geneid | 4286 |
---|---|
ensemblid | ENSG00000187098.18 |
hgncid | 7105 |
symbol | MITF |
name | melanocyte inducing transcription factor |
refseq_nuc | NM_000248.4 |
refseq_prot | NP_000239.1 |
ensembl_nuc | ENST00000394351.9 |
ensembl_prot | ENSP00000377880.3 |
mane_status | MANE Plus Clinical |
chr | chr3 |
start | 69936592 |
end | 69968332 |
strand | + |
ver | v1.2 |
region | chr3:69936592-69968332 |
region5000 | chr3:69931592-69973332 |
regionname0 | MITF_chr3_69936592_69968332 |
regionname5000 | MITF_chr3_69931592_69973332 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 419 | 381 | 94 | 67 | 170 | 12 | 36 | 136 | MITF_chr3_69931592_69973332 | MITF | copy fasta | chr3 | 69931592 | 69973332 |
a0002 | 0/0 | 419 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | MITF_chr3_69931592_69973332 | MITF | copy fasta | chr3 | 69931592 | 69973332 |
a0003 | 0/0 | 419 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | copy fasta | chr3 | 69931592 | 69973332 |
a0004 | 0/0 | 419 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | copy fasta | chr3 | 69931592 | 69973332 |
a0005 | 0/0 | 419 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | copy fasta | chr3 | 69931592 | 69973332 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1260 | 375 | 91 | 67 | 170 | 12 | 33 | MITF_chr3_69931592_69973332 | MITF | copy fasta | chr3 | 69931592 | 69973332 |
c0002 | 0/0 | 1260 | 3 | 0 | 0 | 0 | 0 | 3 | MITF_chr3_69931592_69973332 | MITF | copy fasta | chr3 | 69931592 | 69973332 |
c0003 | 0/0 | 1260 | 2 | 0 | 0 | 2 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | copy fasta | chr3 | 69931592 | 69973332 |
c0004 | 0/0 | 1260 | 2 | 2 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | copy fasta | chr3 | 69931592 | 69973332 |
c0005 | 0/0 | 1260 | 1 | 0 | 1 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | copy fasta | chr3 | 69931592 | 69973332 |
c0006 | 0/0 | 1260 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | copy fasta | chr3 | 69931592 | 69973332 |
c0007 | 0/0 | 1260 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | copy fasta | chr3 | 69931592 | 69973332 |
c0008 | 0/0 | 1260 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | copy fasta | chr3 | 69931592 | 69973332 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 3216 | 198 | 29 | 41 | 99 | 7 | 20 | MITF_chr3_69931592_69973332 | MITF | copy fasta | chr3 | 69931592 | 69973332 |
t0002 | 0/0 | 3218 | 107 | 31 | 15 | 48 | 4 | 9 | MITF_chr3_69931592_69973332 | MITF | copy fasta | chr3 | 69931592 | 69973332 |
t0003 | 0/0 | 3216 | 27 | 23 | 4 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | copy fasta | chr3 | 69931592 | 69973332 |
t0004 | 0/0 | 3216 | 14 | 1 | 2 | 10 | 0 | 1 | MITF_chr3_69931592_69973332 | MITF | copy fasta | chr3 | 69931592 | 69973332 |
t0005 | 0/0 | 3216 | 8 | 1 | 0 | 7 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | copy fasta | chr3 | 69931592 | 69973332 |
t0006 | 0/0 | 3216 | 5 | 0 | 2 | 1 | 0 | 2 | MITF_chr3_69931592_69973332 | MITF | copy fasta | chr3 | 69931592 | 69973332 |
t0007 | 0/0 | 3216 | 4 | 0 | 0 | 4 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | copy fasta | chr3 | 69931592 | 69973332 |
t0008 | 0/0 | 3216 | 4 | 0 | 0 | 4 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | copy fasta | chr3 | 69931592 | 69973332 |
t0009 | 0/0 | 3216 | 3 | 0 | 1 | 0 | 0 | 2 | MITF_chr3_69931592_69973332 | MITF | copy fasta | chr3 | 69931592 | 69973332 |
t0010 | 0/0 | 3216 | 2 | 2 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | copy fasta | chr3 | 69931592 | 69973332 |
t0011 | 0/0 | 3216 | 2 | 2 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | copy fasta | chr3 | 69931592 | 69973332 |
t0012 | 0/0 | 3216 | 2 | 2 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | copy fasta | chr3 | 69931592 | 69973332 |
t0013 | 0/0 | 3216 | 2 | 0 | 2 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | copy fasta | chr3 | 69931592 | 69973332 |
t0014 | 0/0 | 3218 | 1 | 0 | 0 | 0 | 0 | 1 | MITF_chr3_69931592_69973332 | MITF | copy fasta | chr3 | 69931592 | 69973332 |
t0015 | 0/0 | 3218 | 1 | 0 | 1 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | copy fasta | chr3 | 69931592 | 69973332 |
t0016 | 0/0 | 3218 | 1 | 0 | 0 | 0 | 0 | 1 | MITF_chr3_69931592_69973332 | MITF | copy fasta | chr3 | 69931592 | 69973332 |
t0017 | 0/0 | 3216 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | copy fasta | chr3 | 69931592 | 69973332 |
t0018 | 0/0 | 3216 | 1 | 0 | 0 | 0 | 1 | 0 | MITF_chr3_69931592_69973332 | MITF | copy fasta | chr3 | 69931592 | 69973332 |
t0019 | 0/0 | 3216 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | copy fasta | chr3 | 69931592 | 69973332 |
t0020 | 0/0 | 3216 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | copy fasta | chr3 | 69931592 | 69973332 |
t0021 | 0/0 | 3216 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | copy fasta | chr3 | 69931592 | 69973332 |
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 | 0 | 9 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0002 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0003 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0004 | 0/0 | 5 | 0 | 1 | 0 | 0 | 4 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0005 | 1/0 | 4 | 0 | 2 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0007 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0009 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0011 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0016 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0027 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0279 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0280 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0281 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0296 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0297 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0302 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1260 | 375 | 91 | 67 | 170 | 12 | 33 | MITF_chr3_69931592_69973332 | MITF | copy fasta | chr3 | 69931592 | 69973332 |
a0001c0002 | 0/0 | 1260 | 3 | 0 | 0 | 0 | 0 | 3 | MITF_chr3_69931592_69973332 | MITF | copy fasta | chr3 | 69931592 | 69973332 |
a0001c0004 | 0/0 | 1260 | 2 | 2 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | copy fasta | chr3 | 69931592 | 69973332 |
a0001c0008 | 0/0 | 1260 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | copy fasta | chr3 | 69931592 | 69973332 |
a0002c0003 | 0/0 | 1260 | 2 | 0 | 0 | 2 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | copy fasta | chr3 | 69931592 | 69973332 |
a0003c0006 | 0/0 | 1260 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | copy fasta | chr3 | 69931592 | 69973332 |
a0004c0005 | 0/0 | 1260 | 1 | 0 | 1 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | copy fasta | chr3 | 69931592 | 69973332 |
a0005c0007 | 0/0 | 1260 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | copy fasta | chr3 | 69931592 | 69973332 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 4475 | 192 | 28 | 40 | 95 | 7 | 20 | MITF_chr3_69931592_69973332 | MITF | copy fasta | chr3 | 69931592 | 69973332 |
a0001c0001t0002 | 0/0 | 4477 | 104 | 31 | 15 | 48 | 4 | 6 | MITF_chr3_69931592_69973332 | MITF | copy fasta | chr3 | 69931592 | 69973332 |
a0001c0001t0003 | 0/0 | 4475 | 27 | 23 | 4 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | copy fasta | chr3 | 69931592 | 69973332 |
a0001c0001t0004 | 0/0 | 4475 | 14 | 1 | 2 | 10 | 0 | 1 | MITF_chr3_69931592_69973332 | MITF | copy fasta | chr3 | 69931592 | 69973332 |
a0001c0001t0005 | 0/0 | 4475 | 8 | 1 | 0 | 7 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | copy fasta | chr3 | 69931592 | 69973332 |
a0001c0001t0006 | 0/0 | 4475 | 5 | 0 | 2 | 1 | 0 | 2 | MITF_chr3_69931592_69973332 | MITF | copy fasta | chr3 | 69931592 | 69973332 |
a0001c0001t0007 | 0/0 | 4475 | 4 | 0 | 0 | 4 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | copy fasta | chr3 | 69931592 | 69973332 |
a0001c0001t0008 | 0/0 | 4475 | 4 | 0 | 0 | 4 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | copy fasta | chr3 | 69931592 | 69973332 |
a0001c0001t0009 | 0/0 | 4475 | 3 | 0 | 1 | 0 | 0 | 2 | MITF_chr3_69931592_69973332 | MITF | copy fasta | chr3 | 69931592 | 69973332 |
a0001c0001t0010 | 0/0 | 4475 | 2 | 2 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | copy fasta | chr3 | 69931592 | 69973332 |
a0001c0001t0011 | 0/0 | 4475 | 2 | 2 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | copy fasta | chr3 | 69931592 | 69973332 |
a0001c0001t0013 | 0/0 | 4475 | 2 | 0 | 2 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | copy fasta | chr3 | 69931592 | 69973332 |
a0001c0001t0014 | 0/0 | 4477 | 1 | 0 | 0 | 0 | 0 | 1 | MITF_chr3_69931592_69973332 | MITF | copy fasta | chr3 | 69931592 | 69973332 |
a0001c0001t0015 | 0/0 | 4477 | 1 | 0 | 1 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | copy fasta | chr3 | 69931592 | 69973332 |
a0001c0001t0016 | 0/0 | 4477 | 1 | 0 | 0 | 0 | 0 | 1 | MITF_chr3_69931592_69973332 | MITF | copy fasta | chr3 | 69931592 | 69973332 |
a0001c0001t0017 | 0/0 | 4475 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | copy fasta | chr3 | 69931592 | 69973332 |
a0001c0001t0018 | 0/0 | 4475 | 1 | 0 | 0 | 0 | 1 | 0 | MITF_chr3_69931592_69973332 | MITF | copy fasta | chr3 | 69931592 | 69973332 |
a0001c0001t0019 | 0/0 | 4475 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | copy fasta | chr3 | 69931592 | 69973332 |
a0001c0001t0020 | 0/0 | 4475 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | copy fasta | chr3 | 69931592 | 69973332 |
a0001c0001t0021 | 0/0 | 4475 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | copy fasta | chr3 | 69931592 | 69973332 |
a0001c0002t0002 | 0/0 | 4477 | 3 | 0 | 0 | 0 | 0 | 3 | MITF_chr3_69931592_69973332 | MITF | copy fasta | chr3 | 69931592 | 69973332 |
a0001c0004t0012 | 0/0 | 4475 | 2 | 2 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | copy fasta | chr3 | 69931592 | 69973332 |
a0001c0008t0001 | 0/0 | 4475 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | copy fasta | chr3 | 69931592 | 69973332 |
a0002c0003t0001 | 0/0 | 4475 | 2 | 0 | 0 | 2 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | copy fasta | chr3 | 69931592 | 69973332 |
a0003c0006t0001 | 0/0 | 4475 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | copy fasta | chr3 | 69931592 | 69973332 |
a0004c0005t0001 | 0/0 | 4475 | 1 | 0 | 1 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | copy fasta | chr3 | 69931592 | 69973332 |
a0005c0007t0001 | 0/0 | 4475 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | copy fasta | chr3 | 69931592 | 69973332 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0003 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0004 | 0/0 | 5 | 0 | 1 | 0 | 0 | 4 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0005 | 1/0 | 4 | 0 | 2 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0280 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0002g0001 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0002g0007 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0002g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0002g0009 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0002g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0002g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0002g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0002g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0002g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0002g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0002g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0002g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0002g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0002g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0002g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0002g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0002g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0002g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0002g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0002g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0002g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0002g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0002g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0002g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0002g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0002g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0002g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0002g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0002g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0002g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0002g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0002g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0002g0297 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0002g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0002g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0002g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0002g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0002g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0002g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0003g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0003g0011 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0003g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0003g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0003g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0003g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0003g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0003g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0003g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0003g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0003g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0003g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0003g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0003g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0003g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0003g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0003g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0003g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0003g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0003g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0003g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0003g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0003g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0004g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0004g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0004g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0004g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0004g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0004g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0004g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0004g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0004g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0004g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0004g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0004g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0004g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0005g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0005g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0005g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0005g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0005g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0005g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0005g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0006g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0006g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0006g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0006g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0006g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0007g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0007g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0007g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0007g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0008g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0008g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0008g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0009g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0009g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0009g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0010g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0010g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0011g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0013g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0014g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0015g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0016g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0017g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0018g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0019g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0020g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0001t0021g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0002t0002g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0002t0002g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0002t0002g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0004t0012g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0004t0012g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0001c0008t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0002c0003t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0002c0003t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0003c0006t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0004c0005t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
a0005c0007t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0002 | g0170 | EUR | GBR | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0218 | EUR | GBR | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0192 | EUR | GBR | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0302 | EUR | GBR | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG00280 | hp1 | a0001 | c0001 | t0002 | g0297 | EUR | FIN | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0027 | EUR | FIN | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG00323 | hp1 | a0001 | c0001 | t0002 | g0279 | EUR | FIN | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0281 | EUR | FIN | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | CHS | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | CHS | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | CHS | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG00423 | hp2 | a0001 | c0001 | t0002 | g0058 | EAS | CHS | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | CHS | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG00438 | hp2 | a0001 | c0001 | t0002 | g0265 | EAS | CHS | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | CHS | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | CHS | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG00609 | hp1 | a0003 | c0006 | t0001 | g0193 | EAS | CHS | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | CHS | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG00621 | hp1 | a0005 | c0007 | t0001 | g0263 | EAS | CHS | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | CHS | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0251 | AMR | PUR | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG00642 | hp2 | a0001 | c0001 | t0009 | g0153 | AMR | PUR | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG00673 | hp1 | a0001 | c0001 | t0004 | g0142 | EAS | CHS | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | CHS | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0255 | AMR | PUR | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG00735 | hp2 | a0001 | c0001 | t0002 | g0190 | AMR | PUR | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0224 | AMR | PUR | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0205 | AMR | PUR | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0254 | AMR | PUR | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0257 | AMR | PUR | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG01074 | hp1 | a0001 | c0001 | t0006 | g0282 | AMR | PUR | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0200 | AMR | PUR | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG01081 | hp1 | a0001 | c0001 | t0002 | g0165 | AMR | PUR | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0197 | AMR | PUR | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0062 | AMR | PUR | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG01106 | hp1 | a0001 | c0001 | t0002 | g0104 | AMR | PUR | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0171 | AMR | PUR | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0204 | AMR | PUR | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG01167 | hp1 | a0001 | c0001 | t0003 | g0243 | AMR | PUR | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | PUR | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG01169 | hp1 | a0001 | c0001 | t0003 | g0037 | AMR | PUR | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG01169 | hp2 | a0001 | c0001 | t0004 | g0230 | AMR | PUR | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG01243 | hp1 | a0001 | c0001 | t0003 | g0274 | AMR | PUR | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG01243 | hp2 | a0001 | c0001 | t0006 | g0284 | AMR | PUR | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG01255 | hp1 | a0001 | c0001 | t0002 | g0100 | AMR | CLM | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG01255 | hp2 | a0001 | c0001 | t0002 | g0101 | AMR | CLM | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | CLM | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | CLM | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG01257 | hp1 | a0001 | c0001 | t0013 | g0017 | AMR | CLM | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | CLM | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG01258 | hp1 | a0001 | c0001 | t0013 | g0017 | AMR | CLM | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | CLM | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0202 | AMR | CLM | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG01346 | hp1 | a0001 | c0001 | t0004 | g0206 | AMR | CLM | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG01346 | hp2 | a0001 | c0001 | t0002 | g0187 | AMR | CLM | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG01358 | hp1 | a0001 | c0001 | t0002 | g0009 | AMR | CLM | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | CLM | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0220 | AMR | CLM | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG01361 | hp2 | a0001 | c0001 | t0002 | g0162 | AMR | CLM | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG01433 | hp1 | a0001 | c0001 | t0002 | g0176 | AMR | CLM | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG01433 | hp2 | a0001 | c0001 | t0002 | g0145 | AMR | CLM | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | CLM | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0033 | AMR | CLM | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG01516 | hp1 | a0001 | c0001 | t0018 | g0241 | EUR | IBS | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0016 | EUR | IBS | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG01517 | hp1 | a0001 | c0001 | t0002 | g0296 | EUR | IBS | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0016 | EUR | IBS | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG01884 | hp1 | a0001 | c0001 | t0002 | g0012 | AFR | ACB | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG01884 | hp2 | a0001 | c0001 | t0002 | g0191 | AFR | ACB | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG01891 | hp1 | a0001 | c0001 | t0003 | g0010 | AFR | ACB | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG01891 | hp2 | a0001 | c0001 | t0002 | g0020 | AFR | ACB | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | PEL | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0061 | AMR | PEL | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG01952 | hp1 | a0001 | c0001 | t0002 | g0184 | AMR | PEL | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG01952 | hp2 | a0001 | c0001 | t0003 | g0259 | AMR | PEL | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0060 | AMR | PEL | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG01975 | hp2 | a0001 | c0001 | t0002 | g0114 | AMR | PEL | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG01978 | hp1 | a0004 | c0005 | t0001 | g0035 | AMR | PEL | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | PEL | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PEL | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PEL | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0172 | AMR | PEL | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | PEL | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG02027 | hp1 | a0001 | c0001 | t0002 | g0160 | EAS | KHV | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0308 | EAS | KHV | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | KHV | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0290 | AFR | ACB | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | ACB | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | KHV | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG02056 | hp2 | a0001 | c0001 | t0004 | g0025 | EAS | KHV | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG02071 | hp2 | a0001 | c0001 | t0005 | g0320 | EAS | KHV | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG02074 | hp1 | a0001 | c0001 | t0002 | g0129 | EAS | KHV | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG02074 | hp2 | a0001 | c0001 | t0019 | g0126 | EAS | KHV | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | KHV | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | KHV | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | KHV | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG02129 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | KHV | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | KHV | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG02132 | hp2 | a0001 | c0001 | t0002 | g0085 | EAS | KHV | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | KHV | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | KHV | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG02145 | hp1 | a0001 | c0001 | t0002 | g0183 | AFR | ACB | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0272 | AFR | ACB | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0288 | AMR | PEL | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG02148 | hp2 | a0001 | c0001 | t0015 | g0182 | AMR | PEL | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG02257 | hp1 | a0001 | c0001 | t0002 | g0119 | AFR | ACB | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0295 | AFR | ACB | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG02258 | hp1 | a0001 | c0001 | t0003 | g0246 | AFR | ACB | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG02258 | hp2 | a0001 | c0001 | t0002 | g0232 | AFR | ACB | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG02273 | hp1 | a0001 | c0001 | t0002 | g0329 | AMR | PEL | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | PEL | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0219 | AFR | ACB | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG02280 | hp2 | a0001 | c0001 | t0003 | g0011 | AFR | ACB | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0260 | AMR | PEL | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG02293 | hp2 | a0001 | c0001 | t0002 | g0009 | AMR | PEL | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG02451 | hp1 | a0001 | c0001 | t0002 | g0316 | AFR | ACB | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG02451 | hp2 | a0001 | c0001 | t0003 | g0252 | AFR | ACB | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | KHV | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | KHV | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG02572 | hp1 | a0001 | c0001 | t0003 | g0245 | AFR | GWD | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | GWD | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG02602 | hp1 | a0001 | c0001 | t0002 | g0139 | SAS | PJL | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0131 | SAS | PJL | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG02615 | hp1 | a0001 | c0001 | t0002 | g0159 | AFR | GWD | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG02615 | hp2 | a0001 | c0001 | t0010 | g0312 | AFR | GWD | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG02622 | hp1 | a0001 | c0001 | t0002 | g0012 | AFR | GWD | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG02622 | hp2 | a0001 | c0001 | t0003 | g0144 | AFR | GWD | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG02630 | hp1 | a0001 | c0001 | t0002 | g0081 | AFR | GWD | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0285 | AFR | GWD | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG02647 | hp1 | a0001 | c0001 | t0003 | g0250 | AFR | GWD | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG02647 | hp2 | a0001 | c0001 | t0021 | g0315 | AFR | GWD | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0196 | SAS | PJL | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG02683 | hp2 | a0001 | c0001 | t0002 | g0146 | SAS | PJL | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG02717 | hp1 | a0001 | c0001 | t0002 | g0097 | AFR | GWD | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG02717 | hp2 | a0001 | c0001 | t0003 | g0090 | AFR | GWD | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG02723 | hp1 | a0001 | c0001 | t0005 | g0289 | AFR | GWD | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG02723 | hp2 | a0001 | c0001 | t0002 | g0115 | AFR | GWD | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0044 | SAS | PJL | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG02735 | hp2 | a0001 | c0002 | t0002 | g0152 | SAS | PJL | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG02738 | hp1 | a0001 | c0001 | t0009 | g0277 | SAS | PJL | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0198 | SAS | PJL | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG02809 | hp1 | a0001 | c0004 | t0012 | g0305 | AFR | GWD | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG02809 | hp2 | a0001 | c0001 | t0003 | g0271 | AFR | GWD | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0275 | AFR | GWD | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG02818 | hp2 | a0001 | c0001 | t0002 | g0012 | AFR | GWD | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG02886 | hp1 | a0001 | c0001 | t0002 | g0080 | AFR | GWD | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG02886 | hp2 | a0001 | c0008 | t0001 | g0029 | AFR | GWD | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG02896 | hp1 | a0001 | c0001 | t0003 | g0293 | AFR | GWD | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG02896 | hp2 | a0001 | c0001 | t0002 | g0147 | AFR | GWD | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG02897 | hp1 | a0001 | c0001 | t0002 | g0118 | AFR | GWD | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG02897 | hp2 | a0001 | c0001 | t0003 | g0039 | AFR | GWD | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG02922 | hp1 | a0001 | c0001 | t0002 | g0121 | AFR | ESN | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG02922 | hp2 | a0001 | c0001 | t0003 | g0247 | AFR | ESN | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG02965 | hp1 | a0001 | c0001 | t0003 | g0011 | AFR | ESN | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG02965 | hp2 | a0001 | c0001 | t0017 | g0319 | AFR | ESN | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG02970 | hp1 | a0001 | c0001 | t0020 | g0141 | AFR | ESN | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG02970 | hp2 | a0001 | c0001 | t0011 | g0030 | AFR | ESN | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG02976 | hp1 | a0001 | c0001 | t0003 | g0294 | AFR | ESN | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | ESN | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG03017 | hp1 | a0001 | c0001 | t0006 | g0313 | SAS | PJL | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG03017 | hp2 | a0001 | c0001 | t0004 | g0227 | SAS | PJL | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG03041 | hp1 | a0001 | c0001 | t0003 | g0287 | AFR | GWD | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0299 | AFR | GWD | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG03098 | hp1 | a0001 | c0001 | t0002 | g0261 | AFR | MSL | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG03098 | hp2 | a0001 | c0001 | t0003 | g0258 | AFR | MSL | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | ESN | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0318 | AFR | ESN | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG03209 | hp1 | a0001 | c0001 | t0002 | g0059 | AFR | MSL | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | MSL | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG03225 | hp1 | a0001 | c0001 | t0011 | g0030 | AFR | MSL | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0300 | AFR | MSL | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0071 | SAS | PJL | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0209 | SAS | PJL | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG03453 | hp1 | a0001 | c0001 | t0002 | g0148 | AFR | MSL | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | MSL | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG03486 | hp1 | a0001 | c0001 | t0002 | g0298 | AFR | MSL | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0273 | AFR | MSL | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG03490 | hp1 | a0001 | c0002 | t0002 | g0188 | SAS | PJL | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG03490 | hp2 | a0001 | c0001 | t0002 | g0253 | SAS | PJL | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG03491 | hp1 | a0001 | c0001 | t0002 | g0007 | SAS | PJL | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0049 | SAS | PJL | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | ESN | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG03516 | hp2 | a0001 | c0001 | t0002 | g0125 | AFR | ESN | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG03540 | hp1 | a0001 | c0001 | t0003 | g0249 | AFR | GWD | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG03540 | hp2 | a0001 | c0001 | t0002 | g0113 | AFR | GWD | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG03579 | hp1 | a0001 | c0001 | t0002 | g0112 | AFR | MSL | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0225 | AFR | MSL | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0203 | SAS | PJL | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0027 | SAS | PJL | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG03669 | hp1 | a0001 | c0001 | t0014 | g0163 | SAS | PJL | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0212 | SAS | PJL | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG03710 | hp1 | a0001 | c0001 | t0002 | g0186 | SAS | PJL | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG03710 | hp2 | a0001 | c0001 | t0016 | g0207 | SAS | PJL | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG03834 | hp1 | a0001 | c0001 | t0006 | g0283 | SAS | BEB | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0223 | SAS | BEB | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG03927 | hp1 | a0001 | c0001 | t0002 | g0110 | SAS | BEB | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0068 | SAS | BEB | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | BEB | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG03942 | hp2 | a0001 | c0001 | t0009 | g0278 | SAS | BEB | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0133 | SAS | BEB | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0157 | SAS | BEB | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG04199 | hp1 | a0001 | c0002 | t0002 | g0179 | SAS | STU | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | STU | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | STU | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0111 | SAS | STU | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0072 | SAS | STU | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | STU | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0303 | AFR | YRI | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA18522 | hp2 | a0001 | c0001 | t0003 | g0143 | AFR | YRI | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | CHB | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | CHB | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0301 | AFR | YRI | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0286 | AFR | YRI | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA18939 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA18940 | hp1 | a0001 | c0001 | t0005 | g0323 | EAS | JPT | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA18941 | hp2 | a0001 | c0001 | t0002 | g0231 | EAS | JPT | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA18942 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA18943 | hp1 | a0001 | c0001 | t0005 | g0327 | EAS | JPT | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA18943 | hp2 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA18947 | hp1 | a0001 | c0001 | t0008 | g0022 | EAS | JPT | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA18947 | hp2 | a0001 | c0001 | t0004 | g0195 | EAS | JPT | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA18953 | hp2 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA18957 | hp1 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA18962 | hp1 | a0001 | c0001 | t0007 | g0106 | EAS | JPT | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA18966 | hp1 | a0001 | c0001 | t0004 | g0194 | EAS | JPT | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA18966 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA18967 | hp1 | a0001 | c0001 | t0007 | g0292 | EAS | JPT | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA18967 | hp2 | a0001 | c0001 | t0002 | g0267 | EAS | JPT | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA18968 | hp1 | a0002 | c0003 | t0001 | g0047 | EAS | JPT | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA18968 | hp2 | a0001 | c0001 | t0008 | g0321 | EAS | JPT | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA18969 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA18970 | hp2 | a0001 | c0001 | t0005 | g0322 | EAS | JPT | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA18972 | hp1 | a0001 | c0001 | t0002 | g0270 | EAS | JPT | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA18975 | hp1 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA18975 | hp2 | a0001 | c0001 | t0002 | g0266 | EAS | JPT | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA18978 | hp1 | a0001 | c0001 | t0008 | g0022 | EAS | JPT | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA18980 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA18981 | hp2 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA18982 | hp1 | a0001 | c0001 | t0006 | g0314 | EAS | JPT | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA18982 | hp2 | a0001 | c0001 | t0004 | g0088 | EAS | JPT | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA18983 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA18985 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA18987 | hp1 | a0001 | c0001 | t0007 | g0001 | EAS | JPT | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA18988 | hp1 | a0001 | c0001 | t0004 | g0216 | EAS | JPT | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA18988 | hp2 | a0001 | c0001 | t0002 | g0269 | EAS | JPT | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA18989 | hp1 | a0001 | c0001 | t0004 | g0024 | EAS | JPT | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA18990 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA18997 | hp2 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA19000 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA19001 | hp2 | a0001 | c0001 | t0002 | g0325 | EAS | JPT | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA19003 | hp1 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA19004 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA19004 | hp2 | a0001 | c0001 | t0002 | g0326 | EAS | JPT | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA19005 | hp1 | a0001 | c0001 | t0002 | g0120 | EAS | JPT | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA19006 | hp1 | a0001 | c0001 | t0002 | g0317 | EAS | JPT | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA19006 | hp2 | a0001 | c0001 | t0004 | g0024 | EAS | JPT | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA19007 | hp2 | a0001 | c0001 | t0005 | g0031 | EAS | JPT | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA19009 | hp1 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA19010 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA19012 | hp1 | a0001 | c0001 | t0002 | g0268 | EAS | JPT | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA19012 | hp2 | a0001 | c0001 | t0005 | g0324 | EAS | JPT | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | LWK | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA19030 | hp2 | a0001 | c0001 | t0003 | g0010 | AFR | LWK | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA19043 | hp1 | a0001 | c0001 | t0002 | g0117 | AFR | LWK | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA19043 | hp2 | a0001 | c0001 | t0002 | g0102 | AFR | LWK | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA19054 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA19056 | hp1 | a0001 | c0001 | t0002 | g0264 | EAS | JPT | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA19058 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA19060 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA19064 | hp2 | a0001 | c0001 | t0007 | g0116 | EAS | JPT | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA19065 | hp2 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA19070 | hp2 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA19077 | hp2 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA19078 | hp1 | a0001 | c0001 | t0002 | g0210 | EAS | JPT | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA19078 | hp2 | a0001 | c0001 | t0004 | g0311 | EAS | JPT | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA19079 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA19082 | hp2 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA19083 | hp1 | a0001 | c0001 | t0005 | g0031 | EAS | JPT | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA19085 | hp2 | a0002 | c0003 | t0001 | g0156 | EAS | JPT | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA19086 | hp1 | a0001 | c0001 | t0008 | g0069 | EAS | JPT | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA19086 | hp2 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA19087 | hp2 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA19090 | hp1 | a0001 | c0001 | t0004 | g0127 | EAS | JPT | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA19240 | hp1 | a0001 | c0001 | t0002 | g0262 | AFR | YRI | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0304 | AFR | YRI | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA20129 | hp1 | a0001 | c0001 | t0002 | g0149 | AFR | ASW | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA20129 | hp2 | a0001 | c0001 | t0003 | g0248 | AFR | ASW | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG02109 | hp1 | a0001 | c0001 | t0010 | g0328 | AFR | ACB | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG02109 | hp2 | a0001 | c0001 | t0003 | g0244 | AFR | ACB | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG02486 | hp1 | a0001 | c0001 | t0002 | g0020 | AFR | ACB | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG02486 | hp2 | a0001 | c0001 | t0003 | g0010 | AFR | ACB | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | ACB | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG02559 | hp2 | a0001 | c0001 | t0002 | g0122 | AFR | ACB | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG03471 | hp1 | a0001 | c0001 | t0002 | g0056 | AFR | MSL | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG03471 | hp2 | a0001 | c0004 | t0012 | g0057 | AFR | MSL | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | USA | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
HG06807 | hp2 | a0001 | c0001 | t0003 | g0011 | AFR | USA | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA18955 | hp1 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | USA | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0276 | AFR | USA | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA21309 | hp1 | a0001 | c0001 | t0004 | g0310 | AFR | LWK | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0228 | AFR | LWK | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0280 | REF | REF | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0005 | REF | REF | MITF_chr3_69931592_69973332 | MITF | chr3 | 69931592 | 69973332 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:69939138
|
A | G | 1 | a0005 | 1 | HG00621.hp1 | missense_variant | MODERATE | c.302A>G | p.Glu101Gly | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 3/9 | 433/4475 | 302/1260 | 101/419 | chr3 | 69939138 | ||
chr3:69964889
|
C | G | 1 | a0003 | 1 | HG00609.hp1 | missense_variant | MODERATE | c.901C>G | p.Pro301Ala | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 9/9 | 1032/4475 | 901/1260 | 301/419 | chr3 | 69964889 | ||
chr3:69965048
|
C | A | 1 | a0002 | 2 | NA18968.hp1 NA19085.hp2 |
missense_variant | MODERATE | c.1060C>A | p.Leu354Ile | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 9/9 | 1191/4475 | 1060/1260 | 354/419 | chr3 | 69965048 | ||
chr3:69965051
|
G | A | 1 | a0004 | 1 | HG01978.hp1 | missense_variant | MODERATE | c.1063G>A | p.Gly355Arg | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 9/9 | 1194/4475 | 1063/1260 | 355/419 | chr3 | 69965051 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:69937836
|
C | T | 1 | a0001c0008 | 1 | HG02886.hp2 | synonymous_variant | LOW | c.48C>T | p.Leu16Leu | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 2/9 | 179/4475 | 48/1260 | 16/419 | chr3 | 69937836 | ||
chr3:69965233
|
G | A | 1 | a0001c0004 | 2 | HG02809.hp1 HG03471.hp2 |
synonymous_variant | LOW | c.1245G>A | p.Thr415Thr | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 9/9 | 1376/4475 | 1245/1260 | 415/419 | chr3 | 69965233 | ||
chr3:69965236
|
G | A | 1 | a0001c0002 | 3 | HG02735.hp2 HG03490.hp1 HG04199.hp1 |
synonymous_variant | LOW | c.1248G>A | p.Glu416Glu | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 9/9 | 1379/4475 | 1248/1260 | 416/419 | chr3 | 69965236 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:69936687
|
G | A | 2 | a0001c0001t0006a0001c0001t0010 | 7 | HG01074.hp1 HG01243.hp2 HG02109.hp1 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-36G>A | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 1/9 | 36 | chr3 | 69936687 | |||||
chr3:69965296
|
T | C | 2 | a0001c0001t0003a0001c0001t0004 | 41 | HG00673.hp1 HG01167.hp1 HG01169.hp1 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*48T>C | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 9/9 | 48 | chr3 | 69965296 | |||||
chr3:69965695
|
C | A | 1 | a0001c0001t0014 | 1 | HG03669.hp1 | 3_prime_UTR_variant | MODIFIER | c.*447C>A | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 9/9 | 447 | chr3 | 69965695 | |||||
chr3:69965814
|
G | GAA | 5 | a0001c0001t0002a0001c0001t0014a0001c0001t0015others(2): Show | 110 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(107): Show |
3_prime_UTR_variant | MODIFIER | c.*575_*576dupAA | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 9/9 | 577 | INFO_REALIGN_3_PRIME | chr3 | 69965814 | ||||
chr3:69966063
|
C | T | 1 | a0001c0001t0021 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*815C>T | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 9/9 | 815 | chr3 | 69966063 | |||||
chr3:69966072
|
T | A | 3 | a0001c0001t0011a0001c0001t0017a0001c0004t0012 | 5 | HG02809.hp1 HG02965.hp2 HG02970.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*824T>A | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 9/9 | 824 | chr3 | 69966072 | |||||
chr3:69966398
|
T | C | 3 | a0001c0001t0006a0001c0001t0010a0001c0001t0018 | 8 | HG01074.hp1 HG01243.hp2 HG01516.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1150T>C | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 9/9 | 1150 | chr3 | 69966398 | |||||
chr3:69966496
|
T | C | 2 | a0001c0001t0004a0001c0001t0009 | 17 | HG00642.hp2 HG00673.hp1 HG01169.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*1248T>C | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 9/9 | 1248 | chr3 | 69966496 | |||||
chr3:69966620
|
A | G | 1 | a0001c0001t0016 | 1 | HG03710.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1372A>G | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 9/9 | 1372 | chr3 | 69966620 | |||||
chr3:69966739
|
A | G | 1 | a0001c0001t0008 | 4 | NA18947.hp1 NA18968.hp2 NA18978.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1491A>G | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 9/9 | 1491 | chr3 | 69966739 | |||||
chr3:69967123
|
G | A | 1 | a0001c0001t0010 | 2 | HG02109.hp1 HG02615.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1875G>A | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 9/9 | 1875 | chr3 | 69967123 | |||||
chr3:69967316
|
C | T | 13 | a0001c0001t0002a0001c0001t0005a0001c0001t0006others(10): Show | 135 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(132): Show |
3_prime_UTR_variant | MODIFIER | c.*2068C>T | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 9/9 | 2068 | chr3 | 69967316 | |||||
chr3:69967418
|
A | G | 1 | a0001c0004t0012 | 2 | HG02809.hp1 HG03471.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2170A>G | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 9/9 | 2170 | chr3 | 69967418 | |||||
chr3:69967570
|
T | C | 1 | a0001c0001t0021 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2322T>C | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 9/9 | 2322 | chr3 | 69967570 | |||||
chr3:69967701
|
T | C | 1 | a0001c0001t0019 | 1 | HG02074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2453T>C | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 9/9 | 2453 | chr3 | 69967701 | |||||
chr3:69967706
|
G | A | 3 | a0001c0001t0006a0001c0001t0010a0001c0001t0018 | 8 | HG01074.hp1 HG01243.hp2 HG01516.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2458G>A | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 9/9 | 2458 | chr3 | 69967706 | |||||
chr3:69967753
|
C | T | 6 | a0001c0001t0002a0001c0001t0007a0001c0001t0014others(3): Show | 114 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(111): Show |
3_prime_UTR_variant | MODIFIER | c.*2505C>T | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 9/9 | 2505 | chr3 | 69967753 | |||||
chr3:69967836
|
G | A | 1 | a0001c0001t0015 | 1 | HG02148.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2588G>A | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 9/9 | 2588 | chr3 | 69967836 | |||||
chr3:69968116
|
T | C | 1 | a0001c0001t0013 | 2 | HG01257.hp1 HG01258.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2868T>C | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 9/9 | 2868 | chr3 | 69968116 | |||||
chr3:69968281
|
A | G | 1 | a0001c0001t0020 | 1 | HG02970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3033A>G | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 9/9 | 3033 | chr3 | 69968281 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:69936817
|
C | T | 1 | a0001c0001t0002g0329 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.33+62C>T | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 1/8 | chr3 | 69936817 | ||||||
chr3:69936947
|
C | CT | 20 | a0001c0001t0001g0318a0001c0001t0002g0316a0001c0001t0002g0317others(17): Show | 22 | HG02071.hp2 HG02109.hp1 HG02451.hp1 others(19): Show |
intron_variant | MODIFIER | c.33+210dupT | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr3 | 69936947 | |||||
chr3:69936947
|
CT | C | 11 | a0001c0001t0001g0013a0001c0001t0001g0032a0001c0001t0001g0034others(8): Show | 12 | HG00609.hp2 HG01169.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.33+210delT | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr3 | 69936947 | |||||
chr3:69936993
|
A | G | 1 | a0001c0001t0004g0310 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.33+238A>G | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 1/8 | chr3 | 69936993 | ||||||
chr3:69937294
|
C | G | 1 | a0001c0001t0010g0328 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.34-528C>G | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 1/8 | chr3 | 69937294 | ||||||
chr3:69937365
|
G | GGT | 62 | a0001c0001t0001g0013a0001c0001t0001g0021a0001c0001t0001g0034others(59): Show | 69 | HG00642.hp2 HG00673.hp1 HG00673.hp2 others(66): Show |
intron_variant | MODIFIER | c.34-418_34-417dupGT | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr3 | 69937365 | |||||
chr3:69937365
|
G | GGTGT | 44 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0019others(41): Show | 48 | HG00408.hp2 HG00423.hp1 HG00609.hp2 others(45): Show |
intron_variant | MODIFIER | c.34-420_34-417dupGT others(2): Show |
MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr3 | 69937365 | |||||
chr3:69937365
|
G | GGTGTGT | 6 | a0001c0001t0001g0043a0001c0001t0001g0048a0001c0001t0001g0049others(3): Show | 6 | HG00408.hp1 HG02083.hp2 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.34-422_34-417dupGT others(4): Show |
MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr3 | 69937365 | |||||
chr3:69937365
|
G | GGTGTGTG others(1): Show |
6 | a0001c0001t0001g0014a0001c0001t0001g0044a0001c0001t0002g0015others(3): Show | 8 | HG02735.hp1 NA18939.hp2 NA18955.hp1 others(5): Show |
intron_variant | MODIFIER | c.34-424_34-417dupGT others(6): Show |
MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr3 | 69937365 | |||||
chr3:69937365
|
GGT | G | 15 | a0001c0001t0001g0285a0001c0001t0001g0286a0001c0001t0001g0288others(12): Show | 17 | HG01517.hp1 HG01884.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.34-418_34-417delGT | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr3 | 69937365 | |||||
chr3:69937365
|
GGTGT | G | 16 | a0001c0001t0001g0029a0001c0001t0001g0040a0001c0001t0001g0041others(13): Show | 17 | HG00140.hp2 HG00280.hp1 HG02886.hp2 others(14): Show |
intron_variant | MODIFIER | c.34-420_34-417delGT others(2): Show |
MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr3 | 69937365 | |||||
chr3:69937365
|
GGTGTGT | G | 10 | a0001c0001t0002g0325a0001c0001t0002g0326a0001c0001t0005g0031others(7): Show | 11 | HG02071.hp2 HG02809.hp1 NA18940.hp1 others(8): Show |
intron_variant | MODIFIER | c.34-422_34-417delGT others(4): Show |
MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr3 | 69937365 | |||||
chr3:69937388
|
G | A | 1 | a0001c0001t0001g0042 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.34-434G>A | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 1/8 | chr3 | 69937388 | ||||||
chr3:69937394
|
G | T | 4 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(1): Show | 4 | HG02027.hp2 NA18942.hp2 NA18972.hp2 others(1): Show |
intron_variant | MODIFIER | c.34-428G>T | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 1/8 | chr3 | 69937394 | ||||||
chr3:69937404
|
GT | G | 3 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0002g0159 | 3 | HG02083.hp1 HG02615.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.34-414delT | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr3 | 69937404 | |||||
chr3:69937405
|
T | TG | 6 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0103others(3): Show | 6 | HG01255.hp1 HG01255.hp2 NA18939.hp1 others(3): Show |
intron_variant | MODIFIER | c.34-417_34-416insG | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 1/8 | chr3 | 69937405 | ||||||
chr3:69937405
|
T | TGTG | 3 | a0001c0001t0002g0056a0001c0001t0002g0058a0001c0004t0012g0057 | 3 | HG00423.hp2 HG03471.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.34-417_34-416insGT others(1): Show |
MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 1/8 | chr3 | 69937405 | ||||||
chr3:69937406
|
T | G | 5 | a0001c0001t0001g0043a0001c0001t0001g0053a0001c0001t0001g0054others(2): Show | 5 | HG01257.hp2 HG02717.hp1 NA19003.hp2 others(2): Show |
intron_variant | MODIFIER | c.34-416T>G | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 1/8 | chr3 | 69937406 | ||||||
chr3:69937407
|
T | G | 1 | a0002c0003t0001g0156 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.34-415T>G | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 1/8 | chr3 | 69937407 | ||||||
chr3:69937593
|
A | T | 6 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0095others(3): Show | 6 | NA18964.hp1 NA18971.hp1 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.34-229A>T | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 1/8 | chr3 | 69937593 | ||||||
chr3:69937628
|
A | C | 23 | a0001c0001t0001g0092a0001c0001t0001g0154a0001c0001t0001g0318others(20): Show | 25 | HG01074.hp1 HG01243.hp2 HG02071.hp2 others(22): Show |
intron_variant | MODIFIER | c.34-194A>C | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 1/8 | chr3 | 69937628 | ||||||
chr3:69938175
|
C | T | 5 | a0001c0001t0001g0154a0001c0001t0001g0318a0001c0001t0011g0030others(2): Show | 6 | HG02559.hp1 HG02647.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.261+126C>T | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 2/8 | chr3 | 69938175 | ||||||
chr3:69938329
|
C | T | 7 | a0001c0001t0006g0282a0001c0001t0006g0283a0001c0001t0006g0284others(4): Show | 7 | HG01074.hp1 HG01243.hp2 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.261+280C>T | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 2/8 | chr3 | 69938329 | ||||||
chr3:69938355
|
A | G | 1 | a0001c0001t0005g0327 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.261+306A>G | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 2/8 | chr3 | 69938355 | ||||||
chr3:69938540
|
G | A | 1 | a0001c0001t0002g0297 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.261+491G>A | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 2/8 | chr3 | 69938540 | ||||||
chr3:69938556
|
C | T | 7 | a0001c0001t0001g0280a0001c0001t0001g0281a0001c0001t0002g0279others(4): Show | 7 | HG00323.hp1 HG00323.hp2 HG00642.hp2 others(4): Show |
intron_variant | MODIFIER | c.261+507C>T | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 2/8 | chr3 | 69938556 | ||||||
chr3:69938581
|
G | A | 1 | a0001c0001t0002g0298 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.262-517G>A | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 2/8 | chr3 | 69938581 | ||||||
chr3:69938612
|
T | C | 1 | a0001c0001t0001g0154 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.262-486T>C | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 2/8 | chr3 | 69938612 | ||||||
chr3:69938709
|
C | T | 1 | a0001c0002t0002g0152 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.262-389C>T | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 2/8 | chr3 | 69938709 | ||||||
chr3:69939426
|
A | G | 7 | a0001c0001t0006g0282a0001c0001t0006g0283a0001c0001t0006g0284others(4): Show | 7 | HG01074.hp1 HG01243.hp2 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.345+245A>G | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 3/8 | chr3 | 69939426 | ||||||
chr3:69940321
|
T | C | 1 | a0001c0001t0002g0104 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.346-915T>C | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 3/8 | chr3 | 69940321 | ||||||
chr3:69940412
|
G | C | 1 | a0001c0001t0002g0160 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.346-824G>C | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 3/8 | chr3 | 69940412 | ||||||
chr3:69940425
|
A | G | 13 | a0001c0001t0001g0028a0001c0001t0001g0040a0001c0001t0001g0041others(10): Show | 14 | HG01243.hp1 HG02145.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.346-811A>G | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 3/8 | chr3 | 69940425 | ||||||
chr3:69941127
|
A | G | 6 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0092others(3): Show | 6 | HG02818.hp1 HG02976.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.346-109A>G | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 3/8 | chr3 | 69941127 | ||||||
chr3:69941229
|
C | T | 1 | a0001c0001t0006g0284 | 1 | HG01243.hp2 | splice_region_variant&intron_variant | LOW | c.346-7C>T | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 3/8 | chr3 | 69941229 | ||||||
chr3:69941362
|
C | T | 10 | a0001c0001t0002g0001a0001c0001t0002g0038a0001c0001t0002g0264others(7): Show | 17 | HG00438.hp2 NA18966.hp2 NA18967.hp2 others(14): Show |
intron_variant | MODIFIER | c.441+31C>T | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 4/8 | chr3 | 69941362 | ||||||
chr3:69941466
|
C | T | 1 | a0005c0007t0001g0263 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.441+135C>T | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 4/8 | chr3 | 69941466 | ||||||
chr3:69941563
|
C | T | 3 | a0001c0001t0001g0318a0001c0001t0011g0030a0001c0001t0017g0319 | 4 | HG02965.hp2 HG02970.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.441+232C>T | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 4/8 | chr3 | 69941563 | ||||||
chr3:69941698
|
T | G | 32 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0092others(29): Show | 34 | HG01074.hp1 HG01243.hp2 HG02071.hp2 others(31): Show |
intron_variant | MODIFIER | c.441+367T>G | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 4/8 | chr3 | 69941698 | ||||||
chr3:69941729
|
T | C | 1 | a0001c0001t0001g0161 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.441+398T>C | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 4/8 | chr3 | 69941729 | ||||||
chr3:69941750
|
A | G | 32 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0092others(29): Show | 34 | HG01074.hp1 HG01243.hp2 HG02071.hp2 others(31): Show |
intron_variant | MODIFIER | c.441+419A>G | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 4/8 | chr3 | 69941750 | ||||||
chr3:69941901
|
T | C | 1 | a0001c0001t0002g0059 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.441+570T>C | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 4/8 | chr3 | 69941901 | ||||||
chr3:69941924
|
T | C | 5 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062others(2): Show | 5 | HG01099.hp2 HG01928.hp2 HG01975.hp1 others(2): Show |
intron_variant | MODIFIER | c.441+593T>C | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 4/8 | chr3 | 69941924 | ||||||
chr3:69941982
|
G | A | 2 | a0001c0001t0001g0151a0001c0001t0001g0275 | 2 | HG02818.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.441+651G>A | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 4/8 | chr3 | 69941982 | ||||||
chr3:69942039
|
G | A | 4 | a0001c0001t0001g0285a0001c0001t0001g0286a0001c0001t0001g0299others(1): Show | 4 | HG02630.hp2 HG03041.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.441+708G>A | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 4/8 | chr3 | 69942039 | ||||||
chr3:69942258
|
A | G | 1 | a0001c0001t0001g0151 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.441+927A>G | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 4/8 | chr3 | 69942258 | ||||||
chr3:69942343
|
G | A | 3 | a0001c0001t0009g0153a0001c0001t0009g0277a0001c0001t0009g0278 | 3 | HG00642.hp2 HG02738.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.441+1012G>A | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 4/8 | chr3 | 69942343 | ||||||
chr3:69942396
|
G | A | 1 | a0001c0001t0002g0065 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.441+1065G>A | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 4/8 | chr3 | 69942396 | ||||||
chr3:69942555
|
C | T | 3 | a0001c0001t0002g0149a0001c0001t0002g0261a0001c0001t0002g0262 | 3 | HG03098.hp1 NA19240.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.441+1224C>T | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 4/8 | chr3 | 69942555 | ||||||
chr3:69942723
|
G | A | 1 | a0001c0001t0002g0162 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.441+1392G>A | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 4/8 | chr3 | 69942723 | ||||||
chr3:69942989
|
T | G | 12 | a0001c0001t0001g0154a0001c0001t0001g0318a0001c0001t0005g0031others(9): Show | 14 | HG02071.hp2 HG02559.hp1 HG02647.hp2 others(11): Show |
intron_variant | MODIFIER | c.441+1658T>G | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 4/8 | chr3 | 69942989 | ||||||
chr3:69943001
|
G | T | 2 | a0001c0001t0002g0147a0001c0001t0002g0148 | 2 | HG02896.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.441+1670G>T | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 4/8 | chr3 | 69943001 | ||||||
chr3:69943058
|
T | G | 1 | a0001c0001t0014g0163 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.441+1727T>G | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 4/8 | chr3 | 69943058 | ||||||
chr3:69943072
|
C | CT | 16 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0154others(13): Show | 17 | HG00735.hp1 HG01071.hp1 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.441+1762dupT | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr3 | 69943072 | |||||
chr3:69943072
|
CT | C | 20 | a0001c0001t0001g0016a0001c0001t0001g0053a0001c0001t0001g0066others(17): Show | 21 | HG00099.hp1 HG01081.hp1 HG01081.hp2 others(18): Show |
intron_variant | MODIFIER | c.441+1762delT | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr3 | 69943072 | |||||
chr3:69943410
|
A | T | 4 | a0001c0001t0001g0285a0001c0001t0001g0286a0001c0001t0001g0299others(1): Show | 4 | HG02630.hp2 HG03041.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.441+2079A>T | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 4/8 | chr3 | 69943410 | ||||||
chr3:69943621
|
T | C | 10 | a0001c0001t0001g0002a0001c0001t0001g0109a0001c0001t0001g0171others(7): Show | 14 | HG01071.hp1 HG01109.hp1 HG01123.hp2 others(11): Show |
intron_variant | MODIFIER | c.441+2290T>C | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 4/8 | chr3 | 69943621 | ||||||
chr3:69943711
|
G | T | 2 | a0001c0001t0002g0170a0001c0001t0002g0253 | 2 | HG00099.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.441+2380G>T | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 4/8 | chr3 | 69943711 | ||||||
chr3:69943772
|
G | C | 2 | a0001c0001t0002g0110a0001c0001t0002g0176 | 2 | HG01433.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.441+2441G>C | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 4/8 | chr3 | 69943772 | ||||||
chr3:69943791
|
T | G | 1 | a0001c0001t0001g0255 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.441+2460T>G | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 4/8 | chr3 | 69943791 | ||||||
chr3:69943820
|
A | G | 6 | a0001c0001t0001g0092a0001c0001t0001g0154a0001c0001t0001g0318others(3): Show | 7 | HG02559.hp1 HG02647.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.441+2489A>G | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 4/8 | chr3 | 69943820 | ||||||
chr3:69943823
|
G | T | 1 | a0001c0001t0002g0145 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.441+2492G>T | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 4/8 | chr3 | 69943823 | ||||||
chr3:69943829
|
G | A | 1 | a0001c0001t0001g0060 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.441+2498G>A | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 4/8 | chr3 | 69943829 | ||||||
chr3:69943843
|
T | C | 6 | a0001c0001t0001g0092a0001c0001t0001g0154a0001c0001t0001g0318others(3): Show | 7 | HG02559.hp1 HG02647.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.441+2512T>C | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 4/8 | chr3 | 69943843 | ||||||
chr3:69944100
|
A | G | 1 | a0001c0001t0014g0163 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.441+2769A>G | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 4/8 | chr3 | 69944100 | ||||||
chr3:69944104
|
A | G | 1 | a0001c0001t0001g0096 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.441+2773A>G | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 4/8 | chr3 | 69944104 | ||||||
chr3:69944154
|
A | G | 1 | a0001c0001t0003g0294 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.441+2823A>G | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 4/8 | chr3 | 69944154 | ||||||
chr3:69944162
|
G | A | 27 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0019others(24): Show | 33 | HG01081.hp2 HG01256.hp2 HG01257.hp1 others(30): Show |
intron_variant | MODIFIER | c.441+2831G>A | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 4/8 | chr3 | 69944162 | ||||||
chr3:69944176
|
C | T | 1 | a0001c0001t0002g0270 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.441+2845C>T | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 4/8 | chr3 | 69944176 | ||||||
chr3:69944197
|
G | A | 1 | a0001c0001t0001g0154 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.441+2866G>A | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 4/8 | chr3 | 69944197 | ||||||
chr3:69944896
|
A | AT | 11 | a0001c0001t0001g0318a0001c0001t0006g0282a0001c0001t0006g0283others(8): Show | 12 | HG01074.hp1 HG01243.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.441+3571dupT | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr3 | 69944896 | |||||
chr3:69945061
|
A | C | 7 | a0001c0001t0006g0282a0001c0001t0006g0283a0001c0001t0006g0284others(4): Show | 7 | HG01074.hp1 HG01243.hp2 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.441+3730A>C | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 4/8 | chr3 | 69945061 | ||||||
chr3:69945186
|
C | T | 1 | a0001c0001t0001g0260 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.441+3855C>T | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 4/8 | chr3 | 69945186 | ||||||
chr3:69945309
|
G | A | 11 | a0001c0001t0001g0318a0001c0001t0006g0282a0001c0001t0006g0283others(8): Show | 12 | HG01074.hp1 HG01243.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.442-3742G>A | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 4/8 | chr3 | 69945309 | ||||||
chr3:69945378
|
G | A | 70 | a0001c0001t0001g0013a0001c0001t0001g0051a0001c0001t0001g0075others(67): Show | 84 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.442-3673G>A | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 4/8 | chr3 | 69945378 | ||||||
chr3:69945386
|
C | T | 3 | a0001c0001t0002g0012a0001c0001t0002g0097a0001c0001t0002g0159 | 5 | HG01884.hp1 HG02615.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.442-3665C>T | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 4/8 | chr3 | 69945386 | ||||||
chr3:69945494
|
G | C | 1 | a0001c0002t0002g0179 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.442-3557G>C | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 4/8 | chr3 | 69945494 | ||||||
chr3:69945641
|
A | G | 7 | a0001c0001t0006g0282a0001c0001t0006g0283a0001c0001t0006g0284others(4): Show | 7 | HG01074.hp1 HG01243.hp2 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.442-3410A>G | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 4/8 | chr3 | 69945641 | ||||||
chr3:69945654
|
T | C | 10 | a0001c0001t0001g0189a0001c0001t0002g0102a0001c0001t0002g0149others(7): Show | 10 | HG00735.hp2 HG01884.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.442-3397T>C | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 4/8 | chr3 | 69945654 | ||||||
chr3:69945825
|
T | G | 2 | a0001c0001t0001g0068a0001c0001t0013g0017 | 3 | HG01257.hp1 HG01258.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.442-3226T>G | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 4/8 | chr3 | 69945825 | ||||||
chr3:69945916
|
G | A | 1 | a0001c0001t0002g0129 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.442-3135G>A | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 4/8 | chr3 | 69945916 | ||||||
chr3:69945958
|
C | T | 23 | a0001c0001t0001g0251a0001c0001t0003g0010a0001c0001t0003g0011others(20): Show | 27 | HG00642.hp1 HG01167.hp1 HG01169.hp1 others(24): Show |
intron_variant | MODIFIER | c.442-3093C>T | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 4/8 | chr3 | 69945958 | ||||||
chr3:69946105
|
T | C | 1 | a0001c0001t0021g0315 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.442-2946T>C | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 4/8 | chr3 | 69946105 | ||||||
chr3:69946159
|
A | G | 1 | a0001c0001t0001g0049 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.442-2892A>G | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 4/8 | chr3 | 69946159 | ||||||
chr3:69946172
|
G | T | 1 | a0001c0001t0002g0038 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.442-2879G>T | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 4/8 | chr3 | 69946172 | ||||||
chr3:69946254
|
G | A | 1 | a0001c0001t0001g0192 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.442-2797G>A | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 4/8 | chr3 | 69946254 | ||||||
chr3:69946350
|
C | T | 1 | a0001c0001t0001g0042 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.442-2701C>T | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 4/8 | chr3 | 69946350 | ||||||
chr3:69946380
|
T | C | 2 | a0001c0001t0003g0037a0001c0001t0003g0243 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.442-2671T>C | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 4/8 | chr3 | 69946380 | ||||||
chr3:69946467
|
G | A | 1 | a0001c0001t0002g0045 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.442-2584G>A | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 4/8 | chr3 | 69946467 | ||||||
chr3:69946814
|
A | G | 3 | a0001c0001t0011g0030a0001c0001t0017g0319a0001c0001t0021g0315 | 4 | HG02647.hp2 HG02965.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.442-2237A>G | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 4/8 | chr3 | 69946814 | ||||||
chr3:69946827
|
T | G | 1 | a0001c0001t0002g0104 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.442-2224T>G | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 4/8 | chr3 | 69946827 | ||||||
chr3:69946922
|
C | T | 7 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0092others(4): Show | 7 | HG02559.hp1 HG02818.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.442-2129C>T | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 4/8 | chr3 | 69946922 | ||||||
chr3:69946933
|
A | G | 2 | a0001c0001t0002g0015a0001c0001t0002g0046 | 3 | NA18939.hp2 NA19009.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.442-2118A>G | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 4/8 | chr3 | 69946933 | ||||||
chr3:69947114
|
A | G | 1 | a0001c0001t0004g0310 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.442-1937A>G | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 4/8 | chr3 | 69947114 | ||||||
chr3:69947444
|
G | C | 1 | a0001c0001t0001g0157 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.442-1607G>C | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 4/8 | chr3 | 69947444 | ||||||
chr3:69947516
|
A | G | 1 | a0001c0001t0001g0242 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.442-1535A>G | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 4/8 | chr3 | 69947516 | ||||||
chr3:69947581
|
C | A | 1 | a0001c0001t0001g0290 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.442-1470C>A | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 4/8 | chr3 | 69947581 | ||||||
chr3:69948002
|
C | T | 1 | a0001c0001t0001g0089 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.442-1049C>T | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 4/8 | chr3 | 69948002 | ||||||
chr3:69948228
|
G | A | 1 | a0001c0001t0001g0091 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.442-823G>A | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 4/8 | chr3 | 69948228 | ||||||
chr3:69948322
|
T | C | 1 | a0001c0001t0002g0112 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.442-729T>C | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 4/8 | chr3 | 69948322 | ||||||
chr3:69948423
|
T | C | 2 | a0001c0001t0011g0030a0001c0001t0017g0319 | 3 | HG02965.hp2 HG02970.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.442-628T>C | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 4/8 | chr3 | 69948423 | ||||||
chr3:69948491
|
T | C | 1 | a0001c0001t0021g0315 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.442-560T>C | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 4/8 | chr3 | 69948491 | ||||||
chr3:69948507
|
C | T | 1 | a0001c0001t0021g0315 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.442-544C>T | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 4/8 | chr3 | 69948507 | ||||||
chr3:69948634
|
T | G | 1 | a0003c0006t0001g0193 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.442-417T>G | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 4/8 | chr3 | 69948634 | ||||||
chr3:69948665
|
A | T | 1 | a0003c0006t0001g0193 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.442-386A>T | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 4/8 | chr3 | 69948665 | ||||||
chr3:69948712
|
C | T | 1 | a0001c0001t0018g0241 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.442-339C>T | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 4/8 | chr3 | 69948712 | ||||||
chr3:69949309
|
A | G | 1 | a0001c0001t0004g0311 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.559+141A>G | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 5/8 | chr3 | 69949309 | ||||||
chr3:69949429
|
T | A | 7 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0092others(4): Show | 7 | HG02559.hp1 HG02818.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.559+261T>A | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 5/8 | chr3 | 69949429 | ||||||
chr3:69949487
|
A | G | 1 | a0001c0001t0005g0289 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.559+319A>G | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 5/8 | chr3 | 69949487 | ||||||
chr3:69949496
|
C | T | 2 | a0001c0001t0001g0087a0001c0001t0004g0088 | 2 | NA18982.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.559+328C>T | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 5/8 | chr3 | 69949496 | ||||||
chr3:69949543
|
C | T | 1 | a0001c0001t0004g0142 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.559+375C>T | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 5/8 | chr3 | 69949543 | ||||||
chr3:69949716
|
T | TAAAATGG others(9): Show |
1 | a0001c0001t0002g0033 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.559+548_559+549ins others(16): Show |
MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 5/8 | chr3 | 69949716 | ||||||
chr3:69949717
|
T | A | 1 | a0001c0001t0002g0033 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.559+549T>A | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 5/8 | chr3 | 69949717 | ||||||
chr3:69949717
|
T | TGGAGCAA others(5): Show |
1 | a0001c0001t0001g0175 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.559+549_559+550ins others(12): Show |
MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 5/8 | chr3 | 69949717 | ||||||
chr3:69949796
|
T | G | 2 | a0001c0001t0004g0194a0001c0001t0004g0311 | 2 | NA18966.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.559+628T>G | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 5/8 | chr3 | 69949796 | ||||||
chr3:69949981
|
T | A | 7 | a0001c0001t0006g0282a0001c0001t0006g0283a0001c0001t0006g0284others(4): Show | 7 | HG01074.hp1 HG01243.hp2 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.559+813T>A | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 5/8 | chr3 | 69949981 | ||||||
chr3:69950014
|
T | C | 3 | a0001c0001t0004g0194a0001c0001t0004g0195a0001c0001t0004g0311 | 3 | NA18947.hp2 NA18966.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.559+846T>C | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 5/8 | chr3 | 69950014 | ||||||
chr3:69950106
|
A | C | 1 | a0001c0001t0002g0078 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.559+938A>C | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 5/8 | chr3 | 69950106 | ||||||
chr3:69950145
|
G | A | 1 | a0001c0001t0001g0196 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.559+977G>A | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 5/8 | chr3 | 69950145 | ||||||
chr3:69950220
|
A | T | 1 | a0001c0001t0001g0128 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.559+1052A>T | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 5/8 | chr3 | 69950220 | ||||||
chr3:69950351
|
A | G | 1 | a0001c0001t0003g0252 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.559+1183A>G | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 5/8 | chr3 | 69950351 | ||||||
chr3:69950386
|
GA | G | 7 | a0001c0001t0006g0282a0001c0001t0006g0283a0001c0001t0006g0284others(4): Show | 7 | HG01074.hp1 HG01243.hp2 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.559+1227delA | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr3 | 69950386 | |||||
chr3:69950395
|
A | G | 1 | a0001c0002t0002g0188 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.559+1227A>G | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 5/8 | chr3 | 69950395 | ||||||
chr3:69950448
|
T | TTA | 4 | a0001c0001t0001g0079a0001c0001t0001g0197a0001c0001t0001g0198others(1): Show | 4 | HG00408.hp2 HG01099.hp1 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.559+1308_559+1309d others(4): Show |
MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr3 | 69950448 | |||||
chr3:69950448
|
T | TTATA | 6 | a0001c0001t0001g0092a0001c0001t0001g0151a0001c0001t0001g0154others(3): Show | 6 | HG02559.hp1 HG02647.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.559+1306_559+1309d others(6): Show |
MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr3 | 69950448 | |||||
chr3:69950448
|
T | TTATATA | 2 | a0001c0001t0010g0312a0001c0001t0011g0030 | 3 | HG02615.hp2 HG02970.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.559+1304_559+1309d others(8): Show |
MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr3 | 69950448 | |||||
chr3:69950448
|
T | TTATATAT others(3): Show |
4 | a0001c0001t0006g0282a0001c0001t0006g0283a0001c0001t0006g0284others(1): Show | 4 | HG01074.hp1 HG01243.hp2 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.559+1300_559+1309d others(12): Show |
MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr3 | 69950448 | |||||
chr3:69950448
|
TTA | T | 229 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(226): Show | 267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.559+1308_559+1309d others(4): Show |
MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr3 | 69950448 | |||||
chr3:69950448
|
TTATA | T | 32 | a0001c0001t0001g0002a0001c0001t0001g0029a0001c0001t0001g0048others(29): Show | 36 | HG00140.hp2 HG00558.hp2 HG00621.hp2 others(33): Show |
intron_variant | MODIFIER | c.559+1306_559+1309d others(6): Show |
MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr3 | 69950448 | |||||
chr3:69950448
|
TTATATA | T | 11 | a0001c0001t0001g0240a0001c0001t0002g0001a0001c0001t0002g0038others(8): Show | 18 | HG02723.hp1 NA18966.hp2 NA18967.hp2 others(15): Show |
intron_variant | MODIFIER | c.559+1304_559+1309d others(8): Show |
MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr3 | 69950448 | |||||
chr3:69950477
|
T | C | 4 | a0001c0001t0002g0102a0001c0001t0002g0149a0001c0001t0002g0261others(1): Show | 4 | HG03098.hp1 NA19043.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.559+1309T>C | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 5/8 | chr3 | 69950477 | ||||||
chr3:69950512
|
A | G | 1 | a0001c0001t0001g0192 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.560-1300A>G | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 5/8 | chr3 | 69950512 | ||||||
chr3:69950513
|
T | TATATGCA others(25): Show |
2 | a0001c0001t0002g0146a0001c0001t0002g0186 | 2 | HG02683.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.560-1250_560-1219d others(34): Show |
MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr3 | 69950513 | |||||
chr3:69950551
|
C | T | 1 | a0001c0001t0002g0139 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.560-1261C>T | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 5/8 | chr3 | 69950551 | ||||||
chr3:69950627
|
G | GTA | 32 | a0001c0001t0001g0016a0001c0001t0001g0040a0001c0001t0001g0041others(29): Show | 35 | HG00140.hp1 HG00621.hp1 HG01074.hp1 others(32): Show |
intron_variant | MODIFIER | c.560-1165_560-1164d others(4): Show |
MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr3 | 69950627 | |||||
chr3:69950627
|
G | GTATA | 3 | a0001c0001t0001g0131a0001c0001t0001g0154a0001c0001t0001g0275 | 3 | HG02559.hp1 HG02602.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.560-1167_560-1164d others(6): Show |
MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr3 | 69950627 | |||||
chr3:69950627
|
G | GTATATAT others(1): Show |
2 | a0001c0001t0011g0030a0001c0001t0017g0319 | 3 | HG02965.hp2 HG02970.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.560-1171_560-1164d others(10): Show |
MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr3 | 69950627 | |||||
chr3:69950629
|
A | G | 2 | a0001c0001t0002g0145a0001c0001t0018g0241 | 2 | HG01433.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.560-1183A>G | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 5/8 | chr3 | 69950629 | ||||||
chr3:69950661
|
A | G | 7 | a0001c0001t0006g0282a0001c0001t0006g0283a0001c0001t0006g0284others(4): Show | 7 | HG01074.hp1 HG01243.hp2 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.560-1151A>G | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 5/8 | chr3 | 69950661 | ||||||
chr3:69951065
|
T | C | 3 | a0001c0001t0011g0030a0001c0001t0017g0319a0001c0001t0021g0315 | 4 | HG02647.hp2 HG02965.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.560-747T>C | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 5/8 | chr3 | 69951065 | ||||||
chr3:69951093
|
C | CT | 81 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0052others(78): Show | 85 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.560-697dupT | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr3 | 69951093 | |||||
chr3:69951093
|
C | CTT | 6 | a0001c0001t0001g0032a0001c0001t0001g0234a0001c0001t0001g0275others(3): Show | 6 | HG00609.hp2 HG02818.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.560-698_560-697dup others(2): Show |
MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr3 | 69951093 | |||||
chr3:69951093
|
CT | C | 6 | a0001c0001t0002g0115a0001c0001t0003g0143a0001c0001t0004g0195others(3): Show | 7 | HG02647.hp2 HG02723.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.560-697delT | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr3 | 69951093 | |||||
chr3:69951404
|
G | T | 1 | a0001c0001t0005g0289 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.560-408G>T | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 5/8 | chr3 | 69951404 | ||||||
chr3:69951514
|
C | T | 1 | a0001c0001t0001g0044 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.560-298C>T | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 5/8 | chr3 | 69951514 | ||||||
chr3:69951537
|
G | C | 2 | a0001c0001t0001g0028a0001c0001t0001g0150 | 3 | HG02572.hp2 HG03195.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.560-275G>C | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 5/8 | chr3 | 69951537 | ||||||
chr3:69951559
|
A | G | 1 | a0001c0001t0011g0030 | 2 | HG02970.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.560-253A>G | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 5/8 | chr3 | 69951559 | ||||||
chr3:69951576
|
G | GT | 6 | a0001c0001t0001g0234a0001c0001t0002g0067a0001c0001t0011g0030others(3): Show | 7 | HG02647.hp2 HG02965.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.560-227dupT | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr3 | 69951576 | |||||
chr3:69952156
|
C | G | 1 | a0001c0001t0004g0142 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.634+270C>G | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 6/8 | chr3 | 69952156 | ||||||
chr3:69952222
|
A | G | 2 | a0001c0001t0005g0323a0001c0001t0005g0324 | 2 | NA18940.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.634+336A>G | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 6/8 | chr3 | 69952222 | ||||||
chr3:69952354
|
T | TA | 7 | a0001c0001t0006g0282a0001c0001t0006g0283a0001c0001t0006g0284others(4): Show | 7 | HG01074.hp1 HG01243.hp2 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.634+476dupA | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr3 | 69952354 | |||||
chr3:69952435
|
C | A | 1 | a0001c0001t0001g0166 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.634+549C>A | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 6/8 | chr3 | 69952435 | ||||||
chr3:69952498
|
G | A | 1 | a0001c0001t0001g0171 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.634+612G>A | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 6/8 | chr3 | 69952498 | ||||||
chr3:69952649
|
A | C | 1 | a0001c0001t0001g0239 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.634+763A>C | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 6/8 | chr3 | 69952649 | ||||||
chr3:69952869
|
T | C | 3 | a0001c0001t0001g0018a0001c0001t0001g0068a0001c0001t0013g0017 | 5 | HG01257.hp1 HG01258.hp1 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.634+983T>C | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 6/8 | chr3 | 69952869 | ||||||
chr3:69952873
|
T | C | 1 | a0001c0001t0001g0198 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.634+987T>C | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 6/8 | chr3 | 69952873 | ||||||
chr3:69953035
|
A | G | 1 | a0001c0001t0004g0195 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.634+1149A>G | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 6/8 | chr3 | 69953035 | ||||||
chr3:69953260
|
T | C | 2 | a0001c0001t0002g0114a0001c0001t0002g0329 | 2 | HG01975.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.634+1374T>C | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 6/8 | chr3 | 69953260 | ||||||
chr3:69953611
|
GTA | G | 4 | a0001c0001t0001g0103a0001c0001t0001g0189a0001c0001t0001g0240others(1): Show | 4 | HG02132.hp2 NA18985.hp2 NA18990.hp1 others(1): Show |
intron_variant | MODIFIER | c.634+1737_634+1738d others(4): Show |
MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr3 | 69953611 | |||||
chr3:69953617
|
A | G | 1 | a0001c0001t0001g0251 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.634+1731A>G | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 6/8 | chr3 | 69953617 | ||||||
chr3:69953623
|
A | G | 5 | a0001c0001t0001g0066a0001c0001t0001g0071a0001c0001t0001g0072others(2): Show | 5 | HG01081.hp2 HG01256.hp2 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.634+1737A>G | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 6/8 | chr3 | 69953623 | ||||||
chr3:69953625
|
G | A | 1 | a0001c0001t0002g0162 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.634+1739G>A | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 6/8 | chr3 | 69953625 | ||||||
chr3:69953629
|
GTA | G | 115 | a0001c0001t0001g0013a0001c0001t0001g0028a0001c0001t0001g0051others(112): Show | 134 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.634+1755_634+1756d others(4): Show |
MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr3 | 69953629 | |||||
chr3:69953631
|
A | G | 2 | a0001c0001t0002g0085a0001c0001t0002g0162 | 2 | HG01361.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.634+1745A>G | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 6/8 | chr3 | 69953631 | ||||||
chr3:69953639
|
A | ATG | 14 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0092others(11): Show | 15 | HG02071.hp2 HG02559.hp1 HG02886.hp1 others(12): Show |
intron_variant | MODIFIER | c.634+1754_634+1755i others(4): Show |
MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr3 | 69953639 | |||||
chr3:69953641
|
A | G | 1 | a0001c0001t0002g0122 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.634+1755A>G | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 6/8 | chr3 | 69953641 | ||||||
chr3:69953643
|
G | A | 2 | a0001c0001t0001g0275a0001c0001t0002g0122 | 2 | HG02559.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.634+1757G>A | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 6/8 | chr3 | 69953643 | ||||||
chr3:69953645
|
A | G | 1 | a0001c0001t0002g0122 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.634+1759A>G | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 6/8 | chr3 | 69953645 | ||||||
chr3:69953647
|
G | A | 16 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0092others(13): Show | 17 | HG02071.hp2 HG02559.hp1 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.634+1761G>A | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 6/8 | chr3 | 69953647 | ||||||
chr3:69953647
|
G | GTA | 6 | a0001c0001t0001g0055a0001c0001t0001g0083a0001c0001t0001g0135others(3): Show | 6 | HG00099.hp2 NA18951.hp2 NA18955.hp2 others(3): Show |
intron_variant | MODIFIER | c.634+1776_634+1777d others(4): Show |
MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr3 | 69953647 | |||||
chr3:69953656
|
TA | T | 2 | a0001c0001t0001g0019a0001c0001t0001g0070 | 3 | NA18940.hp2 NA18950.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.634+1771delA | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 6/8 | chr3 | 69953656 | ||||||
chr3:69953660
|
T | G | 7 | a0001c0001t0001g0154a0001c0001t0001g0211a0001c0001t0002g0231others(4): Show | 7 | HG02523.hp2 HG02559.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.634+1774T>G | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 6/8 | chr3 | 69953660 | ||||||
chr3:69953660
|
T | TAG | 5 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0151others(2): Show | 5 | HG02148.hp2 HG02976.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.634+1775_634+1776i others(4): Show |
MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr3 | 69953660 | |||||
chr3:69953660
|
TATAGAG | T | 3 | a0001c0001t0001g0107a0001c0001t0008g0022a0001c0001t0008g0069 | 4 | NA18947.hp1 NA18978.hp1 NA18992.hp2 others(1): Show |
intron_variant | MODIFIER | c.634+1776_634+1781d others(8): Show |
MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr3 | 69953660 | |||||
chr3:69953662
|
T | G | 68 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0025others(65): Show | 83 | HG00099.hp1 HG00280.hp1 HG00642.hp2 others(80): Show |
intron_variant | MODIFIER | c.634+1776T>G | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 6/8 | chr3 | 69953662 | ||||||
chr3:69953662
|
T | TAGAG | 3 | a0001c0001t0005g0323a0001c0001t0005g0324a0001c0001t0008g0321 | 3 | NA18940.hp1 NA18968.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.634+1800_634+1803d others(6): Show |
MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr3 | 69953662 | |||||
chr3:69953662
|
T | TAGAGAGA others(1): Show |
2 | a0001c0001t0005g0031a0001c0001t0005g0327 | 3 | NA18943.hp1 NA19007.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.634+1796_634+1803d others(10): Show |
MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr3 | 69953662 | |||||
chr3:69953662
|
T | TATAG | 3 | a0001c0001t0001g0192a0001c0001t0005g0322a0001c0001t0011g0030 | 4 | HG00140.hp1 HG02970.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.634+1777_634+1778i others(6): Show |
MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr3 | 69953662 | |||||
chr3:69953662
|
T | TATAGAG | 11 | a0001c0001t0001g0021a0001c0001t0001g0138a0001c0001t0001g0174others(8): Show | 12 | HG00741.hp1 HG01256.hp1 HG01258.hp2 others(9): Show |
intron_variant | MODIFIER | c.634+1777_634+1778i others(8): Show |
MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr3 | 69953662 | |||||
chr3:69953662
|
TAG | T | 20 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062others(17): Show | 20 | HG00408.hp2 HG01074.hp1 HG01074.hp2 others(17): Show |
intron_variant | MODIFIER | c.634+1802_634+1803d others(4): Show |
MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr3 | 69953662 | |||||
chr3:69953662
|
TAGAGAG | T | 4 | a0001c0001t0001g0053a0001c0001t0001g0108a0001c0001t0001g0166others(1): Show | 4 | NA18971.hp2 NA19003.hp2 NA19082.hp1 others(1): Show |
intron_variant | MODIFIER | c.634+1798_634+1803d others(8): Show |
MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr3 | 69953662 | |||||
chr3:69953662
|
TAGAGAGA others(1): Show |
T | 2 | a0001c0001t0002g0012a0001c0001t0002g0159 | 4 | HG01884.hp1 HG02615.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.634+1796_634+1803d others(10): Show |
MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr3 | 69953662 | |||||
chr3:69953664
|
G | T | 80 | a0001c0001t0001g0013a0001c0001t0001g0016a0001c0001t0001g0019others(77): Show | 87 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(84): Show |
intron_variant | MODIFIER | c.634+1778G>T | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 6/8 | chr3 | 69953664 | ||||||
chr3:69953666
|
G | T | 26 | a0001c0001t0001g0023a0001c0001t0001g0072a0001c0001t0001g0094others(23): Show | 27 | HG01074.hp1 HG01243.hp1 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.634+1780G>T | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 6/8 | chr3 | 69953666 | ||||||
chr3:69953668
|
G | T | 4 | a0001c0001t0006g0282a0001c0001t0006g0284a0001c0001t0006g0314others(1): Show | 4 | HG01074.hp1 HG01243.hp2 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.634+1782G>T | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 6/8 | chr3 | 69953668 | ||||||
chr3:69953670
|
G | T | 1 | a0001c0001t0006g0314 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.634+1784G>T | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 6/8 | chr3 | 69953670 | ||||||
chr3:69953684
|
G | C | 15 | a0001c0001t0001g0021a0001c0001t0001g0034a0001c0001t0001g0138others(12): Show | 16 | HG00099.hp2 HG00140.hp1 HG00735.hp1 others(13): Show |
intron_variant | MODIFIER | c.634+1798G>C | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 6/8 | chr3 | 69953684 | ||||||
chr3:69953684
|
G | GAGAGAC | 26 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0027others(23): Show | 35 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(32): Show |
intron_variant | MODIFIER | c.634+1822_634+1827d others(8): Show |
MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr3 | 69953684 | |||||
chr3:69953684
|
GAGAGAC | G | 27 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0019others(24): Show | 32 | HG00558.hp2 HG01081.hp2 HG01256.hp2 others(29): Show |
intron_variant | MODIFIER | c.634+1822_634+1827d others(8): Show |
MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr3 | 69953684 | |||||
chr3:69953690
|
C | G | 2 | a0001c0001t0008g0022a0001c0001t0008g0069 | 3 | NA18947.hp1 NA18978.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.634+1804C>G | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 6/8 | chr3 | 69953690 | ||||||
chr3:69953814
|
G | A | 8 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0092others(5): Show | 8 | HG02559.hp1 HG02818.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.634+1928G>A | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 6/8 | chr3 | 69953814 | ||||||
chr3:69954054
|
A | G | 1 | a0001c0001t0002g0080 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.634+2168A>G | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 6/8 | chr3 | 69954054 | ||||||
chr3:69954175
|
A | G | 5 | a0001c0001t0001g0027a0001c0001t0001g0161a0001c0001t0001g0192others(2): Show | 6 | HG00140.hp1 HG00280.hp2 HG00741.hp1 others(3): Show |
intron_variant | MODIFIER | c.635-2280A>G | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 6/8 | chr3 | 69954175 | ||||||
chr3:69954189
|
A | C | 2 | a0001c0001t0011g0030a0001c0001t0017g0319 | 3 | HG02965.hp2 HG02970.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.635-2266A>C | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 6/8 | chr3 | 69954189 | ||||||
chr3:69954268
|
G | A | 1 | a0001c0001t0001g0068 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.635-2187G>A | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 6/8 | chr3 | 69954268 | ||||||
chr3:69954422
|
G | A | 4 | a0001c0001t0002g0110a0001c0001t0002g0139a0001c0001t0002g0176others(1): Show | 4 | HG01433.hp1 HG02602.hp1 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.635-2033G>A | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 6/8 | chr3 | 69954422 | ||||||
chr3:69955049
|
C | G | 2 | a0001c0001t0005g0031a0001c0001t0005g0327 | 3 | NA18943.hp1 NA19007.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.635-1406C>G | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 6/8 | chr3 | 69955049 | ||||||
chr3:69955057
|
C | T | 4 | a0001c0001t0001g0130a0001c0001t0001g0197a0001c0001t0001g0204others(1): Show | 4 | HG01099.hp1 HG01109.hp2 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.635-1398C>T | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 6/8 | chr3 | 69955057 | ||||||
chr3:69955093
|
G | A | 1 | a0001c0001t0001g0169 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.635-1362G>A | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 6/8 | chr3 | 69955093 | ||||||
chr3:69955312
|
G | A | 8 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0092others(5): Show | 8 | HG02559.hp1 HG02818.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.635-1143G>A | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 6/8 | chr3 | 69955312 | ||||||
chr3:69955370
|
T | G | 1 | a0001c0001t0001g0196 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.635-1085T>G | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 6/8 | chr3 | 69955370 | ||||||
chr3:69955549
|
C | T | 1 | a0001c0001t0001g0171 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.635-906C>T | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 6/8 | chr3 | 69955549 | ||||||
chr3:69955777
|
G | A | 1 | a0001c0001t0002g0056 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.635-678G>A | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 6/8 | chr3 | 69955777 | ||||||
chr3:69955830
|
C | T | 1 | a0001c0001t0002g0080 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.635-625C>T | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 6/8 | chr3 | 69955830 | ||||||
chr3:69955934
|
G | A | 1 | a0001c0001t0001g0061 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.635-521G>A | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 6/8 | chr3 | 69955934 | ||||||
chr3:69955935
|
T | C | 4 | a0001c0001t0001g0285a0001c0001t0001g0286a0001c0001t0001g0299others(1): Show | 4 | HG02630.hp2 HG03041.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.635-520T>C | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 6/8 | chr3 | 69955935 | ||||||
chr3:69955953
|
T | C | 3 | a0001c0001t0001g0161a0001c0001t0001g0192a0001c0001t0001g0209 | 3 | HG00140.hp1 HG02055.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.635-502T>C | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 6/8 | chr3 | 69955953 | ||||||
chr3:69956130
|
A | G | 244 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0016others(241): Show | 280 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(277): Show |
intron_variant | MODIFIER | c.635-325A>G | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 6/8 | chr3 | 69956130 | ||||||
chr3:69956190
|
T | A | 1 | a0001c0001t0003g0248 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.635-265T>A | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 6/8 | chr3 | 69956190 | ||||||
chr3:69956246
|
G | A | 4 | a0001c0001t0001g0285a0001c0001t0001g0286a0001c0001t0001g0299others(1): Show | 4 | HG02630.hp2 HG03041.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.635-209G>A | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 6/8 | chr3 | 69956246 | ||||||
chr3:69956542
|
C | T | 1 | a0001c0001t0001g0237 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.710+12C>T | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 7/8 | chr3 | 69956542 | ||||||
chr3:69956544
|
C | T | 1 | a0001c0001t0004g0227 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.710+14C>T | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 7/8 | chr3 | 69956544 | ||||||
chr3:69956561
|
T | C | 2 | a0001c0001t0001g0197a0001c0001t0001g0204 | 2 | HG01099.hp1 HG01109.hp2 |
intron_variant | MODIFIER | c.710+31T>C | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 7/8 | chr3 | 69956561 | ||||||
chr3:69956729
|
G | A | 2 | a0001c0001t0001g0151a0001c0001t0001g0275 | 2 | HG02818.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.710+199G>A | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 7/8 | chr3 | 69956729 | ||||||
chr3:69956735
|
A | G | 1 | a0004c0005t0001g0035 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.710+205A>G | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 7/8 | chr3 | 69956735 | ||||||
chr3:69956805
|
A | G | 1 | a0001c0001t0001g0202 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.710+275A>G | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 7/8 | chr3 | 69956805 | ||||||
chr3:69957490
|
C | G | 1 | a0001c0001t0010g0312 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.710+960C>G | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 7/8 | chr3 | 69957490 | ||||||
chr3:69957528
|
T | C | 1 | a0001c0001t0001g0158 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.710+998T>C | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 7/8 | chr3 | 69957528 | ||||||
chr3:69957722
|
A | G | 1 | a0001c0001t0021g0315 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.710+1192A>G | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 7/8 | chr3 | 69957722 | ||||||
chr3:69957727
|
G | T | 1 | a0001c0001t0001g0257 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.710+1197G>T | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 7/8 | chr3 | 69957727 | ||||||
chr3:69957754
|
C | G | 2 | a0001c0004t0012g0057a0001c0004t0012g0305 | 2 | HG02809.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.710+1224C>G | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 7/8 | chr3 | 69957754 | ||||||
chr3:69957872
|
G | C | 1 | a0001c0001t0001g0301 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.710+1342G>C | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 7/8 | chr3 | 69957872 | ||||||
chr3:69957929
|
C | T | 10 | a0001c0001t0006g0282a0001c0001t0006g0283a0001c0001t0006g0284others(7): Show | 11 | HG01074.hp1 HG01243.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.711-1344C>T | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 7/8 | chr3 | 69957929 | ||||||
chr3:69957951
|
C | T | 2 | a0001c0001t0001g0215a0001c0001t0001g0221 | 2 | HG00558.hp1 HG02135.hp1 |
intron_variant | MODIFIER | c.711-1322C>T | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 7/8 | chr3 | 69957951 | ||||||
chr3:69957998
|
A | G | 2 | a0001c0001t0002g0015a0001c0001t0002g0046 | 3 | NA18939.hp2 NA19009.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.711-1275A>G | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 7/8 | chr3 | 69957998 | ||||||
chr3:69958217
|
T | C | 17 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0092others(14): Show | 18 | HG01074.hp1 HG01243.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.711-1056T>C | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 7/8 | chr3 | 69958217 | ||||||
chr3:69958323
|
T | C | 1 | a0001c0001t0001g0201 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.711-950T>C | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 7/8 | chr3 | 69958323 | ||||||
chr3:69958335
|
C | T | 2 | a0001c0001t0002g0279a0001c0001t0002g0296 | 2 | HG00323.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.711-938C>T | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 7/8 | chr3 | 69958335 | ||||||
chr3:69958573
|
TA | T | 6 | a0001c0001t0001g0034a0001c0001t0001g0063a0001c0001t0001g0169others(3): Show | 6 | HG00438.hp1 HG02896.hp1 NA18951.hp2 others(3): Show |
intron_variant | MODIFIER | c.711-686delA | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr3 | 69958573 | |||||
chr3:69958707
|
A | G | 2 | a0001c0001t0001g0093a0001c0001t0001g0155 | 2 | NA18971.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.711-566A>G | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 7/8 | chr3 | 69958707 | ||||||
chr3:69958709
|
A | G | 1 | a0001c0001t0019g0126 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.711-564A>G | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 7/8 | chr3 | 69958709 | ||||||
chr3:69958924
|
G | T | 1 | a0003c0006t0001g0193 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.711-349G>T | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 7/8 | chr3 | 69958924 | ||||||
chr3:69959012
|
G | A | 5 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0095others(2): Show | 5 | NA18964.hp1 NA18971.hp1 NA18981.hp1 others(2): Show |
intron_variant | MODIFIER | c.711-261G>A | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 7/8 | chr3 | 69959012 | ||||||
chr3:69959026
|
T | A | 1 | a0001c0001t0001g0040 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.711-247T>A | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 7/8 | chr3 | 69959026 | ||||||
chr3:69959125
|
A | G | 1 | a0001c0001t0001g0092 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.711-148A>G | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 7/8 | chr3 | 69959125 | ||||||
chr3:69959151
|
C | T | 1 | a0001c0001t0001g0091 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.711-122C>T | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 7/8 | chr3 | 69959151 | ||||||
chr3:69959175
|
T | A | 8 | a0001c0001t0001g0189a0001c0001t0001g0318a0001c0001t0002g0190others(5): Show | 8 | HG00735.hp2 HG01884.hp2 HG02273.hp1 others(5): Show |
intron_variant | MODIFIER | c.711-98T>A | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 7/8 | chr3 | 69959175 | ||||||
chr3:69959189
|
A | G | 2 | a0001c0001t0001g0307a0001c0001t0001g0309 | 2 | NA18972.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.711-84A>G | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 7/8 | chr3 | 69959189 | ||||||
chr3:69959514
|
C | T | 2 | a0001c0001t0011g0030a0001c0001t0017g0319 | 3 | HG02965.hp2 HG02970.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.858+94C>T | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 8/8 | chr3 | 69959514 | ||||||
chr3:69959637
|
G | T | 24 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0092others(21): Show | 26 | HG01074.hp1 HG01243.hp2 HG02071.hp2 others(23): Show |
intron_variant | MODIFIER | c.858+217G>T | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 8/8 | chr3 | 69959637 | ||||||
chr3:69959857
|
G | A | 9 | a0001c0001t0003g0010a0001c0001t0003g0037a0001c0001t0003g0090others(6): Show | 11 | HG01167.hp1 HG01169.hp1 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.858+437G>A | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 8/8 | chr3 | 69959857 | ||||||
chr3:69959915
|
G | C | 3 | a0001c0001t0002g0110a0001c0001t0002g0176a0001c0001t0014g0163 | 3 | HG01433.hp1 HG03669.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.858+495G>C | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 8/8 | chr3 | 69959915 | ||||||
chr3:69960126
|
A | G | 7 | a0001c0001t0006g0282a0001c0001t0006g0283a0001c0001t0006g0284others(4): Show | 7 | HG01074.hp1 HG01243.hp2 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.858+706A>G | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 8/8 | chr3 | 69960126 | ||||||
chr3:69960142
|
AC | A | 24 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0092others(21): Show | 26 | HG01074.hp1 HG01243.hp2 HG02071.hp2 others(23): Show |
intron_variant | MODIFIER | c.858+724delC | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr3 | 69960142 | |||||
chr3:69960406
|
C | T | 1 | a0001c0001t0001g0154 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.858+986C>T | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 8/8 | chr3 | 69960406 | ||||||
chr3:69960585
|
A | G | 24 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0092others(21): Show | 26 | HG01074.hp1 HG01243.hp2 HG02071.hp2 others(23): Show |
intron_variant | MODIFIER | c.858+1165A>G | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 8/8 | chr3 | 69960585 | ||||||
chr3:69960743
|
G | A | 3 | a0001c0001t0002g0076a0001c0001t0007g0106a0001c0001t0007g0116 | 3 | NA18953.hp2 NA18962.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.858+1323G>A | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 8/8 | chr3 | 69960743 | ||||||
chr3:69960747
|
A | T | 2 | a0001c0001t0001g0218a0001c0001t0001g0223 | 2 | HG00099.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.858+1327A>T | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 8/8 | chr3 | 69960747 | ||||||
chr3:69960827
|
T | A | 4 | a0001c0001t0002g0045a0001c0001t0002g0065a0001c0001t0002g0180others(1): Show | 4 | NA18955.hp1 NA18975.hp1 NA19077.hp2 others(1): Show |
intron_variant | MODIFIER | c.858+1407T>A | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 8/8 | chr3 | 69960827 | ||||||
chr3:69960938
|
T | C | 25 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0092others(22): Show | 27 | HG00735.hp2 HG01074.hp1 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.858+1518T>C | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 8/8 | chr3 | 69960938 | ||||||
chr3:69961069
|
G | A | 94 | a0001c0001t0001g0013a0001c0001t0001g0051a0001c0001t0001g0075others(91): Show | 111 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.858+1649G>A | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 8/8 | chr3 | 69961069 | ||||||
chr3:69961080
|
G | A | 118 | a0001c0001t0001g0013a0001c0001t0001g0040a0001c0001t0001g0041others(115): Show | 137 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.858+1660G>A | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 8/8 | chr3 | 69961080 | ||||||
chr3:69961188
|
G | C | 1 | a0001c0001t0001g0044 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.858+1768G>C | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 8/8 | chr3 | 69961188 | ||||||
chr3:69961246
|
G | A | 1 | a0001c0001t0001g0079 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.858+1826G>A | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 8/8 | chr3 | 69961246 | ||||||
chr3:69961256
|
G | A | 11 | a0001c0001t0002g0112a0001c0001t0002g0113a0001c0001t0002g0115others(8): Show | 11 | HG02257.hp1 HG02559.hp2 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.858+1836G>A | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 8/8 | chr3 | 69961256 | ||||||
chr3:69961273
|
C | T | 4 | a0001c0001t0002g0190a0001c0001t0002g0191a0001c0001t0002g0298others(1): Show | 4 | HG00735.hp2 HG01884.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.858+1853C>T | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 8/8 | chr3 | 69961273 | ||||||
chr3:69961306
|
C | T | 2 | a0001c0001t0002g0147a0001c0001t0002g0148 | 2 | HG02896.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.858+1886C>T | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 8/8 | chr3 | 69961306 | ||||||
chr3:69961391
|
C | A | 3 | a0001c0001t0001g0092a0001c0001t0001g0154a0001c0001t0001g0276 | 3 | HG02559.hp1 HG03516.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.858+1971C>A | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 8/8 | chr3 | 69961391 | ||||||
chr3:69961393
|
A | T | 3 | a0001c0001t0001g0092a0001c0001t0001g0154a0001c0001t0001g0276 | 3 | HG02559.hp1 HG03516.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.858+1973A>T | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 8/8 | chr3 | 69961393 | ||||||
chr3:69961444
|
C | T | 2 | a0001c0004t0012g0057a0001c0004t0012g0305 | 2 | HG02809.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.858+2024C>T | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 8/8 | chr3 | 69961444 | ||||||
chr3:69961550
|
C | CA | 7 | a0001c0001t0001g0092a0001c0001t0001g0154a0001c0001t0001g0228others(4): Show | 7 | HG02559.hp1 HG03516.hp1 NA18940.hp1 others(4): Show |
intron_variant | MODIFIER | c.858+2143dupA | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr3 | 69961550 | |||||
chr3:69961550
|
CAA | C | 87 | a0001c0001t0001g0189a0001c0001t0001g0318a0001c0001t0002g0001others(84): Show | 103 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.858+2142_858+2143d others(4): Show |
MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr3 | 69961550 | |||||
chr3:69961564
|
G | A | 24 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0092others(21): Show | 26 | HG01074.hp1 HG01243.hp2 HG02071.hp2 others(23): Show |
intron_variant | MODIFIER | c.858+2144G>A | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 8/8 | chr3 | 69961564 | ||||||
chr3:69961779
|
T | A | 88 | a0001c0001t0001g0189a0001c0001t0001g0318a0001c0001t0002g0001others(85): Show | 104 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.858+2359T>A | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 8/8 | chr3 | 69961779 | ||||||
chr3:69961885
|
T | A | 3 | a0001c0001t0001g0023a0001c0001t0001g0099a0001c0001t0001g0177 | 4 | NA18939.hp1 NA18951.hp1 NA18995.hp1 others(1): Show |
intron_variant | MODIFIER | c.858+2465T>A | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 8/8 | chr3 | 69961885 | ||||||
chr3:69962270
|
T | C | 99 | a0001c0001t0001g0032a0001c0001t0001g0089a0001c0001t0001g0189others(96): Show | 115 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.859-2577T>C | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 8/8 | chr3 | 69962270 | ||||||
chr3:69962328
|
T | C | 1 | a0001c0001t0002g0065 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.859-2519T>C | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 8/8 | chr3 | 69962328 | ||||||
chr3:69962380
|
G | T | 2 | a0001c0001t0001g0189a0001c0001t0001g0318 | 2 | HG03195.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.859-2467G>T | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 8/8 | chr3 | 69962380 | ||||||
chr3:69962515
|
A | G | 2 | a0001c0004t0012g0057a0001c0004t0012g0305 | 2 | HG02809.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.859-2332A>G | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 8/8 | chr3 | 69962515 | ||||||
chr3:69962592
|
G | C | 99 | a0001c0001t0001g0032a0001c0001t0001g0052a0001c0001t0001g0189others(96): Show | 115 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.859-2255G>C | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 8/8 | chr3 | 69962592 | ||||||
chr3:69962819
|
G | A | 1 | a0001c0001t0021g0315 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.859-2028G>A | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 8/8 | chr3 | 69962819 | ||||||
chr3:69963282
|
T | G | 1 | a0001c0001t0002g0261 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.859-1565T>G | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 8/8 | chr3 | 69963282 | ||||||
chr3:69963475
|
T | C | 1 | a0001c0001t0003g0245 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.859-1372T>C | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 8/8 | chr3 | 69963475 | ||||||
chr3:69963508
|
T | A | 1 | a0001c0001t0021g0315 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.859-1339T>A | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 8/8 | chr3 | 69963508 | ||||||
chr3:69963518
|
T | C | 1 | a0001c0001t0002g0267 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.859-1329T>C | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 8/8 | chr3 | 69963518 | ||||||
chr3:69963726
|
A | G | 1 | a0001c0001t0005g0322 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.859-1121A>G | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 8/8 | chr3 | 69963726 | ||||||
chr3:69963739
|
T | C | 2 | a0001c0001t0001g0154a0001c0001t0001g0276 | 2 | HG02559.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.859-1108T>C | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 8/8 | chr3 | 69963739 | ||||||
chr3:69963970
|
C | CT | 26 | a0001c0001t0001g0095a0001c0001t0001g0133a0001c0001t0001g0136others(23): Show | 28 | HG00438.hp1 HG00735.hp2 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.859-854dupT | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr3 | 69963970 | |||||
chr3:69963970
|
C | CTTT | 91 | a0001c0001t0001g0032a0001c0001t0001g0052a0001c0001t0001g0084others(88): Show | 108 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.859-856_859-854dup others(3): Show |
MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr3 | 69963970 | |||||
chr3:69963970
|
C | CTTTT | 8 | a0001c0001t0002g0076a0001c0001t0002g0119a0001c0001t0002g0120others(5): Show | 8 | HG00438.hp2 HG02145.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.859-857_859-854dup others(4): Show |
MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr3 | 69963970 | |||||
chr3:69963970
|
CT | C | 16 | a0001c0001t0001g0026a0001c0001t0001g0036a0001c0001t0001g0053others(13): Show | 18 | HG00673.hp1 HG00735.hp1 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.859-854delT | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr3 | 69963970 | |||||
chr3:69963970
|
CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0009g0277 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.859-863_859-854del others(10): Show |
MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr3 | 69963970 | |||||
chr3:69964182
|
T | A | 1 | a0001c0001t0002g0078 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.859-665T>A | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 8/8 | chr3 | 69964182 | ||||||
chr3:69964198
|
A | G | 127 | a0001c0001t0001g0032a0001c0001t0001g0052a0001c0001t0001g0084others(124): Show | 146 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(143): Show |
intron_variant | MODIFIER | c.859-649A>G | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 8/8 | chr3 | 69964198 | ||||||
chr3:69964226
|
C | T | 2 | a0001c0001t0003g0039a0001c0001t0003g0293 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.859-621C>T | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 8/8 | chr3 | 69964226 | ||||||
chr3:69964264
|
G | A | 3 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0002g0077 | 3 | HG02976.hp2 HG03453.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.859-583G>A | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 8/8 | chr3 | 69964264 | ||||||
chr3:69964323
|
GTGAGAGA others(406): Show |
G | 97 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0008others(94): Show | 114 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(111): Show |
intron_variant | MODIFIER | c.859-521_859-109del | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr3 | 69964323 | |||||
chr3:69964348
|
A | T | 1 | a0001c0001t0021g0315 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.859-499A>T | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 8/8 | chr3 | 69964348 | ||||||
chr3:69964593
|
C | T | 9 | a0001c0001t0005g0031a0001c0001t0005g0289a0001c0001t0005g0320others(6): Show | 11 | HG02071.hp2 HG02723.hp1 HG02965.hp2 others(8): Show |
intron_variant | MODIFIER | c.859-254C>T | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 8/8 | chr3 | 69964593 | ||||||
chr3:69964658
|
C | T | 1 | a0001c0001t0020g0141 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.859-189C>T | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 8/8 | chr3 | 69964658 | ||||||
chr3:69964659
|
G | A | 2 | a0001c0004t0012g0057a0001c0004t0012g0305 | 2 | HG02809.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.859-188G>A | MITF | ENSG00000187098.18 | transcript | ENST00000394351.9 | protein_coding | 8/8 | chr3 | 69964659 |