geneid | 4010 |
---|---|
ensemblid | ENSG00000136944.19 |
hgncid | 6654 |
symbol | LMX1B |
name | LIM homeobox transcription factor 1 beta |
refseq_nuc | NM_001174147.2 |
refseq_prot | NP_001167618.1 |
ensembl_nuc | ENST00000373474.9 |
ensembl_prot | ENSP00000362573.3 |
mane_status | MANE Select |
chr | chr9 |
start | 126613928 |
end | 126701032 |
strand | + |
ver | v1.2 |
region | chr9:126613928-126701032 |
region5000 | chr9:126608928-126706032 |
regionname0 | LMX1B_chr9_126613928_126701032 |
regionname5000 | LMX1B_chr9_126608928_126706032 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 402 | 342 | 84 | 62 | 146 | 10 | 38 | 108 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1209 | 166 | 33 | 30 | 72 | 7 | 22 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
c0002 | 0/0 | 1209 | 132 | 12 | 27 | 74 | 3 | 16 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
c0003 | 0/0 | 1209 | 15 | 13 | 2 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
c0004 | 0/0 | 1209 | 12 | 9 | 3 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
c0005 | 0/0 | 1209 | 6 | 6 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
c0006 | 0/0 | 1209 | 3 | 3 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
c0007 | 0/0 | 1209 | 2 | 2 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
c0008 | 0/0 | 1209 | 2 | 2 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
c0009 | 0/0 | 1209 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
c0010 | 0/0 | 1209 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
c0011 | 0/0 | 1209 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
c0012 | 0/0 | 1209 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 5104 | 24 | 0 | 2 | 22 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0002 | 0/0 | 5097 | 17 | 4 | 5 | 2 | 2 | 4 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0003 | 0/0 | 5099 | 12 | 0 | 1 | 10 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0004 | 0/0 | 5109 | 10 | 0 | 1 | 9 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0005 | 0/0 | 5083 | 6 | 0 | 3 | 3 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0006 | 0/0 | 5089 | 6 | 0 | 2 | 0 | 2 | 2 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0007 | 0/0 | 5097 | 5 | 0 | 0 | 5 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0008 | 0/0 | 5102 | 5 | 0 | 0 | 3 | 0 | 2 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0009 | 0/0 | 5101 | 4 | 0 | 1 | 2 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0010 | 0/0 | 5098 | 4 | 0 | 0 | 4 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0011 | 0/0 | 5104 | 4 | 0 | 1 | 3 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0012 | 0/0 | 5107 | 4 | 4 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0013 | 0/0 | 5099 | 4 | 0 | 2 | 0 | 0 | 2 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0014 | 0/0 | 5106 | 3 | 0 | 0 | 3 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0015 | 0/0 | 5104 | 3 | 0 | 0 | 3 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0016 | 0/0 | 5104 | 3 | 0 | 0 | 3 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0017 | 0/0 | 5097 | 3 | 0 | 0 | 2 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0018 | 0/0 | 5102 | 3 | 0 | 2 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0019 | 0/0 | 5109 | 3 | 0 | 0 | 3 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0020 | 0/0 | 5114 | 3 | 0 | 0 | 3 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0021 | 0/0 | 5104 | 3 | 0 | 1 | 2 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0022 | 0/0 | 5100 | 3 | 0 | 0 | 3 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0023 | 0/0 | 5104 | 3 | 3 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0024 | 0/0 | 5102 | 3 | 0 | 2 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0025 | 0/0 | 5100 | 2 | 0 | 1 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0026 | 0/0 | 5107 | 2 | 0 | 0 | 2 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0027 | 0/0 | 5105 | 2 | 0 | 2 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0028 | 0/0 | 5099 | 2 | 0 | 0 | 0 | 1 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0029 | 0/0 | 5101 | 2 | 0 | 0 | 2 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0030 | 0/0 | 5099 | 2 | 0 | 2 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0031 | 0/0 | 5101 | 2 | 0 | 2 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0032 | 0/0 | 5105 | 2 | 0 | 0 | 2 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0033 | 0/0 | 5095 | 2 | 2 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0034 | 0/0 | 5097 | 2 | 0 | 0 | 2 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0035 | 0/0 | 5092 | 2 | 0 | 0 | 0 | 0 | 2 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0036 | 0/0 | 5097 | 2 | 1 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0037 | 0/0 | 5104 | 2 | 0 | 0 | 2 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0038 | 0/0 | 5102 | 2 | 0 | 1 | 0 | 1 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0039 | 0/0 | 5109 | 2 | 0 | 0 | 2 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0040 | 0/0 | 5107 | 2 | 2 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0041 | 0/0 | 5088 | 2 | 0 | 0 | 2 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0042 | 0/0 | 5114 | 2 | 2 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0043 | 0/0 | 5099 | 2 | 0 | 0 | 2 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0044 | 0/0 | 5094 | 2 | 0 | 2 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0045 | 0/0 | 5102 | 2 | 0 | 2 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0046 | 0/0 | 5104 | 2 | 0 | 0 | 2 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0047 | 0/0 | 5109 | 2 | 0 | 0 | 2 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0048 | 0/0 | 5092 | 2 | 2 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0049 | 0/0 | 5104 | 2 | 0 | 2 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0050 | 0/0 | 5104 | 2 | 2 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0051 | 0/1 | 5099 | 2 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0052 | 0/0 | 5097 | 2 | 1 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0053 | 0/0 | 5099 | 2 | 1 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0054 | 0/0 | 5102 | 2 | 1 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0055 | 0/0 | 5092 | 2 | 2 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0056 | 0/0 | 5091 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0057 | 0/0 | 5094 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0058 | 0/0 | 5092 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0059 | 0/0 | 5107 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0060 | 0/0 | 5100 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0061 | 0/0 | 5107 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0062 | 0/0 | 5105 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0063 | 0/0 | 5107 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0064 | 0/0 | 5112 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0065 | 0/0 | 5117 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0066 | 0/0 | 5105 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0067 | 0/0 | 5105 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0068 | 0/0 | 5105 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0069 | 0/0 | 5117 | 1 | 0 | 0 | 0 | 1 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0070 | 0/0 | 5097 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0071 | 0/0 | 5100 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0072 | 0/0 | 5112 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0073 | 0/0 | 5107 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0074 | 0/0 | 5107 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0075 | 0/0 | 5107 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0076 | 0/0 | 5123 | 1 | 0 | 0 | 0 | 1 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0077 | 0/0 | 5091 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0078 | 0/0 | 5101 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0079 | 0/0 | 5101 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0080 | 0/0 | 5099 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0081 | 0/0 | 5099 | 1 | 0 | 0 | 0 | 1 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0082 | 0/0 | 5099 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0083 | 0/0 | 5099 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0084 | 0/0 | 5101 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0085 | 0/0 | 5106 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0086 | 0/0 | 5104 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0087 | 0/0 | 5104 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0088 | 0/0 | 5091 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0089 | 0/0 | 5096 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0090 | 0/0 | 5099 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0091 | 0/0 | 5101 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0092 | 0/0 | 5101 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0093 | 0/0 | 5101 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0094 | 0/0 | 5106 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0095 | 0/0 | 5106 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0096 | 0/0 | 5098 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0097 | 0/0 | 5100 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0098 | 0/0 | 5105 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0099 | 0/0 | 5084 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0100 | 0/0 | 5108 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0101 | 0/0 | 5105 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0102 | 0/0 | 5100 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0103 | 0/0 | 5100 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0104 | 0/0 | 5105 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0105 | 0/0 | 5103 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0106 | 0/0 | 5093 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0107 | 0/0 | 5109 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0108 | 0/0 | 5104 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0109 | 0/0 | 5089 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0110 | 0/0 | 5089 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0111 | 0/0 | 5089 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0112 | 0/0 | 5094 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0113 | 0/0 | 5097 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0114 | 0/0 | 5104 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0115 | 0/0 | 5102 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0116 | 0/0 | 5104 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0117 | 0/0 | 5092 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0118 | 0/0 | 5097 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0119 | 0/0 | 5094 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0120 | 0/0 | 5099 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0121 | 0/0 | 5099 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0122 | 0/0 | 5099 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0123 | 0/0 | 5099 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0124 | 0/0 | 5099 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0125 | 0/0 | 5099 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0126 | 0/0 | 5097 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0127 | 0/0 | 5097 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0128 | 0/0 | 5097 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0129 | 0/0 | 5099 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0130 | 0/0 | 5102 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0131 | 0/0 | 5102 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0132 | 0/0 | 5104 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0133 | 0/0 | 5104 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0134 | 0/0 | 5102 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0135 | 0/0 | 5104 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0136 | 0/0 | 5102 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0137 | 0/0 | 5104 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0138 | 0/0 | 5083 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0139 | 0/0 | 5083 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0140 | 0/0 | 5083 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0141 | 0/0 | 5109 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0142 | 0/0 | 5107 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0143 | 0/0 | 5112 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0144 | 0/0 | 5112 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0145 | 0/0 | 5114 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0146 | 0/0 | 5119 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0147 | 0/0 | 5104 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0148 | 0/0 | 5102 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0149 | 0/0 | 5117 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0150 | 0/0 | 5102 | 1 | 0 | 0 | 0 | 1 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0151 | 0/0 | 5112 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0152 | 0/0 | 5099 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0153 | 0/0 | 5104 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0154 | 0/0 | 5102 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0155 | 0/0 | 5104 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0156 | 0/0 | 5104 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0157 | 0/0 | 5104 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0158 | 0/0 | 5104 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0159 | 0/0 | 5104 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0160 | 0/0 | 5104 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0161 | 0/0 | 5104 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0162 | 0/0 | 5104 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0163 | 0/0 | 5092 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0164 | 0/0 | 5092 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0165 | 0/0 | 5104 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0166 | 0/0 | 5089 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0167 | 0/0 | 5102 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0168 | 0/0 | 5104 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0169 | 0/0 | 5104 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0170 | 0/0 | 5107 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0171 | 0/0 | 5104 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0172 | 0/0 | 5092 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0173 | 0/0 | 5099 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0174 | 0/0 | 5097 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0175 | 0/0 | 5099 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0176 | 0/0 | 5099 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0177 | 0/0 | 5104 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0178 | 0/0 | 5102 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0179 | 1/0 | 5104 | 1 | 0 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0180 | 0/0 | 5104 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0181 | 0/0 | 5104 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0182 | 0/0 | 5107 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0183 | 0/0 | 5109 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0184 | 0/0 | 5107 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0185 | 0/0 | 5109 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0186 | 0/0 | 5112 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0187 | 0/0 | 5114 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0188 | 0/0 | 5099 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0189 | 0/0 | 5097 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0190 | 0/0 | 5099 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0191 | 0/0 | 5099 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0192 | 0/0 | 5102 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0193 | 0/0 | 5102 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0194 | 0/0 | 5107 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0195 | 0/0 | 5092 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0196 | 0/0 | 5085 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
t0197 | 0/0 | 5092 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0003 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0005 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0075 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0168 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0280 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0281 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1209 | 166 | 33 | 30 | 72 | 7 | 22 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0002 | 0/0 | 1209 | 132 | 12 | 27 | 74 | 3 | 16 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0003 | 0/0 | 1209 | 15 | 13 | 2 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0004 | 0/0 | 1209 | 12 | 9 | 3 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0005 | 0/0 | 1209 | 6 | 6 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0006 | 0/0 | 1209 | 3 | 3 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0007 | 0/0 | 1209 | 2 | 2 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0008 | 0/0 | 1209 | 2 | 2 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0009 | 0/0 | 1209 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0010 | 0/0 | 1209 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0011 | 0/0 | 1209 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0012 | 0/0 | 1209 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002 | 0/0 | 6305 | 16 | 4 | 4 | 2 | 2 | 4 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0001t0003 | 0/0 | 6307 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0001t0004 | 0/0 | 6317 | 10 | 0 | 1 | 9 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0001t0005 | 0/0 | 6291 | 6 | 0 | 3 | 3 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0001t0007 | 0/0 | 6305 | 5 | 0 | 0 | 5 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0001t0008 | 0/0 | 6310 | 5 | 0 | 0 | 3 | 0 | 2 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0001t0010 | 0/0 | 6306 | 4 | 0 | 0 | 4 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0001t0011 | 0/0 | 6312 | 4 | 0 | 1 | 3 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0001t0017 | 0/0 | 6305 | 3 | 0 | 0 | 2 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0001t0018 | 0/0 | 6310 | 3 | 0 | 2 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0001t0019 | 0/0 | 6317 | 3 | 0 | 0 | 3 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0001t0020 | 0/0 | 6322 | 3 | 0 | 0 | 3 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0001t0025 | 0/0 | 6308 | 2 | 0 | 1 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0001t0026 | 0/0 | 6315 | 2 | 0 | 0 | 2 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0001t0027 | 0/0 | 6313 | 2 | 0 | 2 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0001t0028 | 0/0 | 6307 | 2 | 0 | 0 | 0 | 1 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0001t0029 | 0/0 | 6309 | 2 | 0 | 0 | 2 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0001t0034 | 0/0 | 6305 | 2 | 0 | 0 | 2 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0001t0035 | 0/0 | 6300 | 2 | 0 | 0 | 0 | 0 | 2 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0001t0036 | 0/0 | 6305 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0001t0037 | 0/0 | 6312 | 2 | 0 | 0 | 2 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0001t0038 | 0/0 | 6310 | 2 | 0 | 1 | 0 | 1 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0001t0039 | 0/0 | 6317 | 2 | 0 | 0 | 2 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0001t0040 | 0/0 | 6315 | 2 | 2 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0001t0041 | 0/0 | 6296 | 2 | 0 | 0 | 2 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0001t0051 | 0/1 | 6307 | 2 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0001t0052 | 0/0 | 6305 | 2 | 1 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0001t0053 | 0/0 | 6307 | 2 | 1 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0001t0054 | 0/0 | 6310 | 2 | 1 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0001t0059 | 0/0 | 6315 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0001t0060 | 0/0 | 6308 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0001t0061 | 0/0 | 6315 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0001t0062 | 0/0 | 6313 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0001t0065 | 0/0 | 6325 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0001t0066 | 0/0 | 6313 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0001t0067 | 0/0 | 6313 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0001t0068 | 0/0 | 6313 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0001t0069 | 0/0 | 6325 | 1 | 0 | 0 | 0 | 1 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0001t0079 | 0/0 | 6309 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0001t0080 | 0/0 | 6307 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0001t0081 | 0/0 | 6307 | 1 | 0 | 0 | 0 | 1 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0001t0082 | 0/0 | 6307 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0001t0083 | 0/0 | 6307 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0001t0084 | 0/0 | 6309 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0001t0085 | 0/0 | 6314 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0001t0087 | 0/0 | 6312 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0001t0096 | 0/0 | 6306 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0001t0097 | 0/0 | 6308 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0001t0098 | 0/0 | 6313 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0001t0099 | 0/0 | 6292 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0001t0100 | 0/0 | 6316 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0001t0102 | 0/0 | 6308 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0001t0107 | 0/0 | 6317 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0001t0118 | 0/0 | 6305 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0001t0119 | 0/0 | 6302 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0001t0120 | 0/0 | 6307 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0001t0121 | 0/0 | 6307 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0001t0122 | 0/0 | 6307 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0001t0123 | 0/0 | 6307 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0001t0124 | 0/0 | 6307 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0001t0125 | 0/0 | 6307 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0001t0126 | 0/0 | 6305 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0001t0127 | 0/0 | 6305 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0001t0128 | 0/0 | 6305 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0001t0129 | 0/0 | 6307 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0001t0130 | 0/0 | 6310 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0001t0131 | 0/0 | 6310 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0001t0132 | 0/0 | 6312 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0001t0133 | 0/0 | 6312 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0001t0134 | 0/0 | 6310 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0001t0135 | 0/0 | 6312 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0001t0136 | 0/0 | 6310 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0001t0137 | 0/0 | 6312 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0001t0138 | 0/0 | 6291 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0001t0139 | 0/0 | 6291 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0001t0140 | 0/0 | 6291 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0001t0141 | 0/0 | 6317 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0001t0142 | 0/0 | 6315 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0001t0143 | 0/0 | 6320 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0001t0144 | 0/0 | 6320 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0001t0145 | 0/0 | 6322 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0001t0147 | 0/0 | 6312 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0001t0148 | 0/0 | 6310 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0001t0149 | 0/0 | 6325 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0001t0150 | 0/0 | 6310 | 1 | 0 | 0 | 0 | 1 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0001t0166 | 0/0 | 6297 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0001t0171 | 0/0 | 6312 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0001t0172 | 0/0 | 6300 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0001t0173 | 0/0 | 6307 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0001t0174 | 0/0 | 6305 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0001t0175 | 0/0 | 6307 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0001t0176 | 0/0 | 6307 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0001t0177 | 0/0 | 6312 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0001t0178 | 0/0 | 6310 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0001t0179 | 1/0 | 6312 | 1 | 0 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0001t0180 | 0/0 | 6312 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0001t0181 | 0/0 | 6312 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0001t0183 | 0/0 | 6317 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0001t0197 | 0/0 | 6300 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0002t0001 | 0/0 | 6312 | 24 | 0 | 2 | 22 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0002t0002 | 0/0 | 6305 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0002t0003 | 0/0 | 6307 | 11 | 0 | 1 | 10 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0002t0006 | 0/0 | 6297 | 6 | 0 | 2 | 0 | 2 | 2 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0002t0009 | 0/0 | 6309 | 4 | 0 | 1 | 2 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0002t0013 | 0/0 | 6307 | 4 | 0 | 2 | 0 | 0 | 2 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0002t0014 | 0/0 | 6314 | 3 | 0 | 0 | 3 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0002t0015 | 0/0 | 6312 | 3 | 0 | 0 | 3 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0002t0016 | 0/0 | 6312 | 3 | 0 | 0 | 3 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0002t0021 | 0/0 | 6312 | 3 | 0 | 1 | 2 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0002t0022 | 0/0 | 6308 | 3 | 0 | 0 | 3 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0002t0024 | 0/0 | 6310 | 3 | 0 | 2 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0002t0030 | 0/0 | 6307 | 2 | 0 | 2 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0002t0031 | 0/0 | 6309 | 2 | 0 | 2 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0002t0032 | 0/0 | 6313 | 2 | 0 | 0 | 2 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0002t0043 | 0/0 | 6307 | 2 | 0 | 0 | 2 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0002t0044 | 0/0 | 6302 | 2 | 0 | 2 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0002t0045 | 0/0 | 6310 | 2 | 0 | 2 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0002t0046 | 0/0 | 6312 | 2 | 0 | 0 | 2 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0002t0047 | 0/0 | 6317 | 2 | 0 | 0 | 2 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0002t0055 | 0/0 | 6300 | 2 | 2 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0002t0056 | 0/0 | 6299 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0002t0057 | 0/0 | 6302 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0002t0070 | 0/0 | 6305 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0002t0071 | 0/0 | 6308 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0002t0072 | 0/0 | 6320 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0002t0073 | 0/0 | 6315 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0002t0074 | 0/0 | 6315 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0002t0075 | 0/0 | 6315 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0002t0076 | 0/0 | 6331 | 1 | 0 | 0 | 0 | 1 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0002t0078 | 0/0 | 6309 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0002t0088 | 0/0 | 6299 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0002t0089 | 0/0 | 6304 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0002t0090 | 0/0 | 6307 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0002t0091 | 0/0 | 6309 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0002t0092 | 0/0 | 6309 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0002t0093 | 0/0 | 6309 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0002t0094 | 0/0 | 6314 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0002t0095 | 0/0 | 6314 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0002t0101 | 0/0 | 6313 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0002t0104 | 0/0 | 6313 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0002t0105 | 0/0 | 6311 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0002t0106 | 0/0 | 6301 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0002t0108 | 0/0 | 6312 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0002t0152 | 0/0 | 6307 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0002t0153 | 0/0 | 6312 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0002t0154 | 0/0 | 6310 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0002t0155 | 0/0 | 6312 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0002t0156 | 0/0 | 6312 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0002t0157 | 0/0 | 6312 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0002t0158 | 0/0 | 6312 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0002t0159 | 0/0 | 6312 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0002t0160 | 0/0 | 6312 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0002t0161 | 0/0 | 6312 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0002t0162 | 0/0 | 6312 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0002t0163 | 0/0 | 6300 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0002t0164 | 0/0 | 6300 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0002t0165 | 0/0 | 6312 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0002t0168 | 0/0 | 6312 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0002t0188 | 0/0 | 6307 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0002t0189 | 0/0 | 6305 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0002t0190 | 0/0 | 6307 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0002t0191 | 0/0 | 6307 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0002t0192 | 0/0 | 6310 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0002t0193 | 0/0 | 6310 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0002t0194 | 0/0 | 6315 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0002t0195 | 0/0 | 6300 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0003t0023 | 0/0 | 6312 | 3 | 3 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0003t0049 | 0/0 | 6312 | 2 | 0 | 2 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0003t0058 | 0/0 | 6300 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0003t0077 | 0/0 | 6299 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0003t0109 | 0/0 | 6297 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0003t0110 | 0/0 | 6297 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0003t0111 | 0/0 | 6297 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0003t0112 | 0/0 | 6302 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0003t0113 | 0/0 | 6305 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0003t0114 | 0/0 | 6312 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0003t0115 | 0/0 | 6310 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0003t0167 | 0/0 | 6310 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0004t0036 | 0/0 | 6305 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0004t0042 | 0/0 | 6322 | 2 | 2 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0004t0063 | 0/0 | 6315 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0004t0064 | 0/0 | 6320 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0004t0146 | 0/0 | 6327 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0004t0151 | 0/0 | 6320 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0004t0182 | 0/0 | 6315 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0004t0184 | 0/0 | 6315 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0004t0185 | 0/0 | 6317 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0004t0186 | 0/0 | 6320 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0004t0187 | 0/0 | 6322 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0005t0012 | 0/0 | 6315 | 4 | 4 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0005t0169 | 0/0 | 6312 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0005t0170 | 0/0 | 6315 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0006t0050 | 0/0 | 6312 | 2 | 2 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0006t0116 | 0/0 | 6312 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0007t0048 | 0/0 | 6300 | 2 | 2 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0008t0033 | 0/0 | 6303 | 2 | 2 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0009t0103 | 0/0 | 6308 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0010t0196 | 0/0 | 6293 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0011t0086 | 0/0 | 6312 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
a0001c0012t0117 | 0/0 | 6300 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | copy fasta | chr9 | 126608928 | 126706032 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0002g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0002g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0002g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0002g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0002g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0002g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0002g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0002g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0002g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0002g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0003g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0004g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0004g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0004g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0004g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0004g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0004g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0004g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0004g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0004g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0004g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0005g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0005g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0005g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0005g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0005g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0005g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0007g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0007g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0007g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0007g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0007g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0008g0005 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0008g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0008g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0008g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0010g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0010g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0010g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0010g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0011g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0011g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0011g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0011g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0017g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0017g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0017g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0018g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0018g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0018g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0019g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0019g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0019g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0020g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0020g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0020g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0025g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0025g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0026g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0026g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0027g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0027g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0028g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0028g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0029g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0029g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0034g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0034g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0035g0003 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0036g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0037g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0037g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0038g0280 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0038g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0039g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0039g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0040g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0040g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0041g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0041g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0051g0075 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0051g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0052g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0052g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0053g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0053g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0054g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0054g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0059g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0060g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0061g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0062g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0065g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0066g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0067g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0068g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0069g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0079g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0080g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0081g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0082g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0083g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0084g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0085g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0087g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0096g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0097g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0098g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0099g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0100g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0102g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0107g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0118g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0119g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0120g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0121g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0122g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0123g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0124g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0125g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0126g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0127g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0128g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0129g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0130g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0131g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0132g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0133g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0134g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0135g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0136g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0137g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0138g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0139g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0140g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0141g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0142g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0143g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0144g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0145g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0147g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0148g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0149g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0150g0281 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0166g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0171g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0172g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0173g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0174g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0175g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0176g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0177g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0178g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0179g0168 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0180g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0181g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0183g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0001t0197g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0003g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0003g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0003g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0003g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0003g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0003g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0003g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0003g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0003g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0003g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0003g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0006g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0006g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0006g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0006g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0006g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0006g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0009g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0009g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0009g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0009g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0013g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0013g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0013g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0013g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0014g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0014g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0014g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0015g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0015g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0015g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0016g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0016g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0016g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0021g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0021g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0021g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0022g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0022g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0022g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0024g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0024g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0024g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0030g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0030g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0031g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0032g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0032g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0043g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0043g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0044g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0044g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0045g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0045g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0046g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0046g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0047g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0047g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0055g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0055g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0056g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0057g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0070g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0071g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0072g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0073g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0074g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0075g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0076g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0078g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0088g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0089g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0090g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0091g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0092g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0093g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0094g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0095g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0101g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0104g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0105g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0106g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0108g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0152g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0153g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0154g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0155g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0156g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0157g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0158g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0159g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0160g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0161g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0162g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0163g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0164g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0165g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0168g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0188g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0189g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0190g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0191g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0192g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0193g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0194g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0002t0195g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0003t0023g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0003t0023g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0003t0023g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0003t0049g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0003t0049g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0003t0058g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0003t0077g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0003t0109g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0003t0110g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0003t0111g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0003t0112g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0003t0113g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0003t0114g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0003t0115g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0003t0167g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0004t0036g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0004t0042g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0004t0042g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0004t0063g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0004t0064g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0004t0146g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0004t0151g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0004t0182g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0004t0184g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0004t0185g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0004t0186g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0004t0187g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0005t0012g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0005t0012g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0005t0012g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0005t0012g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0005t0169g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0005t0170g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0006t0050g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0006t0050g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0006t0116g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0007t0048g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0007t0048g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0008t0033g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0008t0033g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0009t0103g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0010t0196g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0011t0086g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
a0001c0012t0117g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0038 | g0280 | EUR | GBR | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG00099 | hp2 | a0001 | c0001 | t0002 | g0204 | EUR | GBR | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG00280 | hp1 | a0001 | c0002 | t0006 | g0191 | EUR | FIN | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG00280 | hp2 | a0001 | c0001 | t0069 | g0125 | EUR | FIN | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG00323 | hp1 | a0001 | c0001 | t0081 | g0074 | EUR | FIN | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG00323 | hp2 | a0001 | c0002 | t0006 | g0190 | EUR | FIN | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG00408 | hp1 | a0001 | c0001 | t0005 | g0258 | EAS | CHS | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG00408 | hp2 | a0001 | c0002 | t0001 | g0286 | EAS | CHS | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG00438 | hp1 | a0001 | c0002 | t0001 | g0018 | EAS | CHS | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG00438 | hp2 | a0001 | c0001 | t0008 | g0030 | EAS | CHS | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG00558 | hp1 | a0001 | c0001 | t0011 | g0330 | EAS | CHS | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG00558 | hp2 | a0001 | c0001 | t0136 | g0295 | EAS | CHS | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG00597 | hp1 | a0001 | c0001 | t0039 | g0320 | EAS | CHS | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG00597 | hp2 | a0001 | c0001 | t0008 | g0051 | EAS | CHS | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG00609 | hp1 | a0001 | c0002 | t0193 | g0188 | EAS | CHS | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG00609 | hp2 | a0001 | c0002 | t0047 | g0047 | EAS | CHS | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG00621 | hp1 | a0001 | c0001 | t0020 | g0313 | EAS | CHS | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG00621 | hp2 | a0001 | c0002 | t0009 | g0116 | EAS | CHS | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG00639 | hp1 | a0001 | c0003 | t0049 | g0147 | AMR | PUR | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG00639 | hp2 | a0001 | c0001 | t0018 | g0336 | AMR | PUR | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG00642 | hp1 | a0001 | c0001 | t0005 | g0274 | AMR | PUR | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG00642 | hp2 | a0001 | c0001 | t0025 | g0095 | AMR | PUR | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG00735 | hp1 | a0001 | c0001 | t0124 | g0225 | AMR | PUR | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG00735 | hp2 | a0001 | c0001 | t0018 | g0337 | AMR | PUR | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG00738 | hp1 | a0001 | c0002 | t0013 | g0175 | AMR | PUR | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG00738 | hp2 | a0001 | c0001 | t0066 | g0114 | AMR | PUR | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG00741 | hp1 | a0001 | c0002 | t0088 | g0098 | AMR | PUR | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG00741 | hp2 | a0001 | c0002 | t0190 | g0155 | AMR | PUR | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG01069 | hp1 | a0001 | c0002 | t0024 | g0174 | AMR | PUR | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG01069 | hp2 | a0001 | c0001 | t0137 | g0006 | AMR | PUR | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG01070 | hp1 | a0001 | c0002 | t0024 | g0196 | AMR | PUR | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG01070 | hp2 | a0001 | c0002 | t0030 | g0091 | AMR | PUR | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG01074 | hp1 | a0001 | c0001 | t0148 | g0203 | AMR | PUR | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG01074 | hp2 | a0001 | c0002 | t0030 | g0090 | AMR | PUR | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG01081 | hp1 | a0001 | c0001 | t0038 | g0311 | AMR | PUR | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG01081 | hp2 | a0001 | c0001 | t0060 | g0115 | AMR | PUR | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG01099 | hp1 | a0001 | c0002 | t0001 | g0057 | AMR | PUR | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG01099 | hp2 | a0001 | c0001 | t0126 | g0201 | AMR | PUR | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG01106 | hp1 | a0001 | c0001 | t0080 | g0099 | AMR | PUR | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG01106 | hp2 | a0001 | c0001 | t0002 | g0272 | AMR | PUR | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG01109 | hp1 | a0001 | c0001 | t0053 | g0165 | AMR | PUR | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG01109 | hp2 | a0001 | c0003 | t0049 | g0158 | AMR | PUR | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG01167 | hp1 | a0001 | c0002 | t0031 | g0002 | AMR | PUR | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG01167 | hp2 | a0001 | c0004 | t0036 | g0235 | AMR | PUR | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG01168 | hp1 | a0001 | c0002 | t0045 | g0216 | AMR | PUR | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG01168 | hp2 | a0001 | c0001 | t0143 | g0279 | AMR | PUR | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG01169 | hp1 | a0001 | c0002 | t0031 | g0002 | AMR | PUR | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG01169 | hp2 | a0001 | c0002 | t0045 | g0208 | AMR | PUR | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG01175 | hp1 | a0001 | c0001 | t0128 | g0206 | AMR | PUR | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG01175 | hp2 | a0001 | c0001 | t0027 | g0073 | AMR | PUR | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG01192 | hp1 | a0001 | c0002 | t0104 | g0194 | AMR | PUR | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG01192 | hp2 | a0001 | c0002 | t0105 | g0195 | AMR | PUR | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG01243 | hp1 | a0001 | c0001 | t0054 | g0199 | AMR | PUR | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG01243 | hp2 | a0001 | c0004 | t0187 | g0083 | AMR | PUR | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG01257 | hp1 | a0001 | c0002 | t0013 | g0123 | AMR | CLM | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG01257 | hp2 | a0001 | c0002 | t0021 | g0001 | AMR | CLM | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG01346 | hp1 | a0001 | c0001 | t0004 | g0053 | AMR | CLM | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG01346 | hp2 | a0001 | c0002 | t0006 | g0186 | AMR | CLM | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG01358 | hp1 | a0001 | c0002 | t0044 | g0001 | AMR | CLM | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG01358 | hp2 | a0001 | c0002 | t0192 | g0197 | AMR | CLM | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG01361 | hp1 | a0001 | c0001 | t0011 | g0214 | AMR | CLM | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG01361 | hp2 | a0001 | c0002 | t0044 | g0041 | AMR | CLM | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG01496 | hp1 | a0001 | c0001 | t0027 | g0076 | AMR | CLM | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG01496 | hp2 | a0001 | c0004 | t0064 | g0082 | AMR | CLM | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG01516 | hp1 | a0001 | c0001 | t0028 | g0122 | EUR | IBS | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG01516 | hp2 | a0001 | c0001 | t0150 | g0281 | EUR | IBS | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG01884 | hp1 | a0001 | c0011 | t0086 | g0077 | AFR | ACB | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG01884 | hp2 | a0001 | c0005 | t0012 | g0138 | AFR | ACB | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG01934 | hp1 | a0001 | c0001 | t0002 | g0297 | AMR | PEL | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG01934 | hp2 | a0001 | c0001 | t0005 | g0212 | AMR | PEL | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG01952 | hp1 | a0001 | c0001 | t0002 | g0296 | AMR | PEL | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG01952 | hp2 | a0001 | c0002 | t0006 | g0182 | AMR | PEL | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG01975 | hp1 | a0001 | c0002 | t0009 | g0092 | AMR | PEL | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG01975 | hp2 | a0001 | c0001 | t0166 | g0239 | AMR | PEL | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG01978 | hp1 | a0001 | c0001 | t0142 | g0202 | AMR | PEL | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG01978 | hp2 | a0001 | c0002 | t0070 | g0126 | AMR | PEL | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG01981 | hp1 | a0001 | c0001 | t0052 | g0187 | AMR | PEL | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG01981 | hp2 | a0001 | c0002 | t0001 | g0055 | AMR | PEL | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG01993 | hp1 | a0001 | c0002 | t0003 | g0215 | AMR | PEL | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG01993 | hp2 | a0001 | c0001 | t0138 | g0303 | AMR | PEL | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02004 | hp1 | a0001 | c0002 | t0165 | g0298 | AMR | PEL | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02004 | hp2 | a0001 | c0001 | t0002 | g0205 | AMR | PEL | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02015 | hp1 | a0001 | c0001 | t0177 | g0120 | EAS | KHV | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02015 | hp2 | a0001 | c0002 | t0015 | g0020 | EAS | KHV | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02027 | hp1 | a0001 | c0001 | t0125 | g0253 | EAS | KHV | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02027 | hp2 | a0001 | c0002 | t0016 | g0017 | EAS | KHV | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02040 | hp1 | a0001 | c0002 | t0003 | g0325 | EAS | KHV | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02040 | hp2 | a0001 | c0002 | t0108 | g0025 | EAS | KHV | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02055 | hp1 | a0001 | c0005 | t0012 | g0135 | AFR | ACB | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02055 | hp2 | a0001 | c0004 | t0182 | g0078 | AFR | ACB | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02071 | hp1 | a0001 | c0001 | t0025 | g0102 | EAS | KHV | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02071 | hp2 | a0001 | c0001 | t0007 | g0288 | EAS | KHV | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02074 | hp1 | a0001 | c0002 | t0001 | g0306 | EAS | KHV | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02074 | hp2 | a0001 | c0001 | t0134 | g0019 | EAS | KHV | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02080 | hp1 | a0001 | c0002 | t0015 | g0023 | EAS | KHV | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02080 | hp2 | a0001 | c0001 | t0097 | g0217 | EAS | KHV | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02083 | hp1 | a0001 | c0001 | t0144 | g0282 | EAS | KHV | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02083 | hp2 | a0001 | c0001 | t0007 | g0048 | EAS | KHV | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02129 | hp1 | a0001 | c0002 | t0159 | g0044 | EAS | KHV | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02129 | hp2 | a0001 | c0001 | t0020 | g0269 | EAS | KHV | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02132 | hp1 | a0001 | c0002 | t0003 | g0267 | EAS | KHV | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02132 | hp2 | a0001 | c0002 | t0016 | g0015 | EAS | KHV | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02145 | hp1 | a0001 | c0001 | t0102 | g0153 | AFR | ACB | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02145 | hp2 | a0001 | c0009 | t0103 | g0145 | AFR | ACB | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02155 | hp1 | a0001 | c0002 | t0001 | g0035 | EAS | CDX | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02155 | hp2 | a0001 | c0001 | t0062 | g0124 | EAS | CDX | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02165 | hp1 | a0001 | c0001 | t0017 | g0326 | EAS | CDX | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02165 | hp2 | a0001 | c0001 | t0041 | g0324 | EAS | CDX | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02257 | hp1 | a0001 | c0001 | t0040 | g0308 | AFR | ACB | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02257 | hp2 | a0001 | c0005 | t0012 | g0137 | AFR | ACB | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02258 | hp1 | a0001 | c0001 | t0132 | g0301 | AFR | ACB | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02258 | hp2 | a0001 | c0001 | t0052 | g0164 | AFR | ACB | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02280 | hp1 | a0001 | c0001 | t0175 | g0166 | AFR | ACB | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02280 | hp2 | a0001 | c0002 | t0055 | g0176 | AFR | ACB | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02300 | hp1 | a0001 | c0001 | t0005 | g0285 | AMR | PEL | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02300 | hp2 | a0001 | c0002 | t0002 | g0058 | AMR | PEL | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02523 | hp1 | a0001 | c0002 | t0156 | g0027 | EAS | KHV | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02523 | hp2 | a0001 | c0001 | t0098 | g0318 | EAS | KHV | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02572 | hp1 | a0001 | c0001 | t0183 | g0154 | AFR | GWD | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02572 | hp2 | a0001 | c0002 | t0191 | g0149 | AFR | GWD | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02602 | hp1 | a0001 | c0001 | t0127 | g0275 | SAS | PJL | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02602 | hp2 | a0001 | c0001 | t0003 | g0241 | SAS | PJL | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02615 | hp1 | a0001 | c0002 | t0163 | g0066 | AFR | GWD | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02615 | hp2 | a0001 | c0001 | t0197 | g0222 | AFR | GWD | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02630 | hp1 | a0001 | c0001 | t0002 | g0234 | AFR | GWD | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02630 | hp2 | a0001 | c0002 | t0164 | g0329 | AFR | GWD | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02647 | hp1 | a0001 | c0001 | t0107 | g0232 | AFR | GWD | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02647 | hp2 | a0001 | c0003 | t0111 | g0067 | AFR | GWD | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02683 | hp1 | a0001 | c0002 | t0006 | g0184 | SAS | PJL | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02683 | hp2 | a0001 | c0002 | t0089 | g0117 | SAS | PJL | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02698 | hp1 | a0001 | c0002 | t0013 | g0177 | SAS | PJL | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02698 | hp2 | a0001 | c0002 | t0094 | g0103 | SAS | PJL | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02717 | hp1 | a0001 | c0001 | t0051 | g0167 | AFR | GWD | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02717 | hp2 | a0001 | c0008 | t0033 | g0143 | AFR | GWD | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02723 | hp1 | a0001 | c0002 | t0056 | g0157 | AFR | GWD | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02723 | hp2 | a0001 | c0003 | t0167 | g0139 | AFR | GWD | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02735 | hp1 | a0001 | c0001 | t0065 | g0086 | SAS | PJL | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02735 | hp2 | a0001 | c0002 | t0092 | g0133 | SAS | PJL | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02738 | hp1 | a0001 | c0002 | t0189 | g0178 | SAS | PJL | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02738 | hp2 | a0001 | c0002 | t0024 | g0189 | SAS | PJL | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02818 | hp1 | a0001 | c0003 | t0112 | g0226 | AFR | GWD | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02818 | hp2 | a0001 | c0001 | t0002 | g0223 | AFR | GWD | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02886 | hp1 | a0001 | c0004 | t0151 | g0065 | AFR | GWD | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02886 | hp2 | a0001 | c0001 | t0122 | g0276 | AFR | GWD | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02895 | hp1 | a0001 | c0001 | t0174 | g0079 | AFR | GWD | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02895 | hp2 | a0001 | c0007 | t0048 | g0312 | AFR | GWD | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02897 | hp1 | a0001 | c0007 | t0048 | g0252 | AFR | GWD | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02897 | hp2 | a0001 | c0001 | t0002 | g0233 | AFR | GWD | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02922 | hp1 | a0001 | c0001 | t0171 | g0160 | AFR | ESN | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02922 | hp2 | a0001 | c0002 | t0055 | g0179 | AFR | ESN | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02965 | hp1 | a0001 | c0001 | t0079 | g0085 | AFR | ESN | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02965 | hp2 | a0001 | c0001 | t0121 | g0230 | AFR | ESN | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02976 | hp1 | a0001 | c0001 | t0053 | g0161 | AFR | ESN | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02976 | hp2 | a0001 | c0006 | t0050 | g0150 | AFR | ESN | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG03041 | hp1 | a0001 | c0003 | t0023 | g0200 | AFR | GWD | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG03041 | hp2 | a0001 | c0003 | t0109 | g0254 | AFR | GWD | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG03098 | hp1 | a0001 | c0001 | t0172 | g0163 | AFR | MSL | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG03098 | hp2 | a0001 | c0002 | t0195 | g0148 | AFR | MSL | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG03130 | hp1 | a0001 | c0001 | t0059 | g0084 | AFR | ESN | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG03130 | hp2 | a0001 | c0001 | t0173 | g0159 | AFR | ESN | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG03139 | hp1 | a0001 | c0006 | t0050 | g0151 | AFR | ESN | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG03139 | hp2 | a0001 | c0001 | t0040 | g0322 | AFR | ESN | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG03195 | hp1 | a0001 | c0004 | t0184 | g0162 | AFR | ESN | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG03195 | hp2 | a0001 | c0005 | t0012 | g0136 | AFR | ESN | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG03209 | hp1 | a0001 | c0008 | t0033 | g0142 | AFR | MSL | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG03209 | hp2 | a0001 | c0003 | t0113 | g0220 | AFR | MSL | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG03225 | hp1 | a0001 | c0004 | t0042 | g0210 | AFR | MSL | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG03225 | hp2 | a0001 | c0002 | t0101 | g0141 | AFR | MSL | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG03239 | hp1 | a0001 | c0001 | t0149 | g0335 | SAS | PJL | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG03239 | hp2 | a0001 | c0001 | t0061 | g0101 | SAS | PJL | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG03453 | hp1 | a0001 | c0004 | t0146 | g0213 | AFR | MSL | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG03453 | hp2 | a0001 | c0001 | t0181 | g0193 | AFR | MSL | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG03486 | hp1 | a0001 | c0003 | t0110 | g0134 | AFR | MSL | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG03486 | hp2 | a0001 | c0002 | t0188 | g0131 | AFR | MSL | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG03490 | hp1 | a0001 | c0001 | t0008 | g0005 | SAS | PJL | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG03490 | hp2 | a0001 | c0002 | t0093 | g0108 | SAS | PJL | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG03491 | hp1 | a0001 | c0001 | t0035 | g0003 | SAS | PJL | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG03491 | hp2 | a0001 | c0002 | t0009 | g0093 | SAS | PJL | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG03492 | hp1 | a0001 | c0001 | t0008 | g0005 | SAS | PJL | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG03492 | hp2 | a0001 | c0001 | t0035 | g0003 | SAS | PJL | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG03516 | hp1 | a0001 | c0006 | t0116 | g0228 | AFR | ESN | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG03516 | hp2 | a0001 | c0004 | t0185 | g0096 | AFR | ESN | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG03540 | hp1 | a0001 | c0001 | t0036 | g0227 | AFR | GWD | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG03540 | hp2 | a0001 | c0004 | t0063 | g0080 | AFR | GWD | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG03579 | hp1 | a0001 | c0004 | t0186 | g0081 | AFR | MSL | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG03579 | hp2 | a0001 | c0003 | t0023 | g0171 | AFR | MSL | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG03654 | hp1 | a0001 | c0001 | t0085 | g0068 | SAS | PJL | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG03654 | hp2 | a0001 | c0001 | t0028 | g0089 | SAS | PJL | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG03688 | hp1 | a0001 | c0001 | t0096 | g0245 | SAS | STU | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG03688 | hp2 | a0001 | c0002 | t0006 | g0185 | SAS | STU | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG03704 | hp1 | a0001 | c0002 | t0013 | g0183 | SAS | PJL | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG03704 | hp2 | a0001 | c0001 | t0130 | g0237 | SAS | PJL | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG03710 | hp1 | a0001 | c0001 | t0002 | g0221 | SAS | PJL | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG03710 | hp2 | a0001 | c0002 | t0194 | g0192 | SAS | PJL | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG03834 | hp1 | a0001 | c0001 | t0002 | g0218 | SAS | BEB | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG03834 | hp2 | a0001 | c0001 | t0002 | g0244 | SAS | BEB | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG03927 | hp1 | a0001 | c0001 | t0118 | g0242 | SAS | BEB | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG03927 | hp2 | a0001 | c0001 | t0120 | g0219 | SAS | BEB | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG03942 | hp1 | a0001 | c0001 | t0017 | g0287 | SAS | BEB | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG03942 | hp2 | a0001 | c0001 | t0067 | g0121 | SAS | BEB | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG04184 | hp1 | a0001 | c0002 | t0072 | g0087 | SAS | BEB | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG04184 | hp2 | a0001 | c0001 | t0002 | g0273 | SAS | BEB | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG04204 | hp1 | a0001 | c0002 | t0091 | g0094 | SAS | STU | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG04204 | hp2 | a0001 | c0002 | t0157 | g0305 | SAS | STU | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG04228 | hp1 | a0001 | c0002 | t0073 | g0071 | SAS | STU | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG04228 | hp2 | a0001 | c0001 | t0068 | g0070 | SAS | STU | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA18522 | hp1 | a0001 | c0003 | t0077 | g0130 | AFR | YRI | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA18522 | hp2 | a0001 | c0005 | t0170 | g0170 | AFR | YRI | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA18747 | hp1 | a0001 | c0002 | t0009 | g0104 | EAS | CHB | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA18747 | hp2 | a0001 | c0001 | t0141 | g0268 | EAS | CHB | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA18906 | hp1 | a0001 | c0002 | t0168 | g0180 | AFR | YRI | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA18906 | hp2 | a0001 | c0001 | t0131 | g0229 | AFR | YRI | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA18941 | hp1 | a0001 | c0001 | t0084 | g0128 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA18941 | hp2 | a0001 | c0001 | t0004 | g0261 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA18942 | hp1 | a0001 | c0002 | t0001 | g0321 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA18942 | hp2 | a0001 | c0001 | t0135 | g0064 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA18943 | hp1 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA18943 | hp2 | a0001 | c0001 | t0019 | g0266 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA18945 | hp1 | a0001 | c0002 | t0090 | g0106 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA18945 | hp2 | a0001 | c0001 | t0018 | g0010 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA18946 | hp1 | a0001 | c0002 | t0001 | g0063 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA18946 | hp2 | a0001 | c0001 | t0004 | g0238 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA18950 | hp1 | a0001 | c0002 | t0032 | g0013 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA18950 | hp2 | a0001 | c0002 | t0075 | g0109 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA18953 | hp1 | a0001 | c0001 | t0026 | g0129 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA18953 | hp2 | a0001 | c0002 | t0046 | g0250 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA18954 | hp1 | a0001 | c0002 | t0021 | g0289 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA18954 | hp2 | a0001 | c0002 | t0022 | g0028 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA18959 | hp1 | a0001 | c0002 | t0152 | g0026 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA18959 | hp2 | a0001 | c0001 | t0010 | g0251 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA18960 | hp1 | a0001 | c0002 | t0153 | g0291 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA18960 | hp2 | a0001 | c0002 | t0001 | g0016 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA18961 | hp1 | a0001 | c0001 | t0010 | g0319 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA18961 | hp2 | a0001 | c0002 | t0022 | g0049 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA18962 | hp1 | a0001 | c0001 | t0004 | g0264 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA18962 | hp2 | a0001 | c0002 | t0003 | g0038 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA18963 | hp1 | a0001 | c0001 | t0010 | g0309 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA18963 | hp2 | a0001 | c0002 | t0001 | g0045 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA18966 | hp1 | a0001 | c0002 | t0001 | g0247 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA18966 | hp2 | a0001 | c0002 | t0071 | g0100 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA18970 | hp1 | a0001 | c0001 | t0008 | g0333 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA18970 | hp2 | a0001 | c0001 | t0004 | g0262 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA18971 | hp1 | a0001 | c0002 | t0047 | g0277 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA18971 | hp2 | a0001 | c0001 | t0019 | g0265 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA18973 | hp1 | a0001 | c0001 | t0082 | g0097 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA18973 | hp2 | a0001 | c0001 | t0037 | g0334 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA18975 | hp1 | a0001 | c0002 | t0003 | g0284 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA18975 | hp2 | a0001 | c0001 | t0100 | g0036 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA18980 | hp1 | a0001 | c0001 | t0007 | g0328 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA18980 | hp2 | a0001 | c0002 | t0001 | g0033 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA18983 | hp1 | a0001 | c0001 | t0034 | g0021 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA18983 | hp2 | a0001 | c0001 | t0029 | g0112 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA18984 | hp1 | a0001 | c0002 | t0014 | g0105 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA18984 | hp2 | a0001 | c0001 | t0019 | g0316 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA18985 | hp1 | a0001 | c0001 | t0129 | g0294 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA18985 | hp2 | a0001 | c0002 | t0158 | g0050 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA18986 | hp1 | a0001 | c0002 | t0095 | g0110 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA18986 | hp2 | a0001 | c0002 | t0078 | g0072 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA18993 | hp1 | a0001 | c0002 | t0046 | g0257 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA18993 | hp2 | a0001 | c0001 | t0011 | g0061 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA18994 | hp1 | a0001 | c0001 | t0007 | g0332 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA18994 | hp2 | a0001 | c0002 | t0015 | g0014 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA18995 | hp1 | a0001 | c0002 | t0161 | g0008 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA18995 | hp2 | a0001 | c0002 | t0043 | g0283 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA18997 | hp1 | a0001 | c0001 | t0020 | g0256 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA18997 | hp2 | a0001 | c0001 | t0087 | g0111 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA18999 | hp1 | a0001 | c0001 | t0041 | g0304 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA18999 | hp2 | a0001 | c0002 | t0003 | g0043 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA19000 | hp1 | a0001 | c0001 | t0004 | g0263 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA19000 | hp2 | a0001 | c0002 | t0001 | g0062 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA19002 | hp1 | a0001 | c0002 | t0160 | g0323 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA19002 | hp2 | a0001 | c0001 | t0010 | g0327 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA19003 | hp1 | a0001 | c0001 | t0017 | g0310 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA19003 | hp2 | a0001 | c0002 | t0155 | g0240 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA19004 | hp1 | a0001 | c0002 | t0003 | g0029 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA19004 | hp2 | a0001 | c0001 | t0083 | g0119 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA19005 | hp1 | a0001 | c0001 | t0039 | g0037 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA19005 | hp2 | a0001 | c0001 | t0133 | g0004 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA19006 | hp1 | a0001 | c0001 | t0099 | g0315 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA19006 | hp2 | a0001 | c0002 | t0001 | g0054 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA19007 | hp1 | a0001 | c0002 | t0001 | g0040 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA19007 | hp2 | a0001 | c0001 | t0005 | g0300 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA19009 | hp1 | a0001 | c0002 | t0001 | g0034 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA19009 | hp2 | a0001 | c0001 | t0037 | g0004 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA19010 | hp1 | a0001 | c0002 | t0021 | g0009 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA19010 | hp2 | a0001 | c0002 | t0154 | g0299 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA19012 | hp1 | a0001 | c0001 | t0004 | g0259 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA19012 | hp2 | a0001 | c0001 | t0026 | g0069 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA19030 | hp1 | a0001 | c0012 | t0117 | g0140 | AFR | LWK | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA19030 | hp2 | a0001 | c0004 | t0042 | g0209 | AFR | LWK | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA19054 | hp1 | a0001 | c0002 | t0014 | g0118 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA19054 | hp2 | a0001 | c0002 | t0001 | g0056 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA19056 | hp1 | a0001 | c0001 | t0005 | g0278 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA19056 | hp2 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA19057 | hp1 | a0001 | c0002 | t0003 | g0046 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA19057 | hp2 | a0001 | c0001 | t0004 | g0270 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA19060 | hp1 | a0001 | c0001 | t0004 | g0260 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA19060 | hp2 | a0001 | c0002 | t0032 | g0022 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA19064 | hp1 | a0001 | c0002 | t0043 | g0290 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA19064 | hp2 | a0001 | c0002 | t0001 | g0039 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA19066 | hp1 | a0001 | c0001 | t0004 | g0271 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA19066 | hp2 | a0001 | c0001 | t0002 | g0317 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA19068 | hp1 | a0001 | c0002 | t0001 | g0248 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA19068 | hp2 | a0001 | c0001 | t0007 | g0012 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA19074 | hp1 | a0001 | c0002 | t0001 | g0024 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA19074 | hp2 | a0001 | c0001 | t0011 | g0314 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA19077 | hp1 | a0001 | c0002 | t0014 | g0107 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA19077 | hp2 | a0001 | c0002 | t0016 | g0059 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA19079 | hp1 | a0001 | c0002 | t0022 | g0042 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA19079 | hp2 | a0001 | c0001 | t0119 | g0293 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA19080 | hp1 | a0001 | c0002 | t0001 | g0031 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA19080 | hp2 | a0001 | c0002 | t0003 | g0307 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA19083 | hp1 | a0001 | c0001 | t0002 | g0331 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA19083 | hp2 | a0001 | c0002 | t0074 | g0127 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA19084 | hp1 | a0001 | c0002 | t0003 | g0292 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA19084 | hp2 | a0001 | c0002 | t0162 | g0032 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA19088 | hp1 | a0001 | c0002 | t0001 | g0052 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA19088 | hp2 | a0001 | c0001 | t0139 | g0302 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA19090 | hp1 | a0001 | c0002 | t0003 | g0243 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA19090 | hp2 | a0001 | c0001 | t0029 | g0113 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA19091 | hp1 | a0001 | c0001 | t0140 | g0249 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA19091 | hp2 | a0001 | c0001 | t0034 | g0060 | EAS | JPT | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA19240 | hp1 | a0001 | c0003 | t0114 | g0224 | AFR | YRI | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA19240 | hp2 | a0001 | c0001 | t0147 | g0255 | AFR | YRI | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA20129 | hp1 | a0001 | c0010 | t0196 | g0146 | AFR | ASW | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA20129 | hp2 | a0001 | c0001 | t0002 | g0246 | AFR | ASW | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA20752 | hp1 | a0001 | c0001 | t0002 | g0211 | EUR | TSI | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA20752 | hp2 | a0001 | c0002 | t0076 | g0088 | EUR | TSI | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02109 | hp1 | a0001 | c0003 | t0058 | g0132 | AFR | ACB | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02109 | hp2 | a0001 | c0001 | t0178 | g0173 | AFR | ACB | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02559 | hp1 | a0001 | c0005 | t0169 | g0152 | AFR | ACB | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG02559 | hp2 | a0001 | c0002 | t0057 | g0156 | AFR | ACB | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG03471 | hp1 | a0001 | c0003 | t0115 | g0207 | AFR | MSL | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG03471 | hp2 | a0001 | c0001 | t0123 | g0236 | AFR | MSL | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG06807 | hp1 | a0001 | c0001 | t0054 | g0181 | AFR | USA | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
HG06807 | hp2 | a0001 | c0002 | t0106 | g0144 | AFR | USA | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA20300 | hp1 | a0001 | c0003 | t0023 | g0169 | AFR | USA | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA20300 | hp2 | a0001 | c0001 | t0180 | g0198 | AFR | USA | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA21309 | hp1 | a0001 | c0001 | t0176 | g0172 | AFR | LWK | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
NA21309 | hp2 | a0001 | c0001 | t0145 | g0231 | AFR | LWK | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0051 | g0075 | REF | REF | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0179 | g0168 | REF | REF | LMX1B_chr9_126608928_126706032 | LMX1B | chr9 | 126608928 | 126706032 |
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 |
---|
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:126690950
|
A | G | 9 | a0001c0002a0001c0003a0001c0004others(6): Show | 173 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(170): Show |
synonymous_variant | LOW | c.441A>G | p.Glu147Glu | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 3/8 | 963/6312 | 441/1209 | 147/402 | chr9 | 126690950 | ||
chr9:126691043
|
C | A | 2 | a0001c0010a0001c0011 | 2 | HG01884.hp1 NA20129.hp1 |
synonymous_variant | LOW | c.534C>A | p.Ser178Ser | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 3/8 | 1056/6312 | 534/1209 | 178/402 | chr9 | 126691043 | ||
chr9:126691055
|
C | T | 1 | a0001c0009 | 1 | HG02145.hp2 | synonymous_variant | LOW | c.546C>T | p.Asp182Asp | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 3/8 | 1068/6312 | 546/1209 | 182/402 | chr9 | 126691055 | ||
chr9:126693308
|
G | C | 7 | a0001c0002a0001c0003a0001c0005others(4): Show | 159 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(156): Show |
synonymous_variant | LOW | c.726G>C | p.Ser242Ser | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 4/8 | 1248/6312 | 726/1209 | 242/402 | chr9 | 126693308 | ||
chr9:126693796
|
C | A | 1 | a0001c0008 | 2 | HG02717.hp2 HG03209.hp1 |
synonymous_variant | LOW | c.870C>A | p.Ser290Ser | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 6/8 | 1392/6312 | 870/1209 | 290/402 | chr9 | 126693796 | ||
chr9:126695882
|
G | A | 1 | a0001c0005 | 6 | HG01884.hp2 HG02055.hp1 HG02257.hp2 others(3): Show |
synonymous_variant | LOW | c.930G>A | p.Thr310Thr | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 7/8 | 1452/6312 | 930/1209 | 310/402 | chr9 | 126695882 | ||
chr9:126696301
|
C | T | 1 | a0001c0012 | 1 | NA19030.hp1 | synonymous_variant | LOW | c.1059C>T | p.Asp353Asp | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 1581/6312 | 1059/1209 | 353/402 | chr9 | 126696301 | ||
chr9:126696349
|
C | T | 5 | a0001c0003a0001c0006a0001c0008others(2): Show | 22 | HG00639.hp1 HG01109.hp2 HG02109.hp1 others(19): Show |
synonymous_variant | LOW | c.1107C>T | p.Ser369Ser | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 1629/6312 | 1107/1209 | 369/402 | chr9 | 126696349 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:126613982
|
G | C | 2 | a0001c0002t0056a0001c0002t0057 | 2 | HG02559.hp2 HG02723.hp1 |
5_prime_UTR_variant | MODIFIER | c.-468G>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 1/8 | 468 | chr9 | 126613982 | |||||
chr9:126614010
|
C | T | 1 | a0001c0001t0197 | 1 | HG02615.hp2 | 5_prime_UTR_variant | MODIFIER | c.-440C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 1/8 | 440 | chr9 | 126614010 | |||||
chr9:126614046
|
G | GC | 15 | a0001c0001t0010a0001c0001t0096a0001c0001t0097others(12): Show | 20 | HG01192.hp1 HG01192.hp2 HG02080.hp2 others(17): Show |
5_prime_UTR_variant | MODIFIER | c.-396dupC | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 1/8 | 395 | INFO_REALIGN_3_PRIME | chr9 | 126614046 | ||||
chr9:126614046
|
G | GCC | 26 | a0001c0001t0028a0001c0001t0029a0001c0001t0079others(23): Show | 35 | HG00323.hp1 HG00621.hp2 HG00741.hp1 others(32): Show |
5_prime_UTR_variant | MODIFIER | c.-397_-396dupCC | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 1/8 | 395 | INFO_REALIGN_3_PRIME | chr9 | 126614046 | ||||
chr9:126614046
|
G | GCCC | 21 | a0001c0001t0025a0001c0001t0026a0001c0001t0027others(18): Show | 24 | HG00280.hp2 HG00642.hp2 HG00738.hp2 others(21): Show |
5_prime_UTR_variant | MODIFIER | c.-398_-396dupCCC | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 1/8 | 395 | INFO_REALIGN_3_PRIME | chr9 | 126614046 | ||||
chr9:126614087
|
C | A | 5 | a0001c0001t0034a0001c0001t0107a0001c0002t0015others(2): Show | 10 | HG02015.hp2 HG02027.hp2 HG02040.hp2 others(7): Show |
5_prime_UTR_variant | MODIFIER | c.-363C>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 1/8 | 363 | chr9 | 126614087 | |||||
chr9:126614099
|
T | C | 102 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(99): Show | 209 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(206): Show |
5_prime_UTR_variant | MODIFIER | c.-351T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 1/8 | 351 | chr9 | 126614099 | |||||
chr9:126614230
|
G | A | 1 | a0001c0003t0167 | 1 | HG02723.hp2 | 5_prime_UTR_variant | MODIFIER | c.-220G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 1/8 | 220 | chr9 | 126614230 | |||||
chr9:126614265
|
C | T | 1 | a0001c0001t0166 | 1 | HG01975.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-185C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 1/8 | chr9 | 126614265 | ||||||
chr9:126614345
|
G | GGGGCCGC others(15): Show |
1 | a0001c0002t0076 | 1 | NA20752.hp2 | 5_prime_UTR_variant | MODIFIER | c.-96_-75dupCCTCCCCG others(14): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 1/8 | 74 | INFO_REALIGN_3_PRIME | chr9 | 126614345 | ||||
chr9:126696478
|
G | A | 21 | a0001c0002t0101a0001c0002t0168a0001c0003t0023others(18): Show | 29 | HG00639.hp1 HG01109.hp2 HG01884.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*27G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 27 | chr9 | 126696478 | |||||
chr9:126696489
|
G | A | 2 | a0001c0001t0096a0001c0001t0118 | 2 | HG03688.hp1 HG03927.hp1 |
3_prime_UTR_variant | MODIFIER | c.*38G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 38 | chr9 | 126696489 | |||||
chr9:126696502
|
A | G | 22 | a0001c0002t0057a0001c0002t0101a0001c0002t0168others(19): Show | 30 | HG00639.hp1 HG01109.hp2 HG01884.hp2 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*51A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 51 | chr9 | 126696502 | |||||
chr9:126696530
|
G | A | 22 | a0001c0002t0057a0001c0002t0101a0001c0002t0168others(19): Show | 30 | HG00639.hp1 HG01109.hp2 HG01884.hp2 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*79G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 79 | chr9 | 126696530 | |||||
chr9:126696578
|
C | T | 3 | a0001c0002t0056a0001c0007t0048a0001c0010t0196 | 4 | HG02723.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*127C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 127 | chr9 | 126696578 | |||||
chr9:126696606
|
G | A | 1 | a0001c0001t0010 | 4 | NA18959.hp2 NA18961.hp1 NA18963.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*155G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 155 | chr9 | 126696606 | |||||
chr9:126696624
|
G | A | 5 | a0001c0003t0058a0001c0003t0077a0001c0003t0109others(2): Show | 5 | HG02109.hp1 HG02647.hp2 HG03041.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*173G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 173 | chr9 | 126696624 | |||||
chr9:126696651
|
C | T | 1 | a0001c0012t0117 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*200C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 200 | chr9 | 126696651 | |||||
chr9:126696701
|
G | A | 1 | a0001c0002t0078 | 1 | NA18986.hp2 | 3_prime_UTR_variant | MODIFIER | c.*250G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 250 | chr9 | 126696701 | |||||
chr9:126696731
|
G | A | 2 | a0001c0002t0056a0001c0007t0048 | 3 | HG02723.hp1 HG02895.hp2 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*280G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 280 | chr9 | 126696731 | |||||
chr9:126696891
|
G | T | 1 | a0001c0002t0165 | 1 | HG02004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*440G>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 440 | chr9 | 126696891 | |||||
chr9:126696902
|
C | T | 32 | a0001c0002t0001a0001c0002t0016a0001c0002t0021others(29): Show | 69 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(66): Show |
3_prime_UTR_variant | MODIFIER | c.*451C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 451 | chr9 | 126696902 | |||||
chr9:126696966
|
A | G | 2 | a0001c0002t0056a0001c0007t0048 | 3 | HG02723.hp1 HG02895.hp2 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*515A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 515 | chr9 | 126696966 | |||||
chr9:126697035
|
C | T | 33 | a0001c0001t0003a0001c0002t0003a0001c0002t0006others(30): Show | 62 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(59): Show |
3_prime_UTR_variant | MODIFIER | c.*584C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 584 | chr9 | 126697035 | |||||
chr9:126697083
|
AACAC | A | 1 | a0001c0002t0022 | 3 | NA18954.hp2 NA18961.hp2 NA19079.hp1 |
3_prime_UTR_variant | MODIFIER | c.*640_*643delCACA | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 640 | INFO_REALIGN_3_PRIME | chr9 | 126697083 | ||||
chr9:126697132
|
C | T | 1 | a0001c0002t0154 | 1 | NA19010.hp2 | 3_prime_UTR_variant | MODIFIER | c.*681C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 681 | chr9 | 126697132 | |||||
chr9:126697159
|
G | A | 31 | a0001c0001t0003a0001c0002t0003a0001c0002t0006others(28): Show | 59 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(56): Show |
3_prime_UTR_variant | MODIFIER | c.*708G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 708 | chr9 | 126697159 | |||||
chr9:126697199
|
C | T | 37 | a0001c0001t0003a0001c0002t0003a0001c0002t0006others(34): Show | 67 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*748C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 748 | chr9 | 126697199 | |||||
chr9:126697236
|
C | T | 1 | a0001c0004t0151 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*785C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 785 | chr9 | 126697236 | |||||
chr9:126697246
|
C | T | 1 | a0001c0001t0150 | 1 | HG01516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*795C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 795 | chr9 | 126697246 | |||||
chr9:126697335
|
G | A | 2 | a0001c0001t0059a0001c0001t0171 | 2 | HG02922.hp1 HG03130.hp1 |
3_prime_UTR_variant | MODIFIER | c.*884G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 884 | chr9 | 126697335 | |||||
chr9:126697349
|
C | T | 8 | a0001c0001t0059a0001c0001t0066a0001c0001t0067others(5): Show | 8 | HG00280.hp2 HG00738.hp2 HG01074.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*898C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 898 | chr9 | 126697349 | |||||
chr9:126697383
|
G | T | 51 | a0001c0001t0147a0001c0002t0001a0001c0002t0016others(48): Show | 95 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(92): Show |
3_prime_UTR_variant | MODIFIER | c.*932G>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 932 | chr9 | 126697383 | |||||
chr9:126697519
|
T | A | 1 | a0001c0001t0107 | 1 | HG02647.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1068T>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 1068 | chr9 | 126697519 | |||||
chr9:126697556
|
CTT | C | 7 | a0001c0002t0055a0001c0002t0056a0001c0002t0106others(4): Show | 9 | HG02280.hp2 HG02615.hp1 HG02630.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1106_*1107delTT | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 1106 | chr9 | 126697556 | |||||
chr9:126697582
|
C | T | 1 | a0001c0002t0162 | 1 | NA19084.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1131C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 1131 | chr9 | 126697582 | |||||
chr9:126697706
|
A | G | 51 | a0001c0001t0147a0001c0002t0001a0001c0002t0016others(48): Show | 95 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(92): Show |
3_prime_UTR_variant | MODIFIER | c.*1255A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 1255 | chr9 | 126697706 | |||||
chr9:126697755
|
G | A | 13 | a0001c0001t0147a0001c0002t0057a0001c0002t0101others(10): Show | 17 | HG00639.hp1 HG01109.hp2 HG02559.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*1304G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 1304 | chr9 | 126697755 | |||||
chr9:126697837
|
C | CTGTTT | 15 | a0001c0001t0004a0001c0001t0019a0001c0001t0039others(12): Show | 29 | HG00597.hp1 HG01346.hp1 HG01496.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*1437_*1441dupTGTT others(1): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 1442 | INFO_REALIGN_3_PRIME | chr9 | 126697837 | ||||
chr9:126697837
|
C | CTGTTTTG others(3): Show |
10 | a0001c0001t0020a0001c0001t0065a0001c0001t0069others(7): Show | 13 | HG00280.hp2 HG00621.hp1 HG01168.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1432_*1441dupTGTT others(6): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 1442 | INFO_REALIGN_3_PRIME | chr9 | 126697837 | ||||
chr9:126697837
|
C | CTGTTTTG others(8): Show |
2 | a0001c0001t0149a0001c0004t0146 | 2 | HG03239.hp1 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1427_*1441dupTGTT others(11): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 1442 | INFO_REALIGN_3_PRIME | chr9 | 126697837 | ||||
chr9:126697837
|
CTGTTT | C | 60 | a0001c0001t0002a0001c0001t0003a0001c0001t0007others(57): Show | 110 | HG00099.hp2 HG00323.hp1 HG00621.hp2 others(107): Show |
3_prime_UTR_variant | MODIFIER | c.*1437_*1441delTGTT others(1): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 1437 | INFO_REALIGN_3_PRIME | chr9 | 126697837 | ||||
chr9:126697837
|
CTGTTTTG others(3): Show |
C | 15 | a0001c0001t0035a0001c0001t0119a0001c0001t0172others(12): Show | 18 | HG01978.hp2 HG02280.hp2 HG02559.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*1432_*1441delTGTT others(6): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 1432 | INFO_REALIGN_3_PRIME | chr9 | 126697837 | ||||
chr9:126697837
|
CTGTTTTG others(8): Show |
C | 3 | a0001c0001t0166a0001c0002t0006a0001c0002t0088 | 8 | HG00280.hp1 HG00323.hp2 HG00741.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1427_*1441delTGTT others(11): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 1427 | INFO_REALIGN_3_PRIME | chr9 | 126697837 | ||||
chr9:126697839
|
G | GGTTTT | 4 | a0001c0002t0047a0001c0002t0194a0001c0005t0012others(1): Show | 8 | HG00609.hp2 HG01884.hp2 HG02055.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1388_*1389insGTTT others(1): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 1389 | chr9 | 126697839 | |||||
chr9:126697839
|
GTTTTGTT others(2): Show |
G | 3 | a0001c0002t0044a0001c0008t0033a0001c0012t0117 | 5 | HG01358.hp1 HG01361.hp2 HG02717.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1389_*1397delTTTT others(5): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 1389 | chr9 | 126697839 | |||||
chr9:126697839
|
GTTTTGTT others(7): Show |
G | 5 | a0001c0003t0058a0001c0003t0077a0001c0003t0109others(2): Show | 5 | HG02109.hp1 HG02647.hp2 HG03041.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1389_*1402delTTTT others(10): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 1389 | chr9 | 126697839 | |||||
chr9:126697839
|
GTTTTGTT others(12): Show |
G | 1 | a0001c0010t0196 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1389_*1407delTTTT others(15): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 1389 | chr9 | 126697839 | |||||
chr9:126697840
|
T | G | 25 | a0001c0002t0001a0001c0002t0016a0001c0002t0021others(22): Show | 59 | HG00408.hp2 HG00438.hp1 HG01069.hp1 others(56): Show |
3_prime_UTR_variant | MODIFIER | c.*1389T>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 1389 | chr9 | 126697840 | |||||
chr9:126697844
|
G | T | 24 | a0001c0002t0001a0001c0002t0016a0001c0002t0021others(21): Show | 58 | HG00408.hp2 HG00438.hp1 HG01069.hp1 others(55): Show |
3_prime_UTR_variant | MODIFIER | c.*1393G>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 1393 | chr9 | 126697844 | |||||
chr9:126697853
|
TG | T | 3 | a0001c0002t0044a0001c0008t0033a0001c0012t0117 | 5 | HG01358.hp1 HG01361.hp2 HG02717.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1403delG | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 1403 | chr9 | 126697853 | |||||
chr9:126697858
|
TG | T | 5 | a0001c0003t0058a0001c0003t0077a0001c0003t0109others(2): Show | 5 | HG02109.hp1 HG02647.hp2 HG03041.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1408delG | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 1408 | chr9 | 126697858 | |||||
chr9:126697924
|
G | A | 35 | a0001c0002t0001a0001c0002t0016a0001c0002t0021others(32): Show | 72 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(69): Show |
3_prime_UTR_variant | MODIFIER | c.*1473G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 1473 | chr9 | 126697924 | |||||
chr9:126697989
|
C | G | 2 | a0001c0002t0101a0001c0002t0168 | 2 | HG03225.hp2 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1538C>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 1538 | chr9 | 126697989 | |||||
chr9:126698025
|
G | A | 1 | a0001c0001t0120 | 1 | HG03927.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1574G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 1574 | chr9 | 126698025 | |||||
chr9:126698025
|
G | T | 3 | a0001c0005t0012a0001c0005t0169a0001c0005t0170 | 6 | HG01884.hp2 HG02055.hp1 HG02257.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1574G>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 1574 | chr9 | 126698025 | |||||
chr9:126698033
|
A | G | 78 | a0001c0001t0003a0001c0001t0068a0001c0002t0001others(75): Show | 148 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(145): Show |
3_prime_UTR_variant | MODIFIER | c.*1582A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 1582 | chr9 | 126698033 | |||||
chr9:126698055
|
A | G | 6 | a0001c0003t0058a0001c0003t0077a0001c0003t0109others(3): Show | 7 | HG02109.hp1 HG02647.hp2 HG02717.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1604A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 1604 | chr9 | 126698055 | |||||
chr9:126698088
|
TGGTCTCC others(14): Show |
T | 6 | a0001c0001t0005a0001c0001t0041a0001c0001t0099others(3): Show | 12 | HG00408.hp1 HG00642.hp1 HG01934.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1641_*1661delCTCC others(17): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 1641 | INFO_REALIGN_3_PRIME | chr9 | 126698088 | ||||
chr9:126698095
|
C | G | 6 | a0001c0003t0058a0001c0003t0077a0001c0003t0109others(3): Show | 7 | HG02109.hp1 HG02647.hp2 HG02717.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1644C>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 1644 | chr9 | 126698095 | |||||
chr9:126698115
|
T | A | 1 | a0001c0004t0182 | 1 | HG02055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1664T>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 1664 | chr9 | 126698115 | |||||
chr9:126698117
|
C | T | 34 | a0001c0001t0003a0001c0001t0068a0001c0002t0003others(31): Show | 62 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(59): Show |
3_prime_UTR_variant | MODIFIER | c.*1666C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 1666 | chr9 | 126698117 | |||||
chr9:126698124
|
C | G | 1 | a0001c0001t0019 | 3 | NA18943.hp2 NA18971.hp2 NA18984.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1673C>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 1673 | chr9 | 126698124 | |||||
chr9:126698154
|
C | T | 6 | a0001c0003t0058a0001c0003t0077a0001c0003t0109others(3): Show | 7 | HG02109.hp1 HG02647.hp2 HG02717.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1703C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 1703 | chr9 | 126698154 | |||||
chr9:126698167
|
A | G | 9 | a0001c0003t0058a0001c0003t0077a0001c0003t0109others(6): Show | 13 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1716A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 1716 | chr9 | 126698167 | |||||
chr9:126698226
|
T | C | 1 | a0001c0012t0117 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1775T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 1775 | chr9 | 126698226 | |||||
chr9:126698443
|
T | C | 46 | a0001c0001t0036a0001c0001t0079a0001c0001t0121others(43): Show | 86 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(83): Show |
3_prime_UTR_variant | MODIFIER | c.*1992T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 1992 | chr9 | 126698443 | |||||
chr9:126698446
|
C | G | 3 | a0001c0001t0147a0001c0003t0023a0001c0003t0167 | 5 | HG02723.hp2 HG03041.hp1 HG03579.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1995C>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 1995 | chr9 | 126698446 | |||||
chr9:126698448
|
G | A | 46 | a0001c0001t0036a0001c0001t0079a0001c0001t0121others(43): Show | 86 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(83): Show |
3_prime_UTR_variant | MODIFIER | c.*1997G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 1997 | chr9 | 126698448 | |||||
chr9:126698463
|
A | G | 1 | a0001c0004t0064 | 1 | HG01496.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2012A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 2012 | chr9 | 126698463 | |||||
chr9:126698611
|
C | T | 1 | a0001c0001t0140 | 1 | NA19091.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2160C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 2160 | chr9 | 126698611 | |||||
chr9:126698635
|
A | G | 99 | a0001c0001t0002a0001c0001t0007a0001c0001t0008others(96): Show | 151 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(148): Show |
3_prime_UTR_variant | MODIFIER | c.*2184A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 2184 | chr9 | 126698635 | |||||
chr9:126698686
|
T | G | 1 | a0001c0002t0156 | 1 | HG02523.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2235T>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 2235 | chr9 | 126698686 | |||||
chr9:126698796
|
G | A | 5 | a0001c0001t0121a0001c0003t0109a0001c0003t0110others(2): Show | 6 | HG02559.hp1 HG02717.hp2 HG02965.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2345G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 2345 | chr9 | 126698796 | |||||
chr9:126698844
|
T | C | 171 | a0001c0001t0002a0001c0001t0003a0001c0001t0007others(168): Show | 290 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(287): Show |
3_prime_UTR_variant | MODIFIER | c.*2393T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 2393 | chr9 | 126698844 | |||||
chr9:126698845
|
G | C | 87 | a0001c0001t0002a0001c0001t0007a0001c0001t0008others(84): Show | 128 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(125): Show |
3_prime_UTR_variant | MODIFIER | c.*2394G>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 2394 | chr9 | 126698845 | |||||
chr9:126699034
|
C | A | 1 | a0001c0001t0174 | 1 | HG02895.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2583C>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 2583 | chr9 | 126699034 | |||||
chr9:126699039
|
CTT | C | 71 | a0001c0001t0002a0001c0001t0007a0001c0001t0008others(68): Show | 117 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(114): Show |
3_prime_UTR_variant | MODIFIER | c.*2590_*2591delTT | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 2590 | INFO_REALIGN_3_PRIME | chr9 | 126699039 | ||||
chr9:126699101
|
G | T | 1 | a0001c0001t0060 | 1 | HG01081.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2650G>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 2650 | chr9 | 126699101 | |||||
chr9:126699126
|
C | T | 1 | a0001c0001t0176 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2675C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 2675 | chr9 | 126699126 | |||||
chr9:126699165
|
G | A | 1 | a0001c0010t0196 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2714G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 2714 | chr9 | 126699165 | |||||
chr9:126699190
|
C | A | 1 | a0001c0002t0014 | 3 | NA18984.hp1 NA19054.hp1 NA19077.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2739C>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 2739 | chr9 | 126699190 | |||||
chr9:126699231
|
G | A | 1 | a0001c0002t0158 | 1 | NA18985.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2780G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 2780 | chr9 | 126699231 | |||||
chr9:126699435
|
C | T | 61 | a0001c0001t0003a0001c0001t0007a0001c0001t0008others(58): Show | 102 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(99): Show |
3_prime_UTR_variant | MODIFIER | c.*2984C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 2984 | chr9 | 126699435 | |||||
chr9:126699633
|
A | G | 67 | a0001c0001t0003a0001c0001t0007a0001c0001t0008others(64): Show | 108 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(105): Show |
3_prime_UTR_variant | MODIFIER | c.*3182A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 3182 | chr9 | 126699633 | |||||
chr9:126699682
|
T | C | 1 | a0001c0002t0191 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3231T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 3231 | chr9 | 126699682 | |||||
chr9:126699687
|
G | A | 1 | a0001c0001t0142 | 1 | HG01978.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3236G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 3236 | chr9 | 126699687 | |||||
chr9:126699789
|
C | G | 1 | a0001c0001t0128 | 1 | HG01175.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3338C>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 3338 | chr9 | 126699789 | |||||
chr9:126699793
|
T | C | 64 | a0001c0001t0003a0001c0001t0007a0001c0001t0008others(61): Show | 103 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(100): Show |
3_prime_UTR_variant | MODIFIER | c.*3342T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 3342 | chr9 | 126699793 | |||||
chr9:126699797
|
G | A | 35 | a0001c0001t0003a0001c0001t0026a0001c0001t0039others(32): Show | 66 | HG00280.hp1 HG00323.hp2 HG00597.hp1 others(63): Show |
3_prime_UTR_variant | MODIFIER | c.*3346G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 3346 | chr9 | 126699797 | |||||
chr9:126700023
|
G | C | 1 | a0001c0003t0110 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3572G>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 3572 | chr9 | 126700023 | |||||
chr9:126700222
|
G | T | 119 | a0001c0001t0003a0001c0001t0004a0001c0001t0005others(116): Show | 218 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(215): Show |
3_prime_UTR_variant | MODIFIER | c.*3771G>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 3771 | chr9 | 126700222 | |||||
chr9:126700284
|
A | G | 120 | a0001c0001t0003a0001c0001t0004a0001c0001t0005others(117): Show | 219 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(216): Show |
3_prime_UTR_variant | MODIFIER | c.*3833A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 3833 | chr9 | 126700284 | |||||
chr9:126700315
|
T | C | 120 | a0001c0001t0003a0001c0001t0004a0001c0001t0005others(117): Show | 219 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(216): Show |
3_prime_UTR_variant | MODIFIER | c.*3864T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 3864 | chr9 | 126700315 | |||||
chr9:126700316
|
G | A | 33 | a0001c0001t0004a0001c0001t0005a0001c0001t0011others(30): Show | 61 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*3865G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 3865 | chr9 | 126700316 | |||||
chr9:126700332
|
G | T | 33 | a0001c0001t0004a0001c0001t0005a0001c0001t0011others(30): Show | 61 | HG00408.hp1 HG00558.hp1 HG00558.hp2 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*3881G>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 3881 | chr9 | 126700332 | |||||
chr9:126700408
|
C | A | 115 | a0001c0001t0003a0001c0001t0004a0001c0001t0005others(112): Show | 213 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(210): Show |
3_prime_UTR_variant | MODIFIER | c.*3957C>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 3957 | chr9 | 126700408 | |||||
chr9:126700431
|
T | A | 1 | a0001c0003t0115 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3980T>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 3980 | chr9 | 126700431 | |||||
chr9:126700463
|
C | T | 1 | a0001c0001t0126 | 1 | HG01099.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4012C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 4012 | chr9 | 126700463 | |||||
chr9:126700503
|
A | G | 1 | a0001c0001t0141 | 1 | NA18747.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4052A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 4052 | chr9 | 126700503 | |||||
chr9:126700581
|
G | A | 2 | a0001c0003t0077a0001c0003t0111 | 2 | HG02647.hp2 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4130G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 4130 | chr9 | 126700581 | |||||
chr9:126700616
|
G | A | 4 | a0001c0003t0115a0001c0004t0064a0001c0004t0187others(1): Show | 4 | HG01243.hp2 HG01496.hp2 HG03471.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4165G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 4165 | chr9 | 126700616 | |||||
chr9:126700622
|
T | C | 122 | a0001c0001t0003a0001c0001t0004a0001c0001t0005others(119): Show | 223 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(220): Show |
3_prime_UTR_variant | MODIFIER | c.*4171T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 4171 | chr9 | 126700622 | |||||
chr9:126700661
|
G | C | 1 | a0001c0009t0103 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4210G>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 4210 | chr9 | 126700661 | |||||
chr9:126700824
|
A | G | 2 | a0001c0002t0101a0001c0002t0168 | 2 | HG03225.hp2 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4373A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 8/8 | 4373 | chr9 | 126700824 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:126614787
|
G | A | 1 | a0001c0001t0137g0006 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.139+199G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 1/7 | chr9 | 126614787 | ||||||
chr9:126614797
|
C | T | 3 | a0001c0001t0018g0336a0001c0001t0018g0337a0001c0001t0149g0335 | 3 | HG00639.hp2 HG00735.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.139+209C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 1/7 | chr9 | 126614797 | ||||||
chr9:126614883
|
G | A | 60 | a0001c0001t0004g0053a0001c0001t0007g0012a0001c0001t0007g0048others(57): Show | 60 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.139+295G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 1/7 | chr9 | 126614883 | ||||||
chr9:126614956
|
C | T | 100 | a0001c0001t0002g0244a0001c0001t0002g0246a0001c0001t0002g0272others(97): Show | 101 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.139+368C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 1/7 | chr9 | 126614956 | ||||||
chr9:126615075
|
G | A | 2 | a0001c0002t0163g0066a0001c0004t0151g0065 | 2 | HG02615.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.140-308G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 1/7 | chr9 | 126615075 | ||||||
chr9:126615117
|
A | G | 44 | a0001c0001t0002g0204a0001c0001t0002g0205a0001c0001t0002g0211others(41): Show | 45 | HG00099.hp2 HG00639.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.140-266A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 1/7 | chr9 | 126615117 | ||||||
chr9:126615121
|
C | T | 1 | a0001c0001t0037g0334 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.140-262C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 1/7 | chr9 | 126615121 | ||||||
chr9:126615301
|
G | A | 1 | a0001c0003t0111g0067 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.140-82G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 1/7 | chr9 | 126615301 | ||||||
chr9:126615576
|
G | C | 67 | a0001c0001t0025g0095a0001c0001t0025g0102a0001c0001t0026g0069others(64): Show | 68 | HG00280.hp2 HG00323.hp1 HG00621.hp2 others(65): Show |
splice_region_variant&intron_variant | LOW | c.326+7G>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126615576 | ||||||
chr9:126615747
|
G | C | 291 | a0001c0001t0002g0204a0001c0001t0002g0205a0001c0001t0002g0211others(288): Show | 294 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(291): Show |
intron_variant | MODIFIER | c.326+178G>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126615747 | ||||||
chr9:126615856
|
T | C | 1 | a0001c0001t0004g0238 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.326+287T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126615856 | ||||||
chr9:126615857
|
A | G | 1 | a0001c0003t0023g0200 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.326+288A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126615857 | ||||||
chr9:126615947
|
C | T | 1 | a0001c0001t0054g0199 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.326+378C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126615947 | ||||||
chr9:126616049
|
GCCCC | G | 4 | a0001c0001t0011g0061a0001c0001t0135g0064a0001c0002t0001g0062others(1): Show | 4 | NA18942.hp2 NA18946.hp1 NA18993.hp2 others(1): Show |
intron_variant | MODIFIER | c.326+482_326+485del others(4): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126616049 | |||||
chr9:126616105
|
A | T | 100 | a0001c0001t0002g0244a0001c0001t0002g0246a0001c0001t0002g0272others(97): Show | 101 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.326+536A>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126616105 | ||||||
chr9:126616118
|
C | G | 1 | a0001c0001t0008g0333 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.326+549C>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126616118 | ||||||
chr9:126616193
|
A | G | 60 | a0001c0001t0004g0053a0001c0001t0007g0012a0001c0001t0007g0048others(57): Show | 60 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.326+624A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126616193 | ||||||
chr9:126616213
|
T | C | 1 | a0001c0001t0166g0239 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.326+644T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126616213 | ||||||
chr9:126616304
|
C | T | 5 | a0001c0001t0180g0198a0001c0002t0024g0196a0001c0002t0104g0194others(2): Show | 5 | HG01070.hp1 HG01192.hp1 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.326+735C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126616304 | ||||||
chr9:126616685
|
G | A | 60 | a0001c0001t0004g0053a0001c0001t0007g0012a0001c0001t0007g0048others(57): Show | 60 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.326+1116G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126616685 | ||||||
chr9:126616766
|
C | T | 1 | a0001c0002t0092g0133 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.326+1197C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126616766 | ||||||
chr9:126616951
|
G | C | 67 | a0001c0001t0025g0095a0001c0001t0025g0102a0001c0001t0026g0069others(64): Show | 68 | HG00280.hp2 HG00323.hp1 HG00621.hp2 others(65): Show |
intron_variant | MODIFIER | c.326+1382G>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126616951 | ||||||
chr9:126617028
|
A | G | 1 | a0001c0001t0054g0199 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.326+1459A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126617028 | ||||||
chr9:126617239
|
G | A | 44 | a0001c0001t0002g0204a0001c0001t0002g0205a0001c0001t0002g0211others(41): Show | 45 | HG00099.hp2 HG00639.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.326+1670G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126617239 | ||||||
chr9:126617277
|
G | A | 1 | a0001c0001t0085g0068 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.326+1708G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126617277 | ||||||
chr9:126617492
|
T | TA | 61 | a0001c0001t0003g0241a0001c0001t0004g0053a0001c0001t0007g0012others(58): Show | 61 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(58): Show |
intron_variant | MODIFIER | c.326+1934dupA | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126617492 | |||||
chr9:126617681
|
C | T | 3 | a0001c0002t0188g0131a0001c0003t0058g0132a0001c0003t0077g0130 | 3 | HG02109.hp1 HG03486.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.326+2112C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126617681 | ||||||
chr9:126617801
|
G | A | 1 | a0001c0003t0110g0134 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.326+2232G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126617801 | ||||||
chr9:126617829
|
C | A | 5 | a0001c0003t0167g0139a0001c0005t0012g0135a0001c0005t0012g0136others(2): Show | 5 | HG01884.hp2 HG02055.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.326+2260C>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126617829 | ||||||
chr9:126617864
|
G | A | 1 | a0001c0001t0126g0201 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.326+2295G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126617864 | ||||||
chr9:126617868
|
A | G | 1 | a0001c0001t0181g0193 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.326+2299A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126617868 | ||||||
chr9:126617904
|
C | T | 1 | a0001c0001t0007g0332 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.326+2335C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126617904 | ||||||
chr9:126617918
|
T | TG | 9 | a0001c0001t0026g0069a0001c0001t0118g0242a0001c0001t0142g0202others(6): Show | 9 | HG00741.hp2 HG01978.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.326+2355dupG | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126617918 | |||||
chr9:126618037
|
T | A | 1 | a0001c0001t0002g0244 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.326+2468T>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126618037 | ||||||
chr9:126618273
|
G | A | 1 | a0001c0001t0096g0245 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.326+2704G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126618273 | ||||||
chr9:126618653
|
G | A | 1 | a0001c0001t0068g0070 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.326+3084G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126618653 | ||||||
chr9:126619106
|
G | A | 1 | a0001c0003t0111g0067 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.326+3537G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126619106 | ||||||
chr9:126619287
|
C | A | 2 | a0001c0001t0002g0244a0001c0001t0002g0246 | 2 | HG03834.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.326+3718C>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126619287 | ||||||
chr9:126619560
|
A | G | 1 | a0001c0001t0002g0331 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.326+3991A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126619560 | ||||||
chr9:126619602
|
G | A | 1 | a0001c0002t0073g0071 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.326+4033G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126619602 | ||||||
chr9:126619772
|
G | A | 1 | a0001c0002t0021g0009 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.326+4203G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126619772 | ||||||
chr9:126619946
|
G | A | 1 | a0001c0002t0104g0194 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.326+4377G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126619946 | ||||||
chr9:126620141
|
C | T | 1 | a0001c0001t0011g0330 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.326+4572C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126620141 | ||||||
chr9:126620281
|
A | G | 29 | a0001c0001t0003g0241a0001c0001t0052g0187a0001c0001t0054g0181others(26): Show | 29 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(26): Show |
intron_variant | MODIFIER | c.326+4712A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126620281 | ||||||
chr9:126620519
|
G | A | 1 | a0001c0002t0078g0072 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.326+4950G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126620519 | ||||||
chr9:126620920
|
G | A | 166 | a0001c0001t0002g0244a0001c0001t0002g0246a0001c0001t0002g0272others(163): Show | 168 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.326+5351G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126620920 | ||||||
chr9:126621006
|
G | A | 61 | a0001c0001t0004g0053a0001c0001t0007g0012a0001c0001t0007g0048others(58): Show | 61 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(58): Show |
intron_variant | MODIFIER | c.326+5437G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126621006 | ||||||
chr9:126621063
|
GA | G | 4 | a0001c0001t0026g0069a0001c0001t0026g0129a0001c0001t0084g0128others(1): Show | 4 | NA18941.hp1 NA18953.hp1 NA19012.hp2 others(1): Show |
intron_variant | MODIFIER | c.326+5495delA | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126621063 | ||||||
chr9:126621411
|
T | C | 1 | a0001c0001t0027g0073 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.326+5842T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126621411 | ||||||
chr9:126621620
|
C | T | 14 | a0001c0001t0102g0153a0001c0002t0191g0149a0001c0002t0195g0148others(11): Show | 14 | HG00639.hp1 HG01884.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.326+6051C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126621620 | ||||||
chr9:126621621
|
G | A | 68 | a0001c0001t0025g0095a0001c0001t0025g0102a0001c0001t0026g0069others(65): Show | 69 | HG00280.hp2 HG00323.hp1 HG00621.hp2 others(66): Show |
intron_variant | MODIFIER | c.326+6052G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126621621 | ||||||
chr9:126621652
|
CTTCTTTT others(2): Show |
C | 5 | a0001c0001t0026g0129a0001c0001t0062g0124a0001c0001t0069g0125others(2): Show | 6 | HG00280.hp2 HG01167.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.326+6086_326+6094d others(11): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126621652 | |||||
chr9:126621652
|
CTTCTTTT others(3): Show |
C | 62 | a0001c0001t0025g0095a0001c0001t0025g0102a0001c0001t0026g0069others(59): Show | 62 | HG00323.hp1 HG00621.hp2 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.326+6086_326+6095d others(12): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126621652 | |||||
chr9:126621655
|
C | CT | 10 | a0001c0001t0002g0233a0001c0001t0002g0234a0001c0001t0102g0153others(7): Show | 10 | HG01069.hp2 HG01167.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.326+6112dupT | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126621655 | |||||
chr9:126621655
|
CTTTTT | C | 10 | a0001c0001t0010g0327a0001c0001t0017g0326a0001c0001t0039g0320others(7): Show | 10 | HG00597.hp1 HG02040.hp1 HG02165.hp1 others(7): Show |
intron_variant | MODIFIER | c.326+6108_326+6112d others(7): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126621655 | |||||
chr9:126621655
|
CTTTTTT | C | 87 | a0001c0001t0002g0221a0001c0001t0002g0244a0001c0001t0002g0246others(84): Show | 88 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.326+6107_326+6112d others(8): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126621655 | |||||
chr9:126621655
|
CTTTTTTT | C | 28 | a0001c0001t0002g0204a0001c0001t0002g0205a0001c0001t0002g0211others(25): Show | 29 | HG00099.hp2 HG00639.hp2 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.326+6106_326+6112d others(9): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126621655 | |||||
chr9:126621655
|
CTTTTTTT others(3): Show |
C | 82 | a0001c0001t0003g0241a0001c0001t0004g0053a0001c0001t0007g0048others(79): Show | 82 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.326+6103_326+6112d others(12): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126621655 | |||||
chr9:126621655
|
CTTTTTTT others(4): Show |
C | 4 | a0001c0001t0007g0012a0001c0001t0018g0010a0001c0002t0001g0011others(1): Show | 4 | HG01069.hp1 NA18945.hp2 NA19056.hp2 others(1): Show |
intron_variant | MODIFIER | c.326+6102_326+6112d others(13): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126621655 | |||||
chr9:126621661
|
T | C | 1 | a0001c0012t0117g0140 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.326+6092T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126621661 | ||||||
chr9:126621662
|
T | C | 5 | a0001c0001t0026g0129a0001c0001t0062g0124a0001c0001t0069g0125others(2): Show | 6 | HG00280.hp2 HG01167.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.326+6093T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126621662 | ||||||
chr9:126621663
|
T | C | 62 | a0001c0001t0025g0095a0001c0001t0025g0102a0001c0001t0026g0069others(59): Show | 62 | HG00323.hp1 HG00621.hp2 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.326+6094T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126621663 | ||||||
chr9:126621664
|
T | C | 3 | a0001c0001t0140g0249a0001c0002t0001g0247a0001c0002t0001g0248 | 3 | NA18966.hp1 NA19068.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.326+6095T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126621664 | ||||||
chr9:126621677
|
T | C | 1 | a0001c0003t0111g0067 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.326+6108T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126621677 | ||||||
chr9:126621691
|
G | C | 1 | a0001c0001t0125g0253 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.326+6122G>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126621691 | ||||||
chr9:126621703
|
A | G | 1 | a0001c0001t0002g0218 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.326+6134A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126621703 | ||||||
chr9:126621942
|
C | T | 1 | a0001c0001t0180g0198 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.326+6373C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126621942 | ||||||
chr9:126621943
|
C | T | 1 | a0001c0002t0013g0123 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.326+6374C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126621943 | ||||||
chr9:126622168
|
C | T | 7 | a0001c0001t0036g0227a0001c0001t0121g0230a0001c0001t0123g0236others(4): Show | 7 | HG00735.hp1 HG02818.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.326+6599C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126622168 | ||||||
chr9:126622511
|
G | A | 1 | a0001c0003t0110g0134 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.326+6942G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126622511 | ||||||
chr9:126622530
|
C | T | 1 | a0001c0002t0106g0144 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.326+6961C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126622530 | ||||||
chr9:126622690
|
C | T | 2 | a0001c0001t0002g0221a0001c0001t0097g0217 | 2 | HG02080.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.326+7121C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126622690 | ||||||
chr9:126623171
|
G | A | 15 | a0001c0001t0034g0021a0001c0001t0034g0060a0001c0001t0134g0019others(12): Show | 15 | HG00438.hp1 HG02015.hp2 HG02027.hp2 others(12): Show |
intron_variant | MODIFIER | c.326+7602G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126623171 | ||||||
chr9:126623174
|
G | A | 2 | a0001c0002t0056g0157a0001c0002t0057g0156 | 2 | HG02559.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.326+7605G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126623174 | ||||||
chr9:126623304
|
G | C | 1 | a0001c0003t0109g0254 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.326+7735G>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126623304 | ||||||
chr9:126623391
|
T | C | 321 | a0001c0001t0002g0204a0001c0001t0002g0205a0001c0001t0002g0211others(318): Show | 324 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(321): Show |
intron_variant | MODIFIER | c.326+7822T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126623391 | ||||||
chr9:126623545
|
T | C | 2 | a0001c0001t0037g0004a0001c0001t0133g0004 | 2 | NA19005.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.326+7976T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126623545 | ||||||
chr9:126623752
|
ACCT | A | 44 | a0001c0001t0002g0204a0001c0001t0002g0205a0001c0001t0002g0211others(41): Show | 45 | HG00099.hp2 HG00639.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.326+8188_326+8190d others(5): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126623752 | |||||
chr9:126623764
|
C | T | 61 | a0001c0001t0004g0053a0001c0001t0007g0012a0001c0001t0007g0048others(58): Show | 61 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(58): Show |
intron_variant | MODIFIER | c.326+8195C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126623764 | ||||||
chr9:126623796
|
G | T | 4 | a0001c0003t0023g0169a0001c0003t0023g0171a0001c0003t0023g0200others(1): Show | 4 | HG03041.hp1 HG03579.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.326+8227G>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126623796 | ||||||
chr9:126623850
|
G | A | 1 | a0001c0001t0062g0124 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.326+8281G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126623850 | ||||||
chr9:126623907
|
A | G | 77 | a0001c0001t0002g0204a0001c0001t0002g0205a0001c0001t0002g0211others(74): Show | 78 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(75): Show |
intron_variant | MODIFIER | c.326+8338A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126623907 | ||||||
chr9:126623966
|
G | C | 1 | a0001c0001t0081g0074 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.326+8397G>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126623966 | ||||||
chr9:126623969
|
T | C | 1 | a0001c0001t0145g0231 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.326+8400T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126623969 | ||||||
chr9:126624062
|
G | A | 4 | a0001c0002t0101g0141a0001c0002t0106g0144a0001c0008t0033g0142others(1): Show | 4 | HG02717.hp2 HG03209.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.326+8493G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126624062 | ||||||
chr9:126624196
|
G | A | 1 | a0001c0001t0051g0075 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.326+8627G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126624196 | ||||||
chr9:126624346
|
C | T | 166 | a0001c0001t0002g0244a0001c0001t0002g0246a0001c0001t0002g0272others(163): Show | 168 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.326+8777C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126624346 | ||||||
chr9:126624352
|
G | A | 1 | a0001c0001t0147g0255 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.326+8783G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126624352 | ||||||
chr9:126624485
|
G | T | 1 | a0001c0001t0028g0122 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.326+8916G>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126624485 | ||||||
chr9:126624499
|
T | C | 20 | a0001c0001t0002g0272a0001c0001t0004g0259a0001c0001t0004g0260others(17): Show | 20 | HG00408.hp1 HG00597.hp1 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.326+8930T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126624499 | ||||||
chr9:126624581
|
C | T | 67 | a0001c0001t0025g0095a0001c0001t0025g0102a0001c0001t0026g0069others(64): Show | 68 | HG00280.hp2 HG00323.hp1 HG00621.hp2 others(65): Show |
intron_variant | MODIFIER | c.326+9012C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126624581 | ||||||
chr9:126624652
|
T | G | 1 | a0001c0001t0051g0075 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.326+9083T>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126624652 | ||||||
chr9:126624663
|
C | T | 321 | a0001c0001t0002g0204a0001c0001t0002g0205a0001c0001t0002g0211others(318): Show | 324 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(321): Show |
intron_variant | MODIFIER | c.326+9094C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126624663 | ||||||
chr9:126624666
|
GT | G | 307 | a0001c0001t0002g0204a0001c0001t0002g0205a0001c0001t0002g0211others(304): Show | 310 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(307): Show |
intron_variant | MODIFIER | c.326+9110delT | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126624666 | |||||
chr9:126624683
|
T | C | 1 | a0001c0001t0002g0273 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.326+9114T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126624683 | ||||||
chr9:126624985
|
C | G | 4 | a0001c0002t0101g0141a0001c0002t0106g0144a0001c0008t0033g0142others(1): Show | 4 | HG02717.hp2 HG03209.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.326+9416C>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126624985 | ||||||
chr9:126625044
|
C | T | 3 | a0001c0002t0188g0131a0001c0003t0058g0132a0001c0003t0077g0130 | 3 | HG02109.hp1 HG03486.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.326+9475C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126625044 | ||||||
chr9:126625062
|
C | G | 1 | a0001c0001t0177g0120 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.326+9493C>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126625062 | ||||||
chr9:126625108
|
T | C | 1 | a0001c0003t0023g0169 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.326+9539T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126625108 | ||||||
chr9:126625224
|
T | C | 4 | a0001c0001t0002g0204a0001c0001t0002g0205a0001c0001t0128g0206others(1): Show | 4 | HG00099.hp2 HG01074.hp1 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.326+9655T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126625224 | ||||||
chr9:126625493
|
G | A | 1 | a0001c0001t0027g0076 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.326+9924G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126625493 | ||||||
chr9:126625754
|
C | A | 28 | a0001c0001t0003g0241a0001c0001t0052g0187a0001c0001t0054g0181others(25): Show | 28 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(25): Show |
intron_variant | MODIFIER | c.326+10185C>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126625754 | ||||||
chr9:126625757
|
C | G | 1 | a0001c0001t0083g0119 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.326+10188C>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126625757 | ||||||
chr9:126625947
|
G | C | 1 | a0001c0002t0101g0141 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.326+10378G>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126625947 | ||||||
chr9:126626129
|
T | C | 2 | a0001c0009t0103g0145a0001c0010t0196g0146 | 2 | HG02145.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.326+10560T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126626129 | ||||||
chr9:126626389
|
C | A | 1 | a0001c0001t0008g0005 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.326+10820C>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126626389 | ||||||
chr9:126626435
|
A | G | 1 | a0001c0003t0110g0134 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.326+10866A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126626435 | ||||||
chr9:126626783
|
C | A | 2 | a0001c0007t0048g0252a0001c0007t0048g0312 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.326+11214C>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126626783 | ||||||
chr9:126627183
|
A | AC | 15 | a0001c0001t0034g0021a0001c0001t0034g0060a0001c0001t0134g0019others(12): Show | 15 | HG00438.hp1 HG02015.hp2 HG02027.hp2 others(12): Show |
intron_variant | MODIFIER | c.326+11620dupC | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126627183 | |||||
chr9:126627431
|
C | T | 321 | a0001c0001t0002g0204a0001c0001t0002g0205a0001c0001t0002g0211others(318): Show | 324 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(321): Show |
intron_variant | MODIFIER | c.326+11862C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126627431 | ||||||
chr9:126627449
|
C | T | 2 | a0001c0002t0024g0189a0001c0002t0194g0192 | 2 | HG02738.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.326+11880C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126627449 | ||||||
chr9:126627555
|
G | A | 1 | a0001c0001t0005g0274 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.326+11986G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126627555 | ||||||
chr9:126627556
|
C | A | 1 | a0001c0001t0005g0274 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.326+11987C>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126627556 | ||||||
chr9:126628056
|
G | T | 2 | a0001c0002t0056g0157a0001c0002t0057g0156 | 2 | HG02559.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.326+12487G>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126628056 | ||||||
chr9:126628080
|
A | C | 2 | a0001c0007t0048g0252a0001c0007t0048g0312 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.326+12511A>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126628080 | ||||||
chr9:126628170
|
G | T | 1 | a0001c0003t0049g0158 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.326+12601G>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126628170 | ||||||
chr9:126628229
|
G | C | 1 | a0001c0001t0149g0335 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.326+12660G>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126628229 | ||||||
chr9:126628492
|
G | A | 1 | a0001c0001t0035g0003 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.326+12923G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126628492 | ||||||
chr9:126628521
|
C | T | 68 | a0001c0001t0025g0095a0001c0001t0025g0102a0001c0001t0026g0069others(65): Show | 69 | HG00280.hp2 HG00323.hp1 HG00621.hp2 others(66): Show |
intron_variant | MODIFIER | c.326+12952C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126628521 | ||||||
chr9:126628627
|
C | T | 1 | a0001c0001t0135g0064 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.326+13058C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126628627 | ||||||
chr9:126628956
|
C | T | 1 | a0001c0001t0166g0239 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.326+13387C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126628956 | ||||||
chr9:126628993
|
TA | T | 312 | a0001c0001t0002g0204a0001c0001t0002g0205a0001c0001t0002g0211others(309): Show | 315 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(312): Show |
intron_variant | MODIFIER | c.326+13437delA | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126628993 | |||||
chr9:126629086
|
A | G | 1 | a0001c0001t0149g0335 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.326+13517A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126629086 | ||||||
chr9:126629259
|
C | T | 29 | a0001c0001t0003g0241a0001c0001t0052g0187a0001c0001t0054g0181others(26): Show | 29 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(26): Show |
intron_variant | MODIFIER | c.326+13690C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126629259 | ||||||
chr9:126629405
|
G | A | 4 | a0001c0002t0101g0141a0001c0002t0106g0144a0001c0008t0033g0142others(1): Show | 4 | HG02717.hp2 HG03209.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.326+13836G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126629405 | ||||||
chr9:126629583
|
A | ATG | 29 | a0001c0001t0003g0241a0001c0001t0052g0187a0001c0001t0054g0181others(26): Show | 29 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(26): Show |
intron_variant | MODIFIER | c.326+14015_326+1401 others(6): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126629583 | |||||
chr9:126629589
|
G | C | 5 | a0001c0002t0101g0141a0001c0002t0106g0144a0001c0003t0110g0134others(2): Show | 5 | HG02717.hp2 HG03209.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.326+14020G>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126629589 | ||||||
chr9:126629692
|
T | C | 2 | a0001c0001t0102g0153a0001c0003t0049g0147 | 2 | HG00639.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.326+14123T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126629692 | ||||||
chr9:126629697
|
G | A | 1 | a0001c0001t0125g0253 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.326+14128G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126629697 | ||||||
chr9:126629962
|
G | A | 14 | a0001c0001t0102g0153a0001c0002t0191g0149a0001c0002t0195g0148others(11): Show | 14 | HG00639.hp1 HG01884.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.326+14393G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126629962 | ||||||
chr9:126630086
|
C | T | 39 | a0001c0001t0025g0102a0001c0001t0026g0069a0001c0001t0026g0129others(36): Show | 39 | HG00323.hp1 HG00621.hp2 HG00738.hp2 others(36): Show |
intron_variant | MODIFIER | c.326+14517C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126630086 | ||||||
chr9:126630161
|
C | CA | 22 | a0001c0001t0011g0061a0001c0001t0020g0256a0001c0001t0020g0313others(19): Show | 22 | HG00621.hp1 HG00639.hp1 HG01168.hp1 others(19): Show |
intron_variant | MODIFIER | c.326+14611dupA | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126630161 | |||||
chr9:126630161
|
C | CAA | 101 | a0001c0001t0002g0204a0001c0001t0002g0205a0001c0001t0002g0211others(98): Show | 102 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.326+14610_326+1461 others(6): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126630161 | |||||
chr9:126630286
|
C | G | 1 | a0001c0012t0117g0140 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.326+14717C>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126630286 | ||||||
chr9:126630512
|
C | T | 1 | a0001c0002t0193g0188 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.326+14943C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126630512 | ||||||
chr9:126630636
|
T | G | 1 | a0001c0002t0001g0062 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.326+15067T>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126630636 | ||||||
chr9:126630901
|
G | A | 1 | a0001c0002t0195g0148 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.326+15332G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126630901 | ||||||
chr9:126631073
|
G | A | 6 | a0001c0001t0181g0193a0001c0003t0023g0169a0001c0003t0023g0171others(3): Show | 6 | HG01109.hp2 HG03041.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.326+15504G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126631073 | ||||||
chr9:126631153
|
C | T | 1 | a0001c0001t0004g0271 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.326+15584C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126631153 | ||||||
chr9:126631224
|
A | G | 14 | a0001c0001t0102g0153a0001c0002t0191g0149a0001c0002t0195g0148others(11): Show | 14 | HG00639.hp1 HG01884.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.326+15655A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126631224 | ||||||
chr9:126631345
|
G | A | 1 | a0001c0003t0110g0134 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.326+15776G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126631345 | ||||||
chr9:126631386
|
G | A | 1 | a0001c0003t0110g0134 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.326+15817G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126631386 | ||||||
chr9:126631509
|
G | A | 60 | a0001c0001t0007g0012a0001c0001t0007g0048a0001c0001t0008g0030others(57): Show | 60 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.326+15940G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126631509 | ||||||
chr9:126631509
|
G | T | 1 | a0001c0003t0167g0139 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.326+15940G>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126631509 | ||||||
chr9:126631510
|
G | C | 1 | a0001c0003t0167g0139 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.326+15941G>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126631510 | ||||||
chr9:126631512
|
C | T | 1 | a0001c0003t0167g0139 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.326+15943C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126631512 | ||||||
chr9:126631516
|
C | T | 60 | a0001c0001t0007g0012a0001c0001t0007g0048a0001c0001t0008g0030others(57): Show | 60 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.326+15947C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126631516 | ||||||
chr9:126631517
|
G | A | 1 | a0001c0002t0013g0175 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.326+15948G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126631517 | ||||||
chr9:126631518
|
GGATGGGG others(1160): Show |
G | 1 | a0001c0002t0013g0175 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.326+15950_326+1711 others(4): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126631518 | ||||||
chr9:126631763
|
A | C | 1 | a0001c0002t0108g0025 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.326+16194A>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126631763 | ||||||
chr9:126631772
|
G | A | 60 | a0001c0001t0007g0012a0001c0001t0007g0048a0001c0001t0008g0030others(57): Show | 60 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.326+16203G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126631772 | ||||||
chr9:126632139
|
C | T | 1 | a0001c0001t0002g0218 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.326+16570C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126632139 | ||||||
chr9:126632304
|
G | A | 1 | a0001c0002t0193g0188 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.326+16735G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126632304 | ||||||
chr9:126632650
|
G | A | 1 | a0001c0001t0197g0222 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.326+17081G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126632650 | ||||||
chr9:126632687
|
A | T | 1 | a0001c0002t0013g0175 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.326+17118A>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126632687 | ||||||
chr9:126632691
|
G | A | 1 | a0001c0002t0013g0175 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.326+17122G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126632691 | ||||||
chr9:126632721
|
C | T | 1 | a0001c0003t0110g0134 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.326+17152C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126632721 | ||||||
chr9:126632788
|
G | T | 2 | a0001c0001t0008g0051a0001c0002t0001g0052 | 2 | HG00597.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.326+17219G>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126632788 | ||||||
chr9:126633067
|
C | T | 217 | a0001c0001t0002g0204a0001c0001t0002g0205a0001c0001t0002g0211others(214): Show | 219 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.326+17498C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126633067 | ||||||
chr9:126633084
|
C | G | 2 | a0001c0001t0059g0084a0001c0001t0079g0085 | 2 | HG02965.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.326+17515C>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126633084 | ||||||
chr9:126633285
|
T | C | 217 | a0001c0001t0002g0204a0001c0001t0002g0205a0001c0001t0002g0211others(214): Show | 219 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.326+17716T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126633285 | ||||||
chr9:126633374
|
C | T | 1 | a0001c0001t0007g0328 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.326+17805C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126633374 | ||||||
chr9:126633639
|
A | G | 1 | a0001c0001t0038g0311 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.326+18070A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126633639 | ||||||
chr9:126633758
|
A | G | 217 | a0001c0001t0002g0204a0001c0001t0002g0205a0001c0001t0002g0211others(214): Show | 219 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.326+18189A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126633758 | ||||||
chr9:126633890
|
C | T | 1 | a0001c0002t0013g0175 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.326+18321C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126633890 | ||||||
chr9:126633913
|
G | A | 1 | a0001c0002t0016g0015 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.326+18344G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126633913 | ||||||
chr9:126633986
|
C | G | 217 | a0001c0001t0002g0204a0001c0001t0002g0205a0001c0001t0002g0211others(214): Show | 219 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.326+18417C>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126633986 | ||||||
chr9:126634062
|
G | C | 3 | a0001c0001t0011g0314a0001c0001t0019g0316a0001c0001t0099g0315 | 3 | NA18984.hp2 NA19006.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.326+18493G>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126634062 | ||||||
chr9:126634129
|
C | T | 217 | a0001c0001t0002g0204a0001c0001t0002g0205a0001c0001t0002g0211others(214): Show | 219 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.326+18560C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126634129 | ||||||
chr9:126634155
|
G | A | 138 | a0001c0001t0002g0204a0001c0001t0002g0205a0001c0001t0002g0211others(135): Show | 139 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.326+18586G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126634155 | ||||||
chr9:126634184
|
G | A | 1 | a0001c0001t0082g0097 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.326+18615G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126634184 | ||||||
chr9:126634342
|
C | T | 1 | a0001c0001t0008g0333 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.326+18773C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126634342 | ||||||
chr9:126634444
|
G | A | 1 | a0001c0001t0002g0246 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.326+18875G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126634444 | ||||||
chr9:126634451
|
C | T | 217 | a0001c0001t0002g0204a0001c0001t0002g0205a0001c0001t0002g0211others(214): Show | 219 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.326+18882C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126634451 | ||||||
chr9:126634453
|
T | C | 1 | a0001c0002t0032g0013 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.326+18884T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126634453 | ||||||
chr9:126634514
|
C | T | 3 | a0001c0002t0056g0157a0001c0002t0057g0156a0001c0002t0191g0149 | 3 | HG02559.hp2 HG02572.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.326+18945C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126634514 | ||||||
chr9:126634546
|
A | G | 1 | a0001c0012t0117g0140 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.326+18977A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126634546 | ||||||
chr9:126634602
|
A | AC | 66 | a0001c0001t0025g0095a0001c0001t0025g0102a0001c0001t0026g0069others(63): Show | 67 | HG00280.hp2 HG00323.hp1 HG00621.hp2 others(64): Show |
intron_variant | MODIFIER | c.326+19041dupC | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126634602 | |||||
chr9:126634603
|
C | A | 8 | a0001c0001t0102g0153a0001c0002t0195g0148a0001c0003t0049g0147others(5): Show | 8 | HG00639.hp1 HG02145.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.326+19034C>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126634603 | ||||||
chr9:126634608
|
C | A | 1 | a0001c0003t0115g0207 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.326+19039C>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126634608 | ||||||
chr9:126634610
|
C | A | 3 | a0001c0001t0005g0278a0001c0002t0001g0321a0001c0002t0047g0277 | 3 | NA18942.hp1 NA18971.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.326+19041C>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126634610 | ||||||
chr9:126634735
|
C | T | 79 | a0001c0001t0025g0095a0001c0001t0025g0102a0001c0001t0026g0069others(76): Show | 80 | HG00280.hp2 HG00323.hp1 HG00621.hp2 others(77): Show |
intron_variant | MODIFIER | c.326+19166C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126634735 | ||||||
chr9:126634755
|
C | T | 17 | a0001c0001t0010g0251a0001c0001t0010g0309a0001c0001t0010g0319others(14): Show | 17 | HG00558.hp1 HG02027.hp1 HG02040.hp1 others(14): Show |
intron_variant | MODIFIER | c.326+19186C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126634755 | ||||||
chr9:126634821
|
G | A | 1 | a0001c0002t0088g0098 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.326+19252G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126634821 | ||||||
chr9:126635285
|
G | A | 1 | a0001c0002t0057g0156 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.326+19716G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126635285 | ||||||
chr9:126635476
|
G | A | 48 | a0001c0001t0002g0204a0001c0001t0002g0205a0001c0001t0002g0211others(45): Show | 49 | HG00099.hp2 HG00639.hp2 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.326+19907G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126635476 | ||||||
chr9:126635525
|
G | A | 1 | a0001c0002t0152g0026 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.326+19956G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126635525 | ||||||
chr9:126635529
|
G | A | 5 | a0001c0001t0102g0153a0001c0002t0195g0148a0001c0003t0049g0147others(2): Show | 5 | HG00639.hp1 HG02145.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.326+19960G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126635529 | ||||||
chr9:126635683
|
G | A | 2 | a0001c0002t0046g0250a0001c0004t0151g0065 | 2 | HG02886.hp1 NA18953.hp2 |
intron_variant | MODIFIER | c.326+20114G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126635683 | ||||||
chr9:126635684
|
C | G | 1 | a0001c0002t0046g0250 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.326+20115C>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126635684 | ||||||
chr9:126635824
|
A | G | 60 | a0001c0001t0007g0012a0001c0001t0007g0048a0001c0001t0008g0030others(57): Show | 60 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.326+20255A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126635824 | ||||||
chr9:126635979
|
A | T | 1 | a0001c0002t0014g0118 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.326+20410A>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126635979 | ||||||
chr9:126636057
|
CT | C | 117 | a0001c0001t0002g0244a0001c0001t0002g0246a0001c0001t0002g0272others(114): Show | 118 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(115): Show |
intron_variant | MODIFIER | c.326+20489delT | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126636057 | ||||||
chr9:126636251
|
A | G | 118 | a0001c0001t0002g0244a0001c0001t0002g0246a0001c0001t0002g0272others(115): Show | 119 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.326+20682A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126636251 | ||||||
chr9:126636280
|
T | C | 5 | a0001c0001t0002g0244a0001c0001t0002g0246a0001c0001t0038g0280others(2): Show | 5 | HG00099.hp1 HG01168.hp2 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.326+20711T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126636280 | ||||||
chr9:126636292
|
C | T | 60 | a0001c0001t0007g0012a0001c0001t0007g0048a0001c0001t0008g0030others(57): Show | 60 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.326+20723C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126636292 | ||||||
chr9:126636406
|
T | A | 1 | a0001c0002t0046g0250 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.326+20837T>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126636406 | ||||||
chr9:126636710
|
G | A | 1 | a0001c0001t0002g0218 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.326+21141G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126636710 | ||||||
chr9:126636772
|
A | G | 1 | a0001c0002t0001g0063 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.326+21203A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126636772 | ||||||
chr9:126636801
|
G | A | 5 | a0001c0001t0002g0244a0001c0001t0002g0246a0001c0001t0038g0280others(2): Show | 5 | HG00099.hp1 HG01168.hp2 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.326+21232G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126636801 | ||||||
chr9:126637065
|
A | G | 1 | a0001c0001t0004g0238 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.326+21496A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126637065 | ||||||
chr9:126637176
|
G | GTGCTCTG others(5): Show |
1 | a0001c0001t0051g0167 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.326+21607_326+2160 others(16): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126637176 | ||||||
chr9:126637179
|
A | C | 1 | a0001c0001t0051g0167 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.326+21610A>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126637179 | ||||||
chr9:126637195
|
G | A | 1 | a0001c0001t0040g0322 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.326+21626G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126637195 | ||||||
chr9:126637283
|
A | G | 121 | a0001c0001t0002g0244a0001c0001t0002g0246a0001c0001t0002g0272others(118): Show | 122 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.326+21714A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126637283 | ||||||
chr9:126637383
|
G | A | 121 | a0001c0001t0002g0244a0001c0001t0002g0246a0001c0001t0002g0272others(118): Show | 122 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.326+21814G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126637383 | ||||||
chr9:126637575
|
G | A | 1 | a0001c0001t0002g0223 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.326+22006G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126637575 | ||||||
chr9:126637591
|
A | G | 121 | a0001c0001t0002g0244a0001c0001t0002g0246a0001c0001t0002g0272others(118): Show | 122 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.326+22022A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126637591 | ||||||
chr9:126637598
|
G | A | 1 | a0001c0002t0193g0188 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.326+22029G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126637598 | ||||||
chr9:126637749
|
T | C | 298 | a0001c0001t0002g0223a0001c0001t0002g0244a0001c0001t0002g0246others(295): Show | 300 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(297): Show |
intron_variant | MODIFIER | c.326+22180T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126637749 | ||||||
chr9:126637763
|
G | A | 3 | a0001c0001t0011g0314a0001c0001t0019g0316a0001c0001t0099g0315 | 3 | NA18984.hp2 NA19006.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.326+22194G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126637763 | ||||||
chr9:126637822
|
T | TC | 64 | a0001c0001t0002g0211a0001c0001t0002g0233a0001c0001t0005g0212others(61): Show | 64 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.326+22264dupC | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126637822 | |||||
chr9:126637822
|
TC | T | 120 | a0001c0001t0002g0244a0001c0001t0002g0246a0001c0001t0002g0272others(117): Show | 121 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(118): Show |
intron_variant | MODIFIER | c.326+22264delC | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126637822 | |||||
chr9:126637829
|
C | G | 1 | a0001c0001t0126g0201 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.326+22260C>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126637829 | ||||||
chr9:126637916
|
C | T | 1 | a0001c0001t0098g0318 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.326+22347C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126637916 | ||||||
chr9:126637943
|
C | A | 121 | a0001c0001t0002g0244a0001c0001t0002g0246a0001c0001t0002g0272others(118): Show | 122 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.326+22374C>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126637943 | ||||||
chr9:126637970
|
C | T | 6 | a0001c0003t0110g0134a0001c0003t0167g0139a0001c0005t0012g0135others(3): Show | 6 | HG01884.hp2 HG02055.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.326+22401C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126637970 | ||||||
chr9:126637979
|
G | T | 2 | a0001c0001t0059g0084a0001c0001t0079g0085 | 2 | HG02965.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.326+22410G>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126637979 | ||||||
chr9:126638015
|
C | T | 6 | a0001c0003t0110g0134a0001c0003t0167g0139a0001c0005t0012g0135others(3): Show | 6 | HG01884.hp2 HG02055.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.326+22446C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126638015 | ||||||
chr9:126638168
|
G | A | 27 | a0001c0001t0003g0241a0001c0001t0052g0187a0001c0001t0054g0199others(24): Show | 27 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(24): Show |
intron_variant | MODIFIER | c.326+22599G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126638168 | ||||||
chr9:126638209
|
G | A | 2 | a0001c0002t0001g0062a0001c0002t0001g0063 | 2 | NA18946.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.326+22640G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126638209 | ||||||
chr9:126638335
|
C | T | 1 | a0001c0002t0191g0149 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.326+22766C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126638335 | ||||||
chr9:126638572
|
T | C | 8 | a0001c0001t0004g0259a0001c0001t0004g0260a0001c0001t0004g0261others(5): Show | 8 | NA18941.hp2 NA18943.hp2 NA18962.hp1 others(5): Show |
intron_variant | MODIFIER | c.326+23003T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126638572 | ||||||
chr9:126639184
|
T | C | 1 | a0001c0001t0004g0238 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.326+23615T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126639184 | ||||||
chr9:126639271
|
C | T | 67 | a0001c0001t0002g0223a0001c0001t0025g0095a0001c0001t0025g0102others(64): Show | 68 | HG00323.hp1 HG00621.hp2 HG00642.hp2 others(65): Show |
intron_variant | MODIFIER | c.326+23702C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126639271 | ||||||
chr9:126639290
|
A | C | 124 | a0001c0001t0002g0244a0001c0001t0002g0246a0001c0001t0002g0272others(121): Show | 126 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.326+23721A>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126639290 | ||||||
chr9:126639313
|
C | T | 1 | a0001c0002t0152g0026 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.326+23744C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126639313 | ||||||
chr9:126639465
|
C | G | 1 | a0001c0001t0004g0270 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.326+23896C>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126639465 | ||||||
chr9:126639475
|
G | A | 4 | a0001c0002t0101g0141a0001c0002t0106g0144a0001c0008t0033g0142others(1): Show | 4 | HG02717.hp2 HG03209.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.326+23906G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126639475 | ||||||
chr9:126639620
|
C | T | 1 | a0001c0002t0089g0117 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.326+24051C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126639620 | ||||||
chr9:126639700
|
G | T | 2 | a0001c0001t0122g0276a0001c0001t0147g0255 | 2 | HG02886.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.326+24131G>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126639700 | ||||||
chr9:126640064
|
A | C | 1 | a0001c0001t0084g0128 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.326+24495A>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126640064 | ||||||
chr9:126640184
|
C | T | 300 | a0001c0001t0002g0223a0001c0001t0002g0244a0001c0001t0002g0246others(297): Show | 303 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(300): Show |
intron_variant | MODIFIER | c.326+24615C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126640184 | ||||||
chr9:126640288
|
G | A | 117 | a0001c0001t0002g0244a0001c0001t0002g0246a0001c0001t0002g0272others(114): Show | 119 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.326+24719G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126640288 | ||||||
chr9:126640438
|
A | T | 124 | a0001c0001t0002g0244a0001c0001t0002g0246a0001c0001t0002g0272others(121): Show | 126 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.326+24869A>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126640438 | ||||||
chr9:126640615
|
C | T | 1 | a0001c0001t0084g0128 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.326+25046C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126640615 | ||||||
chr9:126640690
|
G | A | 3 | a0001c0001t0002g0204a0001c0001t0002g0205a0001c0001t0128g0206 | 3 | HG00099.hp2 HG01175.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.326+25121G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126640690 | ||||||
chr9:126640694
|
C | A | 1 | a0001c0001t0084g0128 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.326+25125C>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126640694 | ||||||
chr9:126640926
|
A | C | 1 | a0001c0011t0086g0077 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.326+25357A>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126640926 | ||||||
chr9:126640928
|
G | A | 1 | a0001c0001t0054g0199 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.326+25359G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126640928 | ||||||
chr9:126641162
|
A | G | 1 | a0001c0001t0084g0128 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.326+25593A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126641162 | ||||||
chr9:126641163
|
G | A | 1 | a0001c0001t0084g0128 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.326+25594G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126641163 | ||||||
chr9:126641180
|
C | G | 1 | a0001c0003t0023g0169 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.326+25611C>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126641180 | ||||||
chr9:126641260
|
A | G | 1 | a0001c0004t0036g0235 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.326+25691A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126641260 | ||||||
chr9:126641359
|
A | G | 1 | a0001c0002t0191g0149 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.326+25790A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126641359 | ||||||
chr9:126641570
|
C | G | 1 | a0001c0001t0028g0089 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.326+26001C>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126641570 | ||||||
chr9:126641605
|
C | T | 1 | a0001c0001t0002g0234 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.326+26036C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126641605 | ||||||
chr9:126641817
|
T | C | 1 | a0001c0001t0130g0237 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.326+26248T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126641817 | ||||||
chr9:126641827
|
C | T | 1 | a0001c0001t0174g0079 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.326+26258C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126641827 | ||||||
chr9:126641830
|
G | A | 124 | a0001c0001t0002g0244a0001c0001t0002g0246a0001c0001t0002g0272others(121): Show | 126 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.326+26261G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126641830 | ||||||
chr9:126642003
|
C | A | 6 | a0001c0001t0102g0153a0001c0002t0195g0148a0001c0003t0049g0147others(3): Show | 6 | HG00639.hp1 HG02145.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.326+26434C>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126642003 | ||||||
chr9:126642176
|
C | T | 1 | a0001c0001t0126g0201 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.326+26607C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126642176 | ||||||
chr9:126642246
|
T | A | 337 | a0001c0001t0002g0204a0001c0001t0002g0205a0001c0001t0002g0211others(334): Show | 340 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(337): Show |
intron_variant | MODIFIER | c.326+26677T>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126642246 | ||||||
chr9:126642253
|
G | A | 1 | a0001c0002t0024g0196 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.326+26684G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126642253 | ||||||
chr9:126642254
|
C | A | 1 | a0001c0002t0024g0196 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.326+26685C>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126642254 | ||||||
chr9:126642400
|
C | T | 1 | a0001c0001t0039g0320 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.326+26831C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126642400 | ||||||
chr9:126642401
|
G | A | 2 | a0001c0001t0007g0012a0001c0002t0003g0038 | 2 | NA18962.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.326+26832G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126642401 | ||||||
chr9:126642417
|
C | A | 2 | a0001c0009t0103g0145a0001c0010t0196g0146 | 2 | HG02145.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.326+26848C>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126642417 | ||||||
chr9:126642543
|
G | A | 3 | a0001c0004t0042g0209a0001c0004t0042g0210a0001c0004t0146g0213 | 3 | HG03225.hp1 HG03453.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.326+26974G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126642543 | ||||||
chr9:126642601
|
T | G | 1 | a0001c0002t0190g0155 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.326+27032T>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126642601 | ||||||
chr9:126642619
|
G | A | 1 | a0001c0002t0024g0174 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.326+27050G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126642619 | ||||||
chr9:126642657
|
T | A | 1 | a0001c0001t0002g0221 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.326+27088T>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126642657 | ||||||
chr9:126642725
|
T | C | 123 | a0001c0001t0002g0244a0001c0001t0002g0246a0001c0001t0002g0272others(120): Show | 125 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.326+27156T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126642725 | ||||||
chr9:126642911
|
G | A | 1 | a0001c0001t0002g0211 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.326+27342G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126642911 | ||||||
chr9:126642949
|
C | G | 1 | a0001c0001t0124g0225 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.326+27380C>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126642949 | ||||||
chr9:126643326
|
G | A | 1 | a0001c0012t0117g0140 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.326+27757G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126643326 | ||||||
chr9:126643466
|
G | A | 1 | a0001c0003t0167g0139 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.326+27897G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126643466 | ||||||
chr9:126643484
|
G | A | 1 | a0001c0001t0197g0222 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.326+27915G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126643484 | ||||||
chr9:126643510
|
A | G | 123 | a0001c0001t0002g0244a0001c0001t0002g0246a0001c0001t0002g0272others(120): Show | 125 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.326+27941A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126643510 | ||||||
chr9:126643584
|
G | A | 1 | a0001c0001t0120g0219 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.326+28015G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126643584 | ||||||
chr9:126643600
|
C | A | 1 | a0001c0002t0006g0182 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.326+28031C>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126643600 | ||||||
chr9:126643805
|
C | T | 3 | a0001c0002t0163g0066a0001c0003t0113g0220a0001c0004t0151g0065 | 3 | HG02615.hp1 HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.326+28236C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126643805 | ||||||
chr9:126643820
|
T | C | 122 | a0001c0001t0002g0244a0001c0001t0002g0246a0001c0001t0002g0272others(119): Show | 124 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.326+28251T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126643820 | ||||||
chr9:126643885
|
C | A | 1 | a0001c0001t0005g0274 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.326+28316C>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126643885 | ||||||
chr9:126643898
|
C | T | 1 | a0001c0001t0175g0166 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.326+28329C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126643898 | ||||||
chr9:126644154
|
C | T | 4 | a0001c0002t0024g0189a0001c0002t0045g0208a0001c0002t0045g0216others(1): Show | 4 | HG01168.hp1 HG01169.hp2 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.326+28585C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126644154 | ||||||
chr9:126644365
|
T | C | 41 | a0001c0001t0003g0241a0001c0001t0052g0187a0001c0001t0054g0181others(38): Show | 41 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(38): Show |
intron_variant | MODIFIER | c.326+28796T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126644365 | ||||||
chr9:126644591
|
G | A | 1 | a0001c0002t0001g0007 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.326+29022G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126644591 | ||||||
chr9:126644640
|
G | C | 41 | a0001c0001t0003g0241a0001c0001t0052g0187a0001c0001t0054g0181others(38): Show | 41 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(38): Show |
intron_variant | MODIFIER | c.326+29071G>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126644640 | ||||||
chr9:126644647
|
T | G | 122 | a0001c0001t0002g0244a0001c0001t0002g0246a0001c0001t0002g0272others(119): Show | 124 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.326+29078T>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126644647 | ||||||
chr9:126644670
|
GCCGAGTG others(4): Show |
G | 1 | a0001c0003t0110g0134 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.326+29103_326+2911 others(15): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126644670 | |||||
chr9:126644710
|
C | A | 122 | a0001c0001t0002g0244a0001c0001t0002g0246a0001c0001t0002g0272others(119): Show | 124 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.326+29141C>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126644710 | ||||||
chr9:126644730
|
G | T | 1 | a0001c0002t0191g0149 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.326+29161G>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126644730 | ||||||
chr9:126644840
|
C | A | 7 | a0001c0003t0110g0134a0001c0003t0167g0139a0001c0005t0012g0135others(4): Show | 7 | HG01884.hp2 HG02055.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.326+29271C>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126644840 | ||||||
chr9:126644988
|
G | A | 5 | a0001c0001t0037g0004a0001c0001t0037g0334a0001c0001t0133g0004others(2): Show | 5 | HG02074.hp1 NA18973.hp2 NA19005.hp2 others(2): Show |
intron_variant | MODIFIER | c.326+29419G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126644988 | ||||||
chr9:126645014
|
C | T | 55 | a0001c0001t0002g0272a0001c0001t0002g0273a0001c0001t0002g0296others(52): Show | 57 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.326+29445C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126645014 | ||||||
chr9:126645221
|
G | A | 14 | a0001c0001t0054g0181a0001c0001t0102g0153a0001c0001t0183g0154others(11): Show | 14 | HG00639.hp1 HG02145.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.326+29652G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126645221 | ||||||
chr9:126645264
|
G | A | 36 | a0001c0001t0002g0204a0001c0001t0002g0205a0001c0001t0002g0211others(33): Show | 36 | HG00099.hp2 HG00639.hp2 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.326+29695G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126645264 | ||||||
chr9:126645292
|
C | CA | 75 | a0001c0001t0002g0272a0001c0001t0002g0273a0001c0001t0002g0296others(72): Show | 77 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.326+29724dupA | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126645292 | |||||
chr9:126645560
|
C | G | 1 | a0001c0003t0109g0254 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.326+29991C>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126645560 | ||||||
chr9:126645657
|
C | T | 1 | a0001c0001t0175g0166 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.326+30088C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126645657 | ||||||
chr9:126645801
|
C | G | 13 | a0001c0001t0002g0317a0001c0001t0007g0288a0001c0001t0008g0333others(10): Show | 13 | HG02071.hp2 HG03139.hp2 HG03927.hp1 others(10): Show |
intron_variant | MODIFIER | c.326+30232C>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126645801 | ||||||
chr9:126645801
|
C | T | 1 | a0001c0003t0167g0139 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.326+30232C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126645801 | ||||||
chr9:126645887
|
C | T | 1 | a0001c0002t0152g0026 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.326+30318C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126645887 | ||||||
chr9:126645888
|
G | A | 1 | a0001c0012t0117g0140 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.326+30319G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126645888 | ||||||
chr9:126646011
|
C | T | 176 | a0001c0001t0002g0211a0001c0001t0002g0223a0001c0001t0003g0241others(173): Show | 177 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(174): Show |
intron_variant | MODIFIER | c.326+30442C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126646011 | ||||||
chr9:126646086
|
G | A | 1 | a0001c0003t0110g0134 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.326+30517G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126646086 | ||||||
chr9:126646152
|
C | T | 1 | a0001c0002t0009g0116 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.326+30583C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126646152 | ||||||
chr9:126646166
|
G | C | 302 | a0001c0001t0002g0211a0001c0001t0002g0223a0001c0001t0002g0244others(299): Show | 305 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(302): Show |
intron_variant | MODIFIER | c.326+30597G>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126646166 | ||||||
chr9:126646234
|
G | A | 135 | a0001c0001t0002g0211a0001c0001t0002g0223a0001c0001t0007g0012others(132): Show | 136 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(133): Show |
intron_variant | MODIFIER | c.326+30665G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126646234 | ||||||
chr9:126646317
|
TATCCATC others(13): Show |
T | 126 | a0001c0001t0002g0244a0001c0001t0002g0246a0001c0001t0002g0272others(123): Show | 128 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.326+30774_326+3079 others(24): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126646317 | |||||
chr9:126646323
|
T | C | 14 | a0001c0001t0054g0181a0001c0001t0102g0153a0001c0001t0183g0154others(11): Show | 14 | HG00639.hp1 HG02145.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.326+30754T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126646323 | ||||||
chr9:126646373
|
C | T | 112 | a0001c0001t0002g0244a0001c0001t0002g0246a0001c0001t0002g0272others(109): Show | 114 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.326+30804C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126646373 | ||||||
chr9:126646403
|
C | CCCAT | 74 | a0001c0001t0002g0211a0001c0001t0002g0223a0001c0001t0011g0214others(71): Show | 75 | HG00280.hp2 HG00323.hp1 HG00621.hp2 others(72): Show |
intron_variant | MODIFIER | c.326+30854_326+3085 others(8): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126646403 | |||||
chr9:126646712
|
T | G | 4 | a0001c0002t0101g0141a0001c0002t0106g0144a0001c0008t0033g0142others(1): Show | 4 | HG02717.hp2 HG03209.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.326+31143T>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126646712 | ||||||
chr9:126646722
|
A | G | 62 | a0001c0001t0007g0012a0001c0001t0007g0048a0001c0001t0008g0030others(59): Show | 62 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.326+31153A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126646722 | ||||||
chr9:126646783
|
C | A | 63 | a0001c0001t0007g0012a0001c0001t0007g0048a0001c0001t0008g0030others(60): Show | 63 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.326+31214C>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126646783 | ||||||
chr9:126646838
|
G | A | 49 | a0001c0001t0002g0211a0001c0001t0002g0221a0001c0001t0011g0214others(46): Show | 50 | HG00621.hp2 HG00642.hp2 HG00738.hp2 others(47): Show |
intron_variant | MODIFIER | c.326+31269G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126646838 | ||||||
chr9:126646896
|
A | AG | 24 | a0001c0001t0002g0221a0001c0001t0026g0069a0001c0001t0026g0129others(21): Show | 25 | HG00621.hp2 HG01070.hp2 HG01074.hp1 others(22): Show |
intron_variant | MODIFIER | c.326+31332dupG | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126646896 | |||||
chr9:126646919
|
T | C | 76 | a0001c0001t0002g0211a0001c0001t0002g0218a0001c0001t0002g0221others(73): Show | 77 | HG00323.hp1 HG00621.hp2 HG00639.hp1 others(74): Show |
intron_variant | MODIFIER | c.326+31350T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126646919 | ||||||
chr9:126646919
|
T | G | 1 | a0001c0001t0053g0161 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.326+31350T>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126646919 | ||||||
chr9:126646950
|
G | A | 2 | a0001c0001t0067g0121a0001c0001t0068g0070 | 2 | HG03942.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.326+31381G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126646950 | ||||||
chr9:126647059
|
A | G | 5 | a0001c0005t0012g0135a0001c0005t0012g0136a0001c0005t0012g0137others(2): Show | 5 | HG01884.hp2 HG02055.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.326+31490A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126647059 | ||||||
chr9:126647111
|
C | A | 10 | a0001c0001t0051g0167a0001c0001t0052g0164a0001c0001t0053g0161others(7): Show | 10 | HG01109.hp1 HG02258.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.326+31542C>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126647111 | ||||||
chr9:126647289
|
C | A | 2 | a0001c0007t0048g0252a0001c0007t0048g0312 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.326+31720C>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126647289 | ||||||
chr9:126647418
|
C | G | 2 | a0001c0001t0037g0334a0001c0002t0003g0307 | 2 | NA18973.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.326+31849C>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126647418 | ||||||
chr9:126647783
|
A | C | 258 | a0001c0001t0002g0211a0001c0001t0002g0221a0001c0001t0002g0223others(255): Show | 261 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(258): Show |
intron_variant | MODIFIER | c.326+32214A>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126647783 | ||||||
chr9:126648165
|
C | G | 2 | a0001c0001t0026g0069a0001c0001t0026g0129 | 2 | NA18953.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.326+32596C>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126648165 | ||||||
chr9:126648315
|
C | T | 224 | a0001c0001t0002g0211a0001c0001t0002g0221a0001c0001t0002g0244others(221): Show | 227 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(224): Show |
intron_variant | MODIFIER | c.326+32746C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126648315 | ||||||
chr9:126648328
|
G | A | 1 | a0001c0001t0174g0079 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.326+32759G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126648328 | ||||||
chr9:126648573
|
G | A | 114 | a0001c0001t0002g0272a0001c0001t0002g0273a0001c0001t0002g0296others(111): Show | 116 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.326+33004G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126648573 | ||||||
chr9:126648639
|
G | A | 26 | a0001c0001t0003g0241a0001c0001t0052g0187a0001c0001t0180g0198others(23): Show | 26 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(23): Show |
intron_variant | MODIFIER | c.326+33070G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126648639 | ||||||
chr9:126648811
|
T | G | 2 | a0001c0001t0026g0069a0001c0001t0026g0129 | 2 | NA18953.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.326+33242T>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126648811 | ||||||
chr9:126648963
|
C | A | 26 | a0001c0001t0003g0241a0001c0001t0052g0187a0001c0001t0180g0198others(23): Show | 26 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(23): Show |
intron_variant | MODIFIER | c.326+33394C>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126648963 | ||||||
chr9:126648985
|
C | T | 1 | a0001c0001t0121g0230 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.326+33416C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126648985 | ||||||
chr9:126649159
|
C | T | 2 | a0001c0002t0056g0157a0001c0002t0057g0156 | 2 | HG02559.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.326+33590C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126649159 | ||||||
chr9:126649160
|
G | A | 65 | a0001c0001t0002g0223a0001c0001t0003g0241a0001c0001t0051g0075others(62): Show | 65 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(62): Show |
intron_variant | MODIFIER | c.326+33591G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126649160 | ||||||
chr9:126649282
|
T | A | 1 | a0001c0001t0144g0282 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.326+33713T>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126649282 | ||||||
chr9:126649362
|
A | G | 1 | a0001c0002t0001g0286 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.326+33793A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126649362 | ||||||
chr9:126649787
|
T | C | 1 | a0001c0001t0061g0101 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.326+34218T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126649787 | ||||||
chr9:126649824
|
C | T | 1 | a0001c0003t0110g0134 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.326+34255C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126649824 | ||||||
chr9:126649854
|
C | T | 219 | a0001c0001t0002g0211a0001c0001t0002g0221a0001c0001t0002g0244others(216): Show | 222 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(219): Show |
intron_variant | MODIFIER | c.326+34285C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126649854 | ||||||
chr9:126649958
|
T | G | 1 | a0001c0001t0061g0101 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.326+34389T>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126649958 | ||||||
chr9:126649960
|
T | C | 10 | a0001c0001t0051g0167a0001c0001t0052g0164a0001c0001t0053g0161others(7): Show | 10 | HG01109.hp1 HG02258.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.326+34391T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126649960 | ||||||
chr9:126649997
|
A | G | 1 | a0001c0002t0022g0049 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.326+34428A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126649997 | ||||||
chr9:126650100
|
A | C | 9 | a0001c0002t0191g0149a0001c0003t0167g0139a0001c0005t0012g0135others(6): Show | 9 | HG01884.hp2 HG02055.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.326+34531A>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126650100 | ||||||
chr9:126650252
|
A | G | 1 | a0001c0002t0001g0024 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.326+34683A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126650252 | ||||||
chr9:126650267
|
C | T | 104 | a0001c0001t0002g0272a0001c0001t0002g0273a0001c0001t0002g0296others(101): Show | 106 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.326+34698C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126650267 | ||||||
chr9:126650351
|
C | T | 45 | a0001c0001t0002g0211a0001c0001t0002g0221a0001c0001t0002g0244others(42): Show | 46 | HG00558.hp2 HG00621.hp2 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.326+34782C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126650351 | ||||||
chr9:126650598
|
C | T | 1 | a0001c0001t0131g0229 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.326+35029C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126650598 | ||||||
chr9:126650631
|
C | T | 2 | a0001c0001t0002g0233a0001c0001t0107g0232 | 2 | HG02647.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.326+35062C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126650631 | ||||||
chr9:126650643
|
C | G | 1 | a0001c0003t0167g0139 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.326+35074C>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126650643 | ||||||
chr9:126650659
|
A | G | 222 | a0001c0001t0002g0223a0001c0001t0002g0272a0001c0001t0002g0273others(219): Show | 224 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(221): Show |
intron_variant | MODIFIER | c.326+35090A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126650659 | ||||||
chr9:126650703
|
G | A | 1 | a0001c0001t0082g0097 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.326+35134G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126650703 | ||||||
chr9:126650734
|
C | T | 1 | a0001c0002t0191g0149 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.326+35165C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126650734 | ||||||
chr9:126650798
|
C | T | 1 | a0001c0012t0117g0140 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.326+35229C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126650798 | ||||||
chr9:126650930
|
G | A | 30 | a0001c0001t0003g0241a0001c0001t0102g0153a0001c0001t0180g0198others(27): Show | 30 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.326+35361G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126650930 | ||||||
chr9:126651019
|
C | T | 157 | a0001c0001t0002g0211a0001c0001t0002g0221a0001c0001t0002g0223others(154): Show | 159 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.326+35450C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126651019 | ||||||
chr9:126651203
|
C | T | 2 | a0001c0002t0003g0243a0001c0002t0003g0284 | 2 | NA18975.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.326+35634C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126651203 | ||||||
chr9:126651211
|
C | T | 266 | a0001c0001t0002g0211a0001c0001t0002g0221a0001c0001t0002g0223others(263): Show | 269 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(266): Show |
intron_variant | MODIFIER | c.326+35642C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126651211 | ||||||
chr9:126651296
|
C | CT | 17 | a0001c0001t0003g0241a0001c0001t0180g0198a0001c0002t0006g0182others(14): Show | 17 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(14): Show |
intron_variant | MODIFIER | c.326+35728dupT | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126651296 | |||||
chr9:126651299
|
G | T | 9 | a0001c0001t0102g0153a0001c0001t0183g0154a0001c0002t0055g0176others(6): Show | 9 | HG02145.hp1 HG02280.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.326+35730G>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126651299 | ||||||
chr9:126651317
|
T | G | 2 | a0001c0001t0080g0099a0001c0002t0089g0117 | 2 | HG01106.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.326+35748T>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126651317 | ||||||
chr9:126651399
|
A | G | 236 | a0001c0001t0002g0211a0001c0001t0002g0221a0001c0001t0002g0223others(233): Show | 239 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.326+35830A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126651399 | ||||||
chr9:126651417
|
G | A | 37 | a0001c0001t0002g0221a0001c0001t0002g0244a0001c0001t0002g0246others(34): Show | 38 | HG00621.hp2 HG00738.hp2 HG01070.hp2 others(35): Show |
intron_variant | MODIFIER | c.326+35848G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126651417 | ||||||
chr9:126651496
|
T | C | 2 | a0001c0002t0001g0247a0001c0002t0001g0248 | 2 | NA18966.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.326+35927T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126651496 | ||||||
chr9:126651647
|
G | A | 2 | a0001c0002t0001g0247a0001c0002t0001g0248 | 2 | NA18966.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.326+36078G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126651647 | ||||||
chr9:126651718
|
C | T | 2 | a0001c0004t0186g0081a0001c0004t0187g0083 | 2 | HG01243.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.326+36149C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126651718 | ||||||
chr9:126651854
|
G | A | 2 | a0001c0005t0012g0135a0001c0005t0012g0136 | 2 | HG02055.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.326+36285G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126651854 | ||||||
chr9:126651890
|
G | T | 249 | a0001c0001t0002g0211a0001c0001t0002g0221a0001c0001t0002g0223others(246): Show | 252 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(249): Show |
intron_variant | MODIFIER | c.326+36321G>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126651890 | ||||||
chr9:126652000
|
T | TG | 168 | a0001c0001t0002g0211a0001c0001t0002g0221a0001c0001t0002g0223others(165): Show | 171 | HG00099.hp1 HG00408.hp2 HG00558.hp1 others(168): Show |
intron_variant | MODIFIER | c.326+36440dupG | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126652000 | |||||
chr9:126652009
|
G | T | 1 | a0001c0005t0169g0152 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.326+36440G>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126652009 | ||||||
chr9:126652024
|
G | T | 8 | a0001c0002t0006g0182a0001c0002t0006g0184a0001c0002t0006g0185others(5): Show | 8 | HG00280.hp1 HG00323.hp2 HG00741.hp1 others(5): Show |
intron_variant | MODIFIER | c.326+36455G>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126652024 | ||||||
chr9:126652045
|
C | T | 180 | a0001c0001t0002g0211a0001c0001t0002g0221a0001c0001t0002g0233others(177): Show | 183 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(180): Show |
intron_variant | MODIFIER | c.326+36476C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126652045 | ||||||
chr9:126652164
|
A | G | 1 | a0001c0002t0091g0094 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.326+36595A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126652164 | ||||||
chr9:126652230
|
C | T | 1 | a0001c0001t0041g0324 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.326+36661C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126652230 | ||||||
chr9:126652231
|
G | A | 31 | a0001c0001t0002g0244a0001c0001t0002g0246a0001c0001t0007g0012others(28): Show | 32 | HG00621.hp2 HG01070.hp2 HG01074.hp2 others(29): Show |
intron_variant | MODIFIER | c.326+36662G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126652231 | ||||||
chr9:126652296
|
A | AGG | 123 | a0001c0001t0002g0211a0001c0001t0002g0221a0001c0001t0002g0223others(120): Show | 124 | HG00099.hp1 HG00558.hp1 HG00558.hp2 others(121): Show |
intron_variant | MODIFIER | c.326+36736_326+3673 others(6): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126652296 | |||||
chr9:126652298
|
G | T | 1 | a0001c0002t0047g0047 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.326+36729G>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126652298 | ||||||
chr9:126652304
|
G | C | 2 | a0001c0003t0049g0147a0001c0003t0049g0158 | 2 | HG00639.hp1 HG01109.hp2 |
intron_variant | MODIFIER | c.326+36735G>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126652304 | ||||||
chr9:126652304
|
G | T | 2 | a0001c0001t0119g0293a0001c0001t0144g0282 | 2 | HG02083.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.326+36735G>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126652304 | ||||||
chr9:126652391
|
G | T | 4 | a0001c0001t0002g0223a0001c0001t0145g0231a0001c0001t0172g0163others(1): Show | 4 | HG01496.hp2 HG02818.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.326+36822G>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126652391 | ||||||
chr9:126652453
|
G | A | 50 | a0001c0001t0003g0241a0001c0001t0027g0073a0001c0001t0052g0187others(47): Show | 50 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.326+36884G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126652453 | ||||||
chr9:126652534
|
T | C | 9 | a0001c0002t0188g0131a0001c0003t0058g0132a0001c0003t0077g0130others(6): Show | 9 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.326+36965T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126652534 | ||||||
chr9:126652650
|
G | A | 71 | a0001c0001t0008g0030a0001c0001t0008g0051a0001c0001t0011g0061others(68): Show | 71 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.326+37081G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126652650 | ||||||
chr9:126652659
|
G | A | 50 | a0001c0001t0027g0073a0001c0001t0052g0187a0001c0001t0066g0114others(47): Show | 50 | HG00639.hp1 HG00738.hp2 HG01074.hp1 others(47): Show |
intron_variant | MODIFIER | c.326+37090G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126652659 | ||||||
chr9:126652780
|
G | A | 2 | a0001c0001t0180g0198a0001c0002t0104g0194 | 2 | HG01192.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.326+37211G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126652780 | ||||||
chr9:126652790
|
G | A | 1 | a0001c0010t0196g0146 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.326+37221G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126652790 | ||||||
chr9:126652868
|
A | G | 1 | a0001c0002t0057g0156 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.326+37299A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126652868 | ||||||
chr9:126652873
|
G | A | 1 | a0001c0003t0109g0254 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.326+37304G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126652873 | ||||||
chr9:126652888
|
C | T | 3 | a0001c0004t0042g0209a0001c0004t0042g0210a0001c0004t0146g0213 | 3 | HG03225.hp1 HG03453.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.326+37319C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126652888 | ||||||
chr9:126652889
|
G | A | 1 | a0001c0002t0160g0323 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.326+37320G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126652889 | ||||||
chr9:126653088
|
C | T | 1 | a0001c0001t0007g0332 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.326+37519C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126653088 | ||||||
chr9:126653142
|
C | CT | 37 | a0001c0001t0002g0218a0001c0001t0002g0272a0001c0001t0002g0296others(34): Show | 37 | HG00597.hp1 HG00621.hp1 HG01074.hp1 others(34): Show |
intron_variant | MODIFIER | c.326+37601dupT | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126653142 | |||||
chr9:126653142
|
CT | C | 46 | a0001c0001t0004g0261a0001c0001t0004g0270a0001c0001t0005g0278others(43): Show | 46 | HG00280.hp1 HG00609.hp1 HG00738.hp1 others(43): Show |
intron_variant | MODIFIER | c.326+37601delT | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126653142 | |||||
chr9:126653142
|
CTT | C | 93 | a0001c0001t0002g0244a0001c0001t0002g0246a0001c0001t0007g0012others(90): Show | 94 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.326+37600_326+3760 others(6): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126653142 | |||||
chr9:126653142
|
CTTT | C | 14 | a0001c0001t0069g0125a0001c0001t0081g0074a0001c0001t0143g0279others(11): Show | 14 | HG00280.hp2 HG00323.hp1 HG01069.hp1 others(11): Show |
intron_variant | MODIFIER | c.326+37599_326+3760 others(7): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126653142 | |||||
chr9:126653142
|
CTTTTTTT others(3): Show |
C | 1 | a0001c0002t0057g0156 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.326+37592_326+3760 others(14): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126653142 | |||||
chr9:126653142
|
CTTTTTTT others(5): Show |
C | 1 | a0001c0002t0191g0149 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.326+37590_326+3760 others(16): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126653142 | |||||
chr9:126653143
|
T | C | 1 | a0001c0001t0149g0335 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.326+37574T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126653143 | ||||||
chr9:126653155
|
T | C | 1 | a0001c0002t0191g0149 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.326+37586T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126653155 | ||||||
chr9:126653195
|
C | T | 34 | a0001c0001t0002g0244a0001c0001t0002g0246a0001c0001t0007g0012others(31): Show | 35 | HG00621.hp2 HG01070.hp2 HG01074.hp2 others(32): Show |
intron_variant | MODIFIER | c.326+37626C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126653195 | ||||||
chr9:126653198
|
G | A | 1 | a0001c0012t0117g0140 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.326+37629G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126653198 | ||||||
chr9:126653198
|
G | C | 1 | a0001c0010t0196g0146 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.326+37629G>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126653198 | ||||||
chr9:126653255
|
C | T | 1 | a0001c0002t0072g0087 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.327-37581C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126653255 | ||||||
chr9:126653280
|
G | A | 35 | a0001c0001t0002g0244a0001c0001t0002g0246a0001c0001t0007g0012others(32): Show | 36 | HG00621.hp2 HG01070.hp2 HG01074.hp2 others(33): Show |
intron_variant | MODIFIER | c.327-37556G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126653280 | ||||||
chr9:126653397
|
C | T | 65 | a0001c0001t0003g0241a0001c0001t0027g0073a0001c0001t0052g0187others(62): Show | 65 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.327-37439C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126653397 | ||||||
chr9:126653491
|
G | A | 1 | a0001c0010t0196g0146 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.327-37345G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126653491 | ||||||
chr9:126653496
|
A | G | 69 | a0001c0001t0008g0030a0001c0001t0008g0051a0001c0001t0011g0061others(66): Show | 69 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.327-37340A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126653496 | ||||||
chr9:126653524
|
A | C | 4 | a0001c0002t0003g0243a0001c0002t0003g0284a0001c0002t0003g0292others(1): Show | 4 | NA18960.hp1 NA18975.hp1 NA19084.hp1 others(1): Show |
intron_variant | MODIFIER | c.327-37312A>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126653524 | ||||||
chr9:126653642
|
G | A | 2 | a0001c0002t0022g0028a0001c0002t0022g0049 | 2 | NA18954.hp2 NA18961.hp2 |
intron_variant | MODIFIER | c.327-37194G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126653642 | ||||||
chr9:126653742
|
C | T | 1 | a0001c0001t0120g0219 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.327-37094C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126653742 | ||||||
chr9:126653747
|
C | G | 1 | a0001c0001t0120g0219 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.327-37089C>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126653747 | ||||||
chr9:126653934
|
T | C | 66 | a0001c0001t0003g0241a0001c0001t0027g0073a0001c0001t0052g0187others(63): Show | 66 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.327-36902T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126653934 | ||||||
chr9:126654038
|
C | T | 27 | a0001c0001t0003g0241a0001c0001t0102g0153a0001c0001t0180g0198others(24): Show | 27 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(24): Show |
intron_variant | MODIFIER | c.327-36798C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126654038 | ||||||
chr9:126654294
|
C | G | 1 | a0001c0003t0109g0254 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.327-36542C>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126654294 | ||||||
chr9:126654415
|
T | C | 1 | a0001c0002t0031g0002 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.327-36421T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126654415 | ||||||
chr9:126654571
|
A | G | 65 | a0001c0001t0003g0241a0001c0001t0027g0073a0001c0001t0052g0187others(62): Show | 65 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.327-36265A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126654571 | ||||||
chr9:126654700
|
C | G | 1 | a0001c0012t0117g0140 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.327-36136C>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126654700 | ||||||
chr9:126655159
|
T | C | 1 | a0001c0005t0170g0170 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.327-35677T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126655159 | ||||||
chr9:126655243
|
A | G | 66 | a0001c0001t0003g0241a0001c0001t0027g0073a0001c0001t0052g0187others(63): Show | 66 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.327-35593A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126655243 | ||||||
chr9:126655272
|
C | T | 1 | a0001c0010t0196g0146 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.327-35564C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126655272 | ||||||
chr9:126655302
|
C | T | 1 | a0001c0003t0110g0134 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.327-35534C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126655302 | ||||||
chr9:126655367
|
A | G | 66 | a0001c0001t0003g0241a0001c0001t0027g0073a0001c0001t0052g0187others(63): Show | 66 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.327-35469A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126655367 | ||||||
chr9:126655375
|
TG | T | 22 | a0001c0001t0027g0073a0001c0001t0052g0187a0001c0001t0066g0114others(19): Show | 22 | HG00639.hp1 HG00738.hp2 HG01074.hp1 others(19): Show |
intron_variant | MODIFIER | c.327-35456delG | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126655375 | |||||
chr9:126655452
|
T | G | 77 | a0001c0001t0003g0241a0001c0001t0007g0012a0001c0001t0027g0073others(74): Show | 77 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(74): Show |
intron_variant | MODIFIER | c.327-35384T>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126655452 | ||||||
chr9:126655494
|
G | A | 1 | a0001c0004t0182g0078 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.327-35342G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126655494 | ||||||
chr9:126655530
|
G | C | 65 | a0001c0001t0003g0241a0001c0001t0027g0073a0001c0001t0052g0187others(62): Show | 65 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.327-35306G>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126655530 | ||||||
chr9:126655745
|
T | C | 5 | a0001c0005t0012g0135a0001c0005t0012g0136a0001c0005t0012g0137others(2): Show | 5 | HG01884.hp2 HG02055.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.327-35091T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126655745 | ||||||
chr9:126655770
|
T | C | 182 | a0001c0001t0002g0244a0001c0001t0002g0246a0001c0001t0003g0241others(179): Show | 183 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.327-35066T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126655770 | ||||||
chr9:126655877
|
G | A | 65 | a0001c0001t0003g0241a0001c0001t0027g0073a0001c0001t0052g0187others(62): Show | 65 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.327-34959G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126655877 | ||||||
chr9:126656000
|
G | A | 1 | a0001c0012t0117g0140 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.327-34836G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126656000 | ||||||
chr9:126656074
|
A | G | 1 | a0001c0002t0057g0156 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.327-34762A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126656074 | ||||||
chr9:126656081
|
G | A | 64 | a0001c0001t0003g0241a0001c0001t0027g0073a0001c0001t0066g0114others(61): Show | 64 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.327-34755G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126656081 | ||||||
chr9:126656124
|
A | G | 1 | a0001c0010t0196g0146 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.327-34712A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126656124 | ||||||
chr9:126656146
|
A | T | 2 | a0001c0001t0051g0167a0001c0001t0175g0166 | 2 | HG02280.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.327-34690A>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126656146 | ||||||
chr9:126656169
|
A | G | 16 | a0001c0001t0003g0241a0001c0001t0180g0198a0001c0002t0006g0182others(13): Show | 16 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(13): Show |
intron_variant | MODIFIER | c.327-34667A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126656169 | ||||||
chr9:126656178
|
A | AT | 4 | a0001c0002t0101g0141a0001c0002t0168g0180a0001c0008t0033g0142others(1): Show | 4 | HG02717.hp2 HG03209.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.327-34652dupT | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126656178 | |||||
chr9:126656271
|
C | T | 36 | a0001c0001t0002g0244a0001c0001t0002g0246a0001c0001t0011g0330others(33): Show | 37 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(34): Show |
intron_variant | MODIFIER | c.327-34565C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126656271 | ||||||
chr9:126656381
|
CT | C | 3 | a0001c0001t0004g0262a0001c0001t0008g0333a0001c0001t0084g0128 | 3 | NA18941.hp1 NA18970.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.327-34452delT | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126656381 | |||||
chr9:126656383
|
T | TTAGA | 46 | a0001c0001t0002g0272a0001c0001t0005g0285a0001c0001t0005g0300others(43): Show | 46 | HG00738.hp2 HG01074.hp2 HG01106.hp1 others(43): Show |
intron_variant | MODIFIER | c.327-34401_327-3439 others(8): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126656383 | |||||
chr9:126656383
|
T | TTAGATAG others(1): Show |
12 | a0001c0001t0035g0003a0001c0001t0038g0280a0001c0001t0059g0084others(9): Show | 13 | HG00099.hp1 HG00609.hp2 HG01257.hp2 others(10): Show |
intron_variant | MODIFIER | c.327-34405_327-3439 others(12): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126656383 | |||||
chr9:126656383
|
TTAGA | T | 86 | a0001c0001t0002g0205a0001c0001t0002g0218a0001c0001t0002g0223others(83): Show | 86 | HG00323.hp1 HG00558.hp1 HG00642.hp1 others(83): Show |
intron_variant | MODIFIER | c.327-34401_327-3439 others(8): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126656383 | |||||
chr9:126656383
|
TTAGATAG others(1): Show |
T | 29 | a0001c0001t0002g0317a0001c0001t0004g0260a0001c0001t0007g0288others(26): Show | 29 | HG00639.hp1 HG00738.hp1 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.327-34405_327-3439 others(12): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126656383 | |||||
chr9:126656383
|
TTAGATAG others(5): Show |
T | 13 | a0001c0001t0002g0244a0001c0001t0002g0246a0001c0001t0025g0095others(10): Show | 13 | HG00280.hp1 HG00323.hp2 HG00642.hp2 others(10): Show |
intron_variant | MODIFIER | c.327-34409_327-3439 others(16): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126656383 | |||||
chr9:126656383
|
TTAGATAG others(9): Show |
T | 13 | a0001c0001t0002g0273a0001c0001t0003g0241a0001c0001t0029g0112others(10): Show | 13 | HG00438.hp1 HG00609.hp1 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.327-34413_327-3439 others(20): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126656383 | |||||
chr9:126656383
|
TTAGATAG others(13): Show |
T | 6 | a0001c0001t0007g0048a0001c0001t0020g0256a0001c0001t0025g0102others(3): Show | 6 | HG00558.hp2 HG02071.hp1 HG02083.hp2 others(3): Show |
intron_variant | MODIFIER | c.327-34417_327-3439 others(24): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126656383 | |||||
chr9:126656474
|
C | G | 1 | a0001c0010t0196g0146 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.327-34362C>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126656474 | ||||||
chr9:126656688
|
C | T | 1 | a0001c0006t0116g0228 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.327-34148C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126656688 | ||||||
chr9:126656746
|
G | A | 69 | a0001c0001t0008g0030a0001c0001t0008g0051a0001c0001t0011g0061others(66): Show | 69 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.327-34090G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126656746 | ||||||
chr9:126656778
|
C | CCTAT | 4 | a0001c0001t0003g0241a0001c0002t0013g0175a0001c0002t0013g0177others(1): Show | 4 | HG00738.hp1 HG00741.hp2 HG02602.hp2 others(1): Show |
intron_variant | MODIFIER | c.327-34057_327-3405 others(8): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126656778 | |||||
chr9:126656851
|
C | T | 1 | a0001c0001t0175g0166 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.327-33985C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126656851 | ||||||
chr9:126657011
|
T | C | 100 | a0001c0001t0002g0244a0001c0001t0002g0246a0001c0001t0003g0241others(97): Show | 101 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(98): Show |
intron_variant | MODIFIER | c.327-33825T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126657011 | ||||||
chr9:126657126
|
C | A | 1 | a0001c0012t0117g0140 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.327-33710C>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126657126 | ||||||
chr9:126657144
|
T | C | 1 | a0001c0001t0002g0331 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.327-33692T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126657144 | ||||||
chr9:126657145
|
G | T | 1 | a0001c0001t0004g0260 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.327-33691G>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126657145 | ||||||
chr9:126657146
|
A | G | 1 | a0001c0001t0004g0260 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.327-33690A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126657146 | ||||||
chr9:126657244
|
G | A | 37 | a0001c0001t0002g0244a0001c0001t0002g0246a0001c0001t0005g0300others(34): Show | 38 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(35): Show |
intron_variant | MODIFIER | c.327-33592G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126657244 | ||||||
chr9:126657445
|
C | T | 1 | a0001c0002t0009g0104 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.327-33391C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126657445 | ||||||
chr9:126657530
|
G | T | 27 | a0001c0001t0003g0241a0001c0001t0102g0153a0001c0001t0180g0198others(24): Show | 27 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(24): Show |
intron_variant | MODIFIER | c.327-33306G>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126657530 | ||||||
chr9:126657683
|
C | T | 1 | a0001c0001t0053g0161 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.327-33153C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126657683 | ||||||
chr9:126657711
|
A | G | 109 | a0001c0001t0002g0244a0001c0001t0002g0246a0001c0001t0003g0241others(106): Show | 110 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.327-33125A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126657711 | ||||||
chr9:126657746
|
C | T | 69 | a0001c0001t0008g0030a0001c0001t0008g0051a0001c0001t0011g0061others(66): Show | 69 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.327-33090C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126657746 | ||||||
chr9:126657956
|
C | T | 2 | a0001c0001t0096g0245a0001c0001t0118g0242 | 2 | HG03688.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.327-32880C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126657956 | ||||||
chr9:126657962
|
A | C | 67 | a0001c0001t0003g0241a0001c0001t0027g0073a0001c0001t0066g0114others(64): Show | 67 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.327-32874A>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126657962 | ||||||
chr9:126657962
|
A | T | 4 | a0001c0002t0188g0131a0001c0003t0058g0132a0001c0003t0077g0130others(1): Show | 4 | HG02109.hp1 HG02647.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.327-32874A>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126657962 | ||||||
chr9:126657976
|
G | A | 1 | a0001c0010t0196g0146 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.327-32860G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126657976 | ||||||
chr9:126658037
|
G | A | 1 | a0001c0001t0065g0086 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.327-32799G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126658037 | ||||||
chr9:126658055
|
T | C | 72 | a0001c0001t0003g0241a0001c0001t0027g0073a0001c0001t0066g0114others(69): Show | 72 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(69): Show |
intron_variant | MODIFIER | c.327-32781T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126658055 | ||||||
chr9:126658219
|
G | C | 3 | a0001c0001t0002g0204a0001c0001t0002g0205a0001c0001t0128g0206 | 3 | HG00099.hp2 HG01175.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.327-32617G>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126658219 | ||||||
chr9:126658357
|
G | A | 81 | a0001c0001t0003g0241a0001c0001t0027g0073a0001c0001t0027g0076others(78): Show | 81 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(78): Show |
intron_variant | MODIFIER | c.327-32479G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126658357 | ||||||
chr9:126658380
|
C | T | 1 | a0001c0001t0011g0330 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.327-32456C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126658380 | ||||||
chr9:126658381
|
C | T | 1 | a0001c0001t0011g0330 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.327-32455C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126658381 | ||||||
chr9:126658390
|
C | T | 5 | a0001c0002t0101g0141a0001c0002t0168g0180a0001c0008t0033g0142others(2): Show | 5 | HG02717.hp2 HG03209.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.327-32446C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126658390 | ||||||
chr9:126658396
|
C | CG | 54 | a0001c0001t0008g0051a0001c0001t0034g0021a0001c0001t0034g0060others(51): Show | 54 | HG00323.hp1 HG00438.hp1 HG00597.hp2 others(51): Show |
intron_variant | MODIFIER | c.327-32437dupG | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126658396 | |||||
chr9:126658407
|
G | C | 47 | a0001c0001t0008g0051a0001c0001t0034g0021a0001c0001t0034g0060others(44): Show | 47 | HG00323.hp1 HG00438.hp1 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.327-32429G>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126658407 | ||||||
chr9:126658452
|
C | G | 6 | a0001c0001t0051g0167a0001c0001t0052g0164a0001c0001t0053g0161others(3): Show | 6 | HG01109.hp1 HG02258.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.327-32384C>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126658452 | ||||||
chr9:126658513
|
T | G | 2 | a0001c0003t0167g0139a0001c0012t0117g0140 | 2 | HG02723.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.327-32323T>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126658513 | ||||||
chr9:126658570
|
C | T | 68 | a0001c0001t0008g0030a0001c0001t0008g0051a0001c0001t0011g0061others(65): Show | 68 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.327-32266C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126658570 | ||||||
chr9:126658869
|
A | G | 75 | a0001c0001t0003g0241a0001c0001t0027g0073a0001c0001t0059g0084others(72): Show | 75 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.327-31967A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126658869 | ||||||
chr9:126658873
|
G | C | 4 | a0001c0002t0188g0131a0001c0003t0058g0132a0001c0003t0077g0130others(1): Show | 4 | HG02109.hp1 HG02647.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.327-31963G>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126658873 | ||||||
chr9:126659025
|
C | T | 1 | a0001c0002t0016g0015 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.327-31811C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126659025 | ||||||
chr9:126659052
|
C | T | 1 | a0001c0002t0056g0157 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.327-31784C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126659052 | ||||||
chr9:126659053
|
G | A | 1 | a0001c0001t0128g0206 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.327-31783G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126659053 | ||||||
chr9:126659105
|
G | T | 69 | a0001c0001t0008g0030a0001c0001t0008g0051a0001c0001t0011g0061others(66): Show | 69 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.327-31731G>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126659105 | ||||||
chr9:126659302
|
A | G | 70 | a0001c0001t0008g0030a0001c0001t0008g0051a0001c0001t0011g0061others(67): Show | 70 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.327-31534A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126659302 | ||||||
chr9:126659434
|
T | C | 83 | a0001c0001t0002g0244a0001c0001t0002g0246a0001c0001t0004g0238others(80): Show | 84 | HG00280.hp2 HG00558.hp1 HG00621.hp2 others(81): Show |
intron_variant | MODIFIER | c.327-31402T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126659434 | ||||||
chr9:126659459
|
G | A | 1 | a0001c0002t0057g0156 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.327-31377G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126659459 | ||||||
chr9:126659651
|
G | C | 9 | a0001c0001t0069g0125a0001c0002t0013g0123a0001c0004t0063g0080others(6): Show | 9 | HG00280.hp2 HG01243.hp2 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.327-31185G>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126659651 | ||||||
chr9:126659744
|
G | A | 82 | a0001c0001t0002g0244a0001c0001t0002g0246a0001c0001t0004g0238others(79): Show | 83 | HG00280.hp2 HG00621.hp2 HG00639.hp1 others(80): Show |
intron_variant | MODIFIER | c.327-31092G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126659744 | ||||||
chr9:126659820
|
A | G | 4 | a0001c0002t0188g0131a0001c0003t0058g0132a0001c0003t0077g0130others(1): Show | 4 | HG02109.hp1 HG02647.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.327-31016A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126659820 | ||||||
chr9:126659933
|
A | AGCCTTAG others(65): Show |
82 | a0001c0001t0002g0244a0001c0001t0002g0246a0001c0001t0004g0238others(79): Show | 83 | HG00280.hp2 HG00621.hp2 HG00639.hp1 others(80): Show |
intron_variant | MODIFIER | c.327-30879_327-3087 others(76): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126659933 | |||||
chr9:126659953
|
G | A | 1 | a0001c0002t0057g0156 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.327-30883G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126659953 | ||||||
chr9:126659963
|
C | A | 1 | a0001c0001t0141g0268 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.327-30873C>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126659963 | ||||||
chr9:126660019
|
C | CTGTGTGG others(178): Show |
79 | a0001c0001t0002g0244a0001c0001t0002g0246a0001c0001t0004g0238others(76): Show | 80 | HG00280.hp2 HG00621.hp2 HG00639.hp1 others(77): Show |
intron_variant | MODIFIER | c.327-30807_327-3080 others(189): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126660019 | |||||
chr9:126660019
|
C | CTGTGTGG others(178): Show |
2 | a0001c0001t0080g0099a0001c0002t0089g0117 | 2 | HG01106.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.327-30807_327-3080 others(189): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126660019 | |||||
chr9:126660022
|
T | TGTGGGGG others(215): Show |
1 | a0001c0002t0056g0157 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.327-30807_327-3080 others(226): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126660022 | |||||
chr9:126660104
|
T | C | 1 | a0001c0002t0154g0299 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.327-30732T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126660104 | ||||||
chr9:126660172
|
T | TGGGGGTA others(178): Show |
79 | a0001c0001t0002g0244a0001c0001t0002g0246a0001c0001t0004g0238others(76): Show | 80 | HG00280.hp2 HG00621.hp2 HG00639.hp1 others(77): Show |
intron_variant | MODIFIER | c.327-30630_327-3062 others(189): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126660172 | |||||
chr9:126660172
|
T | TGGGGGTA others(179): Show |
1 | a0001c0002t0072g0087 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.327-30630_327-3062 others(190): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126660172 | |||||
chr9:126660207
|
T | A | 2 | a0001c0003t0058g0132a0001c0003t0077g0130 | 2 | HG02109.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.327-30629T>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126660207 | ||||||
chr9:126660213
|
G | A | 80 | a0001c0001t0002g0244a0001c0001t0002g0246a0001c0001t0004g0238others(77): Show | 81 | HG00280.hp2 HG00621.hp2 HG00639.hp1 others(78): Show |
intron_variant | MODIFIER | c.327-30623G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126660213 | ||||||
chr9:126660227
|
C | CTTCAGAG others(177): Show |
2 | a0001c0003t0058g0132a0001c0003t0077g0130 | 2 | HG02109.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.327-30609_327-3060 others(188): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126660227 | ||||||
chr9:126660235
|
A | G | 2 | a0001c0003t0058g0132a0001c0003t0077g0130 | 2 | HG02109.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.327-30601A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126660235 | ||||||
chr9:126660240
|
T | C | 2 | a0001c0003t0058g0132a0001c0003t0077g0130 | 2 | HG02109.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.327-30596T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126660240 | ||||||
chr9:126660271
|
G | C | 25 | a0001c0001t0003g0241a0001c0001t0059g0084a0001c0001t0079g0085others(22): Show | 25 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(22): Show |
intron_variant | MODIFIER | c.327-30565G>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126660271 | ||||||
chr9:126660479
|
G | A | 1 | a0001c0001t0069g0125 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.327-30357G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126660479 | ||||||
chr9:126660485
|
A | G | 1 | a0001c0001t0019g0265 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.327-30351A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126660485 | ||||||
chr9:126660504
|
G | A | 82 | a0001c0001t0002g0244a0001c0001t0002g0246a0001c0001t0004g0238others(79): Show | 83 | HG00280.hp2 HG00621.hp2 HG00639.hp1 others(80): Show |
intron_variant | MODIFIER | c.327-30332G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126660504 | ||||||
chr9:126660513
|
T | G | 1 | a0001c0001t0085g0068 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.327-30323T>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126660513 | ||||||
chr9:126660676
|
A | G | 1 | a0001c0002t0016g0015 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.327-30160A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126660676 | ||||||
chr9:126660950
|
G | C | 1 | a0001c0001t0134g0019 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.327-29886G>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126660950 | ||||||
chr9:126661099
|
A | G | 178 | a0001c0001t0002g0244a0001c0001t0002g0246a0001c0001t0002g0317others(175): Show | 179 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(176): Show |
intron_variant | MODIFIER | c.327-29737A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126661099 | ||||||
chr9:126661130
|
T | C | 86 | a0001c0001t0002g0244a0001c0001t0002g0246a0001c0001t0004g0238others(83): Show | 87 | HG00280.hp2 HG00558.hp1 HG00621.hp2 others(84): Show |
intron_variant | MODIFIER | c.327-29706T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126661130 | ||||||
chr9:126661174
|
G | A | 1 | a0001c0001t0002g0234 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.327-29662G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126661174 | ||||||
chr9:126661199
|
A | ACCCCACG others(29): Show |
1 | a0001c0001t0002g0273 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.327-29618_327-2961 others(40): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126661199 | |||||
chr9:126661199
|
A | ACCCCACG others(29): Show |
44 | a0001c0001t0002g0244a0001c0001t0002g0246a0001c0001t0004g0238others(41): Show | 45 | HG00558.hp1 HG00621.hp2 HG00741.hp2 others(42): Show |
intron_variant | MODIFIER | c.327-29617_327-2958 others(40): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126661199 | |||||
chr9:126661199
|
A | ACCCCACG others(65): Show |
1 | a0001c0002t0003g0284 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.327-29582_327-2958 others(76): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126661199 | |||||
chr9:126661200
|
C | G | 1 | a0001c0001t0150g0281 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.327-29636C>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126661200 | ||||||
chr9:126661219
|
T | C | 29 | a0001c0001t0003g0241a0001c0001t0037g0334a0001c0001t0059g0084others(26): Show | 29 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(26): Show |
intron_variant | MODIFIER | c.327-29617T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126661219 | ||||||
chr9:126661219
|
TCAGGCCA others(29): Show |
T | 66 | a0001c0001t0002g0317a0001c0001t0008g0030a0001c0001t0008g0051others(63): Show | 66 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.327-29581_327-2954 others(40): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126661219 | |||||
chr9:126661255
|
C | CCAGGCCA others(29): Show |
26 | a0001c0001t0003g0241a0001c0001t0065g0086a0001c0001t0069g0125others(23): Show | 26 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(23): Show |
intron_variant | MODIFIER | c.327-29562_327-2952 others(40): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126661255 | |||||
chr9:126661255
|
C | T | 77 | a0001c0001t0002g0244a0001c0001t0002g0246a0001c0001t0004g0238others(74): Show | 78 | HG00558.hp1 HG00621.hp2 HG00639.hp1 others(75): Show |
intron_variant | MODIFIER | c.327-29581C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126661255 | ||||||
chr9:126661336
|
G | A | 3 | a0001c0001t0059g0084a0001c0001t0079g0085a0001c0001t0147g0255 | 3 | HG02965.hp1 HG03130.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.327-29500G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126661336 | ||||||
chr9:126661392
|
T | A | 47 | a0001c0001t0002g0223a0001c0001t0002g0234a0001c0001t0027g0076others(44): Show | 47 | HG00099.hp1 HG00735.hp1 HG01069.hp2 others(44): Show |
intron_variant | MODIFIER | c.327-29444T>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126661392 | ||||||
chr9:126661416
|
G | A | 1 | a0001c0002t0155g0240 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.327-29420G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126661416 | ||||||
chr9:126661483
|
A | G | 2 | a0001c0002t0001g0062a0001c0002t0001g0063 | 2 | NA18946.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.327-29353A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126661483 | ||||||
chr9:126661489
|
G | A | 14 | a0001c0001t0051g0167a0001c0001t0107g0232a0001c0001t0180g0198others(11): Show | 14 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(11): Show |
intron_variant | MODIFIER | c.327-29347G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126661489 | ||||||
chr9:126661535
|
C | T | 1 | a0001c0001t0177g0120 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.327-29301C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126661535 | ||||||
chr9:126661651
|
T | A | 1 | a0001c0001t0003g0241 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.327-29185T>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126661651 | ||||||
chr9:126661701
|
G | A | 1 | a0001c0001t0132g0301 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.327-29135G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126661701 | ||||||
chr9:126661800
|
G | C | 9 | a0001c0001t0102g0153a0001c0005t0012g0135a0001c0005t0012g0136others(6): Show | 9 | HG01884.hp2 HG02055.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.327-29036G>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126661800 | ||||||
chr9:126661808
|
G | A | 1 | a0001c0003t0167g0139 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.327-29028G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126661808 | ||||||
chr9:126661823
|
G | A | 10 | a0001c0001t0069g0125a0001c0001t0183g0154a0001c0002t0013g0123others(7): Show | 10 | HG00280.hp2 HG01243.hp2 HG01257.hp1 others(7): Show |
intron_variant | MODIFIER | c.327-29013G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126661823 | ||||||
chr9:126661869
|
G | A | 42 | a0001c0001t0002g0244a0001c0001t0002g0246a0001c0001t0004g0238others(39): Show | 43 | HG00558.hp1 HG00621.hp2 HG00741.hp2 others(40): Show |
intron_variant | MODIFIER | c.327-28967G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126661869 | ||||||
chr9:126661970
|
C | T | 1 | a0001c0002t0001g0306 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.327-28866C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126661970 | ||||||
chr9:126661971
|
G | A | 1 | a0001c0003t0112g0226 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.327-28865G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126661971 | ||||||
chr9:126662002
|
T | G | 3 | a0001c0001t0003g0241a0001c0002t0013g0175a0001c0002t0013g0177 | 3 | HG00738.hp1 HG02602.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.327-28834T>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126662002 | ||||||
chr9:126662429
|
T | C | 1 | a0001c0012t0117g0140 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.327-28407T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126662429 | ||||||
chr9:126662440
|
A | G | 171 | a0001c0001t0002g0218a0001c0001t0002g0317a0001c0001t0003g0241others(168): Show | 172 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.327-28396A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126662440 | ||||||
chr9:126662691
|
C | A | 1 | a0001c0001t0002g0221 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.327-28145C>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126662691 | ||||||
chr9:126662751
|
G | A | 13 | a0001c0001t0005g0212a0001c0001t0005g0274a0001c0001t0005g0278others(10): Show | 13 | HG00621.hp1 HG00642.hp1 HG01934.hp2 others(10): Show |
intron_variant | MODIFIER | c.327-28085G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126662751 | ||||||
chr9:126662918
|
G | A | 1 | a0001c0001t0126g0201 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.327-27918G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126662918 | ||||||
chr9:126662922
|
A | G | 14 | a0001c0002t0055g0176a0001c0002t0055g0179a0001c0002t0056g0157others(11): Show | 14 | HG00639.hp1 HG01109.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.327-27914A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126662922 | ||||||
chr9:126662926
|
G | A | 14 | a0001c0002t0055g0176a0001c0002t0055g0179a0001c0002t0056g0157others(11): Show | 14 | HG00639.hp1 HG01109.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.327-27910G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126662926 | ||||||
chr9:126663190
|
GTTGAGGC others(11): Show |
G | 30 | a0001c0001t0003g0241a0001c0001t0102g0153a0001c0001t0147g0255others(27): Show | 30 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.327-27639_327-2762 others(22): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126663190 | |||||
chr9:126663423
|
C | CA | 10 | a0001c0001t0177g0120a0001c0001t0183g0154a0001c0002t0001g0034others(7): Show | 10 | HG01243.hp2 HG01496.hp2 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.327-27398dupA | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126663423 | |||||
chr9:126663423
|
CA | C | 26 | a0001c0001t0034g0060a0001c0001t0065g0086a0001c0001t0138g0303others(23): Show | 26 | HG00639.hp1 HG01109.hp2 HG01993.hp2 others(23): Show |
intron_variant | MODIFIER | c.327-27398delA | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126663423 | |||||
chr9:126663423
|
CAAAAAAA others(3): Show |
C | 52 | a0001c0001t0003g0241a0001c0001t0004g0238a0001c0001t0180g0198others(49): Show | 53 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.327-27407_327-2739 others(14): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126663423 | |||||
chr9:126663466
|
G | A | 16 | a0001c0001t0040g0308a0001c0001t0066g0114a0001c0001t0068g0070others(13): Show | 16 | HG00280.hp2 HG00738.hp2 HG01074.hp1 others(13): Show |
intron_variant | MODIFIER | c.327-27370G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126663466 | ||||||
chr9:126663567
|
G | A | 35 | a0001c0001t0102g0153a0001c0001t0147g0255a0001c0002t0055g0176others(32): Show | 35 | HG00639.hp1 HG01109.hp2 HG01884.hp2 others(32): Show |
intron_variant | MODIFIER | c.327-27269G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126663567 | ||||||
chr9:126663631
|
C | T | 1 | a0001c0005t0170g0170 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.327-27205C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126663631 | ||||||
chr9:126663643
|
A | G | 1 | a0001c0001t0150g0281 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.327-27193A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126663643 | ||||||
chr9:126663927
|
G | C | 17 | a0001c0002t0055g0176a0001c0002t0055g0179a0001c0002t0056g0157others(14): Show | 17 | HG00639.hp1 HG01109.hp2 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.327-26909G>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126663927 | ||||||
chr9:126664190
|
G | T | 85 | a0001c0001t0008g0051a0001c0001t0018g0010a0001c0001t0067g0121others(82): Show | 85 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.327-26646G>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126664190 | ||||||
chr9:126664247
|
C | T | 1 | a0001c0001t0008g0333 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.327-26589C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126664247 | ||||||
chr9:126664248
|
G | A | 1 | a0001c0012t0117g0140 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.327-26588G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126664248 | ||||||
chr9:126664360
|
G | A | 1 | a0001c0001t0007g0332 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.327-26476G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126664360 | ||||||
chr9:126664371
|
C | T | 9 | a0001c0001t0102g0153a0001c0005t0012g0135a0001c0005t0012g0136others(6): Show | 9 | HG01884.hp2 HG02055.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.327-26465C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126664371 | ||||||
chr9:126664410
|
G | A | 1 | a0001c0003t0110g0134 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.327-26426G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126664410 | ||||||
chr9:126664428
|
C | T | 1 | a0001c0002t0193g0188 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.327-26408C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126664428 | ||||||
chr9:126664474
|
A | G | 4 | a0001c0001t0147g0255a0001c0002t0057g0156a0001c0008t0033g0142others(1): Show | 4 | HG02559.hp2 HG02717.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.327-26362A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126664474 | ||||||
chr9:126664527
|
G | A | 1 | a0001c0001t0002g0205 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.327-26309G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126664527 | ||||||
chr9:126664624
|
C | T | 36 | a0001c0001t0004g0238a0001c0002t0003g0038a0001c0002t0003g0215others(33): Show | 37 | HG00621.hp2 HG00741.hp2 HG01070.hp2 others(34): Show |
intron_variant | MODIFIER | c.327-26212C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126664624 | ||||||
chr9:126664645
|
G | T | 9 | a0001c0001t0102g0153a0001c0005t0012g0135a0001c0005t0012g0136others(6): Show | 9 | HG01884.hp2 HG02055.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.327-26191G>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126664645 | ||||||
chr9:126664745
|
C | T | 3 | a0001c0002t0003g0267a0001c0002t0009g0104a0001c0002t0078g0072 | 3 | HG02132.hp1 NA18747.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.327-26091C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126664745 | ||||||
chr9:126664811
|
G | A | 1 | a0001c0003t0167g0139 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.327-26025G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126664811 | ||||||
chr9:126664831
|
C | T | 1 | a0001c0002t0001g0055 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.327-26005C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126664831 | ||||||
chr9:126664837
|
C | T | 337 | a0001c0001t0002g0204a0001c0001t0002g0205a0001c0001t0002g0211others(334): Show | 340 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(337): Show |
intron_variant | MODIFIER | c.327-25999C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126664837 | ||||||
chr9:126664895
|
C | G | 1 | a0001c0002t0057g0156 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.327-25941C>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126664895 | ||||||
chr9:126665096
|
A | G | 12 | a0001c0001t0026g0069a0001c0001t0026g0129a0001c0001t0183g0154others(9): Show | 12 | HG01243.hp2 HG01496.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.327-25740A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126665096 | ||||||
chr9:126665235
|
C | G | 1 | a0001c0002t0057g0156 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.327-25601C>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126665235 | ||||||
chr9:126665593
|
T | A | 1 | a0001c0002t0001g0034 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.327-25243T>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126665593 | ||||||
chr9:126665745
|
T | C | 1 | a0001c0002t0001g0034 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.327-25091T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126665745 | ||||||
chr9:126665746
|
G | T | 1 | a0001c0002t0001g0034 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.327-25090G>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126665746 | ||||||
chr9:126665747
|
C | G | 1 | a0001c0002t0001g0034 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.327-25089C>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126665747 | ||||||
chr9:126666003
|
C | G | 9 | a0001c0001t0183g0154a0001c0004t0063g0080a0001c0004t0064g0082others(6): Show | 9 | HG01243.hp2 HG01496.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.327-24833C>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126666003 | ||||||
chr9:126666089
|
T | G | 9 | a0001c0001t0183g0154a0001c0004t0063g0080a0001c0004t0064g0082others(6): Show | 9 | HG01243.hp2 HG01496.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.327-24747T>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126666089 | ||||||
chr9:126666099
|
G | A | 1 | a0001c0004t0036g0235 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.327-24737G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126666099 | ||||||
chr9:126666143
|
G | T | 3 | a0001c0001t0147g0255a0001c0008t0033g0142a0001c0008t0033g0143 | 3 | HG02717.hp2 HG03209.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.327-24693G>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126666143 | ||||||
chr9:126666168
|
A | G | 1 | a0001c0001t0065g0086 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.327-24668A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126666168 | ||||||
chr9:126666265
|
C | T | 7 | a0001c0001t0102g0153a0001c0005t0012g0135a0001c0005t0012g0136others(4): Show | 7 | HG01884.hp2 HG02055.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.327-24571C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126666265 | ||||||
chr9:126666349
|
G | T | 1 | a0001c0004t0036g0235 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.327-24487G>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126666349 | ||||||
chr9:126666398
|
A | G | 167 | a0001c0001t0004g0238a0001c0001t0018g0010a0001c0001t0067g0121others(164): Show | 168 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(165): Show |
intron_variant | MODIFIER | c.327-24438A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126666398 | ||||||
chr9:126666486
|
A | G | 2 | a0001c0004t0186g0081a0001c0004t0187g0083 | 2 | HG01243.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.327-24350A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126666486 | ||||||
chr9:126666568
|
T | TTAAAA | 165 | a0001c0001t0004g0238a0001c0001t0018g0010a0001c0001t0067g0121others(162): Show | 166 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.327-24265_327-2426 others(9): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126666568 | |||||
chr9:126666675
|
G | A | 1 | a0001c0002t0163g0066 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.327-24161G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126666675 | ||||||
chr9:126666748
|
T | C | 1 | a0001c0002t0191g0149 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.327-24088T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126666748 | ||||||
chr9:126666812
|
A | G | 98 | a0001c0001t0067g0121a0001c0001t0102g0153a0001c0001t0147g0255others(95): Show | 98 | HG00609.hp1 HG00609.hp2 HG00639.hp1 others(95): Show |
intron_variant | MODIFIER | c.327-24024A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126666812 | ||||||
chr9:126667010
|
T | A | 1 | a0001c0005t0012g0135 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.327-23826T>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126667010 | ||||||
chr9:126667038
|
C | T | 1 | a0001c0001t0097g0217 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.327-23798C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126667038 | ||||||
chr9:126667137
|
C | G | 335 | a0001c0001t0002g0204a0001c0001t0002g0205a0001c0001t0002g0211others(332): Show | 338 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(335): Show |
intron_variant | MODIFIER | c.327-23699C>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126667137 | ||||||
chr9:126667296
|
G | A | 1 | a0001c0001t0141g0268 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.327-23540G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126667296 | ||||||
chr9:126667425
|
C | T | 12 | a0001c0001t0180g0198a0001c0002t0006g0182a0001c0002t0006g0184others(9): Show | 12 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(9): Show |
intron_variant | MODIFIER | c.327-23411C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126667425 | ||||||
chr9:126667475
|
C | T | 66 | a0001c0001t0067g0121a0001c0002t0001g0007a0001c0002t0001g0011others(63): Show | 66 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(63): Show |
intron_variant | MODIFIER | c.327-23361C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126667475 | ||||||
chr9:126667502
|
C | T | 2 | a0001c0001t0011g0214a0001c0001t0061g0101 | 2 | HG01361.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.327-23334C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126667502 | ||||||
chr9:126667901
|
G | A | 1 | a0001c0001t0004g0270 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.327-22935G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126667901 | ||||||
chr9:126668059
|
G | A | 54 | a0001c0001t0102g0153a0001c0001t0180g0198a0001c0001t0183g0154others(51): Show | 54 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.327-22777G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126668059 | ||||||
chr9:126668158
|
G | A | 28 | a0001c0001t0183g0154a0001c0002t0056g0157a0001c0002t0101g0141others(25): Show | 28 | HG00639.hp1 HG01109.hp2 HG01243.hp2 others(25): Show |
intron_variant | MODIFIER | c.327-22678G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126668158 | ||||||
chr9:126668191
|
G | A | 1 | a0001c0001t0007g0328 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.327-22645G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126668191 | ||||||
chr9:126668291
|
C | T | 54 | a0001c0001t0102g0153a0001c0001t0180g0198a0001c0001t0183g0154others(51): Show | 54 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.327-22545C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126668291 | ||||||
chr9:126668443
|
T | TTTA | 3 | a0001c0001t0037g0004a0001c0001t0037g0334a0001c0001t0133g0004 | 3 | NA18973.hp2 NA19005.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.327-22369_327-2236 others(7): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126668443 | |||||
chr9:126668443
|
T | TTTATTA | 59 | a0001c0001t0067g0121a0001c0002t0001g0007a0001c0002t0001g0011others(56): Show | 59 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(56): Show |
intron_variant | MODIFIER | c.327-22372_327-2236 others(10): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126668443 | |||||
chr9:126668443
|
T | TTTATTAT others(2): Show |
55 | a0001c0001t0004g0238a0001c0001t0011g0214a0001c0001t0061g0101others(52): Show | 56 | HG00621.hp2 HG00738.hp1 HG00741.hp2 others(53): Show |
intron_variant | MODIFIER | c.327-22375_327-2236 others(13): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126668443 | |||||
chr9:126668443
|
T | TTTATTAT others(5): Show |
15 | a0001c0002t0003g0043a0001c0002t0003g0046a0001c0002t0047g0277others(12): Show | 15 | HG02055.hp1 HG02129.hp1 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.327-22378_327-2236 others(16): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126668443 | |||||
chr9:126668443
|
T | TTTATTAT others(8): Show |
11 | a0001c0002t0188g0131a0001c0002t0191g0149a0001c0003t0049g0147others(8): Show | 11 | HG00639.hp1 HG01109.hp2 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.327-22381_327-2236 others(19): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126668443 | |||||
chr9:126668443
|
T | TTTATTAT others(11): Show |
2 | a0001c0002t0056g0157a0001c0003t0113g0220 | 2 | HG02723.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.327-22384_327-2236 others(22): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126668443 | |||||
chr9:126668443
|
T | TTTATTAT others(14): Show |
13 | a0001c0001t0180g0198a0001c0001t0183g0154a0001c0002t0006g0182others(10): Show | 13 | HG00280.hp1 HG00323.hp2 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.327-22387_327-2236 others(25): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126668443 | |||||
chr9:126668443
|
T | TTTATTAT others(17): Show |
10 | a0001c0002t0006g0185a0001c0002t0013g0183a0001c0002t0101g0141others(7): Show | 10 | HG00609.hp1 HG02055.hp2 HG03195.hp1 others(7): Show |
intron_variant | MODIFIER | c.327-22390_327-2236 others(28): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126668443 | |||||
chr9:126668443
|
T | TTTATTAT others(20): Show |
3 | a0001c0002t0006g0186a0001c0004t0064g0082a0001c0004t0185g0096 | 3 | HG01346.hp2 HG01496.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.327-22367_327-2236 others(31): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126668443 | |||||
chr9:126668443
|
T | TTTATTAT others(23): Show |
2 | a0001c0001t0102g0153a0001c0002t0104g0194 | 2 | HG01192.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.327-22367_327-2236 others(34): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126668443 | |||||
chr9:126668492
|
C | T | 116 | a0001c0001t0004g0238a0001c0001t0011g0214a0001c0001t0061g0101others(113): Show | 117 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(114): Show |
intron_variant | MODIFIER | c.327-22344C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126668492 | ||||||
chr9:126668502
|
G | T | 8 | a0001c0005t0012g0135a0001c0005t0012g0136a0001c0005t0012g0137others(5): Show | 8 | HG01884.hp2 HG02055.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.327-22334G>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126668502 | ||||||
chr9:126668598
|
C | T | 2 | a0001c0002t0003g0215a0001c0002t0013g0123 | 2 | HG01257.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.327-22238C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126668598 | ||||||
chr9:126668618
|
T | A | 1 | a0001c0001t0017g0287 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.327-22218T>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126668618 | ||||||
chr9:126668934
|
C | T | 172 | a0001c0001t0004g0238a0001c0001t0011g0214a0001c0001t0061g0101others(169): Show | 173 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(170): Show |
intron_variant | MODIFIER | c.327-21902C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126668934 | ||||||
chr9:126669085
|
C | T | 2 | a0001c0002t0001g0039a0001c0002t0155g0240 | 2 | NA19003.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.327-21751C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126669085 | ||||||
chr9:126669117
|
G | A | 1 | a0001c0002t0001g0011 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.327-21719G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126669117 | ||||||
chr9:126669139
|
A | T | 29 | a0001c0001t0102g0153a0001c0001t0183g0154a0001c0002t0056g0157others(26): Show | 29 | HG00639.hp1 HG01109.hp2 HG01243.hp2 others(26): Show |
intron_variant | MODIFIER | c.327-21697A>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126669139 | ||||||
chr9:126669177
|
G | A | 2 | a0001c0004t0186g0081a0001c0004t0187g0083 | 2 | HG01243.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.327-21659G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126669177 | ||||||
chr9:126669241
|
CGAG | C | 172 | a0001c0001t0004g0238a0001c0001t0011g0214a0001c0001t0061g0101others(169): Show | 173 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(170): Show |
intron_variant | MODIFIER | c.327-21590_327-2158 others(7): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126669241 | |||||
chr9:126669245
|
G | A | 2 | a0001c0002t0055g0176a0001c0002t0055g0179 | 2 | HG02280.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.327-21591G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126669245 | ||||||
chr9:126669356
|
A | G | 7 | a0001c0005t0012g0135a0001c0005t0012g0136a0001c0005t0012g0137others(4): Show | 7 | HG01884.hp2 HG02055.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.327-21480A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126669356 | ||||||
chr9:126669380
|
C | G | 1 | a0001c0002t0190g0155 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.327-21456C>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126669380 | ||||||
chr9:126669670
|
G | A | 1 | a0001c0001t0002g0273 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.327-21166G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126669670 | ||||||
chr9:126669765
|
T | G | 337 | a0001c0001t0002g0204a0001c0001t0002g0205a0001c0001t0002g0211others(334): Show | 340 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(337): Show |
intron_variant | MODIFIER | c.327-21071T>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126669765 | ||||||
chr9:126669956
|
C | T | 23 | a0001c0002t0001g0033a0001c0002t0001g0035a0001c0002t0001g0040others(20): Show | 23 | HG00408.hp2 HG02027.hp2 HG02040.hp2 others(20): Show |
intron_variant | MODIFIER | c.327-20880C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126669956 | ||||||
chr9:126669957
|
G | A | 1 | a0001c0002t0021g0009 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.327-20879G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126669957 | ||||||
chr9:126670451
|
T | G | 2 | a0001c0010t0196g0146a0001c0012t0117g0140 | 2 | NA19030.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.327-20385T>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126670451 | ||||||
chr9:126670455
|
G | T | 4 | a0001c0004t0151g0065a0001c0004t0184g0162a0001c0004t0186g0081others(1): Show | 4 | HG01243.hp2 HG02886.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.327-20381G>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126670455 | ||||||
chr9:126670460
|
G | A | 6 | a0001c0002t0055g0176a0001c0002t0055g0179a0001c0002t0106g0144others(3): Show | 6 | HG02280.hp2 HG02615.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.327-20376G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126670460 | ||||||
chr9:126670462
|
T | C | 29 | a0001c0001t0102g0153a0001c0001t0183g0154a0001c0002t0056g0157others(26): Show | 29 | HG00639.hp1 HG01109.hp2 HG01243.hp2 others(26): Show |
intron_variant | MODIFIER | c.327-20374T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126670462 | ||||||
chr9:126670473
|
G | A | 1 | a0001c0002t0015g0020 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.327-20363G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126670473 | ||||||
chr9:126670483
|
G | A | 14 | a0001c0001t0180g0198a0001c0002t0006g0182a0001c0002t0006g0184others(11): Show | 14 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(11): Show |
intron_variant | MODIFIER | c.327-20353G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126670483 | ||||||
chr9:126670514
|
G | A | 28 | a0001c0001t0180g0198a0001c0002t0006g0182a0001c0002t0006g0184others(25): Show | 28 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(25): Show |
intron_variant | MODIFIER | c.327-20322G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126670514 | ||||||
chr9:126670519
|
G | A | 2 | a0001c0001t0027g0076a0001c0001t0060g0115 | 2 | HG01081.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.327-20317G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126670519 | ||||||
chr9:126670572
|
G | A | 1 | a0001c0004t0036g0235 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.327-20264G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126670572 | ||||||
chr9:126670589
|
A | G | 2 | a0001c0002t0001g0056a0001c0002t0158g0050 | 2 | NA18985.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.327-20247A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126670589 | ||||||
chr9:126670662
|
C | G | 17 | a0001c0001t0102g0153a0001c0002t0056g0157a0001c0002t0101g0141others(14): Show | 17 | HG00639.hp1 HG01109.hp2 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.327-20174C>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126670662 | ||||||
chr9:126670770
|
C | T | 12 | a0001c0001t0183g0154a0001c0004t0042g0209a0001c0004t0042g0210others(9): Show | 12 | HG01243.hp2 HG01496.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.327-20066C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126670770 | ||||||
chr9:126670859
|
C | T | 29 | a0001c0001t0102g0153a0001c0001t0183g0154a0001c0002t0056g0157others(26): Show | 29 | HG00639.hp1 HG01109.hp2 HG01243.hp2 others(26): Show |
intron_variant | MODIFIER | c.327-19977C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126670859 | ||||||
chr9:126670926
|
G | A | 3 | a0001c0001t0027g0073a0001c0001t0096g0245a0001c0001t0118g0242 | 3 | HG01175.hp2 HG03688.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.327-19910G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126670926 | ||||||
chr9:126670978
|
C | T | 1 | a0001c0002t0001g0054 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.327-19858C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126670978 | ||||||
chr9:126671001
|
G | C | 14 | a0001c0001t0180g0198a0001c0002t0006g0182a0001c0002t0006g0184others(11): Show | 14 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(11): Show |
intron_variant | MODIFIER | c.327-19835G>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126671001 | ||||||
chr9:126671152
|
G | A | 29 | a0001c0001t0102g0153a0001c0001t0183g0154a0001c0002t0056g0157others(26): Show | 29 | HG00639.hp1 HG01109.hp2 HG01243.hp2 others(26): Show |
intron_variant | MODIFIER | c.327-19684G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126671152 | ||||||
chr9:126671163
|
T | C | 2 | a0001c0001t0039g0037a0001c0001t0039g0320 | 2 | HG00597.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.327-19673T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126671163 | ||||||
chr9:126671250
|
T | C | 8 | a0001c0001t0002g0272a0001c0001t0002g0296a0001c0001t0002g0297others(5): Show | 8 | HG01081.hp1 HG01106.hp2 HG01934.hp1 others(5): Show |
intron_variant | MODIFIER | c.327-19586T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126671250 | ||||||
chr9:126671306
|
T | C | 29 | a0001c0001t0102g0153a0001c0001t0183g0154a0001c0002t0056g0157others(26): Show | 29 | HG00639.hp1 HG01109.hp2 HG01243.hp2 others(26): Show |
intron_variant | MODIFIER | c.327-19530T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126671306 | ||||||
chr9:126671514
|
A | C | 14 | a0001c0001t0180g0198a0001c0002t0006g0182a0001c0002t0006g0184others(11): Show | 14 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(11): Show |
intron_variant | MODIFIER | c.327-19322A>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126671514 | ||||||
chr9:126671650
|
A | G | 281 | a0001c0001t0002g0204a0001c0001t0002g0205a0001c0001t0002g0211others(278): Show | 283 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(280): Show |
intron_variant | MODIFIER | c.327-19186A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126671650 | ||||||
chr9:126671659
|
T | C | 1 | a0001c0001t0051g0075 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.327-19177T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126671659 | ||||||
chr9:126671691
|
G | A | 5 | a0001c0005t0012g0135a0001c0005t0012g0136a0001c0005t0012g0137others(2): Show | 5 | HG01884.hp2 HG02055.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.327-19145G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126671691 | ||||||
chr9:126671832
|
G | A | 2 | a0001c0007t0048g0252a0001c0007t0048g0312 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.327-19004G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126671832 | ||||||
chr9:126671860
|
A | G | 12 | a0001c0001t0002g0204a0001c0001t0002g0205a0001c0001t0002g0218others(9): Show | 12 | HG00099.hp2 HG00642.hp2 HG01175.hp1 others(9): Show |
intron_variant | MODIFIER | c.327-18976A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126671860 | ||||||
chr9:126672231
|
G | A | 20 | a0001c0001t0180g0198a0001c0002t0006g0182a0001c0002t0006g0184others(17): Show | 20 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(17): Show |
intron_variant | MODIFIER | c.327-18605G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126672231 | ||||||
chr9:126672308
|
G | A | 5 | a0001c0003t0109g0254a0001c0003t0110g0134a0001c0010t0196g0146others(2): Show | 5 | HG01884.hp1 HG03041.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.327-18528G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126672308 | ||||||
chr9:126672371
|
G | A | 1 | a0001c0001t0143g0279 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.327-18465G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126672371 | ||||||
chr9:126672521
|
C | T | 5 | a0001c0003t0109g0254a0001c0003t0110g0134a0001c0010t0196g0146others(2): Show | 5 | HG01884.hp1 HG03041.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.327-18315C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126672521 | ||||||
chr9:126672551
|
TAAATTGG others(132): Show |
T | 1 | a0001c0002t0001g0054 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.327-18283_327-1814 others(4): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126672551 | |||||
chr9:126672701
|
G | A | 2 | a0001c0004t0186g0081a0001c0004t0187g0083 | 2 | HG01243.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.327-18135G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126672701 | ||||||
chr9:126672742
|
C | T | 55 | a0001c0001t0102g0153a0001c0001t0180g0198a0001c0001t0183g0154others(52): Show | 55 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.327-18094C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126672742 | ||||||
chr9:126672766
|
G | A | 1 | a0001c0011t0086g0077 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.327-18070G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126672766 | ||||||
chr9:126672824
|
C | T | 6 | a0001c0005t0012g0135a0001c0005t0012g0136a0001c0005t0012g0137others(3): Show | 6 | HG01884.hp2 HG02055.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.327-18012C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126672824 | ||||||
chr9:126672875
|
G | A | 3 | a0001c0001t0002g0317a0001c0002t0046g0250a0001c0002t0046g0257 | 3 | NA18953.hp2 NA18993.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.327-17961G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126672875 | ||||||
chr9:126672997
|
C | T | 5 | a0001c0001t0051g0167a0001c0001t0052g0164a0001c0001t0053g0161others(2): Show | 5 | HG01109.hp1 HG02258.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.327-17839C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126672997 | ||||||
chr9:126673177
|
G | C | 1 | a0001c0001t0002g0331 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.327-17659G>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126673177 | ||||||
chr9:126673481
|
A | G | 1 | a0001c0002t0001g0054 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.327-17355A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126673481 | ||||||
chr9:126673494
|
G | A | 2 | a0001c0001t0026g0069a0001c0001t0026g0129 | 2 | NA18953.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.327-17342G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126673494 | ||||||
chr9:126673562
|
C | G | 63 | a0001c0001t0011g0214a0001c0001t0061g0101a0001c0001t0102g0153others(60): Show | 63 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.327-17274C>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126673562 | ||||||
chr9:126673613
|
G | A | 2 | a0001c0001t0002g0233a0001c0001t0176g0172 | 2 | HG02897.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.327-17223G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126673613 | ||||||
chr9:126673653
|
G | A | 1 | a0001c0004t0182g0078 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.327-17183G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126673653 | ||||||
chr9:126673774
|
G | T | 1 | a0001c0002t0001g0054 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.327-17062G>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126673774 | ||||||
chr9:126673790
|
C | G | 1 | a0001c0002t0001g0054 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.327-17046C>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126673790 | ||||||
chr9:126673801
|
G | T | 1 | a0001c0001t0008g0333 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.327-17035G>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126673801 | ||||||
chr9:126673826
|
G | A | 1 | a0001c0002t0057g0156 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.327-17010G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126673826 | ||||||
chr9:126673993
|
C | T | 63 | a0001c0001t0067g0121a0001c0002t0001g0007a0001c0002t0001g0011others(60): Show | 63 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.327-16843C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126673993 | ||||||
chr9:126674097
|
C | T | 11 | a0001c0001t0180g0198a0001c0002t0006g0182a0001c0002t0006g0184others(8): Show | 11 | HG00280.hp1 HG00323.hp2 HG00741.hp1 others(8): Show |
intron_variant | MODIFIER | c.327-16739C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126674097 | ||||||
chr9:126674136
|
G | A | 2 | a0001c0003t0058g0132a0001c0003t0077g0130 | 2 | HG02109.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.327-16700G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126674136 | ||||||
chr9:126674246
|
G | A | 11 | a0001c0001t0180g0198a0001c0002t0006g0184a0001c0002t0006g0185others(8): Show | 11 | HG00280.hp1 HG00323.hp2 HG00741.hp1 others(8): Show |
intron_variant | MODIFIER | c.327-16590G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126674246 | ||||||
chr9:126674283
|
C | G | 3 | a0001c0003t0058g0132a0001c0003t0077g0130a0001c0003t0111g0067 | 3 | HG02109.hp1 HG02647.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.327-16553C>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126674283 | ||||||
chr9:126674389
|
T | TG | 25 | a0001c0001t0180g0198a0001c0002t0006g0182a0001c0002t0006g0184others(22): Show | 25 | HG00280.hp1 HG00323.hp2 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.327-16440dupG | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126674389 | |||||
chr9:126674517
|
T | G | 1 | a0001c0002t0001g0054 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.327-16319T>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126674517 | ||||||
chr9:126674614
|
A | C | 3 | a0001c0001t0126g0201a0001c0001t0172g0163a0001c0001t0174g0079 | 3 | HG01099.hp2 HG02895.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.327-16222A>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126674614 | ||||||
chr9:126674683
|
C | T | 6 | a0001c0002t0057g0156a0001c0003t0109g0254a0001c0003t0110g0134others(3): Show | 6 | HG01884.hp1 HG02559.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.327-16153C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126674683 | ||||||
chr9:126674840
|
C | A | 1 | a0001c0001t0107g0232 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.327-15996C>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126674840 | ||||||
chr9:126674860
|
A | G | 6 | a0001c0002t0057g0156a0001c0003t0109g0254a0001c0003t0110g0134others(3): Show | 6 | HG01884.hp1 HG02559.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.327-15976A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126674860 | ||||||
chr9:126674961
|
G | T | 13 | a0001c0001t0180g0198a0001c0002t0006g0182a0001c0002t0006g0184others(10): Show | 13 | HG00280.hp1 HG00323.hp2 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.327-15875G>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126674961 | ||||||
chr9:126674981
|
G | A | 1 | a0001c0011t0086g0077 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.327-15855G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126674981 | ||||||
chr9:126675056
|
A | G | 35 | a0001c0001t0102g0153a0001c0001t0183g0154a0001c0002t0056g0157others(32): Show | 35 | HG00639.hp1 HG01109.hp2 HG01243.hp2 others(32): Show |
intron_variant | MODIFIER | c.327-15780A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126675056 | ||||||
chr9:126675175
|
AC | A | 60 | a0001c0001t0102g0153a0001c0001t0180g0198a0001c0001t0183g0154others(57): Show | 60 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(57): Show |
intron_variant | MODIFIER | c.327-15654delC | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126675175 | |||||
chr9:126675395
|
G | T | 1 | a0001c0001t0028g0089 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.327-15441G>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126675395 | ||||||
chr9:126675554
|
G | A | 2 | a0001c0008t0033g0142a0001c0008t0033g0143 | 2 | HG02717.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.327-15282G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126675554 | ||||||
chr9:126675595
|
C | T | 3 | a0001c0001t0126g0201a0001c0001t0172g0163a0001c0001t0174g0079 | 3 | HG01099.hp2 HG02895.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.327-15241C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126675595 | ||||||
chr9:126675657
|
A | C | 2 | a0001c0010t0196g0146a0001c0012t0117g0140 | 2 | NA19030.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.327-15179A>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126675657 | ||||||
chr9:126675735
|
T | TA | 30 | a0001c0001t0102g0153a0001c0001t0183g0154a0001c0002t0001g0054others(27): Show | 30 | HG00639.hp1 HG01109.hp2 HG01243.hp2 others(27): Show |
intron_variant | MODIFIER | c.327-15087dupA | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126675735 | |||||
chr9:126675735
|
TA | T | 8 | a0001c0001t0010g0251a0001c0001t0017g0310a0001c0002t0001g0011others(5): Show | 8 | HG01975.hp1 HG02922.hp2 NA18959.hp2 others(5): Show |
intron_variant | MODIFIER | c.327-15087delA | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126675735 | |||||
chr9:126675736
|
A | T | 24 | a0001c0001t0180g0198a0001c0002t0006g0182a0001c0002t0006g0184others(21): Show | 24 | HG00280.hp1 HG00323.hp2 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.327-15100A>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126675736 | ||||||
chr9:126675737
|
A | T | 1 | a0001c0002t0055g0179 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.327-15099A>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126675737 | ||||||
chr9:126675772
|
G | A | 2 | a0001c0002t0015g0014a0001c0002t0015g0020 | 2 | HG02015.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.327-15064G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126675772 | ||||||
chr9:126675816
|
G | C | 2 | a0001c0003t0109g0254a0001c0003t0110g0134 | 2 | HG03041.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.327-15020G>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126675816 | ||||||
chr9:126675831
|
C | T | 6 | a0001c0002t0055g0176a0001c0002t0055g0179a0001c0002t0106g0144others(3): Show | 6 | HG02280.hp2 HG02615.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.327-15005C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126675831 | ||||||
chr9:126675906
|
G | A | 2 | a0001c0002t0101g0141a0001c0002t0168g0180 | 2 | HG03225.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.327-14930G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126675906 | ||||||
chr9:126675909
|
C | T | 2 | a0001c0002t0101g0141a0001c0002t0168g0180 | 2 | HG03225.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.327-14927C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126675909 | ||||||
chr9:126675915
|
A | G | 2 | a0001c0002t0101g0141a0001c0002t0168g0180 | 2 | HG03225.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.327-14921A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126675915 | ||||||
chr9:126675942
|
G | A | 1 | a0001c0002t0104g0194 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.327-14894G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126675942 | ||||||
chr9:126675945
|
A | T | 24 | a0001c0001t0002g0221a0001c0001t0002g0272a0001c0001t0002g0296others(21): Show | 24 | HG00639.hp2 HG00735.hp2 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.327-14891A>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126675945 | ||||||
chr9:126676048
|
C | CA | 20 | a0001c0001t0002g0211a0001c0001t0002g0223a0001c0001t0004g0263others(17): Show | 20 | HG00741.hp1 HG01099.hp1 HG01257.hp2 others(17): Show |
intron_variant | MODIFIER | c.327-14770dupA | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126676048 | |||||
chr9:126676048
|
CA | C | 35 | a0001c0001t0102g0153a0001c0001t0183g0154a0001c0002t0030g0091others(32): Show | 35 | HG00639.hp1 HG01070.hp2 HG01109.hp2 others(32): Show |
intron_variant | MODIFIER | c.327-14770delA | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126676048 | |||||
chr9:126676158
|
G | A | 2 | a0001c0003t0109g0254a0001c0003t0110g0134 | 2 | HG03041.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.327-14678G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126676158 | ||||||
chr9:126676310
|
T | C | 2 | a0001c0002t0071g0100a0001c0002t0090g0106 | 2 | NA18945.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.327-14526T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126676310 | ||||||
chr9:126676312
|
C | A | 37 | a0001c0001t0102g0153a0001c0001t0183g0154a0001c0002t0056g0157others(34): Show | 37 | HG00639.hp1 HG01109.hp2 HG01243.hp2 others(34): Show |
intron_variant | MODIFIER | c.327-14524C>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126676312 | ||||||
chr9:126676454
|
T | G | 1 | a0001c0002t0191g0149 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.327-14382T>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126676454 | ||||||
chr9:126676510
|
G | A | 1 | a0001c0002t0092g0133 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.327-14326G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126676510 | ||||||
chr9:126676582
|
A | G | 335 | a0001c0001t0002g0204a0001c0001t0002g0205a0001c0001t0002g0211others(332): Show | 338 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(335): Show |
intron_variant | MODIFIER | c.327-14254A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126676582 | ||||||
chr9:126676593
|
A | G | 62 | a0001c0001t0102g0153a0001c0001t0180g0198a0001c0001t0183g0154others(59): Show | 62 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(59): Show |
intron_variant | MODIFIER | c.327-14243A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126676593 | ||||||
chr9:126676771
|
C | T | 2 | a0001c0002t0001g0011a0001c0002t0057g0156 | 2 | HG02559.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.327-14065C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126676771 | ||||||
chr9:126676947
|
T | C | 1 | a0001c0001t0135g0064 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.327-13889T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126676947 | ||||||
chr9:126676996
|
C | T | 12 | a0001c0001t0002g0204a0001c0001t0002g0205a0001c0001t0002g0218others(9): Show | 12 | HG00099.hp2 HG00642.hp2 HG01175.hp1 others(9): Show |
intron_variant | MODIFIER | c.327-13840C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126676996 | ||||||
chr9:126676997
|
G | A | 1 | a0001c0001t0085g0068 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.327-13839G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126676997 | ||||||
chr9:126677095
|
C | T | 3 | a0001c0003t0058g0132a0001c0003t0077g0130a0001c0003t0111g0067 | 3 | HG02109.hp1 HG02647.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.327-13741C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126677095 | ||||||
chr9:126677184
|
C | T | 29 | a0001c0001t0102g0153a0001c0001t0183g0154a0001c0002t0056g0157others(26): Show | 29 | HG00639.hp1 HG01109.hp2 HG01243.hp2 others(26): Show |
intron_variant | MODIFIER | c.327-13652C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126677184 | ||||||
chr9:126677286
|
C | T | 2 | a0001c0002t0006g0190a0001c0002t0006g0191 | 2 | HG00280.hp1 HG00323.hp2 |
intron_variant | MODIFIER | c.327-13550C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126677286 | ||||||
chr9:126677681
|
C | A | 1 | a0001c0001t0028g0089 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.327-13155C>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126677681 | ||||||
chr9:126677977
|
T | G | 3 | a0001c0002t0014g0105a0001c0002t0014g0107a0001c0002t0014g0118 | 3 | NA18984.hp1 NA19054.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.327-12859T>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126677977 | ||||||
chr9:126678178
|
C | T | 1 | a0001c0001t0102g0153 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.327-12658C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126678178 | ||||||
chr9:126678309
|
C | CA | 9 | a0001c0001t0002g0331a0001c0001t0007g0332a0001c0001t0062g0124others(6): Show | 9 | HG00735.hp1 HG01175.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.327-12515dupA | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126678309 | |||||
chr9:126678311
|
AAAAAAAA others(11): Show |
A | 6 | a0001c0005t0012g0135a0001c0005t0012g0136a0001c0005t0012g0137others(3): Show | 6 | HG01884.hp2 HG02055.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.327-12514_327-1249 others(22): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126678311 | |||||
chr9:126678314
|
A | G | 1 | a0001c0001t0054g0199 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.327-12522A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126678314 | ||||||
chr9:126678321
|
AC | A | 4 | a0001c0001t0180g0198a0001c0004t0184g0162a0001c0004t0186g0081others(1): Show | 4 | HG01243.hp2 HG03195.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.327-12514delC | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126678321 | ||||||
chr9:126678322
|
C | A | 55 | a0001c0001t0102g0153a0001c0001t0183g0154a0001c0002t0006g0182others(52): Show | 55 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(52): Show |
intron_variant | MODIFIER | c.327-12514C>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126678322 | ||||||
chr9:126678325
|
A | C | 28 | a0001c0001t0102g0153a0001c0001t0183g0154a0001c0002t0056g0157others(25): Show | 28 | HG00639.hp1 HG01109.hp2 HG01243.hp2 others(25): Show |
intron_variant | MODIFIER | c.327-12511A>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126678325 | ||||||
chr9:126678326
|
A | C | 1 | a0001c0003t0109g0254 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.327-12510A>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126678326 | ||||||
chr9:126678329
|
C | A | 58 | a0001c0001t0102g0153a0001c0001t0183g0154a0001c0002t0006g0182others(55): Show | 58 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.327-12507C>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126678329 | ||||||
chr9:126678329
|
C | CA | 9 | a0001c0001t0002g0218a0001c0001t0003g0241a0001c0001t0005g0300others(6): Show | 9 | HG01243.hp1 HG01981.hp1 HG02602.hp1 others(6): Show |
intron_variant | MODIFIER | c.327-12495dupA | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126678329 | |||||
chr9:126678332
|
A | C | 1 | a0001c0001t0069g0125 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.327-12504A>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126678332 | ||||||
chr9:126678335
|
A | AC | 9 | a0001c0001t0180g0198a0001c0002t0055g0176a0001c0002t0055g0179others(6): Show | 9 | HG00741.hp1 HG02280.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.327-12501_327-1250 others(5): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126678335 | ||||||
chr9:126678335
|
A | C | 43 | a0001c0001t0102g0153a0001c0001t0183g0154a0001c0002t0006g0182others(40): Show | 43 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.327-12501A>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126678335 | ||||||
chr9:126678342
|
C | A | 9 | a0001c0003t0058g0132a0001c0003t0077g0130a0001c0003t0111g0067others(6): Show | 9 | HG01884.hp2 HG02055.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.327-12494C>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126678342 | ||||||
chr9:126678561
|
A | C | 54 | a0001c0001t0102g0153a0001c0001t0180g0198a0001c0001t0183g0154others(51): Show | 54 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(51): Show |
intron_variant | MODIFIER | c.327-12275A>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126678561 | ||||||
chr9:126678612
|
G | C | 2 | a0001c0008t0033g0142a0001c0008t0033g0143 | 2 | HG02717.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.327-12224G>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126678612 | ||||||
chr9:126678637
|
C | G | 1 | a0001c0001t0082g0097 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.327-12199C>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126678637 | ||||||
chr9:126678712
|
C | G | 3 | a0001c0003t0058g0132a0001c0003t0077g0130a0001c0003t0111g0067 | 3 | HG02109.hp1 HG02647.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.327-12124C>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126678712 | ||||||
chr9:126678765
|
A | C | 1 | a0001c0001t0143g0279 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.327-12071A>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126678765 | ||||||
chr9:126678773
|
T | G | 1 | a0001c0001t0132g0301 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.327-12063T>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126678773 | ||||||
chr9:126679157
|
C | T | 2 | a0001c0001t0011g0214a0001c0001t0061g0101 | 2 | HG01361.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.327-11679C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126679157 | ||||||
chr9:126679235
|
C | CTA | 29 | a0001c0001t0102g0153a0001c0001t0183g0154a0001c0002t0056g0157others(26): Show | 29 | HG00639.hp1 HG01109.hp2 HG01243.hp2 others(26): Show |
intron_variant | MODIFIER | c.327-11600_327-1159 others(6): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126679235 | |||||
chr9:126679280
|
C | T | 6 | a0001c0002t0001g0033a0001c0002t0001g0035a0001c0002t0001g0045others(3): Show | 6 | HG02155.hp1 NA18950.hp2 NA18963.hp2 others(3): Show |
intron_variant | MODIFIER | c.327-11556C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126679280 | ||||||
chr9:126679422
|
G | A | 2 | a0001c0010t0196g0146a0001c0012t0117g0140 | 2 | NA19030.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.327-11414G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126679422 | ||||||
chr9:126679437
|
G | A | 2 | a0001c0001t0002g0223a0001c0001t0145g0231 | 2 | HG02818.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.327-11399G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126679437 | ||||||
chr9:126679475
|
G | C | 55 | a0001c0001t0004g0238a0001c0001t0180g0198a0001c0002t0003g0029others(52): Show | 56 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.327-11361G>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126679475 | ||||||
chr9:126679518
|
A | G | 97 | a0001c0001t0004g0238a0001c0001t0102g0153a0001c0001t0180g0198others(94): Show | 98 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(95): Show |
intron_variant | MODIFIER | c.327-11318A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126679518 | ||||||
chr9:126679568
|
A | T | 29 | a0001c0001t0102g0153a0001c0001t0183g0154a0001c0002t0056g0157others(26): Show | 29 | HG00639.hp1 HG01109.hp2 HG01243.hp2 others(26): Show |
intron_variant | MODIFIER | c.327-11268A>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126679568 | ||||||
chr9:126679597
|
T | TG | 6 | a0001c0005t0012g0135a0001c0005t0012g0136a0001c0005t0012g0137others(3): Show | 6 | HG01884.hp2 HG02055.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.327-11237dupG | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126679597 | |||||
chr9:126680040
|
G | T | 1 | a0001c0002t0056g0157 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.327-10796G>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126680040 | ||||||
chr9:126680067
|
G | A | 1 | a0001c0001t0149g0335 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.327-10769G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126680067 | ||||||
chr9:126680104
|
G | A | 1 | a0001c0002t0190g0155 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.327-10732G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126680104 | ||||||
chr9:126680104
|
G | T | 64 | a0001c0001t0067g0121a0001c0002t0001g0007a0001c0002t0001g0011others(61): Show | 64 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.327-10732G>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126680104 | ||||||
chr9:126680314
|
G | C | 6 | a0001c0005t0012g0135a0001c0005t0012g0136a0001c0005t0012g0137others(3): Show | 6 | HG01884.hp2 HG02055.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.327-10522G>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126680314 | ||||||
chr9:126680378
|
G | T | 2 | a0001c0002t0003g0043a0001c0002t0003g0046 | 2 | NA18999.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.327-10458G>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126680378 | ||||||
chr9:126680402
|
A | G | 1 | a0001c0001t0002g0221 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.327-10434A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126680402 | ||||||
chr9:126680451
|
C | T | 1 | a0001c0001t0039g0320 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.327-10385C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126680451 | ||||||
chr9:126680557
|
C | G | 338 | a0001c0001t0002g0204a0001c0001t0002g0205a0001c0001t0002g0211others(335): Show | 341 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(338): Show |
intron_variant | MODIFIER | c.327-10279C>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126680557 | ||||||
chr9:126680600
|
A | G | 1 | a0001c0002t0013g0177 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.327-10236A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126680600 | ||||||
chr9:126680780
|
G | A | 3 | a0001c0003t0058g0132a0001c0003t0077g0130a0001c0003t0111g0067 | 3 | HG02109.hp1 HG02647.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.327-10056G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126680780 | ||||||
chr9:126680784
|
A | G | 2 | a0001c0002t0055g0176a0001c0002t0055g0179 | 2 | HG02280.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.327-10052A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126680784 | ||||||
chr9:126680835
|
C | A | 2 | a0001c0001t0002g0273a0001c0001t0011g0330 | 2 | HG00558.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.327-10001C>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126680835 | ||||||
chr9:126681037
|
G | A | 1 | a0001c0001t0171g0160 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.327-9799G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126681037 | ||||||
chr9:126681041
|
C | T | 6 | a0001c0005t0012g0135a0001c0005t0012g0136a0001c0005t0012g0137others(3): Show | 6 | HG01884.hp2 HG02055.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.327-9795C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126681041 | ||||||
chr9:126681055
|
A | G | 17 | a0001c0001t0102g0153a0001c0002t0056g0157a0001c0002t0101g0141others(14): Show | 17 | HG00639.hp1 HG01109.hp2 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.327-9781A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126681055 | ||||||
chr9:126681221
|
A | G | 2 | a0001c0002t0015g0023a0001c0002t0193g0188 | 2 | HG00609.hp1 HG02080.hp1 |
intron_variant | MODIFIER | c.327-9615A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126681221 | ||||||
chr9:126681255
|
A | G | 1 | a0001c0001t0041g0324 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.327-9581A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126681255 | ||||||
chr9:126681371
|
G | T | 6 | a0001c0005t0012g0135a0001c0005t0012g0136a0001c0005t0012g0137others(3): Show | 6 | HG01884.hp2 HG02055.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.327-9465G>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126681371 | ||||||
chr9:126681467
|
G | GC | 173 | a0001c0001t0004g0238a0001c0001t0067g0121a0001c0001t0102g0153others(170): Show | 174 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(171): Show |
intron_variant | MODIFIER | c.327-9366dupC | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126681467 | |||||
chr9:126681573
|
G | GC | 62 | a0001c0001t0004g0238a0001c0001t0180g0198a0001c0002t0003g0029others(59): Show | 63 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.327-9256dupC | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126681573 | |||||
chr9:126681579
|
C | G | 1 | a0001c0001t0138g0303 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.327-9257C>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126681579 | ||||||
chr9:126681616
|
C | A | 6 | a0001c0005t0012g0135a0001c0005t0012g0136a0001c0005t0012g0137others(3): Show | 6 | HG01884.hp2 HG02055.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.327-9220C>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126681616 | ||||||
chr9:126681770
|
G | A | 2 | a0001c0003t0109g0254a0001c0003t0110g0134 | 2 | HG03041.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.327-9066G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126681770 | ||||||
chr9:126681799
|
G | T | 6 | a0001c0002t0057g0156a0001c0008t0033g0142a0001c0008t0033g0143others(3): Show | 6 | HG01884.hp1 HG02559.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.327-9037G>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126681799 | ||||||
chr9:126681887
|
T | C | 6 | a0001c0005t0012g0135a0001c0005t0012g0136a0001c0005t0012g0137others(3): Show | 6 | HG01884.hp2 HG02055.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.327-8949T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126681887 | ||||||
chr9:126681900
|
C | CA | 6 | a0001c0005t0012g0135a0001c0005t0012g0136a0001c0005t0012g0137others(3): Show | 6 | HG01884.hp2 HG02055.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.327-8924dupA | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126681900 | |||||
chr9:126681907
|
A | AAT | 12 | a0001c0001t0183g0154a0001c0004t0042g0209a0001c0004t0042g0210others(9): Show | 12 | HG01243.hp2 HG01496.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.327-8928_327-8927i others(4): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126681907 | |||||
chr9:126681910
|
A | T | 88 | a0001c0001t0002g0218a0001c0001t0004g0238a0001c0001t0028g0089others(85): Show | 89 | HG00280.hp1 HG00323.hp2 HG00597.hp1 others(86): Show |
intron_variant | MODIFIER | c.327-8926A>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126681910 | ||||||
chr9:126681913
|
T | A | 8 | a0001c0001t0010g0251a0001c0001t0010g0309a0001c0001t0010g0319others(5): Show | 8 | HG02165.hp1 NA18959.hp2 NA18961.hp1 others(5): Show |
intron_variant | MODIFIER | c.327-8923T>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126681913 | ||||||
chr9:126681965
|
G | A | 6 | a0001c0005t0012g0135a0001c0005t0012g0136a0001c0005t0012g0137others(3): Show | 6 | HG01884.hp2 HG02055.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.327-8871G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126681965 | ||||||
chr9:126682081
|
G | GCC | 11 | a0001c0001t0067g0121a0001c0002t0001g0033a0001c0002t0001g0034others(8): Show | 11 | HG02027.hp2 HG02074.hp1 HG02738.hp2 others(8): Show |
intron_variant | MODIFIER | c.327-8755_327-8754i others(4): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126682081 | ||||||
chr9:126682081
|
G | GCCTTTTT | 9 | a0001c0001t0102g0153a0001c0002t0003g0038a0001c0002t0009g0116others(6): Show | 9 | HG00621.hp2 HG02109.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.327-8755_327-8754i others(9): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126682081 | ||||||
chr9:126682081
|
G | GCCTTTTT others(1): Show |
33 | a0001c0001t0180g0198a0001c0002t0003g0029a0001c0002t0003g0046others(30): Show | 34 | HG00280.hp1 HG00323.hp2 HG01070.hp2 others(31): Show |
intron_variant | MODIFIER | c.327-8755_327-8754i others(10): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126682081 | ||||||
chr9:126682081
|
G | GCCTTTTT others(2): Show |
23 | a0001c0001t0004g0238a0001c0001t0028g0122a0001c0002t0003g0043others(20): Show | 23 | HG00609.hp1 HG01074.hp2 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.327-8755_327-8754i others(11): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126682081 | ||||||
chr9:126682081
|
G | GCCTTTTT others(3): Show |
13 | a0001c0002t0006g0184a0001c0002t0013g0177a0001c0002t0055g0176others(10): Show | 13 | HG01884.hp2 HG01978.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.327-8755_327-8754i others(12): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126682081 | ||||||
chr9:126682081
|
G | GCCTTTTT others(4): Show |
8 | a0001c0002t0006g0185a0001c0002t0088g0098a0001c0002t0090g0106others(5): Show | 8 | HG00741.hp1 HG00741.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.327-8755_327-8754i others(13): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126682081 | ||||||
chr9:126682081
|
G | GCCTTTTT others(5): Show |
3 | a0001c0002t0013g0175a0001c0002t0195g0148a0001c0005t0170g0170 | 3 | HG00738.hp1 HG03098.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.327-8755_327-8754i others(14): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126682081 | ||||||
chr9:126682081
|
GT | G | 4 | a0001c0002t0057g0156a0001c0004t0036g0235a0001c0008t0033g0142others(1): Show | 4 | HG01167.hp2 HG02559.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.327-8754delT | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126682081 | ||||||
chr9:126682082
|
T | C | 69 | a0001c0001t0183g0154a0001c0002t0001g0007a0001c0002t0001g0011others(66): Show | 69 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(66): Show |
intron_variant | MODIFIER | c.327-8754T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126682082 | ||||||
chr9:126682083
|
C | CT | 64 | a0001c0001t0007g0332a0001c0001t0008g0333a0001c0001t0018g0337others(61): Show | 64 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.327-8728dupT | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126682083 | |||||
chr9:126682083
|
C | T | 101 | a0001c0001t0004g0238a0001c0001t0028g0122a0001c0001t0067g0121others(98): Show | 102 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(99): Show |
intron_variant | MODIFIER | c.327-8753C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126682083 | ||||||
chr9:126682084
|
T | C | 4 | a0001c0002t0057g0156a0001c0004t0036g0235a0001c0008t0033g0142others(1): Show | 4 | HG01167.hp2 HG02559.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.327-8752T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126682084 | ||||||
chr9:126682108
|
T | TTTTTTTT others(6): Show |
5 | a0001c0001t0183g0154a0001c0004t0042g0209a0001c0004t0064g0082others(2): Show | 5 | HG01496.hp2 HG02572.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.327-8728_327-8727i others(15): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126682108 | ||||||
chr9:126682108
|
T | TTTTTTTT others(7): Show |
5 | a0001c0004t0042g0210a0001c0004t0182g0078a0001c0004t0184g0162others(2): Show | 5 | HG02055.hp2 HG03195.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.327-8728_327-8727i others(16): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126682108 | ||||||
chr9:126682108
|
T | TTTTTTTT others(8): Show |
1 | a0001c0004t0187g0083 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.327-8728_327-8727i others(17): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126682108 | ||||||
chr9:126682308
|
G | T | 6 | a0001c0005t0012g0135a0001c0005t0012g0136a0001c0005t0012g0137others(3): Show | 6 | HG01884.hp2 HG02055.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.327-8528G>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126682308 | ||||||
chr9:126682342
|
G | A | 6 | a0001c0002t0057g0156a0001c0008t0033g0142a0001c0008t0033g0143others(3): Show | 6 | HG01884.hp1 HG02559.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.327-8494G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126682342 | ||||||
chr9:126682500
|
A | G | 1 | a0001c0001t0008g0333 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.327-8336A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126682500 | ||||||
chr9:126682763
|
C | A | 1 | a0001c0001t0002g0272 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.327-8073C>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126682763 | ||||||
chr9:126682812
|
T | C | 6 | a0001c0005t0012g0135a0001c0005t0012g0136a0001c0005t0012g0137others(3): Show | 6 | HG01884.hp2 HG02055.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.327-8024T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126682812 | ||||||
chr9:126682820
|
A | G | 6 | a0001c0005t0012g0135a0001c0005t0012g0136a0001c0005t0012g0137others(3): Show | 6 | HG01884.hp2 HG02055.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.327-8016A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126682820 | ||||||
chr9:126682861
|
C | G | 1 | a0001c0001t0197g0222 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.327-7975C>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126682861 | ||||||
chr9:126682877
|
A | G | 1 | a0001c0001t0020g0269 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.327-7959A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126682877 | ||||||
chr9:126682894
|
G | GA | 59 | a0001c0001t0002g0297a0001c0001t0005g0212a0001c0001t0007g0328others(56): Show | 59 | HG00408.hp2 HG00609.hp2 HG01099.hp1 others(56): Show |
intron_variant | MODIFIER | c.327-7921dupA | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126682894 | |||||
chr9:126682894
|
G | GAA | 19 | a0001c0002t0001g0007a0001c0002t0001g0040a0001c0002t0022g0049others(16): Show | 19 | HG01069.hp1 HG01070.hp1 HG01168.hp1 others(16): Show |
intron_variant | MODIFIER | c.327-7922_327-7921d others(4): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126682894 | |||||
chr9:126682894
|
G | GAAA | 19 | a0001c0001t0102g0153a0001c0002t0001g0018a0001c0002t0009g0104others(16): Show | 19 | HG00438.hp1 HG00639.hp1 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.327-7923_327-7921d others(5): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126682894 | |||||
chr9:126682894
|
G | GAAAA | 55 | a0001c0001t0004g0238a0001c0001t0081g0074a0001c0001t0180g0198others(52): Show | 56 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(53): Show |
intron_variant | MODIFIER | c.327-7924_327-7921d others(6): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126682894 | |||||
chr9:126682894
|
GA | G | 8 | a0001c0001t0005g0285a0001c0001t0007g0332a0001c0001t0010g0327others(5): Show | 8 | HG01069.hp2 HG01167.hp2 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.327-7921delA | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126682894 | |||||
chr9:126682894
|
GAA | G | 6 | a0001c0005t0012g0135a0001c0005t0012g0136a0001c0005t0012g0137others(3): Show | 6 | HG01884.hp2 HG02055.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.327-7922_327-7921d others(4): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126682894 | |||||
chr9:126682912
|
A | G | 6 | a0001c0005t0012g0135a0001c0005t0012g0136a0001c0005t0012g0137others(3): Show | 6 | HG01884.hp2 HG02055.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.327-7924A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126682912 | ||||||
chr9:126683096
|
G | A | 1 | a0001c0010t0196g0146 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.327-7740G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126683096 | ||||||
chr9:126683138
|
G | A | 1 | a0001c0002t0089g0117 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.327-7698G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126683138 | ||||||
chr9:126683157
|
C | T | 79 | a0001c0001t0004g0238a0001c0001t0102g0153a0001c0001t0180g0198others(76): Show | 80 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.327-7679C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126683157 | ||||||
chr9:126683183
|
G | A | 6 | a0001c0005t0012g0135a0001c0005t0012g0136a0001c0005t0012g0137others(3): Show | 6 | HG01884.hp2 HG02055.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.327-7653G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126683183 | ||||||
chr9:126683441
|
G | A | 6 | a0001c0005t0012g0135a0001c0005t0012g0136a0001c0005t0012g0137others(3): Show | 6 | HG01884.hp2 HG02055.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.327-7395G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126683441 | ||||||
chr9:126683835
|
G | A | 1 | a0001c0002t0057g0156 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.327-7001G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126683835 | ||||||
chr9:126683972
|
C | T | 2 | a0001c0001t0172g0163a0001c0001t0174g0079 | 2 | HG02895.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.327-6864C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126683972 | ||||||
chr9:126683999
|
C | T | 16 | a0001c0001t0002g0221a0001c0001t0002g0317a0001c0001t0010g0251others(13): Show | 16 | HG00639.hp2 HG00735.hp2 HG01516.hp1 others(13): Show |
intron_variant | MODIFIER | c.327-6837C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126683999 | ||||||
chr9:126684102
|
A | G | 1 | a0001c0002t0195g0148 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.327-6734A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126684102 | ||||||
chr9:126684171
|
G | C | 12 | a0001c0002t0055g0176a0001c0002t0055g0179a0001c0002t0106g0144others(9): Show | 12 | HG01884.hp2 HG02055.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.327-6665G>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126684171 | ||||||
chr9:126684180
|
T | C | 12 | a0001c0002t0055g0176a0001c0002t0055g0179a0001c0002t0106g0144others(9): Show | 12 | HG01884.hp2 HG02055.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.327-6656T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126684180 | ||||||
chr9:126684187
|
G | A | 1 | a0001c0008t0033g0143 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.327-6649G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126684187 | ||||||
chr9:126684237
|
T | C | 1 | a0001c0001t0134g0019 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.327-6599T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126684237 | ||||||
chr9:126684312
|
A | G | 57 | a0001c0001t0004g0238a0001c0001t0180g0198a0001c0002t0003g0029others(54): Show | 58 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.327-6524A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126684312 | ||||||
chr9:126684369
|
G | C | 1 | a0001c0002t0057g0156 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.327-6467G>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126684369 | ||||||
chr9:126684713
|
C | A | 3 | a0001c0004t0042g0209a0001c0004t0042g0210a0001c0004t0146g0213 | 3 | HG03225.hp1 HG03453.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.327-6123C>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126684713 | ||||||
chr9:126684746
|
A | AC | 13 | a0001c0002t0055g0176a0001c0002t0055g0179a0001c0002t0106g0144others(10): Show | 13 | HG01496.hp2 HG01884.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.327-6084dupC | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126684746 | |||||
chr9:126684753
|
G | A | 171 | a0001c0001t0004g0238a0001c0001t0102g0153a0001c0001t0180g0198others(168): Show | 172 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(169): Show |
intron_variant | MODIFIER | c.327-6083G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126684753 | ||||||
chr9:126685060
|
C | T | 63 | a0001c0002t0001g0007a0001c0002t0001g0011a0001c0002t0001g0016others(60): Show | 63 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.327-5776C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126685060 | ||||||
chr9:126685284
|
G | T | 2 | a0001c0001t0096g0245a0001c0001t0118g0242 | 2 | HG03688.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.327-5552G>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126685284 | ||||||
chr9:126685328
|
C | T | 2 | a0001c0010t0196g0146a0001c0011t0086g0077 | 2 | HG01884.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.327-5508C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126685328 | ||||||
chr9:126685334
|
G | A | 1 | a0001c0001t0183g0154 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.327-5502G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126685334 | ||||||
chr9:126685358
|
G | A | 2 | a0001c0001t0002g0244a0001c0001t0002g0246 | 2 | HG03834.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.327-5478G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126685358 | ||||||
chr9:126685363
|
C | T | 1 | a0001c0001t0183g0154 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.327-5473C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126685363 | ||||||
chr9:126685461
|
G | A | 63 | a0001c0002t0001g0007a0001c0002t0001g0011a0001c0002t0001g0016others(60): Show | 63 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.327-5375G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126685461 | ||||||
chr9:126685507
|
G | A | 1 | a0001c0006t0050g0150 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.327-5329G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126685507 | ||||||
chr9:126685679
|
G | A | 2 | a0001c0003t0049g0147a0001c0003t0049g0158 | 2 | HG00639.hp1 HG01109.hp2 |
intron_variant | MODIFIER | c.327-5157G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126685679 | ||||||
chr9:126685795
|
G | A | 12 | a0001c0001t0183g0154a0001c0004t0042g0209a0001c0004t0042g0210others(9): Show | 12 | HG01243.hp2 HG01496.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.327-5041G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126685795 | ||||||
chr9:126685841
|
T | C | 33 | a0001c0001t0002g0204a0001c0001t0002g0205a0001c0001t0002g0218others(30): Show | 33 | HG00099.hp2 HG00558.hp2 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.327-4995T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126685841 | ||||||
chr9:126685852
|
T | G | 172 | a0001c0001t0004g0238a0001c0001t0102g0153a0001c0001t0180g0198others(169): Show | 173 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(170): Show |
intron_variant | MODIFIER | c.327-4984T>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126685852 | ||||||
chr9:126685863
|
T | C | 2 | a0001c0002t0003g0215a0001c0002t0013g0123 | 2 | HG01257.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.327-4973T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126685863 | ||||||
chr9:126685914
|
G | A | 5 | a0001c0005t0012g0135a0001c0005t0012g0136a0001c0005t0012g0137others(2): Show | 5 | HG01884.hp2 HG02055.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.327-4922G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126685914 | ||||||
chr9:126686136
|
C | T | 16 | a0001c0001t0183g0154a0001c0003t0058g0132a0001c0003t0077g0130others(13): Show | 16 | HG01167.hp2 HG01243.hp2 HG01496.hp2 others(13): Show |
intron_variant | MODIFIER | c.327-4700C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126686136 | ||||||
chr9:126686235
|
A | G | 173 | a0001c0001t0004g0238a0001c0001t0102g0153a0001c0001t0180g0198others(170): Show | 174 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(171): Show |
intron_variant | MODIFIER | c.327-4601A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126686235 | ||||||
chr9:126686279
|
C | CA | 16 | a0001c0001t0008g0030a0001c0001t0029g0113a0001c0001t0082g0097others(13): Show | 16 | HG00438.hp2 HG01884.hp2 HG01978.hp1 others(13): Show |
intron_variant | MODIFIER | c.327-4540dupA | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126686279 | |||||
chr9:126686279
|
C | CAA | 88 | a0001c0001t0102g0153a0001c0002t0001g0007a0001c0002t0001g0011others(85): Show | 88 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(85): Show |
intron_variant | MODIFIER | c.327-4541_327-4540d others(4): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126686279 | |||||
chr9:126686279
|
C | CAAA | 47 | a0001c0001t0004g0238a0001c0001t0180g0198a0001c0002t0003g0038others(44): Show | 48 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(45): Show |
intron_variant | MODIFIER | c.327-4542_327-4540d others(5): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126686279 | |||||
chr9:126686348
|
T | G | 1 | a0001c0004t0042g0210 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.327-4488T>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126686348 | ||||||
chr9:126686511
|
A | G | 6 | a0001c0005t0012g0135a0001c0005t0012g0136a0001c0005t0012g0137others(3): Show | 6 | HG01884.hp2 HG02055.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.327-4325A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126686511 | ||||||
chr9:126686521
|
G | A | 63 | a0001c0002t0001g0007a0001c0002t0001g0011a0001c0002t0001g0016others(60): Show | 63 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.327-4315G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126686521 | ||||||
chr9:126686581
|
C | T | 1 | a0001c0001t0177g0120 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.327-4255C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126686581 | ||||||
chr9:126686641
|
C | T | 3 | a0001c0002t0057g0156a0001c0008t0033g0142a0001c0008t0033g0143 | 3 | HG02559.hp2 HG02717.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.327-4195C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126686641 | ||||||
chr9:126686677
|
G | T | 2 | a0001c0010t0196g0146a0001c0011t0086g0077 | 2 | HG01884.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.327-4159G>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126686677 | ||||||
chr9:126686720
|
G | A | 1 | a0001c0002t0162g0032 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.327-4116G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126686720 | ||||||
chr9:126686973
|
G | A | 1 | a0001c0001t0039g0320 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.327-3863G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126686973 | ||||||
chr9:126687030
|
G | A | 1 | a0001c0001t0068g0070 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.327-3806G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126687030 | ||||||
chr9:126687214
|
T | C | 2 | a0001c0001t0011g0061a0001c0001t0135g0064 | 2 | NA18942.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.327-3622T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126687214 | ||||||
chr9:126687217
|
C | CT | 171 | a0001c0001t0004g0238a0001c0001t0026g0129a0001c0001t0102g0153others(168): Show | 172 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(169): Show |
intron_variant | MODIFIER | c.327-3608dupT | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126687217 | |||||
chr9:126687217
|
C | T | 1 | a0001c0001t0131g0229 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.327-3619C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126687217 | ||||||
chr9:126687371
|
G | C | 3 | a0001c0002t0057g0156a0001c0008t0033g0142a0001c0008t0033g0143 | 3 | HG02559.hp2 HG02717.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.327-3465G>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126687371 | ||||||
chr9:126687476
|
C | T | 1 | a0001c0001t0020g0256 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.327-3360C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126687476 | ||||||
chr9:126687626
|
G | T | 6 | a0001c0005t0012g0135a0001c0005t0012g0136a0001c0005t0012g0137others(3): Show | 6 | HG01884.hp2 HG02055.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.327-3210G>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126687626 | ||||||
chr9:126687952
|
G | A | 6 | a0001c0002t0055g0176a0001c0002t0055g0179a0001c0002t0106g0144others(3): Show | 6 | HG02280.hp2 HG02615.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.327-2884G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126687952 | ||||||
chr9:126688058
|
C | T | 1 | a0001c0002t0101g0141 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.327-2778C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126688058 | ||||||
chr9:126688065
|
C | T | 1 | a0001c0001t0175g0166 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.327-2771C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126688065 | ||||||
chr9:126688128
|
C | A | 1 | a0001c0001t0131g0229 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.327-2708C>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126688128 | ||||||
chr9:126688160
|
T | C | 172 | a0001c0001t0004g0238a0001c0001t0180g0198a0001c0001t0183g0154others(169): Show | 173 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(170): Show |
intron_variant | MODIFIER | c.327-2676T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126688160 | ||||||
chr9:126688262
|
G | A | 1 | a0001c0002t0164g0329 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.327-2574G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126688262 | ||||||
chr9:126688315
|
C | T | 1 | a0001c0001t0141g0268 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.327-2521C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126688315 | ||||||
chr9:126688379
|
A | C | 2 | a0001c0010t0196g0146a0001c0011t0086g0077 | 2 | HG01884.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.327-2457A>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126688379 | ||||||
chr9:126688425
|
G | A | 6 | a0001c0002t0055g0176a0001c0002t0055g0179a0001c0002t0106g0144others(3): Show | 6 | HG02280.hp2 HG02615.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.327-2411G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126688425 | ||||||
chr9:126688598
|
C | T | 1 | a0001c0003t0113g0220 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.327-2238C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126688598 | ||||||
chr9:126688641
|
G | C | 2 | a0001c0001t0011g0314a0001c0001t0098g0318 | 2 | HG02523.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.327-2195G>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126688641 | ||||||
chr9:126688781
|
A | G | 1 | a0001c0004t0036g0235 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.327-2055A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126688781 | ||||||
chr9:126688848
|
G | A | 4 | a0001c0002t0055g0176a0001c0002t0055g0179a0001c0002t0106g0144others(1): Show | 4 | HG02280.hp2 HG02630.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.327-1988G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126688848 | ||||||
chr9:126688988
|
C | G | 1 | a0001c0001t0039g0320 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.327-1848C>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126688988 | ||||||
chr9:126688988
|
C | T | 1 | a0001c0001t0065g0086 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.327-1848C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126688988 | ||||||
chr9:126689333
|
G | A | 16 | a0001c0001t0183g0154a0001c0003t0058g0132a0001c0003t0077g0130others(13): Show | 16 | HG01167.hp2 HG01243.hp2 HG01496.hp2 others(13): Show |
intron_variant | MODIFIER | c.327-1503G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126689333 | ||||||
chr9:126689442
|
G | A | 2 | a0001c0001t0079g0085a0001c0001t0173g0159 | 2 | HG02965.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.327-1394G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126689442 | ||||||
chr9:126689479
|
G | A | 1 | a0001c0001t0177g0120 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.327-1357G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126689479 | ||||||
chr9:126689552
|
G | A | 1 | a0001c0001t0039g0037 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.327-1284G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126689552 | ||||||
chr9:126689721
|
TGATGGGA | T | 63 | a0001c0002t0001g0007a0001c0002t0001g0011a0001c0002t0001g0016others(60): Show | 63 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.327-1102_327-1096d others(9): Show |
LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | 126689721 | |||||
chr9:126689774
|
C | T | 63 | a0001c0002t0001g0007a0001c0002t0001g0011a0001c0002t0001g0016others(60): Show | 63 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.327-1062C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126689774 | ||||||
chr9:126689901
|
G | C | 1 | a0001c0010t0196g0146 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.327-935G>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126689901 | ||||||
chr9:126689925
|
T | C | 63 | a0001c0002t0001g0007a0001c0002t0001g0011a0001c0002t0001g0016others(60): Show | 63 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.327-911T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126689925 | ||||||
chr9:126689994
|
G | A | 2 | a0001c0001t0002g0221a0001c0001t0097g0217 | 2 | HG02080.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.327-842G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126689994 | ||||||
chr9:126690110
|
CT | C | 64 | a0001c0001t0002g0317a0001c0002t0001g0007a0001c0002t0001g0011others(61): Show | 64 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.327-725delT | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126690110 | ||||||
chr9:126690498
|
A | G | 69 | a0001c0002t0001g0007a0001c0002t0001g0011a0001c0002t0001g0016others(66): Show | 69 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(66): Show |
intron_variant | MODIFIER | c.327-338A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126690498 | ||||||
chr9:126690508
|
C | G | 1 | a0001c0002t0001g0306 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.327-328C>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126690508 | ||||||
chr9:126690518
|
A | G | 173 | a0001c0001t0040g0322a0001c0001t0180g0198a0001c0002t0001g0007others(170): Show | 174 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(171): Show |
intron_variant | MODIFIER | c.327-318A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126690518 | ||||||
chr9:126690553
|
T | A | 6 | a0001c0005t0012g0135a0001c0005t0012g0136a0001c0005t0012g0137others(3): Show | 6 | HG01884.hp2 HG02055.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.327-283T>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126690553 | ||||||
chr9:126690563
|
G | A | 6 | a0001c0005t0012g0135a0001c0005t0012g0136a0001c0005t0012g0137others(3): Show | 6 | HG01884.hp2 HG02055.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.327-273G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126690563 | ||||||
chr9:126690730
|
C | T | 3 | a0001c0001t0025g0095a0001c0001t0080g0099a0001c0001t0127g0275 | 3 | HG00642.hp2 HG01106.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.327-106C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 2/7 | chr9 | 126690730 | ||||||
chr9:126691088
|
G | A | 9 | a0001c0004t0036g0235a0001c0005t0012g0135a0001c0005t0012g0136others(6): Show | 9 | HG01167.hp2 HG01884.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.559+20G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 3/7 | chr9 | 126691088 | ||||||
chr9:126691518
|
G | A | 3 | a0001c0004t0036g0235a0001c0007t0048g0252a0001c0007t0048g0312 | 3 | HG01167.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.559+450G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 3/7 | chr9 | 126691518 | ||||||
chr9:126691528
|
C | G | 1 | a0001c0002t0055g0176 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.559+460C>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 3/7 | chr9 | 126691528 | ||||||
chr9:126691537
|
T | C | 1 | a0001c0001t0040g0322 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.559+469T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 3/7 | chr9 | 126691537 | ||||||
chr9:126691612
|
C | T | 21 | a0001c0002t0056g0157a0001c0002t0101g0141a0001c0002t0168g0180others(18): Show | 21 | HG00639.hp1 HG01109.hp2 HG02717.hp2 others(18): Show |
intron_variant | MODIFIER | c.559+544C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 3/7 | chr9 | 126691612 | ||||||
chr9:126691638
|
G | T | 1 | a0001c0002t0001g0016 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.559+570G>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 3/7 | chr9 | 126691638 | ||||||
chr9:126691649
|
A | G | 1 | a0001c0012t0117g0140 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.559+581A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 3/7 | chr9 | 126691649 | ||||||
chr9:126691743
|
C | T | 3 | a0001c0001t0025g0095a0001c0001t0080g0099a0001c0001t0127g0275 | 3 | HG00642.hp2 HG01106.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.559+675C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 3/7 | chr9 | 126691743 | ||||||
chr9:126691807
|
G | A | 2 | a0001c0002t0003g0243a0001c0002t0003g0284 | 2 | NA18975.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.559+739G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 3/7 | chr9 | 126691807 | ||||||
chr9:126691809
|
A | G | 2 | a0001c0007t0048g0252a0001c0007t0048g0312 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.559+741A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 3/7 | chr9 | 126691809 | ||||||
chr9:126691822
|
G | A | 70 | a0001c0002t0001g0007a0001c0002t0001g0011a0001c0002t0001g0016others(67): Show | 70 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.559+754G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 3/7 | chr9 | 126691822 | ||||||
chr9:126691917
|
C | G | 1 | a0001c0001t0081g0074 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.559+849C>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 3/7 | chr9 | 126691917 | ||||||
chr9:126692261
|
C | A | 8 | a0001c0001t0036g0227a0001c0001t0079g0085a0001c0001t0121g0230others(5): Show | 8 | HG00735.hp1 HG02886.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.560-881C>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 3/7 | chr9 | 126692261 | ||||||
chr9:126692435
|
G | T | 57 | a0001c0002t0003g0029a0001c0002t0003g0038a0001c0002t0003g0043others(54): Show | 58 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.560-707G>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 3/7 | chr9 | 126692435 | ||||||
chr9:126692483
|
C | T | 1 | a0001c0001t0027g0073 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.560-659C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 3/7 | chr9 | 126692483 | ||||||
chr9:126692484
|
G | A | 1 | a0001c0002t0094g0103 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.560-658G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 3/7 | chr9 | 126692484 | ||||||
chr9:126692602
|
G | A | 2 | a0001c0008t0033g0142a0001c0008t0033g0143 | 2 | HG02717.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.560-540G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 3/7 | chr9 | 126692602 | ||||||
chr9:126692653
|
G | A | 2 | a0001c0007t0048g0252a0001c0007t0048g0312 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.560-489G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 3/7 | chr9 | 126692653 | ||||||
chr9:126692690
|
T | C | 2 | a0001c0007t0048g0252a0001c0007t0048g0312 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.560-452T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 3/7 | chr9 | 126692690 | ||||||
chr9:126692745
|
G | A | 3 | a0001c0002t0001g0034a0001c0004t0184g0162a0001c0012t0117g0140 | 3 | HG03195.hp1 NA19009.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.560-397G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 3/7 | chr9 | 126692745 | ||||||
chr9:126692749
|
G | A | 2 | a0001c0008t0033g0142a0001c0008t0033g0143 | 2 | HG02717.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.560-393G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 3/7 | chr9 | 126692749 | ||||||
chr9:126692809
|
T | G | 1 | a0001c0001t0052g0164 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.560-333T>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 3/7 | chr9 | 126692809 | ||||||
chr9:126692928
|
G | A | 2 | a0001c0001t0002g0223a0001c0001t0107g0232 | 2 | HG02647.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.560-214G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 3/7 | chr9 | 126692928 | ||||||
chr9:126692967
|
T | C | 2 | a0001c0007t0048g0252a0001c0007t0048g0312 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.560-175T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 3/7 | chr9 | 126692967 | ||||||
chr9:126693055
|
A | G | 2 | a0001c0007t0048g0252a0001c0007t0048g0312 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.560-87A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 3/7 | chr9 | 126693055 | ||||||
chr9:126693093
|
C | T | 70 | a0001c0002t0001g0007a0001c0002t0001g0011a0001c0002t0001g0016others(67): Show | 70 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.560-49C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 3/7 | chr9 | 126693093 | ||||||
chr9:126693114
|
A | C | 3 | a0001c0007t0048g0252a0001c0007t0048g0312a0001c0010t0196g0146 | 3 | HG02895.hp2 HG02897.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.560-28A>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 3/7 | chr9 | 126693114 | ||||||
chr9:126693123
|
C | T | 2 | a0001c0007t0048g0252a0001c0007t0048g0312 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.560-19C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 3/7 | chr9 | 126693123 | ||||||
chr9:126693333
|
G | A | 1 | a0001c0002t0031g0002 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.741+10G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 4/7 | chr9 | 126693333 | ||||||
chr9:126693337
|
G | T | 1 | a0001c0001t0008g0005 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.741+14G>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 4/7 | chr9 | 126693337 | ||||||
chr9:126693416
|
C | T | 1 | a0001c0011t0086g0077 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.741+93C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 4/7 | chr9 | 126693416 | ||||||
chr9:126693477
|
G | A | 1 | a0001c0012t0117g0140 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.742-47G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 4/7 | chr9 | 126693477 | ||||||
chr9:126693654
|
G | A | 1 | a0001c0010t0196g0146 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.819+53G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 5/7 | chr9 | 126693654 | ||||||
chr9:126693830
|
C | T | 1 | a0001c0004t0063g0080 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.886+18C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 6/7 | chr9 | 126693830 | ||||||
chr9:126693850
|
G | A | 1 | a0001c0001t0132g0301 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.886+38G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 6/7 | chr9 | 126693850 | ||||||
chr9:126693937
|
G | A | 1 | a0001c0001t0125g0253 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.886+125G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 6/7 | chr9 | 126693937 | ||||||
chr9:126694249
|
G | C | 2 | a0001c0007t0048g0252a0001c0007t0048g0312 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.886+437G>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 6/7 | chr9 | 126694249 | ||||||
chr9:126694251
|
G | A | 102 | a0001c0002t0001g0007a0001c0002t0001g0011a0001c0002t0001g0016others(99): Show | 102 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(99): Show |
intron_variant | MODIFIER | c.886+439G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 6/7 | chr9 | 126694251 | ||||||
chr9:126694302
|
G | A | 4 | a0001c0001t0005g0212a0001c0001t0005g0285a0001c0001t0005g0300others(1): Show | 4 | HG01934.hp2 HG01993.hp2 HG02300.hp1 others(1): Show |
intron_variant | MODIFIER | c.886+490G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 6/7 | chr9 | 126694302 | ||||||
chr9:126694356
|
A | G | 3 | a0001c0001t0011g0214a0001c0001t0061g0101a0001c0001t0085g0068 | 3 | HG01361.hp1 HG03239.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.886+544A>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 6/7 | chr9 | 126694356 | ||||||
chr9:126694401
|
T | C | 6 | a0001c0005t0012g0135a0001c0005t0012g0136a0001c0005t0012g0137others(3): Show | 6 | HG01884.hp2 HG02055.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.886+589T>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 6/7 | chr9 | 126694401 | ||||||
chr9:126694496
|
C | A | 1 | a0001c0001t0082g0097 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.886+684C>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 6/7 | chr9 | 126694496 | ||||||
chr9:126694556
|
C | T | 1 | a0001c0001t0027g0073 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.886+744C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 6/7 | chr9 | 126694556 | ||||||
chr9:126694590
|
C | T | 1 | a0001c0001t0081g0074 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.886+778C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 6/7 | chr9 | 126694590 | ||||||
chr9:126694739
|
G | T | 6 | a0001c0005t0012g0135a0001c0005t0012g0136a0001c0005t0012g0137others(3): Show | 6 | HG01884.hp2 HG02055.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.886+927G>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 6/7 | chr9 | 126694739 | ||||||
chr9:126694782
|
C | T | 1 | a0001c0001t0138g0303 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.886+970C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 6/7 | chr9 | 126694782 | ||||||
chr9:126694933
|
G | A | 3 | a0001c0001t0002g0317a0001c0001t0083g0119a0001c0001t0125g0253 | 3 | HG02027.hp1 NA19004.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.887-906G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 6/7 | chr9 | 126694933 | ||||||
chr9:126694933
|
G | T | 7 | a0001c0003t0058g0132a0001c0003t0077g0130a0001c0003t0109g0254others(4): Show | 7 | HG02109.hp1 HG02647.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.887-906G>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 6/7 | chr9 | 126694933 | ||||||
chr9:126694996
|
C | T | 3 | a0001c0001t0007g0012a0001c0001t0007g0048a0001c0001t0119g0293 | 3 | HG02083.hp2 NA19068.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.887-843C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 6/7 | chr9 | 126694996 | ||||||
chr9:126695203
|
C | T | 5 | a0001c0003t0058g0132a0001c0003t0077g0130a0001c0003t0109g0254others(2): Show | 5 | HG02109.hp1 HG02647.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.887-636C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 6/7 | chr9 | 126695203 | ||||||
chr9:126695320
|
G | A | 98 | a0001c0002t0001g0007a0001c0002t0001g0011a0001c0002t0001g0016others(95): Show | 98 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(95): Show |
intron_variant | MODIFIER | c.887-519G>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 6/7 | chr9 | 126695320 | ||||||
chr9:126695368
|
C | T | 58 | a0001c0001t0003g0241a0001c0002t0003g0029a0001c0002t0003g0038others(55): Show | 59 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.887-471C>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 6/7 | chr9 | 126695368 | ||||||
chr9:126695469
|
CG | C | 58 | a0001c0001t0003g0241a0001c0002t0003g0029a0001c0002t0003g0038others(55): Show | 59 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.887-365delG | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr9 | 126695469 | |||||
chr9:126695473
|
G | C | 58 | a0001c0001t0003g0241a0001c0002t0003g0029a0001c0002t0003g0038others(55): Show | 59 | HG00280.hp1 HG00323.hp2 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.887-366G>C | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 6/7 | chr9 | 126695473 | ||||||
chr9:126695675
|
C | G | 1 | a0001c0002t0001g0054 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.887-164C>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 6/7 | chr9 | 126695675 | ||||||
chr9:126695762
|
T | A | 2 | a0001c0001t0181g0193a0001c0001t0197g0222 | 2 | HG02615.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.887-77T>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 6/7 | chr9 | 126695762 | ||||||
chr9:126695813
|
G | T | 102 | a0001c0002t0001g0007a0001c0002t0001g0011a0001c0002t0001g0016others(99): Show | 102 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(99): Show |
intron_variant | MODIFIER | c.887-26G>T | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 6/7 | chr9 | 126695813 | ||||||
chr9:126696095
|
C | A | 1 | a0001c0010t0196g0146 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1051+92C>A | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 7/7 | chr9 | 126696095 | ||||||
chr9:126696097
|
C | G | 1 | a0001c0001t0002g0234 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1051+94C>G | LMX1B | ENSG00000136944.19 | transcript | ENST00000373474.9 | protein_coding | 7/7 | chr9 | 126696097 |