geneid | 7268 |
---|---|
ensemblid | ENSG00000243725.7 |
hgncid | 12394 |
symbol | TTC4 |
name | tetratricopeptide repeat domain 4 |
refseq_nuc | NM_004623.5 |
refseq_prot | NP_004614.3 |
ensembl_nuc | ENST00000371281.4 |
ensembl_prot | ENSP00000360329.3 |
mane_status | MANE Select |
chr | chr1 |
start | 54715861 |
end | 54742657 |
strand | + |
ver | v1.2 |
region | chr1:54715861-54742657 |
region5000 | chr1:54710861-54747657 |
regionname0 | TTC4_chr1_54715861_54742657 |
regionname5000 | TTC4_chr1_54710861_54747657 |
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 | 0/1 | 387 | 289 | 37 | 46 | 170 | 7 | 28 | 131 | TTC4_chr1_54710861_54747657 | TTC4 | copy fasta | chr1 | 54710861 | 54747657 |
a0002 | 1/0 | 387 | 91 | 40 | 29 | 2 | 7 | 12 | 2 | TTC4_chr1_54710861_54747657 | TTC4 | copy fasta | chr1 | 54710861 | 54747657 |
a0003 | 0/0 | 387 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | copy fasta | chr1 | 54710861 | 54747657 |
a0004 | 0/0 | 387 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | copy fasta | chr1 | 54710861 | 54747657 |
a0005 | 0/0 | 387 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | TTC4_chr1_54710861_54747657 | TTC4 | copy fasta | chr1 | 54710861 | 54747657 |
a0006 | 0/0 | 387 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | copy fasta | chr1 | 54710861 | 54747657 |
a0007 | 0/0 | 387 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | copy fasta | chr1 | 54710861 | 54747657 |
a0008 | 0/0 | 387 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | copy fasta | chr1 | 54710861 | 54747657 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/1 | 1164 | 225 | 22 | 43 | 136 | 6 | 17 | TTC4_chr1_54710861_54747657 | TTC4 | copy fasta | chr1 | 54710861 | 54747657 |
c0002 | 1/0 | 1164 | 91 | 40 | 29 | 2 | 7 | 12 | TTC4_chr1_54710861_54747657 | TTC4 | copy fasta | chr1 | 54710861 | 54747657 |
c0003 | 0/0 | 1164 | 48 | 8 | 0 | 34 | 0 | 6 | TTC4_chr1_54710861_54747657 | TTC4 | copy fasta | chr1 | 54710861 | 54747657 |
c0004 | 0/0 | 1164 | 13 | 6 | 3 | 0 | 1 | 3 | TTC4_chr1_54710861_54747657 | TTC4 | copy fasta | chr1 | 54710861 | 54747657 |
c0005 | 0/0 | 1164 | 6 | 6 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | copy fasta | chr1 | 54710861 | 54747657 |
c0006 | 0/0 | 1164 | 6 | 6 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | copy fasta | chr1 | 54710861 | 54747657 |
c0007 | 0/0 | 1164 | 3 | 0 | 0 | 3 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | copy fasta | chr1 | 54710861 | 54747657 |
c0008 | 0/0 | 1164 | 2 | 0 | 0 | 0 | 0 | 2 | TTC4_chr1_54710861_54747657 | TTC4 | copy fasta | chr1 | 54710861 | 54747657 |
c0009 | 0/0 | 1164 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | copy fasta | chr1 | 54710861 | 54747657 |
c0010 | 0/0 | 1164 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | copy fasta | chr1 | 54710861 | 54747657 |
c0011 | 0/0 | 1164 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | copy fasta | chr1 | 54710861 | 54747657 |
c0012 | 0/0 | 1164 | 1 | 0 | 1 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | copy fasta | chr1 | 54710861 | 54747657 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 1193 | 232 | 24 | 44 | 139 | 5 | 19 | TTC4_chr1_54710861_54747657 | TTC4 | copy fasta | chr1 | 54710861 | 54747657 |
t0002 | 1/0 | 1193 | 83 | 33 | 28 | 2 | 7 | 12 | TTC4_chr1_54710861_54747657 | TTC4 | copy fasta | chr1 | 54710861 | 54747657 |
t0003 | 0/0 | 1188 | 71 | 23 | 4 | 34 | 1 | 9 | TTC4_chr1_54710861_54747657 | TTC4 | copy fasta | chr1 | 54710861 | 54747657 |
t0004 | 0/0 | 1193 | 4 | 4 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | copy fasta | chr1 | 54710861 | 54747657 |
t0005 | 0/0 | 1188 | 2 | 2 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | copy fasta | chr1 | 54710861 | 54747657 |
t0006 | 0/0 | 1193 | 2 | 1 | 0 | 0 | 1 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | copy fasta | chr1 | 54710861 | 54747657 |
t0007 | 0/0 | 1193 | 2 | 2 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | copy fasta | chr1 | 54710861 | 54747657 |
t0008 | 0/0 | 1188 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | copy fasta | chr1 | 54710861 | 54747657 |
t0009 | 0/0 | 1193 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | copy fasta | chr1 | 54710861 | 54747657 |
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 | 7 | 0 | 0 | 5 | 0 | 2 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0002 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0003 | 0/0 | 6 | 0 | 2 | 3 | 0 | 1 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0004 | 0/0 | 6 | 0 | 1 | 4 | 0 | 1 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0005 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0006 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0007 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0008 | 0/1 | 5 | 0 | 0 | 4 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0009 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0010 | 0/0 | 4 | 1 | 2 | 0 | 1 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0011 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0013 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0015 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0016 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0018 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0019 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0020 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0024 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0027 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0028 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0029 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0030 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0031 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0032 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0034 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0037 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0038 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0041 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0042 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0044 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0046 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0047 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0051 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0052 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0053 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0054 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0055 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0056 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0057 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0058 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0059 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0060 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0061 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0084 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 1164 | 225 | 22 | 43 | 136 | 6 | 17 | TTC4_chr1_54710861_54747657 | TTC4 | copy fasta | chr1 | 54710861 | 54747657 |
a0001c0003 | 0/0 | 1164 | 48 | 8 | 0 | 34 | 0 | 6 | TTC4_chr1_54710861_54747657 | TTC4 | copy fasta | chr1 | 54710861 | 54747657 |
a0001c0004 | 0/0 | 1164 | 13 | 6 | 3 | 0 | 1 | 3 | TTC4_chr1_54710861_54747657 | TTC4 | copy fasta | chr1 | 54710861 | 54747657 |
a0001c0008 | 0/0 | 1164 | 2 | 0 | 0 | 0 | 0 | 2 | TTC4_chr1_54710861_54747657 | TTC4 | copy fasta | chr1 | 54710861 | 54747657 |
a0001c0009 | 0/0 | 1164 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | copy fasta | chr1 | 54710861 | 54747657 |
a0002c0002 | 1/0 | 1164 | 91 | 40 | 29 | 2 | 7 | 12 | TTC4_chr1_54710861_54747657 | TTC4 | copy fasta | chr1 | 54710861 | 54747657 |
a0003c0006 | 0/0 | 1164 | 6 | 6 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | copy fasta | chr1 | 54710861 | 54747657 |
a0004c0005 | 0/0 | 1164 | 6 | 6 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | copy fasta | chr1 | 54710861 | 54747657 |
a0005c0007 | 0/0 | 1164 | 3 | 0 | 0 | 3 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | copy fasta | chr1 | 54710861 | 54747657 |
a0006c0012 | 0/0 | 1164 | 1 | 0 | 1 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | copy fasta | chr1 | 54710861 | 54747657 |
a0007c0011 | 0/0 | 1164 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | copy fasta | chr1 | 54710861 | 54747657 |
a0008c0010 | 0/0 | 1164 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | copy fasta | chr1 | 54710861 | 54747657 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 2356 | 217 | 16 | 43 | 135 | 5 | 17 | TTC4_chr1_54710861_54747657 | TTC4 | copy fasta | chr1 | 54710861 | 54747657 |
a0001c0001t0002 | 0/0 | 2356 | 3 | 3 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | copy fasta | chr1 | 54710861 | 54747657 |
a0001c0001t0006 | 0/0 | 2356 | 2 | 1 | 0 | 0 | 1 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | copy fasta | chr1 | 54710861 | 54747657 |
a0001c0001t0007 | 0/0 | 2356 | 2 | 2 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | copy fasta | chr1 | 54710861 | 54747657 |
a0001c0001t0009 | 0/0 | 2356 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | copy fasta | chr1 | 54710861 | 54747657 |
a0001c0003t0003 | 0/0 | 2351 | 45 | 5 | 0 | 34 | 0 | 6 | TTC4_chr1_54710861_54747657 | TTC4 | copy fasta | chr1 | 54710861 | 54747657 |
a0001c0003t0005 | 0/0 | 2351 | 2 | 2 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | copy fasta | chr1 | 54710861 | 54747657 |
a0001c0003t0008 | 0/0 | 2351 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | copy fasta | chr1 | 54710861 | 54747657 |
a0001c0004t0003 | 0/0 | 2351 | 13 | 6 | 3 | 0 | 1 | 3 | TTC4_chr1_54710861_54747657 | TTC4 | copy fasta | chr1 | 54710861 | 54747657 |
a0001c0008t0001 | 0/0 | 2356 | 2 | 0 | 0 | 0 | 0 | 2 | TTC4_chr1_54710861_54747657 | TTC4 | copy fasta | chr1 | 54710861 | 54747657 |
a0001c0009t0003 | 0/0 | 2351 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | copy fasta | chr1 | 54710861 | 54747657 |
a0002c0002t0001 | 0/0 | 2356 | 2 | 2 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | copy fasta | chr1 | 54710861 | 54747657 |
a0002c0002t0002 | 1/0 | 2356 | 73 | 23 | 28 | 2 | 7 | 12 | TTC4_chr1_54710861_54747657 | TTC4 | copy fasta | chr1 | 54710861 | 54747657 |
a0002c0002t0003 | 0/0 | 2351 | 12 | 11 | 1 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | copy fasta | chr1 | 54710861 | 54747657 |
a0002c0002t0004 | 0/0 | 2356 | 4 | 4 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | copy fasta | chr1 | 54710861 | 54747657 |
a0003c0006t0002 | 0/0 | 2356 | 6 | 6 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | copy fasta | chr1 | 54710861 | 54747657 |
a0004c0005t0001 | 0/0 | 2356 | 6 | 6 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | copy fasta | chr1 | 54710861 | 54747657 |
a0005c0007t0001 | 0/0 | 2356 | 3 | 0 | 0 | 3 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | copy fasta | chr1 | 54710861 | 54747657 |
a0006c0012t0001 | 0/0 | 2356 | 1 | 0 | 1 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | copy fasta | chr1 | 54710861 | 54747657 |
a0007c0011t0002 | 0/0 | 2356 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | copy fasta | chr1 | 54710861 | 54747657 |
a0008c0010t0001 | 0/0 | 2356 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | copy fasta | chr1 | 54710861 | 54747657 |
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 | 7 | 0 | 0 | 5 | 0 | 2 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0001g0002 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0001g0003 | 0/0 | 6 | 0 | 2 | 3 | 0 | 1 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0001g0004 | 0/0 | 6 | 0 | 1 | 4 | 0 | 1 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0001g0006 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0001g0007 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0001g0008 | 0/1 | 5 | 0 | 0 | 4 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0001g0009 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0001g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0001g0013 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0001g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0001g0018 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0001g0019 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0001g0020 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0001g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0001g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0001g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0001g0024 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0001g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0001g0037 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0001g0042 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0001g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0001g0046 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0001g0047 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0001g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0001g0051 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0001g0052 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0001g0053 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0001g0054 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0001g0055 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0001g0056 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0001g0057 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0001g0058 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0001g0059 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0002g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0002g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0002g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0006g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0006g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0007g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0007g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0001t0009g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0003t0003g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0003t0003g0015 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0003t0003g0060 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0003t0003g0061 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0003t0003g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0003t0003g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0003t0003g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0003t0003g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0003t0003g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0003t0003g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0003t0003g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0003t0003g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0003t0003g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0003t0003g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0003t0003g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0003t0003g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0003t0003g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0003t0003g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0003t0003g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0003t0003g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0003t0003g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0003t0003g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0003t0003g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0003t0003g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0003t0003g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0003t0003g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0003t0003g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0003t0003g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0003t0003g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0003t0003g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0003t0003g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0003t0003g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0003t0003g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0003t0003g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0003t0003g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0003t0003g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0003t0003g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0003t0005g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0003t0005g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0003t0008g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0004t0003g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0004t0003g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0004t0003g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0004t0003g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0004t0003g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0004t0003g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0004t0003g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0004t0003g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0004t0003g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0004t0003g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0004t0003g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0004t0003g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0004t0003g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0008t0001g0038 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0001c0009t0003g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0002c0002t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0002c0002t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0002c0002t0002g0010 | 0/0 | 4 | 1 | 2 | 0 | 1 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0002c0002t0002g0016 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0002c0002t0002g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0002c0002t0002g0027 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0002c0002t0002g0028 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0002c0002t0002g0029 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0002c0002t0002g0030 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0002c0002t0002g0031 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0002c0002t0002g0032 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0002c0002t0002g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0002c0002t0002g0034 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0002c0002t0002g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0002c0002t0002g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0002c0002t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0002c0002t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0002c0002t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0002c0002t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0002c0002t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0002c0002t0002g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0002c0002t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0002c0002t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0002c0002t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0002c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0002c0002t0002g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0002c0002t0002g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0002c0002t0002g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0002c0002t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0002c0002t0002g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0002c0002t0002g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0002c0002t0002g0084 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0002c0002t0002g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0002c0002t0002g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0002c0002t0002g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0002c0002t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0002c0002t0002g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0002c0002t0002g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0002c0002t0002g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0002c0002t0002g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0002c0002t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0002c0002t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0002c0002t0002g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0002c0002t0002g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0002c0002t0002g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0002c0002t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0002c0002t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0002c0002t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0002c0002t0002g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0002c0002t0002g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0002c0002t0002g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0002c0002t0002g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0002c0002t0002g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0002c0002t0002g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0002c0002t0002g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0002c0002t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0002c0002t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0002c0002t0002g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0002c0002t0002g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0002c0002t0002g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0002c0002t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0002c0002t0003g0011 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0002c0002t0003g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0002c0002t0003g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0002c0002t0003g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0002c0002t0003g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0002c0002t0003g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0002c0002t0003g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0002c0002t0003g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0002c0002t0004g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0002c0002t0004g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0002c0002t0004g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0002c0002t0004g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0003c0006t0002g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0003c0006t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0003c0006t0002g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0003c0006t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0003c0006t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0004c0005t0001g0005 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0004c0005t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0005c0007t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0005c0007t0001g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0006c0012t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0007c0011t0002g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
a0008c0010t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0020 | EUR | GBR | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG00099 | hp2 | a0002 | c0002 | t0002 | g0029 | EUR | GBR | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG00140 | hp1 | a0002 | c0002 | t0002 | g0032 | EUR | GBR | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0020 | EUR | GBR | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG00323 | hp1 | a0001 | c0001 | t0006 | g0041 | EUR | FIN | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0180 | EUR | FIN | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG00408 | hp1 | a0001 | c0003 | t0003 | g0259 | EAS | CHS | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | CHS | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG00423 | hp1 | a0001 | c0003 | t0003 | g0277 | EAS | CHS | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | CHS | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | CHS | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | CHS | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | CHS | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | CHS | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | CHS | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | CHS | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | CHS | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | CHS | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG00621 | hp2 | a0001 | c0003 | t0003 | g0278 | EAS | CHS | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG00639 | hp2 | a0002 | c0002 | t0002 | g0062 | AMR | PUR | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0183 | AMR | PUR | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG00642 | hp2 | a0002 | c0002 | t0003 | g0123 | AMR | PUR | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | CHS | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | CHS | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG00735 | hp1 | a0002 | c0002 | t0002 | g0099 | AMR | PUR | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0210 | AMR | PUR | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG00738 | hp1 | a0002 | c0002 | t0002 | g0114 | AMR | PUR | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG00738 | hp2 | a0002 | c0002 | t0002 | g0102 | AMR | PUR | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0209 | AMR | PUR | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0142 | AMR | PUR | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG01070 | hp2 | a0002 | c0002 | t0002 | g0033 | AMR | PUR | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG01071 | hp1 | a0002 | c0002 | t0002 | g0033 | AMR | PUR | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG01074 | hp1 | a0001 | c0004 | t0003 | g0243 | AMR | PUR | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | PUR | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | PUR | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG01081 | hp2 | a0002 | c0002 | t0002 | g0094 | AMR | PUR | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG01106 | hp1 | a0002 | c0002 | t0002 | g0103 | AMR | PUR | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | PUR | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG01109 | hp2 | a0002 | c0002 | t0002 | g0101 | AMR | PUR | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0196 | AMR | PUR | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG01167 | hp2 | a0002 | c0002 | t0002 | g0095 | AMR | PUR | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG01168 | hp1 | a0002 | c0002 | t0002 | g0080 | AMR | PUR | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG01169 | hp2 | a0002 | c0002 | t0002 | g0079 | AMR | PUR | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG01175 | hp1 | a0002 | c0002 | t0002 | g0108 | AMR | PUR | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG01175 | hp2 | a0002 | c0002 | t0002 | g0067 | AMR | PUR | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG01192 | hp1 | a0002 | c0002 | t0002 | g0031 | AMR | PUR | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG01243 | hp1 | a0002 | c0002 | t0002 | g0090 | AMR | PUR | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG01243 | hp2 | a0001 | c0004 | t0003 | g0237 | AMR | PUR | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0176 | AMR | CLM | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG01255 | hp2 | a0002 | c0002 | t0002 | g0107 | AMR | CLM | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | CLM | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | CLM | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG01257 | hp1 | a0002 | c0002 | t0002 | g0105 | AMR | CLM | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | CLM | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG01258 | hp2 | a0002 | c0002 | t0002 | g0030 | AMR | CLM | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG01261 | hp1 | a0002 | c0002 | t0002 | g0075 | AMR | CLM | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0202 | AMR | CLM | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG01346 | hp1 | a0002 | c0002 | t0002 | g0010 | AMR | CLM | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | CLM | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG01358 | hp1 | a0002 | c0002 | t0002 | g0093 | AMR | CLM | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG01358 | hp2 | a0006 | c0012 | t0001 | g0178 | AMR | CLM | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0213 | AMR | CLM | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | CLM | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0214 | EUR | IBS | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG01516 | hp2 | a0002 | c0002 | t0002 | g0016 | EUR | IBS | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG01517 | hp1 | a0002 | c0002 | t0002 | g0016 | EUR | IBS | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG01517 | hp2 | a0001 | c0004 | t0003 | g0241 | EUR | IBS | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG01891 | hp1 | a0002 | c0002 | t0003 | g0011 | AFR | ACB | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG01891 | hp2 | a0001 | c0004 | t0003 | g0233 | AFR | ACB | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | PEL | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG01943 | hp1 | a0002 | c0002 | t0002 | g0010 | AMR | PEL | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PEL | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG01952 | hp2 | a0002 | c0002 | t0002 | g0092 | AMR | PEL | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0208 | AMR | PEL | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | PEL | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | PEL | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG01981 | hp2 | a0002 | c0002 | t0002 | g0088 | AMR | PEL | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0204 | AMR | PEL | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0212 | AMR | PEL | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | PEL | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG02055 | hp1 | a0001 | c0001 | t0006 | g0018 | AFR | ACB | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0231 | AFR | ACB | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG02056 | hp1 | a0008 | c0010 | t0001 | g0002 | EAS | KHV | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | KHV | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | KHV | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | KHV | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG02080 | hp2 | a0001 | c0003 | t0003 | g0060 | EAS | KHV | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | KHV | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG02083 | hp2 | a0001 | c0003 | t0003 | g0265 | EAS | KHV | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | KHV | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | KHV | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | KHV | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG02135 | hp1 | a0001 | c0003 | t0003 | g0060 | EAS | KHV | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | KHV | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0203 | AMR | PEL | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | CDX | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG02165 | hp2 | a0001 | c0003 | t0003 | g0015 | EAS | CDX | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG02257 | hp1 | a0003 | c0006 | t0002 | g0085 | AFR | ACB | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG02257 | hp2 | a0002 | c0002 | t0002 | g0089 | AFR | ACB | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | ACB | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG02258 | hp2 | a0004 | c0005 | t0001 | g0005 | AFR | ACB | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0141 | AMR | PEL | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG02293 | hp2 | a0002 | c0002 | t0002 | g0016 | AMR | PEL | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG02300 | hp1 | a0001 | c0004 | t0003 | g0239 | AMR | PEL | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG02300 | hp2 | a0002 | c0002 | t0002 | g0027 | AMR | PEL | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | ACB | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG02451 | hp2 | a0002 | c0002 | t0002 | g0066 | AFR | ACB | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | KHV | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | KHV | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG02572 | hp1 | a0001 | c0003 | t0005 | g0252 | AFR | GWD | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG02572 | hp2 | a0002 | c0002 | t0002 | g0071 | AFR | GWD | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG02602 | hp1 | a0001 | c0004 | t0003 | g0242 | SAS | PJL | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG02602 | hp2 | a0002 | c0002 | t0002 | g0028 | SAS | PJL | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG02615 | hp1 | a0002 | c0002 | t0002 | g0109 | AFR | GWD | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG02615 | hp2 | a0002 | c0002 | t0004 | g0117 | AFR | GWD | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG02622 | hp1 | a0002 | c0002 | t0002 | g0069 | AFR | GWD | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG02630 | hp2 | a0002 | c0002 | t0002 | g0111 | AFR | GWD | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG02647 | hp1 | a0001 | c0004 | t0003 | g0234 | AFR | GWD | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | GWD | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0218 | SAS | PJL | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG02683 | hp2 | a0002 | c0002 | t0002 | g0028 | SAS | PJL | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG02698 | hp2 | a0002 | c0002 | t0002 | g0100 | SAS | PJL | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG02723 | hp1 | a0001 | c0003 | t0003 | g0254 | AFR | GWD | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG02723 | hp2 | a0002 | c0002 | t0003 | g0127 | AFR | GWD | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0205 | SAS | PJL | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG02735 | hp2 | a0001 | c0004 | t0003 | g0244 | SAS | PJL | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG02809 | hp1 | a0002 | c0002 | t0002 | g0097 | AFR | GWD | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG02809 | hp2 | a0001 | c0004 | t0003 | g0235 | AFR | GWD | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | GWD | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG02818 | hp2 | a0002 | c0002 | t0003 | g0011 | AFR | GWD | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG02886 | hp1 | a0002 | c0002 | t0003 | g0011 | AFR | GWD | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG02886 | hp2 | a0002 | c0002 | t0002 | g0025 | AFR | GWD | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG02895 | hp1 | a0002 | c0002 | t0002 | g0025 | AFR | GWD | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG02895 | hp2 | a0003 | c0006 | t0002 | g0026 | AFR | GWD | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG02896 | hp1 | a0001 | c0001 | t0002 | g0248 | AFR | GWD | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | GWD | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG02897 | hp1 | a0001 | c0001 | t0002 | g0249 | AFR | GWD | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG02897 | hp2 | a0003 | c0006 | t0002 | g0026 | AFR | GWD | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG02922 | hp1 | a0004 | c0005 | t0001 | g0005 | AFR | ESN | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG02922 | hp2 | a0001 | c0001 | t0007 | g0128 | AFR | ESN | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG02965 | hp1 | a0002 | c0002 | t0002 | g0064 | AFR | ESN | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG02965 | hp2 | a0002 | c0002 | t0003 | g0078 | AFR | ESN | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG02970 | hp1 | a0002 | c0002 | t0002 | g0091 | AFR | ESN | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG02970 | hp2 | a0002 | c0002 | t0003 | g0124 | AFR | ESN | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG02976 | hp1 | a0002 | c0002 | t0002 | g0077 | AFR | ESN | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG02976 | hp2 | a0002 | c0002 | t0003 | g0126 | AFR | ESN | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG03017 | hp1 | a0001 | c0004 | t0003 | g0240 | SAS | PJL | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG03017 | hp2 | a0001 | c0003 | t0003 | g0267 | SAS | PJL | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0211 | AFR | GWD | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG03041 | hp2 | a0002 | c0002 | t0004 | g0119 | AFR | GWD | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG03098 | hp1 | a0001 | c0004 | t0003 | g0238 | AFR | MSL | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG03098 | hp2 | a0002 | c0002 | t0002 | g0110 | AFR | MSL | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG03130 | hp1 | a0002 | c0002 | t0002 | g0010 | AFR | ESN | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG03130 | hp2 | a0004 | c0005 | t0001 | g0005 | AFR | ESN | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ESN | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG03139 | hp2 | a0001 | c0004 | t0003 | g0245 | AFR | ESN | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG03195 | hp1 | a0002 | c0002 | t0001 | g0116 | AFR | ESN | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG03195 | hp2 | a0001 | c0003 | t0003 | g0247 | AFR | ESN | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG03209 | hp1 | a0002 | c0002 | t0002 | g0096 | AFR | MSL | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG03209 | hp2 | a0001 | c0003 | t0005 | g0253 | AFR | MSL | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0230 | SAS | PJL | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG03239 | hp2 | a0002 | c0002 | t0002 | g0083 | SAS | PJL | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG03453 | hp1 | a0002 | c0002 | t0004 | g0118 | AFR | MSL | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG03453 | hp2 | a0004 | c0005 | t0001 | g0005 | AFR | MSL | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG03486 | hp1 | a0003 | c0006 | t0002 | g0086 | AFR | MSL | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG03486 | hp2 | a0002 | c0002 | t0003 | g0035 | AFR | MSL | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG03490 | hp1 | a0002 | c0002 | t0002 | g0082 | SAS | PJL | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG03490 | hp2 | a0001 | c0008 | t0001 | g0038 | SAS | PJL | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG03492 | hp1 | a0001 | c0008 | t0001 | g0038 | SAS | PJL | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG03492 | hp2 | a0002 | c0002 | t0002 | g0031 | SAS | PJL | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG03516 | hp1 | a0002 | c0002 | t0002 | g0068 | AFR | ESN | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG03516 | hp2 | a0001 | c0009 | t0003 | g0255 | AFR | ESN | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | GWD | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG03540 | hp2 | a0002 | c0002 | t0003 | g0011 | AFR | GWD | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG03579 | hp1 | a0002 | c0002 | t0002 | g0070 | AFR | MSL | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG03579 | hp2 | a0002 | c0002 | t0004 | g0122 | AFR | MSL | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG03654 | hp1 | a0002 | c0002 | t0002 | g0106 | SAS | PJL | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0163 | SAS | PJL | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0041 | SAS | PJL | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0216 | SAS | STU | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG03704 | hp1 | a0001 | c0003 | t0003 | g0270 | SAS | PJL | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0199 | SAS | PJL | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0201 | SAS | PJL | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG03710 | hp2 | a0002 | c0002 | t0002 | g0029 | SAS | PJL | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG03831 | hp1 | a0002 | c0002 | t0002 | g0034 | SAS | BEB | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG03831 | hp2 | a0002 | c0002 | t0002 | g0034 | SAS | BEB | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG03834 | hp1 | a0002 | c0002 | t0002 | g0115 | SAS | BEB | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG03834 | hp2 | a0001 | c0003 | t0003 | g0276 | SAS | BEB | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | BEB | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0047 | SAS | BEB | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0182 | SAS | BEB | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG03942 | hp2 | a0001 | c0003 | t0003 | g0261 | SAS | BEB | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG04115 | hp1 | a0001 | c0003 | t0003 | g0274 | SAS | STU | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0044 | SAS | STU | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG04204 | hp1 | a0002 | c0002 | t0002 | g0063 | SAS | STU | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0044 | SAS | STU | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA18522 | hp1 | a0001 | c0001 | t0002 | g0250 | AFR | YRI | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA18522 | hp2 | a0002 | c0002 | t0003 | g0035 | AFR | YRI | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA18612 | hp1 | a0001 | c0003 | t0003 | g0014 | EAS | CHB | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | CHB | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | CHB | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | CHB | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA18906 | hp1 | a0003 | c0006 | t0002 | g0087 | AFR | YRI | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA18906 | hp2 | a0001 | c0004 | t0003 | g0236 | AFR | YRI | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA18939 | hp2 | a0001 | c0003 | t0003 | g0015 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA18942 | hp1 | a0001 | c0003 | t0003 | g0268 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA18943 | hp2 | a0001 | c0003 | t0003 | g0014 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA18944 | hp1 | a0005 | c0007 | t0001 | g0048 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA18944 | hp2 | a0001 | c0003 | t0003 | g0282 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA18946 | hp1 | a0001 | c0003 | t0003 | g0014 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA18953 | hp1 | a0001 | c0003 | t0003 | g0280 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA18967 | hp2 | a0001 | c0003 | t0003 | g0275 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA18970 | hp1 | a0001 | c0001 | t0009 | g0160 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA18971 | hp2 | a0001 | c0003 | t0003 | g0263 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA18973 | hp2 | a0001 | c0003 | t0003 | g0266 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA18974 | hp2 | a0001 | c0003 | t0003 | g0015 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA18990 | hp1 | a0001 | c0003 | t0003 | g0269 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA18991 | hp1 | a0001 | c0003 | t0003 | g0279 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA18992 | hp2 | a0001 | c0003 | t0003 | g0015 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA19000 | hp2 | a0001 | c0003 | t0003 | g0273 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA19009 | hp2 | a0001 | c0003 | t0003 | g0264 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA19010 | hp1 | a0001 | c0003 | t0003 | g0272 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA19011 | hp1 | a0001 | c0003 | t0003 | g0014 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | LWK | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | LWK | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA19043 | hp1 | a0003 | c0006 | t0002 | g0065 | AFR | LWK | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | LWK | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA19056 | hp1 | a0001 | c0003 | t0003 | g0061 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA19058 | hp1 | a0001 | c0003 | t0003 | g0281 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA19062 | hp1 | a0001 | c0003 | t0003 | g0283 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA19067 | hp1 | a0005 | c0007 | t0001 | g0049 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA19067 | hp2 | a0001 | c0003 | t0003 | g0262 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA19072 | hp1 | a0001 | c0003 | t0003 | g0257 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA19072 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA19075 | hp1 | a0001 | c0003 | t0003 | g0284 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA19075 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA19076 | hp2 | a0001 | c0003 | t0003 | g0260 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA19079 | hp1 | a0005 | c0007 | t0001 | g0049 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA19080 | hp2 | a0002 | c0002 | t0002 | g0076 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA19084 | hp2 | a0001 | c0003 | t0003 | g0061 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA19087 | hp2 | a0002 | c0002 | t0002 | g0121 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA19088 | hp1 | a0001 | c0003 | t0003 | g0271 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA19240 | hp1 | a0001 | c0003 | t0003 | g0232 | AFR | YRI | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA19240 | hp2 | a0004 | c0005 | t0001 | g0130 | AFR | YRI | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA20129 | hp1 | a0001 | c0003 | t0003 | g0246 | AFR | ASW | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA20129 | hp2 | a0001 | c0001 | t0007 | g0129 | AFR | ASW | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA20752 | hp1 | a0002 | c0002 | t0002 | g0098 | EUR | TSI | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0019 | EUR | TSI | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA20805 | hp1 | a0002 | c0002 | t0002 | g0113 | EUR | TSI | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA20805 | hp2 | a0002 | c0002 | t0002 | g0010 | EUR | TSI | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA20905 | hp1 | a0001 | c0003 | t0003 | g0258 | SAS | GIH | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0168 | SAS | GIH | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG01123 | hp1 | a0002 | c0002 | t0002 | g0104 | AMR | CLM | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG02109 | hp1 | a0002 | c0002 | t0002 | g0027 | AFR | ACB | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG02109 | hp2 | a0002 | c0002 | t0001 | g0120 | AFR | ACB | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG02486 | hp1 | a0007 | c0011 | t0002 | g0073 | AFR | ACB | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | ACB | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | ACB | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG02559 | hp2 | a0004 | c0005 | t0001 | g0005 | AFR | ACB | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG03471 | hp1 | a0002 | c0002 | t0002 | g0072 | AFR | MSL | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG03471 | hp2 | a0002 | c0002 | t0003 | g0125 | AFR | MSL | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG06807 | hp1 | a0001 | c0003 | t0008 | g0256 | AFR | USA | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
HG06807 | hp2 | a0002 | c0002 | t0002 | g0030 | AFR | USA | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA20300 | hp1 | a0002 | c0002 | t0002 | g0112 | AFR | USA | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA20300 | hp2 | a0002 | c0002 | t0002 | g0032 | AFR | USA | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA21309 | hp1 | a0001 | c0003 | t0003 | g0251 | AFR | LWK | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
NA21309 | hp2 | a0002 | c0002 | t0002 | g0081 | AFR | LWK | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0008 | REF | REF | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
homoSapiens_grch38 | hp1 | a0002 | c0002 | t0002 | g0084 | REF | REF | TTC4_chr1_54710861_54747657 | TTC4 | chr1 | 54710861 | 54747657 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:54715934
|
C | T | 1 | a0006 | 1 | HG01358.hp2 | missense_variant | MODERATE | c.26C>T | p.Thr9Ile | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 1/10 | 74/2356 | 26/1164 | 9/387 | chr1 | 54715934 | ||
chr1:54716627
|
T | A | 5 | a0001a0004a0005others(2): Show | 300 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(297): Show |
missense_variant | MODERATE | c.139T>A | p.Ser47Thr | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 2/10 | 187/2356 | 139/1164 | 47/387 | chr1 | 54716627 | ||
chr1:54717617
|
C | T | 1 | a0005 | 3 | NA18944.hp1 NA19067.hp1 NA19079.hp1 |
missense_variant | MODERATE | c.355C>T | p.Leu119Phe | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 3/10 | 403/2356 | 355/1164 | 119/387 | chr1 | 54717617 | ||
chr1:54717627
|
A | G | 1 | a0008 | 1 | HG02056.hp1 | missense_variant | MODERATE | c.365A>G | p.Asn122Ser | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 3/10 | 413/2356 | 365/1164 | 122/387 | chr1 | 54717627 | ||
chr1:54722716
|
G | A | 1 | a0007 | 1 | HG02486.hp1 | missense_variant | MODERATE | c.511G>A | p.Val171Met | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/10 | 559/2356 | 511/1164 | 171/387 | chr1 | 54722716 | ||
chr1:54722764
|
C | T | 1 | a0004 | 6 | HG02258.hp2 HG02559.hp2 HG02922.hp1 others(3): Show |
missense_variant | MODERATE | c.559C>T | p.Leu187Phe | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/10 | 607/2356 | 559/1164 | 187/387 | chr1 | 54722764 | ||
chr1:54741484
|
C | T | 1 | a0003 | 6 | HG02257.hp1 HG02895.hp2 HG02897.hp2 others(3): Show |
missense_variant | MODERATE | c.1135C>T | p.Arg379Trp | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 10/10 | 1183/2356 | 1135/1164 | 379/387 | chr1 | 54741484 | ||
chr1:54742657
|
A | C | 1 | a0001 | 2 | HG02922.hp2 NA20129.hp2 |
splice_region_variant | LOW | c.*1144A>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 10/10 | chr1 | 54742657 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:54722709
|
C | T | 3 | a0001c0003a0001c0004a0001c0009 | 62 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(59): Show |
synonymous_variant | LOW | c.504C>T | p.Ala168Ala | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/10 | 552/2356 | 504/1164 | 168/387 | chr1 | 54722709 | ||
chr1:54731647
|
G | A | 1 | a0001c0004 | 13 | HG01074.hp1 HG01243.hp2 HG01517.hp2 others(10): Show |
synonymous_variant | LOW | c.843G>A | p.Leu281Leu | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 7/10 | 891/2356 | 843/1164 | 281/387 | chr1 | 54731647 | ||
chr1:54731647
|
G | C | 1 | a0001c0008 | 2 | HG03490.hp2 HG03492.hp1 |
synonymous_variant | LOW | c.843G>C | p.Leu281Leu | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 7/10 | 891/2356 | 843/1164 | 281/387 | chr1 | 54731647 | ||
chr1:54737612
|
C | T | 1 | a0001c0009 | 1 | HG03516.hp2 | synonymous_variant | LOW | c.1009C>T | p.Leu337Leu | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/10 | 1057/2356 | 1009/1164 | 337/387 | chr1 | 54737612 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:54715861
|
G | T | 1 | a0002c0002t0004 | 4 | HG02615.hp2 HG03041.hp2 HG03453.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-48G>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 1/10 | 48 | chr1 | 54715861 | |||||
chr1:54741543
|
T | C | 7 | a0001c0001t0009a0001c0003t0003a0001c0003t0005others(4): Show | 75 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(72): Show |
3_prime_UTR_variant | MODIFIER | c.*30T>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 10/10 | 30 | chr1 | 54741543 | |||||
chr1:54741861
|
T | G | 1 | a0001c0001t0006 | 2 | HG00323.hp1 HG02055.hp1 |
3_prime_UTR_variant | MODIFIER | c.*348T>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 10/10 | 348 | chr1 | 54741861 | |||||
chr1:54741865
|
G | A | 6 | a0001c0003t0003a0001c0003t0005a0001c0003t0008others(3): Show | 74 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(71): Show |
3_prime_UTR_variant | MODIFIER | c.*352G>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 10/10 | 352 | chr1 | 54741865 | |||||
chr1:54741911
|
CACAA | C | 6 | a0001c0003t0003a0001c0003t0005a0001c0003t0008others(3): Show | 74 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(71): Show |
3_prime_UTR_variant | MODIFIER | c.*407_*410delACAA | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 10/10 | 407 | INFO_REALIGN_3_PRIME | chr1 | 54741911 | ||||
chr1:54742081
|
C | G | 17 | a0001c0001t0001a0001c0001t0006a0001c0001t0007others(14): Show | 315 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(312): Show |
3_prime_UTR_variant | MODIFIER | c.*568C>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 10/10 | 568 | chr1 | 54742081 | |||||
chr1:54742112
|
A | G | 1 | a0001c0003t0005 | 2 | HG02572.hp1 HG03209.hp2 |
3_prime_UTR_variant | MODIFIER | c.*599A>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 10/10 | 599 | chr1 | 54742112 | |||||
chr1:54742150
|
CT | C | 6 | a0001c0003t0003a0001c0003t0005a0001c0003t0008others(3): Show | 74 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(71): Show |
3_prime_UTR_variant | MODIFIER | c.*640delT | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 10/10 | 640 | INFO_REALIGN_3_PRIME | chr1 | 54742150 | ||||
chr1:54742245
|
C | T | 5 | a0001c0003t0003a0001c0003t0005a0001c0004t0003others(2): Show | 73 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(70): Show |
3_prime_UTR_variant | MODIFIER | c.*732C>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 10/10 | 732 | chr1 | 54742245 | |||||
chr1:54742310
|
T | C | 6 | a0001c0003t0003a0001c0003t0005a0001c0003t0008others(3): Show | 74 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(71): Show |
3_prime_UTR_variant | MODIFIER | c.*797T>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 10/10 | 797 | chr1 | 54742310 | |||||
chr1:54742311
|
T | C | 6 | a0001c0003t0003a0001c0003t0005a0001c0003t0008others(3): Show | 74 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(71): Show |
3_prime_UTR_variant | MODIFIER | c.*798T>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 10/10 | 798 | chr1 | 54742311 | |||||
chr1:54742531
|
C | T | 6 | a0001c0003t0003a0001c0003t0005a0001c0003t0008others(3): Show | 74 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(71): Show |
3_prime_UTR_variant | MODIFIER | c.*1018C>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 10/10 | 1018 | chr1 | 54742531 | |||||
chr1:54742626
|
G | C | 17 | a0001c0001t0001a0001c0001t0006a0001c0001t0007others(14): Show | 315 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(312): Show |
3_prime_UTR_variant | MODIFIER | c.*1113G>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 10/10 | 1113 | chr1 | 54742626 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:54716170
|
G | T | 43 | a0001c0001t0002g0248a0001c0001t0002g0249a0001c0001t0002g0250others(40): Show | 51 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.111+151G>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 1/9 | chr1 | 54716170 | ||||||
chr1:54716257
|
TACTTA | T | 14 | a0001c0003t0003g0232a0001c0004t0003g0233a0001c0004t0003g0234others(11): Show | 14 | HG01074.hp1 HG01243.hp2 HG01517.hp2 others(11): Show |
intron_variant | MODIFIER | c.111+243_111+247del others(5): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr1 | 54716257 | |||||
chr1:54716363
|
G | C | 2 | a0002c0002t0002g0062a0002c0002t0002g0063 | 2 | HG00639.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.112-237G>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 1/9 | chr1 | 54716363 | ||||||
chr1:54716393
|
T | C | 1 | a0002c0002t0002g0064 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.112-207T>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 1/9 | chr1 | 54716393 | ||||||
chr1:54716556
|
A | G | 32 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(29): Show | 40 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(37): Show |
intron_variant | MODIFIER | c.112-44A>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 1/9 | chr1 | 54716556 | ||||||
chr1:54716775
|
G | A | 43 | a0001c0001t0002g0248a0001c0001t0002g0249a0001c0001t0002g0250others(40): Show | 51 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.229+58G>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 2/9 | chr1 | 54716775 | ||||||
chr1:54716877
|
C | T | 57 | a0001c0001t0002g0248a0001c0001t0002g0249a0001c0001t0002g0250others(54): Show | 65 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(62): Show |
intron_variant | MODIFIER | c.229+160C>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 2/9 | chr1 | 54716877 | ||||||
chr1:54716905
|
G | A | 57 | a0001c0001t0002g0248a0001c0001t0002g0249a0001c0001t0002g0250others(54): Show | 65 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(62): Show |
intron_variant | MODIFIER | c.229+188G>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 2/9 | chr1 | 54716905 | ||||||
chr1:54717022
|
G | A | 2 | a0001c0003t0003g0246a0001c0003t0003g0247 | 2 | HG03195.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.229+305G>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 2/9 | chr1 | 54717022 | ||||||
chr1:54717031
|
A | G | 1 | a0001c0003t0008g0256 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.229+314A>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 2/9 | chr1 | 54717031 | ||||||
chr1:54717428
|
A | G | 13 | a0001c0004t0003g0233a0001c0004t0003g0234a0001c0004t0003g0235others(10): Show | 13 | HG01074.hp1 HG01243.hp2 HG01517.hp2 others(10): Show |
intron_variant | MODIFIER | c.230-64A>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 2/9 | chr1 | 54717428 | ||||||
chr1:54717459
|
A | G | 54 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(51): Show | 62 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.230-33A>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 2/9 | chr1 | 54717459 | ||||||
chr1:54717855
|
C | G | 54 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(51): Show | 62 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.391+202C>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 3/9 | chr1 | 54717855 | ||||||
chr1:54718137
|
T | C | 14 | a0001c0003t0003g0232a0001c0004t0003g0233a0001c0004t0003g0234others(11): Show | 14 | HG01074.hp1 HG01243.hp2 HG01517.hp2 others(11): Show |
intron_variant | MODIFIER | c.391+484T>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 3/9 | chr1 | 54718137 | ||||||
chr1:54718280
|
C | T | 2 | a0001c0003t0003g0246a0001c0003t0003g0247 | 2 | HG03195.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.391+627C>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 3/9 | chr1 | 54718280 | ||||||
chr1:54718287
|
C | T | 36 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(33): Show | 44 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(41): Show |
intron_variant | MODIFIER | c.391+634C>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 3/9 | chr1 | 54718287 | ||||||
chr1:54718288
|
G | A | 11 | a0001c0004t0003g0233a0002c0002t0002g0025a0002c0002t0002g0066others(8): Show | 12 | HG01175.hp2 HG01891.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.391+635G>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 3/9 | chr1 | 54718288 | ||||||
chr1:54718414
|
T | G | 2 | a0001c0001t0001g0074a0001c0003t0003g0232 | 2 | HG02896.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.391+761T>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 3/9 | chr1 | 54718414 | ||||||
chr1:54718416
|
T | C | 40 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(37): Show | 48 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(45): Show |
intron_variant | MODIFIER | c.391+763T>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 3/9 | chr1 | 54718416 | ||||||
chr1:54718458
|
G | A | 5 | a0001c0003t0003g0251a0001c0003t0003g0254a0001c0003t0005g0252others(2): Show | 5 | HG02572.hp1 HG02723.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.391+805G>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 3/9 | chr1 | 54718458 | ||||||
chr1:54718468
|
C | T | 4 | a0001c0003t0003g0251a0001c0003t0005g0252a0001c0003t0005g0253others(1): Show | 4 | HG02572.hp1 HG03209.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.391+815C>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 3/9 | chr1 | 54718468 | ||||||
chr1:54718502
|
C | T | 3 | a0001c0001t0001g0024a0001c0001t0001g0230a0001c0001t0001g0231 | 5 | HG02055.hp2 HG02258.hp1 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.391+849C>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 3/9 | chr1 | 54718502 | ||||||
chr1:54718536
|
C | T | 150 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(147): Show | 233 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(230): Show |
intron_variant | MODIFIER | c.391+883C>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 3/9 | chr1 | 54718536 | ||||||
chr1:54718613
|
C | T | 54 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(51): Show | 62 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.391+960C>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 3/9 | chr1 | 54718613 | ||||||
chr1:54718787
|
A | T | 55 | a0001c0001t0001g0059a0001c0003t0003g0014a0001c0003t0003g0015others(52): Show | 64 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.391+1134A>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 3/9 | chr1 | 54718787 | ||||||
chr1:54718788
|
A | G | 18 | a0001c0003t0003g0232a0001c0003t0003g0251a0001c0003t0005g0252others(15): Show | 18 | HG01074.hp1 HG01243.hp2 HG01517.hp2 others(15): Show |
intron_variant | MODIFIER | c.391+1135A>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 3/9 | chr1 | 54718788 | ||||||
chr1:54718788
|
A | T | 36 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(33): Show | 44 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(41): Show |
intron_variant | MODIFIER | c.391+1135A>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 3/9 | chr1 | 54718788 | ||||||
chr1:54718823
|
C | A | 1 | a0002c0002t0002g0075 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.391+1170C>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 3/9 | chr1 | 54718823 | ||||||
chr1:54718896
|
T | G | 54 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(51): Show | 62 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.391+1243T>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 3/9 | chr1 | 54718896 | ||||||
chr1:54718954
|
G | T | 54 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(51): Show | 62 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.391+1301G>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 3/9 | chr1 | 54718954 | ||||||
chr1:54718984
|
C | CT | 5 | a0001c0001t0007g0128a0001c0001t0007g0129a0001c0003t0003g0246others(2): Show | 5 | HG02922.hp2 HG03195.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.391+1337dupT | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr1 | 54718984 | |||||
chr1:54719116
|
T | C | 54 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(51): Show | 62 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.391+1463T>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 3/9 | chr1 | 54719116 | ||||||
chr1:54719206
|
G | A | 2 | a0004c0005t0001g0005a0004c0005t0001g0130 | 6 | HG02258.hp2 HG02559.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.391+1553G>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 3/9 | chr1 | 54719206 | ||||||
chr1:54719264
|
C | T | 1 | a0001c0001t0001g0024 | 3 | HG02258.hp1 NA19030.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.391+1611C>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 3/9 | chr1 | 54719264 | ||||||
chr1:54719301
|
G | GTACTTTG others(54): Show |
32 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(29): Show | 40 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(37): Show |
intron_variant | MODIFIER | c.391+1663_391+1664i others(63): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr1 | 54719301 | |||||
chr1:54719301
|
G | GTACTTTG others(179): Show |
8 | a0001c0003t0003g0246a0001c0003t0003g0247a0001c0003t0003g0251others(5): Show | 8 | HG02572.hp1 HG02723.hp1 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.391+1698_391+1699i others(188): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr1 | 54719301 | |||||
chr1:54719301
|
G | GTACTTTG others(179): Show |
14 | a0001c0003t0003g0232a0001c0004t0003g0233a0001c0004t0003g0234others(11): Show | 14 | HG01074.hp1 HG01243.hp2 HG01517.hp2 others(11): Show |
intron_variant | MODIFIER | c.391+1698_391+1699i others(188): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr1 | 54719301 | |||||
chr1:54719307
|
T | C | 1 | a0001c0001t0001g0131 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.391+1654T>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 3/9 | chr1 | 54719307 | ||||||
chr1:54719352
|
A | G | 54 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(51): Show | 62 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.391+1699A>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 3/9 | chr1 | 54719352 | ||||||
chr1:54719531
|
C | A | 54 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(51): Show | 62 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.392-1632C>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 3/9 | chr1 | 54719531 | ||||||
chr1:54719689
|
A | C | 1 | a0001c0004t0003g0233 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.392-1474A>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 3/9 | chr1 | 54719689 | ||||||
chr1:54719794
|
G | A | 54 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(51): Show | 62 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.392-1369G>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 3/9 | chr1 | 54719794 | ||||||
chr1:54719811
|
A | T | 1 | a0001c0003t0003g0254 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.392-1352A>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 3/9 | chr1 | 54719811 | ||||||
chr1:54719896
|
C | CT | 11 | a0001c0003t0003g0061a0001c0003t0003g0254a0001c0003t0003g0279others(8): Show | 12 | HG01891.hp2 HG02647.hp1 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.392-1248dupT | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr1 | 54719896 | |||||
chr1:54719896
|
C | CTT | 11 | a0001c0003t0003g0232a0001c0004t0003g0236a0001c0004t0003g0237others(8): Show | 11 | HG01074.hp1 HG01243.hp2 HG01517.hp2 others(8): Show |
intron_variant | MODIFIER | c.392-1249_392-1248d others(4): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr1 | 54719896 | |||||
chr1:54719896
|
CT | C | 14 | a0001c0001t0001g0036a0001c0001t0001g0132a0001c0001t0001g0133others(11): Show | 15 | HG01168.hp2 HG01256.hp2 HG02647.hp2 others(12): Show |
intron_variant | MODIFIER | c.392-1248delT | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr1 | 54719896 | |||||
chr1:54719959
|
T | C | 54 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(51): Show | 62 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.392-1204T>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 3/9 | chr1 | 54719959 | ||||||
chr1:54719971
|
A | T | 54 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(51): Show | 62 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.392-1192A>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 3/9 | chr1 | 54719971 | ||||||
chr1:54720025
|
A | C | 54 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(51): Show | 62 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.392-1138A>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 3/9 | chr1 | 54720025 | ||||||
chr1:54720090
|
G | A | 148 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(145): Show | 227 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(224): Show |
intron_variant | MODIFIER | c.392-1073G>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 3/9 | chr1 | 54720090 | ||||||
chr1:54720285
|
A | G | 3 | a0001c0001t0001g0229a0001c0003t0003g0277a0001c0003t0003g0278 | 3 | HG00423.hp1 HG00621.hp2 NA18953.hp2 |
intron_variant | MODIFIER | c.392-878A>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 3/9 | chr1 | 54720285 | ||||||
chr1:54720314
|
C | A | 1 | a0001c0001t0001g0139 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.392-849C>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 3/9 | chr1 | 54720314 | ||||||
chr1:54720437
|
CT | C | 39 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(36): Show | 60 | HG00438.hp2 HG00558.hp1 HG00597.hp1 others(57): Show |
intron_variant | MODIFIER | c.392-711delT | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr1 | 54720437 | |||||
chr1:54720452
|
T | A | 54 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(51): Show | 62 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.392-711T>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 3/9 | chr1 | 54720452 | ||||||
chr1:54720489
|
T | C | 3 | a0002c0002t0002g0066a0002c0002t0002g0067a0003c0006t0002g0065 | 3 | HG01175.hp2 HG02451.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.392-674T>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 3/9 | chr1 | 54720489 | ||||||
chr1:54720493
|
GT | G | 55 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(52): Show | 86 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(83): Show |
intron_variant | MODIFIER | c.392-655delT | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr1 | 54720493 | |||||
chr1:54720505
|
TTTTA | T | 15 | a0001c0003t0003g0232a0001c0003t0003g0257a0001c0004t0003g0233others(12): Show | 15 | HG01074.hp1 HG01243.hp2 HG01517.hp2 others(12): Show |
intron_variant | MODIFIER | c.392-657_392-654del others(4): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 3/9 | chr1 | 54720505 | ||||||
chr1:54720506
|
TTTA | T | 32 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(29): Show | 40 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(37): Show |
intron_variant | MODIFIER | c.392-656_392-654del others(3): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 3/9 | chr1 | 54720506 | ||||||
chr1:54720507
|
TTA | T | 7 | a0001c0003t0003g0246a0001c0003t0003g0247a0001c0003t0003g0254others(4): Show | 7 | HG02572.hp1 HG02723.hp1 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.392-655_392-654del others(2): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 3/9 | chr1 | 54720507 | ||||||
chr1:54720722
|
C | T | 1 | a0001c0001t0001g0164 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.392-441C>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 3/9 | chr1 | 54720722 | ||||||
chr1:54720818
|
C | G | 8 | a0002c0002t0003g0011a0002c0002t0003g0035a0002c0002t0003g0078others(5): Show | 12 | HG00642.hp2 HG01891.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.392-345C>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 3/9 | chr1 | 54720818 | ||||||
chr1:54720942
|
C | T | 54 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(51): Show | 62 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.392-221C>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 3/9 | chr1 | 54720942 | ||||||
chr1:54720989
|
G | C | 13 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0039others(10): Show | 23 | HG00621.hp1 HG01255.hp1 HG02040.hp2 others(20): Show |
intron_variant | MODIFIER | c.392-174G>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 3/9 | chr1 | 54720989 | ||||||
chr1:54721013
|
G | A | 54 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(51): Show | 62 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.392-150G>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 3/9 | chr1 | 54721013 | ||||||
chr1:54721252
|
G | A | 54 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(51): Show | 62 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.469+12G>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 4/9 | chr1 | 54721252 | ||||||
chr1:54721468
|
T | G | 40 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(37): Show | 48 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(45): Show |
intron_variant | MODIFIER | c.469+228T>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 4/9 | chr1 | 54721468 | ||||||
chr1:54721493
|
C | T | 14 | a0001c0003t0003g0232a0001c0004t0003g0233a0001c0004t0003g0234others(11): Show | 14 | HG01074.hp1 HG01243.hp2 HG01517.hp2 others(11): Show |
intron_variant | MODIFIER | c.469+253C>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 4/9 | chr1 | 54721493 | ||||||
chr1:54721494
|
C | G | 54 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(51): Show | 62 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.469+254C>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 4/9 | chr1 | 54721494 | ||||||
chr1:54721624
|
G | T | 1 | a0001c0009t0003g0255 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.469+384G>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 4/9 | chr1 | 54721624 | ||||||
chr1:54721829
|
A | C | 54 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(51): Show | 62 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.469+589A>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 4/9 | chr1 | 54721829 | ||||||
chr1:54721926
|
G | T | 2 | a0001c0003t0003g0246a0001c0003t0003g0247 | 2 | HG03195.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.469+686G>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 4/9 | chr1 | 54721926 | ||||||
chr1:54722016
|
A | G | 8 | a0001c0003t0003g0246a0001c0003t0003g0247a0001c0003t0003g0251others(5): Show | 8 | HG02572.hp1 HG02723.hp1 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.470-659A>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 4/9 | chr1 | 54722016 | ||||||
chr1:54722052
|
T | C | 1 | a0001c0001t0001g0177 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.470-623T>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 4/9 | chr1 | 54722052 | ||||||
chr1:54722129
|
A | AT | 126 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(123): Show | 196 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(193): Show |
intron_variant | MODIFIER | c.470-529dupT | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr1 | 54722129 | |||||
chr1:54722129
|
A | ATT | 15 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0058others(12): Show | 20 | HG00673.hp1 HG00673.hp2 HG02080.hp1 others(17): Show |
intron_variant | MODIFIER | c.470-530_470-529dup others(2): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr1 | 54722129 | |||||
chr1:54722129
|
ATT | A | 49 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(46): Show | 57 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(54): Show |
intron_variant | MODIFIER | c.470-530_470-529del others(2): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr1 | 54722129 | |||||
chr1:54722349
|
C | G | 54 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(51): Show | 62 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.470-326C>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 4/9 | chr1 | 54722349 | ||||||
chr1:54722516
|
G | A | 54 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(51): Show | 62 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.470-159G>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 4/9 | chr1 | 54722516 | ||||||
chr1:54722518
|
A | G | 40 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(37): Show | 48 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(45): Show |
intron_variant | MODIFIER | c.470-157A>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 4/9 | chr1 | 54722518 | ||||||
chr1:54722576
|
G | A | 40 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(37): Show | 48 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(45): Show |
intron_variant | MODIFIER | c.470-99G>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 4/9 | chr1 | 54722576 | ||||||
chr1:54722581
|
T | C | 1 | a0001c0001t0001g0166 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.470-94T>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 4/9 | chr1 | 54722581 | ||||||
chr1:54722596
|
G | A | 54 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(51): Show | 62 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.470-79G>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 4/9 | chr1 | 54722596 | ||||||
chr1:54722819
|
CAATTAGC others(17): Show |
C | 32 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(29): Show | 40 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(37): Show |
intron_variant | MODIFIER | c.594+31_594+54delTG others(22): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr1 | 54722819 | |||||
chr1:54722974
|
G | T | 1 | a0001c0001t0001g0057 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.594+175G>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | chr1 | 54722974 | ||||||
chr1:54723110
|
CTGTGTTT others(3): Show |
C | 1 | a0001c0001t0001g0163 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.594+321_594+330del others(10): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr1 | 54723110 | |||||
chr1:54723121
|
T | C | 1 | a0001c0001t0001g0166 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.594+322T>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | chr1 | 54723121 | ||||||
chr1:54723158
|
G | A | 1 | a0001c0004t0003g0236 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.594+359G>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | chr1 | 54723158 | ||||||
chr1:54723165
|
A | G | 4 | a0002c0002t0004g0117a0002c0002t0004g0118a0002c0002t0004g0119others(1): Show | 4 | HG02615.hp2 HG03041.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.594+366A>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | chr1 | 54723165 | ||||||
chr1:54723169
|
G | T | 54 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(51): Show | 62 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.594+370G>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | chr1 | 54723169 | ||||||
chr1:54723205
|
T | C | 56 | a0001c0001t0007g0128a0001c0001t0007g0129a0001c0003t0003g0014others(53): Show | 64 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.594+406T>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | chr1 | 54723205 | ||||||
chr1:54723268
|
G | T | 54 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(51): Show | 62 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.594+469G>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | chr1 | 54723268 | ||||||
chr1:54723347
|
C | T | 54 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(51): Show | 62 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.594+548C>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | chr1 | 54723347 | ||||||
chr1:54723406
|
G | C | 1 | a0001c0009t0003g0255 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.594+607G>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | chr1 | 54723406 | ||||||
chr1:54723456
|
C | T | 1 | a0001c0003t0003g0254 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.594+657C>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | chr1 | 54723456 | ||||||
chr1:54723457
|
G | T | 2 | a0001c0001t0001g0021a0001c0001t0001g0137 | 4 | HG02486.hp2 HG02622.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.594+658G>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | chr1 | 54723457 | ||||||
chr1:54723512
|
G | A | 54 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(51): Show | 62 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.594+713G>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | chr1 | 54723512 | ||||||
chr1:54723525
|
A | G | 1 | a0002c0002t0002g0083 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.594+726A>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | chr1 | 54723525 | ||||||
chr1:54723550
|
A | G | 54 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(51): Show | 62 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.594+751A>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | chr1 | 54723550 | ||||||
chr1:54723735
|
G | T | 54 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(51): Show | 62 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.594+936G>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | chr1 | 54723735 | ||||||
chr1:54723762
|
C | T | 287 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(284): Show | 397 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(394): Show |
intron_variant | MODIFIER | c.594+963C>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | chr1 | 54723762 | ||||||
chr1:54723796
|
A | G | 1 | a0001c0001t0001g0218 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.594+997A>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | chr1 | 54723796 | ||||||
chr1:54723826
|
T | C | 18 | a0001c0003t0003g0232a0001c0003t0003g0251a0001c0003t0005g0252others(15): Show | 18 | HG01074.hp1 HG01243.hp2 HG01517.hp2 others(15): Show |
intron_variant | MODIFIER | c.594+1027T>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | chr1 | 54723826 | ||||||
chr1:54723955
|
A | G | 3 | a0001c0001t0001g0058a0001c0001t0001g0227a0001c0001t0001g0228 | 4 | HG02523.hp1 NA19012.hp1 NA19064.hp2 others(1): Show |
intron_variant | MODIFIER | c.594+1156A>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | chr1 | 54723955 | ||||||
chr1:54724040
|
T | C | 1 | a0001c0003t0003g0258 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.594+1241T>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | chr1 | 54724040 | ||||||
chr1:54724107
|
A | C | 1 | a0001c0001t0001g0226 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.594+1308A>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | chr1 | 54724107 | ||||||
chr1:54724120
|
C | T | 44 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(41): Show | 56 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.594+1321C>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | chr1 | 54724120 | ||||||
chr1:54724125
|
G | T | 62 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(59): Show | 74 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.594+1326G>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | chr1 | 54724125 | ||||||
chr1:54724197
|
G | A | 1 | a0001c0003t0003g0259 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.594+1398G>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | chr1 | 54724197 | ||||||
chr1:54724268
|
C | CT | 19 | a0001c0003t0003g0232a0001c0003t0003g0251a0001c0003t0005g0252others(16): Show | 19 | HG01074.hp1 HG01243.hp2 HG01517.hp2 others(16): Show |
intron_variant | MODIFIER | c.594+1481dupT | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr1 | 54724268 | |||||
chr1:54724268
|
C | CTT | 44 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(41): Show | 56 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.594+1480_594+1481d others(4): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr1 | 54724268 | |||||
chr1:54724410
|
C | T | 44 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(41): Show | 56 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.594+1611C>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | chr1 | 54724410 | ||||||
chr1:54724428
|
G | T | 44 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(41): Show | 56 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.594+1629G>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | chr1 | 54724428 | ||||||
chr1:54724574
|
C | T | 54 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(51): Show | 62 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.594+1775C>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | chr1 | 54724574 | ||||||
chr1:54724644
|
C | T | 2 | a0001c0003t0003g0246a0001c0003t0003g0247 | 2 | HG03195.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.594+1845C>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | chr1 | 54724644 | ||||||
chr1:54724677
|
CTT | C | 2 | a0004c0005t0001g0005a0004c0005t0001g0130 | 6 | HG02258.hp2 HG02559.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.594+1879_594+1880d others(4): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | chr1 | 54724677 | ||||||
chr1:54724679
|
T | G | 44 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(41): Show | 56 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.594+1880T>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | chr1 | 54724679 | ||||||
chr1:54724780
|
G | A | 42 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(39): Show | 54 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.594+1981G>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | chr1 | 54724780 | ||||||
chr1:54724865
|
C | G | 62 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(59): Show | 74 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.594+2066C>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | chr1 | 54724865 | ||||||
chr1:54725003
|
T | C | 215 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(212): Show | 310 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(307): Show |
intron_variant | MODIFIER | c.594+2204T>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | chr1 | 54725003 | ||||||
chr1:54725217
|
G | C | 32 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(29): Show | 40 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(37): Show |
intron_variant | MODIFIER | c.594+2418G>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | chr1 | 54725217 | ||||||
chr1:54725330
|
C | G | 2 | a0001c0001t0001g0055a0001c0001t0001g0056 | 4 | HG00423.hp2 HG00438.hp1 HG02071.hp2 others(1): Show |
intron_variant | MODIFIER | c.594+2531C>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | chr1 | 54725330 | ||||||
chr1:54725369
|
A | G | 1 | a0001c0001t0001g0217 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.594+2570A>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | chr1 | 54725369 | ||||||
chr1:54725400
|
C | T | 1 | a0001c0001t0001g0218 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.594+2601C>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | chr1 | 54725400 | ||||||
chr1:54725728
|
A | G | 66 | a0001c0001t0001g0004a0001c0001t0001g0054a0001c0001t0001g0136others(63): Show | 80 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.595-2618A>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | chr1 | 54725728 | ||||||
chr1:54725732
|
G | A | 5 | a0001c0004t0003g0234a0001c0004t0003g0235a0001c0004t0003g0236others(2): Show | 5 | HG01243.hp2 HG02647.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.595-2614G>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | chr1 | 54725732 | ||||||
chr1:54725864
|
A | C | 1 | a0001c0003t0003g0254 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.595-2482A>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | chr1 | 54725864 | ||||||
chr1:54725923
|
G | A | 68 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0132others(65): Show | 88 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.595-2423G>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | chr1 | 54725923 | ||||||
chr1:54725958
|
A | G | 1 | a0001c0001t0001g0212 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.595-2388A>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | chr1 | 54725958 | ||||||
chr1:54725971
|
T | C | 235 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(232): Show | 325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.595-2375T>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | chr1 | 54725971 | ||||||
chr1:54725976
|
C | G | 1 | a0001c0003t0008g0256 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.595-2370C>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | chr1 | 54725976 | ||||||
chr1:54726029
|
G | A | 1 | a0001c0003t0003g0232 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.595-2317G>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | chr1 | 54726029 | ||||||
chr1:54726212
|
C | T | 13 | a0001c0004t0003g0233a0001c0004t0003g0234a0001c0004t0003g0235others(10): Show | 13 | HG01074.hp1 HG01243.hp2 HG01517.hp2 others(10): Show |
intron_variant | MODIFIER | c.595-2134C>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | chr1 | 54726212 | ||||||
chr1:54726337
|
A | G | 1 | a0002c0002t0001g0116 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.595-2009A>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | chr1 | 54726337 | ||||||
chr1:54726608
|
T | G | 215 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(212): Show | 310 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(307): Show |
intron_variant | MODIFIER | c.595-1738T>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | chr1 | 54726608 | ||||||
chr1:54726676
|
T | C | 5 | a0003c0006t0002g0026a0003c0006t0002g0065a0003c0006t0002g0085others(2): Show | 6 | HG02257.hp1 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.595-1670T>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | chr1 | 54726676 | ||||||
chr1:54726767
|
C | T | 54 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(51): Show | 62 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.595-1579C>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | chr1 | 54726767 | ||||||
chr1:54726863
|
C | CCTGG | 33 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(30): Show | 53 | HG00438.hp2 HG00558.hp1 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.595-1482_595-1479d others(6): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr1 | 54726863 | |||||
chr1:54727055
|
C | CA | 5 | a0001c0001t0001g0147a0001c0001t0001g0148a0002c0002t0002g0025others(2): Show | 6 | HG01981.hp2 HG02886.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.595-1275dupA | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr1 | 54727055 | |||||
chr1:54727055
|
CA | C | 117 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(114): Show | 179 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(176): Show |
intron_variant | MODIFIER | c.595-1275delA | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr1 | 54727055 | |||||
chr1:54727068
|
A | AC | 45 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(42): Show | 57 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(54): Show |
intron_variant | MODIFIER | c.595-1278_595-1277i others(3): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | chr1 | 54727068 | ||||||
chr1:54727068
|
A | C | 12 | a0001c0004t0003g0233a0001c0004t0003g0234a0001c0004t0003g0235others(9): Show | 12 | HG01074.hp1 HG01243.hp2 HG01517.hp2 others(9): Show |
intron_variant | MODIFIER | c.595-1278A>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | chr1 | 54727068 | ||||||
chr1:54727074
|
A | G | 62 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(59): Show | 74 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.595-1272A>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | chr1 | 54727074 | ||||||
chr1:54727112
|
G | A | 62 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(59): Show | 74 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.595-1234G>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | chr1 | 54727112 | ||||||
chr1:54727265
|
C | G | 1 | a0004c0005t0001g0130 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.595-1081C>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | chr1 | 54727265 | ||||||
chr1:54727362
|
G | T | 1 | a0001c0001t0007g0129 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.595-984G>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | chr1 | 54727362 | ||||||
chr1:54727509
|
T | G | 9 | a0001c0003t0003g0254a0002c0002t0003g0011a0002c0002t0003g0035others(6): Show | 13 | HG00642.hp2 HG01891.hp1 HG02723.hp1 others(10): Show |
intron_variant | MODIFIER | c.595-837T>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | chr1 | 54727509 | ||||||
chr1:54727539
|
A | AAAGTT | 62 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(59): Show | 74 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.595-804_595-803ins others(5): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr1 | 54727539 | |||||
chr1:54727554
|
G | GA | 62 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(59): Show | 74 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.595-786dupA | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr1 | 54727554 | |||||
chr1:54727607
|
T | G | 1 | a0002c0002t0002g0069 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.595-739T>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | chr1 | 54727607 | ||||||
chr1:54727649
|
C | T | 18 | a0001c0003t0003g0232a0001c0003t0003g0251a0001c0003t0005g0252others(15): Show | 18 | HG01074.hp1 HG01243.hp2 HG01517.hp2 others(15): Show |
intron_variant | MODIFIER | c.595-697C>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | chr1 | 54727649 | ||||||
chr1:54727688
|
C | CA | 35 | a0001c0001t0001g0009a0001c0001t0001g0040a0001c0001t0001g0042others(32): Show | 45 | HG00597.hp2 HG00609.hp2 HG00673.hp2 others(42): Show |
intron_variant | MODIFIER | c.595-636dupA | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr1 | 54727688 | |||||
chr1:54727688
|
CA | C | 6 | a0001c0001t0001g0143a0001c0001t0001g0215a0001c0001t0007g0128others(3): Show | 6 | HG01070.hp1 HG02922.hp2 HG06807.hp1 others(3): Show |
intron_variant | MODIFIER | c.595-636delA | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr1 | 54727688 | |||||
chr1:54727688
|
CAAAAAAA others(4): Show |
C | 44 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(41): Show | 56 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.595-646_595-636del others(11): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr1 | 54727688 | |||||
chr1:54727736
|
C | T | 62 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(59): Show | 74 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.595-610C>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | chr1 | 54727736 | ||||||
chr1:54727743
|
G | T | 64 | a0001c0001t0007g0128a0001c0001t0007g0129a0001c0003t0003g0014others(61): Show | 76 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(73): Show |
intron_variant | MODIFIER | c.595-603G>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | chr1 | 54727743 | ||||||
chr1:54727804
|
A | G | 2 | a0001c0001t0001g0020a0001c0001t0001g0210 | 4 | HG00099.hp1 HG00140.hp2 HG00735.hp2 others(1): Show |
intron_variant | MODIFIER | c.595-542A>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | chr1 | 54727804 | ||||||
chr1:54727845
|
C | T | 44 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(41): Show | 56 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.595-501C>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | chr1 | 54727845 | ||||||
chr1:54727953
|
C | A | 1 | a0001c0001t0001g0168 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.595-393C>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | chr1 | 54727953 | ||||||
chr1:54728016
|
A | G | 62 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(59): Show | 74 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.595-330A>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | chr1 | 54728016 | ||||||
chr1:54728023
|
G | A | 62 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(59): Show | 74 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.595-323G>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | chr1 | 54728023 | ||||||
chr1:54728041
|
G | C | 62 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(59): Show | 74 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.595-305G>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | chr1 | 54728041 | ||||||
chr1:54728043
|
C | G | 18 | a0001c0003t0003g0232a0001c0003t0003g0251a0001c0003t0005g0252others(15): Show | 18 | HG01074.hp1 HG01243.hp2 HG01517.hp2 others(15): Show |
intron_variant | MODIFIER | c.595-303C>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | chr1 | 54728043 | ||||||
chr1:54728199
|
T | G | 9 | a0001c0003t0003g0254a0002c0002t0003g0011a0002c0002t0003g0035others(6): Show | 13 | HG00642.hp2 HG01891.hp1 HG02723.hp1 others(10): Show |
intron_variant | MODIFIER | c.595-147T>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 5/9 | chr1 | 54728199 | ||||||
chr1:54728515
|
C | G | 44 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(41): Show | 56 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.681+83C>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 6/9 | chr1 | 54728515 | ||||||
chr1:54728620
|
A | G | 62 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(59): Show | 74 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.681+188A>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 6/9 | chr1 | 54728620 | ||||||
chr1:54728682
|
T | C | 62 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(59): Show | 74 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.681+250T>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 6/9 | chr1 | 54728682 | ||||||
chr1:54728710
|
C | G | 44 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(41): Show | 56 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.681+278C>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 6/9 | chr1 | 54728710 | ||||||
chr1:54728831
|
T | A | 3 | a0001c0001t0001g0169a0001c0001t0001g0172a0001c0001t0001g0185 | 3 | NA18957.hp1 NA18993.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.681+399T>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 6/9 | chr1 | 54728831 | ||||||
chr1:54728851
|
T | C | 62 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(59): Show | 74 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.681+419T>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 6/9 | chr1 | 54728851 | ||||||
chr1:54729021
|
C | A | 44 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(41): Show | 56 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.681+589C>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 6/9 | chr1 | 54729021 | ||||||
chr1:54729140
|
G | A | 2 | a0001c0003t0003g0246a0001c0003t0003g0247 | 2 | HG03195.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.681+708G>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 6/9 | chr1 | 54729140 | ||||||
chr1:54729169
|
C | T | 32 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(29): Show | 40 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(37): Show |
intron_variant | MODIFIER | c.681+737C>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 6/9 | chr1 | 54729169 | ||||||
chr1:54729198
|
C | T | 62 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(59): Show | 74 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.681+766C>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 6/9 | chr1 | 54729198 | ||||||
chr1:54729298
|
GGTAACTG others(7): Show |
G | 1 | a0001c0003t0003g0260 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.681+868_681+881del others(14): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr1 | 54729298 | |||||
chr1:54729308
|
T | A | 61 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(58): Show | 73 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(70): Show |
intron_variant | MODIFIER | c.681+876T>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 6/9 | chr1 | 54729308 | ||||||
chr1:54729514
|
C | T | 1 | a0001c0001t0001g0059 | 2 | NA18943.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.681+1082C>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 6/9 | chr1 | 54729514 | ||||||
chr1:54729675
|
A | C | 62 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(59): Show | 74 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.681+1243A>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 6/9 | chr1 | 54729675 | ||||||
chr1:54729727
|
G | GT | 100 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0019others(97): Show | 134 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.681+1309dupT | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr1 | 54729727 | |||||
chr1:54729845
|
C | T | 44 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(41): Show | 56 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.681+1413C>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 6/9 | chr1 | 54729845 | ||||||
chr1:54729913
|
G | A | 32 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(29): Show | 40 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(37): Show |
intron_variant | MODIFIER | c.681+1481G>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 6/9 | chr1 | 54729913 | ||||||
chr1:54730001
|
G | A | 62 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(59): Show | 74 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.682-1485G>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 6/9 | chr1 | 54730001 | ||||||
chr1:54730006
|
C | T | 36 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0019others(33): Show | 57 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(54): Show |
intron_variant | MODIFIER | c.682-1480C>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 6/9 | chr1 | 54730006 | ||||||
chr1:54730021
|
G | A | 44 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(41): Show | 56 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.682-1465G>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 6/9 | chr1 | 54730021 | ||||||
chr1:54730024
|
G | A | 62 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(59): Show | 74 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.682-1462G>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 6/9 | chr1 | 54730024 | ||||||
chr1:54730027
|
G | T | 62 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(59): Show | 74 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.682-1459G>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 6/9 | chr1 | 54730027 | ||||||
chr1:54730155
|
T | C | 62 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(59): Show | 74 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.682-1331T>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 6/9 | chr1 | 54730155 | ||||||
chr1:54730235
|
T | A | 62 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(59): Show | 74 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.682-1251T>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 6/9 | chr1 | 54730235 | ||||||
chr1:54730241
|
A | G | 1 | a0001c0001t0001g0205 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.682-1245A>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 6/9 | chr1 | 54730241 | ||||||
chr1:54730247
|
A | G | 62 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(59): Show | 74 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.682-1239A>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 6/9 | chr1 | 54730247 | ||||||
chr1:54730280
|
C | CT | 50 | a0001c0001t0001g0176a0001c0001t0001g0179a0001c0001t0001g0210others(47): Show | 66 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(63): Show |
intron_variant | MODIFIER | c.682-1189dupT | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr1 | 54730280 | |||||
chr1:54730280
|
CT | C | 25 | a0001c0001t0001g0223a0001c0001t0002g0248a0001c0001t0002g0249others(22): Show | 26 | HG01074.hp1 HG01243.hp2 HG01517.hp2 others(23): Show |
intron_variant | MODIFIER | c.682-1189delT | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr1 | 54730280 | |||||
chr1:54730342
|
A | C | 62 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(59): Show | 74 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.682-1144A>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 6/9 | chr1 | 54730342 | ||||||
chr1:54730426
|
G | A | 213 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(210): Show | 308 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(305): Show |
intron_variant | MODIFIER | c.682-1060G>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 6/9 | chr1 | 54730426 | ||||||
chr1:54730434
|
A | G | 2 | a0001c0001t0001g0019a0001c0001t0001g0209 | 4 | HG01069.hp1 HG01071.hp2 HG01257.hp2 others(1): Show |
intron_variant | MODIFIER | c.682-1052A>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 6/9 | chr1 | 54730434 | ||||||
chr1:54730664
|
A | G | 1 | a0001c0003t0003g0254 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.682-822A>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 6/9 | chr1 | 54730664 | ||||||
chr1:54730789
|
T | TTTC | 44 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(41): Show | 56 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.682-694_682-692dup others(3): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr1 | 54730789 | |||||
chr1:54730793
|
T | TTC | 18 | a0001c0003t0003g0232a0001c0003t0003g0251a0001c0003t0005g0252others(15): Show | 18 | HG01074.hp1 HG01243.hp2 HG01517.hp2 others(15): Show |
intron_variant | MODIFIER | c.682-692_682-691ins others(2): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr1 | 54730793 | |||||
chr1:54730807
|
T | A | 2 | a0003c0006t0002g0085a0003c0006t0002g0086 | 2 | HG02257.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.682-679T>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 6/9 | chr1 | 54730807 | ||||||
chr1:54731063
|
G | C | 1 | a0002c0002t0002g0092 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.682-423G>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 6/9 | chr1 | 54731063 | ||||||
chr1:54731066
|
G | A | 62 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(59): Show | 74 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.682-420G>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 6/9 | chr1 | 54731066 | ||||||
chr1:54731134
|
G | T | 1 | a0001c0001t0001g0204 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.682-352G>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 6/9 | chr1 | 54731134 | ||||||
chr1:54731218
|
GTTT | G | 32 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(29): Show | 40 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(37): Show |
intron_variant | MODIFIER | c.682-261_682-259del others(3): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr1 | 54731218 | |||||
chr1:54731224
|
T | TG | 12 | a0001c0003t0003g0246a0001c0003t0003g0247a0001c0003t0003g0254others(9): Show | 16 | HG00642.hp2 HG01891.hp1 HG02723.hp1 others(13): Show |
intron_variant | MODIFIER | c.682-262_682-261ins others(1): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 6/9 | chr1 | 54731224 | ||||||
chr1:54731476
|
T | C | 78 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(75): Show | 121 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.682-10T>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 6/9 | chr1 | 54731476 | ||||||
chr1:54731849
|
T | C | 6 | a0001c0004t0003g0239a0001c0004t0003g0240a0001c0004t0003g0241others(3): Show | 6 | HG01074.hp1 HG01517.hp2 HG02300.hp1 others(3): Show |
intron_variant | MODIFIER | c.896+149T>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 7/9 | chr1 | 54731849 | ||||||
chr1:54731855
|
T | C | 62 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(59): Show | 74 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.896+155T>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 7/9 | chr1 | 54731855 | ||||||
chr1:54731859
|
T | TGAACCTT others(5): Show |
62 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(59): Show | 74 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.896+160_896+171dup others(12): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr1 | 54731859 | |||||
chr1:54731874
|
T | C | 5 | a0001c0003t0003g0061a0001c0003t0003g0279a0001c0003t0003g0280others(2): Show | 6 | NA18953.hp1 NA18991.hp1 NA19056.hp1 others(3): Show |
intron_variant | MODIFIER | c.896+174T>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 7/9 | chr1 | 54731874 | ||||||
chr1:54731875
|
A | G | 13 | a0001c0004t0003g0233a0001c0004t0003g0234a0001c0004t0003g0235others(10): Show | 13 | HG01074.hp1 HG01243.hp2 HG01517.hp2 others(10): Show |
intron_variant | MODIFIER | c.896+175A>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 7/9 | chr1 | 54731875 | ||||||
chr1:54732046
|
T | G | 60 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(57): Show | 72 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(69): Show |
intron_variant | MODIFIER | c.896+346T>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 7/9 | chr1 | 54732046 | ||||||
chr1:54732227
|
A | G | 1 | a0001c0001t0001g0142 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.896+527A>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 7/9 | chr1 | 54732227 | ||||||
chr1:54732287
|
C | T | 1 | a0001c0001t0001g0054 | 2 | NA18968.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.896+587C>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 7/9 | chr1 | 54732287 | ||||||
chr1:54732316
|
G | C | 6 | a0001c0004t0003g0239a0001c0004t0003g0240a0001c0004t0003g0241others(3): Show | 6 | HG01074.hp1 HG01517.hp2 HG02300.hp1 others(3): Show |
intron_variant | MODIFIER | c.896+616G>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 7/9 | chr1 | 54732316 | ||||||
chr1:54732334
|
AAT | A | 9 | a0001c0001t0001g0136a0001c0001t0001g0138a0001c0001t0001g0158others(6): Show | 9 | HG01069.hp1 HG01168.hp2 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.896+636_896+637del others(2): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr1 | 54732334 | |||||
chr1:54732335
|
AT | A | 213 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(210): Show | 309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.896+636delT | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 7/9 | chr1 | 54732335 | ||||||
chr1:54732336
|
T | A | 49 | a0001c0001t0001g0145a0001c0001t0001g0149a0001c0001t0001g0151others(46): Show | 61 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(58): Show |
intron_variant | MODIFIER | c.896+636T>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 7/9 | chr1 | 54732336 | ||||||
chr1:54732393
|
G | C | 62 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(59): Show | 74 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.896+693G>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 7/9 | chr1 | 54732393 | ||||||
chr1:54732448
|
G | A | 62 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(59): Show | 74 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.896+748G>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 7/9 | chr1 | 54732448 | ||||||
chr1:54732452
|
T | G | 118 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(115): Show | 177 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(174): Show |
intron_variant | MODIFIER | c.896+752T>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 7/9 | chr1 | 54732452 | ||||||
chr1:54732459
|
A | AT | 9 | a0001c0001t0001g0151a0001c0001t0001g0159a0001c0001t0001g0181others(6): Show | 9 | HG00597.hp2 HG01175.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.896+775dupT | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr1 | 54732459 | |||||
chr1:54732459
|
AT | A | 44 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(41): Show | 56 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.896+775delT | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr1 | 54732459 | |||||
chr1:54732464
|
T | C | 2 | a0004c0005t0001g0005a0004c0005t0001g0130 | 6 | HG02258.hp2 HG02559.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.896+764T>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 7/9 | chr1 | 54732464 | ||||||
chr1:54732542
|
T | C | 1 | a0001c0001t0001g0151 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.896+842T>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 7/9 | chr1 | 54732542 | ||||||
chr1:54732568
|
C | T | 18 | a0001c0003t0003g0232a0001c0003t0003g0251a0001c0003t0005g0252others(15): Show | 18 | HG01074.hp1 HG01243.hp2 HG01517.hp2 others(15): Show |
intron_variant | MODIFIER | c.896+868C>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 7/9 | chr1 | 54732568 | ||||||
chr1:54732660
|
A | G | 62 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(59): Show | 74 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.896+960A>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 7/9 | chr1 | 54732660 | ||||||
chr1:54732694
|
G | A | 63 | a0001c0001t0001g0152a0001c0003t0003g0014a0001c0003t0003g0015others(60): Show | 75 | HG00408.hp1 HG00423.hp1 HG00609.hp1 others(72): Show |
intron_variant | MODIFIER | c.897-935G>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 7/9 | chr1 | 54732694 | ||||||
chr1:54732709
|
C | G | 1 | a0001c0009t0003g0255 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.897-920C>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 7/9 | chr1 | 54732709 | ||||||
chr1:54732777
|
T | C | 62 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(59): Show | 74 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.897-852T>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 7/9 | chr1 | 54732777 | ||||||
chr1:54732778
|
T | C | 62 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(59): Show | 74 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.897-851T>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 7/9 | chr1 | 54732778 | ||||||
chr1:54732813
|
T | C | 62 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(59): Show | 74 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.897-816T>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 7/9 | chr1 | 54732813 | ||||||
chr1:54732931
|
T | C | 9 | a0001c0003t0003g0254a0002c0002t0003g0011a0002c0002t0003g0035others(6): Show | 13 | HG00642.hp2 HG01891.hp1 HG02723.hp1 others(10): Show |
intron_variant | MODIFIER | c.897-698T>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 7/9 | chr1 | 54732931 | ||||||
chr1:54732950
|
G | A | 4 | a0001c0003t0003g0251a0001c0003t0005g0252a0001c0003t0005g0253others(1): Show | 4 | HG02572.hp1 HG03209.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.897-679G>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 7/9 | chr1 | 54732950 | ||||||
chr1:54732960
|
G | T | 2 | a0004c0005t0001g0005a0004c0005t0001g0130 | 6 | HG02258.hp2 HG02559.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.897-669G>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 7/9 | chr1 | 54732960 | ||||||
chr1:54732961
|
C | A | 1 | a0002c0002t0002g0033 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.897-668C>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 7/9 | chr1 | 54732961 | ||||||
chr1:54732994
|
C | T | 2 | a0001c0003t0003g0246a0001c0003t0003g0247 | 2 | HG03195.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.897-635C>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 7/9 | chr1 | 54732994 | ||||||
chr1:54732995
|
G | A | 1 | a0001c0001t0001g0186 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.897-634G>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 7/9 | chr1 | 54732995 | ||||||
chr1:54733093
|
C | CA | 62 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(59): Show | 74 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.897-525dupA | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr1 | 54733093 | |||||
chr1:54733155
|
C | T | 1 | a0002c0002t0002g0033 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.897-474C>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 7/9 | chr1 | 54733155 | ||||||
chr1:54733156
|
C | T | 1 | a0001c0009t0003g0255 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.897-473C>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 7/9 | chr1 | 54733156 | ||||||
chr1:54733168
|
TA | T | 62 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(59): Show | 74 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.897-459delA | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr1 | 54733168 | |||||
chr1:54733216
|
A | G | 32 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(29): Show | 40 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(37): Show |
intron_variant | MODIFIER | c.897-413A>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 7/9 | chr1 | 54733216 | ||||||
chr1:54733246
|
C | T | 44 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(41): Show | 56 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.897-383C>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 7/9 | chr1 | 54733246 | ||||||
chr1:54733247
|
A | G | 62 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(59): Show | 74 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.897-382A>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 7/9 | chr1 | 54733247 | ||||||
chr1:54733254
|
CA | C | 62 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(59): Show | 74 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.897-367delA | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr1 | 54733254 | |||||
chr1:54733309
|
A | G | 1 | a0001c0001t0001g0215 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.897-320A>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 7/9 | chr1 | 54733309 | ||||||
chr1:54733323
|
G | A | 2 | a0001c0001t0001g0045a0001c0001t0001g0149 | 3 | NA18955.hp2 NA18977.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.897-306G>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 7/9 | chr1 | 54733323 | ||||||
chr1:54733418
|
CAA | C | 18 | a0001c0003t0003g0232a0001c0003t0003g0251a0001c0003t0005g0252others(15): Show | 18 | HG01074.hp1 HG01243.hp2 HG01517.hp2 others(15): Show |
intron_variant | MODIFIER | c.897-200_897-199del others(2): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr1 | 54733418 | |||||
chr1:54733418
|
CAAAAAAA | C | 44 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(41): Show | 56 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.897-205_897-199del others(7): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr1 | 54733418 | |||||
chr1:54733426
|
A | T | 19 | a0001c0003t0003g0232a0001c0003t0003g0251a0001c0003t0005g0252others(16): Show | 19 | HG01074.hp1 HG01175.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.897-203A>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 7/9 | chr1 | 54733426 | ||||||
chr1:54733426
|
AAAAAT | A | 5 | a0003c0006t0002g0026a0003c0006t0002g0065a0003c0006t0002g0085others(2): Show | 6 | HG02257.hp1 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.897-182_897-178del others(5): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr1 | 54733426 | |||||
chr1:54733427
|
A | T | 1 | a0001c0001t0001g0171 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.897-202A>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 7/9 | chr1 | 54733427 | ||||||
chr1:54733431
|
T | A | 152 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(149): Show | 235 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(232): Show |
intron_variant | MODIFIER | c.897-198T>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 7/9 | chr1 | 54733431 | ||||||
chr1:54733432
|
A | AT | 4 | a0001c0001t0001g0021a0001c0001t0001g0137a0001c0001t0001g0179others(1): Show | 6 | HG01516.hp1 HG02486.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.897-197_897-196ins others(1): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 7/9 | chr1 | 54733432 | ||||||
chr1:54733432
|
A | T | 145 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(142): Show | 226 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(223): Show |
intron_variant | MODIFIER | c.897-197A>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 7/9 | chr1 | 54733432 | ||||||
chr1:54733743
|
ATTAATTT others(4): Show |
A | 1 | a0002c0002t0003g0127 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.978+36_978+46delAA others(9): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 54733743 | |||||
chr1:54733746
|
AATTTTTT others(2): Show |
A | 5 | a0001c0003t0003g0232a0001c0003t0003g0251a0001c0003t0005g0252others(2): Show | 5 | HG02572.hp1 HG03209.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.978+37_978+45delAT others(7): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54733746 | ||||||
chr1:54733746
|
AATTTTTT others(3): Show |
A | 17 | a0001c0003t0003g0246a0001c0003t0003g0247a0001c0003t0003g0273others(14): Show | 17 | HG01074.hp1 HG01243.hp2 HG01517.hp2 others(14): Show |
intron_variant | MODIFIER | c.978+37_978+46delAT others(8): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54733746 | ||||||
chr1:54733746
|
AATTTTTT others(4): Show |
A | 38 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(35): Show | 50 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.978+37_978+47delAT others(9): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54733746 | ||||||
chr1:54733746
|
AATTTTTT others(5): Show |
A | 1 | a0002c0002t0003g0123 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.978+37_978+48delAT others(10): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54733746 | ||||||
chr1:54733747
|
A | AT | 18 | a0002c0002t0001g0116a0002c0002t0001g0120a0002c0002t0002g0025others(15): Show | 21 | HG00140.hp1 HG00738.hp2 HG01106.hp1 others(18): Show |
intron_variant | MODIFIER | c.978+63dupT | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 54733747 | |||||
chr1:54733747
|
AT | A | 7 | a0001c0001t0007g0128a0001c0001t0007g0129a0002c0002t0002g0064others(4): Show | 8 | HG01081.hp2 HG01167.hp2 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.978+63delT | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 54733747 | |||||
chr1:54733747
|
ATTTTTTT | A | 8 | a0001c0001t0001g0002a0001c0001t0001g0148a0001c0001t0001g0149others(5): Show | 16 | HG01358.hp2 HG02056.hp1 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.978+57_978+63delTT others(5): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 54733747 | |||||
chr1:54733747
|
ATTTTTTT others(1): Show |
A | 106 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(103): Show | 169 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(166): Show |
intron_variant | MODIFIER | c.978+56_978+63delTT others(6): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 54733747 | |||||
chr1:54733747
|
ATTTTTTT others(2): Show |
A | 28 | a0001c0001t0001g0009a0001c0001t0001g0018a0001c0001t0001g0020others(25): Show | 39 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(36): Show |
intron_variant | MODIFIER | c.978+55_978+63delTT others(7): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 54733747 | |||||
chr1:54733747
|
ATTTTTTT others(3): Show |
A | 7 | a0001c0001t0001g0050a0001c0001t0001g0133a0001c0001t0001g0159others(4): Show | 8 | HG02129.hp1 NA18951.hp1 NA18954.hp1 others(5): Show |
intron_variant | MODIFIER | c.978+54_978+63delTT others(8): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 54733747 | |||||
chr1:54733758
|
T | A | 5 | a0001c0003t0003g0232a0001c0003t0003g0251a0001c0003t0005g0252others(2): Show | 5 | HG02572.hp1 HG03209.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.978+48T>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54733758 | ||||||
chr1:54733759
|
T | A | 17 | a0001c0003t0003g0246a0001c0003t0003g0247a0001c0003t0003g0273others(14): Show | 17 | HG01074.hp1 HG01243.hp2 HG01517.hp2 others(14): Show |
intron_variant | MODIFIER | c.978+49T>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54733759 | ||||||
chr1:54733760
|
T | A | 32 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(29): Show | 40 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(37): Show |
intron_variant | MODIFIER | c.978+50T>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54733760 | ||||||
chr1:54733761
|
T | A | 5 | a0001c0003t0003g0232a0001c0003t0003g0251a0001c0003t0005g0252others(2): Show | 5 | HG02572.hp1 HG03209.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.978+51T>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54733761 | ||||||
chr1:54733762
|
T | A | 13 | a0001c0004t0003g0233a0001c0004t0003g0234a0001c0004t0003g0235others(10): Show | 13 | HG01074.hp1 HG01243.hp2 HG01517.hp2 others(10): Show |
intron_variant | MODIFIER | c.978+52T>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54733762 | ||||||
chr1:54733764
|
T | A | 5 | a0001c0003t0003g0232a0001c0003t0003g0251a0001c0003t0005g0252others(2): Show | 5 | HG02572.hp1 HG03209.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.978+54T>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54733764 | ||||||
chr1:54733814
|
T | G | 18 | a0001c0003t0003g0232a0001c0003t0003g0251a0001c0003t0005g0252others(15): Show | 18 | HG01074.hp1 HG01243.hp2 HG01517.hp2 others(15): Show |
intron_variant | MODIFIER | c.978+104T>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54733814 | ||||||
chr1:54733858
|
T | C | 1 | a0001c0001t0001g0183 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.978+148T>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54733858 | ||||||
chr1:54733907
|
A | G | 1 | a0001c0001t0001g0218 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.978+197A>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54733907 | ||||||
chr1:54734043
|
T | C | 2 | a0001c0001t0007g0128a0001c0001t0007g0129 | 2 | HG02922.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.978+333T>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54734043 | ||||||
chr1:54734079
|
T | A | 5 | a0001c0003t0003g0251a0001c0003t0005g0252a0001c0003t0005g0253others(2): Show | 5 | HG01891.hp2 HG02572.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.978+369T>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54734079 | ||||||
chr1:54734080
|
T | A | 62 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(59): Show | 74 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.978+370T>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54734080 | ||||||
chr1:54734081
|
T | A | 62 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(59): Show | 74 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.978+371T>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54734081 | ||||||
chr1:54734095
|
G | A | 1 | a0001c0001t0001g0198 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.978+385G>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54734095 | ||||||
chr1:54734186
|
C | T | 5 | a0001c0003t0003g0232a0001c0003t0003g0251a0001c0003t0005g0252others(2): Show | 5 | HG02572.hp1 HG03209.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.978+476C>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54734186 | ||||||
chr1:54734212
|
T | C | 62 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(59): Show | 74 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.978+502T>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54734212 | ||||||
chr1:54734272
|
A | C | 1 | a0001c0001t0001g0161 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.978+562A>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54734272 | ||||||
chr1:54734325
|
G | A | 18 | a0001c0003t0003g0232a0001c0003t0003g0251a0001c0003t0005g0252others(15): Show | 18 | HG01074.hp1 HG01243.hp2 HG01517.hp2 others(15): Show |
intron_variant | MODIFIER | c.978+615G>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54734325 | ||||||
chr1:54734347
|
T | C | 62 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(59): Show | 74 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.978+637T>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54734347 | ||||||
chr1:54734363
|
T | C | 62 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(59): Show | 74 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.978+653T>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54734363 | ||||||
chr1:54734463
|
G | A | 64 | a0001c0001t0007g0128a0001c0001t0007g0129a0001c0003t0003g0014others(61): Show | 76 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(73): Show |
intron_variant | MODIFIER | c.978+753G>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54734463 | ||||||
chr1:54734535
|
T | C | 62 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(59): Show | 74 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.978+825T>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54734535 | ||||||
chr1:54734579
|
G | A | 1 | a0001c0004t0003g0234 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.978+869G>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54734579 | ||||||
chr1:54735063
|
C | CT | 9 | a0002c0002t0002g0115a0002c0002t0003g0011a0002c0002t0003g0035others(6): Show | 13 | HG00642.hp2 HG01891.hp1 HG02723.hp2 others(10): Show |
intron_variant | MODIFIER | c.978+1364dupT | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 54735063 | |||||
chr1:54735125
|
G | T | 62 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(59): Show | 74 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.978+1415G>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54735125 | ||||||
chr1:54735127
|
C | T | 62 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(59): Show | 74 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.978+1417C>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54735127 | ||||||
chr1:54735156
|
G | A | 1 | a0001c0001t0001g0199 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.978+1446G>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54735156 | ||||||
chr1:54735156
|
G | T | 13 | a0001c0004t0003g0233a0001c0004t0003g0234a0001c0004t0003g0235others(10): Show | 13 | HG01074.hp1 HG01243.hp2 HG01517.hp2 others(10): Show |
intron_variant | MODIFIER | c.978+1446G>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54735156 | ||||||
chr1:54735163
|
G | A | 1 | a0002c0002t0002g0109 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.978+1453G>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54735163 | ||||||
chr1:54735310
|
C | T | 62 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(59): Show | 74 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.978+1600C>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54735310 | ||||||
chr1:54735338
|
C | G | 2 | a0001c0001t0007g0128a0001c0001t0007g0129 | 2 | HG02922.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.978+1628C>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54735338 | ||||||
chr1:54735370
|
A | C | 62 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(59): Show | 74 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.978+1660A>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54735370 | ||||||
chr1:54735377
|
G | A | 2 | a0001c0001t0001g0177a0001c0001t0001g0230 | 2 | HG00408.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.978+1667G>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54735377 | ||||||
chr1:54735438
|
C | G | 2 | a0001c0003t0003g0246a0001c0003t0003g0247 | 2 | HG03195.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.978+1728C>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54735438 | ||||||
chr1:54735461
|
T | A | 1 | a0001c0001t0001g0224 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.978+1751T>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54735461 | ||||||
chr1:54735516
|
C | T | 1 | a0001c0001t0001g0143 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.978+1806C>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54735516 | ||||||
chr1:54735575
|
C | T | 1 | a0001c0004t0003g0233 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.978+1865C>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54735575 | ||||||
chr1:54735588
|
G | A | 1 | a0001c0003t0003g0254 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.978+1878G>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54735588 | ||||||
chr1:54735592
|
A | ATAATCTC others(4): Show |
1 | a0001c0003t0003g0260 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.978+1884_978+1894d others(13): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 54735592 | |||||
chr1:54735719
|
C | T | 1 | a0001c0001t0001g0145 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.979-1863C>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54735719 | ||||||
chr1:54735748
|
C | T | 1 | a0001c0004t0003g0233 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.979-1834C>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54735748 | ||||||
chr1:54735765
|
A | G | 38 | a0002c0002t0002g0010a0002c0002t0002g0016a0002c0002t0002g0027others(35): Show | 50 | HG00099.hp2 HG00140.hp1 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.979-1817A>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54735765 | ||||||
chr1:54735891
|
T | A | 1 | a0001c0001t0001g0198 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.979-1691T>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54735891 | ||||||
chr1:54736147
|
G | C | 1 | a0002c0002t0002g0068 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.979-1435G>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736147 | ||||||
chr1:54736149
|
G | C | 1 | a0002c0002t0002g0068 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.979-1433G>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736149 | ||||||
chr1:54736155
|
A | C | 9 | a0001c0003t0003g0254a0002c0002t0003g0011a0002c0002t0003g0035others(6): Show | 13 | HG00642.hp2 HG01891.hp1 HG02723.hp1 others(10): Show |
intron_variant | MODIFIER | c.979-1427A>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736155 | ||||||
chr1:54736156
|
A | G | 1 | a0002c0002t0002g0068 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.979-1426A>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736156 | ||||||
chr1:54736157
|
G | C | 1 | a0002c0002t0002g0068 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.979-1425G>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736157 | ||||||
chr1:54736158
|
A | G | 1 | a0002c0002t0002g0068 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.979-1424A>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736158 | ||||||
chr1:54736160
|
A | T | 1 | a0002c0002t0002g0068 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.979-1422A>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736160 | ||||||
chr1:54736163
|
G | C | 1 | a0002c0002t0002g0068 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.979-1419G>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736163 | ||||||
chr1:54736164
|
A | T | 1 | a0002c0002t0002g0068 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.979-1418A>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736164 | ||||||
chr1:54736164
|
AAAGAAAG others(4): Show |
A | 15 | a0001c0003t0003g0246a0001c0003t0003g0254a0001c0003t0003g0264others(12): Show | 19 | HG00642.hp2 HG01891.hp1 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.979-1417_979-1407d others(13): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736164 | ||||||
chr1:54736165
|
A | C | 1 | a0002c0002t0002g0068 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.979-1417A>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736165 | ||||||
chr1:54736165
|
A | G | 47 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(44): Show | 55 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.979-1417A>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736165 | ||||||
chr1:54736168
|
A | T | 1 | a0002c0002t0002g0068 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.979-1414A>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736168 | ||||||
chr1:54736168
|
AAAGAAAG | A | 18 | a0001c0003t0003g0014a0001c0003t0003g0061a0001c0003t0003g0247others(15): Show | 22 | HG00408.hp1 HG00621.hp2 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.979-1413_979-1407d others(9): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736168 | ||||||
chr1:54736169
|
A | C | 1 | a0002c0002t0002g0068 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.979-1413A>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736169 | ||||||
chr1:54736169
|
A | G | 29 | a0001c0003t0003g0015a0001c0003t0003g0060a0001c0003t0003g0232others(26): Show | 33 | HG00423.hp1 HG01074.hp1 HG02080.hp2 others(30): Show |
intron_variant | MODIFIER | c.979-1413A>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736169 | ||||||
chr1:54736170
|
A | C | 1 | a0002c0002t0002g0068 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.979-1412A>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736170 | ||||||
chr1:54736172
|
A | T | 1 | a0002c0002t0002g0068 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.979-1410A>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736172 | ||||||
chr1:54736172
|
AAAG | A | 25 | a0001c0003t0003g0015a0001c0003t0003g0060a0001c0003t0003g0232others(22): Show | 29 | HG00423.hp1 HG01074.hp1 HG02080.hp2 others(26): Show |
intron_variant | MODIFIER | c.979-1409_979-1407d others(5): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736172 | ||||||
chr1:54736173
|
A | G | 4 | a0001c0003t0003g0265a0001c0003t0003g0269a0001c0004t0003g0240others(1): Show | 4 | HG02083.hp2 HG02735.hp2 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.979-1409A>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736173 | ||||||
chr1:54736173
|
A | T | 1 | a0002c0002t0002g0068 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.979-1409A>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736173 | ||||||
chr1:54736173
|
AAGGAGAG others(6): Show |
A | 2 | a0001c0001t0001g0052a0001c0001t0001g0188 | 3 | NA18940.hp1 NA18940.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.979-1406_979-1394d others(15): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 54736173 | |||||
chr1:54736174
|
A | G | 1 | a0002c0002t0002g0068 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.979-1408A>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736174 | ||||||
chr1:54736174
|
AG | A | 4 | a0001c0003t0003g0265a0001c0003t0003g0269a0001c0004t0003g0240others(1): Show | 4 | HG02083.hp2 HG02735.hp2 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.979-1406delG | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 54736174 | |||||
chr1:54736175
|
G | GGA | 11 | a0001c0001t0001g0182a0001c0001t0002g0249a0002c0002t0002g0010others(8): Show | 15 | HG00140.hp1 HG01081.hp2 HG01255.hp2 others(12): Show |
intron_variant | MODIFIER | c.979-1360_979-1359d others(4): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 54736175 | |||||
chr1:54736175
|
G | GGAGA | 11 | a0001c0001t0002g0250a0002c0002t0002g0030a0002c0002t0002g0062others(8): Show | 12 | HG00639.hp2 HG00738.hp1 HG00738.hp2 others(9): Show |
intron_variant | MODIFIER | c.979-1362_979-1359d others(6): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 54736175 | |||||
chr1:54736175
|
G | GGAGAGA | 6 | a0002c0002t0002g0031a0002c0002t0002g0080a0002c0002t0002g0092others(3): Show | 8 | HG01106.hp1 HG01167.hp2 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.979-1364_979-1359d others(8): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 54736175 | |||||
chr1:54736175
|
G | GGAGAGAG others(1): Show |
9 | a0002c0002t0002g0016a0002c0002t0002g0027a0002c0002t0002g0075others(6): Show | 12 | HG01123.hp1 HG01169.hp2 HG01261.hp1 others(9): Show |
intron_variant | MODIFIER | c.979-1366_979-1359d others(10): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 54736175 | |||||
chr1:54736175
|
G | GGAGAGAG others(3): Show |
1 | a0002c0002t0002g0099 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.979-1368_979-1359d others(12): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 54736175 | |||||
chr1:54736175
|
G | GGAGAGAG others(5): Show |
1 | a0002c0002t0002g0072 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.979-1370_979-1359d others(14): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 54736175 | |||||
chr1:54736175
|
G | GGAGAGAG others(7): Show |
3 | a0002c0002t0002g0100a0002c0002t0002g0108a0003c0006t0002g0087 | 3 | HG01175.hp1 HG02698.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.979-1372_979-1359d others(16): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 54736175 | |||||
chr1:54736175
|
GGA | G | 4 | a0002c0002t0002g0028a0002c0002t0002g0076a0002c0002t0002g0090others(1): Show | 5 | HG01243.hp1 HG02602.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.979-1360_979-1359d others(4): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 54736175 | |||||
chr1:54736175
|
GGAGA | G | 5 | a0002c0002t0002g0025a0002c0002t0002g0077a0002c0002t0002g0096others(2): Show | 6 | HG01109.hp2 HG02886.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.979-1362_979-1359d others(6): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 54736175 | |||||
chr1:54736175
|
GGAGAGA | G | 9 | a0001c0001t0001g0056a0001c0001t0001g0141a0001c0001t0001g0146others(6): Show | 10 | HG00423.hp2 HG01175.hp2 HG02132.hp2 others(7): Show |
intron_variant | MODIFIER | c.979-1364_979-1359d others(8): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 54736175 | |||||
chr1:54736175
|
GGAGAGAG others(1): Show |
G | 13 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0048others(10): Show | 24 | HG00438.hp1 HG00558.hp1 HG01123.hp2 others(21): Show |
intron_variant | MODIFIER | c.979-1366_979-1359d others(10): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 54736175 | |||||
chr1:54736175
|
GGAGAGAG others(3): Show |
G | 5 | a0001c0001t0001g0047a0001c0001t0001g0208a0001c0001t0001g0217others(2): Show | 7 | HG01975.hp1 HG01981.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.979-1368_979-1359d others(12): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 54736175 | |||||
chr1:54736175
|
GGAGAGAG others(5): Show |
G | 22 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0037others(19): Show | 33 | HG00323.hp2 HG00558.hp2 HG00621.hp1 others(30): Show |
intron_variant | MODIFIER | c.979-1370_979-1359d others(14): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 54736175 | |||||
chr1:54736175
|
GGAGAGAG others(7): Show |
G | 85 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(82): Show | 134 | HG00323.hp1 HG00408.hp2 HG00438.hp2 others(131): Show |
intron_variant | MODIFIER | c.979-1372_979-1359d others(16): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 54736175 | |||||
chr1:54736175
|
GGAGAGAG others(9): Show |
G | 4 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0184others(1): Show | 4 | NA18954.hp1 NA18954.hp2 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.979-1374_979-1359d others(18): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 54736175 | |||||
chr1:54736175
|
GGAGAGAG others(11): Show |
G | 13 | a0001c0001t0001g0020a0001c0001t0001g0053a0001c0001t0001g0074others(10): Show | 16 | HG00099.hp1 HG00140.hp2 HG00735.hp2 others(13): Show |
intron_variant | MODIFIER | c.979-1376_979-1359d others(20): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 54736175 | |||||
chr1:54736175
|
GGAGAGAG others(13): Show |
G | 2 | a0001c0001t0001g0151a0001c0001t0001g0229 | 2 | NA18953.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.979-1378_979-1359d others(22): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 54736175 | |||||
chr1:54736175
|
GGAGAGAG others(15): Show |
G | 1 | a0002c0002t0004g0118 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.979-1380_979-1359d others(24): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 54736175 | |||||
chr1:54736175
|
GGAGAGAG others(19): Show |
G | 2 | a0004c0005t0001g0005a0004c0005t0001g0130 | 6 | HG02258.hp2 HG02559.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.979-1384_979-1359d others(28): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 54736175 | |||||
chr1:54736177
|
A | T | 1 | a0002c0002t0002g0068 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.979-1405A>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736177 | ||||||
chr1:54736183
|
A | T | 1 | a0002c0002t0002g0068 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.979-1399A>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736183 | ||||||
chr1:54736186
|
G | T | 1 | a0002c0002t0002g0068 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.979-1396G>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736186 | ||||||
chr1:54736187
|
A | T | 1 | a0002c0002t0002g0068 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.979-1395A>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736187 | ||||||
chr1:54736189
|
A | G | 1 | a0002c0002t0002g0068 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.979-1393A>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736189 | ||||||
chr1:54736190
|
G | T | 1 | a0002c0002t0002g0068 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.979-1392G>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736190 | ||||||
chr1:54736191
|
A | T | 1 | a0001c0009t0003g0255 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.979-1391A>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736191 | ||||||
chr1:54736193
|
A | G | 1 | a0002c0002t0002g0068 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.979-1389A>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736193 | ||||||
chr1:54736193
|
A | T | 3 | a0001c0004t0003g0237a0001c0004t0003g0238a0001c0009t0003g0255 | 3 | HG01243.hp2 HG03098.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.979-1389A>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736193 | ||||||
chr1:54736195
|
A | T | 12 | a0001c0003t0003g0015a0001c0003t0003g0060a0001c0003t0003g0257others(9): Show | 16 | HG01243.hp2 HG02080.hp2 HG02135.hp1 others(13): Show |
intron_variant | MODIFIER | c.979-1387A>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736195 | ||||||
chr1:54736197
|
A | T | 17 | a0001c0003t0003g0015a0001c0003t0003g0060a0001c0003t0003g0257others(14): Show | 21 | HG01243.hp2 HG01891.hp2 HG02080.hp2 others(18): Show |
intron_variant | MODIFIER | c.979-1385A>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736197 | ||||||
chr1:54736199
|
A | T | 21 | a0001c0003t0003g0015a0001c0003t0003g0060a0001c0003t0003g0257others(18): Show | 25 | HG01243.hp2 HG01891.hp2 HG02080.hp2 others(22): Show |
intron_variant | MODIFIER | c.979-1383A>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736199 | ||||||
chr1:54736201
|
A | T | 24 | a0001c0003t0003g0015a0001c0003t0003g0060a0001c0003t0003g0257others(21): Show | 28 | HG00423.hp1 HG01243.hp2 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.979-1381A>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736201 | ||||||
chr1:54736203
|
A | T | 36 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(33): Show | 44 | HG00423.hp1 HG00621.hp2 HG01243.hp2 others(41): Show |
intron_variant | MODIFIER | c.979-1379A>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736203 | ||||||
chr1:54736205
|
A | T | 42 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(39): Show | 50 | HG00423.hp1 HG00621.hp2 HG01243.hp2 others(47): Show |
intron_variant | MODIFIER | c.979-1377A>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736205 | ||||||
chr1:54736207
|
A | T | 46 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(43): Show | 54 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.979-1375A>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736207 | ||||||
chr1:54736209
|
A | T | 48 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(45): Show | 56 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.979-1373A>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736209 | ||||||
chr1:54736209
|
AGAGAGAG others(21): Show |
A | 1 | a0001c0001t0001g0043 | 2 | NA18980.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.979-1372_979-1345d others(30): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736209 | ||||||
chr1:54736211
|
A | T | 51 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(48): Show | 59 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.979-1371A>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736211 | ||||||
chr1:54736213
|
A | T | 51 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(48): Show | 59 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.979-1369A>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736213 | ||||||
chr1:54736215
|
A | T | 53 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(50): Show | 61 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(58): Show |
intron_variant | MODIFIER | c.979-1367A>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736215 | ||||||
chr1:54736217
|
A | T | 56 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(53): Show | 67 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(64): Show |
intron_variant | MODIFIER | c.979-1365A>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736217 | ||||||
chr1:54736218
|
GAGAGAAG others(27): Show |
G | 2 | a0001c0004t0003g0233a0001c0004t0003g0245 | 2 | HG01891.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.979-1363_979-1330d others(36): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736218 | ||||||
chr1:54736219
|
A | T | 56 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(53): Show | 68 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(65): Show |
intron_variant | MODIFIER | c.979-1363A>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736219 | ||||||
chr1:54736220
|
GAGAAGAG others(18): Show |
G | 13 | a0001c0003t0003g0251a0001c0003t0003g0258a0001c0003t0003g0262others(10): Show | 13 | HG00423.hp1 HG01074.hp1 HG02300.hp1 others(10): Show |
intron_variant | MODIFIER | c.979-1361_979-1337d others(27): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736220 | ||||||
chr1:54736220
|
GAGAAGAG others(25): Show |
G | 4 | a0001c0003t0003g0268a0001c0003t0003g0283a0001c0004t0003g0237others(1): Show | 4 | HG01243.hp2 HG03098.hp1 NA18942.hp1 others(1): Show |
intron_variant | MODIFIER | c.979-1361_979-1330d others(34): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736220 | ||||||
chr1:54736221
|
A | T | 40 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(37): Show | 52 | HG00408.hp1 HG00621.hp2 HG00642.hp2 others(49): Show |
intron_variant | MODIFIER | c.979-1361A>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736221 | ||||||
chr1:54736222
|
GAAGAGGA others(2): Show |
G | 5 | a0001c0003t0003g0264a0001c0003t0003g0267a0001c0003t0003g0274others(2): Show | 8 | HG01891.hp1 HG02818.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.979-1359_979-1351d others(11): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736222 | ||||||
chr1:54736222
|
GAAGAGGA others(16): Show |
G | 11 | a0001c0003t0003g0014a0001c0003t0003g0061a0001c0003t0003g0259others(8): Show | 15 | HG00408.hp1 HG00621.hp2 HG01517.hp2 others(12): Show |
intron_variant | MODIFIER | c.979-1359_979-1337d others(25): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736222 | ||||||
chr1:54736222
|
GAAGAGGA others(23): Show |
G | 18 | a0001c0003t0003g0015a0001c0003t0003g0060a0001c0003t0003g0246others(15): Show | 22 | HG02080.hp2 HG02083.hp2 HG02135.hp1 others(19): Show |
intron_variant | MODIFIER | c.979-1359_979-1330d others(32): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736222 | ||||||
chr1:54736223
|
A | T | 6 | a0001c0003t0003g0254a0001c0003t0005g0252a0001c0003t0005g0253others(3): Show | 7 | HG02572.hp1 HG02723.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.979-1359A>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736223 | ||||||
chr1:54736224
|
A | G | 5 | a0001c0003t0003g0254a0001c0003t0005g0252a0001c0003t0005g0253others(2): Show | 6 | HG02572.hp1 HG02723.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.979-1358A>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736224 | ||||||
chr1:54736224
|
AGAGGAGA others(37): Show |
A | 1 | a0001c0009t0003g0255 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.979-1357_979-1314d others(46): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736224 | ||||||
chr1:54736225
|
G | T | 5 | a0001c0003t0003g0254a0001c0003t0005g0252a0001c0003t0005g0253others(2): Show | 6 | HG02572.hp1 HG02723.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.979-1357G>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736225 | ||||||
chr1:54736226
|
A | G | 5 | a0001c0003t0003g0254a0001c0003t0005g0252a0001c0003t0005g0253others(2): Show | 6 | HG02572.hp1 HG02723.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.979-1356A>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736226 | ||||||
chr1:54736227
|
G | T | 7 | a0001c0003t0003g0254a0001c0003t0005g0252a0001c0003t0005g0253others(4): Show | 8 | HG00642.hp2 HG02572.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.979-1355G>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736227 | ||||||
chr1:54736229
|
A | T | 8 | a0001c0003t0003g0232a0001c0003t0003g0254a0001c0003t0005g0252others(5): Show | 9 | HG00642.hp2 HG02572.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.979-1353A>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736229 | ||||||
chr1:54736231
|
A | T | 8 | a0001c0003t0003g0232a0001c0003t0003g0254a0001c0003t0005g0252others(5): Show | 9 | HG00642.hp2 HG02572.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.979-1351A>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736231 | ||||||
chr1:54736232
|
G | GT | 8 | a0001c0003t0003g0232a0001c0003t0003g0254a0001c0003t0005g0252others(5): Show | 9 | HG00642.hp2 HG02572.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.979-1350_979-1349i others(3): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736232 | ||||||
chr1:54736232
|
G | T | 5 | a0001c0003t0003g0264a0001c0003t0003g0267a0001c0003t0003g0274others(2): Show | 8 | HG01891.hp1 HG02818.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.979-1350G>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736232 | ||||||
chr1:54736234
|
A | T | 13 | a0001c0003t0003g0232a0001c0003t0003g0254a0001c0003t0003g0264others(10): Show | 17 | HG00642.hp2 HG01891.hp1 HG02572.hp1 others(14): Show |
intron_variant | MODIFIER | c.979-1348A>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736234 | ||||||
chr1:54736236
|
A | T | 13 | a0001c0003t0003g0232a0001c0003t0003g0254a0001c0003t0003g0264others(10): Show | 17 | HG00642.hp2 HG01891.hp1 HG02572.hp1 others(14): Show |
intron_variant | MODIFIER | c.979-1346A>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736236 | ||||||
chr1:54736238
|
A | T | 13 | a0001c0003t0003g0232a0001c0003t0003g0254a0001c0003t0003g0264others(10): Show | 17 | HG00642.hp2 HG01891.hp1 HG02572.hp1 others(14): Show |
intron_variant | MODIFIER | c.979-1344A>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736238 | ||||||
chr1:54736239
|
GAAGAGA | G | 9 | a0001c0003t0003g0254a0001c0003t0003g0264a0001c0003t0003g0267others(6): Show | 12 | HG01891.hp1 HG02572.hp1 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.979-1342_979-1337d others(8): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736239 | ||||||
chr1:54736239
|
GAAGAGAG others(6): Show |
G | 2 | a0002c0002t0003g0035a0002c0002t0003g0127 | 3 | HG02723.hp2 HG03486.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.979-1342_979-1330d others(15): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736239 | ||||||
chr1:54736241
|
A | G | 1 | a0001c0001t0001g0043 | 2 | NA18980.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.979-1341A>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736241 | ||||||
chr1:54736241
|
A | T | 2 | a0001c0003t0003g0232a0002c0002t0003g0123 | 2 | HG00642.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.979-1341A>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736241 | ||||||
chr1:54736243
|
A | T | 2 | a0001c0003t0003g0232a0002c0002t0003g0123 | 2 | HG00642.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.979-1339A>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736243 | ||||||
chr1:54736245
|
A | T | 2 | a0001c0003t0003g0232a0002c0002t0003g0123 | 2 | HG00642.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.979-1337A>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736245 | ||||||
chr1:54736246
|
G | T | 33 | a0001c0003t0003g0014a0001c0003t0003g0061a0001c0003t0003g0251others(30): Show | 40 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(37): Show |
intron_variant | MODIFIER | c.979-1336G>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736246 | ||||||
chr1:54736248
|
A | T | 35 | a0001c0003t0003g0014a0001c0003t0003g0061a0001c0003t0003g0232others(32): Show | 42 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.979-1334A>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736248 | ||||||
chr1:54736250
|
A | T | 35 | a0001c0003t0003g0014a0001c0003t0003g0061a0001c0003t0003g0232others(32): Show | 42 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.979-1332A>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736250 | ||||||
chr1:54736252
|
A | T | 33 | a0001c0003t0003g0014a0001c0003t0003g0061a0001c0003t0003g0232others(30): Show | 40 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(37): Show |
intron_variant | MODIFIER | c.979-1330A>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736252 | ||||||
chr1:54736253
|
G | GT | 33 | a0001c0003t0003g0014a0001c0003t0003g0061a0001c0003t0003g0232others(30): Show | 40 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(37): Show |
intron_variant | MODIFIER | c.979-1329_979-1328i others(3): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736253 | ||||||
chr1:54736253
|
G | T | 28 | a0001c0003t0003g0015a0001c0003t0003g0060a0001c0003t0003g0246others(25): Show | 33 | HG01243.hp2 HG01891.hp2 HG02080.hp2 others(30): Show |
intron_variant | MODIFIER | c.979-1329G>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736253 | ||||||
chr1:54736253
|
GGA | G | 9 | a0002c0002t0002g0025a0002c0002t0002g0066a0002c0002t0002g0067others(6): Show | 10 | HG01175.hp2 HG02451.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.979-1312_979-1311d others(4): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 54736253 | |||||
chr1:54736254
|
G | A | 1 | a0001c0001t0001g0043 | 2 | NA18980.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.979-1328G>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736254 | ||||||
chr1:54736255
|
A | T | 61 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(58): Show | 73 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(70): Show |
intron_variant | MODIFIER | c.979-1327A>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736255 | ||||||
chr1:54736257
|
A | T | 61 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(58): Show | 73 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(70): Show |
intron_variant | MODIFIER | c.979-1325A>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736257 | ||||||
chr1:54736259
|
A | T | 61 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(58): Show | 73 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(70): Show |
intron_variant | MODIFIER | c.979-1323A>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736259 | ||||||
chr1:54736261
|
A | T | 61 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(58): Show | 73 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(70): Show |
intron_variant | MODIFIER | c.979-1321A>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736261 | ||||||
chr1:54736263
|
A | T | 61 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(58): Show | 73 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(70): Show |
intron_variant | MODIFIER | c.979-1319A>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736263 | ||||||
chr1:54736265
|
A | T | 61 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(58): Show | 73 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(70): Show |
intron_variant | MODIFIER | c.979-1317A>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736265 | ||||||
chr1:54736267
|
A | T | 61 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(58): Show | 73 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(70): Show |
intron_variant | MODIFIER | c.979-1315A>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736267 | ||||||
chr1:54736268
|
G | A | 61 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(58): Show | 73 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(70): Show |
intron_variant | MODIFIER | c.979-1314G>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736268 | ||||||
chr1:54736270
|
G | A | 62 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(59): Show | 74 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.979-1312G>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736270 | ||||||
chr1:54736290
|
A | G | 1 | a0001c0001t0001g0228 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.979-1292A>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736290 | ||||||
chr1:54736300
|
CT | C | 287 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(284): Show | 397 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(394): Show |
intron_variant | MODIFIER | c.979-1280delT | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 54736300 | |||||
chr1:54736400
|
A | G | 62 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(59): Show | 74 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.979-1182A>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736400 | ||||||
chr1:54736438
|
TG | T | 62 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(59): Show | 74 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.979-1142delG | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | 54736438 | |||||
chr1:54736442
|
T | C | 75 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(72): Show | 112 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.979-1140T>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736442 | ||||||
chr1:54736473
|
C | T | 1 | a0001c0003t0003g0277 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.979-1109C>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736473 | ||||||
chr1:54736474
|
A | G | 62 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(59): Show | 74 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.979-1108A>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736474 | ||||||
chr1:54736509
|
C | T | 32 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(29): Show | 40 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(37): Show |
intron_variant | MODIFIER | c.979-1073C>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736509 | ||||||
chr1:54736525
|
C | T | 1 | a0002c0002t0002g0098 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.979-1057C>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736525 | ||||||
chr1:54736561
|
A | G | 62 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(59): Show | 74 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.979-1021A>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736561 | ||||||
chr1:54736578
|
C | T | 1 | a0001c0001t0001g0151 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.979-1004C>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736578 | ||||||
chr1:54736607
|
G | C | 2 | a0001c0003t0003g0246a0001c0003t0003g0247 | 2 | HG03195.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.979-975G>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736607 | ||||||
chr1:54736790
|
C | T | 2 | a0001c0003t0003g0246a0001c0003t0003g0247 | 2 | HG03195.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.979-792C>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736790 | ||||||
chr1:54736972
|
C | G | 62 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(59): Show | 74 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.979-610C>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54736972 | ||||||
chr1:54737040
|
T | C | 1 | a0004c0005t0001g0130 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.979-542T>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54737040 | ||||||
chr1:54737117
|
G | A | 62 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(59): Show | 74 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.979-465G>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54737117 | ||||||
chr1:54737201
|
T | C | 62 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(59): Show | 74 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.979-381T>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54737201 | ||||||
chr1:54737219
|
C | T | 24 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(21): Show | 32 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(29): Show |
intron_variant | MODIFIER | c.979-363C>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54737219 | ||||||
chr1:54737314
|
T | C | 287 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(284): Show | 397 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(394): Show |
intron_variant | MODIFIER | c.979-268T>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54737314 | ||||||
chr1:54737321
|
G | C | 2 | a0001c0001t0001g0019a0001c0001t0001g0209 | 4 | HG01069.hp1 HG01071.hp2 HG01257.hp2 others(1): Show |
intron_variant | MODIFIER | c.979-261G>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54737321 | ||||||
chr1:54737423
|
C | T | 1 | a0001c0009t0003g0255 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.979-159C>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54737423 | ||||||
chr1:54737462
|
A | G | 61 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(58): Show | 73 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(70): Show |
intron_variant | MODIFIER | c.979-120A>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54737462 | ||||||
chr1:54737483
|
A | G | 62 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(59): Show | 74 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.979-99A>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 8/9 | chr1 | 54737483 | ||||||
chr1:54737757
|
T | G | 62 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(59): Show | 74 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.1061+93T>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | chr1 | 54737757 | ||||||
chr1:54737760
|
G | A | 62 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(59): Show | 74 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.1061+96G>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | chr1 | 54737760 | ||||||
chr1:54737825
|
C | A | 1 | a0001c0003t0003g0254 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1061+161C>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | chr1 | 54737825 | ||||||
chr1:54737871
|
G | A | 19 | a0001c0003t0003g0232a0001c0003t0003g0251a0001c0003t0005g0252others(16): Show | 19 | HG01074.hp1 HG01243.hp2 HG01517.hp2 others(16): Show |
intron_variant | MODIFIER | c.1061+207G>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | chr1 | 54737871 | ||||||
chr1:54737908
|
C | CT | 18 | a0001c0003t0003g0232a0001c0003t0003g0251a0001c0003t0005g0252others(15): Show | 18 | HG01074.hp1 HG01243.hp2 HG01517.hp2 others(15): Show |
intron_variant | MODIFIER | c.1061+253dupT | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54737908 | |||||
chr1:54737908
|
CT | C | 5 | a0001c0001t0001g0022a0001c0001t0001g0206a0001c0001t0001g0207others(2): Show | 7 | HG02080.hp1 NA18939.hp1 NA18948.hp2 others(4): Show |
intron_variant | MODIFIER | c.1061+253delT | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54737908 | |||||
chr1:54737957
|
A | G | 62 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(59): Show | 74 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.1061+293A>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | chr1 | 54737957 | ||||||
chr1:54737995
|
G | C | 1 | a0001c0001t0001g0176 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1061+331G>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | chr1 | 54737995 | ||||||
chr1:54738045
|
C | T | 1 | a0001c0001t0001g0156 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1061+381C>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | chr1 | 54738045 | ||||||
chr1:54738057
|
C | T | 1 | a0001c0001t0001g0148 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1061+393C>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | chr1 | 54738057 | ||||||
chr1:54738058
|
G | A | 4 | a0001c0001t0002g0248a0001c0001t0002g0249a0001c0001t0002g0250others(1): Show | 4 | HG02896.hp1 HG02897.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1061+394G>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | chr1 | 54738058 | ||||||
chr1:54738061
|
C | T | 13 | a0001c0004t0003g0233a0001c0004t0003g0234a0001c0004t0003g0235others(10): Show | 13 | HG01074.hp1 HG01243.hp2 HG01517.hp2 others(10): Show |
intron_variant | MODIFIER | c.1061+397C>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | chr1 | 54738061 | ||||||
chr1:54738062
|
G | T | 2 | a0001c0001t0001g0190a0001c0001t0009g0160 | 2 | NA18942.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.1061+398G>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | chr1 | 54738062 | ||||||
chr1:54738068
|
CTT | C | 2 | a0004c0005t0001g0005a0004c0005t0001g0130 | 6 | HG02258.hp2 HG02559.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.1061+407_1061+408d others(4): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54738068 | |||||
chr1:54738089
|
C | T | 1 | a0001c0004t0003g0233 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1061+425C>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | chr1 | 54738089 | ||||||
chr1:54738138
|
T | G | 2 | a0001c0003t0005g0252a0001c0003t0005g0253 | 2 | HG02572.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1061+474T>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | chr1 | 54738138 | ||||||
chr1:54738156
|
C | G | 1 | a0001c0001t0001g0046 | 2 | HG01074.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.1061+492C>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | chr1 | 54738156 | ||||||
chr1:54738196
|
C | T | 44 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(41): Show | 56 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.1061+532C>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | chr1 | 54738196 | ||||||
chr1:54738198
|
G | A | 1 | a0001c0001t0001g0230 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1061+534G>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | chr1 | 54738198 | ||||||
chr1:54738249
|
A | G | 6 | a0001c0004t0003g0239a0001c0004t0003g0240a0001c0004t0003g0241others(3): Show | 6 | HG01074.hp1 HG01517.hp2 HG02300.hp1 others(3): Show |
intron_variant | MODIFIER | c.1061+585A>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | chr1 | 54738249 | ||||||
chr1:54738260
|
A | C | 1 | a0001c0001t0001g0214 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1061+596A>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | chr1 | 54738260 | ||||||
chr1:54738276
|
AC | A | 6 | a0001c0004t0003g0239a0001c0004t0003g0240a0001c0004t0003g0241others(3): Show | 6 | HG01074.hp1 HG01517.hp2 HG02300.hp1 others(3): Show |
intron_variant | MODIFIER | c.1061+617delC | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54738276 | |||||
chr1:54738277
|
C | A | 1 | a0001c0003t0003g0271 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1061+613C>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | chr1 | 54738277 | ||||||
chr1:54738354
|
G | A | 2 | a0002c0002t0002g0097a0002c0002t0002g0101 | 2 | HG01109.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1061+690G>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | chr1 | 54738354 | ||||||
chr1:54738448
|
C | T | 1 | a0001c0001t0001g0159 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1061+784C>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | chr1 | 54738448 | ||||||
chr1:54738511
|
T | C | 1 | a0001c0001t0001g0218 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1061+847T>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | chr1 | 54738511 | ||||||
chr1:54738590
|
G | A | 32 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(29): Show | 40 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(37): Show |
intron_variant | MODIFIER | c.1061+926G>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | chr1 | 54738590 | ||||||
chr1:54738661
|
C | CT | 47 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0009others(44): Show | 75 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(72): Show |
intron_variant | MODIFIER | c.1061+1011dupT | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54738661 | |||||
chr1:54738661
|
C | CTTTTTTT others(1): Show |
33 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0061others(30): Show | 44 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(41): Show |
intron_variant | MODIFIER | c.1061+1004_1061+101 others(12): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54738661 | |||||
chr1:54738661
|
C | CTTTTTTT others(2): Show |
25 | a0001c0003t0003g0060a0001c0003t0003g0251a0001c0003t0003g0254others(22): Show | 26 | HG01074.hp1 HG01243.hp2 HG01517.hp2 others(23): Show |
intron_variant | MODIFIER | c.1061+1003_1061+101 others(13): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54738661 | |||||
chr1:54738661
|
C | CTTTTTTT others(3): Show |
1 | a0001c0003t0003g0232 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1061+1002_1061+101 others(14): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54738661 | |||||
chr1:54738689
|
G | A | 1 | a0001c0004t0003g0233 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1061+1025G>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | chr1 | 54738689 | ||||||
chr1:54738758
|
G | T | 1 | a0001c0001t0001g0051 | 2 | HG02559.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1061+1094G>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | chr1 | 54738758 | ||||||
chr1:54738780
|
A | C | 1 | a0002c0002t0002g0113 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1061+1116A>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | chr1 | 54738780 | ||||||
chr1:54738838
|
T | C | 1 | a0001c0001t0001g0189 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1061+1174T>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | chr1 | 54738838 | ||||||
chr1:54738844
|
G | A | 1 | a0001c0001t0001g0205 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1061+1180G>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | chr1 | 54738844 | ||||||
chr1:54738975
|
T | A | 1 | a0001c0001t0001g0230 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1061+1311T>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | chr1 | 54738975 | ||||||
chr1:54738992
|
A | G | 18 | a0001c0003t0003g0232a0001c0003t0003g0251a0001c0003t0005g0252others(15): Show | 18 | HG01074.hp1 HG01243.hp2 HG01517.hp2 others(15): Show |
intron_variant | MODIFIER | c.1061+1328A>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | chr1 | 54738992 | ||||||
chr1:54739011
|
CTTTT | C | 5 | a0002c0002t0001g0116a0002c0002t0004g0117a0002c0002t0004g0118others(2): Show | 5 | HG02615.hp2 HG03041.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1061+1348_1061+135 others(8): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | chr1 | 54739011 | ||||||
chr1:54739037
|
A | ATTT | 27 | a0001c0003t0003g0232a0001c0003t0003g0254a0001c0003t0003g0284others(24): Show | 31 | HG00642.hp2 HG01074.hp1 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.1061+1384_1061+138 others(7): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54739037 | |||||
chr1:54739037
|
A | ATTTT | 33 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(30): Show | 41 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(38): Show |
intron_variant | MODIFIER | c.1061+1383_1061+138 others(8): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54739037 | |||||
chr1:54739092
|
G | A | 1 | a0001c0004t0003g0235 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1061+1428G>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | chr1 | 54739092 | ||||||
chr1:54739111
|
A | G | 1 | a0001c0003t0003g0060 | 2 | HG02080.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.1061+1447A>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | chr1 | 54739111 | ||||||
chr1:54739187
|
T | A | 1 | a0001c0004t0003g0233 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1061+1523T>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | chr1 | 54739187 | ||||||
chr1:54739412
|
C | T | 28 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(25): Show | 48 | HG00438.hp2 HG00558.hp1 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.1061+1748C>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | chr1 | 54739412 | ||||||
chr1:54739526
|
A | G | 64 | a0001c0001t0007g0128a0001c0001t0007g0129a0001c0003t0003g0014others(61): Show | 76 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(73): Show |
intron_variant | MODIFIER | c.1061+1862A>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | chr1 | 54739526 | ||||||
chr1:54739625
|
C | T | 32 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(29): Show | 40 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(37): Show |
intron_variant | MODIFIER | c.1062-1786C>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | chr1 | 54739625 | ||||||
chr1:54739684
|
C | A | 62 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(59): Show | 74 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.1062-1727C>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | chr1 | 54739684 | ||||||
chr1:54739699
|
G | T | 1 | a0001c0001t0001g0224 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1062-1712G>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | chr1 | 54739699 | ||||||
chr1:54739727
|
A | G | 7 | a0002c0002t0003g0011a0002c0002t0003g0035a0002c0002t0003g0078others(4): Show | 11 | HG01891.hp1 HG02723.hp2 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.1062-1684A>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | chr1 | 54739727 | ||||||
chr1:54739807
|
G | T | 1 | a0001c0009t0003g0255 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1062-1604G>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | chr1 | 54739807 | ||||||
chr1:54739907
|
C | T | 2 | a0001c0003t0003g0246a0001c0003t0003g0247 | 2 | HG03195.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1062-1504C>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | chr1 | 54739907 | ||||||
chr1:54739912
|
A | G | 1 | a0001c0001t0001g0145 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1062-1499A>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | chr1 | 54739912 | ||||||
chr1:54739920
|
T | C | 1 | a0002c0002t0003g0123 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1062-1491T>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | chr1 | 54739920 | ||||||
chr1:54740027
|
A | T | 1 | a0001c0001t0001g0224 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1062-1384A>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | chr1 | 54740027 | ||||||
chr1:54740029
|
C | T | 62 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(59): Show | 74 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.1062-1382C>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | chr1 | 54740029 | ||||||
chr1:54740122
|
C | G | 5 | a0002c0002t0001g0116a0002c0002t0004g0117a0002c0002t0004g0118others(2): Show | 5 | HG02615.hp2 HG03041.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1062-1289C>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | chr1 | 54740122 | ||||||
chr1:54740139
|
CACTCCAG others(16): Show |
C | 13 | a0001c0004t0003g0233a0001c0004t0003g0234a0001c0004t0003g0235others(10): Show | 13 | HG01074.hp1 HG01243.hp2 HG01517.hp2 others(10): Show |
intron_variant | MODIFIER | c.1062-1269_1062-124 others(27): Show |
TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr1 | 54740139 | |||||
chr1:54740146
|
G | A | 1 | a0001c0009t0003g0255 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1062-1265G>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | chr1 | 54740146 | ||||||
chr1:54740168
|
C | A | 62 | a0001c0003t0003g0014a0001c0003t0003g0015a0001c0003t0003g0060others(59): Show | 74 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.1062-1243C>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | chr1 | 54740168 | ||||||
chr1:54740192
|
A | G | 2 | a0001c0001t0001g0199a0001c0001t0001g0201 | 2 | HG03704.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.1062-1219A>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | chr1 | 54740192 | ||||||
chr1:54740277
|
T | C | 1 | a0001c0001t0001g0158 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1062-1134T>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | chr1 | 54740277 | ||||||
chr1:54740283
|
G | A | 1 | a0001c0001t0001g0158 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1062-1128G>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | chr1 | 54740283 | ||||||
chr1:54740490
|
T | C | 5 | a0001c0003t0003g0232a0001c0003t0003g0251a0001c0003t0005g0252others(2): Show | 5 | HG02572.hp1 HG03209.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.1062-921T>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | chr1 | 54740490 | ||||||
chr1:54740564
|
C | T | 3 | a0001c0003t0003g0261a0001c0003t0003g0274a0001c0003t0003g0276 | 3 | HG03834.hp2 HG03942.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.1062-847C>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | chr1 | 54740564 | ||||||
chr1:54740624
|
C | G | 5 | a0001c0003t0003g0232a0001c0003t0003g0251a0001c0003t0005g0252others(2): Show | 5 | HG02572.hp1 HG03209.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.1062-787C>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | chr1 | 54740624 | ||||||
chr1:54740764
|
C | G | 1 | a0001c0003t0003g0254 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1062-647C>G | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | chr1 | 54740764 | ||||||
chr1:54740926
|
G | T | 2 | a0002c0002t0002g0076a0002c0002t0002g0121 | 2 | NA19080.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.1062-485G>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | chr1 | 54740926 | ||||||
chr1:54740974
|
G | A | 3 | a0001c0004t0003g0240a0001c0004t0003g0242a0001c0004t0003g0244 | 3 | HG02602.hp1 HG02735.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.1062-437G>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | chr1 | 54740974 | ||||||
chr1:54741157
|
T | A | 18 | a0001c0003t0003g0232a0001c0003t0003g0251a0001c0003t0005g0252others(15): Show | 18 | HG01074.hp1 HG01243.hp2 HG01517.hp2 others(15): Show |
intron_variant | MODIFIER | c.1062-254T>A | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | chr1 | 54741157 | ||||||
chr1:54741379
|
T | C | 18 | a0001c0003t0003g0232a0001c0003t0003g0251a0001c0003t0005g0252others(15): Show | 18 | HG01074.hp1 HG01243.hp2 HG01517.hp2 others(15): Show |
intron_variant | MODIFIER | c.1062-32T>C | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | chr1 | 54741379 | ||||||
chr1:54741405
|
C | T | 1 | a0001c0001t0007g0128 | 1 | HG02922.hp2 | splice_region_variant&intron_variant | LOW | c.1062-6C>T | TTC4 | ENSG00000243725.7 | transcript | ENST00000371281.4 | protein_coding | 9/9 | chr1 | 54741405 |