geneid | 22823 |
---|---|
ensemblid | ENSG00000143033.18 |
hgncid | 29535 |
symbol | MTF2 |
name | metal response element binding transcription factor 2 |
refseq_nuc | NM_007358.4 |
refseq_prot | NP_031384.1 |
ensembl_nuc | ENST00000370298.9 |
ensembl_prot | ENSP00000359321.4 |
mane_status | MANE Select |
chr | chr1 |
start | 93079283 |
end | 93139076 |
strand | + |
ver | v1.2 |
region | chr1:93079283-93139076 |
region5000 | chr1:93074283-93144076 |
regionname0 | MTF2_chr1_93079283_93139076 |
regionname5000 | MTF2_chr1_93074283_93144076 |
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 | 593 | 336 | 88 | 63 | 139 | 14 | 30 | 108 | MTF2_chr1_93074283_93144076 | MTF2 | copy fasta | chr1 | 93074283 | 93144076 |
a0002 | 0/0 | 593 | 3 | 0 | 0 | 3 | 0 | 0 | 2 | MTF2_chr1_93074283_93144076 | MTF2 | copy fasta | chr1 | 93074283 | 93144076 |
a0003 | 0/0 | 593 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | copy fasta | chr1 | 93074283 | 93144076 |
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 | 1782 | 335 | 87 | 63 | 139 | 14 | 30 | MTF2_chr1_93074283_93144076 | MTF2 | copy fasta | chr1 | 93074283 | 93144076 |
c0002 | 0/0 | 1782 | 3 | 0 | 0 | 3 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | copy fasta | chr1 | 93074283 | 93144076 |
c0003 | 0/0 | 1782 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | copy fasta | chr1 | 93074283 | 93144076 |
c0004 | 0/0 | 1782 | 1 | 0 | 1 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | copy fasta | chr1 | 93074283 | 93144076 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 2296 | 153 | 32 | 28 | 74 | 6 | 13 | MTF2_chr1_93074283_93144076 | MTF2 | copy fasta | chr1 | 93074283 | 93144076 |
t0002 | 1/0 | 2294 | 79 | 4 | 17 | 48 | 3 | 6 | MTF2_chr1_93074283_93144076 | MTF2 | copy fasta | chr1 | 93074283 | 93144076 |
t0003 | 0/0 | 2296 | 75 | 35 | 14 | 13 | 4 | 9 | MTF2_chr1_93074283_93144076 | MTF2 | copy fasta | chr1 | 93074283 | 93144076 |
t0004 | 0/0 | 2296 | 6 | 6 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | copy fasta | chr1 | 93074283 | 93144076 |
t0005 | 0/0 | 2296 | 4 | 4 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | copy fasta | chr1 | 93074283 | 93144076 |
t0006 | 0/0 | 2296 | 4 | 3 | 1 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | copy fasta | chr1 | 93074283 | 93144076 |
t0007 | 0/1 | 2296 | 4 | 0 | 2 | 0 | 1 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | copy fasta | chr1 | 93074283 | 93144076 |
t0008 | 0/0 | 2293 | 4 | 0 | 1 | 3 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | copy fasta | chr1 | 93074283 | 93144076 |
t0009 | 0/0 | 2296 | 1 | 0 | 0 | 0 | 0 | 1 | MTF2_chr1_93074283_93144076 | MTF2 | copy fasta | chr1 | 93074283 | 93144076 |
t0010 | 0/0 | 2295 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | copy fasta | chr1 | 93074283 | 93144076 |
t0011 | 0/0 | 2296 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | copy fasta | chr1 | 93074283 | 93144076 |
t0012 | 0/0 | 2296 | 1 | 0 | 1 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | copy fasta | chr1 | 93074283 | 93144076 |
t0013 | 0/0 | 2296 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | copy fasta | chr1 | 93074283 | 93144076 |
t0014 | 0/0 | 2294 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | copy fasta | chr1 | 93074283 | 93144076 |
t0015 | 0/0 | 2294 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | copy fasta | chr1 | 93074283 | 93144076 |
t0016 | 0/0 | 2294 | 1 | 0 | 0 | 0 | 0 | 1 | MTF2_chr1_93074283_93144076 | MTF2 | copy fasta | chr1 | 93074283 | 93144076 |
t0017 | 0/0 | 2294 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | copy fasta | chr1 | 93074283 | 93144076 |
t0018 | 0/0 | 2296 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | copy fasta | chr1 | 93074283 | 93144076 |
t0019 | 0/0 | 2295 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | copy fasta | chr1 | 93074283 | 93144076 |
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 | 4 | 0 | 0 | 4 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0003 | 0/0 | 4 | 0 | 1 | 2 | 1 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0005 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0009 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0010 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0013 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0021 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0073 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0293 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
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 | 1782 | 335 | 87 | 63 | 139 | 14 | 30 | MTF2_chr1_93074283_93144076 | MTF2 | copy fasta | chr1 | 93074283 | 93144076 |
a0001c0003 | 0/0 | 1782 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | copy fasta | chr1 | 93074283 | 93144076 |
a0002c0002 | 0/0 | 1782 | 3 | 0 | 0 | 3 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | copy fasta | chr1 | 93074283 | 93144076 |
a0003c0004 | 0/0 | 1782 | 1 | 0 | 1 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | copy fasta | chr1 | 93074283 | 93144076 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 4077 | 150 | 32 | 27 | 72 | 6 | 13 | MTF2_chr1_93074283_93144076 | MTF2 | copy fasta | chr1 | 93074283 | 93144076 |
a0001c0001t0002 | 1/0 | 4075 | 79 | 4 | 17 | 48 | 3 | 6 | MTF2_chr1_93074283_93144076 | MTF2 | copy fasta | chr1 | 93074283 | 93144076 |
a0001c0001t0003 | 0/0 | 4077 | 74 | 34 | 14 | 13 | 4 | 9 | MTF2_chr1_93074283_93144076 | MTF2 | copy fasta | chr1 | 93074283 | 93144076 |
a0001c0001t0004 | 0/0 | 4077 | 6 | 6 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | copy fasta | chr1 | 93074283 | 93144076 |
a0001c0001t0005 | 0/0 | 4077 | 4 | 4 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | copy fasta | chr1 | 93074283 | 93144076 |
a0001c0001t0006 | 0/0 | 4077 | 4 | 3 | 1 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | copy fasta | chr1 | 93074283 | 93144076 |
a0001c0001t0007 | 0/1 | 4077 | 4 | 0 | 2 | 0 | 1 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | copy fasta | chr1 | 93074283 | 93144076 |
a0001c0001t0008 | 0/0 | 4074 | 4 | 0 | 1 | 3 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | copy fasta | chr1 | 93074283 | 93144076 |
a0001c0001t0009 | 0/0 | 4077 | 1 | 0 | 0 | 0 | 0 | 1 | MTF2_chr1_93074283_93144076 | MTF2 | copy fasta | chr1 | 93074283 | 93144076 |
a0001c0001t0010 | 0/0 | 4076 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | copy fasta | chr1 | 93074283 | 93144076 |
a0001c0001t0011 | 0/0 | 4077 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | copy fasta | chr1 | 93074283 | 93144076 |
a0001c0001t0012 | 0/0 | 4077 | 1 | 0 | 1 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | copy fasta | chr1 | 93074283 | 93144076 |
a0001c0001t0013 | 0/0 | 4077 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | copy fasta | chr1 | 93074283 | 93144076 |
a0001c0001t0014 | 0/0 | 4075 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | copy fasta | chr1 | 93074283 | 93144076 |
a0001c0001t0015 | 0/0 | 4075 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | copy fasta | chr1 | 93074283 | 93144076 |
a0001c0001t0016 | 0/0 | 4075 | 1 | 0 | 0 | 0 | 0 | 1 | MTF2_chr1_93074283_93144076 | MTF2 | copy fasta | chr1 | 93074283 | 93144076 |
a0001c0001t0017 | 0/0 | 4075 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | copy fasta | chr1 | 93074283 | 93144076 |
a0001c0001t0018 | 0/0 | 4077 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | copy fasta | chr1 | 93074283 | 93144076 |
a0001c0003t0003 | 0/0 | 4077 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | copy fasta | chr1 | 93074283 | 93144076 |
a0002c0002t0001 | 0/0 | 4077 | 2 | 0 | 0 | 2 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | copy fasta | chr1 | 93074283 | 93144076 |
a0002c0002t0019 | 0/0 | 4076 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | copy fasta | chr1 | 93074283 | 93144076 |
a0003c0004t0001 | 0/0 | 4077 | 1 | 0 | 1 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | copy fasta | chr1 | 93074283 | 93144076 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0001g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0001g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0001g0010 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0002g0003 | 0/0 | 3 | 0 | 1 | 1 | 1 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0002g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0002g0005 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0002g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0002g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0002g0013 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0002g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0002g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0002g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0002g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0002g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0002g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0002g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0002g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0002g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0002g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0002g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0002g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0002g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0002g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0002g0293 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0003g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0003g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0003g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0003g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0003g0021 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0003g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0003g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0003g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0003g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0003g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0003g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0003g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0003g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0003g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0003g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0003g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0003g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0003g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0003g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0003g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0003g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0003g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0003g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0003g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0003g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0003g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0003g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0003g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0003g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0003g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0003g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0003g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0003g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0003g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0003g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0003g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0003g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0003g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0003g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0003g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0003g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0003g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0003g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0003g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0003g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0003g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0003g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0003g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0003g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0003g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0003g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0003g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0003g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0003g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0003g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0003g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0003g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0003g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0003g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0003g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0003g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0003g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0003g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0003g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0003g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0003g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0003g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0003g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0004g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0004g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0004g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0004g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0004g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0005g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0005g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0005g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0005g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0006g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0006g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0006g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0006g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0007g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0007g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0007g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0007g0073 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0008g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0008g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0008g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0008g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0009g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0010g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0011g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0012g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0013g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0014g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0015g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0016g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0017g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0001t0018g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0001c0003t0003g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0002c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0002c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0002c0002t0019g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
a0003c0004t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00280 | hp1 | a0001 | c0001 | t0001 | g0086 | EUR | FIN | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG00280 | hp2 | a0001 | c0001 | t0003 | g0196 | EUR | FIN | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0095 | EUR | FIN | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG00323 | hp2 | a0001 | c0001 | t0003 | g0220 | EUR | FIN | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG00408 | hp1 | a0001 | c0001 | t0003 | g0304 | EAS | CHS | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG00423 | hp1 | a0001 | c0001 | t0003 | g0022 | EAS | CHS | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | CHS | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | CHS | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | CHS | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | CHS | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG00544 | hp2 | a0001 | c0001 | t0002 | g0173 | EAS | CHS | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG00558 | hp1 | a0001 | c0001 | t0002 | g0167 | EAS | CHS | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG00639 | hp2 | a0001 | c0001 | t0002 | g0148 | AMR | PUR | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG00642 | hp2 | a0001 | c0001 | t0003 | g0212 | AMR | PUR | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG00673 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | CHS | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | CHS | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | PUR | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG00733 | hp2 | a0001 | c0001 | t0002 | g0144 | AMR | PUR | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG00738 | hp2 | a0001 | c0001 | t0007 | g0051 | AMR | PUR | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG00741 | hp1 | a0001 | c0001 | t0003 | g0202 | AMR | PUR | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG00741 | hp2 | a0003 | c0004 | t0001 | g0066 | AMR | PUR | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG01069 | hp1 | a0001 | c0001 | t0003 | g0194 | AMR | PUR | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG01070 | hp1 | a0001 | c0001 | t0003 | g0208 | AMR | PUR | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0088 | AMR | PUR | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG01074 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG01074 | hp2 | a0001 | c0001 | t0003 | g0018 | AMR | PUR | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG01081 | hp1 | a0001 | c0001 | t0002 | g0177 | AMR | PUR | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG01081 | hp2 | a0001 | c0001 | t0003 | g0021 | AMR | PUR | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG01106 | hp1 | a0001 | c0001 | t0002 | g0141 | AMR | PUR | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG01106 | hp2 | a0001 | c0001 | t0003 | g0018 | AMR | PUR | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG01109 | hp1 | a0001 | c0001 | t0006 | g0238 | AMR | PUR | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG01167 | hp1 | a0001 | c0001 | t0003 | g0209 | AMR | PUR | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | PUR | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG01169 | hp2 | a0001 | c0001 | t0003 | g0201 | AMR | PUR | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG01175 | hp1 | a0001 | c0001 | t0012 | g0199 | AMR | PUR | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG01175 | hp2 | a0001 | c0001 | t0007 | g0064 | AMR | PUR | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG01192 | hp1 | a0001 | c0001 | t0003 | g0195 | AMR | PUR | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | CLM | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG01256 | hp2 | a0001 | c0001 | t0002 | g0147 | AMR | CLM | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0078 | AMR | CLM | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG01257 | hp2 | a0001 | c0001 | t0003 | g0019 | AMR | CLM | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG01261 | hp1 | a0001 | c0001 | t0003 | g0019 | AMR | CLM | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG01261 | hp2 | a0001 | c0001 | t0002 | g0138 | AMR | CLM | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG01346 | hp1 | a0001 | c0001 | t0002 | g0180 | AMR | CLM | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0062 | AMR | CLM | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG01358 | hp1 | a0001 | c0001 | t0003 | g0218 | AMR | CLM | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG01361 | hp1 | a0001 | c0001 | t0002 | g0179 | AMR | CLM | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0081 | AMR | CLM | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG01496 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | CLM | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0061 | AMR | CLM | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG01515 | hp1 | a0001 | c0001 | t0003 | g0221 | EUR | IBS | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG01515 | hp2 | a0001 | c0001 | t0002 | g0165 | EUR | IBS | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0189 | EUR | IBS | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG01516 | hp2 | a0001 | c0001 | t0007 | g0039 | EUR | IBS | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0190 | EUR | IBS | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG01517 | hp2 | a0001 | c0001 | t0003 | g0222 | EUR | IBS | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG01884 | hp1 | a0001 | c0001 | t0006 | g0239 | AFR | ACB | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG01884 | hp2 | a0001 | c0001 | t0004 | g0017 | AFR | ACB | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG01891 | hp1 | a0001 | c0001 | t0003 | g0214 | AFR | ACB | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0247 | AFR | ACB | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG01928 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PEL | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0245 | AMR | PEL | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG01934 | hp1 | a0001 | c0001 | t0008 | g0005 | AMR | PEL | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | PEL | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG01943 | hp1 | a0001 | c0001 | t0002 | g0126 | AMR | PEL | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | PEL | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | PEL | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG01952 | hp2 | a0001 | c0001 | t0002 | g0014 | AMR | PEL | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PEL | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG01978 | hp2 | a0001 | c0001 | t0002 | g0014 | AMR | PEL | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG01981 | hp1 | a0001 | c0001 | t0002 | g0137 | AMR | PEL | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | PEL | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG02015 | hp1 | a0001 | c0001 | t0002 | g0228 | EAS | KHV | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | KHV | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | KHV | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG02040 | hp2 | a0001 | c0001 | t0002 | g0183 | EAS | KHV | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0254 | AFR | ACB | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG02055 | hp2 | a0001 | c0001 | t0003 | g0213 | AFR | ACB | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG02056 | hp1 | a0001 | c0001 | t0014 | g0003 | EAS | KHV | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG02056 | hp2 | a0002 | c0002 | t0001 | g0115 | EAS | KHV | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG02074 | hp1 | a0001 | c0001 | t0003 | g0294 | EAS | KHV | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG02074 | hp2 | a0001 | c0001 | t0002 | g0134 | EAS | KHV | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG02080 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | KHV | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | KHV | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | KHV | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG02129 | hp2 | a0001 | c0001 | t0002 | g0182 | EAS | KHV | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG02135 | hp1 | a0001 | c0001 | t0002 | g0133 | EAS | KHV | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | KHV | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG02145 | hp1 | a0001 | c0001 | t0003 | g0286 | AFR | ACB | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG02145 | hp2 | a0001 | c0001 | t0003 | g0192 | AFR | ACB | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0071 | AMR | PEL | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG02148 | hp2 | a0001 | c0001 | t0002 | g0188 | AMR | PEL | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG02155 | hp1 | a0001 | c0001 | t0002 | g0132 | EAS | CDX | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | CDX | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG02257 | hp1 | a0001 | c0001 | t0003 | g0219 | AFR | ACB | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0243 | AFR | ACB | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0260 | AFR | ACB | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG02258 | hp2 | a0001 | c0001 | t0013 | g0109 | AFR | ACB | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | ACB | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG02280 | hp2 | a0001 | c0001 | t0003 | g0204 | AFR | ACB | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | PEL | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG02293 | hp2 | a0001 | c0001 | t0003 | g0235 | AMR | PEL | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0259 | AFR | ACB | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG02451 | hp2 | a0001 | c0001 | t0002 | g0122 | AFR | ACB | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG02523 | hp1 | a0001 | c0001 | t0008 | g0143 | EAS | KHV | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | KHV | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG02572 | hp1 | a0001 | c0001 | t0003 | g0193 | AFR | GWD | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | GWD | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG02602 | hp1 | a0001 | c0001 | t0009 | g0227 | SAS | PJL | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0072 | SAS | PJL | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG02615 | hp1 | a0001 | c0001 | t0018 | g0289 | AFR | GWD | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0246 | AFR | GWD | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG02630 | hp1 | a0001 | c0001 | t0004 | g0229 | AFR | GWD | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0252 | AFR | GWD | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG02647 | hp1 | a0001 | c0001 | t0003 | g0224 | AFR | GWD | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0263 | AFR | GWD | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG02683 | hp2 | a0001 | c0001 | t0003 | g0276 | SAS | PJL | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0077 | SAS | PJL | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG02698 | hp2 | a0001 | c0001 | t0003 | g0284 | SAS | PJL | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG02717 | hp1 | a0001 | c0001 | t0004 | g0017 | AFR | GWD | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG02717 | hp2 | a0001 | c0001 | t0003 | g0301 | AFR | GWD | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG02723 | hp1 | a0001 | c0001 | t0003 | g0287 | AFR | GWD | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0258 | AFR | GWD | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0107 | SAS | PJL | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG02738 | hp2 | a0001 | c0001 | t0016 | g0129 | SAS | PJL | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG02809 | hp1 | a0001 | c0001 | t0003 | g0015 | AFR | GWD | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0257 | AFR | GWD | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | GWD | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG02818 | hp2 | a0001 | c0001 | t0003 | g0226 | AFR | GWD | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG02886 | hp1 | a0001 | c0001 | t0003 | g0225 | AFR | GWD | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG02886 | hp2 | a0001 | c0001 | t0003 | g0306 | AFR | GWD | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG02895 | hp1 | a0001 | c0001 | t0003 | g0295 | AFR | GWD | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0302 | AFR | GWD | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0244 | AFR | GWD | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG02896 | hp2 | a0001 | c0001 | t0004 | g0230 | AFR | GWD | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0270 | AFR | GWD | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG02897 | hp2 | a0001 | c0001 | t0004 | g0231 | AFR | GWD | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG02922 | hp1 | a0001 | c0001 | t0003 | g0274 | AFR | ESN | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | ESN | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG02965 | hp1 | a0001 | c0001 | t0010 | g0232 | AFR | ESN | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG02965 | hp2 | a0001 | c0001 | t0003 | g0203 | AFR | ESN | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG02970 | hp1 | a0001 | c0001 | t0004 | g0233 | AFR | ESN | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | ESN | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0255 | AFR | ESN | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG02976 | hp2 | a0001 | c0001 | t0003 | g0016 | AFR | ESN | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0249 | AFR | MSL | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0264 | AFR | MSL | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0290 | AFR | ESN | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0248 | AFR | ESN | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | ESN | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0269 | AFR | ESN | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0250 | AFR | ESN | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG03195 | hp2 | a0001 | c0001 | t0006 | g0241 | AFR | ESN | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG03209 | hp1 | a0001 | c0001 | t0003 | g0016 | AFR | MSL | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0261 | AFR | MSL | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG03225 | hp1 | a0001 | c0001 | t0005 | g0280 | AFR | MSL | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG03225 | hp2 | a0001 | c0001 | t0003 | g0237 | AFR | MSL | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0307 | AFR | MSL | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0288 | AFR | MSL | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0030 | SAS | PJL | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG03491 | hp2 | a0001 | c0001 | t0003 | g0272 | SAS | PJL | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG03492 | hp1 | a0001 | c0001 | t0003 | g0273 | SAS | PJL | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG03516 | hp1 | a0001 | c0001 | t0006 | g0240 | AFR | ESN | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG03516 | hp2 | a0001 | c0003 | t0003 | g0217 | AFR | ESN | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG03540 | hp1 | a0001 | c0001 | t0002 | g0123 | AFR | GWD | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG03540 | hp2 | a0001 | c0001 | t0003 | g0207 | AFR | GWD | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG03579 | hp1 | a0001 | c0001 | t0003 | g0303 | AFR | MSL | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG03579 | hp2 | a0001 | c0001 | t0003 | g0216 | AFR | MSL | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG03704 | hp1 | a0001 | c0001 | t0003 | g0211 | SAS | PJL | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG03704 | hp2 | a0001 | c0001 | t0003 | g0277 | SAS | PJL | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG03710 | hp1 | a0001 | c0001 | t0003 | g0223 | SAS | PJL | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0099 | SAS | PJL | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG03831 | hp1 | a0001 | c0001 | t0002 | g0174 | SAS | BEB | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0108 | SAS | BEB | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG03834 | hp1 | a0001 | c0001 | t0003 | g0299 | SAS | BEB | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | BEB | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0083 | SAS | BEB | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG03942 | hp2 | a0001 | c0001 | t0002 | g0164 | SAS | BEB | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG04115 | hp1 | a0001 | c0001 | t0002 | g0135 | SAS | STU | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0104 | SAS | STU | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0103 | SAS | BEB | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG04184 | hp2 | a0001 | c0001 | t0002 | g0139 | SAS | BEB | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0102 | SAS | STU | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG04199 | hp2 | a0001 | c0001 | t0002 | g0128 | SAS | STU | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG04204 | hp1 | a0001 | c0001 | t0002 | g0140 | SAS | STU | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG04204 | hp2 | a0001 | c0001 | t0003 | g0291 | SAS | STU | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
NA18522 | hp1 | a0001 | c0001 | t0005 | g0283 | AFR | YRI | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
NA18522 | hp2 | a0001 | c0001 | t0003 | g0197 | AFR | YRI | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | CHB | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
NA18612 | hp2 | a0001 | c0001 | t0002 | g0156 | EAS | CHB | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0253 | AFR | YRI | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
NA18906 | hp2 | a0001 | c0001 | t0003 | g0205 | AFR | YRI | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
NA18940 | hp2 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
NA18941 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
NA18942 | hp2 | a0001 | c0001 | t0008 | g0170 | EAS | JPT | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
NA18943 | hp2 | a0001 | c0001 | t0003 | g0236 | EAS | JPT | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
NA18945 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
NA18946 | hp2 | a0001 | c0001 | t0002 | g0159 | EAS | JPT | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
NA18947 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
NA18948 | hp1 | a0001 | c0001 | t0002 | g0169 | EAS | JPT | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
NA18948 | hp2 | a0002 | c0002 | t0019 | g0058 | EAS | JPT | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
NA18950 | hp2 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
NA18954 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
NA18956 | hp2 | a0001 | c0001 | t0002 | g0146 | EAS | JPT | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
NA18960 | hp1 | a0001 | c0001 | t0002 | g0168 | EAS | JPT | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
NA18961 | hp1 | a0001 | c0001 | t0003 | g0292 | EAS | JPT | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
NA18962 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
NA18963 | hp2 | a0001 | c0001 | t0002 | g0131 | EAS | JPT | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
NA18969 | hp2 | a0001 | c0001 | t0002 | g0149 | EAS | JPT | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
NA18971 | hp2 | a0001 | c0001 | t0002 | g0152 | EAS | JPT | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
NA18975 | hp1 | a0001 | c0001 | t0002 | g0176 | EAS | JPT | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
NA18977 | hp1 | a0001 | c0001 | t0003 | g0285 | EAS | JPT | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
NA18979 | hp2 | a0001 | c0001 | t0002 | g0187 | EAS | JPT | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
NA18981 | hp1 | a0001 | c0001 | t0003 | g0022 | EAS | JPT | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
NA18983 | hp1 | a0001 | c0001 | t0002 | g0145 | EAS | JPT | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
NA18983 | hp2 | a0001 | c0001 | t0003 | g0021 | EAS | JPT | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
NA18986 | hp2 | a0001 | c0001 | t0002 | g0157 | EAS | JPT | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
NA18993 | hp1 | a0001 | c0001 | t0003 | g0278 | EAS | JPT | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
NA18997 | hp2 | a0001 | c0001 | t0008 | g0130 | EAS | JPT | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
NA18998 | hp2 | a0001 | c0001 | t0002 | g0154 | EAS | JPT | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
NA19000 | hp1 | a0001 | c0001 | t0002 | g0163 | EAS | JPT | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
NA19001 | hp2 | a0001 | c0001 | t0002 | g0162 | EAS | JPT | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
NA19002 | hp1 | a0001 | c0001 | t0002 | g0161 | EAS | JPT | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
NA19004 | hp2 | a0001 | c0001 | t0002 | g0186 | EAS | JPT | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
NA19005 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
NA19007 | hp1 | a0001 | c0001 | t0002 | g0142 | EAS | JPT | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
NA19010 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
NA19011 | hp1 | a0001 | c0001 | t0003 | g0234 | EAS | JPT | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
NA19012 | hp2 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
NA19043 | hp1 | a0001 | c0001 | t0003 | g0297 | AFR | LWK | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
NA19043 | hp2 | a0001 | c0001 | t0003 | g0200 | AFR | LWK | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
NA19055 | hp2 | a0001 | c0001 | t0003 | g0300 | EAS | JPT | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
NA19062 | hp1 | a0001 | c0001 | t0017 | g0172 | EAS | JPT | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
NA19062 | hp2 | a0001 | c0001 | t0003 | g0279 | EAS | JPT | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
NA19063 | hp2 | a0001 | c0001 | t0003 | g0275 | EAS | JPT | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
NA19066 | hp2 | a0001 | c0001 | t0002 | g0160 | EAS | JPT | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
NA19070 | hp2 | a0001 | c0001 | t0002 | g0151 | EAS | JPT | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
NA19075 | hp1 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
NA19075 | hp2 | a0001 | c0001 | t0011 | g0105 | EAS | JPT | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
NA19077 | hp2 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
NA19079 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
NA19082 | hp2 | a0001 | c0001 | t0002 | g0166 | EAS | JPT | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
NA19083 | hp1 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
NA19084 | hp1 | a0001 | c0001 | t0002 | g0185 | EAS | JPT | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
NA19090 | hp1 | a0001 | c0001 | t0002 | g0150 | EAS | JPT | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
NA19240 | hp1 | a0001 | c0001 | t0005 | g0281 | AFR | YRI | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0256 | AFR | YRI | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
NA20129 | hp1 | a0001 | c0001 | t0003 | g0206 | AFR | ASW | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0242 | AFR | ASW | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0097 | EUR | TSI | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
NA20752 | hp2 | a0001 | c0001 | t0002 | g0003 | EUR | TSI | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0091 | EUR | TSI | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
NA20805 | hp2 | a0001 | c0001 | t0002 | g0013 | EUR | TSI | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | CLM | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG01123 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | CLM | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG02109 | hp1 | a0001 | c0001 | t0003 | g0305 | AFR | ACB | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG02109 | hp2 | a0001 | c0001 | t0003 | g0015 | AFR | ACB | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG02559 | hp1 | a0001 | c0001 | t0002 | g0155 | AFR | ACB | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG02559 | hp2 | a0001 | c0001 | t0005 | g0282 | AFR | ACB | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG03471 | hp1 | a0001 | c0001 | t0003 | g0296 | AFR | MSL | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG03471 | hp2 | a0001 | c0001 | t0003 | g0198 | AFR | MSL | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG06807 | hp1 | a0001 | c0001 | t0015 | g0298 | AFR | USA | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
HG06807 | hp2 | a0001 | c0001 | t0003 | g0215 | AFR | USA | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
NA18955 | hp1 | a0002 | c0002 | t0001 | g0057 | EAS | JPT | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
NA18955 | hp2 | a0001 | c0001 | t0002 | g0158 | EAS | JPT | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
NA20300 | hp1 | a0001 | c0001 | t0003 | g0210 | AFR | USA | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
NA20300 | hp2 | a0001 | c0001 | t0002 | g0178 | AFR | USA | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0007 | g0073 | REF | REF | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0293 | REF | REF | MTF2_chr1_93074283_93144076 | MTF2 | chr1 | 93074283 | 93144076 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:93110261
|
C | T | 1 | a0003 | 1 | HG00741.hp2 | missense_variant | MODERATE | c.37C>T | p.His13Tyr | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 2/15 | 281/4075 | 37/1782 | 13/593 | chr1 | 93110261 | ||
chr1:93136882
|
A | G | 1 | a0002 | 3 | HG02056.hp2 NA18948.hp2 NA18955.hp1 |
missense_variant | MODERATE | c.1637A>G | p.Asn546Ser | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 15/15 | 1881/4075 | 1637/1782 | 546/593 | chr1 | 93136882 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:93115040
|
A | G | 1 | a0001c0003 | 1 | HG03516.hp2 | synonymous_variant | LOW | c.435A>G | p.Ser145Ser | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 5/15 | 679/4075 | 435/1782 | 145/593 | chr1 | 93115040 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:93079288
|
G | C | 1 | a0001c0001t0009 | 1 | HG02602.hp1 | 5_prime_UTR_variant | MODIFIER | c.-239G>C | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/15 | 239 | chr1 | 93079288 | |||||
chr1:93079313
|
T | C | 2 | a0001c0001t0004a0001c0001t0010 | 7 | HG01884.hp2 HG02630.hp1 HG02717.hp1 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-214T>C | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/15 | 214 | chr1 | 93079313 | |||||
chr1:93137118
|
TA | T | 3 | a0001c0001t0008a0001c0001t0010a0002c0002t0019 | 6 | HG01934.hp1 HG02523.hp1 HG02965.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*105delA | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 15/15 | 105 | INFO_REALIGN_3_PRIME | chr1 | 93137118 | ||||
chr1:93137175
|
G | C | 1 | a0001c0001t0011 | 1 | NA19075.hp2 | 3_prime_UTR_variant | MODIFIER | c.*148G>C | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 15/15 | 148 | chr1 | 93137175 | |||||
chr1:93137177
|
A | T | 1 | a0001c0001t0011 | 1 | NA19075.hp2 | 3_prime_UTR_variant | MODIFIER | c.*150A>T | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 15/15 | 150 | chr1 | 93137177 | |||||
chr1:93137185
|
A | G | 1 | a0001c0001t0018 | 1 | HG02615.hp1 | 3_prime_UTR_variant | MODIFIER | c.*158A>G | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 15/15 | 158 | chr1 | 93137185 | |||||
chr1:93137257
|
A | G | 1 | a0001c0001t0007 | 4 | HG00738.hp2 HG01175.hp2 HG01516.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*230A>G | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 15/15 | 230 | chr1 | 93137257 | |||||
chr1:93137339
|
T | C | 1 | a0001c0001t0005 | 4 | HG02559.hp2 HG03225.hp1 NA18522.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*312T>C | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 15/15 | 312 | chr1 | 93137339 | |||||
chr1:93137390
|
A | G | 1 | a0001c0001t0017 | 1 | NA19062.hp1 | 3_prime_UTR_variant | MODIFIER | c.*363A>G | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 15/15 | 363 | chr1 | 93137390 | |||||
chr1:93137626
|
C | CAT | 16 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(13): Show | 253 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(250): Show |
3_prime_UTR_variant | MODIFIER | c.*599_*600insAT | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 15/15 | 600 | chr1 | 93137626 | |||||
chr1:93137843
|
A | G | 1 | a0001c0001t0016 | 1 | HG02738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*816A>G | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 15/15 | 816 | chr1 | 93137843 | |||||
chr1:93138027
|
G | A | 1 | a0001c0001t0014 | 1 | HG02056.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1000G>A | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 15/15 | 1000 | chr1 | 93138027 | |||||
chr1:93138397
|
A | G | 1 | a0001c0001t0006 | 4 | HG01109.hp1 HG01884.hp1 HG03195.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1370A>G | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 15/15 | 1370 | chr1 | 93138397 | |||||
chr1:93138424
|
G | A | 1 | a0001c0001t0012 | 1 | HG01175.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1397G>A | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 15/15 | 1397 | chr1 | 93138424 | |||||
chr1:93138579
|
T | C | 7 | a0001c0001t0003a0001c0001t0004a0001c0001t0005others(4): Show | 88 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(85): Show |
3_prime_UTR_variant | MODIFIER | c.*1552T>C | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 15/15 | 1552 | chr1 | 93138579 | |||||
chr1:93138748
|
G | A | 1 | a0001c0001t0013 | 1 | HG02258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1721G>A | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 15/15 | 1721 | chr1 | 93138748 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:93079600
|
G | A | 224 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(221): Show | 249 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(246): Show |
intron_variant | MODIFIER | c.5+69G>A | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93079600 | ||||||
chr1:93079897
|
G | T | 1 | a0001c0001t0002g0228 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.5+366G>T | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93079897 | ||||||
chr1:93080079
|
G | A | 6 | a0001c0001t0004g0017a0001c0001t0004g0229a0001c0001t0004g0230others(3): Show | 7 | HG01884.hp2 HG02630.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.5+548G>A | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93080079 | ||||||
chr1:93080186
|
T | C | 5 | a0001c0001t0003g0018a0001c0001t0003g0019a0001c0001t0003g0234others(2): Show | 7 | HG01074.hp2 HG01106.hp2 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.5+655T>C | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93080186 | ||||||
chr1:93080275
|
G | A | 1 | a0001c0001t0003g0237 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.5+744G>A | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93080275 | ||||||
chr1:93080605
|
C | T | 1 | a0001c0001t0009g0227 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.5+1074C>T | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93080605 | ||||||
chr1:93080636
|
T | C | 2 | a0001c0001t0004g0017a0001c0001t0004g0229 | 3 | HG01884.hp2 HG02630.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.5+1105T>C | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93080636 | ||||||
chr1:93080742
|
T | G | 107 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(104): Show | 119 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.5+1211T>G | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93080742 | ||||||
chr1:93080764
|
C | CT | 9 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0118others(6): Show | 9 | HG00738.hp1 HG02056.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.5+1249dupT | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 93080764 | |||||
chr1:93080764
|
CT | C | 83 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0153others(80): Show | 94 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(91): Show |
intron_variant | MODIFIER | c.5+1249delT | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 93080764 | |||||
chr1:93080829
|
A | G | 3 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0114 | 3 | HG02572.hp2 HG02922.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.5+1298A>G | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93080829 | ||||||
chr1:93080997
|
A | T | 1 | a0001c0001t0003g0225 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.5+1466A>T | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93080997 | ||||||
chr1:93081173
|
A | C | 1 | a0001c0001t0001g0307 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.5+1642A>C | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93081173 | ||||||
chr1:93081456
|
G | A | 2 | a0001c0001t0002g0122a0001c0001t0002g0123 | 2 | HG02451.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.5+1925G>A | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93081456 | ||||||
chr1:93081609
|
A | G | 1 | a0001c0001t0001g0111 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.5+2078A>G | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93081609 | ||||||
chr1:93081746
|
C | T | 1 | a0001c0001t0001g0110 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.5+2215C>T | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93081746 | ||||||
chr1:93081920
|
A | G | 2 | a0001c0001t0001g0189a0001c0001t0001g0190 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.5+2389A>G | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93081920 | ||||||
chr1:93081957
|
G | T | 1 | a0001c0001t0013g0109 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.5+2426G>T | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93081957 | ||||||
chr1:93082032
|
G | A | 1 | a0001c0001t0003g0237 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.5+2501G>A | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93082032 | ||||||
chr1:93082273
|
C | CT | 127 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0153others(124): Show | 140 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.5+2758dupT | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 93082273 | |||||
chr1:93082361
|
G | A | 4 | a0001c0001t0001g0242a0001c0001t0001g0243a0001c0001t0001g0244others(1): Show | 4 | HG01928.hp2 HG02257.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.5+2830G>A | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93082361 | ||||||
chr1:93082372
|
T | C | 308 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(305): Show | 339 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(336): Show |
intron_variant | MODIFIER | c.5+2841T>C | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93082372 | ||||||
chr1:93082405
|
C | T | 1 | a0001c0001t0003g0292 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.5+2874C>T | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93082405 | ||||||
chr1:93082448
|
T | TTAAA | 4 | a0001c0001t0006g0238a0001c0001t0006g0239a0001c0001t0006g0240others(1): Show | 4 | HG01109.hp1 HG01884.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.5+2918_5+2919insAA others(2): Show |
MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 93082448 | |||||
chr1:93082566
|
G | A | 2 | a0001c0001t0004g0230a0001c0001t0004g0231 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.5+3035G>A | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93082566 | ||||||
chr1:93082672
|
G | A | 2 | a0001c0001t0002g0128a0001c0001t0016g0129 | 2 | HG02738.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.5+3141G>A | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93082672 | ||||||
chr1:93082789
|
A | G | 1 | a0001c0001t0002g0188 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.5+3258A>G | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93082789 | ||||||
chr1:93083230
|
G | C | 1 | a0001c0001t0001g0246 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.5+3699G>C | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93083230 | ||||||
chr1:93083316
|
A | G | 308 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(305): Show | 339 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(336): Show |
intron_variant | MODIFIER | c.5+3785A>G | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93083316 | ||||||
chr1:93084342
|
A | G | 4 | a0001c0001t0006g0238a0001c0001t0006g0239a0001c0001t0006g0240others(1): Show | 4 | HG01109.hp1 HG01884.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.5+4811A>G | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93084342 | ||||||
chr1:93084529
|
C | T | 1 | a0001c0001t0003g0291 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.5+4998C>T | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93084529 | ||||||
chr1:93084539
|
A | G | 76 | a0001c0001t0001g0108a0001c0001t0001g0153a0001c0001t0002g0003others(73): Show | 87 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(84): Show |
intron_variant | MODIFIER | c.5+5008A>G | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93084539 | ||||||
chr1:93084700
|
T | A | 224 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(221): Show | 249 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(246): Show |
intron_variant | MODIFIER | c.5+5169T>A | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93084700 | ||||||
chr1:93084897
|
G | T | 1 | a0001c0001t0001g0290 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.5+5366G>T | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93084897 | ||||||
chr1:93085138
|
C | G | 1 | a0001c0001t0003g0237 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.5+5607C>G | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93085138 | ||||||
chr1:93085336
|
C | T | 1 | a0001c0001t0003g0225 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.5+5805C>T | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93085336 | ||||||
chr1:93085399
|
G | T | 224 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(221): Show | 249 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(246): Show |
intron_variant | MODIFIER | c.5+5868G>T | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93085399 | ||||||
chr1:93085418
|
G | C | 308 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(305): Show | 339 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(336): Show |
intron_variant | MODIFIER | c.5+5887G>C | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93085418 | ||||||
chr1:93085419
|
C | T | 1 | a0001c0001t0018g0289 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.5+5888C>T | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93085419 | ||||||
chr1:93085476
|
CT | C | 212 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(209): Show | 237 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(234): Show |
intron_variant | MODIFIER | c.5+5964delT | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 93085476 | |||||
chr1:93085495
|
T | C | 1 | a0001c0001t0001g0124 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.5+5964T>C | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93085495 | ||||||
chr1:93085816
|
A | G | 1 | a0001c0001t0003g0291 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.5+6285A>G | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93085816 | ||||||
chr1:93085938
|
C | T | 1 | a0001c0001t0001g0107 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.5+6407C>T | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93085938 | ||||||
chr1:93085978
|
T | C | 2 | a0001c0001t0002g0131a0001c0001t0008g0130 | 2 | NA18963.hp2 NA18997.hp2 |
intron_variant | MODIFIER | c.5+6447T>C | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93085978 | ||||||
chr1:93086128
|
C | T | 308 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(305): Show | 339 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(336): Show |
intron_variant | MODIFIER | c.5+6597C>T | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93086128 | ||||||
chr1:93086146
|
G | A | 2 | a0001c0001t0002g0132a0001c0001t0002g0133 | 2 | HG02135.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.5+6615G>A | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93086146 | ||||||
chr1:93086153
|
A | G | 1 | a0001c0001t0003g0237 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.5+6622A>G | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93086153 | ||||||
chr1:93086411
|
T | C | 1 | a0001c0001t0003g0192 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.5+6880T>C | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93086411 | ||||||
chr1:93086426
|
G | A | 1 | a0001c0001t0003g0193 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.5+6895G>A | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93086426 | ||||||
chr1:93086496
|
C | CA | 136 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(133): Show | 150 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.5+6985dupA | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 93086496 | |||||
chr1:93086496
|
C | CAA | 84 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(81): Show | 95 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(92): Show |
intron_variant | MODIFIER | c.5+6984_5+6985dupAA | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 93086496 | |||||
chr1:93086496
|
C | CAAA | 7 | a0001c0001t0002g0127a0001c0001t0002g0134a0001c0001t0002g0135others(4): Show | 7 | HG01261.hp2 HG01981.hp1 HG02074.hp2 others(4): Show |
intron_variant | MODIFIER | c.5+6983_5+6985dupAA others(1): Show |
MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 93086496 | |||||
chr1:93086580
|
A | G | 1 | a0001c0001t0001g0098 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.5+7049A>G | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93086580 | ||||||
chr1:93086630
|
C | G | 106 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(103): Show | 118 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(115): Show |
intron_variant | MODIFIER | c.5+7099C>G | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93086630 | ||||||
chr1:93086769
|
G | A | 37 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0192others(34): Show | 39 | HG00280.hp2 HG00323.hp2 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.5+7238G>A | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93086769 | ||||||
chr1:93086991
|
C | T | 2 | a0001c0001t0003g0305a0001c0001t0003g0306 | 2 | HG02109.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.5+7460C>T | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93086991 | ||||||
chr1:93087038
|
A | C | 1 | a0001c0001t0001g0097 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.5+7507A>C | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93087038 | ||||||
chr1:93087091
|
A | T | 1 | a0001c0001t0001g0124 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.5+7560A>T | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93087091 | ||||||
chr1:93087104
|
C | A | 1 | a0001c0001t0001g0028 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.5+7573C>A | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93087104 | ||||||
chr1:93087194
|
C | T | 2 | a0001c0001t0001g0288a0001c0001t0001g0290 | 2 | HG03130.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.5+7663C>T | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93087194 | ||||||
chr1:93087231
|
G | A | 308 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(305): Show | 339 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(336): Show |
intron_variant | MODIFIER | c.5+7700G>A | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93087231 | ||||||
chr1:93087284
|
C | A | 224 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(221): Show | 249 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(246): Show |
intron_variant | MODIFIER | c.5+7753C>A | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93087284 | ||||||
chr1:93087291
|
G | T | 1 | a0001c0001t0001g0096 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.5+7760G>T | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93087291 | ||||||
chr1:93087363
|
G | A | 1 | a0001c0001t0003g0294 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.5+7832G>A | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93087363 | ||||||
chr1:93087369
|
C | A | 1 | a0001c0001t0001g0125 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.5+7838C>A | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93087369 | ||||||
chr1:93087446
|
C | T | 2 | a0001c0001t0001g0094a0001c0001t0001g0095 | 2 | HG00323.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.5+7915C>T | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93087446 | ||||||
chr1:93087529
|
A | G | 228 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(225): Show | 253 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(250): Show |
intron_variant | MODIFIER | c.5+7998A>G | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93087529 | ||||||
chr1:93087571
|
C | CA | 221 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(218): Show | 246 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(243): Show |
intron_variant | MODIFIER | c.5+8054dupA | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 93087571 | |||||
chr1:93087571
|
C | CAA | 9 | a0001c0001t0001g0023a0001c0001t0001g0029a0001c0001t0001g0030others(6): Show | 9 | HG01109.hp1 HG01884.hp1 HG01978.hp1 others(6): Show |
intron_variant | MODIFIER | c.5+8053_5+8054dupAA | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 93087571 | |||||
chr1:93087666
|
G | T | 228 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(225): Show | 253 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(250): Show |
intron_variant | MODIFIER | c.5+8135G>T | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93087666 | ||||||
chr1:93087808
|
G | A | 308 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(305): Show | 339 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(336): Show |
intron_variant | MODIFIER | c.5+8277G>A | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93087808 | ||||||
chr1:93087941
|
CT | C | 106 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(103): Show | 118 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(115): Show |
intron_variant | MODIFIER | c.5+8414delT | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 93087941 | |||||
chr1:93088263
|
T | C | 3 | a0001c0001t0003g0194a0001c0001t0003g0195a0001c0001t0003g0196 | 3 | HG00280.hp2 HG01069.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.5+8732T>C | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93088263 | ||||||
chr1:93088458
|
C | G | 2 | a0001c0001t0002g0183a0001c0001t0002g0184 | 2 | HG02040.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.5+8927C>G | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93088458 | ||||||
chr1:93088661
|
G | C | 1 | a0001c0001t0001g0125 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.5+9130G>C | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93088661 | ||||||
chr1:93088768
|
C | T | 1 | a0001c0001t0001g0093 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.5+9237C>T | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93088768 | ||||||
chr1:93088781
|
G | A | 2 | a0001c0001t0001g0248a0001c0001t0001g0249 | 2 | HG03098.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.5+9250G>A | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93088781 | ||||||
chr1:93088995
|
C | CT | 4 | a0001c0001t0006g0238a0001c0001t0006g0239a0001c0001t0006g0240others(1): Show | 4 | HG01109.hp1 HG01884.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.5+9465dupT | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 93088995 | |||||
chr1:93089008
|
G | A | 4 | a0001c0001t0006g0238a0001c0001t0006g0239a0001c0001t0006g0240others(1): Show | 4 | HG01109.hp1 HG01884.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.5+9477G>A | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93089008 | ||||||
chr1:93089443
|
T | G | 224 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(221): Show | 249 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(246): Show |
intron_variant | MODIFIER | c.5+9912T>G | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93089443 | ||||||
chr1:93089444
|
C | T | 224 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(221): Show | 249 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(246): Show |
intron_variant | MODIFIER | c.5+9913C>T | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93089444 | ||||||
chr1:93089533
|
G | C | 1 | a0001c0001t0003g0192 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.5+10002G>C | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93089533 | ||||||
chr1:93089659
|
C | T | 1 | a0001c0001t0003g0237 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.5+10128C>T | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93089659 | ||||||
chr1:93089704
|
C | T | 2 | a0001c0001t0001g0189a0001c0001t0001g0190 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.5+10173C>T | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93089704 | ||||||
chr1:93089849
|
C | CT | 225 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(222): Show | 250 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(247): Show |
intron_variant | MODIFIER | c.5+10331dupT | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 93089849 | |||||
chr1:93089863
|
G | C | 1 | a0001c0001t0002g0140 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.5+10332G>C | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93089863 | ||||||
chr1:93089943
|
G | A | 1 | a0001c0001t0003g0237 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.5+10412G>A | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93089943 | ||||||
chr1:93089996
|
A | G | 3 | a0001c0001t0003g0218a0001c0001t0003g0219a0001c0001t0003g0220 | 3 | HG00323.hp2 HG01358.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.5+10465A>G | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93089996 | ||||||
chr1:93090031
|
C | T | 1 | a0001c0001t0003g0304 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.5+10500C>T | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93090031 | ||||||
chr1:93090125
|
C | T | 107 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(104): Show | 119 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.5+10594C>T | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93090125 | ||||||
chr1:93090169
|
G | C | 4 | a0001c0001t0006g0238a0001c0001t0006g0239a0001c0001t0006g0240others(1): Show | 4 | HG01109.hp1 HG01884.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.5+10638G>C | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93090169 | ||||||
chr1:93090298
|
A | G | 1 | a0001c0001t0001g0092 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.5+10767A>G | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93090298 | ||||||
chr1:93090372
|
A | G | 2 | a0001c0001t0003g0303a0001c0001t0003g0306 | 2 | HG02886.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.5+10841A>G | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93090372 | ||||||
chr1:93090403
|
C | T | 31 | a0001c0001t0003g0018a0001c0001t0003g0019a0001c0001t0003g0021others(28): Show | 36 | HG00423.hp1 HG01074.hp2 HG01081.hp2 others(33): Show |
intron_variant | MODIFIER | c.5+10872C>T | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93090403 | ||||||
chr1:93090428
|
G | A | 37 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0192others(34): Show | 39 | HG00280.hp2 HG00323.hp2 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.5+10897G>A | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93090428 | ||||||
chr1:93090435
|
T | C | 224 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(221): Show | 249 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(246): Show |
intron_variant | MODIFIER | c.5+10904T>C | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93090435 | ||||||
chr1:93090664
|
G | GT | 26 | a0001c0001t0001g0010a0001c0001t0001g0088a0001c0001t0001g0089others(23): Show | 30 | HG00323.hp1 HG01069.hp2 HG01070.hp2 others(27): Show |
intron_variant | MODIFIER | c.5+11150dupT | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 93090664 | |||||
chr1:93090804
|
T | C | 308 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(305): Show | 339 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(336): Show |
intron_variant | MODIFIER | c.5+11273T>C | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93090804 | ||||||
chr1:93090964
|
A | G | 1 | a0001c0001t0003g0301 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.5+11433A>G | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93090964 | ||||||
chr1:93091108
|
C | T | 4 | a0001c0001t0006g0238a0001c0001t0006g0239a0001c0001t0006g0240others(1): Show | 4 | HG01109.hp1 HG01884.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.5+11577C>T | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93091108 | ||||||
chr1:93091229
|
ATAC | A | 3 | a0001c0001t0003g0218a0001c0001t0003g0219a0001c0001t0003g0220 | 3 | HG00323.hp2 HG01358.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.5+11706_5+11708del others(3): Show |
MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 93091229 | |||||
chr1:93091351
|
TG | T | 36 | a0001c0001t0001g0020a0001c0001t0001g0242a0001c0001t0001g0243others(33): Show | 37 | HG01891.hp2 HG01928.hp2 HG02055.hp1 others(34): Show |
intron_variant | MODIFIER | c.5+11821delG | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93091351 | ||||||
chr1:93091381
|
T | TG | 37 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0192others(34): Show | 39 | HG00280.hp2 HG00323.hp2 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.5+11850_5+11851ins others(1): Show |
MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93091381 | ||||||
chr1:93091435
|
A | G | 1 | a0001c0001t0001g0087 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.5+11904A>G | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93091435 | ||||||
chr1:93091920
|
T | G | 1 | a0002c0002t0001g0115 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.5+12389T>G | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93091920 | ||||||
chr1:93092013
|
A | T | 1 | a0001c0001t0002g0176 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.5+12482A>T | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93092013 | ||||||
chr1:93092020
|
C | T | 1 | a0001c0001t0002g0176 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.5+12489C>T | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93092020 | ||||||
chr1:93092025
|
C | T | 1 | a0001c0001t0001g0191 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.5+12494C>T | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93092025 | ||||||
chr1:93092479
|
T | G | 228 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(225): Show | 253 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(250): Show |
intron_variant | MODIFIER | c.5+12948T>G | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93092479 | ||||||
chr1:93092494
|
C | T | 1 | a0001c0001t0003g0237 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.5+12963C>T | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93092494 | ||||||
chr1:93092674
|
A | G | 2 | a0001c0001t0001g0247a0001c0001t0001g0269 | 2 | HG01891.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.5+13143A>G | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93092674 | ||||||
chr1:93092970
|
T | C | 1 | a0001c0001t0002g0141 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.5+13439T>C | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93092970 | ||||||
chr1:93093037
|
C | A | 1 | a0001c0001t0008g0130 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.5+13506C>A | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93093037 | ||||||
chr1:93093076
|
G | C | 67 | a0001c0001t0001g0020a0001c0001t0001g0242a0001c0001t0001g0243others(64): Show | 73 | HG00423.hp1 HG01074.hp2 HG01081.hp2 others(70): Show |
intron_variant | MODIFIER | c.5+13545G>C | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93093076 | ||||||
chr1:93093107
|
G | A | 1 | a0001c0001t0001g0031 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.5+13576G>A | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93093107 | ||||||
chr1:93093152
|
A | G | 1 | a0001c0001t0003g0196 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.5+13621A>G | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93093152 | ||||||
chr1:93093261
|
A | G | 108 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(105): Show | 120 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.5+13730A>G | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93093261 | ||||||
chr1:93093352
|
TCA | T | 7 | a0001c0001t0001g0020a0001c0001t0001g0265a0001c0001t0001g0266others(4): Show | 8 | NA18967.hp2 NA18968.hp1 NA18977.hp1 others(5): Show |
intron_variant | MODIFIER | c.5+13824_5+13825del others(2): Show |
MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 93093352 | |||||
chr1:93093436
|
C | A | 2 | a0001c0001t0002g0132a0001c0001t0002g0133 | 2 | HG02135.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.5+13905C>A | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93093436 | ||||||
chr1:93093514
|
C | T | 228 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(225): Show | 253 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(250): Show |
intron_variant | MODIFIER | c.5+13983C>T | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93093514 | ||||||
chr1:93093566
|
G | A | 8 | a0001c0001t0003g0295a0001c0001t0003g0296a0001c0001t0003g0297others(5): Show | 8 | HG02109.hp1 HG02717.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.5+14035G>A | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93093566 | ||||||
chr1:93093618
|
A | G | 2 | a0001c0001t0001g0263a0001c0001t0001g0264 | 2 | HG02647.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.5+14087A>G | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93093618 | ||||||
chr1:93093690
|
C | T | 1 | a0002c0002t0001g0115 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.5+14159C>T | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93093690 | ||||||
chr1:93093964
|
G | A | 1 | a0001c0001t0002g0183 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.5+14433G>A | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93093964 | ||||||
chr1:93094028
|
G | A | 2 | a0001c0001t0001g0032a0001c0001t0001g0033 | 2 | NA18993.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.5+14497G>A | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93094028 | ||||||
chr1:93094092
|
T | C | 228 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(225): Show | 253 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(250): Show |
intron_variant | MODIFIER | c.5+14561T>C | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93094092 | ||||||
chr1:93094458
|
A | G | 228 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(225): Show | 253 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(250): Show |
intron_variant | MODIFIER | c.5+14927A>G | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93094458 | ||||||
chr1:93094622
|
G | A | 228 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(225): Show | 253 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(250): Show |
intron_variant | MODIFIER | c.5+15091G>A | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93094622 | ||||||
chr1:93094920
|
G | C | 1 | a0001c0001t0001g0093 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.6-15310G>C | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93094920 | ||||||
chr1:93095105
|
C | T | 4 | a0001c0001t0006g0238a0001c0001t0006g0239a0001c0001t0006g0240others(1): Show | 4 | HG01109.hp1 HG01884.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.6-15125C>T | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93095105 | ||||||
chr1:93095214
|
T | A | 1 | a0001c0001t0001g0034 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.6-15016T>A | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93095214 | ||||||
chr1:93095290
|
G | A | 1 | a0001c0001t0001g0124 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.6-14940G>A | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93095290 | ||||||
chr1:93095438
|
T | C | 4 | a0001c0001t0006g0238a0001c0001t0006g0239a0001c0001t0006g0240others(1): Show | 4 | HG01109.hp1 HG01884.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.6-14792T>C | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93095438 | ||||||
chr1:93095560
|
C | T | 36 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0192others(33): Show | 38 | HG00280.hp2 HG00323.hp2 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.6-14670C>T | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93095560 | ||||||
chr1:93095655
|
CT | C | 70 | a0001c0001t0001g0020a0001c0001t0001g0035a0001c0001t0001g0088others(67): Show | 76 | HG00423.hp1 HG01069.hp2 HG01070.hp2 others(73): Show |
intron_variant | MODIFIER | c.6-14557delT | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 93095655 | |||||
chr1:93095899
|
C | T | 1 | a0001c0001t0001g0249 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.6-14331C>T | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93095899 | ||||||
chr1:93096423
|
C | T | 1 | a0001c0001t0001g0086 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.6-13807C>T | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93096423 | ||||||
chr1:93096436
|
G | A | 10 | a0001c0001t0002g0005a0001c0001t0002g0014a0001c0001t0002g0126others(7): Show | 13 | HG01081.hp1 HG01123.hp2 HG01261.hp2 others(10): Show |
intron_variant | MODIFIER | c.6-13794G>A | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93096436 | ||||||
chr1:93096448
|
A | C | 308 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(305): Show | 339 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(336): Show |
intron_variant | MODIFIER | c.6-13782A>C | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93096448 | ||||||
chr1:93096795
|
TTTTTTTC others(6): Show |
T | 1 | a0001c0001t0002g0181 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.6-13428_6-13416del others(13): Show |
MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 93096795 | |||||
chr1:93096813
|
T | C | 1 | a0001c0001t0002g0181 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.6-13417T>C | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93096813 | ||||||
chr1:93096813
|
T | TC | 220 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(217): Show | 245 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(242): Show |
intron_variant | MODIFIER | c.6-13417_6-13416ins others(1): Show |
MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93096813 | ||||||
chr1:93096814
|
T | C | 1 | a0001c0001t0001g0036 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.6-13416T>C | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93096814 | ||||||
chr1:93096832
|
A | G | 224 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(221): Show | 249 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(246): Show |
intron_variant | MODIFIER | c.6-13398A>G | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93096832 | ||||||
chr1:93096902
|
C | T | 1 | a0001c0001t0001g0083 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.6-13328C>T | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93096902 | ||||||
chr1:93097001
|
G | A | 4 | a0001c0001t0006g0238a0001c0001t0006g0239a0001c0001t0006g0240others(1): Show | 4 | HG01109.hp1 HG01884.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.6-13229G>A | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93097001 | ||||||
chr1:93097022
|
C | G | 4 | a0001c0001t0006g0238a0001c0001t0006g0239a0001c0001t0006g0240others(1): Show | 4 | HG01109.hp1 HG01884.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.6-13208C>G | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93097022 | ||||||
chr1:93097292
|
C | G | 1 | a0001c0001t0001g0030 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.6-12938C>G | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93097292 | ||||||
chr1:93097300
|
A | C | 4 | a0001c0001t0006g0238a0001c0001t0006g0239a0001c0001t0006g0240others(1): Show | 4 | HG01109.hp1 HG01884.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.6-12930A>C | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93097300 | ||||||
chr1:93097436
|
T | C | 1 | a0001c0001t0002g0142 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.6-12794T>C | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93097436 | ||||||
chr1:93097690
|
C | T | 1 | a0001c0001t0001g0082 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.6-12540C>T | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93097690 | ||||||
chr1:93097923
|
G | A | 2 | a0001c0001t0003g0286a0001c0001t0003g0287 | 2 | HG02145.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.6-12307G>A | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93097923 | ||||||
chr1:93097950
|
C | G | 1 | a0001c0001t0003g0237 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.6-12280C>G | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93097950 | ||||||
chr1:93098217
|
G | T | 224 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(221): Show | 249 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(246): Show |
intron_variant | MODIFIER | c.6-12013G>T | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93098217 | ||||||
chr1:93098829
|
G | A | 308 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(305): Show | 339 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(336): Show |
intron_variant | MODIFIER | c.6-11401G>A | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93098829 | ||||||
chr1:93099194
|
A | G | 6 | a0001c0001t0004g0017a0001c0001t0004g0229a0001c0001t0004g0230others(3): Show | 7 | HG01884.hp2 HG02630.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.6-11036A>G | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93099194 | ||||||
chr1:93099470
|
G | A | 2 | a0001c0001t0002g0182a0001c0001t0008g0143 | 2 | HG02129.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.6-10760G>A | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93099470 | ||||||
chr1:93099566
|
A | G | 78 | a0001c0001t0001g0108a0001c0001t0001g0153a0001c0001t0001g0189others(75): Show | 89 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(86): Show |
intron_variant | MODIFIER | c.6-10664A>G | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93099566 | ||||||
chr1:93099821
|
A | T | 2 | a0001c0001t0001g0260a0001c0001t0001g0261 | 2 | HG02258.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.6-10409A>T | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93099821 | ||||||
chr1:93099896
|
G | A | 2 | a0001c0001t0004g0233a0001c0001t0010g0232 | 2 | HG02965.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.6-10334G>A | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93099896 | ||||||
chr1:93100171
|
A | G | 1 | a0001c0001t0003g0284 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.6-10059A>G | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93100171 | ||||||
chr1:93100281
|
A | T | 1 | a0001c0001t0001g0083 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.6-9949A>T | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93100281 | ||||||
chr1:93100291
|
A | ATGTT | 25 | a0001c0001t0003g0015a0001c0001t0003g0018a0001c0001t0003g0019others(22): Show | 30 | HG00423.hp1 HG01074.hp2 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.6-9913_6-9910dupGT others(2): Show |
MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 93100291 | |||||
chr1:93100308
|
T | C | 1 | a0001c0001t0009g0227 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.6-9922T>C | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93100308 | ||||||
chr1:93100406
|
G | A | 2 | a0001c0001t0002g0122a0001c0001t0002g0123 | 2 | HG02451.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.6-9824G>A | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93100406 | ||||||
chr1:93100530
|
C | A | 308 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(305): Show | 339 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(336): Show |
intron_variant | MODIFIER | c.6-9700C>A | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93100530 | ||||||
chr1:93100832
|
A | T | 2 | a0001c0001t0003g0219a0001c0001t0003g0220 | 2 | HG00323.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.6-9398A>T | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93100832 | ||||||
chr1:93100995
|
G | A | 1 | a0001c0001t0002g0142 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.6-9235G>A | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93100995 | ||||||
chr1:93101241
|
T | C | 1 | a0001c0001t0001g0260 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.6-8989T>C | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93101241 | ||||||
chr1:93101266
|
T | G | 2 | a0001c0001t0003g0272a0001c0001t0003g0273 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.6-8964T>G | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93101266 | ||||||
chr1:93101366
|
C | CT | 49 | a0001c0001t0001g0033a0001c0001t0001g0079a0001c0001t0001g0080others(46): Show | 51 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(48): Show |
intron_variant | MODIFIER | c.6-8838dupT | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 93101366 | |||||
chr1:93101366
|
CT | C | 29 | a0001c0001t0001g0024a0001c0001t0001g0030a0001c0001t0001g0032others(26): Show | 33 | HG00423.hp1 HG01074.hp2 HG01081.hp2 others(30): Show |
intron_variant | MODIFIER | c.6-8838delT | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 93101366 | |||||
chr1:93101366
|
CTTTTTTT | C | 33 | a0001c0001t0001g0020a0001c0001t0001g0242a0001c0001t0001g0243others(30): Show | 34 | HG01891.hp2 HG01928.hp2 HG02055.hp1 others(31): Show |
intron_variant | MODIFIER | c.6-8844_6-8838delTT others(5): Show |
MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 93101366 | |||||
chr1:93101366
|
CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0012g0199 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.6-8848_6-8838delTT others(9): Show |
MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 93101366 | |||||
chr1:93101366
|
CTTTTTTT others(8): Show |
C | 75 | a0001c0001t0001g0153a0001c0001t0002g0003a0001c0001t0002g0004others(72): Show | 86 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(83): Show |
intron_variant | MODIFIER | c.6-8852_6-8838delTT others(13): Show |
MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 93101366 | |||||
chr1:93101419
|
T | G | 308 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(305): Show | 339 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(336): Show |
intron_variant | MODIFIER | c.6-8811T>G | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93101419 | ||||||
chr1:93101522
|
T | A | 38 | a0001c0001t0002g0144a0001c0001t0003g0015a0001c0001t0003g0016others(35): Show | 40 | HG00280.hp2 HG00323.hp2 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.6-8708T>A | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93101522 | ||||||
chr1:93101568
|
G | GTTTT | 8 | a0001c0001t0003g0286a0001c0001t0003g0296a0001c0001t0003g0301others(5): Show | 8 | HG02145.hp1 HG02630.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.6-8636_6-8633dupTT others(2): Show |
MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 93101568 | |||||
chr1:93101568
|
G | GTTTTT | 12 | a0001c0001t0003g0274a0001c0001t0003g0275a0001c0001t0003g0287others(9): Show | 13 | HG01884.hp2 HG02109.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.6-8637_6-8633dupTT others(3): Show |
MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 93101568 | |||||
chr1:93101568
|
G | GTTTTTT | 8 | a0001c0001t0003g0018a0001c0001t0003g0234a0001c0001t0003g0276others(5): Show | 9 | HG01074.hp2 HG01106.hp2 HG02683.hp2 others(6): Show |
intron_variant | MODIFIER | c.6-8638_6-8633dupTT others(4): Show |
MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 93101568 | |||||
chr1:93101568
|
G | GTTTTTTT | 9 | a0001c0001t0003g0019a0001c0001t0003g0021a0001c0001t0003g0022others(6): Show | 12 | HG00423.hp1 HG01081.hp2 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.6-8639_6-8633dupTT others(5): Show |
MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 93101568 | |||||
chr1:93101568
|
G | GTTTTTTT others(1): Show |
6 | a0001c0001t0001g0042a0001c0001t0001g0189a0001c0001t0001g0191others(3): Show | 6 | HG00408.hp1 HG01168.hp2 HG01516.hp1 others(3): Show |
intron_variant | MODIFIER | c.6-8640_6-8633dupTT others(6): Show |
MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 93101568 | |||||
chr1:93101568
|
G | GTTTTTTT others(2): Show |
49 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(46): Show | 56 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(53): Show |
intron_variant | MODIFIER | c.6-8641_6-8633dupTT others(7): Show |
MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 93101568 | |||||
chr1:93101568
|
G | GTTTTTTT others(3): Show |
60 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0010others(57): Show | 69 | HG00642.hp1 HG00738.hp1 HG01106.hp1 others(66): Show |
intron_variant | MODIFIER | c.6-8642_6-8633dupTT others(8): Show |
MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 93101568 | |||||
chr1:93101568
|
G | GTTTTTTT others(4): Show |
35 | a0001c0001t0001g0006a0001c0001t0001g0027a0001c0001t0001g0038others(32): Show | 42 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(39): Show |
intron_variant | MODIFIER | c.6-8643_6-8633dupTT others(9): Show |
MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 93101568 | |||||
chr1:93101568
|
G | GTTTTTTT others(5): Show |
9 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0112others(6): Show | 9 | HG01516.hp2 HG02135.hp2 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.6-8644_6-8633dupTT others(10): Show |
MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 93101568 | |||||
chr1:93101568
|
G | GTTTTTTT others(6): Show |
5 | a0001c0001t0001g0035a0001c0001t0001g0116a0001c0001t0001g0121others(2): Show | 5 | HG02738.hp2 NA18941.hp2 NA18997.hp1 others(2): Show |
intron_variant | MODIFIER | c.6-8645_6-8633dupTT others(11): Show |
MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 93101568 | |||||
chr1:93101568
|
G | GTTTTTTT others(7): Show |
2 | a0001c0001t0001g0030a0001c0001t0002g0173 | 2 | HG00544.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.6-8646_6-8633dupTT others(12): Show |
MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 93101568 | |||||
chr1:93101568
|
G | GTTTTTTT others(8): Show |
3 | a0001c0001t0001g0100a0001c0001t0002g0131a0001c0001t0003g0294 | 3 | HG02074.hp1 NA18943.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.6-8647_6-8633dupTT others(13): Show |
MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 93101568 | |||||
chr1:93101568
|
G | GTTTTTTT others(9): Show |
7 | a0001c0001t0001g0076a0001c0001t0001g0096a0001c0001t0001g0113others(4): Show | 7 | HG00733.hp1 HG00733.hp2 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.6-8648_6-8633dupTT others(14): Show |
MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 93101568 | |||||
chr1:93101568
|
G | GTTTTTTT others(10): Show |
2 | a0001c0001t0001g0077a0001c0001t0001g0101 | 2 | HG02698.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.6-8649_6-8633dupTT others(15): Show |
MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 93101568 | |||||
chr1:93101568
|
G | GTTTTTTT others(13): Show |
1 | a0001c0001t0002g0175 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.6-8652_6-8633dupTT others(18): Show |
MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 93101568 | |||||
chr1:93101568
|
G | GTTTTTTT others(15): Show |
1 | a0001c0001t0001g0114 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.6-8654_6-8633dupTT others(20): Show |
MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 93101568 | |||||
chr1:93101568
|
G | GTTTTTTT others(17): Show |
1 | a0001c0001t0001g0085 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.6-8656_6-8633dupTT others(22): Show |
MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 93101568 | |||||
chr1:93101568
|
G | GTTTTTTT others(18): Show |
1 | a0001c0001t0008g0130 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.6-8657_6-8633dupTT others(23): Show |
MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 93101568 | |||||
chr1:93101568
|
G | GTTTTTTT others(20): Show |
1 | a0001c0001t0001g0078 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.6-8659_6-8633dupTT others(25): Show |
MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 93101568 | |||||
chr1:93101568
|
GT | G | 16 | a0001c0001t0003g0192a0001c0001t0003g0193a0001c0001t0003g0198others(13): Show | 16 | HG00642.hp2 HG00741.hp1 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.6-8633delT | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 93101568 | |||||
chr1:93101568
|
GTT | G | 23 | a0001c0001t0002g0145a0001c0001t0002g0146a0001c0001t0002g0186others(20): Show | 25 | HG00280.hp2 HG00323.hp2 HG01069.hp1 others(22): Show |
intron_variant | MODIFIER | c.6-8634_6-8633delTT | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 93101568 | |||||
chr1:93101568
|
GTTTTTTT others(3): Show |
G | 2 | a0001c0001t0001g0025a0001c0001t0001g0124 | 2 | HG03139.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.6-8642_6-8633delTT others(8): Show |
MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 93101568 | |||||
chr1:93101568
|
GTTTTTTT others(8): Show |
G | 2 | a0001c0001t0001g0040a0001c0001t0001g0041 | 2 | HG00673.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.6-8647_6-8633delTT others(13): Show |
MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 93101568 | |||||
chr1:93101572
|
T | TTTTTTTT others(1): Show |
8 | a0001c0001t0001g0254a0001c0001t0001g0255a0001c0001t0001g0256others(5): Show | 8 | HG01109.hp1 HG01884.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.6-8651_6-8650insGT others(6): Show |
MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 93101572 | |||||
chr1:93101573
|
T | TTTTTTTG | 9 | a0001c0001t0001g0245a0001c0001t0001g0246a0001c0001t0001g0247others(6): Show | 9 | HG01891.hp2 HG01928.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.6-8651_6-8650insGT others(5): Show |
MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 93101573 | |||||
chr1:93101574
|
T | TTTTTTG | 20 | a0001c0001t0001g0020a0001c0001t0001g0242a0001c0001t0001g0243others(17): Show | 21 | HG02257.hp2 HG02451.hp1 HG02630.hp2 others(18): Show |
intron_variant | MODIFIER | c.6-8651_6-8650insGT others(4): Show |
MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 93101574 | |||||
chr1:93101586
|
T | G | 2 | a0001c0001t0001g0250a0001c0001t0001g0259 | 2 | HG02451.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.6-8644T>G | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93101586 | ||||||
chr1:93101663
|
G | A | 2 | a0001c0001t0001g0125a0001c0001t0001g0191 | 2 | HG01168.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.6-8567G>A | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93101663 | ||||||
chr1:93101812
|
A | T | 31 | a0001c0001t0003g0018a0001c0001t0003g0019a0001c0001t0003g0021others(28): Show | 36 | HG00423.hp1 HG01074.hp2 HG01081.hp2 others(33): Show |
intron_variant | MODIFIER | c.6-8418A>T | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93101812 | ||||||
chr1:93101822
|
C | T | 31 | a0001c0001t0003g0018a0001c0001t0003g0019a0001c0001t0003g0021others(28): Show | 36 | HG00423.hp1 HG01074.hp2 HG01081.hp2 others(33): Show |
intron_variant | MODIFIER | c.6-8408C>T | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93101822 | ||||||
chr1:93101960
|
C | T | 75 | a0001c0001t0001g0153a0001c0001t0002g0003a0001c0001t0002g0004others(72): Show | 86 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(83): Show |
intron_variant | MODIFIER | c.6-8270C>T | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93101960 | ||||||
chr1:93102127
|
C | T | 1 | a0001c0001t0003g0218 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.6-8103C>T | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93102127 | ||||||
chr1:93102591
|
C | CA | 9 | a0001c0001t0001g0254a0001c0001t0001g0255a0001c0001t0001g0256others(6): Show | 9 | HG02055.hp1 HG02258.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.6-7629dupA | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 93102591 | |||||
chr1:93102613
|
C | T | 3 | a0001c0001t0003g0194a0001c0001t0003g0195a0001c0001t0003g0196 | 3 | HG00280.hp2 HG01069.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.6-7617C>T | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93102613 | ||||||
chr1:93102639
|
C | G | 2 | a0001c0001t0003g0286a0001c0001t0003g0287 | 2 | HG02145.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.6-7591C>G | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93102639 | ||||||
chr1:93102701
|
T | C | 1 | a0001c0001t0001g0065 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.6-7529T>C | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93102701 | ||||||
chr1:93103026
|
G | A | 4 | a0001c0001t0002g0147a0001c0001t0002g0155a0001c0001t0002g0165others(1): Show | 4 | HG01256.hp2 HG01515.hp2 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.6-7204G>A | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93103026 | ||||||
chr1:93103032
|
T | C | 1 | a0003c0004t0001g0066 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.6-7198T>C | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93103032 | ||||||
chr1:93103095
|
G | A | 1 | a0001c0001t0002g0148 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.6-7135G>A | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93103095 | ||||||
chr1:93103397
|
A | C | 1 | a0001c0001t0001g0124 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.6-6833A>C | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93103397 | ||||||
chr1:93103399
|
G | A | 31 | a0001c0001t0003g0018a0001c0001t0003g0019a0001c0001t0003g0021others(28): Show | 36 | HG00423.hp1 HG01074.hp2 HG01081.hp2 others(33): Show |
intron_variant | MODIFIER | c.6-6831G>A | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93103399 | ||||||
chr1:93103534
|
A | G | 1 | a0001c0001t0002g0179 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.6-6696A>G | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93103534 | ||||||
chr1:93103680
|
TAATA | T | 36 | a0001c0001t0001g0020a0001c0001t0001g0242a0001c0001t0001g0243others(33): Show | 37 | HG01891.hp2 HG01928.hp2 HG02055.hp1 others(34): Show |
intron_variant | MODIFIER | c.6-6546_6-6543delAA others(2): Show |
MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 93103680 | |||||
chr1:93103836
|
C | T | 224 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(221): Show | 249 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(246): Show |
intron_variant | MODIFIER | c.6-6394C>T | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93103836 | ||||||
chr1:93104015
|
T | C | 1 | a0001c0001t0002g0179 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.6-6215T>C | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93104015 | ||||||
chr1:93104102
|
C | CT | 31 | a0001c0001t0001g0028a0001c0001t0001g0035a0001c0001t0001g0083others(28): Show | 32 | HG00639.hp2 HG01081.hp2 HG01109.hp1 others(29): Show |
intron_variant | MODIFIER | c.6-6110dupT | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 93104102 | |||||
chr1:93104102
|
C | CTT | 44 | a0001c0001t0001g0020a0001c0001t0001g0244a0001c0001t0001g0245others(41): Show | 48 | HG00423.hp1 HG01074.hp2 HG01106.hp2 others(45): Show |
intron_variant | MODIFIER | c.6-6111_6-6110dupTT | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 93104102 | |||||
chr1:93104407
|
G | A | 1 | a0001c0001t0001g0052 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.6-5823G>A | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93104407 | ||||||
chr1:93104665
|
A | G | 4 | a0001c0001t0006g0238a0001c0001t0006g0239a0001c0001t0006g0240others(1): Show | 4 | HG01109.hp1 HG01884.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.6-5565A>G | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93104665 | ||||||
chr1:93104677
|
CA | C | 183 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(180): Show | 206 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(203): Show |
intron_variant | MODIFIER | c.6-5535delA | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 93104677 | |||||
chr1:93104811
|
G | A | 106 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(103): Show | 118 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(115): Show |
intron_variant | MODIFIER | c.6-5419G>A | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93104811 | ||||||
chr1:93104860
|
GAGAC | G | 12 | a0001c0001t0003g0294a0001c0001t0003g0295a0001c0001t0003g0296others(9): Show | 12 | HG00408.hp1 HG02074.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.6-5364_6-5361delGA others(2): Show |
MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 93104860 | |||||
chr1:93104877
|
C | T | 12 | a0001c0001t0003g0294a0001c0001t0003g0295a0001c0001t0003g0296others(9): Show | 12 | HG00408.hp1 HG02074.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.6-5353C>T | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93104877 | ||||||
chr1:93104879
|
G | T | 15 | a0001c0001t0001g0010a0001c0001t0001g0062a0001c0001t0001g0063others(12): Show | 16 | HG00323.hp1 HG00738.hp2 HG01069.hp2 others(13): Show |
intron_variant | MODIFIER | c.6-5351G>T | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93104879 | ||||||
chr1:93104882
|
C | T | 36 | a0001c0001t0001g0020a0001c0001t0001g0242a0001c0001t0001g0243others(33): Show | 37 | HG01891.hp2 HG01928.hp2 HG02055.hp1 others(34): Show |
intron_variant | MODIFIER | c.6-5348C>T | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93104882 | ||||||
chr1:93104938
|
C | T | 1 | a0001c0001t0003g0192 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.6-5292C>T | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93104938 | ||||||
chr1:93105001
|
G | A | 2 | a0001c0001t0001g0189a0001c0001t0001g0190 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.6-5229G>A | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93105001 | ||||||
chr1:93105066
|
C | T | 2 | a0001c0001t0005g0281a0001c0001t0005g0283 | 2 | NA18522.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.6-5164C>T | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93105066 | ||||||
chr1:93105092
|
C | T | 1 | a0001c0001t0001g0081 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.6-5138C>T | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93105092 | ||||||
chr1:93105100
|
C | T | 1 | a0001c0001t0002g0133 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.6-5130C>T | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93105100 | ||||||
chr1:93105126
|
A | T | 2 | a0001c0001t0001g0032a0001c0001t0001g0033 | 2 | NA18993.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.6-5104A>T | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93105126 | ||||||
chr1:93105143
|
C | CA | 71 | a0001c0001t0001g0020a0001c0001t0001g0030a0001c0001t0001g0124others(68): Show | 77 | HG00423.hp1 HG01074.hp2 HG01081.hp2 others(74): Show |
intron_variant | MODIFIER | c.6-5069dupA | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 93105143 | |||||
chr1:93105143
|
C | CAA | 171 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(168): Show | 194 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(191): Show |
intron_variant | MODIFIER | c.6-5070_6-5069dupAA | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 93105143 | |||||
chr1:93105143
|
C | CAAA | 50 | a0001c0001t0001g0043a0001c0001t0001g0053a0001c0001t0001g0112others(47): Show | 52 | HG00280.hp2 HG00323.hp2 HG00642.hp2 others(49): Show |
intron_variant | MODIFIER | c.6-5071_6-5069dupAA others(1): Show |
MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 93105143 | |||||
chr1:93105241
|
T | C | 7 | a0001c0001t0001g0020a0001c0001t0001g0262a0001c0001t0001g0265others(4): Show | 8 | NA18967.hp2 NA18968.hp1 NA18977.hp2 others(5): Show |
intron_variant | MODIFIER | c.6-4989T>C | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93105241 | ||||||
chr1:93105339
|
A | G | 5 | a0001c0001t0003g0295a0001c0001t0003g0301a0001c0001t0003g0303others(2): Show | 5 | HG02717.hp2 HG02886.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.6-4891A>G | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93105339 | ||||||
chr1:93105420
|
C | T | 264 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(261): Show | 290 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(287): Show |
intron_variant | MODIFIER | c.6-4810C>T | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93105420 | ||||||
chr1:93105427
|
G | A | 2 | a0001c0001t0001g0270a0001c0001t0001g0302 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.6-4803G>A | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93105427 | ||||||
chr1:93105585
|
C | T | 1 | a0001c0001t0001g0050 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.6-4645C>T | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93105585 | ||||||
chr1:93105667
|
T | TTG | 65 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(62): Show | 78 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.6-4549_6-4548dupGT | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 93105667 | |||||
chr1:93105681
|
G | T | 1 | a0001c0001t0003g0237 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.6-4549G>T | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93105681 | ||||||
chr1:93105683
|
T | G | 40 | a0001c0001t0001g0020a0001c0001t0001g0242a0001c0001t0001g0243others(37): Show | 41 | HG01109.hp1 HG01884.hp1 HG01891.hp2 others(38): Show |
intron_variant | MODIFIER | c.6-4547T>G | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93105683 | ||||||
chr1:93105793
|
A | G | 2 | a0001c0001t0002g0132a0001c0001t0002g0133 | 2 | HG02135.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.6-4437A>G | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93105793 | ||||||
chr1:93105855
|
A | T | 308 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(305): Show | 339 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(336): Show |
intron_variant | MODIFIER | c.6-4375A>T | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93105855 | ||||||
chr1:93106312
|
A | G | 1 | a0001c0003t0003g0217 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.6-3918A>G | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93106312 | ||||||
chr1:93106438
|
G | A | 308 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(305): Show | 339 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(336): Show |
intron_variant | MODIFIER | c.6-3792G>A | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93106438 | ||||||
chr1:93106441
|
TA | T | 308 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(305): Show | 339 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(336): Show |
intron_variant | MODIFIER | c.6-3787delA | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 93106441 | |||||
chr1:93106520
|
CT | C | 7 | a0001c0001t0001g0046a0001c0001t0001g0069a0001c0001t0001g0116others(4): Show | 7 | HG02040.hp1 NA18941.hp2 NA18942.hp1 others(4): Show |
intron_variant | MODIFIER | c.6-3694delT | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 93106520 | |||||
chr1:93106520
|
CTT | C | 265 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(262): Show | 295 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(292): Show |
intron_variant | MODIFIER | c.6-3695_6-3694delTT | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 93106520 | |||||
chr1:93106520
|
CTTT | C | 36 | a0001c0001t0001g0020a0001c0001t0001g0242a0001c0001t0001g0243others(33): Show | 37 | HG01891.hp2 HG01928.hp2 HG02055.hp1 others(34): Show |
intron_variant | MODIFIER | c.6-3696_6-3694delTT others(1): Show |
MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 93106520 | |||||
chr1:93106641
|
T | G | 6 | a0001c0001t0002g0011a0001c0001t0002g0150a0001c0001t0002g0157others(3): Show | 7 | HG00673.hp1 HG02129.hp2 HG02523.hp1 others(4): Show |
intron_variant | MODIFIER | c.6-3589T>G | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93106641 | ||||||
chr1:93106685
|
A | G | 1 | a0001c0001t0001g0290 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.6-3545A>G | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93106685 | ||||||
chr1:93106853
|
A | G | 1 | a0001c0001t0001g0191 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.6-3377A>G | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93106853 | ||||||
chr1:93106995
|
G | C | 1 | a0001c0001t0007g0051 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.6-3235G>C | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93106995 | ||||||
chr1:93107414
|
G | A | 1 | a0003c0004t0001g0066 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.6-2816G>A | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93107414 | ||||||
chr1:93107504
|
G | A | 1 | a0001c0001t0012g0199 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.6-2726G>A | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93107504 | ||||||
chr1:93107615
|
A | C | 1 | a0001c0001t0003g0291 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.6-2615A>C | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93107615 | ||||||
chr1:93107628
|
C | A | 1 | a0001c0001t0003g0237 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.6-2602C>A | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93107628 | ||||||
chr1:93107692
|
T | C | 1 | a0001c0001t0008g0170 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.6-2538T>C | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93107692 | ||||||
chr1:93107696
|
G | T | 264 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(261): Show | 290 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(287): Show |
intron_variant | MODIFIER | c.6-2534G>T | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93107696 | ||||||
chr1:93107709
|
AT | A | 229 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(226): Show | 254 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(251): Show |
intron_variant | MODIFIER | c.6-2511delT | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 93107709 | |||||
chr1:93107788
|
CTTCTTTT others(11): Show |
C | 1 | a0001c0001t0002g0146 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.6-2437_6-2420delTT others(16): Show |
MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 93107788 | |||||
chr1:93107936
|
A | G | 107 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(104): Show | 119 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.6-2294A>G | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93107936 | ||||||
chr1:93108268
|
T | TTG | 80 | a0001c0001t0001g0108a0001c0001t0001g0153a0001c0001t0002g0003others(77): Show | 92 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(89): Show |
intron_variant | MODIFIER | c.6-1946_6-1945dupGT | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 93108268 | |||||
chr1:93108335
|
A | G | 2 | a0001c0001t0004g0233a0001c0001t0010g0232 | 2 | HG02965.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.6-1895A>G | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93108335 | ||||||
chr1:93108561
|
G | A | 1 | a0001c0001t0002g0164 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.6-1669G>A | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93108561 | ||||||
chr1:93108606
|
A | AT | 53 | a0001c0001t0001g0020a0001c0001t0001g0028a0001c0001t0001g0031others(50): Show | 54 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(51): Show |
intron_variant | MODIFIER | c.6-1604dupT | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr1 | 93108606 | |||||
chr1:93108638
|
T | A | 12 | a0001c0001t0003g0294a0001c0001t0003g0295a0001c0001t0003g0296others(9): Show | 12 | HG00408.hp1 HG02074.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.6-1592T>A | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93108638 | ||||||
chr1:93108926
|
T | A | 1 | a0001c0001t0001g0070 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.6-1304T>A | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93108926 | ||||||
chr1:93109289
|
A | G | 8 | a0001c0001t0003g0295a0001c0001t0003g0296a0001c0001t0003g0297others(5): Show | 8 | HG02109.hp1 HG02717.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.6-941A>G | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93109289 | ||||||
chr1:93109293
|
T | A | 1 | a0001c0001t0001g0111 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.6-937T>A | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93109293 | ||||||
chr1:93109429
|
G | A | 1 | a0001c0001t0001g0062 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.6-801G>A | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93109429 | ||||||
chr1:93109491
|
G | A | 36 | a0001c0001t0001g0020a0001c0001t0001g0242a0001c0001t0001g0243others(33): Show | 37 | HG01891.hp2 HG01928.hp2 HG02055.hp1 others(34): Show |
intron_variant | MODIFIER | c.6-739G>A | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93109491 | ||||||
chr1:93109543
|
C | T | 10 | a0001c0001t0001g0009a0001c0001t0001g0060a0001c0001t0001g0061others(7): Show | 11 | HG00642.hp1 HG00733.hp1 HG01167.hp2 others(8): Show |
intron_variant | MODIFIER | c.6-687C>T | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93109543 | ||||||
chr1:93109566
|
C | T | 2 | a0001c0001t0001g0189a0001c0001t0001g0190 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.6-664C>T | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93109566 | ||||||
chr1:93109625
|
G | T | 31 | a0001c0001t0003g0018a0001c0001t0003g0019a0001c0001t0003g0021others(28): Show | 36 | HG00423.hp1 HG01074.hp2 HG01081.hp2 others(33): Show |
intron_variant | MODIFIER | c.6-605G>T | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93109625 | ||||||
chr1:93109742
|
A | G | 2 | a0001c0001t0003g0234a0001c0001t0003g0236 | 2 | NA18943.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.6-488A>G | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93109742 | ||||||
chr1:93110191
|
C | A | 1 | a0001c0001t0003g0294 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.6-39C>A | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 1/14 | chr1 | 93110191 | ||||||
chr1:93110745
|
T | G | 308 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(305): Show | 339 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(336): Show |
intron_variant | MODIFIER | c.286+119T>G | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 3/14 | chr1 | 93110745 | ||||||
chr1:93110777
|
T | C | 1 | a0001c0001t0012g0199 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.286+151T>C | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 3/14 | chr1 | 93110777 | ||||||
chr1:93111125
|
G | A | 1 | a0001c0001t0003g0294 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.286+499G>A | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 3/14 | chr1 | 93111125 | ||||||
chr1:93111129
|
G | A | 4 | a0001c0001t0006g0238a0001c0001t0006g0239a0001c0001t0006g0240others(1): Show | 4 | HG01109.hp1 HG01884.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.286+503G>A | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 3/14 | chr1 | 93111129 | ||||||
chr1:93111704
|
T | G | 1 | a0001c0001t0003g0203 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.286+1078T>G | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 3/14 | chr1 | 93111704 | ||||||
chr1:93111869
|
A | C | 14 | a0001c0001t0001g0020a0001c0001t0001g0247a0001c0001t0001g0251others(11): Show | 15 | HG01891.hp2 HG02615.hp1 HG02895.hp2 others(12): Show |
intron_variant | MODIFIER | c.286+1243A>C | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 3/14 | chr1 | 93111869 | ||||||
chr1:93111965
|
C | G | 4 | a0001c0001t0003g0015a0001c0001t0003g0193a0001c0001t0003g0197others(1): Show | 5 | HG02109.hp2 HG02572.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.286+1339C>G | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 3/14 | chr1 | 93111965 | ||||||
chr1:93112051
|
A | G | 1 | a0001c0001t0002g0228 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.286+1425A>G | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 3/14 | chr1 | 93112051 | ||||||
chr1:93112371
|
T | G | 1 | a0001c0001t0001g0050 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.286+1745T>G | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 3/14 | chr1 | 93112371 | ||||||
chr1:93112390
|
TAAAG | T | 224 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(221): Show | 249 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(246): Show |
intron_variant | MODIFIER | c.286+1768_286+1771d others(6): Show |
MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 93112390 | |||||
chr1:93112484
|
G | C | 1 | a0001c0001t0001g0009 | 2 | HG01167.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.286+1858G>C | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 3/14 | chr1 | 93112484 | ||||||
chr1:93112572
|
A | G | 37 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0192others(34): Show | 39 | HG00280.hp2 HG00323.hp2 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.286+1946A>G | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 3/14 | chr1 | 93112572 | ||||||
chr1:93112577
|
T | C | 1 | a0001c0003t0003g0217 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.286+1951T>C | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 3/14 | chr1 | 93112577 | ||||||
chr1:93112614
|
T | G | 1 | a0001c0001t0001g0191 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.286+1988T>G | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 3/14 | chr1 | 93112614 | ||||||
chr1:93112680
|
A | G | 1 | a0001c0001t0001g0055 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.287-2008A>G | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 3/14 | chr1 | 93112680 | ||||||
chr1:93112845
|
C | T | 108 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(105): Show | 120 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.287-1843C>T | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 3/14 | chr1 | 93112845 | ||||||
chr1:93112967
|
T | C | 308 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(305): Show | 339 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(336): Show |
intron_variant | MODIFIER | c.287-1721T>C | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 3/14 | chr1 | 93112967 | ||||||
chr1:93112977
|
C | T | 1 | a0001c0001t0003g0215 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.287-1711C>T | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 3/14 | chr1 | 93112977 | ||||||
chr1:93113031
|
A | C | 264 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(261): Show | 290 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(287): Show |
intron_variant | MODIFIER | c.287-1657A>C | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 3/14 | chr1 | 93113031 | ||||||
chr1:93113216
|
C | CA | 86 | a0001c0001t0001g0025a0001c0001t0001g0060a0001c0001t0001g0063others(83): Show | 97 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(94): Show |
intron_variant | MODIFIER | c.287-1455dupA | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 93113216 | |||||
chr1:93113216
|
C | CAA | 37 | a0001c0001t0002g0181a0001c0001t0002g0182a0001c0001t0002g0184others(34): Show | 39 | HG00280.hp2 HG00323.hp2 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.287-1456_287-1455d others(4): Show |
MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 93113216 | |||||
chr1:93113375
|
A | G | 31 | a0001c0001t0003g0018a0001c0001t0003g0019a0001c0001t0003g0021others(28): Show | 36 | HG00423.hp1 HG01074.hp2 HG01081.hp2 others(33): Show |
intron_variant | MODIFIER | c.287-1313A>G | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 3/14 | chr1 | 93113375 | ||||||
chr1:93113467
|
A | G | 1 | a0001c0001t0001g0248 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.287-1221A>G | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 3/14 | chr1 | 93113467 | ||||||
chr1:93113635
|
A | G | 31 | a0001c0001t0003g0018a0001c0001t0003g0019a0001c0001t0003g0021others(28): Show | 36 | HG00423.hp1 HG01074.hp2 HG01081.hp2 others(33): Show |
intron_variant | MODIFIER | c.287-1053A>G | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 3/14 | chr1 | 93113635 | ||||||
chr1:93113641
|
T | A | 14 | a0001c0001t0001g0020a0001c0001t0001g0247a0001c0001t0001g0251others(11): Show | 15 | HG01891.hp2 HG02615.hp1 HG02895.hp2 others(12): Show |
intron_variant | MODIFIER | c.287-1047T>A | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 3/14 | chr1 | 93113641 | ||||||
chr1:93114003
|
GA | G | 36 | a0001c0001t0001g0020a0001c0001t0001g0242a0001c0001t0001g0243others(33): Show | 37 | HG01891.hp2 HG01928.hp2 HG02055.hp1 others(34): Show |
intron_variant | MODIFIER | c.287-684delA | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 3/14 | chr1 | 93114003 | ||||||
chr1:93114060
|
T | TA | 308 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(305): Show | 339 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(336): Show |
intron_variant | MODIFIER | c.287-620dupA | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr1 | 93114060 | |||||
chr1:93114311
|
C | T | 6 | a0001c0001t0002g0011a0001c0001t0002g0150a0001c0001t0002g0157others(3): Show | 7 | HG00673.hp1 HG02129.hp2 HG02523.hp1 others(4): Show |
intron_variant | MODIFIER | c.287-377C>T | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 3/14 | chr1 | 93114311 | ||||||
chr1:93114435
|
G | A | 31 | a0001c0001t0003g0018a0001c0001t0003g0019a0001c0001t0003g0021others(28): Show | 36 | HG00423.hp1 HG01074.hp2 HG01081.hp2 others(33): Show |
intron_variant | MODIFIER | c.287-253G>A | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 3/14 | chr1 | 93114435 | ||||||
chr1:93114547
|
A | G | 1 | a0001c0001t0003g0198 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.287-141A>G | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 3/14 | chr1 | 93114547 | ||||||
chr1:93114578
|
A | G | 4 | a0001c0001t0002g0142a0001c0001t0002g0154a0001c0001t0002g0161others(1): Show | 4 | NA18948.hp1 NA18998.hp2 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.287-110A>G | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 3/14 | chr1 | 93114578 | ||||||
chr1:93114845
|
T | A | 37 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0192others(34): Show | 39 | HG00280.hp2 HG00323.hp2 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.382+62T>A | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 4/14 | chr1 | 93114845 | ||||||
chr1:93114941
|
A | C | 1 | a0001c0001t0001g0249 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.383-47A>C | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 4/14 | chr1 | 93114941 | ||||||
chr1:93115317
|
A | G | 36 | a0001c0001t0001g0020a0001c0001t0001g0242a0001c0001t0001g0243others(33): Show | 37 | HG01891.hp2 HG01928.hp2 HG02055.hp1 others(34): Show |
intron_variant | MODIFIER | c.484-153A>G | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 5/14 | chr1 | 93115317 | ||||||
chr1:93115322
|
T | C | 107 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(104): Show | 119 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.484-148T>C | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 5/14 | chr1 | 93115322 | ||||||
chr1:93115427
|
A | G | 2 | a0001c0001t0001g0263a0001c0001t0001g0264 | 2 | HG02647.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.484-43A>G | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 5/14 | chr1 | 93115427 | ||||||
chr1:93115435
|
C | T | 187 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(184): Show | 210 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(207): Show |
intron_variant | MODIFIER | c.484-35C>T | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 5/14 | chr1 | 93115435 | ||||||
chr1:93115467
|
T | C | 108 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(105): Show | 120 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(117): Show |
splice_region_variant&intron_variant | LOW | c.484-3T>C | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 5/14 | chr1 | 93115467 | ||||||
chr1:93115684
|
T | G | 1 | a0001c0001t0001g0191 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.632+66T>G | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 6/14 | chr1 | 93115684 | ||||||
chr1:93115707
|
T | C | 1 | a0001c0001t0003g0297 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.632+89T>C | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 6/14 | chr1 | 93115707 | ||||||
chr1:93116001
|
A | G | 1 | a0001c0001t0003g0237 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.632+383A>G | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 6/14 | chr1 | 93116001 | ||||||
chr1:93116065
|
A | G | 1 | a0001c0001t0001g0098 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.632+447A>G | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 6/14 | chr1 | 93116065 | ||||||
chr1:93116171
|
T | C | 264 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(261): Show | 290 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(287): Show |
intron_variant | MODIFIER | c.632+553T>C | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 6/14 | chr1 | 93116171 | ||||||
chr1:93116236
|
AT | A | 226 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(223): Show | 250 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(247): Show |
intron_variant | MODIFIER | c.632+629delT | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr1 | 93116236 | |||||
chr1:93116344
|
G | A | 1 | a0001c0001t0003g0213 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.632+726G>A | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 6/14 | chr1 | 93116344 | ||||||
chr1:93116501
|
A | AT | 64 | a0001c0001t0001g0059a0001c0001t0001g0069a0001c0001t0001g0100others(61): Show | 71 | HG00408.hp1 HG00423.hp1 HG01081.hp1 others(68): Show |
intron_variant | MODIFIER | c.632+903dupT | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr1 | 93116501 | |||||
chr1:93116501
|
A | ATT | 32 | a0001c0001t0001g0020a0001c0001t0001g0242a0001c0001t0001g0243others(29): Show | 33 | HG01109.hp1 HG01884.hp1 HG01891.hp2 others(30): Show |
intron_variant | MODIFIER | c.632+902_632+903dup others(2): Show |
MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr1 | 93116501 | |||||
chr1:93116501
|
A | ATTTT | 25 | a0001c0001t0003g0194a0001c0001t0003g0195a0001c0001t0003g0196others(22): Show | 25 | HG00280.hp2 HG00323.hp2 HG01069.hp1 others(22): Show |
intron_variant | MODIFIER | c.632+900_632+903dup others(4): Show |
MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr1 | 93116501 | |||||
chr1:93116501
|
A | ATTTTT | 11 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0192others(8): Show | 13 | HG00642.hp2 HG00741.hp1 HG01517.hp2 others(10): Show |
intron_variant | MODIFIER | c.632+899_632+903dup others(5): Show |
MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr1 | 93116501 | |||||
chr1:93116559
|
A | G | 2 | a0001c0001t0004g0230a0001c0001t0004g0231 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.632+941A>G | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 6/14 | chr1 | 93116559 | ||||||
chr1:93117187
|
G | A | 37 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0192others(34): Show | 39 | HG00280.hp2 HG00323.hp2 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.633-1158G>A | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 6/14 | chr1 | 93117187 | ||||||
chr1:93117574
|
T | C | 1 | a0001c0001t0001g0068 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.633-771T>C | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 6/14 | chr1 | 93117574 | ||||||
chr1:93117793
|
G | A | 1 | a0001c0001t0007g0073 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.633-552G>A | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 6/14 | chr1 | 93117793 | ||||||
chr1:93117892
|
G | A | 40 | a0001c0001t0001g0020a0001c0001t0001g0242a0001c0001t0001g0243others(37): Show | 41 | HG01109.hp1 HG01884.hp1 HG01891.hp2 others(38): Show |
intron_variant | MODIFIER | c.633-453G>A | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 6/14 | chr1 | 93117892 | ||||||
chr1:93118261
|
C | CTT | 33 | a0001c0001t0001g0020a0001c0001t0001g0242a0001c0001t0001g0243others(30): Show | 34 | HG01891.hp2 HG01928.hp2 HG02055.hp1 others(31): Show |
intron_variant | MODIFIER | c.633-66_633-65dupTT | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr1 | 93118261 | |||||
chr1:93118261
|
CT | C | 193 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(190): Show | 216 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(213): Show |
intron_variant | MODIFIER | c.633-65delT | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr1 | 93118261 | |||||
chr1:93118261
|
CTT | C | 8 | a0001c0001t0001g0044a0001c0001t0001g0050a0001c0001t0001g0081others(5): Show | 8 | HG01070.hp2 HG01168.hp2 HG01256.hp2 others(5): Show |
intron_variant | MODIFIER | c.633-66_633-65delTT | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr1 | 93118261 | |||||
chr1:93118280
|
T | TA | 4 | a0001c0001t0006g0238a0001c0001t0006g0239a0001c0001t0006g0240others(1): Show | 4 | HG01109.hp1 HG01884.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.633-62dupA | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr1 | 93118280 | |||||
chr1:93118449
|
G | A | 6 | a0001c0001t0004g0017a0001c0001t0004g0229a0001c0001t0004g0230others(3): Show | 7 | HG01884.hp2 HG02630.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.728+9G>A | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 7/14 | chr1 | 93118449 | ||||||
chr1:93118594
|
C | T | 1 | a0001c0001t0003g0305 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.728+154C>T | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 7/14 | chr1 | 93118594 | ||||||
chr1:93118642
|
G | A | 187 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(184): Show | 210 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(207): Show |
intron_variant | MODIFIER | c.728+202G>A | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 7/14 | chr1 | 93118642 | ||||||
chr1:93118910
|
A | G | 2 | a0001c0001t0005g0281a0001c0001t0005g0283 | 2 | NA18522.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.729-423A>G | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 7/14 | chr1 | 93118910 | ||||||
chr1:93119049
|
G | A | 104 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(101): Show | 116 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.729-284G>A | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 7/14 | chr1 | 93119049 | ||||||
chr1:93119179
|
A | G | 3 | a0001c0001t0001g0045a0001c0001t0001g0054a0001c0001t0001g0067 | 3 | NA18612.hp1 NA19079.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.729-154A>G | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 7/14 | chr1 | 93119179 | ||||||
chr1:93119313
|
C | CT | 38 | a0001c0001t0002g0131a0001c0001t0003g0015a0001c0001t0003g0016others(35): Show | 40 | HG00280.hp2 HG00323.hp2 HG00642.hp2 others(37): Show |
splice_region_variant&intron_variant | LOW | c.729-6dupT | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr1 | 93119313 | |||||
chr1:93119722
|
A | G | 1 | a0001c0001t0001g0191 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.797+321A>G | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 8/14 | chr1 | 93119722 | ||||||
chr1:93119811
|
A | G | 31 | a0001c0001t0003g0018a0001c0001t0003g0019a0001c0001t0003g0021others(28): Show | 36 | HG00423.hp1 HG01074.hp2 HG01081.hp2 others(33): Show |
intron_variant | MODIFIER | c.797+410A>G | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 8/14 | chr1 | 93119811 | ||||||
chr1:93119911
|
A | G | 1 | a0001c0001t0001g0124 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.797+510A>G | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 8/14 | chr1 | 93119911 | ||||||
chr1:93120049
|
G | A | 2 | a0001c0001t0001g0189a0001c0001t0001g0190 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.798-500G>A | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 8/14 | chr1 | 93120049 | ||||||
chr1:93120301
|
G | GA | 105 | a0001c0001t0001g0047a0001c0001t0001g0074a0001c0001t0001g0099others(102): Show | 116 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(113): Show |
intron_variant | MODIFIER | c.798-228dupA | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr1 | 93120301 | |||||
chr1:93120301
|
G | GAA | 10 | a0001c0001t0001g0020a0001c0001t0001g0251a0001c0001t0001g0254others(7): Show | 11 | HG02055.hp1 HG02738.hp2 HG04204.hp1 others(8): Show |
intron_variant | MODIFIER | c.798-229_798-228dup others(2): Show |
MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr1 | 93120301 | |||||
chr1:93120301
|
GA | G | 11 | a0001c0001t0001g0069a0001c0001t0001g0089a0001c0001t0001g0090others(8): Show | 11 | HG00323.hp2 HG01069.hp2 HG01256.hp1 others(8): Show |
intron_variant | MODIFIER | c.798-228delA | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr1 | 93120301 | |||||
chr1:93120302
|
A | G | 8 | a0001c0001t0003g0294a0001c0001t0003g0296a0001c0001t0003g0297others(5): Show | 8 | HG00408.hp1 HG02074.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.798-247A>G | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 8/14 | chr1 | 93120302 | ||||||
chr1:93120303
|
A | G | 4 | a0001c0001t0003g0295a0001c0001t0003g0301a0001c0001t0003g0303others(1): Show | 4 | HG02717.hp2 HG02895.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.798-246A>G | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 8/14 | chr1 | 93120303 | ||||||
chr1:93121505
|
T | C | 4 | a0001c0001t0006g0238a0001c0001t0006g0239a0001c0001t0006g0240others(1): Show | 4 | HG01109.hp1 HG01884.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.921+833T>C | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 9/14 | chr1 | 93121505 | ||||||
chr1:93121564
|
A | G | 3 | a0001c0001t0006g0238a0001c0001t0006g0239a0001c0001t0006g0241 | 3 | HG01109.hp1 HG01884.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.921+892A>G | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 9/14 | chr1 | 93121564 | ||||||
chr1:93121792
|
AT | A | 34 | a0001c0001t0003g0018a0001c0001t0003g0019a0001c0001t0003g0021others(31): Show | 39 | HG00408.hp1 HG00423.hp1 HG01074.hp2 others(36): Show |
intron_variant | MODIFIER | c.921+1146delT | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr1 | 93121792 | |||||
chr1:93121792
|
ATT | A | 8 | a0001c0001t0001g0243a0001c0001t0001g0254a0001c0001t0001g0271others(5): Show | 8 | HG01109.hp1 HG02055.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.921+1145_921+1146d others(4): Show |
MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr1 | 93121792 | |||||
chr1:93121792
|
ATTT | A | 33 | a0001c0001t0001g0020a0001c0001t0001g0242a0001c0001t0001g0244others(30): Show | 34 | HG01891.hp2 HG01928.hp2 HG02258.hp1 others(31): Show |
intron_variant | MODIFIER | c.921+1144_921+1146d others(5): Show |
MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr1 | 93121792 | |||||
chr1:93121792
|
ATTTTTTT others(5): Show |
A | 5 | a0001c0001t0001g0062a0001c0001t0002g0135a0001c0001t0002g0167others(2): Show | 5 | HG00558.hp1 HG01346.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.921+1135_921+1146d others(14): Show |
MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr1 | 93121792 | |||||
chr1:93121792
|
ATTTTTTT others(6): Show |
A | 219 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(216): Show | 244 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(241): Show |
intron_variant | MODIFIER | c.921+1134_921+1146d others(15): Show |
MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr1 | 93121792 | |||||
chr1:93121824
|
C | T | 1 | a0001c0001t0003g0220 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.921+1152C>T | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 9/14 | chr1 | 93121824 | ||||||
chr1:93121862
|
C | T | 12 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0023others(9): Show | 18 | HG00408.hp2 HG00438.hp1 HG00558.hp2 others(15): Show |
intron_variant | MODIFIER | c.921+1190C>T | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 9/14 | chr1 | 93121862 | ||||||
chr1:93121878
|
C | T | 107 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(104): Show | 119 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.921+1206C>T | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 9/14 | chr1 | 93121878 | ||||||
chr1:93122044
|
C | A | 1 | a0001c0001t0001g0026 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.921+1372C>A | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 9/14 | chr1 | 93122044 | ||||||
chr1:93122225
|
T | A | 28 | a0001c0001t0001g0020a0001c0001t0001g0242a0001c0001t0001g0243others(25): Show | 29 | HG01891.hp2 HG01928.hp2 HG02055.hp1 others(26): Show |
intron_variant | MODIFIER | c.921+1553T>A | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 9/14 | chr1 | 93122225 | ||||||
chr1:93122318
|
G | A | 12 | a0001c0001t0003g0294a0001c0001t0003g0295a0001c0001t0003g0296others(9): Show | 12 | HG00408.hp1 HG02074.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.921+1646G>A | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 9/14 | chr1 | 93122318 | ||||||
chr1:93122676
|
A | G | 224 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(221): Show | 249 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(246): Show |
intron_variant | MODIFIER | c.921+2004A>G | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 9/14 | chr1 | 93122676 | ||||||
chr1:93122877
|
T | C | 1 | a0001c0001t0001g0097 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.921+2205T>C | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 9/14 | chr1 | 93122877 | ||||||
chr1:93123001
|
A | G | 40 | a0001c0001t0001g0020a0001c0001t0001g0242a0001c0001t0001g0243others(37): Show | 41 | HG01109.hp1 HG01884.hp1 HG01891.hp2 others(38): Show |
intron_variant | MODIFIER | c.921+2329A>G | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 9/14 | chr1 | 93123001 | ||||||
chr1:93123149
|
T | A | 1 | a0001c0001t0001g0087 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.921+2477T>A | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 9/14 | chr1 | 93123149 | ||||||
chr1:93123210
|
CT | C | 60 | a0001c0001t0001g0025a0001c0001t0001g0037a0001c0001t0001g0038others(57): Show | 65 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(62): Show |
intron_variant | MODIFIER | c.921+2559delT | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr1 | 93123210 | |||||
chr1:93123210
|
CTT | C | 6 | a0001c0001t0002g0150a0001c0001t0003g0295a0001c0001t0003g0300others(3): Show | 6 | HG02895.hp1 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.921+2558_921+2559d others(4): Show |
MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr1 | 93123210 | |||||
chr1:93123214
|
T | C | 6 | a0001c0001t0001g0153a0001c0001t0002g0012a0001c0001t0002g0127others(3): Show | 7 | HG02040.hp2 NA18947.hp1 NA18962.hp2 others(4): Show |
intron_variant | MODIFIER | c.921+2542T>C | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 9/14 | chr1 | 93123214 | ||||||
chr1:93123215
|
T | C | 1 | a0001c0001t0002g0149 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.921+2543T>C | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 9/14 | chr1 | 93123215 | ||||||
chr1:93123244
|
A | C | 264 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(261): Show | 290 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(287): Show |
intron_variant | MODIFIER | c.921+2572A>C | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 9/14 | chr1 | 93123244 | ||||||
chr1:93123258
|
C | G | 40 | a0001c0001t0001g0020a0001c0001t0001g0242a0001c0001t0001g0243others(37): Show | 41 | HG01109.hp1 HG01884.hp1 HG01891.hp2 others(38): Show |
intron_variant | MODIFIER | c.921+2586C>G | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 9/14 | chr1 | 93123258 | ||||||
chr1:93123262
|
CT | C | 6 | a0001c0001t0001g0048a0001c0001t0001g0262a0001c0001t0002g0127others(3): Show | 6 | HG01943.hp2 HG02647.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.921+2603delT | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr1 | 93123262 | |||||
chr1:93123726
|
C | G | 1 | a0001c0001t0001g0258 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.921+3054C>G | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 9/14 | chr1 | 93123726 | ||||||
chr1:93123729
|
T | A | 1 | a0001c0001t0003g0234 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.921+3057T>A | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 9/14 | chr1 | 93123729 | ||||||
chr1:93123761
|
T | TC | 65 | a0001c0001t0001g0040a0001c0001t0001g0056a0001c0001t0001g0094others(62): Show | 72 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(69): Show |
intron_variant | MODIFIER | c.921+3099dupC | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr1 | 93123761 | |||||
chr1:93123761
|
TC | T | 42 | a0001c0001t0001g0020a0001c0001t0001g0072a0001c0001t0001g0078others(39): Show | 43 | HG01109.hp1 HG01257.hp1 HG01884.hp1 others(40): Show |
intron_variant | MODIFIER | c.921+3099delC | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr1 | 93123761 | |||||
chr1:93123902
|
A | G | 1 | a0001c0001t0001g0034 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.921+3230A>G | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 9/14 | chr1 | 93123902 | ||||||
chr1:93124083
|
C | T | 2 | a0001c0001t0002g0122a0001c0001t0002g0123 | 2 | HG02451.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.922-3149C>T | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 9/14 | chr1 | 93124083 | ||||||
chr1:93124335
|
C | T | 36 | a0001c0001t0001g0020a0001c0001t0001g0242a0001c0001t0001g0243others(33): Show | 37 | HG01891.hp2 HG01928.hp2 HG02055.hp1 others(34): Show |
intron_variant | MODIFIER | c.922-2897C>T | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 9/14 | chr1 | 93124335 | ||||||
chr1:93124460
|
T | C | 1 | a0001c0001t0003g0226 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.922-2772T>C | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 9/14 | chr1 | 93124460 | ||||||
chr1:93124588
|
T | A | 1 | a0001c0001t0003g0204 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.922-2644T>A | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 9/14 | chr1 | 93124588 | ||||||
chr1:93124604
|
A | G | 1 | a0001c0001t0003g0207 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.922-2628A>G | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 9/14 | chr1 | 93124604 | ||||||
chr1:93124691
|
A | G | 6 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0250others(3): Show | 6 | HG02451.hp1 HG02630.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.922-2541A>G | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 9/14 | chr1 | 93124691 | ||||||
chr1:93125103
|
A | T | 1 | a0001c0001t0003g0277 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.922-2129A>T | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 9/14 | chr1 | 93125103 | ||||||
chr1:93125111
|
C | T | 74 | a0001c0001t0001g0153a0001c0001t0002g0003a0001c0001t0002g0004others(71): Show | 85 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(82): Show |
intron_variant | MODIFIER | c.922-2121C>T | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 9/14 | chr1 | 93125111 | ||||||
chr1:93125191
|
A | G | 1 | a0001c0001t0001g0072 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.922-2041A>G | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 9/14 | chr1 | 93125191 | ||||||
chr1:93125194
|
T | C | 12 | a0001c0001t0003g0294a0001c0001t0003g0295a0001c0001t0003g0296others(9): Show | 12 | HG00408.hp1 HG02074.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.922-2038T>C | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 9/14 | chr1 | 93125194 | ||||||
chr1:93125270
|
T | A | 1 | a0001c0001t0001g0026 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.922-1962T>A | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 9/14 | chr1 | 93125270 | ||||||
chr1:93125305
|
T | TTG | 6 | a0001c0001t0001g0027a0001c0001t0001g0093a0001c0001t0002g0135others(3): Show | 6 | HG01981.hp1 HG02602.hp1 HG04115.hp1 others(3): Show |
intron_variant | MODIFIER | c.922-1926_922-1925i others(4): Show |
MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr1 | 93125305 | |||||
chr1:93125306
|
T | TG | 178 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(175): Show | 201 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(198): Show |
intron_variant | MODIFIER | c.922-1926_922-1925i others(3): Show |
MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 9/14 | chr1 | 93125306 | ||||||
chr1:93125307
|
T | G | 118 | a0001c0001t0001g0020a0001c0001t0001g0030a0001c0001t0001g0125others(115): Show | 126 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(123): Show |
intron_variant | MODIFIER | c.922-1925T>G | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 9/14 | chr1 | 93125307 | ||||||
chr1:93125308
|
T | G | 1 | a0001c0001t0001g0191 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.922-1924T>G | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 9/14 | chr1 | 93125308 | ||||||
chr1:93125458
|
G | A | 1 | a0001c0001t0001g0106 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.922-1774G>A | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 9/14 | chr1 | 93125458 | ||||||
chr1:93125485
|
C | T | 1 | a0001c0001t0002g0159 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.922-1747C>T | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 9/14 | chr1 | 93125485 | ||||||
chr1:93125489
|
T | A | 308 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(305): Show | 339 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(336): Show |
intron_variant | MODIFIER | c.922-1743T>A | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 9/14 | chr1 | 93125489 | ||||||
chr1:93125605
|
A | G | 37 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0192others(34): Show | 39 | HG00280.hp2 HG00323.hp2 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.922-1627A>G | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 9/14 | chr1 | 93125605 | ||||||
chr1:93125628
|
A | G | 1 | a0001c0001t0001g0261 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.922-1604A>G | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 9/14 | chr1 | 93125628 | ||||||
chr1:93125856
|
A | C | 2 | a0001c0001t0001g0248a0001c0001t0001g0249 | 2 | HG03098.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.922-1376A>C | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 9/14 | chr1 | 93125856 | ||||||
chr1:93126079
|
A | G | 36 | a0001c0001t0001g0020a0001c0001t0001g0242a0001c0001t0001g0243others(33): Show | 37 | HG01891.hp2 HG01928.hp2 HG02055.hp1 others(34): Show |
intron_variant | MODIFIER | c.922-1153A>G | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 9/14 | chr1 | 93126079 | ||||||
chr1:93126158
|
G | GT | 24 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0192others(21): Show | 26 | HG00280.hp2 HG00323.hp2 HG00642.hp2 others(23): Show |
intron_variant | MODIFIER | c.922-1062dupT | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr1 | 93126158 | |||||
chr1:93126158
|
GT | G | 185 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(182): Show | 208 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(205): Show |
intron_variant | MODIFIER | c.922-1062delT | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr1 | 93126158 | |||||
chr1:93126233
|
T | C | 4 | a0001c0001t0006g0238a0001c0001t0006g0239a0001c0001t0006g0240others(1): Show | 4 | HG01109.hp1 HG01884.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.922-999T>C | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 9/14 | chr1 | 93126233 | ||||||
chr1:93126256
|
C | A | 2 | a0001c0001t0001g0125a0001c0001t0001g0191 | 2 | HG01168.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.922-976C>A | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 9/14 | chr1 | 93126256 | ||||||
chr1:93126481
|
CT | C | 274 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(271): Show | 300 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(297): Show |
intron_variant | MODIFIER | c.922-739delT | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr1 | 93126481 | |||||
chr1:93126694
|
T | C | 1 | a0001c0001t0003g0237 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.922-538T>C | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 9/14 | chr1 | 93126694 | ||||||
chr1:93126872
|
A | G | 36 | a0001c0001t0001g0020a0001c0001t0001g0242a0001c0001t0001g0243others(33): Show | 37 | HG01891.hp2 HG01928.hp2 HG02055.hp1 others(34): Show |
intron_variant | MODIFIER | c.922-360A>G | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 9/14 | chr1 | 93126872 | ||||||
chr1:93127020
|
T | A | 187 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(184): Show | 210 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(207): Show |
intron_variant | MODIFIER | c.922-212T>A | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 9/14 | chr1 | 93127020 | ||||||
chr1:93127135
|
A | T | 75 | a0001c0001t0001g0153a0001c0001t0002g0003a0001c0001t0002g0004others(72): Show | 86 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(83): Show |
intron_variant | MODIFIER | c.922-97A>T | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 9/14 | chr1 | 93127135 | ||||||
chr1:93127521
|
A | G | 1 | a0001c0001t0001g0031 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.989+222A>G | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 10/14 | chr1 | 93127521 | ||||||
chr1:93127731
|
A | G | 1 | a0001c0001t0001g0065 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.989+432A>G | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 10/14 | chr1 | 93127731 | ||||||
chr1:93127823
|
C | CT | 308 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(305): Show | 339 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(336): Show |
intron_variant | MODIFIER | c.989+533dupT | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 93127823 | |||||
chr1:93128217
|
C | T | 40 | a0001c0001t0001g0020a0001c0001t0001g0242a0001c0001t0001g0243others(37): Show | 41 | HG01109.hp1 HG01884.hp1 HG01891.hp2 others(38): Show |
intron_variant | MODIFIER | c.989+918C>T | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 10/14 | chr1 | 93128217 | ||||||
chr1:93128296
|
A | G | 1 | a0001c0001t0001g0191 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.990-982A>G | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 10/14 | chr1 | 93128296 | ||||||
chr1:93128323
|
C | T | 12 | a0001c0001t0003g0294a0001c0001t0003g0295a0001c0001t0003g0296others(9): Show | 12 | HG00408.hp1 HG02074.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.990-955C>T | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 10/14 | chr1 | 93128323 | ||||||
chr1:93128333
|
A | G | 264 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(261): Show | 290 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(287): Show |
intron_variant | MODIFIER | c.990-945A>G | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 10/14 | chr1 | 93128333 | ||||||
chr1:93128386
|
T | C | 264 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(261): Show | 290 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(287): Show |
intron_variant | MODIFIER | c.990-892T>C | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 10/14 | chr1 | 93128386 | ||||||
chr1:93128458
|
G | A | 1 | a0001c0001t0007g0051 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.990-820G>A | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 10/14 | chr1 | 93128458 | ||||||
chr1:93128555
|
CA | C | 9 | a0001c0001t0001g0033a0001c0001t0001g0189a0001c0001t0001g0190others(6): Show | 9 | HG01168.hp2 HG01192.hp1 HG01516.hp1 others(6): Show |
intron_variant | MODIFIER | c.990-704delA | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 93128555 | |||||
chr1:93128555
|
CAA | C | 251 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(248): Show | 277 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(274): Show |
intron_variant | MODIFIER | c.990-705_990-704del others(2): Show |
MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | 93128555 | |||||
chr1:93128736
|
A | C | 12 | a0001c0001t0003g0294a0001c0001t0003g0295a0001c0001t0003g0296others(9): Show | 12 | HG00408.hp1 HG02074.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.990-542A>C | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 10/14 | chr1 | 93128736 | ||||||
chr1:93128859
|
A | G | 1 | a0001c0001t0001g0191 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.990-419A>G | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 10/14 | chr1 | 93128859 | ||||||
chr1:93129174
|
T | C | 1 | a0001c0001t0002g0140 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.990-104T>C | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 10/14 | chr1 | 93129174 | ||||||
chr1:93129209
|
T | A | 6 | a0001c0001t0001g0020a0001c0001t0001g0265a0001c0001t0001g0266others(3): Show | 7 | NA18967.hp2 NA18968.hp1 NA18977.hp2 others(4): Show |
intron_variant | MODIFIER | c.990-69T>A | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 10/14 | chr1 | 93129209 | ||||||
chr1:93129490
|
T | A | 1 | a0001c0001t0003g0304 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1160+42T>A | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 11/14 | chr1 | 93129490 | ||||||
chr1:93129558
|
A | AT | 32 | a0001c0001t0001g0041a0001c0001t0001g0052a0001c0001t0001g0053others(29): Show | 35 | HG00558.hp1 HG00673.hp2 HG01192.hp1 others(32): Show |
intron_variant | MODIFIER | c.1160+130dupT | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 93129558 | |||||
chr1:93129558
|
AT | A | 54 | a0001c0001t0001g0023a0001c0001t0001g0095a0001c0001t0001g0246others(51): Show | 59 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.1160+130delT | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 93129558 | |||||
chr1:93129562
|
T | G | 1 | a0001c0001t0003g0224 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1160+114T>G | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 11/14 | chr1 | 93129562 | ||||||
chr1:93129745
|
G | C | 1 | a0001c0001t0001g0007 | 2 | NA18962.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1160+297G>C | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 11/14 | chr1 | 93129745 | ||||||
chr1:93129749
|
G | C | 153 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(150): Show | 170 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(167): Show |
intron_variant | MODIFIER | c.1160+301G>C | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 11/14 | chr1 | 93129749 | ||||||
chr1:93130034
|
T | A | 1 | a0001c0001t0003g0304 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1160+586T>A | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 11/14 | chr1 | 93130034 | ||||||
chr1:93130181
|
A | G | 3 | a0001c0001t0001g0070a0001c0001t0001g0074a0001c0001t0001g0075 | 3 | HG00544.hp1 HG02135.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.1160+733A>G | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 11/14 | chr1 | 93130181 | ||||||
chr1:93130576
|
CA | C | 46 | a0001c0001t0001g0048a0001c0001t0001g0262a0001c0001t0003g0018others(43): Show | 51 | HG00408.hp1 HG00423.hp1 HG01074.hp2 others(48): Show |
intron_variant | MODIFIER | c.1160+1140delA | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 93130576 | |||||
chr1:93130701
|
A | G | 4 | a0001c0001t0006g0238a0001c0001t0006g0239a0001c0001t0006g0240others(1): Show | 4 | HG01109.hp1 HG01884.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1160+1253A>G | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 11/14 | chr1 | 93130701 | ||||||
chr1:93130788
|
A | G | 2 | a0001c0001t0001g0247a0001c0001t0001g0269 | 2 | HG01891.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1160+1340A>G | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 11/14 | chr1 | 93130788 | ||||||
chr1:93130946
|
A | AAC | 52 | a0001c0001t0001g0010a0001c0001t0001g0062a0001c0001t0001g0063others(49): Show | 58 | HG00323.hp1 HG00423.hp1 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.1160+1521_1160+152 others(6): Show |
MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 93130946 | |||||
chr1:93130946
|
A | AACAC | 8 | a0001c0001t0001g0121a0001c0001t0001g0259a0001c0001t0002g0184others(5): Show | 8 | HG01884.hp1 HG02451.hp1 HG02698.hp2 others(5): Show |
intron_variant | MODIFIER | c.1160+1519_1160+152 others(8): Show |
MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 93130946 | |||||
chr1:93130953
|
A | G | 4 | a0001c0001t0001g0253a0001c0001t0001g0270a0001c0001t0001g0302others(1): Show | 4 | HG02615.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1160+1505A>G | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 11/14 | chr1 | 93130953 | ||||||
chr1:93130999
|
C | G | 1 | a0001c0001t0001g0251 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1160+1551C>G | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 11/14 | chr1 | 93130999 | ||||||
chr1:93131017
|
A | G | 36 | a0001c0001t0001g0020a0001c0001t0001g0242a0001c0001t0001g0243others(33): Show | 37 | HG01891.hp2 HG01928.hp2 HG02055.hp1 others(34): Show |
intron_variant | MODIFIER | c.1160+1569A>G | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 11/14 | chr1 | 93131017 | ||||||
chr1:93131379
|
T | C | 233 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(230): Show | 253 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(250): Show |
intron_variant | MODIFIER | c.1160+1931T>C | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 11/14 | chr1 | 93131379 | ||||||
chr1:93131511
|
A | C | 2 | a0001c0001t0001g0189a0001c0001t0001g0190 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1160+2063A>C | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 11/14 | chr1 | 93131511 | ||||||
chr1:93132124
|
T | C | 1 | a0001c0001t0001g0118 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1161-1579T>C | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 11/14 | chr1 | 93132124 | ||||||
chr1:93132350
|
GA | G | 37 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0192others(34): Show | 39 | HG00280.hp2 HG00323.hp2 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.1161-1344delA | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 93132350 | |||||
chr1:93132557
|
T | C | 41 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0192others(38): Show | 43 | HG00280.hp2 HG00323.hp2 HG00642.hp2 others(40): Show |
intron_variant | MODIFIER | c.1161-1146T>C | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 11/14 | chr1 | 93132557 | ||||||
chr1:93132747
|
C | G | 8 | a0001c0001t0002g0005a0001c0001t0002g0014a0001c0001t0002g0126others(5): Show | 11 | HG01081.hp1 HG01123.hp2 HG01261.hp2 others(8): Show |
intron_variant | MODIFIER | c.1161-956C>G | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 11/14 | chr1 | 93132747 | ||||||
chr1:93132894
|
A | G | 1 | a0001c0001t0003g0224 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1161-809A>G | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 11/14 | chr1 | 93132894 | ||||||
chr1:93132985
|
A | T | 37 | a0001c0001t0001g0020a0001c0001t0001g0242a0001c0001t0001g0243others(34): Show | 38 | HG01891.hp2 HG01928.hp2 HG02055.hp1 others(35): Show |
intron_variant | MODIFIER | c.1161-718A>T | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 11/14 | chr1 | 93132985 | ||||||
chr1:93133041
|
T | TGCTTGGT others(5): Show |
12 | a0001c0001t0003g0294a0001c0001t0003g0295a0001c0001t0003g0296others(9): Show | 12 | HG00408.hp1 HG02074.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.1161-657_1161-646d others(14): Show |
MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr1 | 93133041 | |||||
chr1:93133120
|
T | C | 2 | a0001c0001t0001g0189a0001c0001t0001g0190 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1161-583T>C | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 11/14 | chr1 | 93133120 | ||||||
chr1:93133367
|
T | C | 1 | a0001c0001t0001g0253 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1161-336T>C | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 11/14 | chr1 | 93133367 | ||||||
chr1:93133369
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A | G | 2 | a0001c0001t0001g0125a0001c0001t0001g0191 | 2 | HG01168.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1161-334A>G | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 11/14 | chr1 | 93133369 | ||||||
chr1:93133651
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G | A | 1 | a0001c0001t0001g0034 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1161-52G>A | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 11/14 | chr1 | 93133651 | ||||||
chr1:93134216
|
T | C | 1 | a0001c0001t0001g0069 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1424+21T>C | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 14/14 | chr1 | 93134216 | ||||||
chr1:93134511
|
T | C | 2 | a0001c0001t0001g0247a0001c0001t0001g0269 | 2 | HG01891.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1424+316T>C | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 14/14 | chr1 | 93134511 | ||||||
chr1:93134521
|
T | A | 2 | a0001c0001t0003g0286a0001c0001t0003g0287 | 2 | HG02145.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1424+326T>A | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 14/14 | chr1 | 93134521 | ||||||
chr1:93134523
|
A | AT | 40 | a0001c0001t0001g0020a0001c0001t0001g0242a0001c0001t0001g0243others(37): Show | 41 | HG01109.hp1 HG01884.hp1 HG01891.hp2 others(38): Show |
intron_variant | MODIFIER | c.1424+339dupT | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr1 | 93134523 | |||||
chr1:93134642
|
G | A | 36 | a0001c0001t0001g0020a0001c0001t0001g0242a0001c0001t0001g0243others(33): Show | 37 | HG01891.hp2 HG01928.hp2 HG02055.hp1 others(34): Show |
intron_variant | MODIFIER | c.1424+447G>A | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 14/14 | chr1 | 93134642 | ||||||
chr1:93134683
|
C | T | 1 | a0001c0001t0001g0097 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1424+488C>T | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 14/14 | chr1 | 93134683 | ||||||
chr1:93134834
|
TA | T | 192 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(189): Show | 208 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.1424+656delA | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr1 | 93134834 | |||||
chr1:93135073
|
A | G | 121 | a0001c0001t0001g0020a0001c0001t0001g0242a0001c0001t0001g0243others(118): Show | 129 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(126): Show |
intron_variant | MODIFIER | c.1424+878A>G | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 14/14 | chr1 | 93135073 | ||||||
chr1:93135184
|
C | G | 1 | a0001c0001t0002g0173 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1424+989C>G | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 14/14 | chr1 | 93135184 | ||||||
chr1:93135235
|
G | A | 1 | a0001c0001t0001g0055 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1424+1040G>A | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 14/14 | chr1 | 93135235 | ||||||
chr1:93135330
|
G | A | 4 | a0001c0001t0006g0238a0001c0001t0006g0239a0001c0001t0006g0240others(1): Show | 4 | HG01109.hp1 HG01884.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1424+1135G>A | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 14/14 | chr1 | 93135330 | ||||||
chr1:93135633
|
G | C | 44 | a0001c0001t0003g0018a0001c0001t0003g0019a0001c0001t0003g0021others(41): Show | 49 | HG00408.hp1 HG00423.hp1 HG01074.hp2 others(46): Show |
intron_variant | MODIFIER | c.1425-1037G>C | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 14/14 | chr1 | 93135633 | ||||||
chr1:93135674
|
G | A | 37 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0192others(34): Show | 39 | HG00280.hp2 HG00323.hp2 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.1425-996G>A | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 14/14 | chr1 | 93135674 | ||||||
chr1:93135784
|
C | T | 14 | a0001c0001t0001g0020a0001c0001t0001g0247a0001c0001t0001g0251others(11): Show | 15 | HG01891.hp2 HG02615.hp1 HG02895.hp2 others(12): Show |
intron_variant | MODIFIER | c.1425-886C>T | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 14/14 | chr1 | 93135784 | ||||||
chr1:93136387
|
G | A | 2 | a0001c0001t0001g0263a0001c0001t0001g0264 | 2 | HG02647.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1425-283G>A | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 14/14 | chr1 | 93136387 | ||||||
chr1:93136398
|
G | C | 44 | a0001c0001t0003g0018a0001c0001t0003g0019a0001c0001t0003g0021others(41): Show | 49 | HG00408.hp1 HG00423.hp1 HG01074.hp2 others(46): Show |
intron_variant | MODIFIER | c.1425-272G>C | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 14/14 | chr1 | 93136398 | ||||||
chr1:93136504
|
C | T | 4 | a0001c0001t0006g0238a0001c0001t0006g0239a0001c0001t0006g0240others(1): Show | 4 | HG01109.hp1 HG01884.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1425-166C>T | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 14/14 | chr1 | 93136504 | ||||||
chr1:93136637
|
C | T | 233 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(230): Show | 253 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(250): Show |
intron_variant | MODIFIER | c.1425-33C>T | MTF2 | ENSG00000143033.18 | transcript | ENST00000370298.9 | protein_coding | 14/14 | chr1 | 93136637 |