geneid | 94015 |
---|---|
ensemblid | ENSG00000141540.11 |
hgncid | 13877 |
symbol | TTYH2 |
name | tweety family member 2 |
refseq_nuc | NM_032646.6 |
refseq_prot | NP_116035.5 |
ensembl_nuc | ENST00000269346.9 |
ensembl_prot | ENSP00000269346.4 |
mane_status | MANE Select |
chr | chr17 |
start | 74213571 |
end | 74262020 |
strand | + |
ver | v1.2 |
region | chr17:74213571-74262020 |
region5000 | chr17:74208571-74267020 |
regionname0 | TTYH2_chr17_74213571_74262020 |
regionname5000 | TTYH2_chr17_74208571_74267020 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 534 | 182 | 32 | 36 | 87 | 8 | 18 | 57 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
a0002 | 0/0 | 534 | 42 | 3 | 10 | 13 | 4 | 12 | 11 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
a0003 | 0/0 | 534 | 34 | 15 | 8 | 2 | 2 | 7 | 2 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
a0004 | 0/0 | 534 | 19 | 9 | 1 | 3 | 3 | 3 | 3 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
a0005 | 0/0 | 534 | 16 | 11 | 0 | 5 | 0 | 0 | 4 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
a0006 | 0/0 | 534 | 13 | 7 | 3 | 0 | 0 | 3 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
a0007 | 0/1 | 534 | 10 | 5 | 2 | 1 | 0 | 1 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
a0008 | 0/0 | 534 | 9 | 0 | 2 | 5 | 1 | 1 | 5 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
a0009 | 0/0 | 534 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
a0010 | 0/0 | 534 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
a0011 | 0/0 | 534 | 4 | 0 | 0 | 4 | 0 | 0 | 4 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
a0012 | 0/0 | 534 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
a0013 | 0/0 | 534 | 3 | 2 | 0 | 1 | 0 | 0 | 1 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
a0014 | 0/0 | 534 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
a0015 | 0/0 | 534 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
a0016 | 0/0 | 534 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
a0017 | 0/0 | 534 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
a0018 | 0/0 | 534 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
a0019 | 0/0 | 534 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
a0020 | 0/0 | 534 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
a0021 | 0/0 | 534 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/0 | 1605 | 170 | 20 | 36 | 87 | 8 | 18 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
c0002 | 0/0 | 1605 | 40 | 3 | 10 | 13 | 3 | 11 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
c0003 | 0/0 | 1605 | 34 | 15 | 8 | 2 | 2 | 7 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
c0004 | 0/0 | 1605 | 13 | 7 | 3 | 0 | 0 | 3 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
c0005 | 0/0 | 1605 | 10 | 1 | 0 | 3 | 3 | 3 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
c0006 | 0/0 | 1605 | 9 | 8 | 1 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
c0007 | 0/0 | 1605 | 8 | 3 | 0 | 5 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
c0008 | 0/0 | 1605 | 8 | 0 | 1 | 5 | 1 | 1 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
c0009 | 0/0 | 1605 | 7 | 7 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
c0010 | 0/0 | 1605 | 6 | 6 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
c0011 | 0/0 | 1605 | 5 | 4 | 1 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
c0012 | 0/1 | 1605 | 5 | 1 | 1 | 1 | 0 | 1 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
c0013 | 0/0 | 1605 | 4 | 4 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
c0014 | 0/0 | 1605 | 4 | 4 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
c0015 | 0/0 | 1605 | 4 | 0 | 0 | 4 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
c0016 | 0/0 | 1605 | 4 | 4 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
c0017 | 0/0 | 1605 | 3 | 3 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
c0018 | 0/0 | 1605 | 3 | 2 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
c0019 | 0/0 | 1605 | 2 | 0 | 0 | 0 | 1 | 1 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
c0020 | 0/0 | 1605 | 2 | 2 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
c0021 | 0/0 | 1605 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
c0022 | 0/0 | 1605 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
c0023 | 0/0 | 1605 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
c0024 | 0/0 | 1605 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
c0025 | 0/0 | 1605 | 1 | 0 | 0 | 0 | 0 | 1 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
c0026 | 0/0 | 1605 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
c0027 | 0/0 | 1605 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
c0028 | 0/0 | 1605 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
c0029 | 0/0 | 1605 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
c0030 | 0/0 | 1605 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
c0031 | 0/0 | 1605 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
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 | 1/1 | 1829 | 200 | 33 | 39 | 92 | 11 | 23 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
t0002 | 0/0 | 1829 | 62 | 30 | 13 | 7 | 3 | 9 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
t0003 | 0/0 | 1829 | 42 | 3 | 11 | 12 | 4 | 12 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
t0004 | 0/0 | 1829 | 10 | 10 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
t0005 | 0/0 | 1829 | 5 | 5 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
t0006 | 0/0 | 1829 | 5 | 0 | 0 | 5 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
t0007 | 0/0 | 1829 | 4 | 4 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
t0008 | 0/0 | 1829 | 4 | 4 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
t0009 | 0/0 | 1829 | 4 | 3 | 1 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
t0010 | 0/0 | 1829 | 3 | 3 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
t0011 | 0/0 | 1829 | 2 | 0 | 0 | 2 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
t0012 | 0/0 | 1829 | 2 | 2 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
t0013 | 0/0 | 1829 | 1 | 0 | 0 | 0 | 0 | 1 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
t0014 | 0/0 | 1829 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
t0015 | 0/0 | 1816 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
t0016 | 0/0 | 1829 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
t0017 | 0/0 | 1829 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
t0018 | 0/0 | 1829 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
t0019 | 0/0 | 1829 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
t0020 | 0/0 | 1829 | 1 | 0 | 0 | 0 | 0 | 1 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
t0021 | 0/0 | 1829 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
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 | 5 | 0 | 0 | 5 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0002 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0003 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0004 | 0/0 | 3 | 1 | 1 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0006 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0007 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0008 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0012 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0013 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0017 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0018 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0020 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0021 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0066 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0272 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0285 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 1605 | 170 | 20 | 36 | 87 | 8 | 18 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
a0001c0009 | 0/0 | 1605 | 7 | 7 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
a0001c0014 | 0/0 | 1605 | 4 | 4 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
a0001c0026 | 0/0 | 1605 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
a0002c0002 | 0/0 | 1605 | 40 | 3 | 10 | 13 | 3 | 11 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
a0002c0019 | 0/0 | 1605 | 2 | 0 | 0 | 0 | 1 | 1 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
a0003c0003 | 0/0 | 1605 | 34 | 15 | 8 | 2 | 2 | 7 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
a0004c0005 | 0/0 | 1605 | 10 | 1 | 0 | 3 | 3 | 3 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
a0004c0006 | 0/0 | 1605 | 9 | 8 | 1 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
a0005c0007 | 0/0 | 1605 | 8 | 3 | 0 | 5 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
a0005c0010 | 0/0 | 1605 | 6 | 6 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
a0005c0020 | 0/0 | 1605 | 2 | 2 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
a0006c0004 | 0/0 | 1605 | 13 | 7 | 3 | 0 | 0 | 3 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
a0007c0011 | 0/0 | 1605 | 5 | 4 | 1 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
a0007c0012 | 0/1 | 1605 | 5 | 1 | 1 | 1 | 0 | 1 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
a0008c0008 | 0/0 | 1605 | 8 | 0 | 1 | 5 | 1 | 1 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
a0008c0029 | 0/0 | 1605 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
a0009c0016 | 0/0 | 1605 | 4 | 4 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
a0010c0013 | 0/0 | 1605 | 4 | 4 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
a0011c0015 | 0/0 | 1605 | 4 | 0 | 0 | 4 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
a0012c0017 | 0/0 | 1605 | 3 | 3 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
a0013c0018 | 0/0 | 1605 | 3 | 2 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
a0014c0023 | 0/0 | 1605 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
a0014c0024 | 0/0 | 1605 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
a0015c0021 | 0/0 | 1605 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
a0016c0022 | 0/0 | 1605 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
a0017c0025 | 0/0 | 1605 | 1 | 0 | 0 | 0 | 0 | 1 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
a0018c0030 | 0/0 | 1605 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
a0019c0027 | 0/0 | 1605 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
a0020c0028 | 0/0 | 1605 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
a0021c0031 | 0/0 | 1605 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 3433 | 155 | 13 | 34 | 82 | 8 | 17 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
a0001c0001t0002 | 0/0 | 3433 | 8 | 7 | 1 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
a0001c0001t0003 | 0/0 | 3433 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
a0001c0001t0011 | 0/0 | 3433 | 2 | 0 | 0 | 2 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
a0001c0001t0013 | 0/0 | 3433 | 1 | 0 | 0 | 0 | 0 | 1 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
a0001c0001t0014 | 0/0 | 3433 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
a0001c0001t0016 | 0/0 | 3433 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
a0001c0001t0017 | 0/0 | 3433 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
a0001c0009t0005 | 0/0 | 3433 | 5 | 5 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
a0001c0009t0012 | 0/0 | 3433 | 2 | 2 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
a0001c0014t0001 | 0/0 | 3433 | 3 | 3 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
a0001c0014t0010 | 0/0 | 3433 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
a0001c0026t0001 | 0/0 | 3433 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
a0002c0002t0001 | 0/0 | 3433 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
a0002c0002t0003 | 0/0 | 3433 | 38 | 3 | 10 | 11 | 3 | 11 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
a0002c0002t0021 | 0/0 | 3433 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
a0002c0019t0003 | 0/0 | 3433 | 2 | 0 | 0 | 0 | 1 | 1 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
a0003c0003t0001 | 0/0 | 3433 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
a0003c0003t0002 | 0/0 | 3433 | 29 | 12 | 7 | 1 | 2 | 7 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
a0003c0003t0009 | 0/0 | 3433 | 4 | 3 | 1 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
a0004c0005t0001 | 0/0 | 3433 | 10 | 1 | 0 | 3 | 3 | 3 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
a0004c0006t0001 | 0/0 | 3433 | 8 | 7 | 1 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
a0004c0006t0008 | 0/0 | 3433 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
a0005c0007t0006 | 0/0 | 3433 | 5 | 0 | 0 | 5 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
a0005c0007t0008 | 0/0 | 3433 | 2 | 2 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
a0005c0007t0018 | 0/0 | 3433 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
a0005c0010t0002 | 0/0 | 3433 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
a0005c0010t0004 | 0/0 | 3433 | 5 | 5 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
a0005c0020t0001 | 0/0 | 3433 | 2 | 2 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
a0006c0004t0001 | 0/0 | 3433 | 1 | 0 | 0 | 0 | 0 | 1 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
a0006c0004t0002 | 0/0 | 3433 | 12 | 7 | 3 | 0 | 0 | 2 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
a0007c0011t0001 | 0/0 | 3433 | 5 | 4 | 1 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
a0007c0012t0001 | 0/1 | 3433 | 5 | 1 | 1 | 1 | 0 | 1 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
a0008c0008t0002 | 0/0 | 3433 | 7 | 0 | 1 | 5 | 1 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
a0008c0008t0020 | 0/0 | 3433 | 1 | 0 | 0 | 0 | 0 | 1 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
a0008c0029t0002 | 0/0 | 3433 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
a0009c0016t0007 | 0/0 | 3433 | 4 | 4 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
a0010c0013t0004 | 0/0 | 3433 | 4 | 4 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
a0011c0015t0001 | 0/0 | 3433 | 4 | 0 | 0 | 4 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
a0012c0017t0010 | 0/0 | 3433 | 2 | 2 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
a0012c0017t0019 | 0/0 | 3433 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
a0013c0018t0002 | 0/0 | 3433 | 3 | 2 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
a0014c0023t0001 | 0/0 | 3433 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
a0014c0024t0001 | 0/0 | 3433 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
a0015c0021t0004 | 0/0 | 3433 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
a0016c0022t0015 | 0/0 | 3420 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
a0017c0025t0001 | 0/0 | 3433 | 1 | 0 | 0 | 0 | 0 | 1 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
a0018c0030t0002 | 0/0 | 3433 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
a0019c0027t0003 | 0/0 | 3433 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
a0020c0028t0001 | 0/0 | 3433 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
a0021c0031t0008 | 0/0 | 3433 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | copy fasta | chr17 | 74208571 | 74267020 |
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 | 5 | 0 | 0 | 5 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0001g0004 | 0/0 | 3 | 1 | 1 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0001g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0001g0006 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0001g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0001g0066 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0002g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0002g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0002g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0002g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0002g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0002g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0003g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0011g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0011g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0013g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0014g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0016g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0001t0017g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0009t0005g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0009t0005g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0009t0005g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0009t0005g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0009t0012g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0009t0012g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0014t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0014t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0014t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0014t0010g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0001c0026t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0002c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0002c0002t0003g0002 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0002c0002t0003g0007 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0002c0002t0003g0008 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0002c0002t0003g0020 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0002c0002t0003g0021 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0002c0002t0003g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0002c0002t0003g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0002c0002t0003g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0002c0002t0003g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0002c0002t0003g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0002c0002t0003g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0002c0002t0003g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0002c0002t0003g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0002c0002t0003g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0002c0002t0003g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0002c0002t0003g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0002c0002t0003g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0002c0002t0003g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0002c0002t0003g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0002c0002t0003g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0002c0002t0003g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0002c0002t0003g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0002c0002t0003g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0002c0002t0003g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0002c0002t0003g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0002c0002t0003g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0002c0002t0003g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0002c0002t0003g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0002c0002t0021g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0002c0019t0003g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0002c0019t0003g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0003c0003t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0003c0003t0002g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0003c0003t0002g0013 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0003c0003t0002g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0003c0003t0002g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0003c0003t0002g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0003c0003t0002g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0003c0003t0002g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0003c0003t0002g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0003c0003t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0003c0003t0002g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0003c0003t0002g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0003c0003t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0003c0003t0002g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0003c0003t0002g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0003c0003t0002g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0003c0003t0002g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0003c0003t0002g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0003c0003t0002g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0003c0003t0002g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0003c0003t0002g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0003c0003t0002g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0003c0003t0002g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0003c0003t0002g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0003c0003t0002g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0003c0003t0002g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0003c0003t0002g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0003c0003t0002g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0003c0003t0009g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0003c0003t0009g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0003c0003t0009g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0003c0003t0009g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0004c0005t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0004c0005t0001g0012 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0004c0005t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0004c0005t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0004c0005t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0004c0005t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0004c0005t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0004c0005t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0004c0006t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0004c0006t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0004c0006t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0004c0006t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0004c0006t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0004c0006t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0004c0006t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0004c0006t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0004c0006t0008g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0005c0007t0006g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0005c0007t0006g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0005c0007t0006g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0005c0007t0006g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0005c0007t0006g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0005c0007t0008g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0005c0007t0008g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0005c0007t0018g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0005c0010t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0005c0010t0004g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0005c0010t0004g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0005c0010t0004g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0005c0010t0004g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0005c0010t0004g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0005c0020t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0005c0020t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0006c0004t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0006c0004t0002g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0006c0004t0002g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0006c0004t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0006c0004t0002g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0006c0004t0002g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0006c0004t0002g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0006c0004t0002g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0006c0004t0002g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0006c0004t0002g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0006c0004t0002g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0006c0004t0002g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0007c0011t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0007c0011t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0007c0011t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0007c0011t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0007c0011t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0007c0012t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0007c0012t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0007c0012t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0007c0012t0001g0272 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0007c0012t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0008c0008t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0008c0008t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0008c0008t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0008c0008t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0008c0008t0002g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0008c0008t0002g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0008c0008t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0008c0008t0020g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0008c0029t0002g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0009c0016t0007g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0009c0016t0007g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0009c0016t0007g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0009c0016t0007g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0010c0013t0004g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0010c0013t0004g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0010c0013t0004g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0010c0013t0004g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0011c0015t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0011c0015t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0011c0015t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0011c0015t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0012c0017t0010g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0012c0017t0010g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0012c0017t0019g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0013c0018t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0013c0018t0002g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0013c0018t0002g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0014c0023t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0014c0024t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0015c0021t0004g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0016c0022t0015g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0017c0025t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0018c0030t0002g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0019c0027t0003g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0020c0028t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
a0021c0031t0008g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0004 | c0005 | t0001 | g0132 | EUR | GBR | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG00099 | hp2 | a0002 | c0019 | t0003 | g0215 | EUR | GBR | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG00140 | hp1 | a0008 | c0008 | t0002 | g0143 | EUR | GBR | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG00140 | hp2 | a0003 | c0003 | t0002 | g0124 | EUR | GBR | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG00280 | hp1 | a0004 | c0005 | t0001 | g0012 | EUR | FIN | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG00280 | hp2 | a0004 | c0005 | t0001 | g0123 | EUR | FIN | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0285 | EUR | FIN | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0237 | EUR | FIN | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | CHS | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | CHS | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG00438 | hp1 | a0005 | c0007 | t0006 | g0187 | EAS | CHS | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | CHS | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | CHS | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG00597 | hp2 | a0001 | c0001 | t0017 | g0198 | EAS | CHS | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG00639 | hp1 | a0003 | c0003 | t0009 | g0084 | AMR | PUR | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG00639 | hp2 | a0003 | c0003 | t0002 | g0266 | AMR | PUR | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG00733 | hp1 | a0001 | c0001 | t0002 | g0150 | AMR | PUR | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG00733 | hp2 | a0003 | c0003 | t0002 | g0165 | AMR | PUR | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | PUR | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0200 | AMR | PUR | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG00738 | hp2 | a0004 | c0006 | t0001 | g0094 | AMR | PUR | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0300 | AMR | PUR | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0239 | AMR | PUR | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG01069 | hp1 | a0001 | c0001 | t0003 | g0018 | AMR | PUR | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG01069 | hp2 | a0002 | c0002 | t0003 | g0008 | AMR | PUR | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG01074 | hp1 | a0007 | c0011 | t0001 | g0309 | AMR | PUR | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG01081 | hp1 | a0006 | c0004 | t0002 | g0014 | AMR | PUR | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG01081 | hp2 | a0002 | c0002 | t0003 | g0211 | AMR | PUR | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0284 | AMR | PUR | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG01109 | hp1 | a0003 | c0003 | t0002 | g0206 | AMR | PUR | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0254 | AMR | PUR | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG01168 | hp1 | a0002 | c0002 | t0003 | g0007 | AMR | PUR | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0270 | AMR | PUR | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG01169 | hp1 | a0002 | c0002 | t0003 | g0007 | AMR | PUR | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | PUR | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG01192 | hp2 | a0006 | c0004 | t0002 | g0014 | AMR | PUR | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG01243 | hp1 | a0002 | c0002 | t0003 | g0279 | AMR | PUR | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG01243 | hp2 | a0014 | c0023 | t0001 | g0116 | AMR | PUR | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG01255 | hp1 | a0003 | c0003 | t0002 | g0172 | AMR | CLM | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0058 | AMR | CLM | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0256 | AMR | CLM | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0213 | AMR | CLM | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG01261 | hp1 | a0003 | c0003 | t0002 | g0013 | AMR | CLM | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG01261 | hp2 | a0003 | c0003 | t0002 | g0298 | AMR | CLM | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG01346 | hp1 | a0007 | c0012 | t0001 | g0218 | AMR | CLM | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG01346 | hp2 | a0008 | c0029 | t0002 | g0233 | AMR | CLM | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG01361 | hp1 | a0014 | c0024 | t0001 | g0135 | AMR | CLM | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0238 | AMR | CLM | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG01433 | hp1 | a0002 | c0002 | t0003 | g0208 | AMR | CLM | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | CLM | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG01496 | hp1 | a0008 | c0008 | t0002 | g0144 | AMR | CLM | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | CLM | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0111 | EUR | IBS | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG01515 | hp2 | a0002 | c0002 | t0003 | g0205 | EUR | IBS | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG01516 | hp1 | a0003 | c0003 | t0002 | g0073 | EUR | IBS | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0045 | EUR | IBS | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0046 | EUR | IBS | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG01517 | hp2 | a0002 | c0002 | t0003 | g0204 | EUR | IBS | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG01884 | hp1 | a0006 | c0004 | t0002 | g0081 | AFR | ACB | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG01884 | hp2 | a0010 | c0013 | t0004 | g0294 | AFR | ACB | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG01891 | hp1 | a0003 | c0003 | t0002 | g0288 | AFR | ACB | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | ACB | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | PEL | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0241 | AMR | PEL | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG01934 | hp1 | a0003 | c0003 | t0002 | g0115 | AMR | PEL | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | PEL | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG01943 | hp1 | a0002 | c0002 | t0003 | g0002 | AMR | PEL | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0281 | AMR | PEL | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | PEL | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG01952 | hp2 | a0002 | c0002 | t0003 | g0053 | AMR | PEL | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | PEL | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0301 | AMR | PEL | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | PEL | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG02004 | hp1 | a0002 | c0002 | t0003 | g0214 | AMR | PEL | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0071 | AMR | PEL | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | KHV | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | KHV | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | KHV | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | KHV | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG02055 | hp1 | a0001 | c0001 | t0002 | g0148 | AFR | ACB | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG02055 | hp2 | a0001 | c0009 | t0005 | g0096 | AFR | ACB | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | KHV | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | KHV | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | KHV | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG02071 | hp2 | a0002 | c0002 | t0003 | g0002 | EAS | KHV | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG02074 | hp1 | a0007 | c0012 | t0001 | g0225 | EAS | KHV | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG02074 | hp2 | a0001 | c0001 | t0014 | g0181 | EAS | KHV | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | KHV | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | KHV | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | KHV | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | KHV | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | KHV | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | KHV | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG02135 | hp2 | a0002 | c0002 | t0003 | g0002 | EAS | KHV | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG02145 | hp1 | a0003 | c0003 | t0009 | g0085 | AFR | ACB | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG02145 | hp2 | a0021 | c0031 | t0008 | g0108 | AFR | ACB | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | CDX | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CDX | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG02257 | hp1 | a0003 | c0003 | t0002 | g0110 | AFR | ACB | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | ACB | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG02258 | hp1 | a0003 | c0003 | t0002 | g0077 | AFR | ACB | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG02258 | hp2 | a0006 | c0004 | t0002 | g0156 | AFR | ACB | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0235 | AMR | PEL | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | PEL | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG02280 | hp1 | a0004 | c0005 | t0001 | g0128 | AFR | ACB | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG02280 | hp2 | a0006 | c0004 | t0002 | g0157 | AFR | ACB | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG02300 | hp1 | a0002 | c0002 | t0003 | g0210 | AMR | PEL | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG02300 | hp2 | a0006 | c0004 | t0002 | g0137 | AMR | PEL | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | ACB | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG02451 | hp2 | a0005 | c0010 | t0004 | g0102 | AFR | ACB | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | KHV | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG02572 | hp1 | a0003 | c0003 | t0002 | g0010 | AFR | GWD | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG02572 | hp2 | a0001 | c0001 | t0002 | g0154 | AFR | GWD | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG02602 | hp1 | a0002 | c0002 | t0003 | g0216 | SAS | PJL | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG02602 | hp2 | a0003 | c0003 | t0002 | g0125 | SAS | PJL | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG02615 | hp1 | a0004 | c0006 | t0001 | g0106 | AFR | GWD | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG02615 | hp2 | a0003 | c0003 | t0002 | g0267 | AFR | GWD | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG02622 | hp1 | a0010 | c0013 | t0004 | g0293 | AFR | GWD | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG02622 | hp2 | a0013 | c0018 | t0002 | g0316 | AFR | GWD | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG02630 | hp1 | a0003 | c0003 | t0002 | g0133 | AFR | GWD | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG02630 | hp2 | a0003 | c0003 | t0002 | g0268 | AFR | GWD | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG02647 | hp1 | a0004 | c0006 | t0001 | g0082 | AFR | GWD | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG02647 | hp2 | a0005 | c0007 | t0018 | g0097 | AFR | GWD | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0199 | SAS | PJL | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG02683 | hp2 | a0002 | c0002 | t0003 | g0217 | SAS | PJL | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG02698 | hp2 | a0003 | c0003 | t0002 | g0164 | SAS | PJL | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG02717 | hp1 | a0009 | c0016 | t0007 | g0290 | AFR | GWD | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG02717 | hp2 | a0001 | c0001 | t0002 | g0155 | AFR | GWD | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG02723 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | GWD | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG02723 | hp2 | a0001 | c0009 | t0005 | g0269 | AFR | GWD | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG02735 | hp1 | a0002 | c0002 | t0003 | g0299 | SAS | PJL | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0067 | SAS | PJL | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG02738 | hp1 | a0006 | c0004 | t0001 | g0107 | SAS | PJL | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0265 | SAS | PJL | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG02809 | hp1 | a0004 | c0006 | t0008 | g0088 | AFR | GWD | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG02809 | hp2 | a0004 | c0006 | t0001 | g0092 | AFR | GWD | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG02818 | hp1 | a0001 | c0001 | t0002 | g0149 | AFR | GWD | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG02818 | hp2 | a0013 | c0018 | t0002 | g0315 | AFR | GWD | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG02886 | hp1 | a0001 | c0009 | t0005 | g0074 | AFR | GWD | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG02886 | hp2 | a0003 | c0003 | t0009 | g0090 | AFR | GWD | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG02895 | hp1 | a0012 | c0017 | t0010 | g0118 | AFR | GWD | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG02895 | hp2 | a0006 | c0004 | t0002 | g0160 | AFR | GWD | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG02896 | hp1 | a0009 | c0016 | t0007 | g0291 | AFR | GWD | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG02896 | hp2 | a0005 | c0020 | t0001 | g0185 | AFR | GWD | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG02897 | hp1 | a0012 | c0017 | t0010 | g0117 | AFR | GWD | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG02897 | hp2 | a0009 | c0016 | t0007 | g0292 | AFR | GWD | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG02922 | hp1 | a0018 | c0030 | t0002 | g0003 | AFR | ESN | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG02922 | hp2 | a0006 | c0004 | t0002 | g0202 | AFR | ESN | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG02965 | hp1 | a0001 | c0009 | t0012 | g0307 | AFR | ESN | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG02965 | hp2 | a0007 | c0011 | t0001 | g0310 | AFR | ESN | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG02970 | hp1 | a0001 | c0014 | t0001 | g0183 | AFR | ESN | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG02970 | hp2 | a0003 | c0003 | t0002 | g0126 | AFR | ESN | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG02976 | hp1 | a0001 | c0009 | t0012 | g0308 | AFR | ESN | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG02976 | hp2 | a0003 | c0003 | t0002 | g0010 | AFR | ESN | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG03017 | hp1 | a0004 | c0005 | t0001 | g0131 | SAS | PJL | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG03017 | hp2 | a0007 | c0012 | t0001 | g0062 | SAS | PJL | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG03041 | hp1 | a0006 | c0004 | t0002 | g0201 | AFR | GWD | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0297 | AFR | GWD | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG03098 | hp1 | a0015 | c0021 | t0004 | g0119 | AFR | MSL | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG03098 | hp2 | a0012 | c0017 | t0019 | g0087 | AFR | MSL | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG03130 | hp1 | a0001 | c0009 | t0005 | g0019 | AFR | ESN | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG03130 | hp2 | a0004 | c0006 | t0001 | g0104 | AFR | ESN | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG03139 | hp1 | a0010 | c0013 | t0004 | g0296 | AFR | ESN | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG03139 | hp2 | a0004 | c0006 | t0001 | g0079 | AFR | ESN | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG03195 | hp1 | a0005 | c0010 | t0004 | g0103 | AFR | ESN | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG03195 | hp2 | a0001 | c0009 | t0005 | g0019 | AFR | ESN | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG03209 | hp1 | a0001 | c0026 | t0001 | g0075 | AFR | MSL | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG03209 | hp2 | a0003 | c0003 | t0009 | g0089 | AFR | MSL | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG03225 | hp1 | a0002 | c0002 | t0003 | g0317 | AFR | MSL | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG03225 | hp2 | a0005 | c0020 | t0001 | g0184 | AFR | MSL | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG03239 | hp1 | a0003 | c0003 | t0002 | g0236 | SAS | PJL | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0244 | SAS | PJL | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG03453 | hp1 | a0007 | c0011 | t0001 | g0311 | AFR | MSL | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG03453 | hp2 | a0005 | c0010 | t0004 | g0101 | AFR | MSL | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | MSL | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG03486 | hp2 | a0005 | c0010 | t0004 | g0099 | AFR | MSL | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG03490 | hp1 | a0004 | c0005 | t0001 | g0207 | SAS | PJL | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG03490 | hp2 | a0002 | c0002 | t0003 | g0020 | SAS | PJL | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG03491 | hp1 | a0003 | c0003 | t0002 | g0196 | SAS | PJL | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG03491 | hp2 | a0002 | c0002 | t0003 | g0021 | SAS | PJL | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG03492 | hp1 | a0002 | c0002 | t0003 | g0020 | SAS | PJL | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG03492 | hp2 | a0002 | c0002 | t0003 | g0021 | SAS | PJL | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG03516 | hp1 | a0006 | c0004 | t0002 | g0151 | AFR | ESN | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG03516 | hp2 | a0010 | c0013 | t0004 | g0295 | AFR | ESN | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG03540 | hp1 | a0005 | c0007 | t0008 | g0305 | AFR | GWD | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | GWD | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG03579 | hp1 | a0007 | c0011 | t0001 | g0313 | AFR | MSL | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG03579 | hp2 | a0004 | c0006 | t0001 | g0080 | AFR | MSL | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0234 | SAS | PJL | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG03654 | hp2 | a0002 | c0002 | t0003 | g0223 | SAS | PJL | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0282 | SAS | STU | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG03688 | hp2 | a0002 | c0002 | t0003 | g0221 | SAS | STU | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0193 | SAS | PJL | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG03704 | hp2 | a0003 | c0003 | t0002 | g0134 | SAS | PJL | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG03710 | hp1 | a0002 | c0019 | t0003 | g0273 | SAS | PJL | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG03710 | hp2 | a0003 | c0003 | t0002 | g0013 | SAS | PJL | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG03831 | hp1 | a0002 | c0002 | t0003 | g0271 | SAS | BEB | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0059 | SAS | BEB | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG03834 | hp1 | a0006 | c0004 | t0002 | g0025 | SAS | BEB | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0041 | SAS | BEB | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG03927 | hp1 | a0004 | c0005 | t0001 | g0012 | SAS | BEB | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0240 | SAS | BEB | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0034 | SAS | BEB | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0032 | SAS | BEB | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG04115 | hp1 | a0017 | c0025 | t0001 | g0203 | SAS | STU | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG04115 | hp2 | a0001 | c0001 | t0013 | g0245 | SAS | STU | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0038 | SAS | STU | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | STU | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0065 | SAS | STU | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG04204 | hp2 | a0006 | c0004 | t0002 | g0130 | SAS | STU | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG04228 | hp1 | a0002 | c0002 | t0003 | g0008 | SAS | STU | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0033 | SAS | STU | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
NA18522 | hp1 | a0005 | c0007 | t0008 | g0304 | AFR | YRI | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
NA18522 | hp2 | a0005 | c0010 | t0002 | g0098 | AFR | YRI | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
NA18747 | hp1 | a0001 | c0001 | t0011 | g0175 | EAS | CHB | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | CHB | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
NA18906 | hp1 | a0003 | c0003 | t0002 | g0076 | AFR | YRI | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0312 | AFR | YRI | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
NA18939 | hp2 | a0008 | c0008 | t0002 | g0250 | EAS | JPT | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
NA18941 | hp1 | a0013 | c0018 | t0002 | g0220 | EAS | JPT | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
NA18941 | hp2 | a0002 | c0002 | t0003 | g0228 | EAS | JPT | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
NA18942 | hp2 | a0008 | c0008 | t0002 | g0049 | EAS | JPT | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
NA18945 | hp1 | a0008 | c0008 | t0002 | g0068 | EAS | JPT | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
NA18948 | hp2 | a0002 | c0002 | t0003 | g0212 | EAS | JPT | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
NA18949 | hp2 | a0011 | c0015 | t0001 | g0251 | EAS | JPT | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
NA18950 | hp1 | a0002 | c0002 | t0021 | g0303 | EAS | JPT | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
NA18950 | hp2 | a0011 | c0015 | t0001 | g0186 | EAS | JPT | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
NA18956 | hp1 | a0008 | c0008 | t0002 | g0138 | EAS | JPT | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
NA18960 | hp2 | a0004 | c0005 | t0001 | g0011 | EAS | JPT | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
NA18966 | hp2 | a0003 | c0003 | t0002 | g0122 | EAS | JPT | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
NA18973 | hp1 | a0002 | c0002 | t0003 | g0224 | EAS | JPT | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
NA18975 | hp1 | a0002 | c0002 | t0001 | g0229 | EAS | JPT | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
NA18980 | hp1 | a0008 | c0008 | t0002 | g0052 | EAS | JPT | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
NA18980 | hp2 | a0005 | c0007 | t0006 | g0197 | EAS | JPT | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
NA18981 | hp1 | a0005 | c0007 | t0006 | g0189 | EAS | JPT | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
NA18984 | hp2 | a0004 | c0005 | t0001 | g0011 | EAS | JPT | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
NA18994 | hp2 | a0002 | c0002 | t0003 | g0227 | EAS | JPT | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
NA18995 | hp2 | a0002 | c0002 | t0003 | g0002 | EAS | JPT | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
NA18997 | hp1 | a0001 | c0001 | t0016 | g0276 | EAS | JPT | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
NA18997 | hp2 | a0002 | c0002 | t0003 | g0226 | EAS | JPT | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
NA19000 | hp1 | a0002 | c0002 | t0003 | g0222 | EAS | JPT | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
NA19002 | hp2 | a0003 | c0003 | t0001 | g0127 | EAS | JPT | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
NA19007 | hp2 | a0004 | c0005 | t0001 | g0023 | EAS | JPT | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
NA19012 | hp1 | a0005 | c0007 | t0006 | g0277 | EAS | JPT | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
NA19012 | hp2 | a0002 | c0002 | t0003 | g0230 | EAS | JPT | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
NA19030 | hp1 | a0001 | c0014 | t0001 | g0095 | AFR | LWK | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0255 | AFR | LWK | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
NA19043 | hp1 | a0007 | c0012 | t0001 | g0314 | AFR | LWK | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
NA19043 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | LWK | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
NA19063 | hp2 | a0002 | c0002 | t0003 | g0002 | EAS | JPT | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
NA19066 | hp1 | a0005 | c0007 | t0006 | g0188 | EAS | JPT | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
NA19078 | hp1 | a0011 | c0015 | t0001 | g0192 | EAS | JPT | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
NA19079 | hp1 | a0011 | c0015 | t0001 | g0177 | EAS | JPT | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
NA19081 | hp1 | a0019 | c0027 | t0003 | g0024 | EAS | JPT | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
NA19091 | hp2 | a0001 | c0001 | t0011 | g0016 | EAS | JPT | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
NA19240 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | YRI | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
NA19240 | hp2 | a0004 | c0006 | t0001 | g0287 | AFR | YRI | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | ASW | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | ASW | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0258 | EUR | TSI | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0114 | EUR | TSI | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0259 | EUR | TSI | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
NA20805 | hp2 | a0002 | c0002 | t0003 | g0008 | EUR | TSI | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
NA20905 | hp1 | a0003 | c0003 | t0002 | g0136 | SAS | GIH | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
NA20905 | hp2 | a0008 | c0008 | t0020 | g0072 | SAS | GIH | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | ACB | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG02109 | hp2 | a0007 | c0011 | t0001 | g0152 | AFR | ACB | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG02486 | hp1 | a0002 | c0002 | t0003 | g0007 | AFR | ACB | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG02486 | hp2 | a0009 | c0016 | t0007 | g0289 | AFR | ACB | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG02559 | hp1 | a0003 | c0003 | t0002 | g0109 | AFR | ACB | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG02559 | hp2 | a0005 | c0010 | t0004 | g0100 | AFR | ACB | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG03471 | hp1 | a0003 | c0003 | t0002 | g0129 | AFR | MSL | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG03471 | hp2 | a0020 | c0028 | t0001 | g0166 | AFR | MSL | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | USA | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
HG06807 | hp2 | a0016 | c0022 | t0015 | g0167 | AFR | USA | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
NA20300 | hp1 | a0002 | c0002 | t0003 | g0219 | AFR | USA | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
NA20300 | hp2 | a0001 | c0014 | t0001 | g0306 | AFR | USA | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
NA21309 | hp1 | a0001 | c0014 | t0010 | g0260 | AFR | LWK | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | LWK | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
homoSapiens_chm13v2 | hp1 | a0007 | c0012 | t0001 | g0272 | REF | REF | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0066 | REF | REF | TTYH2_chr17_74208571_74267020 | TTYH2 | chr17 | 74208571 | 74267020 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:74230901
|
G | A | 2 | a0012a0015 | 4 | HG02895.hp1 HG02897.hp1 HG03098.hp1 others(1): Show |
missense_variant | MODERATE | c.316G>A | p.Val106Ile | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 3/14 | 333/3433 | 316/1605 | 106/534 | chr17 | 74230901 | ||
chr17:74237420
|
G | A | 5 | a0003a0004a0006others(2): Show | 69 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(66): Show |
missense_variant | MODERATE | c.541G>A | p.Val181Ile | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 4/14 | 558/3433 | 541/1605 | 181/534 | chr17 | 74237420 | ||
chr17:74237466
|
T | C | 1 | a0021 | 1 | HG02145.hp2 | missense_variant | MODERATE | c.587T>C | p.Met196Thr | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 4/14 | 604/3433 | 587/1605 | 196/534 | chr17 | 74237466 | ||
chr17:74243447
|
C | T | 1 | a0009 | 4 | HG02486.hp2 HG02717.hp1 HG02896.hp1 others(1): Show |
missense_variant | MODERATE | c.709C>T | p.Arg237Cys | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 5/14 | 726/3433 | 709/1605 | 237/534 | chr17 | 74243447 | ||
chr17:74244029
|
G | A | 2 | a0002a0007 | 52 | HG00099.hp2 HG01069.hp2 HG01074.hp1 others(49): Show |
missense_variant | MODERATE | c.784G>A | p.Ala262Thr | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 6/14 | 801/3433 | 784/1605 | 262/534 | chr17 | 74244029 | ||
chr17:74244038
|
T | G | 12 | a0002a0003a0004others(9): Show | 147 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(144): Show |
missense_variant | MODERATE | c.793T>G | p.Ser265Ala | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 6/14 | 810/3433 | 793/1605 | 265/534 | chr17 | 74244038 | ||
chr17:74250018
|
C | T | 1 | a0018 | 1 | HG02922.hp1 | missense_variant | MODERATE | c.1013C>T | p.Ser338Phe | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 9/14 | 1030/3433 | 1013/1605 | 338/534 | chr17 | 74250018 | ||
chr17:74252343
|
C | A | 3 | a0006a0016a0017 | 15 | HG01081.hp1 HG01192.hp2 HG01884.hp1 others(12): Show |
missense_variant | MODERATE | c.1226C>A | p.Ala409Glu | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 11/14 | 1243/3433 | 1226/1605 | 409/534 | chr17 | 74252343 | ||
chr17:74252373
|
C | T | 2 | a0002a0019 | 43 | HG00099.hp2 HG01069.hp2 HG01081.hp2 others(40): Show |
missense_variant | MODERATE | c.1256C>T | p.Thr419Ile | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 11/14 | 1273/3433 | 1256/1605 | 419/534 | chr17 | 74252373 | ||
chr17:74253090
|
C | A | 6 | a0003a0006a0008others(3): Show | 61 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(58): Show |
missense_variant | MODERATE | c.1269C>A | p.Asp423Glu | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 12/14 | 1286/3433 | 1269/1605 | 423/534 | chr17 | 74253090 | ||
chr17:74253250
|
C | A | 1 | a0011 | 4 | NA18949.hp2 NA18950.hp2 NA19078.hp1 others(1): Show |
missense_variant | MODERATE | c.1429C>A | p.Pro477Thr | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 12/14 | 1446/3433 | 1429/1605 | 477/534 | chr17 | 74253250 | ||
chr17:74253786
|
C | T | 2 | a0010a0015 | 5 | HG01884.hp2 HG02622.hp1 HG03098.hp1 others(2): Show |
missense_variant | MODERATE | c.1477C>T | p.Arg493Cys | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 13/14 | 1494/3433 | 1477/1605 | 493/534 | chr17 | 74253786 | ||
chr17:74253798
|
G | A | 1 | a0016 | 1 | HG06807.hp2 | missense_variant | MODERATE | c.1489G>A | p.Val497Met | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 13/14 | 1506/3433 | 1489/1605 | 497/534 | chr17 | 74253798 | ||
chr17:74253810
|
G | A | 1 | a0020 | 1 | HG03471.hp2 | missense_variant | MODERATE | c.1501G>A | p.Gly501Arg | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 13/14 | 1518/3433 | 1501/1605 | 501/534 | chr17 | 74253810 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:74222487
|
G | A | 1 | a0002c0019 | 2 | HG00099.hp2 HG03710.hp1 |
splice_region_variant&synonymous_variant | LOW | c.132G>A | p.Ser44Ser | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/14 | 149/3433 | 132/1605 | 44/534 | chr17 | 74222487 | ||
chr17:74230990
|
C | T | 1 | a0021c0031 | 1 | HG02145.hp2 | synonymous_variant | LOW | c.405C>T | p.Ile135Ile | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 3/14 | 422/3433 | 405/1605 | 135/534 | chr17 | 74230990 | ||
chr17:74249962
|
T | C | 23 | a0001c0009a0001c0014a0001c0026others(20): Show | 159 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(156): Show |
synonymous_variant | LOW | c.957T>C | p.Leu319Leu | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 9/14 | 974/3433 | 957/1605 | 319/534 | chr17 | 74249962 | ||
chr17:74250327
|
C | T | 15 | a0001c0014a0002c0002a0002c0019others(12): Show | 134 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(131): Show |
synonymous_variant | LOW | c.1086C>T | p.Thr362Thr | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 10/14 | 1103/3433 | 1086/1605 | 362/534 | chr17 | 74250327 | ||
chr17:74252344
|
A | G | 19 | a0001c0014a0001c0026a0002c0002others(16): Show | 139 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(136): Show |
synonymous_variant | LOW | c.1227A>G | p.Ala409Ala | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 11/14 | 1244/3433 | 1227/1605 | 409/534 | chr17 | 74252344 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:74260222
|
G | T | 1 | a0005c0007t0006 | 5 | HG00438.hp1 NA18980.hp2 NA18981.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*13G>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 14/14 | 13 | chr17 | 74260222 | |||||
chr17:74260366
|
G | A | 1 | a0001c0001t0013 | 1 | HG04115.hp2 | 3_prime_UTR_variant | MODIFIER | c.*157G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 14/14 | 157 | chr17 | 74260366 | |||||
chr17:74260386
|
C | T | 1 | a0002c0002t0021 | 1 | NA18950.hp1 | 3_prime_UTR_variant | MODIFIER | c.*177C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 14/14 | 177 | chr17 | 74260386 | |||||
chr17:74260640
|
TCTGTCCT others(6): Show |
T | 1 | a0016c0022t0015 | 1 | HG06807.hp2 | 3_prime_UTR_variant | MODIFIER | c.*448_*460delTCCTCG others(7): Show |
TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 14/14 | 448 | INFO_REALIGN_3_PRIME | chr17 | 74260640 | ||||
chr17:74260656
|
G | A | 1 | a0001c0001t0014 | 1 | HG02074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*447G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 14/14 | 447 | chr17 | 74260656 | |||||
chr17:74260816
|
G | A | 3 | a0005c0010t0004a0010c0013t0004a0015c0021t0004 | 10 | HG01884.hp2 HG02451.hp2 HG02559.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*607G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 14/14 | 607 | chr17 | 74260816 | |||||
chr17:74260833
|
G | A | 4 | a0004c0006t0008a0005c0007t0008a0009c0016t0007others(1): Show | 8 | HG02145.hp2 HG02486.hp2 HG02717.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*624G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 14/14 | 624 | chr17 | 74260833 | |||||
chr17:74260989
|
A | T | 1 | a0001c0009t0012 | 2 | HG02965.hp1 HG02976.hp1 |
3_prime_UTR_variant | MODIFIER | c.*780A>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 14/14 | 780 | chr17 | 74260989 | |||||
chr17:74261114
|
C | G | 10 | a0001c0001t0002a0003c0003t0002a0005c0010t0002others(7): Show | 64 | HG00140.hp1 HG00140.hp2 HG00639.hp2 others(61): Show |
3_prime_UTR_variant | MODIFIER | c.*905C>G | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 14/14 | 905 | chr17 | 74261114 | |||||
chr17:74261298
|
A | G | 1 | a0012c0017t0019 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1089A>G | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 14/14 | 1089 | chr17 | 74261298 | |||||
chr17:74261438
|
T | C | 1 | a0001c0001t0016 | 1 | NA18997.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1229T>C | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 14/14 | 1229 | chr17 | 74261438 | |||||
chr17:74261475
|
C | G | 3 | a0005c0010t0004a0010c0013t0004a0015c0021t0004 | 10 | HG01884.hp2 HG02451.hp2 HG02559.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1266C>G | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 14/14 | 1266 | chr17 | 74261475 | |||||
chr17:74261529
|
C | T | 1 | a0005c0007t0018 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1320C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 14/14 | 1320 | chr17 | 74261529 | |||||
chr17:74261574
|
C | T | 5 | a0001c0001t0003a0002c0002t0003a0002c0002t0021others(2): Show | 43 | HG00099.hp2 HG01069.hp1 HG01069.hp2 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*1365C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 14/14 | 1365 | chr17 | 74261574 | |||||
chr17:74261578
|
C | T | 1 | a0001c0001t0014 | 1 | HG02074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1369C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 14/14 | 1369 | chr17 | 74261578 | |||||
chr17:74261616
|
G | A | 1 | a0001c0001t0011 | 2 | NA18747.hp1 NA19091.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1407G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 14/14 | 1407 | chr17 | 74261616 | |||||
chr17:74261640
|
G | A | 6 | a0001c0009t0012a0001c0014t0010a0005c0010t0004others(3): Show | 15 | HG01884.hp2 HG02451.hp2 HG02559.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1431G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 14/14 | 1431 | chr17 | 74261640 | |||||
chr17:74261666
|
G | A | 1 | a0003c0003t0009 | 4 | HG00639.hp1 HG02145.hp1 HG02886.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1457G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 14/14 | 1457 | chr17 | 74261666 | |||||
chr17:74261720
|
G | A | 1 | a0012c0017t0019 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1511G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 14/14 | 1511 | chr17 | 74261720 | |||||
chr17:74261756
|
G | A | 1 | a0001c0001t0017 | 1 | HG00597.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1547G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 14/14 | 1547 | chr17 | 74261756 | |||||
chr17:74261793
|
T | C | 15 | a0001c0001t0002a0001c0009t0005a0003c0003t0002others(12): Show | 83 | HG00140.hp1 HG00140.hp2 HG00639.hp2 others(80): Show |
3_prime_UTR_variant | MODIFIER | c.*1584T>C | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 14/14 | 1584 | chr17 | 74261793 | |||||
chr17:74261873
|
G | A | 6 | a0001c0009t0012a0001c0014t0010a0005c0010t0004others(3): Show | 15 | HG01884.hp2 HG02451.hp2 HG02559.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1664G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 14/14 | 1664 | chr17 | 74261873 | |||||
chr17:74261957
|
G | A | 1 | a0008c0008t0020 | 1 | NA20905.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1748G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 14/14 | 1748 | chr17 | 74261957 | |||||
chr17:74261997
|
A | G | 3 | a0005c0010t0004a0010c0013t0004a0015c0021t0004 | 10 | HG01884.hp2 HG02451.hp2 HG02559.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1788A>G | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 14/14 | 1788 | chr17 | 74261997 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:74213719
|
A | G | 267 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0009others(264): Show | 295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
splice_region_variant&intron_variant | LOW | c.129+3A>G | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 1/13 | chr17 | 74213719 | ||||||
chr17:74213809
|
C | G | 9 | a0001c0001t0001g0312a0002c0002t0003g0317a0007c0011t0001g0309others(6): Show | 9 | HG01074.hp1 HG02622.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.129+93C>G | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 1/13 | chr17 | 74213809 | ||||||
chr17:74214378
|
CTGTTGTC others(3): Show |
C | 5 | a0001c0009t0005g0074a0001c0026t0001g0075a0003c0003t0002g0073others(2): Show | 5 | HG01516.hp1 HG02258.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.129+663_129+672del others(10): Show |
TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 1/13 | chr17 | 74214378 | ||||||
chr17:74214503
|
G | C | 1 | a0001c0001t0001g0022 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.129+787G>C | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 1/13 | chr17 | 74214503 | ||||||
chr17:74214674
|
G | C | 1 | a0001c0001t0001g0078 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.129+958G>C | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 1/13 | chr17 | 74214674 | ||||||
chr17:74215036
|
C | A | 41 | a0001c0001t0001g0083a0001c0001t0001g0086a0001c0001t0001g0091others(38): Show | 41 | HG00639.hp1 HG00738.hp2 HG01074.hp1 others(38): Show |
intron_variant | MODIFIER | c.129+1320C>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 1/13 | chr17 | 74215036 | ||||||
chr17:74215043
|
C | T | 1 | a0004c0006t0001g0106 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.129+1327C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 1/13 | chr17 | 74215043 | ||||||
chr17:74215102
|
A | G | 2 | a0001c0001t0001g0105a0004c0006t0001g0104 | 2 | HG03130.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.129+1386A>G | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 1/13 | chr17 | 74215102 | ||||||
chr17:74215170
|
C | CGT | 23 | a0001c0001t0001g0105a0001c0001t0001g0280a0001c0001t0001g0281others(20): Show | 25 | HG00323.hp1 HG01106.hp2 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.129+1487_129+1488d others(4): Show |
TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 74215170 | |||||
chr17:74215170
|
C | CGTGT | 10 | a0001c0001t0001g0086a0001c0001t0001g0300a0001c0001t0001g0301others(7): Show | 10 | HG00741.hp1 HG01099.hp1 HG01261.hp2 others(7): Show |
intron_variant | MODIFIER | c.129+1485_129+1488d others(6): Show |
TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 74215170 | |||||
chr17:74215170
|
C | CGTGTGT | 6 | a0001c0001t0001g0091a0001c0009t0005g0074a0001c0026t0001g0075others(3): Show | 6 | HG02886.hp1 HG03209.hp1 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.129+1483_129+1488d others(8): Show |
TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 74215170 | |||||
chr17:74215170
|
C | CGTGTGTG others(1): Show |
12 | a0001c0001t0001g0093a0001c0009t0005g0096a0001c0009t0012g0307others(9): Show | 12 | HG00738.hp2 HG01074.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.129+1481_129+1488d others(10): Show |
TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 74215170 | |||||
chr17:74215170
|
C | CGTGTGTG others(3): Show |
7 | a0001c0001t0001g0312a0005c0010t0004g0099a0005c0010t0004g0100others(4): Show | 7 | HG02559.hp2 HG03453.hp1 HG03453.hp2 others(4): Show |
intron_variant | MODIFIER | c.129+1479_129+1488d others(12): Show |
TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 74215170 | |||||
chr17:74215170
|
C | CGTGTGTG others(5): Show |
2 | a0003c0003t0002g0076a0005c0010t0004g0102 | 2 | HG02451.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.129+1477_129+1488d others(14): Show |
TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 74215170 | |||||
chr17:74215170
|
C | CGTGTGTG others(7): Show |
4 | a0002c0002t0003g0317a0005c0010t0004g0103a0013c0018t0002g0315others(1): Show | 4 | HG02622.hp2 HG02818.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.129+1475_129+1488d others(16): Show |
TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 74215170 | |||||
chr17:74215170
|
CGT | C | 108 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0015others(105): Show | 121 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(118): Show |
intron_variant | MODIFIER | c.129+1487_129+1488d others(4): Show |
TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 74215170 | |||||
chr17:74215170
|
CGTGT | C | 10 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0113others(7): Show | 11 | HG01175.hp2 HG01515.hp1 HG01934.hp1 others(8): Show |
intron_variant | MODIFIER | c.129+1485_129+1488d others(6): Show |
TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 74215170 | |||||
chr17:74215240
|
C | T | 1 | a0017c0025t0001g0203 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.129+1524C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 1/13 | chr17 | 74215240 | ||||||
chr17:74215241
|
G | A | 5 | a0001c0001t0001g0093a0001c0009t0005g0096a0001c0014t0001g0095others(2): Show | 5 | HG00738.hp2 HG02055.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.129+1525G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 1/13 | chr17 | 74215241 | ||||||
chr17:74215556
|
G | A | 3 | a0001c0001t0001g0086a0001c0001t0001g0105a0004c0006t0001g0104 | 3 | HG01099.hp1 HG03130.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.129+1840G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 1/13 | chr17 | 74215556 | ||||||
chr17:74215561
|
T | C | 4 | a0012c0017t0010g0117a0012c0017t0010g0118a0014c0023t0001g0116others(1): Show | 4 | HG01243.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.129+1845T>C | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 1/13 | chr17 | 74215561 | ||||||
chr17:74215706
|
GT | G | 28 | a0001c0001t0001g0083a0001c0001t0001g0086a0001c0001t0001g0093others(25): Show | 28 | HG00639.hp1 HG00738.hp2 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.129+1995delT | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 74215706 | |||||
chr17:74215850
|
C | T | 3 | a0001c0001t0001g0086a0001c0001t0001g0105a0004c0006t0001g0104 | 3 | HG01099.hp1 HG03130.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.129+2134C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 1/13 | chr17 | 74215850 | ||||||
chr17:74215917
|
G | C | 5 | a0004c0006t0001g0079a0004c0006t0001g0080a0004c0006t0001g0082others(2): Show | 5 | HG01884.hp1 HG02615.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.129+2201G>C | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 1/13 | chr17 | 74215917 | ||||||
chr17:74215927
|
C | T | 3 | a0001c0001t0001g0086a0001c0001t0001g0105a0004c0006t0001g0104 | 3 | HG01099.hp1 HG03130.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.129+2211C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 1/13 | chr17 | 74215927 | ||||||
chr17:74215928
|
G | A | 1 | a0006c0004t0002g0025 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.129+2212G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 1/13 | chr17 | 74215928 | ||||||
chr17:74215940
|
C | T | 4 | a0012c0017t0010g0117a0012c0017t0010g0118a0014c0023t0001g0116others(1): Show | 4 | HG01243.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.129+2224C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 1/13 | chr17 | 74215940 | ||||||
chr17:74216078
|
A | G | 4 | a0003c0003t0009g0084a0003c0003t0009g0085a0003c0003t0009g0089others(1): Show | 4 | HG00639.hp1 HG02145.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.129+2362A>G | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 1/13 | chr17 | 74216078 | ||||||
chr17:74216120
|
A | C | 23 | a0001c0001t0001g0312a0001c0009t0005g0074a0001c0026t0001g0075others(20): Show | 23 | HG01074.hp1 HG01516.hp1 HG02451.hp2 others(20): Show |
intron_variant | MODIFIER | c.129+2404A>C | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 1/13 | chr17 | 74216120 | ||||||
chr17:74216150
|
A | G | 23 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0190others(20): Show | 27 | HG00408.hp1 HG00438.hp1 HG00597.hp2 others(24): Show |
intron_variant | MODIFIER | c.129+2434A>G | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 1/13 | chr17 | 74216150 | ||||||
chr17:74216187
|
C | T | 1 | a0002c0019t0003g0273 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.129+2471C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 1/13 | chr17 | 74216187 | ||||||
chr17:74216327
|
G | A | 2 | a0002c0002t0003g0204a0002c0002t0003g0205 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.129+2611G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 1/13 | chr17 | 74216327 | ||||||
chr17:74216395
|
T | C | 1 | a0001c0001t0001g0026 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.129+2679T>C | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 1/13 | chr17 | 74216395 | ||||||
chr17:74216527
|
TCTCA | T | 2 | a0002c0002t0003g0008a0007c0012t0001g0272 | 4 | HG01069.hp2 HG04228.hp1 NA20805.hp2 others(1): Show |
intron_variant | MODIFIER | c.129+2818_129+2821d others(6): Show |
TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 74216527 | |||||
chr17:74216530
|
C | T | 8 | a0001c0001t0001g0083a0001c0001t0001g0086a0001c0001t0001g0105others(5): Show | 8 | HG00639.hp1 HG01099.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.129+2814C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 1/13 | chr17 | 74216530 | ||||||
chr17:74216538
|
T | A | 1 | a0001c0001t0001g0120 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.129+2822T>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 1/13 | chr17 | 74216538 | ||||||
chr17:74216630
|
G | A | 26 | a0001c0001t0001g0121a0003c0003t0001g0127a0003c0003t0002g0013others(23): Show | 30 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(27): Show |
intron_variant | MODIFIER | c.129+2914G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 1/13 | chr17 | 74216630 | ||||||
chr17:74216702
|
G | T | 12 | a0001c0001t0001g0083a0001c0001t0001g0312a0002c0002t0003g0317others(9): Show | 12 | HG00639.hp1 HG01074.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.129+2986G>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 1/13 | chr17 | 74216702 | ||||||
chr17:74216759
|
T | C | 2 | a0001c0001t0001g0274a0001c0001t0001g0275 | 2 | NA19082.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.129+3043T>C | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 1/13 | chr17 | 74216759 | ||||||
chr17:74216790
|
G | A | 3 | a0002c0002t0003g0007a0002c0002t0003g0020a0002c0002t0003g0208 | 6 | HG01168.hp1 HG01169.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.129+3074G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 1/13 | chr17 | 74216790 | ||||||
chr17:74216914
|
C | T | 1 | a0003c0003t0002g0073 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.129+3198C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 1/13 | chr17 | 74216914 | ||||||
chr17:74216966
|
G | A | 1 | a0001c0001t0001g0209 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.129+3250G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 1/13 | chr17 | 74216966 | ||||||
chr17:74217129
|
G | A | 5 | a0001c0001t0001g0093a0001c0009t0005g0096a0001c0014t0001g0095others(2): Show | 5 | HG00738.hp2 HG02055.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.129+3413G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 1/13 | chr17 | 74217129 | ||||||
chr17:74217191
|
C | G | 2 | a0003c0003t0009g0089a0003c0003t0009g0090 | 2 | HG02886.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.129+3475C>G | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 1/13 | chr17 | 74217191 | ||||||
chr17:74217229
|
C | T | 1 | a0008c0008t0020g0072 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.129+3513C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 1/13 | chr17 | 74217229 | ||||||
chr17:74217235
|
T | C | 1 | a0021c0031t0008g0108 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.129+3519T>C | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 1/13 | chr17 | 74217235 | ||||||
chr17:74217273
|
C | T | 3 | a0001c0001t0001g0086a0001c0001t0001g0105a0004c0006t0001g0104 | 3 | HG01099.hp1 HG03130.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.129+3557C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 1/13 | chr17 | 74217273 | ||||||
chr17:74217287
|
T | C | 14 | a0001c0001t0001g0093a0001c0001t0001g0312a0001c0009t0005g0096others(11): Show | 14 | HG00738.hp2 HG01074.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.129+3571T>C | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 1/13 | chr17 | 74217287 | ||||||
chr17:74217682
|
C | G | 1 | a0003c0003t0002g0076 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.129+3966C>G | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 1/13 | chr17 | 74217682 | ||||||
chr17:74217692
|
C | T | 1 | a0005c0020t0001g0185 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.129+3976C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 1/13 | chr17 | 74217692 | ||||||
chr17:74217818
|
C | T | 1 | a0002c0002t0003g0271 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.129+4102C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 1/13 | chr17 | 74217818 | ||||||
chr17:74217906
|
T | C | 9 | a0001c0001t0001g0312a0002c0002t0003g0317a0007c0011t0001g0309others(6): Show | 9 | HG01074.hp1 HG02622.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.129+4190T>C | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 1/13 | chr17 | 74217906 | ||||||
chr17:74217929
|
TG | T | 9 | a0001c0001t0001g0312a0002c0002t0003g0317a0007c0011t0001g0309others(6): Show | 9 | HG01074.hp1 HG02622.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.129+4214delG | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 1/13 | chr17 | 74217929 | ||||||
chr17:74217931
|
C | T | 9 | a0001c0001t0001g0312a0002c0002t0003g0317a0007c0011t0001g0309others(6): Show | 9 | HG01074.hp1 HG02622.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.129+4215C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 1/13 | chr17 | 74217931 | ||||||
chr17:74217933
|
G | T | 9 | a0001c0001t0001g0312a0002c0002t0003g0317a0007c0011t0001g0309others(6): Show | 9 | HG01074.hp1 HG02622.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.129+4217G>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 1/13 | chr17 | 74217933 | ||||||
chr17:74217936
|
G | A | 1 | a0001c0001t0001g0027 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.129+4220G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 1/13 | chr17 | 74217936 | ||||||
chr17:74217963
|
TGGGAGGC others(3): Show |
T | 2 | a0001c0001t0001g0139a0008c0008t0002g0138 | 2 | NA18956.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.129+4260_129+4269d others(12): Show |
TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 74217963 | |||||
chr17:74218177
|
G | T | 5 | a0001c0001t0001g0297a0010c0013t0004g0293a0010c0013t0004g0294others(2): Show | 5 | HG01884.hp2 HG02622.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.130-4308G>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 1/13 | chr17 | 74218177 | ||||||
chr17:74218180
|
G | A | 1 | a0004c0006t0001g0092 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.130-4305G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 1/13 | chr17 | 74218180 | ||||||
chr17:74218483
|
G | A | 35 | a0001c0001t0001g0213a0002c0002t0001g0229a0002c0002t0003g0002others(32): Show | 45 | HG00099.hp2 HG01069.hp2 HG01081.hp2 others(42): Show |
intron_variant | MODIFIER | c.130-4002G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 1/13 | chr17 | 74218483 | ||||||
chr17:74218517
|
T | TA | 7 | a0001c0001t0001g0026a0001c0001t0001g0028a0001c0001t0001g0029others(4): Show | 7 | HG02015.hp1 HG02027.hp2 HG02080.hp1 others(4): Show |
intron_variant | MODIFIER | c.130-3961dupA | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 74218517 | |||||
chr17:74218518
|
A | T | 4 | a0009c0016t0007g0289a0009c0016t0007g0290a0009c0016t0007g0291others(1): Show | 4 | HG02486.hp2 HG02717.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.130-3967A>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 1/13 | chr17 | 74218518 | ||||||
chr17:74218530
|
TC | T | 6 | a0001c0009t0005g0074a0001c0026t0001g0075a0003c0003t0002g0073others(3): Show | 6 | HG01516.hp1 HG02809.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.130-3954delC | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 1/13 | chr17 | 74218530 | ||||||
chr17:74218531
|
C | A | 4 | a0009c0016t0007g0289a0009c0016t0007g0290a0009c0016t0007g0291others(1): Show | 4 | HG02486.hp2 HG02717.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.130-3954C>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 1/13 | chr17 | 74218531 | ||||||
chr17:74218531
|
C | CA | 26 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0034others(23): Show | 26 | HG00140.hp1 HG00735.hp1 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.130-3939dupA | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 74218531 | |||||
chr17:74218531
|
CA | C | 20 | a0001c0001t0001g0027a0001c0001t0001g0071a0001c0001t0001g0083others(17): Show | 20 | HG00639.hp1 HG01074.hp1 HG01433.hp2 others(17): Show |
intron_variant | MODIFIER | c.130-3939delA | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 74218531 | |||||
chr17:74218532
|
A | T | 2 | a0001c0026t0001g0075a0003c0003t0002g0076 | 2 | HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.130-3953A>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 1/13 | chr17 | 74218532 | ||||||
chr17:74218671
|
G | A | 21 | a0001c0001t0001g0312a0001c0009t0005g0074a0001c0026t0001g0075others(18): Show | 21 | HG01074.hp1 HG01516.hp1 HG02451.hp2 others(18): Show |
intron_variant | MODIFIER | c.130-3814G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 1/13 | chr17 | 74218671 | ||||||
chr17:74218703
|
G | A | 4 | a0001c0009t0005g0074a0001c0026t0001g0075a0003c0003t0002g0073others(1): Show | 4 | HG01516.hp1 HG02886.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.130-3782G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 1/13 | chr17 | 74218703 | ||||||
chr17:74218719
|
G | C | 1 | a0001c0001t0001g0234 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.130-3766G>C | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 1/13 | chr17 | 74218719 | ||||||
chr17:74218724
|
A | C | 22 | a0001c0001t0001g0083a0001c0001t0001g0091a0001c0001t0001g0312others(19): Show | 22 | HG00639.hp1 HG01074.hp1 HG01516.hp1 others(19): Show |
intron_variant | MODIFIER | c.130-3761A>C | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 1/13 | chr17 | 74218724 | ||||||
chr17:74218755
|
G | A | 1 | a0001c0001t0001g0121 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.130-3730G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 1/13 | chr17 | 74218755 | ||||||
chr17:74218900
|
A | G | 7 | a0002c0002t0001g0229a0002c0002t0003g0224a0002c0002t0003g0226others(4): Show | 7 | HG02074.hp1 NA18941.hp2 NA18973.hp1 others(4): Show |
intron_variant | MODIFIER | c.130-3585A>G | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 1/13 | chr17 | 74218900 | ||||||
chr17:74218956
|
G | A | 72 | a0001c0001t0001g0083a0001c0001t0001g0091a0001c0001t0001g0093others(69): Show | 74 | HG00639.hp1 HG00733.hp1 HG00738.hp2 others(71): Show |
intron_variant | MODIFIER | c.130-3529G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 1/13 | chr17 | 74218956 | ||||||
chr17:74218968
|
G | A | 2 | a0001c0026t0001g0075a0003c0003t0002g0076 | 2 | HG03209.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.130-3517G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 1/13 | chr17 | 74218968 | ||||||
chr17:74219103
|
G | T | 2 | a0001c0009t0005g0074a0003c0003t0002g0073 | 2 | HG01516.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.130-3382G>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 1/13 | chr17 | 74219103 | ||||||
chr17:74219133
|
C | T | 1 | a0001c0001t0001g0200 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.130-3352C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 1/13 | chr17 | 74219133 | ||||||
chr17:74219174
|
G | A | 5 | a0002c0002t0003g0007a0002c0002t0003g0020a0002c0002t0003g0208others(2): Show | 8 | HG01168.hp1 HG01169.hp1 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.130-3311G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 1/13 | chr17 | 74219174 | ||||||
chr17:74219176
|
T | C | 7 | a0001c0001t0001g0083a0001c0001t0001g0091a0003c0003t0009g0084others(4): Show | 7 | HG00639.hp1 HG02145.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.130-3309T>C | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 1/13 | chr17 | 74219176 | ||||||
chr17:74219215
|
C | CA | 7 | a0001c0001t0016g0276a0001c0009t0005g0074a0001c0026t0001g0075others(4): Show | 7 | HG01516.hp1 HG02809.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.130-3257dupA | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 74219215 | |||||
chr17:74219215
|
C | CAAAAA | 14 | a0001c0001t0001g0083a0001c0001t0001g0312a0002c0002t0003g0317others(11): Show | 14 | HG00639.hp1 HG01074.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.130-3261_130-3257d others(7): Show |
TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 74219215 | |||||
chr17:74219366
|
C | A | 5 | a0001c0001t0001g0083a0003c0003t0009g0084a0003c0003t0009g0085others(2): Show | 5 | HG00639.hp1 HG02145.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.130-3119C>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 1/13 | chr17 | 74219366 | ||||||
chr17:74219387
|
C | CAAAAAAA others(1): Show |
11 | a0001c0001t0001g0083a0001c0009t0005g0074a0003c0003t0002g0073others(8): Show | 11 | HG00639.hp1 HG01516.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.130-3089_130-3082d others(10): Show |
TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 74219387 | |||||
chr17:74219387
|
C | CAAAAAAA others(2): Show |
7 | a0001c0001t0001g0093a0001c0009t0005g0096a0001c0014t0001g0095others(4): Show | 7 | HG00738.hp2 HG02055.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.130-3090_130-3082d others(11): Show |
TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 74219387 | |||||
chr17:74219387
|
C | CAAAAAAA others(4): Show |
2 | a0004c0006t0008g0088a0005c0020t0001g0184 | 2 | HG02809.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.130-3092_130-3082d others(13): Show |
TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 74219387 | |||||
chr17:74219387
|
C | CAAAAAAA others(6): Show |
1 | a0012c0017t0019g0087 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.130-3094_130-3082d others(15): Show |
TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 74219387 | |||||
chr17:74219387
|
C | CAAAAAAA others(7): Show |
6 | a0001c0001t0001g0297a0002c0002t0003g0317a0007c0011t0001g0313others(3): Show | 6 | HG02622.hp2 HG02818.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.130-3095_130-3082d others(16): Show |
TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 74219387 | |||||
chr17:74219387
|
C | CAAAAAAA others(8): Show |
4 | a0001c0001t0001g0312a0007c0011t0001g0309a0007c0011t0001g0310others(1): Show | 4 | HG01074.hp1 HG02965.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.130-3096_130-3082d others(17): Show |
TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 74219387 | |||||
chr17:74219387
|
C | CAAAAAAA others(11): Show |
1 | a0001c0001t0001g0159 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.130-3082_130-3081i others(20): Show |
TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 74219387 | |||||
chr17:74219387
|
C | CAAAAAAA others(12): Show |
4 | a0001c0001t0001g0158a0001c0014t0001g0183a0005c0020t0001g0185others(1): Show | 4 | HG01106.hp1 HG02896.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.130-3082_130-3081i others(21): Show |
TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 74219387 | |||||
chr17:74219387
|
C | CAAAAAAA others(13): Show |
8 | a0005c0010t0002g0098a0005c0010t0004g0100a0005c0010t0004g0101others(5): Show | 8 | HG02258.hp2 HG02280.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.130-3082_130-3081i others(22): Show |
TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 74219387 | |||||
chr17:74219387
|
C | CAAAAAAA others(14): Show |
9 | a0001c0001t0001g0153a0001c0001t0002g0003a0001c0001t0002g0154others(6): Show | 11 | HG02109.hp1 HG02109.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.130-3082_130-3081i others(23): Show |
TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 74219387 | |||||
chr17:74219387
|
C | CAAAAAAA others(15): Show |
2 | a0001c0001t0002g0149a0001c0001t0002g0150 | 2 | HG00733.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.130-3082_130-3081i others(24): Show |
TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 74219387 | |||||
chr17:74219387
|
C | CAAAAAAA others(16): Show |
2 | a0001c0001t0002g0148a0005c0010t0004g0099 | 2 | HG02055.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.130-3082_130-3081i others(25): Show |
TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 74219387 | |||||
chr17:74219387
|
C | CAAAAAAA others(26): Show |
2 | a0001c0009t0012g0307a0001c0009t0012g0308 | 2 | HG02965.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.130-3082_130-3081i others(35): Show |
TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 74219387 | |||||
chr17:74219387
|
C | CAAAAAAA others(27): Show |
1 | a0001c0014t0001g0306 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.130-3082_130-3081i others(36): Show |
TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 74219387 | |||||
chr17:74219387
|
C | CAAAAAAA others(29): Show |
1 | a0010c0013t0004g0294 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.130-3082_130-3081i others(38): Show |
TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 74219387 | |||||
chr17:74219387
|
C | CAAAAAAA others(30): Show |
1 | a0010c0013t0004g0293 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.130-3082_130-3081i others(39): Show |
TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 74219387 | |||||
chr17:74219403
|
A | AAAAAAAA others(21): Show |
1 | a0005c0007t0008g0304 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.130-3082_130-3081i others(30): Show |
TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 1/13 | chr17 | 74219403 | ||||||
chr17:74219403
|
A | AAAAAAAA others(8): Show |
1 | a0005c0007t0008g0305 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.130-3082_130-3081i others(17): Show |
TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 1/13 | chr17 | 74219403 | ||||||
chr17:74219487
|
A | G | 1 | a0010c0013t0004g0293 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.130-2998A>G | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 1/13 | chr17 | 74219487 | ||||||
chr17:74219569
|
G | A | 1 | a0001c0001t0001g0036 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.130-2916G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 1/13 | chr17 | 74219569 | ||||||
chr17:74219658
|
T | A | 1 | a0001c0001t0001g0083 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.130-2827T>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 1/13 | chr17 | 74219658 | ||||||
chr17:74219710
|
C | A | 1 | a0001c0001t0001g0037 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.130-2775C>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 1/13 | chr17 | 74219710 | ||||||
chr17:74219734
|
C | T | 2 | a0004c0006t0008g0088a0012c0017t0019g0087 | 2 | HG02809.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.130-2751C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 1/13 | chr17 | 74219734 | ||||||
chr17:74219800
|
A | G | 1 | a0001c0009t0005g0074 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.130-2685A>G | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 1/13 | chr17 | 74219800 | ||||||
chr17:74219867
|
C | T | 5 | a0001c0001t0001g0093a0001c0009t0005g0096a0001c0014t0001g0095others(2): Show | 5 | HG00738.hp2 HG02055.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.130-2618C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 1/13 | chr17 | 74219867 | ||||||
chr17:74219911
|
T | C | 1 | a0001c0001t0001g0038 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.130-2574T>C | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 1/13 | chr17 | 74219911 | ||||||
chr17:74219962
|
A | AT | 16 | a0001c0001t0001g0093a0001c0001t0001g0182a0001c0001t0001g0199others(13): Show | 17 | HG00738.hp2 HG01081.hp1 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.130-2508dupT | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 74219962 | |||||
chr17:74220013
|
C | CT | 14 | a0001c0001t0001g0083a0001c0001t0001g0312a0002c0002t0003g0317others(11): Show | 14 | HG00639.hp1 HG01074.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.130-2463dupT | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 74220013 | |||||
chr17:74220101
|
A | C | 75 | a0001c0001t0001g0083a0001c0001t0001g0091a0001c0001t0001g0093others(72): Show | 78 | HG00639.hp1 HG00733.hp1 HG00738.hp2 others(75): Show |
intron_variant | MODIFIER | c.130-2384A>C | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 1/13 | chr17 | 74220101 | ||||||
chr17:74220158
|
A | G | 23 | a0001c0001t0001g0083a0001c0001t0001g0091a0001c0001t0001g0312others(20): Show | 23 | HG00639.hp1 HG01074.hp1 HG01516.hp1 others(20): Show |
intron_variant | MODIFIER | c.130-2327A>G | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 1/13 | chr17 | 74220158 | ||||||
chr17:74220377
|
A | G | 4 | a0003c0003t0002g0266a0003c0003t0002g0267a0003c0003t0002g0268others(1): Show | 4 | HG00639.hp2 HG01891.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.130-2108A>G | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 1/13 | chr17 | 74220377 | ||||||
chr17:74220638
|
T | C | 21 | a0001c0001t0001g0083a0001c0001t0001g0312a0001c0009t0005g0074others(18): Show | 21 | HG00639.hp1 HG01074.hp1 HG01516.hp1 others(18): Show |
intron_variant | MODIFIER | c.130-1847T>C | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 1/13 | chr17 | 74220638 | ||||||
chr17:74220664
|
G | A | 7 | a0001c0001t0001g0083a0001c0026t0001g0075a0003c0003t0002g0076others(4): Show | 7 | HG00639.hp1 HG02145.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.130-1821G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 1/13 | chr17 | 74220664 | ||||||
chr17:74220701
|
GAGCCCC | G | 7 | a0001c0001t0001g0083a0001c0026t0001g0075a0003c0003t0002g0076others(4): Show | 7 | HG00639.hp1 HG02145.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.130-1771_130-1766d others(8): Show |
TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr17 | 74220701 | |||||
chr17:74220890
|
G | A | 11 | a0001c0001t0001g0312a0002c0002t0003g0317a0004c0006t0008g0088others(8): Show | 11 | HG01074.hp1 HG02622.hp2 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.130-1595G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 1/13 | chr17 | 74220890 | ||||||
chr17:74220934
|
A | T | 14 | a0001c0001t0001g0312a0001c0009t0005g0074a0002c0002t0003g0317others(11): Show | 14 | HG01074.hp1 HG01516.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.130-1551A>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 1/13 | chr17 | 74220934 | ||||||
chr17:74221224
|
C | G | 1 | a0001c0001t0001g0070 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.130-1261C>G | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 1/13 | chr17 | 74221224 | ||||||
chr17:74221244
|
C | T | 2 | a0001c0001t0001g0069a0008c0008t0002g0068 | 2 | NA18945.hp1 NA18956.hp2 |
intron_variant | MODIFIER | c.130-1241C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 1/13 | chr17 | 74221244 | ||||||
chr17:74221277
|
C | T | 7 | a0001c0001t0001g0083a0001c0026t0001g0075a0003c0003t0002g0076others(4): Show | 7 | HG00639.hp1 HG02145.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.130-1208C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 1/13 | chr17 | 74221277 | ||||||
chr17:74221501
|
A | G | 1 | a0004c0006t0001g0287 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.130-984A>G | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 1/13 | chr17 | 74221501 | ||||||
chr17:74221523
|
T | C | 32 | a0001c0001t0001g0083a0001c0001t0001g0091a0001c0001t0001g0297others(29): Show | 32 | HG00639.hp1 HG01074.hp1 HG01516.hp1 others(29): Show |
intron_variant | MODIFIER | c.130-962T>C | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 1/13 | chr17 | 74221523 | ||||||
chr17:74221806
|
G | A | 1 | a0001c0001t0001g0235 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.130-679G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 1/13 | chr17 | 74221806 | ||||||
chr17:74221929
|
G | A | 1 | a0003c0003t0002g0109 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.130-556G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 1/13 | chr17 | 74221929 | ||||||
chr17:74221976
|
G | A | 6 | a0005c0010t0002g0098a0005c0010t0004g0099a0005c0010t0004g0100others(3): Show | 6 | HG02451.hp2 HG02559.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.130-509G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 1/13 | chr17 | 74221976 | ||||||
chr17:74222101
|
C | T | 1 | a0001c0001t0001g0147 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.130-384C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 1/13 | chr17 | 74222101 | ||||||
chr17:74222718
|
T | C | 6 | a0005c0010t0002g0098a0005c0010t0004g0099a0005c0010t0004g0100others(3): Show | 6 | HG02451.hp2 HG02559.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.302+61T>C | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | chr17 | 74222718 | ||||||
chr17:74222788
|
C | CT | 30 | a0001c0001t0001g0083a0001c0001t0001g0265a0001c0001t0001g0312others(27): Show | 30 | HG00639.hp1 HG01074.hp1 HG01516.hp1 others(27): Show |
intron_variant | MODIFIER | c.302+144dupT | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 74222788 | |||||
chr17:74222801
|
T | TC | 5 | a0001c0001t0001g0093a0001c0009t0005g0096a0001c0014t0001g0095others(2): Show | 5 | HG00738.hp2 HG02055.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.302+144_302+145ins others(1): Show |
TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | chr17 | 74222801 | ||||||
chr17:74222814
|
G | A | 1 | a0004c0006t0001g0287 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.302+157G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | chr17 | 74222814 | ||||||
chr17:74222936
|
C | T | 1 | a0003c0003t0002g0268 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.302+279C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | chr17 | 74222936 | ||||||
chr17:74222967
|
G | A | 1 | a0001c0001t0001g0093 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.302+310G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | chr17 | 74222967 | ||||||
chr17:74222974
|
C | T | 6 | a0005c0010t0002g0098a0005c0010t0004g0099a0005c0010t0004g0100others(3): Show | 6 | HG02451.hp2 HG02559.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.302+317C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | chr17 | 74222974 | ||||||
chr17:74223052
|
A | ACTGTGAG | 6 | a0001c0001t0001g0083a0003c0003t0009g0084a0003c0003t0009g0085others(3): Show | 6 | HG00639.hp1 HG02145.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.302+395_302+396ins others(7): Show |
TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | chr17 | 74223052 | ||||||
chr17:74223055
|
A | C | 6 | a0001c0001t0001g0083a0003c0003t0009g0084a0003c0003t0009g0085others(3): Show | 6 | HG00639.hp1 HG02145.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.302+398A>C | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | chr17 | 74223055 | ||||||
chr17:74223056
|
G | A | 6 | a0001c0001t0001g0083a0003c0003t0009g0084a0003c0003t0009g0085others(3): Show | 6 | HG00639.hp1 HG02145.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.302+399G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | chr17 | 74223056 | ||||||
chr17:74223060
|
T | G | 6 | a0001c0001t0001g0083a0003c0003t0009g0084a0003c0003t0009g0085others(3): Show | 6 | HG00639.hp1 HG02145.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.302+403T>G | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | chr17 | 74223060 | ||||||
chr17:74223061
|
T | TGAGAAC | 6 | a0001c0001t0001g0083a0003c0003t0009g0084a0003c0003t0009g0085others(3): Show | 6 | HG00639.hp1 HG02145.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.302+404_302+405ins others(6): Show |
TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | chr17 | 74223061 | ||||||
chr17:74223062
|
A | T | 6 | a0001c0001t0001g0083a0003c0003t0009g0084a0003c0003t0009g0085others(3): Show | 6 | HG00639.hp1 HG02145.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.302+405A>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | chr17 | 74223062 | ||||||
chr17:74223068
|
G | A | 1 | a0004c0006t0008g0088 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.302+411G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | chr17 | 74223068 | ||||||
chr17:74223166
|
T | C | 28 | a0001c0001t0001g0083a0001c0001t0001g0093a0001c0001t0001g0312others(25): Show | 28 | HG00639.hp1 HG00738.hp2 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.302+509T>C | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | chr17 | 74223166 | ||||||
chr17:74223285
|
T | G | 15 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(12): Show | 16 | HG01175.hp1 HG01496.hp2 HG01934.hp2 others(13): Show |
intron_variant | MODIFIER | c.302+628T>G | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | chr17 | 74223285 | ||||||
chr17:74223286
|
G | T | 17 | a0001c0001t0001g0312a0001c0009t0005g0074a0002c0002t0003g0317others(14): Show | 17 | HG01074.hp1 HG01516.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.302+629G>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | chr17 | 74223286 | ||||||
chr17:74223290
|
GGC | G | 18 | a0001c0001t0001g0312a0001c0009t0005g0074a0002c0002t0003g0317others(15): Show | 18 | HG01074.hp1 HG01516.hp1 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.302+635_302+636del others(2): Show |
TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 74223290 | |||||
chr17:74223291
|
G | T | 8 | a0001c0001t0001g0091a0005c0007t0018g0097a0005c0010t0002g0098others(5): Show | 8 | HG02451.hp2 HG02559.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.302+634G>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | chr17 | 74223291 | ||||||
chr17:74223291
|
GC | G | 5 | a0001c0001t0001g0083a0003c0003t0009g0084a0003c0003t0009g0085others(2): Show | 5 | HG00639.hp1 HG02145.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.302+635delC | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | chr17 | 74223291 | ||||||
chr17:74223292
|
C | G | 14 | a0001c0001t0001g0091a0001c0026t0001g0075a0004c0006t0008g0088others(11): Show | 14 | HG02451.hp2 HG02486.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.302+635C>G | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | chr17 | 74223292 | ||||||
chr17:74223296
|
G | C | 14 | a0001c0001t0001g0312a0002c0002t0003g0317a0004c0006t0001g0079others(11): Show | 14 | HG01074.hp1 HG01884.hp1 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.302+639G>C | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | chr17 | 74223296 | ||||||
chr17:74223389
|
G | C | 9 | a0001c0001t0001g0312a0002c0002t0003g0317a0007c0011t0001g0309others(6): Show | 9 | HG01074.hp1 HG02622.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.302+732G>C | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | chr17 | 74223389 | ||||||
chr17:74223481
|
C | G | 1 | a0001c0001t0001g0070 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.302+824C>G | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | chr17 | 74223481 | ||||||
chr17:74223554
|
C | G | 2 | a0001c0009t0005g0019a0001c0009t0005g0269 | 3 | HG02723.hp2 HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.302+897C>G | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | chr17 | 74223554 | ||||||
chr17:74223675
|
T | A | 28 | a0001c0001t0001g0083a0001c0001t0001g0093a0001c0001t0001g0312others(25): Show | 28 | HG00639.hp1 HG00738.hp2 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.302+1018T>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | chr17 | 74223675 | ||||||
chr17:74223712
|
G | A | 1 | a0003c0003t0002g0110 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.302+1055G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | chr17 | 74223712 | ||||||
chr17:74223757
|
T | C | 25 | a0001c0001t0001g0083a0001c0001t0001g0093a0001c0001t0001g0312others(22): Show | 25 | HG00639.hp1 HG00738.hp2 HG01074.hp1 others(22): Show |
intron_variant | MODIFIER | c.302+1100T>C | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | chr17 | 74223757 | ||||||
chr17:74223786
|
T | C | 74 | a0001c0001t0001g0083a0001c0001t0001g0091a0001c0001t0001g0093others(71): Show | 77 | HG00639.hp1 HG00733.hp1 HG00738.hp2 others(74): Show |
intron_variant | MODIFIER | c.302+1129T>C | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | chr17 | 74223786 | ||||||
chr17:74223930
|
C | T | 22 | a0001c0001t0001g0153a0001c0001t0001g0158a0001c0001t0001g0159others(19): Show | 25 | HG00733.hp1 HG01106.hp1 HG01891.hp2 others(22): Show |
intron_variant | MODIFIER | c.302+1273C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | chr17 | 74223930 | ||||||
chr17:74223985
|
G | C | 6 | a0005c0010t0002g0098a0005c0010t0004g0099a0005c0010t0004g0100others(3): Show | 6 | HG02451.hp2 HG02559.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.302+1328G>C | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | chr17 | 74223985 | ||||||
chr17:74224004
|
C | T | 1 | a0001c0001t0001g0163 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.302+1347C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | chr17 | 74224004 | ||||||
chr17:74224005
|
G | A | 6 | a0005c0010t0002g0098a0005c0010t0004g0099a0005c0010t0004g0100others(3): Show | 6 | HG02451.hp2 HG02559.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.302+1348G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | chr17 | 74224005 | ||||||
chr17:74224176
|
A | G | 29 | a0001c0001t0001g0083a0001c0001t0001g0093a0001c0001t0001g0312others(26): Show | 29 | HG00639.hp1 HG00738.hp2 HG01074.hp1 others(26): Show |
intron_variant | MODIFIER | c.302+1519A>G | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | chr17 | 74224176 | ||||||
chr17:74224189
|
C | T | 5 | a0004c0006t0008g0088a0009c0016t0007g0289a0009c0016t0007g0290others(2): Show | 5 | HG02486.hp2 HG02717.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.302+1532C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | chr17 | 74224189 | ||||||
chr17:74224212
|
T | C | 1 | a0006c0004t0002g0156 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.302+1555T>C | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | chr17 | 74224212 | ||||||
chr17:74224235
|
C | A | 3 | a0003c0003t0002g0124a0003c0003t0002g0298a0004c0005t0001g0123 | 3 | HG00140.hp2 HG00280.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.302+1578C>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | chr17 | 74224235 | ||||||
chr17:74224362
|
G | A | 2 | a0001c0001t0001g0045a0001c0001t0001g0046 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.302+1705G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | chr17 | 74224362 | ||||||
chr17:74224385
|
T | TAC | 36 | a0001c0001t0001g0213a0002c0002t0001g0229a0002c0002t0003g0002others(33): Show | 46 | HG00099.hp2 HG01069.hp2 HG01081.hp2 others(43): Show |
intron_variant | MODIFIER | c.302+1746_302+1747d others(4): Show |
TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 74224385 | |||||
chr17:74224385
|
TAC | T | 8 | a0001c0001t0001g0091a0005c0007t0018g0097a0005c0010t0002g0098others(5): Show | 8 | HG02451.hp2 HG02559.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.302+1746_302+1747d others(4): Show |
TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 74224385 | |||||
chr17:74224403
|
C | CAG | 4 | a0009c0016t0007g0289a0009c0016t0007g0290a0009c0016t0007g0291others(1): Show | 4 | HG02486.hp2 HG02717.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.302+1748_302+1749d others(4): Show |
TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 74224403 | |||||
chr17:74224403
|
C | G | 68 | a0001c0001t0001g0083a0001c0001t0001g0091a0001c0001t0001g0093others(65): Show | 70 | HG00639.hp1 HG00733.hp1 HG00738.hp2 others(67): Show |
intron_variant | MODIFIER | c.302+1746C>G | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | chr17 | 74224403 | ||||||
chr17:74224419
|
T | C | 17 | a0001c0001t0001g0312a0001c0009t0005g0074a0002c0002t0003g0317others(14): Show | 17 | HG01074.hp1 HG01516.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.302+1762T>C | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | chr17 | 74224419 | ||||||
chr17:74224441
|
C | T | 2 | a0001c0001t0001g0263a0001c0001t0001g0264 | 2 | NA18939.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.302+1784C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | chr17 | 74224441 | ||||||
chr17:74224474
|
A | G | 17 | a0001c0001t0001g0312a0001c0009t0005g0074a0002c0002t0003g0317others(14): Show | 17 | HG01074.hp1 HG01516.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.302+1817A>G | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | chr17 | 74224474 | ||||||
chr17:74224485
|
C | A | 3 | a0003c0003t0002g0124a0003c0003t0002g0298a0004c0005t0001g0123 | 3 | HG00140.hp2 HG00280.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.302+1828C>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | chr17 | 74224485 | ||||||
chr17:74224514
|
G | T | 2 | a0001c0001t0001g0091a0005c0007t0018g0097 | 2 | HG02647.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.302+1857G>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | chr17 | 74224514 | ||||||
chr17:74224536
|
A | G | 1 | a0008c0029t0002g0233 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.302+1879A>G | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | chr17 | 74224536 | ||||||
chr17:74224562
|
G | A | 5 | a0004c0006t0008g0088a0009c0016t0007g0289a0009c0016t0007g0290others(2): Show | 5 | HG02486.hp2 HG02717.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.302+1905G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | chr17 | 74224562 | ||||||
chr17:74224590
|
G | A | 10 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0113others(7): Show | 10 | HG00733.hp2 HG01175.hp2 HG01515.hp1 others(7): Show |
intron_variant | MODIFIER | c.302+1933G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | chr17 | 74224590 | ||||||
chr17:74224744
|
A | C | 5 | a0004c0006t0001g0079a0004c0006t0001g0080a0004c0006t0001g0082others(2): Show | 5 | HG01884.hp1 HG02615.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.302+2087A>C | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | chr17 | 74224744 | ||||||
chr17:74224831
|
C | T | 1 | a0001c0001t0001g0067 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.302+2174C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | chr17 | 74224831 | ||||||
chr17:74224955
|
C | T | 5 | a0001c0001t0001g0093a0001c0009t0005g0096a0001c0014t0001g0095others(2): Show | 5 | HG00738.hp2 HG02055.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.302+2298C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | chr17 | 74224955 | ||||||
chr17:74224993
|
C | T | 1 | a0004c0005t0001g0207 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.302+2336C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | chr17 | 74224993 | ||||||
chr17:74224994
|
G | A | 1 | a0001c0001t0001g0237 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.302+2337G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | chr17 | 74224994 | ||||||
chr17:74224998
|
C | CA | 80 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0017others(77): Show | 89 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(86): Show |
intron_variant | MODIFIER | c.302+2355dupA | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 74224998 | |||||
chr17:74224998
|
C | CAA | 20 | a0001c0001t0001g0121a0001c0001t0001g0312a0001c0009t0005g0074others(17): Show | 20 | HG01074.hp1 HG01516.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.302+2354_302+2355d others(4): Show |
TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 74224998 | |||||
chr17:74225013
|
C | A | 5 | a0004c0006t0001g0079a0004c0006t0001g0080a0004c0006t0001g0082others(2): Show | 5 | HG01884.hp1 HG02615.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.302+2356C>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | chr17 | 74225013 | ||||||
chr17:74225124
|
G | A | 1 | a0003c0003t0001g0127 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.302+2467G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | chr17 | 74225124 | ||||||
chr17:74225149
|
G | A | 1 | a0003c0003t0002g0164 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.302+2492G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | chr17 | 74225149 | ||||||
chr17:74225168
|
A | T | 14 | a0001c0001t0001g0312a0002c0002t0003g0317a0004c0006t0001g0079others(11): Show | 14 | HG01074.hp1 HG01884.hp1 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.302+2511A>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | chr17 | 74225168 | ||||||
chr17:74225275
|
T | C | 2 | a0001c0001t0001g0231a0001c0001t0001g0242 | 2 | NA18990.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.302+2618T>C | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | chr17 | 74225275 | ||||||
chr17:74225306
|
A | G | 17 | a0001c0001t0001g0312a0001c0009t0005g0074a0002c0002t0003g0317others(14): Show | 17 | HG01074.hp1 HG01516.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.302+2649A>G | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | chr17 | 74225306 | ||||||
chr17:74225406
|
G | A | 1 | a0001c0001t0001g0048 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.302+2749G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | chr17 | 74225406 | ||||||
chr17:74225455
|
G | T | 1 | a0002c0002t0003g0223 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.302+2798G>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | chr17 | 74225455 | ||||||
chr17:74225530
|
T | C | 1 | a0002c0002t0003g0212 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.302+2873T>C | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | chr17 | 74225530 | ||||||
chr17:74225796
|
G | A | 1 | a0004c0006t0001g0104 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.302+3139G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | chr17 | 74225796 | ||||||
chr17:74225805
|
C | T | 5 | a0001c0009t0012g0307a0001c0009t0012g0308a0001c0014t0001g0306others(2): Show | 5 | HG02965.hp1 HG02976.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.302+3148C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | chr17 | 74225805 | ||||||
chr17:74225842
|
AG | A | 14 | a0001c0001t0001g0312a0002c0002t0003g0317a0004c0006t0001g0079others(11): Show | 14 | HG01074.hp1 HG01884.hp1 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.302+3189delG | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 74225842 | |||||
chr17:74225862
|
G | A | 18 | a0001c0001t0001g0153a0001c0001t0001g0158a0001c0001t0001g0159others(15): Show | 20 | HG00733.hp1 HG01106.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.302+3205G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | chr17 | 74225862 | ||||||
chr17:74225885
|
T | C | 34 | a0001c0001t0001g0083a0001c0001t0001g0093a0001c0001t0001g0312others(31): Show | 34 | HG00639.hp1 HG00738.hp2 HG01074.hp1 others(31): Show |
intron_variant | MODIFIER | c.302+3228T>C | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | chr17 | 74225885 | ||||||
chr17:74225931
|
G | A | 1 | a0004c0005t0001g0128 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.302+3274G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | chr17 | 74225931 | ||||||
chr17:74225935
|
C | T | 1 | a0006c0004t0002g0081 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.302+3278C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | chr17 | 74225935 | ||||||
chr17:74225956
|
G | T | 1 | a0001c0001t0014g0181 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.302+3299G>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | chr17 | 74225956 | ||||||
chr17:74226052
|
C | T | 20 | a0001c0001t0001g0153a0001c0001t0001g0158a0001c0001t0001g0159others(17): Show | 22 | HG00733.hp1 HG01106.hp1 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.302+3395C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | chr17 | 74226052 | ||||||
chr17:74226053
|
G | A | 2 | a0001c0001t0001g0142a0001c0001t0001g0147 | 2 | NA19081.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.302+3396G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | chr17 | 74226053 | ||||||
chr17:74226192
|
C | T | 29 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0038others(26): Show | 33 | HG00140.hp1 HG00735.hp2 HG01175.hp1 others(30): Show |
intron_variant | MODIFIER | c.302+3535C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | chr17 | 74226192 | ||||||
chr17:74226286
|
C | G | 6 | a0001c0001t0001g0083a0003c0003t0009g0084a0003c0003t0009g0085others(3): Show | 6 | HG00639.hp1 HG02145.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.302+3629C>G | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | chr17 | 74226286 | ||||||
chr17:74226419
|
A | G | 14 | a0001c0001t0001g0312a0002c0002t0003g0317a0004c0006t0001g0079others(11): Show | 14 | HG01074.hp1 HG01884.hp1 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.302+3762A>G | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | chr17 | 74226419 | ||||||
chr17:74226495
|
G | A | 1 | a0001c0001t0001g0243 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.302+3838G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | chr17 | 74226495 | ||||||
chr17:74226511
|
C | T | 1 | a0003c0003t0002g0073 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.302+3854C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | chr17 | 74226511 | ||||||
chr17:74226535
|
C | T | 1 | a0003c0003t0009g0085 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.302+3878C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | chr17 | 74226535 | ||||||
chr17:74226588
|
G | A | 7 | a0001c0001t0001g0234a0001c0001t0001g0243a0001c0001t0001g0244others(4): Show | 7 | HG00408.hp2 HG02040.hp2 HG02056.hp2 others(4): Show |
intron_variant | MODIFIER | c.302+3931G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | chr17 | 74226588 | ||||||
chr17:74226667
|
G | A | 1 | a0003c0003t0002g0165 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.302+4010G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | chr17 | 74226667 | ||||||
chr17:74226733
|
A | T | 1 | a0021c0031t0008g0108 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.302+4076A>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | chr17 | 74226733 | ||||||
chr17:74226984
|
C | T | 4 | a0009c0016t0007g0289a0009c0016t0007g0290a0009c0016t0007g0291others(1): Show | 4 | HG02486.hp2 HG02717.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.303-3904C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | chr17 | 74226984 | ||||||
chr17:74227038
|
G | A | 14 | a0001c0001t0001g0312a0002c0002t0003g0317a0004c0006t0001g0079others(11): Show | 14 | HG01074.hp1 HG01884.hp1 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.303-3850G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | chr17 | 74227038 | ||||||
chr17:74227131
|
T | C | 27 | a0001c0001t0001g0093a0001c0001t0001g0312a0001c0009t0005g0074others(24): Show | 27 | HG00738.hp2 HG01074.hp1 HG01516.hp1 others(24): Show |
intron_variant | MODIFIER | c.303-3757T>C | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | chr17 | 74227131 | ||||||
chr17:74227230
|
C | T | 2 | a0001c0009t0005g0074a0003c0003t0002g0073 | 2 | HG01516.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.303-3658C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | chr17 | 74227230 | ||||||
chr17:74227246
|
A | G | 1 | a0003c0003t0002g0165 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.303-3642A>G | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | chr17 | 74227246 | ||||||
chr17:74227267
|
G | A | 1 | a0006c0004t0002g0151 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.303-3621G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | chr17 | 74227267 | ||||||
chr17:74227366
|
T | C | 319 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(316): Show | 351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.303-3522T>C | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | chr17 | 74227366 | ||||||
chr17:74227367
|
G | T | 6 | a0005c0010t0002g0098a0005c0010t0004g0099a0005c0010t0004g0100others(3): Show | 6 | HG02451.hp2 HG02559.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.303-3521G>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | chr17 | 74227367 | ||||||
chr17:74227471
|
A | C | 1 | a0001c0001t0002g0155 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.303-3417A>C | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | chr17 | 74227471 | ||||||
chr17:74227622
|
G | C | 1 | a0001c0001t0001g0159 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.303-3266G>C | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | chr17 | 74227622 | ||||||
chr17:74227746
|
C | CTTGTTTT others(4): Show |
5 | a0005c0007t0006g0187a0005c0007t0006g0188a0005c0007t0006g0189others(2): Show | 5 | HG00438.hp1 NA18980.hp2 NA18981.hp1 others(2): Show |
intron_variant | MODIFIER | c.303-3139_303-3129d others(13): Show |
TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 74227746 | |||||
chr17:74227749
|
G | GT | 13 | a0001c0001t0001g0015a0001c0001t0001g0065a0001c0001t0001g0069others(10): Show | 14 | HG00597.hp1 HG00597.hp2 HG01255.hp1 others(11): Show |
intron_variant | MODIFIER | c.303-3128dupT | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 74227749 | |||||
chr17:74227749
|
GT | G | 8 | a0001c0009t0012g0307a0001c0009t0012g0308a0001c0014t0001g0306others(5): Show | 8 | HG01884.hp1 HG02615.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.303-3128delT | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 74227749 | |||||
chr17:74227749
|
GTT | G | 9 | a0001c0001t0001g0312a0002c0002t0003g0317a0007c0011t0001g0309others(6): Show | 9 | HG01074.hp1 HG02622.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.303-3129_303-3128d others(4): Show |
TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 74227749 | |||||
chr17:74227750
|
T | TTTTTTTT others(3): Show |
5 | a0004c0006t0008g0088a0009c0016t0007g0289a0009c0016t0007g0290others(2): Show | 5 | HG02486.hp2 HG02717.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.303-3129_303-3128i others(12): Show |
TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 74227750 | |||||
chr17:74227761
|
G | T | 28 | a0001c0001t0001g0153a0001c0001t0001g0158a0001c0001t0001g0159others(25): Show | 30 | HG00438.hp1 HG00733.hp1 HG01106.hp1 others(27): Show |
intron_variant | MODIFIER | c.303-3127G>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | chr17 | 74227761 | ||||||
chr17:74227761
|
GT | G | 34 | a0001c0001t0001g0083a0001c0001t0001g0091a0001c0001t0001g0093others(31): Show | 35 | HG00639.hp1 HG00738.hp2 HG01516.hp1 others(32): Show |
intron_variant | MODIFIER | c.303-3117delT | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 74227761 | |||||
chr17:74227762
|
T | G | 28 | a0001c0001t0001g0153a0001c0001t0001g0158a0001c0001t0001g0159others(25): Show | 30 | HG00438.hp1 HG00733.hp1 HG01106.hp1 others(27): Show |
intron_variant | MODIFIER | c.303-3126T>G | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | chr17 | 74227762 | ||||||
chr17:74227791
|
T | C | 14 | a0001c0001t0001g0083a0001c0001t0001g0091a0003c0003t0009g0084others(11): Show | 14 | HG00639.hp1 HG02145.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.303-3097T>C | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | chr17 | 74227791 | ||||||
chr17:74227983
|
C | CT | 17 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0114others(14): Show | 17 | HG00140.hp2 HG00733.hp2 HG00738.hp2 others(14): Show |
intron_variant | MODIFIER | c.303-2887dupT | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 74227983 | |||||
chr17:74227983
|
C | CTT | 7 | a0001c0001t0001g0064a0001c0001t0001g0093a0001c0009t0005g0096others(4): Show | 7 | HG02055.hp2 HG02976.hp1 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.303-2888_303-2887d others(4): Show |
TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 74227983 | |||||
chr17:74227983
|
C | CTTTTTTT | 26 | a0001c0001t0001g0083a0001c0001t0001g0091a0001c0001t0001g0153others(23): Show | 28 | HG00639.hp1 HG00733.hp1 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.303-2893_303-2887d others(9): Show |
TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 74227983 | |||||
chr17:74227983
|
C | CTTTTTTT others(1): Show |
10 | a0001c0001t0001g0297a0001c0014t0001g0183a0003c0003t0009g0085others(7): Show | 10 | HG01884.hp2 HG02145.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.303-2894_303-2887d others(10): Show |
TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 74227983 | |||||
chr17:74227983
|
C | CTTTTTTT others(3): Show |
8 | a0001c0009t0005g0074a0003c0003t0002g0073a0004c0006t0001g0106others(5): Show | 8 | HG01516.hp1 HG02615.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.303-2896_303-2887d others(12): Show |
TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 74227983 | |||||
chr17:74227983
|
C | CTTTTTTT others(4): Show |
8 | a0001c0026t0001g0075a0004c0006t0001g0079a0004c0006t0001g0080others(5): Show | 8 | HG01884.hp1 HG02486.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.303-2897_303-2887d others(13): Show |
TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 74227983 | |||||
chr17:74227983
|
C | CTTTTTTT others(5): Show |
6 | a0002c0002t0003g0317a0007c0011t0001g0309a0007c0011t0001g0311others(3): Show | 6 | HG01074.hp1 HG02818.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.303-2898_303-2887d others(14): Show |
TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 74227983 | |||||
chr17:74227983
|
C | CTTTTTTT others(6): Show |
2 | a0001c0001t0001g0312a0013c0018t0002g0316 | 2 | HG02622.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.303-2899_303-2887d others(15): Show |
TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 74227983 | |||||
chr17:74227983
|
CT | C | 7 | a0001c0001t0001g0147a0001c0001t0001g0169a0001c0001t0001g0234others(4): Show | 7 | HG01433.hp1 HG02523.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.303-2887delT | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 74227983 | |||||
chr17:74227987
|
T | C | 2 | a0001c0001t0001g0111a0001c0001t0001g0174 | 2 | HG01515.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.303-2901T>C | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | chr17 | 74227987 | ||||||
chr17:74228087
|
G | A | 1 | a0001c0001t0001g0283 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.303-2801G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | chr17 | 74228087 | ||||||
chr17:74228279
|
T | C | 49 | a0001c0001t0001g0083a0001c0001t0001g0086a0001c0001t0001g0091others(46): Show | 49 | HG00438.hp1 HG00639.hp1 HG00738.hp2 others(46): Show |
intron_variant | MODIFIER | c.303-2609T>C | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | chr17 | 74228279 | ||||||
chr17:74228311
|
G | T | 4 | a0001c0009t0005g0019a0001c0009t0005g0269a0005c0020t0001g0184others(1): Show | 5 | HG02723.hp2 HG02896.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.303-2577G>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | chr17 | 74228311 | ||||||
chr17:74228368
|
C | T | 1 | a0002c0002t0003g0223 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.303-2520C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | chr17 | 74228368 | ||||||
chr17:74228369
|
G | A | 13 | a0001c0001t0001g0093a0001c0009t0005g0074a0001c0009t0005g0096others(10): Show | 13 | HG00738.hp2 HG01516.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.303-2519G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | chr17 | 74228369 | ||||||
chr17:74228573
|
T | G | 1 | a0004c0006t0001g0287 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.303-2315T>G | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | chr17 | 74228573 | ||||||
chr17:74228592
|
A | T | 1 | a0001c0001t0001g0169 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.303-2296A>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | chr17 | 74228592 | ||||||
chr17:74228704
|
G | A | 1 | a0001c0009t0012g0308 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.303-2184G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | chr17 | 74228704 | ||||||
chr17:74228705
|
C | T | 1 | a0001c0026t0001g0075 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.303-2183C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | chr17 | 74228705 | ||||||
chr17:74228766
|
C | T | 1 | a0001c0001t0001g0063 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.303-2122C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | chr17 | 74228766 | ||||||
chr17:74228917
|
C | T | 14 | a0001c0001t0001g0153a0001c0001t0001g0158a0001c0001t0001g0159others(11): Show | 16 | HG00733.hp1 HG01106.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.303-1971C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | chr17 | 74228917 | ||||||
chr17:74228987
|
C | T | 46 | a0001c0001t0001g0312a0001c0009t0012g0307a0001c0009t0012g0308others(43): Show | 56 | HG00099.hp2 HG01069.hp2 HG01074.hp1 others(53): Show |
intron_variant | MODIFIER | c.303-1901C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | chr17 | 74228987 | ||||||
chr17:74229014
|
G | A | 2 | a0005c0007t0008g0304a0005c0007t0008g0305 | 2 | HG03540.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.303-1874G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | chr17 | 74229014 | ||||||
chr17:74229255
|
G | A | 1 | a0001c0001t0001g0200 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.303-1633G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | chr17 | 74229255 | ||||||
chr17:74229311
|
C | T | 4 | a0009c0016t0007g0289a0009c0016t0007g0290a0009c0016t0007g0291others(1): Show | 4 | HG02486.hp2 HG02717.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.303-1577C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | chr17 | 74229311 | ||||||
chr17:74229314
|
A | G | 84 | a0001c0001t0001g0091a0001c0001t0001g0297a0001c0001t0001g0312others(81): Show | 95 | HG00099.hp2 HG00438.hp1 HG00738.hp2 others(92): Show |
intron_variant | MODIFIER | c.303-1574A>G | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | chr17 | 74229314 | ||||||
chr17:74229457
|
C | T | 1 | a0001c0001t0001g0286 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.303-1431C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | chr17 | 74229457 | ||||||
chr17:74229472
|
CCCAGCCC others(5): Show |
C | 5 | a0005c0007t0006g0187a0005c0007t0006g0188a0005c0007t0006g0189others(2): Show | 5 | HG00438.hp1 NA18980.hp2 NA18981.hp1 others(2): Show |
intron_variant | MODIFIER | c.303-1415_303-1404d others(14): Show |
TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | chr17 | 74229472 | ||||||
chr17:74229567
|
A | G | 4 | a0012c0017t0010g0117a0012c0017t0010g0118a0012c0017t0019g0087others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.303-1321A>G | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | chr17 | 74229567 | ||||||
chr17:74229763
|
G | A | 3 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0286 | 3 | NA18981.hp2 NA18994.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.303-1125G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | chr17 | 74229763 | ||||||
chr17:74229856
|
T | A | 1 | a0001c0001t0001g0050 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.303-1032T>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | chr17 | 74229856 | ||||||
chr17:74229962
|
T | C | 311 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(308): Show | 343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.303-926T>C | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | chr17 | 74229962 | ||||||
chr17:74230050
|
A | C | 6 | a0004c0006t0001g0079a0004c0006t0001g0080a0004c0006t0001g0082others(3): Show | 6 | HG00738.hp2 HG02615.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.303-838A>C | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | chr17 | 74230050 | ||||||
chr17:74230117
|
C | G | 1 | a0004c0006t0008g0088 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.303-771C>G | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | chr17 | 74230117 | ||||||
chr17:74230169
|
G | A | 1 | a0001c0001t0001g0051 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.303-719G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | chr17 | 74230169 | ||||||
chr17:74230175
|
C | T | 3 | a0001c0001t0001g0091a0001c0026t0001g0075a0005c0007t0018g0097 | 3 | HG02647.hp2 HG03209.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.303-713C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | chr17 | 74230175 | ||||||
chr17:74230246
|
G | A | 5 | a0005c0007t0006g0187a0005c0007t0006g0188a0005c0007t0006g0189others(2): Show | 5 | HG00438.hp1 NA18980.hp2 NA18981.hp1 others(2): Show |
intron_variant | MODIFIER | c.303-642G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | chr17 | 74230246 | ||||||
chr17:74230257
|
A | AT | 12 | a0001c0001t0001g0093a0001c0001t0001g0161a0001c0009t0005g0096others(9): Show | 12 | HG01175.hp1 HG02055.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.303-620dupT | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 74230257 | |||||
chr17:74230257
|
A | ATT | 131 | a0001c0001t0001g0091a0001c0001t0001g0297a0001c0001t0001g0312others(128): Show | 147 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.303-621_303-620dup others(2): Show |
TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 74230257 | |||||
chr17:74230562
|
G | A | 5 | a0005c0007t0006g0187a0005c0007t0006g0188a0005c0007t0006g0189others(2): Show | 5 | HG00438.hp1 NA18980.hp2 NA18981.hp1 others(2): Show |
intron_variant | MODIFIER | c.303-326G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | chr17 | 74230562 | ||||||
chr17:74230589
|
C | T | 1 | a0004c0006t0001g0106 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.303-299C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | chr17 | 74230589 | ||||||
chr17:74230643
|
C | CT | 12 | a0001c0001t0001g0058a0001c0001t0001g0059a0001c0001t0001g0091others(9): Show | 12 | HG00738.hp2 HG01255.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.303-231dupT | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr17 | 74230643 | |||||
chr17:74230806
|
A | G | 89 | a0001c0001t0001g0091a0001c0001t0001g0093a0001c0001t0001g0297others(86): Show | 95 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.303-82A>G | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | chr17 | 74230806 | ||||||
chr17:74230879
|
T | G | 1 | a0001c0009t0005g0019 | 2 | HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.303-9T>G | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 2/13 | chr17 | 74230879 | ||||||
chr17:74231061
|
C | G | 3 | a0001c0001t0001g0312a0007c0011t0001g0152a0007c0012t0001g0314 | 3 | HG02109.hp2 NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.414+62C>G | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 3/13 | chr17 | 74231061 | ||||||
chr17:74231067
|
C | T | 10 | a0001c0001t0001g0297a0001c0009t0005g0019a0001c0009t0005g0074others(7): Show | 11 | HG01884.hp2 HG02622.hp1 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.414+68C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 3/13 | chr17 | 74231067 | ||||||
chr17:74231181
|
G | T | 4 | a0012c0017t0010g0117a0012c0017t0010g0118a0012c0017t0019g0087others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.414+182G>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 3/13 | chr17 | 74231181 | ||||||
chr17:74231439
|
T | A | 145 | a0001c0001t0001g0091a0001c0001t0001g0093a0001c0001t0001g0297others(142): Show | 160 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(157): Show |
intron_variant | MODIFIER | c.414+440T>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 3/13 | chr17 | 74231439 | ||||||
chr17:74231500
|
C | A | 1 | a0002c0002t0003g0214 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.414+501C>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 3/13 | chr17 | 74231500 | ||||||
chr17:74231730
|
G | C | 1 | a0001c0001t0001g0051 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.414+731G>C | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 3/13 | chr17 | 74231730 | ||||||
chr17:74231855
|
T | C | 2 | a0001c0001t0001g0032a0001c0001t0001g0067 | 2 | HG02735.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.414+856T>C | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 3/13 | chr17 | 74231855 | ||||||
chr17:74231901
|
C | T | 5 | a0005c0007t0006g0187a0005c0007t0006g0188a0005c0007t0006g0189others(2): Show | 5 | HG00438.hp1 NA18980.hp2 NA18981.hp1 others(2): Show |
intron_variant | MODIFIER | c.414+902C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 3/13 | chr17 | 74231901 | ||||||
chr17:74231997
|
C | G | 1 | a0003c0003t0002g0206 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.414+998C>G | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 3/13 | chr17 | 74231997 | ||||||
chr17:74232025
|
C | T | 4 | a0012c0017t0010g0117a0012c0017t0010g0118a0012c0017t0019g0087others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.414+1026C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 3/13 | chr17 | 74232025 | ||||||
chr17:74232069
|
C | T | 27 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0028others(24): Show | 31 | HG00140.hp1 HG00735.hp2 HG01175.hp1 others(28): Show |
intron_variant | MODIFIER | c.414+1070C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 3/13 | chr17 | 74232069 | ||||||
chr17:74232079
|
A | T | 1 | a0003c0003t0002g0073 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.414+1080A>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 3/13 | chr17 | 74232079 | ||||||
chr17:74232167
|
G | A | 7 | a0001c0001t0001g0297a0005c0020t0001g0184a0005c0020t0001g0185others(4): Show | 7 | HG01884.hp2 HG02622.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.414+1168G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 3/13 | chr17 | 74232167 | ||||||
chr17:74232210
|
G | C | 1 | a0006c0004t0002g0202 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.414+1211G>C | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 3/13 | chr17 | 74232210 | ||||||
chr17:74232258
|
G | A | 1 | a0003c0003t0002g0206 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.414+1259G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 3/13 | chr17 | 74232258 | ||||||
chr17:74232299
|
C | T | 1 | a0003c0003t0002g0073 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.414+1300C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 3/13 | chr17 | 74232299 | ||||||
chr17:74232436
|
G | A | 5 | a0001c0001t0001g0297a0010c0013t0004g0293a0010c0013t0004g0294others(2): Show | 5 | HG01884.hp2 HG02622.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.414+1437G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 3/13 | chr17 | 74232436 | ||||||
chr17:74232437
|
C | T | 4 | a0012c0017t0010g0117a0012c0017t0010g0118a0012c0017t0019g0087others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.414+1438C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 3/13 | chr17 | 74232437 | ||||||
chr17:74232523
|
G | T | 1 | a0001c0026t0001g0075 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.414+1524G>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 3/13 | chr17 | 74232523 | ||||||
chr17:74232558
|
G | A | 2 | a0005c0020t0001g0184a0005c0020t0001g0185 | 2 | HG02896.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.414+1559G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 3/13 | chr17 | 74232558 | ||||||
chr17:74232583
|
A | C | 1 | a0001c0001t0001g0195 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.414+1584A>C | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 3/13 | chr17 | 74232583 | ||||||
chr17:74232752
|
G | A | 10 | a0004c0006t0001g0079a0004c0006t0001g0080a0004c0006t0001g0082others(7): Show | 10 | HG00738.hp2 HG02615.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.414+1753G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 3/13 | chr17 | 74232752 | ||||||
chr17:74233003
|
C | T | 1 | a0003c0003t0002g0125 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.414+2004C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 3/13 | chr17 | 74233003 | ||||||
chr17:74233183
|
C | G | 6 | a0004c0006t0001g0079a0004c0006t0001g0080a0004c0006t0001g0082others(3): Show | 6 | HG00738.hp2 HG02615.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.414+2184C>G | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 3/13 | chr17 | 74233183 | ||||||
chr17:74233353
|
G | A | 55 | a0003c0003t0001g0127a0003c0003t0002g0010a0003c0003t0002g0013others(52): Show | 60 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(57): Show |
intron_variant | MODIFIER | c.414+2354G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 3/13 | chr17 | 74233353 | ||||||
chr17:74233484
|
C | T | 23 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0028others(20): Show | 27 | HG01175.hp1 HG02015.hp2 HG02074.hp2 others(24): Show |
intron_variant | MODIFIER | c.414+2485C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 3/13 | chr17 | 74233484 | ||||||
chr17:74233485
|
G | T | 1 | a0015c0021t0004g0119 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.414+2486G>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 3/13 | chr17 | 74233485 | ||||||
chr17:74233525
|
A | T | 10 | a0004c0006t0001g0079a0004c0006t0001g0080a0004c0006t0001g0082others(7): Show | 10 | HG00738.hp2 HG02615.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.414+2526A>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 3/13 | chr17 | 74233525 | ||||||
chr17:74233604
|
C | T | 10 | a0004c0006t0001g0079a0004c0006t0001g0080a0004c0006t0001g0082others(7): Show | 10 | HG00738.hp2 HG02615.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.414+2605C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 3/13 | chr17 | 74233604 | ||||||
chr17:74233887
|
C | A | 4 | a0003c0003t0009g0084a0003c0003t0009g0085a0003c0003t0009g0089others(1): Show | 4 | HG00639.hp1 HG02145.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.414+2888C>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 3/13 | chr17 | 74233887 | ||||||
chr17:74233979
|
A | C | 1 | a0003c0003t0002g0073 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.414+2980A>C | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 3/13 | chr17 | 74233979 | ||||||
chr17:74234049
|
C | T | 3 | a0001c0009t0012g0307a0001c0009t0012g0308a0001c0014t0001g0306 | 3 | HG02965.hp1 HG02976.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.414+3050C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 3/13 | chr17 | 74234049 | ||||||
chr17:74234073
|
A | G | 10 | a0004c0006t0001g0079a0004c0006t0001g0080a0004c0006t0001g0082others(7): Show | 10 | HG00738.hp2 HG02615.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.414+3074A>G | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 3/13 | chr17 | 74234073 | ||||||
chr17:74234092
|
G | C | 1 | a0001c0009t0005g0074 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.414+3093G>C | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 3/13 | chr17 | 74234092 | ||||||
chr17:74234140
|
G | A | 10 | a0004c0006t0001g0079a0004c0006t0001g0080a0004c0006t0001g0082others(7): Show | 10 | HG00738.hp2 HG02615.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.414+3141G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 3/13 | chr17 | 74234140 | ||||||
chr17:74234274
|
G | A | 2 | a0001c0001t0001g0060a0001c0001t0001g0061 | 2 | NA18970.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.415-3020G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 3/13 | chr17 | 74234274 | ||||||
chr17:74234282
|
C | T | 2 | a0001c0001t0001g0258a0001c0001t0001g0259 | 2 | NA20752.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.415-3012C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 3/13 | chr17 | 74234282 | ||||||
chr17:74234335
|
C | G | 1 | a0003c0003t0002g0073 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.415-2959C>G | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 3/13 | chr17 | 74234335 | ||||||
chr17:74234428
|
T | C | 2 | a0002c0019t0003g0215a0002c0019t0003g0273 | 2 | HG00099.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.415-2866T>C | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 3/13 | chr17 | 74234428 | ||||||
chr17:74234441
|
A | G | 1 | a0005c0007t0008g0304 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.415-2853A>G | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 3/13 | chr17 | 74234441 | ||||||
chr17:74234572
|
C | G | 1 | a0001c0001t0001g0302 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.415-2722C>G | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 3/13 | chr17 | 74234572 | ||||||
chr17:74234625
|
T | C | 2 | a0003c0003t0002g0122a0004c0005t0001g0011 | 3 | NA18960.hp2 NA18966.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.415-2669T>C | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 3/13 | chr17 | 74234625 | ||||||
chr17:74234647
|
CT | C | 7 | a0001c0001t0001g0297a0005c0020t0001g0184a0005c0020t0001g0185others(4): Show | 7 | HG01884.hp2 HG02622.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.415-2638delT | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr17 | 74234647 | |||||
chr17:74234656
|
T | C | 3 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0286 | 3 | NA18981.hp2 NA18994.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.415-2638T>C | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 3/13 | chr17 | 74234656 | ||||||
chr17:74234662
|
TAAGGAGG others(17): Show |
T | 1 | a0001c0001t0001g0275 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.415-2630_415-2607d others(26): Show |
TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr17 | 74234662 | |||||
chr17:74234690
|
TAACTGTG others(9): Show |
T | 6 | a0005c0010t0002g0098a0005c0010t0004g0099a0005c0010t0004g0100others(3): Show | 6 | HG02451.hp2 HG02559.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.415-2594_415-2579d others(18): Show |
TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr17 | 74234690 | |||||
chr17:74235032
|
G | A | 1 | a0005c0010t0004g0102 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.415-2262G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 3/13 | chr17 | 74235032 | ||||||
chr17:74235065
|
G | A | 44 | a0002c0002t0001g0229a0002c0002t0003g0002a0002c0002t0003g0007others(41): Show | 54 | HG00099.hp2 HG01069.hp2 HG01074.hp1 others(51): Show |
intron_variant | MODIFIER | c.415-2229G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 3/13 | chr17 | 74235065 | ||||||
chr17:74235157
|
G | A | 1 | a0006c0004t0002g0156 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.415-2137G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 3/13 | chr17 | 74235157 | ||||||
chr17:74235161
|
T | C | 153 | a0001c0001t0001g0093a0001c0001t0001g0231a0001c0001t0001g0242others(150): Show | 169 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.415-2133T>C | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 3/13 | chr17 | 74235161 | ||||||
chr17:74235261
|
C | T | 1 | a0001c0026t0001g0075 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.415-2033C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 3/13 | chr17 | 74235261 | ||||||
chr17:74235279
|
T | C | 1 | a0001c0001t0001g0141 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.415-2015T>C | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 3/13 | chr17 | 74235279 | ||||||
chr17:74235380
|
G | A | 1 | a0008c0008t0002g0250 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.415-1914G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 3/13 | chr17 | 74235380 | ||||||
chr17:74235500
|
C | T | 1 | a0001c0001t0001g0031 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.415-1794C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 3/13 | chr17 | 74235500 | ||||||
chr17:74235613
|
G | A | 1 | a0004c0006t0008g0088 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.415-1681G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 3/13 | chr17 | 74235613 | ||||||
chr17:74235746
|
C | T | 3 | a0001c0009t0012g0307a0001c0009t0012g0308a0001c0014t0001g0306 | 3 | HG02965.hp1 HG02976.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.415-1548C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 3/13 | chr17 | 74235746 | ||||||
chr17:74235818
|
C | T | 10 | a0004c0006t0001g0079a0004c0006t0001g0080a0004c0006t0001g0082others(7): Show | 10 | HG00738.hp2 HG02615.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.415-1476C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 3/13 | chr17 | 74235818 | ||||||
chr17:74235895
|
C | CA | 21 | a0001c0001t0001g0016a0001c0001t0001g0027a0001c0001t0001g0064others(18): Show | 21 | HG00738.hp2 HG01433.hp2 HG02074.hp1 others(18): Show |
intron_variant | MODIFIER | c.415-1383dupA | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr17 | 74235895 | |||||
chr17:74235905
|
A | C | 1 | a0001c0001t0001g0051 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.415-1389A>C | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 3/13 | chr17 | 74235905 | ||||||
chr17:74235947
|
A | G | 3 | a0001c0009t0012g0307a0001c0009t0012g0308a0001c0014t0001g0306 | 3 | HG02965.hp1 HG02976.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.415-1347A>G | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 3/13 | chr17 | 74235947 | ||||||
chr17:74236043
|
G | A | 4 | a0009c0016t0007g0289a0009c0016t0007g0290a0009c0016t0007g0291others(1): Show | 4 | HG02486.hp2 HG02717.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.415-1251G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 3/13 | chr17 | 74236043 | ||||||
chr17:74236169
|
G | C | 3 | a0003c0003t0001g0127a0003c0003t0002g0122a0004c0005t0001g0011 | 4 | NA18960.hp2 NA18966.hp2 NA18984.hp2 others(1): Show |
intron_variant | MODIFIER | c.415-1125G>C | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 3/13 | chr17 | 74236169 | ||||||
chr17:74236505
|
A | G | 1 | a0021c0031t0008g0108 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.415-789A>G | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 3/13 | chr17 | 74236505 | ||||||
chr17:74236521
|
T | C | 4 | a0012c0017t0010g0117a0012c0017t0010g0118a0012c0017t0019g0087others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.415-773T>C | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 3/13 | chr17 | 74236521 | ||||||
chr17:74236658
|
C | T | 1 | a0005c0007t0018g0097 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.415-636C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 3/13 | chr17 | 74236658 | ||||||
chr17:74236661
|
G | A | 1 | a0005c0020t0001g0185 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.415-633G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 3/13 | chr17 | 74236661 | ||||||
chr17:74236672
|
G | C | 123 | a0001c0026t0001g0075a0002c0002t0001g0229a0002c0002t0003g0002others(120): Show | 138 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.415-622G>C | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 3/13 | chr17 | 74236672 | ||||||
chr17:74236717
|
C | T | 7 | a0001c0001t0002g0003a0001c0001t0002g0148a0001c0001t0002g0149others(4): Show | 9 | HG00733.hp1 HG02055.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.415-577C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 3/13 | chr17 | 74236717 | ||||||
chr17:74236726
|
G | C | 4 | a0009c0016t0007g0289a0009c0016t0007g0290a0009c0016t0007g0291others(1): Show | 4 | HG02486.hp2 HG02717.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.415-568G>C | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 3/13 | chr17 | 74236726 | ||||||
chr17:74236779
|
A | G | 133 | a0001c0009t0012g0307a0001c0009t0012g0308a0001c0014t0001g0306others(130): Show | 148 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(145): Show |
intron_variant | MODIFIER | c.415-515A>G | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 3/13 | chr17 | 74236779 | ||||||
chr17:74236795
|
C | T | 4 | a0012c0017t0010g0117a0012c0017t0010g0118a0012c0017t0019g0087others(1): Show | 4 | HG02895.hp1 HG02897.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.415-499C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 3/13 | chr17 | 74236795 | ||||||
chr17:74236796
|
G | A | 1 | a0005c0007t0018g0097 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.415-498G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 3/13 | chr17 | 74236796 | ||||||
chr17:74236831
|
G | A | 1 | a0002c0002t0003g0217 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.415-463G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 3/13 | chr17 | 74236831 | ||||||
chr17:74236835
|
G | A | 1 | a0003c0003t0002g0109 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.415-459G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 3/13 | chr17 | 74236835 | ||||||
chr17:74236881
|
G | A | 4 | a0009c0016t0007g0289a0009c0016t0007g0290a0009c0016t0007g0291others(1): Show | 4 | HG02486.hp2 HG02717.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.415-413G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 3/13 | chr17 | 74236881 | ||||||
chr17:74236895
|
C | CT | 24 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0059others(21): Show | 24 | HG00735.hp1 HG01175.hp1 HG01515.hp2 others(21): Show |
intron_variant | MODIFIER | c.415-382dupT | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr17 | 74236895 | |||||
chr17:74236895
|
CT | C | 73 | a0001c0001t0001g0297a0003c0003t0001g0127a0003c0003t0002g0010others(70): Show | 78 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(75): Show |
intron_variant | MODIFIER | c.415-382delT | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr17 | 74236895 | |||||
chr17:74236914
|
G | T | 1 | a0001c0001t0001g0285 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.415-380G>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 3/13 | chr17 | 74236914 | ||||||
chr17:74236927
|
A | G | 5 | a0005c0007t0006g0187a0005c0007t0006g0188a0005c0007t0006g0189others(2): Show | 5 | HG00438.hp1 NA18980.hp2 NA18981.hp1 others(2): Show |
intron_variant | MODIFIER | c.415-367A>G | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 3/13 | chr17 | 74236927 | ||||||
chr17:74236950
|
G | A | 1 | a0005c0007t0018g0097 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.415-344G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 3/13 | chr17 | 74236950 | ||||||
chr17:74236958
|
G | A | 4 | a0001c0001t0001g0252a0001c0001t0001g0280a0008c0008t0002g0250others(1): Show | 4 | NA18939.hp2 NA18949.hp2 NA18957.hp2 others(1): Show |
intron_variant | MODIFIER | c.415-336G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 3/13 | chr17 | 74236958 | ||||||
chr17:74236959
|
C | T | 1 | a0001c0001t0001g0179 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.415-335C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 3/13 | chr17 | 74236959 | ||||||
chr17:74236965
|
T | C | 5 | a0005c0007t0006g0187a0005c0007t0006g0188a0005c0007t0006g0189others(2): Show | 5 | HG00438.hp1 NA18980.hp2 NA18981.hp1 others(2): Show |
intron_variant | MODIFIER | c.415-329T>C | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 3/13 | chr17 | 74236965 | ||||||
chr17:74237074
|
T | TA | 6 | a0004c0006t0001g0079a0004c0006t0001g0080a0004c0006t0001g0082others(3): Show | 6 | HG00738.hp2 HG02615.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.415-220_415-219ins others(1): Show |
TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 3/13 | chr17 | 74237074 | ||||||
chr17:74237086
|
G | T | 1 | a0005c0007t0018g0097 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.415-208G>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 3/13 | chr17 | 74237086 | ||||||
chr17:74237102
|
G | A | 1 | a0004c0006t0008g0088 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.415-192G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 3/13 | chr17 | 74237102 | ||||||
chr17:74237280
|
C | T | 21 | a0003c0003t0001g0127a0003c0003t0002g0013a0003c0003t0002g0076others(18): Show | 24 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(21): Show |
intron_variant | MODIFIER | c.415-14C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 3/13 | chr17 | 74237280 | ||||||
chr17:74237586
|
G | T | 1 | a0001c0001t0001g0280 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.635+72G>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 4/13 | chr17 | 74237586 | ||||||
chr17:74237621
|
AT | A | 49 | a0002c0002t0001g0229a0002c0002t0003g0002a0002c0002t0003g0007others(46): Show | 59 | HG00099.hp2 HG01069.hp2 HG01074.hp1 others(56): Show |
intron_variant | MODIFIER | c.635+117delT | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr17 | 74237621 | |||||
chr17:74237627
|
T | G | 4 | a0001c0001t0001g0242a0002c0002t0003g0223a0003c0003t0002g0073others(1): Show | 4 | HG00733.hp2 HG01516.hp1 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.635+113T>G | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 4/13 | chr17 | 74237627 | ||||||
chr17:74237632
|
G | T | 1 | a0001c0026t0001g0075 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.635+118G>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 4/13 | chr17 | 74237632 | ||||||
chr17:74237806
|
T | C | 6 | a0005c0010t0002g0098a0005c0010t0004g0099a0005c0010t0004g0100others(3): Show | 6 | HG02451.hp2 HG02559.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.635+292T>C | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 4/13 | chr17 | 74237806 | ||||||
chr17:74237831
|
A | G | 72 | a0001c0001t0001g0297a0001c0009t0005g0019a0001c0009t0005g0074others(69): Show | 78 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(75): Show |
intron_variant | MODIFIER | c.635+317A>G | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 4/13 | chr17 | 74237831 | ||||||
chr17:74237913
|
G | A | 1 | a0021c0031t0008g0108 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.635+399G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 4/13 | chr17 | 74237913 | ||||||
chr17:74238062
|
G | T | 58 | a0001c0001t0001g0297a0002c0002t0001g0229a0002c0002t0003g0002others(55): Show | 68 | HG00099.hp2 HG01069.hp2 HG01074.hp1 others(65): Show |
intron_variant | MODIFIER | c.635+548G>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 4/13 | chr17 | 74238062 | ||||||
chr17:74238075
|
G | A | 2 | a0001c0001t0001g0252a0001c0001t0001g0280 | 2 | NA18957.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.635+561G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 4/13 | chr17 | 74238075 | ||||||
chr17:74238085
|
C | T | 1 | a0005c0007t0018g0097 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.635+571C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 4/13 | chr17 | 74238085 | ||||||
chr17:74238167
|
G | A | 6 | a0005c0010t0002g0098a0005c0010t0004g0099a0005c0010t0004g0100others(3): Show | 6 | HG02451.hp2 HG02559.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.635+653G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 4/13 | chr17 | 74238167 | ||||||
chr17:74238191
|
C | T | 1 | a0001c0001t0001g0039 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.635+677C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 4/13 | chr17 | 74238191 | ||||||
chr17:74238456
|
T | C | 5 | a0005c0007t0006g0187a0005c0007t0006g0188a0005c0007t0006g0189others(2): Show | 5 | HG00438.hp1 NA18980.hp2 NA18981.hp1 others(2): Show |
intron_variant | MODIFIER | c.635+942T>C | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 4/13 | chr17 | 74238456 | ||||||
chr17:74238520
|
T | C | 9 | a0001c0001t0002g0003a0001c0001t0002g0148a0001c0001t0002g0149others(6): Show | 11 | HG00733.hp1 HG02055.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.635+1006T>C | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 4/13 | chr17 | 74238520 | ||||||
chr17:74238599
|
G | C | 1 | a0001c0009t0012g0307 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.635+1085G>C | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 4/13 | chr17 | 74238599 | ||||||
chr17:74238622
|
T | C | 2 | a0001c0026t0001g0075a0003c0003t0002g0073 | 2 | HG01516.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.635+1108T>C | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 4/13 | chr17 | 74238622 | ||||||
chr17:74238663
|
C | T | 9 | a0005c0007t0006g0187a0005c0007t0006g0188a0005c0007t0006g0189others(6): Show | 9 | HG00438.hp1 HG02145.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.635+1149C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 4/13 | chr17 | 74238663 | ||||||
chr17:74238728
|
G | A | 1 | a0001c0001t0001g0244 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.635+1214G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 4/13 | chr17 | 74238728 | ||||||
chr17:74238867
|
CA | C | 58 | a0001c0001t0001g0048a0001c0001t0001g0111a0001c0001t0001g0178others(55): Show | 68 | HG00099.hp2 HG00438.hp1 HG01069.hp2 others(65): Show |
intron_variant | MODIFIER | c.635+1369delA | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr17 | 74238867 | |||||
chr17:74238883
|
A | T | 1 | a0005c0007t0018g0097 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.635+1369A>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 4/13 | chr17 | 74238883 | ||||||
chr17:74238967
|
T | A | 3 | a0001c0009t0012g0307a0001c0009t0012g0308a0001c0014t0001g0306 | 3 | HG02965.hp1 HG02976.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.635+1453T>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 4/13 | chr17 | 74238967 | ||||||
chr17:74239069
|
GTGTACAA others(5): Show |
G | 1 | a0001c0026t0001g0075 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.635+1558_635+1569d others(14): Show |
TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr17 | 74239069 | |||||
chr17:74239175
|
C | G | 1 | a0001c0001t0016g0276 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.635+1661C>G | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 4/13 | chr17 | 74239175 | ||||||
chr17:74239281
|
C | T | 1 | a0001c0001t0001g0283 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.635+1767C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 4/13 | chr17 | 74239281 | ||||||
chr17:74239326
|
G | A | 10 | a0001c0001t0001g0112a0001c0001t0001g0237a0001c0001t0001g0238others(7): Show | 10 | HG00323.hp2 HG00741.hp1 HG01106.hp2 others(7): Show |
intron_variant | MODIFIER | c.635+1812G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 4/13 | chr17 | 74239326 | ||||||
chr17:74239419
|
C | T | 44 | a0002c0002t0001g0229a0002c0002t0003g0002a0002c0002t0003g0007others(41): Show | 54 | HG00099.hp2 HG01069.hp2 HG01074.hp1 others(51): Show |
intron_variant | MODIFIER | c.635+1905C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 4/13 | chr17 | 74239419 | ||||||
chr17:74239422
|
C | A | 22 | a0001c0001t0001g0018a0001c0001t0001g0047a0001c0001t0001g0141others(19): Show | 22 | HG00408.hp2 HG00741.hp2 HG01069.hp1 others(19): Show |
intron_variant | MODIFIER | c.635+1908C>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 4/13 | chr17 | 74239422 | ||||||
chr17:74239576
|
G | A | 6 | a0004c0006t0001g0079a0004c0006t0001g0080a0004c0006t0001g0082others(3): Show | 6 | HG00738.hp2 HG02615.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.635+2062G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 4/13 | chr17 | 74239576 | ||||||
chr17:74239780
|
C | T | 3 | a0001c0009t0012g0307a0001c0009t0012g0308a0001c0014t0001g0306 | 3 | HG02965.hp1 HG02976.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.635+2266C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 4/13 | chr17 | 74239780 | ||||||
chr17:74239912
|
G | A | 1 | a0001c0001t0013g0245 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.635+2398G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 4/13 | chr17 | 74239912 | ||||||
chr17:74239915
|
A | C | 3 | a0001c0009t0012g0307a0001c0009t0012g0308a0001c0014t0001g0306 | 3 | HG02965.hp1 HG02976.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.635+2401A>C | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 4/13 | chr17 | 74239915 | ||||||
chr17:74240053
|
T | C | 1 | a0004c0006t0008g0088 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.635+2539T>C | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 4/13 | chr17 | 74240053 | ||||||
chr17:74240094
|
G | A | 120 | a0001c0001t0001g0297a0001c0026t0001g0075a0002c0002t0001g0229others(117): Show | 134 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(131): Show |
intron_variant | MODIFIER | c.635+2580G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 4/13 | chr17 | 74240094 | ||||||
chr17:74240116
|
T | C | 5 | a0005c0007t0006g0187a0005c0007t0006g0188a0005c0007t0006g0189others(2): Show | 5 | HG00438.hp1 NA18980.hp2 NA18981.hp1 others(2): Show |
intron_variant | MODIFIER | c.635+2602T>C | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 4/13 | chr17 | 74240116 | ||||||
chr17:74240161
|
G | A | 1 | a0001c0001t0001g0009 | 3 | NA18975.hp2 NA19007.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.635+2647G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 4/13 | chr17 | 74240161 | ||||||
chr17:74240438
|
CA | C | 8 | a0001c0014t0001g0183a0002c0002t0001g0229a0004c0006t0001g0079others(5): Show | 8 | HG00738.hp2 HG02615.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.636-2921delA | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr17 | 74240438 | |||||
chr17:74240632
|
G | A | 47 | a0001c0026t0001g0075a0002c0002t0001g0229a0002c0002t0003g0002others(44): Show | 57 | HG00099.hp2 HG01069.hp2 HG01074.hp1 others(54): Show |
intron_variant | MODIFIER | c.636-2742G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 4/13 | chr17 | 74240632 | ||||||
chr17:74240633
|
C | A | 47 | a0001c0026t0001g0075a0002c0002t0001g0229a0002c0002t0003g0002others(44): Show | 57 | HG00099.hp2 HG01069.hp2 HG01074.hp1 others(54): Show |
intron_variant | MODIFIER | c.636-2741C>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 4/13 | chr17 | 74240633 | ||||||
chr17:74240634
|
A | G | 47 | a0001c0026t0001g0075a0002c0002t0001g0229a0002c0002t0003g0002others(44): Show | 57 | HG00099.hp2 HG01069.hp2 HG01074.hp1 others(54): Show |
intron_variant | MODIFIER | c.636-2740A>G | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 4/13 | chr17 | 74240634 | ||||||
chr17:74240639
|
A | C | 11 | a0004c0006t0001g0079a0004c0006t0001g0080a0004c0006t0001g0082others(8): Show | 11 | HG00438.hp1 HG00738.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.636-2735A>C | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 4/13 | chr17 | 74240639 | ||||||
chr17:74240643
|
G | A | 125 | a0001c0026t0001g0075a0002c0002t0001g0229a0002c0002t0003g0002others(122): Show | 140 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.636-2731G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 4/13 | chr17 | 74240643 | ||||||
chr17:74240748
|
G | A | 4 | a0012c0017t0010g0117a0012c0017t0010g0118a0012c0017t0019g0087others(1): Show | 4 | HG02145.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.636-2626G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 4/13 | chr17 | 74240748 | ||||||
chr17:74240812
|
G | A | 2 | a0013c0018t0002g0315a0013c0018t0002g0316 | 2 | HG02622.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.636-2562G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 4/13 | chr17 | 74240812 | ||||||
chr17:74240881
|
G | A | 2 | a0005c0020t0001g0184a0005c0020t0001g0185 | 2 | HG02896.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.636-2493G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 4/13 | chr17 | 74240881 | ||||||
chr17:74241057
|
G | T | 1 | a0011c0015t0001g0251 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.636-2317G>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 4/13 | chr17 | 74241057 | ||||||
chr17:74241236
|
C | T | 6 | a0001c0001t0001g0297a0010c0013t0004g0293a0010c0013t0004g0294others(3): Show | 6 | HG01884.hp2 HG02622.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.636-2138C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 4/13 | chr17 | 74241236 | ||||||
chr17:74241248
|
C | T | 67 | a0003c0003t0001g0127a0003c0003t0002g0010a0003c0003t0002g0013others(64): Show | 72 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(69): Show |
intron_variant | MODIFIER | c.636-2126C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 4/13 | chr17 | 74241248 | ||||||
chr17:74241262
|
C | CGT | 21 | a0001c0001t0001g0056a0001c0001t0001g0069a0001c0001t0001g0112others(18): Show | 21 | HG00408.hp1 HG00408.hp2 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.636-2078_636-2077d others(4): Show |
TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr17 | 74241262 | |||||
chr17:74241262
|
C | CGTGT | 16 | a0001c0001t0001g0015a0001c0001t0001g0044a0001c0001t0001g0083others(13): Show | 19 | HG01168.hp2 HG01361.hp1 HG01361.hp2 others(16): Show |
intron_variant | MODIFIER | c.636-2080_636-2077d others(6): Show |
TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr17 | 74241262 | |||||
chr17:74241262
|
C | CGTGTGT | 6 | a0001c0001t0001g0120a0001c0001t0001g0171a0001c0001t0001g0264others(3): Show | 6 | HG02818.hp1 HG03209.hp1 NA18906.hp2 others(3): Show |
intron_variant | MODIFIER | c.636-2082_636-2077d others(8): Show |
TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr17 | 74241262 | |||||
chr17:74241262
|
C | CGTGTGTG others(3): Show |
1 | a0014c0023t0001g0116 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.636-2086_636-2077d others(12): Show |
TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr17 | 74241262 | |||||
chr17:74241262
|
CGT | C | 64 | a0001c0001t0001g0009a0001c0001t0001g0030a0001c0001t0001g0033others(61): Show | 77 | HG00099.hp2 HG00140.hp1 HG00735.hp2 others(74): Show |
intron_variant | MODIFIER | c.636-2078_636-2077d others(4): Show |
TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr17 | 74241262 | |||||
chr17:74241262
|
CGTGT | C | 60 | a0001c0001t0001g0026a0001c0001t0001g0029a0001c0001t0001g0060others(57): Show | 65 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(62): Show |
intron_variant | MODIFIER | c.636-2080_636-2077d others(6): Show |
TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr17 | 74241262 | |||||
chr17:74241262
|
CGTGTGT | C | 11 | a0001c0001t0001g0031a0003c0003t0002g0109a0003c0003t0002g0125others(8): Show | 11 | HG02080.hp1 HG02451.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.636-2082_636-2077d others(8): Show |
TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr17 | 74241262 | |||||
chr17:74241262
|
CGTGTGTG others(5): Show |
C | 1 | a0001c0001t0016g0276 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.636-2088_636-2077d others(14): Show |
TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr17 | 74241262 | |||||
chr17:74241294
|
T | TGTGTGTG others(7): Show |
1 | a0021c0031t0008g0108 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.636-2077_636-2076i others(16): Show |
TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr17 | 74241294 | |||||
chr17:74241296
|
T | C | 4 | a0004c0006t0001g0079a0004c0006t0001g0082a0004c0006t0001g0092others(1): Show | 4 | HG00738.hp2 HG02647.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.636-2078T>C | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 4/13 | chr17 | 74241296 | ||||||
chr17:74241296
|
T | TGTGTGCG others(3): Show |
2 | a0005c0007t0006g0187a0005c0007t0006g0197 | 2 | HG00438.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.636-2077_636-2076i others(12): Show |
TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr17 | 74241296 | |||||
chr17:74241296
|
T | TGTGTGTG others(5): Show |
2 | a0005c0007t0006g0188a0005c0007t0006g0277 | 2 | NA19012.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.636-2077_636-2076i others(14): Show |
TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr17 | 74241296 | |||||
chr17:74241296
|
T | TGTGTGTG others(7): Show |
1 | a0005c0007t0006g0189 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.636-2077_636-2076i others(16): Show |
TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr17 | 74241296 | |||||
chr17:74241354
|
C | T | 1 | a0003c0003t0009g0084 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.636-2020C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 4/13 | chr17 | 74241354 | ||||||
chr17:74241422
|
G | A | 5 | a0005c0007t0006g0187a0005c0007t0006g0188a0005c0007t0006g0189others(2): Show | 5 | HG00438.hp1 NA18980.hp2 NA18981.hp1 others(2): Show |
intron_variant | MODIFIER | c.636-1952G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 4/13 | chr17 | 74241422 | ||||||
chr17:74241650
|
C | T | 1 | a0011c0015t0001g0251 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.636-1724C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 4/13 | chr17 | 74241650 | ||||||
chr17:74241652
|
G | A | 2 | a0001c0026t0001g0075a0014c0023t0001g0116 | 2 | HG01243.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.636-1722G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 4/13 | chr17 | 74241652 | ||||||
chr17:74241705
|
G | A | 1 | a0005c0007t0018g0097 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.636-1669G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 4/13 | chr17 | 74241705 | ||||||
chr17:74241737
|
G | T | 6 | a0001c0001t0001g0297a0010c0013t0004g0293a0010c0013t0004g0294others(3): Show | 6 | HG01884.hp2 HG02622.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.636-1637G>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 4/13 | chr17 | 74241737 | ||||||
chr17:74241786
|
C | T | 68 | a0003c0003t0001g0127a0003c0003t0002g0010a0003c0003t0002g0013others(65): Show | 73 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(70): Show |
intron_variant | MODIFIER | c.636-1588C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 4/13 | chr17 | 74241786 | ||||||
chr17:74241846
|
A | G | 2 | a0001c0026t0001g0075a0014c0023t0001g0116 | 2 | HG01243.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.636-1528A>G | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 4/13 | chr17 | 74241846 | ||||||
chr17:74241916
|
G | A | 1 | a0001c0001t0001g0193 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.636-1458G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 4/13 | chr17 | 74241916 | ||||||
chr17:74242038
|
A | G | 2 | a0001c0026t0001g0075a0014c0023t0001g0116 | 2 | HG01243.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.636-1336A>G | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 4/13 | chr17 | 74242038 | ||||||
chr17:74242098
|
G | C | 1 | a0001c0001t0001g0022 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.636-1276G>C | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 4/13 | chr17 | 74242098 | ||||||
chr17:74242172
|
A | G | 6 | a0003c0003t0002g0073a0003c0003t0002g0165a0005c0020t0001g0184others(3): Show | 6 | HG00733.hp2 HG01516.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.636-1202A>G | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 4/13 | chr17 | 74242172 | ||||||
chr17:74242254
|
G | C | 1 | a0005c0007t0018g0097 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.636-1120G>C | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 4/13 | chr17 | 74242254 | ||||||
chr17:74242281
|
G | A | 1 | a0001c0001t0001g0170 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.636-1093G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 4/13 | chr17 | 74242281 | ||||||
chr17:74242586
|
T | G | 4 | a0001c0001t0001g0035a0001c0001t0001g0054a0001c0001t0001g0055others(1): Show | 4 | HG00735.hp1 HG01169.hp2 HG01256.hp2 others(1): Show |
intron_variant | MODIFIER | c.636-788T>G | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 4/13 | chr17 | 74242586 | ||||||
chr17:74242589
|
C | T | 1 | a0005c0007t0018g0097 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.636-785C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 4/13 | chr17 | 74242589 | ||||||
chr17:74242733
|
G | C | 2 | a0001c0001t0001g0035a0001c0001t0001g0054 | 2 | HG00735.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.636-641G>C | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 4/13 | chr17 | 74242733 | ||||||
chr17:74242881
|
G | A | 42 | a0002c0002t0001g0229a0002c0002t0003g0002a0002c0002t0003g0007others(39): Show | 52 | HG00099.hp2 HG01069.hp2 HG01074.hp1 others(49): Show |
intron_variant | MODIFIER | c.636-493G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 4/13 | chr17 | 74242881 | ||||||
chr17:74242918
|
A | C | 2 | a0001c0026t0001g0075a0014c0023t0001g0116 | 2 | HG01243.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.636-456A>C | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 4/13 | chr17 | 74242918 | ||||||
chr17:74242928
|
T | C | 1 | a0013c0018t0002g0220 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.636-446T>C | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 4/13 | chr17 | 74242928 | ||||||
chr17:74243021
|
GC | G | 57 | a0002c0002t0001g0229a0002c0002t0003g0002a0002c0002t0003g0007others(54): Show | 67 | HG00099.hp2 HG00438.hp1 HG00738.hp2 others(64): Show |
intron_variant | MODIFIER | c.636-351delC | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr17 | 74243021 | |||||
chr17:74243065
|
G | T | 1 | a0001c0001t0001g0065 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.636-309G>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 4/13 | chr17 | 74243065 | ||||||
chr17:74243179
|
G | A | 6 | a0004c0006t0001g0079a0004c0006t0001g0080a0004c0006t0001g0082others(3): Show | 6 | HG00738.hp2 HG02615.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.636-195G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 4/13 | chr17 | 74243179 | ||||||
chr17:74243223
|
C | A | 1 | a0001c0001t0001g0173 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.636-151C>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 4/13 | chr17 | 74243223 | ||||||
chr17:74243227
|
C | A | 1 | a0001c0001t0001g0173 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.636-147C>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 4/13 | chr17 | 74243227 | ||||||
chr17:74243309
|
T | C | 11 | a0004c0006t0001g0079a0004c0006t0001g0080a0004c0006t0001g0082others(8): Show | 11 | HG00438.hp1 HG00738.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.636-65T>C | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 4/13 | chr17 | 74243309 | ||||||
chr17:74243313
|
G | A | 11 | a0004c0006t0001g0079a0004c0006t0001g0080a0004c0006t0001g0082others(8): Show | 11 | HG00438.hp1 HG00738.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.636-61G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 4/13 | chr17 | 74243313 | ||||||
chr17:74243323
|
G | T | 1 | a0001c0001t0001g0173 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.636-51G>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 4/13 | chr17 | 74243323 | ||||||
chr17:74243357
|
C | T | 1 | a0001c0001t0001g0193 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.636-17C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 4/13 | chr17 | 74243357 | ||||||
chr17:74243495
|
G | A | 5 | a0005c0007t0006g0187a0005c0007t0006g0188a0005c0007t0006g0189others(2): Show | 5 | HG00438.hp1 NA18980.hp2 NA18981.hp1 others(2): Show |
intron_variant | MODIFIER | c.731+26G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 5/13 | chr17 | 74243495 | ||||||
chr17:74243508
|
G | T | 1 | a0001c0001t0001g0173 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.731+39G>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 5/13 | chr17 | 74243508 | ||||||
chr17:74243722
|
T | C | 5 | a0005c0007t0006g0187a0005c0007t0006g0188a0005c0007t0006g0189others(2): Show | 5 | HG00438.hp1 NA18980.hp2 NA18981.hp1 others(2): Show |
intron_variant | MODIFIER | c.731+253T>C | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 5/13 | chr17 | 74243722 | ||||||
chr17:74243890
|
G | A | 1 | a0001c0001t0001g0033 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.732-87G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 5/13 | chr17 | 74243890 | ||||||
chr17:74244081
|
G | A | 1 | a0004c0006t0001g0287 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.804+32G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 6/13 | chr17 | 74244081 | ||||||
chr17:74244197
|
G | A | 71 | a0003c0003t0001g0127a0003c0003t0002g0010a0003c0003t0002g0013others(68): Show | 76 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.804+148G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 6/13 | chr17 | 74244197 | ||||||
chr17:74244249
|
C | A | 1 | a0001c0001t0001g0173 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.804+200C>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 6/13 | chr17 | 74244249 | ||||||
chr17:74244367
|
C | A | 1 | a0006c0004t0002g0160 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.804+318C>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 6/13 | chr17 | 74244367 | ||||||
chr17:74244449
|
G | A | 17 | a0003c0003t0002g0196a0004c0005t0001g0023a0004c0005t0001g0131others(14): Show | 18 | HG01081.hp1 HG01192.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.804+400G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 6/13 | chr17 | 74244449 | ||||||
chr17:74244486
|
T | C | 1 | a0001c0001t0001g0173 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.804+437T>C | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 6/13 | chr17 | 74244486 | ||||||
chr17:74244487
|
G | T | 1 | a0001c0001t0001g0173 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.804+438G>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 6/13 | chr17 | 74244487 | ||||||
chr17:74244500
|
G | A | 3 | a0001c0009t0012g0307a0001c0009t0012g0308a0001c0014t0001g0306 | 3 | HG02965.hp1 HG02976.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.804+451G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 6/13 | chr17 | 74244500 | ||||||
chr17:74244542
|
C | T | 119 | a0002c0002t0001g0229a0002c0002t0003g0002a0002c0002t0003g0007others(116): Show | 134 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(131): Show |
intron_variant | MODIFIER | c.804+493C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 6/13 | chr17 | 74244542 | ||||||
chr17:74244597
|
T | TA | 143 | a0001c0001t0001g0297a0001c0009t0005g0019a0001c0009t0005g0074others(140): Show | 159 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.804+559dupA | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr17 | 74244597 | |||||
chr17:74244662
|
G | A | 1 | a0003c0003t0002g0136 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.804+613G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 6/13 | chr17 | 74244662 | ||||||
chr17:74244669
|
T | A | 1 | a0001c0001t0001g0173 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.804+620T>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 6/13 | chr17 | 74244669 | ||||||
chr17:74244697
|
G | A | 2 | a0008c0008t0002g0143a0008c0008t0002g0144 | 2 | HG00140.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.804+648G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 6/13 | chr17 | 74244697 | ||||||
chr17:74244763
|
C | T | 3 | a0004c0005t0001g0123a0009c0016t0007g0291a0009c0016t0007g0292 | 3 | HG00280.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.804+714C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 6/13 | chr17 | 74244763 | ||||||
chr17:74244855
|
A | AGT | 16 | a0001c0001t0001g0009a0001c0001t0001g0026a0001c0001t0001g0029others(13): Show | 18 | HG00140.hp1 HG00323.hp1 HG01099.hp1 others(15): Show |
intron_variant | MODIFIER | c.804+833_804+834dup others(2): Show |
TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr17 | 74244855 | |||||
chr17:74244855
|
A | AGTGT | 9 | a0001c0001t0001g0093a0001c0001t0001g0194a0003c0003t0002g0073others(6): Show | 9 | HG00733.hp2 HG01516.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.804+831_804+834dup others(4): Show |
TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr17 | 74244855 | |||||
chr17:74244855
|
A | AGTGTGT | 9 | a0001c0001t0001g0297a0001c0009t0005g0019a0001c0009t0005g0074others(6): Show | 10 | HG01884.hp2 HG02055.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.804+829_804+834dup others(6): Show |
TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr17 | 74244855 | |||||
chr17:74244855
|
A | AGTGTGTG others(1): Show |
3 | a0001c0014t0001g0095a0001c0026t0001g0075a0014c0023t0001g0116 | 3 | HG01243.hp2 HG03209.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.804+827_804+834dup others(8): Show |
TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr17 | 74244855 | |||||
chr17:74244855
|
A | AGTGTGTG others(3): Show |
6 | a0001c0009t0012g0307a0001c0009t0012g0308a0001c0014t0001g0306others(3): Show | 6 | HG02622.hp2 HG02647.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.804+825_804+834dup others(10): Show |
TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr17 | 74244855 | |||||
chr17:74244855
|
A | AGTGTGTG others(5): Show |
2 | a0005c0020t0001g0184a0005c0020t0001g0185 | 2 | HG02896.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.804+823_804+834dup others(12): Show |
TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr17 | 74244855 | |||||
chr17:74244855
|
A | AGTGTGTG others(11): Show |
2 | a0005c0007t0006g0187a0005c0007t0006g0197 | 2 | HG00438.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.804+817_804+834dup others(18): Show |
TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr17 | 74244855 | |||||
chr17:74244855
|
A | AGTGTGTG others(13): Show |
3 | a0005c0007t0006g0188a0005c0007t0006g0189a0005c0007t0006g0277 | 3 | NA18981.hp1 NA19012.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.804+815_804+834dup others(20): Show |
TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr17 | 74244855 | |||||
chr17:74244855
|
AGTGT | A | 7 | a0001c0001t0001g0253a0003c0003t0009g0084a0004c0006t0001g0079others(4): Show | 7 | HG00639.hp1 HG00738.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.804+831_804+834del others(4): Show |
TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr17 | 74244855 | |||||
chr17:74244855
|
AGTGTGT | A | 66 | a0003c0003t0001g0127a0003c0003t0002g0010a0003c0003t0002g0013others(63): Show | 71 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(68): Show |
intron_variant | MODIFIER | c.804+829_804+834del others(6): Show |
TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr17 | 74244855 | |||||
chr17:74244855
|
AGTGTGTG others(1): Show |
A | 43 | a0002c0002t0001g0229a0002c0002t0003g0002a0002c0002t0003g0007others(40): Show | 53 | HG00099.hp2 HG01069.hp2 HG01074.hp1 others(50): Show |
intron_variant | MODIFIER | c.804+827_804+834del others(8): Show |
TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr17 | 74244855 | |||||
chr17:74245015
|
C | A | 1 | a0001c0001t0001g0173 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.804+966C>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 6/13 | chr17 | 74245015 | ||||||
chr17:74245053
|
A | G | 145 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0312others(142): Show | 162 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.804+1004A>G | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 6/13 | chr17 | 74245053 | ||||||
chr17:74245059
|
C | G | 1 | a0001c0001t0001g0173 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.804+1010C>G | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 6/13 | chr17 | 74245059 | ||||||
chr17:74245060
|
T | C | 1 | a0001c0001t0001g0173 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.804+1011T>C | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 6/13 | chr17 | 74245060 | ||||||
chr17:74245091
|
C | A | 25 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0028others(22): Show | 29 | HG00140.hp1 HG01175.hp1 HG01361.hp1 others(26): Show |
intron_variant | MODIFIER | c.804+1042C>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 6/13 | chr17 | 74245091 | ||||||
chr17:74245139
|
A | C | 53 | a0003c0003t0001g0127a0003c0003t0002g0010a0003c0003t0002g0013others(50): Show | 58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.804+1090A>C | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 6/13 | chr17 | 74245139 | ||||||
chr17:74245211
|
C | T | 2 | a0001c0001t0001g0093a0001c0014t0001g0095 | 2 | HG03540.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.804+1162C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 6/13 | chr17 | 74245211 | ||||||
chr17:74245228
|
C | A | 1 | a0001c0001t0001g0173 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.804+1179C>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 6/13 | chr17 | 74245228 | ||||||
chr17:74245260
|
G | A | 1 | a0007c0011t0001g0310 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.804+1211G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 6/13 | chr17 | 74245260 | ||||||
chr17:74245304
|
C | T | 3 | a0002c0002t0001g0229a0002c0002t0003g0224a0002c0002t0003g0228 | 3 | NA18941.hp2 NA18973.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.804+1255C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 6/13 | chr17 | 74245304 | ||||||
chr17:74245595
|
C | T | 1 | a0001c0001t0001g0195 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.804+1546C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 6/13 | chr17 | 74245595 | ||||||
chr17:74245703
|
C | A | 1 | a0001c0001t0001g0173 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.804+1654C>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 6/13 | chr17 | 74245703 | ||||||
chr17:74245761
|
C | G | 1 | a0001c0001t0001g0173 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.804+1712C>G | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 6/13 | chr17 | 74245761 | ||||||
chr17:74245761
|
C | T | 4 | a0009c0016t0007g0289a0009c0016t0007g0290a0009c0016t0007g0291others(1): Show | 4 | HG02486.hp2 HG02717.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.804+1712C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 6/13 | chr17 | 74245761 | ||||||
chr17:74245809
|
T | A | 1 | a0001c0001t0001g0113 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.804+1760T>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 6/13 | chr17 | 74245809 | ||||||
chr17:74245888
|
C | T | 1 | a0001c0001t0001g0140 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.804+1839C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 6/13 | chr17 | 74245888 | ||||||
chr17:74246017
|
G | A | 2 | a0002c0002t0003g0021a0002c0002t0003g0299 | 3 | HG02735.hp1 HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.804+1968G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 6/13 | chr17 | 74246017 | ||||||
chr17:74246036
|
G | A | 1 | a0001c0001t0001g0234 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.804+1987G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 6/13 | chr17 | 74246036 | ||||||
chr17:74246059
|
G | A | 1 | a0007c0012t0001g0218 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.804+2010G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 6/13 | chr17 | 74246059 | ||||||
chr17:74246062
|
G | A | 1 | a0003c0003t0009g0085 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.804+2013G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 6/13 | chr17 | 74246062 | ||||||
chr17:74246077
|
A | AG | 8 | a0005c0007t0006g0187a0005c0007t0006g0188a0005c0007t0006g0189others(5): Show | 8 | HG00438.hp1 HG02647.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.804+2030dupG | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr17 | 74246077 | |||||
chr17:74246194
|
T | A | 1 | a0001c0001t0001g0173 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.804+2145T>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 6/13 | chr17 | 74246194 | ||||||
chr17:74246229
|
C | A | 1 | a0001c0001t0001g0173 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.804+2180C>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 6/13 | chr17 | 74246229 | ||||||
chr17:74246330
|
T | A | 1 | a0003c0003t0009g0084 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.804+2281T>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 6/13 | chr17 | 74246330 | ||||||
chr17:74246436
|
A | T | 52 | a0001c0001t0001g0064a0003c0003t0001g0127a0003c0003t0002g0010others(49): Show | 56 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(53): Show |
intron_variant | MODIFIER | c.804+2387A>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 6/13 | chr17 | 74246436 | ||||||
chr17:74246441
|
C | T | 1 | a0001c0001t0001g0176 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.804+2392C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 6/13 | chr17 | 74246441 | ||||||
chr17:74246494
|
G | A | 193 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0009others(190): Show | 206 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(203): Show |
intron_variant | MODIFIER | c.804+2445G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 6/13 | chr17 | 74246494 | ||||||
chr17:74246499
|
C | T | 5 | a0005c0007t0006g0187a0005c0007t0006g0188a0005c0007t0006g0189others(2): Show | 5 | HG00438.hp1 NA18980.hp2 NA18981.hp1 others(2): Show |
intron_variant | MODIFIER | c.804+2450C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 6/13 | chr17 | 74246499 | ||||||
chr17:74246504
|
TA | T | 27 | a0001c0001t0001g0158a0001c0009t0012g0307a0001c0009t0012g0308others(24): Show | 27 | HG00639.hp2 HG00738.hp2 HG01106.hp1 others(24): Show |
intron_variant | MODIFIER | c.804+2456delA | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 6/13 | chr17 | 74246504 | ||||||
chr17:74246512
|
C | T | 1 | a0001c0001t0001g0083 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.804+2463C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 6/13 | chr17 | 74246512 | ||||||
chr17:74246517
|
G | A | 1 | a0001c0001t0001g0029 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.804+2468G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 6/13 | chr17 | 74246517 | ||||||
chr17:74246561
|
C | A | 1 | a0001c0001t0001g0173 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.805-2450C>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 6/13 | chr17 | 74246561 | ||||||
chr17:74246607
|
C | A | 1 | a0001c0001t0001g0173 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.805-2404C>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 6/13 | chr17 | 74246607 | ||||||
chr17:74246663
|
T | C | 3 | a0001c0009t0012g0307a0001c0009t0012g0308a0001c0014t0001g0306 | 3 | HG02965.hp1 HG02976.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.805-2348T>C | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 6/13 | chr17 | 74246663 | ||||||
chr17:74246679
|
C | T | 1 | a0001c0001t0001g0055 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.805-2332C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 6/13 | chr17 | 74246679 | ||||||
chr17:74246712
|
A | C | 1 | a0001c0001t0001g0173 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.805-2299A>C | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 6/13 | chr17 | 74246712 | ||||||
chr17:74246743
|
A | T | 1 | a0001c0001t0001g0173 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.805-2268A>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 6/13 | chr17 | 74246743 | ||||||
chr17:74246827
|
G | A | 1 | a0005c0007t0018g0097 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.805-2184G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 6/13 | chr17 | 74246827 | ||||||
chr17:74246914
|
G | C | 3 | a0001c0009t0005g0019a0001c0009t0005g0096a0001c0009t0005g0269 | 4 | HG02055.hp2 HG02723.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.805-2097G>C | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 6/13 | chr17 | 74246914 | ||||||
chr17:74247107
|
G | A | 1 | a0004c0006t0001g0104 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.805-1904G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 6/13 | chr17 | 74247107 | ||||||
chr17:74247119
|
T | C | 1 | a0013c0018t0002g0220 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.805-1892T>C | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 6/13 | chr17 | 74247119 | ||||||
chr17:74247155
|
C | T | 1 | a0006c0004t0002g0137 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.805-1856C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 6/13 | chr17 | 74247155 | ||||||
chr17:74247160
|
C | T | 3 | a0001c0001t0001g0022a0001c0001t0002g0148a0001c0001t0002g0150 | 3 | HG00733.hp1 HG02055.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.805-1851C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 6/13 | chr17 | 74247160 | ||||||
chr17:74247161
|
G | A | 1 | a0001c0001t0001g0145 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.805-1850G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 6/13 | chr17 | 74247161 | ||||||
chr17:74247181
|
C | CA | 28 | a0001c0001t0001g0038a0001c0001t0001g0070a0001c0001t0001g0168others(25): Show | 28 | HG00140.hp2 HG00408.hp2 HG00597.hp1 others(25): Show |
intron_variant | MODIFIER | c.805-1809dupA | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr17 | 74247181 | |||||
chr17:74247181
|
CA | C | 54 | a0001c0001t0001g0045a0001c0001t0001g0063a0001c0001t0001g0093others(51): Show | 65 | HG00099.hp2 HG01069.hp2 HG01074.hp1 others(62): Show |
intron_variant | MODIFIER | c.805-1809delA | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr17 | 74247181 | |||||
chr17:74247181
|
CAA | C | 9 | a0001c0001t0001g0046a0001c0001t0001g0048a0002c0002t0003g0212others(6): Show | 9 | HG01517.hp1 HG02109.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.805-1810_805-1809d others(4): Show |
TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr17 | 74247181 | |||||
chr17:74247335
|
C | G | 4 | a0009c0016t0007g0289a0009c0016t0007g0290a0009c0016t0007g0291others(1): Show | 4 | HG02486.hp2 HG02717.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.805-1676C>G | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 6/13 | chr17 | 74247335 | ||||||
chr17:74247346
|
C | T | 2 | a0001c0026t0001g0075a0014c0023t0001g0116 | 2 | HG01243.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.805-1665C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 6/13 | chr17 | 74247346 | ||||||
chr17:74247387
|
T | C | 11 | a0005c0010t0002g0098a0005c0010t0004g0099a0005c0010t0004g0100others(8): Show | 11 | HG01884.hp2 HG02451.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.805-1624T>C | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 6/13 | chr17 | 74247387 | ||||||
chr17:74247422
|
C | T | 5 | a0005c0007t0006g0187a0005c0007t0006g0188a0005c0007t0006g0189others(2): Show | 5 | HG00438.hp1 NA18980.hp2 NA18981.hp1 others(2): Show |
intron_variant | MODIFIER | c.805-1589C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 6/13 | chr17 | 74247422 | ||||||
chr17:74247478
|
G | A | 1 | a0016c0022t0015g0167 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.805-1533G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 6/13 | chr17 | 74247478 | ||||||
chr17:74247488
|
G | T | 1 | a0006c0004t0002g0025 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.805-1523G>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 6/13 | chr17 | 74247488 | ||||||
chr17:74247491
|
G | A | 1 | a0001c0014t0001g0095 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.805-1520G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 6/13 | chr17 | 74247491 | ||||||
chr17:74247555
|
T | G | 1 | a0001c0001t0011g0175 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.805-1456T>G | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 6/13 | chr17 | 74247555 | ||||||
chr17:74247636
|
T | C | 6 | a0005c0007t0006g0187a0005c0007t0006g0188a0005c0007t0006g0189others(3): Show | 6 | HG00438.hp1 HG02647.hp2 NA18980.hp2 others(3): Show |
intron_variant | MODIFIER | c.805-1375T>C | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 6/13 | chr17 | 74247636 | ||||||
chr17:74247695
|
C | A | 2 | a0005c0020t0001g0184a0005c0020t0001g0185 | 2 | HG02896.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.805-1316C>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 6/13 | chr17 | 74247695 | ||||||
chr17:74247712
|
G | A | 1 | a0001c0001t0001g0038 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.805-1299G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 6/13 | chr17 | 74247712 | ||||||
chr17:74247743
|
C | T | 2 | a0007c0011t0001g0152a0008c0008t0002g0144 | 2 | HG01496.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.805-1268C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 6/13 | chr17 | 74247743 | ||||||
chr17:74247759
|
G | A | 1 | a0004c0006t0001g0080 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.805-1252G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 6/13 | chr17 | 74247759 | ||||||
chr17:74247784
|
T | C | 40 | a0001c0014t0001g0183a0001c0014t0001g0306a0002c0002t0001g0229others(37): Show | 50 | HG00099.hp2 HG01069.hp2 HG01074.hp1 others(47): Show |
intron_variant | MODIFIER | c.805-1227T>C | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 6/13 | chr17 | 74247784 | ||||||
chr17:74247849
|
G | A | 1 | a0001c0001t0001g0159 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.805-1162G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 6/13 | chr17 | 74247849 | ||||||
chr17:74247857
|
G | A | 2 | a0001c0026t0001g0075a0014c0023t0001g0116 | 2 | HG01243.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.805-1154G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 6/13 | chr17 | 74247857 | ||||||
chr17:74247873
|
G | A | 40 | a0001c0014t0001g0183a0001c0014t0001g0306a0002c0002t0001g0229others(37): Show | 50 | HG00099.hp2 HG01069.hp2 HG01074.hp1 others(47): Show |
intron_variant | MODIFIER | c.805-1138G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 6/13 | chr17 | 74247873 | ||||||
chr17:74247930
|
G | T | 40 | a0001c0014t0001g0183a0001c0014t0001g0306a0002c0002t0001g0229others(37): Show | 50 | HG00099.hp2 HG01069.hp2 HG01074.hp1 others(47): Show |
intron_variant | MODIFIER | c.805-1081G>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 6/13 | chr17 | 74247930 | ||||||
chr17:74247937
|
C | T | 2 | a0001c0009t0012g0307a0001c0009t0012g0308 | 2 | HG02965.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.805-1074C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 6/13 | chr17 | 74247937 | ||||||
chr17:74247961
|
G | A | 2 | a0001c0009t0012g0307a0001c0009t0012g0308 | 2 | HG02965.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.805-1050G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 6/13 | chr17 | 74247961 | ||||||
chr17:74248048
|
G | C | 2 | a0001c0009t0012g0307a0001c0009t0012g0308 | 2 | HG02965.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.805-963G>C | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 6/13 | chr17 | 74248048 | ||||||
chr17:74248112
|
C | T | 2 | a0007c0011t0001g0309a0007c0011t0001g0310 | 2 | HG01074.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.805-899C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 6/13 | chr17 | 74248112 | ||||||
chr17:74248227
|
C | T | 3 | a0012c0017t0010g0117a0012c0017t0010g0118a0012c0017t0019g0087 | 3 | HG02895.hp1 HG02897.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.805-784C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 6/13 | chr17 | 74248227 | ||||||
chr17:74248228
|
G | A | 1 | a0002c0002t0003g0216 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.805-783G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 6/13 | chr17 | 74248228 | ||||||
chr17:74248329
|
G | A | 2 | a0001c0001t0001g0274a0001c0001t0001g0275 | 2 | NA19082.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.805-682G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 6/13 | chr17 | 74248329 | ||||||
chr17:74248330
|
C | T | 1 | a0003c0003t0002g0298 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.805-681C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 6/13 | chr17 | 74248330 | ||||||
chr17:74248331
|
G | A | 6 | a0004c0006t0001g0079a0004c0006t0001g0080a0004c0006t0001g0082others(3): Show | 6 | HG00738.hp2 HG02615.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.805-680G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 6/13 | chr17 | 74248331 | ||||||
chr17:74248373
|
C | A | 1 | a0007c0012t0001g0314 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.805-638C>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 6/13 | chr17 | 74248373 | ||||||
chr17:74248390
|
G | T | 1 | a0005c0007t0008g0304 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.805-621G>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 6/13 | chr17 | 74248390 | ||||||
chr17:74248642
|
T | A | 5 | a0005c0007t0006g0187a0005c0007t0006g0188a0005c0007t0006g0189others(2): Show | 5 | HG00438.hp1 NA18980.hp2 NA18981.hp1 others(2): Show |
intron_variant | MODIFIER | c.805-369T>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 6/13 | chr17 | 74248642 | ||||||
chr17:74248704
|
G | A | 5 | a0005c0007t0006g0187a0005c0007t0006g0188a0005c0007t0006g0189others(2): Show | 5 | HG00438.hp1 NA18980.hp2 NA18981.hp1 others(2): Show |
intron_variant | MODIFIER | c.805-307G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 6/13 | chr17 | 74248704 | ||||||
chr17:74248798
|
A | G | 1 | a0001c0001t0001g0199 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.805-213A>G | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 6/13 | chr17 | 74248798 | ||||||
chr17:74248860
|
A | G | 2 | a0001c0026t0001g0075a0014c0023t0001g0116 | 2 | HG01243.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.805-151A>G | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 6/13 | chr17 | 74248860 | ||||||
chr17:74248902
|
C | T | 4 | a0004c0005t0001g0012a0004c0005t0001g0128a0004c0005t0001g0132others(1): Show | 5 | HG00099.hp1 HG00280.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.805-109C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 6/13 | chr17 | 74248902 | ||||||
chr17:74248989
|
C | T | 4 | a0009c0016t0007g0289a0009c0016t0007g0290a0009c0016t0007g0291others(1): Show | 4 | HG02486.hp2 HG02717.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.805-22C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 6/13 | chr17 | 74248989 | ||||||
chr17:74248990
|
G | A | 1 | a0001c0001t0001g0033 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.805-21G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 6/13 | chr17 | 74248990 | ||||||
chr17:74249131
|
CTG | C | 19 | a0001c0009t0005g0019a0001c0009t0005g0074a0001c0009t0005g0096others(16): Show | 20 | HG01884.hp2 HG02055.hp2 HG02451.hp2 others(17): Show |
intron_variant | MODIFIER | c.874+54_874+55delTG | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr17 | 74249131 | |||||
chr17:74249332
|
G | A | 1 | a0001c0001t0013g0245 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.875-12G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 7/13 | chr17 | 74249332 | ||||||
chr17:74249427
|
C | A | 1 | a0002c0002t0003g0317 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.930+28C>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 8/13 | chr17 | 74249427 | ||||||
chr17:74249474
|
A | G | 125 | a0001c0014t0001g0095a0001c0014t0001g0183a0001c0014t0001g0306others(122): Show | 138 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.930+75A>G | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 8/13 | chr17 | 74249474 | ||||||
chr17:74249488
|
G | T | 15 | a0001c0009t0005g0019a0001c0009t0005g0074a0001c0009t0005g0096others(12): Show | 16 | HG01884.hp2 HG02055.hp2 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.930+89G>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 8/13 | chr17 | 74249488 | ||||||
chr17:74249490
|
A | G | 142 | a0001c0009t0005g0019a0001c0009t0005g0074a0001c0009t0005g0096others(139): Show | 156 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(153): Show |
intron_variant | MODIFIER | c.930+91A>G | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 8/13 | chr17 | 74249490 | ||||||
chr17:74249545
|
G | A | 1 | a0005c0007t0018g0097 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.930+146G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 8/13 | chr17 | 74249545 | ||||||
chr17:74249554
|
G | A | 55 | a0003c0003t0001g0127a0003c0003t0002g0010a0003c0003t0002g0013others(52): Show | 58 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.930+155G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 8/13 | chr17 | 74249554 | ||||||
chr17:74249556
|
C | T | 28 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0026others(25): Show | 32 | HG01175.hp1 HG01361.hp1 HG02015.hp2 others(29): Show |
intron_variant | MODIFIER | c.930+157C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 8/13 | chr17 | 74249556 | ||||||
chr17:74249616
|
C | A | 1 | a0001c0001t0001g0026 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.930+217C>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 8/13 | chr17 | 74249616 | ||||||
chr17:74249648
|
G | A | 1 | a0004c0006t0001g0104 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.930+249G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 8/13 | chr17 | 74249648 | ||||||
chr17:74249668
|
A | G | 1 | a0001c0014t0001g0095 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.931-268A>G | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 8/13 | chr17 | 74249668 | ||||||
chr17:74249687
|
G | A | 70 | a0001c0014t0010g0260a0003c0003t0001g0127a0003c0003t0002g0010others(67): Show | 73 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.931-249G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 8/13 | chr17 | 74249687 | ||||||
chr17:74249814
|
G | A | 121 | a0001c0014t0001g0095a0001c0014t0001g0183a0001c0014t0001g0306others(118): Show | 134 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(131): Show |
intron_variant | MODIFIER | c.931-122G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 8/13 | chr17 | 74249814 | ||||||
chr17:74249847
|
CCACTGTG others(22): Show |
C | 314 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(311): Show | 346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): Show |
intron_variant | MODIFIER | c.931-47_931-19delCC others(27): Show |
TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr17 | 74249847 | |||||
chr17:74250062
|
G | T | 2 | a0010c0013t0004g0295a0010c0013t0004g0296 | 2 | HG03139.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1023+34G>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 9/13 | chr17 | 74250062 | ||||||
chr17:74250083
|
C | T | 2 | a0001c0001t0001g0093a0001c0001t0001g0297 | 2 | HG03041.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1023+55C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 9/13 | chr17 | 74250083 | ||||||
chr17:74250243
|
TCTCG | T | 124 | a0001c0014t0001g0095a0001c0014t0001g0183a0001c0014t0001g0306others(121): Show | 137 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(134): Show |
intron_variant | MODIFIER | c.1024-18_1024-15del others(4): Show |
TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr17 | 74250243 | |||||
chr17:74250247
|
G | T | 19 | a0001c0001t0001g0093a0001c0001t0001g0297a0001c0009t0012g0307others(16): Show | 19 | HG01243.hp2 HG01884.hp2 HG02451.hp2 others(16): Show |
intron_variant | MODIFIER | c.1024-18G>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 9/13 | chr17 | 74250247 | ||||||
chr17:74250408
|
C | T | 1 | a0001c0014t0001g0095 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1116+51C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 10/13 | chr17 | 74250408 | ||||||
chr17:74250429
|
C | T | 2 | a0001c0026t0001g0075a0014c0023t0001g0116 | 2 | HG01243.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1116+72C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 10/13 | chr17 | 74250429 | ||||||
chr17:74250439
|
C | T | 1 | a0005c0007t0018g0097 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1116+82C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 10/13 | chr17 | 74250439 | ||||||
chr17:74250497
|
A | C | 6 | a0004c0006t0001g0079a0004c0006t0001g0080a0004c0006t0001g0082others(3): Show | 6 | HG00738.hp2 HG02615.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1116+140A>C | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 10/13 | chr17 | 74250497 | ||||||
chr17:74250509
|
G | A | 5 | a0005c0007t0006g0187a0005c0007t0006g0188a0005c0007t0006g0189others(2): Show | 5 | HG00438.hp1 NA18980.hp2 NA18981.hp1 others(2): Show |
intron_variant | MODIFIER | c.1116+152G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 10/13 | chr17 | 74250509 | ||||||
chr17:74250509
|
G | C | 1 | a0001c0001t0014g0181 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1116+152G>C | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 10/13 | chr17 | 74250509 | ||||||
chr17:74250570
|
G | C | 119 | a0001c0014t0001g0095a0001c0014t0001g0183a0001c0014t0001g0306others(116): Show | 132 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.1116+213G>C | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 10/13 | chr17 | 74250570 | ||||||
chr17:74250589
|
C | T | 123 | a0001c0014t0001g0095a0001c0014t0001g0183a0001c0014t0001g0306others(120): Show | 136 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(133): Show |
intron_variant | MODIFIER | c.1116+232C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 10/13 | chr17 | 74250589 | ||||||
chr17:74250613
|
A | T | 3 | a0001c0001t0001g0069a0001c0001t0001g0139a0001c0001t0001g0182 | 3 | NA18956.hp2 NA18970.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.1116+256A>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 10/13 | chr17 | 74250613 | ||||||
chr17:74250659
|
A | G | 123 | a0001c0014t0001g0095a0001c0014t0001g0183a0001c0014t0001g0306others(120): Show | 136 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(133): Show |
intron_variant | MODIFIER | c.1116+302A>G | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 10/13 | chr17 | 74250659 | ||||||
chr17:74250668
|
C | T | 123 | a0001c0014t0001g0095a0001c0014t0001g0183a0001c0014t0001g0306others(120): Show | 136 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(133): Show |
intron_variant | MODIFIER | c.1116+311C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 10/13 | chr17 | 74250668 | ||||||
chr17:74250825
|
T | G | 2 | a0004c0006t0001g0104a0004c0006t0001g0287 | 2 | HG03130.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1116+468T>G | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 10/13 | chr17 | 74250825 | ||||||
chr17:74250899
|
C | T | 123 | a0001c0014t0001g0095a0001c0014t0001g0183a0001c0014t0001g0306others(120): Show | 136 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(133): Show |
intron_variant | MODIFIER | c.1116+542C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 10/13 | chr17 | 74250899 | ||||||
chr17:74250926
|
C | CACAGAA | 123 | a0001c0014t0001g0095a0001c0014t0001g0183a0001c0014t0001g0306others(120): Show | 136 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(133): Show |
intron_variant | MODIFIER | c.1116+569_1116+570i others(8): Show |
TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 10/13 | chr17 | 74250926 | ||||||
chr17:74250958
|
G | A | 77 | a0001c0014t0001g0183a0001c0014t0001g0306a0001c0014t0010g0260others(74): Show | 80 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.1116+601G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 10/13 | chr17 | 74250958 | ||||||
chr17:74250972
|
A | G | 1 | a0001c0001t0001g0083 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1116+615A>G | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 10/13 | chr17 | 74250972 | ||||||
chr17:74251004
|
G | A | 2 | a0001c0009t0012g0307a0001c0009t0012g0308 | 2 | HG02965.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1116+647G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 10/13 | chr17 | 74251004 | ||||||
chr17:74251048
|
G | A | 2 | a0004c0006t0001g0104a0004c0006t0001g0287 | 2 | HG03130.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1116+691G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 10/13 | chr17 | 74251048 | ||||||
chr17:74251054
|
CTG | C | 123 | a0001c0014t0001g0095a0001c0014t0001g0183a0001c0014t0001g0306others(120): Show | 136 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(133): Show |
intron_variant | MODIFIER | c.1116+708_1116+709d others(4): Show |
TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr17 | 74251054 | |||||
chr17:74251067
|
CGT | C | 30 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0026others(27): Show | 34 | HG01099.hp1 HG01175.hp1 HG01361.hp1 others(31): Show |
intron_variant | MODIFIER | c.1116+718_1116+719d others(4): Show |
TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr17 | 74251067 | |||||
chr17:74251081
|
TGTG | T | 105 | a0001c0014t0001g0095a0001c0014t0001g0183a0001c0014t0001g0306others(102): Show | 118 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(115): Show |
intron_variant | MODIFIER | c.1116+728_1116+730d others(5): Show |
TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr17 | 74251081 | |||||
chr17:74251093
|
GTCTGTGC others(14): Show |
G | 122 | a0001c0014t0001g0183a0001c0014t0001g0306a0001c0014t0010g0260others(119): Show | 135 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(132): Show |
intron_variant | MODIFIER | c.1116+741_1116+761d others(23): Show |
TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr17 | 74251093 | |||||
chr17:74251114
|
T | G | 1 | a0001c0014t0001g0095 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1116+757T>G | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 10/13 | chr17 | 74251114 | ||||||
chr17:74251211
|
T | C | 1 | a0001c0001t0001g0153 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1116+854T>C | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 10/13 | chr17 | 74251211 | ||||||
chr17:74251215
|
T | C | 1 | a0001c0001t0001g0064 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1116+858T>C | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 10/13 | chr17 | 74251215 | ||||||
chr17:74251239
|
T | G | 7 | a0001c0009t0012g0307a0001c0009t0012g0308a0005c0007t0006g0187others(4): Show | 7 | HG00438.hp1 HG02965.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.1116+882T>G | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 10/13 | chr17 | 74251239 | ||||||
chr17:74251287
|
T | C | 123 | a0001c0014t0001g0095a0001c0014t0001g0183a0001c0014t0001g0306others(120): Show | 136 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(133): Show |
intron_variant | MODIFIER | c.1116+930T>C | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 10/13 | chr17 | 74251287 | ||||||
chr17:74251319
|
C | G | 1 | a0003c0003t0002g0136 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1117-915C>G | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 10/13 | chr17 | 74251319 | ||||||
chr17:74251347
|
GGTGCATG others(5): Show |
G | 123 | a0001c0014t0001g0095a0001c0014t0001g0183a0001c0014t0001g0306others(120): Show | 136 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(133): Show |
intron_variant | MODIFIER | c.1117-877_1117-866d others(14): Show |
TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr17 | 74251347 | |||||
chr17:74251377
|
A | G | 123 | a0001c0014t0001g0095a0001c0014t0001g0183a0001c0014t0001g0306others(120): Show | 136 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(133): Show |
intron_variant | MODIFIER | c.1117-857A>G | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 10/13 | chr17 | 74251377 | ||||||
chr17:74251384
|
T | G | 8 | a0001c0001t0001g0162a0001c0001t0013g0245a0005c0007t0006g0187others(5): Show | 8 | HG00438.hp1 HG02647.hp2 HG04115.hp2 others(5): Show |
intron_variant | MODIFIER | c.1117-850T>G | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 10/13 | chr17 | 74251384 | ||||||
chr17:74251386
|
G | C | 33 | a0002c0002t0001g0229a0002c0002t0003g0002a0002c0002t0003g0007others(30): Show | 43 | HG00099.hp2 HG01069.hp2 HG01081.hp2 others(40): Show |
intron_variant | MODIFIER | c.1117-848G>C | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 10/13 | chr17 | 74251386 | ||||||
chr17:74251389
|
G | T | 123 | a0001c0014t0001g0095a0001c0014t0001g0183a0001c0014t0001g0306others(120): Show | 136 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(133): Show |
intron_variant | MODIFIER | c.1117-845G>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 10/13 | chr17 | 74251389 | ||||||
chr17:74251652
|
C | T | 1 | a0003c0003t0002g0010 | 2 | HG02572.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1117-582C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 10/13 | chr17 | 74251652 | ||||||
chr17:74251656
|
T | TC | 70 | a0001c0014t0001g0183a0001c0014t0001g0306a0001c0014t0010g0260others(67): Show | 73 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(70): Show |
intron_variant | MODIFIER | c.1117-575dupC | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr17 | 74251656 | |||||
chr17:74251712
|
A | G | 122 | a0001c0014t0001g0095a0001c0014t0001g0183a0001c0014t0001g0306others(119): Show | 135 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(132): Show |
intron_variant | MODIFIER | c.1117-522A>G | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 10/13 | chr17 | 74251712 | ||||||
chr17:74251724
|
G | A | 123 | a0001c0014t0001g0095a0001c0014t0001g0183a0001c0014t0001g0306others(120): Show | 136 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(133): Show |
intron_variant | MODIFIER | c.1117-510G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 10/13 | chr17 | 74251724 | ||||||
chr17:74251845
|
A | G | 33 | a0002c0002t0001g0229a0002c0002t0003g0002a0002c0002t0003g0007others(30): Show | 43 | HG00099.hp2 HG01069.hp2 HG01081.hp2 others(40): Show |
intron_variant | MODIFIER | c.1117-389A>G | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 10/13 | chr17 | 74251845 | ||||||
chr17:74251938
|
G | GGTCTGAA others(2): Show |
7 | a0002c0002t0003g0007a0002c0002t0003g0020a0002c0002t0003g0208others(4): Show | 10 | HG00099.hp2 HG01168.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.1117-296_1117-295i others(11): Show |
TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 10/13 | chr17 | 74251938 | ||||||
chr17:74251943
|
C | T | 2 | a0001c0026t0001g0075a0014c0023t0001g0116 | 2 | HG01243.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1117-291C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 10/13 | chr17 | 74251943 | ||||||
chr17:74251974
|
T | G | 1 | a0001c0001t0001g0302 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1117-260T>G | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 10/13 | chr17 | 74251974 | ||||||
chr17:74252010
|
T | A | 126 | a0001c0014t0001g0095a0001c0014t0001g0183a0001c0014t0001g0306others(123): Show | 139 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(136): Show |
intron_variant | MODIFIER | c.1117-224T>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 10/13 | chr17 | 74252010 | ||||||
chr17:74252010
|
T | G | 20 | a0001c0009t0005g0019a0001c0009t0005g0074a0001c0009t0005g0096others(17): Show | 21 | HG01884.hp2 HG02055.hp2 HG02451.hp2 others(18): Show |
intron_variant | MODIFIER | c.1117-224T>G | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 10/13 | chr17 | 74252010 | ||||||
chr17:74252143
|
G | A | 6 | a0004c0006t0001g0079a0004c0006t0001g0080a0004c0006t0001g0082others(3): Show | 6 | HG00738.hp2 HG02615.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1117-91G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 10/13 | chr17 | 74252143 | ||||||
chr17:74252146
|
C | G | 1 | a0007c0011t0001g0152 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1117-88C>G | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 10/13 | chr17 | 74252146 | ||||||
chr17:74252176
|
G | C | 4 | a0001c0001t0001g0032a0001c0001t0001g0067a0007c0012t0001g0062others(1): Show | 4 | HG02735.hp2 HG03017.hp2 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.1117-58G>C | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 10/13 | chr17 | 74252176 | ||||||
chr17:74252195
|
C | T | 1 | a0001c0001t0001g0234 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1117-39C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 10/13 | chr17 | 74252195 | ||||||
chr17:74252224
|
C | T | 126 | a0001c0014t0001g0095a0001c0014t0001g0183a0001c0014t0001g0306others(123): Show | 139 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(136): Show |
intron_variant | MODIFIER | c.1117-10C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 10/13 | chr17 | 74252224 | ||||||
chr17:74252385
|
C | T | 78 | a0001c0014t0001g0183a0001c0014t0001g0306a0001c0014t0010g0260others(75): Show | 81 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.1259+9C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 11/13 | chr17 | 74252385 | ||||||
chr17:74252454
|
C | T | 126 | a0001c0014t0001g0095a0001c0014t0001g0183a0001c0014t0001g0306others(123): Show | 139 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(136): Show |
intron_variant | MODIFIER | c.1259+78C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 11/13 | chr17 | 74252454 | ||||||
chr17:74252494
|
G | A | 1 | a0008c0008t0002g0144 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1259+118G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 11/13 | chr17 | 74252494 | ||||||
chr17:74252495
|
GC | G | 6 | a0005c0007t0006g0187a0005c0007t0006g0188a0005c0007t0006g0189others(3): Show | 6 | HG00438.hp1 HG02647.hp2 NA18980.hp2 others(3): Show |
intron_variant | MODIFIER | c.1259+122delC | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr17 | 74252495 | |||||
chr17:74252575
|
C | G | 2 | a0001c0026t0001g0075a0014c0023t0001g0116 | 2 | HG01243.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1259+199C>G | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 11/13 | chr17 | 74252575 | ||||||
chr17:74252692
|
T | C | 148 | a0001c0001t0001g0093a0001c0001t0001g0297a0001c0009t0005g0019others(145): Show | 162 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.1259+316T>C | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 11/13 | chr17 | 74252692 | ||||||
chr17:74252744
|
T | C | 126 | a0001c0014t0001g0095a0001c0014t0001g0183a0001c0014t0001g0306others(123): Show | 139 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(136): Show |
intron_variant | MODIFIER | c.1260-337T>C | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 11/13 | chr17 | 74252744 | ||||||
chr17:74252808
|
G | C | 125 | a0001c0014t0001g0095a0001c0014t0001g0183a0001c0014t0001g0306others(122): Show | 138 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.1260-273G>C | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 11/13 | chr17 | 74252808 | ||||||
chr17:74252815
|
G | A | 4 | a0009c0016t0007g0289a0009c0016t0007g0290a0009c0016t0007g0291others(1): Show | 4 | HG02486.hp2 HG02717.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.1260-266G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 11/13 | chr17 | 74252815 | ||||||
chr17:74252816
|
G | T | 4 | a0009c0016t0007g0289a0009c0016t0007g0290a0009c0016t0007g0291others(1): Show | 4 | HG02486.hp2 HG02717.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.1260-265G>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 11/13 | chr17 | 74252816 | ||||||
chr17:74252841
|
T | G | 126 | a0001c0014t0001g0095a0001c0014t0001g0183a0001c0014t0001g0306others(123): Show | 139 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(136): Show |
intron_variant | MODIFIER | c.1260-240T>G | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 11/13 | chr17 | 74252841 | ||||||
chr17:74252843
|
G | A | 126 | a0001c0014t0001g0095a0001c0014t0001g0183a0001c0014t0001g0306others(123): Show | 139 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(136): Show |
intron_variant | MODIFIER | c.1260-238G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 11/13 | chr17 | 74252843 | ||||||
chr17:74252867
|
G | C | 1 | a0001c0001t0001g0302 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1260-214G>C | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 11/13 | chr17 | 74252867 | ||||||
chr17:74252973
|
C | T | 5 | a0005c0007t0006g0187a0005c0007t0006g0188a0005c0007t0006g0189others(2): Show | 5 | HG00438.hp1 NA18980.hp2 NA18981.hp1 others(2): Show |
intron_variant | MODIFIER | c.1260-108C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 11/13 | chr17 | 74252973 | ||||||
chr17:74253056
|
G | A | 1 | a0001c0001t0001g0244 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1260-25G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 11/13 | chr17 | 74253056 | ||||||
chr17:74253355
|
C | T | 1 | a0003c0003t0002g0134 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1445+89C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 12/13 | chr17 | 74253355 | ||||||
chr17:74253413
|
C | T | 2 | a0001c0026t0001g0075a0014c0023t0001g0116 | 2 | HG01243.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1445+147C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 12/13 | chr17 | 74253413 | ||||||
chr17:74253476
|
C | T | 125 | a0001c0014t0001g0095a0001c0014t0001g0183a0001c0014t0001g0306others(122): Show | 138 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.1445+210C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 12/13 | chr17 | 74253476 | ||||||
chr17:74253507
|
T | C | 125 | a0001c0014t0001g0095a0001c0014t0001g0183a0001c0014t0001g0306others(122): Show | 138 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.1445+241T>C | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 12/13 | chr17 | 74253507 | ||||||
chr17:74253539
|
T | C | 125 | a0001c0014t0001g0095a0001c0014t0001g0183a0001c0014t0001g0306others(122): Show | 138 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.1446-216T>C | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 12/13 | chr17 | 74253539 | ||||||
chr17:74253556
|
G | C | 71 | a0003c0003t0001g0127a0003c0003t0002g0010a0003c0003t0002g0013others(68): Show | 74 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.1446-199G>C | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 12/13 | chr17 | 74253556 | ||||||
chr17:74253564
|
T | A | 125 | a0001c0014t0001g0095a0001c0014t0001g0183a0001c0014t0001g0306others(122): Show | 138 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.1446-191T>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 12/13 | chr17 | 74253564 | ||||||
chr17:74253684
|
C | T | 6 | a0004c0006t0001g0079a0004c0006t0001g0080a0004c0006t0001g0082others(3): Show | 6 | HG00738.hp2 HG02615.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1446-71C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 12/13 | chr17 | 74253684 | ||||||
chr17:74253971
|
G | C | 125 | a0001c0014t0001g0095a0001c0014t0001g0183a0001c0014t0001g0306others(122): Show | 138 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.1524+138G>C | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 13/13 | chr17 | 74253971 | ||||||
chr17:74254010
|
T | C | 125 | a0001c0014t0001g0095a0001c0014t0001g0183a0001c0014t0001g0306others(122): Show | 138 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.1524+177T>C | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 13/13 | chr17 | 74254010 | ||||||
chr17:74254181
|
TTA | T | 64 | a0003c0003t0001g0127a0003c0003t0002g0010a0003c0003t0002g0013others(61): Show | 67 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(64): Show |
intron_variant | MODIFIER | c.1524+350_1524+351d others(4): Show |
TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr17 | 74254181 | |||||
chr17:74254182
|
TA | T | 53 | a0001c0014t0001g0183a0001c0014t0001g0306a0002c0002t0001g0229others(50): Show | 63 | HG00099.hp2 HG00438.hp1 HG01069.hp2 others(60): Show |
intron_variant | MODIFIER | c.1524+350delA | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 13/13 | chr17 | 74254182 | ||||||
chr17:74254183
|
A | T | 5 | a0001c0014t0001g0095a0001c0014t0010g0260a0002c0002t0003g0223others(2): Show | 5 | HG01243.hp2 HG02809.hp1 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.1524+350A>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 13/13 | chr17 | 74254183 | ||||||
chr17:74254187
|
A | T | 125 | a0001c0014t0001g0095a0001c0014t0001g0183a0001c0014t0001g0306others(122): Show | 138 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.1524+354A>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 13/13 | chr17 | 74254187 | ||||||
chr17:74254212
|
A | G | 2 | a0001c0026t0001g0075a0014c0023t0001g0116 | 2 | HG01243.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1524+379A>G | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 13/13 | chr17 | 74254212 | ||||||
chr17:74254237
|
G | A | 72 | a0001c0014t0001g0183a0001c0014t0001g0306a0001c0014t0010g0260others(69): Show | 75 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(72): Show |
intron_variant | MODIFIER | c.1524+404G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 13/13 | chr17 | 74254237 | ||||||
chr17:74254305
|
C | T | 125 | a0001c0014t0001g0095a0001c0014t0001g0183a0001c0014t0001g0306others(122): Show | 138 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.1524+472C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 13/13 | chr17 | 74254305 | ||||||
chr17:74254368
|
A | G | 2 | a0005c0020t0001g0184a0005c0020t0001g0185 | 2 | HG02896.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1524+535A>G | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 13/13 | chr17 | 74254368 | ||||||
chr17:74254378
|
G | C | 2 | a0004c0006t0001g0104a0004c0006t0001g0287 | 2 | HG03130.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1524+545G>C | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 13/13 | chr17 | 74254378 | ||||||
chr17:74254397
|
A | G | 125 | a0001c0014t0001g0095a0001c0014t0001g0183a0001c0014t0001g0306others(122): Show | 138 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.1524+564A>G | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 13/13 | chr17 | 74254397 | ||||||
chr17:74254419
|
C | T | 1 | a0007c0011t0001g0152 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1524+586C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 13/13 | chr17 | 74254419 | ||||||
chr17:74254457
|
C | T | 14 | a0001c0014t0001g0183a0001c0014t0001g0306a0001c0014t0010g0260others(11): Show | 14 | HG01074.hp1 HG02109.hp2 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.1524+624C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 13/13 | chr17 | 74254457 | ||||||
chr17:74254829
|
A | T | 1 | a0001c0001t0001g0297 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1524+996A>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 13/13 | chr17 | 74254829 | ||||||
chr17:74254886
|
G | T | 3 | a0010c0013t0004g0293a0010c0013t0004g0294a0015c0021t0004g0119 | 3 | HG01884.hp2 HG02622.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1524+1053G>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 13/13 | chr17 | 74254886 | ||||||
chr17:74254957
|
G | T | 2 | a0001c0001t0002g0148a0001c0001t0002g0150 | 2 | HG00733.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.1524+1124G>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 13/13 | chr17 | 74254957 | ||||||
chr17:74255038
|
G | A | 72 | a0001c0014t0001g0183a0001c0014t0001g0306a0001c0014t0010g0260others(69): Show | 75 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(72): Show |
intron_variant | MODIFIER | c.1524+1205G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 13/13 | chr17 | 74255038 | ||||||
chr17:74255101
|
G | A | 17 | a0001c0009t0005g0019a0001c0009t0005g0074a0001c0009t0005g0096others(14): Show | 18 | HG01884.hp2 HG02055.hp2 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.1524+1268G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 13/13 | chr17 | 74255101 | ||||||
chr17:74255181
|
G | A | 1 | a0006c0004t0002g0137 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1524+1348G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 13/13 | chr17 | 74255181 | ||||||
chr17:74255460
|
A | AT | 9 | a0004c0006t0008g0088a0005c0007t0006g0187a0005c0007t0006g0188others(6): Show | 9 | HG00438.hp1 HG02145.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.1524+1636dupT | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr17 | 74255460 | |||||
chr17:74255499
|
T | C | 1 | a0001c0001t0001g0040 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1524+1666T>C | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 13/13 | chr17 | 74255499 | ||||||
chr17:74255864
|
G | A | 1 | a0004c0005t0001g0123 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1524+2031G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 13/13 | chr17 | 74255864 | ||||||
chr17:74255919
|
A | G | 272 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0009others(269): Show | 298 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(295): Show |
intron_variant | MODIFIER | c.1524+2086A>G | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 13/13 | chr17 | 74255919 | ||||||
chr17:74256038
|
G | A | 4 | a0009c0016t0007g0289a0009c0016t0007g0290a0009c0016t0007g0291others(1): Show | 4 | HG02486.hp2 HG02717.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.1524+2205G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 13/13 | chr17 | 74256038 | ||||||
chr17:74256058
|
C | A | 1 | a0008c0008t0002g0250 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1524+2225C>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 13/13 | chr17 | 74256058 | ||||||
chr17:74256215
|
G | C | 2 | a0005c0007t0006g0187a0005c0007t0006g0197 | 2 | HG00438.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.1524+2382G>C | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 13/13 | chr17 | 74256215 | ||||||
chr17:74256416
|
G | A | 1 | a0003c0003t0002g0110 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1524+2583G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 13/13 | chr17 | 74256416 | ||||||
chr17:74256471
|
C | T | 1 | a0001c0001t0001g0121 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1524+2638C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 13/13 | chr17 | 74256471 | ||||||
chr17:74256704
|
C | CA | 128 | a0001c0014t0001g0183a0001c0014t0001g0306a0001c0014t0010g0260others(125): Show | 141 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(138): Show |
intron_variant | MODIFIER | c.1524+2871_1524+287 others(5): Show |
TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 13/13 | chr17 | 74256704 | ||||||
chr17:74256785
|
A | T | 7 | a0001c0001t0002g0003a0001c0001t0002g0148a0001c0001t0002g0149others(4): Show | 9 | HG00733.hp1 HG02055.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.1524+2952A>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 13/13 | chr17 | 74256785 | ||||||
chr17:74256795
|
C | T | 1 | a0001c0001t0001g0195 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1524+2962C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 13/13 | chr17 | 74256795 | ||||||
chr17:74256820
|
T | C | 1 | a0001c0001t0001g0113 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1524+2987T>C | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 13/13 | chr17 | 74256820 | ||||||
chr17:74256853
|
A | T | 82 | a0001c0014t0001g0183a0001c0014t0001g0306a0001c0014t0010g0260others(79): Show | 85 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.1524+3020A>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 13/13 | chr17 | 74256853 | ||||||
chr17:74256927
|
G | C | 6 | a0004c0006t0001g0079a0004c0006t0001g0080a0004c0006t0001g0082others(3): Show | 6 | HG00738.hp2 HG02615.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1524+3094G>C | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 13/13 | chr17 | 74256927 | ||||||
chr17:74256929
|
A | G | 43 | a0001c0026t0001g0075a0002c0002t0001g0229a0002c0002t0003g0002others(40): Show | 53 | HG00099.hp2 HG00738.hp2 HG01069.hp2 others(50): Show |
intron_variant | MODIFIER | c.1524+3096A>G | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 13/13 | chr17 | 74256929 | ||||||
chr17:74256940
|
C | T | 131 | a0001c0001t0001g0064a0001c0014t0001g0183a0001c0014t0001g0306others(128): Show | 145 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(142): Show |
intron_variant | MODIFIER | c.1524+3107C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 13/13 | chr17 | 74256940 | ||||||
chr17:74257125
|
A | G | 1 | a0005c0007t0018g0097 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1525-3004A>G | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 13/13 | chr17 | 74257125 | ||||||
chr17:74257153
|
A | G | 1 | a0005c0007t0018g0097 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1525-2976A>G | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 13/13 | chr17 | 74257153 | ||||||
chr17:74257185
|
T | C | 2 | a0005c0020t0001g0184a0005c0020t0001g0185 | 2 | HG02896.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1525-2944T>C | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 13/13 | chr17 | 74257185 | ||||||
chr17:74257250
|
C | A | 1 | a0003c0003t0002g0077 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1525-2879C>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 13/13 | chr17 | 74257250 | ||||||
chr17:74257468
|
C | T | 4 | a0009c0016t0007g0289a0009c0016t0007g0290a0009c0016t0007g0291others(1): Show | 4 | HG02486.hp2 HG02717.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.1525-2661C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 13/13 | chr17 | 74257468 | ||||||
chr17:74257480
|
C | T | 1 | a0001c0014t0001g0095 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1525-2649C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 13/13 | chr17 | 74257480 | ||||||
chr17:74257512
|
G | A | 2 | a0013c0018t0002g0315a0013c0018t0002g0316 | 2 | HG02622.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1525-2617G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 13/13 | chr17 | 74257512 | ||||||
chr17:74257545
|
C | T | 81 | a0001c0014t0001g0183a0001c0014t0001g0306a0001c0014t0010g0260others(78): Show | 84 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.1525-2584C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 13/13 | chr17 | 74257545 | ||||||
chr17:74257638
|
A | G | 5 | a0005c0007t0006g0187a0005c0007t0006g0188a0005c0007t0006g0189others(2): Show | 5 | HG00438.hp1 NA18980.hp2 NA18981.hp1 others(2): Show |
intron_variant | MODIFIER | c.1525-2491A>G | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 13/13 | chr17 | 74257638 | ||||||
chr17:74257750
|
G | A | 9 | a0004c0006t0008g0088a0005c0007t0006g0187a0005c0007t0006g0188others(6): Show | 9 | HG00438.hp1 HG02145.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.1525-2379G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 13/13 | chr17 | 74257750 | ||||||
chr17:74257952
|
G | A | 68 | a0001c0014t0001g0183a0001c0014t0001g0306a0001c0014t0010g0260others(65): Show | 71 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(68): Show |
intron_variant | MODIFIER | c.1525-2177G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 13/13 | chr17 | 74257952 | ||||||
chr17:74258077
|
C | T | 2 | a0004c0006t0001g0104a0004c0006t0001g0287 | 2 | HG03130.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1525-2052C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 13/13 | chr17 | 74258077 | ||||||
chr17:74258192
|
C | T | 2 | a0006c0004t0002g0157a0016c0022t0015g0167 | 2 | HG02280.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1525-1937C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 13/13 | chr17 | 74258192 | ||||||
chr17:74258193
|
G | A | 3 | a0001c0001t0001g0200a0001c0001t0001g0238a0001c0001t0001g0300 | 3 | HG00738.hp1 HG00741.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.1525-1936G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 13/13 | chr17 | 74258193 | ||||||
chr17:74258193
|
G | T | 1 | a0005c0007t0018g0097 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1525-1936G>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 13/13 | chr17 | 74258193 | ||||||
chr17:74258208
|
G | A | 85 | a0001c0001t0002g0154a0001c0014t0001g0183a0001c0014t0001g0306others(82): Show | 88 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(85): Show |
intron_variant | MODIFIER | c.1525-1921G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 13/13 | chr17 | 74258208 | ||||||
chr17:74258274
|
T | C | 1 | a0003c0003t0002g0010 | 2 | HG02572.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1525-1855T>C | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 13/13 | chr17 | 74258274 | ||||||
chr17:74258422
|
C | T | 1 | a0005c0007t0018g0097 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1525-1707C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 13/13 | chr17 | 74258422 | ||||||
chr17:74258518
|
C | T | 2 | a0001c0009t0012g0307a0001c0009t0012g0308 | 2 | HG02965.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1525-1611C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 13/13 | chr17 | 74258518 | ||||||
chr17:74258556
|
C | T | 16 | a0001c0001t0001g0069a0001c0001t0001g0083a0001c0001t0001g0139others(13): Show | 18 | HG00733.hp1 HG01106.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.1525-1573C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 13/13 | chr17 | 74258556 | ||||||
chr17:74258723
|
C | T | 3 | a0012c0017t0010g0117a0012c0017t0010g0118a0012c0017t0019g0087 | 3 | HG02895.hp1 HG02897.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1525-1406C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 13/13 | chr17 | 74258723 | ||||||
chr17:74259029
|
AG | A | 9 | a0001c0001t0002g0154a0001c0014t0001g0183a0001c0014t0001g0306others(6): Show | 9 | HG01074.hp1 HG02109.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.1525-1099delG | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 13/13 | chr17 | 74259029 | ||||||
chr17:74259124
|
C | T | 3 | a0003c0003t0002g0124a0003c0003t0002g0172a0003c0003t0002g0298 | 3 | HG00140.hp2 HG01255.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.1525-1005C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 13/13 | chr17 | 74259124 | ||||||
chr17:74259246
|
G | A | 1 | a0001c0001t0001g0297 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1525-883G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 13/13 | chr17 | 74259246 | ||||||
chr17:74259305
|
G | C | 2 | a0001c0009t0012g0307a0001c0009t0012g0308 | 2 | HG02965.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1525-824G>C | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 13/13 | chr17 | 74259305 | ||||||
chr17:74259435
|
G | A | 33 | a0002c0002t0001g0229a0002c0002t0003g0002a0002c0002t0003g0007others(30): Show | 43 | HG00099.hp2 HG01069.hp2 HG01081.hp2 others(40): Show |
intron_variant | MODIFIER | c.1525-694G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 13/13 | chr17 | 74259435 | ||||||
chr17:74259456
|
C | T | 1 | a0004c0005t0001g0207 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1525-673C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 13/13 | chr17 | 74259456 | ||||||
chr17:74259508
|
G | A | 8 | a0006c0004t0002g0081a0006c0004t0002g0151a0006c0004t0002g0156others(5): Show | 8 | HG01884.hp1 HG02258.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1525-621G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 13/13 | chr17 | 74259508 | ||||||
chr17:74259512
|
T | C | 1 | a0001c0001t0001g0284 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1525-617T>C | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 13/13 | chr17 | 74259512 | ||||||
chr17:74259669
|
C | T | 48 | a0001c0001t0001g0018a0001c0001t0001g0043a0001c0001t0001g0047others(45): Show | 49 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(46): Show |
intron_variant | MODIFIER | c.1525-460C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 13/13 | chr17 | 74259669 | ||||||
chr17:74259835
|
C | A | 1 | a0001c0001t0001g0041 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1525-294C>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 13/13 | chr17 | 74259835 | ||||||
chr17:74259839
|
C | A | 1 | a0001c0001t0001g0264 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1525-290C>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 13/13 | chr17 | 74259839 | ||||||
chr17:74259921
|
G | A | 1 | a0008c0008t0002g0049 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1525-208G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 13/13 | chr17 | 74259921 | ||||||
chr17:74259965
|
T | G | 33 | a0002c0002t0001g0229a0002c0002t0003g0002a0002c0002t0003g0007others(30): Show | 43 | HG00099.hp2 HG01069.hp2 HG01081.hp2 others(40): Show |
intron_variant | MODIFIER | c.1525-164T>G | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 13/13 | chr17 | 74259965 | ||||||
chr17:74260016
|
G | A | 58 | a0001c0001t0002g0003a0001c0001t0002g0148a0001c0001t0002g0149others(55): Show | 63 | HG00140.hp1 HG00140.hp2 HG00639.hp2 others(60): Show |
intron_variant | MODIFIER | c.1525-113G>A | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 13/13 | chr17 | 74260016 | ||||||
chr17:74260034
|
C | T | 1 | a0001c0014t0001g0095 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1525-95C>T | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 13/13 | chr17 | 74260034 | ||||||
chr17:74260057
|
TC | T | 56 | a0001c0001t0002g0003a0001c0001t0002g0148a0001c0001t0002g0149others(53): Show | 61 | HG00140.hp1 HG00140.hp2 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.1525-68delC | TTYH2 | ENSG00000141540.11 | transcript | ENST00000269346.9 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr17 | 74260057 |