geneid | 23548 |
---|---|
ensemblid | ENSG00000113638.14 |
hgncid | 29959 |
symbol | TTC33 |
name | tetratricopeptide repeat domain 33 |
refseq_nuc | NM_012382.3 |
refseq_prot | NP_036514.1 |
ensembl_nuc | ENST00000337702.5 |
ensembl_prot | ENSP00000338533.4 |
mane_status | MANE Select |
chr | chr5 |
start | 40711576 |
end | 40755961 |
strand | - |
ver | v1.2 |
region | chr5:40711576-40755961 |
region5000 | chr5:40706576-40760961 |
regionname0 | TTC33_chr5_40711576_40755961 |
regionname5000 | TTC33_chr5_40706576_40760961 |
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 | 262 | 383 | 91 | 78 | 156 | 16 | 40 | 130 | TTC33_chr5_40706576_40760961 | TTC33 | copy fasta | chr5 | 40706576 | 40760961 |
a0002 | 0/0 | 262 | 10 | 0 | 0 | 10 | 0 | 0 | 4 | TTC33_chr5_40706576_40760961 | TTC33 | copy fasta | chr5 | 40706576 | 40760961 |
a0003 | 0/0 | 262 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | copy fasta | chr5 | 40706576 | 40760961 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 789 | 383 | 91 | 78 | 156 | 16 | 40 | TTC33_chr5_40706576_40760961 | TTC33 | copy fasta | chr5 | 40706576 | 40760961 |
c0002 | 0/0 | 789 | 10 | 0 | 0 | 10 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | copy fasta | chr5 | 40706576 | 40760961 |
c0003 | 0/0 | 789 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | copy fasta | chr5 | 40706576 | 40760961 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 4708 | 92 | 9 | 28 | 36 | 5 | 14 | TTC33_chr5_40706576_40760961 | TTC33 | copy fasta | chr5 | 40706576 | 40760961 |
t0002 | 0/0 | 4708 | 83 | 27 | 14 | 34 | 4 | 4 | TTC33_chr5_40706576_40760961 | TTC33 | copy fasta | chr5 | 40706576 | 40760961 |
t0003 | 0/1 | 4706 | 49 | 1 | 11 | 33 | 1 | 2 | TTC33_chr5_40706576_40760961 | TTC33 | copy fasta | chr5 | 40706576 | 40760961 |
t0004 | 0/0 | 4708 | 45 | 7 | 3 | 26 | 0 | 9 | TTC33_chr5_40706576_40760961 | TTC33 | copy fasta | chr5 | 40706576 | 40760961 |
t0005 | 0/0 | 4708 | 20 | 2 | 4 | 11 | 0 | 3 | TTC33_chr5_40706576_40760961 | TTC33 | copy fasta | chr5 | 40706576 | 40760961 |
t0006 | 0/0 | 4708 | 19 | 0 | 12 | 0 | 4 | 3 | TTC33_chr5_40706576_40760961 | TTC33 | copy fasta | chr5 | 40706576 | 40760961 |
t0007 | 1/0 | 4708 | 10 | 8 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | copy fasta | chr5 | 40706576 | 40760961 |
t0008 | 0/0 | 4708 | 10 | 0 | 0 | 10 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | copy fasta | chr5 | 40706576 | 40760961 |
t0009 | 0/0 | 4708 | 8 | 8 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | copy fasta | chr5 | 40706576 | 40760961 |
t0010 | 0/0 | 4708 | 6 | 6 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | copy fasta | chr5 | 40706576 | 40760961 |
t0011 | 0/0 | 4705 | 4 | 4 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | copy fasta | chr5 | 40706576 | 40760961 |
t0012 | 0/0 | 4708 | 4 | 3 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | copy fasta | chr5 | 40706576 | 40760961 |
t0013 | 0/0 | 4708 | 4 | 3 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | copy fasta | chr5 | 40706576 | 40760961 |
t0014 | 0/0 | 4708 | 4 | 3 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | copy fasta | chr5 | 40706576 | 40760961 |
t0015 | 0/0 | 4715 | 3 | 3 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | copy fasta | chr5 | 40706576 | 40760961 |
t0016 | 0/0 | 4706 | 3 | 0 | 0 | 3 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | copy fasta | chr5 | 40706576 | 40760961 |
t0017 | 0/0 | 4708 | 3 | 3 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | copy fasta | chr5 | 40706576 | 40760961 |
t0018 | 0/0 | 4706 | 3 | 0 | 0 | 3 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | copy fasta | chr5 | 40706576 | 40760961 |
t0019 | 0/0 | 4708 | 2 | 0 | 0 | 2 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | copy fasta | chr5 | 40706576 | 40760961 |
t0020 | 0/0 | 4706 | 2 | 0 | 0 | 2 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | copy fasta | chr5 | 40706576 | 40760961 |
t0021 | 0/0 | 4708 | 1 | 0 | 0 | 0 | 0 | 1 | TTC33_chr5_40706576_40760961 | TTC33 | copy fasta | chr5 | 40706576 | 40760961 |
t0022 | 0/0 | 4706 | 1 | 0 | 0 | 0 | 1 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | copy fasta | chr5 | 40706576 | 40760961 |
t0023 | 0/0 | 4708 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | copy fasta | chr5 | 40706576 | 40760961 |
t0024 | 0/0 | 4706 | 1 | 0 | 0 | 0 | 0 | 1 | TTC33_chr5_40706576_40760961 | TTC33 | copy fasta | chr5 | 40706576 | 40760961 |
t0025 | 0/0 | 4708 | 1 | 0 | 0 | 0 | 0 | 1 | TTC33_chr5_40706576_40760961 | TTC33 | copy fasta | chr5 | 40706576 | 40760961 |
t0026 | 0/0 | 4708 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | copy fasta | chr5 | 40706576 | 40760961 |
t0027 | 0/0 | 4708 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | copy fasta | chr5 | 40706576 | 40760961 |
t0028 | 0/0 | 4708 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | copy fasta | chr5 | 40706576 | 40760961 |
t0029 | 0/0 | 4708 | 1 | 0 | 0 | 0 | 0 | 1 | TTC33_chr5_40706576_40760961 | TTC33 | copy fasta | chr5 | 40706576 | 40760961 |
t0030 | 0/0 | 4708 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | copy fasta | chr5 | 40706576 | 40760961 |
t0031 | 0/0 | 4708 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | copy fasta | chr5 | 40706576 | 40760961 |
t0032 | 0/0 | 4708 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | copy fasta | chr5 | 40706576 | 40760961 |
t0033 | 0/0 | 4708 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | copy fasta | chr5 | 40706576 | 40760961 |
t0034 | 0/0 | 4706 | 1 | 0 | 0 | 0 | 0 | 1 | TTC33_chr5_40706576_40760961 | TTC33 | copy fasta | chr5 | 40706576 | 40760961 |
t0035 | 0/0 | 4706 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | copy fasta | chr5 | 40706576 | 40760961 |
t0036 | 0/0 | 4708 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | copy fasta | chr5 | 40706576 | 40760961 |
t0037 | 0/0 | 4708 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | copy fasta | chr5 | 40706576 | 40760961 |
t0038 | 0/0 | 4708 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | copy fasta | chr5 | 40706576 | 40760961 |
t0039 | 0/0 | 4708 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | copy fasta | chr5 | 40706576 | 40760961 |
t0040 | 0/0 | 4708 | 1 | 0 | 0 | 0 | 1 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | copy fasta | chr5 | 40706576 | 40760961 |
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 | 8 | 0 | 4 | 1 | 1 | 2 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0002 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0003 | 0/0 | 6 | 0 | 0 | 3 | 0 | 3 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0004 | 0/0 | 5 | 0 | 3 | 2 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0006 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0009 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0010 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0015 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0018 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0021 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0025 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0026 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0027 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0028 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0034 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0035 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0037 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0042 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0043 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0044 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0128 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0271 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0293 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0296 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0303 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 789 | 383 | 91 | 78 | 156 | 16 | 40 | TTC33_chr5_40706576_40760961 | TTC33 | copy fasta | chr5 | 40706576 | 40760961 |
a0002c0002 | 0/0 | 789 | 10 | 0 | 0 | 10 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | copy fasta | chr5 | 40706576 | 40760961 |
a0003c0003 | 0/0 | 789 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | copy fasta | chr5 | 40706576 | 40760961 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 5496 | 91 | 8 | 28 | 36 | 5 | 14 | TTC33_chr5_40706576_40760961 | TTC33 | copy fasta | chr5 | 40706576 | 40760961 |
a0001c0001t0002 | 0/0 | 5496 | 83 | 27 | 14 | 34 | 4 | 4 | TTC33_chr5_40706576_40760961 | TTC33 | copy fasta | chr5 | 40706576 | 40760961 |
a0001c0001t0003 | 0/1 | 5494 | 49 | 1 | 11 | 33 | 1 | 2 | TTC33_chr5_40706576_40760961 | TTC33 | copy fasta | chr5 | 40706576 | 40760961 |
a0001c0001t0004 | 0/0 | 5496 | 45 | 7 | 3 | 26 | 0 | 9 | TTC33_chr5_40706576_40760961 | TTC33 | copy fasta | chr5 | 40706576 | 40760961 |
a0001c0001t0005 | 0/0 | 5496 | 20 | 2 | 4 | 11 | 0 | 3 | TTC33_chr5_40706576_40760961 | TTC33 | copy fasta | chr5 | 40706576 | 40760961 |
a0001c0001t0006 | 0/0 | 5496 | 19 | 0 | 12 | 0 | 4 | 3 | TTC33_chr5_40706576_40760961 | TTC33 | copy fasta | chr5 | 40706576 | 40760961 |
a0001c0001t0007 | 1/0 | 5496 | 10 | 8 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | copy fasta | chr5 | 40706576 | 40760961 |
a0001c0001t0009 | 0/0 | 5496 | 8 | 8 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | copy fasta | chr5 | 40706576 | 40760961 |
a0001c0001t0010 | 0/0 | 5496 | 6 | 6 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | copy fasta | chr5 | 40706576 | 40760961 |
a0001c0001t0011 | 0/0 | 5493 | 4 | 4 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | copy fasta | chr5 | 40706576 | 40760961 |
a0001c0001t0012 | 0/0 | 5496 | 4 | 3 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | copy fasta | chr5 | 40706576 | 40760961 |
a0001c0001t0013 | 0/0 | 5496 | 4 | 3 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | copy fasta | chr5 | 40706576 | 40760961 |
a0001c0001t0014 | 0/0 | 5496 | 4 | 3 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | copy fasta | chr5 | 40706576 | 40760961 |
a0001c0001t0015 | 0/0 | 5503 | 3 | 3 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | copy fasta | chr5 | 40706576 | 40760961 |
a0001c0001t0016 | 0/0 | 5494 | 3 | 0 | 0 | 3 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | copy fasta | chr5 | 40706576 | 40760961 |
a0001c0001t0017 | 0/0 | 5496 | 3 | 3 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | copy fasta | chr5 | 40706576 | 40760961 |
a0001c0001t0018 | 0/0 | 5494 | 3 | 0 | 0 | 3 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | copy fasta | chr5 | 40706576 | 40760961 |
a0001c0001t0019 | 0/0 | 5496 | 2 | 0 | 0 | 2 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | copy fasta | chr5 | 40706576 | 40760961 |
a0001c0001t0020 | 0/0 | 5494 | 2 | 0 | 0 | 2 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | copy fasta | chr5 | 40706576 | 40760961 |
a0001c0001t0021 | 0/0 | 5496 | 1 | 0 | 0 | 0 | 0 | 1 | TTC33_chr5_40706576_40760961 | TTC33 | copy fasta | chr5 | 40706576 | 40760961 |
a0001c0001t0022 | 0/0 | 5494 | 1 | 0 | 0 | 0 | 1 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | copy fasta | chr5 | 40706576 | 40760961 |
a0001c0001t0023 | 0/0 | 5496 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | copy fasta | chr5 | 40706576 | 40760961 |
a0001c0001t0024 | 0/0 | 5494 | 1 | 0 | 0 | 0 | 0 | 1 | TTC33_chr5_40706576_40760961 | TTC33 | copy fasta | chr5 | 40706576 | 40760961 |
a0001c0001t0025 | 0/0 | 5496 | 1 | 0 | 0 | 0 | 0 | 1 | TTC33_chr5_40706576_40760961 | TTC33 | copy fasta | chr5 | 40706576 | 40760961 |
a0001c0001t0026 | 0/0 | 5496 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | copy fasta | chr5 | 40706576 | 40760961 |
a0001c0001t0027 | 0/0 | 5496 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | copy fasta | chr5 | 40706576 | 40760961 |
a0001c0001t0028 | 0/0 | 5496 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | copy fasta | chr5 | 40706576 | 40760961 |
a0001c0001t0029 | 0/0 | 5496 | 1 | 0 | 0 | 0 | 0 | 1 | TTC33_chr5_40706576_40760961 | TTC33 | copy fasta | chr5 | 40706576 | 40760961 |
a0001c0001t0030 | 0/0 | 5496 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | copy fasta | chr5 | 40706576 | 40760961 |
a0001c0001t0031 | 0/0 | 5496 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | copy fasta | chr5 | 40706576 | 40760961 |
a0001c0001t0032 | 0/0 | 5496 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | copy fasta | chr5 | 40706576 | 40760961 |
a0001c0001t0033 | 0/0 | 5496 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | copy fasta | chr5 | 40706576 | 40760961 |
a0001c0001t0034 | 0/0 | 5494 | 1 | 0 | 0 | 0 | 0 | 1 | TTC33_chr5_40706576_40760961 | TTC33 | copy fasta | chr5 | 40706576 | 40760961 |
a0001c0001t0035 | 0/0 | 5494 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | copy fasta | chr5 | 40706576 | 40760961 |
a0001c0001t0036 | 0/0 | 5496 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | copy fasta | chr5 | 40706576 | 40760961 |
a0001c0001t0037 | 0/0 | 5496 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | copy fasta | chr5 | 40706576 | 40760961 |
a0001c0001t0038 | 0/0 | 5496 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | copy fasta | chr5 | 40706576 | 40760961 |
a0001c0001t0039 | 0/0 | 5496 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | copy fasta | chr5 | 40706576 | 40760961 |
a0001c0001t0040 | 0/0 | 5496 | 1 | 0 | 0 | 0 | 1 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | copy fasta | chr5 | 40706576 | 40760961 |
a0002c0002t0008 | 0/0 | 5496 | 10 | 0 | 0 | 10 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | copy fasta | chr5 | 40706576 | 40760961 |
a0003c0003t0001 | 0/0 | 5496 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | copy fasta | chr5 | 40706576 | 40760961 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 8 | 0 | 4 | 1 | 1 | 2 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0001g0004 | 0/0 | 5 | 0 | 3 | 2 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0001g0006 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0001g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0001g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0001g0025 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0002g0002 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0002g0009 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0002g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0002g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0002g0018 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0002g0021 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0002g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0002g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0002g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0002g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0002g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0002g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0002g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0002g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0002g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0002g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0002g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0002g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0002g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0002g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0002g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0002g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0002g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0002g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0002g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0002g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0002g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0002g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0002g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0002g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0002g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0002g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0002g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0002g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0002g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0002g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0003g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0003g0010 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0003g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0003g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0003g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0003g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0003g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0003g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0003g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0003g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0003g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0003g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0003g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0003g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0003g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0003g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0003g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0003g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0003g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0003g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0003g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0003g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0003g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0003g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0003g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0003g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0003g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0003g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0003g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0003g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0003g0128 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0003g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0003g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0003g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0003g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0003g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0003g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0003g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0004g0003 | 0/0 | 6 | 0 | 0 | 3 | 0 | 3 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0004g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0004g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0004g0034 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0004g0035 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0004g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0004g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0004g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0004g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0004g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0004g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0004g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0004g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0004g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0004g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0004g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0004g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0004g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0004g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0004g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0004g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0004g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0004g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0004g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0004g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0004g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0004g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0004g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0004g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0004g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0004g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0004g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0004g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0005g0015 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0005g0037 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0005g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0005g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0005g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0005g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0005g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0005g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0005g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0005g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0005g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0005g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0005g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0005g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0005g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0006g0042 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0006g0043 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0006g0044 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0006g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0006g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0006g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0006g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0006g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0006g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0006g0296 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0006g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0006g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0006g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0006g0303 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0006g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0006g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0007g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0007g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0007g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0007g0271 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0007g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0007g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0007g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0007g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0007g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0009g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0009g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0009g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0009g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0009g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0009g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0009g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0010g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0010g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0010g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0010g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0010g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0010g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0011g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0011g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0012g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0012g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0012g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0012g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0013g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0013g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0013g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0013g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0014g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0014g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0014g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0015g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0015g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0015g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0016g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0016g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0017g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0017g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0017g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0018g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0018g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0018g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0019g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0020g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0021g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0022g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0023g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0024g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0025g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0026g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0027g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0028g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0029g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0030g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0031g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0032g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0033g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0034g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0035g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0036g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0037g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0038g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0039g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0001c0001t0040g0293 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0002c0002t0008g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0002c0002t0008g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0002c0002t0008g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0002c0002t0008g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0002c0002t0008g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0002c0002t0008g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0002c0002t0008g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0002c0002t0008g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
a0003c0003t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0027 | EUR | GBR | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG00099 | hp2 | a0001 | c0001 | t0003 | g0010 | EUR | GBR | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG00280 | hp1 | a0001 | c0001 | t0002 | g0146 | EUR | FIN | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0220 | EUR | FIN | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0190 | EUR | FIN | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG00408 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | CHS | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG00408 | hp2 | a0002 | c0002 | t0008 | g0197 | EAS | CHS | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG00423 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | CHS | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | CHS | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG00558 | hp2 | a0001 | c0001 | t0004 | g0007 | EAS | CHS | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG00597 | hp1 | a0002 | c0002 | t0008 | g0012 | EAS | CHS | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG00597 | hp2 | a0001 | c0001 | t0005 | g0276 | EAS | CHS | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0183 | AMR | PUR | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG00673 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | CHS | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG00733 | hp2 | a0001 | c0001 | t0006 | g0290 | AMR | PUR | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0242 | AMR | PUR | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG00735 | hp2 | a0001 | c0001 | t0005 | g0037 | AMR | PUR | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG00741 | hp1 | a0001 | c0001 | t0002 | g0147 | AMR | PUR | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG00741 | hp2 | a0001 | c0001 | t0006 | g0043 | AMR | PUR | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0228 | AMR | PUR | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG01069 | hp2 | a0001 | c0001 | t0003 | g0116 | AMR | PUR | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG01070 | hp1 | a0001 | c0001 | t0004 | g0265 | AMR | PUR | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG01071 | hp1 | a0001 | c0001 | t0004 | g0267 | AMR | PUR | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG01074 | hp1 | a0001 | c0001 | t0006 | g0300 | AMR | PUR | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG01074 | hp2 | a0001 | c0001 | t0003 | g0101 | AMR | PUR | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG01081 | hp1 | a0001 | c0001 | t0006 | g0305 | AMR | PUR | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG01081 | hp2 | a0001 | c0001 | t0027 | g0065 | AMR | PUR | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG01099 | hp1 | a0001 | c0001 | t0004 | g0268 | AMR | PUR | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0227 | AMR | PUR | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG01106 | hp1 | a0001 | c0001 | t0013 | g0050 | AMR | PUR | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG01106 | hp2 | a0001 | c0001 | t0006 | g0299 | AMR | PUR | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG01109 | hp1 | a0001 | c0001 | t0006 | g0288 | AMR | PUR | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG01109 | hp2 | a0001 | c0001 | t0002 | g0021 | AMR | PUR | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG01167 | hp1 | a0001 | c0001 | t0002 | g0164 | AMR | PUR | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | PUR | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0187 | AMR | PUR | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG01168 | hp2 | a0001 | c0001 | t0003 | g0171 | AMR | PUR | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG01169 | hp1 | a0001 | c0001 | t0003 | g0170 | AMR | PUR | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG01175 | hp1 | a0001 | c0001 | t0003 | g0163 | AMR | PUR | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0238 | AMR | PUR | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG01192 | hp1 | a0001 | c0001 | t0012 | g0182 | AMR | PUR | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG01192 | hp2 | a0001 | c0001 | t0038 | g0184 | AMR | PUR | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG01243 | hp1 | a0001 | c0001 | t0003 | g0121 | AMR | PUR | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | CLM | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG01255 | hp2 | a0001 | c0001 | t0003 | g0010 | AMR | CLM | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG01256 | hp1 | a0001 | c0001 | t0002 | g0140 | AMR | CLM | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG01256 | hp2 | a0001 | c0001 | t0006 | g0044 | AMR | CLM | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG01257 | hp2 | a0001 | c0001 | t0002 | g0059 | AMR | CLM | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG01258 | hp1 | a0001 | c0001 | t0006 | g0044 | AMR | CLM | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG01258 | hp2 | a0001 | c0001 | t0002 | g0055 | AMR | CLM | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0176 | AMR | CLM | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG01261 | hp2 | a0001 | c0001 | t0006 | g0304 | AMR | CLM | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG01346 | hp1 | a0001 | c0001 | t0002 | g0144 | AMR | CLM | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG01346 | hp2 | a0001 | c0001 | t0014 | g0152 | AMR | CLM | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0240 | AMR | CLM | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG01358 | hp2 | a0001 | c0001 | t0003 | g0113 | AMR | CLM | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG01361 | hp1 | a0001 | c0001 | t0003 | g0098 | AMR | CLM | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG01361 | hp2 | a0001 | c0001 | t0007 | g0269 | AMR | CLM | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG01433 | hp1 | a0001 | c0001 | t0005 | g0275 | AMR | CLM | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG01433 | hp2 | a0001 | c0001 | t0006 | g0291 | AMR | CLM | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG01496 | hp1 | a0001 | c0001 | t0002 | g0132 | AMR | CLM | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0232 | AMR | CLM | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG01515 | hp1 | a0001 | c0001 | t0040 | g0293 | EUR | IBS | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG01515 | hp2 | a0001 | c0001 | t0002 | g0077 | EUR | IBS | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG01516 | hp1 | a0001 | c0001 | t0006 | g0042 | EUR | IBS | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG01516 | hp2 | a0001 | c0001 | t0002 | g0153 | EUR | IBS | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG01517 | hp1 | a0001 | c0001 | t0006 | g0042 | EUR | IBS | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG01517 | hp2 | a0001 | c0001 | t0002 | g0018 | EUR | IBS | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG01884 | hp1 | a0001 | c0001 | t0002 | g0158 | AFR | ACB | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG01884 | hp2 | a0003 | c0003 | t0001 | g0188 | AFR | ACB | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG01891 | hp1 | a0001 | c0001 | t0007 | g0310 | AFR | ACB | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG01891 | hp2 | a0001 | c0001 | t0002 | g0145 | AFR | ACB | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG01928 | hp1 | a0001 | c0001 | t0005 | g0015 | AMR | PEL | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG01943 | hp2 | a0001 | c0001 | t0002 | g0066 | AMR | PEL | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG01952 | hp1 | a0001 | c0001 | t0006 | g0295 | AMR | PEL | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG01975 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0213 | AMR | PEL | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG01978 | hp1 | a0001 | c0001 | t0005 | g0015 | AMR | PEL | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0233 | AMR | PEL | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0215 | AMR | PEL | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG01981 | hp2 | a0001 | c0001 | t0002 | g0166 | AMR | PEL | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG02004 | hp1 | a0001 | c0001 | t0003 | g0107 | AMR | PEL | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG02015 | hp1 | a0002 | c0002 | t0008 | g0196 | EAS | KHV | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG02015 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG02027 | hp1 | a0001 | c0001 | t0003 | g0112 | EAS | KHV | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | KHV | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG02040 | hp1 | a0002 | c0002 | t0008 | g0201 | EAS | KHV | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG02040 | hp2 | a0001 | c0001 | t0002 | g0056 | EAS | KHV | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG02055 | hp1 | a0001 | c0001 | t0007 | g0248 | AFR | ACB | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG02055 | hp2 | a0001 | c0001 | t0014 | g0022 | AFR | ACB | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG02056 | hp1 | a0002 | c0002 | t0008 | g0012 | EAS | KHV | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG02056 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | KHV | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG02071 | hp1 | a0001 | c0001 | t0005 | g0246 | EAS | KHV | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG02071 | hp2 | a0001 | c0001 | t0030 | g0073 | EAS | KHV | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG02080 | hp1 | a0002 | c0002 | t0008 | g0198 | EAS | KHV | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG02080 | hp2 | a0001 | c0001 | t0002 | g0070 | EAS | KHV | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG02083 | hp1 | a0001 | c0001 | t0016 | g0019 | EAS | KHV | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG02083 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | KHV | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG02129 | hp1 | a0001 | c0001 | t0004 | g0261 | EAS | KHV | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG02129 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | KHV | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG02135 | hp1 | a0001 | c0001 | t0005 | g0277 | EAS | KHV | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG02135 | hp2 | a0001 | c0001 | t0003 | g0099 | EAS | KHV | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG02145 | hp1 | a0001 | c0001 | t0002 | g0138 | AFR | ACB | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG02145 | hp2 | a0001 | c0001 | t0004 | g0251 | AFR | ACB | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG02148 | hp1 | a0001 | c0001 | t0003 | g0108 | AMR | PEL | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG02155 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | CDX | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | CDX | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG02165 | hp1 | a0001 | c0001 | t0002 | g0060 | EAS | CDX | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG02165 | hp2 | a0001 | c0001 | t0004 | g0033 | EAS | CDX | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG02257 | hp1 | a0001 | c0001 | t0039 | g0167 | AFR | ACB | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG02257 | hp2 | a0001 | c0001 | t0010 | g0088 | AFR | ACB | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0211 | AFR | ACB | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG02258 | hp2 | a0001 | c0001 | t0002 | g0141 | AFR | ACB | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG02280 | hp1 | a0001 | c0001 | t0012 | g0194 | AFR | ACB | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG02280 | hp2 | a0001 | c0001 | t0015 | g0314 | AFR | ACB | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG02293 | hp2 | a0001 | c0001 | t0002 | g0084 | AMR | PEL | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0234 | AMR | PEL | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG02300 | hp2 | a0001 | c0001 | t0002 | g0067 | AMR | PEL | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG02451 | hp1 | a0001 | c0001 | t0007 | g0040 | AFR | ACB | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG02451 | hp2 | a0001 | c0001 | t0010 | g0087 | AFR | ACB | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG02572 | hp1 | a0001 | c0001 | t0013 | g0047 | AFR | GWD | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG02572 | hp2 | a0001 | c0001 | t0009 | g0297 | AFR | GWD | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG02602 | hp1 | a0001 | c0001 | t0002 | g0009 | SAS | PJL | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0027 | SAS | PJL | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG02615 | hp1 | a0001 | c0001 | t0005 | g0274 | AFR | GWD | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG02615 | hp2 | a0001 | c0001 | t0004 | g0249 | AFR | GWD | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG02630 | hp1 | a0001 | c0001 | t0010 | g0089 | AFR | GWD | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG02630 | hp2 | a0001 | c0001 | t0002 | g0024 | AFR | GWD | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG02647 | hp1 | a0001 | c0001 | t0010 | g0091 | AFR | GWD | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG02647 | hp2 | a0001 | c0001 | t0007 | g0301 | AFR | GWD | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0243 | SAS | PJL | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG02683 | hp2 | a0001 | c0001 | t0021 | g0225 | SAS | PJL | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG02717 | hp1 | a0001 | c0001 | t0002 | g0143 | AFR | GWD | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG02717 | hp2 | a0001 | c0001 | t0017 | g0193 | AFR | GWD | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0241 | SAS | PJL | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG02735 | hp2 | a0001 | c0001 | t0005 | g0247 | SAS | PJL | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG02738 | hp1 | a0001 | c0001 | t0002 | g0061 | SAS | PJL | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG02738 | hp2 | a0001 | c0001 | t0005 | g0278 | SAS | PJL | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG02809 | hp1 | a0001 | c0001 | t0002 | g0165 | AFR | GWD | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG02809 | hp2 | a0001 | c0001 | t0002 | g0139 | AFR | GWD | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG02818 | hp1 | a0001 | c0001 | t0010 | g0092 | AFR | GWD | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG02886 | hp1 | a0001 | c0001 | t0002 | g0162 | AFR | GWD | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG02886 | hp2 | a0001 | c0001 | t0002 | g0154 | AFR | GWD | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG02895 | hp1 | a0001 | c0001 | t0013 | g0048 | AFR | GWD | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG02895 | hp2 | a0001 | c0001 | t0002 | g0157 | AFR | GWD | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG02896 | hp2 | a0001 | c0001 | t0002 | g0149 | AFR | GWD | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG02897 | hp2 | a0001 | c0001 | t0002 | g0156 | AFR | GWD | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG02922 | hp1 | a0001 | c0001 | t0002 | g0159 | AFR | ESN | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG02922 | hp2 | a0001 | c0001 | t0017 | g0191 | AFR | ESN | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG02965 | hp1 | a0001 | c0001 | t0026 | g0282 | AFR | ESN | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG02965 | hp2 | a0001 | c0001 | t0012 | g0180 | AFR | ESN | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG02970 | hp1 | a0001 | c0001 | t0002 | g0142 | AFR | ESN | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | ESN | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG02976 | hp1 | a0001 | c0001 | t0011 | g0008 | AFR | ESN | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG02976 | hp2 | a0001 | c0001 | t0007 | g0309 | AFR | ESN | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG03017 | hp2 | a0001 | c0001 | t0004 | g0035 | SAS | PJL | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG03098 | hp1 | a0001 | c0001 | t0007 | g0040 | AFR | MSL | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG03098 | hp2 | a0001 | c0001 | t0009 | g0041 | AFR | MSL | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG03130 | hp1 | a0001 | c0001 | t0002 | g0023 | AFR | ESN | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG03130 | hp2 | a0001 | c0001 | t0002 | g0134 | AFR | ESN | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG03139 | hp1 | a0001 | c0001 | t0002 | g0021 | AFR | ESN | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG03139 | hp2 | a0001 | c0001 | t0011 | g0008 | AFR | ESN | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG03195 | hp1 | a0001 | c0001 | t0010 | g0090 | AFR | ESN | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG03195 | hp2 | a0001 | c0001 | t0002 | g0086 | AFR | ESN | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG03209 | hp1 | a0001 | c0001 | t0002 | g0024 | AFR | MSL | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG03209 | hp2 | a0001 | c0001 | t0009 | g0308 | AFR | MSL | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG03225 | hp1 | a0001 | c0001 | t0014 | g0022 | AFR | MSL | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG03225 | hp2 | a0001 | c0001 | t0015 | g0312 | AFR | MSL | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG03239 | hp1 | a0001 | c0001 | t0006 | g0294 | SAS | PJL | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG03453 | hp1 | a0001 | c0001 | t0004 | g0169 | AFR | MSL | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG03453 | hp2 | a0001 | c0001 | t0007 | g0311 | AFR | MSL | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG03486 | hp1 | a0001 | c0001 | t0002 | g0148 | AFR | MSL | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG03486 | hp2 | a0001 | c0001 | t0023 | g0174 | AFR | MSL | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG03490 | hp2 | a0001 | c0001 | t0004 | g0034 | SAS | PJL | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG03492 | hp1 | a0001 | c0001 | t0004 | g0034 | SAS | PJL | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG03516 | hp1 | a0001 | c0001 | t0009 | g0041 | AFR | ESN | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG03516 | hp2 | a0001 | c0001 | t0037 | g0052 | AFR | ESN | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG03540 | hp1 | a0001 | c0001 | t0011 | g0046 | AFR | GWD | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG03540 | hp2 | a0001 | c0001 | t0014 | g0151 | AFR | GWD | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0286 | AFR | MSL | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG03579 | hp2 | a0001 | c0001 | t0017 | g0192 | AFR | MSL | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG03654 | hp1 | a0001 | c0001 | t0004 | g0264 | SAS | PJL | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG03654 | hp2 | a0001 | c0001 | t0024 | g0123 | SAS | PJL | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG03669 | hp1 | a0001 | c0001 | t0004 | g0003 | SAS | PJL | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG03669 | hp2 | a0001 | c0001 | t0003 | g0155 | SAS | PJL | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG03688 | hp1 | a0001 | c0001 | t0002 | g0009 | SAS | STU | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0237 | SAS | STU | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0222 | SAS | PJL | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG03704 | hp2 | a0001 | c0001 | t0003 | g0010 | SAS | PJL | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG03710 | hp1 | a0001 | c0001 | t0006 | g0043 | SAS | PJL | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0186 | SAS | PJL | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG03831 | hp1 | a0001 | c0001 | t0025 | g0068 | SAS | BEB | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG03831 | hp2 | a0001 | c0001 | t0004 | g0003 | SAS | BEB | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0245 | SAS | BEB | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG03834 | hp2 | a0001 | c0001 | t0004 | g0035 | SAS | BEB | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG03942 | hp1 | a0001 | c0001 | t0004 | g0003 | SAS | BEB | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG03942 | hp2 | a0001 | c0001 | t0029 | g0051 | SAS | BEB | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0223 | SAS | BEB | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG04184 | hp2 | a0001 | c0001 | t0034 | g0120 | SAS | BEB | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG04199 | hp1 | a0001 | c0001 | t0006 | g0289 | SAS | STU | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG04199 | hp2 | a0001 | c0001 | t0004 | g0266 | SAS | STU | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG04204 | hp2 | a0001 | c0001 | t0005 | g0037 | SAS | STU | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA18522 | hp1 | a0001 | c0001 | t0004 | g0250 | AFR | YRI | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA18522 | hp2 | a0001 | c0001 | t0002 | g0023 | AFR | YRI | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA18906 | hp1 | a0001 | c0001 | t0011 | g0008 | AFR | YRI | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA18906 | hp2 | a0001 | c0001 | t0009 | g0307 | AFR | YRI | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA18939 | hp1 | a0001 | c0001 | t0003 | g0020 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA18939 | hp2 | a0001 | c0001 | t0004 | g0033 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA18941 | hp2 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA18942 | hp1 | a0001 | c0001 | t0003 | g0104 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA18942 | hp2 | a0001 | c0001 | t0033 | g0206 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA18943 | hp1 | a0001 | c0001 | t0004 | g0262 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA18943 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA18945 | hp2 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA18946 | hp1 | a0001 | c0001 | t0004 | g0253 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA18946 | hp2 | a0001 | c0001 | t0016 | g0103 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA18947 | hp2 | a0001 | c0001 | t0003 | g0115 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA18948 | hp1 | a0001 | c0001 | t0003 | g0125 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA18952 | hp1 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA18952 | hp2 | a0001 | c0001 | t0003 | g0097 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA18953 | hp1 | a0001 | c0001 | t0003 | g0094 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA18954 | hp1 | a0001 | c0001 | t0004 | g0036 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA18956 | hp1 | a0001 | c0001 | t0016 | g0019 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA18956 | hp2 | a0001 | c0001 | t0004 | g0255 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA18957 | hp1 | a0001 | c0001 | t0003 | g0020 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA18957 | hp2 | a0001 | c0001 | t0004 | g0270 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA18960 | hp1 | a0001 | c0001 | t0003 | g0079 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA18960 | hp2 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA18962 | hp1 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA18962 | hp2 | a0001 | c0001 | t0035 | g0110 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA18967 | hp2 | a0001 | c0001 | t0031 | g0315 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA18968 | hp1 | a0001 | c0001 | t0002 | g0316 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA18968 | hp2 | a0001 | c0001 | t0004 | g0036 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA18970 | hp1 | a0001 | c0001 | t0005 | g0038 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA18970 | hp2 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA18972 | hp2 | a0001 | c0001 | t0002 | g0317 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA18973 | hp2 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA18977 | hp1 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA18977 | hp2 | a0002 | c0002 | t0008 | g0200 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA18979 | hp1 | a0001 | c0001 | t0005 | g0038 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA18979 | hp2 | a0001 | c0001 | t0004 | g0257 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA18981 | hp2 | a0001 | c0001 | t0003 | g0127 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA18982 | hp1 | a0001 | c0001 | t0003 | g0111 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA18982 | hp2 | a0001 | c0001 | t0004 | g0263 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA18983 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA18984 | hp1 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA18985 | hp1 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA18986 | hp1 | a0001 | c0001 | t0004 | g0252 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA18986 | hp2 | a0001 | c0001 | t0003 | g0109 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA18987 | hp2 | a0001 | c0001 | t0004 | g0285 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA18988 | hp1 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA18988 | hp2 | a0001 | c0001 | t0018 | g0105 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA18989 | hp2 | a0001 | c0001 | t0005 | g0039 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA18991 | hp1 | a0001 | c0001 | t0003 | g0175 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA18991 | hp2 | a0001 | c0001 | t0004 | g0007 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA18992 | hp1 | a0001 | c0001 | t0004 | g0007 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA18992 | hp2 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA18994 | hp1 | a0001 | c0001 | t0020 | g0045 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA18994 | hp2 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA18995 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA18995 | hp2 | a0001 | c0001 | t0020 | g0045 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA18998 | hp1 | a0001 | c0001 | t0005 | g0281 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA19002 | hp1 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA19002 | hp2 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA19003 | hp1 | a0001 | c0001 | t0003 | g0124 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA19003 | hp2 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA19004 | hp1 | a0001 | c0001 | t0005 | g0280 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA19004 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA19006 | hp1 | a0001 | c0001 | t0005 | g0015 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA19006 | hp2 | a0001 | c0001 | t0003 | g0129 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA19007 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA19009 | hp1 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA19009 | hp2 | a0001 | c0001 | t0003 | g0093 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA19011 | hp1 | a0001 | c0001 | t0005 | g0279 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA19011 | hp2 | a0001 | c0001 | t0032 | g0202 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA19012 | hp1 | a0001 | c0001 | t0019 | g0032 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA19012 | hp2 | a0001 | c0001 | t0003 | g0117 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA19030 | hp1 | a0001 | c0001 | t0004 | g0168 | AFR | LWK | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA19030 | hp2 | a0001 | c0001 | t0009 | g0302 | AFR | LWK | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA19043 | hp1 | a0001 | c0001 | t0013 | g0049 | AFR | LWK | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA19043 | hp2 | a0001 | c0001 | t0005 | g0272 | AFR | LWK | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA19055 | hp1 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA19056 | hp2 | a0001 | c0001 | t0004 | g0287 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA19057 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA19057 | hp2 | a0001 | c0001 | t0004 | g0007 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA19059 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA19059 | hp2 | a0001 | c0001 | t0018 | g0102 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA19060 | hp1 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA19062 | hp2 | a0001 | c0001 | t0004 | g0256 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA19063 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA19064 | hp1 | a0001 | c0001 | t0004 | g0259 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA19064 | hp2 | a0001 | c0001 | t0003 | g0122 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA19066 | hp1 | a0001 | c0001 | t0003 | g0100 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA19068 | hp1 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA19068 | hp2 | a0001 | c0001 | t0005 | g0039 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA19070 | hp2 | a0001 | c0001 | t0036 | g0258 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA19074 | hp1 | a0001 | c0001 | t0003 | g0118 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA19075 | hp1 | a0002 | c0002 | t0008 | g0199 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA19075 | hp2 | a0001 | c0001 | t0003 | g0131 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA19077 | hp1 | a0001 | c0001 | t0018 | g0106 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA19077 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA19078 | hp1 | a0002 | c0002 | t0008 | g0012 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA19078 | hp2 | a0001 | c0001 | t0004 | g0260 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA19079 | hp1 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA19079 | hp2 | a0001 | c0001 | t0003 | g0114 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA19080 | hp1 | a0001 | c0001 | t0003 | g0096 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA19080 | hp2 | a0002 | c0002 | t0008 | g0195 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA19086 | hp2 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA19088 | hp1 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA19088 | hp2 | a0001 | c0001 | t0019 | g0032 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA19089 | hp2 | a0001 | c0001 | t0004 | g0273 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA19090 | hp1 | a0001 | c0001 | t0004 | g0254 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA19090 | hp2 | a0001 | c0001 | t0003 | g0095 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA19091 | hp2 | a0001 | c0001 | t0003 | g0126 | EAS | JPT | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA19240 | hp1 | a0001 | c0001 | t0002 | g0137 | AFR | YRI | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA19240 | hp2 | a0001 | c0001 | t0009 | g0306 | AFR | YRI | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA20129 | hp1 | a0001 | c0001 | t0012 | g0181 | AFR | ASW | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA20129 | hp2 | a0001 | c0001 | t0003 | g0119 | AFR | ASW | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0185 | EUR | TSI | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA20752 | hp2 | a0001 | c0001 | t0006 | g0296 | EUR | TSI | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA20805 | hp1 | a0001 | c0001 | t0022 | g0130 | EUR | TSI | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA20805 | hp2 | a0001 | c0001 | t0006 | g0303 | EUR | TSI | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0212 | SAS | GIH | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA20905 | hp2 | a0001 | c0001 | t0002 | g0172 | SAS | GIH | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG01123 | hp1 | a0001 | c0001 | t0002 | g0150 | AMR | CLM | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG01123 | hp2 | a0001 | c0001 | t0006 | g0298 | AMR | CLM | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG02109 | hp1 | a0001 | c0001 | t0002 | g0133 | AFR | ACB | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG02109 | hp2 | a0001 | c0001 | t0002 | g0161 | AFR | ACB | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG02486 | hp1 | a0001 | c0001 | t0007 | g0318 | AFR | ACB | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG02486 | hp2 | a0001 | c0001 | t0004 | g0283 | AFR | ACB | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG03471 | hp1 | a0001 | c0001 | t0002 | g0135 | AFR | MSL | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG03471 | hp2 | a0001 | c0001 | t0004 | g0284 | AFR | MSL | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0224 | AFR | USA | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
HG06807 | hp2 | a0001 | c0001 | t0009 | g0292 | AFR | USA | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0226 | AFR | USA | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA20300 | hp2 | a0001 | c0001 | t0002 | g0136 | AFR | USA | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA21309 | hp1 | a0001 | c0001 | t0015 | g0313 | AFR | LWK | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
NA21309 | hp2 | a0001 | c0001 | t0028 | g0160 | AFR | LWK | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0003 | g0128 | REF | REF | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0007 | g0271 | REF | REF | TTC33_chr5_40706576_40760961 | TTC33 | chr5 | 40706576 | 40760961 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:40716264
|
T | A | 1 | a0003 | 1 | HG01884.hp2 | missense_variant | MODERATE | c.670A>T | p.Thr224Ser | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 5/5 | 809/5497 | 670/789 | 224/262 | chr5 | 40716264 | ||
chr5:40746814
|
A | T | 1 | a0002 | 10 | HG00408.hp2 HG00597.hp1 HG02015.hp1 others(7): Show |
missense_variant | MODERATE | c.205T>A | p.Leu69Met | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/5 | 344/5497 | 205/789 | 69/262 | chr5 | 40746814 |
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 |
---|
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:40711586
|
T | C | 1 | a0001c0001t0027 | 1 | HG01081.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4559A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 5/5 | 4559 | chr5 | 40711586 | |||||
chr5:40711671
|
G | A | 1 | a0001c0001t0028 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4474C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 5/5 | 4474 | chr5 | 40711671 | |||||
chr5:40711865
|
C | T | 1 | a0001c0001t0032 | 1 | NA19011.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4280G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 5/5 | 4280 | chr5 | 40711865 | |||||
chr5:40711893
|
T | C | 1 | a0001c0001t0024 | 1 | HG03654.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4252A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 5/5 | 4252 | chr5 | 40711893 | |||||
chr5:40712142
|
A | T | 2 | a0001c0001t0006a0001c0001t0040 | 20 | HG00733.hp2 HG00741.hp2 HG01074.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*4003T>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 5/5 | 4003 | chr5 | 40712142 | |||||
chr5:40712196
|
T | G | 1 | a0001c0001t0033 | 1 | NA18942.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3949A>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 5/5 | 3949 | chr5 | 40712196 | |||||
chr5:40712441
|
A | G | 2 | a0001c0001t0012a0001c0001t0023 | 5 | HG01192.hp1 HG02280.hp1 HG02965.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3704T>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 5/5 | 3704 | chr5 | 40712441 | |||||
chr5:40712455
|
A | T | 1 | a0001c0001t0017 | 3 | HG02717.hp2 HG02922.hp2 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3690T>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 5/5 | 3690 | chr5 | 40712455 | |||||
chr5:40712465
|
C | A | 1 | a0001c0001t0009 | 8 | HG02572.hp2 HG03098.hp2 HG03209.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3680G>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 5/5 | 3680 | chr5 | 40712465 | |||||
chr5:40712646
|
C | A | 1 | a0001c0001t0029 | 1 | HG03942.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3499G>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 5/5 | 3499 | chr5 | 40712646 | |||||
chr5:40712671
|
T | C | 1 | a0001c0001t0013 | 4 | HG01106.hp1 HG02572.hp1 HG02895.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3474A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 5/5 | 3474 | chr5 | 40712671 | |||||
chr5:40712695
|
A | C | 20 | a0001c0001t0002a0001c0001t0003a0001c0001t0010others(17): Show | 165 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(162): Show |
3_prime_UTR_variant | MODIFIER | c.*3450T>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 5/5 | 3450 | chr5 | 40712695 | |||||
chr5:40712821
|
C | T | 1 | a0001c0001t0026 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3324G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 5/5 | 3324 | chr5 | 40712821 | |||||
chr5:40712854
|
T | C | 1 | a0001c0001t0030 | 1 | HG02071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3291A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 5/5 | 3291 | chr5 | 40712854 | |||||
chr5:40712859
|
C | G | 1 | a0001c0001t0025 | 1 | HG03831.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3286G>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 5/5 | 3286 | chr5 | 40712859 | |||||
chr5:40713334
|
T | C | 1 | a0001c0001t0031 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2811A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 5/5 | 2811 | chr5 | 40713334 | |||||
chr5:40713543
|
T | C | 1 | a0001c0001t0005 | 20 | HG00597.hp2 HG00735.hp2 HG01433.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*2602A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 5/5 | 2602 | chr5 | 40713543 | |||||
chr5:40713553
|
T | C | 1 | a0001c0001t0016 | 3 | HG02083.hp1 NA18946.hp2 NA18956.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2592A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 5/5 | 2592 | chr5 | 40713553 | |||||
chr5:40713564
|
T | A | 6 | a0001c0001t0001a0001c0001t0021a0001c0001t0032others(3): Show | 96 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(93): Show |
3_prime_UTR_variant | MODIFIER | c.*2581A>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 5/5 | 2581 | chr5 | 40713564 | |||||
chr5:40713847
|
CTA | C | 8 | a0001c0001t0003a0001c0001t0016a0001c0001t0018others(5): Show | 61 | HG00099.hp2 HG00408.hp1 HG01069.hp2 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*2296_*2297delTA | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 5/5 | 2296 | chr5 | 40713847 | |||||
chr5:40713855
|
G | A | 1 | a0001c0001t0019 | 2 | NA19012.hp1 NA19088.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2290C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 5/5 | 2290 | chr5 | 40713855 | |||||
chr5:40713888
|
G | C | 1 | a0001c0001t0034 | 1 | HG04184.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2257C>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 5/5 | 2257 | chr5 | 40713888 | |||||
chr5:40713907
|
G | A | 1 | a0001c0001t0018 | 3 | NA18988.hp2 NA19059.hp2 NA19077.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2238C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 5/5 | 2238 | chr5 | 40713907 | |||||
chr5:40713983
|
C | T | 2 | a0001c0001t0012a0001c0001t0023 | 5 | HG01192.hp1 HG02280.hp1 HG02965.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2162G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 5/5 | 2162 | chr5 | 40713983 | |||||
chr5:40714063
|
C | T | 1 | a0001c0001t0022 | 1 | NA20805.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2082G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 5/5 | 2082 | chr5 | 40714063 | |||||
chr5:40714252
|
C | A | 1 | a0001c0001t0035 | 1 | NA18962.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1893G>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 5/5 | 1893 | chr5 | 40714252 | |||||
chr5:40714507
|
CA | C | 2 | a0001c0001t0011a0001c0001t0015 | 7 | HG02280.hp2 HG02976.hp1 HG03139.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1637delT | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 5/5 | 1637 | chr5 | 40714507 | |||||
chr5:40714579
|
C | T | 1 | a0002c0002t0008 | 10 | HG00408.hp2 HG00597.hp1 HG02015.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1566G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 5/5 | 1566 | chr5 | 40714579 | |||||
chr5:40714635
|
C | A | 2 | a0001c0001t0010a0001c0001t0037 | 7 | HG02257.hp2 HG02451.hp2 HG02630.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1510G>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 5/5 | 1510 | chr5 | 40714635 | |||||
chr5:40714679
|
T | C | 1 | a0001c0001t0036 | 1 | NA19070.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1466A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 5/5 | 1466 | chr5 | 40714679 | |||||
chr5:40714776
|
C | T | 1 | a0001c0001t0021 | 1 | HG02683.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1369G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 5/5 | 1369 | chr5 | 40714776 | |||||
chr5:40714885
|
T | A | 1 | a0001c0001t0037 | 1 | HG03516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1260A>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 5/5 | 1260 | chr5 | 40714885 | |||||
chr5:40714960
|
A | G | 1 | a0001c0001t0012 | 4 | HG01192.hp1 HG02280.hp1 HG02965.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1185T>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 5/5 | 1185 | chr5 | 40714960 | |||||
chr5:40715231
|
T | G | 1 | a0001c0001t0038 | 1 | HG01192.hp2 | 3_prime_UTR_variant | MODIFIER | c.*914A>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 5/5 | 914 | chr5 | 40715231 | |||||
chr5:40715327
|
T | C | 1 | a0001c0001t0039 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*818A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 5/5 | 818 | chr5 | 40715327 | |||||
chr5:40715362
|
A | ACCTATCT others(1): Show |
2 | a0001c0001t0011a0001c0001t0015 | 7 | HG02280.hp2 HG02976.hp1 HG03139.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*775_*782dupCAGATA others(2): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 5/5 | 782 | chr5 | 40715362 | |||||
chr5:40715591
|
T | C | 1 | a0001c0001t0014 | 4 | HG01346.hp2 HG02055.hp2 HG03225.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*554A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 5/5 | 554 | chr5 | 40715591 | |||||
chr5:40716051
|
C | A | 37 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(34): Show | 356 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(353): Show |
3_prime_UTR_variant | MODIFIER | c.*94G>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 5/5 | 94 | chr5 | 40716051 | |||||
chr5:40716134
|
T | C | 1 | a0001c0001t0040 | 1 | HG01515.hp1 | 3_prime_UTR_variant | MODIFIER | c.*11A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 5/5 | 11 | chr5 | 40716134 | |||||
chr5:40755838
|
T | C | 1 | a0001c0001t0020 | 2 | NA18994.hp1 NA18995.hp2 |
5_prime_UTR_variant | MODIFIER | c.-16A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/5 | 8820 | chr5 | 40755838 | |||||
chr5:40755867
|
CCACCCCT others(3): Show |
C | 1 | a0001c0001t0011 | 4 | HG02976.hp1 HG03139.hp2 HG03540.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-55_-46delCCCAGGGG others(2): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/5 | 8850 | chr5 | 40755867 | |||||
chr5:40755887
|
A | G | 1 | a0001c0001t0011 | 4 | HG02976.hp1 HG03139.hp2 HG03540.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-65T>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/5 | 8869 | chr5 | 40755887 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:40716531
|
T | C | 1 | a0001c0001t0001g0186 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.436-33A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40716531 | ||||||
chr5:40716735
|
G | T | 1 | a0001c0001t0004g0264 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.436-237C>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40716735 | ||||||
chr5:40716751
|
G | C | 1 | a0001c0001t0010g0090 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.436-253C>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40716751 | ||||||
chr5:40716852
|
G | A | 1 | a0001c0001t0009g0302 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.436-354C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40716852 | ||||||
chr5:40716957
|
G | C | 8 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0183others(5): Show | 10 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(7): Show |
intron_variant | MODIFIER | c.436-459C>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40716957 | ||||||
chr5:40717003
|
C | T | 143 | a0001c0001t0002g0002a0001c0001t0002g0009a0001c0001t0002g0016others(140): Show | 167 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(164): Show |
intron_variant | MODIFIER | c.436-505G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40717003 | ||||||
chr5:40717041
|
C | A | 1 | a0001c0001t0003g0131 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.436-543G>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40717041 | ||||||
chr5:40717043
|
A | C | 1 | a0001c0001t0003g0131 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.436-545T>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40717043 | ||||||
chr5:40717058
|
G | C | 1 | a0001c0001t0002g0063 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.436-560C>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40717058 | ||||||
chr5:40717143
|
C | T | 1 | a0002c0002t0008g0195 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.436-645G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40717143 | ||||||
chr5:40717229
|
C | CA | 119 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(116): Show | 140 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.436-732dupT | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40717229 | ||||||
chr5:40717229
|
C | CAA | 98 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(95): Show | 129 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(126): Show |
intron_variant | MODIFIER | c.436-733_436-732dup others(2): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40717229 | ||||||
chr5:40717229
|
C | CAAA | 11 | a0001c0001t0001g0215a0001c0001t0001g0220a0001c0001t0001g0222others(8): Show | 11 | HG00323.hp1 HG01099.hp2 HG01978.hp2 others(8): Show |
intron_variant | MODIFIER | c.436-734_436-732dup others(3): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40717229 | ||||||
chr5:40717229
|
CA | C | 6 | a0001c0001t0002g0139a0001c0001t0012g0180a0001c0001t0013g0047others(3): Show | 6 | HG01106.hp1 HG02572.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.436-732delT | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40717229 | ||||||
chr5:40717343
|
T | C | 1 | a0001c0001t0003g0096 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.436-845A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40717343 | ||||||
chr5:40717376
|
A | G | 1 | a0001c0001t0031g0315 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.436-878T>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40717376 | ||||||
chr5:40717439
|
T | C | 5 | a0001c0001t0011g0008a0001c0001t0011g0046a0001c0001t0015g0312others(2): Show | 7 | HG02280.hp2 HG02976.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.436-941A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40717439 | ||||||
chr5:40717507
|
T | A | 5 | a0001c0001t0004g0035a0001c0001t0004g0265a0001c0001t0004g0266others(2): Show | 6 | HG01070.hp1 HG01071.hp1 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.436-1009A>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40717507 | ||||||
chr5:40717640
|
C | T | 2 | a0001c0001t0004g0168a0001c0001t0004g0169 | 2 | HG03453.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.436-1142G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40717640 | ||||||
chr5:40717719
|
A | G | 5 | a0001c0001t0011g0008a0001c0001t0011g0046a0001c0001t0015g0312others(2): Show | 7 | HG02280.hp2 HG02976.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.436-1221T>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40717719 | ||||||
chr5:40717740
|
G | A | 16 | a0001c0001t0004g0249a0001c0001t0005g0015a0001c0001t0005g0037others(13): Show | 21 | HG00597.hp2 HG00735.hp2 HG01433.hp1 others(18): Show |
intron_variant | MODIFIER | c.436-1242C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40717740 | ||||||
chr5:40717789
|
C | A | 1 | a0001c0001t0010g0089 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.436-1291G>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40717789 | ||||||
chr5:40717929
|
G | T | 131 | a0001c0001t0002g0002a0001c0001t0002g0009a0001c0001t0002g0016others(128): Show | 155 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(152): Show |
intron_variant | MODIFIER | c.436-1431C>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40717929 | ||||||
chr5:40717954
|
C | T | 1 | a0001c0001t0001g0243 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.436-1456G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40717954 | ||||||
chr5:40718045
|
A | T | 16 | a0001c0001t0004g0249a0001c0001t0005g0015a0001c0001t0005g0037others(13): Show | 21 | HG00597.hp2 HG00735.hp2 HG01433.hp1 others(18): Show |
intron_variant | MODIFIER | c.436-1547T>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40718045 | ||||||
chr5:40718057
|
C | T | 3 | a0001c0001t0017g0191a0001c0001t0017g0192a0001c0001t0017g0193 | 3 | HG02717.hp2 HG02922.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.436-1559G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40718057 | ||||||
chr5:40718216
|
T | C | 4 | a0001c0001t0013g0047a0001c0001t0013g0048a0001c0001t0013g0049others(1): Show | 4 | HG01106.hp1 HG02572.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.436-1718A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40718216 | ||||||
chr5:40718236
|
T | C | 1 | a0001c0001t0037g0052 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.436-1738A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40718236 | ||||||
chr5:40718252
|
A | G | 1 | a0002c0002t0008g0199 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.436-1754T>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40718252 | ||||||
chr5:40718310
|
G | T | 8 | a0002c0002t0008g0012a0002c0002t0008g0195a0002c0002t0008g0196others(5): Show | 10 | HG00408.hp2 HG00597.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.436-1812C>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40718310 | ||||||
chr5:40718367
|
C | T | 1 | a0001c0001t0010g0089 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.436-1869G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40718367 | ||||||
chr5:40718480
|
G | A | 1 | a0001c0001t0001g0208 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.436-1982C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40718480 | ||||||
chr5:40718496
|
C | G | 1 | a0001c0001t0023g0174 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.436-1998G>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40718496 | ||||||
chr5:40718507
|
G | A | 2 | a0001c0001t0018g0105a0001c0001t0018g0106 | 2 | NA18988.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.436-2009C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40718507 | ||||||
chr5:40718585
|
C | T | 7 | a0001c0001t0003g0010a0001c0001t0003g0098a0001c0001t0003g0121others(4): Show | 9 | HG00099.hp2 HG01168.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.436-2087G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40718585 | ||||||
chr5:40718653
|
G | A | 56 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(53): Show | 78 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.436-2155C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40718653 | ||||||
chr5:40718665
|
G | A | 1 | a0001c0001t0001g0286 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.436-2167C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40718665 | ||||||
chr5:40718682
|
G | C | 2 | a0001c0001t0004g0168a0001c0001t0004g0169 | 2 | HG03453.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.436-2184C>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40718682 | ||||||
chr5:40718686
|
C | T | 141 | a0001c0001t0002g0002a0001c0001t0002g0009a0001c0001t0002g0016others(138): Show | 165 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.436-2188G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40718686 | ||||||
chr5:40718689
|
G | A | 3 | a0001c0001t0012g0180a0001c0001t0012g0181a0001c0001t0012g0182 | 3 | HG01192.hp1 HG02965.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.436-2191C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40718689 | ||||||
chr5:40718788
|
C | T | 41 | a0001c0001t0002g0002a0001c0001t0002g0009a0001c0001t0002g0016others(38): Show | 51 | HG00423.hp1 HG00673.hp1 HG01081.hp2 others(48): Show |
intron_variant | MODIFIER | c.436-2290G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40718788 | ||||||
chr5:40718948
|
T | C | 1 | a0001c0001t0003g0108 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.436-2450A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40718948 | ||||||
chr5:40718991
|
A | G | 7 | a0001c0001t0010g0087a0001c0001t0010g0088a0001c0001t0010g0089others(4): Show | 7 | HG02257.hp2 HG02451.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.436-2493T>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40718991 | ||||||
chr5:40719045
|
A | G | 1 | a0001c0001t0006g0042 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.436-2547T>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40719045 | ||||||
chr5:40719139
|
C | T | 3 | a0001c0001t0017g0191a0001c0001t0017g0192a0001c0001t0017g0193 | 3 | HG02717.hp2 HG02922.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.436-2641G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40719139 | ||||||
chr5:40719160
|
T | C | 1 | a0001c0001t0001g0222 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.436-2662A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40719160 | ||||||
chr5:40719340
|
C | T | 8 | a0002c0002t0008g0012a0002c0002t0008g0195a0002c0002t0008g0196others(5): Show | 10 | HG00408.hp2 HG00597.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.436-2842G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40719340 | ||||||
chr5:40719404
|
T | C | 1 | a0001c0001t0001g0229 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.436-2906A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40719404 | ||||||
chr5:40719412
|
C | T | 5 | a0001c0001t0001g0025a0001c0001t0001g0176a0001c0001t0001g0177others(2): Show | 6 | HG01167.hp2 HG01169.hp2 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.436-2914G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40719412 | ||||||
chr5:40719441
|
T | C | 143 | a0001c0001t0002g0002a0001c0001t0002g0009a0001c0001t0002g0016others(140): Show | 167 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(164): Show |
intron_variant | MODIFIER | c.436-2943A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40719441 | ||||||
chr5:40719442
|
C | G | 1 | a0001c0001t0002g0070 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.436-2944G>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40719442 | ||||||
chr5:40719582
|
C | T | 5 | a0001c0001t0011g0008a0001c0001t0011g0046a0001c0001t0015g0312others(2): Show | 7 | HG02280.hp2 HG02976.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.436-3084G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40719582 | ||||||
chr5:40719597
|
T | C | 2 | a0001c0001t0002g0081a0001c0001t0002g0083 | 2 | NA18977.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.436-3099A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40719597 | ||||||
chr5:40719696
|
C | G | 6 | a0002c0002t0008g0012a0002c0002t0008g0195a0002c0002t0008g0196others(3): Show | 8 | HG00597.hp1 HG02015.hp1 HG02040.hp1 others(5): Show |
intron_variant | MODIFIER | c.436-3198G>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40719696 | ||||||
chr5:40719848
|
T | C | 1 | a0001c0001t0037g0052 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.436-3350A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40719848 | ||||||
chr5:40719999
|
C | T | 5 | a0001c0001t0012g0180a0001c0001t0012g0181a0001c0001t0012g0182others(2): Show | 5 | HG01192.hp1 HG02280.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.436-3501G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40719999 | ||||||
chr5:40720026
|
A | C | 131 | a0001c0001t0002g0002a0001c0001t0002g0009a0001c0001t0002g0016others(128): Show | 155 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(152): Show |
intron_variant | MODIFIER | c.436-3528T>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40720026 | ||||||
chr5:40720057
|
C | G | 5 | a0001c0001t0012g0180a0001c0001t0012g0181a0001c0001t0012g0182others(2): Show | 5 | HG01192.hp1 HG02280.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.436-3559G>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40720057 | ||||||
chr5:40720081
|
G | C | 1 | a0001c0001t0005g0272 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.436-3583C>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40720081 | ||||||
chr5:40720256
|
C | T | 1 | a0001c0001t0012g0194 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.436-3758G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40720256 | ||||||
chr5:40720285
|
G | A | 56 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(53): Show | 78 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.436-3787C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40720285 | ||||||
chr5:40720481
|
T | C | 1 | a0001c0001t0001g0211 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.436-3983A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40720481 | ||||||
chr5:40720514
|
C | T | 1 | a0001c0001t0037g0052 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.436-4016G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40720514 | ||||||
chr5:40720576
|
A | C | 4 | a0001c0001t0013g0047a0001c0001t0013g0048a0001c0001t0013g0049others(1): Show | 4 | HG01106.hp1 HG02572.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.436-4078T>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40720576 | ||||||
chr5:40720593
|
A | G | 8 | a0002c0002t0008g0012a0002c0002t0008g0195a0002c0002t0008g0196others(5): Show | 10 | HG00408.hp2 HG00597.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.436-4095T>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40720593 | ||||||
chr5:40720716
|
G | A | 1 | a0001c0001t0023g0174 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.436-4218C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40720716 | ||||||
chr5:40720905
|
C | T | 2 | a0001c0001t0004g0168a0001c0001t0004g0169 | 2 | HG03453.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.436-4407G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40720905 | ||||||
chr5:40721140
|
G | A | 2 | a0002c0002t0008g0197a0002c0002t0008g0198 | 2 | HG00408.hp2 HG02080.hp1 |
intron_variant | MODIFIER | c.436-4642C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40721140 | ||||||
chr5:40721176
|
T | G | 1 | a0001c0001t0003g0100 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.436-4678A>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40721176 | ||||||
chr5:40721193
|
T | C | 3 | a0001c0001t0002g0139a0001c0001t0002g0148a0001c0001t0002g0149 | 3 | HG02809.hp2 HG02896.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.436-4695A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40721193 | ||||||
chr5:40721297
|
A | G | 8 | a0002c0002t0008g0012a0002c0002t0008g0195a0002c0002t0008g0196others(5): Show | 10 | HG00408.hp2 HG00597.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.436-4799T>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40721297 | ||||||
chr5:40721331
|
C | T | 4 | a0001c0001t0004g0262a0001c0001t0010g0090a0001c0001t0010g0091others(1): Show | 4 | HG02647.hp1 HG02818.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.436-4833G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40721331 | ||||||
chr5:40721336
|
T | C | 236 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(233): Show | 289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.436-4838A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40721336 | ||||||
chr5:40721349
|
C | T | 4 | a0001c0001t0013g0047a0001c0001t0013g0048a0001c0001t0013g0049others(1): Show | 4 | HG01106.hp1 HG02572.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.436-4851G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40721349 | ||||||
chr5:40721395
|
C | A | 1 | a0001c0001t0002g0056 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.436-4897G>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40721395 | ||||||
chr5:40721544
|
G | A | 5 | a0001c0001t0011g0008a0001c0001t0011g0046a0001c0001t0015g0312others(2): Show | 7 | HG02280.hp2 HG02976.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.436-5046C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40721544 | ||||||
chr5:40721560
|
A | G | 5 | a0001c0001t0011g0008a0001c0001t0011g0046a0001c0001t0015g0312others(2): Show | 7 | HG02280.hp2 HG02976.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.436-5062T>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40721560 | ||||||
chr5:40721605
|
C | G | 1 | a0001c0001t0026g0282 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.436-5107G>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40721605 | ||||||
chr5:40721643
|
C | T | 1 | a0001c0001t0004g0266 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.436-5145G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40721643 | ||||||
chr5:40721682
|
A | AAAAAC | 51 | a0001c0001t0003g0005a0001c0001t0003g0010a0001c0001t0003g0011others(48): Show | 61 | HG00099.hp2 HG00408.hp1 HG01069.hp2 others(58): Show |
intron_variant | MODIFIER | c.436-5189_436-5185d others(7): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40721682 | ||||||
chr5:40721821
|
C | T | 1 | a0001c0001t0010g0089 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.436-5323G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40721821 | ||||||
chr5:40722160
|
G | T | 71 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(68): Show | 96 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.436-5662C>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40722160 | ||||||
chr5:40722243
|
T | A | 1 | a0001c0001t0001g0186 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.436-5745A>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40722243 | ||||||
chr5:40722282
|
T | G | 1 | a0001c0001t0021g0225 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.436-5784A>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40722282 | ||||||
chr5:40722321
|
C | T | 8 | a0002c0002t0008g0012a0002c0002t0008g0195a0002c0002t0008g0196others(5): Show | 10 | HG00408.hp2 HG00597.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.436-5823G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40722321 | ||||||
chr5:40722331
|
G | A | 1 | a0001c0001t0035g0110 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.436-5833C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40722331 | ||||||
chr5:40722349
|
G | A | 64 | a0001c0001t0002g0023a0001c0001t0002g0024a0001c0001t0002g0154others(61): Show | 76 | HG00099.hp2 HG00408.hp1 HG01069.hp2 others(73): Show |
intron_variant | MODIFIER | c.436-5851C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40722349 | ||||||
chr5:40722402
|
G | A | 1 | a0001c0001t0002g0134 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.436-5904C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40722402 | ||||||
chr5:40722424
|
C | T | 1 | a0001c0001t0040g0293 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.435+5921G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40722424 | ||||||
chr5:40722434
|
C | T | 1 | a0001c0001t0001g0233 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.435+5911G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40722434 | ||||||
chr5:40722438
|
C | A | 1 | a0001c0001t0002g0138 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.435+5907G>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40722438 | ||||||
chr5:40722486
|
G | C | 1 | a0001c0001t0017g0192 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.435+5859C>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40722486 | ||||||
chr5:40722557
|
G | C | 7 | a0001c0001t0010g0087a0001c0001t0010g0088a0001c0001t0010g0089others(4): Show | 7 | HG02257.hp2 HG02451.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.435+5788C>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40722557 | ||||||
chr5:40722656
|
G | A | 5 | a0001c0001t0011g0008a0001c0001t0011g0046a0001c0001t0015g0312others(2): Show | 7 | HG02280.hp2 HG02976.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.435+5689C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40722656 | ||||||
chr5:40722663
|
C | T | 47 | a0001c0001t0002g0002a0001c0001t0002g0009a0001c0001t0002g0016others(44): Show | 57 | HG00423.hp1 HG00673.hp1 HG01081.hp2 others(54): Show |
intron_variant | MODIFIER | c.435+5682G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40722663 | ||||||
chr5:40722673
|
C | T | 7 | a0001c0001t0010g0087a0001c0001t0010g0088a0001c0001t0010g0089others(4): Show | 7 | HG02257.hp2 HG02451.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.435+5672G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40722673 | ||||||
chr5:40722674
|
C | G | 1 | a0001c0001t0003g0118 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.435+5671G>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40722674 | ||||||
chr5:40722708
|
G | A | 3 | a0001c0001t0013g0047a0001c0001t0013g0048a0001c0001t0013g0050 | 3 | HG01106.hp1 HG02572.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.435+5637C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40722708 | ||||||
chr5:40722714
|
C | T | 1 | a0001c0001t0004g0249 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.435+5631G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40722714 | ||||||
chr5:40722720
|
G | A | 144 | a0001c0001t0002g0002a0001c0001t0002g0009a0001c0001t0002g0016others(141): Show | 168 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(165): Show |
intron_variant | MODIFIER | c.435+5625C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40722720 | ||||||
chr5:40722747
|
C | T | 7 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0183others(4): Show | 9 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(6): Show |
intron_variant | MODIFIER | c.435+5598G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40722747 | ||||||
chr5:40722749
|
C | T | 1 | a0001c0001t0005g0276 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.435+5596G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40722749 | ||||||
chr5:40722763
|
G | A | 2 | a0001c0001t0003g0109a0001c0001t0003g0114 | 2 | NA18986.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.435+5582C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40722763 | ||||||
chr5:40722812
|
A | C | 1 | a0001c0001t0005g0277 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.435+5533T>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40722812 | ||||||
chr5:40722822
|
C | T | 214 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(211): Show | 263 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.435+5523G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40722822 | ||||||
chr5:40722876
|
C | T | 7 | a0001c0001t0004g0168a0001c0001t0004g0169a0001c0001t0011g0008others(4): Show | 9 | HG02280.hp2 HG02976.hp1 HG03139.hp2 others(6): Show |
intron_variant | MODIFIER | c.435+5469G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40722876 | ||||||
chr5:40722918
|
G | A | 1 | a0001c0001t0012g0194 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.435+5427C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40722918 | ||||||
chr5:40722921
|
A | AC | 7 | a0001c0001t0001g0217a0001c0001t0001g0229a0001c0001t0001g0233others(4): Show | 7 | HG01978.hp2 HG02145.hp1 NA18954.hp2 others(4): Show |
intron_variant | MODIFIER | c.435+5423dupG | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40722921 | ||||||
chr5:40722972
|
C | G | 222 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(219): Show | 273 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.435+5373G>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40722972 | ||||||
chr5:40723367
|
C | T | 5 | a0001c0001t0011g0008a0001c0001t0011g0046a0001c0001t0015g0312others(2): Show | 7 | HG02280.hp2 HG02976.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.435+4978G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40723367 | ||||||
chr5:40723443
|
A | C | 1 | a0001c0001t0004g0249 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.435+4902T>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40723443 | ||||||
chr5:40723445
|
T | A | 3 | a0001c0001t0010g0090a0001c0001t0010g0091a0001c0001t0010g0092 | 3 | HG02647.hp1 HG02818.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.435+4900A>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40723445 | ||||||
chr5:40723510
|
A | G | 1 | a0001c0001t0002g0172 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.435+4835T>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40723510 | ||||||
chr5:40723512
|
TAA | T | 144 | a0001c0001t0002g0002a0001c0001t0002g0009a0001c0001t0002g0016others(141): Show | 170 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(167): Show |
intron_variant | MODIFIER | c.435+4831_435+4832d others(4): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40723512 | ||||||
chr5:40723512
|
TAAA | T | 78 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(75): Show | 103 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.435+4830_435+4832d others(5): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40723512 | ||||||
chr5:40723526
|
AAAG | A | 5 | a0001c0001t0011g0008a0001c0001t0011g0046a0001c0001t0015g0312others(2): Show | 7 | HG02280.hp2 HG02976.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.435+4816_435+4818d others(5): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40723526 | ||||||
chr5:40723560
|
A | G | 1 | a0001c0001t0005g0274 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.435+4785T>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40723560 | ||||||
chr5:40723573
|
C | A | 1 | a0001c0001t0001g0238 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.435+4772G>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40723573 | ||||||
chr5:40723592
|
C | T | 1 | a0001c0001t0003g0116 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.435+4753G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40723592 | ||||||
chr5:40723783
|
C | T | 3 | a0001c0001t0001g0173a0001c0001t0001g0230a0001c0001t0001g0231 | 3 | HG00423.hp2 HG00558.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.435+4562G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40723783 | ||||||
chr5:40723818
|
T | C | 1 | a0001c0001t0006g0296 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.435+4527A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40723818 | ||||||
chr5:40723844
|
G | A | 20 | a0001c0001t0002g0021a0001c0001t0002g0132a0001c0001t0002g0138others(17): Show | 22 | HG00280.hp1 HG00741.hp1 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.435+4501C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40723844 | ||||||
chr5:40723864
|
C | CA | 6 | a0001c0001t0002g0164a0001c0001t0002g0316a0001c0001t0003g0107others(3): Show | 6 | HG01167.hp1 HG01358.hp2 HG02004.hp1 others(3): Show |
intron_variant | MODIFIER | c.435+4480dupT | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40723864 | ||||||
chr5:40723870
|
AAAAC | A | 19 | a0001c0001t0004g0007a0001c0001t0004g0033a0001c0001t0004g0036others(16): Show | 25 | HG00558.hp2 HG02129.hp1 HG02165.hp2 others(22): Show |
intron_variant | MODIFIER | c.435+4471_435+4474d others(6): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40723870 | ||||||
chr5:40724120
|
A | C | 5 | a0001c0001t0012g0180a0001c0001t0012g0181a0001c0001t0012g0182others(2): Show | 5 | HG01192.hp1 HG02280.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.435+4225T>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40724120 | ||||||
chr5:40724304
|
G | A | 3 | a0001c0001t0010g0090a0001c0001t0010g0091a0001c0001t0010g0092 | 3 | HG02647.hp1 HG02818.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.435+4041C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40724304 | ||||||
chr5:40724451
|
G | A | 4 | a0001c0001t0013g0047a0001c0001t0013g0048a0001c0001t0013g0049others(1): Show | 4 | HG01106.hp1 HG02572.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.435+3894C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40724451 | ||||||
chr5:40724655
|
C | CA | 5 | a0001c0001t0001g0176a0001c0001t0003g0079a0001c0001t0003g0109others(2): Show | 5 | HG01261.hp1 NA18960.hp1 NA18986.hp2 others(2): Show |
intron_variant | MODIFIER | c.435+3689dupT | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40724655 | ||||||
chr5:40724659
|
A | C | 1 | a0001c0001t0001g0237 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.435+3686T>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40724659 | ||||||
chr5:40724735
|
TACA | T | 4 | a0001c0001t0012g0180a0001c0001t0012g0181a0001c0001t0012g0182others(1): Show | 4 | HG01192.hp1 HG02280.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.435+3607_435+3609d others(5): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40724735 | ||||||
chr5:40724762
|
A | G | 1 | a0001c0001t0004g0268 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.435+3583T>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40724762 | ||||||
chr5:40724853
|
A | AT | 11 | a0001c0001t0002g0067a0001c0001t0002g0082a0001c0001t0002g0083others(8): Show | 11 | HG01261.hp2 HG01433.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.435+3491dupA | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40724853 | ||||||
chr5:40724853
|
AT | A | 40 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(37): Show | 48 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.435+3491delA | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40724853 | ||||||
chr5:40724853
|
ATT | A | 54 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(51): Show | 76 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.435+3490_435+3491d others(4): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40724853 | ||||||
chr5:40724918
|
T | C | 1 | a0001c0001t0002g0069 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.435+3427A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40724918 | ||||||
chr5:40724946
|
A | C | 1 | a0001c0001t0035g0110 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.435+3399T>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40724946 | ||||||
chr5:40725003
|
T | C | 56 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(53): Show | 78 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.435+3342A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40725003 | ||||||
chr5:40725150
|
A | AT | 9 | a0001c0001t0003g0094a0001c0001t0003g0111a0001c0001t0004g0168others(6): Show | 9 | HG02572.hp1 HG02895.hp1 HG03453.hp1 others(6): Show |
intron_variant | MODIFIER | c.435+3194dupA | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40725150 | ||||||
chr5:40725150
|
AT | A | 15 | a0001c0001t0002g0082a0001c0001t0002g0084a0001c0001t0004g0254others(12): Show | 17 | HG01884.hp2 HG02280.hp2 HG02293.hp2 others(14): Show |
intron_variant | MODIFIER | c.435+3194delA | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40725150 | ||||||
chr5:40725278
|
T | C | 2 | a0001c0001t0004g0168a0001c0001t0004g0169 | 2 | HG03453.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.435+3067A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40725278 | ||||||
chr5:40725611
|
G | A | 1 | a0001c0001t0035g0110 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.435+2734C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40725611 | ||||||
chr5:40725632
|
T | C | 1 | a0001c0001t0001g0223 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.435+2713A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40725632 | ||||||
chr5:40725703
|
G | A | 1 | a0001c0001t0005g0039 | 2 | NA18989.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.435+2642C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40725703 | ||||||
chr5:40725716
|
T | C | 41 | a0001c0001t0002g0002a0001c0001t0002g0009a0001c0001t0002g0016others(38): Show | 51 | HG00423.hp1 HG00673.hp1 HG01081.hp2 others(48): Show |
intron_variant | MODIFIER | c.435+2629A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40725716 | ||||||
chr5:40725739
|
A | G | 2 | a0001c0001t0004g0283a0001c0001t0004g0284 | 2 | HG02486.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.435+2606T>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40725739 | ||||||
chr5:40725764
|
C | T | 3 | a0001c0001t0001g0240a0001c0001t0001g0241a0001c0001t0001g0243 | 3 | HG01358.hp1 HG02683.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.435+2581G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40725764 | ||||||
chr5:40725784
|
C | CT | 41 | a0001c0001t0001g0173a0001c0001t0001g0205a0001c0001t0001g0214others(38): Show | 46 | HG00423.hp2 HG00597.hp2 HG00735.hp2 others(43): Show |
intron_variant | MODIFIER | c.435+2560dupA | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40725784 | ||||||
chr5:40725784
|
CT | C | 16 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0183others(13): Show | 18 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(15): Show |
intron_variant | MODIFIER | c.435+2560delA | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40725784 | ||||||
chr5:40725843
|
T | C | 2 | a0001c0001t0013g0047a0001c0001t0013g0048 | 2 | HG02572.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.435+2502A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40725843 | ||||||
chr5:40725987
|
G | A | 7 | a0001c0001t0003g0010a0001c0001t0003g0098a0001c0001t0003g0121others(4): Show | 9 | HG00099.hp2 HG01168.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.435+2358C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40725987 | ||||||
chr5:40726003
|
T | A | 1 | a0001c0001t0010g0089 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.435+2342A>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40726003 | ||||||
chr5:40726004
|
C | T | 1 | a0001c0001t0010g0089 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.435+2341G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40726004 | ||||||
chr5:40726036
|
C | T | 116 | a0001c0001t0002g0002a0001c0001t0002g0009a0001c0001t0002g0016others(113): Show | 138 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(135): Show |
intron_variant | MODIFIER | c.435+2309G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40726036 | ||||||
chr5:40726145
|
A | T | 215 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(212): Show | 264 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.435+2200T>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40726145 | ||||||
chr5:40726160
|
TAC | T | 222 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(219): Show | 274 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(271): Show |
intron_variant | MODIFIER | c.435+2183_435+2184d others(4): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40726160 | ||||||
chr5:40726162
|
C | T | 5 | a0001c0001t0001g0030a0001c0001t0001g0203a0001c0001t0001g0212others(2): Show | 6 | HG02615.hp2 NA18987.hp1 NA19011.hp2 others(3): Show |
intron_variant | MODIFIER | c.435+2183G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40726162 | ||||||
chr5:40726212
|
T | TTA | 3 | a0001c0001t0002g0139a0001c0001t0002g0148a0001c0001t0002g0149 | 3 | HG02809.hp2 HG02896.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.435+2132_435+2133i others(4): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40726212 | ||||||
chr5:40726214
|
T | A | 3 | a0001c0001t0002g0139a0001c0001t0002g0148a0001c0001t0002g0149 | 3 | HG02809.hp2 HG02896.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.435+2131A>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40726214 | ||||||
chr5:40726214
|
T | TTA | 142 | a0001c0001t0001g0053a0001c0001t0002g0002a0001c0001t0002g0009others(139): Show | 166 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.435+2129_435+2130d others(4): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40726214 | ||||||
chr5:40726394
|
A | G | 236 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(233): Show | 289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.435+1951T>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40726394 | ||||||
chr5:40726550
|
C | CA | 64 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(61): Show | 87 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.435+1794dupT | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40726550 | ||||||
chr5:40726616
|
GA | G | 308 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(305): Show | 383 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(380): Show |
intron_variant | MODIFIER | c.435+1728delT | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40726616 | ||||||
chr5:40726699
|
C | T | 222 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(219): Show | 273 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.435+1646G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40726699 | ||||||
chr5:40727081
|
T | G | 1 | a0001c0001t0005g0274 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.435+1264A>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40727081 | ||||||
chr5:40727255
|
T | C | 5 | a0001c0001t0011g0008a0001c0001t0011g0046a0001c0001t0015g0312others(2): Show | 7 | HG02280.hp2 HG02976.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.435+1090A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40727255 | ||||||
chr5:40727385
|
T | C | 3 | a0001c0001t0004g0250a0001c0001t0004g0251a0001c0001t0026g0282 | 3 | HG02145.hp2 HG02965.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.435+960A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40727385 | ||||||
chr5:40727522
|
A | G | 1 | a0002c0002t0008g0199 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.435+823T>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40727522 | ||||||
chr5:40727628
|
C | T | 4 | a0001c0001t0002g0140a0001c0001t0002g0144a0001c0001t0002g0146others(1): Show | 4 | HG00280.hp1 HG00741.hp1 HG01256.hp1 others(1): Show |
intron_variant | MODIFIER | c.435+717G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40727628 | ||||||
chr5:40727672
|
C | T | 1 | a0001c0001t0026g0282 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.435+673G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40727672 | ||||||
chr5:40727702
|
T | C | 1 | a0001c0001t0002g0058 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.435+643A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40727702 | ||||||
chr5:40727907
|
C | A | 1 | a0001c0001t0028g0160 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.435+438G>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40727907 | ||||||
chr5:40728134
|
A | G | 4 | a0001c0001t0013g0047a0001c0001t0013g0048a0001c0001t0013g0049others(1): Show | 4 | HG01106.hp1 HG02572.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.435+211T>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40728134 | ||||||
chr5:40728176
|
C | T | 10 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0183others(7): Show | 12 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(9): Show |
intron_variant | MODIFIER | c.435+169G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40728176 | ||||||
chr5:40728268
|
C | T | 2 | a0001c0001t0004g0283a0001c0001t0004g0284 | 2 | HG02486.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.435+77G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40728268 | ||||||
chr5:40728272
|
A | C | 1 | a0001c0001t0015g0313 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.435+73T>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40728272 | ||||||
chr5:40728281
|
C | CAAAAAA | 5 | a0001c0001t0011g0008a0001c0001t0011g0046a0001c0001t0015g0312others(2): Show | 7 | HG02280.hp2 HG02976.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.435+58_435+63dupTT others(4): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40728281 | ||||||
chr5:40728281
|
C | CAAAAAAA others(3): Show |
7 | a0001c0001t0001g0187a0001c0001t0001g0213a0001c0001t0001g0228others(4): Show | 7 | HG01069.hp1 HG01168.hp1 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.435+54_435+63dupTT others(8): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40728281 | ||||||
chr5:40728281
|
C | CAAAAAAA others(4): Show |
68 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(65): Show | 93 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.435+53_435+63dupTT others(9): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40728281 | ||||||
chr5:40728281
|
C | CAAAAAAA others(5): Show |
72 | a0001c0001t0001g0176a0001c0001t0001g0190a0001c0001t0001g0203others(69): Show | 91 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.435+52_435+63dupTT others(10): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40728281 | ||||||
chr5:40728281
|
C | CAAAAAAA others(6): Show |
32 | a0001c0001t0002g0023a0001c0001t0002g0024a0001c0001t0002g0066others(29): Show | 36 | HG00597.hp1 HG01106.hp1 HG01167.hp1 others(33): Show |
intron_variant | MODIFIER | c.435+51_435+63dupTT others(11): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40728281 | ||||||
chr5:40728281
|
C | CAAAAAAA others(7): Show |
94 | a0001c0001t0001g0053a0001c0001t0002g0002a0001c0001t0002g0009others(91): Show | 116 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.435+50_435+63dupTT others(12): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40728281 | ||||||
chr5:40728281
|
C | CAAAAAAA others(8): Show |
21 | a0001c0001t0002g0055a0001c0001t0002g0062a0001c0001t0002g0063others(18): Show | 21 | HG00741.hp1 HG01258.hp2 HG01346.hp1 others(18): Show |
intron_variant | MODIFIER | c.435+63_435+64insTT others(13): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40728281 | ||||||
chr5:40728281
|
C | CAAAAAAA others(9): Show |
3 | a0001c0001t0003g0115a0001c0001t0006g0042a0001c0001t0006g0043 | 5 | HG00741.hp2 HG01516.hp1 HG01517.hp1 others(2): Show |
intron_variant | MODIFIER | c.435+63_435+64insTT others(14): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40728281 | ||||||
chr5:40728295
|
A | AAAAAAAA others(6): Show |
1 | a0001c0001t0004g0273 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.435+49_435+50insCT others(11): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40728295 | ||||||
chr5:40728296
|
G | T | 1 | a0001c0001t0023g0174 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.435+49C>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 4/4 | chr5 | 40728296 | ||||||
chr5:40728591
|
C | T | 5 | a0001c0001t0001g0025a0001c0001t0001g0176a0001c0001t0001g0177others(2): Show | 6 | HG01167.hp2 HG01169.hp2 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.304-115G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 3/4 | chr5 | 40728591 | ||||||
chr5:40728612
|
C | T | 1 | a0001c0001t0030g0073 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.304-136G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 3/4 | chr5 | 40728612 | ||||||
chr5:40728677
|
G | A | 1 | a0001c0001t0001g0204 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.304-201C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 3/4 | chr5 | 40728677 | ||||||
chr5:40728677
|
G | C | 5 | a0001c0001t0011g0008a0001c0001t0011g0046a0001c0001t0015g0312others(2): Show | 7 | HG02280.hp2 HG02976.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.304-201C>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 3/4 | chr5 | 40728677 | ||||||
chr5:40729047
|
G | C | 1 | a0001c0001t0012g0194 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.304-571C>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 3/4 | chr5 | 40729047 | ||||||
chr5:40729099
|
G | C | 55 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(52): Show | 77 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(74): Show |
intron_variant | MODIFIER | c.304-623C>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 3/4 | chr5 | 40729099 | ||||||
chr5:40729140
|
C | T | 55 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(52): Show | 77 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(74): Show |
intron_variant | MODIFIER | c.304-664G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 3/4 | chr5 | 40729140 | ||||||
chr5:40729329
|
G | T | 1 | a0001c0001t0010g0089 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.304-853C>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 3/4 | chr5 | 40729329 | ||||||
chr5:40729340
|
T | G | 5 | a0001c0001t0011g0008a0001c0001t0011g0046a0001c0001t0015g0312others(2): Show | 7 | HG02280.hp2 HG02976.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.304-864A>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 3/4 | chr5 | 40729340 | ||||||
chr5:40729418
|
C | G | 1 | a0001c0001t0001g0242 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.303+844G>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 3/4 | chr5 | 40729418 | ||||||
chr5:40729440
|
T | C | 1 | a0001c0001t0007g0310 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.303+822A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 3/4 | chr5 | 40729440 | ||||||
chr5:40729542
|
G | A | 1 | a0001c0001t0001g0212 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.303+720C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 3/4 | chr5 | 40729542 | ||||||
chr5:40729648
|
C | T | 1 | a0001c0001t0010g0092 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.303+614G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 3/4 | chr5 | 40729648 | ||||||
chr5:40729761
|
C | A | 2 | a0002c0002t0008g0197a0002c0002t0008g0198 | 2 | HG00408.hp2 HG02080.hp1 |
intron_variant | MODIFIER | c.303+501G>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 3/4 | chr5 | 40729761 | ||||||
chr5:40729872
|
T | C | 139 | a0001c0001t0001g0053a0001c0001t0002g0002a0001c0001t0002g0009others(136): Show | 163 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.303+390A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 3/4 | chr5 | 40729872 | ||||||
chr5:40729919
|
G | A | 1 | a0001c0001t0001g0235 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.303+343C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 3/4 | chr5 | 40729919 | ||||||
chr5:40729969
|
G | A | 5 | a0001c0001t0011g0008a0001c0001t0011g0046a0001c0001t0015g0312others(2): Show | 7 | HG02280.hp2 HG02976.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.303+293C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 3/4 | chr5 | 40729969 | ||||||
chr5:40729983
|
G | A | 1 | a0001c0001t0002g0149 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.303+279C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 3/4 | chr5 | 40729983 | ||||||
chr5:40730024
|
C | T | 8 | a0002c0002t0008g0012a0002c0002t0008g0195a0002c0002t0008g0196others(5): Show | 10 | HG00408.hp2 HG00597.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.303+238G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 3/4 | chr5 | 40730024 | ||||||
chr5:40730435
|
T | C | 5 | a0001c0001t0011g0008a0001c0001t0011g0046a0001c0001t0015g0312others(2): Show | 7 | HG02280.hp2 HG02976.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.222-92A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40730435 | ||||||
chr5:40730572
|
T | A | 2 | a0001c0001t0004g0168a0001c0001t0004g0169 | 2 | HG03453.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.222-229A>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40730572 | ||||||
chr5:40730638
|
A | G | 6 | a0001c0001t0004g0253a0001c0001t0004g0254a0001c0001t0004g0255others(3): Show | 6 | NA18946.hp1 NA18956.hp2 NA18957.hp2 others(3): Show |
intron_variant | MODIFIER | c.222-295T>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40730638 | ||||||
chr5:40730979
|
A | G | 5 | a0001c0001t0012g0180a0001c0001t0012g0181a0001c0001t0012g0182others(2): Show | 5 | HG01192.hp1 HG02280.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.222-636T>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40730979 | ||||||
chr5:40731044
|
G | A | 13 | a0001c0001t0005g0015a0001c0001t0005g0037a0001c0001t0005g0038others(10): Show | 18 | HG00597.hp2 HG00735.hp2 HG01433.hp1 others(15): Show |
intron_variant | MODIFIER | c.222-701C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40731044 | ||||||
chr5:40731052
|
T | C | 55 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(52): Show | 77 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(74): Show |
intron_variant | MODIFIER | c.222-709A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40731052 | ||||||
chr5:40731072
|
T | C | 73 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(70): Show | 98 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.222-729A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40731072 | ||||||
chr5:40731135
|
C | G | 1 | a0001c0001t0002g0060 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.222-792G>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40731135 | ||||||
chr5:40731234
|
A | T | 16 | a0001c0001t0004g0249a0001c0001t0005g0015a0001c0001t0005g0037others(13): Show | 21 | HG00597.hp2 HG00735.hp2 HG01433.hp1 others(18): Show |
intron_variant | MODIFIER | c.222-891T>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40731234 | ||||||
chr5:40731367
|
TAC | T | 232 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(229): Show | 285 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(282): Show |
intron_variant | MODIFIER | c.222-1026_222-1025d others(4): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40731367 | ||||||
chr5:40731382
|
C | A | 1 | a0001c0001t0005g0276 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.222-1039G>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40731382 | ||||||
chr5:40731474
|
G | A | 1 | a0001c0001t0001g0189 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.222-1131C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40731474 | ||||||
chr5:40731647
|
G | A | 2 | a0001c0001t0002g0064a0001c0001t0002g0162 | 2 | HG02886.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.222-1304C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40731647 | ||||||
chr5:40731647
|
G | C | 5 | a0001c0001t0011g0008a0001c0001t0011g0046a0001c0001t0015g0312others(2): Show | 7 | HG02280.hp2 HG02976.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.222-1304C>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40731647 | ||||||
chr5:40731796
|
C | T | 2 | a0001c0001t0004g0168a0001c0001t0004g0169 | 2 | HG03453.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.222-1453G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40731796 | ||||||
chr5:40732029
|
T | A | 2 | a0001c0001t0004g0283a0001c0001t0004g0284 | 2 | HG02486.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.222-1686A>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40732029 | ||||||
chr5:40732224
|
T | C | 5 | a0001c0001t0011g0008a0001c0001t0011g0046a0001c0001t0015g0312others(2): Show | 7 | HG02280.hp2 HG02976.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.222-1881A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40732224 | ||||||
chr5:40732302
|
C | G | 8 | a0002c0002t0008g0012a0002c0002t0008g0195a0002c0002t0008g0196others(5): Show | 10 | HG00408.hp2 HG00597.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.222-1959G>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40732302 | ||||||
chr5:40732327
|
C | T | 1 | a0001c0001t0038g0184 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.222-1984G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40732327 | ||||||
chr5:40732381
|
G | A | 1 | a0001c0001t0004g0251 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.222-2038C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40732381 | ||||||
chr5:40732395
|
T | C | 5 | a0001c0001t0011g0008a0001c0001t0011g0046a0001c0001t0015g0312others(2): Show | 7 | HG02280.hp2 HG02976.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.222-2052A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40732395 | ||||||
chr5:40732556
|
A | G | 1 | a0002c0002t0008g0196 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.222-2213T>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40732556 | ||||||
chr5:40732611
|
A | AT | 8 | a0002c0002t0008g0012a0002c0002t0008g0195a0002c0002t0008g0196others(5): Show | 10 | HG00408.hp2 HG00597.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.222-2269dupA | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40732611 | ||||||
chr5:40732733
|
C | T | 4 | a0001c0001t0013g0047a0001c0001t0013g0048a0001c0001t0013g0049others(1): Show | 4 | HG01106.hp1 HG02572.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.222-2390G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40732733 | ||||||
chr5:40732739
|
G | A | 1 | a0001c0001t0010g0089 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.222-2396C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40732739 | ||||||
chr5:40733101
|
C | T | 5 | a0001c0001t0001g0025a0001c0001t0001g0176a0001c0001t0001g0177others(2): Show | 6 | HG01167.hp2 HG01169.hp2 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.222-2758G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40733101 | ||||||
chr5:40733104
|
T | C | 73 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(70): Show | 98 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.222-2761A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40733104 | ||||||
chr5:40733223
|
T | C | 2 | a0001c0001t0010g0087a0001c0001t0010g0088 | 2 | HG02257.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.222-2880A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40733223 | ||||||
chr5:40733458
|
G | C | 1 | a0001c0001t0003g0093 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.222-3115C>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40733458 | ||||||
chr5:40733475
|
A | C | 2 | a0001c0001t0004g0168a0001c0001t0004g0169 | 2 | HG03453.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.222-3132T>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40733475 | ||||||
chr5:40733592
|
A | G | 227 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(224): Show | 280 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(277): Show |
intron_variant | MODIFIER | c.222-3249T>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40733592 | ||||||
chr5:40733620
|
C | T | 1 | a0001c0001t0004g0250 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.222-3277G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40733620 | ||||||
chr5:40733754
|
C | T | 2 | a0001c0001t0010g0087a0001c0001t0010g0088 | 2 | HG02257.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.222-3411G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40733754 | ||||||
chr5:40733810
|
C | T | 2 | a0001c0001t0009g0041a0001c0001t0009g0308 | 3 | HG03098.hp2 HG03209.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.222-3467G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40733810 | ||||||
chr5:40733999
|
C | T | 1 | a0001c0001t0037g0052 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.222-3656G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40733999 | ||||||
chr5:40734081
|
A | C | 4 | a0001c0001t0013g0047a0001c0001t0013g0048a0001c0001t0013g0049others(1): Show | 4 | HG01106.hp1 HG02572.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.222-3738T>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40734081 | ||||||
chr5:40734290
|
C | G | 3 | a0001c0001t0010g0090a0001c0001t0010g0091a0001c0001t0010g0092 | 3 | HG02647.hp1 HG02818.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.222-3947G>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40734290 | ||||||
chr5:40734314
|
T | TGAACAGA others(1): Show |
132 | a0001c0001t0001g0053a0001c0001t0002g0002a0001c0001t0002g0009others(129): Show | 156 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(153): Show |
intron_variant | MODIFIER | c.222-3972_222-3971i others(10): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40734314 | ||||||
chr5:40734316
|
G | GAACAGAC others(1): Show |
132 | a0001c0001t0001g0053a0001c0001t0002g0002a0001c0001t0002g0009others(129): Show | 156 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(153): Show |
intron_variant | MODIFIER | c.222-3974_222-3973i others(10): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40734316 | ||||||
chr5:40734408
|
A | G | 1 | a0001c0001t0010g0089 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.222-4065T>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40734408 | ||||||
chr5:40734524
|
T | C | 73 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(70): Show | 98 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.222-4181A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40734524 | ||||||
chr5:40734924
|
T | C | 3 | a0001c0001t0010g0090a0001c0001t0010g0091a0001c0001t0010g0092 | 3 | HG02647.hp1 HG02818.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.222-4581A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40734924 | ||||||
chr5:40734929
|
A | G | 1 | a0002c0002t0008g0196 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.222-4586T>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40734929 | ||||||
chr5:40735211
|
T | C | 2 | a0001c0001t0004g0283a0001c0001t0004g0284 | 2 | HG02486.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.222-4868A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40735211 | ||||||
chr5:40735241
|
G | C | 5 | a0001c0001t0011g0008a0001c0001t0011g0046a0001c0001t0015g0312others(2): Show | 7 | HG02280.hp2 HG02976.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.222-4898C>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40735241 | ||||||
chr5:40735461
|
G | C | 2 | a0001c0001t0004g0283a0001c0001t0004g0284 | 2 | HG02486.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.222-5118C>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40735461 | ||||||
chr5:40735737
|
G | C | 5 | a0001c0001t0011g0008a0001c0001t0011g0046a0001c0001t0015g0312others(2): Show | 7 | HG02280.hp2 HG02976.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.222-5394C>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40735737 | ||||||
chr5:40735824
|
G | A | 70 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(67): Show | 95 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.222-5481C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40735824 | ||||||
chr5:40735873
|
G | T | 8 | a0002c0002t0008g0012a0002c0002t0008g0195a0002c0002t0008g0196others(5): Show | 10 | HG00408.hp2 HG00597.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.222-5530C>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40735873 | ||||||
chr5:40736065
|
A | G | 1 | a0001c0001t0029g0051 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.222-5722T>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40736065 | ||||||
chr5:40736187
|
C | A | 1 | a0001c0001t0001g0218 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.222-5844G>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40736187 | ||||||
chr5:40736189
|
G | A | 28 | a0001c0001t0004g0003a0001c0001t0004g0007a0001c0001t0004g0033others(25): Show | 41 | HG00558.hp2 HG01070.hp1 HG01071.hp1 others(38): Show |
intron_variant | MODIFIER | c.222-5846C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40736189 | ||||||
chr5:40736209
|
G | A | 2 | a0001c0001t0001g0240a0001c0001t0001g0241 | 2 | HG01358.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.222-5866C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40736209 | ||||||
chr5:40736225
|
C | A | 1 | a0001c0001t0012g0194 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.222-5882G>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40736225 | ||||||
chr5:40736269
|
C | T | 1 | a0001c0001t0027g0065 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.222-5926G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40736269 | ||||||
chr5:40736702
|
A | G | 2 | a0001c0001t0016g0019a0001c0001t0016g0103 | 3 | HG02083.hp1 NA18946.hp2 NA18956.hp1 |
intron_variant | MODIFIER | c.222-6359T>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40736702 | ||||||
chr5:40736759
|
T | G | 1 | a0001c0001t0003g0101 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.222-6416A>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40736759 | ||||||
chr5:40736802
|
C | T | 1 | a0001c0001t0005g0275 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.222-6459G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40736802 | ||||||
chr5:40736885
|
ATACTCAC others(11): Show |
A | 1 | a0001c0001t0006g0304 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.222-6560_222-6543d others(20): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40736885 | ||||||
chr5:40737087
|
G | A | 5 | a0001c0001t0001g0025a0001c0001t0001g0176a0001c0001t0001g0177others(2): Show | 6 | HG01167.hp2 HG01169.hp2 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.222-6744C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40737087 | ||||||
chr5:40737098
|
T | C | 303 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(300): Show | 377 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(374): Show |
intron_variant | MODIFIER | c.222-6755A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40737098 | ||||||
chr5:40737147
|
A | G | 3 | a0001c0001t0004g0255a0001c0001t0004g0270a0001c0001t0004g0273 | 3 | NA18956.hp2 NA18957.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.222-6804T>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40737147 | ||||||
chr5:40737226
|
A | G | 5 | a0001c0001t0011g0008a0001c0001t0011g0046a0001c0001t0015g0312others(2): Show | 7 | HG02280.hp2 HG02976.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.222-6883T>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40737226 | ||||||
chr5:40737234
|
T | C | 5 | a0001c0001t0011g0008a0001c0001t0011g0046a0001c0001t0015g0312others(2): Show | 7 | HG02280.hp2 HG02976.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.222-6891A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40737234 | ||||||
chr5:40737329
|
C | T | 2 | a0001c0001t0012g0180a0001c0001t0012g0182 | 2 | HG01192.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.222-6986G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40737329 | ||||||
chr5:40737522
|
C | T | 1 | a0001c0001t0006g0305 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.222-7179G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40737522 | ||||||
chr5:40737600
|
A | G | 2 | a0001c0001t0004g0250a0001c0001t0004g0251 | 2 | HG02145.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.222-7257T>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40737600 | ||||||
chr5:40737680
|
A | G | 1 | a0001c0001t0013g0050 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.222-7337T>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40737680 | ||||||
chr5:40737853
|
G | C | 4 | a0001c0001t0002g0086a0001c0001t0002g0133a0001c0001t0002g0134others(1): Show | 4 | HG02109.hp1 HG03130.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.222-7510C>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40737853 | ||||||
chr5:40737921
|
G | A | 3 | a0001c0001t0017g0191a0001c0001t0017g0192a0001c0001t0017g0193 | 3 | HG02717.hp2 HG02922.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.222-7578C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40737921 | ||||||
chr5:40738237
|
C | A | 1 | a0001c0001t0007g0301 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.222-7894G>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738237 | ||||||
chr5:40738283
|
G | A | 1 | a0001c0001t0006g0305 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.222-7940C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738283 | ||||||
chr5:40738284
|
C | A | 55 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(52): Show | 77 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(74): Show |
intron_variant | MODIFIER | c.222-7941G>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738284 | ||||||
chr5:40738291
|
G | A | 10 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0183others(7): Show | 12 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(9): Show |
intron_variant | MODIFIER | c.222-7948C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738291 | ||||||
chr5:40738323
|
G | A | 1 | a0001c0001t0002g0056 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.222-7980C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738323 | ||||||
chr5:40738378
|
G | A | 236 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(233): Show | 289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.222-8035C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738378 | ||||||
chr5:40738426
|
A | T | 5 | a0001c0001t0011g0008a0001c0001t0011g0046a0001c0001t0015g0312others(2): Show | 7 | HG02280.hp2 HG02976.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.222-8083T>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738426 | ||||||
chr5:40738432
|
AAATATAA others(90): Show |
A | 1 | a0001c0001t0015g0312 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.222-8186_222-8090d others(99): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738432 | ||||||
chr5:40738432
|
AAATATAA others(100): Show |
A | 4 | a0001c0001t0011g0008a0001c0001t0011g0046a0001c0001t0015g0313others(1): Show | 6 | HG02280.hp2 HG02976.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.222-8196_222-8090d others(2): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738432 | ||||||
chr5:40738435
|
T | C | 1 | a0001c0001t0004g0261 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.222-8092A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738435 | ||||||
chr5:40738435
|
TATAAA | T | 28 | a0001c0001t0001g0031a0001c0001t0001g0211a0001c0001t0001g0222others(25): Show | 30 | HG01099.hp2 HG01123.hp2 HG01433.hp1 others(27): Show |
intron_variant | MODIFIER | c.222-8097_222-8093d others(7): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738435 | ||||||
chr5:40738439
|
AAATAAAA others(3): Show |
A | 63 | a0001c0001t0001g0205a0001c0001t0001g0207a0001c0001t0001g0224others(60): Show | 81 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.222-8106_222-8097d others(12): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738439 | ||||||
chr5:40738439
|
AAATAAAA others(8): Show |
A | 56 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0053others(53): Show | 70 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.222-8111_222-8097d others(17): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738439 | ||||||
chr5:40738439
|
AAATAAAA others(13): Show |
A | 25 | a0001c0001t0001g0014a0001c0001t0001g0240a0001c0001t0001g0241others(22): Show | 27 | HG00280.hp1 HG00673.hp2 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.222-8116_222-8097d others(22): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738439 | ||||||
chr5:40738439
|
AAATAAAA others(18): Show |
A | 28 | a0001c0001t0001g0006a0001c0001t0001g0028a0001c0001t0001g0029others(25): Show | 36 | HG00423.hp2 HG00558.hp1 HG00597.hp1 others(33): Show |
intron_variant | MODIFIER | c.222-8121_222-8097d others(27): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738439 | ||||||
chr5:40738439
|
AAATAAAA others(23): Show |
A | 5 | a0001c0001t0001g0004a0001c0001t0001g0232a0001c0001t0001g0233others(2): Show | 9 | HG01257.hp1 HG01496.hp2 HG01928.hp2 others(6): Show |
intron_variant | MODIFIER | c.222-8126_222-8097d others(32): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738439 | ||||||
chr5:40738444
|
A | AAATAC | 11 | a0001c0001t0004g0283a0001c0001t0004g0284a0001c0001t0006g0290others(8): Show | 12 | HG00733.hp2 HG01433.hp2 HG01515.hp1 others(9): Show |
intron_variant | MODIFIER | c.222-8106_222-8102d others(7): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738444 | ||||||
chr5:40738444
|
A | AAATACAA others(3): Show |
2 | a0001c0001t0006g0289a0001c0001t0007g0311 | 2 | HG03453.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.222-8111_222-8102d others(12): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738444 | ||||||
chr5:40738444
|
A | C | 10 | a0001c0001t0001g0236a0001c0001t0002g0016a0001c0001t0002g0055others(7): Show | 11 | HG01074.hp2 HG01081.hp1 HG01257.hp2 others(8): Show |
intron_variant | MODIFIER | c.222-8101T>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738444 | ||||||
chr5:40738444
|
AAATAC | A | 22 | a0001c0001t0001g0025a0001c0001t0001g0177a0001c0001t0001g0179others(19): Show | 26 | HG00735.hp2 HG01074.hp1 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.222-8106_222-8102d others(7): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738444 | ||||||
chr5:40738444
|
AAATACAA others(3): Show |
A | 7 | a0001c0001t0004g0033a0001c0001t0004g0270a0001c0001t0005g0038others(4): Show | 11 | HG00741.hp2 HG01261.hp2 HG01516.hp1 others(8): Show |
intron_variant | MODIFIER | c.222-8111_222-8102d others(12): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738444 | ||||||
chr5:40738444
|
AAATACAA others(13): Show |
A | 4 | a0001c0001t0013g0047a0001c0001t0013g0048a0001c0001t0013g0049others(1): Show | 4 | HG01106.hp1 HG02572.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.222-8121_222-8102d others(22): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738444 | ||||||
chr5:40738454
|
C | A | 2 | a0001c0001t0010g0087a0001c0001t0010g0088 | 2 | HG02257.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.222-8111G>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738454 | ||||||
chr5:40738484
|
C | A | 3 | a0001c0001t0012g0180a0001c0001t0012g0181a0001c0001t0012g0194 | 3 | HG02280.hp1 HG02965.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.222-8141G>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738484 | ||||||
chr5:40738489
|
C | A | 2 | a0001c0001t0001g0176a0001c0001t0001g0178 | 2 | HG01243.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.222-8146G>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738489 | ||||||
chr5:40738489
|
C | CAATAAAA others(3): Show |
1 | a0001c0001t0004g0169 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.222-8147_222-8146i others(12): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738489 | ||||||
chr5:40738494
|
C | A | 14 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0177others(11): Show | 16 | HG00099.hp1 HG01167.hp2 HG01168.hp1 others(13): Show |
intron_variant | MODIFIER | c.222-8151G>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738494 | ||||||
chr5:40738499
|
C | A | 16 | a0001c0001t0001g0026a0001c0001t0001g0176a0001c0001t0001g0178others(13): Show | 17 | HG00323.hp2 HG00642.hp1 HG00733.hp1 others(14): Show |
intron_variant | MODIFIER | c.222-8156G>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738499 | ||||||
chr5:40738504
|
C | A | 10 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0176others(7): Show | 14 | HG00099.hp1 HG01167.hp2 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.222-8161G>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738504 | ||||||
chr5:40738509
|
A | C | 13 | a0001c0001t0001g0176a0001c0001t0001g0178a0001c0001t0001g0220others(10): Show | 15 | HG00323.hp1 HG01070.hp1 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.222-8166T>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738509 | ||||||
chr5:40738514
|
C | A | 15 | a0001c0001t0001g0026a0001c0001t0001g0176a0001c0001t0001g0178others(12): Show | 18 | HG00323.hp2 HG00642.hp1 HG00733.hp1 others(15): Show |
intron_variant | MODIFIER | c.222-8171G>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738514 | ||||||
chr5:40738514
|
CAATAA | C | 3 | a0001c0001t0001g0027a0001c0001t0001g0187a0003c0003t0001g0188 | 4 | HG00099.hp1 HG01168.hp1 HG01884.hp2 others(1): Show |
intron_variant | MODIFIER | c.222-8176_222-8172d others(7): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738514 | ||||||
chr5:40738519
|
A | AAATAAAA others(3): Show |
7 | a0001c0001t0002g0021a0001c0001t0002g0138a0001c0001t0002g0141others(4): Show | 8 | HG01109.hp2 HG01361.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.222-8186_222-8177d others(12): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738519 | ||||||
chr5:40738519
|
A | C | 16 | a0001c0001t0001g0026a0001c0001t0001g0176a0001c0001t0001g0178others(13): Show | 17 | HG00323.hp2 HG00642.hp1 HG00733.hp1 others(14): Show |
intron_variant | MODIFIER | c.222-8176T>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738519 | ||||||
chr5:40738524
|
A | C | 11 | a0001c0001t0001g0025a0001c0001t0001g0177a0001c0001t0001g0179others(8): Show | 14 | HG01167.hp2 HG01169.hp2 HG01255.hp1 others(11): Show |
intron_variant | MODIFIER | c.222-8181T>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738524 | ||||||
chr5:40738529
|
C | A | 16 | a0001c0001t0001g0025a0001c0001t0001g0177a0001c0001t0001g0179others(13): Show | 19 | HG01070.hp1 HG01071.hp1 HG01167.hp2 others(16): Show |
intron_variant | MODIFIER | c.222-8186G>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738529 | ||||||
chr5:40738534
|
A | C | 8 | a0001c0001t0001g0025a0001c0001t0001g0177a0001c0001t0001g0179others(5): Show | 11 | HG01070.hp1 HG01071.hp1 HG01167.hp2 others(8): Show |
intron_variant | MODIFIER | c.222-8191T>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738534 | ||||||
chr5:40738539
|
C | A | 27 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(24): Show | 32 | HG00099.hp1 HG00642.hp1 HG00733.hp1 others(29): Show |
intron_variant | MODIFIER | c.222-8196G>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738539 | ||||||
chr5:40738539
|
C | CAATAA | 4 | a0001c0001t0004g0250a0001c0001t0004g0283a0001c0001t0004g0284others(1): Show | 4 | HG02486.hp2 HG03471.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.222-8201_222-8197d others(7): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738539 | ||||||
chr5:40738539
|
C | CAATAAAA others(3): Show |
5 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0203others(2): Show | 7 | NA18966.hp1 NA18966.hp2 NA18987.hp1 others(4): Show |
intron_variant | MODIFIER | c.222-8206_222-8197d others(12): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738539 | ||||||
chr5:40738539
|
C | CAATAAAA others(8): Show |
16 | a0001c0001t0002g0132a0001c0001t0002g0139a0001c0001t0002g0140others(13): Show | 17 | HG00280.hp1 HG00741.hp1 HG01123.hp1 others(14): Show |
intron_variant | MODIFIER | c.222-8197_222-8196i others(17): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738539 | ||||||
chr5:40738539
|
C | CAATAAAA others(13): Show |
74 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0028others(71): Show | 93 | HG00099.hp2 HG00408.hp1 HG00673.hp2 others(90): Show |
intron_variant | MODIFIER | c.222-8197_222-8196i others(22): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738539 | ||||||
chr5:40738539
|
C | CAATAAAA others(18): Show |
31 | a0001c0001t0002g0002a0001c0001t0002g0016a0001c0001t0002g0017others(28): Show | 39 | HG00423.hp1 HG00673.hp1 HG01081.hp2 others(36): Show |
intron_variant | MODIFIER | c.222-8197_222-8196i others(27): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738539 | ||||||
chr5:40738539
|
C | CAATAAAA others(23): Show |
8 | a0001c0001t0001g0286a0001c0001t0002g0009a0001c0001t0002g0072others(5): Show | 10 | HG02602.hp1 HG03579.hp1 HG03688.hp1 others(7): Show |
intron_variant | MODIFIER | c.222-8197_222-8196i others(32): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738539 | ||||||
chr5:40738539
|
C | CAATAAAA others(23): Show |
2 | a0001c0001t0001g0053a0001c0001t0018g0102 | 2 | NA19059.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.222-8197_222-8196i others(32): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738539 | ||||||
chr5:40738539
|
CAATAA | C | 3 | a0001c0001t0004g0034a0001c0001t0004g0035a0001c0001t0004g0268 | 5 | HG01099.hp1 HG03017.hp2 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.222-8201_222-8197d others(7): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738539 | ||||||
chr5:40738539
|
CAATAAAA others(3): Show |
C | 1 | a0001c0001t0026g0282 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.222-8206_222-8197d others(12): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738539 | ||||||
chr5:40738539
|
CAATAAAA others(8): Show |
C | 19 | a0001c0001t0004g0007a0001c0001t0004g0033a0001c0001t0004g0036others(16): Show | 25 | HG00558.hp2 HG02129.hp1 HG02165.hp2 others(22): Show |
intron_variant | MODIFIER | c.222-8211_222-8197d others(17): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738539 | ||||||
chr5:40738544
|
A | C | 4 | a0001c0001t0004g0251a0001c0001t0004g0265a0001c0001t0004g0266others(1): Show | 4 | HG01070.hp1 HG01071.hp1 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.222-8201T>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738544 | ||||||
chr5:40738549
|
A | C | 51 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0013others(48): Show | 66 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(63): Show |
intron_variant | MODIFIER | c.222-8206T>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738549 | ||||||
chr5:40738559
|
A | T | 1 | a0001c0001t0001g0189 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.222-8216T>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738559 | ||||||
chr5:40738562
|
T | A | 1 | a0001c0001t0001g0189 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.222-8219A>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738562 | ||||||
chr5:40738564
|
A | T | 15 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(12): Show | 18 | HG00099.hp1 HG00642.hp1 HG00733.hp1 others(15): Show |
intron_variant | MODIFIER | c.222-8221T>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738564 | ||||||
chr5:40738564
|
AAAT | A | 2 | a0001c0001t0011g0008a0001c0001t0011g0046 | 4 | HG02976.hp1 HG03139.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.222-8224_222-8222d others(5): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738564 | ||||||
chr5:40738567
|
T | A | 20 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(17): Show | 23 | HG00099.hp1 HG00642.hp1 HG00733.hp1 others(20): Show |
intron_variant | MODIFIER | c.222-8224A>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738567 | ||||||
chr5:40738567
|
T | TAAAATAA others(1): Show |
3 | a0001c0001t0003g0100a0001c0001t0003g0101a0001c0001t0003g0125 | 3 | HG01074.hp2 NA18948.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.222-8225_222-8224i others(10): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738567 | ||||||
chr5:40738567
|
T | TAAAATAA others(8): Show |
2 | a0001c0001t0010g0087a0001c0001t0010g0088 | 2 | HG02257.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.222-8225_222-8224i others(17): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738567 | ||||||
chr5:40738567
|
T | TAAAATAA others(13): Show |
1 | a0001c0001t0010g0089 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.222-8225_222-8224i others(22): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738567 | ||||||
chr5:40738567
|
T | TAAAATAA others(6): Show |
3 | a0001c0001t0017g0191a0001c0001t0017g0192a0001c0001t0017g0193 | 3 | HG02717.hp2 HG02922.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.222-8225_222-8224i others(15): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738567 | ||||||
chr5:40738567
|
T | TAAAATAA others(11): Show |
1 | a0001c0001t0002g0137 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.222-8225_222-8224i others(20): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738567 | ||||||
chr5:40738567
|
T | TAAAATAA others(23): Show |
3 | a0001c0001t0002g0074a0001c0001t0002g0075a0001c0001t0030g0073 | 3 | HG02071.hp2 NA18960.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.222-8225_222-8224i others(32): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738567 | ||||||
chr5:40738567
|
T | TAAAATAA others(33): Show |
1 | a0001c0001t0001g0207 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.222-8225_222-8224i others(42): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738567 | ||||||
chr5:40738567
|
T | TAAAATAA others(18): Show |
8 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0224others(5): Show | 8 | HG01175.hp2 HG02683.hp2 HG03704.hp1 others(5): Show |
intron_variant | MODIFIER | c.222-8225_222-8224i others(27): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738567 | ||||||
chr5:40738567
|
T | TAAAATAA others(23): Show |
23 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0173others(20): Show | 36 | HG00280.hp2 HG00423.hp2 HG00558.hp1 others(33): Show |
intron_variant | MODIFIER | c.222-8225_222-8224i others(32): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738567 | ||||||
chr5:40738567
|
T | TAAAATAA others(28): Show |
6 | a0001c0001t0001g0013a0001c0001t0001g0204a0001c0001t0001g0205others(3): Show | 8 | HG00408.hp2 HG02080.hp1 NA18942.hp2 others(5): Show |
intron_variant | MODIFIER | c.222-8225_222-8224i others(37): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738567 | ||||||
chr5:40738567
|
T | TAAAATAA others(33): Show |
1 | a0001c0001t0001g0208 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.222-8225_222-8224i others(42): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738567 | ||||||
chr5:40738567
|
T | TAAAATAA others(13): Show |
3 | a0001c0001t0001g0220a0001c0001t0001g0221a0001c0001t0002g0084 | 3 | HG00323.hp1 HG02293.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.222-8225_222-8224i others(22): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738567 | ||||||
chr5:40738567
|
T | TAAAATAA others(18): Show |
2 | a0001c0001t0001g0240a0001c0001t0001g0241 | 2 | HG01358.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.222-8225_222-8224i others(27): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738567 | ||||||
chr5:40738567
|
T | TAAAATAA others(8): Show |
3 | a0001c0001t0013g0047a0001c0001t0013g0048a0001c0001t0013g0049 | 3 | HG02572.hp1 HG02895.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.222-8225_222-8224i others(17): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738567 | ||||||
chr5:40738567
|
T | TAAAATAT others(3): Show |
1 | a0001c0001t0013g0050 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.222-8225_222-8224i others(12): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738567 | ||||||
chr5:40738567
|
T | TAAAATAT others(8): Show |
1 | a0001c0001t0012g0194 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.222-8225_222-8224i others(17): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738567 | ||||||
chr5:40738567
|
T | TAAAATAT others(13): Show |
1 | a0001c0001t0023g0174 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.222-8225_222-8224i others(22): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738567 | ||||||
chr5:40738569
|
T | A | 85 | a0001c0001t0001g0053a0001c0001t0002g0021a0001c0001t0002g0023others(82): Show | 99 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(96): Show |
intron_variant | MODIFIER | c.222-8226A>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738569 | ||||||
chr5:40738572
|
A | AAT | 8 | a0001c0001t0002g0137a0001c0001t0003g0100a0001c0001t0003g0101others(5): Show | 8 | HG01074.hp2 HG02630.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.221+8224_221+8225d others(4): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738572 | ||||||
chr5:40738572
|
A | AATAAAAT others(5): Show |
2 | a0001c0001t0010g0091a0001c0001t0010g0092 | 2 | HG02647.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.221+8214_221+8225d others(14): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738572 | ||||||
chr5:40738572
|
A | T | 85 | a0001c0001t0001g0053a0001c0001t0002g0021a0001c0001t0002g0023others(82): Show | 99 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(96): Show |
intron_variant | MODIFIER | c.221+8226T>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738572 | ||||||
chr5:40738669
|
T | C | 3 | a0001c0001t0010g0090a0001c0001t0010g0091a0001c0001t0010g0092 | 3 | HG02647.hp1 HG02818.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.221+8129A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738669 | ||||||
chr5:40738838
|
T | C | 70 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(67): Show | 95 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.221+7960A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738838 | ||||||
chr5:40738911
|
C | G | 2 | a0001c0001t0001g0209a0001c0001t0001g0210 | 2 | NA18983.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.221+7887G>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738911 | ||||||
chr5:40738929
|
T | C | 5 | a0001c0001t0011g0008a0001c0001t0011g0046a0001c0001t0015g0312others(2): Show | 7 | HG02280.hp2 HG02976.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.221+7869A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40738929 | ||||||
chr5:40739007
|
T | C | 1 | a0002c0002t0008g0198 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.221+7791A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40739007 | ||||||
chr5:40739137
|
A | G | 236 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(233): Show | 289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.221+7661T>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40739137 | ||||||
chr5:40739159
|
C | T | 139 | a0001c0001t0001g0053a0001c0001t0002g0002a0001c0001t0002g0009others(136): Show | 163 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.221+7639G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40739159 | ||||||
chr5:40739212
|
T | A | 1 | a0002c0002t0008g0198 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.221+7586A>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40739212 | ||||||
chr5:40739333
|
T | C | 5 | a0001c0001t0011g0008a0001c0001t0011g0046a0001c0001t0015g0312others(2): Show | 7 | HG02280.hp2 HG02976.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.221+7465A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40739333 | ||||||
chr5:40739602
|
T | C | 1 | a0001c0001t0004g0268 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.221+7196A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40739602 | ||||||
chr5:40739610
|
G | A | 1 | a0001c0001t0006g0288 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.221+7188C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40739610 | ||||||
chr5:40739921
|
A | C | 5 | a0001c0001t0001g0025a0001c0001t0001g0176a0001c0001t0001g0177others(2): Show | 6 | HG01167.hp2 HG01169.hp2 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.221+6877T>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40739921 | ||||||
chr5:40739936
|
C | CT | 6 | a0002c0002t0008g0012a0002c0002t0008g0195a0002c0002t0008g0196others(3): Show | 8 | HG00597.hp1 HG02015.hp1 HG02040.hp1 others(5): Show |
intron_variant | MODIFIER | c.221+6861dupA | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40739936 | ||||||
chr5:40739943
|
T | TA | 5 | a0001c0001t0011g0008a0001c0001t0011g0046a0001c0001t0015g0312others(2): Show | 7 | HG02280.hp2 HG02976.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.221+6854_221+6855i others(3): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40739943 | ||||||
chr5:40739944
|
T | A | 102 | a0001c0001t0001g0053a0001c0001t0002g0023a0001c0001t0002g0024others(99): Show | 123 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(120): Show |
intron_variant | MODIFIER | c.221+6854A>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40739944 | ||||||
chr5:40740152
|
T | C | 1 | a0001c0001t0037g0052 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.221+6646A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40740152 | ||||||
chr5:40740601
|
C | T | 1 | a0001c0001t0002g0056 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.221+6197G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40740601 | ||||||
chr5:40740716
|
C | T | 1 | a0001c0001t0002g0172 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.221+6082G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40740716 | ||||||
chr5:40740759
|
T | C | 1 | a0001c0001t0002g0165 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.221+6039A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40740759 | ||||||
chr5:40740784
|
C | T | 1 | a0001c0001t0002g0054 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.221+6014G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40740784 | ||||||
chr5:40740909
|
G | A | 2 | a0001c0001t0006g0044a0001c0001t0006g0304 | 3 | HG01256.hp2 HG01258.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.221+5889C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40740909 | ||||||
chr5:40740997
|
A | G | 3 | a0001c0001t0017g0191a0001c0001t0017g0192a0001c0001t0017g0193 | 3 | HG02717.hp2 HG02922.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.221+5801T>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40740997 | ||||||
chr5:40740998
|
G | C | 1 | a0001c0001t0001g0237 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.221+5800C>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40740998 | ||||||
chr5:40741021
|
C | T | 236 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(233): Show | 289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.221+5777G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40741021 | ||||||
chr5:40741406
|
C | T | 285 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(282): Show | 356 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(353): Show |
intron_variant | MODIFIER | c.221+5392G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40741406 | ||||||
chr5:40741522
|
T | C | 1 | a0001c0001t0004g0270 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.221+5276A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40741522 | ||||||
chr5:40741595
|
C | CCAACTGC others(8): Show |
1 | a0001c0001t0006g0305 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.221+5202_221+5203i others(17): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40741595 | ||||||
chr5:40741596
|
A | C | 1 | a0001c0001t0006g0305 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.221+5202T>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40741596 | ||||||
chr5:40741603
|
A | T | 1 | a0001c0001t0006g0305 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.221+5195T>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40741603 | ||||||
chr5:40741609
|
C | A | 1 | a0001c0001t0006g0305 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.221+5189G>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40741609 | ||||||
chr5:40741614
|
C | G | 1 | a0001c0001t0006g0305 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.221+5184G>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40741614 | ||||||
chr5:40741618
|
A | G | 1 | a0001c0001t0006g0305 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.221+5180T>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40741618 | ||||||
chr5:40741620
|
G | C | 1 | a0001c0001t0006g0305 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.221+5178C>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40741620 | ||||||
chr5:40741620
|
G | T | 8 | a0002c0002t0008g0012a0002c0002t0008g0195a0002c0002t0008g0196others(5): Show | 10 | HG00408.hp2 HG00597.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.221+5178C>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40741620 | ||||||
chr5:40741631
|
A | T | 2 | a0001c0001t0003g0096a0001c0001t0003g0097 | 2 | NA18952.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.221+5167T>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40741631 | ||||||
chr5:40741648
|
T | G | 1 | a0001c0001t0006g0305 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.221+5150A>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40741648 | ||||||
chr5:40741661
|
T | G | 1 | a0001c0001t0006g0305 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.221+5137A>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40741661 | ||||||
chr5:40741702
|
A | G | 10 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0183others(7): Show | 12 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(9): Show |
intron_variant | MODIFIER | c.221+5096T>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40741702 | ||||||
chr5:40741713
|
G | A | 2 | a0001c0001t0009g0306a0001c0001t0009g0307 | 2 | NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.221+5085C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40741713 | ||||||
chr5:40741743
|
C | A | 5 | a0001c0001t0011g0008a0001c0001t0011g0046a0001c0001t0015g0312others(2): Show | 7 | HG02280.hp2 HG02976.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.221+5055G>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40741743 | ||||||
chr5:40741890
|
G | A | 1 | a0001c0001t0009g0308 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.221+4908C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40741890 | ||||||
chr5:40741904
|
G | A | 2 | a0001c0001t0002g0150a0001c0001t0002g0153 | 2 | HG01123.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.221+4894C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40741904 | ||||||
chr5:40741977
|
G | A | 1 | a0001c0001t0002g0165 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.221+4821C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40741977 | ||||||
chr5:40742201
|
C | T | 1 | a0001c0001t0010g0089 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.221+4597G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40742201 | ||||||
chr5:40742336
|
T | C | 5 | a0001c0001t0001g0238a0001c0001t0001g0240a0001c0001t0001g0241others(2): Show | 5 | HG00735.hp1 HG01175.hp2 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.221+4462A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40742336 | ||||||
chr5:40742363
|
C | T | 70 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(67): Show | 95 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.221+4435G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40742363 | ||||||
chr5:40742420
|
A | G | 1 | a0001c0001t0037g0052 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.221+4378T>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40742420 | ||||||
chr5:40742440
|
C | T | 236 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(233): Show | 289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.221+4358G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40742440 | ||||||
chr5:40742547
|
G | GC | 5 | a0001c0001t0011g0008a0001c0001t0011g0046a0001c0001t0015g0312others(2): Show | 7 | HG02280.hp2 HG02976.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.221+4250dupG | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40742547 | ||||||
chr5:40742678
|
T | A | 5 | a0001c0001t0011g0008a0001c0001t0011g0046a0001c0001t0015g0312others(2): Show | 7 | HG02280.hp2 HG02976.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.221+4120A>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40742678 | ||||||
chr5:40742759
|
G | C | 2 | a0001c0001t0004g0168a0001c0001t0004g0169 | 2 | HG03453.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.221+4039C>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40742759 | ||||||
chr5:40742910
|
G | A | 1 | a0001c0001t0007g0309 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.221+3888C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40742910 | ||||||
chr5:40742959
|
G | A | 144 | a0001c0001t0001g0053a0001c0001t0002g0002a0001c0001t0002g0009others(141): Show | 170 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(167): Show |
intron_variant | MODIFIER | c.221+3839C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40742959 | ||||||
chr5:40742969
|
T | C | 1 | a0001c0001t0007g0310 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.221+3829A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40742969 | ||||||
chr5:40742992
|
G | C | 5 | a0001c0001t0011g0008a0001c0001t0011g0046a0001c0001t0015g0312others(2): Show | 7 | HG02280.hp2 HG02976.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.221+3806C>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40742992 | ||||||
chr5:40743129
|
C | A | 5 | a0001c0001t0011g0008a0001c0001t0011g0046a0001c0001t0015g0312others(2): Show | 7 | HG02280.hp2 HG02976.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.221+3669G>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40743129 | ||||||
chr5:40743229
|
A | G | 1 | a0001c0001t0011g0046 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.221+3569T>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40743229 | ||||||
chr5:40743237
|
T | C | 2 | a0001c0001t0004g0036a0001c0001t0004g0285 | 3 | NA18954.hp1 NA18968.hp2 NA18987.hp2 |
intron_variant | MODIFIER | c.221+3561A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40743237 | ||||||
chr5:40743415
|
A | G | 17 | a0001c0001t0002g0021a0001c0001t0002g0132a0001c0001t0002g0138others(14): Show | 18 | HG00280.hp1 HG00741.hp1 HG01109.hp2 others(15): Show |
intron_variant | MODIFIER | c.221+3383T>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40743415 | ||||||
chr5:40743575
|
C | T | 1 | a0001c0001t0004g0250 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.221+3223G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40743575 | ||||||
chr5:40743623
|
A | C | 8 | a0002c0002t0008g0012a0002c0002t0008g0195a0002c0002t0008g0196others(5): Show | 10 | HG00408.hp2 HG00597.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.221+3175T>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40743623 | ||||||
chr5:40743852
|
T | C | 232 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(229): Show | 285 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(282): Show |
intron_variant | MODIFIER | c.221+2946A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40743852 | ||||||
chr5:40743870
|
T | C | 70 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(67): Show | 95 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.221+2928A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40743870 | ||||||
chr5:40743884
|
T | A | 1 | a0001c0001t0004g0273 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.221+2914A>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40743884 | ||||||
chr5:40743936
|
C | A | 1 | a0001c0001t0004g0273 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.221+2862G>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40743936 | ||||||
chr5:40743936
|
C | T | 112 | a0001c0001t0001g0053a0001c0001t0002g0002a0001c0001t0002g0009others(109): Show | 134 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.221+2862G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40743936 | ||||||
chr5:40743937
|
A | G | 1 | a0001c0001t0004g0273 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.221+2861T>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40743937 | ||||||
chr5:40743956
|
T | C | 3 | a0001c0001t0017g0191a0001c0001t0017g0192a0001c0001t0017g0193 | 3 | HG02717.hp2 HG02922.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.221+2842A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40743956 | ||||||
chr5:40743972
|
T | A | 5 | a0001c0001t0001g0025a0001c0001t0001g0176a0001c0001t0001g0177others(2): Show | 6 | HG01167.hp2 HG01169.hp2 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.221+2826A>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40743972 | ||||||
chr5:40744083
|
G | A | 3 | a0001c0001t0010g0087a0001c0001t0010g0088a0001c0001t0037g0052 | 3 | HG02257.hp2 HG02451.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.221+2715C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40744083 | ||||||
chr5:40744259
|
TAGTTA | T | 6 | a0001c0001t0001g0013a0001c0001t0001g0204a0001c0001t0001g0205others(3): Show | 8 | HG02155.hp2 NA18942.hp2 NA18945.hp1 others(5): Show |
intron_variant | MODIFIER | c.221+2534_221+2538d others(7): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40744259 | ||||||
chr5:40744299
|
C | T | 3 | a0001c0001t0017g0191a0001c0001t0017g0192a0001c0001t0017g0193 | 3 | HG02717.hp2 HG02922.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.221+2499G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40744299 | ||||||
chr5:40744487
|
G | GT | 166 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(163): Show | 215 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(212): Show |
intron_variant | MODIFIER | c.221+2310dupA | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40744487 | ||||||
chr5:40744487
|
G | GTT | 136 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(133): Show | 163 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.221+2309_221+2310d others(4): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40744487 | ||||||
chr5:40744487
|
G | GTTT | 8 | a0001c0001t0001g0176a0001c0001t0001g0183a0001c0001t0002g0133others(5): Show | 8 | HG00642.hp1 HG01256.hp1 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.221+2308_221+2310d others(5): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40744487 | ||||||
chr5:40744892
|
C | A | 4 | a0001c0001t0012g0180a0001c0001t0012g0181a0001c0001t0012g0182others(1): Show | 4 | HG01192.hp1 HG02280.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.221+1906G>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40744892 | ||||||
chr5:40745105
|
G | A | 1 | a0001c0001t0006g0291 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.221+1693C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40745105 | ||||||
chr5:40745231
|
C | T | 70 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(67): Show | 95 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.221+1567G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40745231 | ||||||
chr5:40745298
|
ATATGT | A | 66 | a0001c0001t0001g0053a0001c0001t0002g0023a0001c0001t0002g0024others(63): Show | 78 | HG00099.hp2 HG00408.hp1 HG01069.hp2 others(75): Show |
intron_variant | MODIFIER | c.221+1495_221+1499d others(7): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40745298 | ||||||
chr5:40745318
|
T | C | 1 | a0001c0001t0002g0165 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.221+1480A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40745318 | ||||||
chr5:40745357
|
T | C | 5 | a0001c0001t0012g0180a0001c0001t0012g0181a0001c0001t0012g0182others(2): Show | 5 | HG01192.hp1 HG02280.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.221+1441A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40745357 | ||||||
chr5:40745566
|
C | A | 1 | a0001c0001t0002g0172 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.221+1232G>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40745566 | ||||||
chr5:40745644
|
C | A | 10 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0183others(7): Show | 12 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(9): Show |
intron_variant | MODIFIER | c.221+1154G>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40745644 | ||||||
chr5:40745657
|
G | A | 5 | a0001c0001t0011g0008a0001c0001t0011g0046a0001c0001t0015g0312others(2): Show | 7 | HG02280.hp2 HG02976.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.221+1141C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40745657 | ||||||
chr5:40745714
|
A | C | 4 | a0001c0001t0013g0047a0001c0001t0013g0048a0001c0001t0013g0049others(1): Show | 4 | HG01106.hp1 HG02572.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.221+1084T>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40745714 | ||||||
chr5:40745810
|
C | G | 4 | a0001c0001t0006g0288a0001c0001t0006g0289a0001c0001t0006g0290others(1): Show | 4 | HG00733.hp2 HG01109.hp1 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.221+988G>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40745810 | ||||||
chr5:40745843
|
T | C | 1 | a0001c0001t0031g0315 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.221+955A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40745843 | ||||||
chr5:40746001
|
TGC | T | 3 | a0001c0001t0015g0312a0001c0001t0015g0313a0001c0001t0015g0314 | 3 | HG02280.hp2 HG03225.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.221+795_221+796del others(2): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40746001 | ||||||
chr5:40746002
|
G | A | 224 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(221): Show | 277 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.221+796C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40746002 | ||||||
chr5:40746005
|
T | C | 3 | a0001c0001t0015g0312a0001c0001t0015g0313a0001c0001t0015g0314 | 3 | HG02280.hp2 HG03225.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.221+793A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40746005 | ||||||
chr5:40746066
|
T | C | 4 | a0002c0002t0008g0012a0002c0002t0008g0199a0002c0002t0008g0200others(1): Show | 6 | HG00597.hp1 HG02040.hp1 HG02056.hp1 others(3): Show |
intron_variant | MODIFIER | c.221+732A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40746066 | ||||||
chr5:40746213
|
A | AAAAGTAA others(58): Show |
1 | a0001c0001t0031g0315 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.221+520_221+584dup others(65): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40746213 | ||||||
chr5:40746439
|
T | C | 1 | a0001c0001t0012g0194 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.221+359A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40746439 | ||||||
chr5:40746783
|
A | T | 132 | a0001c0001t0001g0053a0001c0001t0002g0002a0001c0001t0002g0009others(129): Show | 156 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(153): Show |
intron_variant | MODIFIER | c.221+15T>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 2/4 | chr5 | 40746783 | ||||||
chr5:40747063
|
T | C | 5 | a0001c0001t0011g0008a0001c0001t0011g0046a0001c0001t0015g0312others(2): Show | 7 | HG02280.hp2 HG02976.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.-1-44A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40747063 | ||||||
chr5:40747169
|
T | G | 3 | a0001c0001t0012g0180a0001c0001t0012g0181a0001c0001t0012g0182 | 3 | HG01192.hp1 HG02965.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-1-150A>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40747169 | ||||||
chr5:40747354
|
G | A | 16 | a0001c0001t0004g0249a0001c0001t0005g0015a0001c0001t0005g0037others(13): Show | 21 | HG00597.hp2 HG00735.hp2 HG01433.hp1 others(18): Show |
intron_variant | MODIFIER | c.-1-335C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40747354 | ||||||
chr5:40747442
|
A | G | 5 | a0001c0001t0001g0025a0001c0001t0001g0176a0001c0001t0001g0177others(2): Show | 6 | HG01167.hp2 HG01169.hp2 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.-1-423T>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40747442 | ||||||
chr5:40747508
|
A | G | 5 | a0001c0001t0012g0180a0001c0001t0012g0181a0001c0001t0012g0182others(2): Show | 5 | HG01192.hp1 HG02280.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.-1-489T>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40747508 | ||||||
chr5:40747514
|
C | A | 1 | a0001c0001t0004g0273 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.-1-495G>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40747514 | ||||||
chr5:40747594
|
A | G | 1 | a0001c0001t0010g0089 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-1-575T>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40747594 | ||||||
chr5:40747670
|
G | A | 1 | a0001c0001t0002g0083 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.-1-651C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40747670 | ||||||
chr5:40747830
|
CT | C | 8 | a0002c0002t0008g0012a0002c0002t0008g0195a0002c0002t0008g0196others(5): Show | 10 | HG00408.hp2 HG00597.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.-1-812delA | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40747830 | ||||||
chr5:40747855
|
T | C | 232 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(229): Show | 285 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(282): Show |
intron_variant | MODIFIER | c.-1-836A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40747855 | ||||||
chr5:40747878
|
T | G | 1 | a0001c0001t0001g0244 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.-1-859A>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40747878 | ||||||
chr5:40747897
|
A | C | 227 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(224): Show | 280 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(277): Show |
intron_variant | MODIFIER | c.-1-878T>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40747897 | ||||||
chr5:40747960
|
G | C | 1 | a0001c0001t0003g0128 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-1-941C>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40747960 | ||||||
chr5:40748070
|
G | A | 3 | a0001c0001t0005g0039a0001c0001t0005g0280a0001c0001t0005g0281 | 4 | NA18989.hp2 NA18998.hp1 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.-1-1051C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40748070 | ||||||
chr5:40748107
|
G | A | 1 | a0001c0001t0004g0251 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-1-1088C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40748107 | ||||||
chr5:40748166
|
G | A | 144 | a0001c0001t0001g0053a0001c0001t0002g0002a0001c0001t0002g0009others(141): Show | 168 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(165): Show |
intron_variant | MODIFIER | c.-1-1147C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40748166 | ||||||
chr5:40748252
|
A | G | 5 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(2): Show | 8 | HG03017.hp1 HG03490.hp1 NA18966.hp1 others(5): Show |
intron_variant | MODIFIER | c.-1-1233T>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40748252 | ||||||
chr5:40748266
|
G | A | 14 | a0001c0001t0005g0015a0001c0001t0005g0037a0001c0001t0005g0038others(11): Show | 19 | HG00597.hp2 HG00735.hp2 HG01433.hp1 others(16): Show |
intron_variant | MODIFIER | c.-1-1247C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40748266 | ||||||
chr5:40748575
|
T | C | 1 | a0001c0001t0002g0080 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.-1-1556A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40748575 | ||||||
chr5:40748628
|
C | T | 5 | a0001c0001t0011g0008a0001c0001t0011g0046a0001c0001t0015g0312others(2): Show | 7 | HG02280.hp2 HG02976.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.-1-1609G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40748628 | ||||||
chr5:40748866
|
G | A | 144 | a0001c0001t0001g0053a0001c0001t0002g0002a0001c0001t0002g0009others(141): Show | 168 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(165): Show |
intron_variant | MODIFIER | c.-1-1847C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40748866 | ||||||
chr5:40748873
|
G | A | 2 | a0001c0001t0010g0087a0001c0001t0010g0088 | 2 | HG02257.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.-1-1854C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40748873 | ||||||
chr5:40748960
|
T | C | 1 | a0001c0001t0023g0174 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-1-1941A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40748960 | ||||||
chr5:40749050
|
C | T | 3 | a0001c0001t0017g0191a0001c0001t0017g0192a0001c0001t0017g0193 | 3 | HG02717.hp2 HG02922.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-1-2031G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40749050 | ||||||
chr5:40749113
|
A | C | 1 | a0001c0001t0003g0094 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.-1-2094T>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40749113 | ||||||
chr5:40749429
|
TC | T | 5 | a0001c0001t0012g0180a0001c0001t0012g0181a0001c0001t0012g0182others(2): Show | 5 | HG01192.hp1 HG02280.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.-1-2411delG | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40749429 | ||||||
chr5:40749547
|
G | A | 1 | a0001c0001t0003g0129 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.-1-2528C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40749547 | ||||||
chr5:40749599
|
T | C | 8 | a0002c0002t0008g0012a0002c0002t0008g0195a0002c0002t0008g0196others(5): Show | 10 | HG00408.hp2 HG00597.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.-1-2580A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40749599 | ||||||
chr5:40749681
|
G | C | 6 | a0001c0001t0002g0086a0001c0001t0002g0133a0001c0001t0002g0134others(3): Show | 6 | HG02109.hp1 HG03130.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.-1-2662C>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40749681 | ||||||
chr5:40749731
|
A | G | 1 | a0001c0001t0013g0049 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-1-2712T>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40749731 | ||||||
chr5:40750020
|
A | G | 229 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(226): Show | 282 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(279): Show |
intron_variant | MODIFIER | c.-1-3001T>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40750020 | ||||||
chr5:40750084
|
T | C | 1 | a0001c0001t0022g0130 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-1-3065A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40750084 | ||||||
chr5:40750087
|
C | CA | 11 | a0001c0001t0004g0250a0001c0001t0004g0251a0001c0001t0004g0283others(8): Show | 11 | HG01192.hp1 HG02145.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.-1-3069dupT | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40750087 | ||||||
chr5:40750087
|
CA | C | 216 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(213): Show | 267 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.-1-3069delT | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40750087 | ||||||
chr5:40750087
|
CAA | C | 7 | a0001c0001t0002g0054a0001c0001t0002g0055a0001c0001t0011g0008others(4): Show | 9 | HG01258.hp2 HG02280.hp2 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.-1-3070_-1-3069del others(2): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40750087 | ||||||
chr5:40750143
|
C | T | 5 | a0001c0001t0011g0008a0001c0001t0011g0046a0001c0001t0015g0312others(2): Show | 7 | HG02280.hp2 HG02976.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.-1-3124G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40750143 | ||||||
chr5:40750174
|
C | G | 1 | a0001c0001t0003g0131 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.-1-3155G>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40750174 | ||||||
chr5:40750323
|
A | G | 236 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(233): Show | 289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.-1-3304T>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40750323 | ||||||
chr5:40750360
|
A | C | 2 | a0001c0001t0004g0250a0001c0001t0004g0251 | 2 | HG02145.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-1-3341T>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40750360 | ||||||
chr5:40750386
|
T | C | 2 | a0001c0001t0004g0168a0001c0001t0004g0169 | 2 | HG03453.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-1-3367A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40750386 | ||||||
chr5:40750419
|
G | A | 1 | a0001c0001t0001g0179 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-1-3400C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40750419 | ||||||
chr5:40750421
|
G | A | 1 | a0001c0001t0003g0093 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.-1-3402C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40750421 | ||||||
chr5:40750438
|
G | C | 1 | a0001c0001t0022g0130 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-1-3419C>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40750438 | ||||||
chr5:40750540
|
T | A | 1 | a0001c0001t0001g0286 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-1-3521A>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40750540 | ||||||
chr5:40750767
|
T | A | 1 | a0001c0001t0002g0166 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-1-3748A>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40750767 | ||||||
chr5:40751165
|
G | A | 5 | a0001c0001t0012g0180a0001c0001t0012g0181a0001c0001t0012g0182others(2): Show | 5 | HG01192.hp1 HG02280.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.-1-4146C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40751165 | ||||||
chr5:40751235
|
GA | G | 10 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0183others(7): Show | 12 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(9): Show |
intron_variant | MODIFIER | c.-1-4217delT | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40751235 | ||||||
chr5:40751241
|
A | G | 10 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0183others(7): Show | 12 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(9): Show |
intron_variant | MODIFIER | c.-1-4222T>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40751241 | ||||||
chr5:40751516
|
T | C | 1 | a0001c0001t0004g0287 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.-2+4308A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40751516 | ||||||
chr5:40751632
|
T | C | 8 | a0002c0002t0008g0012a0002c0002t0008g0195a0002c0002t0008g0196others(5): Show | 10 | HG00408.hp2 HG00597.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.-2+4192A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40751632 | ||||||
chr5:40751650
|
C | T | 1 | a0001c0001t0004g0253 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-2+4174G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40751650 | ||||||
chr5:40751730
|
G | A | 33 | a0001c0001t0003g0020a0001c0001t0003g0131a0001c0001t0006g0042others(30): Show | 39 | HG00733.hp2 HG00741.hp2 HG01074.hp1 others(36): Show |
intron_variant | MODIFIER | c.-2+4094C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40751730 | ||||||
chr5:40751768
|
C | T | 6 | a0001c0001t0002g0086a0001c0001t0002g0133a0001c0001t0002g0134others(3): Show | 6 | HG02109.hp1 HG03130.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.-2+4056G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40751768 | ||||||
chr5:40751818
|
G | T | 1 | a0001c0001t0002g0132 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-2+4006C>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40751818 | ||||||
chr5:40751838
|
T | C | 1 | a0001c0001t0020g0045 | 2 | NA18994.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.-2+3986A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40751838 | ||||||
chr5:40751961
|
GA | G | 232 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(229): Show | 285 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(282): Show |
intron_variant | MODIFIER | c.-2+3862delT | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40751961 | ||||||
chr5:40752067
|
C | T | 5 | a0001c0001t0012g0180a0001c0001t0012g0181a0001c0001t0012g0182others(2): Show | 5 | HG01192.hp1 HG02280.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.-2+3757G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40752067 | ||||||
chr5:40752156
|
A | G | 5 | a0001c0001t0001g0025a0001c0001t0001g0176a0001c0001t0001g0177others(2): Show | 6 | HG01167.hp2 HG01169.hp2 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.-2+3668T>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40752156 | ||||||
chr5:40752198
|
G | T | 5 | a0001c0001t0011g0008a0001c0001t0011g0046a0001c0001t0015g0312others(2): Show | 7 | HG02280.hp2 HG02976.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.-2+3626C>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40752198 | ||||||
chr5:40752434
|
A | G | 139 | a0001c0001t0001g0053a0001c0001t0002g0002a0001c0001t0002g0009others(136): Show | 163 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.-2+3390T>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40752434 | ||||||
chr5:40752572
|
G | A | 1 | a0001c0001t0010g0089 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-2+3252C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40752572 | ||||||
chr5:40752590
|
T | C | 8 | a0002c0002t0008g0012a0002c0002t0008g0195a0002c0002t0008g0196others(5): Show | 10 | HG00408.hp2 HG00597.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.-2+3234A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40752590 | ||||||
chr5:40752663
|
T | C | 235 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(232): Show | 288 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.-2+3161A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40752663 | ||||||
chr5:40752707
|
A | G | 8 | a0002c0002t0008g0012a0002c0002t0008g0195a0002c0002t0008g0196others(5): Show | 10 | HG00408.hp2 HG00597.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.-2+3117T>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40752707 | ||||||
chr5:40752732
|
C | A | 1 | a0001c0001t0002g0084 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.-2+3092G>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40752732 | ||||||
chr5:40752792
|
T | C | 1 | a0001c0001t0012g0194 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-2+3032A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40752792 | ||||||
chr5:40752859
|
C | T | 1 | a0001c0001t0003g0093 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.-2+2965G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40752859 | ||||||
chr5:40752876
|
G | A | 3 | a0001c0001t0010g0090a0001c0001t0010g0091a0001c0001t0010g0092 | 3 | HG02647.hp1 HG02818.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-2+2948C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40752876 | ||||||
chr5:40753139
|
C | T | 1 | a0001c0001t0004g0249 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-2+2685G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40753139 | ||||||
chr5:40753149
|
G | A | 1 | a0001c0001t0002g0085 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.-2+2675C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40753149 | ||||||
chr5:40753193
|
C | G | 1 | a0001c0001t0031g0315 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-2+2631G>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40753193 | ||||||
chr5:40753315
|
G | A | 8 | a0002c0002t0008g0012a0002c0002t0008g0195a0002c0002t0008g0196others(5): Show | 10 | HG00408.hp2 HG00597.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.-2+2509C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40753315 | ||||||
chr5:40753372
|
A | AAAAG | 52 | a0001c0001t0001g0053a0001c0001t0003g0005a0001c0001t0003g0010others(49): Show | 62 | HG00099.hp2 HG00408.hp1 HG01069.hp2 others(59): Show |
intron_variant | MODIFIER | c.-2+2448_-2+2451dup others(4): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40753372 | ||||||
chr5:40753509
|
T | C | 54 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(51): Show | 76 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.-2+2315A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40753509 | ||||||
chr5:40753775
|
G | A | 42 | a0001c0001t0002g0002a0001c0001t0002g0009a0001c0001t0002g0016others(39): Show | 52 | HG00423.hp1 HG00673.hp1 HG01081.hp2 others(49): Show |
intron_variant | MODIFIER | c.-2+2049C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40753775 | ||||||
chr5:40753883
|
C | T | 235 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(232): Show | 288 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.-2+1941G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40753883 | ||||||
chr5:40753917
|
G | A | 1 | a0001c0001t0023g0174 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-2+1907C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40753917 | ||||||
chr5:40753919
|
A | T | 1 | a0001c0001t0023g0174 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-2+1905T>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40753919 | ||||||
chr5:40753929
|
A | C | 8 | a0001c0001t0002g0086a0001c0001t0010g0087a0001c0001t0010g0088others(5): Show | 8 | HG02257.hp2 HG02451.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.-2+1895T>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40753929 | ||||||
chr5:40754119
|
G | A | 54 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(51): Show | 76 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.-2+1705C>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40754119 | ||||||
chr5:40754127
|
A | G | 42 | a0001c0001t0002g0002a0001c0001t0002g0009a0001c0001t0002g0016others(39): Show | 52 | HG00423.hp1 HG00673.hp1 HG01081.hp2 others(49): Show |
intron_variant | MODIFIER | c.-2+1697T>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40754127 | ||||||
chr5:40754190
|
C | T | 1 | a0001c0001t0005g0247 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-2+1634G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40754190 | ||||||
chr5:40754298
|
GAGACAAA others(14): Show |
G | 5 | a0001c0001t0011g0008a0001c0001t0011g0046a0001c0001t0015g0312others(2): Show | 7 | HG02280.hp2 HG02976.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.-2+1505_-2+1525del others(21): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40754298 | ||||||
chr5:40754585
|
A | AAGGCCTG others(11): Show |
1 | a0001c0001t0001g0053 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-2+1238_-2+1239ins others(18): Show |
TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40754585 | ||||||
chr5:40754593
|
A | C | 1 | a0001c0001t0001g0053 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-2+1231T>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40754593 | ||||||
chr5:40754602
|
T | G | 1 | a0001c0001t0001g0053 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-2+1222A>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40754602 | ||||||
chr5:40754614
|
G | T | 1 | a0001c0001t0001g0053 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-2+1210C>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40754614 | ||||||
chr5:40754778
|
C | G | 4 | a0001c0001t0013g0047a0001c0001t0013g0048a0001c0001t0013g0049others(1): Show | 4 | HG01106.hp1 HG02572.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2+1046G>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40754778 | ||||||
chr5:40754797
|
C | T | 1 | a0001c0001t0001g0173 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.-2+1027G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40754797 | ||||||
chr5:40754919
|
T | C | 2 | a0001c0001t0003g0170a0001c0001t0003g0171 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.-2+905A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40754919 | ||||||
chr5:40755014
|
A | G | 1 | a0001c0001t0005g0246 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-2+810T>C | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40755014 | ||||||
chr5:40755108
|
T | C | 1 | a0001c0001t0007g0311 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-2+716A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40755108 | ||||||
chr5:40755178
|
G | T | 234 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(231): Show | 287 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(284): Show |
intron_variant | MODIFIER | c.-2+646C>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40755178 | ||||||
chr5:40755412
|
T | C | 5 | a0001c0001t0011g0008a0001c0001t0011g0046a0001c0001t0015g0312others(2): Show | 7 | HG02280.hp2 HG02976.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.-2+412A>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40755412 | ||||||
chr5:40755450
|
G | T | 1 | a0001c0001t0037g0052 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-2+374C>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40755450 | ||||||
chr5:40755466
|
C | T | 140 | a0001c0001t0001g0053a0001c0001t0002g0002a0001c0001t0002g0009others(137): Show | 164 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.-2+358G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40755466 | ||||||
chr5:40755532
|
AG | A | 3 | a0001c0001t0002g0316a0001c0001t0002g0317a0001c0001t0031g0315 | 3 | NA18967.hp2 NA18968.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.-2+291delC | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40755532 | ||||||
chr5:40755724
|
C | T | 1 | a0001c0001t0029g0051 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-2+100G>A | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40755724 | ||||||
chr5:40755753
|
A | C | 4 | a0001c0001t0013g0047a0001c0001t0013g0048a0001c0001t0013g0049others(1): Show | 4 | HG01106.hp1 HG02572.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2+71T>G | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40755753 | ||||||
chr5:40755782
|
C | A | 1 | a0001c0001t0007g0318 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-2+42G>T | TTC33 | ENSG00000113638.14 | transcript | ENST00000337702.5 | protein_coding | 1/4 | chr5 | 40755782 |