variant | MODIFIER | c.1184+2964C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54820086 | ||||||
chr1:54820089
|
C | CTTCT | 33 | a0001c0002t0002g0263a0001c0002t0002g0264a0001c0002t0002g0265others(30): Show | 39 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(36): Show |
intron_variant | MODIFIER | c.1184+2980_1184+298 others(8): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54820089 | |||||
chr1:54820089
|
C | T | 27 | a0001c0002t0001g0078a0001c0002t0002g0009a0001c0002t0002g0053others(24): Show | 34 | HG00408.hp1 HG01167.hp1 HG01884.hp2 others(31): Show |
intron_variant | MODIFIER | c.1184+2967C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54820089 | ||||||
chr1:54820098
|
TTCTTTCT others(5): Show |
T | 2 | a0002c0001t0001g0007a0010c0019t0002g0067 | 5 | HG01884.hp1 HG02145.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.1184+2980_1184+299 others(16): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54820098 | |||||
chr1:54820102
|
T | C | 135 | a0001c0002t0002g0005a0001c0002t0002g0011a0001c0002t0002g0013others(132): Show | 171 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.1184+2980T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54820102 | ||||||
chr1:54820106
|
C | T | 20 | a0001c0002t0002g0010a0001c0002t0002g0023a0001c0002t0002g0046others(17): Show | 27 | HG00280.hp2 HG00639.hp2 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.1184+2984C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54820106 | ||||||
chr1:54820108
|
CTCTCTCT others(5): Show |
C | 134 | a0001c0002t0002g0005a0001c0002t0002g0011a0001c0002t0002g0013others(131): Show | 170 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(167): Show |
intron_variant | MODIFIER | c.1184+2990_1184+300 others(16): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54820108 | |||||
chr1:54820108
|
CTCTCTCT others(9): Show |
C | 1 | a0001c0002t0002g0058 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1184+2990_1184+300 others(20): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54820108 | |||||
chr1:54820112
|
C | CTCTT | 2 | a0003c0006t0001g0051a0003c0006t0001g0279 | 3 | NA18946.hp1 NA19066.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.1184+3014_1184+301 others(8): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54820112 | |||||
chr1:54820112
|
C | CTCTTTCT others(5): Show |
12 | a0003c0006t0001g0274a0003c0006t0001g0280a0003c0006t0001g0281others(9): Show | 13 | HG02165.hp1 HG02451.hp1 HG02886.hp1 others(10): Show |
intron_variant | MODIFIER | c.1184+3006_1184+301 others(16): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54820112 | |||||
chr1:54820112
|
C | CTCTTTCT others(9): Show |
2 | a0003c0006t0001g0276a0003c0006t0001g0286 | 2 | HG02074.hp2 NA18957.hp1 |
intron_variant | MODIFIER | c.1184+3002_1184+301 others(20): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54820112 | |||||
chr1:54820112
|
C | CTCTTTCT others(13): Show |
2 | a0003c0006t0001g0277a0003c0020t0004g0287 | 2 | NA19090.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.1184+2998_1184+301 others(24): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54820112 | |||||
chr1:54820112
|
CTCTTTCT others(1): Show |
C | 55 | a0001c0002t0002g0238a0001c0002t0009g0230a0001c0003t0003g0003others(52): Show | 82 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.1184+3010_1184+301 others(12): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54820112 | |||||
chr1:54820116
|
T | C | 80 | a0001c0002t0001g0078a0001c0002t0002g0009a0001c0002t0002g0010others(77): Show | 104 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.1184+2994T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54820116 | ||||||
chr1:54820124
|
T | C | 55 | a0001c0002t0002g0238a0001c0002t0009g0230a0001c0003t0003g0003others(52): Show | 82 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.1184+3002T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54820124 | ||||||
chr1:54820132
|
T | C | 79 | a0001c0002t0001g0078a0001c0002t0002g0009a0001c0002t0002g0010others(76): Show | 100 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.1184+3010T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54820132 | ||||||
chr1:54820136
|
T | C | 134 | a0001c0002t0001g0078a0001c0002t0002g0009a0001c0002t0002g0010others(131): Show | 182 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(179): Show |
intron_variant | MODIFIER | c.1184+3014T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54820136 | ||||||
chr1:54820148
|
C | CCCTT | 41 | a0001c0002t0001g0078a0001c0002t0002g0263a0001c0002t0002g0264others(38): Show | 50 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(47): Show |
intron_variant | MODIFIER | c.1184+3044_1184+304 others(8): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54820148 | |||||
chr1:54820258
|
C | T | 20 | a0001c0002t0002g0010a0001c0002t0002g0023a0001c0002t0002g0046others(17): Show | 27 | HG00280.hp2 HG00639.hp2 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.1184+3136C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54820258 | ||||||
chr1:54820287
|
T | G | 1 | a0002c0001t0001g0159 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1184+3165T>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54820287 | ||||||
chr1:54820584
|
C | G | 2 | a0001c0002t0002g0265a0001c0002t0002g0271 | 2 | HG02895.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1184+3462C>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54820584 | ||||||
chr1:54820600
|
C | T | 292 | a0001c0002t0001g0078a0001c0002t0002g0005a0001c0002t0002g0009others(289): Show | 381 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(378): Show |
intron_variant | MODIFIER | c.1184+3478C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54820600 | ||||||
chr1:54820750
|
C | T | 1 | a0002c0001t0001g0143 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1184+3628C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54820750 | ||||||
chr1:54820771
|
TTTTG | T | 5 | a0001c0003t0003g0003a0001c0003t0003g0044a0001c0003t0003g0215others(2): Show | 11 | HG00099.hp2 HG00140.hp1 HG00735.hp1 others(8): Show |
intron_variant | MODIFIER | c.1184+3662_1184+366 others(8): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54820771 | |||||
chr1:54820799
|
C | T | 13 | a0001c0002t0001g0078a0001c0002t0002g0263a0001c0002t0002g0264others(10): Show | 13 | HG00408.hp1 HG00423.hp2 HG00621.hp1 others(10): Show |
intron_variant | MODIFIER | c.1184+3677C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54820799 | ||||||
chr1:54820872
|
G | A | 78 | a0001c0002t0001g0078a0001c0002t0002g0009a0001c0002t0002g0010others(75): Show | 99 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(96): Show |
intron_variant | MODIFIER | c.1184+3750G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54820872 | ||||||
chr1:54820960
|
G | A | 55 | a0001c0002t0002g0238a0001c0002t0009g0230a0001c0003t0003g0003others(52): Show | 82 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.1184+3838G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54820960 | ||||||
chr1:54821170
|
T | C | 55 | a0001c0002t0002g0238a0001c0002t0009g0230a0001c0003t0003g0003others(52): Show | 82 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.1184+4048T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54821170 | ||||||
chr1:54821180
|
G | A | 20 | a0001c0002t0002g0010a0001c0002t0002g0023a0001c0002t0002g0046others(17): Show | 27 | HG00280.hp2 HG00639.hp2 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.1184+4058G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54821180 | ||||||
chr1:54821200
|
A | ATTGT | 55 | a0001c0002t0002g0238a0001c0002t0009g0230a0001c0003t0003g0003others(52): Show | 82 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.1184+4080_1184+408 others(8): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54821200 | |||||
chr1:54821208
|
G | C | 1 | a0002c0001t0001g0135 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1184+4086G>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54821208 | ||||||
chr1:54821219
|
G | GC | 134 | a0001c0002t0001g0078a0001c0002t0002g0009a0001c0002t0002g0010others(131): Show | 182 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(179): Show |
intron_variant | MODIFIER | c.1184+4097_1184+409 others(5): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54821219 | ||||||
chr1:54821275
|
T | A | 1 | a0004c0008t0006g0288 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1184+4153T>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54821275 | ||||||
chr1:54821343
|
G | C | 2 | a0006c0014t0003g0048a0006c0014t0003g0233 | 3 | HG02922.hp1 HG03130.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1184+4221G>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54821343 | ||||||
chr1:54821414
|
G | A | 138 | a0001c0002t0002g0005a0001c0002t0002g0011a0001c0002t0002g0013others(135): Show | 177 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.1184+4292G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54821414 | ||||||
chr1:54821732
|
T | C | 55 | a0001c0002t0002g0238a0001c0002t0009g0230a0001c0003t0003g0003others(52): Show | 82 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.1184+4610T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54821732 | ||||||
chr1:54821816
|
T | A | 79 | a0001c0002t0001g0078a0001c0002t0002g0009a0001c0002t0002g0010others(76): Show | 100 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.1184+4694T>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54821816 | ||||||
chr1:54821854
|
T | G | 18 | a0003c0006t0001g0051a0003c0006t0001g0274a0003c0006t0001g0276others(15): Show | 19 | HG02074.hp2 HG02165.hp1 NA18747.hp2 others(16): Show |
intron_variant | MODIFIER | c.1184+4732T>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54821854 | ||||||
chr1:54821878
|
TCTTATTT others(311): Show |
T | 55 | a0001c0002t0002g0238a0001c0002t0009g0230a0001c0003t0003g0003others(52): Show | 82 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.1184+4768_1184+508 others(4): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54821878 | |||||
chr1:54821886
|
C | CT | 48 | a0001c0002t0002g0005a0001c0002t0002g0014a0001c0002t0002g0015others(45): Show | 64 | HG00544.hp2 HG00558.hp1 HG00642.hp1 others(61): Show |
intron_variant | MODIFIER | c.1184+4794dupT | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54821886 | |||||
chr1:54821886
|
C | CTT | 7 | a0001c0002t0002g0025a0001c0003t0003g0217a0002c0001t0001g0034others(4): Show | 10 | HG01109.hp1 HG01109.hp2 HG01261.hp2 others(7): Show |
intron_variant | MODIFIER | c.1184+4793_1184+479 others(6): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54821886 | |||||
chr1:54821886
|
CT | C | 20 | a0001c0002t0002g0097a0001c0002t0002g0098a0002c0001t0001g0165others(17): Show | 21 | HG00423.hp1 HG02074.hp2 HG02165.hp1 others(18): Show |
intron_variant | MODIFIER | c.1184+4794delT | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54821886 | |||||
chr1:54821886
|
CTT | C | 8 | a0001c0002t0002g0065a0001c0002t0002g0066a0001c0002t0002g0079others(5): Show | 9 | HG01891.hp1 HG01891.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.1184+4793_1184+479 others(6): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54821886 | |||||
chr1:54821886
|
CTTTT | C | 9 | a0001c0002t0002g0264a0001c0002t0002g0268a0001c0004t0003g0198others(6): Show | 9 | HG00423.hp2 HG00438.hp2 HG01978.hp2 others(6): Show |
intron_variant | MODIFIER | c.1184+4791_1184+479 others(8): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54821886 | |||||
chr1:54821886
|
CTTTTT | C | 30 | a0001c0002t0002g0050a0001c0002t0002g0263a0001c0002t0002g0265others(27): Show | 40 | HG00408.hp1 HG00408.hp2 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.1184+4790_1184+479 others(9): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54821886 | |||||
chr1:54821886
|
CTTTTTT | C | 24 | a0001c0002t0002g0010a0001c0002t0002g0023a0001c0002t0002g0046others(21): Show | 30 | HG00280.hp2 HG00609.hp1 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.1184+4789_1184+479 others(10): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54821886 | |||||
chr1:54821886
|
CTTTTTTT | C | 20 | a0001c0002t0002g0009a0001c0002t0002g0011a0001c0002t0002g0026others(17): Show | 28 | HG01167.hp2 HG01169.hp2 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.1184+4788_1184+479 others(11): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54821886 | |||||
chr1:54821886
|
CTTTTTTT others(2): Show |
C | 3 | a0002c0001t0001g0007a0002c0001t0001g0174a0010c0019t0002g0067 | 6 | HG01884.hp1 HG02145.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1184+4786_1184+479 others(13): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54821886 | |||||
chr1:54821886
|
CTTTTTTT others(5): Show |
C | 1 | a0001c0004t0003g0190 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1184+4783_1184+479 others(16): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54821886 | |||||
chr1:54821929
|
C | T | 2 | a0007c0013t0002g0029a0007c0013t0002g0080 | 3 | HG02451.hp1 HG02723.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1184+4807C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54821929 | ||||||
chr1:54821960
|
G | A | 19 | a0001c0002t0002g0010a0001c0002t0002g0023a0001c0002t0002g0046others(16): Show | 26 | HG00280.hp2 HG00639.hp2 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.1184+4838G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54821960 | ||||||
chr1:54822010
|
C | T | 79 | a0001c0002t0001g0078a0001c0002t0002g0009a0001c0002t0002g0010others(76): Show | 100 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.1184+4888C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54822010 | ||||||
chr1:54822048
|
A | G | 1 | a0001c0002t0002g0079 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1184+4926A>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54822048 | ||||||
chr1:54822108
|
C | T | 1 | a0004c0008t0001g0052 | 2 | HG01884.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1184+4986C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54822108 | ||||||
chr1:54822140
|
C | T | 52 | a0001c0002t0001g0078a0001c0002t0002g0011a0001c0002t0002g0026others(49): Show | 64 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.1184+5018C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54822140 | ||||||
chr1:54822144
|
C | T | 79 | a0001c0002t0001g0078a0001c0002t0002g0009a0001c0002t0002g0010others(76): Show | 100 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.1184+5022C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54822144 | ||||||
chr1:54822164
|
C | T | 1 | a0001c0002t0005g0064 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1184+5042C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54822164 | ||||||
chr1:54822182
|
G | A | 20 | a0003c0006t0001g0051a0003c0006t0001g0274a0003c0006t0001g0276others(17): Show | 22 | HG02074.hp2 HG02165.hp1 HG02451.hp1 others(19): Show |
intron_variant | MODIFIER | c.1184+5060G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54822182 | ||||||
chr1:54822188
|
G | A | 1 | a0001c0002t0002g0053 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1184+5066G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54822188 | ||||||
chr1:54822189
|
C | T | 1 | a0002c0001t0001g0092 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1184+5067C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54822189 | ||||||
chr1:54822288
|
G | C | 55 | a0001c0002t0002g0238a0001c0002t0009g0230a0001c0003t0003g0003others(52): Show | 82 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.1184+5166G>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54822288 | ||||||
chr1:54822311
|
G | T | 55 | a0001c0002t0002g0238a0001c0002t0009g0230a0001c0003t0003g0003others(52): Show | 82 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.1184+5189G>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54822311 | ||||||
chr1:54822382
|
G | GT | 65 | a0001c0002t0002g0009a0001c0002t0002g0053a0001c0002t0002g0071others(62): Show | 96 | HG00099.hp2 HG00140.hp1 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.1184+5272dupT | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54822382 | |||||
chr1:54822382
|
G | T | 1 | a0001c0003t0003g0244 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1184+5260G>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54822382 | ||||||
chr1:54822430
|
A | C | 45 | a0001c0009t0002g0202a0001c0009t0002g0203a0002c0001t0001g0002others(42): Show | 55 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(52): Show |
intron_variant | MODIFIER | c.1184+5308A>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54822430 | ||||||
chr1:54822628
|
T | C | 2 | a0002c0001t0001g0072a0002c0001t0001g0178 | 2 | NA18967.hp2 NA18970.hp2 |
intron_variant | MODIFIER | c.1184+5506T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54822628 | ||||||
chr1:54822936
|
T | C | 55 | a0001c0002t0002g0238a0001c0002t0009g0230a0001c0003t0003g0003others(52): Show | 82 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.1184+5814T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54822936 | ||||||
chr1:54822950
|
T | C | 1 | a0004c0008t0001g0289 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1184+5828T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54822950 | ||||||
chr1:54823058
|
C | T | 135 | a0001c0002t0001g0078a0001c0002t0002g0009a0001c0002t0002g0010others(132): Show | 183 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.1184+5936C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54823058 | ||||||
chr1:54823162
|
T | C | 1 | a0001c0002t0005g0246 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1184+6040T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54823162 | ||||||
chr1:54823179
|
C | T | 37 | a0001c0002t0002g0009a0001c0002t0002g0010a0001c0002t0002g0023others(34): Show | 49 | HG00280.hp2 HG00639.hp2 HG00741.hp1 others(46): Show |
intron_variant | MODIFIER | c.1184+6057C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54823179 | ||||||
chr1:54823325
|
T | C | 55 | a0001c0002t0002g0238a0001c0002t0009g0230a0001c0003t0003g0003others(52): Show | 82 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.1184+6203T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54823325 | ||||||
chr1:54823345
|
CT | C | 10 | a0001c0002t0002g0011a0001c0002t0002g0026a0001c0002t0002g0058others(7): Show | 13 | HG01167.hp2 HG01169.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.1184+6234delT | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54823345 | |||||
chr1:54823413
|
C | T | 1 | a0001c0002t0002g0050 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1184+6291C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54823413 | ||||||
chr1:54823506
|
A | G | 135 | a0001c0002t0001g0078a0001c0002t0002g0009a0001c0002t0002g0010others(132): Show | 183 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.1184+6384A>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54823506 | ||||||
chr1:54823632
|
C | A | 20 | a0001c0002t0002g0010a0001c0002t0002g0023a0001c0002t0002g0046others(17): Show | 27 | HG00280.hp2 HG00639.hp2 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.1184+6510C>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54823632 | ||||||
chr1:54823784
|
C | T | 292 | a0001c0002t0001g0078a0001c0002t0002g0005a0001c0002t0002g0009others(289): Show | 381 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(378): Show |
intron_variant | MODIFIER | c.1184+6662C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54823784 | ||||||
chr1:54823942
|
TTTTG | T | 5 | a0001c0002t0002g0011a0001c0002t0002g0058a0001c0002t0002g0059others(2): Show | 7 | HG02132.hp2 NA18747.hp1 NA18944.hp1 others(4): Show |
intron_variant | MODIFIER | c.1184+6836_1184+683 others(8): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54823942 | |||||
chr1:54824053
|
G | A | 42 | a0001c0002t0001g0078a0001c0002t0002g0079a0001c0002t0002g0263others(39): Show | 51 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(48): Show |
intron_variant | MODIFIER | c.1184+6931G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54824053 | ||||||
chr1:54824087
|
T | G | 79 | a0001c0002t0001g0078a0001c0002t0002g0009a0001c0002t0002g0010others(76): Show | 100 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.1184+6965T>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54824087 | ||||||
chr1:54824088
|
C | G | 42 | a0001c0002t0001g0078a0001c0002t0002g0079a0001c0002t0002g0263others(39): Show | 51 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(48): Show |
intron_variant | MODIFIER | c.1184+6966C>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54824088 | ||||||
chr1:54824242
|
A | G | 135 | a0001c0002t0001g0078a0001c0002t0002g0009a0001c0002t0002g0010others(132): Show | 183 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.1184+7120A>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54824242 | ||||||
chr1:54824319
|
T | G | 43 | a0001c0002t0001g0078a0001c0002t0002g0079a0001c0002t0002g0263others(40): Show | 52 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(49): Show |
intron_variant | MODIFIER | c.1184+7197T>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54824319 | ||||||
chr1:54824337
|
C | T | 1 | a0001c0003t0004g0027 | 2 | HG00673.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.1184+7215C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54824337 | ||||||
chr1:54824394
|
TG | T | 135 | a0001c0002t0001g0078a0001c0002t0002g0009a0001c0002t0002g0010others(132): Show | 183 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.1184+7277delG | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54824394 | |||||
chr1:54824540
|
G | A | 3 | a0002c0001t0001g0007a0002c0001t0001g0174a0010c0019t0002g0067 | 6 | HG01884.hp1 HG02145.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1184+7418G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54824540 | ||||||
chr1:54824572
|
T | A | 291 | a0001c0002t0001g0078a0001c0002t0002g0005a0001c0002t0002g0009others(288): Show | 380 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(377): Show |
intron_variant | MODIFIER | c.1184+7450T>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54824572 | ||||||
chr1:54824656
|
AGT | A | 19 | a0001c0002t0002g0010a0001c0002t0002g0023a0001c0002t0002g0046others(16): Show | 26 | HG00280.hp2 HG00639.hp2 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.1184+7537_1184+753 others(6): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54824656 | |||||
chr1:54824659
|
G | A | 1 | a0001c0002t0002g0079 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1184+7537G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54824659 | ||||||
chr1:54824723
|
C | T | 55 | a0001c0002t0002g0238a0001c0002t0009g0230a0001c0003t0003g0003others(52): Show | 82 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.1184+7601C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54824723 | ||||||
chr1:54824724
|
T | C | 55 | a0001c0002t0002g0238a0001c0002t0009g0230a0001c0003t0003g0003others(52): Show | 82 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.1184+7602T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54824724 | ||||||
chr1:54824757
|
G | C | 20 | a0001c0003t0003g0008a0001c0003t0003g0234a0001c0003t0003g0235others(17): Show | 28 | HG00408.hp2 HG00609.hp1 HG01978.hp2 others(25): Show |
intron_variant | MODIFIER | c.1184+7635G>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54824757 | ||||||
chr1:54824811
|
T | C | 1 | a0001c0009t0002g0202 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1184+7689T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54824811 | ||||||
chr1:54824835
|
T | C | 7 | a0001c0002t0002g0013a0001c0002t0002g0014a0001c0002t0002g0049others(4): Show | 12 | HG03490.hp2 HG03492.hp2 NA18940.hp1 others(9): Show |
intron_variant | MODIFIER | c.1184+7713T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54824835 | ||||||
chr1:54825035
|
G | A | 1 | a0004c0008t0006g0288 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1184+7913G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54825035 | ||||||
chr1:54825041
|
CT | C | 34 | a0001c0002t0002g0053a0001c0002t0002g0071a0001c0002t0002g0264others(31): Show | 39 | HG00408.hp1 HG00423.hp2 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.1184+7945delT | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54825041 | |||||
chr1:54825041
|
CTT | C | 108 | a0001c0002t0002g0005a0001c0002t0002g0009a0001c0002t0002g0025others(105): Show | 136 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.1184+7944_1184+794 others(6): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54825041 | |||||
chr1:54825041
|
CTTT | C | 66 | a0001c0002t0002g0011a0001c0002t0002g0013a0001c0002t0002g0014others(63): Show | 88 | HG00408.hp2 HG00438.hp2 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.1184+7943_1184+794 others(7): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54825041 | |||||
chr1:54825041
|
CTTTTTTT others(2): Show |
C | 57 | a0001c0002t0002g0238a0001c0002t0005g0064a0001c0002t0009g0230others(54): Show | 84 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.1184+7937_1184+794 others(13): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54825041 | |||||
chr1:54825041
|
CTTTTTTT others(8): Show |
C | 20 | a0001c0002t0002g0010a0001c0002t0002g0023a0001c0002t0002g0046others(17): Show | 27 | HG00280.hp2 HG00639.hp2 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.1184+7931_1184+794 others(19): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54825041 | |||||
chr1:54825070
|
G | A | 17 | a0003c0006t0001g0051a0003c0006t0001g0276a0003c0006t0001g0277others(14): Show | 18 | HG02074.hp2 HG02165.hp1 NA18747.hp2 others(15): Show |
intron_variant | MODIFIER | c.1184+7948G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54825070 | ||||||
chr1:54825096
|
C | G | 55 | a0001c0002t0002g0238a0001c0002t0009g0230a0001c0003t0003g0003others(52): Show | 82 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.1184+7974C>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54825096 | ||||||
chr1:54825136
|
C | T | 13 | a0001c0002t0002g0009a0001c0002t0002g0053a0001c0002t0002g0071others(10): Show | 17 | HG01884.hp2 HG02109.hp2 HG02622.hp1 others(14): Show |
intron_variant | MODIFIER | c.1184+8014C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54825136 | ||||||
chr1:54825176
|
G | A | 1 | a0002c0001t0001g0141 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1184+8054G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54825176 | ||||||
chr1:54825339
|
C | T | 80 | a0001c0002t0001g0078a0001c0002t0002g0009a0001c0002t0002g0010others(77): Show | 101 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.1184+8217C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54825339 | ||||||
chr1:54825342
|
C | T | 1 | a0004c0008t0006g0288 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1184+8220C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54825342 | ||||||
chr1:54825384
|
G | A | 1 | a0002c0001t0001g0137 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1184+8262G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54825384 | ||||||
chr1:54825432
|
T | A | 2 | a0006c0014t0003g0048a0006c0014t0003g0233 | 3 | HG02922.hp1 HG03130.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1184+8310T>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54825432 | ||||||
chr1:54825785
|
G | A | 2 | a0001c0003t0003g0220a0001c0003t0003g0224 | 2 | NA18968.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.1184+8663G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54825785 | ||||||
chr1:54826177
|
C | T | 1 | a0001c0003t0003g0222 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1184+9055C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54826177 | ||||||
chr1:54826481
|
G | C | 20 | a0001c0002t0002g0010a0001c0002t0002g0023a0001c0002t0002g0046others(17): Show | 27 | HG00280.hp2 HG00639.hp2 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.1184+9359G>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54826481 | ||||||
chr1:54826538
|
C | T | 1 | a0001c0002t0002g0259 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1184+9416C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54826538 | ||||||
chr1:54826691
|
C | A | 1 | a0002c0001t0001g0183 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1184+9569C>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54826691 | ||||||
chr1:54826815
|
A | G | 1 | a0009c0021t0004g0291 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1184+9693A>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54826815 | ||||||
chr1:54826875
|
C | T | 55 | a0001c0002t0002g0238a0001c0002t0009g0230a0001c0003t0003g0003others(52): Show | 82 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.1184+9753C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54826875 | ||||||
chr1:54826927
|
A | G | 3 | a0002c0001t0001g0007a0002c0001t0001g0174a0010c0019t0002g0067 | 6 | HG01884.hp1 HG02145.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1184+9805A>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54826927 | ||||||
chr1:54826940
|
C | T | 10 | a0001c0002t0002g0011a0001c0002t0002g0026a0001c0002t0002g0058others(7): Show | 13 | HG01167.hp2 HG01169.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.1184+9818C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54826940 | ||||||
chr1:54827027
|
C | T | 2 | a0002c0001t0001g0116a0002c0001t0001g0150 | 2 | HG01106.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1184+9905C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54827027 | ||||||
chr1:54827211
|
A | G | 55 | a0001c0002t0002g0238a0001c0002t0009g0230a0001c0003t0003g0003others(52): Show | 82 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.1184+10089A>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54827211 | ||||||
chr1:54827340
|
C | G | 1 | a0002c0001t0001g0123 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1184+10218C>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54827340 | ||||||
chr1:54827383
|
C | G | 13 | a0001c0002t0002g0009a0001c0002t0002g0053a0001c0002t0002g0071others(10): Show | 17 | HG01884.hp2 HG02109.hp2 HG02622.hp1 others(14): Show |
intron_variant | MODIFIER | c.1184+10261C>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54827383 | ||||||
chr1:54827705
|
G | A | 4 | a0001c0002t0002g0053a0004c0008t0001g0052a0004c0008t0001g0289others(1): Show | 5 | HG01884.hp2 HG02622.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1184+10583G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54827705 | ||||||
chr1:54828022
|
A | G | 1 | a0009c0021t0004g0291 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1184+10900A>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54828022 | ||||||
chr1:54828067
|
T | G | 43 | a0001c0002t0001g0078a0001c0002t0002g0079a0001c0002t0002g0263others(40): Show | 52 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(49): Show |
intron_variant | MODIFIER | c.1184+10945T>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54828067 | ||||||
chr1:54828116
|
A | G | 1 | a0002c0005t0004g0129 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1184+10994A>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54828116 | ||||||
chr1:54828178
|
T | C | 1 | a0002c0001t0001g0135 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1184+11056T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54828178 | ||||||
chr1:54828210
|
T | G | 1 | a0002c0001t0001g0074 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1184+11088T>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54828210 | ||||||
chr1:54828243
|
A | C | 4 | a0005c0007t0002g0056a0005c0007t0002g0093a0005c0007t0002g0231others(1): Show | 4 | NA18985.hp2 NA19009.hp2 NA19078.hp2 others(1): Show |
intron_variant | MODIFIER | c.1184+11121A>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54828243 | ||||||
chr1:54828268
|
C | T | 1 | a0004c0008t0006g0288 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1184+11146C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54828268 | ||||||
chr1:54828297
|
AAATT | A | 29 | a0001c0003t0003g0008a0001c0003t0003g0234a0001c0003t0003g0235others(26): Show | 38 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.1184+11180_1184+11 others(10): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54828297 | |||||
chr1:54828325
|
AT | A | 12 | a0001c0002t0001g0078a0001c0002t0002g0263a0001c0002t0002g0264others(9): Show | 12 | HG00408.hp1 HG00423.hp2 HG00621.hp1 others(9): Show |
intron_variant | MODIFIER | c.1184+11214delT | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54828325 | |||||
chr1:54828365
|
C | T | 11 | a0001c0002t0001g0078a0001c0002t0002g0263a0001c0002t0002g0264others(8): Show | 11 | HG00408.hp1 HG00423.hp2 HG00621.hp1 others(8): Show |
intron_variant | MODIFIER | c.1184+11243C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54828365 | ||||||
chr1:54828477
|
A | G | 1 | a0002c0001t0001g0134 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1184+11355A>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54828477 | ||||||
chr1:54828661
|
A | T | 1 | a0001c0003t0008g0226 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1184+11539A>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54828661 | ||||||
chr1:54828675
|
C | T | 4 | a0001c0002t0002g0238a0001c0003t0003g0239a0001c0003t0003g0240others(1): Show | 4 | HG00621.hp2 HG02083.hp1 HG02135.hp1 others(1): Show |
intron_variant | MODIFIER | c.1184+11553C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54828675 | ||||||
chr1:54828696
|
C | A | 1 | a0002c0001t0001g0135 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1184+11574C>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54828696 | ||||||
chr1:54828714
|
C | T | 1 | a0002c0001t0001g0092 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1184+11592C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54828714 | ||||||
chr1:54828785
|
A | G | 1 | a0001c0003t0003g0228 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1184+11663A>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54828785 | ||||||
chr1:54828831
|
A | G | 1 | a0001c0002t0002g0266 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1184+11709A>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54828831 | ||||||
chr1:54828850
|
T | A | 3 | a0001c0002t0002g0053a0004c0008t0001g0289a0004c0008t0001g0290 | 3 | HG02622.hp1 HG02647.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1184+11728T>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54828850 | ||||||
chr1:54828927
|
T | C | 1 | a0001c0002t0002g0264 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1184+11805T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54828927 | ||||||
chr1:54829049
|
T | C | 141 | a0001c0002t0002g0005a0001c0002t0002g0011a0001c0002t0002g0013others(138): Show | 181 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.1184+11927T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54829049 | ||||||
chr1:54829081
|
G | A | 1 | a0002c0001t0001g0169 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1184+11959G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54829081 | ||||||
chr1:54829275
|
C | T | 29 | a0001c0003t0003g0008a0001c0003t0003g0234a0001c0003t0003g0235others(26): Show | 38 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.1184+12153C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54829275 | ||||||
chr1:54829300
|
A | G | 55 | a0001c0002t0002g0238a0001c0002t0009g0230a0001c0003t0003g0003others(52): Show | 82 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.1184+12178A>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54829300 | ||||||
chr1:54829330
|
A | G | 55 | a0001c0002t0002g0238a0001c0002t0009g0230a0001c0003t0003g0003others(52): Show | 82 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.1184+12208A>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54829330 | ||||||
chr1:54829347
|
A | T | 17 | a0001c0002t0002g0010a0001c0002t0002g0023a0001c0002t0002g0046others(14): Show | 24 | HG00280.hp2 HG00639.hp2 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.1184+12225A>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54829347 | ||||||
chr1:54829585
|
G | A | 11 | a0001c0002t0001g0078a0001c0002t0002g0263a0001c0002t0002g0264others(8): Show | 11 | HG00408.hp1 HG00423.hp2 HG00621.hp1 others(8): Show |
intron_variant | MODIFIER | c.1185-12216G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54829585 | ||||||
chr1:54829589
|
T | C | 1 | a0001c0009t0002g0203 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1185-12212T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54829589 | ||||||
chr1:54829908
|
T | G | 1 | a0002c0001t0001g0086 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1185-11893T>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54829908 | ||||||
chr1:54830137
|
T | C | 17 | a0001c0002t0002g0010a0001c0002t0002g0023a0001c0002t0002g0046others(14): Show | 24 | HG00280.hp2 HG00639.hp2 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.1185-11664T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54830137 | ||||||
chr1:54830177
|
T | C | 10 | a0001c0002t0002g0011a0001c0002t0002g0026a0001c0002t0002g0058others(7): Show | 13 | HG01167.hp2 HG01169.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.1185-11624T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54830177 | ||||||
chr1:54830249
|
T | A | 19 | a0001c0002t0002g0010a0001c0002t0002g0023a0001c0002t0002g0046others(16): Show | 26 | HG00280.hp2 HG00639.hp2 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.1185-11552T>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54830249 | ||||||
chr1:54830258
|
T | C | 55 | a0001c0002t0002g0238a0001c0002t0009g0230a0001c0003t0003g0003others(52): Show | 82 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.1185-11543T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54830258 | ||||||
chr1:54830441
|
C | G | 55 | a0001c0002t0002g0238a0001c0002t0009g0230a0001c0003t0003g0003others(52): Show | 82 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.1185-11360C>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54830441 | ||||||
chr1:54830551
|
G | T | 4 | a0001c0002t0002g0053a0004c0008t0001g0052a0004c0008t0001g0289others(1): Show | 5 | HG01884.hp2 HG02622.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1185-11250G>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54830551 | ||||||
chr1:54830560
|
T | C | 80 | a0001c0002t0001g0078a0001c0002t0002g0009a0001c0002t0002g0010others(77): Show | 101 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.1185-11241T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54830560 | ||||||
chr1:54830591
|
A | G | 135 | a0001c0002t0001g0078a0001c0002t0002g0009a0001c0002t0002g0010others(132): Show | 183 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.1185-11210A>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54830591 | ||||||
chr1:54830663
|
G | A | 19 | a0001c0002t0002g0010a0001c0002t0002g0023a0001c0002t0002g0046others(16): Show | 26 | HG00280.hp2 HG00639.hp2 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.1185-11138G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54830663 | ||||||
chr1:54830752
|
G | A | 1 | a0002c0010t0001g0151 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1185-11049G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54830752 | ||||||
chr1:54830810
|
A | C | 275 | a0001c0002t0001g0078a0001c0002t0002g0005a0001c0002t0002g0009others(272): Show | 363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.1185-10991A>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54830810 | ||||||
chr1:54830837
|
T | C | 3 | a0002c0001t0001g0007a0002c0001t0001g0174a0010c0019t0002g0067 | 6 | HG01884.hp1 HG02145.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1185-10964T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54830837 | ||||||
chr1:54830943
|
T | C | 1 | a0001c0002t0002g0026 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1185-10858T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54830943 | ||||||
chr1:54831042
|
G | A | 1 | a0004c0008t0001g0052 | 2 | HG01884.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1185-10759G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54831042 | ||||||
chr1:54831132
|
A | T | 4 | a0002c0010t0001g0033a0002c0010t0001g0151a0002c0010t0001g0152others(1): Show | 5 | HG02451.hp2 HG02486.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1185-10669A>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54831132 | ||||||
chr1:54831347
|
A | C | 2 | a0001c0002t0002g0252a0001c0002t0002g0258 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1185-10454A>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54831347 | ||||||
chr1:54831363
|
A | T | 1 | a0002c0001t0001g0090 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1185-10438A>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54831363 | ||||||
chr1:54831426
|
G | A | 1 | a0007c0013t0002g0029 | 2 | HG02451.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1185-10375G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54831426 | ||||||
chr1:54831463
|
G | A | 2 | a0001c0002t0001g0078a0005c0007t0002g0063 | 2 | HG01167.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1185-10338G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54831463 | ||||||
chr1:54831482
|
G | A | 4 | a0002c0010t0001g0033a0002c0010t0001g0151a0002c0010t0001g0152others(1): Show | 5 | HG02451.hp2 HG02486.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1185-10319G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54831482 | ||||||
chr1:54831640
|
C | T | 42 | a0001c0002t0001g0078a0001c0002t0002g0079a0001c0002t0002g0263others(39): Show | 51 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(48): Show |
intron_variant | MODIFIER | c.1185-10161C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54831640 | ||||||
chr1:54831684
|
A | G | 2 | a0001c0002t0002g0218a0001c0002t0002g0219 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1185-10117A>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54831684 | ||||||
chr1:54831709
|
C | T | 1 | a0001c0002t0002g0066 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1185-10092C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54831709 | ||||||
chr1:54831939
|
C | T | 2 | a0001c0002t0002g0045a0001c0003t0003g0217 | 3 | HG01109.hp2 HG02717.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1185-9862C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54831939 | ||||||
chr1:54831978
|
C | G | 1 | a0001c0004t0003g0195 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1185-9823C>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54831978 | ||||||
chr1:54832005
|
C | G | 42 | a0001c0002t0001g0078a0001c0002t0002g0079a0001c0002t0002g0263others(39): Show | 51 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(48): Show |
intron_variant | MODIFIER | c.1185-9796C>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54832005 | ||||||
chr1:54832037
|
G | T | 2 | a0001c0002t0001g0078a0005c0007t0002g0063 | 2 | HG01167.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1185-9764G>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54832037 | ||||||
chr1:54832126
|
T | C | 4 | a0002c0010t0001g0033a0002c0010t0001g0151a0002c0010t0001g0152others(1): Show | 5 | HG02451.hp2 HG02486.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1185-9675T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54832126 | ||||||
chr1:54832311
|
A | G | 127 | a0001c0002t0002g0005a0001c0002t0002g0013a0001c0002t0002g0014others(124): Show | 161 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(158): Show |
intron_variant | MODIFIER | c.1185-9490A>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54832311 | ||||||
chr1:54832358
|
TAGTTAAC others(1): Show |
T | 135 | a0001c0002t0001g0078a0001c0002t0002g0009a0001c0002t0002g0010others(132): Show | 183 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.1185-9434_1185-942 others(12): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54832358 | |||||
chr1:54832375
|
C | T | 1 | a0002c0001t0001g0175 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1185-9426C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54832375 | ||||||
chr1:54832618
|
C | T | 1 | a0001c0004t0003g0199 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1185-9183C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54832618 | ||||||
chr1:54832634
|
A | G | 1 | a0002c0001t0001g0089 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1185-9167A>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54832634 | ||||||
chr1:54832720
|
G | T | 17 | a0003c0006t0001g0051a0003c0006t0001g0276a0003c0006t0001g0277others(14): Show | 18 | HG02074.hp2 HG02165.hp1 NA18747.hp2 others(15): Show |
intron_variant | MODIFIER | c.1185-9081G>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54832720 | ||||||
chr1:54832822
|
G | A | 1 | a0001c0003t0003g0234 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1185-8979G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54832822 | ||||||
chr1:54832835
|
C | T | 20 | a0001c0002t0002g0010a0001c0002t0002g0023a0001c0002t0002g0046others(17): Show | 27 | HG00280.hp2 HG00639.hp2 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.1185-8966C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54832835 | ||||||
chr1:54832993
|
C | T | 1 | a0004c0008t0006g0288 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1185-8808C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54832993 | ||||||
chr1:54833016
|
CA | C | 20 | a0001c0002t0002g0010a0001c0002t0002g0023a0001c0002t0002g0046others(17): Show | 27 | HG00280.hp2 HG00639.hp2 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.1185-8774delA | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54833016 | |||||
chr1:54833139
|
A | T | 1 | a0001c0003t0003g0225 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1185-8662A>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54833139 | ||||||
chr1:54833289
|
C | T | 1 | a0001c0002t0002g0269 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1185-8512C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54833289 | ||||||
chr1:54833332
|
A | G | 55 | a0001c0002t0002g0238a0001c0002t0009g0230a0001c0003t0003g0003others(52): Show | 82 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.1185-8469A>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54833332 | ||||||
chr1:54833466
|
C | T | 80 | a0001c0002t0001g0078a0001c0002t0002g0009a0001c0002t0002g0010others(77): Show | 101 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.1185-8335C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54833466 | ||||||
chr1:54833671
|
T | C | 43 | a0001c0002t0001g0078a0001c0002t0002g0079a0001c0002t0002g0263others(40): Show | 52 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(49): Show |
intron_variant | MODIFIER | c.1185-8130T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54833671 | ||||||
chr1:54833730
|
C | T | 1 | a0001c0002t0002g0096 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1185-8071C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54833730 | ||||||
chr1:54833796
|
C | T | 80 | a0001c0002t0001g0078a0001c0002t0002g0009a0001c0002t0002g0010others(77): Show | 101 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.1185-8005C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54833796 | ||||||
chr1:54833820
|
T | C | 140 | a0001c0002t0002g0005a0001c0002t0002g0011a0001c0002t0002g0013others(137): Show | 180 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(177): Show |
intron_variant | MODIFIER | c.1185-7981T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54833820 | ||||||
chr1:54833841
|
CT | C | 55 | a0001c0002t0002g0238a0001c0002t0009g0230a0001c0003t0003g0003others(52): Show | 82 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.1185-7950delT | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54833841 | |||||
chr1:54833851
|
T | A | 1 | a0002c0001t0001g0174 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1185-7950T>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54833851 | ||||||
chr1:54833913
|
T | C | 1 | a0001c0002t0005g0064 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1185-7888T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54833913 | ||||||
chr1:54833983
|
G | A | 23 | a0001c0002t0002g0013a0001c0002t0002g0014a0001c0002t0002g0015others(20): Show | 32 | HG00558.hp1 HG02080.hp1 HG03490.hp2 others(29): Show |
intron_variant | MODIFIER | c.1185-7818G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54833983 | ||||||
chr1:54833987
|
A | G | 1 | a0002c0001t0001g0186 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1185-7814A>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54833987 | ||||||
chr1:54834190
|
A | T | 3 | a0002c0001t0001g0007a0002c0001t0001g0174a0010c0019t0002g0067 | 6 | HG01884.hp1 HG02145.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1185-7611A>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54834190 | ||||||
chr1:54834674
|
C | T | 1 | a0002c0001t0001g0177 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1185-7127C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54834674 | ||||||
chr1:54834828
|
G | A | 135 | a0001c0002t0001g0078a0001c0002t0002g0009a0001c0002t0002g0010others(132): Show | 183 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.1185-6973G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54834828 | ||||||
chr1:54834855
|
G | A | 17 | a0003c0006t0001g0051a0003c0006t0001g0276a0003c0006t0001g0277others(14): Show | 18 | HG02074.hp2 HG02165.hp1 NA18747.hp2 others(15): Show |
intron_variant | MODIFIER | c.1185-6946G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54834855 | ||||||
chr1:54834869
|
G | C | 1 | a0001c0002t0002g0061 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1185-6932G>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54834869 | ||||||
chr1:54834881
|
A | C | 135 | a0001c0002t0001g0078a0001c0002t0002g0009a0001c0002t0002g0010others(132): Show | 183 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.1185-6920A>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54834881 | ||||||
chr1:54834941
|
A | G | 135 | a0001c0002t0001g0078a0001c0002t0002g0009a0001c0002t0002g0010others(132): Show | 183 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.1185-6860A>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54834941 | ||||||
chr1:54835129
|
G | A | 133 | a0001c0002t0001g0078a0001c0002t0002g0009a0001c0002t0002g0010others(130): Show | 181 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(178): Show |
intron_variant | MODIFIER | c.1185-6672G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54835129 | ||||||
chr1:54835182
|
GGTTT | G | 42 | a0001c0002t0001g0078a0001c0002t0002g0079a0001c0002t0002g0263others(39): Show | 51 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(48): Show |
intron_variant | MODIFIER | c.1185-6606_1185-660 others(8): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54835182 | |||||
chr1:54835259
|
T | G | 236 | a0001c0002t0001g0078a0001c0002t0002g0005a0001c0002t0002g0011others(233): Show | 312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.1185-6542T>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54835259 | ||||||
chr1:54835322
|
GCTGGGAC others(4551): Show |
G | 2 | a0004c0008t0001g0289a0004c0008t0001g0290 | 2 | HG02647.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1185-6461_1185-190 others(4): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54835322 | |||||
chr1:54835352
|
T | C | 96 | a0001c0002t0001g0078a0001c0002t0002g0009a0001c0002t0002g0010others(93): Show | 118 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(115): Show |
intron_variant | MODIFIER | c.1185-6449T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54835352 | ||||||
chr1:54835547
|
T | C | 222 | a0001c0002t0001g0078a0001c0002t0002g0005a0001c0002t0002g0009others(219): Show | 278 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(275): Show |
intron_variant | MODIFIER | c.1185-6254T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54835547 | ||||||
chr1:54835636
|
T | C | 99 | a0001c0002t0001g0078a0001c0002t0002g0009a0001c0002t0002g0010others(96): Show | 124 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.1185-6165T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54835636 | ||||||
chr1:54835765
|
C | T | 18 | a0001c0002t0002g0010a0001c0002t0002g0023a0001c0002t0002g0046others(15): Show | 25 | HG00280.hp2 HG00639.hp2 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.1185-6036C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54835765 | ||||||
chr1:54835805
|
A | G | 109 | a0001c0002t0001g0078a0001c0002t0002g0009a0001c0002t0002g0010others(106): Show | 137 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.1185-5996A>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54835805 | ||||||
chr1:54835842
|
A | G | 12 | a0001c0002t0001g0078a0001c0002t0002g0263a0001c0002t0002g0264others(9): Show | 12 | HG00408.hp1 HG00423.hp2 HG00621.hp1 others(9): Show |
intron_variant | MODIFIER | c.1185-5959A>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54835842 | ||||||
chr1:54836011
|
T | G | 204 | a0001c0002t0002g0005a0001c0002t0002g0013a0001c0002t0002g0014others(201): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.1185-5790T>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54836011 | ||||||
chr1:54836067
|
G | T | 2 | a0001c0002t0005g0246a0004c0008t0006g0288 | 2 | HG02257.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1185-5734G>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54836067 | ||||||
chr1:54836262
|
CTCCCGCC others(17): Show |
C | 1 | a0001c0004t0003g0192 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1185-5538_1185-551 others(28): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54836262 | ||||||
chr1:54836263
|
T | G | 186 | a0001c0002t0002g0005a0001c0002t0002g0013a0001c0002t0002g0014others(183): Show | 247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.1185-5538T>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54836263 | ||||||
chr1:54836282
|
CGCCTGCC others(17): Show |
C | 289 | a0001c0002t0001g0078a0001c0002t0002g0005a0001c0002t0002g0009others(286): Show | 378 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(375): Show |
intron_variant | MODIFIER | c.1185-5494_1185-547 others(28): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54836282 | |||||
chr1:54836299
|
G | A | 1 | a0001c0004t0003g0192 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1185-5502G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54836299 | ||||||
chr1:54836306
|
T | C | 1 | a0001c0004t0003g0192 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1185-5495T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54836306 | ||||||
chr1:54836355
|
C | T | 1 | a0002c0001t0001g0168 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1185-5446C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54836355 | ||||||
chr1:54836407
|
T | C | 4 | a0002c0010t0001g0033a0002c0010t0001g0151a0002c0010t0001g0152others(1): Show | 5 | HG02451.hp2 HG02486.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1185-5394T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54836407 | ||||||
chr1:54836596
|
CAGA | C | 30 | a0001c0002t0002g0010a0001c0002t0002g0023a0001c0002t0002g0046others(27): Show | 41 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(38): Show |
intron_variant | MODIFIER | c.1185-5202_1185-520 others(7): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54836596 | |||||
chr1:54836664
|
C | T | 1 | a0002c0001t0001g0147 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1185-5137C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54836664 | ||||||
chr1:54836716
|
G | T | 61 | a0001c0002t0001g0078a0001c0002t0002g0010a0001c0002t0002g0023others(58): Show | 81 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(78): Show |
intron_variant | MODIFIER | c.1185-5085G>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54836716 | ||||||
chr1:54836784
|
G | T | 1 | a0002c0001t0001g0122 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1185-5017G>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54836784 | ||||||
chr1:54836807
|
G | A | 1 | a0002c0010t0001g0164 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1185-4994G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54836807 | ||||||
chr1:54837024
|
A | G | 187 | a0001c0002t0002g0005a0001c0002t0002g0013a0001c0002t0002g0014others(184): Show | 248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.1185-4777A>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54837024 | ||||||
chr1:54837046
|
A | C | 187 | a0001c0002t0002g0005a0001c0002t0002g0013a0001c0002t0002g0014others(184): Show | 248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.1185-4755A>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54837046 | ||||||
chr1:54837054
|
T | A | 1 | a0002c0001t0001g0176 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1185-4747T>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54837054 | ||||||
chr1:54837159
|
C | T | 1 | a0001c0002t0002g0257 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1185-4642C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54837159 | ||||||
chr1:54837206
|
C | A | 1 | a0004c0008t0001g0272 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1185-4595C>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54837206 | ||||||
chr1:54837668
|
G | T | 34 | a0001c0002t0002g0045a0001c0009t0002g0200a0002c0001t0001g0016others(31): Show | 40 | HG00423.hp1 HG00438.hp1 HG00639.hp1 others(37): Show |
intron_variant | MODIFIER | c.1185-4133G>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54837668 | ||||||
chr1:54837766
|
A | G | 187 | a0001c0002t0002g0005a0001c0002t0002g0013a0001c0002t0002g0014others(184): Show | 248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.1185-4035A>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54837766 | ||||||
chr1:54837790
|
A | G | 290 | a0001c0002t0001g0078a0001c0002t0002g0005a0001c0002t0002g0009others(287): Show | 379 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(376): Show |
intron_variant | MODIFIER | c.1185-4011A>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54837790 | ||||||
chr1:54837845
|
C | G | 187 | a0001c0002t0002g0005a0001c0002t0002g0013a0001c0002t0002g0014others(184): Show | 248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.1185-3956C>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54837845 | ||||||
chr1:54837880
|
G | T | 1 | a0001c0002t0002g0079 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1185-3921G>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54837880 | ||||||
chr1:54837908
|
T | TA | 187 | a0001c0002t0002g0005a0001c0002t0002g0013a0001c0002t0002g0014others(184): Show | 248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.1185-3893_1185-389 others(5): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54837908 | ||||||
chr1:54838073
|
G | A | 1 | a0001c0002t0002g0260 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1185-3728G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54838073 | ||||||
chr1:54838079
|
A | T | 57 | a0001c0002t0002g0238a0001c0002t0009g0230a0001c0003t0003g0003others(54): Show | 84 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.1185-3722A>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54838079 | ||||||
chr1:54838109
|
T | G | 187 | a0001c0002t0002g0005a0001c0002t0002g0013a0001c0002t0002g0014others(184): Show | 248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.1185-3692T>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54838109 | ||||||
chr1:54838110
|
A | G | 1 | a0001c0002t0002g0079 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1185-3691A>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54838110 | ||||||
chr1:54838126
|
G | A | 1 | a0001c0002t0002g0100 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1185-3675G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54838126 | ||||||
chr1:54838129
|
A | G | 1 | a0001c0002t0002g0100 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1185-3672A>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54838129 | ||||||
chr1:54838280
|
C | T | 18 | a0001c0002t0002g0010a0001c0002t0002g0023a0001c0002t0002g0046others(15): Show | 25 | HG00280.hp2 HG00639.hp2 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.1185-3521C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54838280 | ||||||
chr1:54838317
|
T | C | 2 | a0001c0002t0005g0246a0004c0008t0006g0288 | 2 | HG02257.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1185-3484T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54838317 | ||||||
chr1:54838345
|
C | T | 1 | a0002c0001t0001g0145 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1185-3456C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54838345 | ||||||
chr1:54838347
|
G | A | 187 | a0001c0002t0002g0005a0001c0002t0002g0013a0001c0002t0002g0014others(184): Show | 248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.1185-3454G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54838347 | ||||||
chr1:54838360
|
G | A | 23 | a0001c0002t0002g0009a0001c0002t0002g0053a0001c0002t0002g0247others(20): Show | 27 | HG02074.hp2 HG02165.hp1 HG02622.hp1 others(24): Show |
intron_variant | MODIFIER | c.1185-3441G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54838360 | ||||||
chr1:54838361
|
T | C | 1 | a0002c0001t0001g0186 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1185-3440T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54838361 | ||||||
chr1:54838375
|
T | C | 286 | a0001c0002t0001g0078a0001c0002t0002g0005a0001c0002t0002g0009others(283): Show | 375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): Show |
intron_variant | MODIFIER | c.1185-3426T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54838375 | ||||||
chr1:54838376
|
G | C | 1 | a0005c0007t0002g0241 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1185-3425G>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54838376 | ||||||
chr1:54838485
|
T | A | 1 | a0001c0002t0002g0100 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1185-3316T>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54838485 | ||||||
chr1:54838485
|
T | TA | 188 | a0001c0002t0002g0005a0001c0002t0002g0013a0001c0002t0002g0014others(185): Show | 249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.1185-3305dupA | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54838485 | |||||
chr1:54838495
|
A | T | 43 | a0001c0002t0001g0078a0001c0002t0002g0077a0001c0002t0002g0079others(40): Show | 56 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(53): Show |
intron_variant | MODIFIER | c.1185-3306A>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54838495 | ||||||
chr1:54838659
|
A | G | 1 | a0001c0002t0002g0053 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1185-3142A>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54838659 | ||||||
chr1:54838682
|
A | T | 1 | a0002c0001t0001g0137 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1185-3119A>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54838682 | ||||||
chr1:54838740
|
T | C | 29 | a0001c0003t0003g0008a0001c0003t0003g0234a0001c0003t0003g0235others(26): Show | 38 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.1185-3061T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54838740 | ||||||
chr1:54838785
|
C | T | 1 | a0001c0002t0002g0079 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1185-3016C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54838785 | ||||||
chr1:54838935
|
T | TG | 187 | a0001c0002t0002g0005a0001c0002t0002g0013a0001c0002t0002g0014others(184): Show | 248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.1185-2860dupG | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54838935 | |||||
chr1:54839010
|
A | G | 187 | a0001c0002t0002g0005a0001c0002t0002g0013a0001c0002t0002g0014others(184): Show | 248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.1185-2791A>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54839010 | ||||||
chr1:54839050
|
C | T | 14 | a0001c0002t0001g0078a0001c0002t0002g0077a0001c0002t0002g0079others(11): Show | 18 | HG00408.hp1 HG00423.hp2 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.1185-2751C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54839050 | ||||||
chr1:54839051
|
G | A | 4 | a0002c0010t0001g0033a0002c0010t0001g0151a0002c0010t0001g0152others(1): Show | 5 | HG02451.hp2 HG02486.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1185-2750G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54839051 | ||||||
chr1:54839130
|
GA | G | 187 | a0001c0002t0002g0005a0001c0002t0002g0013a0001c0002t0002g0014others(184): Show | 248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.1185-2663delA | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54839130 | |||||
chr1:54839163
|
C | T | 10 | a0001c0002t0002g0011a0001c0002t0002g0026a0001c0002t0002g0058others(7): Show | 13 | HG01167.hp2 HG01169.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.1185-2638C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54839163 | ||||||
chr1:54839297
|
G | A | 130 | a0001c0002t0002g0005a0001c0002t0002g0013a0001c0002t0002g0014others(127): Show | 164 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.1185-2504G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54839297 | ||||||
chr1:54839362
|
A | T | 186 | a0001c0002t0002g0005a0001c0002t0002g0013a0001c0002t0002g0014others(183): Show | 247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.1185-2439A>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54839362 | ||||||
chr1:54839386
|
A | T | 187 | a0001c0002t0002g0005a0001c0002t0002g0013a0001c0002t0002g0014others(184): Show | 248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.1185-2415A>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54839386 | ||||||
chr1:54839397
|
C | CAG | 290 | a0001c0002t0001g0078a0001c0002t0002g0005a0001c0002t0002g0009others(287): Show | 379 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(376): Show |
intron_variant | MODIFIER | c.1185-2403_1185-240 others(6): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54839397 | |||||
chr1:54839412
|
C | G | 187 | a0001c0002t0002g0005a0001c0002t0002g0013a0001c0002t0002g0014others(184): Show | 248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.1185-2389C>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54839412 | ||||||
chr1:54839495
|
A | C | 1 | a0002c0001t0001g0135 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1185-2306A>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54839495 | ||||||
chr1:54839522
|
C | T | 2 | a0001c0003t0003g0217a0002c0005t0004g0084 | 2 | HG01109.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.1185-2279C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54839522 | ||||||
chr1:54839534
|
C | T | 1 | a0001c0003t0003g0224 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1185-2267C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54839534 | ||||||
chr1:54839540
|
A | G | 187 | a0001c0002t0002g0005a0001c0002t0002g0013a0001c0002t0002g0014others(184): Show | 248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.1185-2261A>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54839540 | ||||||
chr1:54839557
|
T | C | 18 | a0001c0002t0002g0010a0001c0002t0002g0023a0001c0002t0002g0046others(15): Show | 25 | HG00280.hp2 HG00639.hp2 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.1185-2244T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54839557 | ||||||
chr1:54839585
|
C | T | 8 | a0001c0004t0003g0041a0001c0004t0003g0055a0001c0004t0003g0188others(5): Show | 9 | HG00438.hp2 HG00609.hp2 NA18952.hp1 others(6): Show |
intron_variant | MODIFIER | c.1185-2216C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54839585 | ||||||
chr1:54839850
|
G | A | 130 | a0001c0002t0002g0005a0001c0002t0002g0013a0001c0002t0002g0014others(127): Show | 164 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.1185-1951G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54839850 | ||||||
chr1:54839858
|
C | T | 5 | a0001c0003t0003g0217a0002c0005t0004g0012a0002c0005t0004g0070others(2): Show | 7 | HG01109.hp2 HG01243.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1185-1943C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54839858 | ||||||
chr1:54839893
|
G | A | 130 | a0001c0002t0002g0005a0001c0002t0002g0013a0001c0002t0002g0014others(127): Show | 164 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.1185-1908G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54839893 | ||||||
chr1:54839940
|
T | C | 1 | a0012c0016t0001g0197 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1185-1861T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54839940 | ||||||
chr1:54840058
|
T | G | 187 | a0001c0002t0002g0005a0001c0002t0002g0013a0001c0002t0002g0014others(184): Show | 248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.1185-1743T>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54840058 | ||||||
chr1:54840094
|
A | C | 187 | a0001c0002t0002g0005a0001c0002t0002g0013a0001c0002t0002g0014others(184): Show | 248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.1185-1707A>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54840094 | ||||||
chr1:54840141
|
TAGTC | T | 24 | a0001c0009t0002g0200a0002c0001t0001g0016a0002c0001t0001g0042others(21): Show | 27 | HG00423.hp1 HG00438.hp1 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.1185-1655_1185-165 others(8): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54840141 | |||||
chr1:54840182
|
C | T | 1 | a0002c0011t0004g0037 | 2 | HG02040.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.1185-1619C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54840182 | ||||||
chr1:54840208
|
G | C | 57 | a0001c0002t0002g0238a0001c0002t0009g0230a0001c0003t0003g0003others(54): Show | 84 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.1185-1593G>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54840208 | ||||||
chr1:54840394
|
C | T | 1 | a0001c0002t0002g0271 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1185-1407C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54840394 | ||||||
chr1:54840718
|
T | A | 12 | a0001c0002t0001g0078a0001c0002t0002g0053a0001c0002t0002g0077others(9): Show | 16 | HG01167.hp1 HG01884.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.1185-1083T>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54840718 | ||||||
chr1:54840728
|
A | G | 1 | a0001c0002t0002g0256 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1185-1073A>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54840728 | ||||||
chr1:54840756
|
A | C | 188 | a0001c0002t0002g0005a0001c0002t0002g0013a0001c0002t0002g0014others(185): Show | 249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.1185-1045A>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54840756 | ||||||
chr1:54840759
|
C | G | 1 | a0001c0002t0002g0265 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1185-1042C>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54840759 | ||||||
chr1:54840828
|
T | A | 1 | a0002c0001t0001g0166 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1185-973T>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54840828 | ||||||
chr1:54840945
|
G | A | 225 | a0001c0002t0001g0078a0001c0002t0002g0005a0001c0002t0002g0013others(222): Show | 297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.1185-856G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54840945 | ||||||
chr1:54840963
|
C | G | 1 | a0001c0002t0002g0100 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1185-838C>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54840963 | ||||||
chr1:54840964
|
G | C | 1 | a0001c0002t0002g0100 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1185-837G>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54840964 | ||||||
chr1:54840970
|
AGAGACAG others(4): Show |
A | 1 | a0003c0006t0001g0286 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1185-829_1185-819d others(13): Show |
LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54840970 | |||||
chr1:54840982
|
G | T | 1 | a0003c0006t0001g0286 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1185-819G>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54840982 | ||||||
chr1:54840985
|
G | C | 1 | a0003c0006t0001g0286 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1185-816G>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54840985 | ||||||
chr1:54840986
|
C | T | 1 | a0003c0006t0001g0286 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1185-815C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54840986 | ||||||
chr1:54840992
|
T | C | 1 | a0003c0006t0001g0286 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1185-809T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54840992 | ||||||
chr1:54840994
|
G | A | 1 | a0003c0006t0001g0286 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1185-807G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54840994 | ||||||
chr1:54840995
|
T | C | 1 | a0003c0006t0001g0286 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1185-806T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54840995 | ||||||
chr1:54840997
|
G | A | 1 | a0003c0006t0001g0286 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1185-804G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54840997 | ||||||
chr1:54840998
|
A | C | 1 | a0003c0006t0001g0286 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1185-803A>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54840998 | ||||||
chr1:54841001
|
T | C | 1 | a0003c0006t0001g0286 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1185-800T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54841001 | ||||||
chr1:54841008
|
T | A | 1 | a0003c0006t0001g0286 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1185-793T>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54841008 | ||||||
chr1:54841012
|
G | A | 1 | a0003c0006t0001g0286 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1185-789G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54841012 | ||||||
chr1:54841013
|
C | G | 1 | a0003c0006t0001g0286 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1185-788C>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54841013 | ||||||
chr1:54841015
|
T | G | 1 | a0003c0006t0001g0286 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1185-786T>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54841015 | ||||||
chr1:54841016
|
G | A | 1 | a0003c0006t0001g0286 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1185-785G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54841016 | ||||||
chr1:54841017
|
G | T | 1 | a0003c0006t0001g0286 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1185-784G>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54841017 | ||||||
chr1:54841018
|
G | C | 1 | a0003c0006t0001g0286 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1185-783G>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54841018 | ||||||
chr1:54841019
|
G | T | 1 | a0003c0006t0001g0286 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1185-782G>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54841019 | ||||||
chr1:54841022
|
G | C | 1 | a0003c0006t0001g0286 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1185-779G>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54841022 | ||||||
chr1:54841030
|
G | A | 1 | a0003c0006t0001g0286 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1185-771G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54841030 | ||||||
chr1:54841032
|
C | G | 1 | a0003c0006t0001g0286 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1185-769C>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54841032 | ||||||
chr1:54841033
|
C | A | 1 | a0003c0006t0001g0286 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1185-768C>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54841033 | ||||||
chr1:54841035
|
T | G | 1 | a0003c0006t0001g0286 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1185-766T>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54841035 | ||||||
chr1:54841036
|
G | A | 1 | a0003c0006t0001g0286 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1185-765G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54841036 | ||||||
chr1:54841038
|
G | A | 1 | a0003c0006t0001g0286 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1185-763G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54841038 | ||||||
chr1:54841039
|
C | G | 1 | a0003c0006t0001g0286 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1185-762C>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54841039 | ||||||
chr1:54841041
|
T | G | 1 | a0003c0006t0001g0286 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1185-760T>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54841041 | ||||||
chr1:54841043
|
G | A | 1 | a0003c0006t0001g0286 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1185-758G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54841043 | ||||||
chr1:54841060
|
A | G | 64 | a0001c0002t0002g0085a0001c0002t0002g0098a0001c0002t0002g0238others(61): Show | 91 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.1185-741A>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54841060 | ||||||
chr1:54841066
|
T | C | 91 | a0001c0002t0002g0085a0001c0002t0002g0098a0001c0002t0002g0238others(88): Show | 127 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.1185-735T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54841066 | ||||||
chr1:54841085
|
G | A | 23 | a0001c0002t0002g0010a0001c0002t0002g0023a0001c0002t0002g0046others(20): Show | 30 | HG00280.hp2 HG00741.hp1 HG01069.hp1 others(27): Show |
intron_variant | MODIFIER | c.1185-716G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54841085 | ||||||
chr1:54841261
|
C | T | 3 | a0001c0002t0002g0065a0001c0002t0002g0066a0004c0008t0001g0272 | 3 | HG01891.hp2 NA19078.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1185-540C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54841261 | ||||||
chr1:54841344
|
G | A | 1 | a0001c0003t0003g0235 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1185-457G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54841344 | ||||||
chr1:54841345
|
A | G | 1 | a0001c0003t0003g0235 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1185-456A>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54841345 | ||||||
chr1:54841352
|
G | A | 1 | a0001c0003t0003g0239 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1185-449G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54841352 | ||||||
chr1:54841368
|
C | T | 1 | a0001c0004t0003g0194 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1185-433C>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54841368 | ||||||
chr1:54841382
|
T | G | 2 | a0001c0002t0002g0071a0001c0002t0002g0250 | 2 | HG02109.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1185-419T>G | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54841382 | ||||||
chr1:54841386
|
A | C | 7 | a0001c0002t0005g0064a0001c0002t0005g0246a0002c0010t0001g0033others(4): Show | 8 | HG02257.hp1 HG02451.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1185-415A>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54841386 | ||||||
chr1:54841387
|
G | A | 4 | a0002c0010t0001g0033a0002c0010t0001g0151a0002c0010t0001g0152others(1): Show | 5 | HG02451.hp2 HG02486.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1185-414G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54841387 | ||||||
chr1:54841409
|
G | A | 3 | a0001c0002t0002g0053a0004c0008t0001g0289a0004c0008t0001g0290 | 3 | HG02622.hp1 HG02647.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1185-392G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54841409 | ||||||
chr1:54841480
|
G | A | 1 | a0001c0002t0005g0064 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1185-321G>A | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54841480 | ||||||
chr1:54841659
|
G | T | 17 | a0001c0002t0002g0238a0003c0006t0001g0051a0003c0006t0001g0276others(14): Show | 18 | HG02074.hp2 HG02165.hp1 NA18747.hp2 others(15): Show |
intron_variant | MODIFIER | c.1185-142G>T | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54841659 | ||||||
chr1:54841784
|
T | C | 1 | a0002c0001t0001g0153 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1185-17T>C | LEXM | ENSG00000162398.12 | transcript | ENST00000371273.4 | protein_coding | 9/9 | chr1 | 54841784 |