geneid | 9654 |
---|---|
ensemblid | ENSG00000135912.11 |
hgncid | 28976 |
symbol | TTLL4 |
name | tubulin tyrosine ligase like 4 |
refseq_nuc | NM_014640.5 |
refseq_prot | NP_055455.3 |
ensembl_nuc | ENST00000392102.6 |
ensembl_prot | ENSP00000375951.1 |
mane_status | MANE Select |
chr | chr2 |
start | 218710835 |
end | 218755416 |
strand | + |
ver | v1.2 |
region | chr2:218710835-218755416 |
region5000 | chr2:218705835-218760416 |
regionname0 | TTLL4_chr2_218710835_218755416 |
regionname5000 | TTLL4_chr2_218705835_218760416 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 1199 | 114 | 43 | 23 | 30 | 4 | 14 | 25 | TTLL4_chr2_218705835_218760416 | TTLL4 | copy fasta | chr2 | 218705835 | 218760416 |
a0002 | 1/1 | 1199 | 99 | 13 | 17 | 45 | 5 | 17 | 30 | TTLL4_chr2_218705835_218760416 | TTLL4 | copy fasta | chr2 | 218705835 | 218760416 |
a0003 | 0/0 | 1199 | 13 | 13 | 0 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | copy fasta | chr2 | 218705835 | 218760416 |
a0004 | 0/0 | 1199 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | copy fasta | chr2 | 218705835 | 218760416 |
a0005 | 0/0 | 1199 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | copy fasta | chr2 | 218705835 | 218760416 |
a0006 | 0/0 | 1199 | 4 | 0 | 0 | 4 | 0 | 0 | 4 | TTLL4_chr2_218705835_218760416 | TTLL4 | copy fasta | chr2 | 218705835 | 218760416 |
a0007 | 0/0 | 1199 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | copy fasta | chr2 | 218705835 | 218760416 |
a0008 | 0/0 | 1199 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | copy fasta | chr2 | 218705835 | 218760416 |
a0009 | 0/0 | 1199 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | copy fasta | chr2 | 218705835 | 218760416 |
a0010 | 0/0 | 1199 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | copy fasta | chr2 | 218705835 | 218760416 |
a0011 | 0/0 | 1199 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | copy fasta | chr2 | 218705835 | 218760416 |
a0012 | 0/0 | 1199 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | copy fasta | chr2 | 218705835 | 218760416 |
a0013 | 0/0 | 1199 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | copy fasta | chr2 | 218705835 | 218760416 |
a0014 | 0/0 | 1199 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TTLL4_chr2_218705835_218760416 | TTLL4 | copy fasta | chr2 | 218705835 | 218760416 |
a0015 | 0/0 | 1199 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | copy fasta | chr2 | 218705835 | 218760416 |
a0016 | 0/0 | 1199 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | copy fasta | chr2 | 218705835 | 218760416 |
a0017 | 0/0 | 1199 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | copy fasta | chr2 | 218705835 | 218760416 |
a0018 | 0/0 | 1199 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | copy fasta | chr2 | 218705835 | 218760416 |
a0019 | 0/0 | 1199 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | copy fasta | chr2 | 218705835 | 218760416 |
a0020 | 0/0 | 1199 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | copy fasta | chr2 | 218705835 | 218760416 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/0 | 3600 | 113 | 42 | 23 | 30 | 4 | 14 | TTLL4_chr2_218705835_218760416 | TTLL4 | copy fasta | chr2 | 218705835 | 218760416 |
c0002 | 1/1 | 3600 | 89 | 5 | 16 | 44 | 5 | 17 | TTLL4_chr2_218705835_218760416 | TTLL4 | copy fasta | chr2 | 218705835 | 218760416 |
c0003 | 0/0 | 3600 | 13 | 13 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | copy fasta | chr2 | 218705835 | 218760416 |
c0004 | 0/0 | 3600 | 6 | 6 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | copy fasta | chr2 | 218705835 | 218760416 |
c0005 | 0/0 | 3600 | 5 | 5 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | copy fasta | chr2 | 218705835 | 218760416 |
c0006 | 0/0 | 3600 | 4 | 0 | 0 | 4 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | copy fasta | chr2 | 218705835 | 218760416 |
c0007 | 0/0 | 3600 | 4 | 3 | 1 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | copy fasta | chr2 | 218705835 | 218760416 |
c0008 | 0/0 | 3600 | 3 | 3 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | copy fasta | chr2 | 218705835 | 218760416 |
c0009 | 0/0 | 3600 | 3 | 3 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | copy fasta | chr2 | 218705835 | 218760416 |
c0010 | 0/0 | 3600 | 2 | 2 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | copy fasta | chr2 | 218705835 | 218760416 |
c0011 | 0/0 | 3600 | 2 | 2 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | copy fasta | chr2 | 218705835 | 218760416 |
c0012 | 0/0 | 3600 | 2 | 0 | 2 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | copy fasta | chr2 | 218705835 | 218760416 |
c0013 | 0/0 | 3600 | 2 | 2 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | copy fasta | chr2 | 218705835 | 218760416 |
c0014 | 0/0 | 3600 | 2 | 2 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | copy fasta | chr2 | 218705835 | 218760416 |
c0015 | 0/0 | 3600 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | copy fasta | chr2 | 218705835 | 218760416 |
c0016 | 0/0 | 3600 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | copy fasta | chr2 | 218705835 | 218760416 |
c0017 | 0/0 | 3600 | 1 | 0 | 0 | 0 | 0 | 1 | TTLL4_chr2_218705835_218760416 | TTLL4 | copy fasta | chr2 | 218705835 | 218760416 |
c0018 | 0/0 | 3600 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | copy fasta | chr2 | 218705835 | 218760416 |
c0019 | 0/0 | 3600 | 1 | 0 | 1 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | copy fasta | chr2 | 218705835 | 218760416 |
c0020 | 0/0 | 3600 | 1 | 0 | 0 | 0 | 1 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | copy fasta | chr2 | 218705835 | 218760416 |
c0021 | 0/0 | 3600 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | copy fasta | chr2 | 218705835 | 218760416 |
c0022 | 0/0 | 3600 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | copy fasta | chr2 | 218705835 | 218760416 |
c0023 | 0/0 | 3600 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | copy fasta | chr2 | 218705835 | 218760416 |
c0024 | 0/0 | 3600 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | copy fasta | chr2 | 218705835 | 218760416 |
c0025 | 0/0 | 3600 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | copy fasta | chr2 | 218705835 | 218760416 |
c0026 | 0/0 | 3600 | 1 | 0 | 1 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | copy fasta | chr2 | 218705835 | 218760416 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 1408 | 128 | 52 | 22 | 34 | 5 | 15 | TTLL4_chr2_218705835_218760416 | TTLL4 | copy fasta | chr2 | 218705835 | 218760416 |
t0002 | 1/1 | 1408 | 104 | 16 | 19 | 46 | 5 | 16 | TTLL4_chr2_218705835_218760416 | TTLL4 | copy fasta | chr2 | 218705835 | 218760416 |
t0003 | 0/0 | 1408 | 8 | 8 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | copy fasta | chr2 | 218705835 | 218760416 |
t0004 | 0/0 | 1408 | 8 | 8 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | copy fasta | chr2 | 218705835 | 218760416 |
t0005 | 0/0 | 1408 | 5 | 5 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | copy fasta | chr2 | 218705835 | 218760416 |
t0006 | 0/0 | 1408 | 2 | 2 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | copy fasta | chr2 | 218705835 | 218760416 |
t0007 | 0/0 | 1408 | 2 | 0 | 2 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | copy fasta | chr2 | 218705835 | 218760416 |
t0008 | 0/0 | 1408 | 1 | 0 | 1 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | copy fasta | chr2 | 218705835 | 218760416 |
t0009 | 0/0 | 1408 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | copy fasta | chr2 | 218705835 | 218760416 |
t0010 | 0/0 | 1408 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | copy fasta | chr2 | 218705835 | 218760416 |
t0011 | 0/0 | 1408 | 1 | 0 | 0 | 0 | 0 | 1 | TTLL4_chr2_218705835_218760416 | TTLL4 | copy fasta | chr2 | 218705835 | 218760416 |
t0012 | 0/0 | 1408 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | copy fasta | chr2 | 218705835 | 218760416 |
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 | 9 | 0 | 5 | 2 | 1 | 1 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0002 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0003 | 0/0 | 4 | 0 | 1 | 0 | 1 | 2 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0004 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0005 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0006 | 0/0 | 3 | 0 | 0 | 2 | 1 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0009 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0010 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0016 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0019 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0020 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0097 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0133 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 3600 | 113 | 42 | 23 | 30 | 4 | 14 | TTLL4_chr2_218705835_218760416 | TTLL4 | copy fasta | chr2 | 218705835 | 218760416 |
a0001c0016 | 0/0 | 3600 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | copy fasta | chr2 | 218705835 | 218760416 |
a0002c0002 | 1/1 | 3600 | 89 | 5 | 16 | 44 | 5 | 17 | TTLL4_chr2_218705835_218760416 | TTLL4 | copy fasta | chr2 | 218705835 | 218760416 |
a0002c0007 | 0/0 | 3600 | 4 | 3 | 1 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | copy fasta | chr2 | 218705835 | 218760416 |
a0002c0011 | 0/0 | 3600 | 2 | 2 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | copy fasta | chr2 | 218705835 | 218760416 |
a0002c0013 | 0/0 | 3600 | 2 | 2 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | copy fasta | chr2 | 218705835 | 218760416 |
a0002c0023 | 0/0 | 3600 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | copy fasta | chr2 | 218705835 | 218760416 |
a0002c0025 | 0/0 | 3600 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | copy fasta | chr2 | 218705835 | 218760416 |
a0003c0003 | 0/0 | 3600 | 13 | 13 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | copy fasta | chr2 | 218705835 | 218760416 |
a0004c0004 | 0/0 | 3600 | 6 | 6 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | copy fasta | chr2 | 218705835 | 218760416 |
a0005c0005 | 0/0 | 3600 | 5 | 5 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | copy fasta | chr2 | 218705835 | 218760416 |
a0006c0006 | 0/0 | 3600 | 4 | 0 | 0 | 4 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | copy fasta | chr2 | 218705835 | 218760416 |
a0007c0009 | 0/0 | 3600 | 3 | 3 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | copy fasta | chr2 | 218705835 | 218760416 |
a0008c0008 | 0/0 | 3600 | 3 | 3 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | copy fasta | chr2 | 218705835 | 218760416 |
a0009c0014 | 0/0 | 3600 | 2 | 2 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | copy fasta | chr2 | 218705835 | 218760416 |
a0010c0012 | 0/0 | 3600 | 2 | 0 | 2 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | copy fasta | chr2 | 218705835 | 218760416 |
a0011c0010 | 0/0 | 3600 | 2 | 2 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | copy fasta | chr2 | 218705835 | 218760416 |
a0012c0026 | 0/0 | 3600 | 1 | 0 | 1 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | copy fasta | chr2 | 218705835 | 218760416 |
a0013c0024 | 0/0 | 3600 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | copy fasta | chr2 | 218705835 | 218760416 |
a0014c0022 | 0/0 | 3600 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | copy fasta | chr2 | 218705835 | 218760416 |
a0015c0021 | 0/0 | 3600 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | copy fasta | chr2 | 218705835 | 218760416 |
a0016c0019 | 0/0 | 3600 | 1 | 0 | 1 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | copy fasta | chr2 | 218705835 | 218760416 |
a0017c0015 | 0/0 | 3600 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | copy fasta | chr2 | 218705835 | 218760416 |
a0018c0017 | 0/0 | 3600 | 1 | 0 | 0 | 0 | 0 | 1 | TTLL4_chr2_218705835_218760416 | TTLL4 | copy fasta | chr2 | 218705835 | 218760416 |
a0019c0018 | 0/0 | 3600 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | copy fasta | chr2 | 218705835 | 218760416 |
a0020c0020 | 0/0 | 3600 | 1 | 0 | 0 | 0 | 1 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | copy fasta | chr2 | 218705835 | 218760416 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 5007 | 103 | 34 | 21 | 30 | 4 | 14 | TTLL4_chr2_218705835_218760416 | TTLL4 | copy fasta | chr2 | 218705835 | 218760416 |
a0001c0001t0003 | 0/0 | 5007 | 6 | 6 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | copy fasta | chr2 | 218705835 | 218760416 |
a0001c0001t0007 | 0/0 | 5007 | 2 | 0 | 2 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | copy fasta | chr2 | 218705835 | 218760416 |
a0001c0001t0009 | 0/0 | 5007 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | copy fasta | chr2 | 218705835 | 218760416 |
a0001c0001t0012 | 0/0 | 5007 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | copy fasta | chr2 | 218705835 | 218760416 |
a0001c0016t0001 | 0/0 | 5007 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | copy fasta | chr2 | 218705835 | 218760416 |
a0002c0002t0002 | 1/1 | 5007 | 87 | 5 | 15 | 44 | 5 | 16 | TTLL4_chr2_218705835_218760416 | TTLL4 | copy fasta | chr2 | 218705835 | 218760416 |
a0002c0002t0008 | 0/0 | 5007 | 1 | 0 | 1 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | copy fasta | chr2 | 218705835 | 218760416 |
a0002c0002t0011 | 0/0 | 5007 | 1 | 0 | 0 | 0 | 0 | 1 | TTLL4_chr2_218705835_218760416 | TTLL4 | copy fasta | chr2 | 218705835 | 218760416 |
a0002c0007t0002 | 0/0 | 5007 | 4 | 3 | 1 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | copy fasta | chr2 | 218705835 | 218760416 |
a0002c0011t0006 | 0/0 | 5007 | 2 | 2 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | copy fasta | chr2 | 218705835 | 218760416 |
a0002c0013t0002 | 0/0 | 5007 | 2 | 2 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | copy fasta | chr2 | 218705835 | 218760416 |
a0002c0023t0002 | 0/0 | 5007 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | copy fasta | chr2 | 218705835 | 218760416 |
a0002c0025t0002 | 0/0 | 5007 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | copy fasta | chr2 | 218705835 | 218760416 |
a0003c0003t0004 | 0/0 | 5007 | 8 | 8 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | copy fasta | chr2 | 218705835 | 218760416 |
a0003c0003t0005 | 0/0 | 5007 | 5 | 5 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | copy fasta | chr2 | 218705835 | 218760416 |
a0004c0004t0001 | 0/0 | 5007 | 5 | 5 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | copy fasta | chr2 | 218705835 | 218760416 |
a0004c0004t0003 | 0/0 | 5007 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | copy fasta | chr2 | 218705835 | 218760416 |
a0005c0005t0001 | 0/0 | 5007 | 5 | 5 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | copy fasta | chr2 | 218705835 | 218760416 |
a0006c0006t0001 | 0/0 | 5007 | 4 | 0 | 0 | 4 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | copy fasta | chr2 | 218705835 | 218760416 |
a0007c0009t0002 | 0/0 | 5007 | 3 | 3 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | copy fasta | chr2 | 218705835 | 218760416 |
a0008c0008t0001 | 0/0 | 5007 | 2 | 2 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | copy fasta | chr2 | 218705835 | 218760416 |
a0008c0008t0003 | 0/0 | 5007 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | copy fasta | chr2 | 218705835 | 218760416 |
a0009c0014t0002 | 0/0 | 5007 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | copy fasta | chr2 | 218705835 | 218760416 |
a0009c0014t0010 | 0/0 | 5007 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | copy fasta | chr2 | 218705835 | 218760416 |
a0010c0012t0002 | 0/0 | 5007 | 2 | 0 | 2 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | copy fasta | chr2 | 218705835 | 218760416 |
a0011c0010t0001 | 0/0 | 5007 | 2 | 2 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | copy fasta | chr2 | 218705835 | 218760416 |
a0012c0026t0002 | 0/0 | 5007 | 1 | 0 | 1 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | copy fasta | chr2 | 218705835 | 218760416 |
a0013c0024t0002 | 0/0 | 5007 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | copy fasta | chr2 | 218705835 | 218760416 |
a0014c0022t0002 | 0/0 | 5007 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | copy fasta | chr2 | 218705835 | 218760416 |
a0015c0021t0001 | 0/0 | 5007 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | copy fasta | chr2 | 218705835 | 218760416 |
a0016c0019t0001 | 0/0 | 5007 | 1 | 0 | 1 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | copy fasta | chr2 | 218705835 | 218760416 |
a0017c0015t0001 | 0/0 | 5007 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | copy fasta | chr2 | 218705835 | 218760416 |
a0018c0017t0001 | 0/0 | 5007 | 1 | 0 | 0 | 0 | 0 | 1 | TTLL4_chr2_218705835_218760416 | TTLL4 | copy fasta | chr2 | 218705835 | 218760416 |
a0019c0018t0001 | 0/0 | 5007 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | copy fasta | chr2 | 218705835 | 218760416 |
a0020c0020t0001 | 0/0 | 5007 | 1 | 0 | 0 | 0 | 1 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | copy fasta | chr2 | 218705835 | 218760416 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0003 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0004 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0010 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0003g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0003g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0003g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0003g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0003g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0003g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0007g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0009g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0001t0012g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0001c0016t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0002t0002g0001 | 0/0 | 8 | 0 | 4 | 2 | 1 | 1 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0002t0002g0002 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0002t0002g0005 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0002t0002g0006 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0002t0002g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0002t0002g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0002t0002g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0002t0002g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0002t0002g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0002t0002g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0002t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0002t0002g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0002t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0002t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0002t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0002t0002g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0002t0002g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0002t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0002t0002g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0002t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0002t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0002t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0002t0002g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0002t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0002t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0002t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0002t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0002t0002g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0002t0002g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0002t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0002t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0002t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0002t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0002t0002g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0002t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0002t0002g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0002t0002g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0002t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0002t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0002t0002g0097 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0002t0002g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0002t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0002t0002g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0002t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0002t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0002t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0002t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0002t0002g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0002t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0002t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0002t0002g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0002t0002g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0002t0002g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0002t0002g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0002t0002g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0002t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0002t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0002t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0002t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0002t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0002t0002g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0002t0002g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0002t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0002t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0002t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0002t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0002t0002g0133 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0002t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0002t0002g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0002t0002g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0002t0008g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0002t0011g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0007t0002g0009 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0007t0002g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0007t0002g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0011t0006g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0011t0006g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0013t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0013t0002g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0023t0002g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0002c0025t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0003c0003t0004g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0003c0003t0004g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0003c0003t0004g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0003c0003t0004g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0003c0003t0004g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0003c0003t0004g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0003c0003t0004g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0003c0003t0004g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0003c0003t0005g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0003c0003t0005g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0003c0003t0005g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0003c0003t0005g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0004c0004t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0004c0004t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0004c0004t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0004c0004t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0004c0004t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0004c0004t0003g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0005c0005t0001g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0005c0005t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0005c0005t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0005c0005t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0006c0006t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0006c0006t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0006c0006t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0006c0006t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0007c0009t0002g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0007c0009t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0007c0009t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0008c0008t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0008c0008t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0008c0008t0003g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0009c0014t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0009c0014t0010g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0010c0012t0002g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0010c0012t0002g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0011c0010t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0011c0010t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0012c0026t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0013c0024t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0014c0022t0002g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0015c0021t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0016c0019t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0017c0015t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0018c0017t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0019c0018t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
a0020c0020t0001g0003 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0002 | c0002 | t0002 | g0006 | EUR | GBR | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0183 | EUR | GBR | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0161 | EUR | GBR | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG00140 | hp2 | a0002 | c0002 | t0002 | g0085 | EUR | GBR | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG00280 | hp1 | a0002 | c0002 | t0002 | g0073 | EUR | FIN | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0019 | EUR | FIN | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG00323 | hp1 | a0002 | c0002 | t0002 | g0001 | EUR | FIN | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0149 | EUR | FIN | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG00438 | hp1 | a0002 | c0002 | t0002 | g0110 | EAS | CHS | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG00438 | hp2 | a0002 | c0002 | t0002 | g0015 | EAS | CHS | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG00558 | hp1 | a0002 | c0002 | t0002 | g0081 | EAS | CHS | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | CHS | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG00597 | hp1 | a0002 | c0002 | t0002 | g0091 | EAS | CHS | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG00597 | hp2 | a0002 | c0002 | t0002 | g0108 | EAS | CHS | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG00621 | hp1 | a0002 | c0002 | t0002 | g0088 | EAS | CHS | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | CHS | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0187 | AMR | PUR | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG00639 | hp2 | a0002 | c0002 | t0002 | g0002 | AMR | PUR | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG00642 | hp1 | a0002 | c0002 | t0002 | g0001 | AMR | PUR | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0180 | AMR | PUR | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG00733 | hp1 | a0002 | c0002 | t0002 | g0090 | AMR | PUR | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG00735 | hp1 | a0002 | c0002 | t0002 | g0076 | AMR | PUR | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | PUR | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG00741 | hp1 | a0002 | c0002 | t0002 | g0005 | AMR | PUR | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG01070 | hp1 | a0002 | c0002 | t0002 | g0135 | AMR | PUR | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0169 | AMR | PUR | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG01081 | hp1 | a0002 | c0002 | t0002 | g0112 | AMR | PUR | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | PUR | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG01109 | hp2 | a0016 | c0019 | t0001 | g0021 | AMR | PUR | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0071 | AMR | PUR | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG01168 | hp2 | a0002 | c0002 | t0002 | g0139 | AMR | PUR | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG01169 | hp1 | a0002 | c0002 | t0002 | g0001 | AMR | PUR | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0070 | AMR | PUR | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0179 | AMR | PUR | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG01175 | hp2 | a0002 | c0002 | t0002 | g0005 | AMR | PUR | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG01192 | hp2 | a0002 | c0002 | t0002 | g0098 | AMR | PUR | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG01255 | hp1 | a0002 | c0002 | t0002 | g0074 | AMR | CLM | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0170 | AMR | CLM | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG01256 | hp1 | a0002 | c0002 | t0002 | g0001 | AMR | CLM | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG01256 | hp2 | a0001 | c0001 | t0007 | g0018 | AMR | CLM | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG01261 | hp1 | a0001 | c0001 | t0007 | g0018 | AMR | CLM | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG01261 | hp2 | a0012 | c0026 | t0002 | g0101 | AMR | CLM | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | CLM | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG01496 | hp2 | a0002 | c0002 | t0002 | g0001 | AMR | CLM | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | ACB | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | ACB | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG01891 | hp2 | a0017 | c0015 | t0001 | g0189 | AFR | ACB | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | PEL | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG01943 | hp2 | a0002 | c0002 | t0002 | g0115 | AMR | PEL | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG01975 | hp1 | a0002 | c0007 | t0002 | g0009 | AMR | PEL | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | PEL | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | PEL | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG01993 | hp2 | a0002 | c0002 | t0008 | g0001 | AMR | PEL | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG02027 | hp2 | a0002 | c0002 | t0002 | g0089 | EAS | KHV | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | ACB | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG02055 | hp2 | a0003 | c0003 | t0005 | g0214 | AFR | ACB | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | KHV | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG02074 | hp2 | a0002 | c0002 | t0002 | g0017 | EAS | KHV | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG02083 | hp1 | a0002 | c0002 | t0002 | g0123 | EAS | KHV | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | KHV | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG02129 | hp1 | a0002 | c0002 | t0002 | g0103 | EAS | KHV | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG02129 | hp2 | a0002 | c0002 | t0002 | g0086 | EAS | KHV | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG02132 | hp1 | a0002 | c0002 | t0002 | g0122 | EAS | KHV | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG02132 | hp2 | a0002 | c0002 | t0002 | g0082 | EAS | KHV | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG02145 | hp1 | a0001 | c0016 | t0001 | g0188 | AFR | ACB | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG02145 | hp2 | a0004 | c0004 | t0001 | g0177 | AFR | ACB | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG02155 | hp1 | a0002 | c0002 | t0002 | g0083 | EAS | CDX | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG02155 | hp2 | a0002 | c0002 | t0002 | g0104 | EAS | CDX | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG02257 | hp1 | a0001 | c0001 | t0003 | g0219 | AFR | ACB | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG02257 | hp2 | a0002 | c0011 | t0006 | g0206 | AFR | ACB | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG02280 | hp1 | a0015 | c0021 | t0001 | g0190 | AFR | ACB | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG02293 | hp1 | a0010 | c0012 | t0002 | g0109 | AMR | PEL | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG02451 | hp1 | a0002 | c0011 | t0006 | g0205 | AFR | ACB | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG02451 | hp2 | a0002 | c0013 | t0002 | g0118 | AFR | ACB | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG02572 | hp2 | a0004 | c0004 | t0001 | g0150 | AFR | GWD | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0159 | SAS | PJL | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG02602 | hp2 | a0002 | c0002 | t0002 | g0005 | SAS | PJL | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG02615 | hp1 | a0003 | c0003 | t0004 | g0216 | AFR | GWD | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG02615 | hp2 | a0009 | c0014 | t0002 | g0111 | AFR | GWD | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG02622 | hp1 | a0003 | c0003 | t0004 | g0213 | AFR | GWD | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG02622 | hp2 | a0002 | c0002 | t0002 | g0016 | AFR | GWD | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG02630 | hp1 | a0002 | c0023 | t0002 | g0119 | AFR | GWD | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG02630 | hp2 | a0003 | c0003 | t0005 | g0023 | AFR | GWD | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG02647 | hp2 | a0019 | c0018 | t0001 | g0061 | AFR | GWD | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG02683 | hp2 | a0002 | c0002 | t0002 | g0072 | SAS | PJL | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG02698 | hp1 | a0002 | c0002 | t0002 | g0079 | SAS | PJL | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG02698 | hp2 | a0002 | c0002 | t0011 | g0131 | SAS | PJL | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG02717 | hp1 | a0001 | c0001 | t0012 | g0207 | AFR | GWD | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG02717 | hp2 | a0007 | c0009 | t0002 | g0137 | AFR | GWD | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG02818 | hp1 | a0003 | c0003 | t0005 | g0210 | AFR | GWD | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG02818 | hp2 | a0004 | c0004 | t0003 | g0024 | AFR | GWD | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG02886 | hp1 | a0011 | c0010 | t0001 | g0197 | AFR | GWD | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG02886 | hp2 | a0007 | c0009 | t0002 | g0136 | AFR | GWD | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | GWD | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | GWD | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG02897 | hp2 | a0005 | c0005 | t0001 | g0012 | AFR | GWD | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG02922 | hp1 | a0009 | c0014 | t0010 | g0100 | AFR | ESN | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG02922 | hp2 | a0005 | c0005 | t0001 | g0051 | AFR | ESN | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | ESN | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG02965 | hp2 | a0002 | c0007 | t0002 | g0009 | AFR | ESN | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG02970 | hp1 | a0004 | c0004 | t0001 | g0158 | AFR | ESN | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | ESN | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG02976 | hp1 | a0007 | c0009 | t0002 | g0138 | AFR | ESN | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG02976 | hp2 | a0001 | c0001 | t0009 | g0025 | AFR | ESN | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0140 | SAS | PJL | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG03041 | hp1 | a0003 | c0003 | t0004 | g0209 | AFR | GWD | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG03041 | hp2 | a0002 | c0007 | t0002 | g0141 | AFR | GWD | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | MSL | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0196 | AFR | MSL | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | ESN | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | ESN | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG03139 | hp1 | a0008 | c0008 | t0001 | g0192 | AFR | ESN | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0199 | AFR | ESN | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG03195 | hp1 | a0002 | c0002 | t0002 | g0095 | AFR | ESN | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG03195 | hp2 | a0003 | c0003 | t0005 | g0218 | AFR | ESN | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0195 | AFR | MSL | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG03209 | hp2 | a0003 | c0003 | t0005 | g0023 | AFR | MSL | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | MSL | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | MSL | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0174 | SAS | PJL | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG03239 | hp2 | a0002 | c0002 | t0002 | g0092 | SAS | PJL | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG03453 | hp1 | a0011 | c0010 | t0001 | g0198 | AFR | MSL | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | MSL | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | MSL | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG03486 | hp2 | a0002 | c0013 | t0002 | g0128 | AFR | MSL | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG03490 | hp1 | a0002 | c0002 | t0002 | g0125 | SAS | PJL | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG03490 | hp2 | a0002 | c0002 | t0002 | g0001 | SAS | PJL | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG03491 | hp1 | a0002 | c0002 | t0002 | g0113 | SAS | PJL | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0154 | SAS | PJL | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG03516 | hp1 | a0008 | c0008 | t0003 | g0194 | AFR | ESN | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG03516 | hp2 | a0001 | c0001 | t0003 | g0024 | AFR | ESN | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG03540 | hp1 | a0008 | c0008 | t0001 | g0193 | AFR | GWD | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG03540 | hp2 | a0005 | c0005 | t0001 | g0012 | AFR | GWD | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | MSL | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG03579 | hp2 | a0003 | c0003 | t0004 | g0208 | AFR | MSL | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG03654 | hp1 | a0002 | c0002 | t0002 | g0027 | SAS | PJL | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG03654 | hp2 | a0018 | c0017 | t0001 | g0042 | SAS | PJL | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG03669 | hp1 | a0002 | c0002 | t0002 | g0075 | SAS | PJL | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0156 | SAS | PJL | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0036 | SAS | STU | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG03688 | hp2 | a0002 | c0002 | t0002 | g0028 | SAS | STU | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0162 | SAS | PJL | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG03704 | hp2 | a0002 | c0002 | t0002 | g0126 | SAS | PJL | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG03831 | hp1 | a0002 | c0002 | t0002 | g0093 | SAS | BEB | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG03831 | hp2 | a0002 | c0002 | t0002 | g0107 | SAS | BEB | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0160 | SAS | BEB | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG03834 | hp2 | a0002 | c0002 | t0002 | g0084 | SAS | BEB | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0176 | SAS | BEB | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG03927 | hp2 | a0002 | c0002 | t0002 | g0030 | SAS | BEB | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG04204 | hp1 | a0002 | c0002 | t0002 | g0069 | SAS | STU | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0142 | SAS | STU | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | YRI | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | YRI | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA18906 | hp1 | a0003 | c0003 | t0004 | g0217 | AFR | YRI | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | YRI | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA18939 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA18940 | hp2 | a0002 | c0002 | t0002 | g0121 | EAS | JPT | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA18950 | hp1 | a0006 | c0006 | t0001 | g0184 | EAS | JPT | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA18950 | hp2 | a0014 | c0022 | t0002 | g0006 | EAS | JPT | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA18953 | hp1 | a0002 | c0002 | t0002 | g0132 | EAS | JPT | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA18953 | hp2 | a0006 | c0006 | t0001 | g0185 | EAS | JPT | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA18960 | hp1 | a0002 | c0002 | t0002 | g0117 | EAS | JPT | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA18960 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA18963 | hp1 | a0006 | c0006 | t0001 | g0172 | EAS | JPT | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA18963 | hp2 | a0002 | c0002 | t0002 | g0106 | EAS | JPT | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA18964 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA18965 | hp1 | a0002 | c0002 | t0002 | g0087 | EAS | JPT | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA18968 | hp1 | a0002 | c0002 | t0002 | g0014 | EAS | JPT | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA18971 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA18977 | hp1 | a0002 | c0002 | t0002 | g0134 | EAS | JPT | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA18981 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA18984 | hp1 | a0006 | c0006 | t0001 | g0173 | EAS | JPT | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA18984 | hp2 | a0002 | c0002 | t0002 | g0099 | EAS | JPT | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA18990 | hp2 | a0002 | c0002 | t0002 | g0032 | EAS | JPT | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA18998 | hp1 | a0002 | c0002 | t0002 | g0130 | EAS | JPT | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA19005 | hp1 | a0002 | c0002 | t0002 | g0127 | EAS | JPT | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA19012 | hp2 | a0002 | c0002 | t0002 | g0014 | EAS | JPT | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA19030 | hp1 | a0003 | c0003 | t0004 | g0212 | AFR | LWK | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA19030 | hp2 | a0001 | c0001 | t0003 | g0202 | AFR | LWK | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA19043 | hp1 | a0002 | c0002 | t0002 | g0116 | AFR | LWK | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | LWK | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA19062 | hp2 | a0002 | c0002 | t0002 | g0078 | EAS | JPT | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA19064 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA19065 | hp1 | a0002 | c0002 | t0002 | g0015 | EAS | JPT | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA19074 | hp1 | a0002 | c0002 | t0002 | g0006 | EAS | JPT | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA19076 | hp1 | a0002 | c0002 | t0002 | g0105 | EAS | JPT | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA19077 | hp1 | a0002 | c0002 | t0002 | g0129 | EAS | JPT | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA19079 | hp1 | a0002 | c0002 | t0002 | g0017 | EAS | JPT | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA19081 | hp2 | a0002 | c0002 | t0002 | g0031 | EAS | JPT | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA19083 | hp2 | a0002 | c0002 | t0002 | g0094 | EAS | JPT | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA19084 | hp2 | a0002 | c0025 | t0002 | g0096 | EAS | JPT | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA19087 | hp1 | a0002 | c0002 | t0002 | g0124 | EAS | JPT | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA19089 | hp2 | a0002 | c0002 | t0002 | g0077 | EAS | JPT | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA19091 | hp2 | a0002 | c0002 | t0002 | g0029 | EAS | JPT | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA19240 | hp1 | a0002 | c0002 | t0002 | g0102 | AFR | YRI | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA19240 | hp2 | a0001 | c0001 | t0003 | g0204 | AFR | YRI | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA20129 | hp1 | a0001 | c0001 | t0003 | g0203 | AFR | ASW | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA20129 | hp2 | a0005 | c0005 | t0001 | g0052 | AFR | ASW | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA20805 | hp1 | a0020 | c0020 | t0001 | g0003 | EUR | TSI | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA20805 | hp2 | a0002 | c0002 | t0002 | g0114 | EUR | TSI | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | GIH | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0040 | SAS | GIH | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0186 | AMR | CLM | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG01123 | hp2 | a0010 | c0012 | t0002 | g0016 | AMR | CLM | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG02109 | hp1 | a0004 | c0004 | t0001 | g0152 | AFR | ACB | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG02109 | hp2 | a0013 | c0024 | t0002 | g0120 | AFR | ACB | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG02486 | hp1 | a0003 | c0003 | t0004 | g0215 | AFR | ACB | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | ACB | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | ACB | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG03471 | hp1 | a0002 | c0007 | t0002 | g0026 | AFR | MSL | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG03471 | hp2 | a0004 | c0004 | t0001 | g0151 | AFR | MSL | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG06807 | hp1 | a0001 | c0001 | t0003 | g0220 | AFR | USA | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
HG06807 | hp2 | a0003 | c0003 | t0004 | g0211 | AFR | USA | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0178 | AFR | USA | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA20300 | hp2 | a0005 | c0005 | t0001 | g0053 | AFR | USA | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA21309 | hp1 | a0002 | c0002 | t0002 | g0080 | AFR | LWK | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | LWK | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
homoSapiens_chm13v2 | hp1 | a0002 | c0002 | t0002 | g0097 | REF | REF | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
homoSapiens_grch38 | hp1 | a0002 | c0002 | t0002 | g0133 | REF | REF | TTLL4_chr2_218705835_218760416 | TTLL4 | chr2 | 218705835 | 218760416 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:218737776
|
G | C | 12 | a0001a0004a0005others(9): Show | 140 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(137): Show |
missense_variant | MODERATE | c.100G>C | p.Glu34Gln | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 3/20 | 480/5007 | 100/3600 | 34/1199 | chr2 | 218737776 | ||
chr2:218737817
|
G | T | 2 | a0008a0015 | 4 | HG02280.hp1 HG03139.hp1 HG03516.hp1 others(1): Show |
missense_variant | MODERATE | c.141G>T | p.Gln47His | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 3/20 | 521/5007 | 141/3600 | 47/1199 | chr2 | 218737817 | ||
chr2:218738014
|
A | G | 1 | a0020 | 1 | NA20805.hp1 | missense_variant | MODERATE | c.338A>G | p.Asn113Ser | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 3/20 | 718/5007 | 338/3600 | 113/1199 | chr2 | 218738014 | ||
chr2:218738031
|
C | T | 1 | a0012 | 1 | HG01261.hp2 | missense_variant | MODERATE | c.355C>T | p.Arg119Cys | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 3/20 | 735/5007 | 355/3600 | 119/1199 | chr2 | 218738031 | ||
chr2:218738089
|
C | T | 1 | a0009 | 2 | HG02615.hp2 HG02922.hp1 |
missense_variant | MODERATE | c.413C>T | p.Ser138Leu | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 3/20 | 793/5007 | 413/3600 | 138/1199 | chr2 | 218738089 | ||
chr2:218738544
|
G | A | 1 | a0014 | 1 | NA18950.hp2 | missense_variant | MODERATE | c.868G>A | p.Ala290Thr | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 3/20 | 1248/5007 | 868/3600 | 290/1199 | chr2 | 218738544 | ||
chr2:218738731
|
C | T | 1 | a0016 | 1 | HG01109.hp2 | missense_variant | MODERATE | c.1055C>T | p.Pro352Leu | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 3/20 | 1435/5007 | 1055/3600 | 352/1199 | chr2 | 218738731 | ||
chr2:218738808
|
C | T | 1 | a0019 | 1 | HG02647.hp2 | missense_variant | MODERATE | c.1132C>T | p.Arg378Trp | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 3/20 | 1512/5007 | 1132/3600 | 378/1199 | chr2 | 218738808 | ||
chr2:218738834
|
G | T | 1 | a0011 | 2 | HG02886.hp1 HG03453.hp1 |
missense_variant | MODERATE | c.1158G>T | p.Gln386His | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 3/20 | 1538/5007 | 1158/3600 | 386/1199 | chr2 | 218738834 | ||
chr2:218738929
|
G | A | 1 | a0003 | 13 | HG02055.hp2 HG02486.hp1 HG02615.hp1 others(10): Show |
missense_variant | MODERATE | c.1253G>A | p.Arg418His | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 3/20 | 1633/5007 | 1253/3600 | 418/1199 | chr2 | 218738929 | ||
chr2:218739067
|
A | G | 1 | a0019 | 1 | HG02647.hp2 | missense_variant | MODERATE | c.1391A>G | p.Asn464Ser | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 3/20 | 1771/5007 | 1391/3600 | 464/1199 | chr2 | 218739067 | ||
chr2:218740102
|
C | T | 1 | a0006 | 4 | NA18950.hp1 NA18953.hp2 NA18963.hp1 others(1): Show |
missense_variant | MODERATE | c.1532C>T | p.Thr511Ile | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 4/20 | 1912/5007 | 1532/3600 | 511/1199 | chr2 | 218740102 | ||
chr2:218745155
|
G | A | 1 | a0007 | 3 | HG02717.hp2 HG02886.hp2 HG02976.hp1 |
missense_variant | MODERATE | c.1708G>A | p.Val570Ile | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 6/20 | 2088/5007 | 1708/3600 | 570/1199 | chr2 | 218745155 | ||
chr2:218747148
|
G | A | 1 | a0017 | 1 | HG01891.hp2 | missense_variant | MODERATE | c.2120G>A | p.Arg707His | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 9/20 | 2500/5007 | 2120/3600 | 707/1199 | chr2 | 218747148 | ||
chr2:218747171
|
C | T | 1 | a0013 | 1 | HG02109.hp2 | missense_variant | MODERATE | c.2143C>T | p.Arg715Cys | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 9/20 | 2523/5007 | 2143/3600 | 715/1199 | chr2 | 218747171 | ||
chr2:218750050
|
A | G | 1 | a0018 | 1 | HG03654.hp2 | missense_variant | MODERATE | c.2777A>G | p.Gln926Arg | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 15/20 | 3157/5007 | 2777/3600 | 926/1199 | chr2 | 218750050 | ||
chr2:218753659
|
A | G | 1 | a0010 | 2 | HG01123.hp2 HG02293.hp1 |
missense_variant | MODERATE | c.3334A>G | p.Ser1112Gly | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 19/20 | 3714/5007 | 3334/3600 | 1112/1199 | chr2 | 218753659 | ||
chr2:218754202
|
C | T | 1 | a0004 | 6 | HG02109.hp1 HG02145.hp2 HG02572.hp2 others(3): Show |
missense_variant | MODERATE | c.3413C>T | p.Thr1138Ile | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 20/20 | 3793/5007 | 3413/3600 | 1138/1199 | chr2 | 218754202 | ||
chr2:218754357
|
A | T | 1 | a0005 | 5 | HG02897.hp2 HG02922.hp2 HG03540.hp2 others(2): Show |
missense_variant | MODERATE | c.3568A>T | p.Ile1190Phe | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 20/20 | 3948/5007 | 3568/3600 | 1190/1199 | chr2 | 218754357 | ||
chr2:218754376
|
C | A | 1 | a0015 | 1 | HG02280.hp1 | missense_variant | MODERATE | c.3587C>A | p.Ala1196Asp | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 20/20 | 3967/5007 | 3587/3600 | 1196/1199 | chr2 | 218754376 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:218737787
|
G | A | 1 | a0002c0011 | 2 | HG02257.hp2 HG02451.hp1 |
synonymous_variant | LOW | c.111G>A | p.Ser37Ser | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 3/20 | 491/5007 | 111/3600 | 37/1199 | chr2 | 218737787 | ||
chr2:218738096
|
G | A | 17 | a0001c0001a0001c0016a0002c0007others(14): Show | 162 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(159): Show |
synonymous_variant | LOW | c.420G>A | p.Pro140Pro | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 3/20 | 800/5007 | 420/3600 | 140/1199 | chr2 | 218738096 | ||
chr2:218738567
|
C | T | 1 | a0002c0025 | 1 | NA19084.hp2 | synonymous_variant | LOW | c.891C>T | p.Thr297Thr | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 3/20 | 1271/5007 | 891/3600 | 297/1199 | chr2 | 218738567 | ||
chr2:218745710
|
A | G | 20 | a0001c0001a0001c0016a0002c0007others(17): Show | 166 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(163): Show |
synonymous_variant | LOW | c.1806A>G | p.Glu602Glu | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 7/20 | 2186/5007 | 1806/3600 | 602/1199 | chr2 | 218745710 | ||
chr2:218752852
|
G | A | 1 | a0002c0023 | 1 | HG02630.hp1 | synonymous_variant | LOW | c.3066G>A | p.Gln1022Gln | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 17/20 | 3446/5007 | 3066/3600 | 1022/1199 | chr2 | 218752852 | ||
chr2:218754293
|
G | A | 1 | a0001c0016 | 1 | HG02145.hp1 | synonymous_variant | LOW | c.3504G>A | p.Thr1168Thr | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 20/20 | 3884/5007 | 3504/3600 | 1168/1199 | chr2 | 218754293 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:218710835
|
C | G | 2 | a0001c0001t0012a0003c0003t0004 | 9 | HG02486.hp1 HG02615.hp1 HG02622.hp1 others(6): Show |
5_prime_UTR_variant | MODIFIER | c.-380C>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/20 | 26842 | chr2 | 218710835 | |||||
chr2:218710849
|
T | C | 7 | a0001c0001t0003a0001c0001t0012a0002c0011t0006others(4): Show | 24 | HG02055.hp2 HG02257.hp1 HG02257.hp2 others(21): Show |
5_prime_UTR_variant | MODIFIER | c.-366T>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/20 | 26828 | chr2 | 218710849 | |||||
chr2:218710964
|
C | A | 1 | a0002c0002t0008 | 1 | HG01993.hp2 | 5_prime_UTR_variant | MODIFIER | c.-251C>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/20 | 26713 | chr2 | 218710964 | |||||
chr2:218727278
|
C | T | 1 | a0002c0011t0006 | 2 | HG02257.hp2 HG02451.hp1 |
5_prime_UTR_variant | MODIFIER | c.-168C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/20 | 10399 | chr2 | 218727278 | |||||
chr2:218727320
|
T | C | 2 | a0003c0003t0004a0003c0003t0005 | 13 | HG02055.hp2 HG02486.hp1 HG02615.hp1 others(10): Show |
5_prime_UTR_variant | MODIFIER | c.-126T>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/20 | 10357 | chr2 | 218727320 | |||||
chr2:218737666
|
G | A | 1 | a0001c0001t0009 | 1 | HG02976.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-11G>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 3/20 | chr2 | 218737666 | ||||||
chr2:218754404
|
A | G | 1 | a0002c0002t0011 | 1 | HG02698.hp2 | 3_prime_UTR_variant | MODIFIER | c.*15A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 20/20 | 15 | chr2 | 218754404 | |||||
chr2:218754552
|
C | T | 1 | a0009c0014t0010 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*163C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 20/20 | 163 | chr2 | 218754552 | |||||
chr2:218754827
|
C | T | 20 | a0001c0001t0001a0001c0001t0003a0001c0001t0007others(17): Show | 142 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(139): Show |
3_prime_UTR_variant | MODIFIER | c.*438C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 20/20 | 438 | chr2 | 218754827 | |||||
chr2:218755043
|
T | C | 20 | a0001c0001t0001a0001c0001t0003a0001c0001t0007others(17): Show | 142 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(139): Show |
3_prime_UTR_variant | MODIFIER | c.*654T>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 20/20 | 654 | chr2 | 218755043 | |||||
chr2:218755100
|
G | T | 1 | a0001c0001t0007 | 2 | HG01256.hp2 HG01261.hp1 |
3_prime_UTR_variant | MODIFIER | c.*711G>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 20/20 | 711 | chr2 | 218755100 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:218711069
|
C | T | 22 | a0001c0001t0003g0024a0001c0001t0003g0202a0001c0001t0003g0203others(19): Show | 23 | HG02055.hp2 HG02257.hp1 HG02257.hp2 others(20): Show |
intron_variant | MODIFIER | c.-178+32C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218711069 | ||||||
chr2:218711120
|
T | C | 1 | a0001c0001t0009g0025 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-178+83T>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218711120 | ||||||
chr2:218711161
|
C | A | 2 | a0002c0007t0002g0009a0002c0007t0002g0026 | 3 | HG01975.hp1 HG02965.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-178+124C>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218711161 | ||||||
chr2:218711249
|
C | T | 2 | a0002c0007t0002g0009a0002c0007t0002g0026 | 3 | HG01975.hp1 HG02965.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-178+212C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218711249 | ||||||
chr2:218711323
|
A | G | 1 | a0001c0001t0009g0025 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-178+286A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218711323 | ||||||
chr2:218711400
|
C | G | 4 | a0001c0001t0003g0024a0001c0001t0003g0219a0001c0001t0003g0220others(1): Show | 4 | HG02257.hp1 HG02818.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-178+363C>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218711400 | ||||||
chr2:218711434
|
C | CT | 15 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0022others(12): Show | 21 | HG01884.hp1 HG02055.hp1 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.-178+402dupT | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr2 | 218711434 | |||||
chr2:218711486
|
C | T | 1 | a0017c0015t0001g0189 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-178+449C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218711486 | ||||||
chr2:218711772
|
A | T | 13 | a0001c0001t0012g0207a0003c0003t0004g0208a0003c0003t0004g0209others(10): Show | 14 | HG02055.hp2 HG02486.hp1 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.-178+735A>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218711772 | ||||||
chr2:218711870
|
C | CAAATCAC others(309): Show |
2 | a0001c0001t0001g0142a0001c0001t0007g0018 | 3 | HG01256.hp2 HG01261.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.-178+849_-178+850i others(318): Show |
TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr2 | 218711870 | |||||
chr2:218711870
|
C | CAAATCAC others(315): Show |
2 | a0001c0001t0001g0143a0001c0001t0001g0144 | 2 | HG01243.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-178+849_-178+850i others(324): Show |
TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr2 | 218711870 | |||||
chr2:218711870
|
C | CAAATCAC others(318): Show |
1 | a0001c0001t0001g0145 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-178+849_-178+850i others(327): Show |
TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr2 | 218711870 | |||||
chr2:218711870
|
C | CAAATCAC others(319): Show |
3 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0148 | 3 | HG02896.hp2 HG02897.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-178+849_-178+850i others(328): Show |
TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr2 | 218711870 | |||||
chr2:218711870
|
C | CAAATCAC others(323): Show |
1 | a0001c0001t0001g0149 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-178+849_-178+850i others(332): Show |
TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr2 | 218711870 | |||||
chr2:218711870
|
C | CAAATCAC others(324): Show |
5 | a0001c0001t0001g0019a0001c0001t0001g0153a0004c0004t0001g0150others(2): Show | 6 | HG00280.hp2 HG00741.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.-178+849_-178+850i others(333): Show |
TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr2 | 218711870 | |||||
chr2:218711870
|
C | CAAATCAC others(325): Show |
24 | a0001c0001t0001g0003a0001c0001t0001g0020a0001c0001t0001g0154others(21): Show | 27 | HG00140.hp1 HG00735.hp2 HG01070.hp2 others(24): Show |
intron_variant | MODIFIER | c.-178+849_-178+850i others(334): Show |
TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr2 | 218711870 | |||||
chr2:218711870
|
C | CAAATCAC others(326): Show |
15 | a0001c0001t0001g0007a0001c0001t0001g0021a0001c0001t0001g0175others(12): Show | 17 | HG00099.hp2 HG00642.hp2 HG00733.hp2 others(14): Show |
intron_variant | MODIFIER | c.-178+849_-178+850i others(335): Show |
TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr2 | 218711870 | |||||
chr2:218711870
|
C | CAAATCAC others(327): Show |
1 | a0001c0001t0001g0187 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-178+849_-178+850i others(336): Show |
TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr2 | 218711870 | |||||
chr2:218711870
|
C | CAAATCAC others(335): Show |
1 | a0001c0016t0001g0188 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-178+849_-178+850i others(344): Show |
TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr2 | 218711870 | |||||
chr2:218711880
|
A | G | 4 | a0001c0001t0001g0004a0001c0001t0001g0199a0001c0001t0001g0200others(1): Show | 7 | HG01884.hp1 HG02055.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.-178+843A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218711880 | ||||||
chr2:218711902
|
T | G | 13 | a0001c0001t0012g0207a0003c0003t0004g0208a0003c0003t0004g0209others(10): Show | 14 | HG02055.hp2 HG02486.hp1 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.-178+865T>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218711902 | ||||||
chr2:218712018
|
A | G | 9 | a0001c0001t0003g0024a0001c0001t0003g0202a0001c0001t0003g0203others(6): Show | 9 | HG02257.hp1 HG02257.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.-178+981A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218712018 | ||||||
chr2:218712026
|
C | T | 2 | a0002c0011t0006g0205a0002c0011t0006g0206 | 2 | HG02257.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.-178+989C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218712026 | ||||||
chr2:218712101
|
G | A | 2 | a0002c0002t0002g0027a0002c0002t0002g0028 | 2 | HG03654.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.-178+1064G>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218712101 | ||||||
chr2:218712243
|
C | T | 1 | a0002c0007t0002g0141 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-178+1206C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218712243 | ||||||
chr2:218712388
|
CT | C | 23 | a0001c0001t0003g0024a0001c0001t0003g0202a0001c0001t0003g0203others(20): Show | 24 | HG02055.hp2 HG02257.hp1 HG02257.hp2 others(21): Show |
intron_variant | MODIFIER | c.-178+1367delT | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr2 | 218712388 | |||||
chr2:218712422
|
C | G | 9 | a0001c0001t0003g0024a0001c0001t0003g0202a0001c0001t0003g0203others(6): Show | 9 | HG02257.hp1 HG02257.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.-178+1385C>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218712422 | ||||||
chr2:218712633
|
C | T | 1 | a0001c0001t0001g0140 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-178+1596C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218712633 | ||||||
chr2:218712650
|
A | G | 22 | a0001c0001t0003g0024a0001c0001t0003g0202a0001c0001t0003g0203others(19): Show | 23 | HG02055.hp2 HG02257.hp1 HG02257.hp2 others(20): Show |
intron_variant | MODIFIER | c.-178+1613A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218712650 | ||||||
chr2:218712702
|
T | G | 1 | a0002c0002t0002g0030 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-178+1665T>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218712702 | ||||||
chr2:218712961
|
G | A | 1 | a0001c0001t0003g0202 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-178+1924G>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218712961 | ||||||
chr2:218713025
|
G | A | 1 | a0001c0001t0001g0154 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-178+1988G>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218713025 | ||||||
chr2:218713130
|
A | G | 1 | a0001c0001t0001g0174 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-178+2093A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218713130 | ||||||
chr2:218713244
|
G | C | 2 | a0002c0002t0002g0031a0002c0002t0002g0032 | 2 | NA18990.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.-178+2207G>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218713244 | ||||||
chr2:218713321
|
A | C | 22 | a0001c0001t0003g0024a0001c0001t0003g0202a0001c0001t0003g0203others(19): Show | 23 | HG02055.hp2 HG02257.hp1 HG02257.hp2 others(20): Show |
intron_variant | MODIFIER | c.-178+2284A>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218713321 | ||||||
chr2:218713426
|
C | T | 1 | a0001c0001t0001g0154 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-178+2389C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218713426 | ||||||
chr2:218713627
|
C | G | 2 | a0011c0010t0001g0197a0011c0010t0001g0198 | 2 | HG02886.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-178+2590C>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218713627 | ||||||
chr2:218713638
|
T | G | 135 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(132): Show | 153 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.-178+2601T>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218713638 | ||||||
chr2:218714309
|
A | G | 2 | a0003c0003t0005g0023a0003c0003t0005g0218 | 3 | HG02630.hp2 HG03195.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-178+3272A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218714309 | ||||||
chr2:218714429
|
C | G | 2 | a0011c0010t0001g0197a0011c0010t0001g0198 | 2 | HG02886.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-178+3392C>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218714429 | ||||||
chr2:218714530
|
T | C | 3 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035 | 3 | NA18971.hp1 NA19012.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.-178+3493T>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218714530 | ||||||
chr2:218714622
|
T | C | 1 | a0001c0001t0001g0155 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-178+3585T>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218714622 | ||||||
chr2:218714645
|
C | G | 1 | a0002c0002t0002g0139 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.-178+3608C>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218714645 | ||||||
chr2:218714797
|
T | TG | 5 | a0001c0001t0001g0004a0001c0001t0001g0199a0001c0001t0001g0200others(2): Show | 8 | HG01884.hp1 HG02055.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.-178+3764dupG | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr2 | 218714797 | |||||
chr2:218714844
|
AACAG | A | 4 | a0002c0007t0002g0141a0007c0009t0002g0136a0007c0009t0002g0137others(1): Show | 4 | HG02717.hp2 HG02886.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.-178+3808_-178+381 others(8): Show |
TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218714844 | ||||||
chr2:218714848
|
G | A | 215 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(212): Show | 251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.-178+3811G>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218714848 | ||||||
chr2:218714912
|
AATATT | A | 21 | a0001c0001t0003g0024a0001c0001t0003g0202a0001c0001t0003g0203others(18): Show | 22 | HG02055.hp2 HG02257.hp1 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.-178+3882_-178+388 others(9): Show |
TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr2 | 218714912 | |||||
chr2:218714958
|
A | G | 1 | a0001c0001t0001g0196 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-178+3921A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218714958 | ||||||
chr2:218715019
|
AAGTT | A | 12 | a0003c0003t0004g0208a0003c0003t0004g0209a0003c0003t0004g0211others(9): Show | 13 | HG02055.hp2 HG02486.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.-178+3988_-178+399 others(8): Show |
TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr2 | 218715019 | |||||
chr2:218715185
|
CAT | C | 10 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(7): Show | 10 | NA18939.hp2 NA18968.hp2 NA18971.hp1 others(7): Show |
intron_variant | MODIFIER | c.-178+4151_-178+415 others(6): Show |
TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr2 | 218715185 | |||||
chr2:218715216
|
T | C | 1 | a0001c0001t0001g0175 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-178+4179T>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218715216 | ||||||
chr2:218715323
|
A | G | 21 | a0001c0001t0003g0024a0001c0001t0003g0202a0001c0001t0003g0203others(18): Show | 22 | HG02055.hp2 HG02257.hp1 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.-178+4286A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218715323 | ||||||
chr2:218715586
|
A | G | 1 | a0002c0002t0002g0129 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-178+4549A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218715586 | ||||||
chr2:218715690
|
C | T | 1 | a0019c0018t0001g0061 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-178+4653C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218715690 | ||||||
chr2:218715699
|
G | C | 2 | a0002c0007t0002g0009a0002c0007t0002g0026 | 3 | HG01975.hp1 HG02965.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-178+4662G>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218715699 | ||||||
chr2:218715724
|
C | T | 21 | a0001c0001t0003g0024a0001c0001t0003g0202a0001c0001t0003g0203others(18): Show | 22 | HG02055.hp2 HG02257.hp1 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.-178+4687C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218715724 | ||||||
chr2:218715947
|
G | A | 1 | a0002c0002t0002g0069 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-178+4910G>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218715947 | ||||||
chr2:218715968
|
A | G | 1 | a0002c0013t0002g0128 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-178+4931A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218715968 | ||||||
chr2:218715975
|
G | C | 2 | a0001c0001t0001g0156a0001c0001t0001g0176 | 2 | HG03669.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.-178+4938G>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218715975 | ||||||
chr2:218716099
|
C | T | 1 | a0001c0001t0001g0186 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-178+5062C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218716099 | ||||||
chr2:218716262
|
A | C | 1 | a0002c0002t0002g0069 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-178+5225A>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218716262 | ||||||
chr2:218716442
|
CAG | C | 21 | a0001c0001t0003g0024a0001c0001t0003g0202a0001c0001t0003g0203others(18): Show | 22 | HG02055.hp2 HG02257.hp1 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.-178+5407_-178+540 others(6): Show |
TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr2 | 218716442 | |||||
chr2:218716554
|
C | G | 12 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0191others(9): Show | 17 | HG01884.hp1 HG02055.hp1 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.-178+5517C>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218716554 | ||||||
chr2:218716555
|
C | T | 2 | a0002c0002t0002g0127a0007c0009t0002g0138 | 2 | HG02976.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.-178+5518C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218716555 | ||||||
chr2:218716606
|
G | A | 12 | a0003c0003t0004g0208a0003c0003t0004g0209a0003c0003t0004g0211others(9): Show | 13 | HG02055.hp2 HG02486.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.-178+5569G>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218716606 | ||||||
chr2:218716862
|
A | G | 2 | a0011c0010t0001g0197a0011c0010t0001g0198 | 2 | HG02886.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-178+5825A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218716862 | ||||||
chr2:218716920
|
G | A | 28 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0033others(25): Show | 30 | HG00558.hp2 HG00621.hp2 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.-178+5883G>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218716920 | ||||||
chr2:218716981
|
A | G | 1 | a0002c0002t0002g0126 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-178+5944A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218716981 | ||||||
chr2:218717074
|
C | G | 4 | a0006c0006t0001g0172a0006c0006t0001g0173a0006c0006t0001g0184others(1): Show | 4 | NA18950.hp1 NA18953.hp2 NA18963.hp1 others(1): Show |
intron_variant | MODIFIER | c.-178+6037C>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218717074 | ||||||
chr2:218717098
|
C | T | 21 | a0001c0001t0003g0024a0001c0001t0003g0202a0001c0001t0003g0203others(18): Show | 22 | HG02055.hp2 HG02257.hp1 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.-178+6061C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218717098 | ||||||
chr2:218717253
|
C | T | 1 | a0001c0001t0001g0068 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-178+6216C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218717253 | ||||||
chr2:218717260
|
G | C | 6 | a0001c0001t0001g0157a0004c0004t0001g0150a0004c0004t0001g0151others(3): Show | 6 | HG01884.hp2 HG02109.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.-178+6223G>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218717260 | ||||||
chr2:218717295
|
T | C | 1 | a0002c0007t0002g0026 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-178+6258T>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218717295 | ||||||
chr2:218717339
|
G | A | 1 | a0001c0001t0001g0049 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-178+6302G>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218717339 | ||||||
chr2:218717578
|
C | A | 2 | a0002c0007t0002g0009a0002c0007t0002g0026 | 3 | HG01975.hp1 HG02965.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-178+6541C>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218717578 | ||||||
chr2:218717801
|
C | CT | 4 | a0001c0001t0001g0022a0001c0001t0001g0196a0011c0010t0001g0197others(1): Show | 5 | HG02886.hp1 HG02896.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.-178+6778dupT | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr2 | 218717801 | |||||
chr2:218717885
|
G | A | 14 | a0002c0011t0006g0205a0002c0011t0006g0206a0003c0003t0004g0208others(11): Show | 15 | HG02055.hp2 HG02257.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.-178+6848G>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218717885 | ||||||
chr2:218717938
|
G | A | 14 | a0002c0011t0006g0205a0002c0011t0006g0206a0003c0003t0004g0208others(11): Show | 15 | HG02055.hp2 HG02257.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.-178+6901G>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218717938 | ||||||
chr2:218718174
|
T | C | 136 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(133): Show | 154 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(151): Show |
intron_variant | MODIFIER | c.-178+7137T>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218718174 | ||||||
chr2:218718247
|
T | G | 4 | a0002c0002t0002g0072a0002c0002t0002g0073a0002c0002t0002g0074others(1): Show | 4 | HG00280.hp1 HG01255.hp1 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.-178+7210T>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218718247 | ||||||
chr2:218718285
|
G | A | 1 | a0001c0001t0001g0187 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-178+7248G>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218718285 | ||||||
chr2:218718409
|
A | C | 1 | a0002c0002t0002g0125 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-178+7372A>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218718409 | ||||||
chr2:218718418
|
G | A | 14 | a0002c0011t0006g0205a0002c0011t0006g0206a0003c0003t0004g0208others(11): Show | 15 | HG02055.hp2 HG02257.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.-178+7381G>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218718418 | ||||||
chr2:218718533
|
C | T | 7 | a0001c0001t0003g0024a0001c0001t0003g0202a0001c0001t0003g0203others(4): Show | 7 | HG02257.hp1 HG02818.hp2 HG03516.hp2 others(4): Show |
intron_variant | MODIFIER | c.-178+7496C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218718533 | ||||||
chr2:218718542
|
C | T | 12 | a0003c0003t0004g0208a0003c0003t0004g0209a0003c0003t0004g0211others(9): Show | 13 | HG02055.hp2 HG02486.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.-178+7505C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218718542 | ||||||
chr2:218718669
|
C | G | 1 | a0001c0001t0001g0195 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-178+7632C>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218718669 | ||||||
chr2:218718789
|
C | G | 4 | a0002c0002t0002g0121a0002c0002t0002g0122a0002c0002t0002g0123others(1): Show | 4 | HG02083.hp1 HG02132.hp1 NA18940.hp2 others(1): Show |
intron_variant | MODIFIER | c.-178+7752C>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218718789 | ||||||
chr2:218718915
|
A | G | 14 | a0002c0011t0006g0205a0002c0011t0006g0206a0003c0003t0004g0208others(11): Show | 15 | HG02055.hp2 HG02257.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.-178+7878A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218718915 | ||||||
chr2:218719067
|
G | A | 12 | a0003c0003t0004g0208a0003c0003t0004g0209a0003c0003t0004g0211others(9): Show | 13 | HG02055.hp2 HG02486.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.-178+8030G>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218719067 | ||||||
chr2:218719135
|
C | T | 3 | a0008c0008t0001g0192a0008c0008t0001g0193a0008c0008t0003g0194 | 3 | HG03139.hp1 HG03516.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-178+8098C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218719135 | ||||||
chr2:218719182
|
C | T | 14 | a0002c0011t0006g0205a0002c0011t0006g0206a0003c0003t0004g0208others(11): Show | 15 | HG02055.hp2 HG02257.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.-177-8087C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218719182 | ||||||
chr2:218719300
|
G | C | 1 | a0015c0021t0001g0190 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-177-7969G>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218719300 | ||||||
chr2:218719302
|
A | G | 3 | a0002c0013t0002g0118a0002c0023t0002g0119a0013c0024t0002g0120 | 3 | HG02109.hp2 HG02451.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.-177-7967A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218719302 | ||||||
chr2:218719355
|
G | A | 1 | a0002c0002t0002g0076 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-177-7914G>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218719355 | ||||||
chr2:218719534
|
A | G | 1 | a0002c0002t0002g0117 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-177-7735A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218719534 | ||||||
chr2:218719570
|
T | TA | 39 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0019others(36): Show | 46 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(43): Show |
intron_variant | MODIFIER | c.-177-7682dupA | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr2 | 218719570 | |||||
chr2:218719570
|
TA | T | 17 | a0001c0001t0001g0048a0001c0001t0001g0060a0001c0001t0001g0148others(14): Show | 18 | HG00099.hp1 HG01943.hp2 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.-177-7682delA | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr2 | 218719570 | |||||
chr2:218720000
|
C | T | 1 | a0001c0001t0001g0142 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-177-7269C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218720000 | ||||||
chr2:218720199
|
C | T | 40 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0013others(37): Show | 43 | HG00558.hp2 HG00621.hp2 HG01109.hp1 others(40): Show |
intron_variant | MODIFIER | c.-177-7070C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218720199 | ||||||
chr2:218720252
|
G | C | 82 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(79): Show | 93 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.-177-7017G>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218720252 | ||||||
chr2:218720266
|
G | T | 2 | a0002c0011t0006g0205a0002c0011t0006g0206 | 2 | HG02257.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.-177-7003G>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218720266 | ||||||
chr2:218720530
|
C | T | 2 | a0005c0005t0001g0012a0005c0005t0001g0053 | 3 | HG02897.hp2 HG03540.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-177-6739C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218720530 | ||||||
chr2:218720668
|
C | T | 12 | a0003c0003t0004g0208a0003c0003t0004g0209a0003c0003t0004g0211others(9): Show | 13 | HG02055.hp2 HG02486.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.-177-6601C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218720668 | ||||||
chr2:218720674
|
C | CA | 9 | a0001c0001t0001g0050a0002c0002t0002g0014a0002c0002t0002g0077others(6): Show | 10 | HG02886.hp1 HG03041.hp1 HG03453.hp1 others(7): Show |
intron_variant | MODIFIER | c.-177-6578dupA | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr2 | 218720674 | |||||
chr2:218720674
|
CA | C | 6 | a0001c0001t0001g0047a0001c0001t0001g0067a0001c0001t0001g0167others(3): Show | 6 | HG00099.hp2 HG01070.hp1 HG01081.hp1 others(3): Show |
intron_variant | MODIFIER | c.-177-6578delA | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr2 | 218720674 | |||||
chr2:218720690
|
A | G | 1 | a0002c0002t0002g0113 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-177-6579A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218720690 | ||||||
chr2:218720707
|
T | C | 3 | a0001c0001t0001g0008a0001c0001t0001g0191a0001c0001t0001g0195 | 5 | HG02258.hp2 HG02486.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.-177-6562T>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218720707 | ||||||
chr2:218720756
|
G | A | 2 | a0002c0007t0002g0009a0002c0007t0002g0026 | 3 | HG01975.hp1 HG02965.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-177-6513G>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218720756 | ||||||
chr2:218720786
|
A | G | 1 | a0009c0014t0002g0111 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-177-6483A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218720786 | ||||||
chr2:218720865
|
G | A | 2 | a0001c0001t0001g0062a0001c0001t0001g0068 | 2 | NA18939.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.-177-6404G>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218720865 | ||||||
chr2:218720888
|
C | T | 12 | a0003c0003t0004g0208a0003c0003t0004g0209a0003c0003t0004g0211others(9): Show | 13 | HG02055.hp2 HG02486.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.-177-6381C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218720888 | ||||||
chr2:218721132
|
A | G | 2 | a0002c0011t0006g0205a0002c0011t0006g0206 | 2 | HG02257.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.-177-6137A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218721132 | ||||||
chr2:218721235
|
CAAT | C | 12 | a0003c0003t0004g0208a0003c0003t0004g0209a0003c0003t0004g0211others(9): Show | 13 | HG02055.hp2 HG02486.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.-177-6033_-177-603 others(7): Show |
TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218721235 | ||||||
chr2:218721235
|
CAATT | C | 133 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(130): Show | 151 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.-177-6011_-177-600 others(8): Show |
TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr2 | 218721235 | |||||
chr2:218721239
|
T | C | 12 | a0003c0003t0004g0208a0003c0003t0004g0209a0003c0003t0004g0211others(9): Show | 13 | HG02055.hp2 HG02486.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.-177-6030T>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218721239 | ||||||
chr2:218721359
|
C | T | 1 | a0002c0002t0002g0117 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-177-5910C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218721359 | ||||||
chr2:218721624
|
C | T | 1 | a0019c0018t0001g0061 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-177-5645C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218721624 | ||||||
chr2:218721667
|
A | G | 1 | a0015c0021t0001g0190 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-177-5602A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218721667 | ||||||
chr2:218721750
|
G | T | 2 | a0002c0002t0002g0017a0002c0002t0002g0110 | 3 | HG00438.hp1 HG02074.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.-177-5519G>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218721750 | ||||||
chr2:218721837
|
A | C | 2 | a0001c0001t0001g0144a0001c0001t0001g0182 | 2 | HG02559.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-177-5432A>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218721837 | ||||||
chr2:218721867
|
A | T | 1 | a0010c0012t0002g0109 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-177-5402A>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218721867 | ||||||
chr2:218721899
|
G | A | 1 | a0001c0001t0001g0149 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-177-5370G>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218721899 | ||||||
chr2:218721962
|
TA | T | 13 | a0001c0001t0001g0008a0001c0001t0001g0022a0001c0001t0001g0060others(10): Show | 16 | HG01943.hp1 HG02258.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.-177-5296delA | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr2 | 218721962 | |||||
chr2:218722022
|
C | T | 4 | a0005c0005t0001g0012a0005c0005t0001g0051a0005c0005t0001g0052others(1): Show | 5 | HG02897.hp2 HG02922.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-177-5247C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218722022 | ||||||
chr2:218722356
|
C | CT | 119 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(116): Show | 136 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.-177-4901dupT | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr2 | 218722356 | |||||
chr2:218722356
|
C | CTT | 6 | a0001c0001t0001g0144a0001c0001t0001g0146a0001c0001t0001g0147others(3): Show | 6 | HG02145.hp1 HG02559.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.-177-4902_-177-490 others(6): Show |
TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr2 | 218722356 | |||||
chr2:218722568
|
A | G | 125 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(122): Show | 142 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.-177-4701A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218722568 | ||||||
chr2:218722617
|
G | A | 12 | a0001c0001t0001g0004a0001c0001t0001g0199a0001c0001t0001g0200others(9): Show | 15 | HG01884.hp1 HG02055.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.-177-4652G>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218722617 | ||||||
chr2:218722698
|
A | G | 1 | a0002c0002t0002g0108 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.-177-4571A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218722698 | ||||||
chr2:218722754
|
C | T | 1 | a0002c0002t0002g0107 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-177-4515C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218722754 | ||||||
chr2:218723015
|
A | G | 2 | a0002c0011t0006g0205a0002c0011t0006g0206 | 2 | HG02257.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.-177-4254A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218723015 | ||||||
chr2:218723051
|
T | C | 1 | a0002c0002t0002g0080 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-177-4218T>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218723051 | ||||||
chr2:218723411
|
A | G | 123 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(120): Show | 140 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.-177-3858A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218723411 | ||||||
chr2:218723974
|
A | G | 125 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(122): Show | 142 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.-177-3295A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218723974 | ||||||
chr2:218724167
|
G | T | 137 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(134): Show | 155 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.-177-3102G>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218724167 | ||||||
chr2:218724245
|
T | A | 13 | a0001c0001t0001g0004a0001c0001t0001g0199a0001c0001t0001g0200others(10): Show | 16 | HG00558.hp1 HG01884.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.-177-3024T>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218724245 | ||||||
chr2:218724441
|
C | T | 123 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(120): Show | 140 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.-177-2828C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218724441 | ||||||
chr2:218724452
|
T | C | 125 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(122): Show | 142 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.-177-2817T>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218724452 | ||||||
chr2:218724525
|
A | G | 1 | a0001c0001t0001g0165 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-177-2744A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218724525 | ||||||
chr2:218724535
|
C | T | 1 | a0008c0008t0003g0194 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-177-2734C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218724535 | ||||||
chr2:218724557
|
T | A | 125 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(122): Show | 142 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.-177-2712T>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218724557 | ||||||
chr2:218724699
|
A | C | 12 | a0001c0001t0001g0004a0001c0001t0001g0199a0001c0001t0001g0200others(9): Show | 15 | HG01884.hp1 HG02055.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.-177-2570A>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218724699 | ||||||
chr2:218724871
|
T | C | 124 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(121): Show | 141 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.-177-2398T>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218724871 | ||||||
chr2:218724872
|
A | C | 1 | a0001c0001t0001g0059 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-177-2397A>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218724872 | ||||||
chr2:218724901
|
G | A | 1 | a0002c0002t0002g0082 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-177-2368G>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218724901 | ||||||
chr2:218725052
|
A | G | 1 | a0002c0002t0002g0106 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.-177-2217A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218725052 | ||||||
chr2:218725077
|
T | G | 3 | a0001c0001t0001g0142a0001c0001t0001g0153a0001c0001t0007g0018 | 4 | HG00741.hp2 HG01256.hp2 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.-177-2192T>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218725077 | ||||||
chr2:218725107
|
A | G | 4 | a0002c0007t0002g0141a0007c0009t0002g0136a0007c0009t0002g0137others(1): Show | 4 | HG02717.hp2 HG02886.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.-177-2162A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218725107 | ||||||
chr2:218725396
|
G | GT | 7 | a0001c0001t0001g0046a0001c0001t0001g0066a0001c0001t0001g0196others(4): Show | 7 | HG00621.hp2 HG03098.hp2 HG03654.hp1 others(4): Show |
intron_variant | MODIFIER | c.-177-1863dupT | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr2 | 218725396 | |||||
chr2:218725415
|
A | G | 1 | a0002c0002t0002g0104 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-177-1854A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218725415 | ||||||
chr2:218725461
|
G | C | 1 | a0002c0002t0002g0083 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-177-1808G>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218725461 | ||||||
chr2:218725544
|
A | G | 2 | a0002c0011t0006g0205a0002c0011t0006g0206 | 2 | HG02257.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.-177-1725A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218725544 | ||||||
chr2:218725546
|
A | G | 12 | a0001c0001t0001g0004a0001c0001t0001g0199a0001c0001t0001g0200others(9): Show | 15 | HG01884.hp1 HG02055.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.-177-1723A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218725546 | ||||||
chr2:218725584
|
C | T | 1 | a0002c0002t0002g0103 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-177-1685C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218725584 | ||||||
chr2:218725602
|
C | T | 7 | a0001c0001t0001g0003a0001c0001t0001g0021a0001c0001t0001g0143others(4): Show | 9 | HG00733.hp2 HG01070.hp2 HG01081.hp2 others(6): Show |
intron_variant | MODIFIER | c.-177-1667C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218725602 | ||||||
chr2:218725625
|
G | A | 2 | a0002c0002t0002g0084a0002c0002t0002g0085 | 2 | HG00140.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.-177-1644G>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218725625 | ||||||
chr2:218725696
|
T | C | 125 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(122): Show | 142 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.-177-1573T>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218725696 | ||||||
chr2:218726148
|
A | G | 125 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(122): Show | 142 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.-177-1121A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218726148 | ||||||
chr2:218726152
|
C | G | 11 | a0001c0001t0001g0008a0001c0001t0001g0022a0001c0001t0001g0191others(8): Show | 14 | HG02258.hp2 HG02280.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.-177-1117C>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218726152 | ||||||
chr2:218726481
|
C | T | 1 | a0001c0016t0001g0188 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-177-788C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218726481 | ||||||
chr2:218726498
|
C | T | 2 | a0002c0011t0006g0205a0002c0011t0006g0206 | 2 | HG02257.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.-177-771C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218726498 | ||||||
chr2:218726568
|
C | T | 7 | a0001c0001t0001g0008a0001c0001t0001g0191a0001c0001t0001g0195others(4): Show | 9 | HG02258.hp2 HG02280.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.-177-701C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218726568 | ||||||
chr2:218726759
|
G | A | 3 | a0001c0001t0001g0144a0001c0001t0001g0182a0001c0016t0001g0188 | 3 | HG02145.hp1 HG02559.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-177-510G>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218726759 | ||||||
chr2:218726898
|
G | A | 2 | a0003c0003t0005g0023a0003c0003t0005g0218 | 3 | HG02630.hp2 HG03195.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-177-371G>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218726898 | ||||||
chr2:218727008
|
C | T | 10 | a0003c0003t0004g0208a0003c0003t0004g0209a0003c0003t0004g0211others(7): Show | 10 | HG02055.hp2 HG02486.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.-177-261C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218727008 | ||||||
chr2:218727060
|
C | T | 1 | a0003c0003t0004g0217 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-177-209C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218727060 | ||||||
chr2:218727261
|
A | G | 2 | a0002c0002t0002g0123a0002c0002t0002g0124 | 2 | HG02083.hp1 NA19087.hp1 |
splice_region_variant&intron_variant | LOW | c.-177-8A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 1/19 | chr2 | 218727261 | ||||||
chr2:218727395
|
A | G | 1 | a0002c0002t0002g0102 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-99+48A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218727395 | ||||||
chr2:218727419
|
C | G | 28 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0033others(25): Show | 30 | HG00558.hp2 HG00621.hp2 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.-99+72C>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218727419 | ||||||
chr2:218727503
|
C | T | 3 | a0001c0001t0003g0202a0001c0001t0003g0203a0001c0001t0003g0204 | 3 | NA19030.hp2 NA19240.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-99+156C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218727503 | ||||||
chr2:218727504
|
A | G | 127 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(124): Show | 145 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.-99+157A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218727504 | ||||||
chr2:218727599
|
G | A | 125 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(122): Show | 142 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.-99+252G>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218727599 | ||||||
chr2:218727864
|
T | C | 2 | a0002c0002t0002g0017a0002c0002t0002g0110 | 3 | HG00438.hp1 HG02074.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.-99+517T>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218727864 | ||||||
chr2:218727908
|
C | A | 2 | a0002c0007t0002g0009a0002c0007t0002g0026 | 3 | HG01975.hp1 HG02965.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-99+561C>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218727908 | ||||||
chr2:218727925
|
A | T | 1 | a0002c0002t0002g0125 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-99+578A>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218727925 | ||||||
chr2:218728136
|
A | G | 2 | a0002c0002t0002g0030a0012c0026t0002g0101 | 2 | HG01261.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.-99+789A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218728136 | ||||||
chr2:218728480
|
T | C | 137 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(134): Show | 155 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.-99+1133T>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218728480 | ||||||
chr2:218728508
|
C | T | 2 | a0002c0011t0006g0205a0002c0011t0006g0206 | 2 | HG02257.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.-99+1161C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218728508 | ||||||
chr2:218728606
|
G | A | 23 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0033others(20): Show | 25 | HG00558.hp2 HG00621.hp2 HG01891.hp2 others(22): Show |
intron_variant | MODIFIER | c.-99+1259G>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218728606 | ||||||
chr2:218728701
|
C | T | 2 | a0002c0011t0006g0205a0002c0011t0006g0206 | 2 | HG02257.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.-99+1354C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218728701 | ||||||
chr2:218728921
|
A | AT | 32 | a0002c0002t0002g0016a0002c0002t0002g0027a0002c0002t0002g0028others(29): Show | 34 | HG01123.hp2 HG01192.hp2 HG01975.hp1 others(31): Show |
intron_variant | MODIFIER | c.-99+1594dupT | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr2 | 218728921 | |||||
chr2:218728942
|
G | T | 14 | a0001c0001t0001g0065a0001c0001t0001g0156a0001c0001t0001g0157others(11): Show | 14 | HG01192.hp1 HG01884.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.-99+1595G>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218728942 | ||||||
chr2:218728943
|
GC | G | 8 | a0001c0001t0001g0065a0001c0001t0001g0156a0001c0001t0001g0164others(5): Show | 8 | HG01192.hp1 HG02257.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.-99+1597delC | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218728943 | ||||||
chr2:218728944
|
C | G | 6 | a0001c0001t0001g0157a0001c0016t0001g0188a0004c0004t0001g0151others(3): Show | 6 | HG01884.hp2 HG02109.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.-99+1597C>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218728944 | ||||||
chr2:218728944
|
CGG | C | 105 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(102): Show | 122 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.-99+1605_-99+1606d others(4): Show |
TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr2 | 218728944 | |||||
chr2:218728945
|
G | A | 1 | a0002c0002t0002g0069 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-99+1598G>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218728945 | ||||||
chr2:218728945
|
G | C | 6 | a0001c0001t0001g0157a0001c0016t0001g0188a0004c0004t0001g0151others(3): Show | 6 | HG01884.hp2 HG02109.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.-99+1598G>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218728945 | ||||||
chr2:218728946
|
G | C | 8 | a0001c0001t0001g0065a0001c0001t0001g0156a0001c0001t0001g0164others(5): Show | 8 | HG01192.hp1 HG02257.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.-99+1599G>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218728946 | ||||||
chr2:218728950
|
G | A | 1 | a0002c0002t0002g0086 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-99+1603G>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218728950 | ||||||
chr2:218728952
|
G | A | 1 | a0001c0001t0001g0063 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.-99+1605G>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218728952 | ||||||
chr2:218728986
|
G | T | 2 | a0002c0011t0006g0205a0002c0011t0006g0206 | 2 | HG02257.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.-99+1639G>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218728986 | ||||||
chr2:218728987
|
C | T | 2 | a0002c0011t0006g0205a0002c0011t0006g0206 | 2 | HG02257.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.-99+1640C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218728987 | ||||||
chr2:218729497
|
C | G | 6 | a0001c0001t0001g0144a0001c0001t0001g0146a0001c0001t0001g0147others(3): Show | 6 | HG02145.hp1 HG02559.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.-99+2150C>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218729497 | ||||||
chr2:218729511
|
A | C | 1 | a0001c0001t0001g0140 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-99+2164A>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218729511 | ||||||
chr2:218729689
|
A | T | 2 | a0001c0001t0001g0070a0001c0001t0001g0071 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-99+2342A>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218729689 | ||||||
chr2:218729747
|
T | TAAA | 4 | a0001c0001t0001g0008a0001c0001t0001g0067a0001c0001t0001g0191others(1): Show | 6 | HG02258.hp2 HG02486.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.-99+2400_-99+2401i others(5): Show |
TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218729747 | ||||||
chr2:218729747
|
TTAAAAAA others(3): Show |
T | 2 | a0008c0008t0001g0192a0008c0008t0003g0194 | 2 | HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-99+2401_-99+2410d others(12): Show |
TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218729747 | ||||||
chr2:218729747
|
TTAAAAAA others(9): Show |
T | 1 | a0001c0001t0001g0035 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.-99+2401_-99+2416d others(18): Show |
TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218729747 | ||||||
chr2:218729748
|
T | A | 7 | a0001c0001t0001g0008a0001c0001t0001g0033a0001c0001t0001g0034others(4): Show | 9 | HG02258.hp2 HG02280.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.-99+2401T>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218729748 | ||||||
chr2:218729748
|
T | TAAAA | 12 | a0001c0001t0001g0013a0001c0001t0001g0036a0001c0001t0001g0046others(9): Show | 13 | HG00621.hp2 HG01243.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.-99+2412_-99+2415d others(6): Show |
TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr2 | 218729748 | |||||
chr2:218729748
|
T | TAAAAA | 11 | a0001c0001t0001g0010a0001c0001t0001g0038a0001c0001t0001g0039others(8): Show | 12 | HG00558.hp2 HG02074.hp1 HG02083.hp2 others(9): Show |
intron_variant | MODIFIER | c.-99+2411_-99+2415d others(7): Show |
TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr2 | 218729748 | |||||
chr2:218729748
|
T | TAAAAAAA | 5 | a0001c0001t0001g0037a0001c0001t0001g0043a0001c0001t0001g0044others(2): Show | 5 | HG02559.hp1 HG03130.hp1 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.-99+2409_-99+2415d others(9): Show |
TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr2 | 218729748 | |||||
chr2:218729756
|
A | AAC | 12 | a0003c0003t0004g0208a0003c0003t0004g0209a0003c0003t0004g0211others(9): Show | 13 | HG02055.hp2 HG02486.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.-99+2410_-99+2411i others(4): Show |
TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr2 | 218729756 | |||||
chr2:218729756
|
A | C | 1 | a0002c0002t0002g0126 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-99+2409A>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218729756 | ||||||
chr2:218729757
|
A | C | 1 | a0002c0002t0002g0097 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-99+2410A>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218729757 | ||||||
chr2:218729759
|
A | AAC | 6 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0149others(3): Show | 6 | HG00323.hp2 HG01168.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.-99+2413_-99+2414i others(4): Show |
TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr2 | 218729759 | |||||
chr2:218729759
|
A | AC | 63 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(60): Show | 73 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.-99+2412_-99+2413i others(3): Show |
TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218729759 | ||||||
chr2:218729759
|
A | C | 1 | a0001c0001t0001g0147 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-99+2412A>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218729759 | ||||||
chr2:218729759
|
A | G | 1 | a0002c0002t0002g0102 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-99+2412A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218729759 | ||||||
chr2:218729760
|
A | C | 12 | a0003c0003t0004g0208a0003c0003t0004g0209a0003c0003t0004g0211others(9): Show | 13 | HG02055.hp2 HG02486.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.-99+2413A>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218729760 | ||||||
chr2:218729762
|
A | C | 1 | a0002c0025t0002g0096 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-99+2415A>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218729762 | ||||||
chr2:218729762
|
AC | A | 3 | a0001c0001t0009g0025a0002c0011t0006g0205a0002c0011t0006g0206 | 3 | HG02257.hp2 HG02451.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.-99+2416delC | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218729762 | ||||||
chr2:218729763
|
C | A | 137 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(134): Show | 155 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.-99+2416C>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218729763 | ||||||
chr2:218729764
|
A | C | 12 | a0003c0003t0004g0208a0003c0003t0004g0209a0003c0003t0004g0211others(9): Show | 13 | HG02055.hp2 HG02486.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.-99+2417A>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218729764 | ||||||
chr2:218729766
|
A | AAC | 4 | a0005c0005t0001g0012a0005c0005t0001g0051a0005c0005t0001g0052others(1): Show | 5 | HG02897.hp2 HG02922.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-99+2420_-99+2421i others(4): Show |
TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr2 | 218729766 | |||||
chr2:218729766
|
A | C | 70 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(67): Show | 80 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(77): Show |
intron_variant | MODIFIER | c.-99+2419A>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218729766 | ||||||
chr2:218729767
|
A | C | 2 | a0002c0011t0006g0205a0002c0011t0006g0206 | 2 | HG02257.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.-99+2420A>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218729767 | ||||||
chr2:218729769
|
A | C | 4 | a0005c0005t0001g0012a0005c0005t0001g0051a0005c0005t0001g0052others(1): Show | 5 | HG02897.hp2 HG02922.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-99+2422A>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218729769 | ||||||
chr2:218729947
|
T | C | 1 | a0017c0015t0001g0189 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-99+2600T>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218729947 | ||||||
chr2:218730054
|
A | G | 2 | a0011c0010t0001g0197a0011c0010t0001g0198 | 2 | HG02886.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-99+2707A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218730054 | ||||||
chr2:218730249
|
C | T | 1 | a0001c0016t0001g0188 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-99+2902C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218730249 | ||||||
chr2:218730278
|
C | T | 125 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(122): Show | 142 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.-99+2931C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218730278 | ||||||
chr2:218730309
|
T | TA | 4 | a0002c0002t0002g0084a0002c0002t0002g0085a0002c0002t0002g0087others(1): Show | 4 | HG00140.hp2 HG03834.hp2 NA18965.hp1 others(1): Show |
intron_variant | MODIFIER | c.-99+2962_-99+2963i others(3): Show |
TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218730309 | ||||||
chr2:218730309
|
TCC | T | 32 | a0002c0002t0002g0002a0002c0002t0002g0005a0002c0002t0002g0006others(29): Show | 40 | HG00099.hp1 HG00558.hp1 HG00597.hp1 others(37): Show |
intron_variant | MODIFIER | c.-99+2963_-99+2964d others(4): Show |
TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218730309 | ||||||
chr2:218730309
|
TCCA | T | 16 | a0002c0002t0002g0001a0002c0002t0002g0027a0002c0002t0002g0028others(13): Show | 23 | HG00280.hp1 HG00323.hp1 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.-99+2963_-99+2965d others(5): Show |
TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218730309 | ||||||
chr2:218730309
|
TCCAA | T | 4 | a0002c0002t0002g0095a0002c0002t0002g0115a0009c0014t0002g0111others(1): Show | 4 | HG01943.hp2 HG02615.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.-99+2963_-99+2966d others(6): Show |
TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218730309 | ||||||
chr2:218730309
|
TCCAAA | T | 3 | a0002c0007t0002g0009a0002c0007t0002g0026a0007c0009t0002g0136 | 4 | HG01975.hp1 HG02886.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.-99+2963_-99+2967d others(7): Show |
TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218730309 | ||||||
chr2:218730309
|
TCCAAAA | T | 3 | a0002c0007t0002g0141a0007c0009t0002g0137a0007c0009t0002g0138 | 3 | HG02717.hp2 HG02976.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-99+2963_-99+2968d others(8): Show |
TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218730309 | ||||||
chr2:218730309
|
TCCAAAAA others(3): Show |
T | 2 | a0002c0002t0002g0017a0002c0011t0006g0206 | 3 | HG02074.hp2 HG02257.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.-99+2963_-99+2972d others(12): Show |
TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218730309 | ||||||
chr2:218730309
|
TCCAAAAA others(4): Show |
T | 1 | a0002c0011t0006g0205 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-99+2963_-99+2973d others(13): Show |
TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218730309 | ||||||
chr2:218730309
|
TCCAAAAA others(5): Show |
T | 1 | a0003c0003t0004g0209 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-99+2963_-99+2974d others(14): Show |
TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218730309 | ||||||
chr2:218730309
|
TCCAAAAA others(6): Show |
T | 1 | a0003c0003t0004g0216 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-99+2963_-99+2975d others(15): Show |
TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218730309 | ||||||
chr2:218730309
|
TCCAAAAA others(11): Show |
T | 4 | a0001c0001t0001g0066a0001c0001t0001g0175a0008c0008t0003g0194others(1): Show | 4 | HG01192.hp1 HG02886.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.-99+2963_-99+2980d others(20): Show |
TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218730309 | ||||||
chr2:218730309
|
TCCAAAAA others(12): Show |
T | 113 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(110): Show | 128 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.-99+2963_-99+2981d others(21): Show |
TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218730309 | ||||||
chr2:218730309
|
TCCAAAAA others(13): Show |
T | 6 | a0001c0001t0001g0013a0001c0001t0001g0022a0001c0001t0001g0049others(3): Show | 8 | HG02280.hp2 HG02896.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.-99+2963_-99+2982d others(22): Show |
TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218730309 | ||||||
chr2:218730310
|
C | A | 34 | a0002c0002t0002g0015a0002c0002t0002g0016a0002c0002t0002g0029others(31): Show | 36 | HG00438.hp2 HG00621.hp1 HG01070.hp1 others(33): Show |
intron_variant | MODIFIER | c.-99+2963C>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218730310 | ||||||
chr2:218730311
|
C | A | 4 | a0002c0002t0002g0084a0002c0002t0002g0085a0002c0002t0002g0087others(1): Show | 4 | HG00140.hp2 HG03834.hp2 NA18965.hp1 others(1): Show |
intron_variant | MODIFIER | c.-99+2964C>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218730311 | ||||||
chr2:218730311
|
C | CAAA | 4 | a0003c0003t0004g0208a0003c0003t0004g0217a0003c0003t0005g0023others(1): Show | 5 | HG02630.hp2 HG02818.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.-99+3000_-99+3002d others(5): Show |
TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr2 | 218730311 | |||||
chr2:218730311
|
CA | C | 20 | a0002c0002t0002g0015a0002c0002t0002g0016a0002c0002t0002g0029others(17): Show | 21 | HG00438.hp2 HG00621.hp1 HG01070.hp1 others(18): Show |
intron_variant | MODIFIER | c.-99+3002delA | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr2 | 218730311 | |||||
chr2:218730313
|
A | C | 32 | a0002c0002t0002g0002a0002c0002t0002g0005a0002c0002t0002g0006others(29): Show | 40 | HG00099.hp1 HG00558.hp1 HG00597.hp1 others(37): Show |
intron_variant | MODIFIER | c.-99+2966A>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218730313 | ||||||
chr2:218730314
|
A | C | 16 | a0002c0002t0002g0001a0002c0002t0002g0027a0002c0002t0002g0028others(13): Show | 23 | HG00280.hp1 HG00323.hp1 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.-99+2967A>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218730314 | ||||||
chr2:218730315
|
A | C | 4 | a0002c0002t0002g0095a0002c0002t0002g0115a0009c0014t0002g0111others(1): Show | 4 | HG01943.hp2 HG02615.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.-99+2968A>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218730315 | ||||||
chr2:218730316
|
A | C | 3 | a0002c0007t0002g0009a0002c0007t0002g0026a0007c0009t0002g0136 | 4 | HG01975.hp1 HG02886.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.-99+2969A>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218730316 | ||||||
chr2:218730317
|
A | C | 3 | a0002c0007t0002g0141a0007c0009t0002g0137a0007c0009t0002g0138 | 3 | HG02717.hp2 HG02976.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-99+2970A>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218730317 | ||||||
chr2:218730320
|
A | C | 1 | a0002c0002t0002g0110 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-99+2973A>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218730320 | ||||||
chr2:218730321
|
A | C | 2 | a0002c0002t0002g0017a0002c0011t0006g0206 | 3 | HG02074.hp2 HG02257.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.-99+2974A>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218730321 | ||||||
chr2:218730322
|
A | C | 1 | a0002c0011t0006g0205 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-99+2975A>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218730322 | ||||||
chr2:218730323
|
A | C | 1 | a0003c0003t0004g0209 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-99+2976A>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218730323 | ||||||
chr2:218730324
|
A | C | 1 | a0003c0003t0004g0216 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-99+2977A>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218730324 | ||||||
chr2:218730329
|
A | C | 4 | a0001c0001t0001g0066a0001c0001t0001g0175a0008c0008t0003g0194others(1): Show | 4 | HG01192.hp1 HG02886.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.-99+2982A>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218730329 | ||||||
chr2:218730330
|
A | C | 113 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(110): Show | 128 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.-99+2983A>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218730330 | ||||||
chr2:218730331
|
A | C | 6 | a0001c0001t0001g0013a0001c0001t0001g0022a0001c0001t0001g0049others(3): Show | 8 | HG02280.hp2 HG02896.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.-99+2984A>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218730331 | ||||||
chr2:218730342
|
A | G | 2 | a0002c0011t0006g0205a0002c0011t0006g0206 | 2 | HG02257.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.-99+2995A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218730342 | ||||||
chr2:218730346
|
A | G | 4 | a0005c0005t0001g0012a0005c0005t0001g0051a0005c0005t0001g0052others(1): Show | 5 | HG02897.hp2 HG02922.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-99+2999A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218730346 | ||||||
chr2:218730437
|
G | A | 123 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(120): Show | 140 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.-99+3090G>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218730437 | ||||||
chr2:218730463
|
A | G | 125 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(122): Show | 142 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.-99+3116A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218730463 | ||||||
chr2:218730508
|
A | G | 4 | a0002c0007t0002g0141a0007c0009t0002g0136a0007c0009t0002g0137others(1): Show | 4 | HG02717.hp2 HG02886.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.-99+3161A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218730508 | ||||||
chr2:218730532
|
T | A | 7 | a0001c0001t0001g0157a0004c0004t0001g0150a0004c0004t0001g0151others(4): Show | 7 | HG01884.hp2 HG02109.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.-99+3185T>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218730532 | ||||||
chr2:218730730
|
CA | C | 6 | a0001c0001t0001g0144a0001c0001t0001g0146a0001c0001t0001g0147others(3): Show | 6 | HG02145.hp1 HG02559.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.-99+3385delA | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr2 | 218730730 | |||||
chr2:218730784
|
A | G | 123 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(120): Show | 140 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.-99+3437A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218730784 | ||||||
chr2:218730825
|
C | T | 1 | a0002c0002t0002g0114 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-99+3478C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218730825 | ||||||
chr2:218730895
|
A | C | 4 | a0005c0005t0001g0012a0005c0005t0001g0051a0005c0005t0001g0052others(1): Show | 5 | HG02897.hp2 HG02922.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-99+3548A>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218730895 | ||||||
chr2:218730906
|
C | A | 1 | a0001c0001t0001g0149 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-99+3559C>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218730906 | ||||||
chr2:218730987
|
T | C | 125 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(122): Show | 142 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.-99+3640T>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218730987 | ||||||
chr2:218731072
|
G | A | 2 | a0002c0007t0002g0009a0002c0007t0002g0026 | 3 | HG01975.hp1 HG02965.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-99+3725G>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218731072 | ||||||
chr2:218731121
|
A | AAT | 8 | a0001c0001t0001g0157a0002c0011t0006g0205a0002c0011t0006g0206others(5): Show | 8 | HG01884.hp2 HG02109.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.-99+3775_-99+3776i others(4): Show |
TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr2 | 218731121 | |||||
chr2:218731121
|
A | AT | 117 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(114): Show | 134 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.-99+3774_-99+3775i others(3): Show |
TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218731121 | ||||||
chr2:218731209
|
G | A | 70 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(67): Show | 80 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(77): Show |
intron_variant | MODIFIER | c.-99+3862G>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218731209 | ||||||
chr2:218731236
|
C | T | 1 | a0002c0002t0002g0092 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-99+3889C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218731236 | ||||||
chr2:218731384
|
G | C | 137 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(134): Show | 155 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.-99+4037G>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218731384 | ||||||
chr2:218731598
|
G | A | 38 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0013others(35): Show | 41 | HG00558.hp2 HG00621.hp2 HG01109.hp1 others(38): Show |
intron_variant | MODIFIER | c.-99+4251G>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218731598 | ||||||
chr2:218731730
|
C | T | 4 | a0002c0007t0002g0141a0007c0009t0002g0136a0007c0009t0002g0137others(1): Show | 4 | HG02717.hp2 HG02886.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.-99+4383C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218731730 | ||||||
chr2:218731787
|
T | C | 1 | a0002c0002t0002g0088 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-99+4440T>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218731787 | ||||||
chr2:218732298
|
A | G | 2 | a0002c0011t0006g0205a0002c0011t0006g0206 | 2 | HG02257.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.-99+4951A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218732298 | ||||||
chr2:218732393
|
G | A | 2 | a0001c0001t0001g0179a0001c0001t0001g0195 | 2 | HG01175.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-99+5046G>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218732393 | ||||||
chr2:218732462
|
T | C | 125 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(122): Show | 142 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.-99+5115T>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218732462 | ||||||
chr2:218732536
|
G | A | 3 | a0001c0001t0001g0008a0001c0001t0001g0191a0001c0001t0001g0195 | 5 | HG02258.hp2 HG02486.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.-98-5043G>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218732536 | ||||||
chr2:218732653
|
C | T | 6 | a0001c0001t0001g0144a0001c0001t0001g0146a0001c0001t0001g0147others(3): Show | 6 | HG02145.hp1 HG02559.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.-98-4926C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218732653 | ||||||
chr2:218732724
|
C | T | 1 | a0002c0002t0002g0083 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-98-4855C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218732724 | ||||||
chr2:218733237
|
A | G | 123 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(120): Show | 140 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.-98-4342A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218733237 | ||||||
chr2:218733318
|
A | T | 123 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(120): Show | 140 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.-98-4261A>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218733318 | ||||||
chr2:218733350
|
G | A | 1 | a0002c0013t0002g0128 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-98-4229G>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218733350 | ||||||
chr2:218733355
|
G | A | 1 | a0002c0013t0002g0128 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-98-4224G>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218733355 | ||||||
chr2:218733369
|
G | A | 123 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(120): Show | 140 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.-98-4210G>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218733369 | ||||||
chr2:218733372
|
C | T | 124 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(121): Show | 141 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.-98-4207C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218733372 | ||||||
chr2:218733873
|
A | G | 1 | a0001c0001t0001g0066 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.-98-3706A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218733873 | ||||||
chr2:218734054
|
G | T | 38 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0013others(35): Show | 41 | HG00558.hp2 HG00621.hp2 HG01109.hp1 others(38): Show |
intron_variant | MODIFIER | c.-98-3525G>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218734054 | ||||||
chr2:218734545
|
G | A | 123 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(120): Show | 140 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.-98-3034G>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218734545 | ||||||
chr2:218734583
|
G | A | 1 | a0015c0021t0001g0190 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-98-2996G>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218734583 | ||||||
chr2:218734593
|
C | T | 1 | a0002c0013t0002g0118 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-98-2986C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218734593 | ||||||
chr2:218734713
|
T | C | 1 | a0001c0001t0001g0157 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-98-2866T>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218734713 | ||||||
chr2:218734758
|
G | A | 12 | a0003c0003t0004g0208a0003c0003t0004g0209a0003c0003t0004g0211others(9): Show | 13 | HG02055.hp2 HG02486.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.-98-2821G>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218734758 | ||||||
chr2:218734761
|
A | G | 2 | a0002c0011t0006g0205a0002c0011t0006g0206 | 2 | HG02257.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.-98-2818A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218734761 | ||||||
chr2:218735034
|
A | G | 1 | a0002c0002t0002g0114 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-98-2545A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218735034 | ||||||
chr2:218735345
|
T | G | 5 | a0004c0004t0001g0150a0004c0004t0001g0151a0004c0004t0001g0152others(2): Show | 5 | HG02109.hp1 HG02145.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.-98-2234T>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218735345 | ||||||
chr2:218735468
|
G | T | 2 | a0002c0011t0006g0205a0002c0011t0006g0206 | 2 | HG02257.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.-98-2111G>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218735468 | ||||||
chr2:218735514
|
C | T | 1 | a0002c0002t0002g0099 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.-98-2065C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218735514 | ||||||
chr2:218735593
|
A | T | 137 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(134): Show | 155 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.-98-1986A>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218735593 | ||||||
chr2:218735712
|
A | G | 125 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(122): Show | 142 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.-98-1867A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218735712 | ||||||
chr2:218735727
|
C | T | 2 | a0002c0011t0006g0205a0002c0011t0006g0206 | 2 | HG02257.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.-98-1852C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218735727 | ||||||
chr2:218735742
|
G | A | 3 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0060 | 3 | HG01891.hp1 HG02965.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-98-1837G>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218735742 | ||||||
chr2:218735967
|
C | CT | 46 | a0001c0001t0001g0022a0001c0001t0001g0034a0001c0001t0001g0036others(43): Show | 52 | HG00140.hp2 HG00438.hp1 HG00438.hp2 others(49): Show |
intron_variant | MODIFIER | c.-98-1589dupT | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr2 | 218735967 | |||||
chr2:218735967
|
C | CTT | 9 | a0001c0001t0001g0046a0002c0011t0006g0205a0002c0011t0006g0206others(6): Show | 10 | HG00621.hp2 HG02055.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.-98-1590_-98-1589d others(4): Show |
TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr2 | 218735967 | |||||
chr2:218735967
|
CT | C | 58 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(55): Show | 71 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.-98-1589delT | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr2 | 218735967 | |||||
chr2:218735967
|
CTT | C | 6 | a0001c0001t0001g0157a0001c0001t0001g0167a0001c0001t0001g0199others(3): Show | 6 | HG01884.hp2 HG02145.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.-98-1590_-98-1589d others(4): Show |
TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr2 | 218735967 | |||||
chr2:218736126
|
C | CACCAT | 12 | a0003c0003t0004g0208a0003c0003t0004g0209a0003c0003t0004g0211others(9): Show | 13 | HG02055.hp2 HG02486.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.-98-1449_-98-1445d others(7): Show |
TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr2 | 218736126 | |||||
chr2:218736147
|
G | C | 12 | a0003c0003t0004g0208a0003c0003t0004g0209a0003c0003t0004g0211others(9): Show | 13 | HG02055.hp2 HG02486.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.-98-1432G>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218736147 | ||||||
chr2:218736276
|
C | T | 1 | a0001c0001t0001g0055 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-98-1303C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218736276 | ||||||
chr2:218736277
|
G | A | 1 | a0002c0002t0002g0093 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-98-1302G>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218736277 | ||||||
chr2:218736425
|
G | C | 12 | a0003c0003t0004g0208a0003c0003t0004g0209a0003c0003t0004g0211others(9): Show | 13 | HG02055.hp2 HG02486.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.-98-1154G>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218736425 | ||||||
chr2:218736527
|
G | A | 2 | a0001c0001t0001g0062a0001c0001t0001g0068 | 2 | NA18939.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.-98-1052G>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218736527 | ||||||
chr2:218736591
|
C | CT | 46 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0019others(43): Show | 53 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(50): Show |
intron_variant | MODIFIER | c.-98-985dupT | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr2 | 218736591 | |||||
chr2:218736603
|
A | G | 1 | a0002c0002t0002g0122 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-98-976A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218736603 | ||||||
chr2:218736609
|
C | T | 1 | a0001c0001t0001g0171 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.-98-970C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218736609 | ||||||
chr2:218736669
|
A | G | 125 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(122): Show | 142 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.-98-910A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218736669 | ||||||
chr2:218736849
|
C | CT | 108 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(105): Show | 121 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.-98-714dupT | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr2 | 218736849 | |||||
chr2:218736849
|
C | CTT | 17 | a0001c0001t0001g0004a0001c0001t0001g0041a0001c0001t0001g0047others(14): Show | 21 | HG01884.hp1 HG02055.hp1 HG02074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-98-715_-98-714dup others(2): Show |
TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr2 | 218736849 | |||||
chr2:218737030
|
C | T | 2 | a0002c0011t0006g0205a0002c0011t0006g0206 | 2 | HG02257.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.-98-549C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218737030 | ||||||
chr2:218737135
|
G | T | 2 | a0002c0002t0002g0027a0002c0002t0002g0028 | 2 | HG03654.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.-98-444G>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218737135 | ||||||
chr2:218737403
|
G | C | 1 | a0015c0021t0001g0190 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-98-176G>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218737403 | ||||||
chr2:218737515
|
C | T | 1 | a0002c0002t0002g0094 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.-98-64C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218737515 | ||||||
chr2:218737533
|
G | A | 2 | a0002c0007t0002g0009a0002c0007t0002g0026 | 3 | HG01975.hp1 HG02965.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-98-46G>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218737533 | ||||||
chr2:218737540
|
T | A | 1 | a0005c0005t0001g0051 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-98-39T>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 2/19 | chr2 | 218737540 | ||||||
chr2:218739209
|
A | G | 1 | a0002c0002t0002g0124 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1487+46A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 3/19 | chr2 | 218739209 | ||||||
chr2:218739462
|
C | T | 1 | a0001c0001t0001g0157 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1487+299C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 3/19 | chr2 | 218739462 | ||||||
chr2:218739603
|
T | C | 58 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(55): Show | 68 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.1487+440T>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 3/19 | chr2 | 218739603 | ||||||
chr2:218740395
|
G | A | 123 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(120): Show | 140 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.1598-126G>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 4/19 | chr2 | 218740395 | ||||||
chr2:218740809
|
C | T | 4 | a0001c0001t0003g0024a0001c0001t0003g0219a0001c0001t0003g0220others(1): Show | 4 | HG02257.hp1 HG02818.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1661+225C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 5/19 | chr2 | 218740809 | ||||||
chr2:218740816
|
G | A | 1 | a0001c0001t0001g0157 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1661+232G>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 5/19 | chr2 | 218740816 | ||||||
chr2:218740847
|
C | T | 12 | a0001c0001t0001g0144a0001c0001t0001g0146a0001c0001t0001g0147others(9): Show | 12 | HG01884.hp2 HG02109.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.1661+263C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 5/19 | chr2 | 218740847 | ||||||
chr2:218740852
|
C | A | 1 | a0002c0002t0002g0093 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1661+268C>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 5/19 | chr2 | 218740852 | ||||||
chr2:218740870
|
C | G | 38 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0013others(35): Show | 41 | HG00558.hp2 HG00621.hp2 HG01109.hp1 others(38): Show |
intron_variant | MODIFIER | c.1661+286C>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 5/19 | chr2 | 218740870 | ||||||
chr2:218740918
|
T | C | 123 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(120): Show | 140 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.1661+334T>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 5/19 | chr2 | 218740918 | ||||||
chr2:218740937
|
G | A | 12 | a0001c0001t0001g0144a0001c0001t0001g0146a0001c0001t0001g0147others(9): Show | 12 | HG01884.hp2 HG02109.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.1661+353G>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 5/19 | chr2 | 218740937 | ||||||
chr2:218741206
|
G | A | 125 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(122): Show | 142 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.1661+622G>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 5/19 | chr2 | 218741206 | ||||||
chr2:218741219
|
A | C | 1 | a0001c0001t0001g0166 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1661+635A>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 5/19 | chr2 | 218741219 | ||||||
chr2:218741329
|
C | T | 125 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(122): Show | 142 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.1661+745C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 5/19 | chr2 | 218741329 | ||||||
chr2:218741355
|
G | C | 1 | a0003c0003t0004g0211 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1661+771G>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 5/19 | chr2 | 218741355 | ||||||
chr2:218741408
|
A | G | 3 | a0002c0002t0002g0029a0002c0002t0002g0079a0002c0002t0002g0134 | 3 | HG02698.hp1 NA18977.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.1661+824A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 5/19 | chr2 | 218741408 | ||||||
chr2:218741454
|
C | T | 135 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(132): Show | 153 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.1661+870C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 5/19 | chr2 | 218741454 | ||||||
chr2:218741495
|
T | G | 137 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(134): Show | 155 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.1661+911T>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 5/19 | chr2 | 218741495 | ||||||
chr2:218741518
|
A | G | 1 | a0001c0001t0009g0025 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1661+934A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 5/19 | chr2 | 218741518 | ||||||
chr2:218741537
|
G | T | 1 | a0001c0001t0001g0157 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1661+953G>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 5/19 | chr2 | 218741537 | ||||||
chr2:218741729
|
T | G | 1 | a0001c0001t0001g0038 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1661+1145T>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 5/19 | chr2 | 218741729 | ||||||
chr2:218741815
|
C | A | 123 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(120): Show | 140 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.1661+1231C>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 5/19 | chr2 | 218741815 | ||||||
chr2:218742025
|
A | G | 28 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0033others(25): Show | 30 | HG00558.hp2 HG00621.hp2 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.1661+1441A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 5/19 | chr2 | 218742025 | ||||||
chr2:218742129
|
A | T | 15 | a0001c0001t0001g0008a0001c0001t0001g0022a0001c0001t0001g0191others(12): Show | 19 | HG02258.hp2 HG02280.hp1 HG02486.hp2 others(16): Show |
intron_variant | MODIFIER | c.1661+1545A>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 5/19 | chr2 | 218742129 | ||||||
chr2:218742153
|
G | A | 1 | a0002c0002t0002g0116 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1661+1569G>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 5/19 | chr2 | 218742153 | ||||||
chr2:218742208
|
A | G | 137 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(134): Show | 155 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.1661+1624A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 5/19 | chr2 | 218742208 | ||||||
chr2:218742236
|
C | T | 1 | a0001c0001t0001g0040 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1661+1652C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 5/19 | chr2 | 218742236 | ||||||
chr2:218742434
|
T | C | 1 | a0001c0001t0001g0040 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1661+1850T>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 5/19 | chr2 | 218742434 | ||||||
chr2:218742638
|
C | T | 1 | a0002c0002t0002g0092 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1661+2054C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 5/19 | chr2 | 218742638 | ||||||
chr2:218742677
|
A | G | 2 | a0002c0011t0006g0205a0002c0011t0006g0206 | 2 | HG02257.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.1661+2093A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 5/19 | chr2 | 218742677 | ||||||
chr2:218742688
|
A | G | 7 | a0001c0001t0001g0008a0001c0001t0001g0191a0001c0001t0001g0195others(4): Show | 9 | HG02258.hp2 HG02280.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.1661+2104A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 5/19 | chr2 | 218742688 | ||||||
chr2:218742750
|
A | G | 1 | a0001c0001t0001g0059 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1661+2166A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 5/19 | chr2 | 218742750 | ||||||
chr2:218743096
|
A | G | 123 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(120): Show | 140 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.1662-2013A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 5/19 | chr2 | 218743096 | ||||||
chr2:218743144
|
C | CA | 12 | a0003c0003t0004g0208a0003c0003t0004g0209a0003c0003t0004g0211others(9): Show | 13 | HG02055.hp2 HG02486.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.1662-1954dupA | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr2 | 218743144 | |||||
chr2:218743268
|
G | T | 2 | a0002c0011t0006g0205a0002c0011t0006g0206 | 2 | HG02257.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.1662-1841G>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 5/19 | chr2 | 218743268 | ||||||
chr2:218743363
|
C | G | 1 | a0001c0001t0001g0191 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1662-1746C>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 5/19 | chr2 | 218743363 | ||||||
chr2:218743420
|
G | A | 2 | a0002c0011t0006g0205a0002c0011t0006g0206 | 2 | HG02257.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.1662-1689G>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 5/19 | chr2 | 218743420 | ||||||
chr2:218743574
|
A | G | 11 | a0001c0001t0001g0008a0001c0001t0001g0022a0001c0001t0001g0191others(8): Show | 14 | HG02258.hp2 HG02280.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.1662-1535A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 5/19 | chr2 | 218743574 | ||||||
chr2:218743678
|
G | GTTTTGT | 12 | a0003c0003t0004g0208a0003c0003t0004g0209a0003c0003t0004g0211others(9): Show | 13 | HG02055.hp2 HG02486.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.1662-1420_1662-141 others(10): Show |
TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr2 | 218743678 | |||||
chr2:218743829
|
G | A | 1 | a0002c0002t0002g0093 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1662-1280G>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 5/19 | chr2 | 218743829 | ||||||
chr2:218743854
|
T | A | 1 | a0001c0001t0001g0054 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1662-1255T>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 5/19 | chr2 | 218743854 | ||||||
chr2:218743931
|
A | G | 123 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(120): Show | 140 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.1662-1178A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 5/19 | chr2 | 218743931 | ||||||
chr2:218744139
|
T | A | 1 | a0003c0003t0004g0212 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1662-970T>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 5/19 | chr2 | 218744139 | ||||||
chr2:218744140
|
C | A | 1 | a0003c0003t0004g0212 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1662-969C>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 5/19 | chr2 | 218744140 | ||||||
chr2:218744246
|
A | T | 1 | a0002c0002t0002g0089 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1662-863A>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 5/19 | chr2 | 218744246 | ||||||
chr2:218744391
|
T | C | 1 | a0002c0002t0002g0091 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1662-718T>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 5/19 | chr2 | 218744391 | ||||||
chr2:218744439
|
T | G | 125 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(122): Show | 142 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.1662-670T>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 5/19 | chr2 | 218744439 | ||||||
chr2:218744717
|
T | C | 123 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(120): Show | 140 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.1662-392T>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 5/19 | chr2 | 218744717 | ||||||
chr2:218744961
|
C | T | 1 | a0001c0001t0001g0162 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1662-148C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 5/19 | chr2 | 218744961 | ||||||
chr2:218745039
|
G | A | 28 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0033others(25): Show | 30 | HG00558.hp2 HG00621.hp2 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.1662-70G>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 5/19 | chr2 | 218745039 | ||||||
chr2:218745053
|
G | A | 123 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(120): Show | 140 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.1662-56G>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 5/19 | chr2 | 218745053 | ||||||
chr2:218745272
|
G | C | 125 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(122): Show | 142 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.1786+39G>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 6/19 | chr2 | 218745272 | ||||||
chr2:218745395
|
A | C | 10 | a0003c0003t0004g0208a0003c0003t0004g0209a0003c0003t0004g0211others(7): Show | 10 | HG02055.hp2 HG02486.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.1786+162A>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 6/19 | chr2 | 218745395 | ||||||
chr2:218745560
|
G | C | 1 | a0002c0023t0002g0119 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1787-131G>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 6/19 | chr2 | 218745560 | ||||||
chr2:218745599
|
G | A | 137 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(134): Show | 155 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.1787-92G>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 6/19 | chr2 | 218745599 | ||||||
chr2:218745930
|
A | T | 1 | a0002c0002t0002g0083 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1897+129A>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 7/19 | chr2 | 218745930 | ||||||
chr2:218745995
|
A | T | 3 | a0001c0001t0001g0039a0001c0001t0001g0046a0001c0001t0001g0047 | 3 | HG00558.hp2 HG00621.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.1898-160A>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 7/19 | chr2 | 218745995 | ||||||
chr2:218746005
|
C | T | 38 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0013others(35): Show | 41 | HG00558.hp2 HG00621.hp2 HG01109.hp1 others(38): Show |
intron_variant | MODIFIER | c.1898-150C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 7/19 | chr2 | 218746005 | ||||||
chr2:218746292
|
A | T | 1 | a0001c0001t0001g0054 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1974+61A>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 8/19 | chr2 | 218746292 | ||||||
chr2:218746711
|
T | G | 123 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(120): Show | 140 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.1975-292T>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 8/19 | chr2 | 218746711 | ||||||
chr2:218746742
|
A | G | 1 | a0005c0005t0001g0053 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1975-261A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 8/19 | chr2 | 218746742 | ||||||
chr2:218747431
|
CCTT | C | 2 | a0002c0007t0002g0009a0002c0007t0002g0026 | 3 | HG01975.hp1 HG02965.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.2249+63_2249+65del others(3): Show |
TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr2 | 218747431 | |||||
chr2:218747559
|
A | G | 125 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(122): Show | 142 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.2250-38A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 10/19 | chr2 | 218747559 | ||||||
chr2:218747904
|
G | A | 1 | a0001c0001t0001g0199 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2378+179G>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 11/19 | chr2 | 218747904 | ||||||
chr2:218748524
|
A | G | 38 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0013others(35): Show | 41 | HG00558.hp2 HG00621.hp2 HG01109.hp1 others(38): Show |
intron_variant | MODIFIER | c.2501+297A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 12/19 | chr2 | 218748524 | ||||||
chr2:218748526
|
G | A | 123 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(120): Show | 140 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.2501+299G>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 12/19 | chr2 | 218748526 | ||||||
chr2:218748587
|
G | A | 1 | a0010c0012t0002g0109 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.2502-249G>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 12/19 | chr2 | 218748587 | ||||||
chr2:218748654
|
C | CA | 95 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(92): Show | 108 | HG00280.hp2 HG00323.hp2 HG00558.hp1 others(105): Show |
intron_variant | MODIFIER | c.2502-161dupA | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr2 | 218748654 | |||||
chr2:218748654
|
C | CAA | 14 | a0001c0001t0001g0142a0001c0001t0001g0147a0001c0001t0001g0148others(11): Show | 15 | HG02257.hp2 HG02280.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.2502-162_2502-161d others(4): Show |
TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr2 | 218748654 | |||||
chr2:218748959
|
G | A | 4 | a0005c0005t0001g0012a0005c0005t0001g0051a0005c0005t0001g0052others(1): Show | 5 | HG02897.hp2 HG02922.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.2600+25G>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 13/19 | chr2 | 218748959 | ||||||
chr2:218749049
|
A | G | 38 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0013others(35): Show | 41 | HG00558.hp2 HG00621.hp2 HG01109.hp1 others(38): Show |
intron_variant | MODIFIER | c.2600+115A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 13/19 | chr2 | 218749049 | ||||||
chr2:218749143
|
C | T | 15 | a0001c0001t0001g0008a0001c0001t0001g0022a0001c0001t0001g0191others(12): Show | 19 | HG02258.hp2 HG02280.hp1 HG02486.hp2 others(16): Show |
intron_variant | MODIFIER | c.2601-110C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 13/19 | chr2 | 218749143 | ||||||
chr2:218749467
|
CT | C | 11 | a0001c0001t0001g0008a0001c0001t0001g0022a0001c0001t0001g0191others(8): Show | 14 | HG02258.hp2 HG02280.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.2735+95delT | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr2 | 218749467 | |||||
chr2:218749480
|
T | C | 2 | a0002c0011t0006g0205a0002c0011t0006g0206 | 2 | HG02257.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.2735+93T>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 14/19 | chr2 | 218749480 | ||||||
chr2:218749483
|
C | T | 2 | a0002c0011t0006g0205a0002c0011t0006g0206 | 2 | HG02257.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.2735+96C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 14/19 | chr2 | 218749483 | ||||||
chr2:218749550
|
C | T | 1 | a0002c0002t0002g0086 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2735+163C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 14/19 | chr2 | 218749550 | ||||||
chr2:218749706
|
A | G | 4 | a0002c0007t0002g0141a0007c0009t0002g0136a0007c0009t0002g0137others(1): Show | 4 | HG02717.hp2 HG02886.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.2736-303A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 14/19 | chr2 | 218749706 | ||||||
chr2:218749718
|
C | T | 12 | a0003c0003t0004g0208a0003c0003t0004g0209a0003c0003t0004g0211others(9): Show | 13 | HG02055.hp2 HG02486.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.2736-291C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 14/19 | chr2 | 218749718 | ||||||
chr2:218749756
|
C | T | 1 | a0001c0001t0001g0165 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.2736-253C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 14/19 | chr2 | 218749756 | ||||||
chr2:218749935
|
C | G | 8 | a0003c0003t0004g0208a0003c0003t0004g0209a0003c0003t0004g0211others(5): Show | 8 | HG02486.hp1 HG02615.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.2736-74C>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 14/19 | chr2 | 218749935 | ||||||
chr2:218749936
|
C | T | 1 | a0001c0001t0001g0161 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2736-73C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 14/19 | chr2 | 218749936 | ||||||
chr2:218750541
|
T | TA | 29 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0033others(26): Show | 31 | HG00558.hp2 HG00621.hp2 HG01891.hp2 others(28): Show |
intron_variant | MODIFIER | c.2873+407dupA | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 15/19 | INFO_REALIGN_3_PRIME | chr2 | 218750541 | |||||
chr2:218750618
|
C | T | 2 | a0002c0007t0002g0009a0002c0007t0002g0026 | 3 | HG01975.hp1 HG02965.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.2873+472C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 15/19 | chr2 | 218750618 | ||||||
chr2:218750867
|
A | AT | 12 | a0001c0001t0001g0008a0001c0001t0001g0191a0001c0001t0001g0195others(9): Show | 15 | HG02258.hp2 HG02280.hp1 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.2873+731dupT | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 15/19 | INFO_REALIGN_3_PRIME | chr2 | 218750867 | |||||
chr2:218751051
|
T | C | 2 | a0002c0011t0006g0205a0002c0011t0006g0206 | 2 | HG02257.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.2874-653T>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 15/19 | chr2 | 218751051 | ||||||
chr2:218751076
|
A | G | 1 | a0002c0002t0011g0131 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2874-628A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 15/19 | chr2 | 218751076 | ||||||
chr2:218751107
|
C | G | 2 | a0003c0003t0005g0210a0003c0003t0005g0214 | 2 | HG02055.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.2874-597C>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 15/19 | chr2 | 218751107 | ||||||
chr2:218751132
|
CT | C | 5 | a0004c0004t0001g0150a0004c0004t0001g0151a0004c0004t0001g0152others(2): Show | 5 | HG02109.hp1 HG02145.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.2874-569delT | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 15/19 | INFO_REALIGN_3_PRIME | chr2 | 218751132 | |||||
chr2:218751155
|
CTCATGTT others(8): Show |
C | 108 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(105): Show | 121 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.2874-546_2874-532d others(17): Show |
TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 15/19 | INFO_REALIGN_3_PRIME | chr2 | 218751155 | |||||
chr2:218751187
|
G | T | 147 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(144): Show | 166 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.2874-517G>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 15/19 | chr2 | 218751187 | ||||||
chr2:218751245
|
T | C | 2 | a0002c0002t0002g0076a0002c0002t0002g0090 | 2 | HG00733.hp1 HG00735.hp1 |
intron_variant | MODIFIER | c.2874-459T>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 15/19 | chr2 | 218751245 | ||||||
chr2:218751279
|
C | A | 108 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(105): Show | 121 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.2874-425C>A | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 15/19 | chr2 | 218751279 | ||||||
chr2:218751640
|
A | G | 1 | a0002c0002t0002g0093 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2874-64A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 15/19 | chr2 | 218751640 | ||||||
chr2:218751887
|
C | CT | 4 | a0005c0005t0001g0012a0005c0005t0001g0051a0005c0005t0001g0052others(1): Show | 5 | HG02897.hp2 HG02922.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.2976+92dupT | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr2 | 218751887 | |||||
chr2:218751887
|
C | CTT | 62 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0011others(59): Show | 68 | HG00558.hp2 HG00621.hp2 HG01109.hp1 others(65): Show |
intron_variant | MODIFIER | c.2976+91_2976+92dup others(2): Show |
TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr2 | 218751887 | |||||
chr2:218751887
|
C | CTTT | 46 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0019others(43): Show | 53 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(50): Show |
intron_variant | MODIFIER | c.2976+90_2976+92dup others(3): Show |
TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr2 | 218751887 | |||||
chr2:218751904
|
C | CT | 75 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(72): Show | 86 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(83): Show |
intron_variant | MODIFIER | c.2976+103dupT | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr2 | 218751904 | |||||
chr2:218751904
|
C | CTT | 8 | a0001c0001t0001g0160a0001c0001t0001g0165a0001c0001t0001g0180others(5): Show | 8 | HG00642.hp2 HG01993.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.2976+102_2976+103d others(4): Show |
TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr2 | 218751904 | |||||
chr2:218751910
|
C | T | 124 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(121): Show | 141 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.2976+104C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 16/19 | chr2 | 218751910 | ||||||
chr2:218751910
|
CT | C | 22 | a0002c0007t0002g0009a0002c0007t0002g0026a0002c0007t0002g0141others(19): Show | 24 | HG01975.hp1 HG02055.hp2 HG02109.hp2 others(21): Show |
intron_variant | MODIFIER | c.2976+118delT | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr2 | 218751910 | |||||
chr2:218751958
|
A | G | 108 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(105): Show | 121 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.2976+152A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 16/19 | chr2 | 218751958 | ||||||
chr2:218752150
|
C | T | 38 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0013others(35): Show | 41 | HG00558.hp2 HG00621.hp2 HG01109.hp1 others(38): Show |
intron_variant | MODIFIER | c.2976+344C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 16/19 | chr2 | 218752150 | ||||||
chr2:218752199
|
C | G | 11 | a0001c0001t0001g0008a0001c0001t0001g0022a0001c0001t0001g0191others(8): Show | 14 | HG02258.hp2 HG02280.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.2976+393C>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 16/19 | chr2 | 218752199 | ||||||
chr2:218752316
|
T | C | 1 | a0002c0002t0002g0108 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.2977-447T>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 16/19 | chr2 | 218752316 | ||||||
chr2:218752372
|
C | T | 1 | a0017c0015t0001g0189 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2977-391C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 16/19 | chr2 | 218752372 | ||||||
chr2:218752470
|
A | C | 4 | a0005c0005t0001g0012a0005c0005t0001g0051a0005c0005t0001g0052others(1): Show | 5 | HG02897.hp2 HG02922.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.2977-293A>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 16/19 | chr2 | 218752470 | ||||||
chr2:218753093
|
A | G | 1 | a0001c0001t0001g0161 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.3188-22A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 17/19 | chr2 | 218753093 | ||||||
chr2:218753452
|
C | T | 1 | a0001c0001t0001g0200 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3259-132C>T | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 18/19 | chr2 | 218753452 | ||||||
chr2:218753514
|
A | C | 137 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(134): Show | 155 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.3259-70A>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 18/19 | chr2 | 218753514 | ||||||
chr2:218753774
|
T | G | 123 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0007others(120): Show | 140 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.3344+105T>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 19/19 | chr2 | 218753774 | ||||||
chr2:218753807
|
A | G | 2 | a0001c0001t0001g0156a0001c0001t0001g0176 | 2 | HG03669.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.3344+138A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 19/19 | chr2 | 218753807 | ||||||
chr2:218753974
|
A | G | 1 | a0001c0001t0001g0059 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.3345-160A>G | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 19/19 | chr2 | 218753974 | ||||||
chr2:218753985
|
T | C | 46 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0019others(43): Show | 53 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(50): Show |
intron_variant | MODIFIER | c.3345-149T>C | TTLL4 | ENSG00000135912.11 | transcript | ENST00000392102.6 | protein_coding | 19/19 | chr2 | 218753985 |