geneid | 286826 |
---|---|
ensemblid | ENSG00000183814.16 |
hgncid | 30830 |
symbol | LIN9 |
name | lin-9 DREAM MuvB core complex component |
refseq_nuc | NM_001366245.2 |
refseq_prot | NP_001353174.1 |
ensembl_nuc | ENST00000681046.1 |
ensembl_prot | ENSP00000505590.1 |
mane_status | MANE Select |
chr | chr1 |
start | 226231157 |
end | 226309164 |
strand | - |
ver | v1.2 |
region | chr1:226231157-226309164 |
region5000 | chr1:226226157-226314164 |
regionname0 | LIN9_chr1_226231157_226309164 |
regionname5000 | LIN9_chr1_226226157_226314164 |
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 | 542 | 361 | 76 | 69 | 162 | 8 | 44 | 125 | LIN9_chr1_226226157_226314164 | LIN9 | copy fasta | chr1 | 226226157 | 226314164 |
a0002 | 0/0 | 542 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | copy fasta | chr1 | 226226157 | 226314164 |
a0003 | 0/0 | 542 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | copy fasta | chr1 | 226226157 | 226314164 |
a0004 | 0/0 | 542 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | LIN9_chr1_226226157_226314164 | LIN9 | copy fasta | chr1 | 226226157 | 226314164 |
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 | 0/1 | 1629 | 260 | 56 | 49 | 121 | 5 | 28 | LIN9_chr1_226226157_226314164 | LIN9 | copy fasta | chr1 | 226226157 | 226314164 |
c0002 | 1/0 | 1629 | 99 | 20 | 19 | 40 | 3 | 16 | LIN9_chr1_226226157_226314164 | LIN9 | copy fasta | chr1 | 226226157 | 226314164 |
c0003 | 0/0 | 1629 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | copy fasta | chr1 | 226226157 | 226314164 |
c0004 | 0/0 | 1629 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | copy fasta | chr1 | 226226157 | 226314164 |
c0005 | 0/0 | 1629 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | copy fasta | chr1 | 226226157 | 226314164 |
c0006 | 0/0 | 1629 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | copy fasta | chr1 | 226226157 | 226314164 |
c0007 | 0/0 | 1629 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | copy fasta | chr1 | 226226157 | 226314164 |
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 | 0/1 | 1370 | 217 | 57 | 44 | 87 | 3 | 25 | LIN9_chr1_226226157_226314164 | LIN9 | copy fasta | chr1 | 226226157 | 226314164 |
t0002 | 1/0 | 1370 | 95 | 19 | 18 | 38 | 3 | 16 | LIN9_chr1_226226157_226314164 | LIN9 | copy fasta | chr1 | 226226157 | 226314164 |
t0003 | 0/0 | 1370 | 45 | 0 | 5 | 35 | 2 | 3 | LIN9_chr1_226226157_226314164 | LIN9 | copy fasta | chr1 | 226226157 | 226314164 |
t0004 | 0/0 | 1370 | 3 | 0 | 3 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | copy fasta | chr1 | 226226157 | 226314164 |
t0005 | 0/0 | 1370 | 2 | 0 | 0 | 2 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | copy fasta | chr1 | 226226157 | 226314164 |
t0006 | 0/0 | 1370 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | copy fasta | chr1 | 226226157 | 226314164 |
t0007 | 0/0 | 1370 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | copy fasta | chr1 | 226226157 | 226314164 |
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 | 0 | 0 | 0 | 2 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0003 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0020 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0230 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0317 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0356 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0357 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0358 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0359 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0360 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
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 | 0/1 | 1629 | 260 | 56 | 49 | 121 | 5 | 28 | LIN9_chr1_226226157_226314164 | LIN9 | copy fasta | chr1 | 226226157 | 226314164 |
a0001c0002 | 1/0 | 1629 | 99 | 20 | 19 | 40 | 3 | 16 | LIN9_chr1_226226157_226314164 | LIN9 | copy fasta | chr1 | 226226157 | 226314164 |
a0001c0004 | 0/0 | 1629 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | copy fasta | chr1 | 226226157 | 226314164 |
a0001c0007 | 0/0 | 1629 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | copy fasta | chr1 | 226226157 | 226314164 |
a0002c0003 | 0/0 | 1629 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | copy fasta | chr1 | 226226157 | 226314164 |
a0003c0005 | 0/0 | 1629 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | copy fasta | chr1 | 226226157 | 226314164 |
a0004c0006 | 0/0 | 1629 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | copy fasta | chr1 | 226226157 | 226314164 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 2998 | 212 | 56 | 44 | 83 | 3 | 25 | LIN9_chr1_226226157_226314164 | LIN9 | copy fasta | chr1 | 226226157 | 226314164 |
a0001c0001t0003 | 0/0 | 2998 | 45 | 0 | 5 | 35 | 2 | 3 | LIN9_chr1_226226157_226314164 | LIN9 | copy fasta | chr1 | 226226157 | 226314164 |
a0001c0001t0005 | 0/0 | 2998 | 2 | 0 | 0 | 2 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | copy fasta | chr1 | 226226157 | 226314164 |
a0001c0001t0006 | 0/0 | 2998 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | copy fasta | chr1 | 226226157 | 226314164 |
a0001c0002t0001 | 0/0 | 2998 | 2 | 1 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | copy fasta | chr1 | 226226157 | 226314164 |
a0001c0002t0002 | 1/0 | 2998 | 93 | 19 | 16 | 38 | 3 | 16 | LIN9_chr1_226226157_226314164 | LIN9 | copy fasta | chr1 | 226226157 | 226314164 |
a0001c0002t0004 | 0/0 | 2998 | 3 | 0 | 3 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | copy fasta | chr1 | 226226157 | 226314164 |
a0001c0002t0007 | 0/0 | 2998 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | copy fasta | chr1 | 226226157 | 226314164 |
a0001c0004t0002 | 0/0 | 2998 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | copy fasta | chr1 | 226226157 | 226314164 |
a0001c0007t0001 | 0/0 | 2998 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | copy fasta | chr1 | 226226157 | 226314164 |
a0002c0003t0002 | 0/0 | 2998 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | copy fasta | chr1 | 226226157 | 226314164 |
a0003c0005t0001 | 0/0 | 2998 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | copy fasta | chr1 | 226226157 | 226314164 |
a0004c0006t0001 | 0/0 | 2998 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | copy fasta | chr1 | 226226157 | 226314164 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0230 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0356 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0357 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0358 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0359 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0360 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0001g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0003g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0003g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0003g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0003g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0003g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0003g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0003g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0003g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0003g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0003g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0003g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0003g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0003g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0003g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0003g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0003g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0003g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0003g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0003g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0003g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0003g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0003g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0003g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0003g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0003g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0003g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0003g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0003g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0003g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0003g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0003g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0003g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0003g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0003g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0003g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0005g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0005g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0001t0006g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0002t0001g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0002t0002g0001 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0002t0002g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0002t0002g0003 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0002t0002g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0002t0002g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0002t0002g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0002t0002g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0002t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0002t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0002t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0002t0002g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0002t0002g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0002t0002g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0002t0002g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0002t0002g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0002t0002g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0002t0002g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0002t0002g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0002t0002g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0002t0002g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0002t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0002t0002g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0002t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0002t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0002t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0002t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0002t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0002t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0002t0002g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0002t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0002t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0002t0002g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0002t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0002t0002g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0002t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0002t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0002t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0002t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0002t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0002t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0002t0002g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0002t0002g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0002t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0002t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0002t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0002t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0002t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0002t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0002t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0002t0002g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0002t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0002t0002g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0002t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0002t0002g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0002t0002g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0002t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0002t0002g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0002t0002g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0002t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0002t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0002t0002g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0002t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0002t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0002t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0002t0002g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0002t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0002t0002g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0002t0002g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0002t0002g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0002t0002g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0002t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0002t0002g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0002t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0002t0002g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0002t0002g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0002t0002g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0002t0002g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0002t0002g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0002t0002g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0002t0002g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0002t0002g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0002t0002g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0002t0002g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0002t0002g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0002t0002g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0002t0002g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0002t0002g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0002t0002g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0002t0002g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0002t0002g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0002t0002g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0002t0002g0317 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0002t0004g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0002t0004g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0002t0004g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0002t0007g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0004t0002g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0001c0007t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0002c0003t0002g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0003c0005t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
a0004c0006t0001g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0029 | EUR | GBR | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG00099 | hp2 | a0001 | c0001 | t0003 | g0157 | EUR | GBR | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG00280 | hp1 | a0001 | c0002 | t0002 | g0172 | EUR | FIN | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0020 | EUR | FIN | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG00408 | hp1 | a0001 | c0002 | t0002 | g0160 | EAS | CHS | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG00408 | hp2 | a0001 | c0002 | t0002 | g0133 | EAS | CHS | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG00423 | hp1 | a0001 | c0001 | t0003 | g0048 | EAS | CHS | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0348 | EAS | CHS | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | CHS | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | CHS | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG00544 | hp1 | a0001 | c0002 | t0002 | g0146 | EAS | CHS | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | CHS | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | CHS | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG00597 | hp2 | a0001 | c0002 | t0002 | g0175 | EAS | CHS | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG00609 | hp1 | a0001 | c0001 | t0003 | g0054 | EAS | CHS | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0333 | EAS | CHS | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0346 | EAS | CHS | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG00621 | hp2 | a0001 | c0002 | t0007 | g0198 | EAS | CHS | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG00639 | hp1 | a0001 | c0002 | t0002 | g0191 | AMR | PUR | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0242 | AMR | PUR | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG00673 | hp1 | a0001 | c0001 | t0003 | g0037 | EAS | CHS | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | CHS | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0315 | AMR | PUR | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0269 | AMR | PUR | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG00738 | hp1 | a0001 | c0002 | t0002 | g0138 | AMR | PUR | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0279 | AMR | PUR | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG00741 | hp1 | a0001 | c0001 | t0003 | g0078 | AMR | PUR | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0274 | AMR | PUR | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG01069 | hp1 | a0001 | c0002 | t0004 | g0150 | AMR | PUR | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG01071 | hp1 | a0001 | c0002 | t0004 | g0151 | AMR | PUR | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG01074 | hp1 | a0001 | c0002 | t0002 | g0180 | AMR | PUR | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0233 | AMR | PUR | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG01099 | hp1 | a0001 | c0001 | t0003 | g0087 | AMR | PUR | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG01106 | hp2 | a0001 | c0004 | t0002 | g0134 | AMR | PUR | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG01109 | hp1 | a0001 | c0002 | t0002 | g0292 | AMR | PUR | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0282 | AMR | PUR | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0243 | AMR | PUR | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG01167 | hp2 | a0001 | c0002 | t0002 | g0296 | AMR | PUR | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG01168 | hp1 | a0001 | c0002 | t0002 | g0291 | AMR | PUR | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG01168 | hp2 | a0001 | c0001 | t0003 | g0121 | AMR | PUR | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG01169 | hp1 | a0001 | c0002 | t0002 | g0293 | AMR | PUR | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0239 | AMR | PUR | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG01192 | hp1 | a0002 | c0003 | t0002 | g0148 | AMR | PUR | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG01192 | hp2 | a0001 | c0002 | t0002 | g0182 | AMR | PUR | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG01243 | hp1 | a0001 | c0002 | t0002 | g0137 | AMR | PUR | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0232 | AMR | PUR | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0248 | AMR | CLM | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | CLM | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG01256 | hp1 | a0001 | c0002 | t0002 | g0158 | AMR | CLM | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0080 | AMR | CLM | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0273 | AMR | CLM | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG01257 | hp2 | a0001 | c0002 | t0002 | g0140 | AMR | CLM | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | CLM | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0240 | AMR | CLM | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0234 | AMR | CLM | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | CLM | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0266 | AMR | CLM | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0277 | AMR | CLM | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG01361 | hp1 | a0001 | c0002 | t0002 | g0142 | AMR | CLM | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG01361 | hp2 | a0001 | c0002 | t0002 | g0206 | AMR | CLM | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | CLM | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0268 | AMR | CLM | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG01496 | hp1 | a0001 | c0002 | t0002 | g0141 | AMR | CLM | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0249 | AMR | CLM | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0241 | EUR | IBS | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG01516 | hp2 | a0001 | c0002 | t0002 | g0143 | EUR | IBS | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | ACB | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG01891 | hp2 | a0001 | c0002 | t0002 | g0295 | AFR | ACB | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0229 | AMR | PEL | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | PEL | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0256 | AMR | PEL | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PEL | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0267 | AMR | PEL | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PEL | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | PEL | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0237 | AMR | PEL | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG01993 | hp1 | a0001 | c0001 | t0003 | g0073 | AMR | PEL | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0226 | AMR | PEL | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | PEL | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0228 | AMR | PEL | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG02027 | hp1 | a0001 | c0001 | t0003 | g0192 | EAS | KHV | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG02027 | hp2 | a0003 | c0005 | t0001 | g0095 | EAS | KHV | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | KHV | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG02040 | hp2 | a0001 | c0001 | t0003 | g0052 | EAS | KHV | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG02055 | hp1 | a0001 | c0002 | t0002 | g0297 | AFR | ACB | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0303 | AFR | ACB | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG02056 | hp1 | a0001 | c0002 | t0002 | g0156 | EAS | KHV | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | KHV | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG02071 | hp1 | a0001 | c0002 | t0002 | g0197 | EAS | KHV | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG02071 | hp2 | a0001 | c0001 | t0003 | g0046 | EAS | KHV | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | KHV | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG02074 | hp2 | a0001 | c0001 | t0003 | g0119 | EAS | KHV | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG02080 | hp1 | a0001 | c0002 | t0002 | g0186 | EAS | KHV | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | KHV | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG02129 | hp1 | a0001 | c0001 | t0003 | g0042 | EAS | KHV | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG02129 | hp2 | a0001 | c0002 | t0002 | g0194 | EAS | KHV | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG02132 | hp1 | a0001 | c0001 | t0003 | g0060 | EAS | KHV | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | KHV | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | ACB | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0318 | AFR | ACB | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG02148 | hp1 | a0001 | c0002 | t0002 | g0204 | AMR | PEL | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG02148 | hp2 | a0001 | c0001 | t0003 | g0075 | AMR | PEL | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | CDX | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG02165 | hp2 | a0001 | c0001 | t0003 | g0050 | EAS | CDX | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG02257 | hp1 | a0001 | c0002 | t0002 | g0287 | AFR | ACB | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | ACB | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG02258 | hp1 | a0001 | c0002 | t0002 | g0290 | AFR | ACB | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | ACB | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0325 | AMR | PEL | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG02273 | hp2 | a0001 | c0002 | t0004 | g0283 | AMR | PEL | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0235 | AMR | PEL | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | PEL | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG02451 | hp1 | a0001 | c0002 | t0002 | g0288 | AFR | ACB | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0258 | AFR | ACB | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | GWD | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0312 | AFR | GWD | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG02602 | hp1 | a0001 | c0002 | t0002 | g0002 | SAS | PJL | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG02602 | hp2 | a0001 | c0002 | t0002 | g0136 | SAS | PJL | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | GWD | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG02622 | hp2 | a0001 | c0002 | t0002 | g0207 | AFR | GWD | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0313 | AFR | GWD | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG02630 | hp2 | a0001 | c0002 | t0002 | g0199 | AFR | GWD | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0306 | AFR | GWD | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | GWD | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG02683 | hp1 | a0001 | c0002 | t0002 | g0200 | SAS | PJL | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG02683 | hp2 | a0001 | c0002 | t0002 | g0188 | SAS | PJL | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG02698 | hp1 | a0001 | c0002 | t0002 | g0001 | SAS | PJL | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0271 | SAS | PJL | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG02735 | hp1 | a0001 | c0002 | t0002 | g0162 | SAS | PJL | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0255 | SAS | PJL | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0250 | SAS | PJL | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0308 | SAS | PJL | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0298 | AFR | GWD | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | GWD | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0320 | AFR | GWD | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0307 | AFR | GWD | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG02886 | hp1 | a0001 | c0002 | t0002 | g0131 | AFR | GWD | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0310 | AFR | GWD | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | GWD | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | GWD | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | GWD | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0261 | AFR | GWD | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0259 | AFR | ESN | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | ESN | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG02965 | hp2 | a0001 | c0002 | t0002 | g0289 | AFR | ESN | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0319 | AFR | ESN | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0309 | AFR | ESN | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0066 | SAS | PJL | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0357 | SAS | PJL | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0322 | AFR | GWD | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG03041 | hp2 | a0001 | c0002 | t0002 | g0164 | AFR | GWD | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0301 | AFR | ESN | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG03139 | hp2 | a0001 | c0002 | t0002 | g0285 | AFR | ESN | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | MSL | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | MSL | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG03225 | hp1 | a0001 | c0002 | t0002 | g0286 | AFR | MSL | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | MSL | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG03239 | hp1 | a0001 | c0002 | t0002 | g0144 | SAS | PJL | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG03239 | hp2 | a0001 | c0002 | t0002 | g0004 | SAS | PJL | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG03453 | hp1 | a0001 | c0002 | t0002 | g0284 | AFR | MSL | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG03453 | hp2 | a0001 | c0002 | t0002 | g0171 | AFR | MSL | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | MSL | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0304 | AFR | MSL | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG03490 | hp1 | a0001 | c0001 | t0003 | g0092 | SAS | PJL | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG03490 | hp2 | a0001 | c0002 | t0002 | g0145 | SAS | PJL | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG03491 | hp1 | a0001 | c0002 | t0002 | g0184 | SAS | PJL | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0253 | SAS | PJL | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0311 | AFR | ESN | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | MSL | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | MSL | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG03654 | hp1 | a0001 | c0002 | t0002 | g0196 | SAS | PJL | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0252 | SAS | STU | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0356 | SAS | STU | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0360 | SAS | PJL | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0359 | SAS | PJL | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0257 | SAS | PJL | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG03831 | hp1 | a0001 | c0001 | t0003 | g0118 | SAS | BEB | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG03831 | hp2 | a0001 | c0002 | t0002 | g0209 | SAS | BEB | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0231 | SAS | BEB | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0067 | SAS | BEB | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0358 | SAS | BEB | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0275 | SAS | BEB | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG03942 | hp1 | a0001 | c0001 | t0003 | g0106 | SAS | BEB | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0105 | SAS | BEB | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG04184 | hp1 | a0001 | c0002 | t0002 | g0208 | SAS | BEB | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG04184 | hp2 | a0001 | c0002 | t0002 | g0187 | SAS | BEB | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0064 | SAS | STU | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG04199 | hp2 | a0001 | c0002 | t0002 | g0185 | SAS | STU | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0236 | SAS | STU | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0251 | SAS | STU | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0238 | SAS | STU | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0065 | SAS | STU | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA18612 | hp1 | a0001 | c0002 | t0002 | g0177 | EAS | CHB | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0327 | EAS | CHB | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | CHB | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0339 | EAS | CHB | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0227 | AFR | YRI | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0300 | AFR | YRI | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA18939 | hp1 | a0001 | c0002 | t0002 | g0167 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA18941 | hp1 | a0001 | c0002 | t0002 | g0178 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA18943 | hp1 | a0001 | c0002 | t0002 | g0176 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA18945 | hp1 | a0001 | c0002 | t0002 | g0007 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA18945 | hp2 | a0001 | c0001 | t0005 | g0053 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA18946 | hp1 | a0001 | c0002 | t0002 | g0132 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0340 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA18947 | hp1 | a0001 | c0002 | t0002 | g0149 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA18947 | hp2 | a0001 | c0001 | t0003 | g0117 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA18948 | hp2 | a0001 | c0001 | t0003 | g0013 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0351 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA18950 | hp1 | a0001 | c0002 | t0002 | g0179 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA18952 | hp1 | a0001 | c0001 | t0003 | g0056 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA18952 | hp2 | a0001 | c0002 | t0002 | g0169 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0334 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA18954 | hp1 | a0001 | c0001 | t0003 | g0083 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA18954 | hp2 | a0001 | c0002 | t0002 | g0168 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA18960 | hp1 | a0001 | c0001 | t0003 | g0049 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA18960 | hp2 | a0001 | c0002 | t0002 | g0163 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA18962 | hp1 | a0001 | c0001 | t0003 | g0061 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0362 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA18963 | hp2 | a0001 | c0001 | t0006 | g0039 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA18965 | hp2 | a0001 | c0002 | t0002 | g0174 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA18966 | hp1 | a0001 | c0001 | t0003 | g0085 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0347 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0336 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA18968 | hp2 | a0001 | c0002 | t0002 | g0173 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0335 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA18970 | hp2 | a0001 | c0001 | t0003 | g0058 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0355 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA18973 | hp2 | a0001 | c0002 | t0002 | g0205 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA18975 | hp1 | a0001 | c0002 | t0002 | g0008 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA18977 | hp2 | a0001 | c0001 | t0003 | g0045 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA18979 | hp1 | a0001 | c0002 | t0001 | g0135 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA18979 | hp2 | a0004 | c0006 | t0001 | g0363 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA18980 | hp1 | a0001 | c0002 | t0002 | g0006 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0331 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0352 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA18983 | hp1 | a0001 | c0002 | t0002 | g0170 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0341 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0338 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0344 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0342 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0329 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0328 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA18993 | hp2 | a0001 | c0001 | t0003 | g0102 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0349 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA18994 | hp2 | a0001 | c0001 | t0003 | g0086 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA18995 | hp1 | a0001 | c0001 | t0003 | g0082 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA18995 | hp2 | a0001 | c0002 | t0002 | g0190 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0326 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA19001 | hp1 | a0001 | c0001 | t0003 | g0113 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA19001 | hp2 | a0001 | c0002 | t0002 | g0181 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA19005 | hp2 | a0001 | c0002 | t0002 | g0153 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA19007 | hp1 | a0001 | c0002 | t0002 | g0183 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0330 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0353 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0350 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0343 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA19012 | hp1 | a0001 | c0001 | t0003 | g0034 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA19012 | hp2 | a0001 | c0001 | t0005 | g0057 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | LWK | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA19030 | hp2 | a0001 | c0002 | t0002 | g0202 | AFR | LWK | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA19043 | hp1 | a0001 | c0002 | t0002 | g0189 | AFR | LWK | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0302 | AFR | LWK | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA19054 | hp1 | a0001 | c0002 | t0002 | g0155 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0324 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0354 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA19056 | hp2 | a0001 | c0002 | t0002 | g0165 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA19062 | hp1 | a0001 | c0001 | t0003 | g0033 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0337 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA19063 | hp2 | a0001 | c0002 | t0002 | g0195 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA19064 | hp2 | a0001 | c0001 | t0003 | g0062 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA19065 | hp2 | a0001 | c0001 | t0003 | g0063 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA19066 | hp2 | a0001 | c0001 | t0003 | g0081 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA19070 | hp2 | a0001 | c0002 | t0002 | g0152 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA19076 | hp1 | a0001 | c0001 | t0003 | g0059 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA19076 | hp2 | a0001 | c0002 | t0002 | g0159 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0323 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA19080 | hp2 | a0001 | c0007 | t0001 | g0038 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA19081 | hp2 | a0001 | c0002 | t0002 | g0154 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA19082 | hp1 | a0001 | c0001 | t0003 | g0114 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA19084 | hp2 | a0001 | c0001 | t0003 | g0079 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA19085 | hp1 | a0001 | c0002 | t0002 | g0166 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA19085 | hp2 | a0001 | c0001 | t0003 | g0051 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0332 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA19088 | hp2 | a0001 | c0002 | t0002 | g0193 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0345 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA19090 | hp2 | a0001 | c0001 | t0003 | g0104 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA19091 | hp1 | a0001 | c0002 | t0002 | g0203 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA19091 | hp2 | a0001 | c0001 | t0003 | g0077 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | YRI | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0260 | AFR | YRI | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | ASW | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | ASW | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA20805 | hp1 | a0001 | c0001 | t0003 | g0074 | EUR | TSI | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA20805 | hp2 | a0001 | c0002 | t0002 | g0317 | EUR | TSI | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA20905 | hp1 | a0001 | c0002 | t0002 | g0001 | SAS | GIH | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0262 | SAS | GIH | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG01123 | hp1 | a0001 | c0002 | t0002 | g0139 | AMR | CLM | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0272 | AMR | CLM | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | ACB | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0281 | AFR | ACB | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0321 | AFR | ACB | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0316 | AFR | ACB | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0305 | AFR | ACB | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG02559 | hp2 | a0001 | c0002 | t0001 | g0361 | AFR | ACB | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | MSL | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG03471 | hp2 | a0001 | c0002 | t0002 | g0294 | AFR | MSL | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG06807 | hp1 | a0001 | c0002 | t0002 | g0147 | AFR | USA | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
HG06807 | hp2 | a0001 | c0002 | t0002 | g0201 | AFR | USA | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA18955 | hp1 | a0001 | c0001 | t0003 | g0103 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0299 | AFR | USA | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | USA | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0270 | AFR | LWK | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0314 | AFR | LWK | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0230 | REF | REF | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
homoSapiens_grch38 | hp1 | a0001 | c0002 | t0002 | g0003 | REF | REF | LIN9_chr1_226226157_226314164 | LIN9 | chr1 | 226226157 | 226314164 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:226233456
|
T | G | 1 | a0002 | 1 | HG01192.hp1 | missense_variant | MODERATE | c.1313A>C | p.Glu438Ala | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 13/15 | 1338/2998 | 1313/1629 | 438/542 | chr1 | 226233456 | ||
chr1:226266247
|
A | G | 1 | a0003 | 1 | HG02027.hp2 | missense_variant | MODERATE | c.902T>C | p.Leu301Ser | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 9/15 | 927/2998 | 902/1629 | 301/542 | chr1 | 226266247 | ||
chr1:226277828
|
T | G | 1 | a0004 | 1 | NA18979.hp2 | missense_variant | MODERATE | c.629A>C | p.Lys210Thr | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/15 | 654/2998 | 629/1629 | 210/542 | chr1 | 226277828 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:226233494
|
T | C | 1 | a0001c0004 | 1 | HG01106.hp2 | synonymous_variant | LOW | c.1275A>G | p.Ala425Ala | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 13/15 | 1300/2998 | 1275/1629 | 425/542 | chr1 | 226233494 | ||
chr1:226286431
|
G | A | 4 | a0001c0001a0001c0007a0003c0005others(1): Show | 263 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(260): Show |
synonymous_variant | LOW | c.426C>T | p.Phe142Phe | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 6/15 | 451/2998 | 426/1629 | 142/542 | chr1 | 226286431 | ||
chr1:226301177
|
T | C | 1 | a0001c0007 | 1 | NA19080.hp2 | synonymous_variant | LOW | c.60A>G | p.Leu20Leu | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 2/15 | 85/2998 | 60/1629 | 20/542 | chr1 | 226301177 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:226231234
|
A | T | 1 | a0001c0001t0005 | 2 | NA18945.hp2 NA19012.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1267T>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 15/15 | 1267 | chr1 | 226231234 | |||||
chr1:226231465
|
G | C | 8 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(5): Show | 265 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(262): Show |
3_prime_UTR_variant | MODIFIER | c.*1036C>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 15/15 | 1036 | chr1 | 226231465 | |||||
chr1:226231536
|
C | G | 8 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(5): Show | 265 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(262): Show |
3_prime_UTR_variant | MODIFIER | c.*965G>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 15/15 | 965 | chr1 | 226231536 | |||||
chr1:226231709
|
A | G | 1 | a0001c0002t0004 | 3 | HG01069.hp1 HG01071.hp1 HG02273.hp2 |
3_prime_UTR_variant | MODIFIER | c.*792T>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 15/15 | 792 | chr1 | 226231709 | |||||
chr1:226232249
|
A | C | 1 | a0001c0001t0006 | 1 | NA18963.hp2 | 3_prime_UTR_variant | MODIFIER | c.*252T>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 15/15 | 252 | chr1 | 226232249 | |||||
chr1:226232339
|
T | C | 3 | a0001c0001t0003a0001c0001t0005a0001c0002t0007 | 48 | HG00099.hp2 HG00423.hp1 HG00609.hp1 others(45): Show |
3_prime_UTR_variant | MODIFIER | c.*162A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 15/15 | 162 | chr1 | 226232339 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:226232711
|
T | C | 3 | a0001c0001t0001g0232a0001c0001t0001g0241a0001c0001t0001g0282 | 3 | HG01109.hp2 HG01243.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.1524-105A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 14/14 | chr1 | 226232711 | ||||||
chr1:226232803
|
C | T | 1 | a0001c0001t0001g0238 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1524-197G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 14/14 | chr1 | 226232803 | ||||||
chr1:226232835
|
C | G | 219 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(216): Show | 220 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(217): Show |
intron_variant | MODIFIER | c.1524-229G>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 14/14 | chr1 | 226232835 | ||||||
chr1:226232920
|
T | C | 1 | a0001c0001t0001g0302 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1523+176A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 14/14 | chr1 | 226232920 | ||||||
chr1:226232953
|
G | A | 2 | a0001c0001t0001g0327a0001c0001t0001g0338 | 2 | NA18612.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.1523+143C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 14/14 | chr1 | 226232953 | ||||||
chr1:226233021
|
A | G | 123 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(120): Show | 123 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.1523+75T>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 14/14 | chr1 | 226233021 | ||||||
chr1:226233674
|
AAC | A | 3 | a0001c0001t0003g0045a0001c0001t0003g0049a0001c0001t0003g0114 | 3 | NA18960.hp1 NA18977.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.1246-153_1246-152d others(4): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 12/14 | chr1 | 226233674 | ||||||
chr1:226233913
|
T | A | 1 | a0001c0001t0001g0098 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1246-390A>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 12/14 | chr1 | 226233913 | ||||||
chr1:226233931
|
A | G | 1 | a0001c0001t0001g0302 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1246-408T>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 12/14 | chr1 | 226233931 | ||||||
chr1:226233979
|
T | C | 265 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(262): Show | 265 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(262): Show |
intron_variant | MODIFIER | c.1246-456A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 12/14 | chr1 | 226233979 | ||||||
chr1:226234015
|
T | G | 2 | a0001c0002t0002g0147a0001c0002t0002g0189 | 2 | HG06807.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1246-492A>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 12/14 | chr1 | 226234015 | ||||||
chr1:226234182
|
T | C | 19 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0212others(16): Show | 19 | HG02040.hp1 HG03017.hp2 HG03688.hp2 others(16): Show |
intron_variant | MODIFIER | c.1246-659A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 12/14 | chr1 | 226234182 | ||||||
chr1:226234219
|
C | T | 1 | a0001c0002t0002g0204 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1246-696G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 12/14 | chr1 | 226234219 | ||||||
chr1:226234531
|
C | T | 2 | a0001c0001t0001g0129a0001c0001t0001g0130 | 2 | NA19240.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1246-1008G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 12/14 | chr1 | 226234531 | ||||||
chr1:226234701
|
AG | A | 4 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0313others(1): Show | 4 | HG02630.hp1 NA19240.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.1246-1179delC | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 12/14 | chr1 | 226234701 | ||||||
chr1:226234893
|
A | AT | 10 | a0001c0001t0001g0218a0001c0001t0001g0222a0001c0001t0001g0298others(7): Show | 10 | HG02055.hp1 HG02809.hp1 HG03139.hp1 others(7): Show |
intron_variant | MODIFIER | c.1246-1371dupA | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 12/14 | chr1 | 226234893 | ||||||
chr1:226234893
|
A | ATTTT | 12 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(9): Show | 12 | HG01069.hp2 HG01074.hp2 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.1246-1374_1246-137 others(8): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 12/14 | chr1 | 226234893 | ||||||
chr1:226234893
|
A | ATTTTT | 79 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0017others(76): Show | 79 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(76): Show |
intron_variant | MODIFIER | c.1246-1375_1246-137 others(9): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 12/14 | chr1 | 226234893 | ||||||
chr1:226234893
|
A | ATTTTTT | 8 | a0001c0001t0001g0047a0001c0001t0001g0055a0001c0001t0001g0126others(5): Show | 8 | HG00673.hp2 HG02027.hp2 HG02300.hp2 others(5): Show |
intron_variant | MODIFIER | c.1246-1376_1246-137 others(10): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 12/14 | chr1 | 226234893 | ||||||
chr1:226234893
|
AT | A | 96 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0088others(93): Show | 96 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(93): Show |
intron_variant | MODIFIER | c.1246-1371delA | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 12/14 | chr1 | 226234893 | ||||||
chr1:226234907
|
T | C | 1 | a0001c0001t0001g0275 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1246-1384A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 12/14 | chr1 | 226234907 | ||||||
chr1:226235179
|
G | A | 1 | a0001c0001t0001g0268 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1246-1656C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 12/14 | chr1 | 226235179 | ||||||
chr1:226235255
|
G | A | 5 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(2): Show | 5 | HG03017.hp1 HG03834.hp2 HG03942.hp2 others(2): Show |
intron_variant | MODIFIER | c.1246-1732C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 12/14 | chr1 | 226235255 | ||||||
chr1:226235322
|
C | CA | 31 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0129others(28): Show | 31 | HG02040.hp1 HG02451.hp2 HG02630.hp1 others(28): Show |
intron_variant | MODIFIER | c.1246-1800dupT | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 12/14 | chr1 | 226235322 | ||||||
chr1:226235322
|
C | CAA | 189 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0012others(186): Show | 189 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.1246-1801_1246-180 others(6): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 12/14 | chr1 | 226235322 | ||||||
chr1:226235322
|
C | CAAA | 22 | a0001c0001t0001g0010a0001c0001t0001g0064a0001c0001t0001g0065others(19): Show | 22 | HG00609.hp1 HG01168.hp2 HG01255.hp1 others(19): Show |
intron_variant | MODIFIER | c.1246-1802_1246-180 others(7): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 12/14 | chr1 | 226235322 | ||||||
chr1:226235322
|
CAAAA | C | 18 | a0001c0001t0001g0298a0001c0001t0001g0299a0001c0001t0001g0300others(15): Show | 18 | HG02055.hp2 HG02145.hp2 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.1246-1803_1246-180 others(8): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 12/14 | chr1 | 226235322 | ||||||
chr1:226235449
|
T | C | 351 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(348): Show | 352 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(349): Show |
intron_variant | MODIFIER | c.1246-1926A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 12/14 | chr1 | 226235449 | ||||||
chr1:226235483
|
C | T | 119 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(116): Show | 119 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.1246-1960G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 12/14 | chr1 | 226235483 | ||||||
chr1:226235559
|
T | C | 1 | a0001c0002t0002g0288 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1246-2036A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 12/14 | chr1 | 226235559 | ||||||
chr1:226235569
|
C | G | 4 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0313others(1): Show | 4 | HG02630.hp1 NA19240.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.1246-2046G>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 12/14 | chr1 | 226235569 | ||||||
chr1:226235871
|
C | T | 263 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(260): Show | 263 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(260): Show |
intron_variant | MODIFIER | c.1246-2348G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 12/14 | chr1 | 226235871 | ||||||
chr1:226236389
|
A | G | 1 | a0001c0002t0002g0184 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1245+2582T>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 12/14 | chr1 | 226236389 | ||||||
chr1:226236437
|
T | C | 19 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0212others(16): Show | 19 | HG02040.hp1 HG03017.hp2 HG03688.hp2 others(16): Show |
intron_variant | MODIFIER | c.1245+2534A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 12/14 | chr1 | 226236437 | ||||||
chr1:226236444
|
CTTTA | C | 3 | a0001c0001t0001g0019a0001c0001t0001g0025a0001c0001t0003g0059 | 3 | NA19005.hp1 NA19054.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.1245+2523_1245+252 others(8): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 12/14 | chr1 | 226236444 | ||||||
chr1:226236581
|
G | A | 2 | a0001c0001t0001g0021a0001c0001t0001g0026 | 2 | HG01255.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.1245+2390C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 12/14 | chr1 | 226236581 | ||||||
chr1:226236754
|
G | C | 1 | a0001c0001t0001g0308 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1245+2217C>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 12/14 | chr1 | 226236754 | ||||||
chr1:226236776
|
C | A | 121 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(118): Show | 121 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(118): Show |
intron_variant | MODIFIER | c.1245+2195G>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 12/14 | chr1 | 226236776 | ||||||
chr1:226236819
|
C | T | 1 | a0001c0002t0002g0145 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1245+2152G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 12/14 | chr1 | 226236819 | ||||||
chr1:226236933
|
G | A | 100 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0088others(97): Show | 100 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(97): Show |
intron_variant | MODIFIER | c.1245+2038C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 12/14 | chr1 | 226236933 | ||||||
chr1:226237103
|
T | A | 1 | a0001c0001t0001g0124 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1245+1868A>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 12/14 | chr1 | 226237103 | ||||||
chr1:226237317
|
A | T | 1 | a0001c0001t0001g0124 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1245+1654T>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 12/14 | chr1 | 226237317 | ||||||
chr1:226237359
|
G | A | 15 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0212others(12): Show | 15 | HG02040.hp1 HG03704.hp1 NA18941.hp2 others(12): Show |
intron_variant | MODIFIER | c.1245+1612C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 12/14 | chr1 | 226237359 | ||||||
chr1:226237360
|
C | T | 2 | a0001c0001t0001g0127a0001c0001t0001g0128 | 2 | HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1245+1611G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 12/14 | chr1 | 226237360 | ||||||
chr1:226237619
|
C | T | 1 | a0001c0002t0002g0204 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1245+1352G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 12/14 | chr1 | 226237619 | ||||||
chr1:226237632
|
C | CA | 106 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0088others(103): Show | 107 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(104): Show |
intron_variant | MODIFIER | c.1245+1338dupT | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 12/14 | chr1 | 226237632 | ||||||
chr1:226237632
|
CA | C | 45 | a0001c0001t0001g0005a0001c0001t0001g0130a0001c0001t0001g0210others(42): Show | 45 | HG00609.hp1 HG01168.hp2 HG01516.hp2 others(42): Show |
intron_variant | MODIFIER | c.1245+1338delT | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 12/14 | chr1 | 226237632 | ||||||
chr1:226237776
|
C | T | 1 | a0001c0002t0002g0206 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1245+1195G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 12/14 | chr1 | 226237776 | ||||||
chr1:226237919
|
C | T | 2 | a0001c0001t0001g0127a0001c0001t0001g0128 | 2 | HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1245+1052G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 12/14 | chr1 | 226237919 | ||||||
chr1:226237940
|
A | C | 5 | a0001c0002t0002g0164a0001c0002t0002g0199a0001c0002t0002g0201others(2): Show | 5 | HG02622.hp2 HG02630.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1245+1031T>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 12/14 | chr1 | 226237940 | ||||||
chr1:226237952
|
CA | C | 259 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(256): Show | 259 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(256): Show |
intron_variant | MODIFIER | c.1245+1018delT | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 12/14 | chr1 | 226237952 | ||||||
chr1:226238089
|
C | G | 19 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0212others(16): Show | 19 | HG02040.hp1 HG03017.hp2 HG03688.hp2 others(16): Show |
intron_variant | MODIFIER | c.1245+882G>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 12/14 | chr1 | 226238089 | ||||||
chr1:226238151
|
A | G | 5 | a0001c0001t0001g0318a0001c0001t0001g0319a0001c0001t0001g0320others(2): Show | 5 | HG02145.hp2 HG02486.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1245+820T>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 12/14 | chr1 | 226238151 | ||||||
chr1:226238588
|
A | T | 17 | a0001c0001t0001g0005a0001c0001t0001g0298a0001c0001t0001g0299others(14): Show | 17 | HG02055.hp2 HG02486.hp2 HG02559.hp1 others(14): Show |
intron_variant | MODIFIER | c.1245+383T>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 12/14 | chr1 | 226238588 | ||||||
chr1:226238609
|
C | T | 1 | a0001c0002t0002g0173 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1245+362G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 12/14 | chr1 | 226238609 | ||||||
chr1:226238636
|
T | A | 261 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(258): Show | 261 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(258): Show |
intron_variant | MODIFIER | c.1245+335A>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 12/14 | chr1 | 226238636 | ||||||
chr1:226238942
|
A | G | 5 | a0001c0001t0001g0017a0001c0001t0001g0028a0001c0001t0001g0041others(2): Show | 5 | HG00438.hp1 HG01346.hp2 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.1245+29T>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 12/14 | chr1 | 226238942 | ||||||
chr1:226239338
|
A | G | 3 | a0001c0001t0001g0036a0001c0001t0001g0047a0001c0001t0001g0093 | 3 | HG00673.hp2 HG02074.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.1120-242T>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226239338 | ||||||
chr1:226239602
|
AAT | A | 4 | a0001c0001t0003g0050a0001c0001t0003g0059a0001c0001t0005g0053others(1): Show | 4 | HG02165.hp2 NA18945.hp2 NA19012.hp2 others(1): Show |
intron_variant | MODIFIER | c.1120-508_1120-507d others(4): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226239602 | ||||||
chr1:226239612
|
T | C | 122 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(119): Show | 122 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(119): Show |
intron_variant | MODIFIER | c.1120-516A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226239612 | ||||||
chr1:226239728
|
C | T | 1 | a0001c0001t0001g0005 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1120-632G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226239728 | ||||||
chr1:226239828
|
A | G | 1 | a0001c0001t0003g0063 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1120-732T>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226239828 | ||||||
chr1:226239951
|
T | C | 1 | a0001c0001t0003g0078 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1120-855A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226239951 | ||||||
chr1:226240265
|
G | A | 1 | a0001c0001t0001g0213 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1120-1169C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226240265 | ||||||
chr1:226240294
|
G | A | 1 | a0001c0002t0002g0170 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1120-1198C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226240294 | ||||||
chr1:226240386
|
G | GT | 7 | a0001c0001t0001g0362a0001c0002t0002g0008a0001c0002t0002g0167others(4): Show | 7 | HG01891.hp2 HG03471.hp2 HG04184.hp1 others(4): Show |
intron_variant | MODIFIER | c.1120-1291dupA | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226240386 | ||||||
chr1:226240386
|
GT | G | 244 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(241): Show | 244 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(241): Show |
intron_variant | MODIFIER | c.1120-1291delA | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226240386 | ||||||
chr1:226240425
|
G | A | 1 | a0003c0005t0001g0095 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1120-1329C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226240425 | ||||||
chr1:226240502
|
C | T | 1 | a0001c0001t0001g0302 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1120-1406G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226240502 | ||||||
chr1:226240640
|
T | C | 5 | a0001c0001t0001g0318a0001c0001t0001g0319a0001c0001t0001g0320others(2): Show | 5 | HG02145.hp2 HG02486.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1120-1544A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226240640 | ||||||
chr1:226240998
|
T | C | 7 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0072others(4): Show | 7 | HG01106.hp1 HG02257.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.1120-1902A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226240998 | ||||||
chr1:226241124
|
A | G | 1 | a0001c0001t0003g0114 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1120-2028T>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226241124 | ||||||
chr1:226241214
|
G | A | 5 | a0001c0001t0001g0318a0001c0001t0001g0319a0001c0001t0001g0320others(2): Show | 5 | HG02145.hp2 HG02486.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1120-2118C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226241214 | ||||||
chr1:226241235
|
C | T | 1 | a0001c0001t0001g0020 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1120-2139G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226241235 | ||||||
chr1:226241313
|
A | G | 1 | a0001c0001t0001g0020 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1120-2217T>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226241313 | ||||||
chr1:226241362
|
A | C | 1 | a0001c0001t0001g0324 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1120-2266T>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226241362 | ||||||
chr1:226241629
|
C | T | 1 | a0001c0002t0002g0132 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1120-2533G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226241629 | ||||||
chr1:226241674
|
C | T | 1 | a0001c0001t0001g0276 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1120-2578G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226241674 | ||||||
chr1:226241724
|
G | A | 1 | a0001c0001t0001g0275 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1120-2628C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226241724 | ||||||
chr1:226241750
|
C | T | 5 | a0001c0001t0001g0318a0001c0001t0001g0319a0001c0001t0001g0320others(2): Show | 5 | HG02145.hp2 HG02486.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1120-2654G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226241750 | ||||||
chr1:226241824
|
C | T | 1 | a0001c0002t0002g0209 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1120-2728G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226241824 | ||||||
chr1:226241857
|
C | CA | 19 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0212others(16): Show | 19 | HG02040.hp1 HG03017.hp2 HG03688.hp2 others(16): Show |
intron_variant | MODIFIER | c.1120-2762dupT | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226241857 | ||||||
chr1:226241892
|
T | C | 5 | a0001c0001t0001g0318a0001c0001t0001g0319a0001c0001t0001g0320others(2): Show | 5 | HG02145.hp2 HG02486.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1120-2796A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226241892 | ||||||
chr1:226242030
|
G | A | 362 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(359): Show | 363 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(360): Show |
intron_variant | MODIFIER | c.1120-2934C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226242030 | ||||||
chr1:226242679
|
C | T | 13 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(10): Show | 13 | HG01074.hp2 HG01099.hp2 HG01978.hp1 others(10): Show |
intron_variant | MODIFIER | c.1120-3583G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226242679 | ||||||
chr1:226242727
|
C | T | 1 | a0001c0001t0001g0023 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1120-3631G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226242727 | ||||||
chr1:226242908
|
T | TTAA | 264 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(261): Show | 264 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(261): Show |
intron_variant | MODIFIER | c.1120-3815_1120-381 others(7): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226242908 | ||||||
chr1:226242943
|
G | C | 1 | a0001c0001t0001g0265 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1120-3847C>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226242943 | ||||||
chr1:226243065
|
G | A | 17 | a0001c0001t0001g0005a0001c0001t0001g0298a0001c0001t0001g0299others(14): Show | 17 | HG02055.hp2 HG02486.hp2 HG02559.hp1 others(14): Show |
intron_variant | MODIFIER | c.1120-3969C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226243065 | ||||||
chr1:226243153
|
T | C | 1 | a0001c0001t0001g0031 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1120-4057A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226243153 | ||||||
chr1:226243379
|
A | C | 3 | a0001c0001t0003g0045a0001c0001t0003g0049a0001c0001t0003g0114 | 3 | NA18960.hp1 NA18977.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.1120-4283T>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226243379 | ||||||
chr1:226243484
|
C | G | 4 | a0001c0001t0001g0044a0001c0001t0001g0055a0001c0001t0001g0068others(1): Show | 4 | HG02622.hp1 HG02895.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1120-4388G>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226243484 | ||||||
chr1:226243682
|
C | T | 2 | a0001c0001t0001g0304a0001c0001t0001g0316 | 2 | HG02486.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1120-4586G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226243682 | ||||||
chr1:226243695
|
C | CA | 61 | a0001c0001t0001g0022a0001c0001t0001g0024a0001c0001t0001g0047others(58): Show | 61 | HG00621.hp2 HG00673.hp2 HG01109.hp1 others(58): Show |
intron_variant | MODIFIER | c.1120-4600dupT | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226243695 | ||||||
chr1:226243695
|
CA | C | 10 | a0001c0001t0001g0014a0001c0001t0001g0040a0001c0001t0001g0098others(7): Show | 10 | HG01256.hp1 HG02630.hp1 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.1120-4600delT | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226243695 | ||||||
chr1:226243735
|
A | C | 222 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(219): Show | 222 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(219): Show |
intron_variant | MODIFIER | c.1120-4639T>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226243735 | ||||||
chr1:226243876
|
A | AATT | 263 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(260): Show | 263 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(260): Show |
intron_variant | MODIFIER | c.1120-4783_1120-478 others(7): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226243876 | ||||||
chr1:226243899
|
G | C | 20 | a0001c0002t0002g0001a0001c0002t0002g0136a0001c0002t0002g0137others(17): Show | 21 | HG00544.hp1 HG00738.hp1 HG01123.hp1 others(18): Show |
intron_variant | MODIFIER | c.1120-4803C>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226243899 | ||||||
chr1:226243931
|
G | A | 1 | a0001c0001t0001g0302 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1120-4835C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226243931 | ||||||
chr1:226244000
|
G | A | 1 | a0001c0001t0001g0211 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1120-4904C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226244000 | ||||||
chr1:226244026
|
T | C | 1 | a0001c0002t0002g0176 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1120-4930A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226244026 | ||||||
chr1:226244166
|
G | A | 1 | a0001c0001t0001g0043 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1120-5070C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226244166 | ||||||
chr1:226244281
|
A | C | 1 | a0001c0001t0001g0023 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1120-5185T>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226244281 | ||||||
chr1:226244304
|
T | C | 217 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(214): Show | 217 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.1120-5208A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226244304 | ||||||
chr1:226244416
|
A | G | 5 | a0001c0001t0001g0318a0001c0001t0001g0319a0001c0001t0001g0320others(2): Show | 5 | HG02145.hp2 HG02486.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1120-5320T>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226244416 | ||||||
chr1:226244819
|
C | T | 1 | a0001c0002t0002g0195 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1120-5723G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226244819 | ||||||
chr1:226244820
|
G | A | 260 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(257): Show | 260 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(257): Show |
intron_variant | MODIFIER | c.1120-5724C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226244820 | ||||||
chr1:226244881
|
G | A | 2 | a0001c0002t0002g0137a0001c0002t0002g0138 | 2 | HG00738.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.1120-5785C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226244881 | ||||||
chr1:226245428
|
TC | T | 260 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(257): Show | 260 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(257): Show |
intron_variant | MODIFIER | c.1119+5410delG | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226245428 | ||||||
chr1:226245429
|
C | T | 57 | a0001c0001t0001g0031a0001c0001t0001g0161a0001c0001t0003g0157others(54): Show | 57 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(54): Show |
intron_variant | MODIFIER | c.1119+5410G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226245429 | ||||||
chr1:226245430
|
C | T | 261 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(258): Show | 261 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(258): Show |
intron_variant | MODIFIER | c.1119+5409G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226245430 | ||||||
chr1:226245431
|
C | T | 261 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(258): Show | 261 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(258): Show |
intron_variant | MODIFIER | c.1119+5408G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226245431 | ||||||
chr1:226245484
|
A | T | 1 | a0001c0001t0001g0010 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1119+5355T>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226245484 | ||||||
chr1:226245551
|
G | T | 237 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(234): Show | 237 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(234): Show |
intron_variant | MODIFIER | c.1119+5288C>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226245551 | ||||||
chr1:226245598
|
T | A | 19 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0212others(16): Show | 19 | HG02040.hp1 HG03017.hp2 HG03688.hp2 others(16): Show |
intron_variant | MODIFIER | c.1119+5241A>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226245598 | ||||||
chr1:226245675
|
CCTCT | C | 260 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(257): Show | 260 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(257): Show |
intron_variant | MODIFIER | c.1119+5160_1119+516 others(8): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226245675 | ||||||
chr1:226245724
|
C | T | 2 | a0001c0002t0002g0166a0001c0002t0002g0174 | 2 | NA18965.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.1119+5115G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226245724 | ||||||
chr1:226245751
|
C | T | 2 | a0001c0001t0001g0268a0001c0001t0001g0269 | 2 | HG00735.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.1119+5088G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226245751 | ||||||
chr1:226245993
|
G | A | 6 | a0001c0001t0001g0215a0001c0001t0001g0218a0001c0001t0001g0219others(3): Show | 6 | NA18941.hp2 NA18966.hp2 NA18967.hp2 others(3): Show |
intron_variant | MODIFIER | c.1119+4846C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226245993 | ||||||
chr1:226246007
|
T | C | 220 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(217): Show | 220 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(217): Show |
intron_variant | MODIFIER | c.1119+4832A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226246007 | ||||||
chr1:226246067
|
A | G | 3 | a0001c0002t0002g0177a0001c0002t0002g0183a0001c0002t0002g0197 | 3 | HG02071.hp1 NA18612.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.1119+4772T>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226246067 | ||||||
chr1:226246563
|
A | G | 1 | a0001c0002t0002g0190 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1119+4276T>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226246563 | ||||||
chr1:226246618
|
T | TA | 6 | a0001c0001t0001g0019a0001c0001t0001g0221a0001c0001t0001g0229others(3): Show | 6 | HG01928.hp1 HG01993.hp1 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.1119+4220dupT | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226246618 | ||||||
chr1:226246725
|
G | A | 17 | a0001c0001t0001g0005a0001c0001t0001g0298a0001c0001t0001g0299others(14): Show | 17 | HG02055.hp2 HG02486.hp2 HG02559.hp1 others(14): Show |
intron_variant | MODIFIER | c.1119+4114C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226246725 | ||||||
chr1:226246780
|
G | A | 17 | a0001c0001t0001g0005a0001c0001t0001g0298a0001c0001t0001g0299others(14): Show | 17 | HG02055.hp2 HG02486.hp2 HG02559.hp1 others(14): Show |
intron_variant | MODIFIER | c.1119+4059C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226246780 | ||||||
chr1:226246792
|
C | CA | 10 | a0001c0002t0001g0135a0001c0002t0002g0008a0001c0002t0002g0149others(7): Show | 10 | HG01106.hp2 HG02622.hp2 HG03041.hp2 others(7): Show |
intron_variant | MODIFIER | c.1119+4046dupT | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226246792 | ||||||
chr1:226246792
|
CA | C | 247 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(244): Show | 248 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(245): Show |
intron_variant | MODIFIER | c.1119+4046delT | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226246792 | ||||||
chr1:226246792
|
CAA | C | 6 | a0001c0001t0001g0011a0001c0001t0001g0229a0001c0001t0001g0254others(3): Show | 6 | HG01257.hp1 HG01928.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1119+4045_1119+404 others(6): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226246792 | ||||||
chr1:226246968
|
TATTCCGT others(5): Show |
T | 1 | a0001c0001t0001g0031 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1119+3859_1119+387 others(16): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226246968 | ||||||
chr1:226247669
|
T | C | 1 | a0001c0001t0003g0013 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1119+3170A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226247669 | ||||||
chr1:226247674
|
C | CT | 144 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(141): Show | 144 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.1119+3164dupA | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226247674 | ||||||
chr1:226247728
|
G | C | 125 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(122): Show | 125 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.1119+3111C>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226247728 | ||||||
chr1:226247900
|
G | A | 1 | a0001c0001t0001g0105 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1119+2939C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226247900 | ||||||
chr1:226248188
|
C | T | 1 | a0001c0002t0002g0205 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1119+2651G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226248188 | ||||||
chr1:226248346
|
A | T | 1 | a0001c0001t0001g0357 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1119+2493T>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226248346 | ||||||
chr1:226248427
|
A | T | 3 | a0001c0001t0001g0300a0001c0001t0001g0301a0001c0001t0001g0303 | 3 | HG02055.hp2 HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1119+2412T>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226248427 | ||||||
chr1:226248437
|
T | TGCAATTA others(14): Show |
1 | a0001c0001t0003g0113 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1119+2381_1119+240 others(25): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226248437 | ||||||
chr1:226248469
|
C | G | 98 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0224others(95): Show | 98 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(95): Show |
intron_variant | MODIFIER | c.1119+2370G>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226248469 | ||||||
chr1:226249040
|
G | C | 1 | a0001c0002t0002g0168 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1119+1799C>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226249040 | ||||||
chr1:226249075
|
G | A | 1 | a0001c0001t0003g0077 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1119+1764C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226249075 | ||||||
chr1:226249209
|
A | G | 1 | a0001c0002t0001g0361 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1119+1630T>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226249209 | ||||||
chr1:226249511
|
T | TA | 6 | a0001c0001t0001g0031a0001c0001t0001g0258a0001c0001t0001g0259others(3): Show | 6 | HG02109.hp2 HG02451.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1119+1327dupT | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226249511 | ||||||
chr1:226249525
|
T | C | 19 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0212others(16): Show | 19 | HG02040.hp1 HG03017.hp2 HG03688.hp2 others(16): Show |
intron_variant | MODIFIER | c.1119+1314A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226249525 | ||||||
chr1:226249607
|
C | A | 1 | a0001c0001t0001g0043 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1119+1232G>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226249607 | ||||||
chr1:226250170
|
GA | G | 22 | a0001c0001t0001g0098a0001c0001t0001g0210a0001c0001t0001g0211others(19): Show | 22 | HG02040.hp1 HG02300.hp1 HG03017.hp2 others(19): Show |
intron_variant | MODIFIER | c.1119+668delT | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226250170 | ||||||
chr1:226250276
|
C | A | 120 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(117): Show | 120 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(117): Show |
intron_variant | MODIFIER | c.1119+563G>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226250276 | ||||||
chr1:226250536
|
T | C | 23 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0298others(20): Show | 23 | HG02055.hp2 HG02145.hp2 HG02486.hp1 others(20): Show |
intron_variant | MODIFIER | c.1119+303A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226250536 | ||||||
chr1:226250748
|
T | C | 317 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(314): Show | 317 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(314): Show |
intron_variant | MODIFIER | c.1119+91A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226250748 | ||||||
chr1:226250753
|
A | T | 1 | a0002c0003t0002g0148 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1119+86T>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226250753 | ||||||
chr1:226250776
|
T | C | 1 | a0001c0002t0002g0171 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1119+63A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226250776 | ||||||
chr1:226250783
|
TCTCA | T | 14 | a0001c0001t0001g0224a0001c0001t0001g0250a0001c0001t0001g0251others(11): Show | 14 | HG00735.hp1 HG02056.hp2 HG02132.hp2 others(11): Show |
intron_variant | MODIFIER | c.1119+52_1119+55del others(4): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226250783 | ||||||
chr1:226250796
|
A | AAATTAGA others(36): Show |
1 | a0001c0002t0002g0154 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1119_1119+42dupGGT others(40): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 11/14 | chr1 | 226250796 | ||||||
chr1:226251020
|
A | G | 19 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0212others(16): Show | 19 | HG02040.hp1 HG03017.hp2 HG03688.hp2 others(16): Show |
intron_variant | MODIFIER | c.1039-101T>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226251020 | ||||||
chr1:226251131
|
A | C | 19 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0212others(16): Show | 19 | HG02040.hp1 HG03017.hp2 HG03688.hp2 others(16): Show |
intron_variant | MODIFIER | c.1039-212T>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226251131 | ||||||
chr1:226251202
|
C | T | 1 | a0001c0001t0001g0357 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1039-283G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226251202 | ||||||
chr1:226251216
|
A | G | 1 | a0001c0002t0002g0131 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1039-297T>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226251216 | ||||||
chr1:226251229
|
A | AT | 127 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(124): Show | 127 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.1039-311dupA | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226251229 | ||||||
chr1:226251517
|
G | A | 1 | a0001c0002t0002g0317 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1039-598C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226251517 | ||||||
chr1:226251656
|
T | A | 47 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(44): Show | 47 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(44): Show |
intron_variant | MODIFIER | c.1039-737A>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226251656 | ||||||
chr1:226251695
|
C | T | 1 | a0001c0001t0001g0005 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1039-776G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226251695 | ||||||
chr1:226252281
|
A | AAAAT | 17 | a0001c0001t0001g0224a0001c0001t0001g0228a0001c0001t0001g0229others(14): Show | 17 | HG01928.hp1 HG02004.hp2 HG02300.hp1 others(14): Show |
intron_variant | MODIFIER | c.1039-1366_1039-136 others(8): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226252281 | ||||||
chr1:226252281
|
A | AAAATAAA others(9): Show |
1 | a0001c0001t0001g0230 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1039-1378_1039-136 others(20): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226252281 | ||||||
chr1:226252281
|
AAAAT | A | 122 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0015others(119): Show | 122 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(119): Show |
intron_variant | MODIFIER | c.1039-1366_1039-136 others(8): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226252281 | ||||||
chr1:226252298
|
A | G | 2 | a0001c0001t0001g0210a0001c0001t0001g0214 | 2 | NA18984.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.1039-1379T>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226252298 | ||||||
chr1:226252302
|
A | G | 15 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0212others(12): Show | 15 | HG02040.hp1 HG03704.hp1 NA18941.hp2 others(12): Show |
intron_variant | MODIFIER | c.1039-1383T>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226252302 | ||||||
chr1:226252306
|
A | G | 19 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0212others(16): Show | 19 | HG02040.hp1 HG03017.hp2 HG03688.hp2 others(16): Show |
intron_variant | MODIFIER | c.1039-1387T>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226252306 | ||||||
chr1:226252310
|
A | G | 19 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0212others(16): Show | 19 | HG02040.hp1 HG03017.hp2 HG03688.hp2 others(16): Show |
intron_variant | MODIFIER | c.1039-1391T>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226252310 | ||||||
chr1:226252314
|
A | AAATG | 9 | a0001c0001t0001g0298a0001c0001t0001g0300a0001c0001t0001g0301others(6): Show | 9 | HG01069.hp1 HG01071.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.1039-1396_1039-139 others(8): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226252314 | ||||||
chr1:226252314
|
A | G | 36 | a0001c0001t0001g0005a0001c0001t0001g0127a0001c0001t0001g0128others(33): Show | 36 | HG02040.hp1 HG02145.hp2 HG02486.hp1 others(33): Show |
intron_variant | MODIFIER | c.1039-1395T>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226252314 | ||||||
chr1:226252318
|
A | AAATAAAT others(1): Show |
7 | a0001c0002t0002g0162a0001c0002t0002g0163a0001c0002t0002g0183others(4): Show | 7 | HG00639.hp1 HG01168.hp1 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.1039-1400_1039-139 others(12): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226252318 | ||||||
chr1:226252318
|
A | AAATG | 48 | a0001c0001t0001g0161a0001c0001t0003g0157a0001c0001t0003g0192others(45): Show | 48 | HG00099.hp2 HG00280.hp1 HG00621.hp2 others(45): Show |
intron_variant | MODIFIER | c.1039-1403_1039-140 others(8): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226252318 | ||||||
chr1:226252318
|
A | AAATGAAT others(1): Show |
3 | a0001c0001t0001g0299a0001c0002t0002g0287a0001c0002t0002g0297 | 3 | HG02055.hp1 HG02257.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1039-1407_1039-140 others(12): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226252318 | ||||||
chr1:226252318
|
A | G | 55 | a0001c0001t0001g0005a0001c0001t0001g0088a0001c0001t0001g0089others(52): Show | 55 | HG01069.hp1 HG01071.hp1 HG01081.hp2 others(52): Show |
intron_variant | MODIFIER | c.1039-1399T>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226252318 | ||||||
chr1:226252322
|
G | A | 89 | a0001c0001t0001g0010a0001c0001t0001g0224a0001c0001t0001g0225others(86): Show | 89 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.1039-1403C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226252322 | ||||||
chr1:226252335
|
A | G | 1 | a0001c0001t0001g0005 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1039-1416T>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226252335 | ||||||
chr1:226252695
|
AGGTGTGG others(8): Show |
A | 1 | a0001c0001t0003g0113 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1039-1791_1039-177 others(19): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226252695 | ||||||
chr1:226252861
|
G | A | 19 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0212others(16): Show | 19 | HG02040.hp1 HG03017.hp2 HG03688.hp2 others(16): Show |
intron_variant | MODIFIER | c.1039-1942C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226252861 | ||||||
chr1:226252923
|
G | A | 1 | a0001c0001t0001g0028 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1039-2004C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226252923 | ||||||
chr1:226252953
|
C | T | 1 | a0001c0001t0001g0315 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1039-2034G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226252953 | ||||||
chr1:226252965
|
T | C | 3 | a0001c0002t0002g0146a0001c0002t0002g0159a0001c0002t0002g0193 | 3 | HG00544.hp1 NA19076.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.1039-2046A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226252965 | ||||||
chr1:226253067
|
A | C | 19 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0212others(16): Show | 19 | HG02040.hp1 HG03017.hp2 HG03688.hp2 others(16): Show |
intron_variant | MODIFIER | c.1039-2148T>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226253067 | ||||||
chr1:226253127
|
G | A | 2 | a0001c0001t0001g0127a0001c0001t0001g0128 | 2 | HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1039-2208C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226253127 | ||||||
chr1:226253265
|
C | CA | 199 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0012others(196): Show | 199 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.1039-2347dupT | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226253265 | ||||||
chr1:226253265
|
C | CAA | 17 | a0001c0001t0001g0111a0001c0001t0001g0304a0001c0001t0001g0305others(14): Show | 17 | HG02145.hp2 HG02486.hp1 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.1039-2348_1039-234 others(6): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226253265 | ||||||
chr1:226253265
|
CA | C | 6 | a0001c0001t0001g0242a0001c0001t0001g0273a0001c0001t0001g0279others(3): Show | 6 | HG00639.hp2 HG00738.hp2 HG01167.hp2 others(3): Show |
intron_variant | MODIFIER | c.1039-2347delT | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226253265 | ||||||
chr1:226253347
|
C | T | 1 | a0001c0001t0001g0005 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1039-2428G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226253347 | ||||||
chr1:226253492
|
C | T | 97 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0224others(94): Show | 97 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(94): Show |
intron_variant | MODIFIER | c.1039-2573G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226253492 | ||||||
chr1:226253549
|
C | T | 2 | a0001c0001t0001g0080a0001c0001t0001g0084 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1039-2630G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226253549 | ||||||
chr1:226253767
|
T | G | 1 | a0001c0001t0001g0005 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1039-2848A>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226253767 | ||||||
chr1:226253828
|
T | C | 1 | a0001c0001t0001g0099 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1039-2909A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226253828 | ||||||
chr1:226254031
|
A | C | 1 | a0001c0002t0002g0195 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1039-3112T>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226254031 | ||||||
chr1:226254057
|
G | A | 1 | a0001c0001t0001g0218 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1039-3138C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226254057 | ||||||
chr1:226254184
|
C | T | 98 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0088others(95): Show | 98 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(95): Show |
intron_variant | MODIFIER | c.1039-3265G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226254184 | ||||||
chr1:226254326
|
C | A | 1 | a0001c0001t0001g0281 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1039-3407G>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226254326 | ||||||
chr1:226254542
|
C | T | 2 | a0001c0001t0001g0129a0001c0001t0001g0130 | 2 | NA19240.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1039-3623G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226254542 | ||||||
chr1:226254686
|
C | T | 6 | a0001c0001t0001g0298a0001c0001t0001g0299a0001c0001t0001g0300others(3): Show | 6 | HG02055.hp2 HG02809.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.1039-3767G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226254686 | ||||||
chr1:226254694
|
G | A | 139 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(136): Show | 139 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(136): Show |
intron_variant | MODIFIER | c.1039-3775C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226254694 | ||||||
chr1:226254836
|
G | A | 22 | a0001c0001t0001g0005a0001c0001t0001g0298a0001c0001t0001g0299others(19): Show | 22 | HG02055.hp2 HG02145.hp2 HG02486.hp1 others(19): Show |
intron_variant | MODIFIER | c.1039-3917C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226254836 | ||||||
chr1:226254910
|
C | CA | 26 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0036others(23): Show | 26 | HG00597.hp1 HG00741.hp2 HG01081.hp2 others(23): Show |
intron_variant | MODIFIER | c.1039-3992dupT | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226254910 | ||||||
chr1:226254910
|
CA | C | 14 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0032others(11): Show | 14 | HG00639.hp2 HG01069.hp2 HG01074.hp2 others(11): Show |
intron_variant | MODIFIER | c.1039-3992delT | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226254910 | ||||||
chr1:226255195
|
T | C | 1 | a0001c0001t0001g0238 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1039-4276A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226255195 | ||||||
chr1:226256058
|
T | C | 19 | a0001c0001t0001g0005a0001c0001t0001g0127a0001c0001t0001g0128others(16): Show | 19 | HG02055.hp2 HG02486.hp2 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.1039-5139A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226256058 | ||||||
chr1:226256153
|
C | T | 1 | a0001c0001t0001g0266 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1039-5234G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226256153 | ||||||
chr1:226256176
|
A | G | 1 | a0001c0002t0002g0209 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1039-5257T>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226256176 | ||||||
chr1:226256524
|
C | T | 1 | a0001c0001t0001g0090 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1039-5605G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226256524 | ||||||
chr1:226256552
|
A | AAT | 23 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0212others(20): Show | 23 | HG02040.hp1 HG02074.hp2 HG03688.hp2 others(20): Show |
intron_variant | MODIFIER | c.1039-5635_1039-563 others(6): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226256552 | ||||||
chr1:226256560
|
T | G | 4 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0268others(1): Show | 4 | HG00735.hp2 HG01433.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1039-5641A>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226256560 | ||||||
chr1:226256569
|
A | T | 19 | a0001c0001t0001g0029a0001c0001t0001g0122a0001c0001t0001g0123others(16): Show | 19 | HG00099.hp1 HG00544.hp1 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.1039-5650T>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226256569 | ||||||
chr1:226256571
|
T | A | 19 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0212others(16): Show | 19 | HG02040.hp1 HG03017.hp2 HG03688.hp2 others(16): Show |
intron_variant | MODIFIER | c.1039-5652A>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226256571 | ||||||
chr1:226256651
|
T | C | 1 | a0001c0001t0001g0275 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1039-5732A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226256651 | ||||||
chr1:226256675
|
C | T | 1 | a0001c0001t0001g0217 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1039-5756G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226256675 | ||||||
chr1:226256949
|
A | C | 1 | a0001c0001t0001g0211 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1039-6030T>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226256949 | ||||||
chr1:226257245
|
T | C | 240 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(237): Show | 240 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(237): Show |
intron_variant | MODIFIER | c.1039-6326A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226257245 | ||||||
chr1:226257659
|
GA | G | 19 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0212others(16): Show | 19 | HG02040.hp1 HG03017.hp2 HG03688.hp2 others(16): Show |
intron_variant | MODIFIER | c.1039-6741delT | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226257659 | ||||||
chr1:226257827
|
C | A | 116 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(113): Show | 116 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.1039-6908G>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226257827 | ||||||
chr1:226257879
|
T | A | 1 | a0001c0001t0001g0276 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1039-6960A>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226257879 | ||||||
chr1:226257915
|
G | A | 1 | a0001c0001t0001g0276 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1039-6996C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226257915 | ||||||
chr1:226257918
|
T | C | 1 | a0001c0001t0001g0276 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1039-6999A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226257918 | ||||||
chr1:226257919
|
C | T | 1 | a0001c0001t0001g0276 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1039-7000G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226257919 | ||||||
chr1:226257920
|
A | T | 1 | a0001c0001t0001g0276 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1039-7001T>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226257920 | ||||||
chr1:226257930
|
T | G | 1 | a0001c0001t0001g0276 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1039-7011A>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226257930 | ||||||
chr1:226257934
|
A | G | 1 | a0001c0001t0001g0276 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1039-7015T>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226257934 | ||||||
chr1:226257937
|
A | C | 1 | a0001c0001t0001g0276 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1039-7018T>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226257937 | ||||||
chr1:226257939
|
T | C | 1 | a0001c0001t0001g0276 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1039-7020A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226257939 | ||||||
chr1:226257946
|
G | A | 1 | a0001c0001t0001g0276 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1039-7027C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226257946 | ||||||
chr1:226257950
|
G | A | 59 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0071others(56): Show | 59 | HG00423.hp1 HG00609.hp1 HG00673.hp1 others(56): Show |
intron_variant | MODIFIER | c.1039-7031C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226257950 | ||||||
chr1:226257957
|
GTCCCATC others(6): Show |
G | 1 | a0001c0001t0001g0276 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1039-7051_1039-703 others(17): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226257957 | ||||||
chr1:226257971
|
G | C | 1 | a0001c0001t0001g0276 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1039-7052C>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226257971 | ||||||
chr1:226258007
|
A | C | 1 | a0001c0001t0001g0347 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1039-7088T>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226258007 | ||||||
chr1:226258008
|
C | A | 1 | a0001c0001t0001g0347 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1039-7089G>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226258008 | ||||||
chr1:226258050
|
G | A | 4 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0313others(1): Show | 4 | HG02630.hp1 NA19240.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.1039-7131C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226258050 | ||||||
chr1:226258102
|
TA | T | 3 | a0001c0001t0003g0045a0001c0001t0003g0049a0001c0001t0003g0114 | 3 | NA18960.hp1 NA18977.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.1039-7184delT | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226258102 | ||||||
chr1:226258123
|
G | A | 13 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0016others(10): Show | 13 | HG01074.hp2 HG01099.hp2 HG01978.hp1 others(10): Show |
intron_variant | MODIFIER | c.1039-7204C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226258123 | ||||||
chr1:226258175
|
A | AAAAC | 26 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0300others(23): Show | 27 | HG00544.hp1 HG00738.hp1 HG01123.hp1 others(24): Show |
intron_variant | MODIFIER | c.1039-7260_1039-725 others(8): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226258175 | ||||||
chr1:226258175
|
A | AAAACAAA others(1): Show |
7 | a0001c0001t0001g0305a0001c0001t0001g0306a0001c0001t0001g0307others(4): Show | 7 | HG02559.hp1 HG02572.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1039-7264_1039-725 others(12): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226258175 | ||||||
chr1:226258175
|
AAAAC | A | 24 | a0001c0001t0001g0055a0001c0001t0001g0129a0001c0001t0001g0130others(21): Show | 24 | HG02040.hp1 HG02080.hp1 HG02622.hp1 others(21): Show |
intron_variant | MODIFIER | c.1039-7260_1039-725 others(8): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226258175 | ||||||
chr1:226258175
|
AAAACAAA others(1): Show |
A | 123 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(120): Show | 123 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(120): Show |
intron_variant | MODIFIER | c.1039-7264_1039-725 others(12): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226258175 | ||||||
chr1:226258175
|
AAAACAAA others(5): Show |
A | 97 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0224others(94): Show | 97 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(94): Show |
intron_variant | MODIFIER | c.1039-7268_1039-725 others(16): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226258175 | ||||||
chr1:226258192
|
AAACAAAC others(4): Show |
A | 1 | a0001c0001t0001g0347 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1039-7284_1039-727 others(15): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226258192 | ||||||
chr1:226258362
|
G | A | 1 | a0001c0002t0002g0131 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1038+7171C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226258362 | ||||||
chr1:226258468
|
C | CA | 29 | a0001c0001t0001g0031a0001c0001t0001g0116a0001c0001t0001g0126others(26): Show | 29 | HG00621.hp1 HG01978.hp2 HG02055.hp2 others(26): Show |
intron_variant | MODIFIER | c.1038+7064dupT | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226258468 | ||||||
chr1:226258662
|
G | A | 1 | a0001c0001t0001g0281 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1038+6871C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226258662 | ||||||
chr1:226258666
|
G | A | 1 | a0001c0001t0001g0021 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1038+6867C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226258666 | ||||||
chr1:226258894
|
C | A | 1 | a0001c0002t0002g0284 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1038+6639G>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226258894 | ||||||
chr1:226258894
|
C | CA | 100 | a0001c0001t0001g0010a0001c0001t0001g0161a0001c0001t0001g0225others(97): Show | 100 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.1038+6638dupT | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226258894 | ||||||
chr1:226258894
|
C | CAA | 69 | a0001c0001t0001g0224a0001c0001t0001g0226a0001c0001t0001g0227others(66): Show | 69 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.1038+6637_1038+663 others(6): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226258894 | ||||||
chr1:226258894
|
C | CAAA | 15 | a0001c0001t0001g0005a0001c0001t0001g0228a0001c0001t0001g0232others(12): Show | 15 | HG00738.hp2 HG00741.hp2 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.1038+6636_1038+663 others(7): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226258894 | ||||||
chr1:226258894
|
C | CAAAAAAA others(5): Show |
1 | a0001c0001t0001g0314 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1038+6627_1038+663 others(16): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226258894 | ||||||
chr1:226258894
|
CAAAAAAA others(1): Show |
C | 33 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0023others(30): Show | 33 | HG00438.hp1 HG00673.hp2 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.1038+6631_1038+663 others(12): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226258894 | ||||||
chr1:226258894
|
CAAAAAAA others(2): Show |
C | 88 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(85): Show | 88 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(85): Show |
intron_variant | MODIFIER | c.1038+6630_1038+663 others(13): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226258894 | ||||||
chr1:226258894
|
CAAAAAAA others(7): Show |
C | 4 | a0001c0001t0001g0220a0001c0001t0001g0222a0001c0001t0001g0356others(1): Show | 4 | HG01516.hp2 HG03688.hp2 NA18967.hp2 others(1): Show |
intron_variant | MODIFIER | c.1038+6625_1038+663 others(18): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226258894 | ||||||
chr1:226258894
|
CAAAAAAA others(8): Show |
C | 16 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0212others(13): Show | 16 | HG02040.hp1 HG03017.hp2 HG03704.hp1 others(13): Show |
intron_variant | MODIFIER | c.1038+6624_1038+663 others(19): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226258894 | ||||||
chr1:226258894
|
CAAAAAAA others(9): Show |
C | 1 | a0001c0002t0002g0207 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1038+6623_1038+663 others(20): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226258894 | ||||||
chr1:226258972
|
A | AT | 119 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(116): Show | 119 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.1038+6560dupA | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226258972 | ||||||
chr1:226258992
|
A | C | 19 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0212others(16): Show | 19 | HG02040.hp1 HG03017.hp2 HG03688.hp2 others(16): Show |
intron_variant | MODIFIER | c.1038+6541T>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226258992 | ||||||
chr1:226258998
|
TCTTGCTC others(6): Show |
T | 1 | a0001c0001t0001g0022 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1038+6522_1038+653 others(17): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226258998 | ||||||
chr1:226259083
|
C | T | 5 | a0001c0002t0002g0164a0001c0002t0002g0199a0001c0002t0002g0201others(2): Show | 5 | HG02622.hp2 HG02630.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1038+6450G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226259083 | ||||||
chr1:226259149
|
G | A | 1 | a0001c0002t0002g0171 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1038+6384C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226259149 | ||||||
chr1:226259179
|
C | T | 5 | a0001c0001t0001g0318a0001c0001t0001g0319a0001c0001t0001g0320others(2): Show | 5 | HG02145.hp2 HG02486.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1038+6354G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226259179 | ||||||
chr1:226259207
|
G | A | 2 | a0001c0001t0001g0254a0001c0001t0001g0278 | 2 | NA18975.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.1038+6326C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226259207 | ||||||
chr1:226259255
|
C | T | 1 | a0001c0001t0001g0218 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1038+6278G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226259255 | ||||||
chr1:226259533
|
G | A | 1 | a0001c0001t0001g0356 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1038+6000C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226259533 | ||||||
chr1:226259649
|
A | G | 1 | a0001c0002t0002g0208 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1038+5884T>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226259649 | ||||||
chr1:226259945
|
A | AAATT | 241 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(238): Show | 241 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(238): Show |
intron_variant | MODIFIER | c.1038+5587_1038+558 others(8): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226259945 | ||||||
chr1:226260565
|
A | C | 3 | a0001c0002t0002g0001a0001c0002t0002g0136a0001c0002t0002g0144 | 4 | HG02602.hp2 HG02698.hp1 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.1038+4968T>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226260565 | ||||||
chr1:226260618
|
G | A | 1 | a0001c0002t0002g0163 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1038+4915C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226260618 | ||||||
chr1:226260628
|
G | GT | 24 | a0001c0001t0001g0010a0001c0001t0001g0217a0001c0001t0001g0227others(21): Show | 24 | HG00408.hp1 HG00438.hp2 HG00597.hp1 others(21): Show |
intron_variant | MODIFIER | c.1038+4904dupA | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226260628 | ||||||
chr1:226260628
|
G | GTT | 7 | a0001c0001t0001g0210a0001c0001t0001g0213a0001c0001t0001g0214others(4): Show | 7 | HG03017.hp2 HG03927.hp1 NA18962.hp2 others(4): Show |
intron_variant | MODIFIER | c.1038+4903_1038+490 others(6): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226260628 | ||||||
chr1:226260628
|
G | GTTT | 12 | a0001c0001t0001g0211a0001c0001t0001g0212a0001c0001t0001g0215others(9): Show | 12 | HG02040.hp1 HG03041.hp2 HG03688.hp2 others(9): Show |
intron_variant | MODIFIER | c.1038+4902_1038+490 others(7): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226260628 | ||||||
chr1:226260628
|
G | GTTTTTTT others(3): Show |
1 | a0001c0001t0001g0304 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1038+4895_1038+490 others(14): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226260628 | ||||||
chr1:226260628
|
G | GTTTTTTT others(12): Show |
3 | a0001c0001t0001g0305a0001c0001t0001g0310a0001c0001t0001g0311 | 3 | HG02559.hp1 HG02886.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1038+4886_1038+490 others(23): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226260628 | ||||||
chr1:226260628
|
G | GTTTTTTT others(13): Show |
3 | a0001c0001t0001g0306a0001c0001t0001g0308a0001c0001t0001g0312 | 3 | HG02572.hp2 HG02647.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.1038+4885_1038+490 others(24): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226260628 | ||||||
chr1:226260628
|
G | GTTTTTTT others(22): Show |
1 | a0001c0001t0001g0307 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1038+4876_1038+490 others(33): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226260628 | ||||||
chr1:226260628
|
GT | G | 85 | a0001c0001t0001g0224a0001c0001t0001g0226a0001c0001t0001g0228others(82): Show | 85 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(82): Show |
intron_variant | MODIFIER | c.1038+4904delA | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226260628 | ||||||
chr1:226260628
|
GTT | G | 26 | a0001c0001t0001g0253a0001c0001t0001g0258a0001c0001t0001g0259others(23): Show | 27 | HG00544.hp1 HG01167.hp2 HG01192.hp1 others(24): Show |
intron_variant | MODIFIER | c.1038+4903_1038+490 others(6): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226260628 | ||||||
chr1:226260628
|
GTTTT | G | 6 | a0001c0001t0001g0014a0001c0001t0001g0127a0001c0001t0001g0128others(3): Show | 6 | HG02486.hp2 HG02976.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1038+4901_1038+490 others(8): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226260628 | ||||||
chr1:226260628
|
GTTTTT | G | 25 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0031others(22): Show | 25 | HG00423.hp1 HG00438.hp1 HG01099.hp2 others(22): Show |
intron_variant | MODIFIER | c.1038+4900_1038+490 others(9): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226260628 | ||||||
chr1:226260628
|
GTTTTTT | G | 92 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0015others(89): Show | 92 | HG00099.hp1 HG00280.hp2 HG00609.hp1 others(89): Show |
intron_variant | MODIFIER | c.1038+4899_1038+490 others(10): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226260628 | ||||||
chr1:226260628
|
GTTTTTTT | G | 7 | a0001c0001t0001g0022a0001c0001t0001g0089a0001c0001t0001g0298others(4): Show | 7 | HG01081.hp2 HG02809.hp1 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.1038+4898_1038+490 others(11): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226260628 | ||||||
chr1:226260630
|
T | G | 3 | a0001c0002t0004g0150a0001c0002t0004g0151a0001c0002t0004g0283 | 3 | HG01069.hp1 HG01071.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.1038+4903A>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226260630 | ||||||
chr1:226260636
|
T | G | 4 | a0001c0001t0001g0014a0001c0001t0001g0127a0001c0001t0001g0128others(1): Show | 4 | HG01192.hp1 HG03209.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1038+4897A>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226260636 | ||||||
chr1:226260637
|
T | G | 25 | a0001c0001t0001g0019a0001c0001t0001g0031a0001c0001t0001g0055others(22): Show | 25 | HG00423.hp1 HG00438.hp1 HG01099.hp2 others(22): Show |
intron_variant | MODIFIER | c.1038+4896A>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226260637 | ||||||
chr1:226260638
|
T | G | 90 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0015others(87): Show | 90 | HG00099.hp1 HG00280.hp2 HG00609.hp1 others(87): Show |
intron_variant | MODIFIER | c.1038+4895A>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226260638 | ||||||
chr1:226260639
|
T | G | 4 | a0001c0001t0001g0022a0001c0001t0001g0089a0001c0001t0003g0083others(1): Show | 4 | HG01081.hp2 NA18945.hp2 NA18954.hp1 others(1): Show |
intron_variant | MODIFIER | c.1038+4894A>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226260639 | ||||||
chr1:226260645
|
T | G | 1 | a0001c0001t0003g0063 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1038+4888A>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226260645 | ||||||
chr1:226260692
|
C | T | 122 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(119): Show | 122 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(119): Show |
intron_variant | MODIFIER | c.1038+4841G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226260692 | ||||||
chr1:226260706
|
A | G | 263 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(260): Show | 263 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(260): Show |
intron_variant | MODIFIER | c.1038+4827T>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226260706 | ||||||
chr1:226260730
|
C | T | 1 | a0001c0001t0003g0063 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1038+4803G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226260730 | ||||||
chr1:226260745
|
C | T | 4 | a0001c0001t0001g0226a0001c0001t0001g0231a0001c0001t0001g0270others(1): Show | 4 | HG00738.hp2 HG01993.hp2 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.1038+4788G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226260745 | ||||||
chr1:226260836
|
G | A | 17 | a0001c0001t0001g0005a0001c0001t0001g0298a0001c0001t0001g0299others(14): Show | 17 | HG02055.hp2 HG02486.hp2 HG02559.hp1 others(14): Show |
intron_variant | MODIFIER | c.1038+4697C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226260836 | ||||||
chr1:226261111
|
T | C | 19 | a0001c0001t0001g0005a0001c0001t0001g0127a0001c0001t0001g0128others(16): Show | 19 | HG02055.hp2 HG02486.hp2 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.1038+4422A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226261111 | ||||||
chr1:226261133
|
C | G | 1 | a0001c0002t0002g0158 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1038+4400G>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226261133 | ||||||
chr1:226261138
|
TA | T | 22 | a0001c0001t0001g0014a0001c0001t0001g0043a0001c0001t0001g0044others(19): Show | 22 | HG01256.hp2 HG01258.hp1 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.1038+4394delT | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226261138 | ||||||
chr1:226261520
|
A | G | 2 | a0001c0001t0003g0073a0001c0001t0003g0074 | 2 | HG01993.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.1038+4013T>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226261520 | ||||||
chr1:226261533
|
T | G | 1 | a0001c0001t0001g0022 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1038+4000A>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226261533 | ||||||
chr1:226261655
|
T | A | 1 | a0001c0001t0001g0022 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1038+3878A>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226261655 | ||||||
chr1:226261741
|
G | A | 1 | a0001c0001t0001g0255 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1038+3792C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226261741 | ||||||
chr1:226261927
|
T | C | 19 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0212others(16): Show | 19 | HG02040.hp1 HG03017.hp2 HG03688.hp2 others(16): Show |
intron_variant | MODIFIER | c.1038+3606A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226261927 | ||||||
chr1:226262130
|
G | T | 1 | a0001c0001t0001g0022 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1038+3403C>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226262130 | ||||||
chr1:226262163
|
T | C | 76 | a0001c0001t0001g0088a0001c0001t0001g0225a0001c0001t0001g0226others(73): Show | 76 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.1038+3370A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226262163 | ||||||
chr1:226262235
|
T | C | 2 | a0001c0001t0001g0268a0001c0001t0001g0269 | 2 | HG00735.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.1038+3298A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226262235 | ||||||
chr1:226262246
|
G | A | 8 | a0001c0002t0002g0165a0001c0002t0002g0166a0001c0002t0002g0167others(5): Show | 8 | NA18939.hp1 NA18941.hp1 NA18952.hp2 others(5): Show |
intron_variant | MODIFIER | c.1038+3287C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226262246 | ||||||
chr1:226262289
|
T | A | 1 | a0001c0001t0001g0022 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1038+3244A>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226262289 | ||||||
chr1:226262293
|
A | T | 1 | a0001c0001t0001g0022 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1038+3240T>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226262293 | ||||||
chr1:226262295
|
T | G | 1 | a0001c0001t0001g0022 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1038+3238A>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226262295 | ||||||
chr1:226262532
|
G | T | 1 | a0001c0001t0001g0022 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1038+3001C>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226262532 | ||||||
chr1:226263093
|
T | G | 1 | a0001c0001t0001g0022 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1038+2440A>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226263093 | ||||||
chr1:226263340
|
G | A | 6 | a0001c0001t0001g0298a0001c0001t0001g0299a0001c0001t0001g0300others(3): Show | 6 | HG02055.hp2 HG02809.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.1038+2193C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226263340 | ||||||
chr1:226263374
|
G | T | 1 | a0001c0001t0001g0234 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1038+2159C>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226263374 | ||||||
chr1:226263676
|
A | G | 3 | a0001c0001t0001g0232a0001c0001t0001g0241a0001c0001t0001g0282 | 3 | HG01109.hp2 HG01243.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.1038+1857T>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226263676 | ||||||
chr1:226263747
|
A | G | 5 | a0001c0001t0001g0318a0001c0001t0001g0319a0001c0001t0001g0320others(2): Show | 5 | HG02145.hp2 HG02486.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1038+1786T>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226263747 | ||||||
chr1:226263801
|
G | A | 1 | a0001c0002t0002g0170 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1038+1732C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226263801 | ||||||
chr1:226263914
|
C | T | 17 | a0001c0001t0001g0005a0001c0001t0001g0298a0001c0001t0001g0299others(14): Show | 17 | HG02055.hp2 HG02486.hp2 HG02559.hp1 others(14): Show |
intron_variant | MODIFIER | c.1038+1619G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226263914 | ||||||
chr1:226263999
|
A | C | 4 | a0001c0001t0001g0356a0001c0001t0001g0357a0001c0001t0001g0358others(1): Show | 4 | HG03017.hp2 HG03688.hp2 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.1038+1534T>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226263999 | ||||||
chr1:226263999
|
A | T | 15 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0212others(12): Show | 15 | HG02040.hp1 HG03704.hp1 NA18941.hp2 others(12): Show |
intron_variant | MODIFIER | c.1038+1534T>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226263999 | ||||||
chr1:226264078
|
A | C | 1 | a0001c0001t0001g0022 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1038+1455T>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226264078 | ||||||
chr1:226264097
|
A | C | 1 | a0001c0001t0001g0022 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1038+1436T>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226264097 | ||||||
chr1:226264148
|
C | T | 8 | a0001c0001t0001g0305a0001c0001t0001g0306a0001c0001t0001g0307others(5): Show | 8 | HG02559.hp1 HG02572.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.1038+1385G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226264148 | ||||||
chr1:226264206
|
C | G | 1 | a0001c0001t0001g0070 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1038+1327G>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226264206 | ||||||
chr1:226264389
|
T | C | 1 | a0001c0002t0002g0179 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1038+1144A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226264389 | ||||||
chr1:226264502
|
A | C | 1 | a0001c0001t0001g0022 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1038+1031T>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226264502 | ||||||
chr1:226264574
|
A | C | 1 | a0001c0001t0001g0022 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1038+959T>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226264574 | ||||||
chr1:226264587
|
T | A | 1 | a0001c0001t0001g0022 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1038+946A>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226264587 | ||||||
chr1:226264675
|
A | C | 1 | a0001c0001t0001g0022 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1038+858T>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226264675 | ||||||
chr1:226264860
|
A | C | 1 | a0001c0001t0001g0022 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1038+673T>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226264860 | ||||||
chr1:226264946
|
A | G | 1 | a0001c0001t0001g0279 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1038+587T>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226264946 | ||||||
chr1:226265201
|
A | G | 2 | a0001c0001t0001g0129a0001c0001t0001g0130 | 2 | NA19240.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1038+332T>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226265201 | ||||||
chr1:226265348
|
G | T | 2 | a0001c0002t0002g0166a0001c0002t0002g0174 | 2 | NA18965.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.1038+185C>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 10/14 | chr1 | 226265348 | ||||||
chr1:226265880
|
T | C | 224 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(221): Show | 224 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(221): Show |
intron_variant | MODIFIER | c.937-246A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 9/14 | chr1 | 226265880 | ||||||
chr1:226265899
|
G | C | 1 | a0001c0002t0004g0283 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.937-265C>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 9/14 | chr1 | 226265899 | ||||||
chr1:226265917
|
T | C | 241 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(238): Show | 241 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(238): Show |
intron_variant | MODIFIER | c.937-283A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 9/14 | chr1 | 226265917 | ||||||
chr1:226265969
|
G | A | 1 | a0001c0001t0003g0113 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.936+244C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 9/14 | chr1 | 226265969 | ||||||
chr1:226266110
|
T | C | 2 | a0001c0001t0001g0210a0001c0001t0001g0214 | 2 | NA18984.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.936+103A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 9/14 | chr1 | 226266110 | ||||||
chr1:226266155
|
A | G | 1 | a0001c0001t0001g0069 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.936+58T>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 9/14 | chr1 | 226266155 | ||||||
chr1:226266161
|
T | C | 1 | a0001c0001t0003g0106 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.936+52A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 9/14 | chr1 | 226266161 | ||||||
chr1:226266530
|
T | C | 2 | a0001c0001t0001g0129a0001c0001t0001g0130 | 2 | NA19240.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.817-198A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 8/14 | chr1 | 226266530 | ||||||
chr1:226266685
|
T | C | 1 | a0001c0001t0001g0357 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.817-353A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 8/14 | chr1 | 226266685 | ||||||
chr1:226266777
|
AT | A | 97 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0224others(94): Show | 97 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(94): Show |
intron_variant | MODIFIER | c.817-446delA | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 8/14 | chr1 | 226266777 | ||||||
chr1:226266843
|
G | A | 1 | a0001c0001t0001g0110 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.817-511C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 8/14 | chr1 | 226266843 | ||||||
chr1:226267023
|
G | A | 2 | a0001c0001t0001g0127a0001c0001t0001g0128 | 2 | HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.817-691C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 8/14 | chr1 | 226267023 | ||||||
chr1:226267055
|
T | C | 1 | a0001c0002t0002g0133 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.817-723A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 8/14 | chr1 | 226267055 | ||||||
chr1:226267164
|
G | C | 4 | a0001c0001t0003g0061a0001c0001t0003g0062a0001c0001t0003g0063others(1): Show | 4 | NA18962.hp1 NA19064.hp2 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.816+793C>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 8/14 | chr1 | 226267164 | ||||||
chr1:226267230
|
G | GAT | 107 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0012others(104): Show | 107 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.816+725_816+726dup others(2): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 8/14 | chr1 | 226267230 | ||||||
chr1:226267230
|
G | GATAT | 23 | a0001c0001t0001g0021a0001c0001t0001g0088a0001c0001t0001g0089others(20): Show | 23 | HG00741.hp1 HG01071.hp2 HG01081.hp2 others(20): Show |
intron_variant | MODIFIER | c.816+723_816+726dup others(4): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 8/14 | chr1 | 226267230 | ||||||
chr1:226267230
|
G | GATATAT | 6 | a0001c0001t0001g0035a0001c0001t0001g0126a0001c0001t0001g0356others(3): Show | 6 | HG02148.hp2 HG02300.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.816+721_816+726dup others(6): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 8/14 | chr1 | 226267230 | ||||||
chr1:226267230
|
GAT | G | 23 | a0001c0001t0001g0305a0001c0001t0001g0306a0001c0001t0001g0307others(20): Show | 23 | HG01109.hp1 HG01167.hp2 HG01168.hp1 others(20): Show |
intron_variant | MODIFIER | c.816+725_816+726del others(2): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 8/14 | chr1 | 226267230 | ||||||
chr1:226267230
|
GATAT | G | 100 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0129others(97): Show | 100 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(97): Show |
intron_variant | MODIFIER | c.816+723_816+726del others(4): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 8/14 | chr1 | 226267230 | ||||||
chr1:226267310
|
T | TTATGTAT others(5): Show |
5 | a0001c0001t0001g0018a0001c0001t0001g0099a0001c0001t0001g0116others(2): Show | 5 | HG01071.hp2 HG01099.hp2 HG01934.hp2 others(2): Show |
intron_variant | MODIFIER | c.816+646_816+647ins others(12): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 8/14 | chr1 | 226267310 | ||||||
chr1:226267310
|
T | TTATGTAT others(9): Show |
50 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(47): Show | 50 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.816+646_816+647ins others(16): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 8/14 | chr1 | 226267310 | ||||||
chr1:226267310
|
T | TTATGTAT others(13): Show |
5 | a0001c0001t0001g0021a0001c0001t0001g0066a0001c0001t0001g0088others(2): Show | 5 | HG01255.hp2 HG01978.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.816+646_816+647ins others(20): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 8/14 | chr1 | 226267310 | ||||||
chr1:226267318
|
A | ATATGTAT others(9): Show |
99 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0076others(96): Show | 99 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(96): Show |
intron_variant | MODIFIER | c.816+623_816+638dup others(16): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 8/14 | chr1 | 226267318 | ||||||
chr1:226267318
|
A | ATATGTAT others(13): Show |
95 | a0001c0001t0001g0005a0001c0001t0001g0069a0001c0001t0001g0070others(92): Show | 95 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.816+619_816+638dup others(20): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 8/14 | chr1 | 226267318 | ||||||
chr1:226267318
|
A | ATATGTAT others(17): Show |
8 | a0001c0001t0001g0127a0001c0001t0001g0239a0001c0001t0001g0243others(5): Show | 8 | HG00609.hp1 HG01167.hp1 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.816+615_816+638dup others(24): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 8/14 | chr1 | 226267318 | ||||||
chr1:226267318
|
A | G | 60 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(57): Show | 60 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(57): Show |
intron_variant | MODIFIER | c.816+639T>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 8/14 | chr1 | 226267318 | ||||||
chr1:226267422
|
C | CA | 117 | a0001c0001t0001g0009a0001c0001t0001g0031a0001c0001t0001g0071others(114): Show | 117 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(114): Show |
intron_variant | MODIFIER | c.816+534dupT | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 8/14 | chr1 | 226267422 | ||||||
chr1:226267422
|
C | CAA | 114 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0012others(111): Show | 114 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(111): Show |
intron_variant | MODIFIER | c.816+533_816+534dup others(2): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 8/14 | chr1 | 226267422 | ||||||
chr1:226267500
|
C | T | 1 | a0001c0001t0001g0308 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.816+457G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 8/14 | chr1 | 226267500 | ||||||
chr1:226267736
|
G | A | 1 | a0001c0002t0002g0131 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.816+221C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 8/14 | chr1 | 226267736 | ||||||
chr1:226268233
|
C | T | 7 | a0001c0002t0002g0162a0001c0002t0002g0170a0001c0002t0002g0182others(4): Show | 7 | HG00639.hp1 HG01192.hp2 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.683-143G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226268233 | ||||||
chr1:226268823
|
A | G | 19 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0212others(16): Show | 19 | HG02040.hp1 HG03017.hp2 HG03688.hp2 others(16): Show |
intron_variant | MODIFIER | c.683-733T>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226268823 | ||||||
chr1:226268865
|
C | T | 4 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0313others(1): Show | 4 | HG02630.hp1 NA19240.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.683-775G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226268865 | ||||||
chr1:226269184
|
A | T | 1 | a0001c0001t0001g0304 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.683-1094T>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226269184 | ||||||
chr1:226269301
|
G | A | 3 | a0001c0001t0001g0300a0001c0001t0001g0301a0001c0001t0001g0303 | 3 | HG02055.hp2 HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.683-1211C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226269301 | ||||||
chr1:226269445
|
G | C | 4 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0313others(1): Show | 4 | HG02630.hp1 NA19240.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.683-1355C>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226269445 | ||||||
chr1:226269473
|
CAA | C | 51 | a0001c0002t0002g0006a0001c0002t0002g0007a0001c0002t0002g0008others(48): Show | 51 | HG00280.hp1 HG00408.hp2 HG00597.hp2 others(48): Show |
intron_variant | MODIFIER | c.683-1385_683-1384d others(4): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226269473 | ||||||
chr1:226269873
|
G | T | 1 | a0001c0002t0002g0193 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.683-1783C>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226269873 | ||||||
chr1:226269993
|
G | A | 3 | a0001c0001t0003g0077a0001c0001t0003g0083a0001c0001t0003g0119 | 3 | HG02074.hp2 NA18954.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.683-1903C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226269993 | ||||||
chr1:226270253
|
G | T | 1 | a0001c0001t0001g0308 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.683-2163C>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226270253 | ||||||
chr1:226270334
|
T | A | 47 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(44): Show | 47 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(44): Show |
intron_variant | MODIFIER | c.683-2244A>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226270334 | ||||||
chr1:226270488
|
A | C | 2 | a0001c0002t0002g0162a0001c0002t0002g0191 | 2 | HG00639.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.683-2398T>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226270488 | ||||||
chr1:226270601
|
C | T | 1 | a0001c0002t0002g0149 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.683-2511G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226270601 | ||||||
chr1:226270702
|
G | A | 8 | a0001c0001t0001g0011a0001c0001t0001g0016a0001c0001t0001g0018others(5): Show | 8 | NA18943.hp2 NA18950.hp2 NA18972.hp1 others(5): Show |
intron_variant | MODIFIER | c.683-2612C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226270702 | ||||||
chr1:226270810
|
G | A | 2 | a0001c0001t0001g0009a0001c0001t0001g0010 | 2 | HG02922.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.683-2720C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226270810 | ||||||
chr1:226270824
|
C | CA | 57 | a0001c0001t0001g0010a0001c0001t0001g0019a0001c0001t0001g0024others(54): Show | 57 | HG00438.hp1 HG00673.hp1 HG00738.hp1 others(54): Show |
intron_variant | MODIFIER | c.683-2735dupT | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226270824 | ||||||
chr1:226270824
|
CA | C | 12 | a0001c0001t0001g0112a0001c0001t0001g0334a0001c0001t0001g0356others(9): Show | 12 | HG01069.hp1 HG01192.hp2 HG01496.hp1 others(9): Show |
intron_variant | MODIFIER | c.683-2735delT | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226270824 | ||||||
chr1:226270824
|
CAAAA | C | 11 | a0001c0002t0002g0285a0001c0002t0002g0286a0001c0002t0002g0287others(8): Show | 11 | HG01109.hp1 HG01167.hp2 HG01168.hp1 others(8): Show |
intron_variant | MODIFIER | c.683-2738_683-2735d others(6): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226270824 | ||||||
chr1:226270834
|
A | T | 1 | a0001c0001t0001g0218 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.683-2744T>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226270834 | ||||||
chr1:226270984
|
C | G | 22 | a0001c0001t0001g0005a0001c0001t0001g0298a0001c0001t0001g0299others(19): Show | 22 | HG02055.hp2 HG02145.hp2 HG02486.hp1 others(19): Show |
intron_variant | MODIFIER | c.683-2894G>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226270984 | ||||||
chr1:226271146
|
T | C | 1 | a0001c0001t0001g0224 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.683-3056A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226271146 | ||||||
chr1:226271162
|
T | C | 2 | a0001c0001t0001g0313a0001c0001t0001g0314 | 2 | HG02630.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.683-3072A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226271162 | ||||||
chr1:226271335
|
C | T | 8 | a0001c0001t0001g0305a0001c0001t0001g0306a0001c0001t0001g0307others(5): Show | 8 | HG02559.hp1 HG02572.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.683-3245G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226271335 | ||||||
chr1:226271792
|
A | T | 1 | a0001c0001t0001g0298 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.683-3702T>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226271792 | ||||||
chr1:226271876
|
G | A | 262 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(259): Show | 262 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(259): Show |
intron_variant | MODIFIER | c.683-3786C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226271876 | ||||||
chr1:226272021
|
C | CT | 217 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(214): Show | 217 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.683-3932dupA | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226272021 | ||||||
chr1:226272051
|
CT | C | 27 | a0001c0001t0001g0005a0001c0001t0001g0026a0001c0001t0001g0298others(24): Show | 27 | HG02055.hp2 HG02145.hp2 HG02273.hp1 others(24): Show |
intron_variant | MODIFIER | c.683-3962delA | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226272051 | ||||||
chr1:226272381
|
C | CT | 8 | a0001c0001t0001g0224a0001c0001t0001g0322a0001c0001t0003g0045others(5): Show | 8 | HG01167.hp2 HG02886.hp1 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.683-4292dupA | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226272381 | ||||||
chr1:226272399
|
A | T | 4 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0313others(1): Show | 4 | HG02630.hp1 NA19240.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.683-4309T>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226272399 | ||||||
chr1:226272465
|
G | C | 22 | a0001c0001t0001g0005a0001c0001t0001g0298a0001c0001t0001g0299others(19): Show | 22 | HG02055.hp2 HG02145.hp2 HG02486.hp1 others(19): Show |
intron_variant | MODIFIER | c.683-4375C>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226272465 | ||||||
chr1:226272487
|
G | C | 257 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(254): Show | 257 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(254): Show |
intron_variant | MODIFIER | c.683-4397C>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226272487 | ||||||
chr1:226272539
|
C | CT | 6 | a0001c0001t0001g0005a0001c0001t0001g0022a0001c0002t0002g0006others(3): Show | 6 | NA18945.hp1 NA18946.hp1 NA18972.hp1 others(3): Show |
intron_variant | MODIFIER | c.683-4450dupA | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226272539 | ||||||
chr1:226272539
|
CT | C | 30 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0212others(27): Show | 30 | HG01069.hp1 HG01071.hp1 HG01169.hp1 others(27): Show |
intron_variant | MODIFIER | c.683-4450delA | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226272539 | ||||||
chr1:226272539
|
CTT | C | 8 | a0001c0001t0001g0216a0001c0001t0001g0217a0001c0001t0001g0319others(5): Show | 8 | HG02486.hp1 HG02818.hp1 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.683-4451_683-4450d others(4): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226272539 | ||||||
chr1:226272539
|
CTTT | C | 96 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0224others(93): Show | 96 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(93): Show |
intron_variant | MODIFIER | c.683-4452_683-4450d others(5): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226272539 | ||||||
chr1:226272558
|
T | A | 2 | a0001c0001t0001g0358a0001c0001t0001g0359 | 2 | HG03704.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.683-4468A>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226272558 | ||||||
chr1:226272559
|
T | A | 19 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0212others(16): Show | 19 | HG02040.hp1 HG03017.hp2 HG03688.hp2 others(16): Show |
intron_variant | MODIFIER | c.683-4469A>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226272559 | ||||||
chr1:226272760
|
C | A | 3 | a0001c0001t0001g0044a0001c0001t0001g0068a0001c0001t0001g0101 | 3 | HG02895.hp1 HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.683-4670G>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226272760 | ||||||
chr1:226272771
|
C | T | 4 | a0001c0001t0003g0077a0001c0001t0003g0083a0001c0001t0003g0102others(1): Show | 4 | HG02074.hp2 NA18954.hp1 NA18993.hp2 others(1): Show |
intron_variant | MODIFIER | c.683-4681G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226272771 | ||||||
chr1:226272924
|
ACTGT | A | 19 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0212others(16): Show | 19 | HG02040.hp1 HG03017.hp2 HG03688.hp2 others(16): Show |
intron_variant | MODIFIER | c.683-4838_683-4835d others(6): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226272924 | ||||||
chr1:226273256
|
A | AT | 145 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0012others(142): Show | 145 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.682+4518dupA | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226273256 | ||||||
chr1:226273256
|
A | ATT | 12 | a0001c0001t0001g0043a0001c0001t0001g0064a0001c0001t0001g0123others(9): Show | 12 | HG00423.hp1 HG01168.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.682+4517_682+4518d others(4): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226273256 | ||||||
chr1:226273256
|
AT | A | 18 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0212others(15): Show | 18 | HG02040.hp1 HG03017.hp2 HG03688.hp2 others(15): Show |
intron_variant | MODIFIER | c.682+4518delA | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226273256 | ||||||
chr1:226273281
|
G | A | 19 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0212others(16): Show | 19 | HG02040.hp1 HG03017.hp2 HG03688.hp2 others(16): Show |
intron_variant | MODIFIER | c.682+4494C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226273281 | ||||||
chr1:226273509
|
T | C | 4 | a0001c0002t0002g0137a0001c0002t0002g0138a0001c0002t0002g0139others(1): Show | 4 | HG00738.hp1 HG01123.hp1 HG01243.hp1 others(1): Show |
intron_variant | MODIFIER | c.682+4266A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226273509 | ||||||
chr1:226273681
|
A | C | 1 | a0001c0001t0003g0103 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.682+4094T>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226273681 | ||||||
chr1:226273798
|
A | G | 2 | a0001c0001t0001g0242a0001c0001t0001g0266 | 2 | HG00639.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.682+3977T>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226273798 | ||||||
chr1:226273834
|
C | CT | 155 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0012others(152): Show | 155 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.682+3940dupA | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226273834 | ||||||
chr1:226273899
|
G | A | 2 | a0001c0001t0001g0313a0001c0001t0001g0314 | 2 | HG02630.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.682+3876C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226273899 | ||||||
chr1:226274060
|
T | G | 1 | a0001c0002t0002g0155 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.682+3715A>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226274060 | ||||||
chr1:226274111
|
G | A | 1 | a0001c0001t0003g0079 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.682+3664C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226274111 | ||||||
chr1:226274671
|
TC | T | 97 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0224others(94): Show | 97 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(94): Show |
intron_variant | MODIFIER | c.682+3103delG | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226274671 | ||||||
chr1:226274735
|
G | A | 8 | a0001c0001t0001g0305a0001c0001t0001g0306a0001c0001t0001g0307others(5): Show | 8 | HG02559.hp1 HG02572.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.682+3040C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226274735 | ||||||
chr1:226275110
|
T | C | 2 | a0001c0002t0002g0147a0001c0002t0002g0189 | 2 | HG06807.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.682+2665A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226275110 | ||||||
chr1:226275252
|
G | T | 93 | a0001c0001t0001g0224a0001c0001t0001g0225a0001c0001t0001g0226others(90): Show | 93 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(90): Show |
intron_variant | MODIFIER | c.682+2523C>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226275252 | ||||||
chr1:226275254
|
T | C | 8 | a0001c0001t0001g0305a0001c0001t0001g0306a0001c0001t0001g0307others(5): Show | 8 | HG02559.hp1 HG02572.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.682+2521A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226275254 | ||||||
chr1:226275390
|
T | TTTA | 5 | a0001c0002t0002g0145a0001c0002t0002g0146a0001c0002t0002g0159others(2): Show | 5 | HG00544.hp1 HG02683.hp2 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.682+2384_682+2385i others(5): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226275390 | ||||||
chr1:226275467
|
G | A | 2 | a0001c0001t0001g0123a0001c0001t0001g0124 | 2 | HG02109.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.682+2308C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226275467 | ||||||
chr1:226275487
|
A | G | 1 | a0001c0002t0002g0172 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.682+2288T>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226275487 | ||||||
chr1:226275491
|
C | T | 1 | a0001c0001t0001g0023 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.682+2284G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226275491 | ||||||
chr1:226275515
|
G | T | 4 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0313others(1): Show | 4 | HG02630.hp1 NA19240.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.682+2260C>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226275515 | ||||||
chr1:226275548
|
T | A | 1 | a0001c0002t0002g0295 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.682+2227A>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226275548 | ||||||
chr1:226275687
|
G | A | 1 | a0001c0001t0001g0324 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.682+2088C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226275687 | ||||||
chr1:226275691
|
C | CA | 23 | a0001c0001t0001g0015a0001c0001t0001g0109a0001c0001t0001g0115others(20): Show | 23 | HG01109.hp2 HG01516.hp1 HG02257.hp2 others(20): Show |
intron_variant | MODIFIER | c.682+2083dupT | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226275691 | ||||||
chr1:226275692
|
AG | A | 5 | a0001c0001t0001g0014a0001c0001t0001g0216a0001c0001t0001g0233others(2): Show | 5 | HG00609.hp1 HG01081.hp1 NA18953.hp2 others(2): Show |
intron_variant | MODIFIER | c.682+2082delC | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226275692 | ||||||
chr1:226275693
|
G | A | 256 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(253): Show | 256 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(253): Show |
intron_variant | MODIFIER | c.682+2082C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226275693 | ||||||
chr1:226275693
|
GA | G | 17 | a0001c0002t0001g0361a0001c0002t0002g0001a0001c0002t0002g0137others(14): Show | 18 | HG00544.hp1 HG00738.hp1 HG01123.hp1 others(15): Show |
intron_variant | MODIFIER | c.682+2081delT | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226275693 | ||||||
chr1:226275721
|
G | GA | 22 | a0001c0001t0001g0324a0001c0002t0001g0361a0001c0002t0002g0001others(19): Show | 23 | HG00544.hp1 HG00738.hp1 HG01123.hp1 others(20): Show |
intron_variant | MODIFIER | c.682+2053dupT | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226275721 | ||||||
chr1:226275740
|
G | A | 97 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0224others(94): Show | 97 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(94): Show |
intron_variant | MODIFIER | c.682+2035C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226275740 | ||||||
chr1:226275755
|
C | T | 4 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0313others(1): Show | 4 | HG02630.hp1 NA19240.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.682+2020G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226275755 | ||||||
chr1:226276604
|
T | C | 1 | a0001c0002t0002g0287 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.682+1171A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226276604 | ||||||
chr1:226276666
|
G | A | 1 | a0001c0002t0002g0184 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.682+1109C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226276666 | ||||||
chr1:226276728
|
T | C | 1 | a0001c0002t0002g0131 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.682+1047A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226276728 | ||||||
chr1:226276806
|
A | G | 1 | a0001c0001t0001g0244 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.682+969T>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226276806 | ||||||
chr1:226276838
|
C | A | 38 | a0001c0002t0002g0006a0001c0002t0002g0007a0001c0002t0002g0008others(35): Show | 38 | HG00280.hp1 HG00408.hp2 HG00597.hp2 others(35): Show |
intron_variant | MODIFIER | c.682+937G>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226276838 | ||||||
chr1:226277004
|
A | G | 1 | a0001c0002t0002g0162 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.682+771T>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226277004 | ||||||
chr1:226277110
|
G | A | 2 | a0001c0001t0001g0009a0001c0001t0001g0010 | 2 | HG02922.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.682+665C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226277110 | ||||||
chr1:226277216
|
G | GA | 17 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0067others(14): Show | 17 | HG01978.hp1 HG02257.hp1 HG02572.hp2 others(14): Show |
intron_variant | MODIFIER | c.682+558dupT | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226277216 | ||||||
chr1:226277230
|
A | C | 98 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0224others(95): Show | 98 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(95): Show |
intron_variant | MODIFIER | c.682+545T>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226277230 | ||||||
chr1:226277360
|
T | C | 19 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0212others(16): Show | 19 | HG02040.hp1 HG03017.hp2 HG03688.hp2 others(16): Show |
intron_variant | MODIFIER | c.682+415A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226277360 | ||||||
chr1:226277584
|
C | CT | 19 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0212others(16): Show | 19 | HG02040.hp1 HG03017.hp2 HG03688.hp2 others(16): Show |
intron_variant | MODIFIER | c.682+190dupA | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 7/14 | chr1 | 226277584 | ||||||
chr1:226278018
|
A | G | 1 | a0001c0001t0003g0049 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.525-86T>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 6/14 | chr1 | 226278018 | ||||||
chr1:226278069
|
T | C | 1 | a0001c0001t0001g0088 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.525-137A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 6/14 | chr1 | 226278069 | ||||||
chr1:226278113
|
T | G | 1 | a0001c0001t0001g0279 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.525-181A>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 6/14 | chr1 | 226278113 | ||||||
chr1:226278199
|
C | A | 1 | a0001c0001t0003g0078 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.525-267G>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 6/14 | chr1 | 226278199 | ||||||
chr1:226278649
|
T | C | 264 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(261): Show | 264 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(261): Show |
intron_variant | MODIFIER | c.525-717A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 6/14 | chr1 | 226278649 | ||||||
chr1:226278658
|
T | C | 19 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0212others(16): Show | 19 | HG02040.hp1 HG03017.hp2 HG03688.hp2 others(16): Show |
intron_variant | MODIFIER | c.525-726A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 6/14 | chr1 | 226278658 | ||||||
chr1:226278666
|
A | G | 1 | a0001c0001t0001g0302 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.525-734T>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 6/14 | chr1 | 226278666 | ||||||
chr1:226278728
|
G | A | 2 | a0001c0001t0001g0313a0001c0001t0001g0314 | 2 | HG02630.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.525-796C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 6/14 | chr1 | 226278728 | ||||||
chr1:226278823
|
C | CA | 141 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(138): Show | 141 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.525-892dupT | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 6/14 | chr1 | 226278823 | ||||||
chr1:226278893
|
G | A | 1 | a0001c0001t0001g0311 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.525-961C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 6/14 | chr1 | 226278893 | ||||||
chr1:226278957
|
T | TA | 124 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0022others(121): Show | 124 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(121): Show |
intron_variant | MODIFIER | c.525-1026dupT | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 6/14 | chr1 | 226278957 | ||||||
chr1:226278957
|
T | TAA | 13 | a0001c0001t0001g0041a0001c0001t0001g0210a0001c0001t0001g0211others(10): Show | 13 | HG01433.hp1 HG01928.hp1 HG01978.hp2 others(10): Show |
intron_variant | MODIFIER | c.525-1027_525-1026d others(4): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 6/14 | chr1 | 226278957 | ||||||
chr1:226279002
|
C | A | 5 | a0001c0001t0003g0061a0001c0001t0003g0062a0001c0001t0003g0063others(2): Show | 5 | HG01106.hp2 NA18962.hp1 NA19064.hp2 others(2): Show |
intron_variant | MODIFIER | c.525-1070G>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 6/14 | chr1 | 226279002 | ||||||
chr1:226279039
|
T | C | 2 | a0001c0001t0001g0252a0001c0001t0001g0253 | 2 | HG03491.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.525-1107A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 6/14 | chr1 | 226279039 | ||||||
chr1:226279301
|
T | C | 24 | a0001c0001t0001g0005a0001c0001t0001g0127a0001c0001t0001g0128others(21): Show | 24 | HG02055.hp2 HG02145.hp2 HG02486.hp1 others(21): Show |
intron_variant | MODIFIER | c.525-1369A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 6/14 | chr1 | 226279301 | ||||||
chr1:226279440
|
C | T | 1 | a0001c0001t0003g0061 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.525-1508G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 6/14 | chr1 | 226279440 | ||||||
chr1:226279608
|
C | CA | 133 | a0001c0001t0001g0015a0001c0001t0001g0041a0001c0001t0001g0055others(130): Show | 134 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(131): Show |
intron_variant | MODIFIER | c.525-1677dupT | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 6/14 | chr1 | 226279608 | ||||||
chr1:226279608
|
C | CAA | 27 | a0001c0001t0001g0009a0001c0001t0001g0127a0001c0001t0001g0128others(24): Show | 27 | HG00544.hp2 HG00741.hp2 HG02055.hp2 others(24): Show |
intron_variant | MODIFIER | c.525-1678_525-1677d others(4): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 6/14 | chr1 | 226279608 | ||||||
chr1:226279608
|
C | CAAA | 6 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0307others(3): Show | 6 | HG02486.hp1 HG02572.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.525-1679_525-1677d others(5): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 6/14 | chr1 | 226279608 | ||||||
chr1:226279609
|
A | C | 4 | a0001c0001t0003g0061a0001c0001t0003g0062a0001c0001t0003g0063others(1): Show | 4 | NA18962.hp1 NA19064.hp2 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.525-1677T>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 6/14 | chr1 | 226279609 | ||||||
chr1:226279690
|
G | C | 1 | a0001c0001t0001g0230 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.525-1758C>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 6/14 | chr1 | 226279690 | ||||||
chr1:226279769
|
G | GA | 119 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(116): Show | 119 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.525-1838dupT | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 6/14 | chr1 | 226279769 | ||||||
chr1:226279769
|
GA | G | 6 | a0001c0001t0001g0231a0001c0001t0001g0337a0001c0001t0001g0338others(3): Show | 6 | HG02258.hp1 HG03834.hp1 NA18960.hp2 others(3): Show |
intron_variant | MODIFIER | c.525-1838delT | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 6/14 | chr1 | 226279769 | ||||||
chr1:226279821
|
A | C | 2 | a0001c0001t0001g0127a0001c0001t0001g0128 | 2 | HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.525-1889T>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 6/14 | chr1 | 226279821 | ||||||
chr1:226279967
|
C | T | 19 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0212others(16): Show | 19 | HG02040.hp1 HG03017.hp2 HG03688.hp2 others(16): Show |
intron_variant | MODIFIER | c.525-2035G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 6/14 | chr1 | 226279967 | ||||||
chr1:226280254
|
T | C | 1 | a0001c0002t0002g0144 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.525-2322A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 6/14 | chr1 | 226280254 | ||||||
chr1:226280347
|
G | A | 19 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0212others(16): Show | 19 | HG02040.hp1 HG03017.hp2 HG03688.hp2 others(16): Show |
intron_variant | MODIFIER | c.525-2415C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 6/14 | chr1 | 226280347 | ||||||
chr1:226280495
|
C | A | 76 | a0001c0001t0001g0161a0001c0001t0001g0225a0001c0001t0001g0226others(73): Show | 76 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.525-2563G>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 6/14 | chr1 | 226280495 | ||||||
chr1:226280495
|
C | T | 1 | a0001c0001t0003g0087 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.525-2563G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 6/14 | chr1 | 226280495 | ||||||
chr1:226280944
|
A | G | 4 | a0001c0001t0003g0045a0001c0001t0003g0049a0001c0001t0003g0082others(1): Show | 4 | NA18960.hp1 NA18977.hp2 NA18995.hp1 others(1): Show |
intron_variant | MODIFIER | c.525-3012T>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 6/14 | chr1 | 226280944 | ||||||
chr1:226281049
|
A | T | 1 | a0001c0002t0002g0196 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.525-3117T>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 6/14 | chr1 | 226281049 | ||||||
chr1:226281131
|
T | C | 14 | a0001c0002t0002g0284a0001c0002t0002g0285a0001c0002t0002g0286others(11): Show | 14 | HG01109.hp1 HG01167.hp2 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.525-3199A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 6/14 | chr1 | 226281131 | ||||||
chr1:226281414
|
TTAA | T | 99 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0161others(96): Show | 99 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(96): Show |
intron_variant | MODIFIER | c.525-3485_525-3483d others(5): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 6/14 | chr1 | 226281414 | ||||||
chr1:226281498
|
T | C | 1 | a0001c0002t0002g0170 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.525-3566A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 6/14 | chr1 | 226281498 | ||||||
chr1:226281632
|
T | A | 2 | a0001c0001t0001g0031a0001c0001t0001g0098 | 2 | NA19055.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.525-3700A>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 6/14 | chr1 | 226281632 | ||||||
chr1:226281673
|
T | G | 4 | a0001c0001t0001g0356a0001c0001t0001g0357a0001c0001t0001g0358others(1): Show | 4 | HG03017.hp2 HG03688.hp2 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.525-3741A>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 6/14 | chr1 | 226281673 | ||||||
chr1:226282526
|
A | G | 20 | a0001c0002t0002g0001a0001c0002t0002g0136a0001c0002t0002g0137others(17): Show | 21 | HG00544.hp1 HG00738.hp1 HG01123.hp1 others(18): Show |
intron_variant | MODIFIER | c.524+3807T>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 6/14 | chr1 | 226282526 | ||||||
chr1:226282538
|
C | T | 3 | a0001c0001t0001g0319a0001c0001t0001g0320a0001c0001t0001g0321 | 3 | HG02486.hp1 HG02818.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.524+3795G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 6/14 | chr1 | 226282538 | ||||||
chr1:226282586
|
C | T | 4 | a0001c0001t0001g0229a0001c0001t0001g0233a0001c0001t0001g0234others(1): Show | 4 | HG01081.hp1 HG01346.hp1 HG01928.hp1 others(1): Show |
intron_variant | MODIFIER | c.524+3747G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 6/14 | chr1 | 226282586 | ||||||
chr1:226282673
|
T | C | 225 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(222): Show | 225 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(222): Show |
intron_variant | MODIFIER | c.524+3660A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 6/14 | chr1 | 226282673 | ||||||
chr1:226282863
|
A | T | 359 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(356): Show | 360 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(357): Show |
intron_variant | MODIFIER | c.524+3470T>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 6/14 | chr1 | 226282863 | ||||||
chr1:226283278
|
A | AT | 73 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0127others(70): Show | 73 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.524+3054dupA | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 6/14 | chr1 | 226283278 | ||||||
chr1:226283278
|
A | ATT | 97 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0015others(94): Show | 97 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.524+3053_524+3054d others(4): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 6/14 | chr1 | 226283278 | ||||||
chr1:226283278
|
A | ATTT | 45 | a0001c0001t0001g0011a0001c0001t0001g0018a0001c0001t0001g0019others(42): Show | 45 | HG00423.hp1 HG00673.hp1 HG00673.hp2 others(42): Show |
intron_variant | MODIFIER | c.524+3052_524+3054d others(5): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 6/14 | chr1 | 226283278 | ||||||
chr1:226283547
|
A | G | 2 | a0001c0002t0002g0152a0001c0002t0002g0154 | 2 | NA19070.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.524+2786T>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 6/14 | chr1 | 226283547 | ||||||
chr1:226283593
|
G | A | 2 | a0001c0001t0001g0313a0001c0001t0001g0314 | 2 | HG02630.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.524+2740C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 6/14 | chr1 | 226283593 | ||||||
chr1:226283891
|
G | A | 1 | a0001c0002t0002g0186 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.524+2442C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 6/14 | chr1 | 226283891 | ||||||
chr1:226283925
|
G | C | 52 | a0001c0002t0001g0135a0001c0002t0002g0006a0001c0002t0002g0007others(49): Show | 52 | HG00280.hp1 HG00408.hp2 HG00597.hp2 others(49): Show |
intron_variant | MODIFIER | c.524+2408C>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 6/14 | chr1 | 226283925 | ||||||
chr1:226283951
|
A | AAG | 6 | a0001c0001t0001g0298a0001c0001t0001g0299a0001c0001t0001g0300others(3): Show | 6 | HG02055.hp2 HG02809.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.524+2380_524+2381d others(4): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 6/14 | chr1 | 226283951 | ||||||
chr1:226284126
|
C | T | 1 | a0001c0002t0002g0152 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.524+2207G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 6/14 | chr1 | 226284126 | ||||||
chr1:226284136
|
G | A | 19 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0212others(16): Show | 19 | HG02040.hp1 HG03017.hp2 HG03688.hp2 others(16): Show |
intron_variant | MODIFIER | c.524+2197C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 6/14 | chr1 | 226284136 | ||||||
chr1:226284463
|
C | T | 4 | a0001c0002t0002g0137a0001c0002t0002g0138a0001c0002t0002g0139others(1): Show | 4 | HG00738.hp1 HG01123.hp1 HG01243.hp1 others(1): Show |
intron_variant | MODIFIER | c.524+1870G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 6/14 | chr1 | 226284463 | ||||||
chr1:226284598
|
C | A | 2 | a0001c0001t0001g0246a0001c0001t0001g0280 | 2 | HG00438.hp2 HG00597.hp1 |
intron_variant | MODIFIER | c.524+1735G>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 6/14 | chr1 | 226284598 | ||||||
chr1:226284698
|
T | C | 2 | a0001c0001t0001g0304a0001c0001t0001g0316 | 2 | HG02486.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.524+1635A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 6/14 | chr1 | 226284698 | ||||||
chr1:226284831
|
T | C | 263 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(260): Show | 263 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(260): Show |
intron_variant | MODIFIER | c.524+1502A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 6/14 | chr1 | 226284831 | ||||||
chr1:226284890
|
C | T | 263 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(260): Show | 263 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(260): Show |
intron_variant | MODIFIER | c.524+1443G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 6/14 | chr1 | 226284890 | ||||||
chr1:226284926
|
AGTTTCAC others(10): Show |
A | 1 | a0001c0001t0003g0192 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.524+1390_524+1406d others(19): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 6/14 | chr1 | 226284926 | ||||||
chr1:226284937
|
T | C | 1 | a0001c0001t0001g0105 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.524+1396A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 6/14 | chr1 | 226284937 | ||||||
chr1:226284945
|
T | A | 1 | a0001c0001t0003g0192 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.524+1388A>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 6/14 | chr1 | 226284945 | ||||||
chr1:226284948
|
A | C | 1 | a0001c0001t0003g0192 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.524+1385T>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 6/14 | chr1 | 226284948 | ||||||
chr1:226284949
|
A | C | 1 | a0001c0001t0003g0192 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.524+1384T>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 6/14 | chr1 | 226284949 | ||||||
chr1:226285024
|
C | T | 1 | a0001c0001t0001g0279 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.524+1309G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 6/14 | chr1 | 226285024 | ||||||
chr1:226285150
|
C | T | 1 | a0001c0001t0001g0218 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.524+1183G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 6/14 | chr1 | 226285150 | ||||||
chr1:226285173
|
T | C | 2 | a0001c0001t0001g0304a0001c0001t0001g0316 | 2 | HG02486.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.524+1160A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 6/14 | chr1 | 226285173 | ||||||
chr1:226285425
|
A | G | 1 | a0001c0001t0001g0319 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.524+908T>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 6/14 | chr1 | 226285425 | ||||||
chr1:226285595
|
A | G | 124 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(121): Show | 124 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.524+738T>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 6/14 | chr1 | 226285595 | ||||||
chr1:226285949
|
T | G | 3 | a0001c0002t0004g0150a0001c0002t0004g0151a0001c0002t0004g0283 | 3 | HG01069.hp1 HG01071.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.524+384A>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 6/14 | chr1 | 226285949 | ||||||
chr1:226285986
|
T | G | 19 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0212others(16): Show | 19 | HG02040.hp1 HG03017.hp2 HG03688.hp2 others(16): Show |
intron_variant | MODIFIER | c.524+347A>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 6/14 | chr1 | 226285986 | ||||||
chr1:226286646
|
G | A | 1 | a0001c0001t0003g0086 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.399-188C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 5/14 | chr1 | 226286646 | ||||||
chr1:226286727
|
C | T | 1 | a0001c0001t0001g0350 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.399-269G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 5/14 | chr1 | 226286727 | ||||||
chr1:226286778
|
A | G | 223 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(220): Show | 223 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.399-320T>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 5/14 | chr1 | 226286778 | ||||||
chr1:226287008
|
T | C | 2 | a0001c0001t0001g0268a0001c0001t0001g0269 | 2 | HG00735.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.399-550A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 5/14 | chr1 | 226287008 | ||||||
chr1:226287405
|
T | C | 2 | a0001c0002t0002g0147a0001c0002t0002g0189 | 2 | HG06807.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.398+259A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 5/14 | chr1 | 226287405 | ||||||
chr1:226287879
|
G | T | 28 | a0001c0001t0001g0005a0001c0001t0001g0127a0001c0001t0001g0128others(25): Show | 28 | HG02055.hp2 HG02145.hp2 HG02486.hp1 others(25): Show |
intron_variant | MODIFIER | c.265-82C>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226287879 | ||||||
chr1:226287981
|
C | CT | 27 | a0001c0001t0001g0005a0001c0001t0001g0080a0001c0001t0001g0127others(24): Show | 27 | HG01109.hp1 HG01256.hp2 HG02055.hp2 others(24): Show |
intron_variant | MODIFIER | c.265-185dupA | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226287981 | ||||||
chr1:226288062
|
C | T | 1 | a0001c0001t0001g0025 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.265-265G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226288062 | ||||||
chr1:226288131
|
C | A | 1 | a0001c0004t0002g0134 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.265-334G>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226288131 | ||||||
chr1:226288298
|
A | G | 2 | a0001c0002t0002g0137a0001c0002t0002g0138 | 2 | HG00738.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.265-501T>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226288298 | ||||||
chr1:226288628
|
A | G | 6 | a0001c0001t0001g0298a0001c0001t0001g0299a0001c0001t0001g0300others(3): Show | 6 | HG02055.hp2 HG02809.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.265-831T>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226288628 | ||||||
chr1:226288746
|
A | ATGT | 319 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(316): Show | 319 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(316): Show |
intron_variant | MODIFIER | c.265-950_265-949ins others(3): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226288746 | ||||||
chr1:226288752
|
T | C | 100 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0224others(97): Show | 100 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(97): Show |
intron_variant | MODIFIER | c.265-955A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226288752 | ||||||
chr1:226288821
|
T | C | 19 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0212others(16): Show | 19 | HG02040.hp1 HG03017.hp2 HG03688.hp2 others(16): Show |
intron_variant | MODIFIER | c.265-1024A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226288821 | ||||||
chr1:226288964
|
C | T | 116 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(113): Show | 116 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.265-1167G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226288964 | ||||||
chr1:226289112
|
G | A | 1 | a0001c0001t0003g0060 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.265-1315C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226289112 | ||||||
chr1:226289234
|
CA | C | 100 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0224others(97): Show | 100 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(97): Show |
intron_variant | MODIFIER | c.265-1438delT | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226289234 | ||||||
chr1:226289330
|
A | C | 7 | a0001c0001t0001g0226a0001c0001t0001g0231a0001c0001t0001g0232others(4): Show | 7 | HG00738.hp2 HG01109.hp2 HG01243.hp2 others(4): Show |
intron_variant | MODIFIER | c.265-1533T>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226289330 | ||||||
chr1:226289334
|
T | TTG | 7 | a0001c0001t0001g0111a0001c0001t0001g0127a0001c0001t0001g0128others(4): Show | 7 | HG01167.hp2 HG01192.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.265-1539_265-1538d others(4): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226289334 | ||||||
chr1:226289551
|
C | T | 1 | a0001c0002t0002g0002 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.265-1754G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226289551 | ||||||
chr1:226289606
|
C | T | 3 | a0001c0001t0001g0228a0001c0001t0001g0230a0001c0001t0001g0271 | 3 | HG02004.hp2 HG02698.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.265-1809G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226289606 | ||||||
chr1:226289834
|
C | CG | 20 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0094others(17): Show | 20 | HG00438.hp1 HG00741.hp2 HG01346.hp2 others(17): Show |
intron_variant | MODIFIER | c.265-2038dupC | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226289834 | ||||||
chr1:226289834
|
C | CGG | 30 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(27): Show | 30 | HG00408.hp1 HG01081.hp2 HG01109.hp1 others(27): Show |
intron_variant | MODIFIER | c.265-2039_265-2038d others(4): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226289834 | ||||||
chr1:226289834
|
C | CGGA | 41 | a0001c0001t0001g0230a0001c0001t0001g0231a0001c0001t0001g0232others(38): Show | 41 | HG00621.hp1 HG00738.hp2 HG01069.hp1 others(38): Show |
intron_variant | MODIFIER | c.265-2038_265-2037i others(5): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226289834 | ||||||
chr1:226289834
|
C | CGGG | 23 | a0001c0001t0001g0021a0001c0001t0001g0036a0001c0001t0001g0080others(20): Show | 23 | HG00280.hp1 HG01071.hp2 HG01255.hp2 others(20): Show |
intron_variant | MODIFIER | c.265-2040_265-2038d others(5): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226289834 | ||||||
chr1:226289834
|
C | CGGGG | 34 | a0001c0001t0001g0009a0001c0001t0001g0019a0001c0001t0001g0020others(31): Show | 34 | HG00280.hp2 HG00621.hp2 HG00735.hp1 others(31): Show |
intron_variant | MODIFIER | c.265-2041_265-2038d others(6): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226289834 | ||||||
chr1:226289834
|
CGGGGGGG others(6): Show |
C | 3 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0067 | 3 | HG03017.hp1 HG03834.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.265-2050_265-2038d others(15): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226289834 | ||||||
chr1:226289835
|
G | GGA | 21 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0241others(18): Show | 21 | HG00438.hp2 HG00544.hp2 HG00597.hp1 others(18): Show |
intron_variant | MODIFIER | c.265-2039_265-2038i others(4): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226289835 | ||||||
chr1:226289836
|
G | GA | 5 | a0001c0001t0001g0333a0001c0001t0001g0343a0001c0001t0001g0344others(2): Show | 5 | HG00609.hp2 NA18949.hp1 NA18986.hp1 others(2): Show |
intron_variant | MODIFIER | c.265-2040_265-2039i others(3): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226289836 | ||||||
chr1:226289840
|
G | A | 1 | a0001c0001t0001g0225 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.265-2043C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226289840 | ||||||
chr1:226289840
|
G | C | 3 | a0001c0001t0001g0245a0001c0001t0001g0246a0001c0001t0001g0280 | 3 | HG00438.hp2 HG00597.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.265-2043C>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226289840 | ||||||
chr1:226289841
|
G | C | 1 | a0001c0001t0001g0014 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.265-2044C>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226289841 | ||||||
chr1:226289841
|
G | T | 2 | a0001c0001t0001g0016a0001c0001t0001g0018 | 2 | NA18989.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.265-2044C>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226289841 | ||||||
chr1:226289843
|
G | GGGGGT | 22 | a0001c0001t0001g0047a0001c0001t0001g0324a0001c0001t0001g0334others(19): Show | 22 | HG00423.hp1 HG00609.hp1 HG00673.hp1 others(19): Show |
intron_variant | MODIFIER | c.265-2047_265-2046i others(7): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226289843 | ||||||
chr1:226289843
|
G | T | 1 | a0001c0001t0001g0017 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.265-2046C>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226289843 | ||||||
chr1:226289844
|
G | GGGGGGGG others(6): Show |
1 | a0001c0001t0001g0210 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.265-2048_265-2047i others(15): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226289844 | ||||||
chr1:226289844
|
G | GGGGGGGG others(4): Show |
3 | a0001c0001t0001g0211a0001c0001t0001g0219a0001c0001t0001g0223 | 3 | NA18966.hp2 NA18990.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.265-2048_265-2047i others(13): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226289844 | ||||||
chr1:226289844
|
G | GGGGGGGG others(3): Show |
2 | a0001c0001t0001g0212a0001c0001t0001g0221 | 2 | HG02040.hp1 NA18949.hp2 |
intron_variant | MODIFIER | c.265-2048_265-2047i others(12): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226289844 | ||||||
chr1:226289844
|
G | GGGGGGGG others(3): Show |
2 | a0001c0001t0001g0356a0001c0001t0001g0358 | 2 | HG03688.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.265-2048_265-2047i others(12): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226289844 | ||||||
chr1:226289845
|
G | GGGGGGGG others(3): Show |
1 | a0001c0001t0001g0214 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.265-2049_265-2048i others(12): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226289845 | ||||||
chr1:226289845
|
G | GGGGGGGG others(3): Show |
1 | a0001c0001t0001g0357 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.265-2049_265-2048i others(12): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226289845 | ||||||
chr1:226289845
|
GT | G | 6 | a0001c0001t0001g0015a0001c0001t0001g0018a0001c0001t0001g0032others(3): Show | 6 | HG01074.hp2 HG01433.hp1 NA18989.hp2 others(3): Show |
intron_variant | MODIFIER | c.265-2049delA | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226289845 | ||||||
chr1:226289846
|
T | G | 183 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0011others(180): Show | 183 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.265-2049A>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226289846 | ||||||
chr1:226289847
|
G | GT | 3 | a0001c0001t0001g0313a0001c0001t0001g0314a0001c0002t0002g0287 | 3 | HG02257.hp1 HG02630.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.265-2051_265-2050i others(3): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226289847 | ||||||
chr1:226289847
|
G | T | 10 | a0001c0001t0001g0337a0001c0001t0001g0340a0001c0001t0001g0341others(7): Show | 10 | NA18946.hp2 NA18949.hp1 NA18973.hp1 others(7): Show |
intron_variant | MODIFIER | c.265-2050C>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226289847 | ||||||
chr1:226289856
|
T | G | 1 | a0001c0001t0003g0103 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.265-2059A>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226289856 | ||||||
chr1:226289867
|
G | A | 4 | a0001c0001t0003g0061a0001c0001t0003g0062a0001c0001t0003g0063others(1): Show | 4 | NA18962.hp1 NA19064.hp2 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.265-2070C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226289867 | ||||||
chr1:226289921
|
G | A | 305 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(302): Show | 305 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(302): Show |
intron_variant | MODIFIER | c.265-2124C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226289921 | ||||||
chr1:226290136
|
C | T | 4 | a0001c0001t0001g0258a0001c0001t0001g0259a0001c0001t0001g0260others(1): Show | 4 | HG02109.hp2 HG02451.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.265-2339G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226290136 | ||||||
chr1:226290333
|
C | CT | 25 | a0001c0001t0001g0005a0001c0001t0001g0015a0001c0001t0001g0096others(22): Show | 25 | HG02027.hp2 HG02055.hp2 HG02071.hp1 others(22): Show |
intron_variant | MODIFIER | c.265-2537dupA | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226290333 | ||||||
chr1:226290333
|
CT | C | 99 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0218others(96): Show | 99 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(96): Show |
intron_variant | MODIFIER | c.265-2537delA | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226290333 | ||||||
chr1:226290372
|
G | A | 1 | a0001c0001t0001g0274 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.265-2575C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226290372 | ||||||
chr1:226290402
|
A | G | 1 | a0001c0002t0002g0194 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.265-2605T>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226290402 | ||||||
chr1:226290452
|
T | C | 19 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0212others(16): Show | 19 | HG02040.hp1 HG03017.hp2 HG03688.hp2 others(16): Show |
intron_variant | MODIFIER | c.265-2655A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226290452 | ||||||
chr1:226290498
|
G | A | 1 | a0001c0001t0001g0089 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.265-2701C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226290498 | ||||||
chr1:226290650
|
C | T | 1 | a0001c0001t0001g0100 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.265-2853G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226290650 | ||||||
chr1:226290655
|
T | C | 1 | a0001c0001t0001g0335 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.265-2858A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226290655 | ||||||
chr1:226290680
|
G | C | 359 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(356): Show | 360 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(357): Show |
intron_variant | MODIFIER | c.265-2883C>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226290680 | ||||||
chr1:226290702
|
G | C | 2 | a0001c0001t0001g0071a0001c0001t0001g0072 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.265-2905C>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226290702 | ||||||
chr1:226290783
|
G | A | 1 | a0001c0001t0001g0214 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.265-2986C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226290783 | ||||||
chr1:226290920
|
C | T | 3 | a0001c0001t0001g0044a0001c0001t0001g0068a0001c0001t0001g0101 | 3 | HG02895.hp1 HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.265-3123G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226290920 | ||||||
chr1:226291025
|
G | C | 98 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0224others(95): Show | 98 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(95): Show |
intron_variant | MODIFIER | c.265-3228C>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226291025 | ||||||
chr1:226291133
|
C | A | 1 | a0001c0001t0001g0005 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.265-3336G>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226291133 | ||||||
chr1:226291231
|
G | C | 100 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0088others(97): Show | 100 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(97): Show |
intron_variant | MODIFIER | c.265-3434C>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226291231 | ||||||
chr1:226291324
|
C | T | 1 | a0001c0001t0001g0005 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.265-3527G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226291324 | ||||||
chr1:226291461
|
A | T | 1 | a0001c0001t0001g0036 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.265-3664T>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226291461 | ||||||
chr1:226291544
|
CTA | C | 5 | a0001c0001t0001g0298a0001c0001t0001g0299a0001c0001t0001g0300others(2): Show | 5 | HG02055.hp2 HG02809.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.265-3749_265-3748d others(4): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226291544 | ||||||
chr1:226291878
|
T | C | 2 | a0001c0001t0001g0268a0001c0001t0001g0269 | 2 | HG00735.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.264+3964A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226291878 | ||||||
chr1:226291879
|
G | C | 1 | a0001c0001t0001g0274 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.264+3963C>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226291879 | ||||||
chr1:226291964
|
A | C | 1 | a0001c0001t0001g0014 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.264+3878T>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226291964 | ||||||
chr1:226292250
|
T | G | 1 | a0001c0002t0002g0205 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.264+3592A>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226292250 | ||||||
chr1:226292387
|
T | C | 1 | a0001c0001t0001g0120 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.264+3455A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226292387 | ||||||
chr1:226292455
|
G | C | 1 | a0001c0001t0001g0336 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.264+3387C>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226292455 | ||||||
chr1:226292625
|
T | A | 1 | a0001c0001t0001g0247 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.264+3217A>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226292625 | ||||||
chr1:226292626
|
A | T | 3 | a0001c0002t0004g0150a0001c0002t0004g0151a0001c0002t0004g0283 | 3 | HG01069.hp1 HG01071.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.264+3216T>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226292626 | ||||||
chr1:226292633
|
AT | A | 19 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0212others(16): Show | 19 | HG02040.hp1 HG03017.hp2 HG03688.hp2 others(16): Show |
intron_variant | MODIFIER | c.264+3208delA | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226292633 | ||||||
chr1:226292634
|
T | A | 1 | a0001c0001t0001g0302 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.264+3208A>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226292634 | ||||||
chr1:226293261
|
T | C | 2 | a0001c0001t0003g0033a0001c0001t0003g0034 | 2 | NA19012.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.264+2581A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226293261 | ||||||
chr1:226293345
|
A | C | 19 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0212others(16): Show | 19 | HG02040.hp1 HG03017.hp2 HG03688.hp2 others(16): Show |
intron_variant | MODIFIER | c.264+2497T>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226293345 | ||||||
chr1:226293395
|
G | A | 1 | a0001c0001t0003g0106 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.264+2447C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226293395 | ||||||
chr1:226293773
|
G | A | 12 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0305others(9): Show | 12 | HG02559.hp1 HG02572.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.264+2069C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226293773 | ||||||
chr1:226293983
|
G | A | 5 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(2): Show | 5 | HG03017.hp1 HG03834.hp2 HG03942.hp2 others(2): Show |
intron_variant | MODIFIER | c.264+1859C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226293983 | ||||||
chr1:226294087
|
C | T | 1 | a0001c0002t0002g0296 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.264+1755G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226294087 | ||||||
chr1:226294277
|
CA | C | 254 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(251): Show | 254 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(251): Show |
intron_variant | MODIFIER | c.264+1564delT | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226294277 | ||||||
chr1:226294429
|
A | G | 14 | a0001c0001t0001g0005a0001c0001t0001g0298a0001c0001t0001g0299others(11): Show | 14 | HG02055.hp2 HG02145.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.264+1413T>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226294429 | ||||||
chr1:226294441
|
A | G | 264 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(261): Show | 264 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(261): Show |
intron_variant | MODIFIER | c.264+1401T>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226294441 | ||||||
chr1:226294464
|
C | T | 52 | a0001c0001t0003g0157a0001c0002t0002g0006a0001c0002t0002g0007others(49): Show | 52 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(49): Show |
intron_variant | MODIFIER | c.264+1378G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226294464 | ||||||
chr1:226294536
|
C | T | 2 | a0001c0001t0001g0127a0001c0001t0001g0128 | 2 | HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.264+1306G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226294536 | ||||||
chr1:226294576
|
A | C | 2 | a0001c0001t0001g0268a0001c0001t0001g0269 | 2 | HG00735.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.264+1266T>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226294576 | ||||||
chr1:226294580
|
A | C | 223 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(220): Show | 223 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(220): Show |
intron_variant | MODIFIER | c.264+1262T>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226294580 | ||||||
chr1:226294582
|
A | C | 14 | a0001c0002t0002g0284a0001c0002t0002g0285a0001c0002t0002g0286others(11): Show | 14 | HG01109.hp1 HG01167.hp2 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.264+1260T>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226294582 | ||||||
chr1:226294588
|
A | C | 236 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(233): Show | 237 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(234): Show |
intron_variant | MODIFIER | c.264+1254T>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226294588 | ||||||
chr1:226294589
|
A | C | 1 | a0001c0001t0001g0080 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.264+1253T>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226294589 | ||||||
chr1:226294721
|
A | C | 5 | a0001c0001t0001g0318a0001c0001t0001g0319a0001c0001t0001g0320others(2): Show | 5 | HG02145.hp2 HG02486.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.264+1121T>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226294721 | ||||||
chr1:226294817
|
T | G | 98 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(95): Show | 98 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.264+1025A>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226294817 | ||||||
chr1:226294869
|
G | A | 21 | a0001c0002t0001g0361a0001c0002t0002g0001a0001c0002t0002g0136others(18): Show | 22 | HG00544.hp1 HG00738.hp1 HG01123.hp1 others(19): Show |
intron_variant | MODIFIER | c.264+973C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226294869 | ||||||
chr1:226295221
|
G | A | 19 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0071others(16): Show | 19 | HG01099.hp1 HG01106.hp1 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.264+621C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226295221 | ||||||
chr1:226295236
|
G | C | 14 | a0001c0001t0001g0224a0001c0001t0001g0250a0001c0001t0001g0251others(11): Show | 14 | HG00735.hp1 HG02056.hp2 HG02132.hp2 others(11): Show |
intron_variant | MODIFIER | c.264+606C>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226295236 | ||||||
chr1:226295282
|
T | C | 14 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0212others(11): Show | 14 | HG02040.hp1 NA18941.hp2 NA18949.hp2 others(11): Show |
intron_variant | MODIFIER | c.264+560A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226295282 | ||||||
chr1:226295418
|
C | T | 4 | a0001c0001t0001g0356a0001c0001t0001g0357a0001c0001t0001g0358others(1): Show | 4 | HG03017.hp2 HG03688.hp2 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.264+424G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226295418 | ||||||
chr1:226295453
|
T | A | 2 | a0001c0001t0001g0129a0001c0001t0001g0130 | 2 | NA19240.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.264+389A>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226295453 | ||||||
chr1:226295484
|
A | T | 216 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(213): Show | 217 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.264+358T>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226295484 | ||||||
chr1:226295689
|
A | T | 2 | a0001c0001t0001g0327a0001c0001t0001g0338 | 2 | NA18612.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.264+153T>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 4/14 | chr1 | 226295689 | ||||||
chr1:226296112
|
A | G | 1 | a0001c0001t0001g0326 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.160-166T>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 3/14 | chr1 | 226296112 | ||||||
chr1:226296151
|
T | C | 2 | a0001c0001t0001g0127a0001c0001t0001g0128 | 2 | HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.160-205A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 3/14 | chr1 | 226296151 | ||||||
chr1:226296225
|
G | A | 1 | a0002c0003t0002g0148 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.160-279C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 3/14 | chr1 | 226296225 | ||||||
chr1:226296421
|
C | T | 1 | a0001c0002t0002g0162 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.160-475G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 3/14 | chr1 | 226296421 | ||||||
chr1:226296573
|
T | A | 1 | a0001c0002t0002g0183 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.160-627A>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 3/14 | chr1 | 226296573 | ||||||
chr1:226296605
|
G | A | 1 | a0001c0001t0001g0115 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.160-659C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 3/14 | chr1 | 226296605 | ||||||
chr1:226296867
|
A | T | 19 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0212others(16): Show | 19 | HG02040.hp1 HG03017.hp2 HG03688.hp2 others(16): Show |
intron_variant | MODIFIER | c.159+852T>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 3/14 | chr1 | 226296867 | ||||||
chr1:226297240
|
T | C | 12 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0305others(9): Show | 12 | HG02559.hp1 HG02572.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.159+479A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 3/14 | chr1 | 226297240 | ||||||
chr1:226297490
|
C | G | 1 | a0001c0001t0001g0043 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.159+229G>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 3/14 | chr1 | 226297490 | ||||||
chr1:226297571
|
T | C | 1 | a0001c0002t0002g0284 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.159+148A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 3/14 | chr1 | 226297571 | ||||||
chr1:226297626
|
A | AT | 225 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(222): Show | 225 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(222): Show |
intron_variant | MODIFIER | c.159+92dupA | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 3/14 | chr1 | 226297626 | ||||||
chr1:226298255
|
C | A | 1 | a0001c0002t0002g0184 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.65-442G>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 2/14 | chr1 | 226298255 | ||||||
chr1:226298364
|
C | T | 1 | a0001c0001t0001g0267 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.65-551G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 2/14 | chr1 | 226298364 | ||||||
chr1:226298511
|
T | C | 1 | a0001c0001t0001g0076 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.65-698A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 2/14 | chr1 | 226298511 | ||||||
chr1:226298631
|
T | C | 265 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(262): Show | 265 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(262): Show |
intron_variant | MODIFIER | c.65-818A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 2/14 | chr1 | 226298631 | ||||||
chr1:226298658
|
C | T | 19 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0212others(16): Show | 19 | HG02040.hp1 HG03017.hp2 HG03688.hp2 others(16): Show |
intron_variant | MODIFIER | c.65-845G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 2/14 | chr1 | 226298658 | ||||||
chr1:226298730
|
A | G | 265 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(262): Show | 265 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(262): Show |
intron_variant | MODIFIER | c.65-917T>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 2/14 | chr1 | 226298730 | ||||||
chr1:226298731
|
C | T | 8 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0212others(5): Show | 8 | HG02040.hp1 NA18949.hp2 NA18962.hp2 others(5): Show |
intron_variant | MODIFIER | c.65-918G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 2/14 | chr1 | 226298731 | ||||||
chr1:226298803
|
C | G | 3 | a0001c0002t0002g0286a0001c0002t0002g0294a0001c0002t0002g0295 | 3 | HG01891.hp2 HG03225.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.65-990G>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 2/14 | chr1 | 226298803 | ||||||
chr1:226298820
|
G | A | 1 | a0001c0001t0001g0255 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.65-1007C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 2/14 | chr1 | 226298820 | ||||||
chr1:226298843
|
G | A | 1 | a0001c0001t0003g0077 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.65-1030C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 2/14 | chr1 | 226298843 | ||||||
chr1:226298909
|
A | G | 1 | a0001c0001t0001g0358 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.65-1096T>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 2/14 | chr1 | 226298909 | ||||||
chr1:226299049
|
A | G | 1 | a0001c0001t0001g0005 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.65-1236T>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 2/14 | chr1 | 226299049 | ||||||
chr1:226299186
|
C | T | 96 | a0001c0002t0002g0001a0001c0002t0002g0002a0001c0002t0002g0004others(93): Show | 97 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.65-1373G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 2/14 | chr1 | 226299186 | ||||||
chr1:226299383
|
A | G | 1 | a0001c0001t0001g0125 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.65-1570T>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 2/14 | chr1 | 226299383 | ||||||
chr1:226299484
|
G | A | 1 | a0001c0002t0002g0185 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.65-1671C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 2/14 | chr1 | 226299484 | ||||||
chr1:226299504
|
CA | C | 210 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0080others(207): Show | 211 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(208): Show |
intron_variant | MODIFIER | c.64+1668delT | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 2/14 | chr1 | 226299504 | ||||||
chr1:226299745
|
C | A | 8 | a0001c0001t0001g0340a0001c0001t0001g0341a0001c0001t0001g0342others(5): Show | 8 | NA18946.hp2 NA18973.hp1 NA18983.hp2 others(5): Show |
intron_variant | MODIFIER | c.64+1428G>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 2/14 | chr1 | 226299745 | ||||||
chr1:226299843
|
T | C | 2 | a0001c0001t0003g0092a0001c0001t0003g0121 | 2 | HG01168.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.64+1330A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 2/14 | chr1 | 226299843 | ||||||
chr1:226299907
|
T | C | 1 | a0001c0001t0003g0113 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.64+1266A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 2/14 | chr1 | 226299907 | ||||||
chr1:226299926
|
C | CT | 18 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0212others(15): Show | 18 | HG02040.hp1 HG03017.hp2 HG03688.hp2 others(15): Show |
intron_variant | MODIFIER | c.64+1246dupA | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 2/14 | chr1 | 226299926 | ||||||
chr1:226299989
|
A | C | 1 | a0001c0001t0001g0089 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.64+1184T>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 2/14 | chr1 | 226299989 | ||||||
chr1:226300001
|
C | T | 1 | a0001c0001t0001g0094 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.64+1172G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 2/14 | chr1 | 226300001 | ||||||
chr1:226300181
|
G | A | 1 | a0001c0001t0001g0093 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.64+992C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 2/14 | chr1 | 226300181 | ||||||
chr1:226300594
|
G | A | 19 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0212others(16): Show | 19 | HG02040.hp1 HG03017.hp2 HG03688.hp2 others(16): Show |
intron_variant | MODIFIER | c.64+579C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 2/14 | chr1 | 226300594 | ||||||
chr1:226300831
|
G | A | 25 | a0001c0002t0002g0002a0001c0002t0002g0004a0001c0002t0002g0149others(22): Show | 25 | HG00408.hp1 HG01109.hp1 HG01167.hp2 others(22): Show |
intron_variant | MODIFIER | c.64+342C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 2/14 | chr1 | 226300831 | ||||||
chr1:226300855
|
A | AAAAC | 8 | a0001c0001t0001g0305a0001c0001t0001g0306a0001c0001t0001g0307others(5): Show | 8 | HG02559.hp1 HG02572.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.64+314_64+317dupGT others(2): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 2/14 | chr1 | 226300855 | ||||||
chr1:226300929
|
T | C | 1 | a0001c0001t0003g0118 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.64+244A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 2/14 | chr1 | 226300929 | ||||||
chr1:226301125
|
A | G | 99 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0088others(96): Show | 99 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(96): Show |
intron_variant | MODIFIER | c.64+48T>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 2/14 | chr1 | 226301125 | ||||||
chr1:226301223
|
A | G | 1 | a0001c0002t0002g0187 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.32-18T>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226301223 | ||||||
chr1:226301325
|
G | A | 1 | a0001c0002t0002g0186 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.32-120C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226301325 | ||||||
chr1:226301384
|
T | A | 10 | a0001c0001t0001g0337a0001c0001t0001g0340a0001c0001t0001g0341others(7): Show | 10 | NA18946.hp2 NA18949.hp1 NA18973.hp1 others(7): Show |
intron_variant | MODIFIER | c.32-179A>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226301384 | ||||||
chr1:226301684
|
C | T | 19 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0212others(16): Show | 19 | HG02040.hp1 HG03017.hp2 HG03688.hp2 others(16): Show |
intron_variant | MODIFIER | c.32-479G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226301684 | ||||||
chr1:226301754
|
A | G | 232 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(229): Show | 233 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(230): Show |
intron_variant | MODIFIER | c.32-549T>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226301754 | ||||||
chr1:226301940
|
G | A | 98 | a0001c0002t0001g0135a0001c0002t0001g0361a0001c0002t0002g0001others(95): Show | 99 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(96): Show |
intron_variant | MODIFIER | c.32-735C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226301940 | ||||||
chr1:226302052
|
G | C | 1 | a0001c0001t0001g0010 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.32-847C>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226302052 | ||||||
chr1:226302227
|
T | A | 19 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0212others(16): Show | 19 | HG02040.hp1 HG03017.hp2 HG03688.hp2 others(16): Show |
intron_variant | MODIFIER | c.32-1022A>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226302227 | ||||||
chr1:226302421
|
T | C | 221 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(218): Show | 221 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(218): Show |
intron_variant | MODIFIER | c.32-1216A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226302421 | ||||||
chr1:226302460
|
G | A | 1 | a0001c0002t0002g0209 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.32-1255C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226302460 | ||||||
chr1:226302547
|
C | CA | 73 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0091others(70): Show | 74 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.32-1343dupT | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226302547 | ||||||
chr1:226302704
|
A | G | 1 | a0001c0002t0002g0317 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.32-1499T>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226302704 | ||||||
chr1:226302978
|
ACT | A | 52 | a0001c0001t0001g0161a0001c0002t0002g0006a0001c0002t0002g0007others(49): Show | 52 | HG00280.hp1 HG00408.hp2 HG00597.hp2 others(49): Show |
intron_variant | MODIFIER | c.32-1775_32-1774del others(2): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226302978 | ||||||
chr1:226303307
|
T | C | 2 | a0001c0001t0001g0218a0001c0001t0001g0220 | 2 | NA18972.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.32-2102A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226303307 | ||||||
chr1:226303437
|
T | C | 11 | a0001c0001t0001g0005a0001c0001t0001g0127a0001c0001t0001g0128others(8): Show | 11 | HG02055.hp2 HG02486.hp2 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.32-2232A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226303437 | ||||||
chr1:226303529
|
G | A | 1 | a0001c0001t0001g0316 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.32-2324C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226303529 | ||||||
chr1:226303803
|
C | T | 5 | a0001c0001t0001g0318a0001c0001t0001g0319a0001c0001t0001g0320others(2): Show | 5 | HG02145.hp2 HG02486.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.32-2598G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226303803 | ||||||
chr1:226303933
|
A | G | 1 | a0001c0001t0003g0042 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.32-2728T>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226303933 | ||||||
chr1:226303955
|
G | A | 99 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0129others(96): Show | 99 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(96): Show |
intron_variant | MODIFIER | c.32-2750C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226303955 | ||||||
chr1:226304376
|
T | A | 1 | a0001c0001t0001g0120 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.32-3171A>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226304376 | ||||||
chr1:226304432
|
A | C | 94 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0088others(91): Show | 94 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(91): Show |
intron_variant | MODIFIER | c.32-3227T>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226304432 | ||||||
chr1:226304453
|
A | T | 268 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(265): Show | 269 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(266): Show |
intron_variant | MODIFIER | c.32-3248T>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226304453 | ||||||
chr1:226304554
|
G | A | 1 | a0001c0002t0002g0186 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.32-3349C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226304554 | ||||||
chr1:226304558
|
C | T | 1 | a0001c0001t0001g0093 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.32-3353G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226304558 | ||||||
chr1:226304560
|
G | C | 1 | a0001c0002t0002g0207 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.32-3355C>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226304560 | ||||||
chr1:226304579
|
T | C | 89 | a0001c0001t0001g0080a0001c0001t0001g0084a0001c0001t0001g0116others(86): Show | 89 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(86): Show |
intron_variant | MODIFIER | c.32-3374A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226304579 | ||||||
chr1:226304771
|
T | C | 5 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0001g0090others(2): Show | 5 | HG01081.hp2 HG01928.hp2 HG01934.hp2 others(2): Show |
intron_variant | MODIFIER | c.32-3566A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226304771 | ||||||
chr1:226305196
|
A | C | 1 | a0001c0001t0003g0013 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.31+3913T>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226305196 | ||||||
chr1:226305287
|
T | C | 2 | a0001c0001t0003g0092a0001c0001t0003g0121 | 2 | HG01168.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.31+3822A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226305287 | ||||||
chr1:226305290
|
G | A | 1 | a0001c0002t0002g0208 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.31+3819C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226305290 | ||||||
chr1:226305315
|
G | A | 1 | a0001c0001t0003g0121 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.31+3794C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226305315 | ||||||
chr1:226305315
|
G | GA | 93 | a0001c0001t0001g0010a0001c0001t0001g0093a0001c0001t0001g0094others(90): Show | 93 | HG00423.hp2 HG00438.hp1 HG00597.hp1 others(90): Show |
intron_variant | MODIFIER | c.31+3793dupT | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226305315 | ||||||
chr1:226305315
|
GA | G | 15 | a0001c0001t0001g0012a0001c0001t0001g0221a0001c0001t0001g0222others(12): Show | 15 | HG00408.hp2 HG01106.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.31+3793delT | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226305315 | ||||||
chr1:226305315
|
GAA | G | 15 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0212others(12): Show | 15 | HG02040.hp1 HG02055.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.31+3792_31+3793del others(2): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226305315 | ||||||
chr1:226305315
|
GAAA | G | 10 | a0001c0001t0001g0011a0001c0001t0001g0298a0001c0001t0001g0299others(7): Show | 10 | HG02809.hp1 HG03017.hp2 HG03139.hp1 others(7): Show |
intron_variant | MODIFIER | c.31+3791_31+3793del others(3): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226305315 | ||||||
chr1:226305315
|
GAAAAAAA others(8): Show |
G | 1 | a0001c0001t0001g0005 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.31+3779_31+3793del others(15): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226305315 | ||||||
chr1:226305315
|
GAAAAAAA others(10): Show |
G | 1 | a0001c0001t0001g0323 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.31+3777_31+3793del others(17): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226305315 | ||||||
chr1:226305330
|
A | C | 2 | a0001c0001t0001g0313a0001c0001t0001g0314 | 2 | HG02630.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.31+3779T>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226305330 | ||||||
chr1:226305333
|
A | C | 1 | a0001c0001t0001g0318 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.31+3776T>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226305333 | ||||||
chr1:226305334
|
A | C | 19 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0212others(16): Show | 19 | HG02040.hp1 HG03017.hp2 HG03688.hp2 others(16): Show |
intron_variant | MODIFIER | c.31+3775T>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226305334 | ||||||
chr1:226305372
|
G | A | 1 | a0001c0002t0002g0002 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.31+3737C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226305372 | ||||||
chr1:226305615
|
G | A | 3 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0124 | 3 | HG02109.hp1 HG02572.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.31+3494C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226305615 | ||||||
chr1:226305621
|
G | T | 1 | a0001c0001t0001g0224 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.31+3488C>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226305621 | ||||||
chr1:226305626
|
G | A | 1 | a0001c0001t0001g0125 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.31+3483C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226305626 | ||||||
chr1:226305669
|
G | C | 1 | a0001c0001t0001g0312 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.31+3440C>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226305669 | ||||||
chr1:226305688
|
G | A | 1 | a0001c0002t0002g0209 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.31+3421C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226305688 | ||||||
chr1:226305728
|
T | C | 100 | a0001c0001t0001g0161a0001c0001t0003g0157a0001c0001t0003g0192others(97): Show | 101 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(98): Show |
intron_variant | MODIFIER | c.31+3381A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226305728 | ||||||
chr1:226305967
|
T | C | 19 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0212others(16): Show | 19 | HG02040.hp1 HG03017.hp2 HG03688.hp2 others(16): Show |
intron_variant | MODIFIER | c.31+3142A>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226305967 | ||||||
chr1:226305984
|
G | A | 9 | a0001c0001t0001g0005a0001c0001t0001g0298a0001c0001t0001g0299others(6): Show | 9 | HG02055.hp2 HG02486.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.31+3125C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226305984 | ||||||
chr1:226306154
|
G | A | 97 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0224others(94): Show | 97 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(94): Show |
intron_variant | MODIFIER | c.31+2955C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226306154 | ||||||
chr1:226306302
|
T | G | 1 | a0001c0001t0001g0360 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.31+2807A>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226306302 | ||||||
chr1:226306323
|
C | CA | 7 | a0001c0001t0001g0126a0001c0001t0001g0282a0001c0001t0001g0318others(4): Show | 7 | HG01109.hp2 HG02145.hp2 HG02300.hp2 others(4): Show |
intron_variant | MODIFIER | c.31+2785dupT | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226306323 | ||||||
chr1:226306373
|
C | A | 1 | a0001c0002t0004g0283 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.31+2736G>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226306373 | ||||||
chr1:226306509
|
G | A | 14 | a0001c0002t0002g0284a0001c0002t0002g0285a0001c0002t0002g0286others(11): Show | 14 | HG01109.hp1 HG01167.hp2 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.31+2600C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226306509 | ||||||
chr1:226306814
|
C | T | 116 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(113): Show | 116 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.31+2295G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226306814 | ||||||
chr1:226307070
|
C | A | 9 | a0001c0001t0001g0005a0001c0001t0001g0298a0001c0001t0001g0299others(6): Show | 9 | HG02055.hp2 HG02486.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.31+2039G>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226307070 | ||||||
chr1:226307361
|
G | A | 2 | a0001c0001t0001g0313a0001c0001t0001g0314 | 2 | HG02630.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.31+1748C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226307361 | ||||||
chr1:226307463
|
A | G | 352 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(349): Show | 353 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(350): Show |
intron_variant | MODIFIER | c.31+1646T>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226307463 | ||||||
chr1:226307494
|
G | T | 2 | a0001c0001t0001g0009a0001c0001t0001g0010 | 2 | HG02922.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.31+1615C>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226307494 | ||||||
chr1:226307648
|
A | AAATC | 3 | a0001c0002t0002g0006a0001c0002t0002g0007a0001c0002t0002g0008 | 3 | NA18945.hp1 NA18975.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.31+1460_31+1461ins others(4): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226307648 | ||||||
chr1:226307758
|
G | A | 1 | a0001c0001t0001g0315 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.31+1351C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226307758 | ||||||
chr1:226307969
|
A | G | 1 | a0001c0001t0001g0005 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.31+1140T>C | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226307969 | ||||||
chr1:226308185
|
C | T | 3 | a0001c0002t0002g0002a0001c0002t0002g0004a0001c0002t0002g0317 | 3 | HG02602.hp1 HG03239.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.31+924G>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226308185 | ||||||
chr1:226308358
|
T | TACTGC | 362 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(359): Show | 363 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(360): Show |
intron_variant | MODIFIER | c.31+750_31+751insGC others(3): Show |
LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226308358 | ||||||
chr1:226308406
|
G | C | 1 | a0001c0001t0001g0316 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.31+703C>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226308406 | ||||||
chr1:226308551
|
G | C | 1 | a0001c0001t0001g0322 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.31+558C>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226308551 | ||||||
chr1:226308695
|
C | A | 2 | a0001c0002t0002g0002a0001c0002t0002g0317 | 2 | HG02602.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.31+414G>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226308695 | ||||||
chr1:226308863
|
G | A | 5 | a0001c0001t0001g0318a0001c0001t0001g0319a0001c0001t0001g0320others(2): Show | 5 | HG02145.hp2 HG02486.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.31+246C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226308863 | ||||||
chr1:226308968
|
G | A | 33 | a0001c0001t0001g0323a0001c0001t0001g0324a0001c0001t0001g0325others(30): Show | 33 | HG00423.hp2 HG00609.hp2 HG00621.hp1 others(30): Show |
intron_variant | MODIFIER | c.31+141C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226308968 | ||||||
chr1:226309050
|
G | C | 5 | a0001c0001t0001g0356a0001c0001t0001g0357a0001c0001t0001g0358others(2): Show | 5 | HG03017.hp2 HG03688.hp2 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.31+59C>G | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226309050 | ||||||
chr1:226309060
|
G | A | 1 | a0001c0002t0001g0361 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.31+49C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226309060 | ||||||
chr1:226309082
|
G | A | 2 | a0001c0001t0001g0362a0004c0006t0001g0363 | 2 | NA18963.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.31+27C>T | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226309082 | ||||||
chr1:226309083
|
G | T | 1 | a0001c0002t0002g0002 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.31+26C>A | LIN9 | ENSG00000183814.16 | transcript | ENST00000681046.1 | protein_coding | 1/14 | chr1 | 226309083 |